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THE
AMERICAN
OURNAL OF Pharmacy.
PUBLISHED HY AUTHORITY OF THE
PHILADELPHIA COLLEGE OF PHARMACY.
EDITED BY
HENRY TRIMBLE.
PUBLISHING COMMITTEE FOR 1897.
HKNRV N. RITTKXHOUvSK, WALLACE PRoCTKR.
SAMUEL P. SADTLER. JOSEPH \V. ENGLAND,
AND THE EDITOR.
VOLUME 69.
PHn.ADIvLPHIA
1897.
LIBRARY OF THE
ONTARIO COLLEGE
OF
PHARMACY
EUCALYPTUS ROSTRATA, SCHLECHT. MURRAY RED GUM.
A, flower buds ; B, fruits ; C, part of leaf, magnified to show venation.
THE AMERICAN
JOURNAL OF PHARMACY
JANUARY, iSgj.
THE MURRAY RED GUM (EUCALYPTUS ROSTRATA,
SCHLECHT) AND ITS KINO.
By J. H. Maiden,
Government Botanist of New South Wales and Director of the Botanic
Gardens at Sydney.
Aboriginal Names. — By the aboriginals of the lower Murrum-
bidgee it used to go by the name of •' Biall," while to those of the
western interior it was known as •• Yarrah," a name which it shared
with some other trees. The specific name, rostrata (beaked), is in
allusion to the way in which the operculum is drawn out to a point
like a beak or snout, as shown in the figure.
Other Vernacular Names. — Iksides being known as •* Red Gum,"
it is the " Flooded Gum " of the interior of Western and South
Australia. In western New South Wales it is called" Creek Gum,"
as it is always found near watercourses. There are several trees
which grow under the name of " Red Gum " in these colonics. One
of them is the smooth-barked apple, Angophora lanceolata, which, in
New South Wales, is often called red gum, but most of the trees
known by that name are Eucalypts. The red gum of Western
Australia is Eucalyptus calophylla, while in the neighborhood of
St. Vincent's Gulf, South Australia, Eucalyptus odorata goes by that
name. In New South Wales two other valuable timbers also go
under the name of red gum, viz.: Eucalyptus tcrcticornis, a tree
bearing close affinity to rostrata, but it is essentially a forest timber,
in contradistinction to rostrata, which is a river timber. Then the
leather-jacket or gray gum, E. punctata, is also known as red gum
occasionally; but the red gum par excellence of these colonics is
Eucalyptus rostrata, and by way of distinction I have denoted it — on
account of its most celebrated 1< cality — Murray Red Gum.
2 Murray Red Giiin and Its Kino. {^"^-JZll^^m^'
Meaning of the Term Gum as Applied to Eucalyptus Trees. — We
have a very large number of species of the protean genus
Eucalyptus, and they differ very much amongst themselves in
(amongst other things) their barks. Some of them have rugged,
dense, hard barks, and are known as *• iron barks." Others have
very fibrous barks, which strip off in long pieces, and even sheets,
used for roofing in the country ; these are called '' stringy barks."
Others have woolly, matted barks, and are known as " box." All
these, and many others, belong to the rough-barked Eucalypts,
But others have smooth barks, smooth as a planed board, and go
by the name of '' gums " or '' gum trees." Now the rough-barked
species produce gum (kino) as abundantly, and often more so,
than the smooth-barked ones, but the stain of the gum is more
apparent on the latter, and that is why, I believe, the term
*' gum " has come to be exclusively applied, in common parlance, to
the smooth-barked forms.
Having distinguished these two great classes, the " gums " are
still further discriminated by means of various adjectives, some re-
ferring to color, e. g., '' white," referring to the color of the bark ;
''blue," referring to the tint of the bark or the glaucous appearance
of the leaves ; " red," referring to the color of the wood, and so on.
And, inasmuch as we have several red gums, I have proposed to
permanently define E. rostrata as •• Murray red gum," for the reason
already indicated. " Red gum " being thus the name of the tree,
"red-gum kino" becomes the name of its product, in spite of its
apparent tautology. It should strictly be written " red-gum kino"
— not " red gum-kino."
Hozv Red-Gum Kino Is Collected. — The manner in which the kino
is procured is as follows : The men employed in getting it look for
the trees from which the substance is or has recently been exuding,
and cut into the tree until they get beyond the gum-vein ; they then
insert a piece of tin (trough-shaped) into the cut or hole, and let the
kino run into a bucket or kerosene tin.^
^ Kerosene tins are rectangular in shape, and hold about 2 gallons ; in them
the kerosene (called paraffin oil in England) is imported from the United
States, and the kerosene, in these original packages, finds its way into the
remotest parts of the colonies. When the top is cut off and a wire handle fixed
across, we have a rough-and-ready pail, which is used in Australia for many
purposes of collection and storage, such as the case we have under considera-
tion now.
Am. Jour. Pharni
jiiSary.i'Sf.'"'} Aft^rraj Red Gum and Its Kino. 3
When the kino exudes it is of the consistency of molasses, and
has a sourish odor. In a few days it dries into a sohd mass, which
subsequently becomes quite friable. It is owing to this property
(shared by other kinos of my " turbid group ") that it cannot be
collected in an indurated condition by simple picking from the bark
of the trees, as can kinos belonging to my " ruby" and " gummy
groups," which do not become friable with age.
As much as 4 gallons have been procured from one tree, but this
is exceptional. On an average, not more than I quart per tree is
obtained, and from the majority of trees no appreciable quantity of
kino is obtained by tapping. Many are all but free from it.
The usual price paid on the Murray River at the present time,
for liquid kino (before induration) is /d. per pound, and a large
quantity could be forthcoming at that price, if a steady demand
were to set in for it. A good workingman can procure between
10 and 12 pounds per day of the liquid kino. It loses but little
weight in drying.
The kino of the red gum is perhaps the best known of all Euca-
lyptus kinos. The following notes of it were published by me in
the Frocccdinjrs of the Linnean Society of Nezv South Wales for Sep-
tember, 1891 :
It is a useful astrmgent, and it seems to be increasing in favor
with medical men in England, America and Australia.
The official kino (Pterocarpus) contains, I believe, no substance
which is not contained in this and some allied kinos, for which they
appear to be a perfect substitute. See Pharm. Jour. [3] 20, 221,
321.
The kino of E. rostrata will be found mentioned in all modern
works on Materia Medica. In Martindale and Westcott's Extra
PharmacopcEia, for instance, we have the following :
" E. rostrata and E. corymbosa, and probably other species
imported from Australia. It is semi-translucent and garnet-colored,
not so dark as, but resembling, kino in appearance, soluble in water,
tough, difficult to powder [not correct as applied to these two kinos.
— J. H. M.] ; it adheres to the teeth when chewed, is intensely astrin-
gent to the mucous membrane, useful in diarrhoea, relaxed throats,
and given with success to check the purging of mercurial pills."
But the following statements pertaining to the percentage of tannic
acid and the .solubility are somewhat misleading, since I have shown
4 Murray Red Gum and Its Kino. {^ januaryfmr'
the enormous variation in the properties of kinos caused by-
age :
"Of 100 parts, 90 are dissolved in cold water, the solution being
clear ; 27 parts of isinglass precipitate all the astringent matter." —
Squire's Companion to the B. P.
Dr. Wiesner says of a sample :
'* Easily soluble in water and alcohol ; solution neutral, free from
gum resin. Broken masses of zircon-red, sometimes light brown,
mixed with bits of bark."
Following are experiments on *' Red Gum " kino purchased in
Sydney, November 22, 1888, of Victorian origin: In lumps up to
the size of peas, though angular. Prevailing color, purplish-brown ;
is readily powdered between the fingers, forming an ochrey-brown
powder. The mass of kino has not the brilliant appearance of the
kinos of the ruby group, owing to this friability.
In cold water it dissolves fairly readily, and almost entirely to a
reddish-brown liquid.
Its composition (determined November, 1888) is:
Catechin and tannic acid 84*3
Ligneous matter, etc "3
Moisture 15*2
Ash -2
lOO'OO
Tannic acid determination (Lbwenthal), 4622 per cent.
A specimen of kino from the "■ Creek Gum," Tarella, Wilcannia,
August 23, 1887 (diameter, 1-2 feet; height, 30-40 feet), gave the
following results : it is only obtainable in rather small quantities
and in rather small pieces ; pale, as kinos go, very bright-looking,
and of a ruby color ; powders fairly readily, forming a powder of a
light-brown tint. It dissolves almost immediately to a pale brown-
ish or almost orange solution, leaving a sediment of a whitish-
salmon color with a few dark-colored particles, like those of E.
goniocalyx, only cleaner-looking.
Its composition, determined October, 1888, is:
Catechin and tannic acid 827
Ligneous matter, etc '6
Moisture 15-8
Ash -9
Tannic acid determination (Lbwenthal), 47746 per cent.
ICO' GO
^ jinua^irlT™} Murray Red Gum and Its Kino. 5
Since the above observations were made, H. G. Smith and the
writer^ have been re examinin^r Eucalyptus kinos. These researches
have been continued by Mr. H. G. Smith.- From these papers it will
be seen that certain kinos of the "Turbid" group contain new
orf;anic bodies, Eudesmin or Aromadendrin, or a mixture of both.
All the kinos of this group (of which E. rostrata is a member) are
at the present time being examined with the view to ascertain
whether they contain these new substances, and in what quantities.
In the first broad grouping of these kinos, Catechin was (from im-
perfect investigation) stated to be present.
Why Eucalyptus Rostrata Kitio is Usually Chosen for Medicinal
Purposes. — Because this species is very gregarious, it cannot, in the
districts in which it occurs, be mistaken for any other species, and
because it is a comparatively free yielder of kino. All these are
important practical considerations, apart from the properties of E.
rostrata kino itself. The discrimination of the various species of
Eucalyptus in a forest is so difficult that considerable botanical
knowledge would be required in the case of a kino collector who
might be set to the task of collecting kinos true to name. As a
matter of fact, such men are not available for the work of kino
collecting in a mixed Eucalyptus forest.
Eucalyptus Rostrata and Its Oil. — In passing, the following notes
may be useful :
The leaves of the red gum emit a pleasant odor when crushed in
the hand, but the P2ucalyptus oil they contain is not a regular article
of commerce, as it is not yielded in payable quantity. Mr. Hosisto
thus reports on it in the Trans. Roy. Soc. of Victoria, Vol. VI, 1 861-4:
*• Plants grown on high ground give an oil of a dark amber color,
possessing an agreeable aromatic flavor, and having the odor of
caraways. The yield from 100 pounds of the frcsh-gathcred leaves
was I ounce 6 drachms. The plants grown on low marshy soil
yielded an oil of a j)ale-}'ellow color, in appearance and smell simi-
lar to that yielded by E. odorata, the quantity being 9*3 drachms
to 100 pounds." Last year M. Mellon, of the Dunolly Scent Farm,
• A Contribution to the Chemistry of Au&traliau Myrtaceout Kinos. Ptoc.
Royal Society N. S. W^., 20, 30 (1895).
'On Aromadendrin or Aroniadendric .\cid from the Turbid Group of Euca-
lyptus Kinos. Proc. Royal Soc. JV. .V. !i\, »o, 135 (•896).
Murray Red Gum and Its Kino. {
Am. Jour. Pharm,
January, 1897.
Victoria, obtained no less than 7 ounces of oil per 100 pounds of
leaves.
In Mueller's edition of Wittstein's work we find the following :
" The essential oil is pale yellow to reddish amber in color ; it
smells and tastes like that of E. odorata. Its specific gravity is
0-918, and it boils at 137° to 181° C."
The celebrated essential oil firm of Schimmel & Co., of Leipzig,
Germany, have also examined this oil [vide \\\€\x Berichtiox October,
1 891). Their oil was prepared by M. E. Mojon, of Algiers, from
trees grown in that country. They determined the specific gravity
of their sample to be 0-924 at 15° C, and the optical activity +12^
58^ in a 100-millimetre tube. The oil has a powerful odor of valerianic
aldehyde, and is rich in cineol. E. rostrata and E. globulus appear
to be the only two eucalyptus oils known to contain valerianic alde-
hyde up to the present.
Quite recently, Mr. W. Percy Wilkinson, of Melbourne, has
made a valuable preliminary investigation of the Eucalyptus oils of
Victoria {Proc, Roy. Soc, Victoria, 1893, P- I95)- Amongst others,
he has examined three specimens of red gum oil, and following are
his results :
Sample.
Specific
Gravity.
Specific
Rotation.
Refractive
Index.
Specific
Refractive
Energy.
I
2
3
-9120
-9216
-9222
+ 87°
-f 2-2°
I -4604
I -4600
I -4607
•5072
•5014
•5018
None of them gave the phellandrene reaction.
Eucalyptus Rostrata. Where Found. — It is widely distributed in
Australia, usually on the banks of rivers, or on river-flats subject to
inundation, or in old water-courses. It becomes dwarfed in the in-
terior; but it attains its greatest development on the banks of the
Murray River, where, on the New South Wales side, there are mil-
lions of acres of land which are periodically flooded (hence the name,
" flooded gum," often applied to this species), and hence unsuited
to agriculture. On this land are countless millions of red gum trees,
the cutting of whose timber affords a large revenue to the New
Am. Jour. PbartD.
januar'y.S^8^':'"} Afurmj' Rcd Gum aud Its Kino. 7
South Wales Government. On this flooded land the propaj^ation of
the tree is largely unchecked, and so the production of timber —
and, indirectly, of kino — is practically unlimited.
The Murray River is a river nearly 2,000 miles long. It forms
the greater part of the boundary between the colonies of New South
Wales and Victoria. There is comparatively little red gum on the
Victorian side, but in New South Wales territory it is very abundant.
Beyond the Dividing Range, in New South Wales, the red gum
has a very wide range, being found on the banks of the Cudgegong,
Castlereagh, Darling, etc. It. is also sparingly found in the coast
country, except from the Victorian boundary to the Hega district.
In Victoria it is found on river-flats and open valleys in most parts
of the colony, and in South Australia it is likewise very extensively
distributed. It is also found in southwest Queensland.
The way in which the red gum (yarra) usually marks the course
of water was early observed by Sir Thomas Mitchell : " The yarra
grew here (Lachlan), as on the Darling, to a gigantic size, the
height sometimes exceeding 100 feet. The yarra is certainly a
pleasing object in various respects; its shining bark and lofty height
inform the traveller of a distant probability of water or. at least, of
the bed of a river or lake, and, being visible over all other trees, it
usually marks the course of the rivers so well that, in travelling
along the Darling and Lachlan, I could trace with ease the general
course of the river without approaching its banks until I wished to
encamp." (" Three ExpeditiQns,"*ii, 54.)
This useful tree has been introduced into several countries (chiefly
through the agency of Baron von Mueller), with varying success.
For particulars of most of the results, see Mueller's "Select Kxtra-
Tropical Plants " (Victorian Edition). For results in Assam, see
Kew Report {ox 1^79, p. 16; and for results in India see Kiw Re-
ports: 1876, p. 23; 1879, p. 16; 1881. p. 12. Vilmorin, of Paris,
has distributed a good deal of red gum in ICuropc. Some years ago
I received, from a correspondent at Oporto, in Portugal, flowers and
fruits raised from such seed, with the report that the SjKxics docs
well in that country. The red gum has been planted by a number
of people in California, and is favorably rept)rted upon by the local
forest conservator. For an account of its growth m that State,
reference may be made to the very interesting monograph on
" Eucalyptus," by Mr. Abbot Kinney, of Los Angeles.
8 Gelsemium. {"-^z^i^,^!^'
GELSEMIUM.
By L. E. Sayre,
Member of the Research Committee C, of the Committee of Revision of the
United States Pharmacopoeia.
RHIZOMES, ROOTS AND STEMS.
Some time ago my attention was called, by members of a class in
microscopy, to the varied structure of this drug. Fragments of
gelsemium root, handed to the different members of the class,
when sectioned and mounted, did not show the same characteristics.
This observation led me to examine samples of gelsemium root from
different sources, and this forced the conclusion that the gelsemium
of the market is composed not only of the rhizome and root, but
also of the stem in varying proportions. Furthermore, that the
description of the drug, supposing it to be composed of rhizome and
root — as is taken for granted by the Pharmacopoeia — is somewhat
ambiguous and misleading. n the present article a more accurate
description of the rhizome and root, and a method of distinguishing
both of these from the stem, is suggested.
I am inclined to think that the stem, present to some extent in the
commercial drug, is an adulterant. Reassuring myself on this
point, I sent a package of the commercial drug to Gerald McCarthy,
botanist of the North Carolina Agricultural Experiment Station,
asking him to report upon the same. In his response to my letter,
he states : " The specimens you submit represent the rhizome and
stem respectively, the latter is the specimen with the bast fibres in
the cortex. The stem was apparently used to adulterate the rhizome
in the original lot. So far as I know, the stem has no medicinal
value."
It is an interesting question whether the stem has any medicinal
virtue. An investigation has been commenced, by which it is hoped
that the relative value of the rhizome, root and stem may be deter-
mined.
Collectors in the South have been applied to for authentic speci-
mens. In the meantime the article of the market is being examined.
It may be of interest to state that Mr. McCarthy, in his letter, re-
marks : " The parts of the plant collected here for medicinal use are
roots, rhizomes, leaves and flowers."
The description given of gelsemium rhizome and root, in one para-
graph, by the U.S. P., 1890, reads asjollows : " Cylindrical, long, or
Am. Jour. Pharm.
Januarj'. 1897.
}
Geise
mitim.
cut in sections, mostly from 5 to 15 millimetres, and occasionally 3
centimetres thick, the roots much thinner, externally li«^ht yellowish
brown, with purplish-brown longitudinal lines ; tough ; fracture
splintery; bark thin, with silky bast fibres, closely adhering to the
Fig, I. — Cross- sections of Gelseinium sempervireus. A, stem ; /?, rhizome ;
C, root.
pale yellowish porous wood, which has fine medullary rays, and in
the rhizome a thin pith ; odor aromatic, heavy; taste bitter."
It will be noted in the above description that the only distinction
made between the root and rhizome is that the latter lias a thin
pith.
Professor Rothrock (Am. Jour. Phar., 1884, p. 130) calls atten-
tion to two structural characteristics of stems and roots, which, he
lO
Gelseinium.
Am. Jour. Pharua.
Januarj', 1897.
says, are peculiar and of positive value. " The first of these char-
acteristics," he says, '' is derived from the medullary rays. These
usually widen in a marked manner, going from centre to circumfer-
ence, being sometimes much more than twice as broad externally as
internally. The second characteristic is the tendency of the pith to
be penetrated by several plates of large, thin-walled cells, which
divide the pith more or less perfectly into four portions. This lat-
ter characteristic is always present and plainly enough marked to
serve as a means of diagnosis."
This, the author seems to indicate, is a characteristic of the stem
Otx
Fig. 2. — Gelsemium, Powder of rhizome. «, wood tissue ; b, cell from
medullary ray ; c, cork cells ; d, bast ; e, parenchyma of cortex.
and root. It is possible he may have meant by the stem the under-
ground stem or rhizome, for the stem is not official. In either case,
whether the stem or rhizome is intended, the statement is- inaccu-
rate and misleading, because it does not make distinction between
the stem (or rhizome) and root. The United States Dispensatory
quotes this description of Professor Rothrock, and does not clear up
the ambiguity and inaccuracy. None of the text-books make any
more definite and lucid description of the root and rhizome of this
plant.
From the growing plant and from the commercial drug numerous
sections have been made and examined microscopically. The ac-
Am. Jour. Pharm.
January, 1897.
}
GelseviiuiH.
I I
companying drawings may, perhaps, more clearly and more briefly
describe these three parts of the plant than any written description
can do.
In an examination of cross-sections of the stem, rhizome and root
of the gelsemium, we find the following microscopical characters
and difference of structure. In the stem (^Fig. /, A) are found com-
paratively large bundles of bast {b) near the wood, just outside the
cambium. In the rhizome (Fig. /, ^) the bast is arranged near the
corky layer, and in an interrupted ring, rather than in bundles. In
Fig. J.— Gelsemium. Powder of root, a, wood tissue ; b, pareuchynia of
cortex ; r, cork cells ; d, catnbium cells.
the root {Fig. /, C) the bast is entirely absent, but there are several
layers of cork. The following table shows the corresponding tissues
in the three plant parts :
stem.
^, Epidermis,
r, Collenchyma.
p, Parenchyma.
b. Bast.
s, Sieve tissue.
ca, Cambium.
w, Wood tissue,
r, Vascular tubes.
Pi, Pith,
w/, Medullary.
Rhizome.
Epidermis.
Collenchyma,
Parenchyma.
Bast.
Sieve tissue.
Cambium.
Woo<l tissue.
Vascular tul)es.
Pith.
Medullary.
Root
Parenchyma.
Sieve tissue.
Cambium.
Wood tissue.
Vascular tube*.
Fig. 4 shows a cro.ss-section of the pith in the rhizome; here the
division into four parts is shown. It seems that, as the rhizome
advances in age, the pith becomes less and less conspicuous, until
12 Gelsemium, {^^.^ri^sir-
in the larger stems and rhizomes it is almost absent, if not entirely
so. In this respect the stem and rhizome are much alike.
The description I have to suggest for gelsemium is as follows :
Rhizome cylindrical, long or cut in sections, mostly 5 to 15 millime-
tres, and occasionally 3 centimetres thick ; externally light yellow-
ish brown, with purplish brown longitudinal lines ; tough and
woody; fracture splintery; bark thin, with silky bast fibres near the
pale-yellowish porous wood, which has fine medullary rays, and a
small pith which, under the lens, is seen to be usually divided into
four segments.
The root is 2 to 10 millimetres thick; externally lighter than the
rhizome ; fracture brittle ; thick bark, closely adhering to the light
Fig. 4. — Gelsemium. Pith of rhizome.
yellowish wood ; odor of both rhizome and root aromatic ; taste
bitter.
POWDERED GELSEMIUM.
No. 60 Powder. — That the official drug is often adulterated with
portions of the stem is very evident, but whether intentionally or
carelessly I am unable to say. To distinguish the adulteration in
powdeied form has been the subject of considerable work, but with
very little attendant success. The root contains no bast, and hence
but a glance will indicate whether the powder be of the root or not.
However, the rhizome and stem both contain the bast and in almost
equal quantities, so this cannot be relied upon to distinguish be-
tween the two. It seems that neither has any characteristic cell
^jaiiCao'^l^^:"} Licorice Root. 13
structure that is not found in the other. The stem, when dried, is cov-
ered with a dark brown, nearly black, layer of cork, while the rhizome
is of a yellowish color. If the bark is in ordinarily coarse powder
and contains a considerable amount of the stem, the dark, almost
black, particles are quite noticeable ; but a fine powder, or a small
amount of adulteration would likely fail to show these characteris-
tics. The ordinary micro-chemical reagents produce the same effect
upon both stem and rhizome.
As before stated, the different parts — stem, rhizome and roots —
are being analyzed. When the analysis is completed the results
will be given.
University of Kansas.
THK COMMERCIAL SOURCES OF LICORICE ROOT.
By H. N. Rittenhouse.
While the commercial varieties of licorice root are well known
to importers of the article, the qualities, values and sources of sup-
ply are no so well known to the pharmacist as they should be, if
any importance is to be attached to accurately dispensing either the
root itself or its preparations.
Previous to the year 1870 the principal source from which the
United States obtained its supplies was Spain. Since then the con-
sumption in the United States has increased so much that the
Spanish root has been utterly inadequate to equal the demand.
Other countries have since then come into the market, and now fur-
nish the greater part of the market recjuirements. These countries
are Southern Russia, Asia Minor (chiefly the province of Anatolia)
and Syria, and about in the order above-named as to quantity,
Russia being the largest exporter and Syria the smallest. Licorice
root from any of the above named sources, when good and sound,
should be acceptable to the pharmacist for his uses, but it is not
always good and sound in a proper sense as found in commerce.
Spanish root is gathered so closely and skilfully sorted and
packed that much of it consists of fine, immature, fibrous roots,
which, while they may be called licorice root, arc pract«cally
worthless as such for the purposes for which licorice root is used,
and besides are 50 per cent, higher in price than the other varie-
ties; yet prejudice and perhaps ignorance on the part of some buy-
14 Licorice Root. {^Vmwy^'Js?:"-
ers still demand Spanish root and Spanish extract. The Spanish
root is sweeter and with less acridity than the other varieties, and
if Spanish root was what it once was in mature condition when
found in the market, the preference above noted might be justified;
but, as it actually is, this prejudice is based on its ancient reputa-
tion, and is now unwarranted. The close digging and limited and
practically exhausted fields of Spain are the causes of this.
Turning now to Russia, with its new and almost unlimited fields,
as yet but lightly worked (exports from Russia only began in 1887),
we find a mature root, rich in glycyrrhizin and extractive, much
better suited for commercial purposes because better and cheaper
than Spanish root, the sole objection to it being in the taste, which,
in addition to the usual sweetness of Spanish root, has a slight
acridity, which is really not objectionable, but gives the impression
of being " stronger."
Anatolian root ranks between Spanish and Russian in the quality
of sweetness (or absence of bitterness). In commerce no attention is
paid to the botanical varieties of licorice root, and from the root
alone it is quite impossible to determine its true botanical origin,
the usual designations being from the countries of growth, as Span-
ish, Russian, Anatolian, etc. ; though all varieties, except Spanish,
are often classified as "■ Greek root," it must be remembered, too,
that all licorice root of commerce is wild root, none being cul-
tivated.
The variety in the market known as '' selected " licorice root,
and put up in small bundles, was formerly selected from Spanish
sources, but as demand increased and supply diminished, other vari-
eties having the requisite straightness and thickness were mixed
with the Spanish, until now " selected root " consists of root from
any and all sources if of the proper quality — straight, sound — and
of the requisite length and thickness.
Peeled Russian root may now be prepared in Russia. I know of
no reason why it should not be, but Syria formerly prepared
" peeled " root for shipment to Europe, some of which found its
way into the market as " peeled Russian." Any variety might be
peeled as well as Russian and be just as good. It would be a satis-
faction, however, to have things called by their correct names and
pay for them accordingly. Peeled "Russian root" has always
commanded a good price, doubtless partly on account of the cost of
^ januaryff^"'} Secoml Pan-Americau Medical Congress. i 5
the labor of peeling and careful drying ; but if so much esteemed
when peeled, why is it not just as much esteemed unpeeled as Span-
ish or any other variety unpeeled ? Besides being much cheaper
and richer in glycyrrhizin and extractive, for all practical purposes it
is the best. Interest always attaches to a knowledge of the true
sources and varieties of drugs, and is frequently a source of profit as
well to the pharmacist.
Batoum is the principal port of export for the Russian root, which
is gathered along the Trans-Caucasian Railroad, running from Ba-
toum on the Black Sea to Baku on the Caspian Sea. The port of ex-
port for Anatolia is Smyrna, while the Spanish root finds its way
into commerce through the principal seaports of Spain.
SECOND PAN-AMERICAN MEDICAL CONGRESS.
By Joseph P. Remington.
The second Pan-American Medical Congress met in the city of
Mexico during the week beginning November 16, 1896. The first
Congress assembled in the city of Washington, in 1893. The pur-
pose of these triennial gatherings is mainly to foster the advance-
ment of medical and pharmaceutical science, and to establish closer
relations between members of-the medical profession and correlative
branches. The large number of delegates in attendance upon the
first Congress surprised the friends of the movement, and, although
the number in attendance upon the second Congress was not as
large, it must be gratifying to the International Executive Com-
mittee to know that over five hundred members testified to their
interest by their presence, many of them contributing papers upon
some subject connected with the work of the Congress. As is cus-
tomary in such bodies, the detailed work was referred to sections or
commissions, the latter having been organized for the purpose of
carrying on continuou.sly important work and reporting at the trien-
nial meetings of the Congress. Two commissions have been organ-
ized, which are of special interest to pharmacists, the Commission on
Pan-American Pharmacopoeia and the Commission on South Ameri-
can Flora.*
' The Commission on Pan-American PharmacoiKL-ia is organizc<l, with Prof.
Jos. P. Remington as Chairman ; that on i^oulh American Plora, Prof. H. H.
Rusby, Chairman.
1 6 Second Pan-American Medical Congress. {'^ January fisK™'
The sections embraced the following: General Medicine, Pathology
and Therapeutics, 89 papers ; General Surgery, 45 papers; Military
and Naval Surgery, 4 papers ; Obstetrics, Gynaecology and Abdom-
inal Surgery, 41 papers; Anatomy and Physiology, 7 papers;
Diseases of Children, 16 papers ; Ophthalmology, 15 papers ; Laryn-
gology, Rhinology and Otology, 3 papers ; Dermatology and Syph-
ilography, 3 papers ; General Hygiene, Demography, Marine
Hygiene and Quarantine, 25 papers; Diseases of the Mind and
Nervous System and Medical Jurisprudence, 17 papers; Dentistry,
6 papers ; Medical Pedagogics, 7 papers. In addition to these, a
large number of volunteer papers were presented. The sections
met in different localities, and the discussions which took place
added largely to the interest of the reading.
The general sessions of the Congress were held in the National
Theatre and Chamber of Deputies. A marked feature of the work
of the Congress was the extraordinary interest manifested by Presi-
dent Diaz, of the Republic, the members of his Cabinet, and, in
fact, all of the officials of the Government. Their attentions were
not only directed to extending hospitality, but public and private
museums and collections were freely accessible, official statistics
were furnished, and every possible facility .afforded for acquiring in-
formation upon any subject. The surgeons were given every oppor-
tunity to visit hospitals and chemists, botanists, mineralogists, arch-
aeologists, paleontologists, geologists and students in any of the re-
lated sciences were furnished with special guides to the valuable
collections. The public and private social entertainments were on a
scale of magnificence rarely approached. The subjects of permanent
interest to pharmacists centre in the permanent commissions.
These will be charged with the duty of investigating the Western
Continent, especially the unknown South American plants, and the
formulation of a plan for a Pan-American Pharmacopoeia. This
will not supersede the special Pharmacopaeias of each country, but
will collect the valuable features of each and endeavor to unify the
strength of the powerful preparations, so that danger to life may be
reduced to a minimum.
The richest collection of palms in the world is said to be in the Botanic
Garden at Buitenzorg, Java. It contains 300 species that are determined, ico-
probably new and still undescribed, and 100 varieties of known species. —
Garden and Forest.
^jaiSJry?'/^'""'} Commercial Ferruginous Pills. \j
COMMERCIAL FERRUGINOUS PILLS— BLAUD'S
FORMULA.
By William B. Thompson.
Manufacturers honestly vie with one another in an endeavor to
produce this pill in an exact condition, and in maintaining its compo-
sition in a state that shall, in all respects, fulfil its therapeutic pur-
pose or intention. Every price schedule issued lists this pill, and
the quantities prescribed, sold and used exceed, perhaps, that of any
other single kind except quinine.
Physicians generally believe that a constitutional effect of the
iron is more promptly assured by a continued use of the Blaud
composition than by that of any other form — not excepting liquid —
and satisfactory results must assuredly follow where the use and
popularity continue to so great an extent. Yet, if we start with
the theoretical principle, and also consider the chemical action
which occurs in the formation of this pill mass, that action being
instantaneous, when an alkaline carbonate is brought into contact
with the ferrous sulphate, and then reflect upon the sensitive and
chemically unstable character of the ferrous salt formed, with its
inevitable tendency towards a ferrous oxide, and finally ferric
oxide, we can scarcely understand in what manner art assumes
to control or retard a chemical law, postponing an action which
is ultimately, if not speedil}-, as sure as that which governs
the planetary systems. Yet it is attempted ; pervious and impervi-
ous coatings are used, as means to protect the iron-salt from the
oxidizing influence of air and moisture. A physical examination,
and the application of a color-test to these various products of the
manufactories, reveal so many conditions and appearances as to
bewilder the judgment when claims to chemical accuracy are made.
The result of the first contact of the iron and the alkali in the
presence of moisture is to produce a compound having a brownish
green color, that of a more positive green hue being accepted as
a more true product of this reaction. Then if this is accepted as
the proper color indication of the true state or condition in which
this ferrous salt should be presented to the human economy as a
remedy, what shall we say in regard to those variable conditions as
to color which the numerous commercial pills present ? Shall we
adopt all these as affording the proper result of a definite chemical
l8 Adulterated Japan Wax. {^TanSary.'isQ^."^-
reaction which the originator of the Blaud pill designed ? Or shall
we admit that varying states of oxidation do not seriously militate
against the therapeutical efficacy of this iron salt, especially when
it has merged into the ferric state. In the numerous essays which
have appeared upon the subject of Blaud's pills are many finely
wrought theories in regard to the action of the normal fluids of the
stomach, most notably the supposed free hydrochloric acid, which
is fancifully conceived to be in waiting in that wondrous receptacle,
ready to claim first seizure upon any congenial substance which
may be ingested — with a predilection for a ferrous salt of iron — and
that an insignificant amount of ferric oxide, now and then, will be
but a small obstacle to the action of this solvent acid.
It would appear to be more reasonable to cease indulging in any
more theories as to the precise behavior of the intestinal processes
towards foreign substances, particularly medicines, or to speculate
upon a probably uniform action regulating animal chemistry. But
rather see to it that the state of combination is exactly such as will
meet the indications suggesting its use ; and that if prepared in
advance of requirement, how much of chemical change or alteration
can occur, and yet demonstrate it a Blaud pill, or what is its precise
character as commonly found in commerce, and wherein does it
differ from that of extemporaneous preparation ?
This paper is presented here for the purpose of eliciting dis-
cussion. Whilst much has been written, the assertions are chiefly
on one side only of the question. Now let us have the other side.
Philadelphia, November 30, 1896.
ADULTERATED JAPAN WAX.
By Chari^ks H. I/AWai.!..
The analytical chemist, whose duty it is to examine the various
commercial products sold by a large wholesale house, encounters
many instances where samples are offered for examination before
purchasing which are inferior in some respects to the official stand-
ard required for the substance, or which contain some unmistak-
able ingredient foreign to their nature.
It frequently occurs that the description of a substance is capable
of several different interpretations, or the requirements are faulty,
^jan^Tyff^."^-} Adulterated J apau Wax. 19
so that the manufacturer or dealer is forced into accepting a sub-
stance which he beUeves to be inferior, but the impurity of which
he cannot conclusively prove.
The watchful care necessarily exercised in a large establishment,
where a high standard is rigidly maintained for all goods purchased,
is a distinct advantage to the retail dealer, and, indirectly, to the
consumer. Only those who are actively engaged in this class of
work, realize the extent to which the nefarious practice of wilful
adulteration is carried on.
Adulterations, according to a standard authority upon definitions,
may be of three kinds:
( i) Adulteration or admixture to suit the public taste or desire in
some respect.
(2) Unintentional admixture of foreign substances, due to faulty
or careless methods of manufacture.
(3) Wilful adulteration for the sake of pecuniary profit.
Adulterators of the latter class are especially to be feared, as
they strive to imitate the genuine product in every respect in order
to obtain the full price for an inferior product.
When a fraud of this kind is detected by a prospective purchaser,
he promptly rejects the goods and usually refuses to purchase further
supplies from the same source. The manufacturer of the fraudulent
goods offers them, in turn, to various other purchasers of large
quantities, until he succeeds in finding one who bu\s without
examining the quality of his purchase ; thus, in almost every case,
the goods eventually reach the consumer, who suffers the greatest
loss.
The extent to which the Japan wax of commerce is adulterated,
at the present time, has never before been equalled, in the case of
a single commercial article, according to the cxjK'rience of the
writer or that of the house with which he is connected.
F*ifty-nine cases of Japan wax, containing from 205 to 225
pounds each, were examined ; twenty-five of these were found to
be adulterated with starchy material to the extent of from 20 to
25 per cent. This means that, in the Japan wax purchased by one
house, about 1,200 pounds of starch were paid for at the price
of Japan wax, which is about three times as great.
Japan wa.x is a vegetable product imported from Japan, where
it is prepared from the berries of several s|>ecies «)f AV/z/i. The use of
20 Adulterated Japan Wax. {^ January fSS"""
this substance has largely increased during the past few years, as
(owing to its low price) it replaces beeswax in many industries.
As imported, it is usually in the form of rectangular blocks or
cakes, weighing several pounds each ; it possesses a yellowish-white
color (becoming darker after age and exposure) and a somewhat
rancid odor. The characteristics, taken from recent authorities, are
as follows: Specific gravity, about 0975 to 0-980; melting point,
about 54° C; saponification number, about 222.
The fraud was detected in the latter part of October, and, since
that time, besides the number of cases enumerated, several samples
have been offered for purchase, identical in the character and extent
of the adulteration ; thus showing that the quantity in the market
is by no means confined to the amount named.
In every case the wax was purchased from agents or brokers in
this country, direct importations, up to the present time, being free
from admixture. The quotation : " For ways that are dark and for
tricks that are vain," can also be applied to individuals of Caucasian
descent.
The appearance of the sophisticated product differed slightly from
that of the genuine wax. The specific gravity was slightly higher,
and a difference was noticed in this respect when cakes of each were
compared ; the adulterated wax was, in most instances, free from the
peculiar network of minute cracks which usually cover the surface
of a cake of pure Japan wax. Upon close examination of a freshly
fractured cake, a variation or gradation in its internal structure was
observed ; this was due to the settling out of the starch while the
wax cooled. The quickest and most effective method found for dis-
tinguishing between a pure and an impure wax is as follows : A
cake is fractured and the freshly exposed surface is scraped slightly
with a knife ; upon the application of several drops of iodine-test
solution the adulterated article turns darker, becoming deep bluish
black after fifteen minutes' time. The pure wax shows no alteration
whatever, nor any coloration, excepting that which is produced by
the iodine solution alone.
Samples for the determination of the constants were obtained by
taking sections squarely across the cake, as the presence of different
proportions of starch in the upper and lower portions of a cake
would produce varying results were the samples taken otherwise.
The averages of the constants obtained from four samples are as
^janJ^.^sS^.'"} Petrolatum vs. Vaseline. 21
follows: specific gravity, 1-0653; melting point, 52^ C; saponifica-
tion number, 173-28. From pure samples examined at the same
time, the following results were obtained: specific gravity, 0-980 ;
melting point, 54° C; saponification number, 22098. The amount
of foreign matter indicated by the lowering of the saponification
number was found upon calculation to be 21-24 per cent. The
starch was estimated directly by treating a weighed sample of the
wax in a flask with chloroform, which dissolves the wax, but does
not take up the starch ; the solution was filtered, the residue upon
the filter was washed well with ether, dried at lOO*^ C. and weighed ;
the percentage obtained by this method of procedure was 23-42,
corresponding favorably with the amount indicated by calculation
from the saponification number.
A microscopical examination was made of the starch, which
showed a lack of uniformity existing in the material used in dif-
ferent cases. In one instance it was unmistakably identified as corn
starch, but in others it was difficult to decide upon the identity of
the starch.
The consumers and handlers of this article will observe that they
are likely to have offered to them a product which is dear at a price
even considerably below the market quotation ; and, as the sophist-
ication is so easily detected, it becomes an important duty to search
out and reject every case of this fraudulent material, in order to
make it impossible for the originators of the compound to find a
market for their product.
305 Cherry Street, Philadelphia.
PETROLATUM VS. VASKLINK.
By Louis Emanuel.
In the advertising pages of the New York Medical Times the
manufacturers of vaseline make the fallowing unjust attack on
petrolatum :
TO THK MEDICAL PROFESSION OF TH8 UNITED STATES.
We consider it our duty to in fonn you that when you presents petrolatum
for a patient (in accordance with the I'harmacop<i'ia) and have the prescription
filled at the nearest druj^ store, you arc much more likely to injure than to
benefit your patient and may do him serious harm. The committee in char^c-
of the last Pharmacopoeia declined to enter therein the word "Vaseline,"
because it was our trade-mark, and we would not a>{ree to »urrcn<!er it, and in
22 Petrolatum vs. Vaseline. {^ januaJyfissr"
place thereof invented and adopted the word " Petrolatum," which was intended
to represent a substance identical to our vaseline. This action has encouraged
the manufacture of worthless imitations of our product, which are sold to the
druggists, the vast majority of whom neither tnow nor care anything about
their quality, and the result is a confusion of ideas amongst physicians and
failure of benefit to the patient. Now it is about time that you should clearly
understand :
(i) That "petrolatum" is not "vaseline," and that the formula given in
the Pharmacopoeia does not and will not make vaseline.
(2) That petrolatum has come to mean a worthless and often noxious petro-
leum product, varying in quality from axle-grease up.
(3) That vaseline is not only useful as a vehicle (as many physicians think),
but that it has extraordinary value as a remedy both externally and internally,
which petrolatum has not.
These reasons ought to be conclusive, to say nothing of the fairness which
should prompt honorable men to recognize those who give time, brains and
money to the benefit of the world, rather than to those who live by appropri-
ating to themselves the creations of others.
It would seem at first sight that the patentee has some rights to
an unlimited monopoly, which the advertisers claim in recompense
for the brains and money which has been largely devoted to the
benefit of mankind. It appears, however, that no mortal born of
woman has yet been endowed with talents sufficient to enable him
to render mankind any service whatsoever without having himself
first profited by the labor and brains of others. For this reason
patents have only a limited existence. The wisdom of this limited
monopoly is clearly demonstrated when we consider that the
patentee of the process for the purification of the crude residue of
petroleum distillation was not the originator of the use of animal
charcoal as a deodorizer and decolorizer, and, in fact, was not the first
person to apply it for this particular purpose; for Fliickiger's Fhar-
maceutische Chemie tells us that "in 1847 C. B. Mansfield, Cam-
bridge, England, patented a process for decolorizing or deodorizing
petroleum sediment by means of animal charcoal; in 1865-66 R.
A. Cheseborough, of New York, U. S. A., patented a process for
the purpose by the use of hot animal charcoal, and in 1872 he
patented the fantastic name of vaseline."
EVOLUTION OF VASELINE.
Patent No. 49,502, dated August 22, 1865, to R. A. Chesebor-
ough, for the use of bone-black for purifying petroleum or coal oils
by filtration.
""janSao-.^^T"} PctroUitum VS. VascliHc. 23
Patent No. 56,179, dated July 10, 1S66, to same, for heating
bone-black by dry steam or otherwise, previous to using the same
for filtering hydrocarbon oils.
Patent No. 127,568, dated June 4, 1872, to same, for the name
vaseline.
In the latter, the claim made by the patentee is as follows :
I have invented -a new and useful product from petroleum, which I have
named Vaseline, and I do hereby declare that the following is a full, clear and
exact description thereof, which will enable those skilled in the art to make
and use the same.
The substance from which vaseline is made is the residuum of petroleum le t
in the still after the greater part of the petroleum has been distilled off. Vas-
eline is the product of the filtration of the said residuum through bone-black,
and varies in color as it comes from the filter. First it is pure white at the be-
ginning of the operation, soon changing to a light straw, and then a deep
claret at the close of the operation.
Vaseline is a thick, oily, pasty substance, is semi-solid in appearance, unob-
jectionable in odor, becomes liquid at temperature varying from 85' to 110° V.
It will not saponify, does not crystallize, and does not contain paraffine.
Vaseline is especially useful in currying, stuffing and oiling all kinds of
leather. It is also a good lubricator, and may be used to great advantage on
all kinds of machinery. It is also an excellent substance for glycerine-cream
for chapped hands.
When we compare the above with the description of petrolatum
of the U. S. P., we must come to the conclusion that the pharma-
copccial committee is grossly misrepresented, and that pharmacy is
unjustly charged with piracy.
The Pharmacopoeia says of petrolatum ;
A mixture of hydrocarbons, chiefly of the marsh-gas series, otuained by dis-
tilling off the lighter and more volatile portions from petroleum, and purifying
the residue when it has the desired melting point. A fat-like mass of about the
consistency of an ointinL*nt, varying from white to yellowish, or yellow, more
or less fluorescent when yellow, especially after being melted, transparent in
thin layers, completely amorphous, and without olor and taste, or gi^nng off,
when heated, a faint odor of p>etroleum.
.\\\ unusually large fasciatc<l stem of meadow thistle (Cnicus alliftsimu.s.
Willd.) was sent to the museum of Purdue University a short lime ago from
northern Indiana. When dry.it measured 12 inches broad at the top and .;
inches at the base. The thickness of this greatly flattened stem was normal,
that is, less than one-fourth inch. It was covered evenly with normal Icavea,
and bore a score or more of immature flower beads sessile along the upper
edge. It 8too<l 3 feet high. The interest in it lies in *' . / .
wedge form, as fasciated stems art- usuallv irrreularly <K
Gazette, Novcml)er, 1896.
24 Modern Surgical Dressings. { ^TanSaryfS" "'
MODERN SURGICAL DRESSINGS.
By F. B. Kii^mer.
The surgical dressings in use at the present time by such practi-
tioners as keep pace with the advancement of the surgical art are
the products of the practical application of scientific knowledge.
They are the outcome of the modifications and amplification of pro-
cedures that have been brought about in the evolution of surgical
science.
Dr. Wm. Pepper states that " medicine and surgery have made
more progress in the last twenty years than in the twenty centuries
preceding." This statement may also be applied to the surgical
dressing.
In the dawn of the present era of surgery, the teachings of Lister
demanded that the dressings to be applied to a wound should be
saturated with chemicals capable of killing germs " within the
wound or coming from without." During this epoch antiseptics
were empirically applied. A dressing that promised sure death to
the microbe was in demand. In those days cloth was plastered
with masses of pitch, paraffin fat and carbolic acid. The products
were unclean — sticky, irritating and non-absorptive — directly the
opposite to those in use at the present time. Crude as was this
beginning, it contained the '' living spark of truth that illuminated
the mysterious darkness which for centuries hovered over wound
infection." It brought blessings that " have soothed and removed
untold suffering and misery — have saved millions of lives. For this
gift to surgery we are indebted to Sir Joseph Lister." — Gerster.
During the decades that have followed the time of which we
speak, the forward progress of the principles of antisepsis has been
continuous.
The accurate scientific observations of bacteriology has determined
the value of antiseptic substances, brought a knowledge of the na-
ture of bacteria, their habits, their life, and shown their influence in
the causation of wound infection. Such knowledge has given to
the surgeon newer and better weapons than those first used in the
combat against wound infection. The surgical dressing has always
been to the front in the revolution and evolution of surgery. Caus-
tic applications were early substituted for those which were mild,
yet more pDtent. Many microbe-killers were found to be man-
^ January^'.'"-} Modcm SuTgical Drcssiugs. 2 5
killers ; others were shown to be valueless. Power to absorb wound
secretion and exclude infection was made an essential requirement
for wound-dressing material.
Prevention became both the watchword and the keystone of sur-
gical technique. What is termed by Gerster " the conscientious
practice of thorough-going cleanliness," was found possible of attain-
ment by the use of antiseptics — "angels of cleanliness." Chemical
sterilization has been combined with mechanical cleansing. Natural
agents, as well as those instituted by the operator, have been called
to the aid of the surgeon. In this transition, antisepsis has not
been abandoned, but has developed into its higher form — asepsis.
The antiseptic dressing has not been discarded, but has become
aseptic. The terms antisepsis — asepsis, are not antagonistic ; the
one is not the antithesis of the other. •' Asepsis is an exalted
degree of cleanliness."
It is reached by the surgeon through the aid of antiseptics. The
antiseptic agents employed to produce the condition of asepsis may
be physical — heat, chemical — carbolic acid, etc., mechanical — wash-
ing. These ma)' be supplemented by measures which exclude all
bacteria. The aim sought is a condition of freedom of septic
material or micro-organisms — asepsis.
The Fundamental Law. — In the transition of surgical practice,
which we have noted, the great guiding principle first recognized by
Lister has been strengthened, viz.: " that the presence of certain
kinds of bacteria is an essential condition of wound infection."
From this has been evolved the fundamental law that all materials
which are to come in contact with the wound must be free from
pathogenic organisms. To i)rcpare a dressing which shall lulhl the
requirements of this law would, at first glance, seem to be a simple
undertaking. We find, however, that the task is not so easy of
accomplishment when we note that over 150 species of bacteria are
classed as pathogenic (6 pyogenic) ; in addition to this we have
nearly 3CX) species of organisms classed as non-pathogenic for lack
of information as to their disease producing power.'
' Bucbn^r has shown that many of the common saprophytes classed as non-
patliogenic, when injected under the skin, cause local abscess. I have recently
witnessed serious results follow nn < cntal inoculation of a clean wound
with mould spores supposed to he li
26 Modern Surgical Dressings. {'^'^kl^.y^ml^'
These bacteria are widely distributed. *
** There is no well-defined dividing line between pathogenic and
non-pathogenic bacteria." — Sternberg.
It would be impossible in the manipulation of dressing material
to separate or remove harmless bacteria from those which may be
virulent. Therefore, in its practical application the fulfillment of
the law demands that surgical dressings shall be free from all forms
of bacteria.
All antiseptic agents do not possess the power to destroy or kill
organisms. Therefore, dressings impregnated with antiseptics will
not, of necessity, meet the demand. Hence, in the preparation
of surgical dressings, the law must be construed to mean that, what-
ever may be the material and whatever may be the methods by
which it may be prepared, in order to meet the requirements of
surgery, the fundamental principle governing its production must
provide that it shall be free from all micro-organisms.
The Infection of Dressings. — The materials which enter into sur-
gical dressings, such as absorbent cotton, gauze, wool, are those
which, in themselves, reach after, absorb and hold bacterial life.
Every person and every object with which the dressing may come
in contact in the course of its preparation, are liable to transfer to it
infection. Infection through air is a possible factor.
Micro-organisms are readily disseminated through the air by the
medium of dust. The air of a crowded room is always laden with
bacterial life. In hospitals, the air is infected through the dis-
charges of patients. The air of a physician's office cannot be kept
free from infected dust. The dust on the drug-store counters, tables
and shelves will always furnish a luxuriant bacterial garden.
Wherever people move about, they must, of necessity, transfer soil
and create dust. If they move from infected centres, as do the
inmates and attendants at hospitals, the visitors to the doctor's
office or the patrons of a drug store, they spread infected dust.
Dressings may also become infected through the water used in
their preparation. The water used upon the dressings should
always be that which is boiling or which has been thoroughly boiled.
A greater source of infection arises from contact with the person
who handles the dressing in the course of its preparation. Here
the clothing of the operator is a possible germ carrier ; his body is
swarming with bacteria numerous in species, in uncountable num-
^Jan'oT/y.^s^T'} Modcru Surgical Dressings, 27
bers. Skin, hair and mucous membranes, even of persons who are
healthy and of cleanly habits, furnish to bacteria a natural home for
growth and multiplication.
In catarrhal conditions, skin disease, or wherever there is an
increase of secretions, the bacteria of the body increase both in kind
and in number. These sources of infection require more than ordi-
nary attention.
Sterilization of the entire surface of the body is impossible. Yet
we are confronted with the fact that the skin secretions, perspira-
tion, dandruff from the hair, all mucous secretions, are a fruitful
source of infectious particles, fatal to asepsis if by any chance they
should be transferred to the dressing. To even touch an aseptic
dressing with hands not disinfected, to touch with prepared hands
the eyes, nose, mouth or clothing, and then touch a dressing, would
mean that infection would surely follow. Such a procedure would
be ap unpardonable violation of surgical cleanliness, a crime against
asepsis. We must further take into account that the objects within
the room where dressings may be prepared, including the air, the
walls, furniture, floors, the tables upon which the dressings are laid
every piece of apparatus, every object of any nature that may come
in contact with the dressing, may be the means of transference of
germ life. If such objects happen to be of the nature of organic
material or those which hold moisture, the more rcadil)- do they
become carriers of infection.
The maker of surgical dressings must have in mind, therefore,
the materials of which the dressings are composed, that they are in
their nature absorptive of infectious particles, that all objects con-
nected with, all surrounding conditions, are sources through which
infection may be carried to dressings during their handling and
manipulation.
The Disinfection of Dressings. — Whatever the term disinfection
has been made to mean elsewhere, when applied to surgical dress-
ings it can only mean one thing — destruction of all micro-organisms
in or upon the material. This process presents many var>'ing prob-
lems. Hacteria show widely varying powers of resistance. Agents
which destroy growing forms will not affect the vitality of their
spores. The conditions of life and environment are all factors which
must be taken into account in the disinfection of dressings. Thus,
utensils and objects with smooth surfaces are readily di-iinfectcd.
28 Modern Surgical Dressings. { ^Tanuao .""isor*
because any bacteria present will be found upon their outer surface ;
but when bacteria are enclosed in a rock-like mass, as they are in
dried dust particles, where we find them surrounded by an almost
impenetrable fortress, in dried pus, sweat, in dried secretions or
flesh tissue, these organisms are protected by a varnish-like coating.
Bacteria, within the fibre of cotton or wool, are enclosed within a
cellulose structure. Therefore, in the disinfection of cotton, wool,
silk, sponge and catgut, we find that there is presented a varying
problem with each material. Chemical reaction is also a factor in
disinfection that has been long overlooked. In the disinfection of
dressings the nature of the materials and their behavior toward the
disinfecting agent must be taken into account. Thus cotton may
be disinfected in a solution of soda, but wool thus treated would be
destroyed.
Wool may be disinfected in an acid solution, which, in turn,
would destroy cotton. Catgut is affected by most chemicals ; it is
destroyed by moisture. Sponge tissue is affected by many chem-
icals ; it is destroyed by moist heat. Oily substances are impene-
trable by watery solutions.
The sole universal disinfectant is fire. It destroys the infection
and the infected material. It is applicable to the disinfection of
asbestos dressings, which have recently been recommended for sur-
gical purposes. There is no one method or agent which, under all
circumstances, will meet all conditions. Generally, more than one
agent and several methods of procedure must be used together or
in succession.
The writer has made a long series of investigations, having in
view the possibility of disinfecting dressings with agents that would
have no reaction with the material composing the dressing, that
could be readily removed from the dressing, or, when allowed to re-
main [within the dressing material, would have no effect upon
wound tissue. In these experiments, such agents as electricity,
gases, vapors, friction and pressure were employed.
The general method pursued was to infect fibres with a nutrient
fluid containing bacteria, to then subject the infected fibres to the
action of the disinfecting agent. The results may be briefly sum-
marized.
Electricity was not effective upon the organisms, except when
electrolysis took place, as was the case when water or a solution
^'j^nu^f'/Sr-} Modern Surgical Dressings. 29
of salts was the medium used in the transmission of electrical
energy.
Oxygen gas when under pressure had a germicidal effect, espe-
cially so when the bacteria were in a moist state. Nascent oxygen
was found to be a powerful germicide. Ozone gave similar results,
as did oxygen. Carbon dioxide was found to be an inhibitant,
but not a germicide. The gaseous oxides of nitrogen, except
NjO were found to be powerful in their action upon bacteria, but
destructive to dressing material and productive of great irritation
upon inhalation. Sulphur dioxide was found to be germicidal in
the presence of moisture, but inapplicable to many classes of the
materials used in surgical dressings. Chlorine gas is a disinfectant,
especially in its reactions which takes place in the bleaching pro-
cess, namely, union with hydrogen, and consequent liberation of
oxygen.
The bleaching process, therefore, effectually destroys germ life.
Iodine and bromine are energetic agents in the presence of mois.
ture, but they react destructively with materials used in surgical
dressings. Formaldehyde vapors possess a high power as a germi.
cide. The vapors are highly irritating and destructive to flesh
tissue. They are, however, applicable in the disinfection of some
classes of material used in dressings, and are utilized in the pro-
cesses hereinafter outlined.
During the mechanical process of carding cotton and other
fibres, the fibres are subjected to prolonged friction, with conse-
quent heat and electrical action. The results upon infected fibre
passed through the process were interesting, and the process was
found to be one of sterilization.
Experiments numbering many hundreds of series were made to
ascertain the value of pressure as a sterilizing agent upon dress-
ing materials. The results show that infected fibres may be steril-
ized by a pressure of 50 to 100 tons to the square inch. This pro-
cess has been utilized in the sterilization of certain forms of surgi-
cal dressings.
With the discovery of a new species of bacteria tlicre is said to
be a new chemical born for its destruction.
I^ut in the present day practice of surgery, only in a few
instances, may we use chemical germicides for the disinfection of
dressings and allow the chemical to remain in the finished pro-
30 Modern Surgical Dressings. { ^ January ffsgT."'-
duct. The active chemical disinfectants are for the most part
destructive to dressing fabrics as well as irritating to flesh tissue.
Out of the many disinfectants lauded in days past for the impregna-
tion of surgical dressings, but few remain. It has been found
that dressings, even when impregnated with antiseptics, may still
harbor germ life. In the presence of dry iodoform, dry corrosive
sublimate, boric acid, germs will retain their vitality for a great
length of time.
Though seemingly a contradiction of terms, it is, nevertheless, a
truth born of experience to state that antiseptic dressings may be
the means of conveying infection to a wound. Hence, the require-
ment that antiseptic dressings shall be free from micro-organisms.
In the list of agents applicable to the disinfection of dressing
materials, heat ranks first in germ-destroying power. Heated air is
precluded for use with cotton and some of the other substances used,
for the reason that the temperature required for efficiency is de-
structive to the material. Heated air is quite inferior in disinfecting
power to boiling water and steam. Boiling water almost instantly
destroys most forms of germ-life ; resistant ^orms succumb to its
action in a few minutes.
Steam, then, holds the first place as a practical agent for the dis-
infection of surgical dressings. To be effective, it must be saturated
(unmixed with air). Saturated or streaming steam circulating under
moderate pressure reaches the efficiency and gives the results at-
tained in boiling.
Practical Application. — Having passed in review some of the prin-
ciples which underlie the preparation of surgical dressings, fitted to
fulfil the requirements of surgery, we can best gain an impression
as to their practical application by a brief review of the methods
instituted by the author, which are now in working operation in the
laboratories of Johnson & Johnson, at New Brunswick, N. J.
The buildings set apart for this work were built for this special
purpose — made plain and tight to exclude dirt. They are admira-
bly situated away from busy and dusty streets. For miles on either
side stretches river and meadow-land, securing an almost dustless
atmosphere. In fitting up the rooms in which the manipulations
take place, the ideas kept in view were the exclusion of bacteria,
easiness of keeping clean.
The walls and ceilings are glass-smooth. The floors are filled and
'"'^jkiZl'/.m^-} Modern Surgical Dressings. 31
polished. There are no closets or shelving, no cracks or crevices to
harbor dust or dirt. The furniture consists of glass-topped tables
with iron frame, allowing effectual and easy cleansing. The princi-
pal part of the work is done in the '• aseptic room," so called be-
cause all things within it are at all times kept surgically clean.
The following is an extract from the rules governing this room :
" Kverything outside of this room, everybody and everything passing
into this room from the outside are to be regarded as infected until subjected to
special cleansing operations.
" Everything required for use in this room, or being brought in, must be ster-
ilized according to the prescribed rules.
" All cleaning, sweeping and dusting must be done at the close of the day's
work. Tools, apparatus, towels, aprons, aseptible clothing, etc., are to be ster-
ilized in the sterilizing chambers. The floor must be well moistened before
sweeping ; dusting must be done with damp cloths. -Xfter sweeping and dust-
ing, the covers upon the tables must remain for at least eight hours.
"As often as may be necessary, the entire wood and iron work of the room
must be washed with soap and water, then with antiseptic solutions ; the
room closed and fumigated with sulphur and steam."
FJverything, whatsoever may be its nature or history outside of
this room, is considered as infected (though, in fact, it may be free
from germ life) ; it is, therefore, disinfected before being taken into
the room. The entrance to this room is through an ante-room,
which is a disinfecting station of the highest type. Through this
quarantine all persons and things pass before entering the aseptic
room. The persons who operate in this room are under charge of
graduate surgical nurses.
The following extracts from the rules in force show the methods
adopted for securing personal cleanliness :
" Kvery person before entering the aseptic room must jmi on the jr*--
scribe<l washable garments (flowers, ornaments, jewelry, etc., must !>« remove
They must thoroughly wash and scrub their hands, forearms and face according
to the prescribed rules.
" //and Disin/t-ctioH. — (i) Scrub hands, face and forearms in a solution of
ammonia and soap with a disinfected brush. By the aid of a knife or niijl-
cleaner, scrape all particles under the nails and on the margins.
" (2) Wash again m ammonia and soap solution, then rinse in clean hui \%.iict
and dry on a sterilized towel."
After this preliminary washing, operatives must pa.ss at once into
the aseptic room. Persons engaged in directly handling dressings
must further put on sterilized over-drcsscs, caps, sleeves, etc., and
again wash their hands with soap and ammonia, rinse ihcm in clean
32 Modern Surgical Dressings. {^"^s'A^y^xm^^
water without drying, rinse in a solution of oxalic acid, finally in
soda and alcohol without drying. After this washing, only such
objects as have been cleansed and sterilized must be handled unless
the hands are rewashed. If for any reason there is cause to leave
the room, the sterilized garments must be taken off, and then, before
re-entering, both the preliminary and final washing be again per-
formed. Tracing the history of a yard of gauze on its way through
these rooms, its course would be somevv^hat as follows : It is first ren-
dered absorbent and bleached (in an adjoining department) and arrives
at the ante-room to be made into dressings. The jars in which it will
be packed, with their tops, fastenings, etc., are brought to the same
point from a bath in hot soda solution. If the gauze is to be im-
pregnated with antiseptics, it is done in this outer or ante-room.
The gauze, the containers, labels and all things pertaining thereto
next pass into the sterilizing chamber. This chamber forms a part
of the dividing wall between the ante-room and the aseptic room.
The chamber is rectangular in form, large enough to hold a wagon-
load of goods. It is constructed with thick walls made of metal,
asbestos and other non-conducting material. The interior is lined
with steam-pipe radiators for producing heated air within the cham-
ber. Doors to the chamber open at both ends, one into the ante-
room and the other into the aseptic room. These doors are steam-
tight and held in place by ratchet screws.
The chambers are fitted with steam supply and escape connec-
tions, gauges for pressure and vacuum, safety valves, exhaust valves,
etc. Cars of iron with trays carry the articles to be treated. Sup-
ply pipes controlled by valves admit live steam to the interior of the
chamber. The actions involved in the operations within the cham-
ber are :
{a) Preliminary warming of the materials to prevent condensa-
tion.
[U) Removal of air.
{c) Circulation of saturated steam unmixed with air under press-
ure through every fibre of the material, subjecting them to the
highest possible action of this agent.
{d) Subsequent exhaustion of steam and substitution of heated
air.
After the gauze passes into this chamber, the doors are closed
and it then becomes a hot-air chamber. The air is then exhausted.
^"jkirry^S^""-} Modern Surgical Dressings. 33
to a vacuum of lo or 12 pounds; saturated streaming steam is then
let in; the temperature soon rises to possibly 240° F., and the press-
ure gauge indicates 5 or 10 pounds. The steam pipes are now
closed ; the vacuum pump is again started until the proper vacuum
is obtained.
Again steam is turned on, and so on, in turn, currents of satur-
ated steam follow each other through the vacuum for from one to
two hours. Every part of the chamber is penetrated, every fibre is
subjected to the action of this highest of bactericides. The most
resistant form of germ life must be reached and destroyed. From
the sterilizing chamber the gauze passes directly into the aseptic
room. In this room, all persons, tables and apparatus having been
previously prepared, the dressings are cut, folded and packed in the
jars, the covers laid on loosely.
(A large portion of this work is done by apparatus, to avoid
touching with the hands.)
This work is rapidly performed, and the filled jars returned to
the sterilizing chambers for a re-sterilization. This final steriliza-
tion effectually secures absolute safety against the remote possibility
of infection by handling. After this final sterilization the jar seals
are locked. For dressings packed in jars, this process is one of
hermetic sealing, a partial vacuum having been formed within the
jars during their heating and cooling. The finished dressings now
pass on to be labelled, put in cartoons and made ready for shipment.
These same chambers are utilized for disinfection with formalde-
hyde vapors, the process being : first heating oC the chambers, ex-
haustion of the air, filling the chamber with formaldehyde vapors,
which penetrate every portion of the material ; finally, exhaustion of
the formaldehyde vapors, which are in turn replaced with heated air.
Sterilization Tests. — The effectiveness of sterilization procedures
can be readily confirmed.
In the writer's laboratory the practice is substantially as follows :
A portion of the dressing material (for example, a piece of gauze)
is impregnated with an infected nutrient fluid. The thus infected
material is then dried in air, that the organisms may, as far as pos-
sible, be placed in a resistant condition. As a check cxijcrimcnt, a
portion of this infected and dried material is placed in sterilized
nutrient jelly in the culture chamber. This is done to ascertain
whether the test material has surelv been infected. The remaining
34 Modern Surgical Dressings. {^'^aJf^^^ySr-
portion of the infected material is then passed through the steriliza-
tion process, care being taken that it passes through like conditions
as would the sterilized dressings.
In the case of gauze or cotton, the writer's practice is to wrap
the test material in the centre of the package.
In testing catgut ligatures, the ligatures are moistened and
untwisted ; the infected material is then rolled up within the tissue
and dried. After the infected material has passed through the
sterilization processes, it is placed in nutrient media in a culture
chamber. After a suitable time (at least three days) if a growth is
found in the check experiment, we are certain that our test material
was infected. If no growth has taken place in the infected material,
that has passed through the sterilization processes, we are certain
that sterilization has been complete in all the dressings. This con-
clusion needs no verification. The dressings have been prepared
and sterilized by methods which exclude contamination. If a cer-
tain portion of material purposely infected, in passing through the
sterilization process with them, is rendered sterile, it is conclusive
proof that the whole of the dressings cannot fail to be sterile and
aseptic.
The above method of procedure applies particularly to dressings
containing no chemical antiseptic. Where the dressings are so
impregnated, the process is varied as follows :
To avoid the restraining influence of the antiseptic upon the
growth of the test organism, portions of the infected material, after
passing through the sterilization processes, are placed in quite a
large body of liquid nutrient media, which is shaken to dilute the
antiseptic below its normal antiseptic potency; to carry this dilution
still farther, a few drops from the first dilution are passed on to a
second tube of culture media.
It has been found in the use of antiseptics that enough may
adhere to the organism (especially to spores) to restrain develop-
ment, though not destroying their vitality. This is obviated even
in the use of strong solutions of an antiseptic by the dilution above
mentioned.
In testing with antiseptics the test material is kept under a culti-
vation for at least a week. Development is often so retarded by
the antiseptic tending to make hasty conclusions erroneous. In
these tests with antiseptics, liquefied flesh— peptone— gelatine of
Koch is usually employed.
^"^aiully^mr} Modern Surgical Dressings. 35
Where no antiseptic has been employed, sterihzed potatoes and
other soHd media have been found convenient.
The required test is the presence or absence of a growth which
will liquefy solid media or produce form, color or odor characteristic
of bacterial colonies.
This is verified when deemed necessary by a microscopical exami-
nation. In surgical bacteriology, the bacillus of anthrax is used as the
standard test organism ; whatever will destroy the vitality of this
bacillus will destroy all the known organisms of wound infection.
Who Should Make Surgical Dressings. — In the past, dressing
materials were largely the product of domestic industry and convict
labor. We could not now tolerate supplies from such disease-
breeding sources. In recent discussions by surgical authorities, the
question has been raised as to the relative fitness of the surgeon,
the pharmacist and the manufacturer as makers and purveyors of
surgical materials.
The apostle of modern surgery manufactured " Lister's Gauze "
in his own kitchen. Sir Joseph's kitchen is doubtless a more fitting
place for such work than is the office of many of his followers.
Doctors' offices are not, as a rule, the most wholesome spots. Their
upholstered furniture is in constant contact with the clothing and
persons of patients carrying infections of ever)' name and kind.
Their tapestried carpets are filled with dust brought from pest-laden
households. In the doctor's ofifice we will find that tables, shelves,
books and apparatus are spattered with debris from urinal examina-
tions, pus from foul sores, dried excretions from diseased skin,
pathological tissue, clotted blood and dried discharges from innumer-
able sources.
Streams of infectious matter continually pour into the rooms ot
the busy doctor and find a lodging-place in its paraphernalia. The
unfitness of such surroundings for the production of surgically clean
dressings is evident.
I claim for the American physician the highest of honors. I all
but reverence the skill and genius of the American surgeon ; but
before I would attempt to prepare aseptic dressings in their offices,
I should, in most cases, require that they be first cleansed and disin-
fected upon the lines adopted by health authorities for the purifica-
tion of infected premises.
A certain hospital claims that its operating room is •• the cleanest
36 Modern Surgical Dressings. {"'^ January, ist?™*
place in the world." All hospitals have not earned such a title.
Many of them are attached to medical colleges where students and
professors gather fresh from the dispensary clinic, from visits to
infected houses, from dissecting rooms, from hundreds of sources
of contagion.
Clinging to their persons and clothing may be found particles
rich in pyogenic and pathogenic bacteria. In hospitals, the aggre-
gation of infectious organisms cannot be avoided. Formerly, they
were •' hot-beds of infection." Now dangers are excluded only
by the most rigorous procedures.
When dressings are prepared by the pharmacist, the work is
generally performed in the drug store back room. This place
comes far short of the conditions known as surgical cleanliness.
The chemically clean graduate is still unclean in the eye of the sur-
geon. Counters covered with vegetable and animal drugs of all
kinds are not suitable places upon which to lay absorbent gauze.
Street and store dust, spatterings of syrups, extracts, oils, and all
manner of decoctions, create a favorable lodging- and breeding-place
for organic life. These are not wanted in surgical dressings. The
pharmacist, though ordinarily clean in person and habits, familiar
with soap and water in the pursuit of his calling, yet he is far from
aseptic. Like the physician, he is constantly in contact with infec-
tion through the person of his patrons.
The hands that dispense beef tea at the soda counter, or that
bring a jar from a mouldy cellar, should not touch sterilized mate-
rial without cleansing. Thus there must be a radical change of
environment before the pharmacist can attain success in aseptic
technique, though he may, perhaps, rightfully claim conditions and
facilities that are above those of the ordinary physician.
The facilities of the manufacturer, whose whole organization is
adapted to the production of surgical dressings, are certainly more
perfect than those of the surgeon, to whom such work is incidental.
The environment of a room from which pathogenic organisms and
septic matters are entirely excluded is superior to that obtained in
the hospital or in the doctor's office. The room in which no work
is undertaken except the handling of aseptic material will certainly
be more nearly surgically clean than one to which infection has
constant access. Persons whose only calling is that of preparing
surgical ma'erial, who have been schooled in the principles under-
^fkiulry^'t^"''} Modern Surgical Dressings. 37
lying the infection and disinfection of dressings, are probably more
competent to handle dressings than the doctor's student or his
attendants, to whom such work is of necessity relegated. In this
work, as in many other instaiices, properly constructed apparatus is
more efficient, more cleanly, more perfect, than hand work.
Further, an organization devoted exclusively to the manufacture
of dressings, once having the details arranged to prepare a yard of
dressing, can produce any number of yards more perfectly than if
done as occasion may require, as is the rule in the hospital or in
private practice.
To the manufacturer and dispensing pharmacist is due the credit
of having made possible the universal application of the principles
of modern surgery. They have supplied to the practitioner in the
most remote regions appliances as perfect as those used in the great
hospital centres. They have placed in the hands of the practitioner
appliances that fulfil every requirement of the advanced art of
surgery.
I hold that the preparation, selling and dispensing of medicinal
and surgical supplies to the doctor, to the surgeon and to the pub
lie belong to pharmacy. Their application is the province of the
practitioner of medicine and surgery, and I maintain that it will be
to the betterment of surgery to receive all dressing materials from
the hands of a competent pharmacist.
Training for the Work. — It is important that persons who are to
handle surgical dressings in any capacity be familiar with the prin-
ciples as well as the details of the work. They should also know
why things are done as well as how to do them. The principles of
surgical asepsis are applicable to the dispensing and sale of these
materials. Therefore, the following epitome oi a course in aseptic
technique, devised for use in the writer's laboratory, may be found
useful to many pharmacists.
In addition to the daily manual training under experienced per-
sons, the operatives are required to attend stated instructions.
These instructions are in the form of demonstrations of the processes,
with an explanation of the principles involved. Those in attend-
ance are given questions to be answered and experiments to per-
form. Text and reference books are furnished. The scheme is
modeled upon the plan of a college extension course. Among the
subjects are the following :
38 Modern Surgical Dressijigs. {^ January ^isgr.""'
( i) The work of preparing surgical materials, its importance, its requirements.
(2) Definition and meaning of terms.
(3) Nature of the material used in dressings. (Fibres, cloth, ligatures, etc.)
(4] Preparation of materials, bleaching, rendering absorbent, etc.
(5) Kinds of dressings used in modern surgical practice.
(6) Uses to which dressings are put in surgery.
(7) Bacteria, their nature, conditions of growth, multiplication, products of
their activity, with demonstrations of the means by which they may be trans-
ferred to and from persons and things.
(^S) Wound infection.
(9) Infection of dressings.
(10) Disinfection — chemical agents and physical agents.
(11) Exclusion of bacteria.
(12) Sterilization.
(13) Disinfection of persons and things.
(14) Asepsis and aseptic technique in the preparation of dressings.
The entire course in my practice occupies several months — in fact,
becomes a continuous course, as additional methods are constantly
brought into practice.
Surgical Dressings in Commerce. — Dr. Gerster, in one of his ad-
dresses, condemned the use of ready-made products as sold in the
drug store, on the ground that the gauge of success is purely com-
mercial, only directed solely to profit.
Another writer affirms that the standard of such dressings iscom-
mercial in nature, the essential requisite being profit, and that they
must be sold to meet competition. That in this the requirements
of surgery are matters of indifference and generally matters of igno-
rance.
These statements were corroborated in a recent instance by a
druggist in one of our large cities, who is commercially wise. He
stated that to him quality, kind or make was no factor. Low prices
were the sole criterion of value. Responsibility hovers over every
field of the pharmacist's activity in dispensing dressings ; we share
the burden with the surgeon. Whoever has stood beside the sur-
geon in his operating room and realized how much depended on
not only the hand, the training and the skill of the operator, but the
absolute cleanliness in every movement, must realize that there
are some things that cannot be expressed in a money ratio.
At such a time and in such a place the integrity of the dressing
rises to supreme importance. Any neglect in its preparation, any
misstep through the ignorance, cupidity and stupidity of any who
"^'janSafy^'i^'""-} ModcTH Suvgical Drcssiiigs. 39
have had to do in its history, is sure to be revealed. The issue of
life or death in such a case should not be subject to the market rates
per pound or yard. What results must follow the very common
practice of dispensers who open packages of dressings, measure and
weigh them over dusty counters with unclean hands, and send them
on their mission ? It would be more humane, perhaps, to send a
lethal dose of strychnine. In the light of asepsis, to dispense mor-
phine for quinine becomes a virtue when compared with the wilful
contamination of a surgical dressing.
Poisons are put under lock and key, dispensed under rigid sys-
tems of precaution and checking.
The importance of the surgical dressing, the nature of its re-
quirements, call for equal care. There is no article in the druggist's
stock which should receive greater care and judgment. Upon every
yard of gauze, sponge or ligature he dispenses hangs, perhaps, the life
and death of a patient and the reputation of a surgeon. They should
be guarded from every chanrtel of direct or indirect infection.
A closet or a room, or a case should be provided for their recep-
tion that is cleanable ; it should be cleaned often and kept clean.
They should be sold within the containers in which they are packed
in their preparation. They should never be broken open for sale or
for any other purpose. They should be delivered to the surgeon so
perfect that there can be no question as to their integrity, placmg
all the responsibility for their subsequent care in his hands. In
dispensing to the public, every purchaser should be cautioned
as to their nature and instructed in their handling and use. The
price should meet the cost of the dressing plus a profit which will
cover this service of advice, trouble and care.
Ninety-five per cent, of the 100,000 physicians in our land who
apply these principles of surgery must look to the pharmacist for
their dressing materials. In filling this demand, the pharmacist
should supply such materials as will meet the highest surgical re-
quirements. As far as the dressing is a factor, the surgeon at the
country cross-roads, by the aid of the pharmacist, should be enabled
to reach the advanced methods of the metropolitan clinic.
To attain this end in the making, in the buying, in the sale and in
the dispensing, even to the most minute detail, there is required
knowledge, skill, ability and finally a faithful application of the same.
40 Analysis of the Bark of Honey Locust, {^"^-^l^l^y^^^!^'
CHEMICAL ANALYSIS OF THE BARK OF HONEY
LOCUST, GLEDITSCHIA TRIACANTHOS.
Bv Louis P. Carstens, Ph.G.
Contribution from the Chemical Laboratory of the Philadelphia College of
Pharmacy. No. i6o.
The specimen analyzed was obtained in central Pennsylvania.
The results of the analysis were as follows :
Petroleum Ether Extract :
Per Cent.
Fat, wax, etc 1*38
Ether Extract:
Resin, 1*15 per cent. ; organic acid, etc IT7
Absolute Alcohol Extract :
Resin, 097 per cent.; alkaloid, etc i 62
Water Extract:
Glucose, o'63 per cent; saccharose, 0*57 per cent.; mucilage,
2"o8 per cent; dextrin, i'92 per cent.; etc 6'5i
Alkaline Water Extract:
Pectin and albuminoids, 4*84 per cent. ; etc 13*68
Acidulated Water Extract:
Pararabin, etc 3-62
Lignin 11-76
Cellulose 42-42
Moisture c-jq
Ash yoo
Loss and undetermined c-y^
'^Otal lOQ-QO
The a.sh contained potassium, calcium, aluminum and ferric iron,
as chlorides, sulphates, carbonates and phosphates.
Starch, tannin and glucosides were not present.
To obtain more of the organic acid and the alkaloid, which were
indicated in the proximate analysis, for further examination, about
500 grammes of the ground bark were percolated with 95 per cent,
alcohol. After reducing the percolate to a small bulk by distilla-
tion, it was diluted with about five times its bulk of distilled water,
distinctly acidified with hydrochloric acid, and the mixture filtered.
After agitating the filtrate with chloroform, it was made alkaline
^"ammryfi^sir} Aualysis of tkc Burk of Honey Locust. 41
with sodium hydrate and again agitated with this solvent. The
chloroformic layers were allowed to evaporate spontaneously. The
residues were dissolved in alcohol, but failed to crystallize on spon-
taneous evaporation. The test solutions for alkaloids were then
applied to the residue from the chloroform shaken with the alkaline
solution, with the following results:
Potassium tri-iodide, no precipitate.
Mayer's solution, precipitate.
Gold chloride, precipitate.
Phospho-tuugstic acid, precipitate.
Picric acid, precipitate.
Platinic chloride, precipitate.
Tannic acid, no precipitate.
Two and one-half kilogrammes of the bark, when operated on in
the manner described above, furnished a larger quantity of this
principle. The residue obtained upon evaporating the chloroform
was dissolved in absolute alcohol, and the solution filtered through
animal charcoal. The filtrate yielded crystals of the principle when
allowed to evaporate spontaneously. The following reagents were
applied to these crystals on a porcelain surface :
Sulphuric acid, dark-red color.
Sulphuric and nitric acids, brownish-red color.
Sulphuric acid and potassium bichromate, dark-brown color.
Nitric acid, brownish-red color.
Gold chloride, brown color.
When the crystals were heated with soda-lime, ammonia was
evolved.
The substance, removed from the acid filtrate by shaking it with
chloroform, was dissolved in absolute alcohol, but failed to crystal-
lize on spontaneous evaporation. Dissolved in water it gave pre-
cipitates with the following reagents for organic acids:
Lead acetate, yellow precipitate.
Silver nitrate, dark precipitate.
Ferric chloride, black precipitate.
Potassium bichromate, brown precipitate.
Gold chloride, black precipitate.
France finds her Algerian cork oaks a convenient and sali^faclory source of
direct revenue. According to a recent official bulletin, the department of
Algiers contains 65,000 acres of cork trees in the hands of the Government. —
The Forester.
Am. Jour. Pharm.
42 Alcohol in tJic Titration of Alkaloids. {^^anuaryfS
ALCOHOL AS A SOURCE OF ERROR IN THE TITRATION
OF ALKALOIDS AND ALKALOIDAL RESIDUES.
By Chas. Caspari, Jr.
In August last, the writer presented a paper on the above sub-
ject at the Montreal meeting of the American Pharmaceutical Asso-
ciation, but not content with the results detailed therein, decided, upon
his return home, to investigate the matter more fully with the view
of presenting a second paper on the same subject at the next annual
meeting. Such a paper has been made unnecessary by the publica-
tion of an article, written by Mr. L. F. Kebler, in the December,
1896, issue of the American Journal of Pharmacy, wherein is
demonstrated the fact that strictly pure alcohol does not interfere
appreciably with the titration of acids by alkalies in the presence of
color indicators, except in the case of methyl orange and a few
others. Having carried out a series of titrations with strictly pure
alcohol prepared by himself, using haematoxylin, Brazil wood and
cochineal as indicators, the writer desires herewith to corroborate
the statements made by Mr. Kebler, that satisfactory results can be
obtained with such alcohol quite as well as with water.
The writer, in his paper (see American Journal of Pharmacy,
September, 1896, p. 473), called attention to the fact that alcohol
and absolute alcohol, as available in the market, exercise a decided
influence on color indicators and may prove the fruitful source of
error in volumetric work, the statement being supported by a large
number of tabulated results obtained in actual work. This was
probably the first time that attention had been publicly called to
this matter, and inquiry made at the time of several leading phar-
macists and chemists failed to elicit any information or experimental
data. The absolute alcohol used in the writer's experiments last
summer and stated to have a slight alkaline reaction was of E. R.
Squibb & Sons' manufacture, and taken from a fresh bottle. That
the error liable to occur from the use of commercial alcohol will
be greater or less in proportion to the impurities present in the
alcohol is, of course, true, and the question arises : Has strictly
pure alcohol always been used in volumetric work, and have
analysts been in the habit of preparing it specially for such
work, the market (at least to the writer's knowledge) not pro-
viding the article? The chairman of the Committee on Indi-
^'january^'isyf.'"} AlcohoUti the Titration of Alkaloids. 43
cators of the American Pharmaceutical Association, Mr. Kebler,
in his instructions to the committee last winter, directed the use of
alcohol, but failed to note his experience of eighteen months ago
{see American Journal of Pharmacy, 1896, p. 667), nor did he
caution the members against the use of commercial alcohol. Did
he assume that all would use strictly pure alcohol, and did he use
such alcohol in his own work done for the committee? This fact
should have been noted in the committee's report.
The explanation offered in the writer's paper for the peculiar
behavior of alcohol, on the basis of electrolytic dissociation, was
made on the assumption that high-grade commercial alcohol, known
as cologne spirit, could scarcely be so impure as to account for the
great disturbance observed, especially as the alcohol employed cor-
responded quite well with pharmacopoeial requirements, and since
Ostwald has directed attention to the action of alcohol on color
indicators. Even now, when using strictly pure alcohol, the writer
has observed that in a mixture of only alcohol and indicator a much
larger (two to four fold) quantity of alkali solution is required for
the characteristic reaction than in a mixture of only distilled water
and indicator; moreover, the same peculiar behavior towards
tropjuolin was observed as recorded in the writer's paper, for 50
c.c. strictly pure alcohol with 3 drops of a very sensitive tropxolin
solution failed to show a decided acid reaction after addition of 45
c.c. y^ H^SO^. This latter circumstance, while confirming the un-
fitness of tropaiolin as an indicator for alcoholic titrations, requires
further investigation.
While the writer regrets his misapprehension of the causes lead-
ing to the observations mentioned in his paper of last August, and
although the conclusions then arrived at have now been shown to be
partly erroneous, both by experiments in his own hands and by the
recently published reports of Mr. Kebler, one good result has at
least been obtained, namely, to show the wholly unreliable character
of commercial alcohol for volumetric work and to direct the attention
of pharmacists and others prominently to this fact, and to the neces-
sity for purifying all alcohol intended for such work.
Baltimore, December 17, 1896.
Pharm.
44 A Rcsuvic of Reairrent Topics. { ^TaimryrfioT
A RESUME OF RECURRENT TOPICS.
By WiIvI^iam B. Thompson.
Tlu Avoirdupois of Odors. — The ingenious are never idle. There
need be but few lost moments to the industrious mind. The povver^
volume, weight of odors can be relatively compared, it is claimed,
by the amount of organic matter obtainable by reducing this to
condensation and solution. Dense and heavy odors must assail the
nerve filaments in our nasal organ with a ponderosity greater than
those of a lighter or more ethereal kind. Experiments may be
made by thoroughly impregnating the warmed and dried air of a
closet or compartment with a chosen odor. Something is certainly
diffused when our sense detects. What is it to be thus appreciable?
Is it organic matter? This being granted, it must have weight.
After a prolonged diffusion of the odor in the air of the closet or
room, it is suddenly filled with the vapor of water, and finally
cooled, when the condensate is collected. This is to be examined
for amount of organic matter, and comparisons instituted. The
actual utility of this does not appear except in the light of scientific
interest ; ordinary tests are all physical. We may, however, desire
to know whether the volume of natural odor in the plant species can
be intensified by natural means. The power and diffusiveness of
fragrance must have a basis of considerable materiality to be so
permanent and enduring. Does it exist there as we recognize it, or
is it not rather the result of the subtle chemistry in which the oxygen
plays the most important part ?
hucainc. — This new therapeutic, similar to cocaine, is a laboratory,
not a vegetable, product. Sixty-seven letters are required to con-
stitute its correct scientific orthography. An abbreviated prescrip-
tion for such an article will not be criticized for ambiguity. The
derivation of eucaine would seem to invest it with an antiseptic
character. Its solubility in aqueous media is very free. It does not
present that tendency to fermentative change or to decomposition
as many vegetable alkaloids in solution are prone to do. Some ob-
servations have been made as to the comparative toxic effect
with cocaine, eucaine being less, and its onset and intensity less.
The pharmaceutical preparations will include an ointment, but its
chief uses will be those of a mydriatic, and as an anaesthetic (lO per
cent, solution) in minor dental surgery. Its composition is said to
^janua/y.^svf."'} ^ Rc'sumc of RcairrcHt Topics. 45
be very complex, and its preparation difficult. The pharmacology
of eucaine, however, is well worthy of attention.
Resemblance with Difference. — The realm of nature abounds in
curious creations, and a fanciful imagination can help many compari-
sons. But with all these freaks, or, to be more reverent, designs,
these objects would almost seem to present the appearance of art
assisting nature. For instance, the fly-orchis, Ophrys muscifera,
and the bee-orchis, Ophrys apifera, produce flowers, the parts of
which bear a very close resemblance to the body forms of these
insects respectively. Then we have, in the mandrake and the gin-
seng, forms which require very slight additions to parts to complete
the figure of human shape. The poetic fancy has given us a tradition
that the ploughman stood aghast as his blade threw upon the surface
the rooted mandrake with its human feet and hands ! Minerals are
often observed to possess outlines of figures which might be mis-
taken for exquisite chiseling.
Professional Cotnpensation. — There seems to exist a somewhat
fixed law of compensation in almost all affairs except those of hu-
man agency, and even there, if we look carefully into the subject,
will be found causes for which we ourselves are directly responsible.
We honor the individual who honors himself; we respect the man
who gives evidence of an innate self-respect, especially in a profes-
sional character. That man who degrades the value of a prescrip-
tion down to that point of a commercial bartering standard creates
a torment which will return to plague him all the remaining days of
his business life. There should be no autocratic rates on prescrip-
tions ; but there should be a just and fair compensation when all the
elements of expense are duly considered. Some estimates have bet n
given as to what should be a fair basis of calculation in attaching
the value, commercially and scientifically, to a physician's prescrip-
tion. The value to the patient may be incalculable; but this is
never computed. A curative compound is of inestimable worth to
illness, suffering and pain. And when the compounder is justly re-
warded for his knowledge, skill and science, what a twopenny com.
parison is the cost of the remedy to the man's or woman's health,
strength and enjoyment of life! Tliis is the way in which the public
should be educated to view it. In the meanwhile, let no reputable
pharmacist consent to gauge the value of a presented prescription
by the price to which some mercenary competitor, some commercial
46 A Rl'suiiii: of Recurrent Topics. {"^Tanuaryj
Am. Jour. Pharm.
897.
apothecary, whose existence is made possible by our loose, lax laws,
has degraded it and himself. The value of the service in compound^
ing a prescription, omitting the cost of material, bears the just ratio
of 50 per cent, of the price charged, yet what a dignified recompense
on a ten-cent prescription !
Fruits and Juices. — Those who are in the habit of observing may
often wonder why tropical fruits are so much less perishable than
those grown in temperate regions. The first impression is that the
high degrees of heat and the strong, direct light would both con-
duce to relaxed tissue and vapid juice ; yet exactly the reverse of
this is true. The provision which guards against this, and so wisely
adjusts the productions to the clime, is seen in the structure of the
orange and the lemon. The volatile oil and fixed oils, which exist
in the pellicle of the rind, absorb and check the penetrative power
of the heat, whilst the soft, white substance, the inner pulpy coat-
ing, is as good a barrier against both cold and heat as the fur on an
animal's body or the soft down on the bird's breast. As the result
of this the orange species, when uninjured in the picking and hand-
ling, can be carried, without deteriorating, to great distances and to
all varieties of climate.
How very different is the case with our Northern berries and
fruits ! But few of these, if any, will keep their flavor for forty-eight
hours, and none of them retain their form for any considerable dur-
ation of time. Another curious and striking fact is that the juices
of tropical fruits are all of a cool temperature in the native or natu-
ral stale, being shielded from vicissitudes. The milky juice of the
cocoanut is of an even temperature, refreshingly cool, being well
protected in that dermic coire, or skin, which is between the outer
shell and the meat of the fruit. Then again, our now indigenous
watermelon gets an abundance of sweet juice and retains it, no mat-
ter how dry and arid may be the soil of its habitat, the largest —
and much the finest — variety of these fruits being grown in the In-
dian Desert, between the valley of the Indus and the Ganges, where
not a drop of water falls from the clouds during the annual cycle,
and the rainy monsoon often passes over the region without shed-
ding one sympathetic tear of moisture upon the parched soil ; yet
the melon secures its quota of sweet, watery juice, and keeps it,
under its varnished rind, comparatively cool. Verily, before the
magic of Nature, the feats of art and legerdemain are insignificant!
^janaaryl'ST.'"'} Cvichotia Cultivation iti Bengal. 47
CINCHONA CULTIVATION IN BENGAL.^
The Thirty-fourth Annual Report of the Cinchona Plantations of
the Government of India in British Sikkim and Bhutan has lately
been submitted to the Ben^^al Government by Dr. George King,
C.I.E., F.R.S , Superintendent of the Royal Botanic Garden, Cal-
cutta, and of cinchona cultivation in Bengal, and Government quin-
ologist.
The number of trees uprooted for their bark during the year
1895-96 was 453,000, comprising 65,000 of C. succirubra, used for
the manufacture of " G3vernment Cinchona Febrifuge," and
388,000 of the kinds which yield yellow or quinine-producing bark
chiefly hybrid cinchona and Calisaya ledgeriana, a large proportion
of the trees uprooted being small. The number of plants was in-
creased during the year by 9,200 hybrids ; the total census of living
cinchona plants at the close of the year, including nursery stock,
was 3,807,701.
The crop collected during the year amounted to 467,190 pounds
of dry bark, consisting of 53,380 pounds of red and 413,810 pounds
of yellow bark. The whole of this crop, with the exception of
79^/i pounds supplied to the Government Medical Stores Depart-
ment or sold to Government institutions, was made over to the cin-
chona factory for manufacture into quinine and febrifuge. In addi-
lion to the bark cropped at the Government plantations, 170,000
pounds of quinine-yielding bark was purchased from private culti-
vators in the district. Seventy-four thousand pounds of red bark,
worked up in the factory during the year, yielded 3,124 pounds of
cinchona febrifuge, valued at Rs. 10 (about 12s.) per pound, and
from 387,200 pounds of yellow bark, 9,004 pounds of quinine sul-
phate, valued at Rs. 14 (about i6s.) per pound, were manufactured.
An additional 1,500 pounds of quinine were purchased from the
quinine factory of the Madras Government at Ootacamund.in order
to meet the greatly increased demand for the 5-grain packets, which
are issued to the people at all post-offices throughout the province,
at the rate of i pice each (less than a farthing).
The total issue of quinine for the year amounted to 10,287
pounds, an increase of 2,725 pounds on the previous year, 1,145
pounds of this increase being due to the growth of the post-office
' niarmaceuticat Jounial, October 17, 1896.
48 Literature Relating to Pharmacy, {^'^dnZy'^im'^'
demand for pice-packets, and 937 pounds issued on account of the
Chitral expedition. Of cinchona febrifuge there were issued during
the year 3,830 pounds, 554 pounds more than in the previous year,
the amount purchased by the pubhc having increased by 194
pounds, showing that the preparation is held in high estimation by
the pubhc as a cheap and rehable remedy for fever, notwithstanding
that cinchonidine and cinchonine can be purchased at a cheaper rate
in the Calcutta bazaar. The febrifuge is an unbleached quinetum,
and represents the total alkaloids in the bark.
The net profit on the year's operations amounted to Rs. 4,598, a
sum which Dr. King says would form but a small dividend on the
capital which has been sunk in these plantations since they were
first begun. There has not been for many years, however, any
capital to pay interest upon, as the cost of the plantations was
extinguished long ago by profits made during the early years of
the manufacture of cinchona febrifuge. As the Government of
India desires only to secure for the people, without loss to itself, a
cheap remedy for fever, the Lieutenant-Governor of Bengal con-
siders this result entirely satisfactory. The demand for quinine in
the popular 5-grain powders has increased with such rapidity that it
has been found necessary to limit the sale to post-offices in Bengal
and Assam, and to discontinue the regular supply to other prov-
inces.
The acknowledgments of Government are again accorded to
Dr. King and to Mr. G. Gammie, the Deputy Superintendent, for
their efficient management of the department during the j^ear.
RECENT LITERATURE RELATING TO PHARMACY.
IODINE MANUFACTURE IN JAPAN. [Chemist and Dvuggist,
October 2^, 6og.)
It is well known that enormous quantities of seaweed containing
iodine are gathered along the coasts of Japan, and were it not for
the fact that the manufacture of iodine from kelp is scarcely profita-
ble in view of the competition of the Chilian product, Japan would
no doubt be one of the principal iodine-producing countries. In
fact, even under the present circumstances, Japanese iodine and
iodides find a market locally, and have even been seen in Eu-
rope in commercial quantities. A proposal has now been made
^Tan2"yri8^™'} Literature Relating to P liar mac y. 49
to the Japanese Government by certain native chemists that the
customs duty on iodine and iodides in Japan should be increased to
such an extent as to enable the Japanese industry to be self-support-
m^. — TJie Journal of the Society of Chemical Industry, Octobtr ^i ,
iSg6.
BARIUM PLATING CYANIDE.
The text-book way of preparing barium platino cyanide is to pass
gaseous hydrocyanic acid through a mixture of platinous chloride
2 parts and barium carbonate 3 parts, suspending in twice their
weight of water. Schertel, in a recent issue of Berichte, describes a
safer process, viz. : Platinum chloride is precipitated by hydrogen
sulphide at 60° to 70° C, and the well-washed platinum sulphide is
dissolved in a warm solution of potassium cyanide. On evaporation,
the potassium platino cyanide (K.^PcCy^3H^O) crystallizes out, and
equal parts of potassium sulphide and potassium thiocyanate remain
in the mother-liquor. If a solution of barium cyanide be used, the
barium platino cyanide is obtained, and from this, by double decom-
position with uranium sulphate, the platino cyanide of uranium may
be gotten in beautiful crystals. — The Chemist and Druggist, October
J/, i8g6,
PKODL'CTION OF QUICKSILVER IN CALIFORNIA.
The Engineering and Mining Journal (New York) states that
quicksilver production in California has shown this year a consider-
able increase, the total receipts at San Francisco for the six months
ending with June having been 18,439 flasks, a gain of 4,743 flasks,
or 346 per cent., over the first half of 1895, and of 6,033 flasks, or
487 per cent., over 1894. While these receipts gauge the rate of
production very fairly, they do not give the whole amount, as the
reports do not include the quicksilver sold directly from the mines,
nor that shipped from them to the East by rail, which does not
come to San F'rancisco at all.
The larger output seems to have been absorbed without difficulty.
In addition to the greater demand from the California mines, there
has been a growth in exports very nearly corresponding to that in
the production. The trade with China, which had been suspended
for several years, has been renewed, and has aided materially in dis-
posing of the increased production — The Journal of the Society of
Chemical Industry, October jr, rSgd.
50 Literature Relating to Pharmacy. {"^Tanuary.^
Am. Jour. Pharru.
1897.
MAPLE SUGAR.
The Production of Maple Sugar, G. H. Grimm {Cult, and Country
Gent., 6 1 (1896). No. 2247, p. 146) — The author urges the neces-
sity of absolute cleanliness in everything connected with the pro-
cess; the sap should come in contact with tin only; tin spouts
should be used ; and the buckets should be covered. The sap
should be evaporated as soon as possible after it leaves the tree.
With suitable apparatus a barrel of sap can be converted into a gal-
lon of syrup weighing 1 1 pounds in 20 minutes. This syrup will make
8 pounds of sugar. The natural color of the syrup is a translucent
white ; if it weighs less than 1 1 pounds per gallon it will ferment ; if
more, it will crystallize. The syrup is far superior to that from re-
melted sugar.
In putting it up for the market it should be poured into tin cans
at 83° C, and hermetically sealed. It will keep better in an attic
than in a cellar, unless the cellar is very dry.
GOLD AND SILVER IN SEA WATER.
Gold and silver in sea-water may not be plentiful enough to war-
rant the formation of limited companies to extract them, yet
those metals exist in the ocean in appreciable amounts. Professor
A. Liversidge, in a long paper read before the Royal Society of
New South Wales [vide Chemical News, Sept. 18, et seq.), gives the
results of some experiments made with the object of determining
the amount of precious metal in the sea-water off the coast of New
South Wales. The evidence obtained indicated the presence of
gold in the proportion of about 0-5 to I grain per ton, or in round
number^ from 1 30 to 260 tons of gold per cubic mile. Assuming that
the cubic contents of the whole of the ocean equal 400,000,000 cubic
miles, the above proportion would be equivalent to a total amount
of 100,000,000,000 tons of gold. With regard to silver, Malaguti
obtained 00005 S"^- ^^om 50 litres of sea-water, representing more
than 40 tons per cubic mile. The metal sheathings of vessels have
been proved to remove both gold and silver from sea-water, that
from one old trader yielding silver, 4 ozs. 15 dwts. 92 grs., and gold,
I dwt. 24 grs. per ton, together with a good deal of iodine. Muntz
metal sheathings from the piles of wharves have also yielded con-
siderable proportions of both gold and silver. — Pharmaceutical
yoidrnal, October ly^ i8g6.
^jan'ryr'^'"-} Editorial. 51
EDITORIAL.
The sixty-eighth volume of the Amkricak Journal of Pharmacy, which
closed with the December uumber, contained 708 pages of reading matter and
index, and was the largest volume of this journal ever issued. It is but justice
to our contributors to say that we believe the quality of the reading matter has
never been excelled in previous volumes. Many of the papers called for illus-
trations, and the call was liberally answered by the publishing committee, so
that every number contained one or more illustrated papers.
The present issue opens the sixty-ninth volume with an array of original
matter, which we have no hesitation in designating as highly meritorious.
Mr. Maiden's paper on red gum is one of the first published in this country
oi that subject. Mr. Rittenhouse's contribution on the present sources of lico-
rice root contains information derived from first hands ; and Mr. LaWall's
article calling attention to a new and easily detected sophistication of Japan
wax is of the greatest importance. It is no detraction from the other papers
that they are not mentioned here, yet we cannot refrain from especially calling
attention to the address by Mr. Kilmer on modern surgical dressings, in which
the pharmacist will find information about the dispensing of these commodi-
ties which should cause him to redouble his vigilance in the direction of clean-
liness, and encourage him to insist on the physician ordering such quantities
as to enable the dressings to be dispensed without danger of their becoming
infected.
THE PATENT MEDICINE AI.MANAC.
This is the season of the year when the pharmacist is liberally supplied with
almanacs, bearing his own business card, for distribution to his customers.
Many fall into the trap, and pass these wretched advertisements on to their
customers, and thereby commit a grievous error which injures them in a uum-
ber of ways.
If every pharmacist who reads this Journal, would either return the alma-
nacs to the sender or consign them to the fire, it would, in some sections of the
country at least, break up this system of making him the advertising agent of
the nostrum manufacturers.
EXIT LUCIUM.
Some three months ago, a new element was announced in monazile sand.
It was soon found, however, that the enterprising discoverer had patented it,
and proposed to use it in incandescent gas lighting.
Dr. William Crookes, editor of the Chemical \cius, has been supplied with
the nitrate and oxalate of the alleged element by the patentee, Mr. V. Rarritire,
and finds, by spectroscopic and chemical examinations, " that lucium is nothii g
but impure yttrium."
In the same issue of the Chemical News, Dr. R. Fresenius calls attention to
the fact that his name had been used in connection with the so-called element
without authority.
52 Reviews. {""^^J.^Sm^-
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
Inorganic Chemical Preparations. By Frank Hall Thorp, Ph.D.,
Instructor iu Industrial Chemistr}^ in the Massachusetts Institute of Tech-
nology. Boston : Ginn & Co., publishers.
We have several excellent small manuals in the English language for the
manufacture of organic preparations, such as those of Cohen and Fischer, but
this is the first one covering the ground of inorganic chemistry in the same
waj'. It has, moreover, several new and distinctive features which we think
are of value. After stating the formula and molecular weight of each com-
pound, it gives the materials and quantities of the same needed for the prepa-
ration, and full working directions for the carrying out of the manufacture,
followed by the reactions involved and the properties of the product. Under
the latter head, the author gives, in a large number of cases, tables showing
the solubility of the salt in water at different temperatures, and the specific
gravity of solutions of different strengths. For these tables the authorities are
invariably given. While the book wants a table of contents, the substances
are alphabetically arranged and an index follows.
A valuable introductory chapter on solution, precipitation, filtration, decan-
tation, washing, evaporation and crystallization, abounding in valuable sug-
gestions, has not been overlooked. S. P. S.
The Principi.es of Theoreticai. Chemistry, with special reference to
the constitution of chemical compounds. By Ira Remsen, Professor of
Chemistry iu the Johns Hopkins University. Fifth Edition. Lea Brothers &
Co., Philadelphia and New York. 1897.
It has been the aim of the author, in the latest edition of this valuable work,
to bring it in accord with all the recent advances of chemical science. The
salient features of this book are, that it contains a clear statement of theoretical
chemistry in a moderate space. It is therefore not so formidable to the
beginner as several of the larger works on this subject, yet it contains abun-
dant information to equip the student for almost any amount of research work.
Semi-Annual Report of ScHiMMEi< & Co. (Fritzsche Brothers. ) Leip-
zig and New York : October, 1896.
On Certain Derivatives of Trichlordinitrobenzol. By C. Loring
Jackson and W. R. Lamar. Reprint horn American Chemical Journal , October,
1896.
A Guide to the Organic Drugs of the U. S. Pharmacopceia. By John
S. Wright. First Revision, Twelfth Thousand. Indianapolis: Eli Lilly &
Co. 1896.
Chemists' and Druggists' Diary for 1897.
British and Coi.oniai, Druggists' Diary for 1897.
Fourth and Fifth Annuai. Reports of the California State Board
OF Pharmacy, 1H94-96.
^ January ^/Sf.""} Pharmaceutical Meeting. S3
MINUTES OF THE PHARMACEUTICAL MEETING.
Phii.adkli'HIa, December i6, 1S96.
The regular pharmaceutical meeting of the series of 1S96-97 was held in the
Museum of the College. Mr. J. \V. England presided. The minutes of the
previous meeting were allowed to stand as published,
Mr, F. B. Kilmer, of the firm of Johnson .S: Johnson, of New Brunswick,
N. J., was the first speaker on the programme, and addressed the meeting on
the subject of " Modern Surgical Dressings." (See page 24. ) This address was
not only interesting from the technical standpoint, but embodied many valua-
ble suggestions of a practical character. The speaker said that the pericd
marked by the introduction of Sir Joseph Lister's principles of antisepsis was a
distinct epoch in the history of surgery. The wound dressings made at the
beginning of this epoch were characterized as crude in contrast with those
manufactured at the present time. Formerly they were caustic, irritating and
non -absorptive, while to day the essential requirements are power to alsorb
wound secretion and to exclude infection. The author stated that observations
of bacteriological life had determined the value of antiseptic agents, and an
interesting feature of his address was his description of the various methods
and agents used for making sterilized dressings at the present time. Accompa-
nying the address were samples of present-day surgical dressings, and, by way
of comparison, one of gauze cloth that was made in 1887. The speaker said
that this sample was the type of the first antiseptic dressing ; that in making it
cloth was impregnated with wax, rosin and carbolic acid ; and that, in the light
of present knowledge, it was as antiquated as though it were a thousand years
old. Microscopic slides of bacilli and tubes containing cultures of the harm-
less kinds were also exhibited.
Prof. Joseph P. Remington delivered an address on the " Second Pan Ameri-
can Medical Congress," which was held in the city of Mexico during the week
beginning November 16, 1896. (Seepage 15,) The speaker defined the purposes
of the Congress and gave a concise statement of the work that was accom-
plished at the recent meeting. The Congress was held under the auspices of
the Mexican Government, and all of the entertainments and social features
connected therewith were on a magnificent scale. An invitation to hold the
next meeting in Caracas, V^enezuela, in 1S99, was received from the Venezuelan
Government, and was accepted. The speaker also related some other incidents
of his trip, which were both entertaining and instructive. One thing in par-
ticular he spoke of, and that was the harmonious relations existing between
this country and Mexico. He believed that more could be done by scientists
in strengthening and promoting these relations than by diplomats or poli-
ticians.
"Spermaceti" was the subject of a paper presented by Mr. Lyman I".
Kebler. About a year ago the author made a chemical examination of a large
number of samples of spermaceti, but as a cjueslion was raised as to their
genuineness, he determined to procure, if possiljlc. samples which would fulfil
this requirement. These were accordingly procured, antl the results obtained
with them agreed in every particular, except that of specific gravity, with those
obtained with the previous samples. In the former work but one mclho^l was
employed for determining the specific gravity, anil in the latter several niethoils
54 Phar^naceiitical Meeting. {'"^January. is"™*
were applied, the figures varying with the method used. The paper was
accompanied bv specimens, and was the occasion for considerable discussion.
" Murray Red Gum, Eucalyptus rosirata, and Its Kino," was the subject of a
communication by Mr. J. H. Maiden, Government Botanist at Sydney, New
South Wales. (See page i.) This paper is not only a valuable one from the
botanical standpoint, but is of interes t as bearing on the commercial and medic-
inal products of the Australian colonies. In connection with this subject
attention was called to the following samples : Syrupus eucalypti rostrati,
made from the kino, and recommended as a valuable astringent remedy ; Eu-
calyptus red gum, and samples of oil of several species of eucalyptus. These
were sent by Mr. J. Bosisto, of Richmond, Melbourne, who is an honorary
member of this College.
Mr. Wm. B. Thompson contributed a paper entitled, " Ferruginous Pills
{Blaud's Pills):' (Seepage 17.) The writer suggested examinations of the
commercial and extemporaneous preparations for the purpose of ascertaining
the precise character of the former, and of determining wherein it differed
from the latter. He doubted whether ferrous carbonate was superior in medic-
inal efficacy to the other compounds of iron formed by the oxidation of this
constituent. He thought it was time to stop theorizing, and offered these sug-
gestions for the purpose of stimulating investigation along this line.
"The Commercial Sources of Licorice Root" was the subject of a paper by
Mr. H. N. Rittenhouse. (See page 13.) This paper was a concise statement of
the sources of commercial licorice root, together with the qualities of the vari-
ous kinds, and was mainly intended to aid the retail pharmacist in making
purchases of the article.
Mr. Chas. H. LaWall contributed the last paper, which was on "Adulterated
Japan Wax." (Seepage 18.) The facts presented by the author were timely, in
that they showed to what extent fraud may be perpetrated, and in warning
buyers against the efforts of the purveyors of the article to obtain a market for
their product. Samples of both the pure and the adulterated Japan wax were
shown.
On motion of Professor Trimble, a unanimous vote of thanks was tendered
Mr. Kilmer for his interesting address and accompanying specimens.
On motion, the meeting adjourned.
T. S. WiEGAND,
Registrar.
The tenth volume of Professor Sargent's Silva of North America was pub-
lished on the 28tli of November. It contains figures and descriptions of the
arborescent species of Yucca, which grow north of the Mexican boundary, the
Arborescent Palms of the United States, the Cupressinese and Taxaceae, and
the following genera of Coniferae : Juniperus, Cupressus (including Chamsecy-
paris), Thuya, Libocedrus, Sequoia and Taxodium. Two additional volumes
will complete the work. The eleventh, now in course of preparation, will be
devoted entirely to the genus Pinus, and in the twelfth and final volume will
be described the Spruces, P^'irs, Hemlocks, Larches and a few trees of earlier
orders which have been found since the publication of this work was begun.
— Garden and Forest.
Am. Jour. Pharm.
January. 1897
Catalogue of the Class,
ss
CLASSES
— OF THK—
PHILADELPHIA COLLEGE OF PHARMACY,
SEVENTY-SIXTH ANNUAL SESSION, 1896-1897.
FIRST YEAR CLASS LIST.
Name.
Allen, Milton Deronda,
Andrews, Willard Crandall,
Anstock, Arthur David,
Arnott, William,
Aughinbaugh, John Keely,
Bacliman, Herbert Keck,
Ball. ClifTord Arthur,
Balliet. Howard Paul,
Bamford, Melvin William,
Barker, Laura Alice.
Barker, Raymond Clark,
Barnett, Eldredge Kwing,
Bayles. John Wickoff,
Bear, Benj. vSam'l Janney,
Beddow, Llewellyn Jenkins,
Blankemeyer, Henry John,
Booth. John Henry,
Bounds, Jesse Vastine,
Bowers, Howard Lewin,
Brown, James Lawrence,
Bulger. Walter John,
Camplxjll, William Lester,
Chalquest, Gustave F)mil.
Chamberlin, William Allen,
Clark, John Hdwanl,
Cochran, Harry Barr,
Cockroft, David Ilolidav,
Collins. Mary O..
Crain, Charles Edward,
Crawford. Horace Victor,
Culbv, Walter Gibson,
Curtis, Henry.
Davis, Benjamin Winter,
Davis, Samuel Bond,
Dichl, (reorge Kdward,
Dixon, John Glaspey.
Do<lson, Henry ^Lllcolm,
Dohcrty, Harry Aloysius,
Donnelly, Clarence Kugene,
Doubler, George Hogen,
Dunn, P^lwin Alfred,
Place.
State.
Preceptor.
Med ford,
N. J.
D. W. Flemming.
Cortland,
O.
Mahanoy City,
Pa.
L. Oliphant.
Wilmington,
Del.
Jos. P. Williams.
Greenvillage,
Pa.
Eberly Bros.
S. Bethlehem,
Pa.
Luther Gerhard.
Hellertown,
Pa.
El wood Ball.
Allentown,
Pa.
John P. Frev.
Reading,
Pa.
R. P. Wilkinson.
Coalport,
Pa.
Dr. Woods
Philadelphia.
Pa.
Van Dvke Bros.
Cape Mav Citv,
, N.J.
D. C. Guthrie, ^LD.
Mt. HollV,
N.J.
Edward B. Jones.
Mt. Joy. '
Pa.
James C. Perrv.
Mahanoy City,
Pa.
M. R. Stein.
Philadelphia,
Pa.
Kennedy & Burke.
Philadelphia,
Pa.
Long 6i: Neely.
Wortham,
Tex.
P'aston.
Pa.
H. B. Sample & Son.
Philadelphia,
Pa.
R. T. Marshall & Co.
Conshohocken,
Pa.
Thos. F. McCoy.
Mt. Pleasant
la.
Frank L. Kreider.
Morristown,
N. J.
E. A. Carrell.
Indianapolis,
Ind.
Frank Morse.
Lock Haven,
Pa.
Franciscus ^: Co.
Millerstown,
F'a.
J. C. Altick .S: Co.
Phila<lelphia,
Pa.
-■\rthur S. Hollojjeter.
Atlanta.
Ga.
Springfield,
O.
G. cS: S. Coblentz.
>Iifllinburg,
Pa.
G. W. Rowland.
Philadelphia,
Pa.
Jose])!! Healy.
Minneapolis,
Minn.
(). J. Thompson, M.D.
Camden,
N.J.
(U'o. L. (;eiger & Co.
Bridgelon,
N. J.
Reeve M: 1-ithian.
Charh stown,
W. \a.
Light N: Watson.
Salem,
N. J.
J il. Lock, M.D.
Delta,
Pa.
M. L. Hollowav.
Atlantic City,
N.J.
F. F:imer Post.'
Bridgtton,
N. J.
F. Seilz. M D.
Milton,
Pa.
W. H. Galbraith.
Meadville,
Pa.
P. Heury I'tech.
56
Catalogue of the Class.
r Am. Jour. Pharm.
t January, 1897.
Name.
Egel, rrederick William,
Engler, Robert Savior,
Evans, Alex. Cornelius,
Evans, Fannie Cheney,
Falkenhainer, Charles,
Faulhaber, Gustave Adolph,
Fenncr, Harvey Albert,
Finger, Philip Charles,
Fishburn, Richard Levis,
Fleming, Arthur Bowles,
FYeeman, William Joseph,
Gasslein, Richard Joseph,
Gillan, Charles McDowell,
Grady, William Patrick,
Greisamer, Henry Franklin,
Gruel, John I{dward,
Gryning. John Francis,
Hammond, Nathan Brown,
Hance, Plovvard Ivins,
Hannum, John Lewis,
Harrison, Walter B.,
Hartman, Harry Kessler,
Hartman, Henry Loelke,
Harvey, Charles John,
Hays, Samuel Smith,
Heckman, John George,
Heineberg, Alfred,
Hess, Percy Dudley,
Hesse, Frederick William,
Hetrick, Harry Leady,
Heyke, John Kricson,
Heyl, Charles Ambrose,
Hicks, George Wellington,
High, Raymond,
Hill, George Price
Hillan, Joseph Jame",
Hoagland, Robert John,
Hoch, (2uintus,
Holland. Albert James Fowler,
Holloway, Paul P'undenberg,
Holt, Edwin Merrimon,
Hostetter, Harry Jacob,
Hottenstein, Peter David.
Humma, (J.smond Bernard,
Hungerbuehler, John Conrad,
Hunt, P^arl Robert,
Huzzard, Kurtz,
Jackson. Charles Henry,
James, Arthur Bernstein,
Jenkins, David livans,
Kaderly, Eugene John,
Keiser. I'rederick,
Kelchner, I'rederick Victor,
Kemp, Lousian Scott.
Kimberlin. P'red, William,
Kincaid, Raymond Keck,
Klusmeyer, Henry Chester,
Koch, Chri.stc)])her. Jr.,
Kraus, Wm. I'red. Constance,
Place.
State.
Bound Brook, X. J.
Temple, Pa.
Brookhaven, Miss.
Reading, Pa.
Guttenburg, la.
Loudenville, O.
S. Bethlehem, Pa.
Lancaster, Pa,
Lock Haven, Pa.
Chambersburg, Pa.
Trenton, N. J.
Philadelphia, Pa.
Chambersburg, Pa.
Philadelphia, Pa.
East Greenville, Pa.
Lancaster, Pa.
Philadelphia, Pa.
W^est Chester, Pa.
Philadelphia, Pa.
Media, Pa.
INIcKeesport, Pa,
Pensauken, N. J.
Lebanon, Pa.
Butler, Pa.
Greensburg, Pa.
Meadville, Pa.
Selma, Ala.
vS3'racuse, N. Y.
Savannah, Ga.
Altoona, Pa.
Dayton, O.
Philadelphia, Pa.
Trenton, N. J.
Norristown, Pa.
Lansford, Pa.
St. Clair, Pa,
Peoria, 111.
Philadelphia, Pa.
Philadelphia, Pa,
Mifflintown, Pa,
Goldsboro, N, C,
Reading, Pa.
Kutztown, Pa.
Reading, Pa,
Philadelphia, Pa,
Bethlehem, Pa.
Norristown, Pa.
Salem, N. J.
Kingston, N. Y.
Danville, Pa.
New Philadelphia, O,
Milton, Pa.
Fleetwood, Pa.
Dayton, Q.
Norristown, Pa.
Allentown, Pa.
Easton, Pa.
Philadelphia, Pa.
Philadelphia, Pa.
Preceptor.
Chas. L. Manning.
John B. Raser.
George Dejan.
W. C. Rowe.
James Hervey.
Gustav Appenzeller.
Campbell & Bro.
J. A. Brown.
Andrew Blair.
J, S. Barnitz.
M. Tidd,
James J. Ottinger.
P, B. White,
F, W, E, Stedem.
Emil Jungmann.
John C, Long, dec'd.
Geo. B. Evans.
Arthur B. Hammond.
R. A. Hance.
W. E. Dickeson.
J. C. Smith.
J. W. Kohlerman.
Dr. Geo. Ross & Co.
D, H. Waller.
S. Logan Waltham.
J. G. Lindemau,
Selma Drug Co.
J. LeRoy Webber.
W. M. C. Craine.
C. E. Martin,
P. M. Kelly, M.D.
A. D. Cuskaden,
W, M. Rickert.
W. M. Hill.
John M. Hillan.
B. G, Clapham,
Aquila Hoch,
Geo. Holland, M.D.
Jos. W\ England.
C. B. Miller,
Harry Bitler.
C. L. Shoemaker.
F. X. Wolf.
C. E. Keeler.
Eugene Fillman.
Harry Lippen.
J. Wohlgemuth.
Henry C. Blair.
C. Carroll Meyer.
C. A. Eckels.
Justus Schmitt.
Chas. B. Ashton.
Harvey I. Keiper.
Fred. L. Mevus.
C, A, Eckels.
Otto Kraus.
Am. Jour. Pbarra.
January, IP97.
Catalogue of tJie Class.
57
Name.
Krehl, Benjamin,
Lacy, Burdett Seldon,
Lauer, Julius Paul,
Lawton, Oliver Halton,
Lehman, Charles Luther,
Lehman, George Theodore,
Leonard, Emma,
Lincoln, John Hamilton,
Lingle, John McXit,
Lock, William,
Longstreet, Chalmer Joseph,
Love, Thomas B.,
Place.
Titusville,
Gloucester,
Millersville,
Philadelphia,
Boiling Springs,
Portsmouth,
Davisville,
Bowling Green,
Bellefonte,
Philadelphia,
Mexico,
Philadelphia,
J-
Luckenbach, Harry Windfield, Bethlehem,
McClure, Richard Terris,
McCoUin, James Garrett,
McCoy. James Edward,
McCullough, Ed. Leonard,
McDonnell. Joseph Francis,
McElwain, William Thomas,
McEall. John Allen,
McGarrah, William Henr}-,
McGuire, Thomas Edward,
McKane. Francis Joseph,
McKeever, William Henry,
MacMurray, Annie,
MacPherran, Ivan LeRoy,
Maghee, Griffith Holme,
Malone, Charles FMward,
Wilmington,
Philadelphia,
New York,
Salladasburg,
Centralia,
Chambersburg,
Charleston,
Scranton,
Mahanoy City,
Philadelphia,
Philadelphia,
Upland,
Pittsburg,
Rawlins,
Philadelphia,
Matlison, Richard Van Selous, Jr., Ambler,
Meister, Samuel Emil,
Meredith, Harry Lionel,
Mervine, Graydon Duncan,
Metzger, Chiis. Washington,
Mitchel, F^lward,
Mooney, I'rank,
Mountain, Lloyd Lott,
Moury, Joseph Daniel,
Mutly, Walter Clement,
Nicklas, David Ivlward,
Norris, Clarence Augustus,
Orf, George Marion,
Orr, James Alexander,
Osterlund. Otto William,
Patrick, William Smith,
Pechin, Ivdward Charles,
Pflieger, FUlwoo<^l Keech,
Phillips, John Henry,
Pile, Wilson,
Popp, .\ndrew Martin Ralph,
Potts, Samuel Lawrence,
Price, .Vrthur Chew,
Pullen, Ro«lney Woolston,
Radefeld, Robert,
Rains, FMward Lee,
Ranck, David Walter,
Reice, William.
Reigel, M. Calvin,
Reinhart, Robert Lucian,
Lancaster,
Hagerstown,
Milton,
Abbottstown,
Philadelphia,
Philadelphia,
Confluence,
Shamc^kin,
South Hrt-wer,
Chambersburg,
Manasquan,
Philadelphia,
Philadelphia,
Kinekulle,
Salem,
Philadelphia,
York,
Red field,
Philadelphia,
Reading,
Newtown,
Wilmington,
Camden.
Philadelphia,
Mein])his,
Phila«lelphia,
Bloomsl)urg,
Linglestown,
Shepherdstown,
State
Pa.
N.
Pa
Pa.
Pa.
O.
Pa.
O.
Pa.
Pa.
N. Y.
Pa.
Pa.
Del.
Pa.
N. Y.
Pa.
Pa.
Pa.
S. C.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Wv.
Pa.
Pa.
Pa.
Md
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Me.
Pa.
N.J.
Pa.
Pa.
Sweden.
X.J.
Pa.
Pa.
N. Y.
Pa.
Pa.
Pa.
Del.
N. J.
Pa.
Tenn.
Pa.
Pa.
Pa.
W. Va.
Preceptor.
Theo. W. Renting.
Wm. E. Lee.
C. E. Keeler.
Lawson C. Funk.
R. T. Blackwood.
Fisher & Streich.
J. C. Lincoln.
F'. Potts Green.
James Huston.
Norval D. Hart.
Bullock & Crenshaw.
Simon Rau 6s: Co.
N. B. Danforth.
Wm. H. Milliken.
H. G. Shinn.
G. W. Davis.
Charles D. Keefer.
A. C. McClennan, M.D.
F. W. F:. Stedem.
Shenandoah Drug Store.
Wm. H. Farley.
Thos.G. Maghee, M.D.
R. V. Mattison, M.D.
James F. Ro>s
D. C. Auginbaugh & Son.
J. S. I-ollmer, M.D.
A. Dalton.
E. R. Gatchel.
F. Schwartz, M.D.
W. S. Mountain. M D.
L. W. Hensvl, >LD.
F. W. K. Sledem.
J. S. Barnitz.
.\ndrew Blair.
J. V. Slaughter, M.D.
Theo. Cam])bell.
W. Henrv Dunn.
G. J. Pfchin.
Dale, Hart vS: Co.
Wm. H. Phillips.
Gustavus Pile.
John B. Raser.
Richard W. Livezey.
Joseph C. Roberts.
J. S. Haer. >LD.
Fred. Radefild.
Jas. S. Robinson.
J. W Ranck, M.D.
Jas, H. Mercer.
G. n. Evans.
S. I*. Loughridgc.
58
Name.
Revnolds. Alver Carroll,
Rh'oads. Robert Elliott,
Rice, Albert Ainsworth,
Robbins, Edward Cruise,
Roesstier, Benjamin,
Rogers, Edward Bancroft,
Ross. Dell Noblitt,
Rossell, Edward Wood,
Ryan, William Stephen,
Sample, James Turner,
Savior, Byron Centennial,
Schreiner, Charles Herman,
Schwaenmile, Fred. Philip,
Seitz, John Alphonsus,
Seubert, Charles Aloysius,
Shannon, Samuel Coward,
Sh^iro, Henry,
Sheehan, William Henry,
Shirey, Orville Ludwig,
Shoffner. John Perry,
Simcox, Howard Leon,
Sipes, Clarence Lessly,
Skinner, Clarence Russel,
Sleifer. Jay Ward,
Smith, Chas. El wood Rupert,
Smith, George Carroll,
Smith, Silas Alfred,
Smith, Wellington Gordon,
Snyder, Herman Hugo,
Stable, Robert Xevin,
Stancill. George Walter,
Stang, Peter,
Steel, Chalmers Alexander,
Stern, Wilson C. A.,
Stinson, William vSamuel,
Stout. Philip Samuel,
Strode, Richard Clark,
Suhn, Minnie,
Tanzola, Angelo,
Turner, Kenneth Beymer,
Turner, Joseph Constant,
Turner, James Deaver,
Tye, Frank John,
Van Dyke, James Wiiber,
Van Senden, James,
Wagner, Charles, Jr.,
Waite, William Crigler,
Walters, I'red. Robert,
Warrington, Henry,
Watson, James Nathaniel,
Weakley, William Stair,
Wehn, Clyde P)dwards,
Wenner. Ilarvey PUitjene,
West, Katheriiie Powell,
Wiiber, John Arthur,
Wf.lf, Charles.
Wright. John Franklin,
Wyckoff, Elmer Leroy,
ilogue of the
Class.
/Am. Jour. Pharm,
I January . 1897.
Place.
State.
Preceptor.
Rising Sun,
Md.
C A. Eckels.
Reading,
Pa.
Irviu J. Brandt.
P'lemington,
N.J.
Franklin C. Burk.
Glassboro,
N.J.
F. G. Thoman.
Philadelphia,
Pa.
Decatur Milligan.
Mt. Holly,
N.J.
Elmer D. Prickitt.
Rosemont,
Pa.
Frank W. Prickitt.
Springfield,
N.J.
Charles B. Mathis.
Philadelphia,
Pa.
Albert D. Forrest.
Roaring Spring,
, Pa.
C. J. Biddle.
Annville,
Pa.
Henrv T. Hayhurst.
Philadelphia,
Pa.
L.W. Hildenbrand, M.D.
Philadelphia,
Pa.
E. H. Fienhold.
Wilmington,
Del.
Z. James Belt.
Lebanon,
Pa.
John F. Loehle.
Philadelphia,
Pa.
D. M. Harris.
Vitebsk,
Russia.
F. W. E. Stedem.
Philadelphia,
Pa.
H. M. CampbeU.
Chambersburg,
Pa.
Cressler & Keefer.
Xorristown,
Pa.
Harrv H. Stallman.
Philadelphia,
Pa.
G. W. Bo wen, M.D.
McConnellsburg, Pa.
W. H. Perkins, M.D.
Chambersburg,
Pa.
Samuel E. Wagaman,
Philadelphia,
Pa.
J. A. Wamsley, M.D.
Philadelphia,
Pa.
Shoemaker & Busch..
Pottstown,
Pa.
C. A. Smith.
Philadelphia,
Pa.
Wm. ISIcCorkle.
Lykens,
Pa.
A. B. Schminky.
Philad-lphia,
Pa.
Frank C. Davis.
Gettysburg,
Pa.
Jesse W. Pechin.
Selma,
N. C.
G. T. Williams.
Philadelphia,
Pa.
Henry Mueller, M.D.
Huntingdon,
Pa.
H. E. Steel.
S Bethlehem,
Pa.
D. B. Richards, M.D.
Titusville,
Pa.
Geo. B. H. Brown.
Quakertown,
Pa.
Oliver Stout.
Philadelphia,
Pa.
Funk & Groff.
Vitebsk,
Russia.
Marcus Peisakhovitch.
Philadelphia,
Pa.
Victor Michelotti.
Washington,
D. C.
Philadelphia,
Pa.
W. F. Steinmetz.
Baltimore,
Md.
Gordon,
Pa.
'j. E. Gregory.
Hightstown,
N.J.
H. G. Rue.
Philadelphia,
Pa.
Philadelphia,
Pa.
J. A. Fajans, M.D.
Culpeper,
Va.
R. B. Macoy.
Philadelphia,
Pa.
Philadelphia,
Pa.
C. W. Warrington.
Elizabethtown,
Pa.
Henrv C. Blair.
Vork,
Pa.
J. J. Weakley.
Johnstown,
Pa.
Charles Young.
Allentown,
Pa.
Geo. D. Feidt.
Xorristown,
Pa.
Jos. C. Roberts.
Malone,
N. Y.
A. A. Allen.
Philadelphia,
Pa.
S. K. Loder.
Caiion City,
Col.
Hunter Palmer.
Ithaca,
N. Y.
Fred, H. Blackmer.
Am. Jour. Phamj.i
January, 1897. /
Catalogue of the Class.
59
Name.
Young, Annie Hawkins,
Zeller, Earl Emanuel,
Ziegler, Chester Winsor,
Place. State. Preceptor.
Henderson, X. C. Geo. B. Evans.
Mifflinburg, Pa. James Kleckner.
Gettysburg, Pa. Shinn ^: Baer.
SECOND YEAR CLASS LIST.— 1896-97.
Name.
Abrams, I-'rederick Arthur,
Albert, Harry Clay,
Albright, Charles Henr\',
Anderson, George Charles,
Baer. Lemuel ^Iiles,
Bartholomew, .\rthur,
Beane, George Ridenour,
Beardsley, Carolyn Frances,
Berbericii. Herman,
Berry, Robert Taylor,
Beyerle, Charles Wellington,
Bishop, David Kerlin,
Black, Robert Morris,
Bloor, Alfred Wainright,
Booth, Thomas,
Brach, Cornelius,
Bradford, Edward Burton.
Bready, William Ramsey. Jr.,
Brennan, Thomas Francis,
Brewton, Swain Hoffman,
Brown, Hampton Housman,
Buckingham. Harry Sheldon,
Calloway, Harry Willis,
Cassel, Oscar Heebner,
Cohen. John Thomas,
Coleman. John FMward,
Cooper, Walter Greenlee,
Cox, Lin wood,
Cunningham, Orrick Sim,
Dale, David,
Davis, George I-'ckley,
DeBeust, William Hare,
Decker. William Robert,
DeHaven, Ida Valeria,
Dirmitt, Charles Walter,
Downing, William Henry,
Dubell, Alexander,
Eason, David Clark,
Estlack, Walter Forrest,
Evans, Abner Thomas,
Evans, Samuel, Jr.,
Farrow, I'rederick Reeves,
Felty, Harvey Long,
F'ishcr, Samuel Keim,
Fleming, John Halbert,
Foltz, Ivdgar Daniel (irant,
Friel)ely, Harry luigene,
Funk, Robert Rowland,
Place.
Philadelphia,
Maysville,
Philadelphia,
Meadville,
Lancaster.
Golden City,
Bainbridge,
Chicago,
Baden,
Charlestown,
Bernville.
Mifflintown.
Philadelphia,
Manor,
Philadelphia,
Kerzenhcim,
Newport,
Philadelphia,
New London,
Cape May City,
Pleasant Grove
Clayton,
BaltimoT e,
Norristown,
Chester,
Carbondale,
Savannah,
Norristown,
Clear S])ring,
Philadelphia,
Eckley,
Philadelphia,
York,
Bayonne,
Philadelphia,
Wilmington,
Mt. Holly,
Brookville,
Philadelphia,
Greensburg,
Circleville,
Philadelphia,
Palmvra,
Litit/,
Mi-dia.
Hflhlchem,
S. Hethlchem,
Hagerstown,
State.
Pa.
Kv.
Pa.
Pa.
Pa.
Col.
Pa.
111.
Germany.
W. Va'.
Pa.
Pa.
Pa.
Tex.
Pa.
Germany
N.J. '
Pa.
Conn.
N. J.
Pa.
X. J.
Md.
Pa.
Pa.
Pa.
Mo.
Pa.
Md.
Pa.
Pa.
Pa.
Pa.
N.J.
Pa.
DeL
N.J.
Pa.
Pa.
Pa.
O.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Md.
Preceptor.
John Wyeth & Bro.
John P. Frey.
A. L. Ballinger.
Breidinger & Comber.
J. W. Higgins.
H. C. Blair.
James MofTet.
P. H. Franklin.
E. M. Boring.
W. G. Nebig.
P. M. Kelly, M.D.
Alexander Wilson.
W. E. Miller.
\. La Dow.
A. J. Frankelberger.
W. Higbee Whitcomb.
W'm. Porter.
B. L. Brown, M.D.
H. G. Shinn.
H. Browning.
William vStahler.
R. H. Henderson.
Geo. V. Eddy.
J. P. Cooper.
Atwood Veakle.
George W Hurd
John Wyeth 8: Bro.
Charles J. Schneider.
R. H. DeBeust, M.D.
R. Wm. Ziegler.
C. H. Dirmitt. M.D.
N. B. Dan forth.
R. C. Barrington.
Shinn vS: Baer.
H. W. Ivsllack.
S. P. Brown.
pA'ans ^y: Kimmel.
F'bcrlv Bros.
A. CHersh.
J. C. Broh^t. M.D.
A. W. - v,dec'd.
N. B. i n.
HA Bur k hart, M.D.
Blew ^c Luca.s.
6o
Catalogue of the Class.
Am. Jour. Pharm.
January, 1897.
Name.
Gag;e, Porciiis Silkinan,
Geitrer. Kdward George,
Gibb, Andrew,
Gladhill, James White,
Greer, Mary C,
Groff, Harry Musselman,
GrofT, William,
Grunden, Percival Edward,
Guth, Herbert Wallace,
Hans, Ralph Leonard,
Heintzelman, Joseph August,
Helmbold, Anna Palmer,
Heverly, Frederick Chase,
Hoffman, William Anthony,
Hubbert, William Ernest,
Hudson, Harr}-. Jr.,
Hukill, Oscar k.,
Huntington, Joseph,
Jenkins, Frank Huston,
Joffe, Jacob Leopold,
Kain, John Kauffman,
Keen, George Carll,
Keen, Geo. Samuel Jacob,
Keenan, John Joseph,
Keim, Joseph Paxson,
Kepner, Weldon vStover,
King, James David,
Kintzer, Harry Augustus,
Kirby, Frank Brennand,
Kohl, George ]\Iichner, Jr.,
Krewson, William Egbert, Jr. ,
Kyser, George Herbert,
Latchford, Orwan Luther,
Lee, Walter Evan,
Lefever, John Matthew,
Lerch, William Abraham,
Levy, Joseph Jacob,
Lindig, Charles Warren,
Luebert, August Gustav,
:McCleary, Harry Walter,
Mahoney, J. Norris,
Mathers, Grace,
Met/.ler, Walter Scott,
Midflleton, Claude Ruoff,
Miller, William I-'rederick,
Mills, John Leopold,
Monaghan, Thomas Francis,
Monroe, William Robeson,
Morell, Charles Joseph,
Morgan, I'rank William,
Mountain, Lloyd Lott,
Xey, Howard Jacob,
Obear, Josiali Julian,
Otto, Glenn Frazier,
Page, (ieorge Ralph,
Parse, Andrew Con net,
Perse, James Woodlock,
Pettebone, Thomas J.,
Preston, Gilbert Kent,
Place.
State.
Vineland,
N.J.
Peoria,
111.
Lock Haven,
Pa.
Jersey Shore,
Pa.
Philadelphia,
Pa. ]
Lancaster,
Pa.
Quarryville,
Pa.
Steelton,
Pa.
Allentown,
Pa.
Mifflinburg,
Pa.
Philadelphia,
Pa.
Philadelphia,
Pa.
Wilkes-Barre,
Pa.
Renovo,
Pa.
Hico,
Texas.
Philadelphia,
Pa.
Hot Springs,
Ark.
Philadelphia,
Pa.
Hanover,
Pa.
Kovno,
Russia,
York,
Pa.
Vineland,
N.J.
Wiconisco,
Pa.
Philadelphia,
Pa.
Bristol,
Pa.
Shippensburg,
Pa.
Easton,
Pa.
Womelsdorf,
Pa.
Philadelphia,
Pa.
Jenkintown,
Pa.
Philadelphia,
Pa.
Richmond,
Ala.
Markelsville,
Pa.
Vineland,
N.J.
York,
Pa.
Allentown,
Pa.
Philadelphia,
Pa.
Lewisburg,
Pa.
Philadelphia,
Pa.
Carlisle,
Pa.
Bridgeport,
Pa.
Philadelphia,
Pa.
Baltic,
O.
Philadelphia,
Pa.
Erie.
Pa.
Cardington,
O.
Philadelphia,
Pa.
P'resno,
Cal.
Philadelphia,
Pa.
Pass Christian,
Miss.
Confluence,
Pa.
Harrisburg,
Pa.
W^innsboro,
S. C.
La Crosse,
Wis.
vScranton,
Pa.
I'lemington,
N. J.
Plymouth,
Pa.
Dorranceton,
Pa.
Philadelphia,
Pa.
Preceptor.
F. H. Vonachen.
W. C. Franciscus.
George M. Beringer.
, K. Richardson, M.D.
C. W. Warrington.
T. M.Rohrer, M.D.
G. A. Gorgas,
Peters & Smith.
W. H. F. Vandegrift.
Jos. A. Heintzelman.
F. W. E. Stedem.
R. D. Williams.
E. T. Swain.
W. E. Hubbert.
Wm. C. Walter.
Andrew Blair.
J. C. Perry.
J. L. Emlet.
E. J. Lupin.
J. B. Kain, M.D.
J. J. Ottinger.
C. D. Christman, M.D.
J.J.Burk.
Enilen Martin.
J. C. Altick & Co.
Rowland Willard.
F. T. Landis.
Lawson C. Funk.
Thos C. Coltman.
Wm. E Krewson.
G. W. Kyser.
D. H. Ross.
Bidwell & Co.
S. M. Gable.
Peters & Smith.
J. H. B. Amick, M.D.
H. N. Hoffman.
David A. Over.
J. E. vSipe.
E. A. Stabler.
Susan Havhurst. M.D.
A. S. Metzler, M.D.
Shinn & Baer.
Wm. Fischer.
A. C. Schofield.
H. D. Stichter, M.D.
G. H. Monroe.
Chas. M. Morell.
Wm. Greve.
W. S. Mountain, M.D.
Chas. F. Kramer,
O. Y. Owings.
Oscar Houck.
Horatio M. Cole.
J. Sherman Cooley.
J. V. Perse.
C. \Y- vSpayd, M.D.
David Preston.
Am. Jour. Pharm,
January, 18i>7.
Catalogue of the Class.
6\
Name.
Putt, Milton Thomas,
Raker, John Wilson
Randolph, Edward Fitts,
Richardson. James,
Ringer, Lewis Johnson,
Rinker, Henry Paul,
Ritz, Charles August,
Roberts, DeWilton Smith,
Rose, Frank,
Ross, Annie Catherine,
Sausser, Howard Elmer,
Schlauch, Theodore Storb,
Scott, Emma Love,
Seiberling, Joseph Dallas,
vSheitz, Lloyd A.,
Shemp, Russell Nicholas,
Shwab, George Augustus,
Sieber, Isaac Grafton,
Slobodkin, Rose,
Smith, Alfred Homer,
Smith, Benjamin James,
Suavely, Clarence Osborne,
Snyder, John Paul,
Steinmetz, William Baer,
Stimus, Howard George,
Stokien, Francis Joseph,
Stott, Horatio Allen,
Strawinski, Jacob Franklin,
Swartley, Harry Mahlon,
Thomas, Frank Hartwell,
Thompson, Henry Kirk,
Thompson, Harry Merril,
Tomlinson, George Walton,
Troth, Finest Augustine,
Tyler. William Walston,
Underwood, James Harris,
Waldner. Herman Theodore,
Walter, William liell,
Wilt, Geo. Washington, Jr.,
Winkler. Oscar Charles,
Winslow, John Hayes,
Wiza, Joseph Louis,
Zane, William Spence,
Zimmeniian, Thos. Edmonds,
Place.
Lebanon,
Pillow.
Plainfield,
Pickering.
Hagerstown,
Hellertown,
Ashland,
Xorristown,
Philadelphia,
Philadelphia,
Schuylkill Hav
New Holland,
Richmond,
Hvnemansville
York,
Philadelphia,
Nashville,
Harrisburg,
Minsk,
Smyrna,
Trenton,
Lebanon,
Lancaster,
Ephrata,
Moorestown,
Charleston,
Coatesville,
York,
Philadelphia,
Yaldosta.
Titusville,
Selins Grove,
Rydal,
Palmyra,
Onancock,
Woodbury,
Ashland,
Gettysburg,
F'lemingsburg,
Philadelphia,
Vineland.
Philadel])hia,
Seabright,
Carlisle,
State.
Pa.
Pa.
N- J.
Out.
Md.
Pa.
Pa.
Pa.
Pa.
Pa.
en. Pa.
Pa.
Ya.
, Pa.
Pa.
Pa.
Tenn.
Pa.
Russia,
Del.
N.J.
Pa.
Pa.
Pa.
N. J.
S. C.
Pa.
Pa.
Pa.
Ga.
Pa.
Pa.
Pa.
N J-
Ya.
N.J.
Pa.
Pa.
Ky.
Pa
N.J.
Pa.
N.J.
Pa.
Preceptor.
\\\ B. Means
Chas. H. Tatem.
L. W. Randolph.
Geo. Y. Wood.
M. L. Bvers & Co.
C. W. Albright.
A. Schoenenberger.
O. F. Lenhardt.
G. W. Bo wen.
W^ E). Supplee.
John B. Raser.
C. J. Seltzer.
Susan Hayhurst, M.D.
Frank Morse.
Harrv A. Hav.
\V. E' Supplee & Bro.
J. Wilson Hoffa.
Susan Hayhurst, M.D.
Wm. F. Dunn.
Aquila Hoch
Wm. G. Shugar.
W. T. Hock.
G. S. Rover
G. H. W'ilkinson.
R. P. Wilkinson.
W. S. Young.
Dale, Hart & Co. "
Y. P. Streeper.
R. C. Cadmus.
T. C. Tomlinson.
S. T. Hamberg.
Shoemaker & Busch.
George B. F'vans.
W. S. Reeve.
T. H. Strouse.
H. C. Blair.
John J. Reynolds.
Milton S. Apple.
A. C. Taylor.
A. A. Pochner.
G. B. Minton.
B. F. Emrick.
SENIOR CLASS LIST.— 1896-97.
Xame.
Althouse, Harry B.,
Anderson. Ralph.
Baker, Newton Claire,
Barth, Charles.
Place.
Harrisburg,
I^atrobe,
Sunbury,
Philadelphia,
Bartholomew, Claude Lafayette, Bath.
Bates, John Phillips, Mansfield.
Becht. Frederick, Philadel])hia,
Beh, Edward, Philadelphia,
State.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Preceptor.
F. J. Althou.se.
R. T. Blackwood.
Charles Leedom.
W G. Nebjj^'.
Peters & Smith.
J. M. Smith.
Bullock ^: Crenshaw
David J. Reese.
62
Catalogue of tJie Class.
Am. Jour. Pharm.
January, 1897.
Name.
Breilliaupt, Alphons Peter,
Brown, Roscoe James,
Briieckmann, Walter,
Brumbaugh, Albert Sylvester,
Carson, James Thompson,
Clapp, Samuel Clarence, Jr. ,
Clark, Kdward B ,
Clark, Robert Hall,
Cloud. Norman Henderson,
Codori, Simon Jacob, Jr.,
Compton, Richard Hal,
Cooper, Morris,
Cope, Edward Kreidler,
Cornell Horace Hogeland,
Craig, Ralph Butz,
Criswell, Edward Ott,
Deibert, William Henry,
Eckels, Frank Huston,
Eddy, Volora Doolittle,
Entwistle, Albert Henry,
Eschbach, Clarence Derbie,
Failing, William Clark,
Farley, Levi James,
Few, Colin Spangler,
Filer, Bunitt Boynton,
Frederici, John Koch,
Funches, Cardoza Marion,
Garrison, Joseph Miller, Jr.,
Gessford, Otice Eugene,
Godshall, Samuel R.,
Place.
Philadelphia,
Oxford,
Philadelphia,
Mansfield,
Philadelphia,
INIilton,
Reading,
Union City,
West Chester,
Gettysburg,
Allen,
Friedensburg,
Philadelphia,
Newtown,
Allentown,
Waynesboro,
Northampton,
Carlisle,
S. Chester,
Philadelphia,
Milton,
Albany,
Chester,
Middletown,
Hammonton,
Auburn.
Rowesville,
Elmer,
Lippincott,
Soudertown,
Goodfellow, Charles Rumney, Philadelphia,
Grakelow, Ralph,
Gross, Paul Herbert,
Harry, Hamilton Maxwell,
Hebden, William.
Heim, Christian, Jr.,
Hildfbrand, Howard Ovid,
Hill, William Maurice,
HofTman, William Shalter,
Horst, Harry Lewis,
Hostellcy, John Jos. hVancis,
Howard, Horace Emory,
Howell, Plarvey I'ield,
Hundertmark, John Charles,
Ingling, Howard Ivdgar,
Jacoby, William Lawless,
Jaeger, Charles I'rederick,
Janisch, Frederick Wm.,
JelTeris, David Strode,
Jennings, Isaac Astor,
Johns, I'rank James,
JoUey, John James,
Kessler, Lawrence Anthony
Tower City,
York,
Conshohocken,
Philadelphia,
Philadelphia,
York,
Lansford,
Danville,
Lock Haven,
Collingdale,
S. Hadley,
Easton,
Cleveland,
Riverton,
Philadelphia,
Philadelphia,
Philadelphia,
Philadelphia,
Philadelphia,
Pleasant Mount
Philadelphia,
Logan,
J-
State.
Pa.
Pa.
Pa.
O.
Pa.
Pa.
Pa.
Ind.
Pa.
Pa.
Tex.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
N. ^
Pa.
Pa.
N.
Pa
S. C
N.J
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Mass
Pa.
O.
N.J.
Pa.
Pa.
Pa.
Pa.
Pa.
, Pa.
Pa.
O
Kirlin, Chas. Coleman Hagenbach Shenandoah, Pa.
Kf)ehler, George,
Konover, Harold Doble,
Kramer, CVeorge Henry,
Ku])fer, John Harry,
Langham, John Williams,
Philadelphia,
Trenton ,
Philadelphia,
Butte City,
Philadelphia,
Pa.
N.J.
Pa.
Mont.
Pa.
Preceptor.
George H. Ochse.
W. T. J. Brown.
E. W^ Herrmann.
Silas Shull.
Dr. Meredith.
C. E. Stout.
F. X. Wolf.
J. P. Frey.
Luther Gerhard.
J. M. Hillan.
Geo. F". McKinstry.
G. D. Borton.
F. H. Cope.
Robert Gleuk.
Kennedy & Burke.
J. W. Harrigan.
J. H. Stermer.
J. B. Moore.
A L. Castle.
Chas. H. Roberts.
JohnS. Follmer, M.D.
H. C. Blair.
Wm. H. Farley.
Geo. B. Evans.
J. F. Meade, M.D.
E. F. Haenchen.
J. M. Hillan.
Theodore Campbell.
Funk & Groff.
Smith, Kline & French Co.
E. M. Wallington & Co.
Ira P. Amick.
R. Wm. Ziegler.
Jas. W. Harry.
Caleb Scattergood.
Henry Mueller, M.D.
A. H. Lafean & Bro.
Wm M. Hill.
G. C. Devine.
T. C. Hilton & Co.
T. W. Hargreaves.
J. J. Ottinger.
Geo. B. Evans.
Acker Bros.
Milton Cowperthwaite.
Bullock & Crenshaw.
E. E. Bostick.
F. H. Davis.
Funk & Grofif.
Theodore Campbell.
H. C. Blair.
F. M. Apple.
E. F. Kessler.
P. P. D. Kirlin.
E. F". Kaempfer.
D. W. Baker.
Robert McNeil.
C. W. Newton, M.D.
E. B Kyle.
Am. Jour. Pharm.
January. 1897.
Catalogue of the Class.
63
Name. Place.
•Laughlin, Albert Russell, Newville,
Lenhart, Enos Samuel, Philadelphia,
Levan, Walter, Nuniidia,
Lewis, Daniel William. Catasauqiia,
Liebert, Charles Frederick, Philadelphia,
Lincoln, George Washington, Philadelphia,
IvOngshaw. Thomas Elmer, Philadelphia,
Luhr, Frederick A., St. Marys,
Lukens, Charles Baker, Philadelphia,
MacKride, W^illiam Vaiighan, Jr., Philadelphia,
McGehee, Hanford Bell, Staunton,
McNeil, Thomas Hunter,
Malin, George Lawrence,
Matusow, Harn^-,
Metzler, Claude Dallas,
Morgan. Clayton Edward,
Morse, Thomas,
Mueller, Charles August,
Nebel, Charles William,
Parry, Edward,
Parry, William Hough,
Pasold, Julius Martin,
Pearce, Sanmel Robert,
Peiffer, Charles Oscar,
Peterson. Walter Nickerstaff,
Pierson, Wm. Harry. Jr.,
Pipes. William Henry,
Praul, Walter I'rancis,
Prosser, David Davis, Jr., _,
Punt, Arnold Anthony Joseph, Philadelphia,
Reese, John Bull, Centralia.
Reifsnyder, David Ernest, X. Heidelberg,
Rieben, Ernest, Philadeli)hia,
Robertson, Henry Edward, Jr., Philadelphia,
Philadelphia,
Atlantic City, X.
Minsk,
Harrisonville,
Lynn,
Montgomen.-,
Philadelphia,
Philadelphia,
Cramer Hill,
Xewtown,
Joliet,
Manasquan,
Morton,
Philadelphia,
Wilmington,
Millington,
Philadelphia,
Hellertown,
Roth, Frans Johan,
Rowe. Thomas Maurer,
Seipel, Harry Bertram,
Smiley, Geo. Washington,
Smiley, Laura ^L1rgucrite,
Smith, Justin Tone,
Sny<ler, Harry Lamar,
Stommel. Henry Aloysius Jos.,
Strayer, Otho O'Burn,
Streeper. Austin.
Swinehart, Daniel Harrison,
Test, Ivllwoo<l Allen,
Tobias, Is.'iac Herbert,
Toelke, Cliarles,
Troxell, John Isaac Peter,
Tyson, Warren Sunderland,
Watson, Joseph Shaffer,
Weber, Howard Elmer,
Weiss, Hervev Beale,
Weit/el, Sue C.,
Wells, James Ralston, Jr.,
Went/.ler. Hartman Gotthanl,
Wet/el, S.imuel,
Wilson, Oliver I'awcett,
Winger, John Bowman,
Yates, John Julius, Jr.,
Lund,
Reading,
Philadelphia,
Philadelphia,
Philadel])hia,
Windsor,
Aniiaiid tie,
Doylestown,
Wilmington.
Xorristown,
Pottstown,
Philadelphia,
Canal Winchester, O.
Philadel])hia,
Allentown,
Xorristown,
Mt Holly,
Mahanoy City,
Philadelphia,
Greensburg,
Philadelphia,
Muncv,
Carli-sie.
Pittsburg.
Philadelphia,
Wilmington,
State. Preceptor.
Pa. B. F. Emrick.
Pa. Harry E). Jones.
Pa. J. E. Gregory.
Pa. Wm. H. Faunce.
Pa. A. G. Keller.
Pa. Howard G. Shinn.
Pa. Henrv Sunderland, ^LD.
Pa. A.'Mulhaupt, ^LD.
Pa. D. A. Over.
Pa. W\ F Seiler.
\'a. Lawson C. I'unk.
Pa. Robert C. McXeil.
Willard W^right. M.D. ( dec'd).
Russia C. H. Bohn.
J. A. I'erguson.
Frank E. Morgan.
H. G. Eakin.
Alex. G. Keller.
A. S. Hollopeter.
W. H. Kensinger.
M. B. Fretz.
H F. Voshage.
Andrew Blair.
J. ^L Sharp.
C. W. Shull.
J. S. Beetem.
Dr. Todd.
J. H. Masholder.
J. Howard Evans, >LD.
W. H. Pile cS: Sons.
Geo. W. Davis.
Wm. P:. Donough, M.D.
A. A. G. Starck, M.D.
Shinn ^: Baer.
E. W. Shaq).
B. A. Hertsch.
Leidy Seipel.
F:. R. Smiley, M.D.
E. R. Smiley, >LD.
W. .A.. Rumsev.
H. A. Xolte. '
E. M. Boring.
A. W. Tavlor, M.D.
H. R. Stallman.
L. L Shuler.
John H. Kerr.
Shinn cS: Baer.
Pa. I'rank \\. Morgan.
Pa. J. Iv. Bennett, >LI).
Pa. .\twood Vcakle.
X. J. Wm F. Simes ^c Son.
Pa. M. R. Stein
Pa. Bullock ^: Crenshaw.
Pa. Susan Hay hurst. .M.D.
Pa. Bullock iS: Crenshaw.
Pa. John W. McLeer.
Pa. W. F. Horn.
Pa. v.. F. Kessiler.
Pa W. L. Hartzcll.
Dil. H. K Watson.
Pa.
Mass.
Ala.
Pa.
Pa.
X.J.
Pa.
111.
N.J.
Pa.
Pa.
Del.
Md.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Pa.
Sweden.
Pa.
Pa.
Pa.
Pa.
Vt.
X.J.
Pa
Del.
Pa.
Pa.
Pa.
64
Catalogue of the Class.
Am. Jour. Pharm.
January. 1897.
LIST OF SPECIAL STUDENTS.— 1896-97.
Name.
Bailey, Esther,
Carrington,Thos. Specs, M.D,
Case, Luella. Ph.Cx.,
Cheney, Millwood C,
Collings, Walter Xagle,
De Graffe, Bertha Leon, Ph.G
Frislimiith, H. H.,
Heckeroth, William Conard,
Hoft, William Irving,
Ketterer, Martin, Ph.G.,
Kinzey, Calvin Otto,
Krider, C. Richard,
Leas. Fred. C, B.S.",
Mavs, Edmund Anstie,
Post, Edward Meigs, Ph.G.,
Rowe, William C, Ph.G.,
Silverthorn, Alfred P.,
Stroup, Freeman Preston, Ph.G
Suhr. Charles Louis,
Toplis, William G.. Ph.G.,
Tucker, Stephen Allen,
White, William Clements,
Place.
State.
KiefF,
Russia,
Philadelphia,
Pa.
Delaware,
0.
Brooklyn,
N. Y.
Philadelphia,
Pa.
Albany,
N. Y.
Philadelphia,
Pa.
Philadelphia,
Pa.
Philadelphia,
Pa.
Philadelphia,
Pa.
Cumberland,
Md.
Philadelphia,
Pa.
Philadelphia,
Pa.
Philadelphia,
Pa.
Chester,
Pa.
Philadelphia,
Pa.
Ridley Park,
Pa.
r.. Rouseville,
Pa.
Oil City,
Pa.
Philadelphia,
Pa.
Philadelphia,
Pa.
Philadelphia,
Pa.
Department.
Pharmacy.
Chemistry.
Chemistr}-.
Chemistry.
Chemistr3\
Chemistry.
Chemistry.
Chemistr3\
Chemistr^^
Chemistry.
Chemistry.
Chemistry.
Chemistry.
Chemistry.
Chemistry.
Chemistry.
Chemistry.
Chemistry.
Chemistry.
Chemistry.
Chemistry.
Chemistry.
THE AMERICAN
JOURNAL OF PHARMACY
FEBRUARY, iSgj.
ON THE VOLUxMETRIC ESTIMATION OF ACETONE.
Bv Lyman F. Kebler,
Since the modern developments in the manufacture of acetone, the
application of this product has been developed in many directions.
As a solvent its uses appear to be almost unlimited, in both analy-
tical and technical operations. Ethyl alcohol, wood alcohol, ether
and acetic ether have been displaced by it in many instances, not
only as being a more economical solvent, but a better general solv-
ent. Prof. S. P. Sadtler' has proposed its use for the technical anal-
ysis of asphalt ; C. Kippenberger- has employed it as a solvent in
volumetric determinations of alkaloids by means of Wagner's rea-
gent ; and H. Trimble and J. C. Peacock'' have used it in the pre-
paration of tannic acid. These are only instances of the possibilities
of acetone.
Now, it can reasonably be expected that the manufacture of this
product will be materially cheapened in due time, and, with this
cheapening, samples of various degrees of purity will be met with ;
then the analyst will be called on to devise ways and means for
deciding in favor of the deserving products.
At present, we are not in position to determine the acetone, or
dimethyl ketone, in various mixtures with accuracy. The commer-
cial acetone generally contains bodies, besides acetone, that respond
to the iodoform reaction, on which all of our analytical methods are
' 1-^95. /• Frank. Inst., 140. 383. •
' 1896, Zlschr. anal. Chctn., .m. 10, aud 422.
' 1893, Am. J. PiiARM., ea, 435 ; /V<><. ./;//. Phatm. Assoc, 41, iia
(65)
66 Vohimetric Estimation of Acetone, {^Y^^r^lxyAm^'
based. The writer examined a sample of acetone that contained 6
per cent, of material (higher ketones?) that possessed a boihng
point of 80" C. and above ; yet it proved on analysis to contain 20
per cent, of iodoform-yielding substances by our present methods.
The specific gravity is of little value, since there are a number of
products formed during the destructive distillation of the acetates
that possess practically the same specific gravity as acetone. An
actual case will illustrate this fact admirably. A certain make of
acetone was examined, and on submitting the results of the analysis
the producer protested loudly. He maintained that their product
contained 98 per cent, of pure acetone according to the alcoholo-
meter. Would methyl alcohol contain 98 per cent, of acetone if, on
immersing the alcoholometer, it sank to the 98 per cent, mark ?
Comment is unnecessary.
The boiling point is of considerable value, but some allowance
must be made even for this constant. A sample, assaying 91-96
per cent, of acetone, yielded, on distilling 100 c.c, the following frac-
tions : from 55°-58° Z. = 6 c.c; 58^-59° C. = 20 c.c; 590-60° C.
= 30 c.c; 6o°-62° C. = 25 c.c; 62^-65° C. =. 10 c c; 65^-70° C.
=r 3 C.c; 70° and above = 6 c.c Another sample, assaying 96*95
per cent, of acetone, boiled between 56° and 61° C, with a small
amount of residue.
A word about the stability of acetone at this point may not be
inappropriate. On assaying a drum of acetone, it was found con-
siderably below the requirements. On informing the manufacturer
concerning it, he made the assertion that acetone deteriorated very
materially in a month. This information was quite contrary to the
writer's experience. For example, a sample of acetone had been
kept by the writer for two years, about one-half of the time in a
dark, dry cellar, in an ordinary greenish, cork-stopped, glass bottle;
the remainder of the time the bottle and contents were kept in
direct and diffused sunlight. This acetone assayed 97-12 per cent.
This product certainly did not deteriorate much in these two years;
for the best commercial acetone obtainable contains only from 97 to
98 per cent, of pure acetone. Dr. Squibb, in a private communica-
tion, writes thus on this point : " Nothing within our knowledge or
experience has ever led us to suspect any spontaneous change in
acetone by keeping, and I do not believe there is any such change
either in full or partly filled vessels."
^Februar/?^!''} Vohinietric Esthfiatioyi of Acetone. 67
A. Lieben,^ in 1870, discovered that certain organic groups, such
as CH3, COC — , CH3 CH(OH)C — . CH3CH2OH, etc.. when treated
with iodine in the presence of an alkali, yield iodoform. Iodoform
itself, however, was discovered in 1822, by SeruUas.- With some
of the groups the application of heat is necessary to bring about the
reaction. Lieben also observed that methyl alcohol did not re-
spond to this test, and suggested at the same time that this fact
might be of service in establishing the purity of this alcohol.
Ten years later, G. Kramer^ devised a gravimetric process, based
on the iodoform reaction for estimating acetone in wood alcohol.
The results obtained by this method were rarely concordant, conse-
quently it was unsatisfactory.
From 1884 to 1888 much interest was manifested in this country
concerning the manufacture of chloroform from acetone. During
this period, \V. R. Orndorff* and H. Jessel studied the action of
chlorinated lime on acetone in the manufacture of chloroform. On the
results of this investigation J. Messinger^ based the first volumetric
method for estimating acetone in wood alcohol. The method has
been applied with success to all* mixtures in which acetone gener-
ally occurs.
The reactions^ involved for this volumetric process are as fol-
lows :
I3 -f 2KOH = KIO 4- KI + H2O.
CH3COCH3 -I- 6KIO = CH3COCI3 + 3KOH -f 3KI.
CH3COCI3 -f KOH = CHI3 -f KCH3O2.
KIO -f KI -}- 2HCI = I, + 2KCI -f H.b.
KIO3 -i- 5KI -:- 6HC1 = 31, -f 6KC1 + 3H2O.
The solutions required for the process are as follows : 56
grammes of potassium hydroxide, free from nitrite, dissolved in dis-
tilled water and made up to i litre.
* 1876, Ann. (Liebig) Supp., 7. 218 and 377.
' 1822, Ann. chem. phys., 20, 165.
* 1S80, Brr, d. chem. Ges., 13. 1000; Ztschr. anal. Chrm., 19,498.
* 1888, Atn. Chrm.J., 10. 363.
* 1888, Bfr. d. chem. Ges., 3366.
* Sec Hteraturc at the end of the article.
^ There may be some question concerning the actual reactions, but the basis
of calculation is not involved. Kramer expresses it in a single equation :
CHjCOCH, 4- 61 i- 4KOH = CHIj 4 3KI - KC,H,0, -f 3H,0.
68 Volumetric Estimation of Acetone. { "^reb^ruary^JsT?!"*
Solution of hydrochloric acid, specific gravity 1-025.
A decinormal solution of sodium thiosulphate.
A starch solution.
A dilute solution of acetone containing from i to ij^ per cent, of
acetone by weight. This is prepared from the acetone or ace-
tone solution to be examined. The writer prepares this by weigh-
ing the acetone in a beaker containing water, transferring to a gradu-
ated cylinder, rinsing the beaker well with water and making up to a
definite volume.
Having prepared the above solutions, place from 25 to 30 c.c. of
the potassium hydroxide solution into a suitable flask, add I or 2
c.c. of the diluted acetone solution, very carefully measured, or if
greater accuracy is desired, carefully weigh the aqueous acetone, mix
well, and run in from a burette, while rotating the flask, from 25 to
30 c.c. of the iodine solution ; insert the stopple quickly and agitate
vigorously for one minute. After shaking, render the mixture acid
by means of the hydrochloric acid solution; add, while rotating, an
excess of the sodium thiosulphate solution. Allow the mixture to
stand several minutes, add the starch indicator, and re-titrate the
excess of the sodium thiosulphate with the iodine solution. From
the above data the per cent, of acetone can readily be calcu-
lated ; thus I molecule of acetone (58) requires 3 molecules of iodine
(762) to form I molecule of iodoform. Expressing it in the form
of a proportion, letting j/ equal the amount of combined iodine, and
X equal the amount of acetone, we have ;
762 \ i^Z \\y\ X or x = y. A_ or x = y. 0-07612.
762
Before leaving the process, it may be well to direct attention to
several important points. After adding the iodine solution, agita-
tion must not be delayed if concordant results are desired, since
the active agent KIO is rapidly converted into KI and KIO3.
Experiments have proven that it becomes inactive in one-half an
hour. It is essential to allow the mixture to stand a few minutes
after adding the sodium thiosulphate solution, in that the reaction is
not immediate. It is necessary to add an excess of the iodine and
sodium thiosulphate solution, respectively, at the time of adding
them, in order to secure completed reactions.
^FeDruaryT?^""} Volufftetric Estimation of Acetone. 69
MM. F. Robineau^ and G. Rollin, in 1893, proposed another volu-
metric method for estimating acetone. This method was first
brought to the writer's notice through the generosity of Dr. Squibb
and the kindness of his chemist, Dr. L. L. Jackson, while visiting
the laboratory of the former last summer. Prior to this time
Messinger's process had been used exclusively by the writer. R.
and R.'s method is applied by mixing an aqueous acetone solution
with a strongly alkaline solution of potassium iodide and convert-
ing the acetone into iodoform by means of a titrated solution
of sodium hypochlorite, the end reaction being determined by
means of a bicarbonated starch solution.
The writer has not applied the above process to any extent, but
has studied and worked with Dr. Squibb's- modification of the same
considerably.
The solutions required for this modification and the methods
of preparing them are as follows :
Pure acetone made by the bisulphite process.
An alkaline solution of potassium iodide. Dissolve 250 grammes
of pure potassium iodide in distilled water and make up to i litre.
Dissolve 257 grammes of sodium hydroxide, purified by alcohol, in
distilled water and make up to I litre. Allow the insoluble
part to subside and mix 850 c.c. of the clear solution with the litre
of potassium iodide.
Solution of hypochlorite, containing about 2^ per cent, of
available chlorine. To each litre add 25 c.c. of sodium hydroxide
solution, specific gravity 1-29.
l^icarbonated starch solution. Treat 01 25 gramme of starch
with 5 c.c. of cold water, then add 20 c.c. of boiling water
and boil a few minutes, cool and add 2 grammes of sodium
bicarbonate. The keeping quality of this solution is certainly
an agreeable surprise. A sample prepared four months ago is as
delicate to-day as a freshly prepared one.
The manner of application. Prepare an aqueous solution of the
pure acetone of such a strength that each 10 c.c. contains exactly
-jIq^ gramme of the acetone. Of this solution, accurately measure,
' 1893, Moniteur Scitntijiquf (4), 7. pt. i, 272 ; translation \nj. Am. Cfum
Soc, 18, 106S.
' 1896, y. Am. Chem. Sac, is. 1068.
70 Volumetric Estimation of Acetone. {'^Feb'I-uaryTJf/?"''
with a pipette, lO c.c. into a 50 c.c. beaker, add 20 c.c. of the alka-
line potassium iodide solution and mix well. To this mixture add,
from a burette, while vigorously agitating the contents of the beaker,
the standard solution of sodium hypochlorite in rapid drops until
about 9 c.c. have been run in. Allow the iodoform to subside*
which it does rapidly, then add a drop or two of the hypochlo-
rite solution ; should a cloudiness result, add another J^ c.c. of
the hypochlorite solution ; agitate well ; allow the iodoform to sub-
side, etc., until just a faint turbidity results on adding the hypo-
chlorite solution. Now agitate the solution well ; transfer a small
drop to a white porcelain tile ; in a similar manner, bring a drop
of the bicarbonated starch solution near this drop, then connect the
two drops by means of a glass rod. If a blue color does not
develop at the point of union, not enough of the hypochlorite solu-
tion has been added. Continue adding the hypochlorite solution,
a small quantity at a time, agitating and testing, until a blue line
is just formed at the meeting of a drop of the starch solution and
a drop of the mixture titrated. Ordinary starch solution is value-
less for this end reaction.
The number of c.c. of the hypochlorite solution required to com-
plete the reaction is the amount of this active agent needed to con-
vert J^ gramme of acetone into iodoform. From this basis calcu-
lations for any amount of acetone are readily made.
In estimating the amount of acetone in any solution, first prepare
an aqueous solution containing from i to 2 per cent, of acetone by
weight, then proceed as above for establishing the standard with
pure acetone. For fuller details the reader is referred to the origi-
nal communication.
The two latter methods will meet with two objections: first, 2, pure
acetone, and second, the tedious, time-consuming drop end reaction.
Pure acetone is not so readily prepared. It necessitates the prepa-
ration of an acetone absolutely free from other ketones, before the
bisulphite process can be applied. The writer has not been able to
secure acetone that assayed more than 9973 per cent, of pure ace-
tone by either Messinger's process or the one presently to be
described. This small quantity may have volatilized, but the loss
would be practically constant for all the methods, consequently, the
basis of calculation for the pure acetone methods would be 100,
when in reality it is less. The difference may again be due to some
^Febroary^^S?*} Vohinietric Estimation of Acetone. yi
slight inaccuracies in the volumetric solutions. Grant that abso-
lutely pure acetone is made, it is not readily secured when desired.
The writer has adapted Dr. Squibb's modification so that both
the pure acetone and the drop end reaction are eliminated. In this
process the following solutions are employed :
A 6 per cent, solution of hydrochloric acid.
The alkaline solution of potassium iodide of Dr. Squibb.
A decinormal solution of sodium thiosulphate.
Sodium hypochlorite solution, about ^ normal, or containing from
2^g- to 3 per cent, of available chlorine. To prepare this solution,
intimately mix lOO grammes of bleaching powder (35 per cent.) in
400 c.c. of distilled water. Dissolve 120 grammes of crystallized
sodium carbonate in 400 c.c. of hot distilled water, and immediately
pour the latter into the former. Cover the vessel and allow to cool,
then decant the clear liquid, filter the remainder and to the filter
add enough water to make up to i litre. To each litre add 25
c.c. of sodium hydroxide solution, specific gravity 1-29.
An aqueous solution of acetone containing from i to 2 per cent,
by weight. Prepared as for Messinger's process above. To esti-
mate the acetone, place 20 c. c. of the alkaline potassium iodide
solution into a suitable flask add lO c.c. of the diluted aqueous ace-
tone solution, or weigh if greater accuracy is desired; mix well, and
run in from a burette, while rotating the flask, an excess of the
sodium hypochlorite solution, insert the stopple quickly and shake
well for one minute. After agitating, render the mixture acid by
means of the hydrochloric acid solution, add, while rotating the
flask, an excess of the sodium thiosulphate solution, and allow the
mixture to stand a few minutes. Then add the starch indicator and
re-titrate the excess of the sodium thiosulphate.
The relation of the sodium hypochlorite solution to the sodium
thiosulphate solution being known, the percentage of acetone can
readily be calculated from the above data. One atom of available
chlorine will liberate I atom of iodine from the potassium iodide
of the alkaline solution, or i c.c. will liberate just enough iodine to
make I c.c. of iodine solution of the same normal strength as the
sodium hypochlorite solution originally was ; therefore, by reading
the number of c.c. of sodium hyp>ochlorite solution consumed as so
many c c. of iodine solution of the same normal strength, we reduce
the calculation to the basis of iodine. For explanation from here
see Messinger's process above.
/2
Volumetric Estimation of Acetone, {^FebrXyasw"'
Example of calculation. Ten c.c. of the acetone solution, con-
taining I gramme of the solution to be analysed, required 14-57 cc.
of N X 0806 sodium hypochlorite solution, which formed 14-57 c.c.
of iodine solution of the same strength ; or combining we have :
14-57 X 0-806 X 01265 X 0-07612 _ ^^^^^^^ ^^ ^^^^^^^ _
I gramme of solution.
11-307 per cent.
On comparing Messinger's, Dr. Squibbs' and the writer's adapta-
tion with the same solution, the following results, in per cent, were
obtained :
Messinger.
Squibb.
Author.
Pure acetone
99-69
99:95
9973
Residue 80° C. and above .
20*00
19-67
20-39
Purified by fraction . . .
99*03
99-00
99-41
Commercial acetone
96-23
96-00
9663
98-00
97-83
97-93
94 "30
94-00
94-46
94-80
94-70
94-81
97-12
96-23
96-42
94-93
94-80
94-39
96-b8
96-56
96-79
97-32
97-28
97*45
90-74
89-03
90-51
98-82
96-11
9862
92-32
92-20
92-94
Wood alcohol
14-61
14-49
14-78
1 ( ( (
ii-8i
11-73
12-00
Crude wood alcohol
11-23
1 1 00
11-42
The above table clearly shows that the results obtained by Dr.
Squibb's process are a trifle too low, notwithstanding the fact that
its basis of calculation gives it some advantage. The method is
represented to yield satisfactory results for ordinary work, and that
it certainly does. The difficulty with this method lies in the end
reaction. According to some experiments made by the writer, it is
necessary to have present a larger excess of the active agent, to
bring about the completed reaction, than the end reaction allows.
The iodoform reaction with ethyl alcohol is an endothermic one,
consequently its presence does not interfere with the estimation of
acetone, which does not require the presence of external heat to
bring about the reaction. The same holds true for all other groups
of endothermic reaction.
^Feb',?."/r,^?S^"} Terpin Hydrate. 73
LITERATURE NOT IN THE BODY OF THK ARTICLE.
1888, E. Hintz, " Zur quantitativen Bestimniung von Aceton in Methyl-
alcohol, Holzgeist und Aceton," Ztschr. anal. Cfion., -ii. 182.
1890, Fr. Collischonn, " Ueber die gebrauchlichen Methoden zur quantita-
tiven Bestimniung des Acetous," Ztschr. anal. Chem., 29,562.
1890, H. Huburt, "Zur quantitativen Bestimniung des Acetons im Harn,"
Ztschr. anal. Chem., 29, 632, from Neubauer und Vogel ; " Anleitung zur
Analyse des Harns," 9 Auf., 471.
1890, L. Vignon, " Dosage de I'ac^tone dans I'alcool m^thylique et dans les
methylenes de ddnaturation," Comp. rend., 110, 534.
1890, G. Arachequesne, " Dosage de I'acdtone par I'iodoforme," Comp. rend.,
110, 642 ; Ztschr. anal. Chem., 27, 695.
1894, N. Savelieff, " Ueber das Vorkommen von Aceton ira Mageninhalt bei
Erkrankung en des Magens ;" Berliner klin. Wochenschrift, No. 33 ; und
Malys Jdhresberichte iiber die Fortschrittc der Thierchemie, 24, 352; 1896,
Ztschr. anal. Chem., 35, 507.
1896, Chr. Geelmnyden, '* Ueber die Messinger'sche Methode zur Bestimmung
des Acetons," Ztschr. anal. Chem., 35, 503.
1896, M. Klar, " Zur Bestimniung des Acetons in Denaturirungs-Holzgeist
und Rohaceton," Die chetn. Ind., 19, 73 ; Ztschr. anal. Chem., 37, 595.
305 Cherry Street, Philadelphia, Pa,
TERPIN HYDRATE.
By Edward T. Hahn.
In 1840, A. Wiggers contributed an article to the Annaicn der
Chemic, 33, 358, on the crystalline substance from turpentine oil, to
which, however, he applied the name turpentine camphor. He em-
ployed a mixture of nitric acid, alcohol and turpentine oil, and in
1846^ i^Annalen der Chemie, 57, 247) reported a formula for making
the substance on a large scale, stating that it could only be obtained
from that variety of turpentine which yielded a crystalline com-
pound with hydrochloric acid.
The method suggested by Wiggers was tried with commercial
oil of turpentine, but it failed to produce any crystalline compound.
Knowing that the oil of turpentine found on the market at the pre-
sent time is occasionally adulterated with some of the heavier
petroleum oils, a quantity of the commercial oil was procured and
distilled with lime and water. An oil having a sf)ecific gravity of
• Am. JoiR. Pharm., i». 286.
T' J.:. U..^^^/^ / Am. Jour. Pharm.
74 lerpin nyarale. | February, 1897.
0-856, and a boiling point of from 154° to 157° C, was obtained,
and this product was used in all my experiments.
The first method tried was one suggested by Carl Hempel {An-
nalen der Chemie, 153, 71), using the following quantities:
(i) Oil of turpentine 120 c.c.
(2) Alcohol (sp. gr., o-8i6) 30 "
(3) Nitric acid (sp. gr., 1-35) 30 "
These liquids were mixed in a flask in the order indicated by the
numbers, and allowed to stand three days, shaking occasionally.
The mixture separated into two layers, the lower one becoming
quite dark in color. On the third day it was poured into a flat dish
and 15 c.c. of alcohol added, and allowed to stand in a room having
a temperature of about 18° C.
Crystals began to form within five days, and at the end of two
weeks they had separated from the mother liquor. About 13
grammes of crystals were thus obtained. This product was puri-
fied by recrystallization in a solution of boiling alcohol, and yielded
8 grammes of terpin hydrate, which was found to answer all the
U.S.P. requirements.
The mother liquor was allowed to stand for a short time, and
another crop of crystals was obtained ; but these, when tested with
sulphuric acid, did not give the characteristic deep orange color,
but a light, pinkish one, which quickly faded.
The next method tried was one suggested by Wm. A. Tilden
{Jour. Client. Soc. Lond., 33, 247), the following being the propor-
tions of liquids used :
Oil of turpentine 60 c.c.
Alcohol 30 "
Nitric acid (sp. gr., 1-40) 60 "
In this method and all others suggested by Tilden, nitric acid
having the specific gravity of 1-40 was employed, but the writer's
experience with acid of this strength was that a thick resinous-like
mass was obtained, which showed no signs of crystallization.
A method was also given by F. Flawitzky {Jour. Chem. Soc. Lond.,
38, 264), in which he used sulphuric instead of nitric acid, and
obtained a compound having the formula CioH^gO.
As ethyl alcohol commands a comparatively high price at the
present time, methyl alcohol was substituted for it, and the follow-
ing formula was found to be very satisfactory :
''fd^ln''%"'} Terpin Hydrate. 75
(i) Oil of turpentine 120 c.c.
(2) Methyl alcohol (sp. gr., o-8oi) 30 **
(3) Nitric acid (sp. gr., 1-35) 30 '•
These liquids were mixed in the order indicated and allowed to
stand in a flask three days and then poured into a flat dish. Taking
advantage of the very slight solubility of terpin hydrate in water,
30 c.c. of this liquid were added to the mixture, with the result that
the crystals separated in a much shorter time than they did with
the methods previously employed. No additional crystals were
formed dn allowing the mixture to stand several days. The weight
of the crystals obtained was 7-32 grammes, and these, on purifying
from hot solution of methyl alcohol, yielded 32 grammes of terpin
hydrate, which answered to all the tests for the U.S.P. compound.
By further evaporation an additional quantity of crystals may
be obtained.
The crystals obtained by the use of methyl alcohol had a closer
resemblance to the article which is found in the market, and also a
more aromatic odor than those obtained by the employment of
ethyl alcohol.
Amyl alcohol likewise may be used in making terpin hydrate.
An explosion occurred a few years ago {Proc. Am. Pharm. Assoc. y
1887) in a Parisian laboratory during the manufacture of terpin
hydrate. The following proportions of liquids were employed :
Oil of turpentine 72 L.
Alcohol 50 "
Nitric acid 17 Kg.
The mixture was usually cooled in stone jars set in water, but as
these were all in use at the time, a part of the mixture was poured
into a wooden cask, to cool off, and as the wood did not conduct
the heat away rapidly enough, a violent explosion took place, doing
much damage.
Indian podophyllum, according to W. R. Dunstan {Imp. Inst. Jour., Decem-
ber, 1896), is derived from Podophyllum emodi, and contains two to three
times as much resin as the American podophyllum from P. peltatnm. Dr.
Mackenzie finds that the two resins 1 Indian and American 1 are idcMitical in
their medicinal effects, and that there is no reason why the resin obtained
from the Indian drug should not be substituted for the American resin.
76
Solanuni Carolinense.
{
Am. Jour. Pharm.
February, 1897.
SOLANUM CAROLINENSE.
By Chari^ton G. Johnson, Ph.G.
(Abstract from Thesis.)
Since its introduction to the medical profession by Dr. J. L.
Napier, in 1889, several contributions to the chemistry of Solanum
/-Vir. / represents a portion of a branch of Solanum Carolinense. It shows
the spiny stem, bearing the rather irregularly shaped leaves, with the small
axillary leaves and the racemose flowers.
Carolinense have appeared in this Journal. In the meantime phar-
macists have become better acquainted with the botany of this plant.
Am. Joar. Pbarm. "»
February, 1897. /
Solatium Carolviense.
77
The microscopical characters, however, have not been so fully
investigated. But, at the beginning of this article, the author
wishes to call attention to a slight difference which was observed in
the fruit (or berry, as it is called), obtained from two sections of the
country. In the specimens obtained from the South, mainly
Georgia and Florida, the calyx, though adherent, was recurved,
while the berries gathered near Philadelphia had the calyx adhering
to the fruit.
A transverse section of the root {Fig. ^) shows it to have a con-
centric structure caused by irregular, alternating zones of wood-
Fif^. 2 shows a small portion of a branch bearing the fruit. Natural size.
The berries frequently grow much larger.
parenchyma and vascular tissues. The cork tissue replacing the epi-
dermis is composed of about three layers of cells, with the rough
fissured remains of older cork cells exterior. The cork meristem in
the root, as well as in the stem, shows quite plainly. The paren-
chyma cells of the cortex are larger in the middle bark than near
the epidermis, becoming very much smaller and elongated longi-
tudinally near the cambium zone, while in the outer and inner por-
tions of the cortex they are, from mutual pressure, much distorted
and elongated tangentially. The ducts of the xylcm are large and
-8
Solanum Carolinense.
/Am. Jour. Pbarm.
I February, 1897.
numerous ; and seen in longitudinal-radial section {Fig- 5), they
prove to be pitted, the pits showing an elliptical marking within a
larger circular one. Spiral, annulate and reticulate ducts are also
^m^
Fig. J is a drawing of the root of vSolanum Carolinense in the fresh state. It
shows the natural size of the root when about two years old.
I)resent. The libriform cells show markings from the pressure of
adjacent cells, and are usually forked at one end. In the portions of
the wood studied no collenchyma was found and bast-fibres were
Am. Jour. Pharm.
February. 1887.
Solatium Carolinense.
79
also absent. The medullary rays are distinct and slightly undulate,
the number of rows varying from two to five or six.
^^£^- /. portion of a transverse section of a root of Solanum Carolinense,
magnified 45 diameters. ./, rnptured cork tissue ; h and b', secretion cells
containing calcium oxalate ; c, cambium zone ; d, medullary ray; r, one of the
concentric layers of ducts, alternating with wood parenchyma.
The underground stem {Fi^. 6) shows the pericyclc relatively
thicker and the corte.x thinner than in the root. The cork tissue
8o
Solamim Carolinense.
Am. Jour. Pharm
February, 1897.
resembles that of the root, except that a part of the epidermis is
present. Collenchyma is found in the younger parts of the stem,
though absent from the older portions. No bast-fibres were found.
A
/S.
^'.
aa^
t.
Fig. 5, longitudinal-radial section, made from a young root of Solanum
Carolinense having a thick cortex, magnified 35 diameters. A, cork tissue;
b, b\ secretion cells of calcium oxalate ; c, the cambium, with the ducts of the
xylem on one side and the phloem tissue on the other.
Am. Jour. Pbarm.
February, 1897.
Solatium Carolinetise.
8i
The cortex is mainly composed of parenchyma tissue ; the cells
are round, but otherwise correspond to the same tissue in the root.
The woody tissue is rather irregular in width, and beside the phloem
tissue on its exterior, there is a distinct inner phloem, which, though
narrower in some places than in others, is distinctly discernible.
The pith is composed of large parenchyma cells.
Fig. 6, transverse section of underjjround stem of Solanum Carolincnsc
(from a portion just at or beneath the ground), magnified 56 diameters. A,
epidermis ; d, cork cells ; r, c/, secretion cells of the cortex ; d, cambium ; ^,
xylem ; p, secondary or inner phloem, l>eneath which arc the soft, parenchy-
matous cells of the pith.
The petiole, as seen in transverse section in Fi^. 7, shows three
bi-coUateral bundles. Heneath the epidermal tissue are several rows
of collenchyma cells, and next to these are the parenchyma cells
surrounding the vasal bundles. Two large secretion reservoirs are
found, one on each side, near the upper surface. Some starch is
present in the parenchymatous cells of the stem, principally in the
f^i]^- 7. transverse section of a younger portion of a petiole of Solanum Caro-
linense. Magnification, 65 diameters, a, epidermis ; b, collenchyma tissue ;
c, c\ large secretion reservoirs ; d, d\ upper and lower phloem tissues, respec
tively ; r, xylem ; /, meristem, found only on the lower side ; g, stellate hair.
Am. Jour. Pharm.
February, 18y7.
Soianum Carolinense.
83
cortex, but it is more especially found in the cortical tissue of the
root, chiefly near the pericycle. In some of the specimens exam-
ined, the whole of the cortex seemed filled with starch granules,
while others failed to show its presence so profusely. The grains
Fig. S, starch grains found in the root of Soianum Carolinense*; magnified
about 40f) diameters.
show distinct stratification lines. In shap>e some were oblong, some
ellipsoidal and others in clusters of two, three or four, the oval or
oblong-ovate being, however, the most common form. The hilum
is distinct, eccentric, and usually presents a fissured appearance.
84 Solannm Carolinense. {^Y^J>r^Iiy^m^'
Some of the grains were bi-nucleated and others possessed a pecu-
liar, contorted shape. The starch grains resemble somewhat in
shape those of another plant of the same genus, Solanum tuberosum,
the potato. Scattered irregularly through the cortex of the root,
and less profusely in the stem, are secretion cells containing a pecu-
liar, mucilaginous-like matter. On treating these cells with potas-
sium hydrate test solution they were rendered clear, and their con-
tents now shown to be a white, granular or crystalline substance.
This substance, by dissolving in warm hydrochloric acid, without
-effervescence, proved to be calcium oxalate. The tests for tannin
failed to show its presence. On testing for resins and oils, with
alcannin solution, small quantities of these substances were found
in some of the starch-bearing cells and also in some of the lignified
tissues.
In conclusion, the author wishes to express his thanks to Messrs.
Parke, Davis & Co. for specimens kindly furnished, and to Dr. M.
V. Ball for his valuable assistance in the microscopical work.
SOLANUM CAROLINENSE.
By M. C1.AYT0N Thrush, Ph.G.
(Abstract from Thesis.)
The author found the fruit to contain the largest amount of alka-
loidal constituents ; consequently, it is the most active therapeuti-
cally. The leaves came next in strength, then the root, and finally
the stem, which is the least active.
In order to study the drug microscopically, sections were cut by
means of the microtome from specimens of the plant which had
been preserved in strong alcohol. They were then placed in Labar-
raque's solution until properly bleached, except those intended for
the tests for tannin and oleoresin. They were then treated as fol-
lows : For double staining some of the sections were treated with
iodine green, then washed to separate excess, then passed through
dilute, strong and finally absolute alcohol, to anhydrate them.
They were then treated with eosin, oil of cloves, and from that
through pure oil of cloves, and mounted in xylol balsam. The
others, after being treated with the reagent, were washed to sep-
arate excess, anhydrated by absolute alcohol and mounted in xylol
Am. Joar. Pbarm.
February, 1897.
Solan Jim Carolinensc.
85
balsam. The sections which were tested for tannin and oleoresin
were treated direct with ferric chloride in absolute alcohol and
alcannin, respectively, then mounted in xylol balsam. These latter
tests were confirmed by treating dry sections with ammonio-
FiK' '• un<lerground portion of the plant, one-half natural size.
ferric alum. By treatinpj dry sections of the younp^ root for
tannin with ferric chloride in absolute alcohol, tannin precipitates
were produced in the central parenchyma and the cortical
parenchyma. In the old root tannin precipitates were produced in
S6 Solanum Carolinense. V^Y^iv^lryMT^'
a great number of the cells of the cortical parenchyma, also in a
itw cells of the phloem tissue and the medullary rays. In the
mature stem, indications of tannin were obtained in abundance, in
the pith parenchyma, medullary rays, cambium zone, phloem, corti-
cal parenchyma and suberous tissue. In the leaf indications were
produced in all of the different tissues. In the fruit tannin indica-
tions were obtained in the cells of the section irregularly scattered.
The tannin was estimated by the *' hide powder method," and
found to be 3-10 per cent, in the leaves; 2-27 per cent, in the root ;
Fig. 2, transverse section of rootlet of Solanum Carolinense, magnified 75
diameters. A, epidermis ; b, collenchyma tissue ; c, cortical parenchyma ; d,
endodermis ; e, phloem tissue ; / cambium zone ; g, duct of xylem ; h, xylem
tissue, consisting of wood cells and ducts.
806 per cent, in the fruit ; 5-06 per cent, in the stem— all calculated
for absolutely dry material.
Fig. I represents the underground portion of the plant.
/e^^/._Phloroglucin and hydrochloric acid stain the xylem tissue,
which is strongly lignified, a bright red. In the young undeveloped
root central parenchyma exists, but as the root becomes older the
xylem of the radial bundle extends to the centre with the develop,
ment of rings of growth, medullary rays and a cambium zone, and
Am. Jour. Pbarm
February, 1897
^•}
Solanuin Carolineiise.
87
has a similar appearance to the structure of a dicotyl stem. Zinc
chloriodide iodine shows an abundance of starch in the cells of the
medullary rays, phloem, collenchyma and cortical parenchyma.
Chloral hydrate iodine gives the same indications. The epidermis
of the mature root consists of several rows of suberous tissue,
which exfoliates at the surface ; beneath this is a circle consisting of
Fig. J, longitudinal section of younj;^ root of Solanuni CaroHnense, magni-
fied 75 diameters. A, epidermis, not yet displaced by cork cells forming
beneath ; c, cortical parenchyma ; d, phloem tissue ; ^, cambium zone ; /, xy-
lem tissue, consisting of wood cells and ducts ; g, central parenchyma, not
yet develof>ed into xylem tissue ; h, duct of xylcm.
several rows of collenchyma tissue ; interior to this a layer of cortical
parenchyma, consisting of several tiers of cells, then the phloem tis-
sue and finally the xylem, which extends to the centre and is sepa-
rated from the phloem by the cambium zone. The different rays
are separated by the medullary rays.
Fig. 4, transverse section of the mid-rib of a leaf of Solanum Carolinense,
with one of the prickles, which is shown in longitudinal section, attached ;
magnification, 150 diameters. A, epidermal cells ; b, parenchyma of upper
portion of mid-rib ; c, a portion of the lamina of the leaf; d, xylem tissue of
mid-rib ; c, cambium zone ; /, phloem tissue of mid-rib ; g, parenchyma of
lower portion of mid-rib ; h, collenchyma tissue ; i, slightly lignified tissue of
the prickle, which occurred on the mid-rib and was cut through longitudinally;
k, epidermal tissue, more lignified.
Am. Jonr. Pbarm. )
February. Ift97. j
Solatiion Carolinense.
89
Steyn. — Zinc chloriodide iodine shows starch in the central paren-
chyma, in the cells of the medullary rays, in the cortical paren-
chyma, and in the cambium zone. Chloral hydrate iodine gives the
same results, as does also potassium iodide iodine, but much more
prominently, especially in the central parenchyma tissue, which
contains an abundance of the substance. Phloroglucin and hydro-
chloric acid stain the xylem tissue, which is strongly lignified, a
Fig. 5, portion of transverse section of fruit of Solanum Carolinense, showinj^
the succulent tissues, magnified 200 diameters. A, epidermal tissue ; b and
c, succulent tissues, farther interior ; d, parenchyma tissue, adjacent to the pla-
centa.
bright red. The stem possesses open collateral bundles, which are
in wedge-shaped rays, and which are separated from one an other
by medullary rays. In the mature stem the outer portion of the
section consists of several rows of cork tissue, which are exfoliat-
ing at the surface. In the mature stem indications of tannin are
obtained in abundance in the pith parenchyma, medullary rays,
cambium zone, phloem, cortical parenchyma and suberous tissue.
Artificial whalebone is prepared from bones by removing fat, then irraim^
with hydrochloric acid to extract lime ; the cartilaginous residue is then
steeped in concentrated chrome alum solution until saturated. It is then dried
and cut into strips for use.
90 North American Conifer a;. {'^Februaryfisg?"'*
A CONTRIBUTION TO THE KNOWLEDGE OF SOME
NORTH AMERICAN CONIFER.©.
By Edson S. Bastin and Henry Trimbi^K.
{^Continued from Vol. 6S,page 648.)
TSUGA CANADENSIS.
CHEMICAL COMPOSITION.
Considering the enormous commercial importance of this tree
and its products, it has received very little attention by the botanist
or chemist. No investigations have been reported recently, except
two on the volatile oil, so that the text-books at the present time
give the results of observations made from twenty-five to fifty years
ago.
The Leaves. — The most important constituent of the leaves is the
volatile oil. The preparation of this product was described by
Stearns^ in a report to the American Pharmaceutical Association in
1858. He had, from a practical distiller, the information that in
Michigan, at least, the oils of hemlock and spruce (Picea nigra) were
one and the same thing, and distilled from the boughs of Tsuga
Canadensis, a statement which is probably true to-day.
" The proceeding is as follows : The trees are cut down and
the boughs collected only ; they are cut up fine and subjected to a
distillation with water, in a portable copper still and worm, capable
of holding about one hundred gallons, which is so arranged that it
can be transported in the woods, and erected quickly upon a tem-
porary arch ; two pails full of boughs (about 8 pounds) are
calculated to yield I ounce of oil. The distilling is done only in
winter, when the tree is richest in oil."
Bertram and Walbaum,^ in 1894, examined oil of spruce, said to
have been prepared from Abies Canadensis (Tsuga Canadensis), and
found it to consist of laevogyrate pinene, laevogyrate bornyl acetate
(36 per cent.) and a sesquiterpene. It had a specific gravity of 0-907
at 15° C. Carl G. HunkeP considered it a question whether this
sample was derived from Tsuga Canadensis, or from Picea nigra ; he,
therefore, collected the leaves and twigs of Tsuga Canadensis him-
self in the month of September, and submitted them, while fresh, to
distillation with water vapor. The yield was small, of a yellowish
' Report on the Medical Plants of Michigan, Am. Jour. Pharm. 1859, P- 28.
"^Archil der Pharm., 231, 294.
' Pharmaceutical Review^ 14, 34.
''FebiSalryT?^"} Novth American Conifcm. 91
color and it possessed the characteristic odor of hemlock. The
specific gravity of the dried oil at 20^ C. was 09288, [«]u = —
18399° ^t the same temperature. His conclusion was that this oil
of hemlock was very similar in composition to that examined by
Bertram and Walbaum, and also to the oil of black spruce, Picea
nigra, previously examined by himself.
Our own experiments on the leaves have been limited to an esti-
mation of the tannin, resin and ash. For this work the leaves were
collected in November, and, after a short exposure to dry air, were
found to still contain 1280 per cent, of moisture. The ash esti-
mated on absolutely dry substance was found to be 378 per cent.,
and tannin, similarly calculated, amounted to 1-48 per cent. The
ash contained calcium and potassium sulphates, phosphates and
traces of carbonates and chlorides. The leaves submitted to the
action of absolute alcohol yielded 22-97 per cent, of their weight to
that solvent. From the residual extract, after recovery of the alco-
hol, petroleum ether removed 583 per cent, of the weight of the
leaves, consisting of fat, volatile oil, wax, chlorophyll and resin.
Water then removed from the residual alcohol extract 14/O per
cent, of the weight of the leaves, which consisted of tannin, sugar
and extractive, leaving 2-44 per cent, of resinous matter and chlo-
rophyll.
The Root Bark. — This portion of the hemlock was collected for
examination on the first day of August, and yielded the following
results :
I'er Cent.
Moisture 11*83
Ash in dry bark 3 96
Tannin in dry bark . 24*46
This large amount of tannin was equivalent to 21-57 per cent, in
the air-dry sample.
Tkc Trunk. — The wood portion of the hemlock tree supplies the
chief amount of the resin, which is found in commerce under the
name of Canadian pitch.
Probably the first pharmaceutical literature concerning this resin
was by Charles Ellis,* in 1830, and the full title of the paper, as
^ "Finns Canadensis, Willd.; Abies Canadensis, Mich. Sylv. A lar^ tree
belonging lo the natural order Conifera.', Mon(i.*cia, Monodelphia of Linnaeus.
Officinal Resin Pini Canadensis. Hemlock Resin. By Charles KUis." Jour-
nal of the Philadelphia College of Phartnaey, Vol. 2, p. 18.
/Am. Jour. Pharm.
92 North American Conifer ce. { February. isT?'
given in the foot-note, indicates that the tree and its products were
not well known at that time. The paper opens by stating this tree
is " known only in the United States by the name of hemlock
spruce, and in Canada by the French is called perusse." That
the resin had not been an article of commerce very long is indicated
by the following : " The resin which exudes from it was first intro-
duced into this City (Philadelphia) about twelve years since, and was
obtained in this State (Pennsylvania) near Silver Lake, Susquehanna
County. But its history even here has been but little known, and
still less elsewhere." That the wood of the hemlock was not much
esteemed is evidenced by the statement that "of all the great
resinous trees of America, its wood is of least value." The pro«
cess of collecting the resin at that time was different from that given
by more recent writers. Then it was prepared by boiling the bark
with water and skimming off the melted resin as it rose to the
surface. The quantity yielded by a single tree with this process
was said to be from 4 to 6 pounds. The product was more or less
contaminated with pieces of bark and was submitted to a process
of purification by melting and straining.
A more recent report, by Stearns, in 1858, already referred to,^
gives the process of preparation as wholly from the wood, two
methods for this purpose being employed, one by making cup-like
incisions in the body of the living tree and allowing the resin to
flow out, after the manner of collecting turpentine ; the other, by
chopping out the knots in the wood, which are rich in resin, and
boiling them with water. The latter method is not considered as
good as the former, as the boiling with water deprives the resin
of most of its volatile oil, which is present in the resin obtained by
exudation.
Canada pitch is considered to be equal, if not superior, to Bur-
gundy pitch in the manufacture of plasters ; but both have given
way, in the modern methods, to caoutchouc and asphalt, chiefly
the latter.
Very little is known of the chemistry of Canada pitch ; the vola-
tile oil contained in it is probably similar to that obtained from the
leaves, and just described ; but the resin or resins, which constitute
a large proportion of it, have not been studied.
The bark of the trunk is, from both chemical and industrial
standpoints, of great importance; nevertheless, there does not ap-
""Febi^a'iV^?^'"} North American Cofiifem. 93
pear to have been published anything concerning its composition.
It is evident that it contains resin, volatile oil and tannin, and a
closer examination will show the presence of a considerable amount
of red coloritig, as has already been shown in the description of
microscopical structure.
The following results were obtained by us on a sample of bark
collected in June, 1896, in eastern Tennessee. The sample was
taken from the trunk of a large tree, near the ground, and repre-
sents an average sample of the hemlock bark used in that district
by tanners. The whole bark was taken; that is, it had not been
" rossed." After having been finely powdered, 50 grammes were
submitted successively to the following solvents, moisture and ash
being added in the proportions they were found to exist in the air-
dry drug :
Per Cent.
Petroleum ether dissolved 070
Ether
Absolute alcohol
Water
Alkaline water
Acid
Boiling
350
1574
392
75'
o-8i
147
Ash in air-dry bark i 42
Moisture in air-dry bark 673
Residue and undetermined 5820
loooo
The petroleum ether extract consisted of 0036 per cent, volatile
oil, 0564 per cent, of fat melting at 50*^, and o 10 per cent, of wax
melting at 65°.
The ethereal extract consisted chiefly of resin and red coloring
matter, with a small amount of tannin.
The alcohol extract contained 7-90 per cent, of resin and decom-
posed tannin, known as hemlock red, the balance being pure tannin,
soluble in water.
The water extract contained neither mucilage, sugar nor tannin,
and only a small amount of coloring matter ; its composition was not
further studied.
The alkali extract contained 229 per cent, of albuminoids, and the
hot water extract consisted almost entirely of starch.
The ash was found to be composed of magnesium in greatest
abundance, aluminum, calcium, manganese, potassium and traces of
phosphoric, hydrochloric and sulphuric acids.
94
North American Coniferce.
( Am. Jour. Pharm.
t February, 1897.
It will be seen from this analysis of the bark that the important
constituents are tannin, resin and hemlock red; all of these con-
stituents vary with the season of the year. Hemlock red may be
an intermediate product between the resins and the tannin ; its pro-
portion in the bark is very variable.
HEMLOCK TANNIN.
The tannin of hemlock bark has received so little attention at
the hands of investigators, and is of so much importance industrially,
that it is considered worthy of especial notice here.
Occurrence. — The few results that have been published concern-
ing the amount of tannin in hemlock bark are widely at variance
with one another. Procter^ says it contains nearly 14 per cent.; he
probably quoted Mulligan and Dowling,^ who, m 1859, found 13*9
per cent. Mafat,'^ 1892, gives 8 to 10 per cent, as the average
amount. The following results will show that there may be a great
variation in the proportion present, according to the season of the
year and other circumstances:
PERCENTAGES OF MOISTURE, ASH AND TANNIN IN THE BARK OF TSUGA CANADENSIS.
Date of
Collection.
Moisture.
May 12, 1895 . . . 20'o6
June 30, 1895 . . . 15-54
August I, 18951 . . 1000
October 27, 1895 . irgo
November 28, 1895 14-01
January 17, 1897 . 13-45
May, 1896 .... 10-73
June, 1896 .... 1043
July, 1896 .... 10-98
Ash in
Absolutely
Dry Bark.
Tannin in
Absolutely
Drj^ Bark.
I "46
8-22
3 '03
9-82
2-51
1477
1-21
15-12
I '43
I5*45
1-58
13'05
1-56
io-6o
I "40
14-96
1-29
11 "34
Remarks.
Small tree.
Taken from a branch.
Small tree. Bark from trunk.
(( K l( tl ((
Medium" " " "
<( i< 11 (< i<
I^arge " '• " "
Near Philadelphia.
Tennessee.
1 This sample was taken from the same tree that yielded the root bark, the composition of which ha
been given on a previous page of this article.
Hemlock bark is usually collected during the months of May,
June and July, and the three samples in the foregoing table which
' Text-Book of Ta^ming, p. 31.
2 Chemical Gazette, 17, 430.
^Bulletin de la Socicte industrielle de Mulhouse, 63, 130. Am. Jour.
Pharm., 64,531.
Am. Jour. Pharm.
Februarj'. 1897.
North American Conifer ce.
95
were collected in 1896 were taken from similar trees for the especial
purpose of determining their relative tannin value.
Preparation. — For the purpose of investigating its composition
and properties, a considerable quantity of the tannin was prepared
by extracting hemlock bark with acetone. The solvent was recovered
by distillation and the syrupy residue was poured into several times
its bulk of water; the insoluble resin and anhydrides were separated
by agitation with paper pulp and filtration. The clear aqueous liquid
was saturated with sodium chloride and shaken with acetic ether,
which removed the tannin,' the solvent in this case being removed
by distillation under reduced pressure. The residue was redissolved
in water, salt added and the tannin again removed by acetic ether,
and the operation repeated until a tannin resulted which formed
a clear solution with water. It was then treated with absolute
ether, in which it was insoluble, and, after removal of the ether,
dried.
Properties and Composition. — The product was a reddish porous
powder, completely and readily soluble in water and in alcohol. A
I per cent, solution gave the following reactions:
Reagent.
Ferric chloride
and
Ammonium
hydrate.
Ammonio-ferric
sulphate.
Calcium hydrate.
Bromine water.
Hemlock Tannin.
Brownish -green
color and ppt.
Purple color
and ppt.
Brownish-green
color and ppt.
Pinkish ppt.,
turning red.
Yellow ppt.
Chestnut Oak
Tannin.
Gallotannic Acid.
Green color
and ppt.
Purple ppt.
Green color
and ppt.
Precipitate
turning pink.
Yellow ppt.
Blue color
and ppt.
Purple ppt.
Blue color
and ppt.
Precipitate
turning blue.
No ppt.
A Study of the decomposition products of hemlock tannin was
made in the usual way. The product resulting from the action of
heat on a solution of the tannin in glycerin was identified as
' It has since been found that methyl acetate with salt answers the purpose
of an immiscible solvent, for the removal of tannin, equally as well as ethyl
acetate, and is much cheaper.
96 North American Conifer ce. {^F^bSyT^s"!"'
catechol. Boiling hydrochloric acid containing 2 per cent, of HCl
gas, resolved the tannin into an amorphous, reddish-brown, in-
soluble phlobaphene and soluble protocatechuic acid. The phlo-
baphene was of the same character as that obtained from the
tannins of several oak barks. When heated with fused potassium
hydrate the tannin yielded protocatechuic acid. Although the
above reactions and decomposition products indicated a great
similarity between the tannins of the barks of the hemlock and
oaks, an ultimate analysis was made in order to further establish
their relationship. The results which were obtained show that
the tannins from these two sources are very closely related, if,
indeed, not identical. For comparison, the figures which represent
the composition of chestnut oak bark tannin, gallotannic acid and
the average composition of the tannins from nine species of oak
bark are given :
Average on
Chestnut Oak Tannins from Nine Gallotannic
Hemlock Tannin. Tannin. Species of Oaks. Acid.
Carbon 60*09 59'69 5979 52 "17
Hydrogen 5*18 5"o6 5*08 3*10
Oxygen 3473 35*25 35-13 4473
IGO'OO IQG'GG lOO'OO lOO'OO
The several tannins used in the combustions were dried at 120° C.
The conclusion from this study of the properties and composition
of hemlock tannin is that it is identical with the other tannins
of this natural order, which have thus far been studied by us, as
well as with the tannin of oak bark, and a number of others from a
variety of sources.
The only other investigation of hemlock tannin on record was
made by Boettinger\ in 1884, who, by precipitating a commercial
extract of hemlock bark with bromine, and estimating the halogen in
the product, deduced the formula Z^^^fixf)^^ from which he con-
cluded that the tannin had a composition expressed by the formula
^zo^igOio- Such a formula would require the following percentage
composition :
C . .
• • • 57*41
^ 4-31
O 38-28
100 GO
' Berichtcder deut. chem. Gesell., 17, 1041 and 11 23.
^Febmary^iS"''} NortJi American Co ni fern. 97
This is a considerable variation from our figures given for hemlock
tannin and, in fact, from those of a larger number of other tannins,
and it appears reasonable to attribute this difference to the fact that
Boettinger operated on a commercial extract of hemlock. To those
familiar with the manufacture of tanning extracts this would be a
sufficient reason for allowing his results to await further research on
the bark. Much assistance on the chemical investigation of this
tannin was given by J. C. Peacock and VV. E. Ridenour, who also
aided in the collection of the various samples used in the estimations.
ECONOMICS.
When Ellis wrote concerning this tree in 1830, the wood
was considered of very little value, but the steady diminution
of our forests has brought this wood to the front, and it is now one
of the most important lumber trees in northeastern United States.
The hemlock trunks also found use before iron became so cheap, in
conveying water. A case was reported in 1862^ where pipes of this
wood had been in service thirty-two years, and where the earth was
moist they had not decayed. The resin has had extensive use in
the manufacture of plasters, and is still employed for that purpose.
The volatile oil from the branches is used as a flavoring and for dis-
infecting purposes. The bark is used to an enormous extent in the
manufacture of heavy leather. In recent years, many tanneries have
been built in the hemlock districts, so as to be near the supply of
bark. For the finer grades of leather the hemlock bark is mixed
with that of the oak, in order to avoid the reddish color produced
by the former.
An extract of the bark is employed by tanners in place of the
bark, or to strengthen their bark liquors, and in a variety of
other ways, notably by dyers, in conjunction with logwood coloring,
to modify the shades of the latter, especially when copper sulphate
is used as the mordant. Large quantities of hemlock extract go to
the European markets, where it finds ready sale. All parts of the
tree are used except the root, and from what we have seen of its
contents of tannin we may look forward to the day when it, too,
will not be allowed to go to waste.
( To be continued.)
* Am. Jour. Pharm., 34. 377.
98 Correspondence, {^^.i?^lr?^^^i^'
CORRESPONDENCE ON THE MANUFACTURE OF SOME
GALENICALS FROM FLUID EXTRACTS.
By Edward R. Souibb, Charles Rice and John Uri IvLoyd.
Brooklyn, N. Y., January 8, 1897.
Mr. L. F. Kebler, Philadelphia.
Dear Sir: — Your favor of yesterday is received. I am not in a
condition to enter upon this discussion, but must confine myself to
my chief argument against the general practice of making tinctures
from fluid extracts ; and this single argument has been sufficient to
control my practice ever since fluid extracts were introduced.
The objection to the practice is that it is not authorized by the
U.S.P., and that, therefore, such tinctures are not officinal, but are
substituted for the officinal tinctures.
To make them so is to break through our own authority, or law,
as to how they should be made, and to substitute them for the
U.S.?. tinctures is an immoral act of dangerous influence and ex-
ample.
The convenience of such a practice has been known to the suc-
cessive Committees of Revision ever since fluid extracts were ad-
mitted to the U.S. P., since the practice antedated the admission,
and in some of the committees, at least, it was fully discussed and
rejected by majority vote. A prominent reason for rejecting the
practice was that it doubled the risks of quality in the tinctures so
made, and pushed the responsibility for quality back from the dis-
penser to some one behind. If a dispenser makes a tincture from a
drug, he is bound to know, and does know, whether it be the offici-
nal drug or not, and responsibility for the quality of the tincture is
direct and, therefore, right and proper. If he makes his tincture
from a fluid extract, according to the formula of the fluid-extract
maker, he goes entirely behind his only legitimate authority, the
U.S.P., both for material and process, and supposes he avoids the
responsibility for quality. If he says : " I buy standardized fluid
extracts because they are better than unassayed drugs," he brings
the practice to depend on the standardization, which is still further
back from the legitimate responsibility, for then, who standardizes
the standardizer, and who authorizes his assay process ?
When the Pharmacopoeia finds a set of assay processes simple
""Fe'rZ'rri^oi^] CoTrespondcncc. 99
enough to be trusted for general use, it will probably direct some
such practice. It has not done so yet, and until it does it is but
right, and it is the part of wisdom and safety, to conform to its
authority and obey its commands. Why sacrifice the advantages
of having an excellent Pharmacopoeia by trying to set up individual
or popular authority against it. Change the law, if you will — but
don't change the practice against the law.
I have no objection whatever to your using what I have said in
your approaching discussion of the subject on the 20th. Indeed, I
would very much like to have this letter read in the discussion at
the Pharmaceutical Meeting on January 20th, and published in the
Minutes of the College Meeting, Very truly yours,
E. R. Squibb.
New York, January 9, 1897,
Lyman F. Kcblcr^ Esq.
My Dear Sir: — You ask me what my opinion is regarding the
propriety of making tmctures and other liquid preparations from the
corresponding fluid extracts, citing as an example the case of nux
vomica, where the U.S.P. directs the tincture to be made from the
assayed extract, and then raising the question why a tincture of
aconite (35 per cent.) prepared from an assayed fluid extract should
be less reliable than one made direct from the drug of unknown
strength.
In compliance with your request, I submit the following, which
you are at liberty to use, as coming from me, in any way agreeable
to you :
When fluid extracts were first suggested and introduced, the prin-
cipal claim made for them was that they represented the correspond-
ing tinctures, wines, etc., in a more concentrated form and in a
smaller bulk. No one claimed for them a different therapeutic
action, except, of course, that a proportionately smaller quantity of
them was required to produce the same effect as a corresponding
dose of the respective tinctures. No authority in therapeutics to
this day has maintained that tinctures and fluid extracts prepared
from the same drug differed by more than the degree of effect, ex-
cept, perhaps, in a few cases, and then for reasons well understood.
Now, if a tincture or a fluid extract is properly made from the
same, uniformly mixed and comminuted lot of a drug, either of them
lOO Correspondence. { ^^^ebiuarV^'fsT-
should and will contain all the desired active principles of the drug.
If this is true, it follows logically and necessarily that if such a
fluid extract be diluted by the proper menstruum to the strength of
the corresponding tincture, the resulting dilution will be equal in
therapeutic effect to the latter. But one reservation must be made
here. The equality will be disturbed,if the liquid added as diluent
to the fluid extract causes such a disturbance of the dissolved mat-
ters that some of the latter, either at once or gradually, lose their
solubility and become precipitated. That there are drugs behaving
in such a manner cannot be denied, and it must, at the same time, be
stated that, while the matters first thrown out of solution are proba-
bly, m theynselves, always inert, yet they are apt to carry along with
them some of the useful, active constituents, thereby causing the
tincture made by dilution from the fluid extract to become weaker
in therapeutic strength than that made originally as a tincture from
the drug direct. Moreover, it is well known that when such pre-
cipitation once begins, it is liable to progress for a long time, so that
even filtration will not interrupt the process of deterioration. A
notable example of this class of drugs is cinchona bark, particu-
larly the red variety.
If the statements thus far made are agreed to, it seems to me
that we may formulate a few propositions regarding the subject,
which will probably also be accepted, though there is likely to arise
a difference of opinion as to whether it is practicable at all, or at
least as to how far it is practicable to apply the propositions. It
should be understood that in comparing any fluid extract and tinc-
ture made from one and the same drug, they are assumed to have
been prepared from known quantities of the drug of known strength,
and, therefore, to be commensurate. The propositions which I wish
to make are as follows :
(i) If a fluid extract differs from a tincture only in the quantity
of the solvent or menstruum, and if the dilution of the former to
the strength of the tincture by the addition of more of the solvent
throws nothing out of solution, the two tinctures must be alike in
the quantity of active constituents, and, therefore, be alike in thera-
peutic effect.
(2) If the dilution of a fluid extract to the strength of the corre-
sponding tincture by the addition of even the most favorable men-
struum causes a precipitation, the two tinctures may still be re-
^Febtuary!'?^"^} Correspondcftcc . lOI
garded as alike in therapeutic effect, if the precipitate contains none
of the useful medicinal constituents.
These propositions are almost self-evident, and will probably not
be gainsaid. But it is a well-known fact that, in many cases, the
dilution of a fluid extract produces, sooner or later, more or less
precipitation. And as it is not at all practicable to classify drugs
into groups representing such as will or will not yield precipitablc
fluid e.xtracts, though it is possible to mention some from which no
precipitate is derived, it seems to me unwise to give a general en-
dorsement to the practice of preparing tinctures from fluid extracts,
at least at the present time, and in the present state of our knowl-
edge. If the manufacturing houses could put on the market fluid
extracts of full official strength, made with menstrua, the further
addition of which would cause no precipitate, or at most only one
known or guaranteed to be inert, the practice might be approved.
But as this is not the case, nor likely to happen in the near future,
no general license to make tinctures from fluid extracts should be
given. On the other hand, if a pharmacist has the knowledge and
ability to examine and assay his preparations, and is willing to as-
sume full responsibility for the quality of the medicines he dispenses,
he should have full liberty as to how he arrives at any preparation,
say at a tincture, and it is then immaterial whether he prepares it
from the fluid extract or the drug. I would, therefore, offer as a
third proposition the following :
(3) The practice of preparing tinctures from fluid extracts, in all
cases where dilution causes obvious physical changes (such as pre-
cipitation, gelatinization, etc.), is not to be recommended for general
use, but may be adopted in cases of necessity or urgency, when a
prescription calls for the tincture of a drug of which only the fluid
extract is available or obtainable.
Now as to the labels you sent me. To judge from exj>erience, I
should say that no trouble will be encountered in preparing a tinct-
ure from the fluid extracts of aconite and ipecac. But it is probable
that some precipitate will form in the case of belladonna leaves and
coca leaves, particularly as different persons are apt to use different
menstrua, in spite of your direction. Still, we should not pay any
attention to what may happen if your directions are disobeyed. If
it can be shown that the i)rccipitate in these cases is free from alka-
loids, there can be no objection raised against the method.
r ^A^^V^^^^ f Am. Jour. Pharm.
102 Lorresponaence. \ February. 1397.
I have been more profuse than I intended ; but I do not regret it
now, since it gave me a chance to discuss a subject which has often
been brought to my notice. Very truly yours,
Charles Rice.
Cincinnati, O., January 9, 1897.
My Dear Mr. Kebler : — Permit me to strongly urge you not to
commit yourself without reserve to the tincture-from-fluid-extract
method. In my opinion there is more than one side to the subject.
In the case of preparations in which the therapeutical constituent or
constituents of the drug are firmly established and known, and in
which no question exists concerning the exact value of the fluid
extract, there seems to me to be no question but that the tincture
may be made by diluting the fluid extract ; this, of course, being in '
cases where the menstruum will not be considered at all as a thera-
peutical part of the product.
In such cases as nux vomica, where the therapeutical constituents
are permanent, I will go further, and say that, owing to the difficulty
of extraction, in my opinion, unless the tincture is assayed in order
to establish its value, the method of preparation from an unexcep-
tional fluid extract (standardized) is to be preferred to blind extrac-
tions from a standardized drug.
In some cases, however, as, for example, ipecac, I question if it
has been demonstrated that a standardized fluid extract will retain
its therapeutical value as fully as will the drug. Indeed, I am of
the opinion that the advantage is decidedly with the drug. Hence,
in such cases as this, which might be illustrated more markedly,
perhaps, with other drugs, the element of time may play an import-
ant part in the subject
On the other hand, with drugs that deteriorate more rapidly than
a bottled preparation made promptly from the drug when in its
best condition, the preference must, in my opinion, rest with the
fluid extract. Among these may be cited those substances con-
taining volatile bodies that escape by age ; as, for example, penny-
royal, peppermint, etc. (of course, the fluid must carry full amount
of tannates, etc.), and included in this class must be such substances
as disintegrate on exposure in drug form, as exemplified in Pulsa-
tilla, arum, etc.
Passing now to the great class of drugs in which nothing has been
""rebrrr-ri^™} Correspondence, 103
recorded as to the therapeutical constituents, and in which the men-
struum employed in making the official tincture is different from
that used in making the fluid extract, in my opinion the question is
open yet, and I hardly venture to express a view for or against.
Indeed, I would prefer to place these among emergency prepara-
tions, in which, in cases demanding prompt action, the making of
a tincture from the fluid extract is permitted, but in which the
general stock should be made, as yet, from the drug.
Among the preparations where tinctures may be made, I would
include all these fluid extracts not official and of which no standard
menstruum exists for making either the tincture or fluid extract.
These the pharmacist should be permitted (expected) to mix from
the respective fluid extract when he has a call for the tincture.
Finally, in cases where the menstruum directed by the U.S. P. is
decidedly different from that used in making the fluid extract, espe-
cially in those cases where the tincture is given in large doses and
in which the alcoholic strength of the tincture is very much less
than that of the fluid extract, the question ot therapy extends beyond
the drug question. If the fluid extract is mixed with the official
menstruum, an unscientific product results ; if it be not mixed with the
tincture menstruum, the superabundance of alcohol may prove objec-
tionable. In these cases, until the U.S. P. is corrected and identical
solvents used in making both tincture and fluid extract (which, in
my opinion, should be accomplished, and with few exceptions can
easily be done), the making of the tincture from the fluid extract
should be avoided, unless an emergency case renders it absolutely
necessary, which now and then will be the case.
In my opinion this subject is one worthy of some study and con-
sideration. I see no reason why manufacturers of fluid extracts
should not give directions for making tinctures from fluid extracts;
but, in my opinion, although such information is useful in emergency
cases, and in certain cases to be preferred, I would not advocate
the substitution of a line of tinctures made in this way without
Pharmacopceial authority. I feel that the skill required in making
these simplest of pharmaceutical preparations is not such as to pre-
vent their preparation from the drugs, and I believe it is the duty of
the Pharmacist to make them according to the PharmacopcL-ia, until
the Pharmacopoeia gives him the privilege of selecting either
method. This, I believe, in face of the fact that in my opinion ccr-
r Am. Jour. Pharm.
104 Ptire Spermaceti. { February, I897,
tain tinctures can in a general way be made as reasonably (or even
cheaper) from the fluid extract, and with greater uniformity than
from the drug. Of course, you are at liberty to use this letter in
your society if my personal opinion will be of service. Bear
in mind that the subject is considered in a rambling way and super-
ficially, but still it voices opinions gained by more than a little
thought in this direction. Very sincerely yours,
John Uri Lloyd.
PURE SPERMACETI.
By Lyman F. Kebi.e;r.
About a year ago, the writer presented^ some data on the ques-
tion of spermaceti. The conclusions arrived at then raised a ques-
tion concerning the absolute purity of the material operated on.
While it was impossible to state that the spermaceti was absolutely
pure, yet there was every reason to think that such was the case.
In order to settle the question as completely as possible, specimens
of spermaceti were secured as close to the natural source as the
nature of the case permitted. To bring this about most effectually,
every person who was likely to be in a position to secure a sample
of pure material was interviewed, either personally or through corre-
spondence. The original producers were also requested to furnish
samples that they were willing to guarantee absolutely pure. This
they cheerfully did.
By the above procedure, three specimens were received from the
Pacific Coast, through the kindness of Prof. W. R. Searby, of San
Francisco, Cal. Prof. E. L. Patch, kindly secured a sample himself
at New Bedford, Mass. Profs. J. P. Remington and W. R. Scoville
each obtained a sample from the same source, through friends closely
connected with the spermaceti trade there. The writer himself
secured five samples from the original producers, with guarantees of
absolute purity. Dr. Chas. Rice also assisted in the way of sugges-
tions. No. 12 was a specimen obtained by melting together several
samples taken from a purchase of 2,000 pounds. These specimens,
coming directly from the centres of supply of the United States, can
reasonably be expected to be pure, at least purer material cannot be
secured in this country.
^ 1896, Am. Jour. Pharm., 68, 7.
Am. Jour. Pharm.
February, 1897,
Pure Spermaceti.
los
Having accumulated the samples, they were carefully examined.
Physically, they resembled one another very closely, and did not
differ in any respect from the commercial material examined during
the past three years. They were all tested in the same manner
that those reported on last year were ; in addition, however, the
specific gravity was taken in a liquid lighter than the spermaceti, by
means of the sinker attached, and at the boiling point of water in a
pycnometer. Two methods lor attaching the sinker were employed.
In the first case, the sinker was simply tied to the spermaceti ; in
the second case, the sinker covered the spermaceti so that only one
surface was exposed to the liquid, thus reducing the question of
attached air-bubbles to a minimum. This was done in the follow-
ing manner : Porcelain crucible covers were carefully cleansed, dried
and their weight taken. The melted spermaceti was poured into
these covers, allowed to cool at the temperature of the working-
room and the specific gravity taken at the end of two days with
the spermaceti in situ. The congealing points were also observed.
The results are as follows :
1
)
\o
?
u
0
J .
0 ^
^-6
0 0
S
es
6
cd
°o
•o
'J
=
>»
^3
^b
u
3
(A
"p
I
be
a
u
u
s
u
CI
a
9
2s;
«2
fit
1-
2o
St
0%
* a
a
be
a
"5
y.
£^
£^
it
a—
U V
^ s
u 3
1
«<
c
be
a
0
1
JO
y
•c .
11
u
1--
s
u
-<
W
(A
(A
(A
tfl
(0
KemiDKton .
43*5°
42°
0-47
13962
08406
0*8083
0*8981
0*8979
08902
0*9381
Scoville . . .
44V
43°
O'lO
>25*
0*8405
0*8083
0*8989
08992
08987
09385
Patch ....
45°
43°
0-25
124*8
08404
0-8083
09042
09009
0*9036
0*9401
Scarby ....
44°
42-5°
0'2I
131*06
0-8458'
08124
0*9066
O9UO7
0-8954
0-9510
Searby ....
43°
4X°
om6
136-31
08432
0 81C9
0-8960
019099
0*8118
0-9413
Searby ....
43-5°
42°
043
129-91
0*8452
0*8160
0*8969
o*9uu9
0-9420
Kebler ....
44°
43°
o\V>
13030
0*8412
0*8089
1 0*8960
1
0*8972
0-8993
0-9394
Kebler ....
43°
42°
035
130*20
0*8412
0*8089
0*8899
08974
08937
Keblcr ....
44°
43°
023
I258I
0*8410
O.80&7
' 0*8982
0*8983
0*8982
0-9421
Kebler ....
46P
44-5°
019
129'oa
0*8412
08089
0-9079
09079
0-9013
0*9410
Kebler ....
44 5°
43°
039
12813
08419
08097
1
09103
0*9018
0-8992
0*9500
Commercial .
44°
43°
009
125*1
0*8409
0*8093
0*8991
0*8993
0*9010
0*9400
io6 Pure Spermaceti. {"^Y^i^^liyM^^-
The melting- points, acid numbers and ether numbers correspond
very closely with those reported last year. The anomalous specific
gravities are unique and require an explanation. The highest spe-
cific gravities were obtained by the same method that was used to
ascertain the specific gravities reported on in a previous paper, viz.:
alcohol diluted to such an extent that the small pellets floated
indifferently. This method, for convenience, will be called the sus-
pensory method.
In making the pellets for the suspensory method, the melted (on
a water-bath) spermaceti was dropped on a moistened plate having
a temperature of about 20° C. This was cool enough to chill the
melted spermaceti quickly, so that the molecules were not given
time to assume a crystalline form ; at least, the pellets were very
slightly crystalline, if at all.
For the other methods in which the solid material was employed,
the melted spermaceti was poured into porcelain crucible covers and
allowed to cool in a room at about 22° C. After cooling, the sper-
maceti was removed from the covers. All material worked on was
given at least two days' time to assume a normal state before the
specific gravity was taken. These prepared forms were 30 mm. in
diameter and about 6 mm. thick ; thicker in the centre, tapering
towards the circumference. The manner of congealing allowed
ample time for the spermaceti to assume crystalline forms.
Normally, spermaceti is crystalline. From the fact that the pel-
lets prepared for the suspensory method were non-crystalline, and
of a higher specific gravity than the crystallized material, the writer
is led to think that the specific gravity for normal spermaceti is not
much above o 9000 and not much below 08900 at 15° C. The spe-
cific gravity obtained by the suspensory method is probably abnor-
mal, due to the non-crystalline character of the pellets.
The writer, on referring td his memorandum, finds that the low
specific gravities obtained by the suspensory method, reported in a
former contribution (0905, 0-915. 0-920, etc.), were taken during the
months of August and early September ; while the higher specific
gravities (0935, 0939, etc.) were taken in November and Decem-
ber.
In the former case the elevated temperature was conducive to
the formation of more highly crystalline pellets than in the latter
case, when the temperature was considerably lower. The specific
^Febrnary^?S^"} P^^rc Spcrmaceti. lOJ
gravities embodied in the present paper were all taken during the
cold weather of December, 1896.
To throw further light on this point, further observations were
made. The writer has in his possession a sample of crude sperm
oil; on cooling, spermaceti crystallizes out and floats indifferently
on the liquid at about 22° C; the specific gravity of this mixture at
22° C is o 8846, which would approximate 08900 very closely at 1 5°
C. Next, a sample of spermaceti, having a specific gravity of o 9385
at 15° C. by the suspensory method, was dissolved with 20 per
cent, of paraffin, having a specific gravity of 09132 at 15° C. by the
same method. This mixture possessed a specific gravity of o 945
by the same method. The same spermaceti, with an admixture
of 33 per cent, of paraffin, had a specific gravity of 0-946 at 15° C.
by the suspensory method. The experiments again indicate that
the conclusion arrived at above is correct.
In view of the possibility of obtaining such variable results for
the specific gravity of solid spermaceti it is necessary to detail ex-
actly the conditions under which the observations are made, or the
results are worthless.
The writer recommends that the specific gravity of this substance
be taken at the boiling point of water. The results by this process
are uniform and concordant. This is done as follows : Pour the
melted spermaceti into the warmed pycnometer, insert the stopple
and plunge the bottle immediately into boiling water, to such a
depth that the neck of the bottle only projects. Keep the water
boiling for one hour, remove the bottle, wipe well, cool and weigh.
This gives the weight of a given volume of spermaceti at the
temperature of boiling water.
The conclusions arrived at in the previous article are fully sup-
ported by the observations made in this communication, except the
specific gravity of the solid material. To this constant a greater
degree of variableness must be ascribed, depending entirely on the
crystalline or non-crystalline condition of the spermaceti oper-
ated on.
Before closing the writer desires to kindly thank all who
assisted him with this work.
305 Cherry Street, Philadelphia, Pa.
io8 Solninc— Pilocarpine Hydrochloride. { ^ February! 1^97°"'
SOLNINE NOTE.
By John Uri Lloyd.
The American Journal of Pharmacy, April, 1894, contained a
paper from my pen concerning the alkaloid of Solamnn Caroli-
nense. To this alkaloid I ventured to affix the name Solnine, " in
order to give it an existence in literature." I also stated that
'• having never made a study of Solanine, I am not prepared to de-
cide concerning the identity of Solnine and that substance. If Witt-
stein's description of Solanine is correct, they are different." After-
ward (September, 1895) ^ determination was accurately made of the
melting point of crystallized solnine. This, together with the
characteristics noted in the paper of April, 1895, may be said to
fairly establish that Solnine is not the same as Solanine.
Melting point of Solnine 127-2° C.
Melting point of Solanine (as per current literature) . . . . 235-0° C.
A fresh supply of Solnine is now in process, and then I hope to
supply combustion figures.
PILOCARPINE HYDROCHLORIDE.!
By Dr. B. H. Paui^ and A. J. Cowni^ey.
In the last issue of the Pharmacopoeia of the United States of
America an addition was made to the characters of this salt by giv-
ing the melting point as 197° C, and an American journal has re-
cently expressed the opinion that an observation of the melting
point is the best means of ascertaining the purity of the salt met
with in commerce. It might therefore be inferred that the hydro-
chloride has in that respect an advantage over the nitrate, some
samples of which we have shown differ considerably in the melting
point. The question, however, is not so much as to the purity of
any particular salt, but whether the alkaloid obtained from jabor-
andi consists of more than one chemical individual. The results
already described by us'-^ point to the probability that the salts met
with in commerce under the name of pilocarpine nitrate do contain
more than one base, and there is consequently some uncertainty as
to which of those bases has the medicinal action peculiar to
jaborandi.
^ Pharmaceutical Journal, November 21, 1896.
"^ Pharm. Jour., 1896, p. i. Am. Jour. Pharm., 1896, p. 445.
'^Februa'ry^?^,™} Pilocarpine Hydrochloride. 109
A similar want of homogeneity might be expected to obtain with
the hydrochloride and other pilocarpine salts.
In examining some samples of pilocarpine hydrochloride as to
the melting point, we have found that this salt gives indications of
being a mixture of more than one chemical compound. Taking
the melting point in a Roth apparatus, we found that two different
temperatures might be read as the melting point, one at which the
substance in the capillar)' tube showed signs of partial liquefaction,
and a higher point, at which the contents of the tube became en-
tirely liquid. The results obtained with two samples of pilocarpine
hydrochloride are given in the following table :
Sample. Befjan to Run. Clear Liquid.
A 1927° 1967°
B 192-2° 1967°
This behavior appears to point to the probable presence of two
substances in both of the samples, judging from the partial melt-
ing at the lower temperature, and the way the salt becomes a clear
liquid at a point about 4° higher.
For one of these samples of pilocarpine hydrochloride we are
indebted to Messrs. Domeier, who were good enough to procure it
specially from the makers, Messrs. C. F. Boehringer & Sons. At
the same time they sent an account of the result of some pharma-
cological examinations they have had made in consequence of the
statement as to abnormal action of pilocarpine salts. ^ They have
found that a salt of high melting does not differ in its action from the
one of low melting point which can be separated by purification —
presumably fractional recrystallization. In regard to the medicinal
use of pilocarpine salts, this result would appear to show that the
possible presence of two substances is, from that point of view, a
matter of no account ; but, at the same time, it would do away
with the value of the melting-point test as a criterion of the quali-
ties of pilocarpine salts.
In reference to the abnormal action of pilocarpine salts analogous
to that of atropine, Messrs. Boehringer suggest that it may prob-
ably be due to the presence of jaborine ; but as the existence of
that base is somewhat questionable, such a mode of explanation
would require to be supported by more definite proof than is at
present available.
' Ibid. , p. 2.
Am. Jour Pharm.
no Literature Relating to Pharmacy. {^FebSiary!
1897.
RECENT LITERATURE RELATING TO PHARMACY.
NOTES ON THE TREES YIELDING MYRRH.
E. M. Holmes read an interesting paper on this subject at
an evening meeting of the Pharmaceutical Society, of Great
Britain (Pharmaceutical Journal, December 12, 1896), in which he
detailed his own investigations and at the same time incorporated
some literature on this subject, which appeared in the Kew Bulletin
for March and April, 1896.
Myrrh is imported into England chiefly from Aden, to which port
it is sent from Arabia and Abyssinia. Some comes from Bombay,
and is known in the London market as '' red Zanzibar " myrrh.
Writers on materia medica distinguish four varieties : Somali myrrh ;
Arabian myrrh, of Hanbury ; Arabian myrrh, of Dymock, or
Meetiya, and Yemen myrrh. There are also three others men-
tioned in Pharmacographia Indica, I, p. 307, as occurring in the
Bombay market : Persian myrrh, sent principally from Mekran,
Chinese myrrh and Siam myrrh or Meetiya ; the same authority
states that myrrh appears to have been shipped from China as early
as A. D. 1340.
Judging from the taste and odor of the four principal varieties of
myrrh mentioned above, it might reasonably be supposed that they
are the product of one species of Commiphora, or of varieties of
the same species modified by conditions of soil, elevation and
climate.
Concerning the plant which yields Somali myrrh, we have no
exact information, for there exists very little evidence connecting
the gum resin with the trees supposed to yield, owing partly to the
fact that collectors of plants are not usually well acquainted with
the drugs of commerce.
With respect to Arabian myrrh the case is different. About the
year 1820, Ehrenberg collected specimens of a myrrh tree at Gezan,
in South Arabia. These were referred to Balsamodendron myrrha,
Nees. Subsequently, however, Berg showed that two species were
mixed under this name, and he separated the second, which has
obcordate leaflets, under the name of B. Ehrenbergiana, Berg. The
first of these, Balsamodendron, or, as it is now called, Commiphora
myrrha, has recently been stated by Schweinfurth to yield no resin
at all, and the second has been identified as a variety of the Balm of
'^Febr**uao^?«^' ; Literature Relating to Pharmacy, III
Gilead tree, C. opobalsamum. Professor Schweinfurth has recently
stated that Arabian myrrh is the product of Commiphora Abyssinica,
Engl., and of C. schimperi [Berichte dcr Pliarin. Gcsellschaft, 1893,
pp. 218 and 237), but the Director of Kevv Gardens, in a lengthy
paper on the subject in the Kew Bulletin, 1896, p. 91, in which he
differs somewhat from the views of Professor Schweinfurth, expresses
the opinion that Commiphora simplicifolia may be accepted as the
source of Yemen myrrh, and that Fadhli myrrh be yielded by both
C. myrrha and C. simplicifolia.
Professor Schweinfurth supplied the herbarium of the Pharma-
ceutical Society with specimens of C. Abyssinica, C. schimperi, C.
simplicifolia, C. Africana and C. opobalsamum, and it occurred to Mr.
Holmes that some light might be thrown on this difficult question
by tasting the bark and fruits of these specimens, especially as true
myrrh has a very bitter taste, and a peculiar aroma, hardly likely to
be entirely absent in the plant itself. In none of these did Mr.
Holmes detect the odor and taste of myrrh, and he says we are
driven to the conclusion that Arabian myrrh is the produce of the
plant named Balsamodendron myrrha, by Nees.and not of C. Abys-
sinica, nor of C. simplicifolia, nor of C. schimperi. There are several
acrid gum resins that occur mixed with myrrh as imported. The
most abundant of these is opaque bdellium, which, as pointed out
by R. H. Parker [Pharm. Jour. [3], il, p. 41), differs from hotai in
its greater toughness, and in giving an intense greenish-black color
with ferric chloride. These are, doubtless, yielded by other species
of Commiphora. Thirty-five species of Commiphora are described
in A. DeCandolle's MonographicB Phancrogajnarutn Proiiro)ni, Vol.
4, pp. 9-^9.
RELATION OF THE GROWTH OF FOLIAGE LEAVES AND THE CHLORO-
PHYLL FUNCTION.
The following conclusions have been reached by D. T. MacDougal
{The Journal of the Linnean Society, 31, 526), after a practical study
of a number of plants:
(i) Material constructed in active chlorophyll areas and stored in
special organs may be transported to inactive chlorophyll-bearing
organs in some plants in light and in darkness, and be used in such
manner as to allow of the perfect development of these organs.
(2) The removal of concurrent members in darkness may have
112 Literature Relating to Pharmacy. {''^^i^^lrjAm^'
no effect, may cause an exaggerated development of the petioles, or
may result in the perfect development of the entire leaf. The
nature of the regulatory mechanism in each instance must be
entirely specific.
(3) It is possible for some plants to form perfect leaves in dark-
ness, some when a portion of the stem only is darkened, and others
when the entire plant is etiolated. It is thus shown that no invari-
able connection exists between the phototonic condition and leaf-
development.
(4) The conclusion of Jost, that pathological conditions ensue
more quickly in inactive leaves in light than in darkness, is not
capable of general application. The deterioration in certain plants
appears as quickly in darkness as in others in light.
(5) Placing a leaf under such conditions that it cannot construct
food material, sets in motion the specific regulatory mechanism of
the organism in such manner that the plastic material may be with-
drawn and the organ cast off. An exaggerated development of the
petioles may be induced in darkness by this mechanism.
(6) It is to be noted that plants may not be entirely ? as to their
reaction to an atmosphere devoid of COg upon the basis of species,
since a given plant may be capable of developing inactive leaves at
one stage of its development, and not at another. This is evident
upon consideration of the fact that such capacity is entirely depend-
ent upon the availability of the reserve food for this purpose.
In addition to this summary, the article contains an interesting
historical introduction and a short bibliography of the subject.
ORANGE GROVES OF NAPLES.
The Orange Groves of Naples are planted with wild trees, which
are grafted in the usual way, and grow with bare trunks to 4 or 5
feet from the ground. The branches then run out and form the
fruit-bearing portion of the tree. An ingenious and beautiful inno-
vation has been introduced into one grove, and is described by
Consul Neville-Rolfe in his latest report. Lemons are grafted upon
the bare and non-productive stems of the oranges, about 2 feet
from the ground, and trained in garlands from tree to tree, thus not
only increasing the productiveness of the grove very materially, but
adding greatly to the picturesqueness of its appearance. Orange
trees being usually planted in rows at a measured distance apart, a
"^Februao^r^T™} Liter uUirc Relating to Pharmacy. 113
grove has usually a geometrical appearance which is unsatisfactory,
but this appearance is very much modified by the lemons, which
break the lines in all directions. There is a legend which most
people firmly believe, that the grafting of a second fruit on the parent
stem materially alters the type and quality, not only of the original
fruit, but also of the graft, and it is sometimes gravely asserted that
•• blood oranges " are obtained by grafting the pomegranate on to
the orange. This, says the Consul, is a complete fallacy. Both
fruits retain their original quality, and neither borrows anything from
the other. There is thus no difference between the lemons grown
in the orange grove from those grown in the grove where lemons
alone are cultivated. — Pharmaceutical Journal, October //, i8g6.
DETERMINATION OF THEOBROMINE IN CACAO. (Eminger, in
Forschungsberichte, 1896, 275.)
The author first extracts vegetable fat by digesting 10 grammes
of the finely powdered material with 150 parts of petroleum
spirit ; the residue is then dried and a weighed portion boiled for
about half an hour, or until the formation of cacao-red is completed,
with 100 cubic centimetres of dilute sulphuric acid (3-4 per cent.)
in a flask fitted with a reflux condenser. The contents of the flask
are then turned into a beaker and, whilst hot, exactly neutralized
with the calculated quantity of baryta ; the whole is evaporated to
dryness with some sand, and the residue extracted in a Soxhlet
apparatus with 150 parts of chloroform for five hours; the chloro-
form is then distilled off and the residue dried at 100° C. This
residue is then washed with not more than 1 00 cubic centimetres of
carbon tetrachloride, which dissolves the fat and caffeine ; the theo-
bromine, being quite insoluble in carbon tetrachloride at 18° C., is
collected on a filter, dissolved in boiling water, the solution filtered
and evaporated and the residue weighed. By this method the
theobromine in different kinds of cacao was found to vary from 105
to 234 per cent., and the caffeine, from 005 to 036 per cent.
Theobromine is soluble in 736-5 parts of water at 18 C, in 136
parts at 100° C, in 818 parts of boiling absolute alcohol, in 21,000
parts of ether at 17° C, in 2,710 parts of boiling chloroform, and in
5,808 parts at 18^ C. "Theobromine begins to sublime at 220° C.
without melting, whilst caffeine sublimes at 180° C. and begins to
melt at 220° C." Theobromine is more or less decomposed if
114 Literature Relating to Pharmacy. {Tebruaryfis^'!"'
warmed for any length of time with alkalies, earthy oxides or hy-
d rated lead oxide. — The Journal of the Society of Chemical Industry ^
October ^i, iSg6.
ANALYSIS OF CHLOROFORM. {Gay, in y. Pharm. Chim., i8g6, ^, ^5P-)
(i) A piece of filter paper saturated with the chloroform should
dry completely, and the odor remain pleasant to the end. The con-
trary indicates the presence of amyl alcohol.
(2) Shake 6 c.c. with 3 c.c. of water and test with litmus paper ;
this should not be reddened.
(3) Shake with an equal volume of 10 per cent, silver nitrate ; a
white precipitate on standing indicates the presence of hydrochloric
acid, and a black precipitate on boiling, that of aldehyde or acetone.
(4) To 5 c.c. add 2 c.c. of a solution of I part of potassium bi-
chromate in 100 parts of strong sulphuric acid, and warm gently;
if alcohol be present a green coloration appears. A quantitative
test for alcohol is necessary, since 0-5 per cent, may be added to
preserve the chloroform. To 5 c.c. add I c.c. of Mohr's solution
(i part of potassium permanganate and 10 parts of alcoholic potash
dissolved in 25 parts of water) in such a manner that the liquids do
not mix ; then shake whilst slowly turning the tube, and observe
the time between the mixture and the appearance of a green color.
Time : 5 minutes Very pure chloroform.
25 " o*oi percent, alcohol.
" 3*5 seconds q-i " "
" 5 " 0-5
" Less than 5 seconds . . more than 0*5 " *'
One agitation 10 ** "
(5) Shake violently 10 c.c. with an equal volume of strong sul-
phuric acid and let stand. The mixture remains colorless, even for
an hour, if the product is pure, but if it becomes brown, the pres-
ence of chloro-derivatives of ethyl alcohol or of the higher homo-
logues is indicated.— r/^c- Journal of the Society of Chemical Indus-
try, October ji^ i8g6.
The quantity of quicksilver exported by the mines of Auerbach & Co. , at
Nikotovka, Russia, in the course of last year, amounted to 10,706 bottles, which
went to various European countries, China, India and to the Transvaal. For
consumption in Russia 1,596 bottles were sold. The output is steadily increas-
ing.—CA^wrj/ and Druggist, December 5, 1896.
Am. Jour. Pharm.
February. 1897.
Editorial.
IIS
EDITORIAL.
MINERAL STATISTICS FOR 1896.
The Etie^iyieering and ^fining Journal, of New York, in its issue of January
2, 1897, presents the statistics of the mineral and metal production of the I'ni-
ted States for the year 1896. These statistics are gathered from official sources,
or irom reports of producers, and will be found to be very close to those which
are made up later in detail. From these statistics we glean some facts of inter-
est to pharmacists.
1^5.
Non-Metallic Products.
Metric
Tons.
Alum 68,035
Bromine 179
Borax 6,126
Copperas 12,805
Copper sulphate 20,413
GypJsum 270,804
Petroleum, crude 6,420,741
Salt. evap>orated 1,539.178
Salt, rock 173.662
Soda, natural 1.724
Soda, manufactured 167,000
Sulphur 1,676
Metals.
Aluminum 408
Antimony 393
Copper 175.294
Oold 70,470 kilos.
Iron, pig 9.597,449
Lead (New York value) 142.29S
Platinum 150 ozs.
Quicksilver 1,179
Silver (commercial value) 1,441,087 k.
Zinc (spelter) 74 245
Value.
$2,225,000
102,662
742,850
69,846
1,350,000
974,219
42,547,701
5,844,34s
518.740
47.500
3,841,000
136.950
495.000
68847
36,944,9**
46,830,200
ioS.632,542
10,132,7^8
2,250
1.313.589
30.254,087
5.942,890
1896.
Metric
Tons.
72,900
2495
6,SiB6
10.796
20,412
241,900
5,731,920
1. 39 1. 349
146,998
».524
5893
579
205.853
85,773 kilos.
8,909 000
159.410
150 ozs.
1.160
1,414.'48
74.925
Value.
13,225,000
143.074
759.094
53112
1,350.000
867,071
42,116,184
5,43', J 05
138,840
3,500,000
100,000
520,000
83.440
48,786,080
S7, 000 ,000
87.688,690
10,472.733
2,250
1.222,444
30.461,665
6,074,319
s. p. s.
FIKLD BOTANY IN WINTER.
The Pharmaceutical Journal, in its issue of January 2, 1S97, says the wild
flowers most likely to be found in blossom in England during the early part
of January arc Capsella Bursa-pastoris, Ulex Europieus and Senecio vulgaris.
This leads us to speak of the winter-blooming plants in the I'nited States,
where in the latitude of Philadelphia one does not need to await the arrival of
spring to pursue outdoor botanical studies, since there is probably no month
in the year in which plants cannot be found in bloom in this latitude. It is
also of peculiar interest to observe the winter habits of a great number of
plants, even if they are not in flower.
A walk of four or five miles in the vicinity of Philadelphia, on November
26, 1896, revcale<l the following eighteen plants in bloom ; they were not
unusually protected, although many of them were found on banks having a
southern exposure: Sisymbrium ofllicinale, Lepidiuni virginicum, Stellaria
media, Ccrastium viscosum, Malva rotundifolia, Trifolium pratense, Daucus
carota. Solidago serotina, S. nemoralis, S. rugosa. Taraxacum officinale,
, r> ' ^ f Am. Jour. Pharm.
no KeVteWS. \ February,! 897.
Chrysanthemum leucanthemum, Aster ericoides, A. cordifolius, Autennaria
plantagiuifolia, Guaphalium polycephalum, Erigeron Canadense and Lobelia
inflata. Two other plants, Symplocarpus fcetidus and Claytonia virginica,
were found, which showed the floral organs well developed and only awaiting
a suitable time in which to bloom.
On December 31, the following were found in blossom : Taraxacum officinale,
Stellaria media, Veronica Buxbaumii, Lamium amplexicaule and Symplocarpus
foetidus.
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
EiNFUHRUNG IN DAS Studium der Ai.kat^oide, mit besoudercr Beriick-
sichtigung der vegetabilischen Alkaloide und der Ptomaine. Von Dr. Icilio
Guareschi, O. O. Professor an der konigl. Universitat Turin, und Director des
pharmaceutisch-chemischen und toxicologischen Instituts. Mit Genehmigung
des Verfassers in deutscher Bearbeitung herausgegeben von Dr. Hermann
Kunz-Krause, dozent fiir allgemeine und pharmaceutische Chemie an der
Universitat Lausanne. Erste Halfte. Berlin, 1896. R. Gaertner's Verlags-
buchhandlung, Hermann Heyfelder.
In publishing a German translation of Guareschi' s ** Introduzione alio Studio
degli Alcaloidi," Dr. Kunz-Krause has made available to a large number of
readers what would otherwise be a sealed book. The first half is now obtain-
able, and the second half will appear during the year 1897. After a brief intro-
duction , the work very properly begins with a historical review, in which the
development of the alkaloids is shown to have been the work of chemists of the
nineteenth century. Beginning with the discovery of morphine, by Sertiirner,
in 1805, this historical summary is divided by the author into six periods, as
follows :
Period i. — Discovery of numerous vegetable alkaloids, 1806-1835.
Period 2. — Investigation of the coal-tar bases (aniline), 1834-1848.
Period 3. — Discovery of pyridine and quinoline bases.
Period 4. — Synthesis of the oxy-ethylene bases and of the paraconiines ; the-
ory of the constitution of pyridine and quinoline.
Period 5. — Discovery of ptomaine and leucomaine.
Period 6. — vSynthesis of a large number of basic pyridine and quinoline
derivatives, and the investigation of the constitution of the natural alkaloids.
The history is followed by a brief description of the properties of the various
organic bases and a discussion of their structural relations. Several pages are
devoted to the alkaloidal reagents, and the behavior of each towards the alka-
loids is explained. Following this is a short summary on classification and
nomenclature, in which the great body of the book is divided into five sections,
as follows : I, Bases of the Open Chain Series ; II, Bases of the Closed Chain
Series; III, Metal Amines; IV, Alkaloids in the Narrower Sense; V, Pto-
maines and Leucomaines. The present volume is largely occupied by the first
two sections, and consequently embraces most of the synthetic organic bases,
as well as those natural alkaloids whose structure has been established.
The whole book is very systematically arranged, and furnishes abundant
material for prolonged study by everyone who is interested in this important
Am. Jour. Pharm.) ReVte'WS 11/
February, 1897. / yvrt/to/J. /
branch of organic chemistry. It is a great credit to both author and translator,
and we look forward with interest to the appearance of the second half.
Commercial Organic Analysis. A treatise on the properties, proximate
analytical examination, and modes of assaying the various organic chemicals
and products employed in the arts, manufactures, medicine, etc., with concise
methods for the detection and determination of their impurities, adulterations,
and products of decomposition. By Alfred H. Allen, F.I.C., F.C.S. Second
Edition. Vol. Ill, Part III. Philadelphia: P. Blakistgn, Son & Co. 1S96.
The installment of this work now published is nominally Part III of Volume
III, though practically it forms Volume V of the book. One more volume,
treating of proteids and albuminoid compounds, will complete the work. The
part now issued treats of the less important vegetable alkaloids, left over from
Part II ; non-basic vegetable bitter principles ; animal bases, including
ptomaines ; animal acids, and cyanogen compounds. Although considered by
the author as less important alkaloids, still there are among them those derived
from ipecac, colchicum, calabar bean and jaborandi, which makes them of con-
siderable importance.
The same systematic treatment has been accorded these alkaloids that was
given to those in Part II, and it serves to make the two volumes the most
important works on this subject in the English language. About one hundred
pages are devoted to the non-basic vegetable bitter principles. The literature
concerning these important compounds is very voluminous, and the author has
sifted that so as to make it available to other chemists. Not the least in this
class is his condensed statement concerning the constituents of digitalis, about
which so much has been written that in many minds the whole subject is
decidedly mixed.
Under the animal bases we have the whole subject of estimating urea as
well as the latest information concerning creatine and creatinine; these have
also been exhaustively treated in the author's Chemistry of the Urine, published
over a year ago.
The whole book is fully equal in value to its predecessors, and the final
volume is looked forward to with interest.
Popular German Names of Domestic Drigs and Medicines (Volks-
thiimliche deutsche .\rzneimittel-Namen). Compiled by Dr. Fr. Hoffmann.
Revised and enlarged edition. Pharmaceutical Review Publishing Company,
Milwaukee. 1.S96.
Dr. Hoffmann has performed a real service for the American druggist by com-
piling this list of popular German names and arranging them so as to be
available to every one but the most stupid. In nearly all parts of the United
States the pharmacist is confronted in his daily practice with the (lernian
names of many of the simpler drugs. The book can be had of the Pharma-
ceutical Review Publishing Company, at the moderate cost of fifty cents ^x
copy.
LE CoM.MERCE .\CTrEL I>E L'HkRBORLSTERIE I»\v^ TNI Ric.ioN DU
Langueix)C. Par le Dr. Ix>uis Planchon.
Ke^nni irom Journal de Pharmacie et deChimie, 1H96. An mtrrcsting con-
tribution to the local flora of a region very rich in medicinal plants.
Am. Jour. Pharm.
1 1 8 Pharmaceutical Meeting. { ^^ebrnarVT isp'
La Composition des Peptones de Viande. Par A. Denaeyer. A com-
munication to the second International Congress of Applied Chemistry at
Paris. 1896. Reprinted from ^«wa/^5t/^ /%arwa^/>.
Prospectus of the Twenty-fifth Annual. Session of the Cai^ifornia.
College of Pharmacy. Session of 1897.
MINUTES OF THE PHARMACEUTICAL MEETING.
Philadelphia, January 20, 1897.
The regular Pharmaceutical Meeting was held in the Museum of the College.
Mr. J. W. England was chairman. The minutes of the previous meeting were
allowed to stand as published.
Professor Trimble called attention to a sample of the genuine kino of Euca-
lyptus rostrata, which had been sent by Mr. J. H. Maiden, of Sydney, New
South Wales ; also to a sample of Texas rhatany Kramerie secundiflora, which
was collected in Mexico and presented by Prof. Alfonso Herrera ; and also to
some specimens of cultivated canaigre root, which were grown in California
and were unusually large.
Mr. Lyman F. Kebler read a paper on the "Volumetric Estimation of
Acetone" (see p. 65), which was considered to be particularly opportune,
inasmuch as the various applications of acetone as a solvent have only just
begun.
The author stated that the methods for estimating the percentage of acetone
were not yet perfected, and that only the amount of iodoform producing
bodies could be determined in the commercial product.
Mr. Edward T. Hahn read a paper on " Terpin Hydrate " (see p. 73), and
said that his experiments had been made with a view of producing the crystals
of this substance, rather than studying its therapeutic properties, or of deter-
mining its ultimate composition. Samples which had been made with ethyl
alcohol and also with methyl alcohol accompanied the paper.
After the reading of the papers, an interesting discussion on the subject of
the manufacture of some galenicals from fluid extracts ensued, and was par-
ticipated in by Mr. Kebler, Mr. England, Professor Remington and others.
The question was introduced at the December meeting by Mr. Kebler, but was
deferred on account of lack of time, and in the meantime he received letters
on the subject from Dr. E. R. Squibb (see p. 98), Dr. Chas. Rice (see p. 99) and
Prof. J. U. Lloyd (see p. 102).
Mr. Kebler prefaced his remarks by saying that the commercial aspect of the
question could not be taken into consideration ; that human life was too valua-
ble for this phase of the subject to merit any attention in this connection.
He said in considering the merits and demerits of the main subject that
" when it comes to the question of making infusions from the fluid extracts,
it must be admitted, on the one hand, that it is wrong in many cases, in the
light of our present knowledge ; but, on the other hand, it remains to be
demonstrated that an infusion made from a fluid extract is less active, thera-
peutically, than one from the drug direct. In some cases an aqueous meustuum
will educe active constituents that are insoluble in alcoholic solutions and vice
'^FebrX/^S:"} Pharinaccjitical Meeting. 119
versa. But when we enter the field of manufacturing tinctures and some other
preparations from the respective fluid extracts, debatable ground is invaded."
Before taking up this question he deemed it necessary to state that if the
position were taken that a U.S. P. preparation was U.S. P. only when made
strictly according to the directions therein laid down, and could not be made
in any other way, there was only a single answer to the question.
Some of the faulty and imperfect tests and methods of the Pharmacopoeia
were referred to, as well as some of the duplicate processes sanctioned by it,
as in the case of the processes for the manufacture of fluid extracts, and thus
the Pharmacopceia itself was considered to justifj-, in a measure, the applica-
tion of processes which seemed best adapted to the needs of the case.
Standardized preparations and the manufacture of other preparations from
them then claimed the speaker's attention. He said that the 1890 Pharma-
copoeia had incorporated methods for assaying the crude drugs cinchona, nux
vomica and opium, as well as some of their preparations ; and that the next
revision would, undoubtedly, be enriched by methods for assaying a number of
other drugs and their preparations. The assay processes already authorized
had been introduced on account of the great variability of the drugs to which
they were applied. Then referring to his analytical records the speaker said
that these showed that there were other drugs equally variable in character ;
for instance, one bale of aconite root assayed 0*4 per cent, total alkaloids, and
another I 14 per cent., or one root was nearly three times as potent as the
other. It was evident that tinctures and fluid extracts, made according to the
Pharmacopceia from these roots, would vary accordingly. In other words, the
tincture made from the root containing the high percentage of alkaloids would
be as powerful as the fluid extract made from the lower assaying root. This
was not an isolated case, but similar data could be furnished for other drugs.
The problem of extracting the active principles from the drugs completely
was next considered, and the speaker said that again and again cases had come
to his notice where only one-half, three-fifths, two-thirds or three-fourths of
these principles had been extracted from the drug operated upon. The fore-
man of the fluid-extract department of a large wholesale house was quoted as
saying: "The manufacture of unassayed preparations and of standardized
preparations are two diff"erent things. Before assaying was adopted, appear-
ance was the only requirement, whether one-half or one-third of the active
principles was extracted."
Then, summarizing his opinions, with reference to the foregoing statements,
the speaker said : " In view of the variableness of the drugs, and the element
of uncertainty introduced in manufacturing the various preparations, which is
the most rational course to pursue : to make tinctures, varying in strength
from a very small potency to the strength of fluid extracts, and fluid extracts,
solid extracts, etc., varying in the same degree ; or to make preparations that
are uniform in strength ?" In his mind there was only one answer. And again :
"What tinctures, for example, will possess the greater degree of uniformity —
those made from crude drugs varying extremely in potency, or those prepared
from standardized fluid extracts, etc.'"
It was stated that, in preparing tinctures from their respective fluid extracts,
the menstrua directed to be used were usually of such a strength that precipita-
tion was obviated. In some cases, a small precipitate settled out on standing ;
I20 Pharmaceutical Meeting, {^FebruaryTJsT;!"-
but this was also true of tinctures freshly prepared from the drug. If it was
inert in one case, it remained to be demonstrated that it was not in the other.
The chairman, Mr. Joseph W. England, was opposed to the manufacture of
other galenicals from fluid extracts, and referred to a paper prepared by him
and published in the September, 1893, number of this Journai,, upon the
question : " Is it possible to produce fluid extracts of such strength that they
can be diluted with proper menstrua to standard tinctures?" Much of the
argument then presented was brought forward by the speaker in support of
his views on the subject proposed for discussion.
One of the statements which he emphasized was that different classes of
proximate principles were yielded to menstrua of varying strength, and hence
oflScial tinctures could not be made from the respective fluid extracts, inasmuch
as the menstrua for these two classes of preparations varied greatly in their
proportions of alcohol and water as applied to different drugs, and in evidence
of this, the menstrua for a number of these preparations were given in tabular
form.
The claim was also made that an officially made tincture was relatively
stronger than the corresponding fluid extract, the relatively larger dose of the
fluid extract confirming this opinion.
The speaker stated that many manufacturers did not make their fluid extracts
according to Pharmacopoeial directions, but according to methods which their
own experience suggested. Another point was the variation in menstrua which
they used, which neither agreed with the Pharmacopoeial requirements nor
among themselves.
He, therefore, concluded that it was impossible to make tinctures uniform in
strength from fluid extracts, whether these were assayed or not, inasmuch as
the assay processes used likewise varied, as well as the standards assumed for
many drugs.
Professor Remington said that the main question was in reference to the
objects had in view concerning these two classes of preparations ; that fluid
extracts were intended to be permanent preparations and were made strongly
alcoholic, while on the other hand, the menstrua for tinctures were made as
aqueous as possible, and still extract and retain the desirable constituents of
the drug.
He also said that some principles which could not be obtained with a small
amount of dilute menstruum could be extracted from the drug by the use of
a larger quantity of the solvent, whereas in the case of fluid extracts the object
was to limit the quantity of menstruum.
In his opinion, to consider the question in reference to standardized fluid ex-
tracts was to limit it, as many manufacturers, who do not standardize these prep-
arations, nevertheless give directions for diluting them in the preparation of
tinctures.
The speaker remarked upon the custom among manufacturers of storing fluid
extracts for a time and then removing the precipitates formed, and questioned
the propriety of making tinctures from fluid extracts thus deprived of some of
their constituents.
On motion, the meeting adjourned.
T. S. WiEGAND,
Registrar.
THE AMERICAN
JOURNAL OF PHARMACY
MARCH, iSgj.
ACETIC ACID AS A MENSTRUUM AND SOLVENT.
By Joseph P. Remington.
Any one who has delved, even moderately, into the pharmacy of
the ancients, must have noticed the frequency with which the vine-
gar of that time was used as a solvent, but the nineteenth century
has witnessed the gradual decline of the use of acetic acid in phar-
macy.
The alcohol question, which is so perplexing, and which is still
unsettled, furnishes a reason for diverting the attention of the phar-
macist to some liquid which will, occasionally, take its place.
The object of the following experiments is to determine whether
acetic acid cannot be made to replace alcohol in at least some of the
preparations now in common use.
The antiseptic power of acetic acid is frequently overlooked, and
there is no question that the vinegars, if properly made, could ad-
vantageously replace many tinctures.
Slightly acidulated liquids are palatable to most patients, and
these, when combined in prescriptions with .syrups, are particularly
acceptable, inasmuch as the acid counteracts the cloying sweetness of
the syrups.
Then again, it is very desirable for physicians to have alternative
preparations of the same drug to give to patients who are liable to
become victims of the alcohol habit, and it cannot be denied that
the prescribing of tinctures, elixirs and other alcoholic preparations
have been the innocent means of working disaster.
The writer, four years ago, made a number of lluid extracts, using
acetic acid in place of alcohol. I hesc* liave been allowed to stand
( 121 )
122 Acetic Acid as a Menstruum and Solvent. {"^'^iS'SK''""*
alongside of others which have been made with alcohol, and most
of them have proved their superiority. It is the intention to report
upon these later.
It will at once occur to the reader that the presence of strong
acetic acid in a fluid extract would be objectionable on account of
its taste; but it can be shown that it is possible to evaporate the fluid
extract at a very low temperature, thus getting rid of the acetic acid,
and then re-dissolving a proper portion of the extract in a sol-
vent. If this extract be standardized, a definite preparation is se-
cured. It is true that a portion of the extractive seems to be ren-
dered insoluble during the evaporation ; but the experiments will
show that this can be re-dissolved by varying the menstruum, and,
in addition, it can be shown that this insoluble extractive usually
represents inert substances.
In the following experiments the acetic extract of nux vomica
was prepared with a lo per cent, acetic acid, made by Dr. E. R.
Squibb & Sons, and proved by assay to contain 15 per cent, of
alkaloids.
These acetic extracts can be made dry and pulverulent, and to dis-
tinguish them the writer proposes for them the name of " Acetracts."
No. I. — 2 gm. acetract nux vomica, treated with 100 c.c. alcohol,
sp. gr. 819, yielded a light colored tincture; the residue weighed
I 1 12 gm., and was not devoid of bitterness, plainly indicating that
the alcohol was too strong.
No. 2. — 2 gm. acetract nux vomica, treated with a menstruum of
75 c.c. alcohol and 25 c.c. water, yielded a residue weighing 0502
gm. The residue was very slightly bitter and practically an inert
substance. The tincture was limpid, transparent and of a dark
amber color.
No. 3. — 2 gm. acetract nux vomica, treated with a menstruum of
70 c.c. alcohol and 30 c.c. water, yielded a residue weighing 0-4<4
gm. This had a very slightly bitter taste, and was practically
exhausted, producing a limpid, dark brownish-red liquid.
No. 4.-2 gm. acetract nux vomica, treated with a menstruum of
65 c.c. alcohol and 35 c.c. water, yielded a residue weighing 0-360
gm. The liquid was not clear, a fine, brownish-red precipitate mak-
ing its appearance. The liquid could not be filtered satisfactorily,
and a small portion which was filtered continued to let fall a pre-
ci[jitate.
^'"M^ch.^Sw^"'} Acetic Acid as a Menstruum and Solvent. 123
No. 5. — 2 gm. acetract nux vomica, treated with a menstruum of
60 c.c. alcohol and 40 c.c. water, yielded a residue weif;hing 04 10
gm. The liquid was not clear, filtering with great difficulty, the
precipitate not settling.
No. 6. — 2 gm. acetract nux vomica, treated with a menstruum of
55 c.c. alcohol and 45 c.c. water, yielded a residue weighing 0340
gm. Ihe liquid was not clear, filtering with great difficulty, the
precipitate not settling.
No. 7. — 2 gm. acetract nux vomica, treated with a menstruum
of 50 c.c. alcohol and 50 c.c. water, yielded a residue weighing o 320
gm. The liquid was muddy, precipitate not settling, and not easily
filtered.
No. 8. — 2 gm. acetract nux vomica, treated with a menstruum of
45 c.c. alcohol and 55 c.c. water, yielded a residue weighing 0-246
gm. Liquid cloudy, precipitate settling in three days, filtering
with difficulty.
No. 9. — 2 gm. acetract nux vomica, treated with a menstruum
of 40 c.c. alcohol and 60 c.c. water, yielded a residue weighing 0450
gm. Liquid muddy, not easily filtered. The addition of a little
talc improved filtering.
No. 10. — 2 gm. acetract nux vomica, treated with a menstruum
ot 35 c.c. alcohol and 65 c.c. water, yielded a residue weighing O 338
gm. Liquid not clear; not easily filtered.
No. II. — 2 gm. acetract nux vomica, treated with a menstruum
of 30 c.c. alcohol and 70 c.c. water, yielded a residue weighing 0360
gm. Liquid not clear, filtered with difficulty, and filtrate does not
remain clear.
No. 12. — 2 gm. acetract nux vomica, treated with a menstruum
of 25 c.c. alcohol and 75 c.c. water yielded a residue weighing 0378
gm. Liquid not clear, but filtered more easily than No. 11.
No. 13. — 2 gm. acetract nux vomica, treated with a menstruum
of 20 c.c. alcohol and 80 c.c. water, yielded a residue weighing o 476
gm. Liquid not quite clear, filters without much difficulty, but
slowly.
No. 14. — 2 gm. acetract nux vomica, treated with a menstruum of
15 c.c. alcohol and 85 c.c. water, yielded a residue weighing 0426
gm. The liquid was not quite clear, but filtered fairly well.
No. 15. — 2 gm. acetract nux vomica, treated with a menstruum
of 10 c.c. picohol and 90 c.c. water, yielded a residue weighing 0-376
Am. Jour. Pharm.
124 Acetic Acid as a Menstruum and Solvent. {^^iAxcl'Xm.
gm. Liquid not clear, deposits some sediment, and showed evi-
dence of decomposition ten days after preparation.
No. 16. — 2 gm. acetract nux vomica, treated with a menstruum
of 65 c.c. alcohol, 10 c.c. glycerin, and 25 c.c. water, left very slight
residue, filtered easily and remained clear.
No. 17. — 2 gm. acetract nux vomica, treated with a menstruum
of 50 c.c. alcohol, 25 c.c. glycerin and 25 c.c. water, left very slight
residue, filtered easily but slowly, and remained clear.
No. 18. — 2 gm. acetract nux vomica, treated with a menstruum of
40 c.c. alcohol, 30 c.c. glycerin and 30 c.c. water, left very little res-
idue, filtered easily, and remained clear.
No. 19. — 2 gm. acetract nux vomica, treated with a menstruum of
20 c.c. alcohol, 20 c.c. glycerin and 60 c.c. water, left very slight
residue, filtered very slowly, but clear.
No, 20. — 2 gm. acetract nux vomica, treated with a menstruum of
10 c.c. alcohol, 10 c.c. glycerin and 80 c.c. water, left very slight
residue, filtered easily, but not quite clear.
No. 21. — 2 gm. acetract nux vomica, treated with a menstruum of
100 c.c. diluted acetic acid, and I gm. ground nux vomica added to
the percolate to aid in filtration. The liquid was not quite clear.
No. 22. — I gm. acetract nux vomica, treated with a menstruum of
100 c.c. diluted acetic acid, gave a liquid which was not easily filtered,
but which remained clear.
No. 24. — 2 gm. extract nux vomica, treated with 100 c.c. alcohol,
left a residue 0352 gm. The liquid was light-colored, filtered
easily and remained perfectly clear.
No. 25. — 2 gm. extract nux vomica, treated with a menstruum of
75 c.c. alcohol and 25 c.c. water, left a residue weighing 01 22 gm.
The liquid was dark brownish-red, remaining perfectly clear, but
throwing down a very slight dark precipitate after filtering.
No. 26. — 2 gm. extract nux vomica, treated with a menstruum of
70 c.c. alcohol and 30 c.c. water, left a residue weighing o-i88 gm.
The liquid remained clear after filtering, but with a slight precipi-
tate.
No. 27. — 2 gm. extract nux vomica, treated with a menstruum of
65 c.c. alcohol and 35 c.c. water, left a residue of 0-212 gm. The
liquid was clear, a slight precipitate settling after the liquid was
filtered.
No. 28. — 2 gm. extract nux vomica, treated with a menstruum of
^"iurch.^s^'"'} Acetic Acid as a Mcnstruuin and Solvent. 125
60 c c. alcohol and 40 c.c. water, left a residue of 0-232 gm. The
liquid was clear.
No. 29. — 2 gm. extract nux vomica, treated with a menstruum of
55 c.c. alcohol and 45 c.c. water, left a residue of 031 gm. The
liquid was clear, a slight precipitate settling after filtration.
No. 30 — 2 gm. extract nux vomica, treated with a menstruum of
50 c.c. alcohol and 50 c.c. water, left a residue of 0-316 gm. The
liquid was not quite clear, a slight precipitate settling after
filtration.
No. 31. — 2 gm. extract nux vomica, treated with a menstruum of
45 c.c. alcohol and 55 c.c. water, left a residue of 031 gm. The
liquid was not clear, a precipitate settling.
No. 32. — 2 gm. extract nux vomica, treated with a menstruum of
45 c.c. alcohol and 60 c.c. water, left a residue of 0342 gm. The
liquid was cloudy, a very slight precipitate after filtration.
No. 33. — 2 gm. extract nux vomica, treated with a menstruum of
35 c.c. alcohol and 65 c c. water, left a residue of 040 gm. The
liquid was cloudy.
No. 34. — 2 gm. extract nux vomica, treated with a menstruum of
30 c.c. alcohol and 70 c.c. water, left a residue of o 430 gm. The
liquid was cloudy.
No. 35. — 2 gm. extract nux vomica, treated with a menstruum of
25 c.c. alcohol and 75 c.c. water, left a residue of 040 gm. The
liquid was cloudy.
No. 36. — 2 gm. extract nux vomica, treated with a menstruum of
20 c c. alcohol and 80 c.c. water, left a residue of 0372 gm. The
liquid was cloudy.
No. 37. — 2 gm. extract nux vomica, treated with a menstruum of
15 c.c. alcohol and 85 c.c. water, left a residue of 0-420 gm. The
liquid was cloudy.
No. 38. — 2 gm. extract nux vomica, treated with a menstruum of
10 c.c. alcohol and 90 c.c. water. The residue not weighed. The
liquid was not clear.
No. 39. — 2 gm. extract nux vomica, dissolved in 100 c.c. water,
left residue 040 gm. The liquid was muddy, and, upon stand-
ing, showed evidence of decomposition.
No. 40. — 2 gm. extract nux vomica, di.ssolved in 100 c.c. diluted
acetic acid. The liquid was a clear, light amber color.
No. 41. — 2*4 gm. extract nux vomica, dissolved in 2,400 c.c.
126 Frangula and Cascara Barks. {^^iv^l\^Jm^.^'
diluted acetic acid. The liquid was clear and of a light amber
color.
It will be observed that the object of these experiments is to as-
certain whether acetic acid can advantageously replace alcohol in the
extraction of a drug like nux vomica. The answer is decidedly in
the affirmative. Acetic acid may be used for exhausting a drug
known to be difficult to exhaust, like nux vomica.
A solid preparation can be made from it ; this can be assayed and
standardized, and the liquid preparations made by re-dissolving the
solid in various mixtures of alcohol and water, with or without gly-
cerin, and of different strengths of acetic acid.
If the proper menstruum be chosen, the residue will be inert, and
may be filtered out. A number of other drugs have been exhausted
with varying strengths of acetic acid, such as sanguinaria, kola,
ipecac, squill, cinchona and colchicum seed.
A number of samples are presented, and especial attention is called
tosanguinaria with acetic acid 60 percent. This fluid extract has been
made four years, and does not show the least sign of precipitation.
It, doubtless, would be just as satisfactory if made with U.S. P.
acetic acid, and experiments are being conducted now, which will
prove this view.
FRANGULA AND CASCARA BARKS.
TO DISTINGUISH BETWEEN RHAMNUS PURSHIANA AND RHAMNUS FRAN-
GULA, AND TO EXCLUDE RHAMNUS CALIFORNICA, IN THE
STATE OF POWDER,
By L. E. SayrE,
Member of the Research Committee C, of the Committee of Revision of the
United States Pharmacopoeia.
One of the problems submitted to this committee is embraced in
the title to the present paper. For the purpose of the investi-
gation, authentic specimens of the barks were received from the
chairman of the sub-committee. Dr. Rusby, who had them specially
collected for the work.
In order to arrive at a conclusion as to the best method of distinguish-
ing the barks in the state of powder, it was, of course, necessary,
first to study them microscopically, and, if possible, find distinctive
elements which might survive pulverization, and be recognizable in
the state of powder.
Am. Jour. Pharm.
March. 18y7.
} Frangula and Cascara Barks.
127
The description of the gross characteristics of these barks may
contribute Httle to the purpose of the investigation; but these should
be stated, as they have a bearing upon {)harmacop(jL*ial description,
an item of interest to every worker in pharmacoprjeial revision.
Taking the specimens, furnished as above stated, I should say
that the pharmacopoeial description of Rhamnus Purshiana is some-
what faulty ; the color of the bark on the outside cannot be con-
sidered as a •• brownish gray," but a dark gray ; the thickness,
instead of being "about 2 millimeters," is about I millimeter. For
Fig. I, Rhamnus Purshiaua, cross section. .7, epidermis ; b, collenchyma ;
r, sclerenchyma ; d, stone cells ; e, medullary ray ; J\ bast bundle ; g, paren-
chyma ; //, crystals of calcium oxalate.
a description of the external characteristics of the three barks,
using the specimens furnished as a guide, I should perhaps adopt
in substance the following :
Rhamnus Purshiana. — In quills or curved pieces, about 3 to 10
centimeters long, and about i millimeter thick ; outer surface dark
gray and much encrusted by ashen gray lichen patches, with longi-
tudinal grooves from 3 to 10 millimeters apart ; inner surface
yellowish to light brownish, becoming darker by age ; smooth,
glossy and finely striate ; fracture short. \'ellowish ; in the insitic
128
Frans:ula and Cascara Barks.
/Am. Jour. Pharm.
t March, 1897.
When
layer of thick bark, somewhat fibrous and sHghtly bitter,
chewed the bark imparts a yellowish color to the saliva.
Rhamnus Californica. — In quills or curved pieces about 3 to lo
centimeters long, and about 1-5 millimeters thick; outer surface
grayish brown, beset with numerous lenticels, which are from round
to transversely elongated, infrequently longitudinally elongated, and
often longitudinally confluent. On scraping the surface of the bark
a reddish brown color is observed, which is due to the contents of
Fig. 2, Rhamnus Purshiana, longitudinal section. A, epidermis ; b, collen-
chyma ; c, sclerenchyma ; d, stone cells ; e, medullary ray ; f, bast bundle ; gy
parenchyma ; h, crystals of calcium oxalate.
the cork cells. Inner surface reddish brown to dark brown ; smooth,
glossy and finely striate ; fracture short (inner layer of thick bark,
although somewhat fibrous ; breaks with a short fracture); inodorous
and slightly bitter. When chewed the bark imparts an orange-red-
ish color to the saliva.
Frafigida. — See U.S.P. External character of this baric answers
well to official description.
From the marked physical distinction between these barks, one
^"Ma°rchj^'""} Frangula and Cascara Barks. 129
might suppose it an easy task to distinguish between them in pow-
der; but such is not the case; although differing widely in ap-
pearance, they possess very similar microscopical or anatomical
structure. The points of similarity may be stated briefly as fol-
lows:
(l) Narrow medullary rays, which extend nearly to thejcork,
these rays in Rhamnus Purshiana convcrgijig at their outer ends.
Fig. J, Rhamnus Frangula, cross section. A, epidermis ; b, collenchyma ; r,
sclerenchyma ; e, medullary ray ; f, bast bundle ; .1^, parenchyma ; /;, crystals
of calcium oxalate.
(2) Numerous small groups of bast scattered somewhat regularly
throughout nearly the whole bark, the number of fibres in the bast
bundle varying from 2 to 3 to perhaps 25 in each bundle.
(3) P^ch bundle of bast is bordered by a layer of thin. walled
cells, filled with cubical crystals of calcium oxalate ; these crystal
cells appearing very distinctly in longitudinal section, and in the
powder. (See drawings.)
130
Frangiila and Cascara Barks.
A.m. Jour. Pharm.
March, 1897.
(4) In each, the relative amount of cork, of collenchyma and of
parenchyma is about the same.
These structural similarities would seem to make the distinction
between the pulverized barks quite difficult, but fortunately, for this
purpose, there are a very few points of dissimilarity revealed by the
compound microscope and reagents, which may serve the pharma-
cologist.
Fig. 4, Rhamnus Frangula, longitudinal section. A, epidermis ; b, collen-
chyma ; c, sclerenchyma ; e, medullary ray ; /, bast bundle ; gy parenchyma ;
h, crystals of calcium oxalate.
Rhamnus Frangula contains no stone cells, while the Rhamnus
Californica and the Rhamnus Purshiana contain a large number of
them, scattered in large, irregular groups below the cork, and usually
outside the region of bast. The presence or absence of stone cells
is very easily noted by one familiar with vegetable tissues, and this
one characteristic is suggested as a means of distinction between
Rhamnus Frangula and the other two barks.
In the case of Rhamnus Purshiana and Rhamnus Californica, it
/
dm^ ^^es
^^S^' S> Rhamnus Californica. powder. B, collenchyma ; r, sclerenchyma
(cross); ^'', sclereuchyma (longitudinal); d, stone cells; e, medullary ray ; _/",
bast bundle ; ^, parenchyma ; h, crystals of calcium oxalate.
Fig^. 6, Rhamnus Frangula, powder. /?, collenchynia ; <', sclerenchyma
(cross); r' sclerenchyma (longitudinal ); e, medullary ray; /, bast bundle;^,
parenchyma ; h, crystals of calcium oxalate.
n2
Fran^ula and Cascara Barks.
( Am. Jour. Pharm.
\ March, 1897.
seems that no microscopical element can be detected sufficiently
reliable to depend upon as a means of distinguishing the two species,
the one from the other. However, if the powder be macerated
several days in diluted alcohol, a very marked difference may be
noted ; the powder of Rhamnus Purshiana will be of an orange-
yellow color, when mounted for microscopical examination, and
when viewed by a moderately high power the various tissues will
come out clearly, while the powder of Rhamnus Californica, sub-
FiIq-. 7, Rhamnus Californica, cross section. A, epidermis ; 5, collenchyma ;
c, sclerenchyma ; ^, stone cells ; e, medullary ray ; /. bast bundle ; ^, paren-
chyma ; h, crystals of calcium oxalate.
jected to the same treatment, assumes a purplish color, and when
viewed through the lens the tissues seem to be obscured more or
less by a dark coloring matter. If to a small quantity of the
powdered barks an alkaline solution be added, the color developed
in the Rhamnus Californica is a deep red, while that of the Purshi-
ana is orange. This test may be briefly stated as follows: If 0-2
gramme of the powdered bark be placed in a small test tube, and
Am. Jour. Pharm.
March, 1&97.
Frayigula and Cascara Barks.
133
there be added 2 c.c. of solution of potassa, T. S., Rhamnus Californica
will immediately produce a blood-red color, while Rhamnus Purshi-
ana will produce an orange-red. These differences in intensity of
color, thus developed, are very marked.
The deep red coloring matter so abundant in Rhamnus Califor-
nica is just beneath the outer cork layer, including the phellogen.
It can be very plainly seen in the whole bark by the aid of a simple
lens.
I
i
I
Fig. 8, Rhamnus Californica, lonj^itudinal section. A, epidermis; h, colleu-
chyma ; c, sclerenchyma ; d, stone cells ; i\ medullary ray ; /, bast bundle ;
g, parenchyma ; //, crj'stals of calcium oxalate.
The above outline seems to answer well the purpose of distin-
guishing between tlie three barks named ; but to detect one powder
mixed with another would, perhaps, be very difficult even to one
perfectly familiar with the drugs. Rhamnus Californica, when used
as an adulterant for Rhamnus Purshiana, could be distinguished by
the color test if in considerable cjuantit)'; small amounts could hardly
be detected.
The following addition to the descriptions of the two official
134 Phytolacca Decandra. {^iSSr"-
barks, Frangula and Rhamnus Purshiana is suggested. To the de-
scription of Frangula add : Medullary rays not converging at the
outer ends (distinction from Rhamnus Purshiana). Stone cells absent
(distinction from Rhamnus Purshiana and Rhamnus Californica).
To the description of Rhamnus Purshiana add: Medullary rays in
groups converging at their outer ends (distinction from Rhamnus
Californica). Stone cells present (distinction from Rhamnus Fran-
gula).
Drawings. — The description accompanying each one of the draw--
ings presented will aid somewhat in pointing out the structural
characteristics above referred to. Figures were drawn, using a i
inch ocular and i objective.
A CHEMICAL STUDY OF PHYTOLACCA DECANDRA.^
By G. B. Frankforter.
part first.
The important medical properties of the root of the common
poke weed, Phytolacca decandra, have made it the subject for a
number of investigations. While many important facts have been
learned, yet nothing of a definite character in connection with the
chemical side of it has been discovered. Crystalline substances
have been obtained, but none of them seem to have been carefully
studied. It has been with the hope of adding more to the present
knowledge of this interesting plant that the following experiments
have b^en conducted.
The -root, which has been the principal part of the plant under
investigation, was personally obtained, dried and prepared for exami-
nation.' It has been stated that the root undergoes a change, so
that after a year it virtually loses its medicinal properties. The
writer has been unable to corroborate this statement. Samples
were examined shortly alter the roots were gathered, and again
after two years. There was no apparent change. The writer there-
fore believes that if the root is carefully dried immediately after
gathering, it will retain its properties for a long time.
' Read before the American Chemical Society, Aug;ust, 1896, aud communi-
cated by the author.
''"March.'ISi^:"} Phytolacca Decandra. 135
ANALYSIS OF THE ASH.
It seldom occurs that a common plant is characterized by the
inorganic substance it contains. In this respect the poke weed
seems to be an exception to the rule. Mention has been made of
the large per cent, of potassium present, but beyond this the writer
has been unable to find any analyses of the inorganic part of the
plant. In order to verify the above statement, and to throw more
light on the inorganic side of the plant, a complete analysis of the
ash was made. The root was carefully cleaned, in order to remove
any soil from the surface, carefully dried and analyzed. Three
analyses gave the following average :
Per Cent.
Ash or inorgauic matter 13*38
The ash contained the following constituents :
Per Cent.
Potassium oxide 41*62
Sodium oxide 4 41
Calcium oxide 4*13
Aluminum oxide 1-62
Iron oxide . . 0*59
Magnesium oxide 6"25
Carbon dioxide 30*01
Chlorine 225
Phosphorus pentoxide 3 54
Silicon dioxide 5*21
Total 99 63
It will be observed that the plant is exceptionally rich in potas-
sium. It was at first suspected that this high per cent, of potassium
was characteristic of the locality from whence the samples came.
Samples from different localities were examined with practicall}' the
same results, so that there is little doubt that the plant has the power
of assimilating large quantities of potassium. It has been stated
that the leaves and stems of the plant contain as high as 4 2 per
cent, of potassium hydroxide. This is low as compared with the
above analysis, inasmuch as the leaves and stems of plants invari-
ably run higher than the roots in inorganic matter.
ANALYSIS OF THE GASES GIVEN OFF BY A DESTRLCIIVK DISTILLATION
OF THE KOOT.
The gas obtained by a destructive distillation of the root of this
plant has been briefly referred to as having a peculiar odor and pro-
136
Phytolacca Decandra.
f Am. Jour. Pharm.
t March, 1897.
ducing dizziness if inhaled.^ With the hope of throwing some
light on this physiologically active gas, a complete analysis of it
was made. The gas was prepared by placing a known quantity of
the dried root in a hard glass retort, removing the air and heating
as long as gas was given off. The gas was collected over mercury.
It was found to vary widely at different stages of the distillation.
That given off early in the process contained as high as 60 per
cent, of gas soluble in water, while that near the end of the process
contained less than 2 per cent. The gas at various stages of the
distillation was tried on several persons without producing any
physiological effects. There is a characteristic odor of ammonia
and pyridine derivatives throughout the whole process.
Owing to the wide variation in the composition of the gas given
off at different stages of the distillation, a series of analyses were
made by heating the substance just long enough to drive off suffi-
cient gas for a single analysis. For the experiment, 72 grammes of
the dried root were taken. The apparatus used was that already
mentioned. The distillation was continued until the gas ceased to
come off at a bright red heat.
The following is the result of the twelve analyses in the order
in which they were made :
Analysis.
I.
2.
3.
4-
5-
6.
7.
8.
9-
17-6
22-3
I"
CO"
10-8
6-1
9'
33'2
10.
II.
6-
12'
I'
GO"
10"
10"
i6-
45"
12.
Ammonia
Carbon dioxide . . .
Heavy hydrocarbons .
Oxygen
Carbon monoxide . ,
Hydrogen
Methane
Nitrogen
65-
13*
0-8
0-4
12*2
CO'
0-6
8-
6o-2
13"
0-8
GO'
i8-6
•6
1-8
5-
55*
H"
1-4
CO'
201
r
3-
5*5
46-
19-4
2*
00'
14*
2-6
^^
12*
37-
23-
2"
GO*
15-8
4'
4*
14*2
32-
24"6
2" 2
CO"
14*
6-
3"
l6*2
26-
24-
17
00*
12'
8-6
5-2
22-5
24*2
25"
I '5
00*
6-
9"
8-
26-3
15'
13*
1-8
GO-
8-8
6-4
IG*
45"
2"
10".
I*
00*
9"
17-8
19-4
4G-8
Total
100 '0
lOO'O
lOO'O
lOO'O
1
lOO'G I00"0
lOG'O
IGO'G
IOO"0
lOO'O
lOG'G
100"0
The gas estimated as ammonia, upon examination, was found to
contain other gases, as the amines, but no determinations of the
latter have as yet been made. The gas estimated as carbon dioxide
' American Journai, of Pharmacy, 1888, p. 123.
^VrchriS^'"."'} Estimation of Ash in Various Drugs. I37
was largely the peculiar-odored gas which is under examination.
It will be seen that the gases increase and decrease quite uniformly.
The variations which occur were undoubtedly due to the uneven
application of heat.
In order to determine whether or not the nitrogen estimated as
such was pure, the hydrocarbons were removed by combustion with
pure oxygen, and the residue sparked with excess of oxygen over
potassium hydrate until no further change took place. About 2CX)
c c. of the residue were taken, and at the end of the process there
remained 2-6 c.c. of gas, which remained unchanged after several
days' sparking gave the spectrum for argon. No satisfactory ex-
planation for this spectrum can as yet be given. The process is
being repeated with larger quantities of gas. It seems impossible
that this quantity could have come from the air which was left after
exhausting the retort with a mercury pump.
University of Minnesota,
Minneapolis, Minn.
ESTIMATION OF ASH IN VARIOUS DRUGS.
By Charles H. La Wall.
Sub-Committee of Research of the United States Pharmacopoeial Committee
of Revision.
The subject of the inorganic constituents of plants has received
very little attention in itself; the existing data are scattered, and, in
many cases, obtainable only after a laborious search. One exten-
sive work on the ash in plants was published in 1871.^
This concerns itself mainly, however, with the per cent, of ash in
various agricultural products. The work is in very few libraries in
this country, and jt was due to the kindness of Professor Trimble
that the author was enabled to consult it before tabulating his
results upon this subject.
Works on materia medica usually contain a list of the proximate
organic constituents of each plant considered ; percentages of these
constituents are only given in few cases, and then with no reference
to the authority whose figures are used. This is often unsatisfactory,
' 1871, Aschen-analysen von landivirihschaftlichcn ProJuctcn, Fabrikabf alien
und wildwachsetidrn Pflanzen. Dr. Va\\\\ Wolf.
Am. Jour. Pharm.
138 Estimation of Ash in Various Drugs. {^^i^^l^X^l
as in one case which came under the author's notice, the percentage
of ash present in a certain drug was stated as " about 8 per cent.;"
and, as authentic samples collected by the author gave a maxi-
mum of 5-20 per cent., and the highest amount in the commercial
drug was 342 per cent., the accuracy of the authority quoted is
questionable.
Some scattering contributions to this subject have been made in
the past few years, but in most cases the data are incomplete in
some one respect. It is a matter of surprise to note what little
importance has been attached to the moisture in the sample taken
for estimation. It is obvious that the moisture content varies with
the atmospheric changes to which the drug is exposed, and that
the only reliable basis for comparison is the per cent, of ash calcu-
lated to, or estimated in, the moisture-free substance.
The therapeutic activity of any given drug is attributable to the
constituents peculiar to that drug, irrespective of the physiological
effects produced by so-called inert cellular tissue. It might, there-
fore, truthfully be said that : The therapeutic effect of any given drug
is the algebraic sum of the effects of its proximate constituents. Effect
is used in a relative sense only ; no uniform or fixed value can be
given, in view of the fact that, in no two cases of administration, are
the conditions exactly similar. The inorganic constituents may play
a very small part in the physiological action of a drug, but, in the
present state of our knowledge, no factor, however slight, should
be ignored.
Certain groups of plants show marked peculiarities in the amount
of ash present. The leaves of those plants belonging to the Natural
Order Solanaceae are noted for the large amount of inorganic mat-
ter present ; in some instances over 25 per cent., or more than
one-fourth their weight, is obtained as ash, upon ignition of a
sample.
This work was begun for the purpose of collecting data on a
number of the more commonly-used drugs, with the hope that they
might be found of service in subsequent studies concerning identifi-
cation of drugs. The subject proved to be one of great interest,
and the results accompanying the present paper are published with
the idea that by making occasional contributions of a limited num-
ber each time, the tedium of a long, uninteresting list (dry reading
at its best) would be avoided, and also that others who are in a po-
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142 F lores DaturcE AlbcB. {^"mSSSt^'"'"'
sition to verify or add to the figures here given may be interested
enough to contribute additional data.
The general arrangement has been made alphabetical, the offi-
cial drugs being distinguished by printing them in italics, using the
pharmacopceial titles.
The present contribution contains all of the estimations made by
the author to date, the lack of uniformity in many respects being
due to an imperfect knowledge of what was required when the
work was begun.
Those which are incomplete are merely included for comparative
effect, and duplications will be made in every case, and, in the
future, only those results will be published which are complete as
regards the per cent, of ash, percent, of moisture in the air-dried
drug and qualitative examination of ash.
The ash estimations were made in a platinum crucible in the usual
manner; the moisture was estimated by drying about 5 grammes to
a constant weight at 1 10° C. In certain cases the alkaloidal or ex-
tractive value is included, but this is merely for the purpose of gen-
eral comparison ; the processes used for the estimation of such con-
stituents are at all times obtainable upon application to the author,
as a detailed record is kept of all estimations made.
FLORES DATURA ALB^.
By J. B. NAGE1.V00RT.
The task of investigating the alkaloidal strength of the flowers of
Datura Alba, L., was undertaken after reading the article by Mr. Van
der Wal, in Nederlandsch Tijdschrift voor PJiarmacie, 1895, and re-
produced in the Bulletin of Pharmacy^ 1896, p. 153.
It was my intention to go a step further and extend Van der
Wal's experiments over the Solanaceae, then Atropa and Hyoscya-
mus, on which he reported, and to begin with Datura.
There was not, however, as much material on hand for the work
as an English analyst, Mr. Frank Brownei had at his disposal.
The flowers of Datura are not used in the United States save for
ornamental purposes, while Browne reports that they are considera-
bly used in China as a medicine, as well as for criminal purposes.
' " Datura Alba," by Frank Browne, Pharm. four., 1896, p 197.
"^^^Mareh.^Sfr!"'"} F lores Daturce Albcc. 143
It will be wise to take particular notice of this, because the
Chinese element in our large cities amounts to something. Browne
reports that the drug is easily administered in tea.
I might be allowed to remark that the use of Datura as a stupe-
fying agent is practised, on a large scale, by all Asiatics, not by
the Chinese exclusively.
Mr. Browne's communication, with its local color, disposes effect-
ually of a doubt expressed in Gehe's BerichtCy for September, 1896,
p. 6. That firm state that they feel bound to call the attention of
the public to the irregularity that Naou-yang-hwa is the Chinese
name of a flower, which is mixed with aconite tubers, and that this
mixture is used, in powder form, in surgery, to alleviate pain. Gehe
further states: " Hanbury records that the above name is the Chi-
nese vernacular for Hyoscyamns. Naou-yang-hwa and Nau-young-fa
(Datura) are semi-successful European experiments to reproduce
one and the same Chinese hieroglyph." This seems to be a small
matter and easily disposed of. Of greater importance is what fol-
lows in the same Berichte, in regard to Datura.
Dr. Pienemann made an analysis of the seeds, of the root, and of
the leaves of Datura alba according to Keller's process, so that we
have now a fairly accurate knowledge of the value of this drug.
Compare also a later investigation by R. A. Cripps in No. 1290,
March 16, iS95,of the Pharm. Journal.
Dr. Pienemann has, in all probability, exhausted his plants with
Prollius' fluid.
Pienemann presumed that the alkaloid he obtained was atropine ;
he intended to prove this by Vitali's test. He mentioned also the
hypothetical " stramonine ;" but Vitali's test is a test for mydria-
tics in general, is a group reagent, not an identity reaction for atro-
pine only.
Above is said that not as much material could be gathered for
this investigation as Browne had at his command. I had about 60
grammes of dry flowers.
Browne found in the dry flowers, Chinese growth, 0485 f>er
cent, of an alkaloid which he called hyoscine.
I found in flowers grown in parks in Chicago, 0464 per cent, al-
kaloid by weight. I presume that Browne's figures are also obtained
on the balance, and not by titration and calculation.
Of course, the coincidence of these figures is remarkable. But it
144 F lores DaturcB AlbcB. {^'"mS;£9T°'-
is wise not to attach too much importance to this. I assayed the
flowers only once. I do not know if Mr. Browne repeated his analysis.
If I had obtained a higher result than Mr. Browne, that would not
have been proof that American-grown Datura alba flowers were
richer in alkaloid than those collected in China. Neither could the
reverse be argued if conditions differed. Let us take it simply as
a contribution in favor of the original Van der Wal's investigation,
and deduce a recommendation to our U. S. P. Revision Committee
from it. When the article, Stramonii folia, is revised for the eighth
decennial revision, I would like to see it read *' Herba Stramonii,
collected in blossom," instead of folia S., so as not to throwaway the
most valuable part of the plant any longer.
Assay. — The flowers, after being dried without the application of any artifi-
cial heat, were reduced to a fine powder. Fifty grammes of this air-dry powder
was exhausted by percolation with alcohol of 90 volume per cent. Exhaustion
was proved according to analytical rules. Alcohol was recovered in vacuo.
Residue was taken up with acidulated water (HgSOj^), whereby all the waxy
and resinous matter was left behind. The aqueous fluid, which was carefully
kept to a small amount, was, in a separator, thoroughly washed with chloro-
form, the latter removed. The fluid was made alkaline with ammonia water,
agitated again with chloroform. This was collected and the operation repeated
to exhaustion. The chloroform was evaporated spontaneously. The residue
was dissolved in acidulated water, because the alkaloid was not pure enough,
washed with chloroform ; the acid fluid being made alkaline again, yielded to
chloroform an amorphous, nearly colorless residue, which, being dried over sul-
phuric acid to constant weight, weighed 0*232 gramme, or o" 464 per cent. This
was dissolved in very diluted hydrochloric acid, precipitated with gold chloride,
the precipitate dissolved in slightly acidulated (HCl) water and recrystallized
from boiling water. The crystals thereby obtained had the form published on
page 67 of Fliickiger's Reaction, American edition. "Hyoscin goldchloride. "
Dried over H2SO4 in vacuo. M.p., 5 determinations, 792° C.
Atropine goldchloride has a melting point of 137°, Hyoscyamine goldchlor-
ide a melting point of 160°.
An extract of the flowers of Datura alba, was free from that large amount
of oil that bothers one so much in Sol. Ex. Sem. Stramonii, U.S.P.
Will the Revision Committee take it kindly under consideration to replace
stramonium seed with 20 per cent, useless fat, by stramonium flowers with
hardly any ?
Will a colorless petrolatum preparation of those flowers not make an elegant
sub-siitute for the unsightly ointment?
I want to see retained in our U.S.P. the very useful Datura. The flowers are
stronger tliaii the seed.
Conclusion. — I have made arrangements to repeat this examina-
tion on a larger scale, in the fall of 1897, and will plant a vacant lot
next to my laboratory with Datura alba.
^"i/aTh.^^""-} Ideyttifying Fats and Oils. 145
Mr. Frank Browne concluded that he obtained hyoscine,
goldchloride, m.p., 198°. This will have to be verified also, but
material is lacking now. The reader interested herein is referred to
the works of E. Schmidt, Max Biechele, Hager, F'isher and Hart-
wich, and especially to Blythe on •• Poisons, their Effects and Detec-
tion," London, 1895, P- 37^-
School of Pharmacy, Northwestern University.
HEAT OF BROMINATION AS A MEANS OF IDENTIFY-
ING FATS AND OILS.
By Wm. BR0MWE1.L, Ph.D., and Joseph L. Mayer, Ph.G.
A contribution from the Chemical Laboratory of the Brooklyn College of
Pharmacy.
Among other work required of the students in the Brooklyn Col-
lege of Pharmacy in the course in analytical and applied chem-
istry, is the examination of fats and oils, with a view to identifying
them and their adulterants.
In addition to the regular color tests, we had been employing
Maumene's method of identifying them by the rise in temperature
produced on the addition of sulphuric acid.
This method is a good one in the hands of an expert analyst, but
our experience with the students here proved it was not the
method for pharmacists ; it is somewhat unsatisfactory and the re-
sults not always regular and concordant, so much so that Professor
Bartley suggested that Professor Bromwell and myself adopt
Hehner and Mitchell's method of recognizing them by the rise in
temperature produced on the addition of I c.c. bromine to i gramme
of oil, and that the table published by them be extended so as to
include as many other fats and oils as could be obtained.
This method, which is quite recent (having been introduced to
the chemical world through the Analyst, July, 1895). depends for its
action on the fact that the oils are natural glycerides containing un-
saturated radicals capable of combining with the halogens.
This fact had been taken advantage of by Hlibl, whose iodine ab-
sorption method is so well known that it needs but to be mentioned.
Fawsitt (Journal Society Chemical Industry, 1888) tried to utilize
the heat evolved by sulphur chloride (SXI..). but nut with sufficient
success to make it popular.
146
Identifying Fats and Oils.
Am. Jour. Pharm.
March, 1897.
To prevent as far as possible loss of heat by radiation, Mitchell
and Hehner used Professor Devvar's vacuum jacketed tube, which
he had employed in his experiments with liquefied air. It is a small
inner tube soldered at the neck to a larger outer tube, from which
the air is practically exhausted, leaving almost a perfect vacuum and
consequently making it a non-conductor of heat.
The expense of such a tube determined us to make our experi-
ments with a cheaper apparatus, so that our method could be
applied and our results obtained at any time or place without special
apparatus.
X
?^^^
^^
^ISS
:-^-5t^
*«fy^ti
r^-g^cc
hm.*i'^^^mT.''.y»j
Fig. I.
Magnesia and Cotton.
.^ Magnesia.
The apparatus we adopted consisted of a larger beaker (a gradu-
ate or other glass vessel will do when a beaker is not at hand), with
about one-fourth of an inch of calcined magnesia in the bottom, a
test tube about 7 inches in length, around the bottom of which was
wrapped a small piece of cotton ; it was then put in the beaker and
imbedded in alternate layers of cotton and calcined magnesia,
being packed quite tightly so that the tube could be withdrawn and
replaced at will without disturbing the nest so made.
A Centigrade thermometer graduated to fifths of a degree com-
pleted the apparatus, which, when ready for use, presented the
appearance shown in Fig, /.
Am. Jour. Pbarm.
March, 1897.
} Identifying Fats and Oils.
147
Mitchell and Hehner added the bromine directly to the oil, but
the difficulty of conveniently handlinf]^ i c.c. of it was recognized
by Dr. Wiley {Journal American Chemical !£ociety, April, 1896),
who su<Tgested that it be diluted with chloroform.
Acting upon his suggestion, we diluted in the proportion of i c.c.
of bromine to 4 c.c. of chloroform.
The action of the bromine on some of the oils being so violent,
we diluted or dissolved them in chloroform in the proportion of 6
grammes of oil and made up to 30 c.c. with chloroform. We made
up this quantity, so that we might conduct a number of determina-
tions on each oil without having to prepare a fresh solution for each
determination.
Fig. 2.
Of the chloroform bromine solution, we made up enough to last for
one day's work, fearing that the action of the bromine on the chlo-
roform might, in due time, generate hydrobromic acid, which would
interfere with the results.
It is of great importance to accurately measure the 5 c.c. of oil
solution ; this is best accomplished by using a glass-stopped burette,
care being taken to avoid any loss by contact with the walls of the
tube during the flowing in.
In the oil solution a thermometer is inserted, to .sec that it lias
the same tcm()erature as the bromine solution ; if such is not the
f Am. Jour. Pbarm.
148 Identifying Fats and Oils. {^"^ii^lliXii.
case, it must be brought to the same temperature. As the action of
the bromine on the oil is instantaneous, it is necessary to have the
thermometer in the oil solution before adding the bromine.
The bromine being largely in excess of the amount required, the
5 c.c. of the solution need not be so accurately measured ; we
adopted Dr. Wiley's apparatus for measuring it {Fig. 2).
It is simply a wash bottle arrangement ; through one opening
in the stopper a pipette (graduated on the stem to 5 c.c.) passes
nearly to the bottom, through the other a short tube which con-
nects on the outside with an atomizer bulb ; by pressing this bulb
the solution is forced up in the pipette to the 5 c.c. mark ; the in-
dex finger is then used to close the top, the stopper and tube are
withdrawn from the bottle, the point of the pipette directed into the
oil, and, the finger being withdrawn, the solution flows in.
Our experiments proved that if the solution was allowed to run
in very quickly the temperature would be reduced, in some instances^
2°, there being much ebullition, which would throw the hot liquid
against the cold sides of the tube and thus reduce the temperature;
this result was also brought about by stirring the mixture with the
thermometer. We would, therefore, recommend that the bromine
solution be slowly run in, consuming about a half minute in adding
it. The figures in the table are the results of four determinations
on each oil, the average of these being given.
In making the tests we had in use about twelve of the beaker
test tube apparatus, so that after making the four tests the tubes
were withdrawn from the nests, washed out with petroleum benzine
and inverted so that they would dry. For the next set of tests we
took four more tubes and beakers, and so on, until we had used all ;
we then come back to the first set, having them, in the meantime,
cleaned, and the temperature of the nest reduced to that of the room.
Experiments made with a beaker with cotton loosely packed,
without any magnesia, proved that in this way the temperature
was also considerably lowered.
In the table will be found Hehner and Mitchell's figures for the
oils on which they worked. There will also be found Dr. Wiley's,
who worked on a few oils in the laboratory of the Washington
Bureau of the Department of Agriculture.
We are still at work on this subject, and hope in our next paper
to give a factor which, when multiplied by the rise in temperature
of the oil, will approximately give Hiibl's iodine number.
Am. Jour. Pharm
March, 1867.
} Identifying Fats and Oils.
149
We would also take this opportunity to thank the members of
the Class of 1897 for valuable assistance rendered us, under our
supervision and direction.
The oils were all supplied gratuitously by the dealers mentioned
in the table, and were supplied as the purest obtainable. For their
kindness and promptness in complying with our request, our thanks
are due.
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AMMONOL.
By George M. Beringer.
The manufacturers state that "Ammonol is a product of the
Amide- benzene series (CgH^NH.,). It differs essentially from the
other m.edicinal coal-tar products, especially in that it contains am-
monia in an active form and has a stimulating action on all the vital
functions." Its medicinal action is claimed " to be stimulant, anti-
pyretic and analgesic." The chemical composition is given as
•* Ammoniated-Phenylacetamide," but the chemical formula giv^en
on the label, '• CgHgNHo," is the accepted formula {ox amido-benzene,
which is commonly spoken of as aniline.
The writer was induced to make an examination of this valuable
mzu coaitar derivative {?^ It is a powder, having a very faint yel-
low color, put up in i-ounce vials. The odor is strongly ammo-
niacal, and on smelling the vial one can readily detect the peculiar
empyreumatic odor of commercial ammonium carbonate. On closer
examination, even with the naked eye, one can detect small parti-
cles of a crystalline character, indicatmg imperfect comminution of
a cr^'stalline ingredient. This is the so-called auiorphous micro
crystals of the manufacturer's description.
One gramme of the powder was rubbed up with 20 c.c. of water
and poured on a tared filter, and the mortar and filter carefully
washed v>-ith an additional 10 c.c. of water added in small portions.
After drying, the residue was a white powder, weighing -360 gm.
A portion left no ash on incinerating. On boiling with concentrated
potassa solution it was converted into aniline, and with chloroform
readily yielded the isonitrile reaction. From these tests, also sup-
ported by solubilitj' and color reactions, I was led to conclude that
this was pure phenylacetamide, or acetanilid. According to the
U. S. Pharmacopoeia, acetanilid is soluble in 194 parts of water, and
so the 30 c.c. of water used would have extracted -154 gm., and this,
added to the undissolved portion on the filter, would give the total
amount of acetanilid as -514 gm., or about 50 per cent.
'I he filtrate was a light canary-yellow-colored solution, and, on
testing, showed the presence of sodium and ammonia as carbonates.
The filtered solution of i gm. of ammonol in 30 c.c. of water, evapo-
rated on the water-bath, yielded a residue of -222 gm., and on pro-
longed heating, minute micaceous crystals separated and sublimed
^^March ';S^^"- } A mmonol. 1 5 1
into loose tufts on the surface. These crystals proved to be acetanilid,
showing that, as stated above, it had been partly extracted by the
water, and that it was more or less volatile at the temperature of
the water-bath. On incineration, the residue left -158 gm. ash,
which required 29- c.c. ^,j sulphuric acid for neutralization, which,
calculated for sodium bicarbonate, would be -24317 gm.
One gm. of ammonol was incinerated, and left an ash weighing
•157 gm., which, titrated with f-^ sulphuric acid, required 30 c.c, or,
calculated as sodium bicarbonate, -25 i 5 gm. This would indicate the
presence of about 25 per cent, of sodium bicarbonate in the product,
and leave 25 per cent, for ammonium carbonate.
On adding hydrochloric acid in excess to the canary-colored
aqueous solution, the color is changed to a rosy pink, which is again
changed to the pale yellow on adding ammonia water. With nitric
acid, the color is also changed to pink, but in excess is destroyed,
the solution becoming colorless, and ammonia does not again
restore the original color. From these reactions I became con-
vinced that a small amount of some aniline color had been added
as a disguise, and not for medicinal action. An examination of a
number of so-called aniline orange and yellow colors, for one possess-
ing similar reactions and tinctorial properties, was made, and the
dye known as Dietanilycllaiv was found to give similar reactions.
According to Allen (Commercial Organic Analysis, Vol. Ill, Pt. I,
p. i84),metanil-yellowor orange MN, is the sodium salt of diphenyl-
amine-azobenzene-meta-sul phonic acid.
From my examination, I am compelled to conclude that •• ammo-
nol," instead of being a new " coal-tar derivative," is merely an
admixture of the well-known acetanilid, sodium bicarbonate and
ammonium carbonate, and that the following formula represents its
real composition :
Gramme*.
li Acetanilid
Stxlium bicarbonate -5'
Ammonium carl>onate .... • ■ 5'
Metauil-yellow 0*005
Mixtures of acetanilid and sodium bicarbonate, as an antacid and
antipyretic and analgesic, have been in daily use by nearly every
physician for at least a decade. The addition of ammonium carbo-
nate as an arterial stimulant is not unusual, and in many cases such
a mixture must undoubtedly prove serviceable. Mr. Joseph \V.
152 Chemical Analysis of Sage Brush. {'^'^^^^11^^^'^'
England informs me that at the Philadelphia Hospital they use an
ammoniated acetanilid, the formula of which is :
Grains.
Ammonium carbonate ^
Sodium bicarbonate i/^
Pulv. acetanilid 2^
Misce.
Dose, one to three powders.
Ammonol thus appears to be another of the numerous mixtures
of acetanilid that are being palmed off on the gullable physicians
as new and valuable discoveries. The names published in their
circulars would indicate that the Ammonol Chemical Company have
been unusually successful in playing on the credulity of quite a
number of prominent practitioners, and medical as well as pharma-
ceutical journals.
CHEMICAL ANALYSIS OF SAGE BRUSH, ARTEMISIA
TRIDENTATA, NUTT.
By Griffith H. Maghke.
Contribution from the Chemical Laboratory of the Philadelphia College of
Pharmacy. No. 161.
The sage brush, or sage bush, is a small shrub, 5 or 6 feet in
height, which grows abundantly on the Western plains, covering
hundreds of square miles on the foot-hills of Nevada and Utah, and
extending from Arizona to Oregon and Sonora, and as far east as
Nebraska. It does not thrive where there is an abundance of water,
but rather prefers a dry, barren soil ; ranchmen very often clear their
ground of it by flooding with water.
When fired, it burns rapidly and with an intense heat, affording
excellent fuel, and the Indians employ the smoky flame in curing or
smoking their buckskins ; they also use an infusion of the leaves
for colds, headache and mountain fever (considered by many physi-
cians to be a modification of typhoid lever).
The leaves and flower heads used in the present analysis were
collected in Fremont County, Wyoming, at an elevation of 5,000
feet. F'ifty grammes of the fine powder were used, and the usual
method of plant analysis was employed, except that the drug, after
extraction with alcohol, was enclosed in a strong piece of muslin
and suspended in the water and succeeding solvents, with the result
that a much smaller amount of liquid was necessary for complete
^ V^h.^STi"" } Fluid Extracts. 1 5 3
exhaustion, and some loss in handling the drug by the ordinary
method was avoided ; it also admitted of expression being employed
without loss of material.
The following results were obtained :
Per Cent.
Moisture 848
Ash 492
Petroleum ether extract, containing volatile oil 084, fixed oil
and fat 041, wax melting at 61^ C. o 61, and caoutchouc
026 212
Ether extract, consisting of resins 4' 25
Absolute alcohol extract, containing resins, glucosidal bitter
principle, etc •• • 332
Water extract, composed of mucilage 3*22, glucose 052, ex-
tractive 4*90 8*63
Alkali extract, containing pectin 274, extractive 3 36 610
Acid extract 114
Lignin 6*44
Cellulose 54"6o
loooo
The ash was composed of calcium, potassium, manganese and
iron, combined with hydrochloric, sulphuric, phosphoric and car-
bonic acids.
The alcohol extract yielded a bitter principle by treating with
acidulated water and agitating this solution with ether or chloroform,
which removed the principle and deposited it, on evaporation, in
an amorphous condition.
Tannin and starch were not found in the drug.
FLUID P:X TRACTS.
By William B. Thompson.
Reasonable and well-tempered discussion on subjects in contro-
versy ought to be improving to knowledge. The natural tendency
of such would be to turn thought into new channels, or to broaden
its scope in directions already pursued. Events which, at times,
seem adverse and disappointing, may often be turned into fortune-
ate advantage. The use and ;///5-use of fluid e.xtracts in extempor-
izing the preparation of the lesser galenicals, as tinctures, wines,
syrups and infusions, has evoked the expression of some opinions
and is likely to arouse more. It would seem to be within the con-
154 Zanzibar Copal. {
f Am. Jour. Pharm.
March, 1897.
fines of truth to say that at least 90 per cent, of the pharmacists of
this country resort, in a more or less extent, to the practice of dilut-
ing fluid extracts to form the minor preparations. That this prac-
tice would inevitably follow the advent of this class of preparations
(fluid extracts) having official sanction, as well as unauthoritative
origin, was obvious, and plainly foreseen at the various periods of re-
vision, adoption and introduction. And it now has the appearance
of an eleventh-hour conversion for pharmacists to criticize the
natural sequence of their own acts. No protest having come from
the medical profession in regard to any deficient therapeutic value
of the lesser galenicals so made, may we not be straining a point or
principle somewhat in making too broad a condemnation of the
practice ?
If the fluid extract is right exactly, and in every particular just
what it should be, the addition or dilution (provided it be made
without material disturbance of permanent solubility) must be right.
There are two dilemmas and two horns ! If the result of contro-
versy should be to induce pharmacists to discriminate more intelli-
gently between the true and the false — between the good and the bad
— much good will undoubtedly arise from a seeming evil. But that
the 90 per cent, of pharmacists can be induced by any persuasion
or argument to abandon that national penchant for a short-cut to
the goal, is an idea too un-American to be entertained. Had w^e
not better wisely adapt the fluids to the dilutions ?
Philadelphia, February, 1897.
ZANZIBAR COPAL.i
By a. Stephan.
Copal is a collective name for a number of resins that exhibit
great differences in their chemical and physical properties ; they
may, according to the author, be arranged in the following groups :
[a) East African, probably derived from Trachylobium mossam-
bicense and Hymenea verrucosa.
{b) West African, said to be obtained from Guibourtia copallifera,
or from species of Copaifera.
* Pharmaceutical Journal, December 19, 1896.
^VaTh.^g^^"} Zanzibar Copal. I55
[c) Kauri copal from New Zealand, the botanical origin of which
is Dammara australis.
{d) Manilla copal, obtained from Vateria indica.
(e) South American copal, derived from Hymenea coubaril, H.
stilbocarpa, Trachylobium martianum, T. hornemannianum.
The first three are fossil resins, and are dug up out of the earth,
whilst the last two are collected from the plants yielding them.
To the East African copals belong the following three varieties:
(i) Copal from Mozambique.
(2) Copal from Madagascar.
(3) Copal from Zanzibar.
The purity and hardness of the last variety render it the most
valuable, and the principal object of the author's work was to
investigate the constituents of Zanzibar copal ; the details that
follow relate, therefore, to that variety only. This must be empha-
sized, because many statements are met with without any mention
of the variety of copal to which they refer.
From Bagamoyo, in East Africa, the author received raw
(unwashed) copal, pure copal, and specimens of the tree yielding it.
The resin is brought down by the natives to Kiboa from districts
from the coast ; the botanical specimens came from Usegna, which
lies inland westward from Bagamoyo. The commercial resin,
obtained from a German firm, agreed in its characters with the
genuine specimens sent from East Africa.
Zanzibar copal, finely powdered, melts at about 140^ C; it is
slowly but completely soluble in alcohol ; benzol, chloroform and
glacial acetic acid dissolve about 30 per cent., ether about 34 per
cent., petroleum spirit and carbon bisulphide about 10 per cent.
When boiled with alcohol the resin caked, and only a slight pro-
portion dissolved, but by repeated digestion with alcohol it could be
brought entirely into solution and precipitated with water. The
resin thus jjurified was more soluble in the menstrua previously
mentioned, and dissolved also in boiling very dilute solution of pot-
ash (o I). All attempts to separate it into other constituents were
unsuccessful, nor could it be saponified. It appeared to consist of
resin-acids, the principal of which, constituting about 80 per cent, of
tlie resin, was called trachylolic acid. This acid could be obtained
with difficulty in minute sphiero-crystalline masses, melting at
168° C. From it the potassium, copj^er and iron salts were pre-
Am. Jour. Pharm.
1897.
156 Literature Relating to Pharmacy. {"^"MaS
pared. A second acid, present to the extent of about 4 per cent,
only, was also obtained ; to this the name isotrachylolic acid was
assigned. These two acids, together with about 6 per cent, of
^/-copal resin and /9-copal resin, a bitter principle and volatile oil,
form the constituents of Zanzibar copal as far as the author could
succeed in separating them.
An examination of the stems sent from Usegna showed that^
although the primary cortex contains schizogenous secretion ducts,
these are soon thrown off as the secondary cortex is produced, and
in the bark of older twigs and of the stem no ducts could be found.
The resin appears, therefore, to the author to be a pathological
product.
RECENT LITERATURE RELATING TO PHARMACY.
ASSAY OF JOHORE GAMBIER.
\V. O. Richtmann {Pharmaceutical Review^ 15, 27) has examined
six specimens of Johore gambier obtained by the University or
Wisconsin from the Columbian Exposition. The tannin was esti
mated by the process recommended by the Commission of German
Technical Chemists and published in 1885; the catechin was deter-
mined by extracting it from the aqueous solution of the gambier,
and the ash and moisture according to the usual methods. The
following are the results in per cent. :
Specimen No. Moisture. Ash. Tannin. Catechin.
2,900 12-37 4'35 39*63 ii'ic.
2,901 II*20 3-63 32'5I 9*22
2,902 1-38 3-65 40-51 9-39
2.904 1-50 1-87 46-95 5-25
.2,905 8-37 3-77 22-21 8*68
2,906 7-00 4-13 29-94 6-98
The presence of two fungi, Penicillium glaucum and Aspergillus
niger, was demonstrated.
ON THE SEPARATION OF NITRATE OF COPPER FROM NITRATE OF
SILVER IN THE MANUFACTURE OF CAUSTIC.
C. J. H. ^ dixd^n [Pharmaceutical yournal, January 23, 1897) gives
the following method for separating these two salts : It is not gen-
erally known that strong nitric acid precipitates nitrate of silver
from concentrated aqueous solutions, and this action has been used
Am. Jour. Pharm. •
SiarchT^?.''"'} Literature Relating to Pliarmacy, 157
in the manufacture of caustic at the Calcutta Medical Depot. The
silver employed always contains a certain amount of copper, and
after solution of the metal in nitric acid and separation of the gold,
as much as possible of the nitrate of silver is crj'stallized out, and
the deep blue mother liquor evaporated to dryness. The dry salt
is then powdered and placed in a glass funnel, stopped with a plug of
asbestos, and percolated with strong nitric acid, specific gravity 1-42.
The nitric acid dissolves the whole of the nitrate of copper, leaving
the nitrate of silver perfectly white, while only a very small amount
of the latter salt is dissolved. The nitric acid can, of course, be re-
covered by distillation, and the small amount of nitrate of silver
separated from the nitrate of copper by precipitation with salt, and,
when sufficient has accumulated, reduced to the metallic condition
by one of the usual methods. In preparing nitrate of silver by
crystallizing out the salt, a point is reached when the mother liquor
is too highly charged with nitrate of copper to permit of a suffi-
ciently pure silver salt separating by crystallization, and this impure
or •* blue nitrate of silver" has hitherto been returned to the mint.
By the adoption, however, of the method above described, these
residues can be worked up and nearly the whole of the silver
obtained in the form of nitrate, and as the nitric acid can be recov-
ered the process is decidedly economical, while it affords a salt
practically free from copper.
TONKA BEANS.
The following information concerning this drug is furnished by
Superintendent J. H. Hart, of the Royal Hotanic Gardens, Trinidad,
in the Bulletin of Miscellaneous Information for January, 1897,
p. II.
The tonga, tonquin or tonka bean is the product of a tree known
to botanists as Dipterix odorata, Willd., and less frequently as the
Coumarouna odora of Aublet. The latter, however, is given in the
Kew Index as the nonun prius.
The tree thrives well in Trinidad when planted in shady, damp
situations, and is very abundant in the forest of the neighboring
mainland of Venezuela. The fruit or seed ripens in June and July,
and in these months large shipments are received in Trinidad
from South American ports. In the newspaper of July 10, 1896,
the arrival is reported of a consignment of 260 bags" Tonca Heans,"
Am. Jour. Pharm.
158 Literature Relating to Pharmacy. {^^ilxcx^Jm.
by S. S. Bolivar, an Orinoco trader. The beans are sent to Trinidad
for preparation for European and American markets ; for this pur-
pose they are conveyed to warehouses, where, under customs regu-
lations, they are steeped in rum for a certain time, and are then
spread on the floors in layers 9 to 12 inches in thickness, to undergo
a kind of fermenting and decaying process, during which white
crystals are developed on the outside of the bean. As much as
;^30,ooo worth have been imported and reshipped during a single
year. The tree grows some 60 or more feet high. It belongs to
the Leguminosae or bean family, but is one of the few members of
this order that produces a single-seeded drupe- like pod, which does
not open at maturity. The seed, when ripe, so soon loses its vitality
that it is difficult at times to procure supplies for raising plants.
A SOLVENT CAPABLE OF SEPARATING CODEINE FROM MORPHINE.
L. Fouquet (Jour, de Pharm. et de Chim,, [O], 5, 49) has found
that morphine is insoluble in anisol in the cold, and only slightly
soluble at the boiling temperature. Codeine, on the contrary, is
soluble in the same solvent cold, and its solubility rapidly rises with
the temperature according to the following :
Temperature. Morphine. Codeine.
9° Insoluble. 7*80 per 100, by weight.
16° .... '« 15-28 " "
32°
100° o"95 per 100. i64"oo *' **
150° 4-80
These investigations were made with a very pure anisol, boiling
at 150° C, and having a specific gravity of 0-991.
Morphine was found to crystallize in beautiful, colorless, anhy-
drous prisms by chilling the solution made in boiling anisol ; these
crystals did not melt at 120^, like the hydrated morphine, but
became brown at 210°, and were converted into an oily black liquid
at 247°.
It should be noted that the solubility of the codeine is increased
by crystallization from anisol ; since after one crystallization the
alkaloid dissolves in the proportion of 1075 P^rts per 100 at the
temperature of 0°, whereas the proportion is only 7-80 per 100 at
9° with the codeine of commerce.
The author concluded that he could, with anisol, effect a separa-
Am.Joar. PhHrm.
Ma^rch.TS""} Literature Relating to Pharmacy. 159
tion of the two alkaloids when mixed, and to establish this he made
a mixture of 1044 grammes codeine and 0-7 10 grammes of mor-
phine; he exhausted this with 20 c.c. of anisol at 15°, and washed
the residue with 10 c.c. more of the solvent poured on the filter;
after drying he found the residual morphine to weigh 0702 grammes,
corresponding to a loss of a little over i per cent. From these re-
sults he concluded that anisol is applicable in many ways as a
laboratory solvent in toxicological investigations.
NATIVE FOOD PLANTS OF THE COEUR d'ALENE INDIANS.
The following is taken from a "Report on a l^otanical Survey
of the Coeur d'Alene Mountains in Idaho," by John B. Leiberg.
Conttibutiotis from the ♦• U. S. National Herbarium^' Vol. 5, No. I.
The native food plants are few. The paucity of plants suitable
for human food is one of the most remarkable circumstances in
a region which supports such vast quantities of vegetation as
does this in its forest covering. Probably, for this reason mainly,
it contained only a small aboriginal population, and the only
localities in which there appear to have been permanent settle-
ments of the Indians were in the slack-water portion of the Coeur
d'Alene — possibly some existed in the lower valley of the St.
Joseph. The rest of the country was visited by them only in
their migratory summer and fall excursions in pursuit of game
and fish, with which the St. Mary and St. Joseph Valleys for-
merly abounded.
The most valuable food plant in the dietary of the Coeur d'Alene
Indians was undoubtedly the camass (Camassia esculenta), a plant
belonging to the lily family, therefore related to the onion, but lack-
ing all trace of alliaceous flavor and smell. The esculent part of
the plant is the bulb, which, in the fresh state, is of an oblong
shape, seldom more than 25 cm. (i inch) in diameter and 4 cm.
(l J^ inches) long. It is mucilaginous, and possesses very little, if
any, flavor. The flowers are bright or deep blue, and a cnmass
meadow in full bloom, seen from an elevation, gives the impression
that one is looking at a body of very clear water reflecting a cloud •
less sky. The lower portion of the valley of the St. Joseph, and, in
particular, that of the St. Mary and its tributaries, were, before the
advent of settlements, among the classic camass grounds of the
Coeur d'Alenes. Here the tribe came in large numbers each sum-
Am. Jour Pharm.
1 60 Literature Relating to Pharmacy. {^"^MaSfsS:
mer to dig the root and to hunt the deer and elk, which roamed
by the thousand in the surrounding forest, and to catch the trout
with which the streams teemed. Every meadow was a camass field.
The plant was so plentiful in many places that it is no exaggera-
tion to say that in the upper St. Mary basin more than one-half of
the total herbaceous vegetation in the lowlands was composed of
this one species. With the advance of settlements came the utili-
zation of the camass fields as hay meadows. This ended the exist-
ence of the plant, except as a weed in the farmers' fields, and the
camass digging in the Coeur d'Alene basins, like the game, is
now a thing of the past. Strangely enough, the plant seems to
have been entirely absent from the North Fork areas, at least I do
not know of a single locality where it occurs.
Two species of lichens, Alectoria fremontii and Alectoria ochro-
leuca, principally the form sarmentosa of the latter species, were
eaten by the Coeur d'Alene tribe. Both are extremely plentiful at
all elevations. Boiled, or rather baked, in which latter condition
they were mainly used, together with venison, they become some-
what gelatinous in their consistency, and lose the bitter taste which
they possess in a fresh state.
Of fruits, they had huckleberries (Vaccinium myrtilloides princi-
pally), raspberries (Rubus leucodermis and R. strigosus), black-
berries (Rubus ursinus or vitifolius) and service berries (Amelanchier
alnifolia). These fruits are gathered and used at the present time
by the white settlers, but none are abundant in the region except
the huckleberries and service berries, and these not every year.
The Coeur d'Alene Indians draw no more native plant foods from
these mountains. They are now mostly farmers, have large and
fairly well-cultivated ranches, and find in the raising of the cereals
and vegetables of civilization a far more bountiful supply of food,
and much more palatable withal, than they ever obtained from the
laboriously gathered camass of their mountain meadows.
Professor Dr. R. Kobert has left Dorpat, Russia, and will, in future, be
located at the Brehmenschen Liingciihcilanstalt in Gorbersdorf, Germany,
where he will occupy the position of director. Dr. Robert's ten years as Pro-
fessor of Pharmacology at the University of Dorpat have been eminently success-
ful ones, and many expressions of regret have been heard from those with whom
he was associated.
Dr. Hans Hermatm Julius Hager recently died at Neuruppin, Germany, at
the advanced age of eighty-nine years. We hope to furnish a suitable sketch
of this eminent pharmacist in our next issue, written by one of his friends.
"""MaThJS^:"} Editorial. l6i
EDITORIAL.
EIGHTH INTERNATIONAL PHARMACEUTICAL CONGRESS.
The General Pharmaceutical Association, of Belgium, has decided to hold the
Eighth International Congress of Pharmacy in Brussels, August 14 to 19,
1897.
There will be six sections organized :
(i) Legislation and questions of professional interest, Deontology and Phar-
maceutical Education.
(2) Practical Pharmacy, Pharmaceutical Chemistry and Pharmacopceia.
(3) Food.
(4) Sanitary Matters, Public Health.
(5) Microscopical, Bacteriological and Biological Researches.
(6) Toxicology.
The following questions have been suggested by the Committee of Organi-
zation to be discussed at the meetings :
(i) In the actual state of science, is it not advisable to enforce in all drugs
and medicines a normal quantity of active principles ?
(2) Is it not necessary to unify the modes of analysis of medicine and of
their active principles ? If so, what are the best ways of doing so ?
(3) As a question of public safety, what are the best regulations of the prac-
tice of pharmacy ?
(4) From a bacteriological point of view, what is the best system of analysis
of drinking water? How far can the methods actually known, be relied
upon ?
(5) Has the chemist the right of preparing and selling organic essences and
the substances employed in organotherapy ? Which are the best ways of insur-
ing the chemist of the value of these substances, and also of serums ?
(6) Show the best ways of encouraging the manufacture of new medicines ?
Is it possible, in patents, to amalgamate the protection of private trade and
public good? Would it not be preferable for the chemist to sell them and the
doctor to presenile them under names more appropriate to their composition ?
(7) Prepare the plan of a programme of pharmaceutical studies.
In addition to these queries, the committee has offered a list of twenty sub-
jects for papers, on which some six prizes will be awarded. Those who desire
to take part in the Congress should send their names to M. Maurice Duyk,
secretary, or Dr. Fernand Ranwez, president, 102 Chauss(5e de Wavre, Brussels,
Belgium.
AMERICAN MILK SUGAR.
Previous to the year 1890, milk sugar from Switzerland was largely used in
the United States. The establishment of a large number of " creanu-ries, "
however, has changed this condition of affairs materially. After making but-
ter and cheese, milk sugar is the only by-pro<luct. The vacuum pan appears
to have made this substance available to such an extent that it not only
largely supplies the demand at home, but it has become a factor in foreign
markets. The milk sugar manufacturers of (lermany have petitione<l their
Government for a protective tariff, not against the Swiss product, but against
that from .America, which, the petitioners claim, will gain such a foothold that
it will be difficult to exclude it. Consul Germain, at Ziirich, says that the
export of Swiss milk sugar to America has almost ceased.
i62 Reviews, {^"M^ll^J^'"^-
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
Principles and Practice of Agricultural. Analysis. By Harvey W.
Wiley, chemist of the U. S. Department of Agriculture. Volume III, Agricul-
tural Products. Chemical Publishing Company, Baston, Pa. 1897.
The third and final volume of this valuable work has recently been com-
pleted, and occupies 665 octavo pages. The three volumes cover about 1600
pages. Volume I deals with soils and their analysis ; Volume II treats of ferti-
lizers, and Volume III of agricultural products. All are full of special informa-
tion for the analyst, but the third volume appeals especially to the pharmacist.
It first considers the operations of sampling, drying, incinerating and extract-
ing, and then takes up the special processes involved in estimating sugars and
starches, carbohydrates in crude or manufactured agricultural products, fats
and oils, nitrogenous bodies, dairy products and miscellaneous agricultural pro-
ducts. The citation of authorities throughout the work has been on a liberal
scale, so that one has at his command a complete view of the whole subject.
There is no other book like it in the English language, and its possession is
almost a necessity to every one having to do with the analysis of organic sub-
stances.
Proceedings of the American Pharmaceutical Association at the
Forty-fourth Annual Meeting, held at Montreal, Canada, August, 1896, also
the constitution, by-laws and roll of members. Published by the American
Pharmaceutical Association. Baltimore. 1896.
It is with considerable satisfaction that we note the publication of th^ Pro-
ceedings some three months earlier than they appeared last year. It is to be
hoped that ere long they may appear within three months of the adjournment
of the meeting.
The something over 500 pages of Report on the Progress of Pharmacy are a
part of this volume, which will be of lasting value. Professor Diehl has made
an excellent collection of abstracts, which are both readable and instructive.
The original papers are an improvement over those which have appeared in
some previous volumes, although, as many of them were not thought suffi-
ciently well of by the members at the meeting to admit of their being more
than read by title, it is a question whether they should not have been curtailed
somewhat or omitted altogether.
A Simple Method of Water Analysis, especially designed for the use
of medical officers of health. By John C. Thresh, M.D. (Vic), D.Sc. (Lond.),
D.P.H. (Camb.). J. & A. Churchill, London. 1897.
What we took for a valuable work on water analysis for health officers and
physicians came to an untimely end in our estimation before we passed the
introduction. The claims for recognition by this book appear to be based on
the use by the author of a prepared reagent, called a " soloid," whereby he is
able to give the free ammonia, chlorine, nitrites, nitrates, hardness, absorbed
oxygen, etc., in water, with a facility that is little short of magical. It is a
kind of tablet medication applied to chemistry.
The author apologizes for this mechanical method of conducting water
examinations on the score of necessity, but it strikes us that the water had
Am. Jour. Pharm.l JP/^^'i/rncie \f\1
March, 18y7. / KCcieWS. IO3
better be let alone rather than to be tested with reagents of which the
so-called analyst can know nothing. A medical officer, with a case of ready-
made reagents and this book, would be a dangerous man. We believe there is
no better waj' to explain the character of the book than to quote the following
test for nitrites :
"Take about 70 c.c. of the water in one of the tubes, dissolve therein i
soloid of compound potassium iodide, add a soloid of acid sulphate and dis-
solve. Note whether any blue color develops within five minutes, and record
whether faint, distinct, very distinct or dark blue. If no blue color develops
in five minutes, nitrites are absent. The blue color, if produced, will be pro-
portionate to the amount of nitrites present."
H.\NDBOOK OF Structural Formulae, for use of students. By Henry
Leffmann. P. Blakiston, Son & Co. Philadelphia. 1S97.
Almost every one having to do with chemistry has felt the need of a book
with the foregoing title. Dr. Leffmann has, in compiling such a work, done a
real service to students, and, we might add, especially to those who are inter-
ested in the relation between chemical composition and physiological action.
Only alternate pages have been printed, in order to admit of the addition of
new compounds and of notes. A table of elements and an index add to the
completeness of the work/
Proceedings of the Seventeenth Annual Meeting of the North
Carolin.\ Pharmaceutical Association, lield at Moorehead City, July 22
and 23, 1896. Raleigh, North Carolina. 1896.
The two original papers are : " Guaiacol," by E. V. Howell, and " Expenses
in Comparison with Purchases of Drugs, and Expenses in Comparison with
Sales of Soda Water for a Period of Ten Years," by H. R. Home.
Des AcanthaceES Medicinales. By Georges Dethan. These ; Ivcole
Supcrieure de Pharmacie de Paris. 1S96-97.
This is a complete illustrated monograph on the medicinal members of
the natural order Acanthaceiu. The work is divided into two parts. In the
first part, the author treats the members of the order in general, giving the
geographical distribution, history, general morphological and anatomical
characters, principles of classification, properties and uses. In the second
part, the individual plants receive special treatment in regard to their
morphology, anatomic structure, properties and uses. The whole comprises
192 pages of valuable reading matter, with a complete index.
On the Toxic Action of Dissolved Salts and Their Elkctrolstic
Dissociation. By Louis Kahleuljerg and Ro<luey H. True. Reprint from
Botanical Gazette, August, 1896.
Native Drugs of Ceylon. By Professor Rodney H. True. Reprint from
Pharmaceutical Review, January, 1897. Bassia longifolia constitutes the special
subject of this interesting communication.
Gf.nhkal Rf,im)rt on a Hotanical Survey of thk C<»i:rR i» .Alhnk
Mou.NTAiNS IN Idaho DURIN<v thi: Summfr of 1895. Hy John \\. Lcilnrrg.
1 64 Pharmaceutical Meeting. { ^ VaS S?^''"'
Contributions from the U. S. National Herbarium, Vol. 5, No. i. Issued Janu-
ary 25, 1897. A number of interesting subjects are discussed concerning the
Coeur d'Alene region, notably, the mineral deposits, native food plants and
forest resources. Some of these we shall take occasion to notice elsewhere in
this Journal.
Electro-Germination, Bulletin No. 43. Hatch Experiment Station of
the Massachusetts Agricultural College, January, 1897.
This interesting coutribution shows that electricity exerts an appreciable
influence upon the germination of seeds. As a result of experiment it has
been found that at the end of twenty-four hours, over 30 per cent, more
seeds were germinated in the treated lots than in the normal, at the end of forty-
eight hours about twenty per cent., and in seventy -two hours six per cent.
Calendar of the Pharmaceutical Society of Great Britain. Besides
giving information to members and others concerning the Society, this book
contains many other valuable matters of interest to the pharmacist in general.
Les Drogues Recemment Inscrites au Codex. Par le Dr. Louis Plan-
chon. I. Les Strophanthus. II. Le Cascara Sagrada. Reprints from Bulletin
de Phannacie du Sud-Est. 1896. These are illustrated contributions on the
two drugs, from a French standpoint, and are a valuable addition to the subject.
The Journal of Pharmacology is the title of the successor to the Alumni
Journal of the New York College of Pharmac}'. The first number makes a
good start with a contribution on "The Comparative Anatomy of the Roots of
Rio Ipecac (Uragoga Ipecacuanha, Baill) and Carthagena Ipecac (Uragoga
Granatensis, Baill)." By Albert Schneider, M.S., M D.
Practical Druggist and Pharmaceutical Review of Reviews is the
title of a new pharmaceutical journal ; it is conducted by Benjamin Lillard, 108
Fulton Street, New York.
The Physician's Vest-Pocket Formula Book. Fourteenth Edition.
Published by McKesson and Robbins. New York. 1897.
MINUTES OF THE PHARMACEUTICAL MEETING.
Philadelphia, February 17, 1897.
The fifth of the present series of Pharmaceutical Meetings was held in the
Museum of the College at 3.30 p.m. Mr. J. W. England presided. The minutes
of the last meeting were allowed to stand as published.
The presentation of specimens was next in order, and the registrar called
attention to the following, which were sent by Mr, E. M, Holmes, Curator of
the Pharmaceutical Society of Great Britain : False Buchu, False Maranham
Jaborandi, Drimys Granatensis (pepper bark). Adulterated Hellebore, Aracati
Jaborandi, Ceylon Nux Vomica, Pilocarpus Microphyllus and Chinese Colo-
cynth. On motion, it was ordered that an expression of thanks be sent Mr.
Holmes for his donation.
Prof. Remington reported the results of a large number of experiments in a
paper entitled " Acetic Acid as a Menstruum and Solvent " (see p. 121). The
Am. Jour. Pl)arm.
March. 18tC.
Pharmaceutical Meeting.
165
paper was accompanied by samples of liquid preparations of various drugs,
and in calling attention to these, Prof. Remington said that acetic acid as a
menstruum was unsuited for some drugs, but that it could be used to replace
alcohol in a number of instances.
He also remarked upon the question of the cost of these solvents, and stated
that an extract made with alcohol was six times as expensive as one made with
acetic acid.
The subject proved to be of special interest to the retail pharmacists present,
and several of them reported favorably upon its use in making preparations of
such drugs as sanguinaria, ergot and gentian.
In connection with this subject, Professor Remington showed a convenient
device for controlling the flow of percolates, which he recommended as much
superior to the rubber tubing directed by the Pharmacopceia. The principle
embodied was that of a valve regulated by a screw adjustment.
The Micrometer Balance.
A paper on "-Vnimoiiol " was ])resented by Mr. Geo. M. Reringer (see p. 150).
Samples of ammonol from an original jxickage and ammonol made according
to a formula, which the author proposed for the compound after examination
of the manufacturer's product, were exhibited, and attention directed to the
complete similarity in appearance of the two products The paper elicited
considerable discussion, during which the frequency with which physicians
directed ammoniated acetanilid was remarked upon.
"A Chemical Analysis of Sage Hrush, .Artemisia Triilentata, Nutt." was the
subject of a contribution, by Mr. (irifiith II. Maghee (see p. 1521. The flo>*cis
and leaves were the parts examined, and in addition to the usual plant con-
stituents, a bitter glucosidal principle was obtained, which was found diflicult
to separate.
The last paper on the programme was presented by Mr. Chas. II. LaWall,
and was entitled, " I^stimalion of -Ash in Various Drugs" 1 see p. n;). This
was the fust of a series of papers on this subject which the author inieuds to
1 66 Obituary. {''^i^^S.-Xm^'^-
present. Results of examinatious of more than loo samples, official and unoffi-
cial, were tabulated. If completeness in the analysis of plants is at all desir-
able, then the importance of such work is at once apparent, and to the
future collaborators of materia medica such knowledge will prove extremely
valuable.
Professor Remington called attention to a new form of prescription balance,
which is manufactured by the Micrometer Balance Scale Company, of Troy,
N. Y., and is illustrated by the accompanying engraving. The arms are of
unequal length and there is but one pan. The knife edges are delicately
adjusted and the ordinary weights are discarded. The principal feature of the
device is embodied in two graduated cylinders, in combination with a screw.
The inner cylinder is rigidly attached to the arm, and by moving the outer
cylinder either to or from the fulcrum, weighing is accomplished, the weight
being read on the index.
There being no further business, a motion to adjourn was affirmed.
T. S. WlKGAND,
Registrar.
OBITUARY.
Auguste Tread, the eminent French plant anatomist, died in Paris, October
1 6, 1896. His most noteworthy papers pertained to the vascular system of
plants. Under the auspices of the French Government he explored various
regions of North America in 1848 and 1849, and many of the cactus species of
European gardens, as well as the Yucca, which bears his name, were introduced
by him.
On August 9, 1896, /<9/z7^ C. Allen died at his home, 335 South Fifth Street,
this city, in the ninetieth year of his age. He was educated as a druggist,
having graduated with honor from the Philadelphia College of Pharmacy in
1829, He was elected a member of the College in 1829, and for many years
was noted as being the oldest living alumnus. He was a direct descendant of
Nathaniel Allen, one of the commissioners of Penn, for laying out Phila-
delphia.
Henry Bower, a well-known business man of this city, died at his late resi-
dence, 130 South Twenty-third Street, March 26, 1896, aged sixty -three years.
He graduated from the Philadelphia College of Pharmacy in 1854, and after
graduation, entered business as a chemical broker. Subsequently, he engaged
in the manufacture of chemicals. Glycerin was one of the products made, and
several years ago he received the Elliott-Cresson Medal from the Franklin
Institute for the process for the utilization of crude glycerin. He was con-
si lered an authority on subjects relating to the manufacture of chemicals, and
was the author of a number of articles on these subjects. He was one of the
Board of Managers of the Franklin Institute and a member of the American
Pharmaceutical Association.
IleJiry Trimen, M.B., F,RS., F.L.S., died at Peradeniya, Ceylon, October
i6th, in his nfty-third year. He was appointed Director of the Botanical Gar-
All). Jour, Pharm.1 (Ihitunrv \f\n
March, 1897. / UUllUar). lO/
den, Ceylon, in 1879, ^"^ held that position until July last, when he retired,
on account of serious ill health. Dr. Trimen's administration was signalized
by great success, for not only did the gardens at Peradeniya take front rank
among the great botanical establishments of the world, but three volumes of
the " Hand-book of the Flora of Ceylon " were completed, and the fourth and
last volume was in course of preparation. The work entitled, " Medicinal
Plants," he prepared in conjunction with Professor Bentley, while he was an as-
sistant in the botanical department of the British Museum. He was also one of
the authors of Trimen and Dyer's " Flora of Middlesex," and for a number of
years editor of the Journal of Botany.
Alfred Henry Mason ^ Ph.C, F.C.S.y F.R.M.S., died at his home in New
York City, November 2, 1896. His illness was only of short duration, and by
his death pharmacy lost one of its most active and efficient representatives.
Mr. Mason was identified with a large number of societies and scientific bodies,
and had served in many of these in an official capacity, and was equallv well
known in professional and trade circles, not only in this country, but abroad
as well. He was born at Newcastle-Under-Lyme, England, fifty-three years
ago, and at an early age began his pharmaceutical career. In 1866, he became
identified with the wholesale trade, and had been actively interested in this
branch of business ever since. In 1892, he began his residence in New York,
when he was appointed secretary of the firm of Seabury ^i Johnson, of that
city. About a year ago he was elected secretary of the College of Pharmacy,
and for five months previous to his death had been editor of the Alumni
Journal.
George Frederick Schacht, a pharmaceutical chemist of Clifton, Bristol, Eng-
land, died at his home, December 26, 1896, in the seventy-fourth year of his age.
Mr. Schacht was one of the best-known pharmacists in England, and, by his
death, the cause of pharmacy has sustained a distinct loss, for he was not only
an accom])lished practical pharmacist, but was earnestly devoted to the cause of
pharmaceutical education.
We quote the following from the Pharmaceutical Journal, of January 2, 1897 :
"Asa pioneer of pharmaceutical advancement, Schacht will long be remem-
bered as having originated the idea which led to the foundation of the British
Pharmaceutical Conference, for his advocacy of provision being made for pro-
vincial education, and of a compulsory curriculum.
" He joined the British Pharmaceutical Society in 1S42, shortly after its organi-
zation, and served it officially in one capacity or another during a number of
years. He was also a member of the Bristol Pharmaceutical Association, and
had long l>een actively engaged in connection with the University College of
Bristol, of which institution he was treasurer at the time of his death." He
was a corresponding member of the Philadelphia College of Pharmacy.
Aionzo Robhins, Ph.M., a member of the Philadelphia College of Pharmacy,
died suddenly at his home in this city, December i, i.S9h. The decease<l had
been in ill health for more than a year, but the immediate cause of his deatli
was an acute attack of pneumonia.
Mr. Robbins was lK>rn in Pottstown, Pa., about sixty-three years ago. He
^o r)U:*^,^^A, / Am. Jour. Pharm.
1 68 Ubltuary. \ March, I897.
graduated from the Philadelphia College of Pharmacy in 1855, was elected a
member in 1868, and in 1878 became a member of its Board of Trustees.
After graduation he was engaged for the most part as a drug clerk until the
close of the Civil War, when he engaged in the retail drug business for himself
at Eleventh and Vine Streets, this city, where he remained until his death.
Mr. Robbins took an interest in all matters pertaining to pharmacy, and was
an occasional contributor to this Journai.. He did considerable work in con.
nection with the formation of the pharmaceutical laws of this State, and when
the Board of Pharmacy was appointed, became, on June 23, 1887, its first presi-
dent. This position he held until May, 1895, when he resigned.
No small share of credit was due him for his efiforts in helping to found the
Pennsylvania Pharmaceutical Association, of which he was a member. He was
also a member of the American Pharmaceutical Association.
He was a member of the Committee of the Philadelphia College of Phar-
macy for carrying on work for the Revision Committee of the 1880 Pharma-
copoeia. His subject was fluid extracts, and he performed a large number of
experiments for determining the most satisfactory formulae for these prepa-
rations.
Theodore George Wormley, M.D., Ph.D., LL.D., a member of the Faculty
of the University of Pennsylvania, died at his home, in this city, January 3d,
1897, after an illness of about two months.
Prof. Wormley was born at Wormleysburg, Pa., in 1826. His collegiate
training began at Dickinson College, Carlisle, Pa., where he spent several
years, but left before the completion of his course in order to enter the Phila-
delphia College of Medicine, from which institution he graduated in 1849.
After graduation Dr. Wormley was engaged in the practice of his profession,
first in Carlisle and then in Columbus, O., until 1852, when he was appointed
professor of chemistry and the natural sciences in Capital University of that
city, which position he held until July, 1865. In 1854 he received the appoint-
ment of professor of chemistry and toxicology in Starling Medical College, of
the same city, and retained the position until 1877, when, in June of the latter
year, he was chosen successor of Dr. Robert E. Rogers as professor of chemis-
try and toxicology, in the department of medicine of the University of Penn-
sylvania, which position he held until his decease.
During his professional career Dr. Wormley held many other positions of
honor and trust, calling into account his abilities as a chemist and scientist.
He was a member of a number of scientific bodies in this country and a Fellow
of the Chemical Society of Ivoudon.
His scientific papers were numerous, and quite a number of these were pub-
lished in the American Journai, of Pharmacy. As long ago as 1870 a very
valuable article of his, entitled "A Contribution to Our Knowledge of the
Chemical Composition of Gelsemium Sempervirens," appeared in its columns.
His last contribution to its pages was in 1894, on the subject of "Some Tests
for Quinine."
His most notable work was his book, " Micro-Chemistry of Poisons," which
was extensively reviewed by Professor Maisch in the September, 1867, number of
this Journal and needs no comment here, other than to say that its value
as a standard authority is recognized throughout the world.
Parthenium Hysterophorous. Flowering branch, three-quarters natural size.
At side, flower heads about twice natural size.
THE AMERICAN
JOURNAL OF PHARMACY
APRIL, 1897.
PARTHENIUM HYSTEROPHOROUS.
By H. V. Arxy, Ph.G., Ph.D.
The Pharmaceutical Journal and Transactions, in its issue of May
30, 1885, called the attention of the pharmaceutical world to this
♦' common weed of Jamaica," quoting from La Cronica Medico-Qui-
rurgica, of Havana, the physiological experiments of Dr. Jose R.
Tovar with a so-called alkaloid, which he named parthenine, ob-
tained from the plant. Another reference to the body parthenine
is found in Pharmaceutical Journal, June 26, 1886, where the inves-
tigations of M. Guyet, as reported to the Societe de Thcrapeutique of
Paris, are set forth. The next reference to the plant is found in
Merck s Bulletin, October, 1888, where an alkaloid, discovered in
the plant by Dr. Carlos Ulrici, and called parthenicine, is described.
At this point the writer undertook an investigation of the plant
as a graduation thesis, and as reported in Am. Jour. Pharm. (1890,
p. 121) no evidences of an alkaloid were found. The alcoholic ex-
tract, however, yielded a body which was supposed to be a glucoside.
Believing that the plant, one of the most common weeds of
Louisiana, may have a future, and realizing that its active princi-
ple might prove interesting chemically, investigations were resumed
with general results herein stated.
BOTANICAL CHARACTERISTICS.
Parthenium hysteroi)horous is a composite plant, sub-order
Tubulifcra, with radiate heads, pistillate rays and sterile disc florets.
It is a pubescent annual, having diffuse stem, pinnatifid leaves, with
linear toothed lobes and {)r()minent nervature (Prontisf>iece).
(169)
I/O Parthenium Hysterophorous. {^^' llxiiXm^."^'
Its heads are loosely panicled with involucre of five ovate scales,
arranged in two rows, (Fig. i). There are in each head five ray
florets in a single row, each resting within an oval chaffy scale which
is hairy above, and which, on separating, usually divide in three
portions. The ray florets are short, pistillate, ripening to smooth,
compressed achenia, with pappus composed of oval scales {Fig. 2).
The disc florets are tubular, five-toothed and sterile, having syn-
genesious anthers producing pollen grains, which are prickled simi-
larly to those of malva. Those nearest the ray florets are attached in
pairs to each of the chaffy scales mentioned above {Fig. j). Each
Fig. I. Parthenium Hysterophorous. Outer involucre, magnified twenty
diameters.
inner floret has its own chaffy scale, which is more narrow than
those on the outer rim. The receptacle is conical and not very
prominent.
The plant commonly called Bastard Feverfew grows in the West
Indies (where it is known as Escoba amargo), in Florida and in
Louisiana. It has been introduced in Europe as Absinthe sauvage
des Antilles. It attains the height of three feet, possesses a peculiar
heavy odor, while the leaves and flowers have an intensely bitter
taste.
The anatomy of the active part of Parthenium hysterophorous is
simple. The chaff is composed of longitudinally elongated cells in
Am. Jour. Pharnj.
April, 18OT.
Partheniu m Hysterophoroiis.
171
single layers, through which pass branching fibro-vascular bundles,
the prominent constituent of which are spiral ducts. The scales
terminate in a mass of hairs composed of two to four cells, of which
the terminal one is the largest. The cells of the corolla of the
disc florets are more symmetrical than those of the chaff, the
vascular system is identified by the spiral ducts. The walls of the
Fig. 2. Ray floret, magnified about forty-eight diameters.
anther cells possess reticulate markings which are quite character-
istic. The pollen grains, as mentioned above, are prickled {^Ftg. ./).
A cross- section of a leaf lobe shows the prominence of even the
secondary veins. These project chiefly on the under side. The
closed fibro-vascular bundle is bi- collateral. The lower half of the
leaf is of spongy parenchyma, while the upper consists of a palisade
layer {Fig. 5). The epidermis of the under side is interrupted by
172
Parthenmm Hysterophoroits. {
Am. Jour. Pharm.
April, 1897.
stomata and beset with several-celled tapering hairs {^Fig. (5).^; The
important characteristics of the powder are the prickled pollen
di^^etfrs. ^''^'' '^''' ^''''^' ^"^"^^"^ ^^ '^^^' magnified about forty-eight
grains, the hairs and longitudinally striate tissue of the chaff, the
tapenng hairs of the leaves, the reticulated anther walls and numer-
ous spiral cells of various sizes {Fig 7)
ApXS^'"} Parthenium Hysterophorous. 173
CHEMICAL COMPOSITION.
The writer's analysis of the plant in 1889 showed, beside such
normal plant constituents as starch, wax, gum and mineral salts, the
presence of an active principle to which the bitterness of the plant
is due. It was obtained from the alcoholic extract of the drug by
Fig. 4. United anthers, magnified about 150 diameters.
evaporation to dryness, solution in water and extraction by agitation
of the aqueous liquid with chloroform, and is supposed to corres-
pond to the parthcnine of Tovar, as well as to Uirici's parthenicine,
all the products being in a more or less impure form. Tovar's origi-
nal article has not yet been procured, despite efforts in that direction,
and the reference in tlie Pkarniaccutical journal gives no inkling
Fig. 5. Cross section of leaf, magnified about 600 diameters, p. /., palisade
layer ; s. p., spongy parenchyma ; s, stomata ; x, xylem ; p, phloem.
Am. Jour. Pharm.
April. 1897.
} Parthenunn HysteropJiorous.
175
of the mode of preparation. Guyet's paper, as reported in full in
La Cronica Medico- Qtiirurgica, of Havana, is a resume of the chemi-
cal researches of Ulrici, with an account of the therapeutical proper-
ties of the drug, as deduced by the author of the article. Ulrici
obtained from the plant black shining scales, from an alcoholic solu-
tion of which he separated, by means not stated, a white amorphous
residue which crystallized in fine needles.
Fif^. 6. Under surface of leaf, magnified about 600 diameters, s, stomata ;
/j, hairs ; d, spiral ducts.
He then dissolved another portion of the black scales in water,
cleared of coloring matter by slight excess of potassa and extracted,
with chloroform, a substance to which he assigned the formula
C„H^NO..
Aferck's Builetiu, October, 1888, describes, without method of
manufacture, the alkaloid parthenicine of Ulrici, without reference
to the original article. As this statement is two years older than
1/6
PartJienhnn Hysterophorous.
Am. Jour. Pharm.
April, 1897.
the researches of Ulrici published in Guyet's paper, it is presumed
that the substance is a purified form of that to which was assigned
the formula CjgHogNOg. It is described as follows : *' Large rectan-
gular prisms, with pyramids on four lateral sides. It is odorless,
very bitter, quite readily soluble in water — still more so, however,
in hot water — in alcohol, ether and chloroform. It gives colored
identity-reactions with sulphuric acid and with potassium bichro-
mate."
Fig. 7. Particles from powder, magnified about 200 diameters, c. h., chaff
hairs; c, fragment of chaff; a, fragment of anther wall ; p, pollen grain ; d,
spiral ducts.
Such is the scanty knowledge of Tovar's parthenine and Ulrici's
parthenicine. In neither case is that very important means of
identity — the melting point — nor the color of stated reactions
given.
So the means of identification of the active principle isolated
by the writer with the so-called parthenine and parthenicine are
almost missing.
On resuming the study of the plant, the first efforts were in
estimating the loss of water in desiccation.
^VpXiSr""'} Parthemum Hysterophorous. i77
The following figures were obtained :
Weight in Weight in
Month of Grammes. C.rammes. Percentage
Collection. Fresh. Dried. of Loss.
April I34'66 30-3 77*49
May 737- 150-5 79*5
June 552*8 127-6 76*91
July 885-9 177-2 79'99
August 680-4 106-3 8437
September 538*65 I55"9 7i'50
In each case the sample was dried by hanging in a room ac-
cessible to draughts of air for six to eight weeks. While, of
course, owing to the complex structure of the drug and the vary-
ing proportion of cellular and ligneous tissue, such data cannot
be exact, it is, nevertheless, useful in establishing the fact that
the amount of water in the fresh herb is somewhere between 70 and
80 per cent.
The average percentage of active principle was the next problem,
and its extraction was performed by exhausting the drug with
diluted alcohol ; distilling off the alcohol ; filtering the aqueous
residue ; washing the filter with water until the filtrate was tasteless,
and extracting the aqueous liquid by agitation with chloroform. In
this way a slightly impure yellow amorphous mass was obtained,
and the yield was as follows :
25 grammes air-dried drug, collected in April, yielded .
100
100
100
75
100
" May,
" June,
" July,
" August,
" September,
Per Cent.
. 0-31
. 0-84
• I 03
• i*I3
. 066
• 053
It will be seen that the quantity of active principle in the plant
gradually increases to the maximum in July, when it diminishes
with the length of days until in October the plant is almost free
from bitterness.
The process of extraction described above was not satisfactory,
as the product was invariably contaminated with coloring matter ;
so other methods were tried. That used in the preparation of
salicin — treatment of a decoction with lead oxide, removal of excess
with sulphuric acid and neutralization of free acid with barium sul-
phide— did not prove .satisfactory, as the lead oxide failed to remove
all the coloring matter.
Am. Jour. Pharm.
178 Parthe7iium Hysterophorous. {^"aphusJ?
The process followed with best results was treating an infusion
with lead acetate, filtering and agitating the filtrate with chloroform,
distillation of the chloroformic extract, thereby recovering the sol-
vent. The residue, by crystallization once or twice from alcohol, to
which a small quantity of water had been added, was obtained pure
in well-formed crystals — some 5 centimeters long — melting at i68°-
169° C. The yield of pure substance from drug collected in June
and July was about I per cent.
It proved soluble in 160 parts water, at 20° C; 5 parts 95 per
cent, alcohol ; 2^ parts boihng alcohol; no parts ether, and in
chloroform and acetic ether. It was soluble both in solution of soda
and in ammonia water, the former solution turning red-brown on
standing, the latter remaining colorless. It dissolved in concen-
trated sulphuric acid without change of color, but the solution
became green on the addition of a crystal of potassium bichro-
mate.
The aqueous solution was neutral to litmus paper.
That it is not an alkaloid was shown by the non-appearance of a
precipitate on addition of Mayer's reagent to its aqueous solution,
as well as by its solubility in solution of soda.
It failed to respond to tests for nitrogen, namely, heating with
soda-lime and also heating with metallic potassium, and attempted
conversion of the fused mass into Prussian blue by treatment with
alkali, ferrous sulphate, ferric chloride and hydrochloric acid ; while
Schonn's test for sulphur gave negative results.
The substance has been analyzed and the empirical formula de-
duced therefrom, but this will not be stated until confirmed by an
estimation of molecular weight and by analysis of derivatives.
The substance not being an alkaloid, the name parthenin can be
safely bestowed upon it.
The rather superficial examination made by the writer in 1889
suggested the glucosidal character of parthenin. Careful investiga-
tion does not, however, confirm this surmise. As a glucoside, par-
thenin should, under the action of a diluted acid, be converted into
glucose and some other body. This, as experiment showed, does not
occur, although the reaction was atternpted in two different ways. In
the first method, several portions of parthenin were heated with
diluted sulphuric acid for periods varying from boilingfor one minute
to heating; on water-bath for four hours. The liquid in each case, after
^"apXi^*'"'} Partheniiun Hysterophorous. 179
its special method of heating, was agitated with successive portions
of ether until the last ethereal portion possessed no bitter taste.
The aqueous liquid after such extraction was carefully examined for
glucose. Trommer's, Bottger's and the picric acid test were applied
in each case with negative result.
The ethereal extract on evaporation yielded a brown syrupy mass.
Crystallization from alcohol and acetic ether was attempted without
success. By treatment with a small quantity of water, the substance
solidified to an amorphous mass, which was still yellow from con-
tamination with a resinous substance that reddened with solution
of soda. This body melted at about 1 70° C. and is supposed to be the
original substance. Other portions of the residue, after careful
washing with ether, melted at 170°.
The second method was in boiling an alcoholic solution of parthenin
with a small quantity of diluted sulphuric acid, addition of water,
evaporation of the alcohol and extraction with ether. The aqueous
residue gave no indication of glucose.
Since not a glucoside, parthenin was expected to possess reactions
similar to some of the proximate principles. Its solubility in solu-
tion of soda suggested an analogy to santonin, and in that case a
sodium compound, similar to sodium santoninate, might be produced.
To this end, parthenin was treated with a diluted solution of soda,
carbon dioxide passed in until saturated and the solution evaporated
to dryness, the passage of carbon dioxide being continued to the
end of the heating. The perfectly dry residue was treated with
absolute alcohol, when the filtered alcoholic extract yielded on spon-
taneous evaporation a yellow syrup, which, on addition of a small
quantity of water, solidified to a brownish yellow mass, which gave
the sodium flame and charred on heating, melting irregularly but
not completely, until at red heat. This was sparingly soluble in
water, and the aqueous solution, which was neutral, yielded a pre-
cipitate with silver nitrate.
An effort to obtain the product after the method used in the
manufacture of sodium santoninate, dissolving in solution of soda
and crystallizing the resulting product by concentration of the solu-
tion, has not yet met with success.
This somewhat sup)erficial effort seems to indicate rather clearly
the formation of a sodium compound of parthenin, which can be
converted into a silver salt. The investigation of this sodium com-
f)Oun(l is still continued.
i8o Parthenium Hysterophorous. {^"^- l^rl-Jm^"^'
The fact being clearly established that parthenin is not a gluco-
side, but rather a proximate principle somewhat akin to santonin,
suggests a more practical method of preparation than by extraction
with chloroform. A process in which the lead acetate dissolved in
the cleared decoction was dissociated by addition of sulphuric acid,
which would precipitate the lead as sulphate, was not attempted
lest the acetic acid set free would react with the parthenin. This
fear is groundless, and a practical process of extraction on these
lines will be devised.
On distillation of the drug with steam there passed over a minute
quantity of volatile oil possessing the distinctive odor of the plant,
and from which, on standing, there separated a stearopten possessing
camphoraceous taste. As yet the quantities won have been too
small for investigation, but attention will be turned to it during the
coming summer.
In conclusion, a few words as to the medical properties of
parthenin. Tovar reported it as a remedy in facial neuralgia,
and it also proved beneficial in a case of fever and anaemia
where quinine failed. Guyet confirmed its efficiency in neuralgia,
especially the cranial variety ; but he found it utterly without effect
as antipyretic. In Jamaica the plant is used as a remedy for
ulcerated sores and certain skin diseases, especially such as are of a
herpetic or pustular character. The dose of Ulrici's parthenicine is
stated as 0-05 gramme every hour in neuralgia, while gramme
doses are used in intermittent fever.
The subject is worthy of further consideration on the part of
therapeutists, and to this end the writer proposes preparing during
the summer considerable parthenin, which will be furnished in
limited quantities to those physicians who will agree to conscien-
tiously test its merits and publish the results, whatever they may
be.
The writer's thanks are due Miss S. E. Bres for the artistic sketch
of the flowering branch.
New Orleans, March 8, 1897.
Formaldehyde is detected by dissolving o"! gramme of morphine hydrochlo-
ride in I c.c. of concentrated sulphuric acid, and adding an equal volume of
the solution to be tested, without mixing ; in the presence of formaldehyde
I I : ous solution will become a clear red-violet color in a few minutes.
^VpXi^^'""} Vie Shaddock or Grape Fruit. i8i
THE SHADDOCK OR GRAPE FRUIT.
By J. H. Hart,
Superintendent of Botanical Department, Trinidad.
The March, 1896, number of the American Journal of Pharmacy
is especially interesting to me, and as I am a twenty-one-years resi-
dent (constantly employed in botanical matters in the West Indies),
I venture to make a few remarks on it. As a rule we look at pict-
ures before the readin^^ matter, and I did so in the case of the shad-
dock paper. Now, as I know the plant, the illustration No. i is
certainly not a shaddock, but a grape fruit, or forbidden fruit,
and as I find, page 123, paragraph 4, that the terms grape fruit and
shaddock are interchangeable, this may explain.
It is quite true that " no reliance ca?t be placed upon the cojnnion
jiames of plafits or flowers, etc., etc.,'' and this sentence contains the
gist of the whole controversy as to names.
I know Jamaica well, having resided there eleven years, and know
the districts of Macfadyen well, and the fruits in them.
The home (English) botanist, however, makes the citron, lemon
and lime one species. Macfadyen made them three ; and various
other changes, etc. The true fact is, no two men can see alike. If
asked to classify the citrus tribe, I should make Citrus inedica in-
clude all the lemons and limes and their hybrids, which are legion.
I should let Citrus aurantium represent the orange of the St.
Michael's type (sweet orange), with all its varieties, and I would let
Citrus deciimana cover all the shaddocks, grape fruit, or pumelows,
etc., and their varieties, which are also very numerous. Citrus nobilis,
or the tangerine and mandarin (also interchangeable names), appear
to maintain themselves fairly distinct. These oranges are sometimes
called "Portugal oranges" in Trinidad. We have one, however,
imported from Grenada, W. I., that approaches the grape fruit in
size ; at the same time, I recognize intermediate varieties between
many of those mentioned.
We have a sweet lime, a fruit with an orange skin, with a lime
flesh, but with a distinct mixture of orange and lime in flavor. We
have a lime, larger than a lemon, with none of the characters of a
lemon. There is a sweet orange called the bergamot in Jamaica,
which is very clear and distinct from that I recently received from
Italy as bergamot ; and unless we agree to adopt special Horticul-
/Am. Jour. Pharm.
182 Hermann Hager. {^^pTuiisJr
tiira! names, I do not really see how the botanists can help out of
the muddle, for muddle indeed is the classification of citrus. I had
lately one of the finest shaddocks sent me I ever saw ; it was deli-
cious in flavor and of a bright red. I have grafted plants on lemon
and orange stocks, and have two fine unions growing freely.
In Jamaica, shaddock is shaddock and nothing else ; although an
old " nigger," to please a questioner, if asked : Is that shaddock ?
pointing to a grape fruit, would say : yes, massa ! Shaddock, sa ' ! or
vice versa. Shaddock, however, in the market, is shaddock, or the
largest fruit of the citrus tribe. Grape fruit, or forbidden fruit, pre-
sents as many characters as other varieties of citrus. Red flesh, white
flesh ; sour, bitter, sweet ; but the one called grape fruit hangs in
clusters like grapes (6 to 10 together), hence the name ; and there is
evidence that the larger kind comes from the smaller. — " The Shad-
dock from the Grape Fruit" (see Bulletin No. 9 of this department,
p. 19).
I must take exception to the statement, p. 126, << which are ex-
tremely acid." The author should have stated that Jamaica
oranges were extremely acid. Trinidad oranges and Grenada oranges
are extremely sweet; but while you can get good oranges in Jamaica,
there are truly many sour ones there. In both Jamaica and Trinidad,
the wisdom of planting seedlings is being almost universally doubted,
and my article 225, Bulletin, was especially directed to this point.
Trinidad, January 26, 1897.
HERMANN HAGER.
By Fred. Hoffmann.
On the gloomy afternoon of the 29th of January, 1897, ^ small
company, consisting of a few relatives, of some townspeople, includ-
ing several local pharmacists, and of the representatives of two
pharmaceutical papers, followed a plain hearse to the graveyard of
the town of Neu Ruppin, located a few miles northwest of the Ger-
man capital. Such was the funeral of the Nestor of German phar-
macy of our generation, Dr, Hermann Hager. Flowers and palms
sent as a last tribute of gratitude and respect by his publishers, and
by the editors of the Pharmaceutische Zeitung, and of the Pharma-
ceutische Wochenschrift, in Berlin, covered the coffin and the grave,
Am. Jour. FbariD.
April, 1897.
Herinaiin Ilager.
183
and a wreath of flowers had been sent by the President of the Ger-
man Apothecaries' Association, Although less than two hours by
rail from the German capital, not one representative pharmacist, no
delegate from any of the national or metropolitan pharmaceutical
societies, nor from the journal founded by Dr. Hager in 1859, and
graced by his famous name ever since, attended his funeral.
What a representative gathering would the funeral of such a man
of national, nay, of world-wide reputation, have drawn together any-
where in the United States ! The foremost representative men of
American pharmacy hastened to Philadelphia to pay a last respect
to Procter at his funeral in February, 1874, and to MaiscJi in Sep-
tember, 1893. No such tender sense of gratitude and veneration
seems to pulsate in the hearts and among the ranks of the repre-
sentative men and members of pharmaceutical associations on this
side of the Atlantic. A profession as well as a country honor them-
selves by honoring the life work and the memory of their great men
during their lifetime as well as at their demise, even if the saying
should apply : " a man lives by his excellencies and not by his
faults." It is the more gratifying that the Continental pharmaceuti-
cal press has promptly and nobly offset this apparent show of a
want of veneration for the departed master of German pharmacy by
unanimous and warm-hearted obituaries.
1 84 Hermmtn Hager. {'''^•l^tXm^'^'
Hans Hermann Julius Hager was born in Berlin on January 3,
1 8 16, where his father was an army surgeon. After having passed
the elementary schools, he attended the high schools at Torgan and
Brandenburg, and in April, 1832, entered upon an apprenticeship in
the pharmacy of the town of Salzwedel. Then apprenticeship in
German pharmacies included the performance of all the common
handiwork, of keeping the store, the laboratory and the storage
rooms in proper order, of cleansing and dusting counters, shelves,
containers, utensils, oil-lamps, etc., of delivering medicines to
customers, etc. Young Hager was by no means spared this hard
ordeal. Little leisure time was left for study, and but very few
pharmaceutical books were placed at his disposal, while his means
were insufficient to purchase any. But bent upon study, and of an
inquisitive mind, young Hager made good use of the few text-books
of pharmacy accessible to him, among them, " Hagen's Treatise on
the Art of Pharmacy," as well as of his old school-books. During
the four years of apprenticeship he perfected his knowledge of Latin
so much that he retained for life the ability to write fluently in
Latin. He also closely applied himself to the study of French, of
history and of natural philosophy. Incidentally he obtained a
small treatise on chemical stoichiometry, which induced him during
the last year of apprenticeship to elaborate a text-book of stoichi-
ometry for pharmacists, which, however, never has been published.
At the close of his apprenticeship Hager passed the obligatory
examination with much credit, and subsequently served as assistant
for some years in pharmacies in several towns. During these years
he read all books accessible to him, and applied himself with much
interest and assiduity to becoming familiar with the flora of the
diluvial plains of Northern Germany. He then served for one year
as army pharmacist in the garrison hospital in the capital of Silesia,
Breslau, whither his father had been removed as army surgeon.
Here young Hager found time and opportunity to attend lectures at
the University on natural philosophy, chemistry and botany. After
having passed his one year of army service, he had the good for-
tune to obtain a place as assistant with an apothecary in the town
of Perleberg, who was an accomplished pharmacist, a sympathetic
man and the possessor of a good pharmaceutical library. Of this
Hager made good use, so much so that in 1841 he ventured to
apply to the highest examination board in medicine and pharmacy
^VpXiST""'} Hermann Hager. 185
in Prussia for permission to pass his State examination as apothecary
without the customary preceding attendance of at least one year
of university lectures. He was admitted and passed this ordeal
with credit.
Hager subsequently served two more years as assistant, always
applying his leisure time to study in almost every branch of natural
science. He also succeeded in obtaining the degree of Doctor of
Philosophy at the University of Jena, and, in 1843, he managed to
purchase a pharmacy in the town of Fraustadt in the Prussian pro-
vince of Posen. Here he attended to his comparatively small busi-
ness most of the time with but one apprentice, married, raised a
family and passed seventeen of the most studious and well-applied,
and, perhaps, also happiest years of his life.
Besides a good prescription business, Dr. Hager attended, with
his apprentices, to the preparation of all galenicals and most phar-
maceutical chemicals, including all metallic salts and solutions, even
to the preparation of the few alkaloids then in use. With his sense
of practical application and great skill he attained to perfect master-
ship in the art and practice of pharmacy in every direction, as also
in the performance of analytical and microscopical work and exam-
inations, and accumulated a vast amount of knowledge and expe-
rience in all branches of the theory and practice of pharmacy and
of related application.
While, during the years of assistanceship. Dr. Hager had occa-
sionally contributed miscellaneous writings and some poetical efforts
to local papers, he seems to have abstained from any contribution
from the wealth of his knowledge and experience to pharmaceutical
periodicals during the years of his activity as apothecary in Frau-
stadt. Hut there he soon entered upon his successful career as a
writer and author. His first publications of repute seem to have
been an essay on *' Weather and Its Considerations," in 1845 ; his
" Handbook of the Art of Dispensing," •* Cosmos Diluvialis," or the
deluge, an historical study; "Treatise on the Manufacture of Min-
eral Waters;" •• Commentary on the Pharmacopujias of Northern
Germany" (1854); •• Manuale Pharmaceuticum ;" " Adjumcnta
Varia ;" •* PharmacopoL-ia HomcLopatica."
The success of several of these works, and the want of incitement
as well a% of literary and scientific resources in the small town, in-
duced Dr. Hager the more to dispose of his pharmacy, as he, in
1 86 Hermann Hager. {^"Aprn/S"""
1859, had commenced the pubhcation of a strictly scientific periodi-
cal, the Pharmacculischc Centralhallc. Early in i860 he removed
to Berlin, with a view to applying his entire time and labors to sci-
entific and literary work. Henceforth his little private laboratory
became the prolific starting point for the solution of many a scien-
tific or technical problem in the practice of pharmacy, and of a vast
amount of analytical and microscopical work. In 1864 Dr. Hager
established, with his friend, Dr. E. Jacobsen, of Berlin, the Industrie
Blatter, in which he inaugurated a fearless exposure of the nostrum
fraud. Of these specialties he analyzed in the course of years more
than any contemporary. He provided his two journals largely with
material from his own pen and laboratory work.
In Berlin Dr. Hager contracted the friendship of the brothers,
Ferdinand and Fritz Springer, of the eminent publishing firm of
Julius Springer, who henceforth became his publishers and life-long
friends. Here he elaborated and published " First Lessons in the
Practice of Pharmacy," *' First Lessons in Pharmaceutical Botany,"
"The Microscope," ''Commentary on the Prussian Pharmacopoeia,"
«' Latin-German Vocabulary to the Pharmacopoeia," and revised
some of his former books for republication in new editions. In
Berlin he also commenced the elaboration of his greatest and most
enduring work, the " Handbook of the Practice of Pharmacy."
Dr. Hager's increasing reputation drew more and more callers to
his quiet home and study in the German capital. Being of a retir-
ing disposition, and carefully estimating the value of time, he gradu-
ally longed for a refuge Vv^here he could attend to and accomplish his
life work in less disturbed solitude. He acquired a modest farmer's
home, located m a rather isolated and unattractive place, called Pul-
vermiihle, near the village of Fijrstenberg, a few miles distant from
the old university city of Frankfort, on the Oder River. He re-
moved thither in October, 1871. Here Dr. Hager enjoyed, for ten
years in full retirement, a studious and active life, applying all his
time and interests to research and literary work. During these
busy years he continued his analytical work, edited his two journals,
one in Berlin, the other in Dresden, translated the first Pharmaco-
poeia of the newly consolidated German Empire, and in 1872 and
1873 wrote a comprehensive commentary on this work.
In 1876 he completed and published his " Handbook of the Prac-
tice of Pharmacy," in two large volumes, to which he added a third
"^""ApXiJ^t!"""} Hermann Hager. 187
volume in 1 880. This master work fully represented the accumu-
lated knowledge of the past, largely enriched by his own vast stock
of theoretical knowledge and practical experience in all branches of
pharmacy, and of analytical and microscopical application, and of
the examination and estimation of drugs, chemicals and of foods.
It at once superseded all similar older works and became the
standard text and guide book, as well as an almost never-failing
reference work for pharmacists and druggists far beyond the limits of
the Fatherland. It made the name of Hager a household word in phar-
macy and the drug trade all over the world, and, at least abroad, is
still a widely used pharmaceutical reference book.
During the remaining years of his residence in Pulvermijhle,
Dr. Hager accomplished a great deal of analytical work for revis-
ion and verification, elaborated a study on oil of turpentine and its
detection as an adulterant of essential oils, and revised a number of
his works for republication in new editions. In 1881 Dr. Hager re-
moved, after the death of his only friend in his lonely retirement, a
physician, to Frankfort-on-the-Oder, where he lived in strict retire-
ment until 1896. Here he continued his customary laboratory and
literary work, completed several revisions of his larger books and
furnished various periodicals with occasional contributions. From
the editorship of the Centrallialle and the Industrie Blatter \\^ had
retired in 1879, allowing his name to be retained on the title-pages.
Until 1890 Dr. Hager enjoyed excellent health and the full powers
of his inquisitive and prolific mind and activity, always occupying
himself with literary work or study, and in later years collecting
minerals and conchyts ; but in this year he became a victim to influ-
enza, and since then his health failed in consequence of occasional
relapses of this malady. In anticipation of the approach of the end
of his struggles, the octogenarian resorted, with the most sympa-
thetic and affectionate companion of his life, his wife, in July, 1896,
to the home of one of their sons, living in the town of Neu Rup-
pin, near Berlin. Here he spent the last few months of his earthly
life in peaceful meditation, kindly remembered by a few noble friemls.
In December, Dr. Hager suffered a severe relapse of influenza from
which he did not recover. On the 24th of January he (juietly tell
asleep to eternal rest, from an active and most useful life, replete
with superior work and generous efforts for his fellow-men, but
devoid of public recognition and honors at home. His devoted
1 88 Hermann Hager. {^'^•l^^llm''^'
wife, who also suffered from influenza, on being informed, on the
day of her husband's funeral, of his death, closed her eyes forever
on the very same day.
More than any other of his German contemporaries, Dr, Hager
was, in the American sense, a self-made man. The stamp of the
autodidact remained impressed upon his character, his labors and
his .writings and imparted to them the charm and the force of orig-
inality. He was a man of rare talents, with a keen and discrimi-
nating intellect and an excellent memory. The style of his writings
was lucid and attractive ; he also was a clever draughtsman, drawing
with his own pen nearly all the sketches for the abundant illustra-
tions of his works. Intense work was to him always a labor of love.
Like most men of originality and genius. Dr. Hager was also bent
upon critical reflection and upon an unreserved candid expression of
his opinion. However stern and straightforward his intellectual
powers and the courage of his honest conviction made him, his
mind was as gentle and forbearing as that of a child. In his long
and active career, by no means free from cares and disappointments,
and in a profession replete with antagonistic and uncharitable
elements, Dr. Hager has not been spared the cruel stings and even
the calumnies of adversaries, particularly of those more fortunate in
inheritance and patronage, and more successful in public position
and honors, which favors he never sought by submission or flattery.
Although a recognized master of his profession, a prolific and excel-
lent writer, and expert in pharmacopceial work and a man of world-
wide fame. Dr. Hager has never been called upon to participate in
the elaboration or the revision of a pharmacopoeia ; nor has he ever
received, from the Government or the State authorities, any public
recognition or distinction for his eminent merits for the advance-
ment and the reputation of German pharmacy ; whereas the pro-
fession of many countries has paid its respects to the great master
by enrolling his famous name in the lists of honorary member-
ship in their national associations — first among them the American
Pharmaceutical Association and several colleges of pharmacy in the
United States.
As long as pharmacy remains a distinct profession and retains its
glorious history, the names oi Hermann Hager and F. A. Fliickiger^
»Amkr. Jour, of Phar. (1895), Vol. 67, p. 65.
''"Vprn'iS}"'"} Estimation of Merit ho 1 . 189
will stand foremost among the few bright stars in the galaxy of
pharmaceutical master minds during the second half of the nine-
teenth century. Hager has set himself the most enduring monu-
ment by his life work and writings, and should the present or the
succeeding generation of pharmacists erect some worthy memorial to
the most deserving pharmaceutical author and mentor of his time,
these words might well be inscribed with particular application and
truth :
•' Das Edle in der Menschenwelt,
Es lebt im nienschlichen Geniiithe.
Es ist nicht Macht, nicht Gut uud Geld,
Es ist ein Herz voll Lieb' und Giite,
Es ist ein Sinn voll Thatenkraft,
Der zielbewusst das Hochste schafft."
Leipzig, March, 1897.
A BRIEF RfeSUME 0¥ ACETIC ANHYDRIDE IN OIL
ANALYSIS, AND A MODIFICATION OF THE
METHOD FOR ESTIMATING MENTHOL
IN OIL OF PEPPERMINT.
By Lyman F. Kebler.
It is well known that the official requirements for some of the
essential oils are not rigid enough, on the one hand, to detect all forms
of adulterations or manipulated products, while, on the other hand,
some of the qualitative tests are so exacting as frequently to dis-
criminate very unfavorably against genuine oils produced in large
quantities in the United States. Just where to draw the line at
present is, in many cases, a difficult problem — a problem which
will probably never be solved in some cases, for the ingenious adul-
terator always aims to debase his goods in such a manner as to make
the fraud difficult of detection.
The chemical investigations of essential oils, during recent years,
are contributing much toward laying the foundation on which to
base analytical methods. In some cases simple and efficient pro-
cesses for estimating certain valuable constituents have already been,
formulated. Methods that are no more difficult of application than
those commonly employed for determining the quality of fixed oils.
In fact, some methods are common to both, as the one in which
acetic anhydride is used.
I90 Estimation of Menthol, {^""apSSt^'""-
The value of acetic anhydride as a chemical reagent has long
been known to organic chemists. But it was left for the genius of
the late Dr. R. Benedikt^ to formulate a qualitative method embody-
ing the well-known property of acetic anhydride.
The method is based on the principle that alcohols and hydroxy
acids on being heated with acetic anhydride, have the hydrogen
atom of the hydroxyl group replaced by the acetyl group, thus form-
ing compound ethers.
The process, according to Benedikt and to Benedikt^ and Ulzer,
is briefly as follows : from 20 to 50 grammes of the fatty acids are
boiled with an equal weight of the acetic anhydride for two hours
in a flask provided with an inverted condenser. The mixture is
then transferred to a suitable vessel, about 600 c.c. of hot water
added and boiled for half an hour. The mixture is then allowed to
separate into two layers, the aqueous portion withdrawn and the oily
layer treated thrice more in the same manner. The acetylized pro-
ducts are then filtered in a drying oven to eliminate all moisture.
From 3 to 5 grammes are carefully weighed off and dissolved in pure
alcohol. In this alcoholic solution the acid and the ether values
are determined as usual. The former is called the acetyl acid value^
the latter the acetyl value and the sum of both is termed the acetyl
saponification value.
The theory of the process can readily be seen from the following
equations :
C„H330H + (C,H30),0 = QeH3,O.QH30 + HQH3O2.
Cetyl Acetic Cetyl Acetic
Alcohol. Anhydride. Acetate. Acid.
Q6H33O.QH3O + KOH ^ QeH330H + KQH3O2
Cetyl Potassium Cetyl Potassium
Acetate. Hydroxide. Alcohol. Acetate.
Q7H32(OH)C02H-f (C2H30)20=^C,7H320.C2H30.C02H + HC2H3O2
Ricinoleic Acetic Acetyl Acetic
Acid. Anhydride. Ricinoleic Acid. Acid.
C17H32O.C2H3O.CO2H ^ KOH = C17H32O.C2H3O.CO2K -L H2O
Acetyl Potassium Acetyl
Ricinoleic Acid. Hydroxide. Ricinoleate of Potassium.
*i887, Ztschr.f.d. Chem. Ind., i, 149, communicated Feb. 26, 1886.
21887, Mojiatshefte fur Chemie, 8, 47; 1892, Die Analyse der Fette und
Wachsarten, zweite Auf , p. 113; 1895, Chemical Analysis of Oils, Fats,
Waxes, etc., by Benedikt and Lewkowitsch, p. 127.
^'VpXiSt"'"} Estimation of Menthol. 191
CnH320.C2H30.CO,K -f- KOH = C,7H3,(OH)COoK + KQHjO,
Acetyl Potassium Potassium Potassium
Ricinoleate of Potassium. Hydroxide. Ricinoleate. Acetate.
J. Lewkowitsch* has studied the above process very thoroughly,
and is continuinfj his work at present.
In 1894 F. B. Power- and C. Kleber proposed an analoj^ous
method for estimating menthol in oil of peppermint. The method
is briefly as follows : About 20 grammes of the oil are mixed with
30 c.c. of normal alcoholic sodium hydroxide, in a flask provided
with a reflux condenser and heated to boiling for one hour. The
uncombined alkali is estimated by means of normal sulphuric acid,
using phenolphthalein as indicator. F^ach cubic centimeter of the
standard alkaline solution consumed represents 0156 gramme of
menthol in the form of ethers.
The contents of the above flask are repeatedly washed with
water, to remove the alcohol present and the oily portion boiled one
hour with an equal volume of acetic anhydride and 2 grammes of
fused sodium acetate in a flask provided with an inverted condenser,
the end of the condenser tube being so ground as to fit accurately
into the neck of the flask. On cooling, the contents of the flask
are washed with ample water, then with a dilute alkaline solution,
the alkalinity removed by washing with water again, and the oily
portion ultimately dried with calcium chloride and filtered. From
8 to 10 grammes of the acetylized oil are treated as above for esti-
mating the combined menthol.
From the data obtained by the above procedure the total per
cent, of menthol, free and in the form of ethers, may be calculated
by the following formula :
y^ =
fl X 15*6
.9 — {a — 0042)
/^equals total menthol ; .S" equals grammes of acetylated oil used ; a
equals the number of cubic centimeters of normal sodium hydroxide
required for saponification ; and 0042 is a constant obtained by
'1890, Proc. Chem. ^Ktety, 72 and 91; /. Soc. Chem. fnd., 9, 660.
1890, y. Soc. Chem. InJ., e, 846; Chemical .Vualysis of Oils, Fats. Waxes,
etc., 1895, by Bene<likt and Lewkowitsch, p. 129.
'1S91, Pharm. h'uudsihau, !'»• 157; Circular of Infotmativu^ .\,' ,-, by
Fritzsche Brothers, p. 1 1.
192 Estimation of Menthol. { ^'"aS'S^''"''
subtracting^ the normal factor of menthol (0156) from the normal
factor of menthyl acetate (0-198).
The two following equations form the basis of the process :
C,<,H„OH + (QH,0),0 = QoHi,O.QH,0 + HQH,©.
Menthol. Acetic Anhydride. Menthyl Acetate. Acetic Acid.
C.<,H„O.QH,0 + KOH = C,oH„OH + KaH30,
Potassium Potassium
Menthyl Acetate. Hydroxide. Menthol. Acetate.
Being frequently requested to estimate the amount of menthol in
peppermint oils on short notice, the writer has modified the above
procedure so that the per cent, of this constituent can readily be
estimated in three hours, while the original method requires the
greater part of a day for execution.
For Estimating the Combined Menthol. — Place from 10 to 12
grammes (accurately weighed) of the oil into a suitable flask, add
about 12 c.c. of normal alcoholic sodium hydroxide, connect the
flask with an inverted condenser and boil for one hour. Retitrate
the excess of alkali by means of standard sulphuric acid, using phenol-
phthalein as indicator. Each cubic centimeter of standardized alkali
consumed corresponds to 0-156 gramme of menthol as esters. This
part of the process embodies the well-known principle of Koettstorfer.
To Estimate the Total Menthol. — Place from 12 to 1 5 grammes
(accurately weighed) of the oil into a suitable flask (the writer uses
an ordinary Kjeldahl digesting flask), add an equal weight of acetic
anhydride, 2 grammes of anhydrous sodium acetate, attach to a reflux
condenser and boil the contents of the flask one hour. Allow the
mixture to cool somewhat, transfer to a 250 c.c. separatory funnel,
with successive portions of distilled water, using about 1 50 c.c. Agi-
tate the funnel and contents well, set aside a few minutes, so that
the mixture will separate into two layers. Withdraw the aqueous
layer and wash again with 150 c.c. of water as above. Having re-
moved the second wash water, add 50 c.c. of water, a few drops of
phenolphthalein solution, and just enough of a 5 per cent, aqueous
sodium hydroxide solution to render the contents of the funnel
pinkish, after thoroughly agitating ; then add enough water so that
the aqueous portion will amount to about 150 c.c; agitate well,
allow the mixture to separate and withdraw the alkaline aqueous
solution. Wash the oily layer again with 150 c.c. of water as above.
Remove the water as completely as possible and transfer the acety-
^"kSiS^^""} Estimation of Menthol. 193
lized oil to a suitable flask, using a small amount of alcohol to
transfer the last portions. To the oil in the flask add from 50 to 60
c.c. of normal alcoholic sodium hydroxide, connect the flask to an
inverted condenser and boil for one hour. Retirrate the excess of
the alkaline solution by means of normal sulphuric acid. Each cubic
centimeter of normal alkali combined corresponds to 0-156 gramme
of menthol.
On deducting the amount of menthol contained in the oil in the
form of esters from the total menthol found, we have the amount of
free menthol.
The table on next page contains the results obtained by the
above process for commercial menthol and a number of samples of
oil of peppermint in connection with the specific gravities, boiling
points and residues. The boiling points were determined with
metallic bath.
It requires only a casual review of the contents of the table
to show that oil of peppermint is a most variable product. Then
when we call to mind that normal Japanese oil generall)' con-
tains about 75 per cent, of menthol, the variation is still greater.
But it must also be remembered that an oil containing a high per-
centage of menthol frequently does not possess the desired fine
aroma so valuable in essential oils. The quality of the aroma is
generally indicated by the amount of menthol esters. Yet, there
may be some disturbing elements present, such as the sulphur com-
pound, recently discovered,^ which will vitiate an otherwise fine
aroma very materially.
The writer has every reason to think that the oils examined
above are genuine, excepting, of course, the sample marked " Un-
known." This was highly adulterated with turpentine, as the boil-
ing points clearly show.
In e.xamining oil of peppermint it is necessary to determine: (i)
the specific gravity, although this is only an indication ; (2) the
boiling point, varying from a few degrees below 200^ C. to about
230° C. (uncorrected), with some residue ; (3) the amount of men-
thol. The combined menthol varies from 3 to 16 per cent. The
total menthol may vary from 30 to 80 per cent. These data, in
connection with the aroma and identity tests, will undoubtedly show
the character of any oil of peppermint.
'1896, C. Klcbcr, Phann. Kciiciv, 14, 269 ; Schimmci cV Lo. s :^ifHt-anttudl
Report, October, p. 48.
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^"AiXiS:"'"} Observations on Acacia of Commerce. 195
It is hoped that the Pharmacopceial Committee will find it desir-
able to introduce the boiling point of this oil, at least, into the next
revision of the Pharmacopouia, if they do not see their way clear to
admit a method for determining the per cent, of menthol. But the
writer cannot see any reason why a simple method like the above
should not be made serviceable, seeing that good acetic anhydride
can be so reasonably secured.
305 Cherry Street, Philadelphia, Pa.
SOME OBSERVATIONS ON ACACIA OF COMMERCE.
Bv J. Henry Schroeder, Ph.G.
Of all the drugs sent forth into the commerce of the world, there
is, perhaps, no single one of which there exist so many varieties as
of acacia. A difference in the source of production is one cause
for the variableness in quality of the commercial article. In some cases
the quality of the gum is lowered by the season of collection, and
a secondary grade is obtained by assorting the other varieties.
The chemical literature relating to the exact nature of the
gums of different species of acacia is only limited, and they have,
so far, been subjected to little thorough stud\'.
As their habitats vary greatly, they are usually known by the
names of the localities where they are collected, or by the names of
the ports from which they are shipped.
For pharmaceutical uses the U. S. Pharmacopoeia directs that the
gum of Acacia Senegal be employed.
It was with a view of determining the presence of dextrin in the
powdered commercial " gum arabic," that an examination of differ-
ent samples was undertaken.
It has been alleged that the high price of a good quality of gum
has tempted those who handle the product, and that many of them
have resorted to adulteration for pecuniary gain, dextrin being the
substance usually employed for the purpose. While for merely
technical purposes an addition of dextrin might not be a disadvan-
tage, such adulterated gum is, of course, unfit for pharmaceutical
purposes, especially for the preparation of emulsions.
Observations were made during the work, which I think of suffi-
cient interest to the pharmacist to report.
Before submitting in detail the results of the examination, I desire
196 Observatmis on Acacia of Commerce. {^"^'l^xiXm^^'
to state that they are presented solely on account of the interest
which they seem to possess for the practical pharmacist, with the
consciousness that, considered as a scientific investigation, the
important factor, completeness, is lacking.
According to the U. S. Pharmacopoeia, acacia is <* a gummy exu-
dation from Acacia Senegal, Willdenow (nat. ord. LeguminoscB).
Besides the description of the physical appearance of the gum, the
following tests are also given :
{a) Acacia should be soluble in 2 parts of water; it should yield a
gelatinous precipitate with basic lead acetate, T. S., ferric chloride,
T. S., or concentrated solution of sodium borate, and does not
reduce alkaline cupric tartrate, V. S.
(b) The powder is not colored blue (absence of starch), or red
(absence of dextrin), by iodine, T. S.
In addition to these tests, it may be of interest to refer to two
others for the presence of dextrin.
One, which is from Hager, Hartwich and Fischer's Commentar
zur Pharm., B. II, p. 44, is as follows :
"Three c.c. of a solution composed of 15 drops of solution of fer-
ric chloride, 15 drops of saturated solution of potassium ferricyan-
ide, 5 drops of diluted hydrochloric acid (sp. gr. 1-165) ^"<^ 60 c.c.
of distilled water, are added to 6 c.c. of a solution of the suspected
gum (strength of solution should be 20 per cent). If the gum be
devoid of dextrin, it will be colored a pure yellowish-brown tinge,
this color remaining permanent during eight to ten hours. If dex-
trin be present, the color will change in about one hour to blue."
The other test, which is evidently a modification of the above
method, is described in El Memorandum}
It seems to be erroneous, inasmuch as it contains potassium /^rr^-
cyanide instead of potassium /^mcyanide, in presence of ferric
chloride. Tlie sulphuric acid present in the solution does not
prevent the precipitation of ferric ferrocyanide. This test seems,
therefore, inapplicable.
The foregoing are the tests upon which the examination of sam-
ples of commercial gum arabic was based.
While I was examining samples of the powdered gum in regard
to their action upon alkaline cupric tartrate, V. S., I noticed that,
^ Pharm. Jour., October 12, 1895, p. 322, and Proc. Am. Pharm. Assoc.,^o\
44, p. 625.
'^"aIj'hi'.'iSt"™} Observations on Acacia of Commerce. 197
in every instance, a marked reduction was taking place. A ref>e-
tition of the experiments verified this observation, I decided to
apply the test to a sample of the whole gum. For this purpose the
best gum (answering the Pharmacopaial description in physical
appearance) obtainable was employed. One gramme was pulver-
ized in a clean mortar, and dissolved in 10 c.c. of recentl}' distilled
water.
Just sufficient potassium hydrate solution wasadded to give an al-
kaline reaction, and this solution heated with alkaline cupric tartrate,
V. S., in a water-bath (boiling temperature), during twenty minutes.
Here, too, a well-defined reduction was observed, though seemingly
less prominent than that produced by an equal amount of the pow-
dcred substance. When the test solution was heated, without the so-
lution of gum, for an equal length of time, it remained clear. A like
behavior of acacia is described in Hager, Hartwich and Fischer's C^;//-
w/^;//fzr, as follows : "Acacia does not reduce Fehling's solution at
6o°-70°, but has a i educing action after being boiled with the rea-
gent," and " dried gum in solution reduces Fehling's solution at
temperature of water bath." I have observed, however, that gum,
not otherwise than air-dried, reduces Fehling's solution without
being boiled, upon heating a solution for some time at watei bath
temperature.
The increased reduction by the powdered gum is probabl}' due to
drying previous to powdering it.
The iodine test for dextrin and starch was applied to each
sample in powder and in the form of solution. When applied to the
same powder it imparts to the powder only a light yellowish color
of the iodine. If only traces of dextrin are present a dark red tint
is produced. When a larger quantity of dextrin is present, the color
produced by a few drops of the reagent is almost black. If starch
and dextrin be present in the same sample, the}' can hardly be dis-
tinguished. One minim of the official T. S. of iodine will produce a
decisive tint in solution of dextrin in distilled water, in proportion
of I of the former to 2,000 of the latter. The presence of gum
does not interfere with this reaction.
As commercial dextrin is not a product of definite comjxjsition
and constant proportions, the delicacy of the iodine test may, of
course, vary accordingly.
As all the samples of gum gave negative results with iodine.
Am. Jour. Pliarm.
198 Observations on Acacia of Commerce. { '^'^Aprii." S
traces of dextrin and starch were added to the sample under exam-
ination ; the reagent in all cases gave prompt indication of their
presence, showing that there was present in the original sample
nothing to mask the reaction.
The potassium ferricyanide reaction did not give satisfactory
results. The test solution was prepared as above described from
clear crystals of potassium ferricyanide, previously washed with
distilled water to free it from any adherent ferrous salt, which might
have formed by exposure to light. By reduction with the ferric
chloride it produced a pure yellowish brown color, without a bluish
shade, proving the absence of ferrous salt.
(a) When diluted with distilled water, it remained unchanged
during twelve hours.
{b) A I per cent, solution of dextrin in distilled water caused
almost immediate reduction and consequently a blue color.
{c) The reaction with finely powdered gum arabic proved some-
what less rapid than that with pure dextrin, but the blue color was
produced within twenty minutes (powder free from dextrin by iodine
test).
{d) Powdered gum arabic, adulterated with dextrin, reduced the
solution after a few minutes' time.
[e) When a tear of the gum was dropped into the solution of
potassium ferricyanide, the solution did not acquire a blue color
within two hours; but after standing a few minutes the outer sur-
face of the tear of gum was colored a decidedly bluish tinge. When
a tear of the gum was powdered, and then some of the potassium
ferricyanide solution added, reduction with formation of a blue color
took place more rapidly, agitation increasing the action.
Is it not possible that the drying of the gum or that other influ-
ences cause a change to take place in the gum acacia, which might
account for the reaction with alkaline cupric tartrate and potassium
ferricyanide solutions ?
In order to determine the quality of the commercial powdered
acacia, the samples were obtained, as far as possible, from the source
of supply of the market, though the majority were obtained in phar-
macies in Ohio, Indiana, New York, Pennsylvania and New Jersey.
All the samples were tasteless, and all reduced Fehling's solution,
as described in the first part of this contribution.
^'"kp^riiViSL"'' ! Proximate Analysis of Orris Root,
199
TABULATHD RESULTS OF EXAMINA TKJN.
Sample.
(
Color of
Sample.
Color of
Solution.
Ver>' light.
Dextrin.
Nont
Starch
Color, when
Heated with
KUH.
U. S. P
Almost white.
Amber.
Gran, gum
White.
Very light.
Nont
Amber.
Powder a ■ .
White.
Yellow.
Xont-.
\ i;i.
.\mber.
b. . .
White.
Yellow.
None
Nour.
.\mber.
c
Gray.
Dark brown.
None.
N..1U
Yellowish-brown.
1
White.
Very light.
None.
N ■ . I , ■
.\mber.
e . .
Yellowish.
Yellow.
None.
None
Amber.
•' /• . .
White.
Light.
Noue.
None.
—
S • ' •
White.
Light.
None.
None.
Amber.
h . . .
White.
Yellow.
None.
None.
.\mber.
White.
Light.
None.
None.
—
White.
Light.
None.
None.
—
I .
White.
Light.
None.
None.
—
m . .
White.
Very light.
None.
None.
Amber.
These results seem to indicate that the cheaper grades of gum
are most frequently employed in the preparation of the powdered
article, and that adulteration with dextrine is not generally prac-
tised.
Of course, the samples examined were only such as are used in
pharmacies ; and, no doubt, for technical purposes, one might be
able to purchase gum wherein dextrin might be revealed.
To all who have favored me with samples of the gum, ni)' sincere
thanks are due.
Cincinnati. O , March, 1897.
PROXIMATE ANALYSIS OF ORRIS ROOT.
Hy S. Allen Ticker.
Coutribulion from the Chemical Laboratory of the Philadelphia Colle>^e of
Pharmacy. No. 162.
What is known in commerce as orris root is the rhizome of Iris
florentina, which has been deprived of its cortex and dried by expo-
sure to sunlight. Orris root has a delicate aroma, and for this rea-
son it finds extensive use in the manufacture of perfumes, floral ex-
tracts and tooth-powders. F*or these purposes the prepared rhizome
Am. Jour. Pharm.
2CX) Proximate Analysis of Orris Root. {^™aSi897
is reduced to a granular form or a fine powder. It was on account
of the extensive use of orris root, and because no statement of the
effect of solvents on the article is given, that the writer undertook
this proximate analysis. It is well known, however, that some of the
proximate principles have been pretty thoroughly investigated by
Dumas, Landerer, Fliickiger and Hager ; especially is this true of
the volatile oil and its stearopten.
A sample of the granular form of the prepared rhizome was
ground to a very fine powder. Petroleum ether extracted wax and
fat to the extent of 1-34 per cent. Ethyl ether afterward dissolved
1-83 percent, of substances which were soluble in alcohol and ben-
zole, but not soluble in acidulated water. This extract had a strong
odor of orris root. The substances to which this odor was due
were not soluble in water. The alcoholic solution of the extract
gave precipitates with alcoholic solutions of ferric chloride and lead
acetate.
Absolute alcohol removed 4-13 per cent, of the weight of the
rhizome. About three-fourths of the extract were soluble in water-
This solution contained small amounts of glucose and sucrose. It
gave a precipitate with lead acetate solution.
The distilled water extract amounted to 14-02 per cent. This in-
cluded 831 per cent, of glucose, 1-27 per cent, of sucrose and a
small amount of substances precipitable by alcohol. The total or-
ganic solids dissolved by water made alkaline with sodium hydrate
were found to be 30-30 per cent. This extract consisted almost en-
tirely of mucilaginous and albuminous substances which were pre-
cipitated by acidifying with acetic acid and adding a large volume
of alcohol. Water acidulated with hydrochloric acid extracted
10-30 per cent, of organic matter. Starch was present to the extent
of 16-85 P^^ cent. A cold infusion of the rhizome gave no precip-
itate with gelatin for tannin. The sample of orris root examined
contained 8-74 per cent, of moisture and 2-12 per cent of ash. The
ash contained calcium, magnesium and potassium as carbonates*
chlorides and phosphates.
In addition to the foregoing percentages representing the extracts,
starch, moisture and ash, 10-37 per cent, of cellulose and undeter-
mined substances were present.
"^"AiXiac"""-; Marrubiin and its Dichlorine Derivative, 201
MARRUBIIN AND ITS DICHLORINE DERIVATIVE.
By Harry Matusow.
Contribution from the Chemical Laboratory of the Philadelphia College of
Pharmacy. No. 163.
This crystallizable principle, obtained from Marrubium vulgare,
a plant belonging to the natural order Labiata;, was first isolated by
Mein in 1855, and investigated by Harms, to whom the former pre-
sented it for investigation.
Harms (Archiv dcr PJiannacie, No. ^^i, p. 144, August, 1855),
then, upon investigation, ascribed to marrubiin the following prop-
erties :
" Marrubiin forms stellate groups of colorless needles ; it melts
at 148^ C, and at a higher temperature it breaks up with the
development of an unbearable odor ; it is almost insoluble in water,
easily soluble in alcohol — particularly in hot alcohol — and soluble
in ether. Its taste is persistently bitter ; and it possesses a tend-
ency to become colored when exposed to the air."
The next investigator to take up the subject was Kromayer
[Archiv der Pharmacic, No. 108, p. 258, 1861), who extracted the
plant with boiling water precipitated the infusion with lead
acetate, removed the excess of lead with hydrogen sulphide, and
then concentrated the infusion to a syrupy consistence. He then
obtained the crystals from the infusion by means of alcohol and
purified them by treating with animal charcoal.
Kromayer's results, which were published simultaneously with
the process of extraction briefly described above, were as follows :
" F'rom ethereal solutions it crystallizes in colorless rhombic
plates, or thick, four-sided, double, gypsum-like crystals.
" From alcoholic solutions it crystallizes in needles.
'• The crystals are gritty between the teeth. On account of their
sparing solubility in water, their bitter taste is not perceived until
after being kept in the mouth for some time.
" Alcohol or ether dissolves it readily.
" The alcoholic solution tastes intensely bitter, and has a some-
what acrid after-taste.
" The alcoholic solution reacts perfectly neutral. Almost com-
pletely insoluble in cold water and only sparingly soluble in hot
water.
"The hot-water solution of marrubiin tastes strongly bitter.
202 Marriibiin and its Dichlorine Derivative. {'^'^Apri'ialG?""*'
** On the addition of water to the alcoholic solution, the marru-
biin separates as an oily liquid, and the mixture becomes milky; on
adding some alcohol and allowing the solution to rest, the marrubiin
crystallizes out in needles.
**When heated on platinum foil, marrubiin melts to a colorless
liquid ; more strongly heated, it gives off white fumes of a biting
and irritating odor, and finally burns away completely without leav-
ing any ash.
♦* When heated in a glass tube closed at one end it distills over in
oily drops without leaving a residue, developing at the same time
mustard-oil-like, piercing fumes.
" The melting point of marrubiin lies at i6o° C; on cooling it
solidifies to a beautiful, radiating, crystalline mass.
" Marrubiin is not a glucoside. Concentrated sulphuric acid dis-
solves it rapidly, with a brown-yellow color. On the addition of
water the color disappears with the separation of gray flakes.
'' Concentrated hydrochloric acid, whether hot or cold, has no effect
on marrubiin.
" Cold concentrated nitric acid does not affect it, but on heating
dissolves it with a yellow color.
" Tannin does not precipitate a solution of marrubiin.
" By the action of alkalies, cold or warm, marrubiin is not per-
ceptibly affected.
" Ammoniacal silver nitrate solution, on being boiled with mar-
rubiin, is only slightly reduced. Marrubiin, consequently, is not an
aldehyde-like body.
" Marrubiin is not precipitated by metallic salts, namely, ferric
chloride, when applied, did not produce any change.
"In its properties marrubiin stands nearest to coumarin, C^gHgO^;
to cinnamein (meta-cinnamein) = CgaHj^O^ = Q^^^O, C^gH^Og
(benzoyl-cinnamate); and to styracin = C36H16O4 = CjgHgO, CigH^Og
(cinnamyl-cinnamate)."
In addition to the foregoing results quoted from him, Kromayer
remarks that marrubiin is the first instance of a crystalline separated
bitter principle from a plant belonging to the Labiatae, a family
which is so rich in ethereal oils, and that all the characters of mar-
rubiin indicate its intimate relation to the ethereal oils.
In 1863 Harms published a second communication on the prop-
erties of marrubiin, in Archiv der Pharmacie, No. 1 16, p. 141.
Am. Joar. Pharm
ApXi^"'"' } Marrubiin and its Dichlorine Derivative. 203
In this case Harms obtained the bitter principle by treating the
herb with three successive portions of hot water, evaporating the
water extractions to a syrupy consistence, and treating them with
alcohol; to the alcoholic solution he added a large quantity of
sodium chloride and about one-third its volume of ether ; the whole
was then agitated and the separated ethereal layer, when drawn off
and allowed to evaporate spontaneously, left tabular crystals of
marrubiin, which, after two re-crystallizations from alcohol, appeared
pure. From 25 pounds of herb Harms obtained 2 grammes of the
crystalline bitter principle.
With reference to the properties of marrubiin, Harms says he
found them, in general, to agree with those given by Kromayer.
An elementary analysis, which Harms made on a portion of the
crystals presented to him by Mein, yielded from 0-3 13 gramme of the
principle, dried at 90°-ioo° C, 0240 gramme of H2O, or 8.52 per cent,
of H. The carbon estimation, unfortunately, was lost, but it showed
that the marrubiin contained more than 69 per cent, of carbon.
Harms also stated that on recrystallizing marrubiin from hot solutions
a portion of it assumes an amorphous form. On dissolving the amor-
phous bitter principle in alcohol, and allowing the solution to stand
at the ordinary temperature in the air, it goes over into its original
form, and separates in a crystalline, wart-shaped mass. Marrubiin
crystallizes easily — best when to a boiling alcoholic solution boiling
water is added until it begins to become turbid, and the solution
allowed to cool slowly.
In the American Journal of Pharmacy for June, 1890, Hertel
published the following experience :
On making a fluid extract of marrubium, using diluted alcohol as
a menstruum, it was noticed that, after standing for a week, a de-
posit of well-defined crystals separated from the extract. The de-
posit from 10 pounds of herb was nearly I ounce, the extract,
however, still being as bitter as before. The slight yellow
color of the needle-shaped crystals was removed by several recrys-
tallizations from alcohol. The crystals still retained their slowly-
developing but persistently bitter taste. When heated on platinum
foil the crystals melted, then charred and finally volatilized without
leaving any residue. They were quite soluble in chloroform, alco-
hol and ether, and slightly soluble in water. The princijile is insolu-
ble in benzin, is not colored by acids, docs not respond to I'^ehling's
204 Marrnbiin and its Dichlorine Derivative. {^^'llx\iXm!^'
test for sugar, nor to the alkaloidal group-reagents, and from its
alcoholic solution is not precipitated by lead subacetate. It crystal-
lizes best from cold alcohol.
A menstruum prepared from 2 parts of alcohol and i part of
water, with 5 per cent, of glycerin, yielded a fluid extract remain-
ing free from crystalline deposit.
The investigation of marrubiin was next taken up by Morrison,
who published his results in the American Journal of Pharmacy,
July, 1890. Morrison obtained the marrubiin by extracting the
herb with ether, and purified it by repeated crystallization from hot
95 per cent, alcohol, and subsequent treatment with animal char-
coal. Morrison describes the properties of marrubiin as follows :
The crystals were insoluble in water and in solution of potassium
hydrate, very sparingly soluble in boiling water and in cold alcohol.
It is soluble in hot 95 per cent, alcohol, also in ether and chloro-
form. The crystals melt at 152°-! 5 3° C. They were at first taste-
less, but developed, when held on the tongue, a decided bitterness.
The alcoholic solution was very bitter. Sulphuric or nitric acid
gave a dark brown color ; hydrochloric acid produced no change,
and ferric chloride produced no change. This principle reduced
Fehling's solution by boiling in a water-bath, without first heating
with an acid. On boiling it first with acidulated water, a peculiar
aromatic odor was developed ; then on heating with Fehling's solu-
tion, an abundant precipitate of cuprous oxide was produced, thus
showing it to be an easily decomposable glucoside.
The average of two combustions was :
Calculated for
Found. (C40H58O9.)
Per Cent. Per Cent.
C 70*25 70-38
H 8-42 8-50
O 21*33 21*12
The melting point of the marrubiin, obtained by Hertel, was also
determined by Morrison and found to be i53-5°-i54-5° C. Morrison
remarks that this marrubiin was evidently nearly pure, and states
that the average ot three combustions made by him was :
Per Cent.
C 70-54
H 9-08
O 20*38
^"'AiXi^*'''"*} Marrubiin and its Dichlorinc Derivative. 205
Morrison further states that his results indicate the composition
of marrubiin to be very close to that of absinthiin, C4yH;^^09. a crys-
talline bitter principle obtained from wormwood, and described by
Kromayer in Arcliiv dcr Pharmacie, No. 108, p. 120, but that it does
not af^ree with all the properties described by Kromayer, who states
that absinthiin melts at 120° to 125° C.
Thus far I have reviewed the history of marrubiin, and described
the investif^ations and results of preceding workers. I shall now
detail my own experience with the extraction of marrubium, for the
isolation and purification of marrubiin, and describe the properties
of that substance as observed by myself.
The herb was collected by the writer at Lawnside, N. J., in the
months of July, August and September, 1896. It was carefully
dried in a room, without exposure to direct sunlight. The herb
was then finely ground, and trial extractions made with alcohol,
benzol and acetone as menstrua, 500 grammes of the herb
being subjected to the solvent action of each of the solvents named.
Of the three different menstrua mentioned, acetone was found to be
the most satisfactory one, extracting the largest quantity of the
bitter principle and the least amount of foreign matter, with
smallest quantity of menstruum.
Two and a half kilogrammes of the herb were now
extracted with acetone, the acetone being, from time to time, recov-
ered from the extract, and used again as menstruum. When the
herb was practically exhausted, the acetone was recovered from the
extract, by distillation, and the thick, syrupy mass which was left
was treated repeatedly with hot benzol. The benzol solution was
allowed to stand for twenty-four hours for marrubiin and resinous
matter to separate. The mother liquid was then poured off, and
the residue treated with a fresh portion of hot benzol and allowed
^to stand as before. This treatment was continued until relatively
pure crystals of a yellowish color were obtained. The crystals were
then repeatedly crystallized from hot alcohol, by solution and chill-
ing, which, owing to the prevalent cool weather, afforded a rapid
means of crystallization. They still retained a slight yellow tinge,
which, however, was removed by treating them with animal char-
coal. A portion of the syrupy mass obtained above, on distilling
off the acetone, was treated repeatedly with hot alcohol, and allowed
to stand ft)r twenty-four hours after each treatment, without previous
2o6 Mamibim and its Dichlorine Derivative. {^^'l^xxXm^^'
treatment with benzol, but without success ; the reason for this, I
think, is the following : the crystals are accompanied in the extract,
besides the coloring and other foreign matter, by what seemed to
be a resinous substance, which was dissolved along with them by the
alcohol, and separated with them from its solution, thus rendering it
difficult for the bitter principle to crystallize ; hot benzol, on the other
hand dissolved the crystals and the resinous substance at first, but
when allowed to stand for twenty-four hours, retained the greater part
of the resinous substance in solution, and deposited the crystals with
only a small quantity of the resinous substance adhering. When
these impure crystals were treated with a fresh portion of hot
benzol, the marrubiin was dissolved, but the contaminating resin,
for the most part, did not go into solution. From the 2J^ kilo-
grammes of herb extracted about 20 grammes of purified crystals
were obtained.
These crystals melted at 154°-! 5 5° C, and on cooling solidified to
a crystalline mass.
When treated with strong sulphuric acid a dark brown color was
produced.
Strong nitric acid produced a similar reaction.
Strong hydrochloric acid produced no change, even on heating.
When Fehling's solution was heated with a hot-water solution of
marrubiin on a water-bath for thirty minutes, it was not reduced.
Fehling's solution, when heated on a water-bath for thirty minutes
with a hot-water solution of marrubiin, which had previously been
boiled with hydrochloric acid, was not reduced.
The alcoholic solution of marrubiin has a neutral reaction.
The alcoholic solution of marrubiin, when treated with alcoholic
ferric chloride, was not changed ; alcoholic lead acetate produced no
change ; alcoholic tannin solution produced no change ; ammoniacal
silver nitrate solution, in the cold, was not reduced by a hot aqueous
solution of marrubiin ; the same reagent when heated in a water-
bath was not reduced ; but as the solution became more concen-
trated, the marrubiin gradually separated from solution on the bot-
tom of the tube.
The alcoholic solution, as well as the crystals, had a persistently
bitter taste. On the addition of water, the alcoholic solution be-
comes turbid white. Marrubiin crystallizes in lustrous needles ar-
ranged in star- shaped groups, from hot alcohol when not concen-
'^''^Aprii".'!^"™'} Marrubiin and its Die Jilorinc Derivative. 207
trated. From concentrated hot alcoholic solutions, it crystallizes
in dull-white plates.
It is soluble in acetone, ether, alcohol, chloroform, but most readily
in hot benzol.
It is insoluble in petroleum benzin and cold water, and only spar-
ingly soluble in hot water.
Marrubiin, when tested for nitrogen, by fusing a small quantity of
it with a fragment of metallic sodium, agitating the heated mass
with water filtering, and adding ferrous sulphate, ferric chloride and
hydrochloric acid in excess, did not give the characteristic blue
precipitate or color of ferric ferrocyanide, (Fejj (F^ (CN)g)3, thus
indicating the absence of nitrogen.
The crystals obtained by recrystallization from hot alcohol, pre-
vious to being treated with animal charcoal, melted at 158°-! 59° C.
They were subjected to ultimate analysis ; the combustions were
made in an open tube with copper oxide and a current of oxygen,
the substance being, in all cases of combustion, previously dried in
a desiccator over sulphuric acid for twenty-four hours.
The following are the results of two combustions :
(0 '^93' gramme of the substance yielded:
•5113 gramme of COj = 72-19 per cent, of C.
•1500 " " H20= 8-59 " " " H.
19-22 " " " O.
lOO'OO
(2) -1659 gramme of the substance yielded :
•4414 gramme of CO, = 72*57 per cent, of C.
•1293 " '• HjO= 8-68 " " '* H.
1875 •• •'. •• O.
lOO'OO
The crystals were then recrystallized six times from hot alcohol,
and a second determination of the melting point gave the same
result as that obtained in the previous case, viz.: 158^-159° C.
They were, therefore, treated with animal charcoal in several suc-
cessive applications, and the melting point, as proven by several
trials, was found to be 154°-! 55° C. A combustion of the purified
substance showed the following to be its percentage composition.
2oS Marrnbiin and its Dichlorine Derivative. {^'^i^'^^^Xm^'^'
which is practically the same as that previously obtained; -1654
gramme of the substance yielded :
•4372 gramme of CO., = 72*07 per cent, of C.
•1305 " " H2O = 877 " " " H.
19-16 " " " O.
100 '00
The average of the three combustions was :
Calculated for
Found. (C30H43O6).
Per Cent. Per Cent.
C 72*28 72'14
H . 8-68 8-62
O 19*04 I9'24
lOO'OO lOO'OO
My results confirm Kromayer's, in general, excepting the melting
point, which he determined to be 160° C. They also differ from
the melting point stated by Harms to be 148° C.
The melting point obtained by myself is nearest to the one ob-
tained by Morrison.
My results show that marrubiin is not a glucoside ; so they also
differ in that respect, as well as in the matter of its formula from the
results obtained by Morrison.
Dichlorine Derivative of Marrnbiin. — A small quantity of marru-
biin was dissolved in ether and dry chlorine gas passed into the
ethereal solution, until no more of the gas was absorbed.
The ethereal solution, which was of a yellow color, was divided
into two portions, one portion being allowed to evaporate and the
other poured into an excess of water. The portion poured into the
water was stirred, the water poured off and the precipitated sub-
stance washed with successive portions of water and carefully dried.
When dry, it was found in the form of a yellowish-white, hard, wax-
like mass, adhering to the sides of the beaker. The portion of the
ethereal solution which was allowed to evaporate left a thick, oily,
yellowish-brown substance, which, when redissolved in ether and
allowed to evaporate several times and then washed repeatedly with
water, assumed a form similar to the substance obtained by pouring
a portion of the ethereal solution into water.
A preliminary test for chlorine was made by heating a small por-
'*^'"Ai,ri'i':iS^*'""*} ^^ote on Ointment of Mercuric Nitrate. 209
tion of the thoroughly washed substance with chlorine-free calcium
carbonate on platinum foil. The mass was allowed to cool, then
dissolved in water by the aid of nitric acid, and silver nitrate, T. S.,
added. This reagent produced a white, curdy precipitate of silver
chloride insoluble in nitric acid.
To estimate the chlorine quantitatively, 0813 gramme of the
chlorine derivative was intimately mixed with chlorine-free calcium
carbonate, and heated in a glass tube, closed at one end, until the
carbon was completely burned off. The tube was then broken, and
it and the contents were introduced into a beaker. Water was
added, and the whole warmed and complete solution of contents
effected by the aid of nitric acid. The solution was filtered clear,
the filter carefully washed, adding the washings to the filtrate, and
then precipitated with silver nitrate. The precipitate was collected,
washed with hot water and dried at 130° C. to constant weight.
The weight of silver chloride so produced was -0425 gramme,
which corresponds to 0105 gramme of chlorine, or 12-91 per cent,
of the weight of the derivative taken. Assuming that one hydro-
gen atom is replaced by every chlorine atom introduced, the for-
mula of the derivative — admitting the formula for marrubiin to be
CjoH^Og — would be CaoH^iCloOg. the theoretical amount of chlorine
in which is 12-47 per cent.
Marrubiin dichloride is a yellowish-white, hard, wax-like sub-
stance, soluble in ether and alcohol, from which solvents, however,
it could not be obtained in crystalline form, even after repeated at-
tempts at crystallization.
When heated it becomes transparent at 63° C.
NOTK ON ointmp:nt of mkrcuric nitrate.
By Josp:ph W. England.
Probably no official ointment has been more carefully studied
than has the familiar citrine ointment. To the physician its medi-
cinal action is peculiar and full of interest. Through its free nitric
acid, when applied to an epidermis more or less altered by patho-
logical change, it rapidly penetrates the superficial tissue, and
sharply stimulates the subdcrmal tissue to absorb the soluble mer-
curic .salt, thus inducing a local, and possibly, to some extent, a con-
stitutional alterative action. The danger of salivation from a too
f Am. Jour. Pharm,
2IO Note on Ointment of Mercuric Nitrate. {^'^•llr\imi.
speedy absorption is such that many physicians dilute the ointment
with fatty diluents in all cases, save those requiring strong stimula-
tion. Whether the elaidin of the ointment is of any value in pro-
moting absorption or not has not been determined.
Not alone from the medical standpoint, however, has the ointment
been of interest, but its making has been the fruitful source of much
study by pharmacists. Under the title of ** Unguentum Hydrargyri
Nitratis," an able paper by P. W. Squire, has been published in the
PJiarmaceutical jfournal of London (February 27, 1897, 172), in
which are given the results of experiments upon the nature of the
fat, the relative quantity of nitric acid, and the manipulation used
in making the ointment. Especial attention is paid to the differ-
ences between the processes of the British and United States Phar-
macopoeias. It is not necessary to here dwell upon these, save only
in a general way.
Regarding the fat to be used, Mr. Squire prefers the British
Pharmacopoeia mixture of lard and olive oil, rather than the lard oil
of the United States Pharmacopoeia. He says that with lard oil the
oxidation takes place at a lower temperature than with lard and
olive oil, the resulting product being somewhat darker; otherwise,
he frankly adds, there is not much to choose between the two fatty
bases.
The relative quantity of nitric acid used in the B.P. process is
considerably more than in the U.S.?., and while the U.S.P. treats the
lard oil with a part of the nitric acid previous to the addition of the
solution of mercuric nitrate, the B.P. directs that the acid solution of
mercuric nitrate be added to the ointment base without any previous
treatment with acid. The advantage of the first procedure over the
second Mr. Squire admits, giving an alternative formula based on the
B.P. formula, in which the fatty base is treated with half the nitric
acid before the mercurial solution is added.
Mr. Squire finds that the temperature at which effervesence takes
place varies with the nature of the mixture of acid and fat. With
nitric acid and lard oil the reaction is slight at 100° C. (212° F.) and
brisk at 110° C. (230° F.) ; with nitric acid, lard and olive oil, the
reaction takes place at 120° 0.(248° F.) ; with acid solution of
mercuric nitrate and lard oil it occurs at about 90° C. (194° F.), and
with acid solution of mercuric nitrate, lard and olive oil, at 95° C.
(203° F.). The relatively higher temperatures of the first two in-
^"^ April; Sr™ } ^ote on Ointment of Mercuric Nitrate. 21 1
stances have no practical bearing if there be no mercuric salt
present.
The important practical point to observe is that the temperature
be kept low after the addition of the mercuric solution, when the
tendency to blacken increases as the temperature rises. This change
will occur even if the ointment be kept at 100° C. (212° F.) for any-
thing like an hour, and possibly in much less time.
The interesting nature of Mr. Squire's communication suggested
to the writer the advisability of reporting its data to American
pharmacists, and also of making a few practical suggestions regard-
ing the present U.S. P. process.
The following formula is suggested for trial :
Grammes.
Red mercuric oxide 755
Nitric acid 175"
Lard oil 760'
Heat the lard oil in a glass or porcelain vessel to 100° C. (212° F.),
withdraw heat, and gradually add 75 grammes of nitric acid. When
the reaction moderates, reapply the heat until brisk effervescence
takes place, and then withdraw heat until active effervescence sub-
sides. Then gently heat until effervescence ceases. (During the
effervescence stir the mixture with a wooden spatula or paddle.)
Allow the mixture to cool to about 60° C. (140° F.). Having dis-
solved the red oxide of mercury in 100 grammes of nitric acid, with
the aid of sufficient heat, add the solution gradually to the oxidized
fat, and stir the product until cold. When nearly cold, add 50
grammes of glycerin, and admix thoroughly.
The advantage in using red mercuric oxide over mercury rests in
the fact that small quantities of it are more easily weighed, and it is
probably purer than commercial mercury. If it be desirable to employ
red mercuric oxide for making the official solution of mercuric nitrate,
it should be equally useful in making the ointment. The small
quantity of water formed in the reaction is of no practical
moment.
In the U.S. P. process, no directions are given for stirring the
fatty mixture during oxidation, and the inference is that such a
practice is to be tabooed. As a matter of fact, a diligent stirring of fat
and oxidizing material facilitates oxidation, and in the writer's opin-
ion is of decided advantage in hastening the end- reaction. If the
212 Aqua Pur a. {'"'^■iSrnJmi"'^-
ingredients be not stirred during effervescence, there is a danger
that the contents may be thrown from the container.
The reaction between the fat and acid is sometimes slow in re-
sponding, and when it responds it does so very quickly. For this
reason the writer prefers to withdraw the heat on active effervescence,
and then after the reaction is in operation, to heat gently until effer-
vescence ceases, rather than to follow the official directions of heat-
ing until effervescence ceases after the addition of acid with
primary reaction.
There is no apparent need of waiting until the temperature of the
oxidized fat falls to 40° C. (104° F.) before adding the mercurial so-
lution. Squire cools his product to 60° C. (140° F.), and this would
seem to be a low enough temperature.
The red oxide of mercury " lumps " slightly on adding it to the
acid, but heat soon brings it into solution.
Objection may be made to the addition of glycerin to ointment of
mercuric nitrate, on the ground that nitro-glycerin may be formed.
The objection is not well founded. The production of nitro-glycerin
requires a large excess of concentrated sulphuric acid over the
quantity of nitric acid used in order probably to absorb rapidly the '
water formed in the reaction, as follows :
C3H, (0H)3 + sNO^-OH .^ C3H, (N03)3 + 3H2O
This condition does not obtain in this ointment. In addition,
the fat present doubtless inhibits such a change. Further, the
writer has followed the practice of adding glycerin to the ointment
for three years past, and there has been no complaint of untoward
therapeutic effects, as there would have been had any nitro-glycerin
been present ; the latter is rapidly'absorbed by the skin.
AQUA PURA.
Bdilor American Journal of Pharmacy.
Dear Sir : — In consideration of the condition of the drinking
water supplied to the citizens of Philadelphia and some other cities,
too, by their public works, it seems to me there is an excellent
opportunity for the pharmacist to do a stroke of business as well as
to assist his suffering fellow-beings to preserve their lives and en-
joy a drink of pure water while still living. My suggestion is that
^"aSiSt*""'*} Common Sense on the AlcoJiol Question. 213
he constitute himself a purveyor of pure drinkinf^ water to his cus-
tomers and neighbors by supplying them with filtered water. He
can either sell this pure filtered water at a merely nominal price,
say, 4 or 5 cents a gallon at his store, not delivered, or else give it
away as an advertisement, and which, I think, would be more pro-
fitable than the selling of postage stamps for a similar purpose.
There are several good filters on the market that can be attached
to the hydrant in the store, and need no attention except for clean-
ing every two or three days, and a proper receptacle for the filtrate ;
they will work on day and night alone. From this arrangement
down to simple filtration through paper with a little magnesia, many
ways of filtration will occur to the competent and skilful gentlemen
for whose information and ultimate benefit this hint is intended.
I fancy I can see an extensive and profitable application of this
hint to the business of many pharmacists.
A little admixture of plain carbonated water added to the filtrate
would make it sparkle and be an improvement possibly.
The highest-priced filter on the market that I know of, filtering
about 10 gallons an hour when clean, can be put up for $25, per-
haps less, and from this through an endless variety of filters and
methods, home-made or otherwise, the outfit can be reduced to a
very small sum, according to quantity of filtered water required or
attention needed to keep the work continuously going on.
Yours truly.
Pro Hono Publico.
COMMON SENSE ON THE ALCOHOL QUESTION.^
However temperate a man's own views may be on any such question
as that of the use of alcohol, he is tempted to lean in his public
utterances toward the contention of fanatics. He may not go to the
extremes that they contend for ; indeed, he is almost sure not to.
Hut he is apt to make statements by which they can strengthen
their case with the public and especially with the legislators. It is
refreshing to notice a recent exception in the case of Mr. Pellcw, of
the department of chemistry of Columbia University, who recently
^Editorial in New York Afedical Journal, March 8, 1897.
214 Common Sense on the Alcohol Question. {^"Aj?ii?i897^™*
concluded a course of lectures in the Museum of Natural History on
the subject of the good and bad effects of alcohol.
Mr. Pellew stated without reserve, and backed up his statement
by citing the most careful observations and experiments of well-
known investigators, that " there was no doubt that, even in health,
a small amount of alcohol, if given in divided doses, could be
burned up in the blood and serve as food, without producing any
injurious effects." We are quoting from the Sun's report of Mr.
Pellew's last lecture. He went on to say that in diseased condi-
tions, where nutrition was impaired, alcohol could be given in
greatly increased amounts without any intoxicating effect, and was
then of enormous value. An ounce of it, he said, gave as much
heat as seven or eight ounces of beef, and that without having to
undergo the process of digestion and assimilation. In other words,
it burned, " as in a lamp, without wasting the wick."
On the other hand, the popular notion that alcohol will keep up
the heat of the body under exposure to great cold was declared to
be a mistake. Alcohol, said Mr. Pellew, actually reduced the tem-
perature of the blood, but it was ot service to restore equilibrium
after the exposure was over. The lecturer was not backward in
depicting the horrors of drunkenness, to which, of course, no rea-
sonable man can shut his eyes. He spoke of the dram-drinking
habit as a nervous disease rather than a vice. He properly insisted
that, in health, the only good effects of alcohol, ** except, indeed, its
action as a ' scavenger of mankind,' " came from its moderate use.
To show the astonishing amount of intemperance in the so-called
temperance doctrines at present promulgated, Mr. Pellew read pas-
sages from the books on " physiology " to which the law now re-
quires the teachers and pupils in the public schools of the State of
New York to devote a large proportion of their time. He pointed
out the " absurd doctrines, not to say absolute falsehoods," which
in many cases were thus crammed into the children's heads. The
Sun's account concludes as follows : " In his opinion it is confusing
to a child to learn that it is a sin to pick a pocket and to drink a
glass of wine, and he suggested the state of mind of a Teutonic
father or grandfather, when his young hopeful would read to him,
from his school books, how the ' use of beer, more than of any
other liquid, tends to make the drinker selfish, cruel and brutal.' "
t^Airti'i^*^"''} Recent Literature Relating to Pharmacy. 215
RECENT LITERATURE RELATING TO PHARMACY.
SOME COLOR REACTIONS OF TARTARIC, CITRIC AND MALIC ACIDS.
According to E. Pinerua [Annates de Chimie Aiialytique, 2, 66), the
reagent for producing these color reactions is made by dissolving
0'02 gramme of ^9-naphthol in i c.c. of sulphuric acid, specific grav-
ity 1-83.
The test is made by warming cautiously in a porcelain capsule
005 gramme of the organic acid with 10 to 15 drops of the reagent.
Tartaric acid, when thus treated, produces a blue color, which,
under the gradual action of heat, becomes a pure green. If to the
cooled mixture 15 to 20 times its volume of water are added, the
green coloration passes to a reddish-yellow.
With citric acid the color at first produced is an intense blue,
which does not become green on the further application of heat, and
the mixture becomes colorless or only slightly yellow on the addi-
tion of 1 5 to 20 times its volume of water. If the citric acid contain
only a small quantity of tartaric acid, the green color is produced
by the latter.
Malic acid, when treated like the others, produces a greenish-yel-
low, quickly passing to yellow. The addition of water furnishes an
orange color. All the reactions are produced quickly, and care and
judgment must be used in applying heat.
THE ALLEGED CONVERSION OF CINCHONINE INTO CINCHONIDINE.
Messrs. B. H. Paul and A. J. Cownley [Pharmaceutical Journal,
February 20, 1897) have investigated the alleged conversion of cin-
chonine into cinchonidine and reached the following conclusions
with reference to their experiments : An endeavor to corroborate
Koenig and Hussmann's statement as to the possibility of convert-
ing cinchonine into cinchonidine by the action of dilute potash was
unsuccessful. The authors stated that if the supposition be made
that the base obtained was really cinchonidine, it must be presumed
that the cinchonine operated upon had not been sufficiently puri-
fied. It is well known to quinologists that the cinchona alkaloids
are very prone to form double compounds with each other, either as
alkaloids when separating from various solvents, such as ether and
alcohol — the latter having been used by the authors — or as salts
from aqueous solutions. Cupreine, for instance, which they isolated
from Remijia pedunculata, forms a compound with quinine, viz.: homo-
Am. Jour. Pharui,
2i6 Recent Literature Relating to Pharmacy, {^^'l^xii
1897
quinine, which reacts whether as an alkaloid or as a salt, differing
in many respects from either cupreine or quinine.
ESTIMATION OF MORPHINE IN OPIUM AND ITS PRINCIPAL PREPARATIONS.
Al. Grandval and H. Lajoux {Jour, de Pharui. et de Chini. [6], 5,
153) recommend a process for the estimation of morphine which
they claim is easy and rapid of execution, and yields a pure white
morphine.
Opium is estimated by taking 10 grammes, triturating in a glass
mortar with 40 grammes of distilled water, until the drug is finely
divided, throwing on a folded filter and washing the mortar with 40
grammes of water, which are also poured on the filter. The mass is
allowed to drain well, the filter and its contents are then returned to
the mortar and triturated with 40 grammes of water added in seve-
ral portions. The whole is then poured on a plain filter and washed
with water until the washings are free from color and taste. The
filtered liquid and washings are then evaporated on a water-bath to
13 grammes; to this residue are added 13 grammes of 95° alcohol,
and the mixture is allowed to stand a half hour for the sulphate
and meconate of calcium to deposit ; it is then filtered through a
small filter moistened with 60° alcohol, and the filter and precipitate
are washed with alcohol applied drop by drop, so that not more than 10
grammes of alcohol have been used when the washing is complete.
The edges of the filter are kept from drying during the washing by
covering the funnel with a watch crystal. Ammonia is next added,
drop by drop, to the liquid until the odor is just apparent, and the
whole is agitated for some minutes, then set aside for twelve hours
in a cool place. The precipitate of morphine and narcotine is col-
lected on a plain filter, previously dried at 100°, tared and moistened
with alcohol of 60°. When the liquid has run through, the precipi-
tate is washed with alcohol of 40° until the filtrate runs colorless,
when not more than 25 c.c. should have been used. The filter and
its contents are then dried at 100°, weighed and returned to the
funnel, where 5 c.c. of ether are added in order to permit the mor-
phine being moistened by the chloroform; then 10 grammes of
chloroform are added, which dissolve the narcotine. Finally the
morphine and filter are dried at 100^ and weighed. The morphine,
being in the state of hydrate and crystalline, is not dissolved by the
chloroform, which only dissolves morphine when in the state of
anhydride.
Am. Jour. Pbarm. ) Fditorinl -t i --
April. 1897. / CilUUTiai. 21/
Extract of opium is assayed by dissolving: 5 grammes of the
extract in 5 grammes of water, adding 5 grammes of alcohol of 95°,
allowing to stand, and then transferring to a plain filter moistened
with alcohol of 60°. The precipitate is washed with alcohol of 40^,
there being required about 10 c.c; the operation is then conducted
in the same manner as under opium.
The liquid preparations of opium are assayed by slight modifi-
cations of the process which readily suggest themselves.
EDITORIAL.
SUBSTITUTION.
There has been a great deal said at the Natioual and the various State Pharma-
ceutical .Associations about substitution, and it is probable that much more will
be said this year than ever before. It is scarcely necessary, however, to waste
nmch time on a subject in which the plain line of duty is so clearly marked
out for the pharmacist. Certainly, every physician has a right to specify any
particular manufacturer's preparation, and the patient has a right to receive it.
If the pharmacist to whom the prescription is presented for compounding does
not care to furnish the pro<luct of the specified manufacturer, he has a right
to decline and to return the prescription. He has no right, however, to sub-
stitute his own or anybody else's preparation for the one specified, even if he
is sure the substitute is as good or, as he may think, better.
It is only justice to Fairchild Brothers 6c Foster to give them credit for going
to considerable expense to bring certain guilty parties to justice, who have been
palming off, not only substitutes but poor substitutes, in prescription for their
essence of pepsin. The pharmacist who does not wish to <lispense anybody's
preparation but his own has a remedy ; he can visit the physicians in his local-
ity, load them up with samples of his own manufacture, and perhaps convince
them that they are the best. \i the same time it will pay him, morally, legally
and financially, to supply just what is ordered.
THE EVOLUTION OF THE NOSTRUM.
We sincerely trust that certain nostrum manufacturers will not garble the
preceding remarks and publish them as reading matter (i)aid for at double the
advertising rates) in the newspapers; they are not intended for the patent
medicine nabobs.
Substitution, as already defined, is almost impossible in the sale of patent
medicines, but at the same time the pro<lucts of the retail druggist are in many
localities taking the place of nostrums. This has l)eeu l>rought about by the
e<lucation of the public by the pharmacist as to the real nature of the numerous
patent remedies whose virtues lie more in printers' ink than in intrinsic merit.
To offset this disastrous warfare against their remedies, the nostrum manufac-
turers resort fre<|uently to paragraphs like the following, which start in the city
pai>ers and gradually find their way into those of ihc smallest country towns
o n ^^-f/^vt/yJ f Am. Jour. Pharm.
2l8 naitortaL. \ Aprii,i897.
GET WHAT YOU ASK FOR.
Certain Druggists Who Bring Keproacli
Upon Tlieir Business by tlie Practice of
Palming Oft" " Substitutes " on tlie Public.
When a person goes to a drug store for a
standard remedy and the druggist tries to palm
off some other preparation of a pretended simi-
lar nature, urging the customer to buy the latter
concoction on the plea that " it is just as good "
or "really better" than the standard remedy
called for, it is proper to avoid that drug store
ever afterwards.
The profit to the druggist on the standard
preparations is not large. The few remedies
that the whole world recognizes as meritorious
are prepared by able phj-sicians and chemists,
with every facility of modern science at their
command, from the formulas of the most learned
physicians that this generation has produced.
A tremendous amount of capital is invested in
the laboratories where these remedies are made.
They have gained their reputations by the great
good they have done in curing disease and reliev-
ing pain. It costs a great deal to keep up their
necessary excellence.
The unscrupulous and generally ignorant drug-
gist referred to sees a chance to make a big profit
by mixing together a number of cheap ingredi-
ents, giving the mixture a name, and taking ad-
vantage of the gullibility of some people, who
seem to like to experiment with their health.
These preparations are frauds, and are never
advertised, because they will not bear the light
of any public investigation.
This appeared as reading matter in the Philadelphia Public Ledger^ and
claimed to have been taken from the Boston Globe.
What is the " standard remedy " spoken of?
Evidently, from what follows, it is one which has been advertised.
When a customer asks for one of these so-called standard remedies, the
pharmacist will not go far astray if he undertakes a little missionary work, and
either sends the patient to a physician or supplies him (after due recommenda-
tion) with a standard preparation of his own manufacture, which, perhaps, has
not been so extensively advertised, but which has real merit. The editor who
admits such "stuff" and calls it reading matter should be waited on by the
druggists of his locality and be enlightened as to the real facts of the case.
Such notices have appeared quite frequently of late, and, no doubt, will con-
tinue to appear unless some active measures are taken by pharmacists. They
indicate the desperate efforts of the nostrum manufacturers to neutralize the
warfare which is being waged by druggists in nearly every part of the country
against the patent medicine ; but sooner or later the persistent aggressiveness
of the 40,000 druggists in the United States will win. It is nonsense to talk of
going back to the day of 33 or 50 per cent, profits on " patents, " nothing moves
that way in this world, the process of evolution is seen in everything, and this
^""aSiS^""""- } Reineivs. 2 1 9
miserable patent medicine traffic cannot go backward, it must gradually grow
into something which we trust will be better.
A TESTIMONIAL TO PROFESSOR ATTFIELD.
The retirement of Dr. Attfield from professional life is an event in the history
of pharmacy which should be marked by an acknowledgment of his long
labors and important services.
Now some of his past pupils, who have been students personally, or students
of one or more of the fifteen editions of his Manual of Chemistrj*, also a few
of his public friends, have decided that the time has arrived for them to show,
in some appropriate manner, the esteem and warm regard they have for him,
and to ask fellow-students and their friends to join them in a scheme for this
purpose.
Just what form the recognition will take has not been settled. Those who
are willing to join in this testimonial should address Mr. John Moss, 39 Tres-
sillian Road, London, S. E., for circulars and other information. The cash
contribution, if any, is not to exceed ten shillings.
OHIO PHARMACEUTICAL ASSOCIATION.
The pharmacists of Ohio have decided to hold their annual meeting this
year in Cleveland, during the second week of June. Detailed information can
be had of Lewis C. Hopp, Secretary, 19S Euclid Avenue, Cleveland, Ohio.
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
North Carolina and Its Resources. Illustrated. Issued by the State
Board of Agriculture, Raleigh, N. C, 1S96. 8vo., pp. 413.
This handsomely illustrated volume opens with a historical and general
sketch of the State, and then treats of climate, forests, flora, fauna, geology,
economic minerals, gems and gem stones, agriculture, horticulture, education,
etc., etc. North Carolina has long been known as a State rich in economic
products, and this lx)ok will do much to extend the knowledge of these pro-
ducts. The flora is especially rich in medicinal plants, and the supply of many
native vegetable drugs has for years come from this State. The Welsl)ach and
other incandescent lamps are dependent on the supply of monazite from
McDowell and adjoining counties.
Hiltmore, the famous estate of the Vanderbilts, receives careful consideration
in this book, and it is shown to be a superior educator in agricultural matters
to the farmers of the State.
I/eaving the mountainous districts, as we approach the coast we find the
turpentine industry of great importance. The annual value of the resinous
products sold from the State aggregates over |i, 500 ,000, being, in fact,
about one-third of the entire product of these commodities in the world.
On the coast the fish industry is of considerable magnitude. On reading
this book one is almost forced to the conclusion that North Carolina is able to
produce, within her boundaries, everything necessary for the comfort and
well-being of the human race, and therefore is capable of being a small world
within herself.
2 20
,-, • ( A.m. Jour. Pharm.
Kevieivs, \ April, 1897
DIE Fabrication der Kunsti.ichen Minerawasser und anderer
Moi-ssiRKXDER Getranke. Voii Dr. B. Hirsch uud Dr. P. Siedler. Dritte
ueu-bearbeitete Auflage. Druck uud Verlag vou Friedrich Vieweg uud Sohn,
Braunschweig. 1S97.
The whole subject of miueral waters is comprehensively treated under the
following titles : A, Mineral waters in general ; B, half-natural mineral waters ;
C artificial mineral waters ; D, mineral-water ingredients ; E, apparatus ; F,
preparation of mineral waters ; G, calculation of analyses ; H, artificial medi-
cinal waters not occurring in nature ; 7, testing of artificial mineral waters ; K,
beverages ; L, laws, etc. In the first chapter the general subject is concisely
and iuterestiuglv stated. The half-natural mineral waters are those which, on
account of their'agreeable taste, are desirable for table waters, but it is found
necessary to fortify them by a further proportion of carbon dioxide, and, in
some cases, also by the addition of common salt.
Much valuable information is given concerning the composition of natural
mineral waters, and how the various acids and bases are combined with one
another. Attention is called to the fact that many of these bases and acids do
not ordinarily occur together in solution, but that their presence in the same
mineral waters is made possible by carbon dioxide, and, in some cases, heat
and pressure.
That portion of the book devoted to mineral water apparatus and the prep-
aration of artificial waters is very full. Much of the apparatus is figured in
the beautiful manner of Vieweg & Son, and for which they have a world-wide
reputation.
The manufacture of carbonated waters is described in detail and fully illus-
trated. The manufacturer, chemist and pharmacist will all find this book one
of value.
The Year-Book of Treatment for 1897. A critical review for practi-
tioners of medicine and surgery. Lea Brothers & Co. , Philadelphia and New
York, 1S97.
The thirteenth issue of the " Year-Book of Treatment " has appeared, with
but few changes in the staff" of contributors. Every branch of medicine has
received careful attention in this summary. The conclusions regarding
antitoxine are quite full, and the weight of evidence in favor of it as a remedial
agent is overwhelmingly in the affirmative. The chapter on therapeutics of the
year is chiefly in reference to new remedies, and contains much information of
especial value to pharmacists.
AnnuaIv of the Medical Sciences and Analytical Index. A yearly
report of the progress of the general sanitary sciences throughout the world.
Tvdited by Charles E. Sajous, M.D., Paris, and seventy associate editors. Five
volumes. The V. A. Davis Company, publishers, Philadelphia, New York and
Chicago.
The editor states in the preface to Volume I that his aim has been to add to
the practical value possessed by the previous issues. From a general examin-
ation of the work, we can say that he has fully accomplished his purpose.
Rapport dk Mis.sion a la Martinique ET a Guyane. Par Emmanuel
Gcoffroy. Macon, France, 1897.
J
Am. Jour. Pharm. ) Revitin C -> -> i
April, 1897. / ixiuuiv:^. 221
On account of the death of the author, the introduction to this report was
written by Dr. E. Heckel, who clearly sets forth the object of the journey of
exploration to Martinique and French Guiana ; this object was to find, if possible,
in the French colonies, trees yielding caoutchouc or other substance that
would take its place, and to determine if the Araucarias of Brazil were to be
found in French Guiana. The author himself answered these questions in his
conclusions, by stating that the search for the forests of Araucarias was com-
pletely fruitless, and he did not believe they existed in that colony, as they are
ver)- conspicuous trees, and could not have escaped the observations of Aublet,
Guisan and others. On the other hand, the trees yielding milky juice coagu-
lable by alcohol, the Balatas, were found in great abundance. They were, how-
ever, in difficultly accessible regions, covered by water for two-thirds of the year.
The most favorable time for collecting the product was thought to be the com-
paratively short season while the ground was dry.
Les Plantes Medicinales et ToxiguES DE LA GuYANE Fran^aise. Par
le Dr. Kdouard Heckel. Macon, 1897.
The I-'rench nation is giving more attention than formerly to its colonies and
their products : and this volume of ninety-three pages is evidence of an effort
to render available the medicinal plants of French Guiana.
The descriptions of the various plants are arranged alphabetically, each
having one or more common names, followed by the botanical name, natural
order, part employed, its use and method of administration. Among those
described are to be found some well-known representatives of our own materia
medica, as for example, Phytolacca decandra and Ricinus communis ; the
former is given as an introduced plant.
No one interested in the science of applied botany can read this contribution
without being greatly benefited thereby, and the author, who has published it
with the sole object of rendering some service to this branch of science deserves
the gratitude of many outside of his own country.
Digest of Criticisms on the United States Pharmacopckia. Seventh
decennial revision (1890). Published by the Committee. Part I, pp. 183.
New York, 1897.
The Committee has again been fortunate in securing the services of Mr. Hans
M. Wilder in compiling this Digest. It is a valuable summary of nearly all
the papers on the preparations of the Phannacopci.*ia to July i, 1S96. The book
is not for sale, but copies may be obtained by remitting seven cents in postage
stamps to Dr. Charles Rice, Bellevue Hospital, New York.
A Rkcaixii.ation of the Atomic Weioiits. By I'rank Wigjik-sworth
Clarke. New edition, revised and enlarged. Published by the Smithsonian
Institution, 1897.
The first edition of this work was j)ublishe<i in 1882. Since then, new matter
has been constantly accumulating, and the result in most cases has been a
slight lowering of the figures representing the atomic weights of the elements.
Clarke's figures are in nearly every case lower than those of Meyer and Seul^erl,
which was published in the I'.S.P. 1890. With hydrogen as 1,000, oxygen is
given as 1588.
222 Pharmaceutical Meeting. \^^' p^^x\\ml^'
CoNTRim-TION II TO THE COASTAL AND PLAIN FLORA OF YUCATAN.
Hy Charles Frederick Millspaugh, M.D. Field Columbian Museum, publica-
tion 15. Botanical series, Vol. i, No. 3. Chicago, December, 1896.
This is a valuable contribution to the botanical knowledge of the almost
unknown country of which it treats.
Proceedings ok the Fifteenth Annual Meeting of the Virginia
Pharmaceutical Association, held at Hampton, Va., July 21 to 23, 1896.
Several interesting papers add to the value of these proceedings. One paper,
bv Geo. R. Barksdale, is devoted to a description of a new form of percolator,
to which a stirrer is attached.
Complete Price List and Catalogue of Parke, Davis & Co. Detroit,
Mich., 1897.
MI^JUTES OF THE PHARMACEUTICAL MEETING.
Philadelphia, March 17, 1897.
The sixth of the present series of Pharmaceutical Meetings was held in the
College Museum at 3.30 P.M. J. W. England presided. The minutes of the
last meeting were allowed to stand as published.
The chairman called for the presentation of specimens and the following
were exhibited : A sample of 'the matrix of the diamond, which is a kind of
blue clay, from Kimberly Mine, South Africa, presented by Mr. Chas. Bullock ;
and two photographs, one of two beech trees which had grown together in
several places, and the other of a birch tree, which was 17 feet in circumference,
4 feet from the ground. The trees grew in Sullivan County, Pa., and the photo-
graphs were presented by Mr. Chas. H. LaWall.
The first paper, which was on the subject of " Parthenium Hysterophorous,"
by Dr. H. V. Arny, was read by Professor Trimble (see p. 169). The active
principle, or principles, of this plant have heretofore generally been regarded
as an alkaloid by investigators. However, an examination of the plant, in 1889
by the author, gave no evidences of an alkaloid, but a substance was isolated
which was then believed to be a glucoside. It was, therefore, with a view of
clearing up the chemistry of the bitter principle of the plant that the present
investigation was undertaken.
The second paper presented was on a '* Proximate Analysis of Orris Root,"
by S. Allen Tucker (see p. 199). This analysis was undertaken for the purpose
of ascertaining the effects of solvents on orris root, as it was believed that such
knowledge would be found of service in determining the percentage of this
root in tooth powders and like preparations. An interesting result of the
analysis was the large amount of starch which was i6"85 per cent.
A paper entitled "A Brief R6sum^. of Acetic Anhydride in Oil Analysis,
and a Modification of the Method for Estimating Menthol in Oil of Pepper-
mint" was read by Lyman F. Kebler (see p. 189). The author referred to
the difficulties which have attended the examination of essential oils, but said
that methods are being established which will render their analysis quite easy.
Among other factors to be considered, he emphasized the importance of the
boiling point.
Am. Jour. Pharoj.
April. 1897.
Pharmacejitical Meeting.
223
uscocs roRMAiaeiYoc
£^<J«ZSHB)E
Replying to an inquiry in reference to the production of the esters of essen-
tial oils, Professor Sadtler referred to a recent report of Schimmel and Co. on
this subject, and mentioned some of the compound ethers which are being
sold in concentrated form by that firm,
"Some Observations on Acacia
of Commerce " was the subject of a
contribution by J. Henry Schroe-
der (see p. 195). The chairman re-
marked upon the great change in
the character of acacia, and said
that it did not possess the ad-
hesiveness that it formerly had.
Professor Ryan said that twenty
years ago no gum but that of Acacia
Senegal was sold, while the pres-
ent supply is obtained from a va-
riety of sources, and as a result
much of it is of inferior quality.
He advised care in buying the
powdered or granulated gum, and
said that he had examined a sam-
ple of powder which contained 40
per cent, of starch.
Messrs. Boring and Procter also
remarked on the unsatisfactory
quality of the drug.
The last paper on the pro-
gramme was read by Harry Matu-
sow, the subject being *• Marru-
biin and its Chlorine Derivative"
(see p. 201 ). This paper gave evi-
dence of much careful work on the
part of its author, and the import-
ance of the study and classification
of the active constituents of vari-
ous plants cannot be overesti-
mated.
At the close of the consideration
of the papers, a lamp, which was
presented ))y Messrs. I'll Lilly &
Co., of Indianapolis, Ind., and
which is known as the Moffatt
I'ormaldehyde (".cnerator, was cx-
liibited. Professor Trimble de-
scribed the method of using it, and
its general coiislrurtion is illustrated by the accompanying drawing. The
device is recommcndeil for disinfecting purposes, its usefulness in this respect
Ijeing due to the conversion of methyl alcohol into formaldehyde gas. The
amount of gas generated from one pint of alcohol is said to effectually disin-
Am, Jour. Pharm.
224 Notes and News.— Obituary. {""^vrixSm.
feet a capacity of 3,000 cubic feet. A photograph of a battery of twelve
generators was also exhibited. The generators are all connected with one
large reservoir for containing the alcohol, and this form of the apparatus may
be used for the disinfection of large spaces.
An expression of thanks was voted Messrs. Bli Lilly & Co. for their present,
and those who furnished papers.
On motion, the meeting adjourned.
Thos. S. WieGand,
Registrar.
NOTES AND NEWS.
Wild Garlic. —SXywvcQ. vineale is the most injurious weed at the present time
in the INIiddle Atlantic States. From Pennsylvania to South Carolina and
Tennessee, it is known to townspeople as disfiguring lawns ; to farmers and
millers as a pest in wheat, and to dairymen and their customers as ruining
dairy products when eaten by cows in the pastures. It is not native in this
country, but was introduced at an early date from the Old World. One of the
earliest authentic records of its presence in America is contained in Pursh's
American Flora, published in 1814, in which it is said to be "in old fields ;
common." — Circular No. p, U^iited States Department of Agriculture, Divisiofi
of Botany.
Sandahvood oil should not have a specific gravity less than 0*975 at 15°, and
it should dissolve in 5 parts of alcohol of 70 per cent, by volume. The follow-
ing process for its examination has been devised by A. J. Hendrix {four, de
Pharm. et de Chim. [6] 4, 499) : Weigh into a flask of 10 c.c. capacity 2
grammes of a solution of 3 parts crystallized phenol in i part of alcohol, add
o"5 gramme of the oil and mix perfectly. Add 0*5 gramme- concentrated
hydrochloric acid without shaking. At the intersection of the liquids there is
formed in pure sandalwood oil a yellow coloration, changing to a bright red in
a few minutes. With oil of copaiba the upper quickly becomes mauve -colored.
With oil of cedar the upper liquid becomes cloudy, and a brownish color is
developed at the intersection.
OBITUARY.
William Kline Mattern, M.D., Ph.C, died suddenly April 16, 1896, at the
Coroner's private office, No. 632 Chestnut Street, this city. Death was caused
by rupture of the pulmonary artery as a result of blood-poisoning.
Dr. Mattern was in the forty -ninth year of his age, having been born at Here-
ford, Jvehigh County, Pa., August 5, 1847.
He came to this city in 1870, and graduated from the Philadelphia College of
Pharmacy in 1874. Since 1886 he had been engaged in the retail drug business
at 2602 (iermantown Avenue.
After having taken a course at Jefferson Medical College, he received the
degree of Doctor of Medicine in 1882. Dr. Mattern was officially connected
with the Twenty-eighth Sectional School Board for several years, and, in 1895,
was appointed a member of the Board of Education.
In 1892 he received the appointment of Coroner's Physician, which position
he had held since that time.
\_/2^^^^^^-t:^:^t^---^:^-*r c:^^^^^^
THE AMERICAN
JOURNAL OF PHARMACY
MA]\ i8gj.
MEMOIR OF ROBERT SHOEMAKER.
Robert Shoemaker deceased on the 17th day of December. 1896,
at his residence, 1 736 Green Street, in this city, at the age of 80 years.
Notwithstanding^ the bodily infirmities which attend advanced
aj^e, he continued his attention to business until November, when
serious illness obliged him to retire. He was the oldest druggist in
Philadelphia who continued actively in business up to the time of
his decease.
The ancestors of Robert Shoemaker came from Kriegsheim,a vil-
lage on the right bank of the Rhine, about eight miles from the
town of Worms. The family name was Schumacher, anglicized to
Shoemaker after their arrival in America.
In 1677 William Penn visited Kriegsheim, attracted by the rclig-
ous persecution of Dissenters, whose religious views were somewhat
in accord with those of the Friends, or Quakers as they were then
called.
Penn tendered to them an invitation to join his colony in Pennsyl-
vania. In 1683 a part of the family emigrated, and were followed
by others in the next three years. They settled near Philadelphia
in the locality known as Germantown.and their names are associated
with the early history of Germantown and the adjacent districts.
Robert Shoemaker was the son of Richard M. and Sarah Shoe-
maker. His mother's maiden name was Sarali Clever. He was
born in Shoemakertown, Montgomery County, Pa., February 2.
1817 ; his father conducted a country store at that place. His early
education was acquired at Abington school, and at the school of
Solomon Jones, in Cheltenham township.
(225)
Am. .Tour. Pharm,
226 Memoir of Robert Shoemaker. {"""^-^^^l-xm:
In 1 83 1 Robert was apprenticed to William Scattergood, a mem-
ber of the Society of Friends, to learn the drug business. Many of
the prominent apothecaries of this city were, at that period, mem-
bers of this religious society.
The store of Wm. Scattergood was at the corner of Second and
Green Streets, Philadelphia.
Tiie aptitude and ability of the young apprentice was shown by
his purchase of the store in 1*837, when only twenty years of age.
In 1837 Robert commenced the preparation of the plasters of the
U. S. Pharmacopoeia. While engaged in the manufacture of plasters,
his attention was directed by the late Prof. William Procter to the
value of the residuum liquid which had been allowed to run to waste.
By his request and advice he prepared for him some glycerine from
this waste liquor, which was presented by Prof. Procter as the first
glycerine made in this city, if not in America (1846).
Glycerine had not then come into use, medicinally or in the arts,
and there was no demand for it. In 1848 the French medical jour-
nals called attention to its use in pulmonary complaints. This notice
of its use created a demand among the medical profession, and in
1848 Mr. Shoemaker made the first glycerine that was sold in this
market ; the quantity was small and the price was ^^4.00 per pound.
The entire product sold in 1848 was 15 pounds. As the demand in-
creased, importation of glycerine commenced, and the price fell. In
1849 Mr. Shoemaker made about 200 pounds, the price averaging
about $2.70 per pound.^
In 1852 his brother, l^enjamin H. Shoemaker, was taken into
partnership with him, A specialty of the firm was the manufacture
of spread plasters, which acquired a high reputation in the trade ;
they were the first in this city to engage in this specialty. Adhesive
plasters, spread on muslin, had been in use many years, but the
apothecary had been obliged to spread all other plasters on sheep-
skin, as the occasion required.
During his apprenticeship Robert Shoemaker was denied the
advantages of attending the instruction given by the College of
Pharmacy.
The lecture course was in the evenings, generally the most busy
time with the apothecary. He was obliged to make good, as far as
possible, the loss of this opportunity by self-instruction, and in con-
' All interesting paper, by Mr. Shoemaker, on this subject will be found in
the American Journai, of Pharm-acy, June, 1879.
"""•May'iSj*""'} Memoir of Robert Shoemaker. 227
sequence was not a graduate of the Collefre, a circumstance which he
often spoke of with regret.
After entering into business on his own account, he became a
member of the College, and was made a member of its Board of
Trustees March 27, 1843, and first vice-president 1869, continuing
in that office up to the time of his death. In 1S94 the degree of
Master in Pharmacy was conferred upon him by the College.
After conducting business for nearly twenty years at Second and
Green Streets, the firm removed, in 1856, to Fourth and Race
Streets, and greatly enlarged their business.
In 1864 two sons of Robert, Wm. M. and Richard M., were taken
into partnership. In Januar)% 1866, Benjamin H. Shoemaker with-
drew from the firm, and, taking an adjoining store, gave his atten-
tion exclusively to plate and window glass, a branch of the business
whith had grown to such large proportions as to make its separa-
tion from the drug business of the firm desirable. The firm now
consists of Richard M., Thomas E. and Benjamin H. Shoemaker, jr.
His experience in business convinced Robert Shoemaker of the
advantage to be derived from a meeting of those engaged in the
wholesale drug and manufacturing business, and on January 22,
1861, he signed the call for such a meeting, which eventuated in
the founding of the Drug F^xchange of Philadeljjhia.
He was president of this body from 1867 to 1870, and in 1890
was made an honorary member, in recognition of his valuable
services.
He was one of the incorporators of the Consolidation Bank, and
one of its directors from the time of its founding.
For many years he was a member of the Fire Insurance Associa-
tion of Philadelphia, and of the Delaware Mutual Fire Insurance
Company.
After the failure of Jay Cooke, in 1873, he was appointed one of
the trustees for the settlement of their affairs.
He took great interest in public school education, was a director
in the Cheltenham District, Montgomery County, for over fifteen
years, giving active service in every detail pertaining to the welfare
of the scholars and teachers, the school at Shoemakertown being
named after him.
Robert Shoemaker was married to hlizabcth Moore, daughter of
the Rev. William Moore, of Philadelphia, November 25, 1837.
/^ J • /I -J f Am. Jour. Pharm.
228 Gelseniic Acid. \ May, 1897.
She died February 26, 1857, leaving the following children:
William M.. Richard M., Sarah C, Joseph M., Thomas E. and Ben-
jamin H. Shoemaker, Jr.
He was again married to Ann Summers, of Alexandria, Va., to
whom were born the following children : James, Roberta, Mary and
Ellis C. Shoemaker, and who survive him.
Robert Shoemaker was a representative man in the drug trade of
Philadelphia; conservative, yet progressive, he conducted business
for sixty years with skill and good judgment, and with a conscien-
tious regard to its close connection with the public welfare.
The sharp competition in trade in his latter years did not disturb
his broad views of honorable business methods.
The benefit of his long experience and good judgment was often
sought for by younger men, and the kindly manner in which he
received such applicants gained for him their confidence and respect.
As a member of the Episcopal Church, he took an active interest
in the congregation of St. Paul's Church, Chelten Hills, near which
he resided for many years. For a long time he was accounting
warden of the church, and continued as such up to the time of his
death. In the ground adjoining this church his mortal remains
were consigned to rest.
A life extending to four score years may not be marked by great
events; but measured by the quiet and steady pursuit of duties well
performed, and with a just regard of the interests of his fellow-men,
and continuing to the end of his sojourn here, erects a monument
to his memory in the esteem and affection of all who knew him.
C. B.
GELSEMIC ACID.
By Virgil Coblentz.
The following notes are intended to serve as a preliminary notice
concerning investigations on the above subject, which have been
carried on at intervals for some years.
The subject was taken up at the suggestion of Professor Lloyd,
who al.so kindly supplied the author with about 50 grammes of an
unusually fine crystalline sample of undoubted purity.
This principle was first isolated by Professor Maisch in 1869, named
and fully described by Professor Wormley in 1870. Professor Worm-
ley, in his investigation, simply restricted himself to applying various
^'^MayViS;^''"''} Gelscmic Acid. 229
color tests for the purpose of identifying:; the principle from the
standpoint of a toxicologist.
Dr. Chas. Robbins, in his work on " Ueber die wesentlichen
Bestandtheile von Gelsemium sempervirens " (1876), published
analyses and claimed that this so-called gelsemic acid of VVormley
was not a distinctive new principle, but simply a,*sculin. This
assumption was later contradicted by Wormley (Am. Jour. Phak.,
1872).
At present, attention will be directed to Dr. Robbins' analyses of
this substance, but two having been made, the results being as
follows :
(I) C = 5204 percent. H := 5 189 per cent.
(II) C= 51-82 " H = 4-9S
Dr. Robbins carried on his combustions in a s'mple bayonet tube
with copper oxide, as was customary at that time. This being the
case, the author questions the value of the analyses and formula
deducted therefrom, even though the figures correspond within a
reasonably close limit.
Gelsemic acid is one of those few organic substances which, upon
heating with copper oxide or any oxidizing agent, gives up only a
portion of its carbon as carbonic oxide, the rest separating as a
graphitic-like deposit on the sides of the combustion-tube, which
cannot be removed even at the highest possible temperature. Some
twenty combustions of gelsemic acid were made after various
methods; in several instances two of these corresponded closely, but
subsequent results did not justify that any reliance should be placed
upon them. The various methods employed were : first, combus-
tion with copper oxide in a bayonet tube; second, with copper
oxide in an open tube with a current of oxygen; in the third
method of combustion, lead chromate was employed ; the fourth
method attempted consisted in mixing the gelsemic acid with
powdered fused potassium bichromate in a platinum boat, and
then burning in an open tube with copper oxide in a current of
oxygen.
In each of the above cases every possible device was attempted
to avoid the separation of carbon in the tube, but without success.
Finally, the well-known method of wet combustion with a mixture
of chromic anhydride and sulphuric acid was attempted, a number
230
Ge hemic Acid.
( .A.m.Jour. Pharm.
I Ma> , 1897.
of analyses beinsr made with no better success than before. A
description of this latter method with apparatus is given here, since
it has answered admirably in the analyses of various derivatives of
gelsemic acid.
In the combination flask (Fto^, i) from lo to 20 grammes of chro-
mic anhydride are introduced, followed by the gelsemic acid which
has been accurately weighed off in a small thin glass tube, this is
placed in a nearly upright position in the flask, in order to avoid
contact with the CrOg before the proper time. After securing all
the joints of the apparatus, a slow current of pure oxygen gas is
passed through the entire apparatus until practically all of the air
has been removed, after which the current is regulated to about 20
Pe.Oa.
O ^
"■^
w^
Fig. t.
bubbles a minute, which is continued throughout the entire combus-
tion, unless the reaction becomes violent, when the current should
be temporarily closed. By slightly shaking the flash the gelsemic
acid is caused to spill out, and is distributed through the chromic
oxide, then the concentrated sulphuric acid which is contained in
the separation funnel is allowed to trickle over the mixture very
slowly, regulating the flow according to the energy of the reaction.
Finally, when the reaction is over, sufficient acid is added to make
a bulk of about 20 to 30 c.c. The flask and contents are then cau-
tiously heated, increasing gradually till just short of boiling tem-
perature, which is kept up for a period of fifteen to twenty minutes.
The gases given off pass up through a well-cooled condenser into a
tube which is filled with spun glass, well covered with lead peroxide,
^"-May'ia!^^"} Gelsemic Acid. 231
which serves to retain any sulphur dioxide which is carried over
with the mixed oxygen and carbonic oxide. After passing this tube,
and before the latter is absorbed by the potash bulb, the gases are
dried by passing through two calcium chloride tubes. It is scarcely
necessary to note that in carrying out an analysis by this method,
the greatest of care must be exercised in regulating the current to
as slow a degree as possible. The analysis of acetyl and bromo
derivatives of gelsemic acid by this method gave very close concord-
ant results, whereas, as already mentioned, no reliable data could be
obtained from the mother substance, owing to the fact that a small
portion of the carbon escapes combustion.
The complete analyses of the acetyl and brom gelsemic acid are
not given here, as the author desires to complete some molecular
weight determinations before assigning a definite formula. In this
connection attention is called to the differences in the melting-points
of gelsemic acid, and some of its derivations, and the same of
icsculin:
Melting-point of gelsemic acid is between . ... . 206 and 205*5^ C.
" " iL-sculiu is 160° C.
" acetyl gels, acid is iSo° C.
" '* ** iesculin is . . 130- C.
" " bromo gels, acid is 250^ C.
" *' cesculin is . . . . 193-195^ C.
Gelsemic acid readily neutralizes solutions of sodium and potas-
sium hydrate, but fails to yield any definite crystalline salts. Vari-
ous attempts were made to prepare salts with barium and magne-
sium with no success.
Attention is here directed to a peculiarity of the potassium gel-
semium mixture, which, upon heating or igniting, becomes very
voluminous, exhibiting the same phenomena as the *• Pliaroah's
Serpent," which results on heating the sulphocyanate of mer-
cury.
From the various data obtained in the course of my investiga-
tions, I hope, at a near future date, to be able to shed some light
upon the constitution of this interesting substance, as well as to
prove my surmise that gelsemic acid is a principle distinct from
arsculin.
New York, April 20, 1.S97.
232 Ointment of Mercuric Nitrate. { '"'•.Aia^y'is^T."'"-
CONSIDERATION OF SOME RECENT SUGGESTIONS
CONCERNING OINTMENT OF MERCURIC
NITRATE.
Bv Charlies H. La Wali..
The Pharmaceutical Journal, of February 27, 1897, page 172,
contained an article by P. W. Squire, upon the processes now offi-
cial for the preparation of ointment of mercuric nitrate, commonly
called citrine ointment.
Mr. Squire's experiments were mainly devoted to the considera-
tion of the differences now existing between the quantities and
manipulations directed by the U.S.P. and B.P.
While he slightly favored the use of a combination of lard and
olive oil (as is authorized in the B.P.) instead of lard oil (directed by
the U.S.P.), Mr. Squire acknowledged the superiority of our process
in previously acting on the fatty base with a portion of the nitric
acid, instead of adding the mercury dissolved in the whole quantity
of nitric acid, as the B.P. directs. His observations on the varia
tions produced by the influence of different temperatures show the
necessity of guarding against over-heating the compound after the
addition of the mercuric nitrate solution.
In commenting upon Mr. Squire's paper in the last number of
The American Journal of Pharmacy (Vol 69, p. 209), Mr. J. W.
England suggests some improvements on the present officinal pro-
cess, which are offered for trial and discussion.
Mr. England's improvements consist in (i) using a proportionate
amount of red oxide of mercury in place of the metal ; (2) chang-
ing the temperature to which the mixture should be permitted to
cool before adding the mercuric nitrate solution ; (3) incorporating
about 5 percent, of glycerin with the finished product when nearly
cold.
The reasons given for the substitution of red mercuric oxide for
metallic mercury are: (i) because small quantities of the oxide
are more easily weighed; and (2) because the oxide is probably
purer than the commercial mercury.
There are altogether six official preparations in which metallic
mercury is directed by the U.S.R, so that a certain amount of
dexterity ought to be acquired in the weighing of this elusive sub-
stance by a pharmacist who does his own manufacturing. As to
Am.jo^ur.pharm.j Oiutmoit of Mcrciiric Nitnitc. 233
the relative purity of the two substances, the experience of a lar^e
manufacturing establishment shows that the commercial metallic
mercury is of far f^reater uniformity and purity than the " red
oxide " of commerce. Many samples of the red mercuric oxide
have been encountered, which yielded a brownish colored nitric
acid solution and left an insoluble residue resemblin^^ brick-dust ; so
that it would be better to use the metallic mercury in the prepara-
tion of the official solution of mercuric nitrate, in order to ensure a
satisfactory product. The purity of commercial mercury was, in all
cases noticed, very good; 'in purifying 156 pounds only y^
pound of impurity was obtained, or less than i/< per cent. The
use of the red oxide of mercury was suggested first in i862\ and
more recently in 1886, by R. Rother, who " finds advantages in the
use of mercuric oxide " without explaining what these advantages
are.
The suggestion as regards temperature is one of great importance,
as experience has shown in the manufacture of a total of hundreds
of pounds by the process outlined in the American Journal of
Pharm.xcv, 1894, p. 523, that careful observance and control of
temperature is essential for the production of a satisfactory product.
The directions might be supplemented by advising the maintenance
of the temperature at 60° C. until all reaction ceases, in order to
obviate the development of the spongy condition so often noticed
in this product.
The addition of glycerin may be advantageous in some respects,
but in the formula as proposed by Mr. Kngland, the addition of 50
grammes of glycerin to 1,000 grammes of ointment of officinal
strength, reduces the percentage of mercuric nitrate below that
required by the U.S. P.; this, however, could be easily remedied by
diminishing the quantity of lard oil by 50 grammes.
It is well for those who have difficulty with officinal ])rocesses to
suggest improvements for the same ; but in the case of citrine oint-
ment, it is extremely likely that those who fail to produce a satis-
factory preparation by the U.S.P. process would not succeed with
any method.
A final consideration, not to be altogether ignored, is the raising
of the cost of manufacture of the preparation, which would happen
* Am. Jour. Piiar.. 34, p. 344.
/- 7 • ^ / Am. Jour. Pbarm.
2:^1 (jClSejmUin. \ May.lSg?.
were the oxide of mercury used in place of the metal. Calculations
show that the finished product would cost about one and one-sixth
times as much as it does by the present process.
305 Cherrv Street, Philadelphia, Pa.
GELSEMIUM.
analysis of root, rhizome and stem.
By L. E. Sayre.
In the January issue of this journal, af^ention was called to the fact
that in the commercial drug gelsemium, which should consist of
rhizome and root, were frequently found portions of the stem in
varying proportions. It was stated on the authority of Gerald
McCarthy, botanist of the North Carolina Agricultural Experi-
ment Station, that the stem was apparently collected and used ta
adulterate the drug.
It was further stated that the stem probably had no medicinal value^
but of this no definite statement could be made until an analysis,
then in progress, was completed. Mr. W. V. Ingham, a pharmacy
student of the University of Kansas, has made this analysis, and
also made a comparison of the active constituents in the three
parts of the plant mentioned.
Since the time above referred to, gelsemium root has been ob-
tained from different quarters, with a view of ascertaining the quality
of the market's supply. As a result, it is safe to state that there is
no difficulty in obtaining a drug free from stem from houses hav-
ing an established reputation as dealers in crude drugs. The article
supplied from several quarters was remarkably free from fragments
of stem.
For analytical purposes a supply of the stem was obtained, not
only from the commercial drug, but from a living plant of six years'
growth, cultivated in a nursery.
Mr. Ingham, in order to perfect himself in the work, made a
number of trial analyses of reliable powders of gelsemium, and thor-
oughly studied the process of isolation and quantitative determina-
tion of the active constituents.
The report of his analysis is briefly stated as follows :
Am. Jour. Pharm.
Ma.v, 1897.
} The Structure of Lcptandra.
23s
Constituents.
Ingrredient Ing^redient Ingredient
Percentage in Percentage in Percentage in
Rhizome. Root. Stem.
Moisture
Volatile oil
Fixed oil
Resins
Gums
Gelsemine alkaloid . . .
Gelsemic acid
Starch
Ash
Other organic acids ...
Inert material, cellulose, etc.
Total
3'i
5'
3-S
0-5
04
Trace.
5-6
74
3'2
4'4
24
3-8
0-8
07
\\
0-2
017
—
0-37 j
i 03
—
6-8 '
7-6
6-3
26
2'2
2-7
27
2-8
19
27-17
26-97
22-S
7283
100'
7303
77-2
i *''®* i
lOQ-
Dragendorffs method was followed except in the case of the ^else-
mine and gelsemic acid, where a modified method was used. (See
p. 332, Blyth, " Poisons; Effects and Detection," 1884.)
The gelsemic acid was obtained in transparent needle-shaped crys-
tals. The alkaloid was obtained only in the amorphous state, and
in that state estimated.
It would seem from the above analysis that the principles upon
which the drug depends for its activit)' are absent or present only in
small quantities in the stem, so that the admixture of any apprecia-
ble amount of stem must correspondingly reduce the value of the
drug as a medicine.
THE STRUCTURE OF LEPTANDRA.
By a. I». Hrhithaipt, Ph.G.
Contribution from the Botanical Laboratory of the Philadelphia College of
Pharmacy.
The official Leptandra consists of the rhizome and roots of
Veronica virginica, Linne, belonging to the natural order Scrophu-
lariacese, growing throughout the United States east of the Missis-
sippi, being found in mountainous meadows in the South and rich
woods in the North.
Fig. /. Rhizome aud roots of Veronica virginica, L., natural size.
The plant is an herbaceous perennial, having a simple, erect
stem, from 2 to 6 feet high, bearing leaves in whorls, and termin-
ated by a long-panicled spike of whitish flowers.
Fig. 2. Cross-section of the root, magniaed lo diameters ; a, cortex ; b,
central cylinder.
^^S- 3' Cross-section \a\ of rhizome, magnified lo diameters; a, outer
layer of bark ; b, middle layer of bark ; c, interrupted circle of sclerenchyma
fibres ; d, inner layer of bark ; e, wood ; /, pith.
Fi^, f. Cross-section (/>. ol rhi/ou.c. inaKuitit'l ii> «lianielcrs; a, outer
layer of bark ; b, middle layer of bark ; <. internit.tfd rinlr <.f scU-riiu'hvnia
fibres ; d, inner layer of bark ; e, wood ; J\ pith
Fig. 5. Cross-section of rhizome, magnified 500 diameters ; a, epidermis ;
b, cork or periderm ; c, hypoderma of collenchyma ; d, cortical parenchyma ;
e, endoderniis ; /, sclerenchymatous pericycle ; g, phloem or bast ; //, xylem
or wood ; i, parenchyma of pith.
^^
Fig. 6. Cross-section of the root, magnified 500 diameters ; <;, epiblema or
ej)i«lermis of the root ; b, exo<lermis or hypo<lernia of the root ; <*, cortical
parenchyma ; </, endo<lermis ; f, parenchymatous ]HTicvcle ; /'. phUcni of the
vasal bundles ; g^ xylem of the vasal bundles.
240 Liquor Poiassce and Liquor SodcB. {^^Mayjg^?.^'"'
The leaves, from four to seven in each whorl, are short-peti-
oled, lanceolate and minutely serrate.
The flowers are small and white, having a four-parted calyx and
a tubular corolla, with two exserted stamens.
The fruit is an ovate, two-celled and many-seeded capsule.
The plant flowers in July and August.
The rhizome, from 4 to 6 inches in length and i<( inch in thick-
ness, is horizontal, somewhat bent and branched with short stem
remnants or cup-shaped scars on the upper side, and beset with
numerous long, straight and brittle rootlets. The rhizome is hard
and breaks with a woody fracture, is almost inodorous, and has a
bitter and feebly acrid taste. Internally it shows a blackish bark,
and a hard, yellowish circle of wood enclosing a three- to six-rayed
purplish pith.
The roots, which may be several inches in length, are about
y2 inch in diameter, somewhat longitudinally wrinkled, pur-
plish-brown, and break with a short fracture.
A transverse section of the rhizome shows a relatively thick bark,
consisting of ordinary parenchyma, covered by a hypoderma of col-
lenchyma and a thin cork, the whole being enclosed by a persistent
epidermis. The inner layer of the bark shows a distinct endoder-
mis, beneath which is found an interrupted circle of lignified fibres,
constituting a sclerenchymatous pericycle. The wood is disposed
in a single circle, and consists of ducts and lignified fibres arranged
in more or less distinct radial rows. The pith is large, from three-
to six-rayed, consisting of ordinary parenchyma.
A cross-section of the root shows a very thick cortex, sharply
marked off from the woody cylinder by a distinct endodermis. The
cortical tissues consist of ordinary parenchyma covered by a strongly
cutinized epidermis, beneath which is seen a single layer of exoder-
mal cells. Immediately beneath the endodermis is found a single-
layered parenchymatous pericvcle which encloses the wood bundles.
LIQUOR POTASS^ AND LIQUOR SOD^.
Bv John P. Batks, Ph.G.
Coutribution from the Chemical Laboratory of the Philadelphia College of
Pharmacy. No. 164.
According to the United States Pharmacopoeia, liquor potassse is
"an aqueous solution of potassium hydrate [KOH=55-99], contain-
Am.Joar. Pbarm
May'iS:""'} Liquor Fotasscd and Liquor SodcB. 241
ing about 5 per cent, of the hydrate." The same authority de-
scribes it as "a clear, colorless liquid, odorless; having a very acrid
and caustic taste, and a strongly alkaline reaction."
** To neutralize 28 grammes of solution of potassa should
require about 25 c.c. of normal sulphuric acid (each c.c. of the
volumetric solution indicating 02 per cent, of absolute potassium
hydrate), phenolphthalein being used as indicator."
The Pharmacopoeia also says : •• Solution of potassa should be kept
in bottles made of green glass, and provided with glass stoppers,
coated with paraffin or petrolatum." Desiring to ascertain the
strength and purity of the preparation, as dispensed by wholesale
and retail drug firms, six samples were procured and examined, two
being purchased from the former and four from the latter ; all of
the houses were in Philadelphia.
Samples 2, 3 and 5 were colorless, while I, 4 and 6 had straw-
colors. Sample 4 was translucent ; all the other samples were clear.
All contained insoluble foreign matter except sample 2.
All of the samples were odorless and decidedly alkaline to litmus
paper. All gave a violet color to the non-luminous flame. Two
pharmacists took the precaution to dispense the solution in colored
glass bottles, and labelled poison.
The writer also examined the samples for potassium, by acidifying
the solution with acetic acid and adding sodium cobaltic nitrite.
All of the solutions showed this base. Number 3 showed a small
amount of calcium, when some of it was acidulated with acetic acid
and mixed with ammonium oxalate; the other samples were free
from it. Carbonate was found in samples i, 2, 3 and 5.
By titrating with decinormal sulphuric acid volumetric solution,
the samples were found to contain, respectively, 318, 8-74, 4- 10,
374, 018 and 4-38 per cent, of absolute potassium hydrate.
Attention is directed to sample No. 5, which showed about
•018 j)er cent, of potassium hydrate as calculated from the acid used.
But in view of the fact that the sample showed much carbonate, it is
likely that the solution owed its alkalinity almost entirely, if not
altogether, to potassium carbonate.
Liquor sodit, or solution of soda, should be, in order to comply
with the requirements of the United States Pharmacopcria *• an
aqueous solution of sodium hydrate (NaOH =^ 3996), containing
about 5 per cent, of the hydrate." The Pharmacopoeia also dcsig-
Am. Jour. Pharm.
1897.
242 Valuation of Liquor lodi Compositus. {^"^Mly!
nates it as " a clear, colorless liquid, odorless, having a very acrid
and caustic taste, and a strongly alkaline reaction." " To neutral-
ize 20 grammes of solution of soda should require about 25 c.c. of
normal sulphuric acid (each c.c. of the volumetric solution indicating
0-2 per cent, of absolute sodium hydrate), phenolphthalein being
used as indicator."
The Pharmacopoeia recommends the solution to be dispensed in
the manner ordered for liquor potassae. In order to determine the
exact quality of the article as sold by manufacturing pharmacists,
six samples were purchased and examined. Four of these were ob-
tained at retail stores and two at wholesale houses. When the
samples were subjected to the flame test for sodium, samples I,
3 and 6 gave evidence of potassium. These behaviors were after-
wards confirmed by means of the sodium cobaltic nitrite test.
Sample 3 was translucent, the other samples were clear. Samples
I, 3 and 4 had straw or yellow colors; the others were colorless.
Sample 3 was the only one containing insoluble foreign matter.
All were odorless and strongly alkaline to litmus paper. No. 3
contained calcium. Carbonate was present in samples I, 2, 3 and
5. Three pharmacists dispensed the samples in colored vials. Two
of these vials bore poison labels.
Upon titrating the samples with decinormal sulphuric acid volu
metric solution, they were found to range from one-half to twice the
official strength, as follows:
1000, 4*47, 2-31, 5-25, 4-21 and 4-93 percent.
VALUATION OF LIQUOR lODI COMPOSITUS.
By Richard Hai. Compton, Ph.G.
Contribution from the Chemical Laboratory of the Philadelphia College of
Pharmacy. No. 165.
Lugol's solution is required by the United States Pharmacopoeia
to be a 5 per cent, solution of iodine, dissolved in water by the
addition of 10 per cent, of potassium iodide. The same authority
directs that if " 1266 grammes of the solution be mixed with a few
drops of starch test solution, it should require for complete decol-
oration from 49 3 c.c. to 50 c.c. of sodium hyposulphite decinormal
volumetric solution (each cubic centimeter of the volumetric solu-
tion corresponding to o-i per cent, of iodine)."
^"^'yilV.'i^'^} Valuation of Liquor lodi Compositus. 243
Being desirous of knowing to what degree the retail dispensers
were governed by the Pharmacopojial requirements for liquor iodi
compositus, I obtained a few samples at different ])harmacies and
estimated the per cent, of iodine by the official method. The
results of my titrations indicated the following percentages for the
samples: 496, 482, 4-72 and 4-17.
As there is no test given under Lugol's solution for estimating the
potassium iodide present, I have made some experiments for the j)ur-
pose of devising one. The following was found to be the best of sev-
eral methods tried, and can be recommended on the concordant
results which it furnished :
Take a definite amount (12-66 grammes) of the solution and
titrate it according to the official method of estimating the iodine.
The amount of the latter is thus obtained. Now titrate the residual
liquid with decinormal silver nitrate volumetric solution, using potas-
sium chromate as an indicator if desired, until all of the iodides
which the solution contains have reacted with the silver nitrate and
formed insoluble silver iodide.
The iodides of the solution consist of the potassium iodide
originally present and the sodium iodide produced in the reaction
between the sodium thiosulphate and the free iodine of the sample.
The volume of the solution of sodium hyposulphite is the measure
of the free iodine of the sample, and therefore the equivalent of the
volume of silver nitrate required to react with the sodium iodide
which it forms. Hence, if the volume of sodium hyposulphite
required to decolorize the iodine of the sample be deducted from
the volume of silver nitrate required to completely precipitate the
decolorized liquid, the remainder will be the volume of decinormal
silver nitrate volumetric solution required for the potassium iodide
that was present. Multiply the number of cubic centimeters so
found by 00 1 65 56, the value of I c.c. of the silver nitrate solution in
potassium iodide, to find the amount of potassium iodide. Then
by proportion calculate the percentage amount of it.
It was also found that practical results could be gotten by boiling
the Lugol's solution after dilution with water until all the free
iodine was expelled, and then titrating with standard silver nitrate
solution, which indicated at once the amount of potassium iodide
present.
244 Starch and Strontium in Opium, {'''^£jri£?f'""*
THE PRESENCE OF STARCH AND STRONTIUM SUL-
PHATE IN OPIUM AND THEIR INFLU-
ENCE ON ASSAYING.
By Lyman F. Kebi^ER and Chari.ES H. LaWai,!..
Although poppy juice does not contain any starchy matter, yet
the presence of this article in opium has been reported in a number
of instances. According to the Pharmacographia, p. 47, Egyptian
opium sometimes contains an abundance of starch. Mr. Mjoen,^
who has probably made the most exhaustive microscopic study of
opium on record, reports that Persian opium is abundantly contam-
inated with wheat and leguminous starch. More recently Mr. Jel-
liffe,- in a report at the regular meeting of the New York College of
Pharmacy, stated that from 5 to 10 per cent, of starch was found in
the samples examined.
We ourselves have found wheat starch in opium assayed dur-
ing the past two years. Mr. Moerk kindly sent us six samples
of opium from three to five or six years old and every one con-
tained wheat starch. The amount varied from a trace to 8
per cent., but it was always present. Why the starch is there
and how it came to be there we can only surmise. In some
cases it may have been added for gain, but from the small
quantity present in some samples its presence may be accidental.
Persian opium is exported to Constantinople, by way of Trebizond,
and is there worked up into forms to imitate the Asia Minor opium.
Here is probably the source of contamination with starch, since Per-
sian opium contains much of this.
Before leaving the question of starch, a few words about its esti-
mation in this connection may not be out of place. There are two
ways of arriving at approximate results — microscopically and chem-
ically. The one is probably as accurate as the other.
Microscopically, dry the opium, note moisture and reduce to a
fine powder. Weigh out i gramme of the powder, introduce it
into a mortar containing 2 c.c. of alcohol; with a pestle rub up the
opium well, add 8 c.c. of simple syrup and mix intimately. Of this
mixture prepare a slide and by means of an ocular micrometer,
divided into square millimeters, count the number of granules in a
' 1895, Arch. d. Pharm., 233» 533.
' 1897, Am. Drug., 30, 41.
Am. Jour. Pharm.
Ma""!^*"'"} Starch and Strontium in Opium. 245
square of 100 square millimeters. Should any worker be without
a micrometer, the total number of granules in a field may be
counted. Repeat the counting with successive drops three or
four times, and take the average of the several countings. Having
approximated the number of starch granules in the above mix-
ture, prepare a syrupy mixture of the same starch as that con-
tained in the opium, say a I per cent, mixture, and deter-
mine the number of starch granules as above. If the number of
starch granules is greater or less than those contained in the opium
mixture, dilute the mixture or make a more concentrated one, as
the case in hand requires. If the number of granules is the same
in both mixtures, the per cent, of adulterant is readily calculated.
When more than one kind of starch is present, the per cent, of
adulterant is more difficult to determine.
Fig. I. Epidermis of capsule, magnified 500 diameters.
Chemically, the starch can be estimated as follows: PLxhaust 10
grammes of the opium with cold water, place the residue into a flask,
add 200 c.c. of alcohol containing 5 per cent, of potassium hydrox-
ide, and boil vigorously on the water bath for about fifteen minutes.
Filter while hot and wash the residue with hot alcohol, until the
filtrate is nearly colorless. Dissii)ate the alcohol from the residue
and introduce the latter into a suitable flask, add 200 c c. of water,
16 c c. of hydrochloric acid (specific gravity ri6), attach to a reflux
condenser and boil gently for three hours. Cool the contents of
the flask, neutralize with sodium carbonate, filter and make up to a
definite volume. In this estimate the reducing sugar by Fehling's
solution, either volumetrically or gravimctrically. The weight of
reducing sugar multiplied by 09 equals the amount of starch con-
tained in 10 grammes of opium.
246
Starch and Strontium in Opium.
/Am. Jour. Pharm
1 May, 1897.
By this process there is estimated as starch, the pentosans and
other carbohydrate bodies, which will undergo hydrolysis when
boiled with hydrochloric acid. We have reasons for thinking that
starch estimations made in plant analysis by means of hydrochloric
acid are frequently wide from the truth.
Fig. 2. Epidermal tissue of leaf, magnified 500 diameters.
Let us now turn our attention to the general microscopical appear-
ance of the opium. On clarifying some opium with chloral hydrate
the structure of the pericarp of the poppy was clearly brought
out, as shown in Fig. i. In the same clarified material were
found scalariform and spiral vessels. An abundance of calcium
O&o- o
G
® c&
&
Fig' 3' Wheat starch granules, magnified 500 diameters.
oxalate crystals and some wheat brand were found in several cases.
Leafy epidermal tissue was also abundant on every slide. Fig. 2.
The starch was brought out by the usual iodine reaction. Fig. j.
All these substances that do not increase the yield of morphine,
by our present methods of assay, must, in our opinion, be considered
^'"'iay'".'!^""'} StarciL and Strontium in Opium. 247
of minor importance, so long as it is only required of opium to con-
tain a certain amount of morphine. Substances that do increase
the yield of morphine are the ones that annoy the analyst.
About a year ago^ one of us (K.) called attention to the fact that
the amount of impurity associated with the crystallized morphine,
as obtained by the U.S. P. process, was abnormally great. The
situation has not changed for the better, at this writing. During the
past few months some of the opium assayed, yielded unusually high
results. The perplexing part in some cases was the fact that one
duplicate contained a much larger amount of impurity associated
with the morphine than that of the other duplicate. The amount
of impurity was estimated by the ash method. This, of course,
indicated that some inorganic substance or substances were influenc-
Fig . 4. Crystals from alcohol-ether precipitate, magnified 500 diameters.
ing the results. The ash was repeatedly examined, and in every
case strontium was indicated.
It has frequently been observed, and commented on,- that when
the 10 grammes of alcohol are added to the 20 grammes of opium
extractive, a turbidity frequently results. We now extracted 40
grammes of opium, preparatory to making a 40 gramme, instead of
the usual lO-gramme, assay. The customary proportions of alcohol
and ether were added and the assay allowed to stand over night. In
the morning, it was found that 16 per cent, of material had precipi-
tated out. On igniting this precipitate, 193 per cent, was volatil-
ized. The residue consisted of strontium, Fig, ^, calcium and
* 1896, Am. J. PiiARM., 68, 257.
' 1895,/. Soc. Chcm. Itid., 14. 464.
Am. Jour. Pharm.
248 Starch and Strontium in Opium. {^"MajsiS?
pota.ssium sulphates. Since no effervescing was produced when the
ash was treated with acid, there was probably no calcium meconate
present in the original precipitate.
Several experiments were now undertaken to ascertain the cause
of the variation of the amount of impurity contained in the crystal-
lized morphine. One case was sampled tv/ice, by two persons, each
using different lumps. These samples were assayed in the usual
manner with the following results ; average of duplicates :
Morphine. Morphine, Crude Morphine Pure Morphine
Crude. Pure. Moisture. in Dry Opium, in Dry Opium.
Sample I . . .11-48 io-68 22-68 14-86 13-81
Sample 2 . . . 10-83 10-43 i9"52 13*48 12-97
The variation in the crude morphine is chiefly due to the impurity
present, as is clearly shown from the fairly uniform results obtained
for the pure morphine.
These same samples were now assayed by both of us, varying the
conditions of precipitation, such as temperature, time of shaking,
etc., with results as follows :
Sample i . . -^ L.
iK.
.K.
Sample 2 . . ^^ K.
U.
The above results are average of duplicates. They show that
ordinary variations in assaying influence the results very little,
when referred to pure morphine. The greatest variations appear
to be due to the sampling, and to the impurity associated with the
morphine as obtained by the U.S. P., method of assay. The
impurity contained in the crude morphine was estimated by the ash
method. This method probably gives higher results than any other,
and is perhaps the best, considering the present impurities in
opium.
In order to ascertain whether or no we had unconsciously lapsed
into a trend, Dr. Squibb's chemist, Mr. Smith, kindly checked our
work, and with his permission we append his results below in con-
nection with our own. Mr. Smith employed Dr. Squibb's process
as Joutlined in the Ephemeris, 3, p. 1 152, and the U.S.P. method
with the lime water correction. We used the U.S.P. process and
Crude
orphine.
Pure
Morphine.
Moisture.
Crude Morphine
in Dry Opium.
11-48
IO-68
22-68
14-86
11-56
I0-8I
22-68
14-96
10-94
1058
22-68
14-16
10-96
10-58
19-52
13*63
10-90
10-35
19-52
13*54
10-84
10-43
19-52
13*48
Am. Jour. Pharm.
May, 1897.
} Starch and Strontium in Opium.
249
applied a correction by means of the ash method. The results are
given below :
Crude
Morphine
Smith [ ^7-27
\ 1678
LaWall
f 17-11
I 17-04
Pure
Morphine.
Sqiiibb's process .... 1613
U.S.P. process i6i9
16-09
1603
Ten cases of opium from one consignment were assayed under
most favorable conditions, in reference to temperature, amount of
washinfTs and time of shakin^r out the morphine. The first five cases
were assayed one day, and the remaining five, two days later. The
results were as follows : —
No. Crude Pure
Morphine. Morphine.
Moisture.
Crude Morphine
in Dry Opium.
I
12-34"
2052
1553
2
1238
20-35
15-55
3
12-39
11-36
20-81
15.65
4
12-33
20*04
15-35
5
6
1234.
12-65'
19-58
20-32
15-34
15-88
7
8
12-78
12-74
1 1 64
19-55
I951
15-89
1583
9
1279
1248,
19-17
15-82
TO
2079
T5-75
A glance at the above figures shows a uniformity in the quality of
opium hitherto unnoticed in assaying large consignments. The
additional circumstances of the presence of wheat starch in the
opium, and strontium in the ash, would indicate a previous manipu-
lation of a large quantity of opium, before packing it into cases for
shipment.
The perplexing part of this view lies in the fact that the yield of
morphine is still .several per cent, higher than the hmit rec|uired by
the custom house ; since it would be just as easy to reduce the mor-
phine to 10 per cent., thus making an additional profit and still be
above the legal standard.
The question naturally arises, can starch or epidermal tissue, or
rumex seed, or strontium sulphate, or the calcareous salts found in
Turkey opium be classed as adulterants of opium in the true sense
of the word ? We all know that the opium as it comes into the
market is the concrete juice of the poppy, mixed with various and
sundry substances, and to say that this or that is an adulterant of
250 Pharmacopmal Preparations, {^""May^iso?*'""*
opium, would require an explicit and comprehensive description of
what is, and what is not, an adulterant. For an analyst to condemn
a case of opium, on the ground that it contained starch, when the
only requirement is a certain amount of morphine, would lay himself
open to criticism. We, however, do think that a substance like
strontium sulphate, which increases the apparent yield of morphine,
oueht to be looked on as an adulterant of a fraudulent nature.
305 Cherry Street, Philadelphia.
ON THE PRESERVATIVES OF PHARMACOPGEIAL
PREPARATIONS.!
By WiIvIvIAM Martindai^e.
In the work of compiling formulae for the use of medical prac-
titioners and pharmacists, care is necessary to test the keeping prop-
erties of the various solutions and preparations, and having prepared
and kept a number of these preparations, I thought a few notes on
them might prove interesting. They are purely pharmaceutical,
and must not be considered as having bacteriological importance.
The vehicle mostly used for the internal administration of medi-
cines, of course, is water in some form or other, but distilled water
alone is recognized by the Pharmacopoeia, and probably this, as
frequently met with, is more defective from a standard of purity
than most preparations in the Pharmacopoeia. It is even more
prone to develop minute organisms than many of the spring waters
that are to be met with, although these may contain inorganic salts,
which render them unsuitable as solvents and vehicles in which to
administer medicinal preparations. So much has distilled water ob-
tained this evil reputation that a bacteriologist of eminence is
reported to have said that one of the best incubating fluids was a
certain manufacturer's distilled water.
Various means have, therefore, been adopted for sterilizing it and
rendering it aseptic for pharmaceutical use, such as keeping it in a
cool place, and, of course, free from dust, and having it recently well
boiled and cooled. The best and only method to be depended upon,
however, care having been taken to select a good water for distilla-
tion, as well as to refuse the first and last products, and to ensure
^ Pharmaceutical Journal, March, 13, 1897.
Am. Jour. Pbarm.
Ma^ri^T.*''™'} Pharmacopaial Preparations. 25 1
freedom from contamination afterwards, is to have it freshly dis-
tilled ; in fact as regards the whole of the preparations of the Phar-
macopoeia, they should be as freshly prepared as possible, and the
use of preservatives should be avoided unless absolutely necessary,
but from a practical point of view we cannot do without them. For
example, the public demand for pills is now that they must be well
preserved and look nice, although they may be insoluble.
Alcohol — The most common preservative used officially is alcohol
in one form or another ; it is true that it is not used solely as a pre-
servative, but as a solvent ; it enters more or less into the composi-
tion of nearly all our tinctures, liquid extracts, wines, and many of
our official solutions. The germination of most of the micro-organ-
isms occurring in aqueous solutions of vegetable and animal sub-
stances is inhibited by the presence of 20 per cent, by volume of
absolute alcohol, but it is inhibitory only, and in this proportion or up-
wards ; it is in no way germicidal, as on evaporation the anaesthetized
germs, if I may so term them, readily take up life and propagate.
This applies to most of the volatile antiseptics, in fact, for organic
tissues, such as strong mineral acids, alkalies and halogens. K.xcep-
tions to this are carbolic acid, creosote, and weak solutions of corro-
sive sublimate, which act probably by coagulating the albuminous
substance of the microbe. Wines I have mentioned ; unless forti-
fied, from their very origin, that of fermentation, they are too weak
to prove of useful service in pharmacy, and in lact medical wines are
anachronisms.
Glycerin. — The abuse of alcohol has led those who take extreme
views on this subject to endeavor to use other solvents and pre-
servatives for pharmaceutical preparations. Among these, avoiding
ethylic alcohol, whose physiological properties are too well known,
they have selected glycerin, which is but another alcohol whose
action physiologically is not so well ascertained, nor is it so inhibi-
tory to the development of micro-organisms. Its strong solvent
action on vegetable extractives, its non-volatility, and its stability in
other respects would have rendered glycerin a useful pharmacopcL-ial
solvent, but although it has been tried again and again and was
made official, more especially in i)reparing some of the liquid
extracts of the United States I'harmacopcL-ia, it has not met with
general acceptance. It nevertheless has a curious preservative
action over some inorganic compounds in preventing oxidation.
252 Pharmacopoeial Preparations, {'^'^•I^Sa^^"'^'
For example, black mercurial lotion can be preserved in its normal
black color by the addition of 5 per cent, by volume of glycerin, but
I find that 10 per cent, of mucilage of tragacanth will produce the
same result, and have the advantage, from its viscosity, of holding
mercurous oxide well suspended ; the addition of both these to the
preparation would be an advantage. It has further been suggested
that glycerin should be used to preserve sublimate solution, espec-
ially the official liquor hydrargyri perchloridi, as it has been thought
necessary that this solution requires preserving, from the chemical,
not, of course, from the biological point of view. But both glycerin
and alcohol added to this solution, especially if exposed to light,
cause a reduction of the salt and deposition of mercurous chloride,
as in the official solution of the Codex, which contains 10 per cent,
of alcohol. Notwithstanding statements to the contrary, I find that
a simple solution of mercuric chloride in distilled water, or even in
spring waters containing supercarbonate of lime in solution, is more
stable than it is with a preservative added, especially one of such a
nature as chloride of ammonium in the official solution. This, as
I showed so long ago as 1870,^ instead of being a preservative, forms
a double salt in solution (sal alembroth plus an excess of chloride of
ammonium), and the solution, if prepared with common water in
place of distilled water, or even if prepared with distilled water and
diluted, throws down a quantity of one of the white precipitates of
mercury. To such an extent is this the case that I found in pre-
paring a pint of the official solution with new river water in place
of distilled water, that 27 grains of this precipitete was deposited,
thus about one-fourth of the mercurial salt was rendered insoluble
in preparing the solution, and more deposited on further dilution
with the water. In fact, a time arrived when there was scarcely a
trace of mercury salt in solution, and as this preparation is most
largely used in hospitals where common water is always used to
dilute the medicines, it leads to very discrepant results therapeu-
tically. It has also been suggested that chloride of sodium should
replace chloride of ammonium in the official solution, as this salt is
largely used in making the sublimate tablets for the convenience of
surgeon's use, but I have found that although sodium chloride helps
these tablets to disintegrate readily it has no advantage, in fact it is
detrimental to the keeping properties of the solution. I have here
^ Pharuiaceutical Journal, [2] Vol. XI. p. 544.
Am. Jour. Phariu.
May'iw?^'"'"} Pharmacopixial Preparations. 253
two specimens prepared in November, 1895, with water from the
Brighton constant supply, which is a very calcareous water ; one is
a simple solution of the perchloride, and the other has an equal
weight of pure chloride of sodium added. The latter you will
observe has deposited much more than the former, in which there
is hardly a trace of deposit. This strongly illustrates ihe undesira-
bility of tampering with solutions in order to make them, as we
consider, more stable ; in fact, with few exceptions no preservative
should be added to a pharmacopoeia preparation unless the label
indicates boldly that it is there. While on the subject of mercuric
salts, I should like to illustrate the importance of having our lime
water of full strength, and well preserved.
In making the yellow mercurial lotion of the B.P., which has 18
grains of sublimate to 10 ounces of lime water ; if the lime water be
only three-fourths, or from keeping, so low as one-half the pharma-
copotial strength, a brick-red preparation, an oxychloride is pro-
duced, rather than the yellow mercuric oxide.
Acetic Acid. — Of other preservatives, which are also solvents used
officially, acetic acid of varying strengths is employed, as in acetum
cantharidis and acetum scillar. This, as I notice Prof. Remington
recently points out,' was much employed in the pharmacy of the
ancients, sometimes combined with honey to form oxymels, of which
we have inherited both the vinegar and the oxymel of squill. Acetic
acid has the disadvantage, however, unless in a very concentrated
form, of growing micro-organisms abundantly, and the fungi and
animalcula; developed in brown vinegar must be well known to all
of you. Acetic acid, therefore, besides being incompatible with
alkalies, is not a good preservative, although in some cases it may
be a useful solvent.
Sugar. — Of the preservatives used officially which are not sol-
vents, this is employed most extensively, not only with us, but in
France and in the United States ; in fact, so much is this the case in
I'Vance, that Mr. Ince once remarked in this room that French
pharmacy might be summed up in one word, "sugar." On account
of its palatability it of course meets with favor, especially among
children. It enters into the composition of all the syrups and
lozenges, and most of the confections and powders, and is a useful
preservative from oxidation of the ferrous preparations, such as the
^American Journal of Pharmacy, March, 1897, p. 121.
Am. Jour, Pharm.
254 Pharniacopmal Preparations. {^'^•i^^y:mi\
saccharated carbonate of iron, mixture of iron, Blaud's pill, and
iodide of iron pill. It also preserves lime in solution, as in the
well-known liquor calcis saccharatus, of a strength about sixteen
times that of the official lime water ; if a pure marble lime be used,
I find as much as 177 per cent, is dissolved, or 816 grains in a fluid
ounce. This preparation is more conveniently made by using an
equivalent weight of syrup, i.e., three ounces in place of two of
sugar, and adding it to nineteen ounces of distilled water containing
the lime in suspension. The «' caking " which is apt to occur is thus
avoided.
Salicylic Acid. — The well-known uses antiseptically of this for sur-
gical purposes, although prohibited from being used for preserving
wines in France, have rendered it servicable in preserving the offi-
cial solution of hydrochlorate of cocaine, which contains ij^ per
mille of the acid, with 10 per cent, of the cocaine salt. I find that
this solution, even if diluted with four times its volume of water, still
keeps free from fungoid growths. The use of this acid might be
objected to in the solution, because salicylic acid forms with cocaine
an indefinite compound rather than a salt, the so-called salicylate of
cocaine ; but it appears not to throw the hydrochloric acid out of
combination, and has proved very serviceable in preserving the solu-
tion of this cocaine salt, which has a great tendency to develop
fungoid growths. The salicylic compound appears to be allied to
the benzoic compound, benzoyl-ecgonine. It forms a pasty mass
which has not, that I am aware of, been studied. If any defence
were needed for using a preservative, perhaps this official solution of
cocaine is a typical case. The use of this solution of salicylic acid,
11^ per mille, which is nearly saturated, as a vehicle, might be ex-
tended to other solutions, for example, the official solution of sul-
phate of atropine, but I have not found this solution, if made with a
well-crystallized salt, prone to grow fungi. Its use, however, cannot
be extended to the hypodermic injection of morphine ; if a solution
of tartrate of morphine, I in 12, or even i in 20, be prepared in it, a
crystallized salicylate of morphine separates; 16^ tartrate keeps
well alone.
Of the salts of morphine suitable for hypodermic injection, the
tartrate seems to be now favored ; the acetate solution, prepared
by dissolving pure morphine in just enough acetic acid, has till
lately been mostly used, but it has the objection of possessing a
Am. Jour. Pbarm.
MajyiS?*'''"'} Pharmacopmal Preparations. 255
tendency to decomposition and becoming muddy and dark-colored.
Still I have two solutions here over 18 years old, no extra sterilizing
precautions were taken when made ; they are well preserved and
are perfectly transparent, although they have slightly changed color.
One is of the strength of i grain in 6 minims, which I advocated
in a paper in 1870,^ the other is I grain in 12 minims. A small
dose is generally preferred for hypodermic injection, but the strength
of I grain in 6 minims is considered now to be dangerously strong
in the hands of an unskilled operator. The more nearly saturated,
however, the aqueous solution of any salt or crystalline principle is,
the better it will keep ; in fact, it was a curious argument of an
advocate for spontaneous generation that there was a debatable land
between that of crystallization and the germination of organisms in
these solutions — that is, between the growth of crystals and of
organisms ; this applies widely in pharmacy, as we well know, in
keeping syrups for example. A nearly perfect syrup consists of two
parts of sugar and one of distilled water ; kept at a uniform temperate
heat, this neither crystallizes nor grows fungi ; and our solid medici-
nal extracts are preserved if they contain no excess of moisture.
Further, these remarks especially apply to the official solutions of
acetate and citrate of ammonium, which are much better kept in a
concentrated form.
The salicylic acid solution cannot either be used for preparing the
hypodermic injection of apomorphine ; a I per cent, solution of the
hydrochlorate of apomorphine prepared in it gives a quantity of a
crystalline deposit.
Hydrochlorate of apomorphine in aqueous solution rapidly devel-
ops a green color; this has been attributed to the influence of
ammonia in the atmosphere, but although a drop of solution of
ammonia does develop the green color immediately, it is apparently
not due to this alone. This salt is now prepared much purer than
formerly, and it is also not so soluble. The official strength of the
hypodermic injection, I grain in 50 minims, i.e., \ in 45.5 parts, of
camphor water is not held in solution at 60° F. Dott gives the
solubility in water as I in 50.89, Squire as I in 56 to 60. I find
I part in 60 of boiled and cooled distilled water dissolves,
but turns green within a few hours, but if acidulated with a trace of
hydrochloric acid, say an equal weight of the official diluted hydro-
^ Pharmaceutical Journal, [2] Vol. XI, p. 480.
256 Pharmacopmal Preparations, {^'"mT/.-iIq'?^"'^'
chloric acid, the color is preserved, but it is rendered less soluble.
More than i per cent, solution, if acidulated, is not certain to keep
free from crystals at the variable temperatures to which it may be
exposed, and less than the quantity of acid I have named does not
keep it free from color.
Sulphurous Acid. — A trace of sulphurous acid, say one-quarter
per cent., added to a 2 per cent, solution of the apomorphine salt,
keeps the solution for a moderate time, but not indefinitely, and the
use of such a deoxidizing agent is not desirable, as its action on the
apomorphine salt is not clearly understood. Nevertheless, sulphur-
ous acid is largely used as a preservative of such preparation as
orange wine.
Boric Acid. — Of the preservatives suggested for keeping apomor-
phine injection, boric acid has been mentioned, but this I find, in a
solution containing 2 per cent, of each, boric acid and hydrochlorate
of apomorphine, forms an opaque white jelly, and even with i per
cent, of each, a curious translucent jelly is formed, quite unsuitable
for hypodermic injection. Boric acid has been recommended and is
used largely for preserving solutions for hypodermic injection, but
as a solution of it, i in 30 parts of water, which is nearly saturated,
will itself develop some peculiar fungi, I can see little advantage in
employing such a preservative pharmaceutically. Mr. Lee has
mounted a specimen of a torula which has been grown in a satur-
ated solution of boric acid in distilled water.
Camphor Water. — The same remarks apply to camphor water,
the favorite of Raspail, as to boric acid. It is a weak inhibitor, and
it further has the disadvantage of the camphor being volatile.
Camphor water is official as the solvent of atropine in the solution
of sulphate of atropine, but oculists complain of the irritating action
of camphor in the eye.
Chloroform. — The addition of chloroform to vegetable infusions
and other aqueous preparations of vegetable and animal substances
was recommended by Mr. J. B. Barnes^ in the proportion of from
one eighth to one-half per cent, by volume. The addition of chloro-
form as an inhibitory in suspended pharmaceutical operations is of
great service, and it has the advantage that by gently warming the
solution for a short time it can be easily dissipated, but it has also
the disadvantage that the chloroform evaporates too easily for pro-
* Pharmaceutical Journal, [3], Vol. V., p. 441.
Am. Jour. Pharm
MayriS:.*''"} Pharmacopaial Preparations. 257
longed preservation, yet I have tried the experiment of preserving
fruit (damsons) in stoppered bottles, adding about one three-
hundredth part of their weight of chloroform to them. The preser-
vation was complete, but the flavor of the chloroform was not dis-
sipated by even baking the fruit in pies.
Hydrate of Chloral has been used as possessing similar prop)erties
to chloroform, being more readily soluble and less volatile, but its
taste is nauseous.
Carbolic Acid. — The odor and flavor of this most powerful anti-
septic is against its use for internal administration, excepting for
hypodermic injections ; it is the best preservative for ergotin in
aqueous solution. Boric acid in this solution fails ; Mr. Severn
kindly infected for me three solutions of ergotin with Pcnicillium
glaucum\ No. I, without preservative added, developed in forty-
eight hours ; No. 2, with I per cent, of phenol added, is undeveloped
yet, after five days ; No. 3, with 2 per cent, of boric acid, developed
on the side of the bottle, just above the surface of the liquid, in
seventy-two hours. Creosote also, although one of the best preserva-
tives, as its name indicates, is not admissable, on account of its odor.
Cherry Laurel Water. — This is recommended in France for pre-
serving hypodermic injections. So, also, are the distilled waters of
meadow sweet and eucalyptus. I am not aware that
Formaldehyde has been much used pharmaceutically, although it
has, I understand, been used for milk preserving for some time. Its
peculiar action on gelatin in rendering it insoluble would tend to
prove that it was not desirable for internal administration, as it
might seriously interfere with digestion.
Ilvpophosphorus Acid. — This and citric acid tLte employed com.
mercially to prevent the change of color of the ferrous syrups ; as
traces only are needed, it may be considered a venial offense. But
preservatives are sometimes used, or are added even officially, which
are often disadvantageous. For example we have two arsenical
solutions official, one acid and the other alkaline. A simple solution
of arsenic anhydride in water of the same strength, colored if desired,
is perfectly stable. It would be compatible with both acids and
alkalies, and might take the place of both the official solutions.
Carbonic Acid. — This in solution in water is inhibitory to organic
growths, and is largely used in preparing carbonatetl waters and
" Fluid Magnesia,'" but otherwise it is not of much service.
258 Pharmacopceial Preparations. {'^'^i^^l?^^''^'
Benzoic Acid. — For preserving lard and some official ointments,
the melted fats are macerated with powdered benzoin, by which
means they obtain an agreeable odor and become impregnated with
benzoic acid. Both these tend to preserve the fats from becoming
rancid. But in using these fats for preparing the ointments of the
alkaloids, apparently some change takes place ; they become dis-
colored, and in the case of cocaine we know, as I have before men-
tioned, a comparatively inert compound of benzoyl-ecgonine, etc.,
is formed, so that the use of benzoated lard is to be avoided for pre-
paring these ointments.
Paraffin Basis. — Where quick absorption is not required, the pre-
servative action of the soft paraffins renders them all that can be
desired, as also is oil of theobroma for suppositories.
Aromatic Waters and Essential Oils. — The oils of clove, cinnamon,
peppermint, and many others are preservatives; so are their aqueous
solutions, but I can only mention them.
Heat and Cold. — A gentle heat assists the incubation of nearly all
micro-organisms ; a greater heat, that of boiling water for example,
is a sterilizer; whereas a still higher temperature is a disorganizer,
and is destructive to all organic growths. Cold, on the contrary,
the freezing point of water and below, as a rule, is only inhibitory
to the development of the lower organisms, their vitality is but sus-
pended, and they spring into life again with the first application of
a gentle warmth. It may appear irrelevant to my subject, but the
important bearing preservatives have on our food supplies, including
frozen meat, makes them of great importance commercially. In
fact, in viewing the pharmaceutical aspect of preservatives, I have
but touched the fringe of the subject of their utility. Without the
aid of boric acid and other preservative, many of our articles of daily
food would be at famine prices. In such a condensed population as
that of London, it would now be almost impossible to supply the
necessary quantities of butter, milk and fish in a fresh condition.
We have long been dependent to a great extent on the importation
of flour and corn. The same has now become the case in regard to
our animal food products.
"^"■ia"/;!^"™} Camphor in China. 259
THE PRODUCTION OF CAMPHOR IN CHINA.^
By Augustine Henry.
The camphor tree, Cinnamomum camphora, Nees et eberm, is
indigenous to Japan, Formosa and the central and southern provin-
ces of China. It has been known to the Chinese from ancient times,
but apparently until 300 or 400 years ago only as a valuable timber
tree.
The camphor first in use was undoubtedly the Malay camphor,
and as Hanbury says (** Pharmacographia," p. 51 1), " at what period
and at whose instigation the Chinese began to manufacture camphor
from the camphor laurel is not known." Hanbury further states
that •' The camphor of European commerce is produced in Formosa
and in Japan, and we have no evidence that any is now manufactured
in China, although very large trees, often from 8 to 9 feet in
diameter, are common ; for instance, in Kiangsi, a camphor wood is
an important timber in the Hankow market." The latest references
to camphor production (" Index Flora: Sinensis " II., p. 371) further
would confirm this, viz., '• Kwangtung, common around Pakhoi, but
not utilized" (Playfair). Again, " Dr. Henry states that the wood
is much used in Central China, but no camphor is extracted."
Until a few years ago, then, no camphor was produced on the
mainland of China, but it is interesting to note that the camphor
industry has been started in China, and that there are signs that it
will become important. This is all the more noteworthy, as For-
mosa has become Japanese territory, and it seemed likely that
camphor would become an entirely Japanese article, not a desirable
contingency in view of the fact that the Japanese Government is
striving to establish a monopoly in the production of camphor in
P'ormosa, and has no doubt in contemplation the creation of a large
revenue by enhanced prices in the future.
For a history of the vicissitudes of the camphor trade in For-
mosa itself the reader is referred to the •• Chinese I. M. Custom,
Decennial Reports'' for 1882-91, pp. 439, 466. hn passant, this is
a most valuable work for all questions connected with Chinese com-
merce, the history of the treaty ports, etc. It is replete with infor-
mation of all kinds, and is illustrated with maps, plans, and diagrams.
* Pharmaceutical Journal^ March 6, ii>97.
26o Camphor in China, { ^'"•£y?il?7"'""'-
GROWTH OF THE CHINESE CAMPHOR INDUSTRY.
The growth of the camphor industry on the mainland of China
is shown by the following facts taken from various China Customs'
Yellow-books. From the ** List of Chinese Medicines," miscel-
laneous series, No. 17, which gives details of the trade in drugs of
all kinds for the year 1885, it appears that camphor was unknown
as a product of the mainland, except in the single province of
Chekiang, there being the small export that year from Ningpo of
25 piculs. Ningpo exported 32 piculs in 1889, 40 piculs in 1890,
and none since, apparently. The Customs' "Trade Reports," for
the different years show the gradual appearance of camphor pro-
duction in other parts. Kowloon exported 88 piculs in 1888, 106
piculs in 1892, 87 piculs in 1893. This was conveyed in junks, and
its provenance is doubtful, but it was perhaps from the province of
Kwangsi. Canton exported 122 piculs in 1893, 37 piculs in 1894,
and 237 piculs in 1895. This is Kwangsi camphor. The Pakhoi
Trade Report for 1894 states that the first record of the article was
in 1892; in 1893 ^^^^ export was 23 piculs, which increased to 128
piculs in 1894, and '* it comes from Lu-chuan, near Yii-linchow, and
is likely to grow in importance, as plantations in that and other
places in the neighborhood are coming to the bearing age." In
the Pakhoi Trade Report for 1895, the export is given as 596
piculs, and the writer says that this gratifying increase is due to the
extended cultivation in Kwangsi. In Formosa, only old and
enormous camphor trees are utilized, and I am inclined to doubt
the existence of camphor plantations in Kwangsi ; the camphor
produced is more likely to be from old forest trees. The Chinese,
at any rate, did not plant any trees with a view to the manufacture
of camphor.
EXPORT OF CAMPHOR FROM CHINA.
In 1895 the exports of camphor from different Chinese ports was :
Foochow, 187 piculs ; Amoy, 668 piculs ; Canton, 237 piculs ; Kow-
loon, 68 piculs, and Pakhoi, 596 piculs. In the Fukien province
there are large forests and camphor trees abound. Some years ago,
a party of Japanese went into the interior of Fukien to manufacture
camphor, but nothing came of this attempt. The Foochow export
is probably the product of this province, but that of Amoy is doubt-
ful, as it maybe Formosan camphor smuggled over to the mainland
in junks. The export of the other three ports is produced in the
"""-Ma^iS^""- } Editorial- Reviews. 26 1
Kwangsi province, and this will probably grow into large figures, if
camphor continues high enough in price to encourage the Chinese
in its manufacture.
To sum up, the production of camphor on the mainland of China
is an affair of the last few years. It began in Chekiang, but has
practically ceased in that province. In Kwangsi it commenced a
short time ago, and promises to develop irto importance. The
Fukein product is only trifling so far.
EDITORIAL.
EDSON SEWELL BASTIN.
On the morning of April 6, 1897, Edson S. Bastin passed away, after an ill-
ness of several months. His funeral took place at Merchantville. on the 9th,
and was largely attended by members of the College and students.
The Board of Trustees was in session when the sad news reached them, and a
series of resolutions were directed to be drawn up for approval at a subsequent
meeting. Two days later a special meeting of the College was held, and
appropriate resolutions were directed to be drawn up to express the sentiments
of that body.
It is merely desired to record the foregoing facts at the present time ; a
memorial will be prepared and published in a subsequent number of this JouR-
N.\L. It is but justice to say, at this time, that while Professor Bastin's occu-
pation of the Chair of Botany and Materia Medica in this College was short in
duration, it was long when measured by results accomplished. More than that,
he won the respect, confidence and admiration of every one with whom he
came in contact during the short four years he was with us.
THE AMERICAN MKDICAI. ASSOCIATION.
The fiftieth annual meeting of the Association will be held this year in
Philadelphia, during the first week in June. As the Association originated in
this city fifty years ago, more than ordinary efforts will be made to have a
notable meeting. Elaborate preparations have already been made by the Com-
mittee of Arrangements for the extraordinary attendance which is anticipated.
The section on Materia Medica ind Therapeutics has been invited to hold its
sessions at the Philadelphia College of Pharmacy.
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
DBS ACANTHACKES Medicinales. Par Georges Dethan. Deuxieme Edi-
tion. Paris : A. Malone, 1897. Pp. 192.
Two months ago we briefly reviewed the first edition of this work, which was
issued as a thesis which had been presente<l to the Ecolc Sup<^rieure de Phar-
macie dc Paris. The present edition has been revised, corrected and enlarged.
Oh NERVATIONS ET E.KPERIENCKS SUR l/OUVERTL'RK DKS FI.El'RS OS
I/(EvoTHERA LAMARKiANA. SKR . Par M. Louis PlanchoH. Reprint from the
/>'w//<7/n de la Sjci<5t<5 botanifjue de I'rance, November, 1H96. This is a close
study of the process of opening of the flowers of renothera, and it throws much
light on the subject in general.
262 Examination Questions, {^'^•yLZ]\l^^''^'
Viola tricolor, L., in morphilogischer, anatomischer und biolo-
GISCHER Beziehung. Vou Henry Kraemer. Universitats-Buchdurckere's
von Jh. Aug. Koch, Marburg, Germany, 1897.
Professor Kraemer has carefully worked out the life history of this interest-
ing plant, and at the same time has added to the value of the work by an elab-
orate series of illustrations. The results are presented in twelve sections, the
last being a short account of what is known at the present time of the chem-
istry of the plant. As pointed out by earlier investigations, salicylic acid is
the most interesting compound ; it exists partly as a methyl salicylate, and
partly in combination with various inorganic salts. A valuable biblio-
graphical index completes the work.
On the Constituents of the Sap of the "Silky Oak," Grevillea
RoBUSTA, R. Br., and the presence of Butyric Acid therein. By Henry
G. Smith, F.C.S. Read before the Royal Society of New South Wales, October
7, 1896. In a previous communication on the timber of this tree, the author,
in conjunction with J. H. Maiden, has pointed out the presence of a deposit of
aluminum succinate. Now, having demonstrated the presence of butyric acid
in the sap, he is led to believe that the succinic acid is derived from butyric
acid by natural oxidation in the tree.
The Dyeing Properties of Aromadendrin and of the Tannins of
Eucalyptus kinos. By Henry G. Smith, F.C.S. Reprint from the Journal
0/ the Society 0/ Chemical Industry, November 30, 1896.
Ueber Flechtenstoffe. Von Dr. O. Hesse. Reprint from Berichte d.
dent. chem. Gesellschaft, 30, 357.
EXAMINATION QUESTIONS OF THE PHILADEL-
PHIA COLLEGE OF PHARMACY, 1896-97.
first y'ear examination,
pharmacy.
A — Crystallization, (i) Describe the method of obtaining crystals by depo-
sition from supersaturated solution. (2) Define pellicle. (3) Water of crys-
tallization. (4) Interstitial water. (5) Efflorescence. (6) Deliquescence. (7)
Mother liquor. (8) What is intermediate crystallization ?
B— Syrups, (i) Define syrups. (2) Name five methods for official syrups.
(3) What kind of sugar is best adapted for making syrups, and give the reasons
for preferring this kind of sugar. (4) Describe a method of preserving fruit
juices in bottles, and state the causes which lead to the decomposition of solu-
tions containing organic matter, if not protected.
chemistry.
C—Hnlo^ren Group, (i) Enumerate the elements belonging to the Halogen
group, and briefly describe the physical appearance of each of them. (2) Give
the formulas of their hydrogen compounds, and state which of them are official
compounds. (3) Write a chemical reaction for the production of one of these
elements and a chemical reaction for the production of one of the hydrogen
compounds above mentioned.
D— Phosphorus, (i) Describe the element phosphorus in its several forms
'^"'■MayViS:^'"} Examination Questions. 263
(2) From what sources do we obtain it, and what are its practical uses? (3)
Give the chemical formula for hydrogen phosphide, and state how it is obtained.
BOTANY.
E—y\) In what group of plants are the sporophyte and gametophyte gen-
erations nearly equal in development ? ( 2) In flowering plants, what two
kinds of spores are produced, and in what organs are they borne respectively?
(3) In most of the higher plants, into what organs are root and shoot differen-
tiated? (4) Define the terms sporophyll and hypsophyll, and give examples
of each as they occur in the flowering plant. ( 5) What are the microsporangia
and macrosporangia commonly called, respectively, in the flowering-plant?
(6) What peculiarities in the leaf venation and in the numerical plan of the
flowers enable us, usually, to distinguish a monocotyl from a dicotyl ? (7)
Name examples of each of the following kinds of fruits : a syconium, a drupe»
a legume, a pepo, and an akene.
F^Materia Medica. (8) Describe Uva-ursi as to the following points:
length, shape, surfaces, venation, margin, texture, taste, a medicinal constitu-
ent, and the chief use of the drug. (9) Name two official leaves which possess
internal glands. (10) State the important structural diff"erences between Ger-
man and Roman chamomile.
COMMITTEE.
G — Glyurifi. 1 n Name three principal reasons showing its value in phar-
macy. (2 1 What official class of preparations contains glycerin as a base ? (3)
What is glycerin, and what is its principal use?
H — Chctnical Terms. Write concise definitions of each of the following
chemical terms : ( i ) matter ; (2 ) elements ; ( 3 ) atoms ; ( 4) atomic weight ; (5)
equivalence or valence; (6) molecules; (7) molecular weight; (S) equation ;
(9) chemical reaction ; ( 10) acids.
/ — Prohlem. A laboratory formula called for 85 kilos of 50 f)er cent, ortho-
phosphoric acid. How much of the U.^^.P. phosphoric acid (85 per cent.)
would be required to take its place in the formula? Show the figures used to
obtain your result.
K—The Flower, (i) Define the term sporophyll. ( 2 ) State what tvo kinds
of sporophylls occur in the flowers of most of the higher plants. (3) State
what they are commonly called, respectively, and what is the function of each.
• 4 ; State, also, what other modified leaves the flower may possess.
OPERATIVE PHARMACY.
(/) Specific Gravity.
Determine the specific gravity of the licjuid contained in the four-ounce
bottle ; put all calculations on the ^^heet of paprr, with v«)ur iiaine and exam-
ination numl>er.
'-') I'ercolation.
Percolate 100 grammes of gentian, with 500 c.c. of water. Label the per-
colator with your name and examination number.
(j) Granulated Salt.
Aci<l Salicylic ... . 7 gni.
Soiiiura Carlx)nate C. I' . . 6*5 gni.
Distilled Water q. s
Make Sotlium Salicylate. Put in the widc-nioulh bolllc.
264 Examination Questions. {'"'"May.'ifQ?.^'"''
PHARMACOGNOSY.
In this branch each student was given specimens of ten official vegetable
drugs, and was required to give the official name and common names, if any,
and also describe the chief characteristics of each specimen.
SECOND YEAR EXAMINATION.
PHARMACY.
A—^i) What is the official name for Solution of Hydrogen Dioxide? (2)
What is the synonym ? (3) What is the official description ? (4) Give a brief
outline of the process for preparing it. (5) What are its uses?
^_(i) What is the official name for Solution of Ferric Chloride ? (2) What
is the official description ? (3) Give a brief outline of the process for preparing
it. (4) If the finished solution has a blackish tint, what is it due to ? (5) How
may this be removed ?
C—{\) What is the official name for Ether? (2) What is its specific gravity ?
(3) How is it made on the large scale? (4) What are its physical properties
and uses ? (5) Is Ether vapor heavier or lighter than air ?
D—{i) Explain the natural changes which occur in the pulpy constituents
of unripe fruits during ripening. (2) Have fleshy roots any of the constituents
of unripe fruits? If so, name them. (3) Explain the reasons for adding
ammonia-water to preparations of glycyrrhiza and senega. (4) How do acids
and heat affect the constituents of fleshy roots ?
^_\Vhat are the essential points of diff"erence between a volatile oil and a
fixed oil ? By what test may one be distinguished from the other ? What is
oleic acid ? How is it prepared ? What are its uses in pharmacy and medicine ?
Describe the manufacture of Soap ? What is Sapo Mollis ? How is it prepared ?
What is Castile Soap chemically ? And what useful by-product results from
the manufacture of Soap ?
CHEMISTRY.
-F— (i) Give the reactions for the production of Sodium Carbonate by the
Leblanc process? (2) Give the reactions for the production by the Ammonia-
Soda and Cryolite processes? (3) State what are the by-products in each of
these processes and which of them are of value.
G — (i) Describe the metal Copper and state from what ores it is obtained.
(2) Describe Cupri Sulphas U.S. P. What is the change of appearance effected
in it by prolonged heating? What is the result of the addition of aqua ammo-
nia to copper sulphate solution ? (3) Mention the more important alloys of
copper, stating the several components of each.
H—{i) How is the metal Aluminum obtained? (2} Give the chemical
{ormula. of A lumen U.S. P. (3) Describe silicate of aluminum and state its uses.
/ — (i) Describe the more important tests for the detection of Arsenic. (2)
How would you distinguish Arsenic from Antimony in these tests ? (3) Describe
Acidum Arsenosum U.S. P.; give its chemical formula and its common name.
K — (r) Enumerate the several varieties of glass and state their approximate
chemical composition. (2) What is " soluble glass ? " (3) Mention some of the
materials used in coloring glass ?
MATERIA MEDICA AND BOTANY.
J^ — Tissues, (i) Enumerate the different kinds of tissues found in plants.
(2) Define meristem and state how its cells differ from ordinary parenchyma
^""May?!^!^} Exaviitiat 10)1 Questions. 265
cells. (3) In what parts of an ordinary' tree, such as the elm, for example, does
meristem occur? (4) State how the wall of an ordinary parenchyma cell,
that of an ordinary epidermal cell, and that of an ordinary wood fibre differ
from each other in their chemical and physical properties.
M—The Structure 0/ Stetns, Roots and Leaves. (5) In what respect does
the growing tip of a Fern stem differ from that of a Dicotyl stem? (6)
What three layers are recognizable at the growing tip of a Dicotyl stem, and
into what regions do these layers develop, respectively, as the stem matures?
(7) What kind or kinds of vasal bundles are characteristic in each of the follow-
ing organs : the root of vSarsaparilla. the trunk of a Pine, the stem of Lyco-
podium, the rhizome of Aspidium, and the stem of the Pumpkin. (8) Define
the terms centric, bifacial, and iso-bilateral as applied to leaves.
A — Root and Rhizome Drugs. 1 9 1 Write the official name, the comtnon
name, the natural order, botanical name, the name of the country from ichich
derived, the most iviportant chemical constituent, and the most itnportaut
medicinal property of each of four official root-drugs. ( 10^ Write the oflficial
names of two root-drugs which contain milk-tissue. (11) Name two official
root-drugs that owe their activity to poisonous alkaloids, giving also the name
of the alkaloid in each case. 112^ Name two root drugs and one rhizome drug,
all of which are official and all characterized by an intensely bitter taste.
O — Root and Rhizome Drugs. (13) State the sources of each of the follow-
ing principles, giving the official name of the drug in each case : Leontin,
Cheleryihrine, Sylvacrol, Atropine, Chrysophan, Ilmetine, Pelosine, Filicic
Acid, Jervine, and Aristolochine. (14) Name four official drugs belonging to
the groups of Roots and Rhizomes that are powerful narcotic poisons. (15)
Describe the structure of Belladonna Root. (16) Write the official names of
each of the following drugs : Pinkroot, Blue Cohosh, Mayapple, Cranesbill
and Marshmallow.
P— Barks, Woods, etc. (17) Name three official barks, each of which
possesses three layers, and three others, each of which consists of the inner
layer only. (18) What official bark is very tough and flexible, has silky bast-
fibers, is very sternutatory when powdered, is acrid to the taste, and is capable
of producing a blister when moistened and applied to the skin? (19 Name
two official barks which have short and rigid bast-fibers, two which possess
long and flexible ones, and two that possess none. (20) Name an official bark
that '\% febrifuge, one that is pectoral, one that is taenifuge, one that is cathartic,
and one that is demulcent.
SPECIMENS FOR RECOGNITION.
(I) Acidum sulphurosum. (2) Plumbi oxidum. (3) Sodii hyposulphis.
(4) Alumen. (5) Plumbi .\cetas. (6) BelladonniL- radix. (7) Podophyllum.
IS) Aspidosperma I (Quebracho). (9I Eriodict} on (Verba Santa), i loi Stroph-
anthus. (11) Pulvis rhei compositus. 112) Aqua chloroformi. (13) Spiritus
juniperi compositus. (14) Emulsum chloroformi. (15) Tinclura calumb;i;.
SENIOR EXAMINATION.
THEORY AND PRACTICE OP PHARMACY.
Put down on your paper all the figures used in making your calculations.
A — How many fluid ounces are there in a kilogramme of each of the follow-
266 Examination Questions. {^'"Ma?!"i£?.*''""*
ing official liquids? (i) Water. (2) Hydrochloric acid. (3) Ether. (4)
Syrup. (5) Diluted Alcohol.
^_Give the unabbreviated official name ; ingredients in preparing ; describe
the appearance of— (i) Compound Infusion of Gentian. (2) Fluid Extract of
Ginger. (3) Soap lyiuiment. (4) Compound Syrup of Rhubarb. (5) Spirit
of Peppermint. (6) Emulsion of Chloroform. (7) Compound Extract of
Colocyuth. (8) Plummer's Pills.
(f__Give the English name, ingredients, and brief outline of process of the
following : (i ) Calx Sulphurata: (2) Argenti Nitras Fusus. (3) Ferri et Strych-
nin^e Citras. (4) Emplastrum Plumbi. (5) Pilulse Ferri Carbonatis. (6)
Unguentum Aquae Rosae. ( 7) Pulvis Purgans. (8) Spiritus Glonoini.
D—{\) What is Monsel's Solution? (2) How is it prepared? (3) What
are its uses? (4) What antidote is prepared from it? (5) How is the anti-
dote made? (6) How is the antidote administered ?
E—{\) How is Chloroform prepared? (2) What is its specific gravity?
(3) What are its uses? (4) What is the official test for purity? (5) How is it
preserved? (6) Is its vapor inflammable? (7) Name three official prepara-
tions in which Chloroform is used.
F—{\) What is Copaiba? (2) What are its constituents? (3) What official
preparation is made from Copaiba ? (4) Give the process for this preparation.
(5) How is this preparation administered ? (6) What is the dose ?
G—{\) What is Chocolate? (2) How is it made? (3) What is the official
name of the fatty constituent ? (4) What is the English name of this con-
stituent? (5) How is this constituent prepared? (6) What are the pharma-
ceutical uses of this constituent ? (7) What is its melting point?
H — ( I ) Describe the apparatus for making Compressed Pills. (2) What are
the advantages of Compressed Pills ? (3) What are the disadvantages ? (4) How
are Tablet Triturates made ? (5 ) How are Tablet Saturates made ?
/—Criticise the following prescriptions. Write out the English name of
each ingredient ; state how you would compound each, and if any incompati-
bility would be developed in either ; state what it is, and what would be the
proper procedure.
R Chloral Hyd gr. xl
Camph. Pulv gr. x
Syr. Zingib • f ^ij
AquiE ad f ^ij
M. ft. Solutio.
S. A teaspoonful every three hours.
R Ferri et Quin. Cit
Amnion. Carb. aa^j
Sp. Ammon. Arom ^iv
Tinct. Opii ^ij
Aqu£e ad ^ viij
M. ft. S. One teaspoonful three times a day. A.
A'— Criticise the following prescriptions. Write out the English names,
with ingredients and quantities ; state whether you would compound them as
written, or what course you would pursue upon receiving them.
^^Miy'i^*'"'"'} Examination Questions. 267
R Quinin. Sulph ■ • • gr. j
Ext. Xucis Vomicae gr. v
Morph. Sulph gr. viij
M. ft. pil. No. X.
Sig. One pill every three hours.
R Potass. Permang • • .tJ
Alcohol • oj
Glycerin ... • oU
M. ft.
Sig. Use as directed. X.
CHEMISTRY.
A — (i) What are the native sources of Borax ? Give the chemical formulas
for Sod a Boras and for Acidum Boricum. (2) How would you prepare Borax
from Boric Acid ? 13) How would you prepare Boric Acid from Borax? (4)
Give the most characteristic tests, both physical and chemical, for both these
compounds.
B — (i) Describe the metal Sodium. (2) Give two of the methods used for
its production. ( 3 ) Give the formulas of Sodii Chloridum, Sodii C/itoras, Sodii
Hyposulphis, Sodii Phosphas, and Sodii Ilypophosphis. (4) What are the
analytical tests for vSodium and its Salts?
C — ( i) What are the chief ores of Zinc, and how is the metal obtained from
them ? Describe the metal, and enumerate its properties, both physical and
chemical. (31 Mention the uses of Zinc, and state which alloys of it are of
practical value. (4) Give the names and formulas of the official Salts of
Zinc.
D — (i) Give the formula of ^r/^/«;// Chromicum. '2) Give the formula of
Potaasii Bichtotnas, and of the normal Potassium Chromate, and explain the
chemical difference between these formulas. (3) What takes place when an
excess of Sulphuric .\cid is added to a concentrated aqueous solution of Potassium
Bichromate ? (4) What takes place when an alkaline hydrate solution is added
to a solution of Potasii Bichroinas ? (5) What pigments may be formed
from Potassium Bichromate ?
E — (1) Write the chemical formulas o{—Ferri Chloridum, Ferri Oxidum
Hydralum, Ferri Sulphas, Ferri Ilypophosphis, Potassii Ferrocyaniduni, Frrri
Lactas. (2) Slate by what tests Ferrous Salts can be distinguished from Ferric
Salts? (3) State how a Ferrous Compound can be converted into a Ferric
one?
/*— (i) Give the general formulas for the Paraffin, the Olefine, and the Ben-
zene series of Hydrocarbons. (2 1 State the occurrence in nature or conditions
of artificial formation of each of these series. (3) How could you distinguish,
by chemical tests, between these three series?
G — (I) Name an official compound belonging to the class of Triatomic
Alcohols. (2) State the source of the compound and how it is prepared from
the naturally occurring products, i 3 1 Write the reaction for its production
from one of these snl>stance8. (4) Name the other products of the reaction
just referred to.
//— <i) Write the graphic formulas of Alcohol, Chloral, Acidum Car-
bolicum, Acidum Bcnzoicum, and Acidum (,'allicum.
268 Examination Questions. {^"""Mayyis^T.*''"'-
/__(!) What is Phenol? (2) Name such ofi&cial compounds as belong
to the class of Phenols, and write their graphic formulas. (3) What is a Phenol-
Acid? (4) Name such official compounds as belong to the class of Phenol-
Acids, and write their graphic formulas.
A'— (i) Name the compounds indicated by graphic formulas, and where
official give both chemical and official names. .
(I) (2) (3) (4) (5)
CO OH CH, CH, C.NH.C2H3O C.NH.C2H3O
I I I ' ^\ //\
CH OH CO CH OH HC CH HC CH
I II I II I II
CH OH CH., CO OH HC CH HC CH
I " %/ %/
CO OH CH C.OC2H5
MATKRIA MEDIC A.
(i) Name and describe the different forms of Proteid that may exist in a
cell.
(2) State how a wall of a cell may vary in composition.
(3) What are the distinctive characteristics of Meristem Tissue?
(4) Describe the characteristics of Epidermal Tissue and name its varieties.
(5) Under what circumstances is the Epidermis not cutinized ?
(6) Describe the structure and state the use of a Stoma. How are Stomata
distributed on the plant ?
(7) Describe the usual form or shape of Chloroplast and their mode of
increase.
(8) What relation does Chlorophyll bear to Chlorophyll-Bodies, and of what
use to the plant is Chlorophyll ?
(9) What are Conjoint Fibro -Vascular Bundles ?
(10) What kind of bundles are characteristic of the following stems: The
Fern, the Lycopodium, the Equisetum, the Monocotyl, and the Dicotyl?
(11) Write such a description of Aconitum as would serve for its certain
identification.
(12) Name one of the most important structural characteristics of each of
the following drugs : Taraxacum, Senega, Rheum, Cimicifuga, and Cinchona
Calisaya.
(13) How, without aid from the senses of taste and smell, may Serpentaria be
distinguished from Spigelia ?
(14) By what chemical test may Guaiac Wood be readily recognized ?
(15) By what simple test may chips of Red Saunders be readily distinguished
from those of Logwood ?
(16) By what s mple means may Granatum be easily distinguished from other
drugs?
(17) Name three official barks which are destitute of bast-fibers.
(18) Name three official barks that consist of the inner layer only.
(19) In the botanical classification of fr aits, to what group do each of the
following belong : Colocynth, Prunum, Foeniculum, Piper Nigrum, and Car-
dauiomum ?
( 20) Name three official seeds that are albuminous and three that are exal-
buuiiuous.
^"'May?ir97*'"*} Examination Questions. 269
(21) Write the botanical name and natural order of Crocus, and state what
part of the plant is official.
(22) Name an acid and three important alkaloids found in Opium. Name au
acid and three important alkaloids found in Cinchona.
( 23) Write the botanical name and natural order of the plants from which each
of the following drugs is derived : Elaterium, Manna, Opium, Guarana, and Zea,
(24) Name the source of each of the following alkaloids : Thebaine, Emetine.
Pelosine, Chelerythrine, Cornutine, Menispine, and Hygrine,
(25) Name the source of each of the following non-alkaloidal principles :
Meconic Acid, Rottlerin, Chrysophau, Cathartic Acid, Saponin, ^Elaterin, and
Rhamnoxanthin.
(261 Name five official drugs that are powerful hydragogue cathartics.
(27) Name three powerful drugs that act as tonics to the heart, strengthen-
ing its beat ; and three that powerfully depress the heart's action.
(28 I Define the terms Cholagogue, -Antiseptic, Antiperiodic, Mydriatic, and
Anthelmintic.
(29) What are the most marked symptoms of opium poisoning, and what
treatment is indicated ?
(30) Name two powerful official drugs which, in medicinal doses, stimulate
the respiratory function.
COMMITTEE.
A — ( I ) A solid body weighs 50 ounces in the air and 30 ounces in water.
What is its specific gravity? (2) What is the volume of the body? (3) What
is the weight of an equal volume of water? (4) What would it weigh if it
were immersed in official Glycerin ? (5) If two avoirdupois pounds of official
Sulphuric Acid were poured into a measure graduated to show fluid ounces,
to what number would it be filled?
B — Asii/utida. (i) Give botanical name, natural order, and habitat of the
plant which yields Asaftetida. (2) Describe the characteristics of the natural
order to which the plant l>elongs. (3) What appearance does the drug present
in commerce? (4) Why does it form an emulsion when mixed with water?
(5) What are its chief constituents, and to what is its odor due? (6) Name
three official preparations of Asafcctida. (7) Give the dose of Asafcutida.
C— Materia Medica. — Belladonna Root, (i) Enumerate the characters by
means of which Belladonna Root may be distinguished from any other official
root. (2) What is the important alkaloid of Belladonna? (3) What is the
most characteristic constitutional effect of Belladonna or of its alkaloid ? (4)
What is the dose of Belladonna Root? (5) Name the official drugs which in
physiological action are closely related to Belladonna. 16) Why is the official
name Belladonna Radix and not Belladonna ?
D—{i) Name five official Tixexl Oils, giving the Latin and English titles.
(2) Describe briefly the processes for making the fixe<l oils of commerce used
medicinally. (3) Name five official volatile oils, giving both Latin and I-inglish
titles. (4) Descrilje briefly three processes by which volatile oils are procured.
/t — (I) Give Symbol, Ivcjuivalence and Atomic Weight of the metal .M.ignc-
sium. (2) What two kinds of Magnesium Oxide are official, and how is each
made? Whatistheessentialdifl"ercnccin chemical reaction with watert>et ween the
two? (3) Which variety of Magnesium Carbonate is the official? (4) Give
the chemical reactions that take place in making Liquor Magnesii Citratis.
270 Examiyiation Questions. {^'^•i^^S^^^'^'
F—{ I ) Give the antidotes for the following poisons : Arsenic, Corrosive
Sublimate, Oxalic Acid. (2) What antidote would you administer for a corro-
sive liquid of unknown identity ? (3) For what class of poisons are antidotes
usually unavailing ? In such cases how may the patient's life be saved ?
G—Strophanthus. (i) Give its official name ; botanical name. (2) To what
region is it indigenous? (3) What is the active principle of Strophanthus ?
(4) What is the dose of Strophanthus ? (5) What preparation of Strophan-
thus is official? (6) Give the dose of this preparation. (7) What are the
medical properties of Strophanthus ?
H — The molecular weight of Crystallized Alum is 946.46, and that of abso-
lutely dry Sodium Carbonate is 105*85. How much of the Sodium Carbonate
would be required for one kilogramme of Alum in the manufacture of Alum-
inum Hydrate?
/—Complete prescription No. i by inserting the quantities of the several
ingredients, the patient being an adult and suffering from a mild dropsical
condition.
Write out, in an unabbreviated form, what you would dispense in prescrip-
tion No. 2.
I.
JR Potass. Acetat
Infus. Digitalis .
Ext. Tritici Fluid
Spt. ^ther Nit
Infus. Buchu
M. Sig. Take a tablespoonful three times a day for four days.
2.
B Pot Chlor 5j
Aq. Chlor f^iv
Spt. Syr. Nig f^^ij
Syr. Zingib q. s. ad ^ viij
M. Sig. Tablespoonful every two hours until relieved.
A%- (i ) Write a metric prescription for 100 pills, each to contain one-eighth
grain Morphine Sulphate, one-sixtieth grain Strychnine Sulphate, and one
twelfth grain Arsenous Acid, with the quantity of a suitable excipient, expressed
metrically, to make one-grain pills.
(2) Translate the following prescription, giving the equivalents in apothe-
cary's system :
GERMAN PRESCRIPTION.
H Chloroform ^o.
-i?£theris 5o'
01. Sesami i^o*
M. ft. Iviniment.
S. Use externally.
SPECIMENS.
The following specimens were placed before the senior students for recogni-
tion during the several examinations :
^'"May'i?^*'''"} Examination Questions. 271
Pharmacy. Chemistry.
Aqua creosoti, Aqua destillata,
Spiritus £etheris nitrosi, Aniylum,
Spiritus a;theris compositus, Sodii salicylas,
Ceratum plumbi subacetatis, Naphtaliuum,
Pulvis ipecacuanhiE et opii, Sodii bicarbonas,
Extractum sennae fluidum, Sodii acetas,
Tinctura benzoini composita, Saccbaruni lactis,
Syrupus ferri iodidi, Mangani dioxidum,
Extractum cinchonae fluidum, Potassii nitras,
Tinctura calumbae. Benzinum.
Materia Medica. Committee.
Bryonia, Tinctura cardamomi composita,
Stillingia, Linimentum chloroformi,
Geranium, Extractum ergotae fluidum,
Calamus, Extractum gentianae fluidum,
Euonymus, Potassii bicarlx)nas,
Salvia, Zinci acetas,
Cheuopodium, Ammonii chloridum,
Conium, Senega,
Pbysostigma, Guaiaci lignum,
Colchici semen. Cascarilla.
OPERATIVE PHARMACY.
(/) Ointment of Mercuric Nitrate.
Mercury 25 gm.
Nitric Acid 2* c.c.
Nitric Acid 3' c.c.
Lard Oil 30* cc.
Make Ointment of Mercuric Nitrate by the official process.
{2) Pills.
Ferric Citrate 3. gni.
Cinchonine Sulph i. gni.
Oil of Caraway 15 Drops.
Mix; make 15 pills.
Write in English, upon the label, all the ingredients and quantities used in
making the pills, and put the lal>el on the bottom of the 1k)x.
(j) Suppositories.
Ext. Belladonna Leaves .50 gm.
Tannic Acid "50 gm.
Oil of Theobroma 6 00 gm.
Make 6 suppositories, by rolling.
{4) Prescription.
Put up a prescription, secundum artem, each teaspoonful dose of which shall
contain five minims each of Tincture of Guaiac and Spirit of Nitrous Ether, with
sufficient water to make two fluid ounces. Write upon a separate label the
contents of the bottle, and attach it.
Am. Jour. Pharm.
272 Commencement Exercises. {^^'-^ty,^'.
(5) Plaster.
Spread a breast-plaster, about 6 inches in diameter. Soap plaster will be
found in the dipper.
ANALYTICAI. CHEMISTRY.
{Students of the second-year class were also given this examination.')
The examination in this branch consisted in the examination of a compound
powder for metals and inorganic and organic acids.
VEGETABLE HISTOLOGY.
{Students of the second-year class were also given this examination.)
(i) To which of the following plant types does the specimen belong : The
Fern, the Monocotyl, the Gymnosperm, or the Dicotyl ? (2) Which of the
following organs does it represent : a root, the petiole of a leaf, or a stem ?
Give the reason for your conclusion. (3) Make a diagram of the cross-section
and locate such of the following parts as are represented : the epidermis, the
periderm, the pith, the cambium zone, a medullary ray, the xylem of a bundle,
the endodermis and the pericycle. (4) Enumerate the tissues which you find
present. (5 ) Is starch present ? What test did you employ to determine? In
what parts of the section is it most abundant ? (6) What tissues are lignified ?
In what part of the section were the lignified tissues most abundant ? Describe
your method of testing for lignified structures. (7) What varieties of secretion
tissue do you find, and how are they distributed ? (8) If milk tissue is present,
state which variety it represents and how it is distributed. (9) For clearing
sections of starch and proteid matters, what reagents may be employed ? (10)
Suppose you find crystals in a cell, bv what means could you tell whether they
are protein crystals or mineral crystals ? Having determined that the crystals
are inorganic, how could you tell whether they are composed of calcium car
bonate or of calcium oxalate ?
SEVENTY-SIXTH ANNUAL COMMENCEMENT.
The exercises connected with conferring the degree of Graduate in Pharmacy
were held at the College Building, Wednesday evening, April 14, at 8 o'clock.
Prayer was offered by Rev. B. L. Agnew, D.D.
President Bullock conferred the degree upon the following :
Xante. Subject of Thesis. State.
Althouse, Harry B., Pharmacy journals., Pennsylvania.
Anderson, Ralph Samuel Lloyd, Progress in pharmacy^ Pennsylvania.
Baker, Newton Claire, Arsenic and its preparations, Pennsylvania.
Bartholomew, Claude Lafayette, Antipyrine, Pennsylvania.
Bates, John Phillips, Liquor potasses et liquor sodcs, Pennsylvania.
Breithaupt, Alphons Peter, Structure of leptandra, Pennsylvania.
Brumbaugh, Albert Sylvester, Digestive value of Carica papaya, Ohio.
Clapp, Samuel Clarence, Kola nut, Pennsylvania.
Clark, Edward B., Glycerinum, Pennsylvania.
Cloud, Norman Henderson, Copaiba, Pennsylvania.
Codori, Simon Jacob, Jr., Cinchona bark, Pennsylvania.
Compton, Richard Hal, Valuation of liquor iodi cotnpositus, Texas.
Cooper, Morris, Testing in retail pharmacies, Pennsylvania.
All). Jour, riiarm.l
May. 1897. /
Covuncncemcnt Exercises.
273
Same. Subject 0/ Thesis. State.
Cope, Edward Kreidler, Opium and its us^s, Pennsylvania.
Criswell. Edward Ott, Cascara sagrada, Pennsylvania.
Deibert, William Henry, Tasteless Cascara sagrada compounds, Pennsylvania.
Eschbach, Clarence Derbie, Syrupus acidi hydriodici,
Farley, Levi James, / 'egetahle histology.
Few, Colin Spangler, Olive oil,
Garrison, Joseph Miller, Jr., Value of pharmacognosy,
Gessford, Otice Eugene, The pharmacists,
Godfrey, Swain Townsend, Coal,
Godshall, Samuel R., Acidu)n a'/ticuui dilutum,
Goodfellow, Charles Rumney, PhatDiacists and their imitators, Pennsylvania.
Gross, Paul Herbert, Oliie oil and its product ion, Pennsjlvania.
Harry, Hamilton Maxwell, Camphor,
Heim, Christian, Liquor plumbi subacetatis,
Hildebrand, Howard Ovid, Coca,
Horst, Harry Lewis, The pharmacy of brewings
Howell, Harry Field, Cocaine^
Hukill, Oscar K., Phartnaceutical education,
Ingling, Howard Edgar, Cinchona,
Opium,
The relation of the druggist to the
physician.
Koumys,
Kessler, Lawrence Anthony, Assay of spirit us tether is nittosi,
Kirlin, Charles Coleman Hagenbuch, Attar or otto of rose,
Kramer, George Henry, Syrupus ferri iodidi,
Gossypium herbaceum.
Sulphuric acid.
Ergot,
Opium,
Jefferis, David Strode,
Jennings, Isaac Astor,
Johns, Frank James,
Pennsylvania.
Pennsylvania.
Pennsylvania.
New Jersey.
Pennsylvania.
New Jersey.
Pennsvlvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Arkansas.
New Jersey.
Pennsylvania.
Laughlin, Albert Russell,
Lenhart, linos Samuel,
Levan, Walter,
Lewis, Daniel William,
Liebert, Charles Frederick, Concentrated infusions,
I^ngshaw, Thomas I-Hmer, Poisons and their antidotes
Luhr, Frederick A.,
Lukens, Charles Baker,
McGehee, Hanford Bell,
McNeil, Thomas Hunter,
Matusow, Harry,
Metzlcr, Claude Dallas,
Morgan, Clayton ICdward,
Mueller, Charles August,
Nel)el, Charles William,
Parry, I'dward,
Parry, William Hough,
I'earce, Samuel Rol>crt,
Peiffer, Charles Oscar,
Praul, Walter I'rancis,
Cascara sagrada.
Hydrogen dioxide,
Ointments,
Kola ,
Kalmia latifolia,
/belladonna,
Adulteration,
Abstracts,
Ointments and cerates.
Powdered extract of liiorue.
Medicated waters.
Camphor,
Acacia,
Rheum,
Punt, Arnold Anthony Joseph, Density of solutions,
Reese, John Bull, Cinchona,
Riebcn. Ernest, Stramonium,
Virginia.
Pennsylvania.
Ohio.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Virginia.
Pennsylvania.
Russia
Pennsvlvania-
Massachusetts-
Pennsylvania.
Pennsylvania.
Wales.
Pennsylvania.
New Jersey.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsvlvania.
274
Commencement Exercises,
f Am. Jour. Pharm.
1. May, 1897.
Xamf.
Roth, Fraus Jobau
Seipel, Harry Bertram,
Smiley, Laura Marguerite,
Stommel, Henry Aloysius,
Streeper, Austin,
Tobias, Isaac Herbert,
Troxell, John Isaac Peter,
Weitzel, Sue C,
Subject of Thesis.
Arsenic and its compounds ,
Zingiber^
Podophyllum,
Liquorice in pharmacy,
Cinchona barks,
Preservative for syrup of ferrous
iodide.
Ergot,
Veratrum viride,
Wentzler Hartman Gotthard, Percolation of every tincture of
U.S.P,
Wetzel, Samuel, Belladonna,
Wilson, Oliver Fawcett, Solid extracts by acetic acid.
Winger, John Bowman, Gelatin capsules.
stale.
Sweden.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Ohio.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
Pennsylvania.
STATES AND COUNTRIES REPRESENTED BY THE GRADUATING CI^ASS.
Arkansas i Pennsylvania ... 58 Virginia 2
Massachusetts i Russia i Wales, i
New Jersey 4 Sweden i —
Ohio 3 Texas i Total, 73
Special certificates for a two years' course in general, applied and analytical
chemistry were awarded to :
Bertha Leon DeGrafFe, New York.
Freeman Preston Stroup, Pennsylvania.
S. Allen Tucker, Pennsylvania.
W^m. Clements White, Pennsylvania.
The degree of Master in Pharmacy was conferred on the following :
Virgil Coblentz, New York.
John Uri Lloyd, Ohio.
Charles T. George, Pennsylvania.
Jacob H. Redsecker, Pennsylvania.
Lucius Elmer Sayre, Kansas.
The following members of the class attained the grade of Distinguished :
Albert Sylvester Brumbaugh.
Harry Matusow.
Clayton Edward Morgan,
AWARD OF PRIZES.
The Maisch Memorial Prize of a Zentmayer microscope, offered by the
family of the late Professor Maisch, for original histological work oh American
plants, was awarded to Alphons Peter Breithaupt.
The William B. Webb Memorial Prize, consisting of a gold medal and
certificate, for the highest general average in operative pharmac}', specimens
and committee examinations, offered by Mrs. Rebecca T. Webb, was awarded
to Albert Sylvester Brumbaugh.
The Chemical Prize of $25 in gold, offered by Prof. Samuel P. Sadtler,
for original quantitative analysis, was given to Harry Matusow. The following
'^"■Ma^iS?.^""-} Alumni Association, 27^
graduate received honorable mention in connection therewith : Lawrence
Anthony Kessler.
The American Joirnal of Pharmacy Prize of ^■2^, offered by Prof.
Henry Trimble, for a paper (not intended for a thesis) involving original work
in the Chemical Laboratory, was awarded to Harr^- Matusow.
The John M. Maisch Prize of ^20 in gold, offered by Mr. J. H. Redsecker, of
Lebanon, Pa., for histological knowledge of drugs, was awarded to Claude
Dallas Metzler, with honorable mention of John Phillips Bates and Albert Syl-
vester Brumbaugh.
The Operative Pharmacy Prize of ^25 in gold, offered by Prof. Joseph
P. Remington, for the best examination in op>erative pharmacy, was awarded
to Clayton Hdward Morgan, with honorable mention of the following gradu-
ates : Kuos Samuel Lenhart, Alphons Peter Breithaupt, Oliver 1-awcett Wilson,
Richard Hal Compton and Albert Sylvester Brumbaugh.
The Robinson Chemical Prize of a gold medal and certificate, offered by Mr.
James S. Robinson, of Memphis, Tenn., for the best examination in general
and analytical chemistry, was awarded to Clayton Hdward Morgan.
The valedictory address to the graduating class was delivered by Professor
Joseph P. Remington.
The farewell supper of the professors to the graduating class was given in the
Museum of the College, Tuesday evening, April 13th. The officers and trustees
of the College were present, together with some other invited guests. Professor
Remington, as Dean of the Faculty, was master of ceremonies, and after the
)netiu was disposed of speeches were made by the President of tlie College,
members of the faculty, some of the trustees, members ol the class and invited
guests.
ALUMNI ASSOCIATION OF THE PHILADELPHIA
COLLEGE OF PHARMACY.
The Thirty-third Annual Meeting of the Alumni Association of the Phila-
delphia College of Pharmacy convened in the Auditorium of the College Build-
ing, 145 North Tenth Street, on Monday afternoon, April 12, 1S97.
President Dr. J. Louis D. Morison, '88, presided, and called the meeting to
order at 2.30 p.m., 22 members being present.
The President read his address, in which he said : "With the close of the
exercises attending the reception to the seventy-sixth graduating class lo night,
we shall have rounded out nearly a third of a century of existence as an active
organization ; and while the past year has not shown any very conspicuous evi-
tlences of activity beyond that of mere routine work, yet I am happy to say we
are still quite healthy. Notwithstanding the fact that there has been observcil
at times slight symptoms of inertia of the interest in the work of the Association
which, during the past year has, at times, seemed to flag, I am by no means con-
vince<l that she is, therefore, losing her vitality as an organization. " I le advised
the infusion of more new blood into her veins by every member giving to the
.Association a more lively interest, and he did not share with some lh«- n
that because the .Association has relinquished its interests in the <Jni//<
therefore, no important work to do. On the contrary, he felt there never was
a time in its history when its field for work was larger and more full of promise
2;r) Alumni Association. {^'^ii^ylmi':''^-
than it is to-day, and the advent of the session of 1897-98 will see our College
doors thrown open to receive for the first time in her history three distinct
classes.
He recommended the publishing of the A1.UMNI Report twelve times a year,
and believed the question was already uppermost in the minds of very many of
the active members, and urged the advisability of giving to this important mat-
ter early and earnest consideration.
He also advised the holding of the Alumni Social Meetings in the future in
the evenings instead of the afternoons, as heretofore.
In closing, he expressed what he believed to be the sense of the meeting, and
that was the profound sorrow felt by all at the death of Prof. Edson S. Bastin.
" By his untimely departure we sustain the loss of an honored member and the
College a valued and distinguished teacher ; and while we lament the passing
away of Edson S. Bastin, we, at the same titne, rejoice that it was our great
privilege to have had him in Our midst, for, by his genius and indomitable
energy, there has been added to our College a microscopical laboratory second
to none in any teaching institution in the country— a work that will ever remain
a glorious monument to his memory.
The Secretary, Wm. E. Krewson, '69, presented his seventeenth annual
report as Secretary, in which he reviewed the work of the Association for the
past year, but regretted that the Association had not been more active.
During the year sixty-five members have been added, seven who paid the
required fee and fifty-eight who were members of the College Review Quiz
Classes.
The membership now numbers 2,749, after deducting those who died during
the year, making a net gain of thirty-nine new members for the year.
The report of the Memorial Committee showed that twenty-six of the active
members had died during the year ; also eleven of our graduates who were not
active members.
The Secretary also reported that two of our honorary members had died, viz :
First Vice-President Robert Shoemaker and Prof. Edson S. Bastin.
Twenty of the members had procured the Alumni badges during the year,
making a total of 285 members who had procured the badge.
The Secretary suggested the dispensing of the Social Meetings altogether
or the holding them in the evenings ; also to petition the Committee on Prop-
erty of the Board of Trustees to have the College Museum open every day for
the use of the students and pharmacists who might wish to avail themselves of
visiting it, and have a suitable person in charge to care for the room and its
valuable collections.
He also suggested the publishing of the Alumni Report each month in
the year.
The Treasurer, Wm. Lincoln Cliffe, '84, reported that he had received from
all sources during the year 12,658.83, which, added to the balance in the treas-
ury at the commencement of the year, made a total of $2,925.77. The disburse-
ments amounted to $2,849.37, leaving a balance in the treasury of I76.40.
John Tri Lloyd, of Cincinnati, O.; Dr. Edward Robinson Squibb, of Brook-
lyn, N. Y., and Dr. Chas. Rice, of New York City, were unanimously elected
as liDuorary members of the Alumni Association.
^'"Ma?!"*!^?*'™} Alumni Association. 27J
The following officers were elected for the ensuing year, vi/
President, Harry L. Stiles, 'S5 ; First Vice-President, James L. I'cirry, '91 ;
Second Vice-President, F. Wm. K. Stedem, '82 ; Treasurer, Wm. Lincoln
Cliffe, '84 ; Secretary, Wm. ¥,. Krewson, '69 ; Corresponding Secretary, Theo-
dore Campbell, '93. Board of Directors, for three years : Henry Trimble, '76 ;
David H. Ross, '78; Wm. N. Stem, '73 ; Dr. J. Louis D. Morison, "88.
John H. Hahn, '81, was elected to fill the vacancy of two years caused by the
election of Theodore Campbell, '93, as Corresponding Secretary. The present
Recording Secretary', Wm. E. Krewson, was re-elected for the eighteenth time.
The Thirty-third Annual Reception to the seventy -sixth graduating class was
held on the evening of the same day in the College Auditorium, and was one of
the most successful ever held. The hall was beautifully decorated with the
College colors and the American flag.
An interesting concert programme was rendered by Bastert's Parlor Orchestra.
The President, Dr. J. Louis D. Morison, presided, and made a few introductory
remarks and welcomed the new members.
The Secretary called the roll of those elected during the year.
The annual class oration was delivered by Howard Ovid Hildebrand of York,
Pa.
The reciting of the poem dedicated to the seventy-sixth graduating class was
rendered by Samuel R. Godshall, of Soudertown, Pa.
Samuel Clarence Clapp. Jr., of Milton, Pa., gave the history of the Class of
1897, and Harry Lewis Horst, of Lock Haven, Pa., foretold the future of the
Class of 1S97.
The Alumni gold medal was presented to Clayton Edward Morgan, of Phila-
delphia, Pa., a son of our fellow member of the Alumni Association, Frank V..
Morgan, of the Class of '81 ; and it was presented in a very pleasing manner
by Dr. Clement B. Lowe, '84. The eight prize certificates for the highest
general average in each of the branches were awarded to the following
students, viz. :
CERTIFICATES.
Pharmacy —John Phillips Bates, Mansfield, Pa.
Chemistry — Walter Francis Praul, Philadelphia, Pa.
Materia Medica — Harry Matusow, Minsk, Russia.
General Pharmacy (Committee)— Samuel Robert Pearce, Manasquan. N. J.
Operative Pharmacy — Oliver Fawcett Wilson, Pittsburg, Pa.
Analytical Chemistry — .Mbert Sylvester Bruml)augh, Mansfield. ().
Pharmacognosy (Specimens) — Claude Dallas Mct/.ler, Harrisonville, Pa.
Microscopy (Vegetable Histology i -Miss I^ura Marguerite Smiley, Philadel
phia. Pa.
The Testimonial Prize certificates to the undergraduates receiving the high-
est general averages in the first- and second-year class examinations were
awarded to Mclvin William Bamford, of the first-year class, of Reading. Pa .
and to George Carll Keen, of Vinelaiid, N. J., of the second year class.
The Lust named certificate was awarded for the first time this year, it l>cing
the first examination for second course slmlenls under the new curriculum.
W. E. K.
278 Minutes of College Meeting. {
Am. Jour. Pharin.
May, 1897.
MINUTES OF THE ANNUAL MEETING OF THE
COLLEGE.
The aunual meeting of the members of the College was held March 29, 1897.
Wm. J. Jenks, Second Vice-President, presided. Xhe minutes of the meetings of
the Board of Trustees for January, February and March were read and adopted.
The next in order was the presentation of the annual reports of officers and
permanent committees.
The following was submitted by the Editor of the American Journai, of
Pharmacy:
This report covers the issues from April i, 1896, to March i, 1897, inclusive.
During that time there have been published 708 pages of reading matter, an
increase over that reported last year of 66 pages ; the average for each of the
twelve numbers being 59 pages against an average of 53>^ pages last year.
This is the greatest number of pages ever issued by the Journai^ in one year.
The number of original papers published during the year was 83, an increase
of nine over last year ; these occupied 397 pages, against 374, 297 and 159 in
each of the immediately preceding years. These papers were prepared
expressly for the Journal, and the number given does not include those read
before other societies, abstracts, translations or editorials.
The number of authors contributing were 51, of whom i6 were members of
the College and 35 were non-members.
Illustrations were published in every number of the Journal, and amounted
to a total of 89 during the year, making an average of 7*4 for each issue, against
a total of 76 last year, averaging 63 for each issue.
No difficulty has been experienced during the year in securing original mat-
ter for publication; in fact the more serious question has been, how to utilize
all that is offered without considerably enlarging the size of the Journal.
The latter alternative may be better considered in connection with the Report of
the Committee on Publication,
The Publication Committee reported the regular issue of the Journal
during the year. There was a gain in the number of new subscribers, and the
character of these was such as to give decided encouragement to the committee.
The financial part of the report was likewise gratifying in character.
The following was presented by the Librarian :
Philadelphia, March 29, 1897.
The Librarian respectfully reports that, during the past year, there have been
added to the library 440 volumes, besides the various periodicals which are
received in exchange for the American Journal of Pharmacy. There
has been expended I430.71 for books, and for binding, $68.90.
The library has been consulted by very many of our students, and by sev-
eral parties who were referred to our books for information not to be found
elsewhere.
T. S. WiEGAND, Librarian.
The Curator submitted the following :
Philadelphia, March 29, 1897,
Philadelphia College of Pharmacy.
Gentlkmen :— Your Curator would respectfully report that the Museum is
in a good condition and has received a number of valuable accessions during
^"■.Miy'iS?*'"'} Pharmaceutical Meeting. 279
the year. Among those who contributed were Prof. J. W. Tourney, of the
University of Arizona ; Mr. J. H. Maiden, of Sydney, New South Wales ; Prof.
Alfonso Herrera, of Mexico; Mr. J. Bosisto, of Melbourne, Australia, and Mr.
\\. M. Holmes, of the Pharmaceutical Society of Great Britain.
The need exists for more shelf room in the Museum, and this will be imper-
atively required, if a certain promised collection of drug products — which is
extensive and valuable — is secured.
There is another matter that should be referred to. While the College is
rich in its splendid herbarium, in its collection of plants and plant-products,
in its collection of chemical and pharmaceutical products, it lacks one thing,
and that is a collection of minerals representing the origin of the elements
and of the inorganic chemical compounds — not a geological collection, but a
collection of raw material — so to speak — that will exhibit to the pharmaceu-
tical student the primary source of his elements and inorganic chemical
compounds. Such a collection need not be very expensive, and would add
much to the value of the Museum. Your Curator would therefore respectfully
suggest that, as soon as the condition of the treasury will permit, that such
a collection be bought. I am,
Yours respectfully,
J. W. England, Curator.
The various reports having been presented and accepted, the next matter of
business was the annual election of officers. The death of Mr. Robert Shoe-
maker having left void the office of First Vice-President, the order of succes-
sion was accorded to Mr. William J. Jenks, Second Vice-President, and he was
thereupon elected to the position made vacant by Mr. Shoemaker's death. Mr.
Howard B. French having been elected to succeed Mr. Jenks as Second Vice-
President, the total number of officers elected was as follows :
President, Charles Bullock ; First Vice-President, William J. Jenks ; Second
Vice-President, Howard B. French; Treasurer, James T. vShinn; Corresponding
Secretary, Dr. A. W. Miller ; Recording Secretary, William H. Thomj)son ;
Librarian, Thos. S. Wiegand ; Curator, Jos. W. luigland ; Editor, Prof. Henry
Trimble; Publication Committee, Henry X. Rittenhouse, et. al., Editor H.
Trimble, ex-otf'icio . Trustees for Three Years, Wallace Procter, Gustavus Pile.
W. Nelson Stem ; Trustees for Unexpired Terms, F. W. F:. Stedem, Richard M.
Shoemaker.
.\s the annual meeting of the American Medicil Associatioti will be held in
Philadelphia in June, Professor Remington moved that an invitation be ex-
tended to the Association to hold the sessions of the section on Materia Medica
al this College, and it was so ordered.
On motion, the meeting adjourne<l.
Wii.i.i AM B. Thompson, Sfcrctaty.
MINUTES OF THE PHARMACEUTICAL MEETING.
Pnii,Ai)Ki,i'HlA, April 20, 1897.
The regular Pharmaceutical Meeting of the present series was held in the
Museum of the College at 3.30 p.m. Dr. C. B. Ix>we presided. The minutes
of the previous meeting were allowed to aland as published.
28o Pharmaceutical Meeting, {^^'^i^^y'Jm''^-
The first paper presented was on " Observations on Some Recent Suggestions
Concerning Ointment of Mercuric Nitrate," by Charles H. lyaWall. This
paper furnished the occasion for an interesting discussion, during which several
important practical points were brought out.
In reference to the permanence of Citrine ointment, Mr. F. W. E. Stedem
said that he had kept it for more than six months without any apparent
change having taken place. He also remarked that by thorough oxidation of
the oil previous to the addition of the mercuric nitrate solution, granulation,
which so often occurs, was prevented.
Mr. LaWall believed that the variability in quality of this ointment was
largely due to difference in manipulation. He also spoke in reference to its
keeping quality, and said that this property was enhanced by heating the
mixture after addition of the mercuric nitrate solution, until effervescence
ceased.
The next paper, which was on a comparative analysis of the root, rhizome
and stem of "Gelsemium," by L. E. Sayre, was read by T. S. Wiegand.
The results showed that the constituents upon which the therapeutic value
of the drug depends were not present in the stem, and the author, there-
fore, concluded that an admixture of this part of the plant must reduce the
value of the drug.
With reference to the use of gelsemium as a remedial agent, Mr. W. L. Cliffe
said that other drugs possessing similar properties appeared to be more fre-
quently prescribed.
Dr. Lowe considered it valuable in cases of facial neuralgia, but did not favor
its use where aconite was indicated.
An interesting contribution on "The Presence of Starch and Strontium Sul-
phate in Opium and their Influence on Assaying," prepared by Lyman F.
Kebler and Charles H. LaWall, was read by the former.
The authors stated that starch had been found in opium in a number of
instances, they themselves having found wheat starch in opium assayed during
the past two years. The amount found by them varied from a trace to 8 per
cent. But as this substance does not influence the results in assaying they
(juestioned whether or not it could be regarded as an adulterant in the true
sense of the word, since the only requirement for opium is that it shall contain
a certain amount of morphine.
A matter for more serious consideration was the presence of strontium sul-
phate in opium, which substance, even in the most carefully conducted assays,
according to the U.S. P. method, was found to increase the percentage of
crude morphine.
For correcting the results the authors recommeded the ash method as prob-
ably being the best, considering the present impurities in opium.
In addition to the consideration of the papers, a number of subjects possess-
ing particular interest for the retail pharmacist were presented for discussion,
and altogether the meeting was one of the most profitable of the present series.
On motion, the meeting adjourned.
Thos. S. Wiegand,
Registrar.
THE AMERICAN
JOURNAL OF PHARMACY
JUNE, iSgj,
THE ROOT OF PHYTOLACCA DECANDRA.
A Contribution to the Knowledge of its Chemical Constituents.
PART II.
By George B. Frankfortek and Francis Ramaley.
This plant was recorded as emetic by Griffith/ in 1833, and as
cathartic by Allen- the following year. The latter writer remarks
that it is difficult to administer without producing emesis, and that
large doses are followed by narcotic symptoms.
The earliest record of chemical investigation, fourd by the writers,
that would seem to be of present interest, is by C. Reichel.^ He
studied the pharmacology, therapeutical properties and chemical
composition of the root of Phytolacca drastica, a Chilean species,
but related to our own. Of organic substances there were found :
resin, wax, coloring matter, proteids and malates.
P2. Donelly,^ in 1844, published an analysis of Phytolacca
decandra. This is interesting because it is the first analysis of
which any record could be found. The following is a summary of
the results :
^Griffith, R. E. On the Vegetable Kmctics of the United States. Joi k.
rini.A. Com., of Pharm.,4, 276, 1S33.
'All^n, John C. Remarks on the Vegetal)le Cathartics of the I'uited Stairs.
Jour. Phila. Coix. of Pharm., 5, 205, 1834.
^Keichel, C. Phytolacca Drastica. Chnn. Centrbl., b&i, 1836.
^Donelly, E. On Phytolacca Decandra. Am. Joi r. Piiarm., 0. 165, 1S44.
(28l)
2Z2 Root of Phytolacca Decandra. { '"/une'iSr'"-
Woody fibre 66*500
Starch 20*000
Tannin, gum and saccharine matter 5 "375
Gum resin 2*625
Potassa • 2'ooo
Iron "875
Fixed oil "500
Silica and carbonaceous matter 1 'ooo
98-875
In the Chem. Centrbl. for 1849 a short note states that, accord-
ing to Landerer,^ all parts of the Phytolacca decandra, when fresh,
have an emetic and purgative effect, which disappears on cooking.
In Greece the young shoots and leaves are eaten as greens. They
are employed as a vermifuge.
An account by C. H. Cressler^ records the fact that the inhalation
of the powdered root produces soreness of the throat and chest,
severe coughing and inflammation of the eyes.
Terreil,' in 1880, described phytolaccic acid which he obtained
from the fruit of P. decandra and P. Kaempferi. The acid is uncrys-
tallizable and dries without alteration. It forms a translucent,
gummy syrup, yellow-brown in color,. not deliquescent; easily solu-
ble in water and alcohol, scarcely in ether. The watery solution
has an acid reaction. It can be heated to boiling without change,
but on addition of hydrochloric or sulphuric acid, is converted into
a gelatinous mass, easily soluble in weak alkalies, ammonia, etc.
Balland examined the berries of P. dioica. He determined the
percentages of water, wax, sugar, gum, etc. There was 2 6 per
cent, of an organic undetermined acid, which was thought to be
similar to the phytolaccic acid of Terreil.
\Vm. F. Pape^ found in the root of P. decandra a dark-brown fixed
oil, tannin, gum, starch, sugar, resin, organic acid and coloring mat-
ter. The ash contained potassium, iron, calcium, chlorine, sulphuric
and phosphoric acids. Crystals of potassium nitrate were obtained
from an alcoholic extract of the root. Tests with iodo-hydrargyrate
^Landerer. (Quoted in an editorial note.) Phytolacca Decandra als Heil-
iiiittel. Chcm. CentrbL, 831, 1849.
''Cressler, Chas. H. Poke Root. Poisonous eflfects from inhalation of the
powder. Am. Jour. Phakm., 47. 196, 1875.
"^Terreil, A. Compies rendus, 91, S56-58, 1880.
"Pape Wm. F. On Phytolaccae Radix. Am. Jour. Pharm., 53. 597, 1881.
^'"w.-rsS:""*^} Root of Phytolacca Decandra. 283
of potassium and with iodine solutions indicated the probable pres-
ence of an alkaloid.
\V. Cramer' found the juice of the berries to contain gum, sugar,
malic acid and coloring matters.
An elaborate investigation of the root was made by Edmond
Preston, Jr.^" He found traces of hydrochloric, phosphoric and sul-
phuric acids, with 5-5 per cent, of potassium hydroxide. A small
amount of free acid was found; this had the characteristic odor of
the root ; its potassium salt was decomposed with effervescence on
treatment with acids. From the purified aqueous extract of the
root there was obtained a small quantity of nearly white crystals,
which in solution gave precipitates with the usual alkaloidal rea-
gents. The crystals were entirely dissipated when heated on plat-
inum foil, and when treated with strong mineral acids simply dis-
solved, giving no characteristic color test. "An alcoholic solution
of the crystals neutralized with dilute hydrochloric acid on concen-
tration yielded nearly colorless acicular crystals, moderately soluble
in alcohol, quite soluble in water and possessing a strong, acrid
taste." It was concluded that the crystals were those of an alka-
loid and of its hydrochloride. For this alkaloid the name •• phyto-
laccine " was proposed.
Coscera^' found that tender shoots and leaves show slight, and
the roots more, toxic qualities. The same parts of the plant, at time
of fruiting, have a marked emetic and purgative action. He
obtained what he considered a glucoside by the following means :
The root was extracted by 90 per cent, alcohol ; the filtrate, on
cooling, showed the substance as a white powder, insoluble in
ether, scarcely in absolute alcohol, somewhat in 50 per cent, alcohol,
readily in water. It was also soluble in dilute acids. The substance
reduced alkaline copper sulphate only after heating with dilute sul-
phuric acid.
In an alcoholic extract of the root ** a fen- cr)stals " were found by
Partee," but these were not investigated. He also obtained some
*Cramer, Walter. Phytolacca Bacctt. Am. Jour. Piiakm.. a:». 59H, 1H81.
^'^Prfslon, luimomi, Jr. The Root of Phytolacca Decandra, I.imu'. Am. Toir.
Pharm., fto, 567, 1884.
^^Coscfra, .\. Heitriige /ur cliemische-toxischc-K-cntmss von I'hylolacca
nccan<lra. L. Review in Chem. C^ntrhl., pp. 576, 643, 808, 18S7.
^^/*arlce, H'fu. .1. Analysis of Poke Root. Am. JoiR. Pharm.. 00. 123,
JSSS.
Am. Jour. Pharn .
284 Root of Phytolacca Decandra. {^""jSeriS?"
acicular crystals from the absolute alcohol extract. The residue
from the ether extract contained a wax, melting at 109°. The other
substances found were : gum, glucose and tannin, with indications
of a possible glucoside.
The investigations of Haverland^^ were directed to the fruit of
Phytolacca. This investigator found phytolaccic acid, with small
quantities of acetic, citric and tartaric acids. Phytolaccin, which he
found in seeds on analysis, was found to be a non-nitrogenous body
related to the tannins, and containing 65 95 per cent, of carbon,
28-15 per cent, of hydrogen, and 5-9 per cent, of oxygen.
A substance obtained from the root, and suggested as being a
saponin, was described by Trimble^^ in 1893. It was precipitated
by water from the alcoholic percolate. Solutions frothed on
shaking. The taste was slightly bitter and acrid. Analysis indi-
cated the formula ^^^^f^2%'
The latest contribution to a knowledge of the chemical properties
of the root is by one^^ of the present authors. A complete quantita-
tive analysis of the ash was made, and the gases given off during
destructive distillation of the root were investigated. As the results
have been so lately published it is unnecessary to summarize them here.
In the foregoing account reference has been made to investiga-
tions on the fruit of Phytolacca only when it seemed that these
might throw light upon the constituents of the root. It will be
sufficient here to mention the investigations of Bischoff^^ and
Macagno/' which were directed to the coloring matter of the fruit,
and those of Claussen^^ on the active principle of the seed ; and of
Eberhardt,^^ who examined the root but made no quantitative analy-
sis and whose work was mostly corroborative of previous results.
^^Haverland, Franz. Beitrage zur Kentniss der in den Friichten von Phyto-
lacca Decandra euthaltenen Bestandtheile. Inaug. Dissertation. Erlaugen. 1892.
'♦ Trimble, Henry. A Proximate Principle from Phytolacca Decandra. Am.
Jour. Pharm., 05, 273, 1893.
^■'Frankforter, Geo. B. A Chemical Study of Phytolacca Decandra. Am.
Jour. Pharm., go, 134, 1897.
^^Bischojf.H. Inaug. Dissertation. Tiibingen, 1876. Ueber den Farbstoffe, etc.
Ivandwirthsch. Versuchsst., 33, 456-61, 1878.
^^Macagno.J. In atti R. Stazione chemico-agraria di Palermo, 47, 1886.
Chem. Centrbl., 123, 1886.
'"^Claussen. In Husemann-Hilger's " Pflanzenstoffe," p. 531, 1882.
^^Eberhardt, E. G. Chemical Examination of Poke Root. Lilly's Bulletin^
No. 23, p. 3. 1893.
'""•/unl'iSr'"} Koot of Phytolacca Dccandra. 285
It is to be noted that the •' phytolaccin " of Claussen was
described five years before the '♦ phytolaccine " of Preston. Should
the latter's discovery be confirmed, it would be necessary to rename
the substance described by him.
The authors desire, at this point, to express their thanks to Mr.
C. P. Berkey, instructor in mineralogy at this University, for his
careful examination of the sugar crystals, and to Dr. Wm. Trelease
and Mr. John S. Wright, for assistance in securing the literature on
the subject.
RECORD OF INVESTIGATIONS.
The work of investigation was begun in October, 1895, and has
been carried on more or less continuously since that time. Two
proximate analyses were made. Besides these, various quantities of
the root were extracted in different ways for certain of the constituents.
Three partial analyses were also made. Air-dried material was
used. This was obtained from three different wholesale houses and
personally garbeled before grinding. The latter process is an
extremely unpleasant task when done with a hand-mill, for the
inhalation of the dust produces, as has been noted in the historical
summary, most severe inflammation of the membranes of the nose
and throat.
Most of the substances previously reported were found in the
present investigation. Preston's phytolaccine was, however, not
obtained, nor could the presence of tannin or of chlorides be shown.
The crystallized sugar which was found is undoubtedly the " glu-
coside " of Coscera and the *• few crystals " of Partee. The " acicular
crystals" of the latter were probably potassium nitrate. The large
amount of potassium in the root is easily recognized. Its character-
istic flame is observed when a splinter of the root is held in the
Hunsen flime.
The percentages extracted by the various solvents were as follows :
Petroleum ether . . '627
Sulphuric ether . . 'loo
Absolute alcohol . 1 1 734
Cold water . >^^32
Dilute sulphuric acid . ^-'^'i^
Dilute alkali 4744
kemovec! by potasftiuin hypohroiniie . r2o6
Residue of cellulose .
100*407
286 Root of Phytolacca Decandra. {^'"•/un"e':-i897"'"'
Great care was taken that the extraction by each solvent should
be complete. The petroleum ether extract was of light amber tint ;
the ether extract was of a burnt sienna color, and probably contained
little else than coloring matter. All the other extracts were of
about the same rich reddish-brown tinge. The water extract showed
an acid reaction.
A summary of the analyses may be given in tabulated form.
When two or more determinations have been made the results have
been averaged :
Oil and wax '627
Resin I'oio
Non-reducing sugar calculated as sucrose 9*457
Reducing sugar calculated as dextrose *435
Proteids i*944
Amido-compounds (calculated as asparagin) 1*634
Free acid calculated as formic '360
Combined organic acid calculated as potassium formate .... 1*891
Starch 11*677
Calcium oxalate 6*225
Nitrates calculated as potassium nitrate 2*408
Cellulose 16*378
Lignin, etc 3*206
Gum, coloring matter, ash, moisture and undetermined .... 42*748
100 000
The oil is non-volatile, of a brownish color and readily saponifi-
able with cold, fixed alkalies. The wax is light yellow in color. It
was not studied. The resin found in the alcohol extract was dark
brown in color, and of a very bitter taste.
The sugar can only be crystallized with great difficulty and best
from absolute alcohol, as the various other substances soluble in
alcohols of less concentration seem to interfere with the crystalli-
zation. In one analysis 26 per cent, of crystallized sugar was
obtained. It can generally be had only in much smaller quantities.
This crystallized sugar is completely soluble in large excess of
hot absolute alcohol. From such a solution it is sometimes obtained
in a very fine crystalline powder. From thick, syrupy water solu-
tions prismatic crystals can, with difficulty, be obtained. These
crystals are clear, colorless, transparent prisms, belonging to the
orthorhombic system. Their most common forms are represented
in the accompanying figure. The longer lateral axis is in nearly all
cases cut by pinnacoid planes, so that the crystals, when seen from
Am. Joar. Pharm.
June. 1897.
} Root of Phytolacca Decandra,
287
above, are almost perfectly hexagonal in outline. The lengths of
the lateral axes are i and -767. Since only prismatic crystals were
found, the length of the vertical axis could not be determined.
The commonest forms are shown in the accompanying figure.
The sugar began to melt at 146°, and was completely melted at
153°. It boiled at from 180° to 185°, turning brown. Warmed
with sodium hydroxid solution, it turned yellow. When warmed
with concentrated sulphuric acid, charring did not take place, though
there was a brown coloration.
r<-
>
^:
>1
»
^
Sugar Cry.stals from Phytolacca Uecaiulra.
Polarization of a clear solution showed 87-6 per cent, sucrose.
The reaction with Fehling's solution indicated 4 4 per cent, anhydrous
dextrose. Polarization was not affected by warming the solution nor
by allowing it to stand in the tube for some hours.
Proteids were determined in the alkali extract by KJcldahl's
method.
Amido-compounds were determined by the use of potassium hy-
pobromite, the nitrogen evolved measured and calculated to aspara-
gin.
The water extract of the root had a decidedly acid reaction. Two
288 Root of Phytolacca Decandra, {
Am. Jour. Pharm.
June, 1897.
grammes of the drug were extracted with 200 c.c. of cold water,
and the filtered solution titrated against a standard alkali solution.
By this means the percentage of free acid, calculated as formic acid,
was determined.
On distilling a 90 per cent, alcohol extract of the root a small
quantity of the acid was obtained. This was exactly neutralized
with fixed alkali and brought to dryness on the water bath. When
the alkali was added the solution became light yellowish in color.
The dry salt was distilled with phosphoric acid, to obtain the organic
acid in the free state. It distilled between 98° and 100°.
The acid responded to the ferric chloride test for formic acid.
Neutralized solutions slowly reduced silver nitrate, but without the
appearance of a mirror. The potassium salt crystallized in beautiful
stellate tufts. The free acid was found to be soluble in water and
weak alcohols, somewhat soluble in 95 per cent, alcohol, and almost
insoluble in absolute alcohol. It was insoluble in ether, benzene,
petroleum ether, etc. The taste and smell of the acid were similar to
those of formic acid, though not quite identical. It is, however,
possible that impurities were present.
When the dry root was distilled with steam the distillate had
only a very slight acid reaction. This may, perhaps, be accounted
for on the supposition that the acid was, in this case, neutralized by
carbonates in the root with which it came in contact in a not too
dilute form. When the root was distilled with dilute sulphuric acid
the free acid was readily obtained.
Careful examination of aqueous and alcoholic extracts of the root
failed to reveal even traces of the following acids : acetic, citric,
malic, tartaric, benzoic and salicylic. The first four named acids
were tested for with particular care, since they have been found by
various investigators in the fruit of the same plant. Although cal-
cium oxalate was found to the extent of 6 per cent., no free oxalic
acid or soluble oxalates were discovered. Phytolaccic acid may or
may not be present. From the descriptions given by its discoverer
it would appear that the acid he described was by no means
pure.
It has seemed proper to calculate the acids in combination as
potassium salts, since such a large amount of potassium is present.
It is certainly reasonable to suppose that the salts exist as such in
the root.
'"""juii?!^"'"} Koot of Phytolacca Decandra. 289
A portion of the dilute sulphuric acid extract was heated in a
closed tube at 120°. The percentage of glucose was determined,
and from this the amount of starch calculated.
Potassium nitrate crystallized from the alcohol extracts. Under
the most favorable conditions a little less than i per cent, was ob-
tained by careful crystallization.
After extracting the root with 90 per cent, and with 60 per cent,
alcohol, an extract made with cold water was, after drying, 6-6 per
cent, by weight of the dry root. The extract has a strong cathartic
action, this property being tested by two persons. It is to be noted
that the 95 per cent, and 60 per cent, extracts also possessed the
same property, but to a less extent. These extracts, when strongly
heated, emit an odor of popping corn.
A quantity of the root, first exhausted with water, was percolated
with 95 per cent, alcohol. The tinctures frothed on boiling. On
cooling there was deposited a whitish powder, the particles usually
somewhat spherical in shape, each one with a short appendage.
This substance is nearly insoluble in water, but rather soluble in
alcohol.' This may be the proximate principle described by Trim-
ble. Only a small quantity was obtained. It has not been further
examined.
Extended investigations were made to establish the presence of
an alkaloid or glucoside. Although the examination was quite thor-
ough, no substances of this nature were isolated. Further investi-
gations will, however, be made as soon as fresh material is obtain-
able.
Tests were made for the alkaloids and the glucosides commonly
occurring in plants, but with negative results in every case. \'ari-
ous methods of extraction were employed; e.g., treatment of the
aqueous extract with alcohol and with metliyl and amyl alcohol ;
also with acidulated water and acidulated alcohols.
In purified aqueous extracts, precipitates were thrown down with
some of the usual alkaloidal reagents, but not with picric acid or
phosphomolybdic acid.
Attempts were made at every step to obtain the substance in
crystalline form, but always without success. Purified extracts, acid
and alkaline, were shaken with various solvents, as ethyl acetate,
chloroform, ether, petroleum ether, and benzol. In many cases
tests applied to the dissolved residues indicated the presence of an
290 Verba Del Polio. {'^'^i^^l^.T'^-
alkaloid from both the acid and alkaline solutions. From this we
are led to infer that the alkaloid — if one and only one be present —
exists in the root as a salt, and also in its basic condition.
University of Minnesota, Minneapolis, Minn.
VERBA DEL POLLO.
By Ai^fonso Herrera, of Mexico.
Several plants of the family Commelinaceae are known in Mexico^
by this name, and are to be found in cold as well as in warm and
temperate regions. They grow on the sandy banks of rivers and
brooks, and flourish from July until September.
Hernandez calls them Matlaliztic prima, secunda, texcocana,.
tercia, asphodelea, and coapatli. According to this author, the Aztecs-
used this plant to cure fevers, headaches, tumors and hemorrhages)
and to give relief in child-birth. The hemostatic properties of the-
Verba del Polio were therefore known to the Indians, but this-
precious plant was forgotten, together with many other good andl
useful products of the conquered country.
Almost three centuries later, Alzate made known to his country-
men the remarkable activity of this plant in stopping the blood from*
wounds, but his efforts were useless, for the plant remained unnoticed
until 1863. at which time we began to read about it in the works of
Hernandez and Alzate ; we repeated the experiments of these illus-
trious authors, induced physicians to use it, and began to seek for
its active principle.
A short time afterwards, Mr. Touraine read the work of Padre
Alzate, and, on trying the efficacy of the drug as a hemostatic, he
met with great success ; the results of his experiments and investi-
gations he laid before the Academia de Medicina de Mexico, on Feb-
ruary 21, 1866; the paper was published in the Gaceta Medica,
Vol. II. He asserted that nobody had studied the plant since
Alzate's time, and he suggested for it the name Tradescantia erecta ;,
the president of the Academy, Dr. Jimenez, observed that we had
attracted his attention to the subject in the year 1863, and its
extract had been applied to a number of patients with success.
Synonyms. — Commelina tuberosa, Linn. Sp. PL Ed. I, page 41 ;.
C. B. Clarke, in D. C. Monogr. Phanerog. HI, page 149 ; Andr. Bot.
Rep., t. 399; Schnizl Iconogr., t. 48. Commelina parviflora, Reichl..
^"■j-iT.iS^"'"'} y^rba Del Polio. 291
Fol. Exot. II, p. 17, t. 142, non Link. Commelina undulata, Lodd.
Bot. Cab , t. 1553, non R. Br.
Matlaliztic, Coapatli, Zoyol, Xochitl, Yerba del Polio, Rosilla.
Habitat. — Valle de Mexico, Orizaba.
Analysis. — The juice obtained by a simple pressure of the fresh
plant has an acid reaction towards litmus paper. We have obtained
some perfectly neutral liquid of a peculiar odor by placing the juice
in a retort and distilling by means of a water bath, then adding to
the bath calcium chloride in several portions, to increase the boiling
temperature, and collecting the different fractions which came over.
When but little juice remained in the retort its odor was found to
have changed, and it possessed a strongly acid reaction ; when this
acid liquid was neutralized with bases, salts were obtained which
were found to be acetates.
Another portion of the juice was heated to 80°, when a precipi-
tate was formed which was found to be vegetable albumin. The
liquid, filtered from the albumin, was concentrated to half its
volume and treated with alcohol 33° Cartier, when a cheesy precipi-
tate separated, which was found to be of an albuminoid nature.
The residual liquid, after separation of this precipitate, was concen-
trated anew to remove alcohol, reduced to a small volume, and set
aside for a while; potassium chloride separated as a result of this
treatment, and on further concentration, more of the same salt sepa-
rated, mixed with e.xtractive matter.
An e.xtract of the juice was obtained by evaporating the latter
on a water-bath. It was partly soluble in water; when treated in
the same manner as the juice, similar compounds were obtained. A
small amount of ammonium acetate was also found in the extract,
due, no doubt, to the pre-existence of acetic acid in the plant, and to
the formation of ammonia from the proteid principle on the applica-
tion of heat.
We obtained also a product neutral to litmus paper — smelling like
the liquid produced by distilling the juice — by distilling the dry
plant with simple water. If distilled with lime it afforded a liquid
smelling like the foregoing, but reacting alkaline towards litmus
paper. On saturating this alkaline liquid with acid an ammonium
salt was obtained.
Ammonia may be obtained even in an ordinary temperature by
wetting the powdered plant and mixing it with lime or the carbon-
292 Verba Del Polio. {^"/une^iSr"'"-
ate of potassium or sodium. The dried plant also yielded chloro-
phyll when treated with ether.
In short, the Verba del Polio contains the following principles :
hi the juice, acetic acid.
Ifi the extract, ammonium acetate, potassium chloride, albumi-
noids, vegetable albumin, chlorophyll, extractive and cellulose.
In his paper about this plant, Padre Alzate owned that he
believed the hemostatic influence of a mucilaginous plant could
never be accounted for. Mr. Touraine proposed to seek and isolate
the active principle. Some four years ago we determined to solve
the problem, and undertook a series of experiments, that were too
long to enumerate, since there are no fixed rules for arriving at an
absolutely correct result, and determining certainly which one of
these principles is the active one.
We can assert from the present moment, with regard to the
extract, that it is not the extractive, chlorophyll, ammonium ace-
tate or vegetable albumin. There remain the potassium chloride
and the proteid principle, though it may be questioned if either of
these has any hemostatic properties. We have seen, however, that
the wet powder of the plant and the solution of the extract are
most active hemostatics, and the analysis points out no principle
worthy of notice in this connection but these two, so that it seems
rational to attribute the hemostatic properties to them.
If it is the proteid principle and potassium chloride which act,
in what manner is it ? The question is rather difficult to solve,
since proteid principles are of a very complex nature, and their
molecules stand in such unstable equilibrium that the slightest
modification in the conditions of their existence suffices to decom-
pose them. Such are the albuminoid principles of Commelina, of
blood, and of animal cells. We have observed in the analytical part
with regard to the Commelina, that an elevation of temperature, the
presence of alkali hydrates or their carbonates suffice to alter it,
heat transforms it into an insoluble principle and a small quantity
of ammonium acetate.
We need say nothing about blood, for its composition and alter-
ability are perfectly well known, except to make the following
quotation from Mialhe : " The three principal liquids of the animal
economy, chyle, lymph and blood, are, when normal, alkaline."
With regard to contractibility of capillary vessels, we will quote
'"'"•/uZ.iS':"'"} ^>^^^ ^'i Polio. 293
from Bcclard's Physiology : *• Pourinfj cold water on the natatory
membrane of a frog, the calibre of its capillary vessels diminishes to
a half or three-quarters of its normal size at least. Common salt
produces the same effect. This contractibility can also be made
evident by acid or diluted alkaline solutions."
Taking all these facts into consideration, we will hazard a theory
which, though in no way invulnerable, might perhaps help us to
explain a physiological fact. Applying on a broken vessel the pow-
der of the plant, in a cataplasm, or a concentrated solution of the
extract, the proteid principle of the herb mixed with the blood
whose alkali reacts upon the former and affords a separation of am-
monia ; this reacts upon the vessels, irritating their tissue and con-
tracting them, as Bcclard observed ; for it constitutes a very dilute
alkaline solution, and has hemostatic properties sufficient to produce
a complete obliteration of the vessels.
Mr. Touraine affirms to have seen this contraction of the vessels
in several physiological experiments, and we have made similar
observations, although not quite so certain of the results.
When we used the powder of the plant or the solution of the
extract, the potassium chloride added its own action to that of the
ammonia, and substituted the sodium chloride, whose action has
been observed by Bcclard.
Internally, Commelina cures metrorrhagia, which fact might be
explained by the aforesaid chemical reactions; the proteid principle
enters the current of the circulation. We will copy Hernandez
according to the text, for it is both elegant and clear, and leaves no
doubt about the latter application we have mentioned. With
regard to the Matlaliztic texcocana, he says : '• Radix discutit
tumores praeter naturam a causa calida ortos, tusa, atque applicata,
aut devorata, duarum drachmarum mensura, humore impetum
cocrcet, sanguinis redundantiam reprimit destunujue refrigerat.'*
Therapeutic Uses. — The most distinguished physicians of Mexico
use the extract of Commelina as a kind of a hemostatic in the treat-
ment of metrorrhagia and hemoptysis, administering it in pills in
the latter case, and in injections in the former. They employ it, too,
as an active remedy against leucorrhcca, and as a general hemostatic
in capillary hemorrhage.
Posology — The extract is to be given in pills of I or 2 grains,
which shall be taken to the number of twenty-four to forty-eight a
294 ^^'^^^ ^^ ^^^'^^- {^"juZ-ifr"'
day. Injections are made by adding from i drachm to i ounce
to a pound of water. In wounds, cataplasms may be made from the
powder of the plant, or a concentrated solution of the extract may
be applied by means of lint.
We copy from the proceedings of the Academia de Medicina de
Mexico, session of February 21, 1866: "■ Dr. Lucia has repeatedly
used Commelina to cure metrorrhagia, and always with success. Dr.
Villagran has also used the extract in injections, the dose being a
drachm to a pound of water, to cure metrorrhagia, and has always
obtained the most satisfactory results. He has lately used it in an
instance of cancer in the stomach, and has attained most unexpected
success. Dr. L, Jimenez has also been fortunate in the use of injec-
tions of extract in two cases of uterine cancer, and in leucorrhoea
accompanied with chlorosis. Dr. Miguel Jimenez has used the ex-
tract since the year 1864, and has made many experiments with the
plant which prove its activity as a hemostatic. The greatest results
are obtained according to this physician by the dose of a drachm in
a pound of water. Its utility is incontestable in uterine cancer, but
it is also useful in other forms of hemorrhage. Dr. M. Jimenez
remembers an instance of hemoptysis in which he was surprised by
the good results obtained with this medicine, for it prolonged the
life of the patient in an unexpected manner. He has also used it to
cure hemorrhoidal flux with success. He has failed, however, in
some other cases of hemoptysis, on account, perhaps, of the patient
vomiting, which prevented the action of the remedy."
RIEGLER'S METHOD FOR ESTIMATING SUGAR IN
URINE.
By Henry C. C. Maisch, Ph.G., Ph.D.
This method, as described on p. 228 of the American Druggist,
estimates the amount of sugar contained in urine indirectly by means
of Fehling's solution. The reaction on which this depends is the
liberation of nitrogen when Fehling's solution is brought in contact
with phenylhydrazine hydrochloride.
The manner of applying this test is to boil the urine and Fehling's
solution, and, after connecting the apparatus, the phenylhydrazine
solution is added. In other words, the balance of the Fehling's
■^"•jun"e"iS^"'"} Sugar in Urine. 295
solution remaining after the reduction with urine, reacts with the
phenylhydrazine hberating the nitrogen.
In theory, and then only with pure solutions, this method for the
•estimation of sugar is good; but I do not consider the method of any
great utility with urine, basing my opinion entirely on theoretical
grounds and experiments carried on with Fehling's solution itself.
In handling a solution as complex as the urine, we must not forget
that there are a number of compounds present, or might be present,
which have more or less of a reducing action on Fehling's solution.
Bodies of this character are uric acid, creatinine, allantoin, nucleoal-
bumin, lactic acid and biliary coloring matters, consequently, all
probable constituents of urine. These compounds, however, are
usually present in such small quantities that their presence becomes
of especial importance where the percentage of sugar is small, and
just in a case of this kind it is of the utmost importance to have a
method which can be used in all cases without fearing that by the
action of the reagent on other constituents of the urine a smiilar
reaction might be brought about. This, to my mind, is the most
serious objection to this method — in fact, to all the methods using
the copper salts.
In my laboratory practice I have repeatedly proven to my own
mind the statement just made in reference to Fehling's solution. I
recall one case especially. The urine was furnished me with the
statement that it showed Fehling's reaction rather strongly. It was
from a lady looking forward to an early confinement, and a careful
examination, with the elimination of all possible errors, was abso-
lutely necessary. I found that the Fehling's test and the Roett-
ger's test were both strongly reduced; but on subjecting the urine to
the action of yeast, no fermentation took place and no difference \\\
specific gravity, as by the Roberts method, was observed. Making
t:xaminations daily, I found that in about three or four days this appar-
ent sugar reaction had entirely disappeared. This lady had been suf-
fering from headache and had used one of the many headache remedies
found in the market at the present time. This "sugar" reaction
was very likely caused by one of the conjugate glycuronic acids.
At the present time I do not depend entirely on Fehling's test or
lk)ettger's test, but run through the principal chemical tests, and in
cases of uncertainty I use the Roberts differential specific rravit\
method for the quantitative estimation of glucose.
296 Strontium in Plants. {^"^/u^n^'if^""'
One of the reactions on which I depend to some extent is that of
Rijbner, and also its modification by Penzoldt; but even here the
question will arise whether or not the same reaction is given by
other compounds. RiJbner uses 3 grammes lead acetate to 10 c.c.
urine, filters, and adds ammonia water until a permanent precipitate
is formed and then warms to about 80° C. The presence of sugar is
indicated by the precipitate becoming pink or red, depending on
the percentage. Penzoldt uses the subacetate of lead in place of the
neutral acetate, and proceeds as in the original reaction.
ON THE OCCURRENCE OF STRONTIUM IN PLANTS.
By Henry Trimbi^e.
Contribution from the Chemical Laboratory of the Philadelphia College of
Pharmacy. No. 166.
Some months ago a number of barks were received from Dr. H.
N. Ridley, of the Botanic Gardens at Singapore. They were
chiefly barks representing the several species of the genus Castan-
opsis in that locality, and two species of oaks. The primary object
in examining these barks was to learn the character of their
tannins, but that is reserved for a later article.
In examining the ash of these barks a slight precipitate was
noticed for strontium in the first one ; this was passed by as
being a small quantity of calcium, which was the most abundant
constituent in the ash. But the ash of other samples also yielded
precipitates indicating strontium, some of them in such quantity
that the precipitate was washed thoroughly, treated with a few
drops of concentrated hydrochloric acid, and the flame test applied ;
the result in every case was a distinct strontium flame. The stron-
tium precipitate was gotten by three methods, viz.: precipitating
with very dilute sulphuric acid, precipitating with an alkaline solu-
tion of potassium chromate, and, finally, by precipitating with solu-
tion of calcium sulphate.
The samples of Castanopsis were from the following : C. Walli-
chiana, C. Curtisii (two samples), C. Javanica, and C. Hulettii. The
oak samples were from Quercus hystrix and Q. discocarpa. The
Quercus hystrix was probably the richest in strontium of all the
samples. None of them contained more than traces of the stron-
tium salt. A sample of our American Castanopsis, C. chrysophylla.
^"•ju°n"e':i^"'"} Strontium in Plants. 297
from California, failed to show a trace of strontium, and yielded
only about one-half the amount of ash that was obtained from the
East India samples. One sample of Rhizophora, from a number
recent!)* received from Sinf^apore, also indicated the presence of
strontium. A letter from Dr. Ridley states that little, if any, stron-
tium occurs in the soil of Singapore.
It is such a natural conclusion that strontium may replace calcium
in plants, that the foregoing statement concerning its existence in
plants may appear almost unnecessary. It was found, however, that
most authors, in speaking of the ash constituents of plants, were
either silent on the subject of strontium, or else referred to the one
case where it has been found in seaweed. Dr. Emil Wolff, in his
Aschcn-Analyscn, among some thousands of results, does not appear
to mention strontium, not even among the seaweeds. Roscoe ^^v:
Schorlemmer {Treatise of Chemistry, Vol. II, Part I, p. 213) state:
" Strontium has also been found in sea water and in the ashes of
Fucus vesiculosis."
Ebermayer {^Pliysiologischc Chemie der Pflanzen, p. 715) mentions
strontium with some other metals as occurring in traces in a few
plants, but he gives no definite information. Sachs {Lectures on the
Physiology of Plants, p. 383) merely states that strontium may
replace calcium in the fungi. Sorauer {A Popular Treatise on the
Physiology of PI ants, \i. 36) calls attention to the fact that strontium
has been discovered in several seaweeds. Goodale {Physiological
Potany^ p. 256) mentions strontium with some other metals as
occurring in Fucus.
Messrs. Kebler and La Wall, in the May number of this Journal,
p. 244, pointed out the presence of strontium in opium. It was
looked on as an adulteration, although we must admit the possi-
bility of it occurring naturally in opium.
It may be that the writer has failed to discover all the literature
relating to this subject, and he is free to admit the possibility of it,
since the literature concerning the ash constituents of plants is very
voluminous. Any information bearing directly on this subject will
be thankfully received.
David Hooper, who has held the post of Quinologist to the Madras Govern-
ment, at Ootacamund, India, for the past twelve and ? half years, has l)eeu
appointe*! to the Curatorship of the Kconomic and Art Sections of the Indian
Museum, Calcutta.
298 Alexandria and India Senna. {^""•/uXifo'^'"'"'
alp:xandria and india senna.
METHOD OF DISTINGUISHING THEM IN POWDER.
By L. E. Sayre,
Member of Research Committee C, Revision Committee of United States
Pharmacopoeia.
The question of distinction and identification of the two sennas,
Alexandria and India, was the subject of a recent preliminary paper
by the author. Since the appearance of this, more careful and elabor-
ate work has been done upon the same subject, the results of which
are embodied in the present article. Some criticisms having been
made upon this early work, due attention will also be paid to the
disputed points in the endeavor to arrive at as truthful conclusions
as possible. To aid in this, a series of photomicrographs have been
carefully made, and are here reproduced. The accuracy of the
drawings may be the subject of dispute, owing to the large personal
factor that enters into their preparation, but the appearances shown
by a photograph admit of no misconstruction, provided they be
truly representative. It is unnecessary to state that in the present
instance all reasonable precautions have been taken to show in a
few reproductions as representative appearances as could be found
in such limited areas. As contributing to a truthful understanding
of the results obtained, a brief outline of the methods employed is
given, and this is followed by the interpretations and conclusions.
While the true character of the tissues has been made the subject
of careful study, the fact has constantly been borne in mind that the
object of the whole matter is to secure a sijnple and accurate test
for senna powders that shall be applicable to the uses of those for
whom it is intended. It has been recognized that no one feature is
found constant throughout the extent of the leaf, and that before
any appearance can be pronounced representative, due care must be
exercised by taking a sufficient number of observations. It is
believed that all precautions have been taken in this investigation^
and that the test proposed will prove reliable and sufficient.
Methods. — The photomicrographs of the epidermis were made
from thin sections cut directly from the surface of the leaf, and sub-
jected to no more treatment than was necessary to mount them in
plain glycerin. The negatives were all made from these sections in
a vertical camera of fixed length, attached to a Van Heurck micro-
Am. Jour. Pharm.
June. 1W7.
Alexandria and India Senna.
299
scope whose optical parts were a Zeiss 8 mm. apochromatic objec-
tive and a No. 2 projection eye-piece. The source of illumination
was the arc light, the crater of which was carefully focussed upon
the object by the condenser. The actual magnification, measured
by projecting the image of a stage micrometer upon the ground
glass of the camera, is 240 diameters. No retouching or other
alterations of the negative have been made. The drawings of parts
.-C
1
Fig. I. India seuna, under side of leaf; a, epidermal cell ; b^ stomata ; r,
hair ; d, hair scar ; e, ncbenzellen.
found in the powder were all made by the camera lucida under like
conditions of preparation and magnification. The amplification
here is 200 diameters.
At the commencement of the work, in order to find some point
of characteristic importance, the parts were thoroughly studied in
their natural relations by means of sections, and the app>caranccs
there observed were then made the object of study in the powder.
300
Alexandria and India Senna. {
Am. Jour. Pharm.
June, 1897.
Commencing in this manner with the ordinary epidermal cells, the
following results were obtained: The size and shape of the epider-
mal cells are extremely variable (see Figs. 6 and 7), and are, as was
stated in the former paper, little to be depended upon as a means of
identification. However, no mistake was made in ascribing some-
what larger cells to the Alexandria variety, as the following table
of careful measurements will show:
Tabi,e I.
India Senna.
Lower side of leaf.
Long diameter. Short diameter.
13 X 10
13 X 8-5
13 X 7
15 X 12
Av., 13-5
9-38
Alexandria Senna.
Lower side of leaf.
Long diameter. Short diameter.
145 X II
17 X 10
10-5 X 9
Av., 14
10
Tabi,e 2.
India Senna.
Taken at random with two-thirds
objective. Some long and
some short diameters.
I '4
1-6
15
1*2
12
Alexandria Sejina.
Two-thirds objective
diameter, taken at random.
2-2
17
i'4
1^5
1-8
1-6
Av., 1-38
Av., 17
Tabi,e 3.
India Senna.
Adjacent cells of upper side
of leaf, two-thirds objective.
17
1-8
0-6
15
Av., 1-4
Alexandria Senna.
Adjacent cells of upper side
of leaf, two-thirds objective.
I "9
1-8
1*5
2*3
r6
0-6
07
Av., 1-48
Am. .Tour. Pliarm.
June, 1»<7.
Alexatidria and India Senna.
\o\
AVERAGES EXPRESSED IN MICRON! ILLIMETERS.
T.\BLE I.
India Senna.
Lower side of leaf.
38-61 X 26-815
India Senna.
Average diameter, 4002
India Senna.
Upper side of leaf, 40-6
Tablk 2.
Tablk 3.
\r-
Alexandria .Senna.
Lower side of leaf.
4004 X 286
Alexandria Senna.
Average diameter, 49-3,
Alexandria Senna.
4309
.-o/
fi^. 2. India Aenna, upper side of leaf; a, epidermal cell ; />, stomata ; r,
hair (scarcely in focus) ; e, uebeuzellen.
Nevertheless, it is not to be denied that sections of epidermis
may be found in which the India senna may exhibit the larger
cells. A series of about forty measurements, made by a student in
the school here, .showed that while the larj^cst cells are found in
\02
Alexandria and India Senna. {
Am. Jour. Pharm.
June, 1897.
the Alexandria senna, the average size of the cells of the India
senna may be somewhat greater than those of the Alexandria
senna. Likewise, the cell walls alone will not serve as a point of
differentiation, owing to the same lack of uniformity. As regards
the shape of the cells, no distinctive value whatever can be placed
upon it, owing to the great variability present. The same may also
be said concerning the arrangement of cells around the hairs. The
Fig. J. Alexandria senna, under side of leaf ; a, epidermal cell ; d, stomata ;
c, hair (scarcely in focus) ; d, hair scar ; e, nebenzellen.
distinction here made by Schneider does not hold, as a rule, although
a small majority of cases may be found to accord with the state-
ments made by this authority .^
In thirty cases, the stomata of Alexandria senna showed sixteen
with two neighbor-cells (nebenzellen) and fourteen with three.
Forty stomata on the epidermis of India senna exhibited twenty-
' Americati Druggist, April lo, 1897, p. 195.
Am. Jour. Fharm.
June. 18»:.
}
Alexandria and India Senna.
303
two with two nebenzellen, fifteen with three, and three with four.
These results seem to eliminate the epidermal cells from further
consideration, but more of value may be expected of the stomata.
Exception will have to be taken, however, to the statements made
by[^ Schneider concernincr the number and size of the neighbor-cells
(nebenzellen). That the India senna usually possesses two, and
Fig. 4. Alexandria senna, upper side of leaf; a, epidermal cells ; h, stomata ;
<", hair (in focus) ; d, hair scar ; e, nebenzellen.
the Alexandria senna a larger number, is easily disproved by the
accompanying figures.
Likewise the statement that when two are present in the
Alexandria senna they are of equal size, cannot be confirmed by
examination. (See Figs, j; and ./.) Hut whatever number may obtain
in either case, it is so inconstant a character as to be of no value
as a discriminating factor. There is, on the contrary, a point of
great distinctive valuj to be found in the size and shape of the
304 Alexandria and India Senna. {^•^jire'-iSr^'"'-
stomata themselves, a feature that was overlooked in the prelimi-
nary paper. Here it will be noticed that almost invariably the
stomata of the Alexandria senna are smaller and much rounder
than those of the India. References to Figs, i and 4. will make
this clear. Measurements of a considerable number of stomata in
each case gave the following ratio between the longer and shorter
diameters : In Alexandria the shorter diameter bore a ratio to the
larger of 0-84 to I ; in the India, of 0-6 to I.
Occasionally stomata of a rounded form may be found in the
India senna, but they do not look like the Alexandria and are
e^
Fig. 5. Alexandria senna, showing number of hairs in a limited area ;
d^ hair scars ; e, nebenzellen.
larger. At the present state of the investigation, this character
represents by far the most characteristic difference between the two
species and, together with the number of hairs, affords the best
means of detecting a mixture of the two in powdered form.
The opinion reached by the author in the former paper, that the
number of hairs shown by the two species is a valuable means of
distinguishing them apart, is, after yet more careful research, again
advanced. It would seem at first sight that the test proposed by
Schneider, i. e., estimating the number of hair scars upon the epi-
Am. Jour. Pharm
June, 1897.
}
Alexandria and India Senna.
305
dermis, would be more accurate than counting the free hairs in the
powder ; but it is really unreliable, because the distribution of the
hairs is not uniform. This objection does not apply to the countin;^
Fig, 6. Alexandria senna, No. 60 powder ; /», stomata ; c, hairs ; </, hair
scars ; r, nebenzellen.
of the free hairs, for by powderinfj the leaves and shaking the pow-
der up in a liquid, the distribution is made comparatively uniform.
3o6
Alexandria and India Senna, {
Am. Jour. Pbartn.
June. 1897.
The objection that fragments may be counted as whole hairs is
easily overcome by choosing some readily distinguishable part of
the hair, such as the tip, and using only it as the unit of estimation.
From the results obtained in the latest series of experiments the
following test appears sufficient to distinguish either senna alone,
or a mixture of the two, and it is therefore proposed for these pur-
poses : Take a portion of the No. 60 powder and place it in a small
homoeopathic vial, and add to it twice its volume of a mixture
Fig. 7. India senna, No. 60 powder ; b, stomata ; c, hair ; d, hair scar ;
e, nebenzelleu.
of water and glycerin in equal parts. Thoroughly shake this mix-
ture, and while still turbid with the suspended powder, place a drop
on each of several glass slips, and cover with cover glasses. If air
bubbles or too great opacity exist, heat to boiling over an alcohol
lamp. Search for hairs showing the tips present, and if they appear
abundant, one to four in each field of a i^-inch objective, Alexandria
senna is present. To further confirm this, examine several frag-
""""•jun^eVig^""} Spirit of Nitrous Ether. 307
ments of the normal epidermis for the stomata. If many are found
that are quite round in outHne (b. Fig. ^), the presence of Alexan-
dria senna is assured. As confirmatory to this, the number of hair
scars upon the epidermal fragments may be employed. These
should be found frequently at a distance of from two to five epider-
mal cells apart. A sample of India senna, on the contrary, will
exhibit few hairs, often none in the field, and the great majority of
the stomata will be found with the long diameter much longer than
the short one {b. Fig. /). The hairs should not frequently be closer
than five epidermal cells apart. In simple powders the mere
number of hairs present will at once distinguish between the two
sennas, but in cases of mixture of the two, the shape of the stomata
will have to be examined. Many of the elongated oval form always
indicate the presence of India senna.
However good a test may be theoretically, it is of no value unless
it works practically. The only way to tell whether it will do this
or not, is to put it in practice under conditions which will represent,
as nearly as may be, those of its usual employment. In this par-
ticular instance the test proposed was given a thorough trial in the
hands of eighteen students of representative abilities, and in no case
did it fail to work, either with simple powders or mixtures.
ASSAY OF SPIRIT OF NITROUS HTHFR.
Bv Lawrence A, Kessler, Ph.G.
Contribution from the Chemical Laboratory of the Philadelphia College of
Pharmacy. No. 167.
My attention was attracted to this subject by a series of papers
which ap]:)eared in the American Druggist and Pliarmaceutieal
Record. To the number of that journal for December 25, 1895,
Professor David Walker contributed an article in which he pro-
posed a rapid method for the volumetric assay of spirit of nitrous
ether. His process of assaying was based on the measurement of
the iodine liberated from potassium iodide, through the decomjx)-
sition of spirit of nitrous ether by the United States Pharmacopcria
process of assay.
The proposed test was made by carciuUy measuring 5 c.c. of
spirit of nitrous ether into a 4-ounce ICrlenmcyer flask, from a
pipette ; this was followed with 10 c.c. of 6 per cent, acetic acid and
308 Spirit of Nitrous Ether, {^^jfreyiSr*''"'-
10 c.c. of potassium iodide test solution. The mixture was occa-
sionally agitated during ten or fifteen minutes, a few drops of starch
test solution added, and the mixture titrated with decinormal sodium
thiosulphate volumetric solution, until the bluish-green color was
discharged. The mixture afterwards assumed a dark color ; but
if the time of maceration does not exceed fifteen minutes, the num-
ber of cubic centimeters required to first discharge the color will
give nearly or quite as accurate results as the nitrometer. Prof.
Walker also said: " While the titration process may not be quite as
accurate in its figures as the modified Allen method, it involves
much less expense, and the results are sufficiently accurate for prac-
tical purposes." This last claim Prof. Walker seemed to have sub-
stantiated by the figures of a table which he gave to show the
results of the assay of ten samples by the two methods.
On January 25, 1896, the same journal published a letter from
Mr. Peter MacEwan, of London, England, in which that gentleman
directed attention to the fact that the method proposed by Professor
Walker had been suggested by Mr. D. B. Dott a dozen years ago,
and had to be abandoned on account of the fallacious results, for
whenever the nitric oxide liberated by decomposition of the ethyl
nitrite comes in contact with the air of the flask, nitrogen tetroxide
is formed. This at once decomposes more of the alkaline iodide;
indeed, decomposition might go on indefinitely if the supply of air
and iodide were large enough. Mr. Dott endeavored to obviate
this objection by various means, such as working with an open dish
in which carbon dioxide was simultaneously generated, but with
modified success. It was his knowledge of the difficulties of this
method which led Mr. A. H. Allen to effect the reaction in an air-
free space and estimate the nitric oxide instead of the iodine; the
method was adopted by many chemists, and simultaneously indirect
estimation through the iodine factor was deservedly forgotten. A
man who knows all the worries of the latter process may get fairly
accurate results, but the novice or careless worker may return a 3
per cent, ethyl nitrite spirit as containing anything between that
and, say, 30 per cent., because he is never sure about the end point.
Professor Walker defended the utility of the titration method in a
reply to Mr. MacEwan in the issue of February 10, 1896, and stated
that further investigation had shown that five minutes' maceration
was ample for the completion of the reaction. As stated at the begin-
"^'"jlaT;!^""} ^//r/V of Nitrous Ether. 309
ning of this article, my attention was attracted by the controversy
referred to, and I undertook some experiments with the titration
method as proposed by Professor Walker, in order to ascertain if it
could be placed in the hands of pharmacists as a practical method.
In the first set of titrations, sufficient decinormal sodium thio-
sulphate volumetric solution was added to discharge the bluish-
green color, so that it did not return in thirty seconds. The reason
for adopting this plan was to afford the operator proof that decolor-
ation had been effected. The color quickly reappeared after decolor-
ation on account of the liberation of iodine by the nitrogen tetroxide,
as pointed out by Mr. MacEwan. This reaction is also, of course,
going on from the time the materials are mixed, and even during
titration, so that iodine is being alternately liberated and titrated.
The tendency of the method must, therefore, be toward high results,
for the same iodine is repeatedly taken into account. The rapidity
with which the volumetric solution of sodium thiosulphate is added,
as also the quantity added at a time, influences the amount required
for decoloration. The more rapid the addition of sodium thiosul-
phate and the larger the portion added, the less the total quantity
required for the first decoloration.
The following figures show the amounts of decinormal sodium
thiosulphate volumetric solution required for the titration of the
iodine liberated by portions of 5 c.c. of a few of the samples of spirit
of nitrous ether examined :
c.c. of V. S. Re«iuircd.
247, 23-1, 14-4, 140
142, 161, 10-2, 107
205, 20-2, 18-9, 19-4
28-2, 283, 322
r 30-4, 30-8, 33-6, 345
U53. 37*3. 373. 3»*o
25"2, 273
24'6, 206
The titrations were conducted as nearly alike as jx)ssible. The
figures for sample 5 also show the effects of the time of maceration.
After concluding that the titration method was not trustworthy,
even when conducted under the conditions and restrictions proposed,
I made a scries of tests with the nitrometer according to the United
States Pharmacopa'ia process of assay. Two difficulties were
Simple
Minutes
No
Macerated.
I
15
2
15
3
15
4
15
5
15
5
10
5
5
Am. Jour. Pharm.
310 Spirit of Nitrous Ether. {^"^'.'^Z'i^'.
encountered in this method. One of these difficulties attended the
assaying of samples of the spirit which were acid in reaction ; it
consisted of a decomposition between the acid spirit and the potas-
sium iodide, with evolution of nitrogen dioxide before the normal
sulphuric acid was added. Spirit of nitrous ether is usually acid; of
the sixteen samples examined during the course of this work, not one
was neutral, but most of them were very acid. To overcome the
difficulty referred to, the sample to be assayed was neutralized by
mixing it with one-fifth its volume of an alcoholic solution of potas-
sium hydrate. Six c.c. of this mixture instead of 5 c.c. of the origi-
nal sample were then taken for each estimation.
The following figures show the results which were obtained by
the official method on the same sample, before and after neutral-
izing :
Sample A. Acid. Neutralized.
(i) 5 C.C. gave 22"o C.C. NO and 2i'o c.c. NO.
(2) 5 " " 24-0 " " " 20-4 ''-
(3) 5 " " 24-4 " " " 20'4 "
The other difficulty encountered in the official assay process was
the displacement of air from the aqueous solution of potassium
iodide when this liquid was let into the burette of the nitrometer
containing the spirit on top of the brine. Any inaccuracy which
might arise from this cause could be prevented by raising the level
tube and then opening the stopcock so the air could pass out. But
this could not be done unless the sample was free from acid, on
account of the premature reaction which takes place between the
potassium iodide and the spirit in the presence of acid. To obviate
this difficulty, I tried using a saturated alcoholic solution of potas-
sium iodide in place of the aqueous solution, as directed by the
United States Pharmacopceia. The results were satisfactory, as but
little or no air bubbles collected in the burette. In order to supply
the required amount of potassium iodide, which is not so soluble in
alcohol as in water, 20 c.c. of a saturated alcoholic solution were
used instead of the 10 c.c. of aqueous solution of potassium iodide.
Three samples were neutralized with the alcoholic solution of
potassium hydrate, and submitted to the official method of assay
with the nitrometer, the alcoholic solution of potassium iodide being
used in place of the aqueous solution ordered by the Pharmacopceia.
The results were as follows :
'^'"■jiinMST*''"} Red Mercuric Oxide. 311
Sample.
( (i) 5 c.c. gave 21-6 c.c. NO.
c
D
The displacement of air from the aqueous solution of the potas-
sium iodide might also be overcome by boiling the solution and
allowing it to cool out of contact with air just previous to use, but
this method was not tried.
The quality of the spirit of nitrous ether dispensed is remarkably
poor.
• (2) 5 c.c.
" 21-6
( (i) 5 c.c.
" 50-0
C ( 2) 5 c.c.
" 500
• (I) 5 c.c.
" 47-0
U2) 5 C C.
" 472
NOTE ON RED MERCURIC OXIDE.
By Joseph W. England.
I have read with interest Mr. Charles H. La Wall's paper on the
" Consideration of Some Recent Suggestions Concerning Ointment
of Mercuric Nitrate," as published in the current issue of the Amkki-
c.\N Journal of Ph.akmacy.
It will be recalled that I urged the use of red mercuric oxide in
place of metallic mercury, in the making of citrine ointment. This
practice was suggested as an alternative, and not as a substitute for
the official formula. The average pharmacist always has red mer-
curic oxide in stock ; he does not always have metallic mercury,
and it was thought to be directly on the line of increased convenience
to urge the substitution of the oxide, in proportionately larger
quantity, for the metal, when occasion required.
To the use of red mercuric oxide in place of metallic mercury for
this purpose, Mr. La Wall says: "As to the relative purity of the
two substances, the experience of a large manufacturing establish-
ment shows that the commercial metallic mercury is of far greater
uniformity and purity than the red oxide of commerce."
This statement does not accord with the writer's information. A
letter from one of the leading firms of manufacturing chemists says :
•• We would state that our red mercuric o.xide conforms strictly to
the requirements of the United States Pharmacopaia, and we regard
it as equal in purity to metallic meicury."
12
Red Mercuric Oxide. {'"^jSe^isy^T"''""-
Another firm of manufacturing chemists, equally as prominent,
writes : *' Our analysis shows that red mercuric oxide contains 997
per cent.'HgO, and 0-3 per cent, of SiO^. The silica is, no doubt,
derived from the vessels in which the mercuric oxide is manufac-
tured. Commercial metallic mercury varies between 99 and 100
per^cent., while the distilled mercury is pure."
Another prominent chemical firm writes : " We would state that
our levigated mercuric oxide conforms to all the requirements of the
U.S.P. 1890, save as regards absolute freedom from HNO3; it con-
tains very small traces of the latter. It conforms strictly to all the
requirements of the Ph.G. iii, also, in regard to HNO3. There is no
doubt that the U.S.P. is hypercritical in the case of red mercuric
oxide, as it is also in several other instances ; for the faint traces of
HNO3 that our levigated grade contains are not known to interfere
with any of the chemical applications of the preparation, and cannot
possibly have any influence on the therapeutic action of the medi-
cament. To provide an oxide absolutely free from HNO3, is practi-
cally impossible commercially, and there is no necessity for the
preparation."
Now, the point the writer would make is this : If the statements
of three of the leading chemical firms of the country, regarding
the purity of their red mercuric oxide, be true, then there should be
no difficulty whatever in the pharmacist procuring an oxide that
could be used as a substitute, if necessary, for metallic mercury in
the making of ointment of mercuric nitrate.
Further, the writer recommended the addition of glycerin to the
finished ointment, not to prevent sponginess — that is a condition due
to the application of insufficient heat — but to prevent the hardening
and ultimately friable condition that obtains in the ointment on
long standing. Regarding the criticism that the addition of 50
grammes of glycerin to 1,000 grammes of ointment of official
strength reduces the percentage of mercuric nitrate below that
required by the U.S.P., there is this to say : that the resulting differ-
ence in strength is of no practical moment therapeutically , as phy-
sicians almost invariably — save in those cases requiring great stimu-
lation— dilute the ointment they prescribe — oftentimes in equal pro-
portions— with lard or other fatty diluent.
The final criticism of increased cost is hardly worth consideration.
The alternative use of 75-5 grammes of mercuric oxide (costing
-^"•jlme^iSJ''""} A Sample of Scammony. SIJ
about 6 cents an ounce avoirdupois) as against 70 f;rammes of
metallic mercury (costing about 5 cents an ounce, avoirdupois), to
make the official quantity of ointment, or a little over 2 pounds,
is of no practical moment whatever.
A sample of the ointment made on March 17, 1897, t>y the use
of red mercuric oxide, is presented to this Pharmaceutical Meeting.
While it has slightly darkened in color, it has retained its smooth-
ness, and has undergone no hardening whatever.
NOTE ON A SAMPLE OF SCAMMONV.
By I. \V. Thomson.
Some time ago a parcel was handed to me, marked •• Scammo-
nium," accompanied by a statement that it contained 84864 per
cent, of scammonium, and, that there might be no mistake, gave
the chemical formula, which is generally accepted as representing
that body Cf^H-^Oig. It was said to be of German origin.
A very cursory examination of the sample so completely belied its
certificate of character, that I concluded it could hardly claim more
than a very remote relationship with scammony.
Having mentioned the circumstance to Mr. Hill, he suggested
that I might exhibit the sample and submit the result of my exami-
nation of it at an evening meeting.
The sample consists of irregular broken pieces, apparently por-
tions of a cake, about half an inch in thickness, greenish-black,
hard and horny, breaking with a resinous fracture, and very diffi-
cult to powder. On submitting it to a systematic examination, the
following results were obtained :
Per Cent.
Soluble in ether 0*4
** '* alcohol 2*0
" " water 42'6
Starch and a little cellular tissue . 43*0
Moisture . ... i2'o
lOO'O
It yielded 212 per cent, of ash, of which 093, equal to 436 per
cent, was soluble in water. The ash contained K, Mg, Ca, Fc, and
Si, as carbonate, sulphate, and a trace of chloride.
The water-soluble portion was evidently gum, apparently gum
314 Siimbul in England. {^"jS/.-ifs""'^"-
arable. The insoluble portion consisted very largely of starch, with
a small quantity of cellular tissue.
So far as I know, the specimen is unique, and the Germans must
think us very gullible when they attempt to foist such an article
upon us as scammony. — Pharmaceutical yournal, March 20, 1 897.
THE CULTIVATION OF SUMBUL IN ENGLAND.i
By E. M. Holmes.
The sumbul root of commerce has of late years been of very
inferior quality compared with the fragrant root imported twenty-
five years ago or more, and usually consists of smaller and more
cylindrical pieces, with only a very faint musky odor. The structure
is also much firmer, and the resinous parts are usually blackish and
cirty, in strong contrast to the paler non-resinous portions. The
upper or rootstock portion, which is marked with rings like the true
sumbul, is evidently often branched, which I have never seen in the
true sumbul, in which the upper portion usually tapers to a rounded
fibrous apex.
The sumbul of the present day is, therefore, probably derived
from a different plant with a more cylindrical root, branched near
the apex, and having a firmer substance. It was suggested some
years ago by Dr. J. E. Aitchison (7m;25. Linn. Soc, ser. 2, Bot., p. 69,
pi. 20-21) that it might possibly be derived from Ferula suaveolens,
which has only a faint musky odor. He states that the root is
scented, and is one of the kinds of sumbul exported from Persia to
Bombay by the Persian Gulf (/. c, p. 69).
It seems to be desirable, therefore, that the true sumbul should
be cultivated to meet a trade desideratum. The use of an inferior
drug will otherwise probably lead in time to the entire disuse of the
drug. Under these circumstances my own experience in the culti-
vation of the true sumbul plant may prove interesting to some of
the readers or the Pharmaceutical Journal.
Some years since, one of our corresponding members, M. Andrew
Ferrein, of Moscow, sent me some young plants of Ferula foetidissima,
and with them two young plants of F. sumbul. They arrived in
autumn, packed in husks of buckwheat, like ordinary bulbs. The
fleshy roots at that period of the year appear to lose all the small
' Pharmaceutical Journal, April 24, 1897.
i^
2
c
E
cr
c
o
o
If.
^A^*^
"^^>
3i6 Sn nib III in England. {-^
m. Jour. Pharri'
June, 1897.
rootlets, and will then bear digging up and transplanting without
injury, the tuberous root sending out, in the following early spring,
new rootlets.
Tn February, or, in late winters, in March, as soon as the ground is
ao longer hard from continued frost, the sumbul plant sends up one
or more young leaves. These may be a little injured if exposed to
hard frost, although not injured by white frost, but as a rule new
leaves come on, and the plant stands our winters as well as most
indigenous plants oi the same natural order. The fully developed
leaves appear in April, and continue to grow until July, when they
turn yellowish and gradually wither. The root increases in size
every year, retaining its oval form, presumably, until it attains a
sufficient reserve of nutrition to enable it to throw up a large fruiting
stem. The inflorescence of the specimen that flowered in the Kew
Gardens some years ago attained a height of about 8 feet, and
the plant then died.
To secure the healthy growth of the plant, it is necessary to give
it plenty of water, and a little weak manure water, during the grow-
ing season, from April to July. A mulch of well-rotted manure
around the plant in the autumn, taking care to protect the crown by
a covering of clean sand, also helps its growth. My plants, which
are now about six years old, have not flowered, but the root of one,
which I took up a few days ago for transplanting, measured about
6 inches long by 3j^ broad, and had a strong, persistent musky
odor where injured, exuding abundance of white, milky juice. The
roots are somewhat twisted, and spread nearly horizontally below
the ground. It is obvious from the shape that such a root might
furnish two tapering and one cylindrical sections of the thickness of
the old-fashioned, but that it could not furnish the cylindrical pieces
2 or 3 inches long, of small diameter, that occur in the drug
of the present day. Provided that good seed could be obtained,
there is little doubt that sumbul might be cultivated in temperate
or mountainous districts in the colonies, or in ordinary gardens or
fields in this country without any difficulty.
The chief difficulty in obtaining good seed is due to the fact that
in this country the fruit are apt to be ruptured by the rains. In their
native country, the fruits are produced in the hot weather. In this
country, therefore, it is necessary to protect the ripening fruits from
rain.
Am. Jour. Pbarm. >
juXi^!"'"} Proprietary Preparations. 317
THE ETHICS AND ECONOMICS OF PROPRIETARY
PREPARATIONS.'
Dr. Charles Rice, a member of the Committee of Revision of the
United States Pharmacopoeia, and the chemist of the New York
department of public charities, has lately thrown a good deal of
the light of common sense on the question of the advisability of
using proprietary preparations. What he says is in the form of a
report to the committee on the apothecary's department of the
medical board of Bellevue Hospital, made in compliance with a
request from that body. The report was adopted by the medical
board on April ist,and has been approved by the board of commis-
sioners.
Dr. Rice defines a proprietary article as one of which some person
or persons have exclusive control of the production, sale or use —
of all three of these features in some cases, of one or two of them
only in others. He divides such articles into natural and artificial
products, and again into these three classes : (i) Products of nature
prepared under patents and mostly sold under copyrighted names.
(2) Products of nature that have never been made under patents or
are no longer so made, but are sold under copyrighted names.
(3) Artificial preparations sold under copyrighted names. As regards
patented articles, it is a principle in patent law, says Dr. Rice, that
a product of nature cannot be patented ; hence no patent is granted
on any chemical substance of a definite and constant comj^osition,
even though it may, at the time when the patent is applied for, not
yet have been found occurring ready-formed in nature. Hut any
process, not previously known or used, by which such a product can
be formed is patentable. Certain articles that are made by patented
processes may also be made by processes that are not patented, and,
as it is impossible for the purchaser to distinguish by which process
they have been made, nobody, says Dr. Rice, would think of raising
any objection against their use in medicine. As an exam[)le, he
mentions salicylic acid, which, in the form of methyl salicylate,
exists in oil of wintergreen and some other volatile oils, from which
the acid may readily be prepared ; but as these oils would be utterly
inadequate to supply the demand, more than 95 per cent, of the
salicylic acid used in medicine is produced by a process that was
* Editorial in the New York Medical Journal, May 22, 1897.
3i8 Proprietary Preparations, {^"^ji^neaS"'"^*
patented in 1874, but on which the patent has now expired. A
patent, says Dr. Rice, not only does away with all secrecy — which
is usually considered the objectionable feature of a proprietary article
— but it commonly acts also as a sort of guarantee of the uniformity
of the product in composition, strength and purity.
Dr. Rice thinks that if all these points are taken into consider-
ation, it will probably be conceded that, if an article is protected by
a patent alone — the feature of a copyrighted name being disre-
garded— it becomes practically impossible to separate patented sub-
stances into classes of which one may, and the other may not, be
used without a violation of ethics, and, therefore, none of these
articles should be rejected for the reason alone that they are
patented. He then proceeds to consider the three classes of pro-
prietary articles previously mentioned. •
As to products of the first class, inasmuch as copyrights on
names never expire, whereas a patent has a definite term of years
to run, it is evident, says Dr. Rice, that the proprietors of the copy-
rights would have a perpetual monopoly unless, after the expiration
of the patents, other producers should put the same articles on the
market under new names not copyrighted. All these bodies — such
as antipyrine, aristol, phenacetine, salol, salophene, sulphonal, trional,
and vanillin (the last-named substance being now sold only under
its proper chemical name) — will undoubtedly. Dr. Rice thinks, be
rescued from their present monopolistic control, when the patents
on them have expired. There is no secret whatever about them, he
says. They are definite chemicals of known composition and prop-
erties, and, since some of them have been found to have real thera-
peutical value, no objection, it is believed, will be raised against the
whole class.
Dr. Rice next considers the products of nature which have never
been, or are not now, made under patents, but are sold under
copyrighted names, familiar examples of which are antifebrine
(acetanilid), dermatol (bismuth subgallate), formalin or formol
(formaldehyde), pyrozone (hydrogen-dioxide solution), diuretin
(sodium-theobromime salicylate), and lanolin (hydrous wool fat).
The owner of the copyrighted name, he remarks, usually professes
that his product is "purer" or more "refined" than the article
found on the market under the common name, and this pretension,
he says, is true in some instances, particularly in those articles first
"^"juDMoS*™*} Proprietary Preparations. 319
put on the market under copyrighted names, although at present
the best grades of the several articles sold under their common
names appear to answer every purpose. These products, he thinks,
are unobjectionable, but he says it seems preferable, as it is certainly
more economical, to order them under their common names, espe-
cially acetanilid, bismuth subgallate and formaldehyde.
His third class preparations that are not products of nature, sold
under copyrighted names, Dr. Rice divides into three groups. The
first group, which he considers unobjectionable, comprises prepara-
tions the origin and composition of which are not kept secret, such
as ichthyol, creolin, Mellin's food, malted milk, etc. The second
group, which he thinks to be of doubtful value, includes all the
preparations of the class that do not belong to either the first or
the third group, which last, by far the largest, consists of the " se-
cret nostrums," such as '* soothing syrups," " female regulators,"
" blood purifiers," etc.
Incidentally, Dr. Rice justly complains that for years the name of
Bellevue Hospital has been taken in vain by a number of persons and
firms without any authority whatever. It is a common occurrence,
he says, for samples of proprietary medicines, foods, mineral waters,
plasters, etc., to be sent to the hospital or to members of the house
staff for " trial," whereupon the subsequent advertisements of the
articles in question often assert that the latter are ♦• used in l^ellevue
Hospital," leaving the impression upon the mind of the reader that
the article or articles have been used with the sanction of some
member of the medical board. It is probably impossible, says Dr.
Rice, to find a remedy for this evil, from which many other institu-
tions of repute likewise suffer. To publish a denial of such false
assertions, he thinks, would only aggravate the evil. The utmost
that can be done appears to be to caution the medical staff against
any entanglements with the agents of the interested parties, or en-
couragement of them.
The existence of philippium is claimed by M. Marc Delafontaiuc, in the
Chemical News for May 14, 1897. Its chief characters arc dcacril>e<l. Ita
symbol is Pp., and its atomic weight 80, 120 or 160, according to whether the
oxide is FpO, PpjO^, or PpOj.
Philippium is more closely allied to cerium and terbium than to any other
of the yttrium and cerium metals. It is to yttrium what cerium is to lantha-
num.
320 Literature Relating to Pharmacy. {^""ju^e'iS:*'''""
RECENT LITERATURE RELATING TO PHARMACY.
PAS5I0X FLOWER, PASSIFLORA INCARNATA, IN FPILEPSY AND OTHER
NEUROSES.
S. D. Bullington, M.D. (Nashville Journal of Medicine and
Surgery, March, 1897), reported some very favorable results from
the administration of the fluid extract of passion flower, either
alone or in conjunction with other medicines, in a number of cases
of nervous disorder.
A case of epilepsy of twenty-six years' standing showed marked
improvement after treatment with this drug, although, of course, it
was not hoped to effect a cure in a case of so long standing.
Various cases of insomnia, hysteria and neurasthenia were like-
wise treated with the drug with satisfactory results.
The author stated that the fluid extract, mixed well with water
or simple elixir, was pleasant to take, and an admirable substitute for
•bromide.
Another feature in its favor was that no ill effects seemed to
follow its use, either temporary or continued.
COMMERCIAL GINGER AND ESSENCE OF GINGER.
VV. S. Glass [Pharmaceutical Journal, March 20, 1897) examined
samples of Jamaica, Cochin and African ginger, with a view to
obtaining a satisfactory essence. His results are given in the follow-
ing table, the percentages of oleoresin obtained by three other
writers being also given for comparison :
Author Thresh. Siggins.* Riegbl.
Jamaica
Cx:hiii .
African
' Am. Jour. Pharm.. Vol. 60, p. 278.
Moisture.
Ash.
5-3
Kxtract
or
' Oleoresin.
Extract
or
Oleoresin.
Extract
or
Oleoresin.
Extract
or
Oleoresin.
9'33
5-00
3 "290
5 '00
5
I I "00
4-6
4 33
4*965
—
8-00
5*5
6-33
I
^ojs
(A 6-17
1^ 7-00
—
The extract was prepared by exhausting the drug with ether and
evaporating at a low temperature. The African variety required
most ether and yielded the highest percentage of extract; but, as
Am. Jour. Pharm
janeViS:""} Literature Relating to Pharmacy. 321
stated by the author, this variety was unsuited for many pharma-
ceutical purposes on account of its brown, coarse appearance.
For the preparation of a soluble essence possessing all the flavor
of the ginger it was recommended to add 3 drachms of powdered
pumice-stone to i fluid ounce of the essence, and shake occasionally
during twelve hours. Then add gradually 3 fluid ounces of distilled
water ; allow the mixture to stand six hours and filter.
REPORT OF COMMITTEE ON ATOMIC WEIGHTS.
The fourth annual report of the Committee of the American
Chemical Society on Atomic Weights, has recently been published
{^joiir. Ai/nr. Chcm. Soc., i<)^ 359)- The chairman. Dr. V . \V,
Clarke, gives the following illustration of the practical value of a
correct knowledge of atomic weights in the commercial world :
'•There are two rival values for the atomic weights of chromium.
One, 525 approximately, based on the old work of Berlin, is still
used by European analysts. The other, 5 2- 1, dep>ends upon later
and more accurate researches, and is used in this country. Mr.
William Glenn, of the Baltimore Chrome Works, informs me that
that establishment imports chrome iron ore by the shipload, the
value being determined by a volumetric assay, in which the atomic
weight of chromium is involved. It is assayed in Glasgow, with the
older value for chromium, and in Baltimore with the modern datum.
A cargo amounts to about 3,500 tons, and the difference in price
due to the difference between 52-1 and 525 for chromium amounts
to about S367.50 per shipload."
The following are the recalculated atomic weights according to
the best authorities, compiled down to January i, 1897:
Aluminuai . .
Antimony ...
Argon
Arsenic
Barium
Bismuth .
Boron
Bromine .
Cadmium ...
Calcium
CarlK)n
Cerium
C;esium
H - I
0-16
2691
2711
119-52
1 20-43
(?)
l?^
74 44
750'
13639
13743
.^ ■.''.•; I
20S1 1
I, ,>'j
1 095
79 34
7995
1 1 1 If)
M I 95
3976
4OC17
ir92
12 01
139-10
Mm- 20
131-89
•32 «9
322 Literature Relating to Pharmacy, {'^'^-IT^-J^T''^^
H = I O = i6
Chlorine 35'i8 35"45
Chromium 51*74 52*i4
Cobalt 58-49 58-93
Columbium 93*02 9373
Copper 63-12 63-60
Erbium 165-06 166-32
Fluorine 18-91 19-06
Gadolinium I55'57 156-76
Gallium 69-38 69-91
Germanium 71 '93 72*48
Glucinum 901 9*08
Gold 195*74 197*23
Helium (?) (?)
Hydrogen i-ooo i*oo8
Indium 112-99 113*85
Iodine 125-89 126-85
Iridium 191-66 193*12
Iron 55-60 56-02
Lanthanum i37*59 13S-64
Lead 205*36 206-92
Lithium 6*97 7*03
Magnesium 24-10 24-28
Manganese 54-57 54-99
Mercury 198-49 200-00
Molybdenum 95*26 95*99
Neodymium 139*70 140-80
Nickel 58-24 58-69
Nitrogen 13-93 14-04
Osmium 189-55 190-99
Oxygen 15-88 16-00
Palladium 105-56 106-36
Phosphorus 30-79 31-02
Platinum 193-41 ^^ 94*89
Potassium 38*82 39*ii
Praseodymium 142-50 143*60
Rhodium 102-23 103-01
Rubidium 84-78 85-43
Ruthenium 100-91 101-68
Samarium 149*13 150-26
Scandium 43-78 44-12
Selenium 78-42 79-02
Silicon 28-18 28-40
Silver 107-11 107-92
Sodium 22-88 23-05
Strontium 86-95 87-61
Sulphur 31-83 32-07
Tantalum 181-45 182-84
Tellurium 126-52 127-49
I
"""^•june' iS^""'} Editorial— Reviews. 325
H ^ I O = 16
Terbium i5S"8o 16000
Thallium 202'6i 20415
Thorium 230*87 232 63
Thulium 169-40 170-70
Tin iiS'i5 11905
Titanium 47*79 48*15
Tungsten 183*43 184*83
Uranium 23777 23959
Vanadium 50*99 5i'38
Ytterbium 171 88 I73"i9
Yttrium ... 88*35 8902
Zinc 64*91 6541
Zirconium 89*72 9040
EDITORIAL.
NEW PROFE.SSORS IN THE PHILADELPHIA COLLEGE OF PHARMACY.
When it became necessary to fill the vacancy in the chair of Botany and
Materia Medica in the College, caused by the death of Professor Bastin,
it was decided by the Board of Trustees to create two new chairs in place of
the old one. Dr. Clement B. Lowe, already an Instructor in the College,
was accordingly nominate<l to occupy the chair of Materia Medica, and Pro-
fessor Henry Kraemer, Professor of Botany, Pharmacognosy and Materia
Medica in the Northwestern University, of Chicago, to fill the chair of Botany.
Both men are amply qualified, by education and experience, to fill the posi-
tions they have been selected to occupy. Dr. I^^we is a graduate of Bucknell
University, of the Philadelphia College of Pharmacy and of the Jefferson
Medical College. He conducted a pharmacy for a num])er of years, and has
been Instructor and Quiz Master in the College for over ten years.
Professor Kraemer is a graduate of Girard College, of the Philadelphia
College of Pharmacy, of the School of Mines, Columbia College, New York,
and of the University of Marburg, Germany, where he received the degree of
Doctor of Philosophy. His thesis for this degree was an elaborate study
of Viola tricolor. He likewise had several years' e.xperience in the retail
drug business. In addition to his lectures on ijotany, Professor Kraemer will
conduct the Botanical Laboratory so successfully organized by Professor Bastin.
Dr. J. L. D. Morison will become Instructor in Materia Medica, in addition to
his present position as Assistant in the Botanical Laboratory.
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
HiNFi HKi,*N(; IN DAS Stidu'M i»kk Alkaloidk. mit besondercr Itcruck-
sichtigung der vegetabilischen Alkaloide uod dcr Ptomaine, Von Dr. Icilio
Guareschi, (). (). Professor an dcr konigl. Universitiit Turin, und Director dc«
pharmaceutisch-cheniiftcben und toxicologischen Institut*. Mil Genehnngung
des Verfassers in deutscher Bearbeitung herausgegeben von Dr. Hermann Kuu/.-
E>^„. •^^,,_ f Am. Jour. Pharra.
324 KeVteiVS. { June,1897.
Krause, Dozeut fiir allgemeine uud pharmaceutische Chemie an der Universitat
Lausanne. Zweite Halfte, Berlin, 1897. R. Gaertner's Verlagsbuchhandlung,
Hermann Heyfelder.
The first half of this valuable work was reviewed in this Journai, for February
of this year. It may be well to repeat what was pointed out at tliat time, in
regard to the sections into which the whole work is divided, viz :
I. Bases of the Open Chain Series.
II. Bases of the Closed Chain Series.
III. Metal Amines.
IV. Alkaloids in the Narrower Sense.
V. Ptomaines and Leucomaines.
The first half, in addition to the historical introduction, included all of the
open chain series and a part of the closed chain series. The second half covers
all the remaining sections, in addition to completing the consideration of the
closed chain series. The fourth section is one of the most important in the
whole work, since it very fully considers the natural alkaloids, their distribu-
tion in the vegetable kingdom, method of extraction, estimation, etc. It also
contains a tabular list of the alkaloids, with their sources, according to natural
orders, and their formulas ; this section is also enriched by a number of para-
graphs from the pen of the translator. As now completed, the book consists of
657 large pages, including an index. It is an indispensable work to every one
who has to do with the alkaloids in any of their varieties.
Reagents and Reactions known by the names of their authors. Based
on the original collection by A. Schneider, revised and enlarged by Dr. Julius
Altschul for the Pharmaceutische Centralhalle. Translated from the German
by Richard Fischer, Instructor in Pharmacy at the University of Wisconsin.
Pharmaceutical Review Publishing Company, Milwaukee, Wisconsin. 1897.
The difficulty experienced by many chemists in determining the nature of a
reagent when, as is frequently the case, the name of the author only is given,
is reason enough for issuing a work like this. The list as now published is
very complete, and occupies 82 pages. There is an index of subjects given at
the end which will materially assist locating certain tests. The pamphlet is
well printed, and appears to be remarkably free from errors.
Warner's Pocket Medicai. Dictionary of To-Day, comprising the pro-
nunciation and definition of 10,000 essential words and terms used in medicine
and associated sciences. By William R. Warner. Philadelphia : William R.
Warner & Co. 1897.
The foregoing title sufficiently explains the scope of this work. By omitting
the very common terms, whose meaning is obvious or known to everybody, the
author has been able to gain space and so keep the book down to his original
intention, thereby making it strictly a pocket dictionary. It is a very complete
list of words and their definitions, which are especially desired by both phy-
sician and pharmacist.
Formaldehyde. By Eli Lilly & Co. Indianapolis. 1897.
This pamphlet is devoted to a description of the chemistry of formaldehyde,
its use as a disinfectant, and its generation in the Moffatt Formaldehyde Lamp,
which was fully described and illustrated in the April number of this Journal.
I
"^""jine^i^f""*} PJiarmaccutical Associations. 325
The Pharmacologist is the title of a quarterly journal devoted to Materia
Medica, Pharmacy and Therapy. It is edited by F. E. Stewart,'M.D., Ph.Cf.
and published by Trederick Kimball Stearns, of Detroit, Mich. ^ The first
number, recently issued, is full of interesting matter. It contains comments
and editorials on a variety of subjects, and two original communications,
one on .\conite and another on Diastatic Ferments.
Semi-Annual Report of Schimmei, & Co. i Fritzsche Brothers. 1
Leipzig and New York, April, 1S97,
This number is superior in many respects to its predecessors. After the usual
information in regard to a large number of oils, the following novelties are
noted : Cardamom oil, Bengal Schinus fpepper-tree 1 oil;Valerian oil, Mexican;
camphor-wood oil, Venezuelan; and golden-rod oil, Canadian.
The latter half of the Report is devoted to a list of essential oils, giving their
botanical origin, the part or products of the plant from which the oil is ob-
tained, the yield and the physical constants and principal chemical constituents
of each oil. This is especially useful for reference. A map is appended, show-
ing the producing districts of oil of peppermint (menthol) and camphor in
Japan.
Proceedings of the Twentieth Anniai, Meeting of the Pharma-
ceutical Association of the State t)F Soith Carolina.
The twentieth annual meeting of this association met in Columbia. S. C,
November ir, 1S96. A goo<i number of original communications in the form
of addresses were delivered.
Strophanthfs ; a Clinical Study. By Reynold W. Wilcox. M.I>.,
LL. D. VromXh^ American Journal 0/ the Medical Sciences, May, 1897.
The author is of the opinion that the variety Komb^ is a distinct species. The
present report is confined to a clinical study of the tincture made from Stro-
phanthus Komb^*; the author reserves for another occasion the presentat on of
similar studies upon what he believes to be four absolutely independent species
of strophanthus.
ZuR PrI FUNG DES Chinins. Von O. Hesse, from Archiv. der Pharm., i«5
114, 1897. This is a subject on which Dr. Hesse is especially well fitted •«>
speak.
Natural History Charts and Ili.u.strations. By John W. Harshl)erg«.,
Ph.D. Reprinted from Education, .\pril, 1897. Dr. Harshberger gives some
valuable suggestions on the best means of conducting a short course ou l>otany.
PHARMACEUTICAL ASSOCIATIONS.
PENNSYLVANIA PHARMACEUTICAL ASSOCIATION.
The twentieth annual meeting of this .XHSOciatiou will be held in the Kilta-
tinny Hotel, Delaware Water Cap, commencing Tues<lay, June a2<l. «t ^ v>
P.M.
The Del iw.irt W.iit-r « ..ip !•> ?»«j delightfully situated, and »o easily ri-,»riied.
^26 Pharmaceutical Associations. {^^"zw\^,\m^.^'
especially by members living in the eastern part of the State, that a large
number will no doubt avail themselves of this opportunity for a few days' recre-
ation and enjoyment.
The Trunk Line Association has granted permission to the railroads running
to the place of meeting to sell tickets at a rate of two cents per mile. Orders
for these tickets can be had on application to the Secretary, J. A. Miller, Harris-
burg, Pa. The hotel will furnish entertainment at $2.65 per day.
The Entertainment Committee will have a programme ready at the time of
the meeting that will please everybody.
NEW YORK STATE PHARMACEUTICAL. ASSOCIATION.
The nineteenth annual meeting of this Association will be held at Manhattan
Beach, commencing Tuesday, July 13, 1897. The Committee on Pharmacy and
Queries is very desirous of presenting a large number of papers on topics of scien-
tific, technical and trade interest, and is making direct appeals to the members
who have occasionally demonstrated their ability to prepare papers on subjects
of interest to the pharmacists of the State. A list of queries has been pre-
pared, which embodies suggestions that should appeal to every working
pharmacist in the Association.
The meeting promises to be a splendid success so far as social features are
concerned, and the Committee on Pharmacy and Queries is determined to
make the pharmacy section of the meeting an interesting and valuable feature
of it. With this object in view members are urged to select one or more sub-
jects from the list of queries and prepare papers thereon. Albert H. Brundage,
Ph.G., M.D., Chairman, 1153 Gates Avenue, Brooklyn, should be addressed on
all matters relating to papers and queries.
THE ARKANSAS ASSOCIATION OF PHARMACISTS.
The Association met in annual session on May nth, 12th, 13th, in Little Rock.
The attendance was not large, but was very enthusiastic, and the meeting was
a very entertaining and successful one. Ten new members were added to the
list, which now numbers 175, consisting of many of the most influential phar-
macists in the State.
President Sparks read his annual address, which was referred to a comfnittee
on distribution. The treasurer's report showed a balance on hand of $293.91.
The president appointed a committee of three, consisting of Dr. Bond, Mr. R.
B. King and Dr. John W. Morton, to convey the fraternal greetings of the
Association to the Arkansas Medical Society, which was in session in this city.
During the session a number of interesting papers were read, among which
were the ' ' Future Supply of Coal," by Mr. R. B. King, of Helena. This paper,
which shows that there can be no dearth in the coal supply of the world, was
referred to the Committee on Publication. Mr. Ginnochio treated the " Influ-
ence of Moisture on Drugs" very instructively.
The report of the Secretary of the Arkansas Board of Pharmacy was read by
Dr. Bond. It showed a registration of 28 during the last year, and a total regis-
tration of 921. Graduates of reputable Colleges of Pharmacy and licentiates
of some of the State Boards are occasionally recognized by our Board.
The query box afforded much interesting and instructive discussion.
^""june'i^^*'" } Pharviaceutical Meeting. 327
A display of chemicals made by Mr, Germain, of Fort Smith, attracted much
attention, particularly the dry chemicals. The prize for Pharmaceutical display
was awarded to him.
The special committee appointed to convey the fraternal greetings of this
body to the Medical Society reported they had been received in a very cordial
manner, and invited to address that body, which invitation was acceptetl, and
much gratification was expressed by the physicians for the visit and the
address.
The following gentlemen were elected officers for the ensuing year :
Mr. J. F. Dowdy. Little Rock, President.
Dr. H. C.Johnson, Van Buren, First Vice-President.
Dr. J. W. Morton. Fort Smith, Second Vice-President.
Mr. John B. Bond, Jr.. Little Rock, Secretary. Re-elected.
Mr. J. A. Jungkind, Little Rock, Treasurer. Re-elected.
Mr. Dowdy, being elected president, made a vacancy in the Executive Com-
mittee, which was filled by the election of Mr. Shachleiter.
After some discussion, it was agreed that the next meeting should be held in
Little Rock on the second Tuesday in May, 1S98.
On motion of Dr. Bond, it was ordered that the president, secretary and
treasurer should compose the Publication Committee.
No further business appearing, the new officers were severally installed, and
the meeting adjourned.
MINUTES OF THE PHARMACEUTICAL MEETING.
PHiL.\nKLPHi.\, May 18, 1S97.
The last Pharmaceutical Meetingof the present series was held in the Museum
of the College at 3.30 p.m. Mr. F. W. K. Stedem presided. The reading of
the minutes of the previous meeting was omitted.
.\n interesting paper on "Verba del Polio," by Prof. Alfonso Herrera, of
Mexico, was read by Prof. Henry Trimble (see page 290).
The usefulness of this plant as a remedy in medical practice, and as affirmed
by the writer, dates back to the time of the A/.tecs, it having been eniplove<l
by them in the treatment of several diseases. But when their power was over-
come it was forgotten, together with other useful pro<lucts of their countrv.
Nearly three centuries elapsed before it again attracted the attention of investi-
gators, and It has been only within the latter half of this century that anv con-
siderable study has l>een given to it. It is valued chiefly as a hemostatic,
although, as stated by the writer, there seems to be some difficulty in determin-
ing to what constituent this property is due.
"On the Occurrence of Strontium in Plants" was the subject of a somewhat
timely paper presented by Prof Henry Trimble (sec page 2961.
The author had discovered strontium in a number of samples of bark from
different species of Castanopsis growing at Singapore, ln<lia, while a sample of
American Cr».stanop)sis growing in California gave no indication of the presence
of this metal. Two samples of oak and one of mangrove from India aUo con-
taineil strontium. A comparison of the data so obtainc<l led the writer to
believe that the presence of strontium salts in the samples from Singapore was
•lue to the composition of the soil in that country.
Am. Jour. Pharro
328 Pharmaceutical Meeting, {'^^'jnne',mil
Prof. Samuel P. Sadtler referred to the use of strontium hydrate in sugar
refining, and to the objectionable feature of its cost when first suggested for
this purpose, on account of the limited supply of the minerals of strontium.
The discovery of other mines since then had had their influence in decreasing
the cost of the metal, and in regard to its occurrence in India he thought it
probable that the government or mining reports would give some information.
Professor Trimble replied that the government officials reported only a trace
oi strontium salts in the Singapore soil.
A paper, entitled a "Note on Red Mercuric Oxide." was contributed by Mr.
J. \V. England (see page 311 ). This was intended as a reply to the criticisms
presented by Mr. Charles H. LaWall, at the meeting last month, on citrine
ointment. The principal remarks of the author were on the question of the
relative purity of red mercuric oxide and metallic mercury, and the advisability
of substituting the former for the latter in the formula for citrine ointment, as
a matter of convenience. His information in regard to the purity. of these
substances did not accord with Mr. LaWall's statement concerning them, and
in evidence of this, extracts from letters from three firms of manufacturing
chemists were presented.
Mr. Lyman F. Kebler casually made reference to a subject which had recently
been brought to his notice. He said that a resinous substance, which had been
applied to the trunks of some of the trees in the public squares of this city
to serve as an obstruction to insects, had been found to be harmful to the trees.
In experimenting with solvents with the object of removing it, he found ace-
tone to answer the purpose most effectually.
Some specimens and other objects added to the interest of the meeting as
follows :
A curious specimen of a growing plant of Japanese cultivation was loaned by
Mr. Howard B. French. It belonged to the natural order Coniferse, and
in outline strikingly resembled a fowl, the fictitious name "Ibis firma" being
significant of this.
A copy of letters patent, which was an elaborate and formidable document,
granted during the reign of George II of Bngland, for a medicine "Oleum
Anodinum," was presented by Mr. Chas. Bullock.
Professor Trimble called attention to a large specimen of canaigre root, show-
ing the influence of cultivation, and to one of natural growth, much smaller in
size, both of them having grown at Rialto, California.
Among the samples was one of calcium carbide, presented by Mr. J. O.
McHenry, of this city.
An improved attachment for the " Moffatt Formaldehyde Generator," pre-
sented by the agents, Messrs. Eli Lilly & Co., of Indianapolis, Ind., was
exhibited.
The chairman believed in the efficacy of the apparatus as a disinfecting
agent, but said that, in order to insure the generation of the gas, it was neces-
sary to carefully adjust the wick.
On motion, the meeting adjourned.
Thos. S. WiEGand, Registrar.
THE AMERICAN
JOURNAL OF PHARMACY
JULY, iSgy.
THE CALIFORNIA MANNA.'
By John Uri Li.oyd, Ph.M.
MENTIONED BY FATHER PICOLO. [IVit/i a sunimary.)
Query by Prof. Fllickiger :
" What was the manna mentioned by one Father Picolo in CaH-
fornia and alluded to by Proust, in Ann. d. Chvn., 57 f 1806), p. 145 ?"
Answer by John Uri Lloyd.
Dear Prof. FlCckiger : — I find, on reference to the paper citedi
that the statement is as follows :
Proust. Ann. d. Chim., 57, p. 145. On the Suf^ar of the Grape.
The manna seems to abound in America, accordinj^ to the
reports of travellers. Herera says : '• It falls in the season in the
quantity of a dew, which congeals like sugar, and which is so whole-
some that it is named Manna. Father Picolo, one of the first
' When Prof. Fliickiger visited America (July, 1894) he hoped to obtain his-
torical data that would enable him to give the records of several interesting
American productions. In this he failed, and he then associated in his behalf
the services of the author of this paper, .\fter much of the work hid K.-.n
done, the death of Prof. Fliickiger interrupte<l the investigation
These papers (some of them) passed into possession of Prof. IM. Schner, of
the Strasburg University, who translated into Gennan the accompanying work
by Professor IJoyd on .American Manna, for the patfes of t}je /irti,htt- Jrr
detilschen pharmaceulischen Gesellscha/t.
We present herein, with the kr. ' ' ' ■ iii 01 rroj, ' ihc
author, the original i)apcr on .\t: litor Am. J"
329 I
330 California Manna. { ^'"juT/jSr^'-
spiritual conquerors of California, assures us that it exudes in con-
siderable amounts from the shrubs (arbrisseaux) in April, May and
June."
It will be shown hereafter that this is not a literal abstract from
the original source, where the word roseaux is used instead of the
word arbrisseaux.
In tracing this subject, first the biography of Father Picolo
presents itself as follows :
BIOGRAPHY OF FRANCOIS MARIE PICOLO."
Abstracted from Bibliotheque des Ecrivains de la Compagnie de
Jesus, Liege A. Lyon, 1872, p. 1957.
•' Picolo, Francois Marie, a Sicilian Jesuit, was born in Palermo,
March 24, 1654, entered the Society of Jesus in 1673, and made the
four vows in Mexico in 1689. He founded the Mission of Jesus of
Carichic, where he resided for fourteen years, and afterwards united
with Father Jean de Salvatierra in order to open the missions in
California.
" After a stay of forty years with the missions, he received the
reward of his toil on February 22, 1729."
His writings, as far as known to me,^ are contained in the follow-
ing communication :
" Memoir, with regard to the conditions of the missions lately
established in California, by the Fathers of the Society of Jesus ;
presented to the Royal Council of Guadalaxara, in Mexico, Feb-
ruary 10, 1702, by Father Francois Marie Picolo, of the same
society, and one of the original founders of this Mission."
This memoir of F. M. Picolo is reprinted literally in W. I. Kip's
Historical Scenes from the old Jesuit Missions, New York, 1875,
which is an abstract of American topics from the following work :
" Lettres Edifiantes et cnrietcses, ccrites des Missions Etrangcres,
in ^7 volumes, containing the letters of the Jesuit missionaries from
about 16 jo to ly^oy this collection being purchased by W. L Kip
from the library of the Bishop of Durham.
Speaking in Chapter II, Missions in Lower California, 1702, he
states, p. 57, in the months of April, May and June, a kind of maiina
' Thanks are extended St. Xavier's College, Cincinnati, for library courtesies,
thus enabling this biography to be presented.
■• J. U. L.
^""•/.Sy^ST""^-} California Manna. 331
falls with the dew, ichich congeals and hardens on the leaves of the
reeds* {roseaux) from which it is gathered. I have tasted tt.
It is a little darker than sugar, but has all its szceetness.'*
Endeavoring to identify Father Picolo's manna, the following
reference to manna-like bodies (false mannasj was noted in the U. S.
Dispensatory, 17th Ed., Philadelphia, 1894, p. 850, which, however,
are not the same manna as that of Picolo.
" American False Manna. A substance resembling manna, of a
sweet, slightly bitter, and terebinthinate taste, and actively purga-
tive, exudes from incisions in Pinus Lambertiana of Oregon, and is
used by the natives." (Nar. of U. S. Expl. Exp., v. 232.)
•' M. Berthelot has abstracted from this product a peculiar saccha-
rine principle which he calls • pinite.' " (See A. J. P., vol, 28, p. 157.)
The strongly cathartic properties of this manna of the pinus and
its resemblance to manna are emphasized in the following descrip-
tion of this substance :
I. Wilkes, Narrative of the U. S. Exploring Exped., Philadelphia,
1850, Vol. 5.
P. 232. Speaking of the Pinus Lambertiana, w'hich they found
frequently when crossing the Umpgua Mountains in Southern Ore-
gon. " Some of the sugar produced by this tree was obtained ; it
is of a sweet taste, with a slightly bitter and piny flavor ; it resem-
bles manna, and is obtained by the Indians by burning a cavit}* in
the tree, whence it exudes. It is gathered in large quantities.
" This sugar is a powerful cathartic, and affected all the party who
partook of it ; yet it is said that it is used as a substitute for sugar
among the trapi)ers and hunters."
II. John S. Newberry, botanist in charge of the U. S. Pacific R. R.
Surveys, California and Oregon. Botanical Report, 1855, p. 44. On
the Pmus Liimbertiana, the Sugar Pine.
" The resin of the sugar pine is less abundant than that of the
P. ponderosa ; is white or transparent like that of P. strobus.
"That which exudes from partially burnt trees, for the most part,
loses its terebinthine taste and smell, and acquires a sweetness
nearly equal to that of sugar.
♦•This sugar gives the tree its name, and is sometimes used for
« Roseaux, iu the original Lettrts idifiantes, etc., Tome V, p. 264. Kip't tr«n»-
Ution, ia literal, as we have verified from the original letter— J. T. L.
332 California Manna, {^""/uiy'is^g?.^'"'
sweetening food. It has, however, decided cathartic properties, and
is oftener used by the frontier men as a medicine than a condiment.
•♦Its resemblance in taste, appearance and properties to manna
strikes one instantly ; and but for a slight terebinthine flavor, it
might be substituted for that drug without the knowledge of the
druggist or physician, its physical and medical properties are so
very like."
It is not possible that Father Picolo refers to the sugar from
these trees, as he failed to record any cathartic properties as an
attribute of his sugar ; furthermore, the manner which he describes
of collecting the sugar hardly conforms to the description just given
as to the manner of collecting it from these trees. It is most prob-
able, according to his brief statement on the subject (for he men-
tions it as occurring *' on the leaves of the reeds "), that high trees
carrying sugar in their sap are out of question, although such sugar
trees were not unlikely to have been met by him. For example,
also, {white maple, Acer macrophyllum, see appended list of refer-
ences, No. 8).
Only reed grasses are likely to come into consideration with the
manna of Picolo, and of these we have recorded as follows :
(i) Manna grass, Glyceria. This seems to be out of the
question, as text-books on botany (Gray, etc.) state that the
name, denoting sweet, is given in allusion to the taste of the grain.
(2) Phragmites communis, Trin. Described by U. S, Geological
Exploration of the 4.0th parallel. C. King, 5th vol. Botany. S.
Watson, p. 390.
*' Found from Florida to Canada and westward to the Pacific. On
the banks of fresh-water streams and springs from the Truskee to
the East Humboldt Mountains, Nevada, 4-6000 feet altitude. Sugar
is said by Durand and Hilgard'^ to be extracted from the stalks of
this grass by the Indians, but the scanty juice is not at all
saccharine.
"A sweet secretion, however, is sometimes formed upon it in con-
siderable quantity by aphides, as well as upon the leaves of cotton-
ivood and other trees, and is collected by both the Utes and
the Mormons."
If this is correct [there is no higher authority to be found than
^Pacific R. R. Surveys, Bot. Rep. By Durand and Hilgard, Washington,
D. C, iSs5. P- 15-
Am. Jour. Pbarm.
July, 1897.
California Manna.
333
Sereno Watson], the " manna " observed to form on these plants is
the secretion of an insect and not an exudation from the plant.
Phragmites communis, thus far, comes nearest the plant described by
Father Picolo.
All the plants cited before were found to occur in locations alto-
gether different from the locality where Father Picolo made his
observations, which' does not, however, preclude them from his
territory.
(See accompanying^ map.)
334 California Marina. {^°'•/u^^•lS^'"■
Father Picolo's range of observation never extended north of
Lower Cahfornia, and, on the other hand, the information we have
of this Cahfornia (which is really a part of Mexico) is rather scant.
The following publications present two sources of information on
Lower California :
First : J. Ross Browne, Resources of States and Territories West
of the Rocky Mountains, New York, i86g, zvith an appendix, p. 6jo, on
Loivcr California, and with an historical addition, a Sketch of the Settle-
mcjit ajid Exploration of Lower California, by Alex, S. Taylor.
The Description of Lower California by J. Ross Browne, contains
the following passage :
Page dj7, " Fields of sugar cane are too common to excite remark,
and the manufacture of sugar is one of the most important interests
of the southern part of the peninsula. * * ^^^ The cane fields extend as
far as the eye can reach from San Jose." (This place is situated at
the extreme southern coast.) " Sugar mills in Comondu * * * sugar
exported in Purisima." This does not refer to the manna under dis-
cussion, and it will be mentioned later that this sugar cane is not
indigenous, but was imported by later settlers.
Second: Encyclopcedia Britannica, ninth ed. On California;
makes mention of Lower California also, introducing it as follows :
" The interior of Lower California is chiefly known to us as to its
physical and geological structure, from a reconnoissance made by
Messrs. Gabb and Lochr of the State Geological Survey of California,
in iSdy. '* This exploration was set on foot in order that some
information might be obtained relative to the value of a concession
made by the Mexican Government to an American company. This
grant was expected to lead to a settlement of the country, but the
whole thing turned out a failure."
The work referred to, The State Geological Survey of California in
i86y in charge of Messrs. Gabb and Loehr, is unfortunately not at our
command, and may possibly name that " reed " which yielded sugar,
as observed by Father Picolo.
However, the first-named book, by J. Ross Browne, in its second
part, A Sketch of the Settlement and Exploration of Lower California,
by Alex. S. Taylor, that appeared in 1869, makes mention of the
exploration of Lower California that had taken place in 1867 by
Messrs. Gabb and Loehr, under the direction of Mr. J. Ross Browne,
the results of which, however, were not then published.
''"'•juTiS^""'} California Manna, 335
Mr. J. Ross Browne, however, gives a general outline of this
exploration, based on detailed letters he received from Mr. Gabb
while on his exploring tour.
P. 66, a description of vegetation in Lower California is given,
which may be condensed as follows :
''Agaves (century plant) are also abundant, may be useful in the
future to extract spirits from the root. * * * Acacias, palms
with edible fruits, conifers, oaks, wild plums, cottonwoods, syca-
mores, willows, elder. The Arabian date palm, introduced by mis-
sionaries, is thriving, llie sugar cane has been cultivated for more
than a century, and yields a su^ar as strong and as sweet as that
of Peru, and very abundant in juice."
P. 82. Letter of Mr. Gabb to Mr. J. Ross Browne, May, 1867:
•* At Santiago, there are extensive plantations of sugar cane, and a
sugar mill was in active operation. The process throughout is of
the most primitive kind, but the result is a very palatable sugar
moulded into cakes somewhat like maple sugar, and known as
panoche." " Sugar industry ^ ^ ^ also at Todos Santos."
P. 143 of J. Ross Browne, Sketch and Settlement of Lower Cali-
fornia. Report of Dr. Jo Jin A. Veateh on Garros or Cedros Island,
p. 152, Soil and Productions, pine trees.
"The two interesting species of Rhus (R. Lentiana and R.
Veatchiana) form marked features in the island flora, the former for
the delicious acid exudation of its fruit." - *
••A beautiful, yellow-flowered agave or aloe plant, about 12 feet
in height, with a stem from 4 to 6 inches diameter at the base,
branching and spreading at the top and terminating in a profusion
of golden blossoms, was tolerably abundant. The flower cups were
filled with a fragrant, sweet liquor."
The same book of J. Ross l^rowne points to a third source of infor-
mation on Lower California ; this, however, was not obtainable in
the original.
P. /j;j, Extracts from a history of Old or Lower California. A pos-
thumous work written originally in Spanish by Padre Franc. }av.
Clavijero, of the Society of Jesus. Translated into Italian, I 'entce,
l'jSg,and back again into Spanish by Nicolas (iarcia de San /V-
cente (Juan R. Navarro, editor), iSj2, was translated into Knclish
BV A. G. Rand.all. Secretary and Translator of the Lo7c'er California
Company's Exploring Expedition^ San Erancisco, May, iSOj.
336 California Manna. {'^'^i^xyAm:"'^'
P. 164 of J. Ross Browne's Book, loc. cit., says, as bearing on our
subject :
" In some parts there grows, near running streams, reed grass, of
the thickness of the little finger.
"This LITTLE reed is the only plant in California in which
MANNA IS FOUND. At the present time there are large growths of
this imported from abroad."
Biography of Francisco Javier Clavijero. Taken from Biblio-
theque de la Compagnie de Jesus. Tome II, Bruxelles and Paris,
1891, p. 1210.
Francisco Javier Clavijero, born in Vera Cruz, on the 9th of Sep-
tember, 1 73 1. Was received in the province of Mexico, February
13th, 1748. He taught rhetoric in Mexico, philosophy at Valla-
dolid and at Guadalaxara in New Spain. He was exiled and
depoited to Italy, and died at Bologna April 2, 1787.
Historia de la Antigua a Baya California. Obra posthuma del
padre Francisco Javier Clavijero de la compaiiia de Jesus.
[Note. — Some time after this paper was placed in the hands of
Professor FlUckiger, the following information was found in the
Lloyd Library, and a copy at once forwarded to Prof. Ed. Schaer,
Strasburg, for the purpose of supplementing the present paper.
From the U. S. Agricultural Report for 1870, Food Products of
the North American Indians, p. 423, "Bent grass (Arundo phrag-
mites)" (which is a synonym for Phragmites communis, Trin.).
"This species of reed, which grows abundantly around St,
Thomas, in southern Utah, during the summer months, produces a
kind of white, sweet gum. The Utah Indians cut down the reeds
and lay them in piles on blankets or hides, and let them remain for
a short time to wilt, when the bundles are beaten with rods to
release the gum. The small particles so detached are pressed into
balls to be eaten at pleasure. It is a sweet, manna-like substance."
In the returned manuscript we find a foot-note by Professor
Schaer, giving the substance of the foregoing quotation, which Pro-
fessor Fluckiger had gathered from the same authority while he
was in Brooklyn.]
SUMMARY.
Sugar and two kinds of" manna " are described in Western litera-
ture.
1st, Sugar. Sugar was derived from the sugar cane, which wa
^"/ui^riS?.'^^"} California Manna. 337
introduced into Lower California at least one hundred years ago.
This was not '* manna."
2dL, Father Picolo s Manna. Father Picolo observed a saccharine
deposit on a species of grass that he called reeds (roseaux) and not
shrubs (arbrisseaux) as Proust recorded the word. Of the plants
likely to have yielded this manna, the reed grasses only are to be
considered. Of the reed grasses, Phragmites communis undoubtedly
answers all the conditions that are cited by Father Picolo, and in
my mind this plant is the origin of Picolo's Manna. This manna
is (or was recently) still collected by the Indians.
3d, Manna of tJie Finns. This is \'ielded by Finns Lambertiana of
Oregon, and is cathartic as well as sweet, but no evidence e.xists to
indicate that Picolo had any knowledge of its existence.
Finally, I would decide that without question Father Picolo
described, as he saw it, the saccharine deposit on Fhragmites com-
munis, which, according to Watson, is caused by aphides.
REFERENCES ON THE SUBJECT OK FATHER PICOLO'S MANNA.
( I ) Proust, Ann. d. Chimie, 57 (1806), p. 145, mentioning Father Picolo and
his manna; this occurnng on "arbrisseaux " shrubs.
(2j Bibliothlque des Ecrivains de la Co}npai:nii- de Jisus, Li^ge & Lyon, 1877,
p. 1957. Biography of Father Picolo, and mentioning his " Memoir."
(3) Letlres edifiantes et curicuses, ecrites des Missions HrangereSy in 47 vol-
umes, containing the letters of the Jesuit missionaries from about 1650-1750.
Translated from the Spanish, Vol. V, p. 264. Containing the memoir of Father
Picolo. mentioned under 2 in French, manna occurring on "roseaux" reeds.
(4) W. I. Kip, Historical Scenes from the old Jesuit Missions, New York,
1875, p. 50. Containing the "memoir" of Father Picolo, literally translated
into Knglish.
(5) U. S. Dispensatory, seventeenth edition, Philadelphia, 1894, p. 850. On
American False Manna, From Pinus Lambertiana, Sugar Pine. Points to
Reference No. 6.
(6) Wilkes, Narrative of the U. S. Expiorinff Expedition, Philadelphia,
i^5<^. Vol. \, p. 232. On Pinus Lambertiana. The sugar has strongly cathar-
tic properties.
(7) John S. Newberry, botanist in charge of the U. S. Pacific R. R. Sur-
veys in California and Oregon, 1855. liotanical Report, p. 42. Describiug
Pinus Lambertiana and corroborating statement in Reference No. 6.
(8) J. C;, Cooi'EK, botanist in charge of the V . S. Pacific R. R. Survey Route
near the 47th and 48th parallels, explored by L L Stevens, 1853-55. liotanical
Report, No. i, p. 28. Mentions White Maple, Acer macrophyllum, as contain-
ing sugar in its sap.
(9) Asa Gray and others. Botany. Manna grass, sweet principle is con-
tained in the grain.
(10) Skreno Watson, botanist in charge off. S. Geological Fxploration of
338 Corrosive Sublimate in Calomel, {^"-AT/'S^""-
the 40th pirallel, under C. King, 5th Vol. Botany, p. 390. On Phragmites
communis. Reed-sap not saccharine. Aphides cause sweet secretions on its
leaves and those of cottouwood and other trees.
(11) DURAXD AND HiLGARD, Pacific R. R. Survey. Botanical Report,
Washington, D. C , 1855, p. 15. The Indians are said (by D. and H.) to extract
sugar from Phragmites communis. This seems to be contrary to the statement
in Reference 10.
(12) J. Ross Browne. Resources of States and Territories west of the
Rocky Mountains, New York, 1869, («) with an appendix, p. 630, on Lower
California, and with an historical addition, [h) A sketch of the settlement and
exploration of Lower California, by Alex. S. Taylor. In 12 (a) it is mentioned
that sugar cane abounds in Lower California ; 12 [b) contains further references.
(13 ) Encyclopcsdia Britannica, 9th ed. On California, also on Lower Califor-
nia, points to Reference No. 14.
( 14) Gabb and Loehr, with the State Geological Survey of California in 1867.
The original was not accessible. A brief excerpt is contained in Reference 12
ib), p. 66.
(15) Report of John A. Veatch, On Carros or Cedros Islaiid. Original not
accessible. Brief excerpt is to be found in Reference 12 [b), p. 152. Mentions
an "agave," which contains a sweet liquid in its flowering cups.
(16) Extracts from a History of Old or Lower California. A posthumous
work, written originally in Spanish by Padre Franc, favier Clavijero, of the
Society of Jesus. Translated into Italian, Venice, 1789, and back again into
Spanish by Nicolas Garcia, de San Vicente (Juan R. Navarro, editor), 1852.
Was translated into English by A. G. Randall, Secretary and Translator of the
Lower California Company's Exploring Expedition, San Francisco, May, 1867.
Original not accessible. An abstract to be found in 12 {b), p. 164. It states
that there is a reed growing in Lower California near running streams that
yields manna.
CORROSIVE SUBLIMATE IN CALOMEL.^
BY IvYMAN F. KEBI^ER.
The 1890 U.S.P., among other requirements, describes calomel as
** A white, impalpable powder, showing only small, isolated crystals
under a magnifying power of 100 diameters. Insoluble in water*
alcohol or ether. In contact with calcium hydrate T. S., the salt is
blackened. If i gramme of the salt be shaken with 10 c.c. of water
or alcohol, the respective filtrates should not be affected by hydrogen
sulphide T. S. or silver nitrate T. S. (absence of mercuric chloride^!'
Several years ago the writer received a sample of calomel that
gave a prominent yellow coloration when treated with lime-water.
Yellow wash instead of black wash, if you please. The question
immediately arose — is it possible that any manufacturer will put such
a valuable medicinal agent as calomel on the market containing
such an apparent quantity of corrosive sublimate ? Further exami-
^ Presented at the meeting of the Penna. Pharm. ^55^?^., June, 1897.
^'"■ju'i"-!^.*''"-} Corrosive Sublimate in Calomel. 339
nation showed that the calomel contained an appreciable quantity of
this poisonous af^ent. Other makes were secured and all developed
a fjreater or lesser yellowish coloration when treated with lime-
water. The various available products were then critically exam-
ined according to the U.S. P. requirements, with the following results:
The color varied from a white to a decided cream. Isolated broken
crystals were present in all material examined. Minute traces of
mercuric chloride were indicated in every instance.
Since examining the above samples the writer has watched the
quality of this article with much interest ; but thus far all efforts
have failed to find a calomel absolutely free from corrosive sublimate
when the U.S. P. tests were rigidly applied. In two cases, however,
both the silver nitrate and the hydrogen sulphide failed to give
absolute evidence of the mercuric chloride, but a transitional yellow
was developed with even these when treated with lime-water. One
of these was a beautiful crystalline (plates) product of Japanese
origin, the other an old sample found in the laboratory.
Several questions arise in this connection. First, the yellowish
coloration, and second, the relative solubilities of mercurous chloride,
silver chloride and mercurous sulphide.
It is well known that the color of the various compounds of mer-
cury is readily modified. In precipitating mercuric mercury with
hydrogen sulphide, the resulting product frequently varies in color
from white to black. The writer on several occasions has repeatedly
washed calomel with water, to remove the soluble mercury com-
pounds, but in every instance a yellowish coloration was develojjed
at the point of contact, when the washed calomel was treated with
lime-water. This would suggest the conclusion that calomel
develops a transitional )'ellowish coloration at the point of contact
when treated with lime-water.
The second question, viz.: the relative solubility of the above-
named compounds, is an interesting one. We are informed by the
Pharmacopoeia, and other standard works, that calomel is insoluble.
Silver chloride and mercurous sulphide are generally considered
insoluble. According to A. M. Comey's •• Dictionary of Chemical
Solubilities " calomel and silver chloride are nearly or almost insoluble
in water, while mercurous sulphide is insoluble.
V. Kohlrausch' and F. Rose, calculating from the electrical c«>n-
» 1893, Ztschr. phys. Chrm., fJ, 241.
Am. Jour. Pharm.
340 Corrosive Sublimate in Calomel. {^"""/vliy^isS
ductivity of calomel in water, at 18° C, have found that I litre
of water dissolves 3-1 mg. of mercurous chloride. The same authori-
ties,- by'the [electrolytic method, have found that i litre of water,
at iS° C, dissolves 1-52 mg. of silver chloride. The difference of the
relative solubilities of silver chloride and mercurous chloride is 1-58
mg. per litre. According to these experiments, there would be
formed a certain amount of silver chloride, when a saturated aqueous
solution of calomel is treated with silver nitrate. When we remem-
bered that one part of silver can be detected in 800,000 parts of
water, it can readily be seen why calomel is so often reported as
containing corrosive sublimate.
Then aeain, if mercurous chloride is soluble at all in water, and
mercurous sulphide is insoluble in the same menstruum, it naturally
follows that hydrogen sulphide will produce a reaction with a satu-
rated aqueous solution of calomel.
According to the writer's observations, calomel is nearly as soluble
in alcohol as in water, but is insoluble in ether ; at least, an alcoholic
solution of calomel frequently gives a reaction with hydrogen sul-
phide, while an ethereal solution will not leave a residue when
evaporated in a pure atmosphere.
While it is impossible to countenance any laxness in a matter of
this kind, still the writer is of the opinion that the official require-
ments are slightly too rigid. As the matter now stands, the analyst
must practically take it upon himself, if he reports favorably on any
material submitted, or he must reject every sample submitted
to him. Calomel does occasionally contain corrosive sublimate, and
it is necessary to keep a strict surveillance over this product. But
according to the most rigid tests, with the above noted exception,
all calomel examined by the writer during the past few years has not
contained over ^^^-^^^^^ of i per cent, of corrosive sublimate.
305 Cherry Street, Philadelphia.
Volatile oil of lavage, according to E. Braun {Archiv der Pharm., 235, i),
contains {a) a terpene, CioHj^,, resembling limonene, but not giving crystalline
compounds with the halogen acids ; {b) cineol, CjoHiyO ; {c) isovalerianic acid ;
{d) acetic acid, as an oxidation product ; [e) benzoic acid. The oil commences
to boil at 170°, and begins to decompose at 200° C.
M893, Thid., 12, 242.
"^"■/uiy'-iS?"""*} ^oot of Kalmia Lati folia, 34 1
ANALYSIS OF THE ROOT OF KALMIA LATIFOLIA.
By Harry Matusow, Ph.G.
Contribution from the Chemical Laboratory of the Philadelphia College of
Pharmacy. Xo. 168.
This plant is a well-known evergreen of the natural order Eri-
caceae, and is known under the various synonyms of laurel, mountain
laurel, broad-leaved laurel, calico bush and spoonwood. It inhabits
all sections of the United States, from the Atlantic Ocean to the
Mississippi River, being especially abundant on the sides of hills
and mountains. It is a shrub, from three to ten feet in height, and
bears beautiful flowers.
The leaves of the plant are said to possess poisonous properties,
due to andromedotoxin, which is found in a number of plants belong-
ing to the EricacecTc. As far as was learned, the root has not been
previously examined ; so in order to ascertain its constituents, a
quantity of the root was collected by the writer at Lawnside, New
Jersey, in July, 1896. The root was well cleaned,' allo^ved to become
air-dry and afterwards reduced to fine powder for proximate analysis.
The results may be outlined in the order of their succession as
follows :
Petroleum Ether Extract. — This amounted to -34 per cent, of the
weight of the root. It consisted of caoutchouc, wax and a resin-
like substance. The last had a dark brown color, and was insoluble
in hot aqueous solution of potassium hydrate. Alcoholic solution
of potassium hydrate dissolved it. From the solution so obtained
diluted sulphuric acid precipitated a white substance which was
soluble in alcohol, and gave precipitates with alcoholic solutions of
ferric chloride and lead acetate.
EJher Extract. — Ether dissolved -89 per cent, of the root. Only
a small quantity of the extract was soluble in water. The water
solution was neutral in reaction. Treatment with I'ehling's solution
and acid showed the absence of glucosidcs. The common alkaloidal
reagents failed to indicate the presence of alkaloids. That part of
the extract which was insoluble in water was completely soluble in
alcohol. The solution was acid in reaction. Water precipitated it.
as did also alcoholic solutions of ferric chloride and lead acetate.
The solution contained resin and phlobaphene. A portion of the
alcoholic solution was evaporated to dryness, and the residue treated
with potassium hydrate solution at the water-bath temperature. The
342 Root of Kalmia Latifolia. { ^"^/u^i^^^sg'^^'"'-
solution was filtered off from the undissolved portion, and when
treated with diluted sulphuric acid in excess, it deposited a floccu-
lent precipitate of resinous matter which showed no color reactions
with strong mineral acids. The filtrate from the fiocculent precipi-
tate was shaken with chloroform in a separating funnel. The
chloroformic layer was separated and evaporated. The following
tests were applied to the residue:
Strong sulphuric acid — one drop produced a red color, which
became more pronounced on warming. Strong nitric acid — a few
drops produced a red color which intensified on warming.
Strong hydrochloric acid, even when warmed, produced no change.
These reactions correspond, except in the case of hydrochloric
acid, with those obtained by previous investigators of the leaves of
this plant, and ascribed by them to andromedotoxin.
Absolute Alcohol Extract. — The extract amounted to 3 68 per
cent. It was of a dark brown color and had a porous character.
Water dissolved an "amount equal to 1-48 per cent, of the root. The
residue consisted of phlobaphene. The water solution was acid in
reaction. It contained a small amount of tannin, which reacted as
follows :
Lead acetate, flesh-colored precipitate. Ferric chloride, brownish
precipitate. Ammonia ferric sulphate, brownish-green precipitate.
Gelatin, flesh-colored precipitate. Bromine water, yellow precipitate-
Calcium hydrate, reddish precipitate.
These reactions were confirmed by tests apphed to a cold-water
infusion of the original root. They indicate a tannin similar to that
of the oak barks and to the one found in the leaves of Kalmia latifolia,
as described by DeGraffe in this Journal for June, 1896. The alco-
holic solution of the phlobaphene gave the same reaction with ferric
chloride as the tannin. Traces of glucose and saccharose were
present. Alkaloids, glucosides and neutral principles v/ere not found
after a complete system of application of immiscible solvents to both
acid and alkaline water solutions of the extract.
Water Extract. — Cold water extracted 3-2 per cent, of organi'c
matter from the root. This comprised -92 per cent, of mucilage and
albuminous matter, a trace of glucose and nearly I per cent, of
saccharose.
Alkaline Water Extract. — Water made alkaline with sodium
hydrate dissolved 544 per cent, of organic solids. The extract
showed 98 per cent, of mucilagre and albuminous matter.
"""•/uTiSS""^-} ^'otcs on Opium Assaying. 343
Acidulated Water Extract. — The root yielded 117 per cent, of
organic solids to water acidulated with hydrochloric acid. Pararabin
was present. The next treatment was with boiling acidulated water,
but the e.xtract was not worked.
Starch. — This constituent was determined on a separate portion
of the original root. Two determinations were made; one showed
1 1 38 per cent., the other 1 1-43 per cent. — an average of 1 1-40 per
cent.
Treatment of the residue from the boiling with acidulated water
with chlorine water, produced a loss which indicated 20 1 8 per cent,
of lignin.
The residue from this treatment was ignited. The loss indicated
47-40 per cent, of cellulose and allied substances. Moisture was
found in the root to the extent of 5-06 per cent. The amount of
ash was 124 per cent. A qualitative analysis of the ash showed
the presence of the following :
Water dissolved 16 16 per cent, of the ash. The solution con-
tained aluminum and potassium combined with hydrochloric and
sulphuric acids. Hydrochloric acid dissolved 33- 14 per cent, of the
ash. The solution contained calcium, magnesium, aluminum, iron
and manganese combined with phosphoric acid. The remainder of
the ash consisted of adhering soil.
NOTES ON OPIUM ASSAYING.'
BY FRANK X. MOERK, PH.C,.
For several years past the writer has adopted certain procedures
in as.saying gum opium, the results of which were expected to assist
in perfecting this assay process.
The sample of gum opium received for analysis is weighed and
dried for about twelve hours at 80-85^ C; drying is facilitated by cut-
ting the sample into pieces about the size of cherries before weigliing.
The loss in weight is noted, and the partly dried opium is coarsely
powdered and thoroughly mixed ; of this, 2 grammes are taken lor
the residual moisture estimation, and 8 grammes for the morphine
estimation, according to the US. P. The latter quantity, as a ruk\
corresponds very closely to 10 grammes moist opium ; the exact quan-
^Read at the meeting of the Pennsylvania Pharmaceutical A»»*»cialion. June
32, 1897.
344 ^otcs on Opium Assaying. { '"^^jj?;:i8?7.^'"-
tities of moist and perfectly dry opium are, however, to be calculated
from the loss sustained in drying. This procedure enables a uni-
form sample from which concordant results can be obtained when
assayed at some subsequent time, and calculated to opium contain-
ing the original quantity of moisture.
In powdering the partly dried opium in glass or iron mortars,
electricity is developed and there is difficulty in avoiding loss from
particles being thrown about; this phenomenon was not noticed
when using wedgewood mortars.
The crude morphine obtained by the U.S.P. process was first
weighed on counterbalanced filters and again after transferring to a
watch-glass ; it will be noticed that there is, in the majority of cases,
a difference due to but a few milligrammes. In transferring, a camel's
hair pencil has to be used with some force to remove all of the
morphine from the filter, and this generally results in loosening some
of the fibres of the paper, which then contaminate the morphine.
The purity of the morphine is an important matter ; for its deter-
mination, several methods are in use, as the solubility in lime-water,
the solubility in alcohol and the ash method. If we look into the
question of the impurities which can be present in crude morphine,
there may be other opium alkaloids, particularly narcotine, sulphates
of calcium and strontium, phosphates of calcium and magnesium,
meconates of potassium, calcium and magnesium, and generally a
little coloring matter ; this does not exhaust the list of substances
that are possible, or even of those that have been found, but it is
sufficiently comprehensive to allow some reflections upon the prob-
able accuracy of these several methods of correction. The alcohol
method will give as morphine everything soluble in alcohol, hence,
narcotine and coloring matter will be returned as morphine ; it
reveals the ash-yielding constituents, particularly if absolute alcohol
be used ; and if, after weighing the insoluble matter, this be ignited
and weighed, the factor for calculating ash into impurity can be
obtained and compared with the present factor, which is simply
theoretical. The objection to the alcohol method has been the
expense and the difficulty of filtering out the very fine precipitate.
The lime-water method was the one first proposed for ascertaining
the purity of the morphine and was particularly recommended as a
means of detecting narcotine. After Stillwell proposed the alcohol
method Squibb, in a series of experiments, obtained almost identical
^"jiri^""-} -^^otes on Opium Assaying. 345
results in comparing these two methods. The ash obtained by
igniting crude morphine, was considered to be pure calcium oxide or
carbonate (depending upon the temperature of ignition), derived
from calcium meconate, until the writer in Am. Jour. Pharm., Sep-
tember, 1894, proved that the ash was a very complex mixture, and
this has since been verified by Mr. L F. Kebler. The writer also
raised the question as to the effect of lime-water upon this complex
mixture of salts, giving rise to the ash ; experiments made since that
time enable me to say that the lime-water solution, even after repre-
cipitation of the morphine, is always more or less colored ; the
reprecipitated morphine dissolved in dilute sulphuric acid frequently
yields a pink to rose-red colored solution, due to some foreign
organic substance which requires several reprecipitations for its
elimination ; in dissolving crude morphine in lime-water I have
observed that, if perfect solution does not result, a fine white precipi-
tate deposits at first, which, in the course of the half hour allowed
for the solvent action of the lime-water, changes to a yellow floccu-
lent precipitate ; o 050 gramme of a precipitate (obtained from the
mother-liquor of an opium assay), allowed to stand for half an hour
with 10 c.c. lime-water, then filtered, and washed first with lime-
water, then with distilled water, dried at 50-55° C, and weighed,
showed an increase in weight of 0004 ; it had also changed in
appearance as just described. These experiments confirm my pre-
vious supposition of the chemical change taking place by the lime-
water solution, but I had rather expected a decrease in the weight,
because of the presence of potassium meconate, and its possible
reaction with lime-water to form calcium meconate and soluble
potassium hydrate ; but the insoluble part in lime-water gave appar-
ently as good a test for potassium salts with platinic chloride as did
the original substance. An interchange between magnesium meco-
nate or phosphate and calcium hydrate, because of the formation of
insoluble calcium meconate or phosphate and insoluble magnesium
hydrate, will cause an increase in weight and seems probable. F'rom
these experiments, we must say that all of the organic matter is not
revealed by this test, and that the ash-yielding substances arc, at
least in part, chemically changed ; so that this correction can also
not be considered an accurate one.
The ash method will not reveal organic matter, and based upon
the assumption that the ash consists entirely of calcium oxide or
346 Notes on Opium Assaying. {^"^-/uT/.-S""^
carbonate derived from calcium meconate, and to which the ash is
calculated by the use of factors (4-55 for calcium oxide and 2-56 for
calcium carbonate), despite the fact that considerable potassium
carbonate is present (which should require a different factor), and
disregarding entirely that the sulphates and phosphates of the
metals present sustain comparatively little loss by ignition (the
factor for which cannot be foretold), the result being that the
correction based entirely upon the weight of the ash will be too
high unless counterbalanced by the presence of foreign organic
matter, an assumption which cannot be proven at the present time.
A number of comparisons of the lime-water and ash methods
have been published and agreed very well. Any difference between
the corrections could be allowed for from the above statements. In
May, 1896, Mr. L. F. Kebler published in the American Journal
OF Pharmacy a series of comparisons in which some new possibili-
ties were brought forward. Of the seventeen samples reported, one
yielded no ash and no correction by either method ; 07ie the same
correction by both methods ; seven a higher correction by the lime-
water method with the percentage of ash normal, i. e., below either
correction ; Jive a higher correction by the ash method, with the
percentage of ash normal; and three di higher correction by the ash
method, with the percentage of ash abnormal, i. e., greater than the
lime-water correction. To explain these results it must be admitted
that in some cases there is an iash-yielding substance which is solu-
ble in lime-water, whi)st in other cases there must be present some
organic impurity which is not soluble in lime-water, and of course
yields no ash.
While not one of these methods of correction can be considered
satisfactory, the writer has given preference to the lime-water
method as involving on the one hand less change during the man-
ipulation, and on the other hand because of the easier filtration of
the solution, and the possible reprecipitation of the morphine ; care
must be taken, by keeping the funnel covered with a watch-glass to
prevent the formation of calcium carbonate if working near a flame.
In the assays to be detailed, the lime-water correction was used ; 0-5
gramme of the well-mixed crude morphine was weighed into a
flask and thoroughly moistened with 5 c.c. lime-water before adding
the remaining 45 c.c. ; rotate the contents of flask repeatedly during
half an hour, and then filter the solution through counterbalanced
^"•jii?:i£7.*'"^'} yotes on Opium Assaying. 347
filters (7 centimetres), rinsing the precipitate in the flask upon the
filter by the use of small portions of the filtrate ; wash the flask and
filter with 5 c.c. lime-water, added in portions of i c.c. After the
last c.c. drains off, set aside the filtrate and washings and wash the
filter with 5 c.c. distilled water applied in portions of i c.c. ; after
draining press the filter between bibulous paper and dry at 50-5 5 ^ C.
to constant weight ; this weight is then calculated to entire weight
of crude morphine, and, subtracted from the weight of the crude
morphine as weighed on a watch-glass, gives the weight of the pure
morphine, which is then calculated to 100 parts of opium.
The lime-water solution of the crude morphine is thoroughly
agitated after adding 6 c.c. ether (just enough to saturate the solu-
tion, and for the purpose of rendering the precipitation of morphine
as complete as possible; morphine, particularly in presence of
foreign organic matter, is less soluble in water saturated with ether
than in pure water); 0150 gramme ammonium chloride is next
added and agitation continued for ten minutes before setting aside
for 10 to 12 hours, or over night (the 55 c.c. lime-water require
0140 gramme ammonium chloride for neutralization, so that there
is but a slight excess added) ; filter through counterbalanced filters
(7 centimetres) ; rinse the flask several times with a little of the
filtrate to remove the remaining morphine crystals, and then wash
the morphine and filter with 15 c.c. distilled water, applied in por-
tions of I c.c; dry the filter as above described, at 50-55° C, and
weigh. The combined weights of the recovered morphine and of
the correction subtracted from 0500 gives the loss sustained in the
purification, and represents chiefly the morphine remaining dis-
solved in the 55 c.c. of mother-liquor.
In looking over these results it will be seen that the impurity m
the crude morphine does not depend so much upon the length of
time in which the assay is allowed to stand as upon variations in
the samples of opium (the assays standing 15 hours, for instance,
illustrate this point) ; it has previously been proven that in any given
sample of opium the impurity increases with the time allowed for
precipitation.
Believing that the great difference in the quantity of the impurity
was due to variation in the ash-yielding constituents, a number of
the samples of opium, kept in the partly dried condition, were ex-
amined. Two grammes of the sample were dried at lOO^ C, then in-
148
Notes on Opiiun Assaying,
/Am. Jour. Pharm.
\ July, 1897.
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Notes on Opium Assayitig.
349
cinerated for total ash ; this, macerated with loc.c. water for one-half
hour, filtered, and filter and contents washed with water, i c c. at a
time, until the filtrate measured 20 c.c; the filter, with insoluble
portion of the ash, was dried, ignited and weighed, the difference
between that and the total ash giving ash soluble in water. The fig-
ures are in terms of percentage and relate to perfectly dried opium ;
for convenience of comparison the percentage of impurity in the
crude morphine is appended. The figures in the last column are
results of another series of experiments, to be mentioned a little later.
Number.
Moisture.
ToUl .\sh.
Soluble Ash.
Insoluble
Ash.
Impurity iu
Crude
Morphine.
Ash of
Dregs.
8
5*oo
6-37
3"2t
316
0"20
2-68
TO
522
55t
2*95
=•56
0'20
2-56
14
4-90
6-6S
350
3-iS
I4"20
2-92
15
527
5-36
3 >7
219
I3'20
1S7
16
5-65
7-15
360
3-55
lo-oo
2-94
17
5-05
5 "53
3"53
2"00
10 60
X 79
18
495
759
31:
442
10 80
371
19
3'47
5-36
329
207
470
rSi
There is no clue here for an explanation, as comparison of No. 8
with Nos. 15, 18 and 19 will prove, unless it were by quantitative
analysis, which the quantity of ash did not permit. The aqueous
solutions, excepting Nos. 8 and 15 and all of the insoluble ashes
moistened with water, gave j)ink or red colorations with phenol-
pthalein, but a single drop of a very dilute sulphuric acid dis-
charged the color; the insoluble ashes were mixed with water and
titrated with dilute sulphuric acid using methyl-orange as indicator,
but the results were as conflicting as the above ash determinations.
As a further probable explanation was based upon the acidity of
the aqueous opium infusion dissolving some of what in the preceding
table is called insoluble ash, and the addition of ammonia afterwards
reprecipitating this, a series of experiments were made, in which 2
grammes were extracted with water, as in the official assay, to make
64 c.c. filtrate ; the dregs were dried and ignited, and the results,
representing percentage of ash left in the dregs of perfectly dried
opium, are found in the last column of the preceding table. The
determination with No, 8 was nude last, and was sufficient to shatter
350 Processes and Laboratory Notes. { ^'^ j-Sy'ifo^^"*""'
conclusions based upon the other seven samples ; it will be seen
that there is a decrease of from 02 1 to 0-71 per cent, between the
insoluble ash and the ash of the dregs, in the case of those samples
yielding an impure crude morphine, whilst No. 10, yielding a pure
morphine, showed no decrease.
While these experiments were going on, I also tried in various
ways and with different indicators to determine the acidity of the
opium or opium infusion directly, but these efforts were fruitless.
The loss in the reprecipitation of the morphine varies from 0033
to o 0635 gramme., and while all of this may not be morphine, owing
to the influence of the lime-water upon the impurities in the crude
morphine, it opens up the question of the morphine left in the mother-
liquor in the assays proper. When it is remembered that this opera-
tion was carried out so as to minimize the loss, that the use of alco-
hol and of larger quantities of ether in the assays will necessarily
cause greater loss, and that the morphine actually weighed must be
subjected to a correction which itself is arbitrary, one can realize
that much work will yet have to be done before a satisfactory or
accurate opium assay process is arrived at. Of the two problems
to be solved, the one disclosing accurately the quantity of morphine
in mother-liquors is considered the more difficult ; in fact, the solving
of this will practically also solve the purity of any isolated morphine.
ANALYTICAL PROCESSES AND LABORATORY NOTES.
By Charles H. La Wall.
ASSAY PROCESSES FOR KOLA, GUARANA AND COFFEE.
A method for the estimation of caffeine in kola, guarana and
coffee, which obviates the use of the Soxhlet extraction apparatus,
has been used with success during the past year. The results agree
closely with those obtained by the long and tedious processes for-
merly employed, and can be obtained within a much shorter space
of time. It resembles closely the process recently suggested by Dr.
Keller for the determination of caffeine in tea. The directions are
as follows: Into a separatory funnel of convenient size, place 5
grammes of the drug and 5 c.c. 10 per cent, ammonia water. Allow
the mixture to stand for thirty minutes, then shake out the alkaloid
with chloroform, using three portions of 20 c.c. each.
"^ "" jaT/.iS^""" } Processes and Laboratory Notes. 3 5 i
If emulsification occurs, add powdered magnesium carbonate in
small quantities until separation takes place. Transfer the mixed
chloroform washings to a tared flask, recover the solvent in the cus-
tomary manner, and weigh the residue, which consists of fat and
alkaloid together.
Dissolve the fat with warm ether, using successive fractions of
20 c.c, until the ethereal washings leave no perceptible residue upon
evaporation of a small quantity. With careful manipulation, the
ether can be decanted each time without loss of caffeine ; but as a
precautionary measure, the ethereal washings may be filtered, the
filter washed well, first with ether and then with chloroform, trans-
ferring the chloroform washings back to the flask for evaporating
and weighing. The residue in the flask is almost pure caffeine, and
the difference between the weights of the first residue and the last
is the amount of fat present in the drug.
In the case of kola, the ether also removes the theobromine,
which is usually but a small percentage and may be ignored.
The following comparative results have been obtained :
KOLA NUTS.
No. I, Exhausted with chloroform in Soxhlet i •39 per cent, caffeine.
No. 2, Exhausted by the foregoing process 137 " '*
No. 3, " " " " . . 1-48 "
No. 4, " '• " " i'43 " *'
No. 5, *• •• " " I 40 "
GUARANA.
No. I, Exhausted with chloroform in Soxhlet 4 32 per cent.
No. 2, Exhausted by the foregoing process 4'68 "
No. 3, " " " " 462 '•
In assaying the fluid extracts of the drugs above mentioned, how-
ever, the Lloyd ferric hydrate process gives the most satisfactory
results.
ESTIMATION OF ALKALOIDS IN WHITE HELLEBOKL.
In answer to query No. 48 of the proceedings of this Association
for 1896, the following results are submitted. The well-known gen-
eral assay process of Dr. Keller was used with satislactory results,
the details being as follows : Place in a dry flask —
White hellel>ore . logrammcR.
Chloroform . .
ivther
10 per cent, ammonia water . .
Am. Jour. Pharm.
352 Processes and Laboratory Notes. {^'"•juT.'iS:
Shake vigorously, and allow to stand for six hours or over night,
then add 5 c.c. 10 per cent, ammonia water, shake well and pour off
50 grammes of the clear solution (representing 5 grammes of the
white hellebore). Transfer the solution to a separatory funnel and
shake out the alkaloid with acidulated water, using three fractions of
20 c.c. each. Place the aqueous washings in a separatory funnel, and,
after rendering alkaline with ammonia water, shake out the sepa-
rated alkaloid with a mixture of chloroform 3 volumes, ether i
volume. Transfer these washings to a tared flask, recover the
solvent, if desired, and weigh the residue, which is the total amount
of alkaloid in 5 grammes of the drug.
The results shown below were obtained by the foregoing process,
using the commercial drug in the form in which it is sold for an
insecticide. Five different samples assayed respectively :
No. I, 1-20 per cent.; No. 2, 1-24 per cent.; No. 3, 1-25 per cent.;
No. 4, ri2 per cent.; No. 5, i-i8 per cent, alkaloids.
A sample of the whole drug was also ground and assayed. This
yielded 1-75 per cent. — a somewhat higher yield, which should be
verified by assaying numerous different samples before accepting it
as a standard. The results as obtained show the commercial
drug to be uniform and about i per cent, would be a fair limit for
the minimum allowable yield of alkaloids by this process.
ARE C. p. CHEMICALS CHEMICALLY PURE?
In answer to query No. 44, requesting information upon the sub-
ject, it is difficult to give a definite reply. The term Chemically
Piire^ commonly abbreviated C. P., is used with such frequency when
applied to inorganic compounds, that it loses its force in a great
degree. To comply with this description accurately, a chemical
should be absolutely free from all foreign compounds, an ideal
requirement seldom found in practice. As generally applied, it has
come to mean simply a very high degree of purity, such as is re-
quired for analytical reagents, and, according to this interpretation
of the term, the quality of most C. P. chemicals sold, is in accord-
ance with the description. As an illustration of this accepted mean-
ing, sulphuric acid may be mentioned. This acid is listed as " C. P.,"
and also " C. P., free from arsenic." The latter commands the higher
price, thus indicating a degree of purity higher than " C P."
Some cases have been observed in which the term was clearly
^"''juiy'.i^'^''^} Processes and Laboratory Notes. 353
misapplied. Among these were " C. P. chemicals for photographic
purposes," as sodium thiosulphate and sulphite containing iron and
zinc; also sodium carbonate containing large quantities of chlorides
and sulphates. Fortunately, instances of this kind are rare, and,
with the exception of one manufacturer who evaded the question
by claiming that C, P. meant commercially pure, it has been found
that chemicals when designated C. P. conform to these requirements
as closely as is practicable. In this connection, the fact that even the
U.S. P. is somewhat inconsistent in its requirements for the purity
of certain chemicals may be new to some persons. The require-
ments of the U.S P. for the purity of carbonate and bicarbonate of
sodium allow a limit of chlorides and sulphates in each case. In
benzoate, salicylate and other salts of sodium, which are
made from one of the first-mentioned bases, absolute free-
dom from chlorides and sulphates is required, with no apparent
reason for such an increase in the standard of purity ; the result
being that the salts of sodium, such as those mentioned, are found,
in most cases, to contain traces of chlorides and sulphates, even
when labelled U.S. P. The fulfillment of such increased requirements
generally means an increase in the cost of the compound, with no
practical benefit resulting therefrom.
In criticising the quality of C. P. chemicals, care should be taken
not to overstep the bounds of reason, as in a certain case where a
bottle of C. P. ferrous suli)hate was returned after some weeks as not
answering the tests for a pure salt. As the bottle was only partly
filled, and loosely stoppered, the complaint was unreasonable. It is
easier to find fault with an article than it is to make excuses for
any deficiencies discovered ; but, for the interests of commercial har-
mony, let us avoid being hypercritical. For use as reagents, chemi-
cals should be required of the highest standard possible, but for pre-
scription u.se it is unnecessary to require conformity to a standard
of purity which raises the cost of the compound without increasing
its practical value.
A chart of the Mineral Products of the t'uited. States from 1S87 to 1896
inclusive, has recently been issued by the U. S. Geological Survey. The pro-
ducts are divided into two classes, metallic and non-mt-tallic. The >;raiul total
in value of both metallic and non-metallic products amounted in 1S87 to J520,-
714,474, and gradually rose to 1:648,670,798 in 1892, when it droppct! off some
|74,QOo,ooo in 1893, the values thereafter being somewhat variable, and in 1896
they had risen to 5611,510,700.
354 North American Conifer ce. {'^'^zXAm^"'^
A CONTRIBUnON TO THE KNOWLEDGE OF SOME
NORTH AMERICAN CONIFER^.^
By Edson S. Bastin and Henry Trimble.
{Concluded from page p/, of this Volume.')
TSUGA MERTENSIANA, CARR.
DISTRIBUTION AND GENERAL CHARACTERS.
This species is known as Western hemlock or Californian hemlock
spruce. It was first named and described by the Russian botanist,
Bongard, who gave it the name Pinus Mertensiana, and the locality
Sitka, in Alaska. It occurs, however, on the Pacific Coast, from the
vicinity of San Francisco through Oregon to Alaska.
While similar in appearance to our Eastern species, it is, when
fully developed, a tree of much larger size, sometimes attaining a
height of 200 feet. It is also straighter grained, and has a redder
and usually thicker bark, but the most distinctive difference, per-
haps, is in the fruits and seeds, the scales of the cones being more
elongated, and the wings of the seeds being relatively longer and
straighter.
MICROSCOPICAL STRUCTURE.
The barks of the Eastern and Western species are the only ones
that have been examined microscopically. They showed, as might
have been expected, a great similarity in structure, though there
appeared to be some characters which we may rely on for distin-
guishing them. In both it was seen that cOrk formation begins
early, and, in all cases, where the bark was taken from stems more
^ The death of Professor Bastin has necessarily brought the publication of
this series of papers to a close. As there was sufficient material left by him to
nearly complete the structural description of the Tsuga, it was thought the
publication of this paper, by completing the genus, would make a more accept-
able ending. Professor Bastin was working on the structure of Tsuga Caro-
liniana until shortly before his death, but it is to be regretted that the drawings
were not completed. As all the originals of the illustrations in this series of
papers were from his pen, no attempt has been made to have the few remaining
ones of this genus completed by others.
A number of reprints have been prepared, and copies will be mailed to any
one applying for them, until the supply is exhausted.
It is the hope and expectation of the surviving author to continue the
chemical work on this natural order, as a large number of samples have been
collected, much work has been completed, and the results will be published as
rapidly as possible.
Am. Jour. Pbarm.
July. 1897.
} North Avierican Conifer cp.
355
than two years old, the secondary cork formations had invaded the
inner layer of the bark and bands of cork were observed crossing
at various angles the medullary rays. The cork in both was colored
C^L
I-IO. 57.
^^S- 57' — Small portion of cross-section of bark of Tsuga Mtrtetisiana, mag-
nified about 50 diameters, c, r, c, bands of secondary cork ; </, intervening
dead tissues, composed of sieve and parenchymatous elements, and, like the
other species, rich in tannic, resinous and coloring matters; j, j,7group9 of
stone cells ; w, ;//, relatively large, fusiform me<lullary-ray cells ; b, band of
large parenchymatous cells ; cr, crystal cell ; ca, cambium cells.
356
NortJi American Conifer cb.
{
Am. Jour. Pharm.
July. 1897.
a deep purple, and this coloring matter was bleached out with diffi-
culty, even by Labarraque's solution. This coloring matter appeared
to be different in character from the reddish-brown coloring sub-
stance found in the tissues between the bands of cork, for not only
was the latter a different shade of red, but it bleached more
readily.
C/r-
FlG. 58.
^^^- 5<^.— Small portion of longitudinal-tangential section of bark of Tsuga
Mertcnsiaiia, magnified about 75 diameters, s, cluster of stone cells ; cr^ crys-
tals of calcium oxalate ; w, m, medullary rays ; r, oleo-resin cell.
Tests for tannin showed in Tsuga Mertensiana that the white or
colorless younger portions of the bark contained but little of it,
while the older portions, particularly the dead sieve and parenchyma
tissues between the bands of secondary cork, were observed to be
particularly rich in it.
Stone cells of large size, and often quite irregular, occurred, either
^"•/uiy'-iS^""'-} ^orth American Cottifenr. 357
isolated or clustered in groups of several or many, throughout all
except the youngest portions of the inner bark. They were quite
numerous, but distributed without apparent order. They were
marked with numerous very fine pore-canals, and very numerous
and fine concentric lines. Although abundance of starch was found
in the bark of Tsuga Canadensis, none was observed in the bark of
T. Mertensiana. It is possible, indeed probable, that a sample of
the latter collected at some other season of the year would show the
presence of starch. The medullary rays in both barks were
observed to be composed of single rows of cells, and these were
radially elongated and of large size as compared with those of
adjacent tissues; but those of T. Mertensiana were, on the average,
larger, and the rays in this species, as seen in a longitudinal-tangen-
tial section were composed, on the average, of a larger ^number of
cells.
These differences in the medullary rays are, perhaps, the most
constant ones between the two barks. In both barks an abundance
of calcium oxalate crystals was observed. (See Fi^. jj) They
were mostly in the form of long prisms, and were contained in rows
of elongated cells of narrow diameter, which traversed the bark in
the direction of its length. The crystals were frequently associated
in the contaming cells with resinous and coloring matters. In form
and arrangement they did not differ in the two barks, but appeared
to be rather more abundant in the Pacific Coast species.
Oleoresin cells appeared to be about equally abundant in the two
species. Those that did not also contain crystals were isolated or
in rows of two or three, and the cells were shorter and broader
than the crystal cells, though they were not usually so large as the
parenchyma cells, with which they were associated. They were
scattered through the inner bark without apparent order. Besides
the oleoresin cells proper, just described oleoresin, was seen to occur
in many cells not especially devoted to secretions; this was particu-
larly true of the cells in the older portions of the bark.
CHEMICAL COMPOSITION.
The constituents of Tsuga Mertensiana do not appear to have
been investigated. The work for this paper was mostly confined to
an estimation and examination of the tannin in the stem bark. The
sample used in the investigation was collected by Professor F. K.
358 North American Conifer ce, {^'"jj^y^?^!™-
Lloyd, of Forest Grove, Oregon. The following results were
obtained:
Per Cent,
Moisture 5'76
Ash iu absolutely dry substance 1*42
Tannin in absolutely dry material ii'37
A quantity of the tannin was prepared, purified and submitted,
after drying at 120° C, to elementary analysis, whereby the follow-
ing percentages were obtained:
Per Cent.
Carbon 59'ii
Hydrogen 4'93
Oxygen - 35*96
$100 '00
These results and the qualitative reactions indicate that the tan-
nin of Tsuga Mertensiana is identical with that from T. Canadensis,
and, therefore, with that from the bark of a large number of species
of oak.
ECONOMICS.
The wood of Tsuga Mertensiana is pale, tough and soft, and is
often used for building purposes. The bark of the roots yields a
strong fibre that is said to be employed for seines and nets, prob-
ably by the Indians. Authorities differ somewhat in regard to the
resin, Kellogg stating that it yields a considerable quantity, while
others report the resin as scarce. The bark of the trunk, with its
rich percentage of tannin, has always been in demand for making
leather.
TSUGA CAROLINIANA, ENGELM.
DISTRIBUTION AND GENERAL CHARACTERS.
The Carolina hemlock is found along the Allegheny mountains
from southwestern Virginia to South Carolina. It has been found
at an elevation of 4,200 feet. It does not occur very abundantly,
and, because it is said to be a rather handsomer tree than T.
Canadensis, it is cultivated somewhat at the North.
Carolina hemlock is not a very large tree ; its height is given
by different authorities as 40 to 80 feet. The wood is brownish
in color, soft and brittle. The cones and leaves resemble those
of the common hemlock, but both are a trifle larger.
^'"■/u'ly'iS^*""''} ///^^^/ Poiuders of Commerce. 359
CHEMICAL COMPOSITION.
The specimen used in this investigation was obtained from the
Highlands Nursery, near Kawana, North CaroHna. No pubHshed
record can be found of an examination into the composition of any
part of this tree. The leaves, the stem bark and the root bark were
partly examined with the following results :
Ash in absolutely Tannin in absolutely
Moisture. dry material. dr\- material.
Leaves 7*07
Stem bark . 8*22
Root bark . 5-95
The ashes of these several parts contained potassium and calcium as
phosphates and carbonates, and silica ; besides these, the ashes of
both barks contained sulphates. No further investigation was made
of the tannin, but it is safe to predict its identity with that from the
other species.
ECONOMICS.
On account of the scarcity of this tree, it does not appear to have
been put to any practical use, although a comparison indicates that
it could be applied to all the uses now possessed by the common
hemlock.
270
452
I "44
18-35
2-20
17 02
INSECT POWDERS OF COMMERCE.^
By Georce Reynolds Durr.\nt.
During the past quarter of a century at least twenty eminent
chemists, pharmacists, and microscopists have devoted some atten-
tion to the physical characteristics, chemical constituents, and toxic
properties of the insect powders of commerce. In the earlier part
of this period the references were exclusively to the powder from
the flowers of Crysanthemum caucasicum, or Persian variety, which
gradually gave way to the Dalmatian kind produced from the
flowers of the Crysanthemum cinerariiufolium, and it is possible that
the Dalmatian replaced the Persian variety because the latter was
the first kind to be grossly adulterated ; at least it is true in my
experience that both kinds are equally useful if equally free from
sophistication.
A careful study of the whole of the subject is more likely, in the
absence of much personal experiment and thought, to confuse the
' Jiiarfnaceudcal Journal, June la, 1897.
360 Insect Powders of Commerce. {
Am. Jour. Pharm.
July, 1897.
reader than to provide him with such information as will enable him
to distinguish the true powder from sophistications, which are still
as common, although changed in character, as they have been at any
time since the Persian powder gave way to its honester rival. To
any one who has worked on this subject for a few years, the last
paragraph may appear to be superfluous, but it is evident that there
is still a plentiful lack of knowledge on the part of the majority of
buyers, or it would be impossible to account on any other hypothesis
for the enormous amount of grossly sophisticated insect powder which
is sold as genuine every season.^
The object I have had in view in recording the results of several
years' attention to this subject, is to provide a ready means of quickly
and cheaply ascertaining if a given sample of insect powder is what
it is represented to be by the seller, but before proceeding to this
part of the subject, it will be profitable to briefly set forth the
results of the work of other investigators. These references will
not be by any means exhaustive of the subject, but will include
most of the literary notices which have come within my own knowl-
edge.
^ While engaged in preparing this paper for the press, a curious confirmation
of my contention has been supplied by a correspondence with a provincial firm
of dealers in insect powder. I have no reason to doubt the bona fides of the
firm, and must therefore conclude that such large sellers of insect powder as
they claim to be are yet profoundly ignorant of the characteristics of true
insect powder. I fear my charity is not sufficiently broad to give credit for
good faith in this firm's opinion on the Loudon trade in insect powder ! The
following short extracts are reproduced from this correspondence : In reply to
my request for samples and quotations, '* Thank you for your enquiry, and are
sending samples of insect powder from closed flowers, 100 5. per cwt., and from
half open flowers at 75 j. per cwt."
My reply to this quotation expressed regret at the misleading description, as
both samples were grossly adulterated, which drew a most indignant letter.
" In reply to your letter, we think the party conducting the analysis must have
made some miscalculation, as we are direct importers from Austria, and have,
from the grinders there, the fullest assurance of its genuineness, and that the
' closed ' and ' half-closed ' are from flowers of that description and from flowers
only. We have sold the same article for seven years, and our sale has greatly
increased. As regards the London price for insect powder, the import offered
in Loudon is second rate, both in quality and quantity, and consists only of odd
lots that have passed through several dealers' hands. We write strongly on
this subject because we should not have been able to advance our trade in this
article to its present state if we had been capable of misdescription ! "
""'"iuiy'iS^"'"} ^'^-^^^'^ Powders of Comvtcrce, 361
It will be found that the hterature of the subject divides itself
into the foUovvinfr sections :
{a) Toxic constituents.
(b) Microscopic appearance.
[c) Adulterations.
It is intended to keep this division of the subject so far as may be
possible and convenient.
So far back as 1863, Hanaman Roch (National Dispensatory)
attributed the insecticidal value of the povsdeied flowers of Crys,
caucasicum to a volatile oil. Some years after, in the seventies,
Semenoff appeared to be practically in agreement with this state-
ment, but treated the matter more broadly, if less definitely, by
substituting "volatile substance " for the more definite, if less ac-
curate, "volatile oil." Immediately after in (1876), Jousset de
Belle^me stated that, in his opinion, the active toxic principle was a
crystalline alkaloid. In 1877 this la.'t statement was corrected by
R. Rother {Druggists' Circular and Chem. Gazette), in a paper giv-
ing the results of a very systematic and practical investigation ; the
conclusions at which this writer arrived are as follows : There is
no crystalline alkaloid ; there are (^) an oleoresinous greenish-yel-
low acid, •' persicein ;" {b) another acid body, " persiretin," both
inactive; {c) active principle, a glucoside converted by boiling into
" persiretin " and glucose. These constituents are all soluble in
ether alcohol, benzine and petroleum ether, and insoluble in chloro-
form. With the latter part of the statement, referring to the solu-
bility of all the constituents of any value in ether, etc., I can cor-
dially agree. Very shortly after the appearance of this article by
Rother, a notice appeared in the Bulletin Soc. Chun, by G. Dal Sie,
in which he claims that the active toxic principle is to be found in
a volatile acid existing in the flowers in a free state. M. Finzclberg
(Pliarui, CentralhalU\ 1880) proved that a concentrated tincture of
the flowers had definite insecticidal properties, and this statement
has been confirmed by my own ex|:erimcnt.s on flies. O. Tester
{Phann. lourn. [3]. XII, 359, states that the active principle is a
soft resin. At the British Pharmaceutical Conference, lS88,apa|x:r
was read by William Kirkby on the microscopical characteristics of
the flowers of C. caucasicum and C. cincrari-efolium. The paper
was valuable so far as the subject was treated, but it was less com-
plete than the author intended, inasmuch as sophistications were net
362 Insect Powders of Commerce, {'''^- inxlim""^'
taken into consideration. Although the paper itself was thus
limited in scope, the discussion which followed covered the whole
ground. Mr. Robinson expressed his incredulity at the presence of
any toxic agent, but this bold skeptic was crushed by the President,
assisted by Mr. Howie and Mr. Martindale.
In the Pliarm. ZeitscJir.fur Ricssland, 1890, E. Hirschsohn states
that the active principle is neither a volatile oil nor an acid resin ;
this statement is neutralized by F. Schlagdenhauffen in an article in
the Pharm. Zeitung, 1892, in which he states that he found the
toxic properties to be {a) yellow volatile oil, and {U) uncrystallizable
soft resinous mass, pyrethrotoxic acid very soluble in ether. It
seems to me that the average buyer of insect powder, after careful
consideration of the foregoing evidence by so many able men, would
remain more or less doubtful as to the properties and characteristics
for which he ought to look in deciding upon the value of the various
qualities to be found in the insect powders of commerce. The
results of my own work on this part of the subject may be briefly
stated as follows :
The toxic properties are due to —
{a) A volatile oil amounting to 05 per cent, in picked specimens
of closed flowers, and much less in open flowers.
{b) A soft acid resinous body, this is the principal source of the
toxic effect. It is found to the amount of 48 per cent, in selected
closed flowers, less than 4 per cent, in half open flowers, and still
less in flowers that are fully open ; the whole plant, apart from the
flowers, contains mere traces of resin.
The fine dry powder, after exhaustion with ether, has no decided
toxic properties, but numerous experiments on beetles convince me
that this exceedingly fine powder contributes something to the
insecticidal properties by its physical action, perhaps by its effect on
respiration, reducing the vitality of the insect, and also by impeding
locomotion, and preventing a speedy retreat from noxious surround-
ings, and a safe return to the customary lodgings. The toxic proper-
ties of the volatile oil and resin may be proved by isolating them
and mixing them with an inert powder, whose physically deterrent
equation has been ascertained by experiment on beetles. I believe
no vivisection license is required for this.
Having referred to the toxic constituents of, and the proportions
in which they exist in, genuine powder of the flowers of C. cinerarise-
^""'juTy';-!^""'} Jfistxt Poivdirs of Commcrcc. 363
folium, it is very important to mention the fact that chlorophyll, in
its green unchanged form, is not found in selected dried, closed
insect flowers, as this fact has an important bearing on one (and I
think the most prevalent) form of sophistication to be found in the
present insect powders of commerce. 1 cannot fully explain why it
is that insect powder from half-open, and from flowers that are fully
developed, should show a certain amount of chlorophyll coloring in
the ether extract, but it may possibly be that less care is taken in
collection of these than is the case with the more valuable closed
flowers. But whatever may be the cause, the fact remains that
insect powder ground from selected closed flowers is sensibly free
from chlorophyll, whereas traces of it (less than 05 per cent.) will be
found in powders prepared from mixed and half-open flowers, and
in the foreign-ground insect powders it often amounts to from 50 to
80 per cent, of the total ether extract. Samples have been recently
examined by me yielding 6 per cent, of ether extract, of which
more than two-thirds was owing to chlorophyll. It will therefore
be seen that any estimate of the value of insect powder based upon
the percentage of ether extract would be quite fallacious unless the
chlorophyll be also determined and deducted from the total.
Microscopical examination is useful in distinguishing the grosser
forms of admixture, such as powdered quassia and the woody tissue
of the leaves and stems of the plant, but this latter form of sophisti-
cation can be determined by the method given further on. [For
full particulars of the microscopical appearance of true insect
flowers, the reader is referred to the paper by Mr. William Kirkby,
F.R.M.S. {Proc. Brit. Pliann. Con/., 1888).]
Adulterants — In using the term adulterants as applied to our sub-
ject, it is intended to imply the presence in insect powder of any-
thing but the flowers of i\. cinerariiufolium. Adulterators of insect
powder have for their first object the cheai)ening of the article sold,
and occasionally they have a second object, /. <•., to improve its color.
The first object has been achievec in the past by the addition of
powder of quassia, aloes, senna and Hungarian daisy, and the artistic
eye of the ignorant buyer has been satisfied by the addition of the
powder of fustic, turmeric and chrome-yellow. The presence of
quassia, fustic and turmeric may be detected by the aid ol the
microscope, and chrome-yellow (salt of lead) chemically. The pres-
ence of the lowdcr of Hungarian d.iisv is more difTicult to detect
364 Insect Pozvders of Commerce. {
Am. Jour. Pharm.
July, 1897.
microscopically, but it yields lO per cent, of ash, whereas true insect
powder yields but 65 per cent. On this point the reader is referred
to an extract from a paper by J. Schrenk (American Journal of
Pharmacy, 1889) in the "Year Book," 1890.
It is hoped that it will not be difficult to accept my contention
that by the term insect powder it is intended by both buyers and
sellers that powder of the flowers of the C. cinerarisefolium is under-
stood, at least so far as transactions in the open market are con-
cerned. Owners of proprietary insect powders have a right to com-
pound them as they please, and this right has been freely exercised
by the use of powdered quassia, colocynth, etc., as well as by the
addition of various coloring agents. Although powdered quassia
mixed with powdered insect flowers must be considered to fall
under our definition of adulteration, it is quite possible that a small
proportion is useful in insect powder, increasing or broadening the
base of its usefulness. The same remarks apply to other admix-
tures, such as powdered bitter apple, and the only criticism to be
made on this point is that if powdered quassia or other powders
having insecticidal properties be added to insect powder, let it be
done with the knowledge of buyers and at the proper price.
The adulterants just referred to are for the most part things of
the past, with the exception of added coloring matters, which are
still very commonly used to meet the too general want of knowl-
edge of the proper appearance of true insect powder. At the pres-
ent time the insect powders of commerce may be divided into the
following classes:
(i) Ground from closed {a) wild, or {p) cultivated flowers of C.
cinerarisefolium.
(2) Ground from half-open or mixed half-open and open flowers.
(3) Ground from damaged flowers.
(4) Foreign-ground, divided into grades of badness under the
meaningless terms: "closed flowers," " half-open flowers," etc., etc.
Of these sorts there appears to be as many as there are of hens*
eggs, which embrace all the kinds between "new-laid" at the top
of the list, and "political" at the bottom. The English-ground
insect powders do not always justify the description given, but in
my experience, the foreign-ground specimens never do, and it is
with much satisfaction that it is noted that a ready method of dis-
tinguishing "foreign-ground" is to hand.
^'"■jub-'iSJ"'"-} ^''-f^^^ Pozi'dcrs of Commerce. 365
It will be seen from the remarks made on the toxic constituents
of the flowers of C. cineraria^fohum that the following statement
embraces the results of my own experience as well as that of the
majority of laborers in the same field :
That the value of insect powder is in direct pro})ortion to the
combined amount of essential oil and soft acid resin, and in inverse
proportion to the amount of chlorophyll, both statements to be read
together.
Jt has not been my good fortune, up to the time of writing this,
to have met with one sample of 'foreign-ground" insect powder
that was not grossly sophisticated.
A perfect sample of insect powder should pass a sieve having at
least eighty meshes to the linear inch ; the particles would be, there-
fore, approximately -^^ of an inch in greatest magnitude. (The
powder has been passed through a sieve with 100 meshes to a linear
inch, but 90 is the more usual number.j The powder should yield
5-25 per cent, of combined essential oil and soft resin ; chlorophyll
should be absent, or present in the merest trace.
The following simple method of testing the value of insect powder
should be adopted by all chemists who wish to sell a genuine pow-
der, or, to put the matter on lower grounds, who wish to increase
their sale of this really important commercial product. Place ICXD
grains of the powder to be tested in the cylinder of a glass syringe
(l oz.). The powder should be pressed down compactly on to a
piece of absorbent cotton, to act as a filter. Moisten with ether 7-35.
Close the top of the syringe, and macerate for thirty minutes ; perco-
lation may then proceed ; the powder being repercolated with the
same fluid four times, and finally washed through with sufficient
ether to make up one fluid ounce. The resulting percolate should
be of a rich yellow color ; if a pronounced green color be the result,
the sample may be discarded at once.
In the absence of much green coloring matter, the fluid may be
carefully evaporated (temperature not exceeding 200° F.), and the
residue weighed in a tared watch-glass. The resulting soft mass
should not weigh less than 3-75 grains, and in the finest samples
reaches 55 grains, and should have the pleasant and characteristic
odor of the flowers.^ At the present time the price of insect powder
* Exactness may require the determiuation of the chlorophyll. If an appre-
ciable amount be present, this may be ilone by l>oiling the residue in dilute iul>
366 Liquefaction of Fluorine. {^"^-/u^y?!!'?""^'
varies between S^., and 2s. 2d. per lb., the highest price represent-
ing the value of English-ground powder from closed flowers and the
lowest powder " foreign-ground " from the whole plant. This
ground whole plant appears to be the principal sophistication,
apart from the coloring matter, found in commerce at the present
time.
I desire to acknowledge my indebtedness to Mr. Charles Umney
for very fine specimens of the dry flowers of C. cinerariaefolium.
THE LIQUEFACTION OF FLUORINE.^
By H. Moissan and J. Dewar.
The physical properties of a large number of mineral and organic
compounds of fluorine indicated, theoretically, that the liquefaction
of fluorine could only be accomplished at a very low temperature.
Whilst the chlorides of boron and silicon are liquid at ordinary
temperatures, the fluorides are gaseous, and very far from their
points of liquefaction. This is also true with the organic com-
pounds; chloride of eth} 1 boils at -f 12° C, and the fluoride of
ethyl at 32°.^ Chloride of propyl boils at -f- 45°, and the fluoride
of propyl at — 2°.^
Similar observations have been made by Paterno and Oliver!/
and by Vallach and Heusler.^
phuric acid and volumetrically determining the converted chlorophyll as glu-
cose with a suitable copper solution. For my own purposes I should unhesi-
tatingly reject the sample rather than take this unnecessary trouble, unless a
fee were attached to the operation.
' M. Moissan brought all his apparatus for the production of fluorine to the
Royal Institution on the occasion of his lecture there on Friday, the 28th of
May. The next day the writer had the good fortune to witness in the labora-
tories of the Institution, by M. Moissan and Professor Dewar, some of the
experiments which resulted in the liquefaction of fluorine. These experiments
mainly owed their success to the unrivalled appliances for the production of
intense cold possessed by the Institution, and the skill and experience of Pro-
fessor Dewar and his assistants in preparing a special apparatus suitable for the
examination of, and experimenting with, fluid fluorine, and in the manipula-
tion of large quantities of liquid air. — W, C.
■^H. Maissan, " Propriet^s et Preparation du Fluorure d'ethyle," ^«^/. de
Chim. etde Phys., Series 6, Vol. X[X, p. 266.
•' Meslans, Comptes Rendus, Vol. CVIII, p. 352.
* Paterno and Oliveri, " Sur les trois Acides Fluobenzoiques Isomeres, et sur
les.\cides Fluotoluidique et Fluoanisque," GazeiLa ChUnica Italiana, Vol. XII,
p. 85, and Vol. XIII, p. 583.
'Vallach and Ileusler, Annales de Liebig, Vol. CCXLIII, p. 219.
^'"■j'uTy'iSj*'''"} Uque faction of Fluorine. 367
Gladstone's experiments on ato-nic refraction'"' can well be com-
pared with these facts.
In fact fluorine by certain of its properties resembles oxyf^en,
though at the same time it is distinctly at the head of the chlorine
group.
The conclusion to be drawn from these observations appears to
be that fluorine can only be liquefied with great difficulty. One of
us showed that at a temperature of — 95", at the ordinary pressure,
there is no change at all."
In the new experiments which we now publish, fluorine was pre-
pared by the electrolysis of fluoride of potassium in solution in
anhydrous hydrofluoric acid. The fluorine gas was freed from vapors
of hydrofluoric acid, by being passed through a serpentine of plati-
num, cooled by a mixture of solid carbonic acid and alcohol.
Two platinum tubes filled with perfectly dry fluoride of sodium com-
pleted the purification.
The apparatus used for liquefying this gas consisted of a small
cylinder of thin glass, to the upper part of which was fused a plati-
num tube. This latter contained in its axis another smaller tube,
likewise of platinum. The gas to be liquefied enters by the annular
space, passes through the glass envelope, and escapes through the
smaller inner tube. This apparatus was fused to the tube by which
the fluorine was supplied.
In these experiments we used liquid oxygen as the refrigerant.
It was prepared according to the method already described by one
of us, and this research, we may remark, required several litres.*
The apparatus being cooled down to the temperature of quietly
boiling liquid oxygen (183^), the current of fluorine gas passed
through the glass envelope without becoming li(juid. Hut at this
low temperature it has lost its chemical activity, and no l<>n'.:tfr
attacks the glass.
If we now make a vacuum over the oxygen, we see, as soon as
rapid ebullition takes place, a liquid collecting in the glass envelope,
"J. H. Gladstone and G. Gladstone, "Rerraction and Dispersion of Fluoben-
zine and .Mlied Compounds," Phil. Mag., Series 5. Vol. XXXI. p. i.
\\. Moissan, " Nouvelles Recherches siir h* Fluor." An^t. iff Chim. et de
Phys., Series 6, Vol. XXIV, p. 224
"J. Dewar, "New Researches on Liquid .\ir, ' Royal Inslilulion ol Ureal
Britain, 1896, and Proc. /Coy. Inst., 1S93.
368 Literature Relating to Pharmacy. { ''"' ju'iyrisT '""'
while gas no longer escapes from the apparatus. At this moment
we stop with the finger the tube by which the gas had been escap-
ing, so as to prevent air from entering, and the glass bulb soon
becomes full of a clear yellow liquid, possessed of great mobility ;
the color of this liquid is the same as that of fluorine gas when
examined in a stratum one metre thick. According to this experi-
ment, fluorine becomes liquid at — 185°.
As soon as this little apparatus is removed from the liquid oxy-
gen the temperature rises, and the yellow liquid begins to boil with
an abundant disengagement of gas, having all the energetic reac-
tions of fluorine.
We took advantage of these experiments to study some of the
reactions of fluorine on bodies kept at extremely low temperatures.
Silicon, boron, carbon, sulphur, phosphorus, and reduced iron
cooled in liquid oxygen and then placed in an atmosphere of fluor-
ine, did not become incandescent. At this low temperature fluorine
did not displace iodine from iodides. However, its chemical energy
is still sufficiently great to decompose benzine and essence of tur-
pentine with incandescence as soon as their temperatures rose to
— 180°. It would thus seem that the powerful affinity of fluorine for
hydrogen is the last to disappear.
There is still another experiment we ought to mention. When
we pass a current of fluorine gas through liquid oxygen, a flocculent
precipitate of a white color, which quickly settles to the bottom, is
rapidly formed. If we shake up this mixture and throw it on a fil-
ter, we separate the precipitate, which possesses the curious prop-
erty of deflagrating with violence as soon as the temperature rises.
We intend to follow up the study of this body, as well as that of
the liquefaction and solidification of fluorine, which demand further
experiments. — Comptes Rendus, Vol. CXXIV, No. 22, p 1202,
through Chemical News, ]\i^Q. 11, 1897.
RECENT LITERATURE RELATING TO PHARMACY.
A REACTION FOR DISTINGUISHING «-NAPHTOL FROM /9-NAPHTOL.
E. Leger {your, de Pharm. et de Cliim., [6], 5, 527), distinguishes
/znaphtol and ^9-naphtol by adding to saturated aqueous solutions of
each a solution of sodium hypobromite. The solutions of naphtol
are prepared by rubbing the respective compounds in a mortar w/th
"""iur/iS:^""} Literature Relating to Pharmacy. 369
water, since by simply shaking in a test tube the naphtol frequently
does not become moistened. The solution of sodium hypobromite
is made by adding 30 c.c. of soda solution, 36° B. to 100 c.c. of
water, and adding 5 c.c. of bromine.
To make the test, one takes of either naphtol solution 10 c.c, to
which are added two drops of the sodium hypobromite solution.
(1) With the ^/-naphtol the reagent produces a violet color and
precipitate. This reaction is so delicate that if the solution of a-
naphtol is diluted with nine volumes of water the color is readily
distinguished.
(2) The solution of ^if-naphtol is turned yellow by the reagent,
then greenish and finally back to yellow.
It will be seen that this test is only applicable in a mixture of the
two to a detection of ^t-naphtol. That fact, however, does not les-
sen its value materially in this country, where it is chiefly desired
to prove the freedom of ^^-naphtol from the a-variety.
ASH OF PINEAPPLE.
J. J. Bowrey {^Bulletin of the Botanical Department, Jamaica, 3,
236), gives the following composition of the ash of the pineapple,
and draws conclusions concerning its cultivation:
Per Cent.
Potash, K,C) . . 4942
Potassium chloride, KCl 088
Sodium chloride, NaCl . 1701
Magnesia, MgO 8'So
Lime, CaO . 1215
Phosphoric acid, P/J 4 oS
Sulphuric acid, H^SC), . trace
Silica, SiOj .; :
Ferric phosphate . . . 293
9929
Judging from this analysis, potash is the most important mineral
substance which the pineapple requires. Of course, phosphoric
acid is also necessary, and so are lime, magnesia and iron ; but it
must be a very rare soil which does not contain iron and magnesia
in ample quantity, and usually there is enough lime also present.
It is difficult to make suggestions respecting manuring in total ig-
norance of the nature of the soil to be manured. But certainly no
harm can be done and probably much good by adding {)hosr)horic
Am. Jour. Pharru.
3;o Literature Relating to Pharmacy, {"^"'•/u'ly^S'
acid and potash to the soil, the former is best appHed as " basic
slag" or "Thomas slag;" 5 to 10 cvvt. per acre will supply
phosphoric acid for three to four years. The potash can be obtained
as chloride for about £Z per ton. From 50 to 100 pounds per
acre would be a dressing for a year. The pineapple also needs
nitrogen for its growth , this might be supplied as nitrate of soda,
at ^10 per ton, giving 100 pounds per acre when the plants have
started to grow rapidly.
COLLECTING JUICE OF PAPAW.
F. B. Kilmer, in Bulletin of the Botanical Department, Jamaicay
4, 68, describes the method to be followed in collecting the juice
from the fruit of Carica papaya in the Island of Jamaica. Cut
an incision lengthwise of the fruit, not over ^ of an inch in
depth ; if it is made much deeper the milk is apt to be carried into
the fruit and not run outside. The milk will run quite freely for a short
time, but soon coagulates so that it will no longer run. To catch
the milk that drops and flows I place under the tree tin pans made
in such a way as surround the trunk of the tree and catch the drip-
ping milk.
I found it well to tap the fruit early in the morning, before the
sun was very high, as it quickly dried the milk and stopped the
flow. After the flow had ceased it was found to be a good practice
to brush off all the coagulated milk into the pans and make a fresh
incision, when another, but smaller, yield was obtained. The scor-
ings should be made about ^ inch apart all around the fruit. The
time to tap the fruit is before it is ripe, and when it is green
and full. The yield is much larger just after a rain storm or a spell
of wet weather. Still, you can tap a green fruit at any time and
obtain more or less of the white milk. This milk must be dried
the same day that it comes from the tree, and must be dried in the
sun. Artificial heat will not do. It can be dried right away on
the tin pans, spread out thin, or spread out on sheets of glass. It
will dry in an hour or so in the sun. Any amount of exposure to
the sun will not harm it in drying, but artificial heat destroys it. If
it should so happen in gathering that, owing to stormy weather, it
cannot be dried in the sun the day it is gathered, you can mix it
with some naphtha or benzine, turning it into a sort of milk.
^"•/u'iy?iSr°''} Literature Relating to Pharmacy. 371
CUTCH EXTRACTION.
When commercial cutch enters the domain of pharmacy it be-
comes catechu ; but whether cutch or catechu, it is a substance of
rather uncertain origin and of very variable composition. The fol-
lowing, from the Indian Pliarmacologist, -♦ 7, January i, 1897, indi-
cates that there is still much to be learned about this substance-
" One of the most recent issues of the Agricultural Ledger series
contains a brief account of the examination of a sample of Burma
cutch received by a Glasgow firm through Dr. Watt. It is interest-
ing if only for the fact that it brings out strongly the divergence
that sometimes exists between chemical analysis and commercial
opinion. Dr. Watt suggested that cutch should be manufactured in
India by the superior European method of extracting dyes from
timber. Twenty tons of the Acacia Catechu timber were procured
here and shipped to Glasgow. Dr. Watt saw the timber before it
was shipped and considered it to be of average quality. The tim-
ber was treated by the vacuum process, and the resulting product
was described by Dr. Watt as a cutch of great purity and very good
appearance. A chemical analysis by Dr. Leather showed that the
cutch thus produced contained 6 58 per cent, of crude catechin and
78-20 per cent, of catechu tannin. At the same time a sample was
submitted to the Calcutta Chamber of Commerce for professional
opinion, and this was completely opposed to the conclusion of the
chemist. Commercial opinion described it as ' very inferior to that
imported from Rangoon.' The sample was described as overboiled,
and would fetch only Rs. 3 a maund as against Rs. 8 for the best
brands of Burma cutch. Clearly the commercial expert who re-
ported on the sample made a mistake in his identification of it. lor
he reported that it was shipped to the Calcutta market in 2-ounce
tins for mixing with paints, 'and in this form it has a special value*
but for medicinal purposes, or for bazaar use, that is, for mixing with
pan, it has no .sale.'
" Dr. Watt, in a brief note on this curious divergence of opinion,
says that the only explanation is that trade opinions arc based
mainly upon external appearances. The sample is unlike the ordi-
nary article met with in the market, and probably bears some resem-
blance to an inferior grade known to dealers. • As a general rule,
the commercial expert is lost if carried out of the field of compara-
tive valuations. Me knows little or nothing of chemistry.' That
3/2
Literature Relating to Pharmacy. {^"'•/u°y:-i?9*^^'"'-
is true, of course, but the trade opinion shows that cutch prepared
by the vacuum process, though pronounced by chemical examina-
tion to be of great purity and good appearance, will not, for the
present at least, secure anything like a good price in the market."
THE ALKALOIDS OF VERATRUM.
George B, Frankforter, in Minnesota Botannical Studies, Bulletin
No. 9, May 31, 1897, gives ^"^ elaborate review of the veratrums, but
especially mentions V. viride, which is the only one occurring in
Minnesota. Its general range in North America, under the popular
name of Hellebore, is a broad one.
The substance commonly known in pharmacy as veratrine, varies
widely in its composition, chemical, physical and physiological prop-
erties. The introduction of the so-called "■ Merck veratrine " has
changed matters somewhat, although samples of the Merck alkaloid
have been found to vary considerably in their general properties.
One of the chief causes of this exceptional variation is the extreme
difficulty with which the alkaloid crystallizes, thus almost excluding
the most important means oi purification. Another, and perhaps
the most important reason for this wide variation, lies in the fact
that almost every one of the early investigators of the *' veratria "
has given the name to a different alkaloid, or to a mixture of
alkaloids.
The foregoing introduction is followed by a concise history, be-
ginning in 1 8 19 with the work of Pelletier and Caventou on Vera-
trum sabadilla and following it step by- step down to Salzberger,
who in 1890 made an exhaustive examination of Veratrum album.
Then follows the •* experimental part " in which the author oper-
ated on a sample of crystallized veratrine which was of a light gray
color, and appeared, when highly magnified, in imperfect granular
crystals. It was slightly soluble in water, very soluble in methyl,
ethyl and amyl alcohols, and in ether, acetone, chloroform and car-
bon disulphide. Its melting point after repurifying was 146 to
148° C, and its identity with that described by Merck and Ahrens
was established by elementary analysis, as well as by the melting
point of the gold double salt. The formula was made out to be C30
H,„NO,H,0.
Am. Jour. Phaim. 1 ZT /,/-.*..-. / ^ « -.
July, 1897. ; hititorial. ^ 373
The following iodine compounds were prepared and studied :
Veratrine tetraiodide, C3..H^.,NO.,l4. jH-^O
triiodide, C3,H,.>'OJ,
" monoiodide, C3._.H,,,X0yI
Other compounds were prepared and investigated as follows:
Chloralhydroveratride, C CI, CH (OC,,H,.,NO0,,
Veratrine methyliodide, C;,,H«,,NOyCHJ.
uiethylhydroxide, C;,H,,XO,CH,,OH.
methylhydroxyhydrochloride. C3,,H,.,N0.,CH .OH. HCl.
eth}lbroraide, C,,H,,,NO,C,H.Br.
allyliodide, C,.,H,.jNO<,C,H5l.
The author concludes with the statement that the structural for-
mula of veratrine is still a mystery. From the odor of picoline by a
destructive distillation, and the isolation of ^^ Picoline by Ahrens, it
is evident that veratine is a pyridine derivative, resembling in many
respects nicotine. Whether both cevadicand tiglic acids are present,
remains for future experiments to determine. The work of Schmidt
and Koppen indicates the presence of both acids, while the careful
researches of Wright and Luff would indicate that these isomeric
acids are converted into each other by special reagents. Assuming
that but one acid is present, the following formula may be assigned
to veratrine :
fOCHj
! OOCCH (CH3) CH3
[nh,c,
Experiments at present are being conducted along this line, with
the hope of throwing more light on the structure of this important
compound.
EDITORIAL.
THE AMKRICAN MKDICAI. ASSOCIATION.
The Jubilee Mcetinj< of this Association, held in Thiladelphia, June 1104.
inclusive, was a notable one in many rcj-pects. Not only whstlic atln dMicc
of 2,500 members unusual, but the deluj^e of paptrrs j)res<rntcd in the various
sections attested the industry of the members during the past year. The founder
of the .\ssociation. Dr. N. S. Davis, of Chicago, and one of the first secretaries.
Dr. .Alfred Slille. of Philadelphia, were both pretenl at the meeting. The
former delivered an address entitled : " \ Brief Ilihtory of the Origin of the
374 Editorial. {*'"jX';-,?£''""-
Americau Medical Association." This address is uot 011I3' very interesting, but
it is a document of considerable historical value, for Dr. Davis is almost the
onlv one who can speak with authority on this subject. He first briefly out-
lined the earl}' history of the country, and called attention to the fact that,
springing as it did from a few States, which had achieved independence, the
Government was confronted with many difficult problems, the one of educa-
tion by no means being the least; but it w^as decided to leave that important
subject to the regulation of individual States.
Our educational historj' as an independent people commenced thus, during the last half
of the last quarter of the eighteenth century, in a new and sparsely populated country,
extending from Maine to Florida, with only four medical schools organized, all as depart-
ments of literary colleges or universities, and all attracting annualh' attendance of less than
300 students, of whom not more than fifteen annualh' received the degree of Doctor of Medi-
cine, and no two of them controlled hy the laws of the same State. And it must be noted,
also, that a very large majority' of those who entered upon the practice of medicine at that
time gained their education in the office of some established practitioner, and were licensed
b\- the censors of medical societies, the judges of courts, or even by the certificates of their
preceptor, without ever having spent a da3'^ in a medical college.
After thus outlining the early history, the speaker came to the years 1846-47,
when the Association was organized, when it was found that colleges had mul-
tiplied until thirty were in existence, with an annual attendance of 3,500 stu-
dents, of whom uot less than i,ogo received the degree of Doctor of Medicine.
This rapid increase in the number of colleges necessarily led to the most active
rivalry.
So potential was the question : " In which school can I obtain the degree of Doctor of Medi-
cine for the least expenditure of time and monej'?' on the several medical schools, that,
although the three medical schools originalh' organized in Philadelphia, New York and Boston
had been founded on the same basis or curriculum as the University of Rdinburgh, requiring
a good academic education as a preliminary for entering the medical course, then from three
to five years of medical study, with annual college terms of not less than six months, long
before the number of our medical schools had reached thirty, all preliminary' requirements
had been abandoned, the term of medical study limited to a nominal three j-ears, and the
medical college instruction to two annual repetitional courses of from twelve to sixteen weeks
each. Under this inadequate and unsystematic medical education it really cost less in time
and money to obtain the degree of Doctor of Medicine than it had previousl}' cost to serve
an apprenticeship in the office of a respectable practitioner, and obtain a license from the
censors of a local medical society.
Such a deplorable condition naturally led to a desire on the part of many for
reform, which, it was said, could only be effected by organization. As early as
1835 the faculty of the Medical College of Georgia urged, through the medical
press and by correspondence, the holding of a National Convention. This and
several other attempts failed, until, in 1846, Dr. Davis and a few associates
effected organization in New York, and arranged for meeting in Philadelphia
in May, 1847.
The speaker then detailed the business of the first meeting, named the
officers of that meeting, and concluded as follows :
Such is a brief history of the origin, objects and organization of the American Medical
Association, which, with the exception of the first two years of the great war for the preser-
vation of the Union of these States, has held its regular annual meetings in all the important
parts of our widely-extending country, still adhering tenaci nisly to the fundamental princi-
ples on which it was founded. And I am most happy to add that every leading object sought
to be acconii)lishe(l by its founders has been substantially obtained ; that is, universal, free
and friendly, social and professional intercourse has been established ; the advancement of
July. 1897. / I\et'lCu.'S.
375
medical science and literature in all their relations has l)een promoted, and the long agitated
subject of medical education has reached the solid basis of a fair academic education as a
preparatory, four years of medical study, attendance on four annual courses of gnided medi-
cal college instruction of from six to nine months each, and licenses to practice to be granted
only by State Boards of Medical Examiners.
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
The Standard Manlal of Soda and Othkr Reverages. By A. I^mil
Hiss, Ph.G. G. P. Kngelhard & Co., Chicago. 1897.
Quite recciitl}' we reviewed iti this Journal. The Statidard Formulary, m
which the atJthor of the present work was associated in joint authorship with
iMr. A. E. Ebeil. The Standard Manual is, therefore, a fitting companion to its
predecessor.
Chapter I is devoted to historical considerations, and is a compact statement
of the growth of the enormous industry in which *' soda water" is the founda-
tion.
The second chapter is made up of such general directions as making carbon-
ated water, discharging thegenerator, aii<l all theother manipulations connected
with making and dispensing beverages. The remainder of the book, amounting
to nine-tenths, is devoted to formulas, in which nearly every conceivable, and
some inconceivable, " soda water " beverages receive attention. " In the soda
water drinks, all spirituous preparations have been omitted, except in certain
well-known standard articles, and in the formulas received '"rem special
cotitributors.''
Flowers of Field, Hill and Swami*. By Caroline A. Creevy, author of
Recreations in Botany. The foregoitig is the title of a book recently published
by Harper ^i Brothers, New York.
It is a botanir-al work, intended to instruct persons who have no technical
knowledge of botany in the art of classifying and naming many of our common
Maslern flowering plants.
Such works, when properly presented, are of great benefit. Tliey appeal to
])er»ons who are interested in flowers, but who are deterred fiom taking up the
study of botany on account of the dreaded "technical names" which in such
cases are administered in a palatable form.
It is a matter of great regret that a book indicating such a large amount of
j)ainstaking work on the part of the author, and re])resenting sucli a hi^ h
degree of typographical skill, should be matred by so many inaccuracies in the
illustrations which accompany the descriptions of many of the plants
Written descriptions are often ambiguous because of their great latitude ; but
in illustrating a p'ant it shoul 1 be remeinbeied that the i>ersons recci ■
instruction are apt to look upon a cut as an abM>lute likeness of the \\
whereas, in many cases, a do/en illustrationH would l)e necessary lo f^ive an idea
of the variety of forms assumed by a single species under • '
In the present work some of the cuts are not of typual :
mal species, l)eing probably taken from a single herbarium s|)ec men in nunv
instances. The illustrations of spearmint, on page u^. and bti-
71, might l)e transjmsed to a<1vantage, as neither i>> .orn.t
change would l)e an improvement tipou accuracy.
, Z?^^,-^,- r Am. Jour. Pharni.
376 AevteiK'S. { juiy.isg?.
The frontispiece shows Hepatica triloba, or liverleaf, in a most luxuriant
state, with numerous flowers and fully-developed leaves at the same time ; the
early spring leaf-buds, which invariably accompany the typical specimen, being
entirely absent, while the previous year's leaves, which in nature are usually
flat on the earth and covered up, are erect and flourishing in appearance.
Oxalis corniculata, var. stricta, yellow- wood sorrel, as seen on page 182, is a
midsummer form of the plant, very diff"erent from that commonly observed
and almost unrecognizable,
Lysimachia quadrifolia, four-leaved loosestrife, page 337, is another illus-
tration very misleading in its character. Instances multiply rapidly, but the
following are all liable to similar criticism : Hypericum perforatum, St. Johns-
wort, page 237 ; Campanula rotundifolia, harebell, page 291 ; Apocynum
androsoemifolium, dogsbane, page 5 21, and Linaria canadensis, blue toad-flax,
page 421.
The work contains descriptions of a very large number of plants, the arrange-
ment being upon a novel basis, and one of doubtful advantage, i. e.^ the charac-
ter of the habitat, such as "banks of streams, in swamps, in w^ater, in low
meadows, along waysides and in dry fields, escaped from gardens, weeds, open
dry woods, deep cool woods, etc."
In nature no boundaries exist that will allow of certain classification of
plants in general in this manner, and it is to be feared that the person who
attempts to classify plants by this book will not care to go further into the
science. Charles H. LaWai.1..
Notes on the Plants Used by the Ki.\math Indians of Oregon. By
Frederick V. Coville. Contributions from the U. S. National Herbarium, Vol.
5, No. 2. Issued June 9, 1897.
While engaged in a botanical survey of the plains of southeastern Oregon,
in the summer of 1896, the author spent three days, August 21st to 23d, at Fort
Klamath and the Klamath Indian Agency, where he was ena )led to secure
information as to the principal plants used by the Klamath Indians. Most of
the information was obtained from Joe Kirk, an educated Klamath Indian, and
from White Cindy, a Klamath medicine woman. The Government agents living
at the fort also furnished much information. A large number of plants, covering
nearly the whole range of natural orders are given. Two lichens are repre-
sented ; one, Alectoria fremontii, as a famine food; and the other, Evernia vul-
pina, on account of its yellow dye. Equisetum hyemale is used to smooth arrow
shafts just as a carpenter uses sand-paper. A number of the Pinaceae are used
for various purposes. The seeds of Pinus Lambertiana are used as food, but no
mention is made of the sugar, which is used as food or medicine by the California
Indians. Some of the pines are used as twirling sticks, to produce fire by
friction, although the sage brush,- Artemisia tridentata, is said to be better for
this purpose. These illustrations will serve to give an idea of the scope of
this work, which, however, is only a pamphlet of 32 pages. Nevertheless,
it is full of valuable information.
Minnesota Botanical Studies. Bulletin No. 9, Parts X and XI. Geo.
logical and Natural History Survey of Minnesota. Conway MacMillan, State
Botanist.
Am. Jour. Pharm. ) P/^,i\ <- ,e -tTT
This large bulletin of 342 pages and 42 plates is full of interesting matter
relating to botany.
The following are the contents :
"Contributions to a Knowledge of the Lichens of Minnesota." II. "Lichens
of Minneapolis and Vicinity." By Bruce Fink.
"A Rearrangement of the North American Hypomycetes." By Roscoe
Pound and Frederic E- Clements,
"On Some Mosses at High Altitudes." By J. M, Ilolzinger.
"The Forces Determining the Position of Dorsiventral Leaves." By R. X.
Day.
"On the Genus Coscinodon in Minnesota." By J. M. Holzinger.
" Observations on the Ferns and Flowering Plants of the Hawaiian Islands."
By A. A. Heller.
" The Phenomena of Symbiosis." By Albert Schneider.
" Observations on the Distribution of Plants Along the Shore at Lake of the
Woods." By Conway MacMillan.
" The Alkaloids of Veratrum." By George B. Frankforter.
The last article is given in abstract on page 372 of this Journal.
A Series OF Papers on the Origin and Chemical Composition of
Petroleum. Read before the American Philosophical Society, February 5,
1S97.
This interesting series has been reprinted from the Proceedings of the
Society, and bound together, so as to make a comj)act pamphlet for reference.
The following are the subjects and authors :
" The Genesis and Chemical Relations of Petroleum and Natural Gas." By
Samuel P. Sadtler, Ph.D.
" On the Nature and Origin of Petroleum." By S. F. Peckham.
"A Suggestion as to the Origin of Pennsylvania Petroleum." By David T.
Day.
"On the Genesis of Natural Gas and Petroleum." By Francis C. Phillips.
" On the Occurrence of Petroleum in the Cavities of Fossils." Hy Fr.uiris C.
Phillips.
" On the Composition of American Petroleum." By Charles F. Mabcry.
The discussion which followed the reading of these papers is also included in
the pamphlet.
A Review ok Recent Synthktic \V»ikK in thk Class of Cardohv-
dratES. By Helen Abbott Michael.
This is a lecture delivered before the Franklin Institute, and reprinted from
the Institute's y<>«;;/j/. It is a valuable summary of the present knowledge of
the sugar group.
Si'R LK Dosage dk la Cafeine. Thesis presented to the A'rn/^ Supt-rieun-
de Phatvtacie de Paris. By Eugene Tassilly. The author haa examined acme
of the methods already proposed, and offered one which he thinks po«w<
advantages of all the earlier processes, ami, at the same time, avoids t; _
advantages. A summary of the literature on the subject is given from 187a to
the present.
QUKLyLRS OXYDKS DoUHLES CrI.STALLISES OBTKNUS A HaUTK TKMPERA-
37S Pkarm.iceutkal Association. {^^jaiy.'is??^''"-
TURK. Thesis presented to t\iQ: Ecole Supcrieure de Pharmacie de Paris . By
M. Dufau (Louis-Emile-Ren6).
Bur<LETiN. Vol. II, No. 7. Imperial University, Cotlege of Agricutture,
Tokyo, Japan.
This number, like its predecessors, is full of valuable matter relating chiefly
to physiological botany. The first article is a continuation by Dr. Loew, of the
stud}' of living protoplasm. We have also received one of the articles, as a sepa-
rate, "On the Formation of Asparagiue in Plants under Different Conditions."
By U. Suzuki. Bulletin, Vol. Ill, No. i, has also been received. Its 113 pages
are devoted entirely to an exhaustive consideration by Professor Dr. Dire Kitao,
to the one subject — "Ueber die Wasserbewegung in Boden."
Papain ; the vegetable pepsin, its origin, properties, and uses. Lehn &
Fink, New York.
Antitoxins, The G. F. Harvey Company. An illustrated pamphlet,
giving much historical matter and considerable clinical data on the use of this
important remedy.
The Action of Taka-Diastase in Various Gastric Disorders. By
Julius Friedenwald, A.B., M.D. Reprinted from the New York Medical
Journal, for May 29, 1897.
Report of Proceedings of the Ili^inois Pharmaceuticai, Association.
Seventeenth Annual Meeting, 1896.
PENNSYLVANIA PHARMACEUTICAL ASSOCIATION.
The twentieth annual meeting of the Pennsylvania Pharmaceutical Associa-
tion convened in the parlor of the Kittatinny House, Delaware Water Gap,
Pennsylvania, on Tuesday, June 22, 1897.
The first session was called to order by President Joseph P. Remington, at
4.48 P.M. About seventy-five persons were present. The Secretary was asked
to read a letter of welcome, which had been received from the chief burgess of
the borough of the Delaware Water Gap, Mr. E. R. Johnson. The President
asked Mr. M. N. Kline to reply to this courtesy. The routine of business was
then begun by the Secretary acknowledging the receipt of the credentials of
delegates from the following bodies: Philadelphia College of Pharmacy,
National Wholesale Druggists' Association, New Jersey Pharmaceutical Associa-
tion, Maryland Pharmaceutical Association and the Proprietors' Association.
The President then delivered his address. It was referred to a committee for
consideration.
The reports of the Committee on Entertainment and of the Secretary were
then presented ; they were referred to the Committee on Publication. The
report of the Treasurer showed a comfortable balance, and that the association
had at the time of the report 312 members in good standing. It was referred
to an auditing committee appointed by the chair. The report of the Executive
Committee stated that the project of holding a joint meeting of the Pennsylvania
and Maryland Pharmaceutical Associations had met with favor. The chair-
man of this committee reported two applications for membership which had
^'^'juiV.'i^""''} Pharmaceutical Association. 379
been made since the last meeting, also seven deaths among members. The
report was referred to the Committee on Publication. The President then
appointed committees on nominations and place of next meeting. It ua> then
voted to adjourn until 9.30 the following morning.
The second session, which met on Wednesday morning, was mainly occupied
by the reading of reports of committees and of delegates to pharmaceutical and
medical associations. The following officers were elected for the ensuing year :
President, J. H. Redsecker ; Vice-Presidents, J. H. Knouse and W. L. Cliffc ;
Treasurer, J. L. Lemberger ; Secretary, J. A. Miller ; Executive Committe. G.
W. Roland, C. L. Hay nnd W. F. Horn. The Committee on Adulteration
reported that they had been successful in securing a new law against this prac-
tice. Under the old law it was difficult to conduct prosecutions, owing to the
wording of the Act ; in the new law this was thought to have been overcome.
The committee reported that comparatively few adulterations had presenteil
themselves during the past year. Attention was directed to the fact that if
pharmacists insist upon jobbers supplying goods which meet the standards of
the United States Pharmacopoeia and the National I-ormulary, without regard
to brands, they will get them, and without additional cost. President Reming-
ton advised the Association, when it undertook a prosecution, to select some
article upon which it would undoubtedly win the case, and not one upon which
the Association might be liable to defeat by the lawyers proving that the
impurity or adulteration was as good for the purpose as the article said to be
adulterated. He cited the contamination of carbolic acid with cresylic acid as
an illustration of an impurity which was of ecjual or greater value as a disin-
fectant than the substance with which it was mixed.
The next report was that of the Committee on Botany. It was chiefly con-
fined to an enumeration of plants and trees of that part of Pennsylvania east
of the Susquehanna River. The committee suggested the adoption, as far as
possible, of the proper scientific names for plants, as their meanings are usually
sufficiently specific to distinguish one plant from its congeners. The report
directed the attention of pharmacists to the deforestration of our immense nat-
ural woodlands and the changes in meteorological and climatic conditions
which follow the destruction of forests. It suggested that an effort be ma<le to
mitigate the evil by enacting and enforcing suitable laws.
The principle issue of the report of the committee to attend the National
Wholesale Druggists' Association, was a ({uestion as to the legitamacy of phar-
macists buying phenacctiHi through oiher channels than the authorized agents,
who charge much more for what is represented to be the same article and sold for
less by the unauthorized dealers. This feature of the report elicited considerable
discussion, and it was made apparent that the Association objected to the pro-
tection which the present copyright laws give to manufacturers who try to sell
a well-defined and well-known chemical under a fancy name. To overcome
this state of affairs, V. W. E. Stedem moved that ': " -ocialion se.
co-operation of the .\merican Pharmaceutical Ass' 1 an«l the A:
Medical Association in an effort to have the copyright laws of the United States
on tlefinite chemical compounds revise<l. It was stated that the Pennsylv
State Mrd'cal Society has pledged itself to co-operate with the Viti.t . ,ti M. ..
cal Association for the repeal of such copyright laws.
The committee on time and place of meeting, announce<l thitt ihr next annual
38o Pharmaceutical Association. {^"'•ju'iy'i?^^''"'
meeting will be held at Buena Vista Hotel, Franklin County, Pa. The time
will be reported later, as it will be a joint meeting with the Maryland Pharma-
ceutical Association, which will convene in its own State, just across the Mason
and Dixon line. F. B. Flemmings, of Shippensburg, was appointed local sec-
retary. The delegates to the State Medical Society reported that samples of
about 2,000 preparations had been exhibited before the meeting of this body in
Pittsburgh. It was evident that this committee, of which Prof. Louis Emanuel
was chairman, had done a great work toward attracting the attention of the
members of the foregoing society to the preparations of the United States Phar-
macopceia and the National Formulary. Prof. Emanuel proposed that a com-
mittee be appointed to consider the feasibility of establishing a literary bureau
from which printed matter on National Formulary and other preparations
might be drawn for distribution among physicians, for the purpose of combat-
ting the advertisements of copyrighted articles. This, and the other consider-
ation of copyrighted articles, were referred to a committee composed of Messrs.
Stedem, George, Emanuel, Redsecker and Kennedy. During the discussion
which followed the last report, F. W. E. Stedem proposed a mixture of the
spirit of orange of the National Formulary, and glycerin in equal quantities,
as a vehicle for bromoform ; its advantages are pleasant taste and solvent
power on the medicament. Prof. Emanuel moved that Prof. Beal's ideal phar-
macy law, which was distributed among the State associations and boards of
pharmacy, by the American Pharmaceutical Association, be referred to the
Committee on Legislation. It was so ordered. The auditing committee approved
the treasurer's report. The presentation of papers then followed.
"The Flora of Bushkill Falls" was the title of a paper read by Adolph W.
Miller, M.D., Ph.D. This contribution was an account of a botanizing tour
made by the Philadelphia Botanical Club and the Torrey Botanical Club, of
New York, through the district of Bushkill, Pike County, Pa., on May 28th last.
Dr. Miller was one of the party which explored this rich region. He called
particular attention to the following plants : the American yew, the gold
thread, Rhododendron maximum, R. nudiflorum, R. cauescens, Kalmia latifolia,
K. angustifolia, Vacineum stamineum, Cypripedium hirsutum (formerly called
C. pubescens), Orchis spectabilis, Cystopteris bulbifera, Camptosorus rhizo-
phyllus, Osmunda struthiopteris, many forms of the Napoleon flower, and
Scrophularia leporella (recently separated from S. nodosa by Bicknell).
Attention was also called to the abundance, in the neighborhood of the Tarax-
acum erythrosperma, Andrz, which, until quite recently, was included in the
official species, the Taraxacum officinale, although it was described as early as
1821, by Anton Andrzejowski, whose name is attached to it. It differs in many
particulars from the official plant, notably in the color of its achenes, which
are crimson, bright red or reddish-brown, whence it received the title " erythro-
sperma." Its pappus is slightly tawny, or dirty white in color ; its leaves are
far more deeply divided into narrowly triangular segments, and the whole plant
is rather smaller in size than the Taraxicum officinale. While a head of the
latter may be made up of 160 to 170 individual florets, one of the red seeded
species does not contain more than 70 to 80. The head itself is smaller, being
scarcely an inch in diameter, and the fruiting receptacle is rarely more than
one-quarter inch broad. There seems to be also a slight difference in the color
of the head, that of the Taraxacum erythrosperma being rather more of a sul-
^"■yuiy'iS-"'"} Pharmaceutical Association. 381
phur or lemon-yellow color than the other. The inner bracts of the involucre
are nearly all furnished witli a peculiar corniculate appendage, half a line or
so below the whitish tip, and the outer ligules of the head are somewhat
purplish on the external surface. A specimen of the T. erythrosi>erma pre-
sents a much more matted, or interlaced apf>earance in its growth than the
taller species. As the T. officinale ' Weber ' is undoubtedly an introduced plant
from Europe, it is just possible that the T. erythrosperma is a native of America.
Appended to the paper was a list of 275 plants, most of which were found in
bloom. The next paper was "On the Presence of Corrosiue Sublimate in
Calomel," by Lyman F. Kebler. It is printed in full on page 33S of this issue.
In reply to the query: Should drug store experience in pharmaceutical edu-
cation precede or follow college training / Theodore Campbell presented a paper
in which he earnesth' urged ever}- druggist to see that his clerks have not less
than one year of experience in the store before attending lectures at a college
of pharmacy. The author showed that a clerk who has had such experience
will be better prepared to receive the college instruction, and that drug store
training previous to attendance at college qualifies a person to open a store and
conduct the business in all its phases immediately after graduation from a college.
William B. Thompson contributed a paper entitled "A Pertinent yuery,"
which was, in effect, a presentation and discussion of the question as to whether
the practice of pharmacy may rightly be regarded as a profession. His argu-
ments were convincing, and left little doubt that he who fills the various
requirements of this calling is justly entitled to a professional standing.
Another paper by Mr. Thompson was on the subject of " Chlorinate<l Lime
in Zinc Containers." In this he stated that the method of packing chlorinated
lime in cans made of sheet zinc had been employed a sutTicient length of time
to thoroughly test its merits. He observed that the article stored in this man-
ner preserved its condition unimpaired for a reasonable period.
Wm. Mclntire suggested that the package be labelled with the date of pack-
ing and the strength of the substance at that time.
The query: should druggists study nitdicine f was answered in the affirma-
tive by W. H. Keed. The ethical relations of the professions of pharmacy and
medicine as such, and as they were formerly practiced, were first defined by the
author. He then considered the complications of the two classes as they now
exist, and favored the adoption by druggists of measures adapted to the changed
conditions brought about by modern business innovations.
He said that druggists were protected by legal enactments only in the dis-
pensing of poisons and compounding of prescriptions ; and he believed that
not more than one-fourth of the present drug stores could subsist on this kind
of patronage alone. He also sai<l that the average drug store now without the
aid of a physician is not a success financially. He, therefore, rccommentled
the practice of medicine in connection with that of pharmacy, under certain
conditions, l>oth as a means of success and to meet the <lcmnn<ls of certain
classes of patrons, namely, those affected with disorders of a tr.msient iialuic.
and those with limited means.
The writer furthermore l)elicvc<l that where he is legally qu«hhe»l, the drug-
gist is as morally justifie<l in practicing medicine in connection with pharmacy
as the physician is justifietl in supplying his patients with drugs, and thereby
injuring the business interests of the pharmacist.
382 Pharmaceutical Association. { ^'''•/uuriS'T^'^'-
Another reason which he advanced for druggists studying medicine, even
though they did not intend to practice it, was that a medical training would be
of inestimable value to them in the practice of general pharmacy.
Under the head of " Rocks and Shoals of Pharmacy," Prof. C. B. Lowe pre-
sented some common-sense doctrine, which was particularly intended for
young men beginning the drug business. Of the hindrances to success in this
business, he considered the following : Immorality, insufficient capital, extrava-
gance in fitting up the store, purchase of large quantities of stock ahead of the
demand, or purchase of stock on account of its cheapness, too early marriage,
insufficient education, lack of business methods with regard to the workings of
the store, carelessness in financial details, want of politeness, neglect of health,
neglect of certain kinds of advertising, and finally, lack of pharmaceutical
literature.
" Cold Cream " was the subject of a paper by F. W. E. Stedem.
It was as follows : "Since the last revision of the United States Pharma-
copoeia, many complaints have been made by physicians as to the deterioration
of ointments of metallic oxides and other medicinal substances, when made
with unguentum aquae rosae as the unction vehicle. The cause of these rapid
changes is due to admixture of a small per cent, of borax, which has been
added because of its saponifying the oil of almond partially, and thereby hold-
ing the rose water in suspension all the more readily. My experience with both
formulas has led me to the firm conviction that the change to the use of borax
was a ver\' unwise one, for many reasons. The first objection is illustrated in a
series of ointments of various mercurials in daily use, and the results are, on
inspection, obvious. These preparations were made on INIay lo, 1897, a little
over a month ago, and in all cases one w^ould be unable to recognize the mix.
tures. The preparation of ointment of yellow oxide of mercury is particularly
objectionable, and its unsightliness is not the least of its failings. This oint"
ment is frequently ordered by physicians for use on the eye, and when made
with official cold cream, is totally unfit for use, because of the terribly irritat-
ing properties of the reduction product. It is not the desire of the writer to
prolong the line because of its length, beyond submitting these specimens,
including an ointment of yellow oxide of mercury, a dilution of ointment of
nitrate of mercury, and an ointment of red oxide of mercurj-. It is a question
as to whether the change from the Pharmacopceia of 1880 was not made in
deference to a demand from those who are simply unwilling to work hard in
an effort to get a good or fit preparation. There is no difficulty iu making a
good and sightly mixture by the old process when worked right and long
enough. It would be much better to drop the preparation entirely from the
Pharmacopceia than to continue it and make it necessary for us to keep both
preparations in stock, for the reasons given before."
This paper was commented on at length ; other members reported trouble
from the same source, and also dissatisfaction with the changes which had been
made iu some other official preparations. Prof. Moerk mentioned the discolor-
ation which happens when resorcin or hydroqinone is mixed with official cold
cream or other substances which contain alkaline bodies. The paper was
referred to the Association's committee on the revision of the United States
Pharmacop<jeia.
^"''jX'mi^'"'} Pharmaceutical Association. 383
Prof. F. X. Moerk then read an interesting contribution entitled " Notes on
Opium Assaying ;" see page ^44 of this number.
"Analytical Processes and Laboratory Notes," by C. H. I, aWall followed.
This paper may be seen in full by referring to page 350.
The Committee on Membership reported thirteen new members. The Secre-
tary read a telegram bearing fraternal greeting from the Colorado Pharma-
ceutical Association, which was in session at the time. He returned the cour-
tesy on behalf of the Pennsylvania Association.
The Committee on Legislation reported that the pharmacy law known as an
act to regulate the practice of pharmacy, sale of prisons, etc., approved May
24, 1887, and subsequently amended in June, 1891 and June, 1S95, upon being
tested as to its efficiency to meet the requirements and purposes for which it
had been enacted, failed to withstand the crucial test of the courts. The first
section was declared unconstitutional by the Superior Court on January 29,
1897, on account of the so-called unlimited widow's clause, which decision, on
an apf>eal, was sustained by the vSupreme Court on May 7, 1897. Tlie com-
mittee at once began work to secure the speedy enactment of a new law, which
would be free from the objections that had brought such disastrous results to
the former law. With this object in view, a bill was introduced in the House
on March i, 1897, and one of like import was introduced in the Senate on
March 15, 1897. This latter bill passed second reading in the Senate, The
House bill met with a formidable resistance, and was amended in such manner
as to require compulsory registration of physicians as pharmacists without the
semblance even of an examination by tlie pharmacy board. This provision met
with a determined opposition, and its advocates were notified that the pharma-
cists of the State would never accept legislation of that character, but would
demand and insist upon the enactment of such legislation as would place them
on a parity with the laws governing the medical profession. Some 12,000 to
15,000 circulars and reprints of bills, including petitions to be signed and for-
warded to the members of the Senate and House, were mailed to llie druggists
throughout the State, with the gratifying effect of arousing an almost united
sentiment in favor of the original measure and against the proposed amend-
ment ; and the committee had the satisfaction of the prompt passage bv the
House of the bill without the objectionable amendment. The bill was next
passed by the Senate, but with a further slight amendment, which the committee
feels sure will be accepted and promptly concurred in by the House. The fol-
lowing is a copy of the bill :
An net supplementary to an act entitled An act to re{(u1ate the practice of pharmacy nnd
sale of poisons and to prevent adulterations in drugs and medicinal preparations in the State of
Pennsylvania, approved the twenty fourth day of May .\nno Domini one thiMi - Mt hun-
dred and eighty-seven, further rcgtilating the practice of pharmacy, the c<.; ng und
dispensing of prescriptions and the sale of drugs, chemicals, medicines and puiiH>us. and pro-
viding a penalty for the violation thereof.
Section i.— Be it enacte<l by the Senate and Hou.se of Representatives of the Common-
wealth of Pennsylvania in (#eiicral .Assembly met, and it is hereby enacted by the same. That
hereafter no person whosoever shall, directly or indirectly, open or cany on In the State of
Pennsylvania any retail drug store or chemical store, or comiraund or dispense ii: ,)f
prescriptions of physicians, or engage in the busiiieKS ut sriling at retail niivdt ,|.
cals, poisons or medicines without having obtained ■ ' ,^.
tion so to do frum the State Pharmaceutical Hxaintniii. ,,ly
384 Pharmaceutical Association, {^"^i^xylS:^"^'
registered bv said board. Any person who shall violate or fail to comply with the provisions
of this section shall be guilty of a misdemeanor, and on conviction before anj' court shall be pun-
ished by a fine not exceeding one hundred dollars ; Provided, however, that nothing in this act
contained shall in any manner whatever be taken or construed to prohibit any practitioner of
medicine from supplying to his patients ?uch articles as he may deem proper, nor to interfere
with the making and dealing in proprietary medicines, nor to prevent storekeepers from
dealing in and selling the commonly used medicines and poisons as now permitted by the
sixth section of the act to which this is a supplement. And provided, also, that the legal rep-
resentatives of any deceased registered pharmacist may, for the purpose of administration of
his estate, be permitted by the Orphans' Court of the proper county to continue the business
for not exceeding one year under the management of a duly registered pharmacist.
Section 2.— The term commonly used medicines and poisons relating to storekeepers is
defined as simple and harmless household remedies which can be handled with safety by the
uneducated, as essence of ginger, peppermint, Hoffmans anoydyne, castor oil, sweet oil and
drugs of like character, and to exclude all dangerous and highh' concentrated remedies,
alkaloids, fluid and solid extracts, and drugs, such as opium, morphine, cocaine, chloral
hvdrate and drugs of like character, and poisons in the same case to mean only such well
known drugs and chemicals as are used by farmers and truckers as insecticides, as Paris
green, royal purple, powdered hellebore, sulphate of copper and drugs of like character.
A bill already referred to in this report and known as the "Adulteration
Bill," was signed by Governor Hastings on May 25th last. It is :
An act to prevent the adulteration, alteration and substitution of drugs and medicinal
preparations; and providing penalties for violation thereof.
Section i. — Be it enacted by the Senate and House of Representatives of the Common-
wealth of Pennsylvania in General Assembly met, and it is hereby- enacted by the authority
of the same, That no person shall within this State manufacture for sale, offer for sale or sell
any drug which is adulterated within the meaning of this act. The term drug used herein
shall include any medicinal substance or any preparation authorized or known in the Phar-
macopceia of the United States or the National Formulary ox the American Homcepathic Phar-
macopieia or the American Homcepathic Dispensatory. A drug shall be deemed to be adulter-
ated within the meaning of this act,
I n If any substance or substances have been mixed with it so as to depreciate and weaken
its strength, purity or quality.
(21 If any quality, substance or ingredient be abstracted so as to deteriorate or affect injuri-
ously the quality or potenc\- of the drug.
(3) If any inferior or cheaper substance or substances have been substituted in whole or
part for it.
(4) If it is an imitation or is sold under the name of another drug.
(5) If the drug shall be so altered that the nature, quality, substance, commercial value or
medicinal value of it will not correspond to the recognized formulae or tests of the latest edi-
tion of the National Formulary or of the Phartnacopceia of the United States or the American
Honuepathic Pharmacopoeia or the American Homcepathic Dispensatory regarding quality or
purity.
On complaint being entered the State Pharmaceutical Examining Board is hereby empow-
ered to employ an analyst or chemical expert, whose duty it shall be to examine into the
so-called adulteration and report upon the result of his investigation, and if said report justifies
such action, the board shall duly cause the prosecution of the offender as provided in this law.
Whoever violates any of the provisions of this act shall be guilty of a misdemeanor, and upon
conviction shall be fined a sum not exceeding one hundred dollars nor less than fifty dollars,
or undergo an imprisonment not exceeding ninety days nor less than thirty days, or both.
Section 2.— All laws or parts of inconsistent laws herewith are hereby repealed.
A vote of thanks was extended to the Committee on Legislation and to the
members of the Legislature who had worked for and supported the measures.
The officers for the coming year were installed at the last session, on Thurs-
day evening. The entertainment provided for the meeting by the committee
in charge was of an interesting character, well attended and much enjoyed by
all present.
THE AMERICAN
JOURNAL OF PHARMACY
AUGUST, 1897.
MEMOIR OF EDSON SEWELL BASTIN.
Death at best is a sad subject, but it becomes doubly so when, as
was the case with Professor Bastin, the victim is cut down in the
very zenith of his strength and usefulness. Beginning as a pioneer
in what was then the far West, he naturally reached his full scientific
development later than those who start surrounded with every edu-
cational facility, and who need to give no thought to the financial
questions which usually attend the attainment of an education.
But what he lost in time he gained in having a broader and more
practical knowledge, which enabled him to more than make up in
later years what he lost in early life.
The subject of this memoir was born May 29, 1843, >" the south-
ern part of Ozaukee County, Wis., on the southern shore of Lake
Michigan, near what was then the village of Milwaukee. His parents,
probably of remote French ancestry, had come there from north-
ern New York some time previously. His father was a strong-
resolute and daring man, with rather a restless temperament. His
mother was sought for in that sparsely settled district by the neigh-
bors in times of sickness; their ailments she relieved to the best of
her knowledge and ability by the use of medicinal herbs, gathered
and prepared by her own hands.
The boyhood of Professor Bastin was divided between farm work
in summer and attendance at the district schools in winter. The
family afterward moved to Wauwatsa, Wis., and then to Wau-
kesha, in the same State.
(385)
386 Memoir of Edson Sewell Bastin. {'^'^-^^^^^x'^mi^-
The rugged life on a pioneer farm developed the latent energies
of the boy, and he became self-reliant and fearless. He would en-
gage in hunting in the depths of the forest, either day or night, and
he was as successful in that important part of the pioneer's life as
he was in the numerous other duties. His mother died when he
was but twelve years of age, and his father was killed by accident
some ten years later.
In 1859, while in his sixteenth year, he entered Carroll College,
at Waukesha, Wis., and remained there until 1862, when the war
spirit took possession of him, as it did of many others at that time.
He entered the Twenty-eighth Wisconsin Infantry, which regiment
became attached to the Army of the West, and engaged in the
Arkansas campaign. This regiment experienced long, severe
marches, much sickness and other privations, with the tedium unre-
lieved by the presence of the enemy until they reached Helena,
Ark., where a battle was fought and won on July 4, 1863, and in
the same year Little Rock was captured.
Soon after this, partly on account of illness, which unfitted him
for field duty, and partly because of his clerical abilities. Professor
Bastin was detached from his company and employed as a clerk at
headquarters. After a year's service in this capacity, he was, in
1864, commissioned captain of the Fourth Arkansas Cavalry; this
appointment was the result of a competitive examination. The
young captain was, from this time to the end of the war, engaged
actively in scouting and picket service, in which he won a high
reputation for ability and bravery, and, through the voluntary re-
commendations of his superior officers, he was offered a cadetship
at West Point. He, however, had no taste for military life in times
of peace, and declined the honor. Instead of this, he entered
Chicago University as a student, where he graduated in 1867.
Following this, he took a course of some three years in the same
institution, in theology, which course he completed in 1870, with the
degree of Bachelor of Divinity. His character at this time can
best be understood by the following extract from an address at his
funeral by one of his classmates, the Rev. Dr. John Gordon :
I became acquainted with Professor Bastin while in his senior year in the
old University of Chicago, and was associated with him for four years in the
class-rooms of the college and Theological Seminary. He first impressed me
as bemg somewhat cold in manner, but on better acquaintance I found this
^'"AugTtT^'" } Memoir of Edson Sewell Basiin, 387
was simply his natural reserve, and that he possessed a warm and tender heart,
which bestowed its affection more and more as the years went by.
Asa student he was respected by professors and classmates because of his
deportment, faithfulness and sincerity. He was always well prepared for reci-
tation or examination, and never did things in a slip-shod manner. The testi-
mony of his students in the Philadelphia College of Pharmacy to his exacting
demands for honest work from them fittingly expresses his own early convic-
tions and habits when a student.
Professor Bastin was a modest, unassuming young man, and never, until to-
day, did I know that he had served in the army during the late civil war. His
record as a soldier is one of which any man might justly be proud, and yet
during all my four years' acquaintance with him I never heard him speak of
the war.
We now come to a turning-point in the life of Professor Bastin,
where, instead of following the ministry, for which his education had
prepared him, he became interested in the natural sciences, particu-
larly the science of botany. This subject had been studied by him
in a variety of ways from his early youth, and the writer has heard
him speak of the observations he made on the flora of Arkansas,
while doing duty as a soldier there ; consequently, " true as the
needle to the pole," when in 187 1 he was deciding on his life-work
he came back to this same subject. He selected the drug busi-
ness as a means to the end which he wished to accomplish, and for
the next few years, while engaged in the duties of apothecary in
Chicago, he gave much time to the study of botany and its allied
sciences. In 1873 he married Christina Hoyd, and shortly after dis-
posed of his drug business. His reputation won in the civil war
secured for him an appointment as United States Marshal, and he
moved with his wife to the scene of his duty in Indian Territory.
The experience in this lawless region was of the most thrilling
character, and often exposed him to great danger, but his cool
judgment, thorough horsemanship, as well as his ability to use fire-
arms to the greatest advantage, brought him safely through evciy
conflict. His wife, however, could not endure the nerve strain of
such an exciting life, and after nearly a year of service he returned
to Chicago, where he accepted, in 1874, the position of registrar in
the University of Chicago. In this institution he almost immc
diately commenced teaching, first as Instructor in Hotany, and two
years later, in 1876, as Professor of Botany and Geology. In this
same year he was chosen to lecture on botany in the Chicago College
of Pharmacy, and for a short time conducted a class in analytical
388 Memoir of Edson Sewell Bastin, {'''\i^lif',l^!!^
chemistry, a fact which points to his broad knowledge of nearly all
branches of science. Soon, however, he was assigned to the chair
of Materia Medica and Botany. In 1878 he met a sad loss in the
death of his wife, who left him one son, Edson S , only three months
old.
In 1883 he resigned from the Chicago University in order to give
his whole time to the College of Pharmacy, and in the same year he
was married to Ellen Beardsley Reed.
During the next several years the world commenced to see some
of the results of Professor Bastin's labors. He first established a
botanical and microscopical laboratory, then issued, in 1887, his
first book, the '• Elements of Botany," which in 1889 appeared in a
second edition, enlarged and entirely rewritten, under the title of
" College Botany." It has been adopted by a large number of insti-
tutions not connected with pharmacy.
In 1890, after having resigned his position in the Chicago College
of Pharmacy, Professor Bastin entered upon his duties as Professor
of Botany and Materia Medica in the school of Pharmacy in North-
western University. Here he organized his second botanical and
microscopical laboratory, which was a model of completeness. In
May, 1 89 1, he was again left desolate by the loss of his wife, ^nd in
August, 1892, he was married to Abbie Beardsley, who, with two
little daughters, survives him.
Up to this time Professor Bastin's writings had been largely con-
fined to his text-books; but in 1892 several papers appeared in The
Apothecary from his pen, viz.: " The Flora of the South Shore of
Lake Michigan," and " Starches in Root Drugs." He also published
contributions on " Plant Hairs," " Notes on Vegetable Histology,"
*' Plant Crystals," and '« Detection of Stem Admixtures in Root
Drugs."
In the autumn of 1893, Professor Bastin was called to the chair
of Botany and Materia Medica in the Philadelphia College of Phar-
macy. This position gave him the opportunity to carry on the
research work which it had long been his aim to do, and he
entered upon his duties with an immense amount of enthusiasm.
Notwithstanding the interruption and distraction necessarily accom-
panying the moving of his family to a new city, he had in one year
established the third botanical and microscopical laboratory organ-
ized by him, he had conducted two large classes through a college year
"^"Aur^'j^""} Memoir of Edson Scicell Basiin. 389
of instruction, had published his important work, " Laboratory
Exercises in Botany," containing several hundred illustrations from
his own pen, and finally, he had made several contributions to the
American Journal of Pharmacy. The few succeeding years were
no less active ones ; during 1895 he published no less than nine
illustrated papers on our local medicinal plants ; one of these, *• Vera-
trum Viride," contained a plate in colors, the original being from his
brush. His research work during 1896 was devoted to the structure
of the " North American Conifer.ne." This series of papers was pub-
lished in joint authorship with Henry Trimble, and was only partly
completed at the time of Professor Hastin's death. All the draw-
ings were from his pen. He was also engaged in preparing an
elaborate work on materia medica, and he had mounted a great
many sections of drugs for the purpose of making drawings from
them. His inability to make rapid progress with this work was a
great trial to him, and he persisted in it at intervals until March 18,
1 897, when, after mounting two sections, he laid down his work forever.
Death came to his relief on April 6, 1897, the immediate cause
being cerebral hemorrhage. He had not been well since the pre-
vious summer, but he continued to attend to all his teaching duties
until the middle of December. What at first appeared to be nervous
prostration, developed into exophthalmic goiter. His tremendous
will-power kept him on his feet almost tc the last, and as late as
February he delivered one lecture, but it was like the last flaring
up of a flickering light.
Professor Hastin was a member of several scientific societies, viz.:
The Chicago Academy of Science, The Evolution Club, the Illinois
Microscopical Society, The American Association for the Advance-
ment of Science, and the Royal Microscopical Society of London.
A short time before his death he was elected a member of the
American Philosophical Society. He was also a member and
trustee of the Philadelphia College of Pharmacy.
In studying the character of this man one cannot but be impressed
with the wide range of exp>erience he covered in 54 years, yet no
one can say that he was not a master in every station in which he was
placed. Whether as student, soldier, teacher, author or artist, he was
a man, and a thoroughly honest one. His strict honesty with him-
self caused him to expect honesty in everyone else. An anecdote
will best illustrate how binding he considered his own promise.
390 Memoir of Edson Sezucll Bastin. {'^^Ai^L't.Tso'':'"-
When he first came to Philadelphia he arranged for the publication
of his book on Materia Medica, which was unfinished at the time of
his death. It was afterwards shown very clearly to him that he
could, with great advantage, give the publication to another firm,
and he expressed his desire to do so but for his promise; and when
asked : " Is there no way out of it?" the prompt reply was : " Yes,
there is a way out of it, but there is no honest way out of it." It is
almost unnecessary to add that the question of publication was con-
sidered settled from that time.
As a teacher, Professor Bastin was noted for his conscientious
thoroughness; no amount of labor was too great for him to under-
take in the interest of his students. He was an earnest advocate of
the practical study of the natural sciences. When asked, during his
preliminary visit to the College in 1893, if he would be willing to
establish a laboratory for the practical study of materia medica and
botany, his reply was that he would 'not be willing to undertake to
teach those branches in any other way. In his ''College Botany" are
some introductory paragraphs, entitled, "A Word to the Student,"
a few sentences of which should be read and re-read by every one
engaged, or about to engage, in the study of botany. He says :
Remember that the study of botany is primarily the study of
plants, and not the study of books about plants. If you study
the book only, you will almost certainly find it dry and unprofit-
able, but if you use it as a guide to the study of plants, and
study it PLANT IN HAND, verifying- its descriptions by obser-
vations of your OAvn, you vs^ill find the work not only profitable,
but intensely interesting.
These {^\m sentences say more than whole volumes could be made
to say against the entire race of "Quiz Compends," "Aids,"
"Lecture Notes," " Home Studies," and all the other " short cuts"
which are devoured but not digested by the great army of unpre-
pared applicants for State Board Certificates. Professor Bastin's
method of studying botany was either in the field, or with the micro-
scope, but always with the plant or drug in hand, and his method of
imparting instruction was the same. It remains but to speak of his
domestic life, which, by those who knew, has been declared to have
been an ideal one. He was especially fortunate in his matrimonial
alliances, which caused the losses to bear more heavily upon him.
He brought into his family the enthusiasm which he himself possessed
^"Au^Jt.^^!"'} Heloderma Siispectiim, Cope. 391
for the study of nature, and thereby drew the members into sym-
pathy with him and his busy Hfe. His funeral was from his resi-
dence in Merchantville, N. J., and was largely attended by his
students and college associates. The burial was in the beautiful
and historic cemetery of Colestown, a few miles distant. H. T.
RESEARCHES IN REGARD TO THE VENOM OF THE
HELODERMA SUSPECTUM, COPE.
From the Physiological Laboratory of the Caroline Institute, Stockholm,
Sweden.
By C. G. Santesson, Professor of Pharmacology.
Having had the opportunity to examine the saliva from three
lizards of the above-named species, Heloderma suspectiun, Cope,
which were caught in Arizona and sent alive to the Zoological Insti-
tute at the Stockholm High School, and thinking that any new
information in regard to this wonderful species of animals might
possibly interest American readers, especially since the question of
its poisonous nature has been enthusiastically discussed in American
papers, I venture to submit for their perusal a short account* of the
results of my experiments in this line.
Before beginning to relate the results of my own experiments,
I must, however, call attention to several features in the discussion
carried on in America, adding a few remarks of my own.
The fact that the anatomical structure of the heloderms suggests
the probability of their being to a certain degree poisonous has
been pointed out by Cope.^ Numerous experiments made on ani-
mals by Sumichrast,^ Houlenger,* J. Fayrer, in the Zoological
* My studies on this subject have been more completely published in German
in a treatise with the title : " Ueber das Gift von Helo<lerma suspectum Cope,
einer giftigen Hidechse, " No. 5 of the festival volumes ot Xordiskl Mtdidnskt
Arkii\ dedicated to Prof. Axel Key, March, 1897.
' Cope : I^oceedings of the Academy of Natural Sciences of Philadelphia,
^^^^7, P- 5 ; »ce also a postscript to an article by Shufeldt, The American Naiu-
ra/ist, Vol. 16 I 1882 j, p. 907.
'Cfr. letter to Bocourt : Comp. rend, de I'acad, des sciences, t. 80 (1875), p.
676 ; furthermore, Sumichrast : liulleiin de la soc, tool, de France, Vol. 5
(1S80), p. 178.
♦ Boulenger : Proceedings of the Zoological Society of London, 1881, p. 631 \
gives an account of Payrer's observations
392 Heloderma Snspectum, Cope, {^'"Augusl'^iSr-
Gardens, London,'* of Weir Mitchell and Reichert,^ and Garman/
have shown that the secretion from the salivary glands of the helo-
derms is more or less venomous. Frogs, hens, doves, guinea-pigs
and rabbits always died of it, the two last-named kinds of animals
generally very quickly. Cats and dogs did not die, but showed
local effects of the poison (pains, swelling, extravasations, etc.). Two
experimenters are said to have arrived at entirely negative results,
viz.: Irwin, U. S. A., about whose experiments (made in 1867?) I
have no explicit knowledge, and Yarrow,^ who discovered no positive
residts worth mentioni?ig, neither after bites nor after subcutaneous
ifijections, the animals always recovering soo7i.
In regard to this last-named research, I beg to call attention to
the possibility for individual variations to exist in the venomous
nature of the heloderms, some individuals always or periodically
being in a much smaller degree venomous.
The accounts of the influence of heloderma bites on man are of
the greatest interest, as for instance the misadventure of Shufeldt^
In spite of the severe pains, swelling, etc., after the bite, this investi-
gator still regards the animal to be harmless, and points out the
fact that even the bites of men or cats may sometimes have a
poisonous effect, although neither men nor cats are classified among
the specifically poisonous animals. It seems to me that Shufeldt here
mixes up two quite different things ; the bites of men or of cats can
certainly not be said to be specifically poisonous (as for instance is
the case with snake-bites); but, on the other hand, they may very
easily cause bacterial infection or " blood-poisoning." The symp-
toms observed by Shufeldt much resemble those brought about by
the bite of our common viper {Vipera berus), i. e., they resemble a
slight specific poisoning, but not " blood-poisoning." It may,
besides, be pointed out that an animal is not *' harmless " because it
does not kill. The bite of our above-mentioned viper does not, as a
rule, kill grown-up persons, and still everybody looks upon it as a
specifically venomous animal, and so it is, beyond all question.
• Short notice in the American Naturalist, Vol. 16 (1882), p. 842.
•' Weir Mitchell and Reichert : The Medical News, Vol. 42, No. 8, Feb. 24,
1883, pp. 209-212.
' Garman : Bulletin of the Essex Institute, Salem, Mass., Vol. 22 (1890), pp.
60-69.
® Yarrow: Forest arid Stream, New York, June 14, 1888, p. 412 and sue.
'•♦ Shufeldt : The American Naturalist, Vol. 16 (1882), p. 907 and sue.
""""Ai^SstjS^""} Helodenna Suspectum, Cope. 393
There is another account of a person bitten by a heloderma, which
is perhaps not so well known by our American readers. Mr. J.
Stein, of Mexico, who once sent two heloderms to Fischer for
anatomical and histological examination of their poison apparatus,^^
was on one occasion deeply bitten in a finger by one of them. The
finger and the whole arm szvelled up considerably, causing the most
violent pain, and his general condition was greatly disturbed. For a
long time afterwards the skin of the arm had a yellow, parchment-
like appearance. Short as it is, this description of the specific local
effect of a poison could scarcely be clearer. In accounts of death as
a consequence of heloderma bites, it may, perhaps, not be worth
while to place too great confidence.
Even the experience hitherto gained seems decidedly to show
that the heloderms are specifically venomous, although their bites
are less dangerous than those of poisonous serpents, and generally
not fatal to men.
The heloderma on whose venom I have made the most of my
experiments (from October, 1895, ^i^^ February, 1896) was a female
H. susptctum (Cope), 40 centimeters long, in good health. It could
not be induced to bite animals, was sluggish and good-natured. The
venom was gained in the following manner : With a pair of long,
crooked tongs, I took a clean, dry sponge, about as large as a wal-
nut, and forced the animal to bite it. When I had sufficiently
irritated the reluctant animal, it would seize the sponge, and I then
generally succeeded in pressing it into the animal's mouth. The
venom in the sponge was then drawn out by means of a little quan-
tity of 06 per cent, solution of common culinary salt. The fluid
thus obtained was turbid, slimy, slightly alkaline, having an aro-
matic smell not at all unpleasant. Some simple preliminary tests
showed that the fluid contained protein substances ; these could
almost completely be precipitated by alcohol in excess, the fluid
having first been rendered slightly sour by the addition of acetic
acid. If, after thus having acidified it, the fluid was instead boiled
for a short time, a part of the albumen coagulated, while the rest
remained in solution.
**J. O. PiAcher: *'Antttoni!sche Notizen T'et>€r Ifetoder^na 'u^ t unnn '.'
Verhandl. d. Verens J. natup-u tssemsch. I'nterhaltung zu HamI >3,
pp. 2-16.
394 Heloderma Suspectum, Cope. { ^""aJ^IJ^I^s^!'"'
The poisonous liquid drawn out of the sponge by means of the
weak solution of salt was afterwards subcutaneously injected into
frogs, white mice and rabbits, which all died of it. By special
experiments, I convinced myself that there was no other poison in
the sponge, syringe, canula, etc. The common symptom was a
paralyzation of the nervous system^ setting in gradually after a short
lapse of time and ultimately causing death. Convulsions were not
observed in rats, and in rabbits only in a very sHght degree towards
the end (suffocating convulsions slightly indicated). In frogs the
poisoning lasted from 57 minutes to several hours, a day and a
night, etc.; in rats 56 to 85 minutes ; a little rabbit lived 112 minutes.
The frogs died of paralyzation of the heart ;^^. the animals, on the
contrary, seemed to die of the gradual paralyzation of the nervous
system and the centres of respiration. If, on prolonged irritation of
these latter systems, the heart had been primarily paralyzed, signs
of acute inner suffocation, accompanied by dyspnoea and violent con-
vulsions should have appeared, as was the case in the experiments
of Weir Mitchell and Reichert (see note 6) ; but such was not
the case to any degree worth mentioning. The difference between
the results of these investigators and my own surely depend chiefly
on their having, as a rule, used much greater doses than I did ; they
have, therefore, obtained a sudden paralyzation of the heart, while
my experiments have brought about very gradual paralyzation of
the nervous system.
On account of the way in which I collected the poison, I cannot
say how great the doses were. The quantity of saliva taken
amounted on one occasion to about 0-3 gramme, but surely both
the quantity and the toxicity varied much on different occasions.
That the poison is effective in very small quantities was proved by
the following experiment: r8 milligrammes of dried poison was dis-
persed in a little water, only partly dissolved ; was filtered and in-
jected into a frog. The animal grew very weak and languid, but
was, however, not totally paralyzed ; did not completely recover
until after a week. The poisonous part of this dose was certainly
not more than a fraction of i milligramme.
A more minute examination of the development of the paralysis
" Frogs can, as a rule, hardly die from paralyzation of the respiratory organs,
since they breathe so sufficiently through their skin that they can lie alive for
weeks without lung respiration and afterwards recover.
Am. Jour. Pharm
Au'grt-.?^"} Helodcrma Suspectum, Cope. 395
in frogs showed that the central nervous system, the brain and the
spinal cord were first affected by it, but afterwards it also attacked
the termini of the motor-nerves in the muscles, producing a com-
plete curare effect, while the irritability of the muscular tissues re-
mained unaffected.
In the heart of a frog observed in situ without opening the
thorax, the rate of pulsation after subcutaneous injection of the
poison was observed at first to increase a little, then gradually to de-
crease until it stopp>ed entirely. Shortly after the heart had stopped,
or while the auricles were still beating slightly, the ventricle (after
opening the thorax) usually seemed contracted and stiff, surely in-
dicating a direct effect of the poison on the muscular tissues.
Weir Mitchell and Reichert have not observed any local effect of
the heloderma venom. Probably this depended upon the hasty
death of the animals on whom they experimented. In several ex-
periments on frogs, I have discovered cedema, small extravasations,
discoloring and fragility of the muscular tissues, etc., at the place of
injection (mostly in the walls of the lymph-sinus of the thorax and
abdomen). In a rat I once observed a greenish-brown discoloring
of the tissue around the place of injection. Furthermore, in many
accounts of former experiments on animals, and also in accounts of
cases in which people have been bitten (Shufeldt, Stein), we read of
more or less marked local effects of the poison. Local gangrene
is, however, not mentioned, and, as a rule, the local effects have
soon disappeared.
On mucous membranes (the mucous membrane of the stomach and
the conjunctiva) the heloderma poison does not seem to have any
injurious effect.
By means of some special e.xperiments, I have furthermore tried
to discover how the poisonous part of the heloderm saliva is affected
by alcohol and boiling. If to the poisonous fluid, which has been
rendered a trifle sour by the admixture of acetic acid, alcohol is
added in excess, all the poison may be precii)itated, in case the pro-
cess is carefully carried out. If the alcoliol is then filtered off from
the poison and allowed to evaporate, and if the residues, after the
evaf>oration of the alcohol are dispersed in acid water, the liquid thus
obtained is uneffectivc. Thus, poisonous alkaloid substances, which
ought to have dissolved in alcohol and then in acid water, «Yfr not
to be found.
396 Heloderma Suspectunt, Cope, {
Am. Jour. Pharm.
August. 1897.
The alcoholic precipitate was again partly dissolved in water
(after the alcohol had been removed), and this solution always had
a fatal effect, accompanied by the usual symptoms, sometimes so
suddenly (a frog died in fifty-seven minutes) that there is all reason
to suppose that the whole of the poison had again been dissolved.
From this the important conclusion may be drawn that the poison
probably does not, or at least only to a small degree, belong to the
group of common albuminous substances {albumin, globulin), which
soon become so altered in alcohol that they cannot be again dis-
solved in water. On the contrary, the venomous principle ought,
probably, to be looked for among the nuclein substances, the albu-
moses (albuminoses?), the peptons, the mucoid substances, etc.
If the poisonous liquid rendered slightly sour by acetic acid is
boiled, coagula are formed, as before mentioned. These are not
poisonous if well washed with water ; but if not washed, a more or
less considerable amount of the venom is liable to adhere to them,
and this venom may afterwards be soaked out of the coagula, and it
is then even able to cause fatal poisoning. That which is coagulated
by boiling and is insoluble in water probably consists of common,,
harmless albumen. Thus it may be seen that the poison, when
boiled with acid, remains in solution. On the contrary, with alco-
hol it may be precipitated from this solution, but may again be dis-
solved in water. These circumstances also point out that the
venom is not an albumin or a globulin, but belongs to the latter of
the above-named groups of protein substances. The fact that the
poison is not destroyed by boiling shows that it is not an enzym {an
unorganized ferment), as these are usually conceived.
When the poisonous solution is brought into a slightly sour reac-
tion by means of a small quantity of acetic acid, there is no pre-
cipitation. Consequently, true mucine is not present in any great
quantity.
Since the supply of material which I was able to obtain was very
small, it was rather difficult to determine the chemical nature of the
venomous substance or substances. I therefore applied to my col-
league, K. A. H. Mbrner, Professor of Medical Chemistry in Stock-
holm, who had the kindness to undertake this work, while I myself
made the experiments on animals required for these tests.
The poisonous solution, rendered a little sour by acetic acid, was
precipitated by alcohol in excess; this precipitate was dissolved in
I
Am. Jour. Pharm. 1
Augim.iaf:^"} Heloderma Suspect urn. Cope. 39;
water and was again precipitated by acetic acid and brought to a
tolerably strong sour reaction. In this precipitate there was found
phosphorus, organically bound ; here there was, therefore, undoubt-
edly, some nucleimferous protein substance present.
But was this substance poisonous? From another quantity of the
poisonous secretion, the nuclein substance was again isolated, dis-
solved in water with a little soda, and injected into a frog. The
animal soon grew weak, bled continually, though slowly, from a
small wound on one of its lips, and died after three days. On dis-
section, I found a great number of small extravasations of blood in
the muscles of the thorax and even some in other places. We see
here (at least partially) the characteristic effects of nuclein sub-
stances on the blood (diminished coagulating power, extravasations).
If a stage of increased coagulating power had preceded, I do not
know. If the solution of heloderm poison is directly applied to
defibrinized blood (of a rabbit), the blood-corpuscles seem to take a
spherical form, which reminds us of the effect of the snake-poison
globuiiues^^ of Weir Mitchell and Reichert.
The solution from which the above-named poisonous nuclein sub-
stance was removed by precipitation with acetic acid did not contain
any albumin which coagulated on boiling. On the other hand,
Millon's reaction showed the presence of some protein substance.
With sulphate of ammonium in. substance, a considerable downy
precipitate of albutnoses was obtained. After these had been filtered
off, the liquid (the filtrate) gave no '' biuret-rcaction ;'' consequently
true peptons were not present. In the liquid from which the nuclein
substances had been removed, albumoses could still be displayed by
means of ordinary culinary salt and acetic acid ; these called forth a
turbidness which disappeared on boiling and reappeared when
exposed to cold.
From another sample, the albumoses were isolated in the above-
described manner with neutral sulphate of ammonium in substance,
were then separated as much as possible from the ammonium salt,
were dissolved in water and precipitated with alcohol. The latter
treatment was repeated once more, and at last the new alcohol pre-
cipitate was dissolved again in water. This solution of albumoses,
which still contained some sulphate o( ammonium, was injected into
" Weir Mitchell and Reichert : '* Re«c*rchc» upon the Venom of Poihonout
Serpents," Washington, 1886.
398 The Pharmacist and the Microscope, {^*"iSt,%'"'
a frog. The frog soon grew weak, almost paralyzed, but did not
die. On the contrary, it gradually recovered, but after ten days
was not yet quite normal. It was then killed ; no extravasations
were visible. (With a larger dose of sulphate of ammonium injected
into another frog, it was shown that this salt called forth quite dif-
ferent symptoms.)
From the experiments here related, it may be seen that the prin-
cipal venomous elements of the heloderm saliva consist partly of nucle-
iniferous substances and partly of albumoses.
By special experiments it was at last shown that aqueous extract
from the poisonous glands of the heloderma and the blood of that
animal possessed poisonous qualities.
Consequently, my observations most decidedly support the asser-
tion of the majority of experimenters, especially Weir Mitchell and
Reichert, that the heloderms are specifically poisonous animals, even
if, as a rule, they are not aggressive towards men, and, on account
of their sluggishness, only seldom do any harm. A heloderma is,
at all events, an individual to be suspected, even if it does give but
very little reason for the name " horridum." As a playmate for
children (Cfr. Weir Mitchell and Reichert, note 6), it is certainly
not suitable.
Stockholm, June, 1897.
THE PHARMACIST AND THE MICROSCOPE.^
By Henry Kraemer.
The topic of " The Microscope in Pharmacy " is by no means a
new one. In this country for at least the past twenty years it has
been a theme upon which comparatively many have written. Upon
looking over some of these papers one is struck with the loyalty of
the authors to the microscope, in describing its construction, uses
and even possibilities. Nevertheless, one cannot but feel that the
situation has been viewed in most cases from some other stand-
point rather than the practice of the profession of pharmacy. The
idea that seems to pervade the atmosphere is that all that is neces-
sary for the pharmacist is to procure the necessary apparatus (mi-
croscopes, reagents, etc.) and books and to follow the directions
given. One furthermore receives the impression that, because
' Presented at the New York State Pharm. Assoc, July 13, 1897.
Am. Joar. Pharm
A^si i5l^^°} The Pharmacist and the Microscope. 399
vegetable drugs possess characteristic structures, therefore, the
pharmacist ought to use his microscope in determining all of the
drugs that he buys. The result of this kind of writing has, to
some extent, hindered our progress in practical pharmacognosy in
this country.
ONE MUST BE T.\UGHT.
To possess a microscope and not know how to use it, or to think
one knows how to use it, and spend one's time by one's self in en-
deavoring to interpret what is revealed there, is both money and
time wasted. In order to obtain results that are reliable in using a
microscope for any purpose, one must know how to use the instru-
ment and understand the structures in the department (say botany)
where it is to be used. This necessary knowledge can come only by
being instructed properly. Of all the instruments yet devised in
the prosecution of scientific research, there is none that requires
that its user shall be better taught in the foundation and guiding
principles of the science in which he engages, than the micro-
scope. It is extremely unprofitable for any one to have the idea
that he can teach himself the use of the microscope in the science
in which he proposes to apply it. It looks very inviting to see a
good illustration and to read of sectioning, mounting and examin-
ing a drug with the microscope. It is another thing to do the work
and see the points. Experience teaches us that a beginner finds no
help in the illustrations of books. What the beginner needs in
doing microscopical work are not illustrations or facts, but ability to
use his hand, eye and brain rightly. One must be taught, i. e., guided
to knowledge. Time must first be consumed under a competent
teacher in mastering the construction of the instrument and in be-
coming familiar with the methods of doing microscopical work and
in learning the foundation and guiding principles of morpholog)-
(both outer and inner) of the plant kingdom. After this is accom-
plished the student will find books helpful. Now he can use his
hands properly, see with his eyes correctly and interpret with his
brain rationally. The more knowledge that is gained by personal
observation the stronger and more self-reliant will the student be-
come.
A broad botanical or even biological university training is the
best foundation and is necessary to accomplish the best work witli
the rnicroscope. It cannot be said, however, that this is absolutely
\iii. Jour. Pharm.
400 The P/mrjnacist and the Microscope. {^"i^S.is^^
necessary in the prosecution of the microscopical work by the phar-
macist. It is necessary for him, however, to have mastered the
foundation principles of physics, botany and chemistry in order to
get the results that are of practical value to him. Some of our
schools and colleges of pharmacy are now prepared to give their
students a good start in this direction. The student must not be
dismayed, but, on the contrary, expect "to make haste slowly" at
first. He must exercise patience in learning to section drugs and
work persistently under a competent instructor until he understands
the principles of his subject. Nature does not unfold herself unless
you work patiently and incessantly at her. When one problem is
well worked out, the next is easier, so that by the time the student
is master of his subject, results come comparatively easily.
TIME AND PLACE FOR USE OF THE MICROSCOPE.
Having shown that instruction is necessary in order to secure
reliable results from the use of the microscope in pharmacy, the
illusion that the microscope is necessary on all occasions must be
dispelled. While it is an indispensable instrument sometimes, it
does not follow that it must be used always, any more than because
an axe is used to chop down a large tree, that therefore an axe is
necessary to break up every piece of wood. The microscope has its
time and its place for use by every one who is accustomed to using it
in his special line of work. It is as superfluous for the educated
pharmacist to use his microscope in the examination of each lot of
nux vomica or calumbo that he buys as it would be for the field
botanist to require to make a microscopical examination before he
could determine, say, Castanea dentata or Quercus alba. In fact, it
bespeaks lack of knowledge in the botanist. It likewise reflects on
the professional pharmacist who wishes to make sections of those
drugs which are so characteristic in a crude condition, and which by
experience he ought to distinguish at once. The microscope is to be
employed only when more refined tests are necessary.
APPLICATIONS OF THE MICROSCOPE IN PHARMACY.
Upon the completion of a proper laboratory course, and being
well grounded in the various sciences necessary for the use of the
microscope in pharmacy, we must also recognize that .in the use of
the microscope there is a training of the eye (a sharpening of it, so
to speak), so that the trained eye, with the other senses (educated
^"iug,mt.^85^f'"} The Pharmacist and the Microscope. 40 1
too), are all to be employed where necessary in determination of
drugs. Now, there are times when the use of the microscope alone
is essential, whereas at other times it is rather a convenience in the
practice of pharmacy. Some of the applications of the microscope
in pharmacy are the following :
(i) Examination of Some Crude Drugs. — While appearance,
odor, taste, etc., are generally sufficient aids in determining most of
the commercial crude drugs one from another, still there are
instances where a microscopical examination is desirable and neces-
sary. This is especially so when certain drugs occur in relatively
small pieces, or when two or more drugs that possess similar charac-
teristics are supposed to be intermixed or incorrectly labelled. The
microscopic structure will generally enable one to quickly dispose
of such doubtful cases. The following crude drugs of the U.S.P.
require not infrequently a microscopical examination for their
accurate determination, especially when they do not appear in the
forms usually seen in commerce :
Mexican sarsaparilla from Honduras sarsaparilla.
Belladonna,' radix (the horny kind) from Inula.
Belladonna folia from Stramonii folia.
Serpentaria,' from Spigelia.
Granatum from Xanthoxylum.
There are a few cases in the examination of crude drugs where
microscopical examinations have been advocated, and while some-
times necessary, the quality and nature of adulterant may frequently
be told by the eye alone, as Crocus, etc.
(2) Examination of Powdered Drugs. — In recent years powdered
drugs have been introduced to such an extent that in many retail
pharmacies few crude drugs are to be found. Drugs in the powdered
condition may be obtained pure, but adulteration is more easily
effected. The reason for this is owing to the inability of the average
pharmacist in detecting it. We notice that some State Boards in
their examinations give the candidates very few, if any, crude drugs
for determination. In time there can be no doubt but that the
candidates for the State Board examinations will be required to
identify powdered drugs and pronounce on their quality. This
is desirable for the sake of the profession of pharmacy, and in accord
* The microscope is not neceMary here, as will he shown in an article to be
published later.
402 TJie Pharmacist and the Microscope. {"^""auS.^S^""''
with the spirit of the State Boards in giving the candidates as practi-
cal examinations as may be possible. The microscope must, in this
province, be used, as only by means of it can one determine most
of the powdered drugs and pronounce on the quality of all. By
means of the microscope, drugs of different origin may readily be
determined, as the various sarsaparillas, sennas, ipecacs, etc.
(3) As a Preliminary Step in the Study of Plant Constituents, —
The microscope is of undoubted service as a preliminary step in con-
ducting chemical examinations of drugs. The nature of inorganic
substances (as CaC03, CaC204, Si02, etc.) may readily be detected.
The nature of some carbon compounds (as starch, sugar), and active
principles (as oils, resins, tannins or other substances) may be
detected qualitatively.
(4) In Determining the Relative Value of Drugs. — It not infre-
quently happens that two drugs of different origin or habitat are
used in medicine, and that the cheaper contains the larger percent-
age of active principles. A chemical assay may be resorted to ; but
when purchasing a small quantity of a drug this might not pay.
By means of the microscope, however, an approximate comparison
may be instituted, even quantitative results may be obtained, as
has already been shown, and will be further demonstrated in a
forthcoming paper. This applies not only to powdered, but also to
crude drugs. The following instances may be cited :
(«) Gingers. — The African ginger is cheaper than the Jamaica
ginger, but the former contains more secretion cells, which are
about the same size in both. Hence, the African, though cheapest,
assays a higher percentage of oleoresin.
(^) Biichus. — The short buchu is cheaper than the long buchu,
but resembles the former, and contains much larger and more
numerous secretion reservoirs than the latter; hence the "short
buchu" assays more oil than the other.
(5) /« Determining Loss of Active Principles. — It is possible in
some cases, without resorting to a chemical assay, to determine
whether the active principles have been removed. This is notably
so in drugs that contain alkaloids, secretion reservoirs or secreting
hairs, as cinchona, ginger, cloves, or any labiatae.
(6) In Determining Identity and Quality of Spices and Foods. —
Since the introduction of spices in a powdered condition into the
household there has been the most flagrant kind of adulteration
^"AuguJt.VS?!""} Tfi^ Pharmacist and the Microscope. 403
practised. In many cases the microscope is the only satisfactory
means for determining the purity and nature of adulterant.
A few illustrations may be given :
{a) Pepper is adulterated with mustard hulls, wheat flour, etc.
(b) Bermuda Arrowroot with other arrowroots and starches.
(c) Tea with the leaves of Salix alba, Sambucus nigra, etc.
(7) In Determining Unknoivn Drugs. — It often occurs that a
pharmacist receives for identification samples of drugs that are un-
known to him. It may be that they are common indeed and in-
digenous to this country. The microscopic exammation at once
gives one a start. The compound microscope is, indeed, playing a
very important part to-day throughout systematic botany. Certain
groups or families or genera are found to possess a certain charac-
teristic inner morphology, and this is the key to the solution. It
may be that the arrangement of the elements of the fibro-vascular
bundle is peculiar, or that the shape of the element (root, stem,
etc.) is characteristic, or the identification may be based on the
nature of secretion cells, or form and nature of hairs, etc. In leaves
the habitat may sometimes be determined by reason of the structure.
(8) In Biological and Sanitary Analysis. — The advancing phar-
macist is taking upon himself the study of these branches, which
are more or less directly related to medicine, and for which there is
evidently a growing demand. He is making the biological as well
as chemical analysis of water and reporting on the condition of
sputum, urine, etc., of the patients of the physician. In all this
kind of work the microscope is necessary.
(9) For Other Practical Purposes. — Recently some one wished to
examine the number of meshes in some sieves. The compound
microscope was recommended for the purpose, the principle of the
method followed being the same as that used in measuring the
lengths of cells, etc.
The microscof)e may be used in detecting forgery, in determining
the writing on soiled labels ; also in ascertaining the kind of writing
paper, labels, etc., that are purchased, etc.
THE INFLUENCE OF THE USE OF THE MICROSCOPE,
From what has preceded it is seen that the microscope has a
very important bearing on the practical work of the pharmacist.
It would not be proper in an essay of this kind to fail to record the
404 The Pharmacist and the Microscope, {^"^kl^^x^^^^i!^-
influence of the microscope in the training of the pharmacist. The
use of the microscope does for him — as it does for all — an infinite
amount of good that must not be overlooked. It makes better ob-
servers of all. The early workers with the microscope often re-
marked that it enabled tJie zvorker to see with the naked eye after-
wards structures that were invisible to him before he used the instru-
ment. By means of the simple lens one is enabled frequently to
make out those characteristics of a drug that he has seen with the
compound microscope. Finally, with the naked eye alone, one can,
by experience, obtain results in determining the quality of drugs
that are based on structure and not on ephemeral external charac-
ters.
RESULTS OF THE USE OF THE MICROSCOPE.
We must not be discouraged by reason of the sceptic and his
oft-repeated question : *' What is the use?" The sceptic is as use-
ful in treating this subject as he is in other problems. In the ap-
plied sciences this question is ever before the student. The pure
scientist, in his pure science, need pay no attention to the query.
But the business and professional man feels it necessary to devote
his energies to those things only that will bring forth useful fruits.
There is, however,an insurmountable difficulty in following the applied
sciences ; one cannot predict what scientific fact or discovery will be
the basis or part of a principle in the construction of some useful
invention. Hence we find it necessary to take in more than we can
use practically, and are silenced for the time sometimes by the ques-
tion : '• What is the use ?" Nevertheless, we are safe in recording
some of the results that accrue to the educated pharmacist from his
use of the microscope. The benefits are two-fold, viz.: to the phar-
macist and to the public.
(i) To the Pharmacist. — The pharmacist is able to dispense drugs,
foods and spices, the purity of which he can guarantee. This
means to him and for him :
(a) The most efficient of co-operative work with the physician.
{b) The building up of a good pharmacy, the name of which shall
endure.
{c) The establishment of confidence in him by the best physi-
cians and the public. To have a good custom one must sell good
drugs.
'""iSi.^iS^';'"'} The Pharmacist and the Microscope. 405
(^) The pharmacist receives the value of his money for his pur-
chases. He does not pay a high price for an inferior drug, as a
Honduras price for a Mexican or other sarsaparilla.
(e) The conscience of the pharmacist is clear, as he knows what
he is selHng.
(/) It is also an advertisement to the pharmacist, and he may
judiciously utilize it in the building up of his estate here.
(2) To the Public. — The public receive in return pure drugs, foods
and spices. This means to them :
{a^ Confidence in the pharmacist, which sometimes may prolong
and even save life.
(b) Satisfaction in the goods for the money paid.
ARGUMENTS AGAINST THE USE OF THE MICROSCOPE.
(i) It requires an educated person to use the microscope to any
advantage. A mere merchant could not use it with profit. It
requires that one shall have spent time and money in acquiring a
proper education. Hence, they who have never been instructed by
a competent teacher cannot practically avail themselves of the bene-
fits of the use of the microscope.
(2) The cost of the outfit, being at least $25, makes some per-
sons, who might use it profitably, think too long about purchasing
a microscope.
(3) Time must be given to the use of the microscope. Many
pharmacists feel that if there is any time to spare it ought to be
given to *' resting up" or waiting for the next rush of business.
(4) It takes " nerve " or backbone for one to go to college, to buy
a microscope, to give the time that is necessary for securing results
and to believe that all will pay in the end.
(5) The merchant who wishes to purchase his goods at the lowest
price, regardless of quality, does not care to be able to know
whether the guarantee of the seller for purity is correct. He would
rather sell impure and adulterated goods with the clear conscience
of wilful ignorance.
CONCLUSION.
A good education is necessary for a professional pharmacist, and
he alone who is taught properly can use the microscope advan-
tageously.
The microscope may be utilized in so many practical ways by the
4o6 The Tannin of Castanopsis. {^^ASM^^sor'
educated pharmacist that the receipts far outweigh the cost and
time. The Hght in the sky is already appearing, the clouds are
rising higher and higher on the mountain side, and the practical
pharmacists are ascending one by one to higher flights than where
they rested yesterday, and they follow those who it sometimes may
seem are working in the clouds, yet who, nevertheless, when the
light shines, are seen to be laboring for the benefit and the future of
pharmacy.
THE TANNIN OF CASTANOPSIS.
By Henry Trimbi^e.
In the June number of this Journal, p. 296, attention was
called to the presence of strontium in the bark of several species of
castanopsis received from Dr. H. N. Ridley, of the Singapore Botani-
cal Gardens, India. These barks have also been examined for tan-
nin; and the results are now tabulated along with those from two
species of oak also from Singapore, and two samples of the one
species of our native castanopsis, C. chrysophylla. The results on
one sample of the latter were published in the Garden and Forest,
8, 293, July 24, 1895 \ the editor, Professor C. S. Sargent, adding
some remarks concerning the genus, which, by reproduction here,
will throw additional light on the subject.
As is well known, the bark of Quercus densiflora, of California, is popularly
considered the most valuable tanning material produced in the Pacific States of
North America. This oak is the only American representative of a peculiar
group of trees which inhabit southeastern Asia, and are intermediate iu botanical
characters between the true oaks and the chestnuts.
There is another genus, Castanopsis, which is also intermediate between the
oaks and the chestnuts, and also of southeastern Asia, but, curiously enough,
with a single representative in Oregon and California, Castanopsis chry-
sophylla, a very beautiful tree, which the Californians call the gold-leafed
chestnut, from the bright golden scurf which covers the lower surface of the
leaves. Some botanists treat Castanopsis as a section of Castauea, while others,
like Dr. King, of Calcutta, who made a special study of the genus, although
finding no very good characters by which it can be distinguished from one of
the Asiatic sections of Quercus, maintain the genus for the purposes of conve-
nience. The relationship of this tree to Quercus densiflora on one hand, and to
the chestnut on the other, suggested that its wood and bark might contain
valuable tanning properties.
The result of a comparison of the American Quercus and Castan-
opsis, was to show that the tannin of Castanopsis chrysophylla is
Am. Jour. Pharm.
August. 1&97.
The Tannm of Castanopsis.
407
identical with that from Quercus densiflora, and, therefore, with all
the other species of oak which have hitherto been examined by me.
Since chestnut tannin is identical with gall tannin, and that from the
oak is quite a different substance, the result from a chemical stand-
point, placed the Castanopsis chrysophylla with quercus.
The natural sequence of this investigation was a desire to examine
the several species of castanopsis of India, where all the other mem-
bers of the genus grow, and through the kindness of Dr. Ridley this
has been possible. It is to be regretted, however, that only the
percentage amount of tannin and some general characters can be
given at this time, since there was not sufficient material to admit of
a final decision in regard to the composition of the tannin. The
attempt was made to purify two lots of tannin from these barks, but
it is only safe at present to state that the indications point to the
presence of oak tannin in all the Indian species. An additional
liberal supply of the bark from the American species was also
received from Miss Alice Eastwood, of the California Academy of
Science, collected by Dr. Geo. McCowen, Ukiah, California.
Castanopsis Wallichiana . . .
Curtisii (old tree)* .
" (young tree)-
" Javauica
Hullettii
Quercus hystrix ...
** discocarpa
Castanopsis chrysophylla . . .
Quercus densiflora
--^. ,„_^ Aah in absolutely Tannin in
MOisiure. dry sample. absolutely dry sample.
894
4-40
5 "37
8-53
2-03
1 6 07
6-8i
441
721
693
461
806
651
377
673
7 'CO
6-20
8 60
727
3'93
528
4272
370
iS 92
i'>'43
061
8-58
10-31
2 46
16 12
' Collected In Penang.
* Singapore.
The two specimens of Castanopsis chrysophylla were quite different
in character; the one showing the large i>crccntagc of moisture was
4o8 Resume of Recurrent lopics. {
Am. Jour. Pharm.
August. 1897.
taken from a shrub, and was received while in the moist green state,
a condition favorable to a large yield of tannin ; the other was
apparently from a much older tree, and apparently much of the
tannin was changed to an insoluble red coloring. The low ash can-
not be accounted for.
In connection with this the following description of the Indian
species by Dr. Ridley may be of interest.
Castanopsis Wallichiana. Nuts commonly eaten. If there are not two
species mixed under this name, the leaves are very variable.
C. Curtisii, King. Native name, " Berangan Janthong." One from the type
tree in Penang, marked " old tree," the other marked " young tree," brought
by a native collection from our forests here ; though the collector persists it is
Curtisii, I have never myself seen this species in Singapore.
C. Javanica, King. Native name, "Berangan Gajah." I think two species
may have been placed under this name by Dr. King. The fruits of the sample
sent are very large ; nuts single, oblong, about three inches in length; they are
purgative when eaten.
C. HuUettii, King, Native name ** Berangan Papan, i. e., plank chestnut.
A big tree, nuts bitter, not eaten,
Quercus hystrix. Native name, "Mempening." A very common oak in
Singapore,
O. discocarpa, from Penang, I hardly see why this is not a Castanopsis; the
fruit is just that of one.
RESUME OF RECURRENT TOPICS.
By W11.1.1AM B, Thompson.
The Gradations of Chemistry. — In the classification of the various
branches of this science (and the divisions are very numerous, as
well as comprehensive), it will be observed that some attach natur-
ally to therapy and others to that of pharmacy. In a general
sense we may say that the physician who fails to give full consid-
eration to biological and physiological chemistry cannot be correct at
diagnosis. Whilst, on the other hand, the pharmacist who omits to
comprehend the relations of toxicological and pharmaceutical chem-
istry cannot proceed intelligently in applying knowledge to his art.
A pharmacist appreciating the aids to the pursuit of his business
could wisely adopt as a special study one of the many divisions of
chemical science. Practice in this might, in time, be made remun-
erative. Apart from the utility, it is a most enticing and absorb-
ing theme, and furnishes the key which unlocks some of the most
profound and amazing mysteries of the material world. A taste of
^Vugus-t.^b^/"'} Resume of Recurrent Topics. 409
this knowledge begets a thirst for more. Chemistry' might be
selected by choice and made an auxiliary to business, and to busi-
ness titles, a deserved or earned title being more worthy than an
assumed one. Once rescued from the commercial slough by the
absorption of its numerous allied sciences, pharmacy ought to rise
again to its true sphere and mission.
Herbs and Simples. — In the earlier days of medical and domestic
practice, when vegetable substances were chiefly in vogue as reme-
dies, there was quite an original subdivision according to their prop-
erties— suggestive, sensible properties. For instance, there were
the so-called five great aperitive roots — smallage, or celery; fennel,
parsley, petty-whin, and asparagus — the title aperitive having the
same derivation as our modern word aperient, the latter being con-
sidered more in euphony. Then there were the four lesser cold
seeds — succory, or chicory; lettuce, purslane, etc., — and the four les-
ser liot seeds — celery, parsley, bishop weed and wild carrots. Next,
the four greater cold seeds, of which the pumpkin is a type, and the
four greater hot seeds, and so on. It will be noticed that these dis-
tinctions were not medical in any sense, but based on the plainest
descriptions, hot and oold, our present pungent carminatives consti-
tuting the former, and the mucilaginous and saccharine the latter.
Many of these were in established repute, and the observations upon
their properties are so specific as to convince us that the effects were
based upon absolute demonstration. With a large class of [x^rsons
there yet lingers a strong predilection in favor of vegetable medi-
cines. If we except the tonic varieties, their reasonable use can
never be harmful. Can we say as much for the minerals? We
cannot, however, revive the faith that once existed, and these sub-
stances are now the drug-store stock of indefinite age, and often
indistinguishable.
Artificial Peptic Action on Food Substances. — That food may be
partially digested, or pre-digested or peptonized by artificial pro-
cess, and yet preserve such elementary state or condition as adapts
it to the needs of the human body, is an open and debatable cjues-
tion. If the primary digestion only produces so-calied peptones,
and true peptones (which have never been isolated or identity cstab.
lished) are inseparable from the acting function of the human slom.
ach or the animal chemistry o( foodconversion, then wc arc some-
what at sea without a chart, for wc Cctnnoi produce j)cptoncs arti-
4IO Resume of Recurrent Topics. {'^'^ki^^C^i^'
ficially. It is quite a simple process to cause the animal ferments in
certain favorable media, and, under the influence of heat, to act
upon substance, and also to change the molecular or physical char,
acter of such substance; but it is a wide stretch of assertion to say
that this altered condition is an exactly similar result to that change
which food undergoes in the animal alimentary receptacle. This
subject is, perhaps, more of a physiological than of pharmaceutical
import; but as articles which come under this category are offered
to the public for self-use and adoption, the knowledge of the apothe-
cary is often sought in explanation of many things the lay commun-
ity do not understand. It never meets the question of scientific
adaptation, to merely say, *'0h, such articles are popular and sell
largely." We all know how popularity may be secured through
the free medium of printers* ink. If there is that which should be
or can be understood, let us have the true knowledge to either
guide our judgment or correct our errors.
Chemistry as Applied to Industrial Arts. — The thought occurs that,
when knowledge in special branches of science becomes an applica-
tion to industrial pursuit to art and to trade, there should arise,
in this country, a national spirit to foster and encourage technical
education in these arts, etc., etc. Take the production of chemicals
of the synthetical class, for instance, as an applied industry, and also
consider the science with non-general adaptations. There must
exist a constant need of educated knowledge and skill in the depart-
ments of work and labor. This want is likely to increase by natural
growth, but could be vastly extended by a systematic encourage-
ment. The pharmaceutical student who imbibes a taste for, and
inclination to pursue the study of this fundamental rather than col-
lateral branch of science, and to make of it a special vocation, has
very meagre stimulus here. How can we avoid seeking the neces-
sary aid of foreign talent when we have, comparatively at least,
none of our own ? We have never promoted enlarged and liberal
views on this and many other subjects of national economic import-
ance. The student in chemistry, out of his novitiate, seeking to
apply his knowledge, finds but limited opportunity open, and he
must search and hope with discouraging result. A self-constituted
committee of patrons, or patronage composed of manufacturers and
others whose capital is embarked in the application of chemical
science, either wholly or partially to the operations of industrial
^^AugusMS^'"} The Normal Urine. 411
arts and trades, or those who regard the aid of this special science,
should ally themselves in some movement or purpose having the
education of the American youth in view. Beyond the pale of com-
merce there is indeed very little conception of the vast inroad which
German manufacturing chemists have made upon our industries.
We are paying a very expensive tribute to their foresight in foster-
ing a talent among their own people, which we neglect or overlook
in ours. We are paying large annual sums to foreign firms and
corporations for products which we can, and should make. In no
region are crude materials so abundant as in our own country. A
utility of these would add to our national wealth — give employment
to our educated labor — instead of contributing to foreign capital.
We need, now, urgently, ev^ery possible advance of occupation
availed of in this country; our hands stand ready reaching for
employment. In this also, we have involved a most serious social
problem, a growing condition which will require adjustment in the
not distant future, when it may require more wisdom to adjust
than the present need demands.
THE NORMAL URINE.'
Bv Charles Platt.
The various compilations current as "Text-books of Urine Analy-
sis" differ materially in their statements as to the average compo-
sition of a normal urine. In many cases, indeed, the authors have
not even attempted to reconcile their "totals" with the figures given
for individual constituents; but aside from this, which is, of course,
the result of carelessness on the part of the compiler, we find great
variations in the original figures, due not so much to errors of deter-
mination as to failure to secure representative samples for analysis.
Normals determined for one nationality, or for one class of one
nationality, are commonly applied indiscriminately to all without
regard to fundamental differences in conditions. For instance, the
average American's habit of life is not that of the German student,
and yet it is a fact that the majority of figures given in our text-
books have originated with the observations of German professors,
working in conjunction with their student assistants.
In view of this laxity in text-book statement, the utiiLt u.i^ i-i
^Jour. Amer, Chevt. Soc, 19, 389.
412
The Normal Urine.
Am. Jour. Pharm.
August, 1897.
several years made careful records of all urine analyses with due
attention to the age, sex and health of the individuals supplying the
samples, and these figures (in all cases compared with and in some
cases averaged with those of foreign observers) are now given in
the following table : ^
The Normai. Urine.
Color Pale amber, straw-yellow.
Appearance Clear or with faint cloud of mucus.
Odor "Aromatic."
Reaction Acid. Acidity in 24 hours equivalent to
2-4 grammes oxalic acid.
Specific gravity at 15° C. . . Range for adults, i'oi5-i*025.
Averages: Man, i'02o; Woman, i*oi8.
Quantity .... , . . . . 1 100-1600 c.c. in 24 hours.
Averages : Man, 1450 c.c. (22 c.c. per kilo
of body-weight) ; woman, 1250 cc.
Averages for adults.
Man. Woman.
Normal urine.
Gram.mes.
Total solids 45*0 -65*0
Urea 20*0 -50*0
Uric acid o'3 - 08
Creatiniu 0*4 - i'3
Hippuric acid 0*4 - i*o
Xanthine, sarcine, etc o'ooi-o'oio
Oxalic acid 0*020-0 '030
Glycero-phosphoric acid o*oiC)-o*o2o
Propionic, valeric, caproic and buty-
ric acids o*oo8-o*o8o
Phenol, cresol, etc o*oo5-o*02o
Sulphur dioxide in ethereal sul-
phates o*090-o*5oo
Indoxyl sulphuric acid (calculated as
indigo) 0005-0019
Thiocyanic acid o-ooi-o-oo8
Grammes
urine in
24 hrs.
Grammes
per kilo-
gramme
of body-
7veight.
Grammes
urine in
24 hrs.
60 "O
o'9i
51-0
34*o
0-51
30-0
0-6
0*009
0-5
0-9
0-014
0-8
07
o-oio
0-6
0-005
—
—
0-025
—
—
0015
—
—
0-040
—
—
Q-OIO
—
—
0-250 —
0-008 —
0-005 —
- Authors consulted : J. Vogel, l,oebisch, Kerner, Dalber, Hammarsten, Neubauer, Pfluger,
Voit, Salkowski, Liebermann, Brieger, Hoffmann, Dragendorff, Munk, Hoppe-Seyler, Yvon
and Berlioz, I^ehmann, Uhle, Ranke, Furbriuger, Geschleiden, Moritz, von Jacksch, Planer
and Morin, Magnier, Robuteau, Gautier, Becquerel, M6hu, Halliburton, Charles, Parkes,
Black, Bence-Jones, Tidy and Woodman, Beale, Parrot, Breed, Oliver, Thudichum, Weidner,
Purdy, Tyson, Griiner, Jaff6, Rankin, von Franque, Oppenheim and Meyer.
Am. Joar. Pharm. )
August. 1897. /
The Nor)fiai Urine
413
Averages for adults.
Man.
Grammes
Xormal urine. urine in
Grammes. 24 hrs.
Paraoxyphenylacetic, paraoxyphen-
ylpropionic, dioxyphenylacetic,
and paraoxyphenylglycollic acids ooio-o'030 o'020
Bile salts o*o -o"oio oooS
Urobilin, urochrome, etc o"o8o-o*i4o 0*125
Carbohydrates o"oi4-o'075 0*044
(Reducing power of normal urine
equivalent to an average of three-
tenths of one per cent, glucose. )
Sarco-lactic, succinic, glycuronic and
oxaluric acids, acetone, inosite,
cystin, taurin, urorubinogen, uro-
rubin, pigment of Giacosa, sca-
toxylsulphuric acid (often in con-
siderable amount), scatoxylglycu-
ronic acid ; nephrozymase, pepsin,
and other ferments ; pseudoxan-
thine, paraxanthine, heteroxan-
thine, guanine, adenine, etc.; py-
rocatechin, hydroquinone, proto-
catechuic acid, etc traces —
Chlorine 50 -lo'o 7*3
Phosphorus pentoxide 2*0 - 3*5 3*0
Sulphur trioxide . . 15 - 30 2'2
Potassium oxide 25 - 35 3*0
Sodium oxide 4*0 - 6'o 4*5
Ammonia . 0*5 - o*8 0*72
Calcium oxide 02 - 0*4 0*30
Magnesium oxide 03 - 0*5 0*40
Iron u'ooi- o'oio 0*007
Silicic acid, carbonic acid, hydrogen
peroxide, nitrates, nitrites and
metals : c. r.. manganese and cop-
per . traces —
Gasks' in Normal Urine.
/n ICO fr'/w "ir-
of i-.l'.
Carbon dioxide '>5'4'>
Oxygen 2-74
Nitr<n'«-!i 3i'b<)
100 'OO
Chemical Laboratorv,
Hahnf.ma.sn Mkdical College, Philadelphia.
' Morin, after Locbiach.
Grammfs
pf-r kilo-
gramme
of body^
•weight.
Woman.
Grammes
urine in
24 hrs.
0110
60
0-045
25
0-033
1*9
0045
2-S
006S
40
O'OIO
0-6
0*0045
0-28
0*0066
035
^ urin4.
c c.
15-957
0658
7 775
24 ".^QO
414 Official Primus Virginiana. {^\i^liS^^J^
AN INVESTIGATION OF THE OFFICIAL PRUNUS
VIRGINIANA, TO DISTINGUISH IT FROM
BARKS COLLECTED AT OTHER
SEASONS.!
By Grace E. Cooi.ky.
A contribution to the work of Research Committee C, of the Revision
Committee U.S. P.
The U.S. P. prescribes that wild cherry bark be collected irt
autumn, when it yields the greatest amount of hydrocyanic acid.
This investigation has failed to furnish any distinctive histological
mark of the bark collected in autumn, and the results have tended
to the belief that the suitable test is a chemical one, not readily to
be found by the use of the microscope.
The following results are presented with tests which are found
accurate, so far as they have been applied.
The researches of Fischer^ have shown us the phases which
starch undergoes in the bark and wood of most trees during the
year. These have been verified with regard to Prunus serotina, and
give us an easy means for rejecting all barks collected in summer
and winter, for they contain no starch at all, or very little. During
September and late summer the starch is being stored up in the
bark, and reaches its maximum amount in October and the first
days of November, just after leaf-fall. At this time all the cells of
the medullary rays, and the bast parenchyma, as well as the chloro-
phyll-bearing cells, are crowded with starch, which occurs in Pnmus
serotina, in small round grains. This gradually disappears, first
from the parenchyma of the bast, and last from the medullary rays.
By the last of November the bark is nearly, if not quite, free from
starch, and remains so during the winter. During the last days of
February, or early in March, a process of starch regeneration
begins. In specimens collected March 2ist the parenchyma cells of
the bast contained a few scattered grains, and there was a little in
those cells of the medullary rays which lay close to the wood.
Specimens of April 6th showed an increase in all the cells of the
bark, and April 2 1st, the maximum was nearly reached, for the bast
parenchyma and medullary rays, as well as the green cells, contained
^ Jour. Pharmacology, 4, 167.
^ Dr. Alfred Fischer, PhysiologiederHolzgewdchseJahrbucherfiir Wiss. Bot.y
1891, vSec. 73-
^"ii^i^t.^sS^"-} Official Prunus Virginiana. 415
much starch. At this time the bud scales were open far enough to
disclose the leaves, which were, however, still folded closely together.
Bark collected in May contained very little starch ; in some
samples none appeared to be present, and in others a very little
could be made out by the use of dilute iodine, when the specimen
was heated. Collections of August 5th exhibited no starch in the
cells of the bark.
The seasons of maximum amounts of starch in the bark are, then,
autumn and spring, and if the bark, whether powdered or whole,
contains much starch in all the parenchymatous cells, we are sure
the collection was made shortly after the time of leaf-fall in autumn
or before the leaves unfolded in the spring. A test based upon the
presence of starch cannot exclude the spring collection, and spring
is the time when the bark is least valuable, so far as the amount of
hydrocyanic acid which it may yield is concerned.
To distinguish between the collections of spring and autumn, I
have found the following color test for tannin applicable to those
samples of Prunus serotina which I have been able to obtain. The
amount of tannin in barks collected in spring is noticeably greater
than that found in the collections of the autumn. I hesitate to sub-
mit the following as an authentic test, because I have not made
extended tests for amounts of tannin to be found in the bark 01
Prunus serotina throughout the year, and because the reasons for the
periodicity in amount and the phases of its fluctuation in plants
have not, so far as I am aware, been fully made out. It seems a
matter of observation that when great activity of growth is going
on, tannin appears in greater amounts than usual. This observation
seems to receive support in the case of Prunus serotina, as a much
greater amount of tannin seems present in the bark during the active
growth of spring than in the autumn.
The following test shows this to be the case :
Upon the surface of distilled water in a watch-glass, sprinkle a
little of the powdered drug, which will spread, forming a thin film.
Let it stand ten seconds, and then drop into it one drop of a I per
cent, solution of ferric chloride. If the bark was collected in the
spring, a cloudiness will appear in the water from the greenish pre-
cipitate, which is immediately formed. If the bark was collected in
autumn, there will be no noticeable precipitate under twenty seconds.
Powders of Nos. 20 and 50 exhibit this test equally well.
4i6 Burdock as a Vegetable. { ^"iigus^Sl^'"-
Tests for hydrocyanic acid and emulsin, though successfully
carried out upon bitter almonds as first tried by Guignard,^ failed of
results when tried with the barks of Primus serotina.
Wellesley, Mass., May, 1897.
BURDOCK AS A VEGETABLE.^
By Ixazo Xitobe.
The well-known definition of a weed by Emerson as " a plant
whose virtues have not yet been discovered," is confirmed by the
better agricultural authority of Schwerz, according to whom " a
weed is a plant of which the direct uses are unknown to man."
Both the poet-philosopher and the scientific farmer implicitly
admit, I think, that as man brings more and more of nature under
his control — in other words, as he brings more and more plants
under cultivation, many of them, hitherto scorned as weeds, must
cease to be considered as such. I have often seen ridiculed the
Chinese custom of eating birds' nests, bears' claws and other in-
comprehensible delicacies, but I cannot help admiring the power of
pantophagy on the one hand and the refinement of culinary skill on
the other, which can convert into means of human enjoyment things
apparently worthless and revolting. If, as philosophers say, civili-
zation consists mainly in bringing natural forces under man's sub-
jection, China must be given a high place in the scale of civilization
from a culinary point of view.
Is it not a real triumph of art to extract food for man from so
coarse and ugly a weed as burdock ? Most books on botany in the
English tongue describe burdock. Lappa major or officinalis, as a
pestiferous weed, and many an agricultural bulletin gives careful
instruction how to destroy it. Perhaps the only use that has been
made of Lappa in America is for medicine. The root contains a
bitter principle, a resin and tannin, and it is said to have an aperient
and diuretic effect. It also has some reputation as an alterative in
constitutional blood diseases, and the readers of Garden and Forest
may have used the so-called *' burdock tea." In Germany, where
the three species, L. major, L. minor, L. tomentosa, are widely
^ Guignard. Sur. la localisation dans les plantes, des principes qui fournsi-
sent I'acide cyanhydrique. Comptes rendus, 1890, p. 249.
' Garden and Forest, 10, 143.
^""iZl'S^^r-} Burdock as a Vegetable. 417
spread, they were formerly much used as medicines under the name
Radix Bardana2, and they are even now regarded by some as good
blood purifiers. Perhaps from the burr of the seeds the plant has
the repute of power to stimulate a rich growth of hair, and an
extract for this purpose is made from the roots. The peasants from
the south of England use the roots as an antiscorbutic, and the
leaves are employed in making a green elder ointment for the use
of farriers.
All these medicinal uses are not to be despised, but they are un-
important when compared to the value of the plant as an edible
vegetable ; since the kitchen is more important than the drug store,
the cook is nearer our hearts than the apothecary. Even in Eng-
land the alimentary value of burdock was not always despised.
Sowerby writes in his " Useful Plants of Great Britain :" " The
stalks of the burdock-, cut before the flowers open and stripped of
their rind, form a delicate vegetable when boiled, similar in flavor
to asparagus. In the raw state they may be eaten with oil and
vinegar as salad. They were sometimes candied with sugar in the
time of Bryant, as those of Angelica are. They are slightly laxa-
tive, but are perfectly wholesome. The roots of the plant are
mildly diuretic and diaphoretic, and have been used with advan-
tage in gout, rheumatism and calculous com])laints. The decoction
of the root is generally employed, but the seeds and leaves possess
nearly the same properties, though the latter are slightly purgative.
The bruised leaves are applied by the peasantry in some districts, in
cataplasms to the feet, as a remedy for hysterical disorders."
In Japan, burdock grows wild in several places, but it is also ex-
tensively cultivated as a vegetable. Every one knows and eats '• Go-
bo," the usual appellation for this plant, although a more refined and
almost obsolete name is •' kitakisu ;" sometimes it is called " Uma
(horse)-fuki (Nardosmia) " It is familiar to the Ainu under the
name of •• Seta (dog) koroki (Nardosmia)." Both the Ainu and
the Japanese j)refixes, •• seta " and " uma," when applied to plants,
seem to have much the same sense as the English " dog," m d(»g-
wood, dogbane, etc., and the •• horse " in horse-radish, horse-chest-
nut, horse-mint, etc. The Ainu use it as food as well as medicine.
They boil the tender shoots with beans, and the roots are put into
soup. F'or medicinal uses the young leaves are softened by rolling
them between the palms, and applied to skin eruptions. The Jap-
4i8
Burdock as a Vegetable.
/Am. Jour. Pharna.
t August, 1897.
anese esteem Lappa for similar purposes. It is used in many pre-
parations for its medicinal properties, which they believe — at least
the old-fashioned empirics believe — consist in counteracting the
action of some kinds of poisons. Grated and made into pulp, the
roots are applied as a poultice in eruptions of the skin. But by
far the more important use is made in the kitchen. As regards this
plant we have outstripped the pantophagous Chinese, for they have
not raised the plant to the dignity of a market vegetable. " When
young," says a Chinese book on botany, "■ the tender leaves of the
Lappa are cut and eaten as greens ; the roots may be boiled or
steamed and eaten, but people nowadays rarely use the plant."
Among the Japanese, however, it has been under cultivation for
years, and possibly for centuries. It enters the kitchen of every
household, not being ostracised from the menu of the most high-
toned restaurant. Thousands of acres are devoted to its culture.
Official statistics for 1888 give the total production of Lappa in the
country at about 72,000,000 pounds, valued at 422,134 yen. The
roots average 350 grains in weight.
The production of so large a quantity is not at all to be wondered
at when we recollect that Lappa ranks high in the scale of nutritive
plants. In the amount of nitrogen it stands higher than potatoes,
beets, carrots or turnips ; in fact, few roots or tubers approach it.
I append here its chemical composition, as compared with some
other commonly used vegetables :
H2O N ; Ash K2O NaaO CaO iMgOPoOs
Potatoes ! 750
Sugar Beets 815
Turnips i 720
Carrots \ 850
Burdock 1 738
I
3*4
1-6
1-8
2*2
5-6
9*5
7'i
6-4
8-2
10-5
5-8
3-8
29
3"o
4*3
0*3
0-6
0-6
1*7
0"2
03
0-4
07
0*9
I"I
0-6
0"2
0*4
20
I 6
0-9
0-8
i"i
0-9
so.
0-6
03
0*5
07
sio, I a
0"2
0"2
O'l
0*2
01
0*3
0*3
0*3
0-4
So important a crop as burdock has, of course, many varieties de-
veloped, but the best known among them are few in number. They
are usually named from the localities where they were first devel-
oped or where they thrive best. A variety known as the Takino-
zawa, raised chiefly near Tokyo, has a slender root, about 4 feet
long, and is of very fine quality. In the vegetable market of Tokyo it
commands a respectable price. TheOwura varietv,named from a small
I
"'"ii^Hrt.?^"} Burdock as a Vegetable, 419
place in the province of Shimosa, where they produce only about
2,oco roots a )'ear, attains the huge size of i ^ feet in circumference,
and 2Y2 feet in length ; this kind is sold at the rate of about 20 sen
(a sen being a hundredth part of a Japanese dollar) apiece. In its
form this variety is like the beet. The two kinds most popular in
the markets of Kyoto are the Yamato and the Horikawa ; in fact,
these seem to be only different names of the same variety.
In raising Lappa much attention is naturally devoted to the right
selection of the soil. It is a common belief among cultivators that
that a light sandy soil is specially adapted to it, and it is true that
roots grown from such soil are long and slender, but they are prone
to be hollow at the centre and rather tough at the rind. A stronger
and deeper soil, say clayey loam, seems to impart firmness to the
root and a better flavor. To gain the most satisfactory results, the
soil must be plowed deep and finely pulverized, or else an undue
amount of labor will be required in harvesting the roots. Indeed,
digging burdock is a proverbially hard task ; it has become almost
a fine art to do it well. Many an old writer recommends digging
the soil to the depth of some 4 or 5 feet, and then putting in green
leaves, stalks, turf, and so forth, in a layer a foot deep, and cover-
ing that with the earth that was excavated. The surface must
then be well hoed in both directions. So much care, however, is
only necessary when exceptionally fine specimens, for show or
otherwise, are aimed at. One peculiarity of I^ppa is that it is not
adapted to rotation ; that is, it thrives better if planted continuously
on the same soil ; in new land the roots are likely to become forked.
It is also grateful for good manures — compost, night-soil, and espe-
cially to rice-bran — but if compost is applied it must be well decom-
posed, or else the roots will throw off too many branches.
When the soil is properly prepared seeds are planted in rows 3
feet apart, five or six seeds being placed every 6 to 8 inches in a
row. In Owura, the usual time for sowing is the early part of May
or late in April. Hefore the early part of June the young plants
are thinned out, leaving but one in the hill. Very often liquid
manure is applied two or three times before the roots are harvested
late in December. Another method is to plant the seeds in Au-
gust, so as to have the vegetable ready for spring use, in which case
they are sown more closely, since they do not grow as vigorously as
those planted in spring. Lappa is a slow grower, and takes over
420 Brimstone in Sicily. {^"^Airustfisgr-
220 days to mature. Seeds retain their vitality for five years, and
many a gardener asserts that the best crop is obtained from those
three years old. They say that new seeds produce roots which
throw off too many branches and flower-stalks. This statement,
however, is not always verified. For keeping and marketing, the
vegetable may simply be left where it was grown, or kept buried in
the earth like beets or turnips.
I am aware that a discourse on burdock will be of little interest
to Americans unless it contains some information regarding the
mode of using it, but it must be remembered that Japanese cuisine
differs widely from the American. I need only state in general
terms that, after their skin is scraped or peeled off, the roots may
be sliced into long strips or cut into pieces of less than an inch in
length, and boiled with soy, salt or Spanish pepper, to impart savor
to them ; or, if boiled alone, they may afterwards be browned in
sesame oil, which of itself will flavor them. Another common way
of cooking them is to scrape off the outer skin and cut them into
pieces about 2 inches long, then, when they are boiled soft, to take
them out of the pan and mash them; then make them into cakes
much as you treat oyster-plants. A kind of salad, though not un-
cooked, is also made of them. A rather unique and more elegant
process consists in stuffing the roots with sea-eel, and boiling them,
after dipping them in a preparation containing soy and pepper.
Slices of Lappa fried and eaten with some condiments form one of
the commonest dishes with us. The roots are sometimes pickled
in miso. There are many other ways of preparing this valuable
vegetable for table use, but a longer description would be interesting
or amusing only to the curious. Each country has its own taste and
national cookery.
BRIMSTONE IN SICILY.^
Through the courtesy of Messrs. Ferd. Bailer & Co., of this city, I
am enabled to submit the following statistics of Sicily brimstone,
which, at this time, when the Anglo-Sicilian sulphur trust is en-
deavoring to absorb the business, will be of special interest. The
currency quoted is not the gold lire to be estimated at 5-18 to the
dollar, but that of paper, the average value of which for the period
covered was about 5 50 to the dollar.
' Consular Report, Vol. 54, page 202.
Am. Jour. Pharai.
August, ley?.
Brimstone in Sicily.
421
Exports from Girgenti, Licata, Catania, Termini and PlaU* mo.
January to December.
To—
(ireat Britain
South of France
North of France
Holland
Belgium
Germany :
Hlbe
Baltic
Aiistria-TIungary
Russia
Sweden and Norway and Denmark .
Spain
Portugal
Italy
Greece, Turkey, and Balkan States .
Morocco. Tunis, Algiers, and Tripoli .
South Africa . .
United States and Canada 1 Atlantic) .
ITnited States ( Pacific*
South America
Asia
Australia
Other countries
Total «63.i53 '49.996 »37.220
•Tons of 13 Sicilian cantars.
Production, exports, stocks, and prices 0/ Sicily brimstone.
Description.
1896.
1895-
Tons.
342,150
356.i'^4
1894.
1893.
189a.
1891.
rroduction,* official
figures (in tons
Tons.
. . . .
Tons.
355.023
335.548
Tons.
363.414
347.304
I '5. 235
50.5 > 2
38.077
Tons.
362.948
309.912
Tons.
336975
I'ixportst ...
end
of Decem-
400.082
78.987
S8.415
»93.620
Visible stocks at the
her at—
Girgenti . . .
I icata
85.3' I
61.785
49.«54
78^12
50.028
53.>^46
I02.7tl
30.385
33.423
65 MO
17.69a
Catania . . .
42.V)0
4.S92
200.5f>9
33.077
Terminit ....
Palermo ....
ToUl . . . .
I the
1,000
onds
31st of De
kilograms.
i:.4<*^
2I3.6^S
2- ■
/.ire.
81.00
75-50
U5.969
Prices at f'.irgenti ot
cemher, per ton of
first co^t :
Best unmixed sec
Best thirds . . .
Lire.
0
.0
Lire.
55-00
52 20
Lire
Lire.
life.
I2V0O
11890
>iis ot 13
•Quantities csrried by rail fiom the stations in the ii.teritir to'
cantars. during the financial year July to June, isys-v'-*- aga>a»t ■'''
V In the exports for the years 1891. 189a and 1^93. thos* from Termini and Palermo are not
included, which, during iS«>4 to 18-^. amounted to6.rx» to 13.000 tons per annum. To calculate
the total consumption, io.c<» tonshave to be added, representing the estimated yearly con-
sumption in Sicily.
: Stocks at Termini for the years prece<ling ts« ■»'' wanting, but were probably smaller.
\ Since the tat of Octot>er, ^89^ the export duty of 1 1 lire per 1.000 kllocram* was abollaheU
422 Brimstone in Sicily, {
Am. Jour. Phflrm.
August, 1897.
After a careful study of the above figures, I think the readers of
this report will recognize the truth of the following deductions :
(i) The exports of sulphur from Sicily in 1896 were 44,00c tons
in excess of 1895, ^^ which 31,000 tons were exported from January
to July. This increase is to be attributed to the exceedingly low
prices which prevailed toward the close of 1895 ^^^^ the beginning
of 1896, at which figures the working of a majority of the mines was
unprofitable. The increase of 13,000 tons in the last six months of
1896 is undoubtedly due to the sudden advance in prices, which in-
duced consumers to lay in heavy stocks in anticipation of a further
rise. These i^tocks, however, cost them relatively low prices.
(2) By reference to the table of exports, stocks and prices for
1 891-1896, it will be observed that, although prices steadily declined
during those years, the production, as estimated by the mining bu-
reau, frequently increased and never decreased. Stocks show a con-
stant increase. These facts unquestionably prove that the cost of
production has diminished, cheaper transportation has been gained
by the construction of roads and railways, and improvements have
been made in mining and smelting. It follows, therefore, that pro-
duction at the lower prices has continued steadily, because it was
found profitable.
(3) The increase of exports during these years is natural, because
the large production had to be sold, and this was made possible by
the fall in prices.
(4) The Italian Parliament abolished the export duty of 8^. 6d.
($2.06) per ton with the object of favoring exports, since this duty
increased the cost to the foreign consumer. The artificial advance
which the Anglo-Sicilian sulphur trust wishes to establish is, there-
fore, in opposition to all the above facts, although the latter are re-
sponsible both for the decline in price for several years and the abo-
lition of the export duty.
(5) It is stated that the production in 1896 shows an increase, and
although the statistics are not yet published, there is the best au-
thority for estimating it at about 385,000 tons. That there really
was an increase is confirmed by the following facts : There were
shipped, in 1896, 44,000 tons more than in 1895, but nevertheless the
visible stock in the ports of Sicily on the 31st of December, 1896,
was only 18,000 tons less than on the same date in 1895. The dif-
ference of 26,000 tons must, therefore, come from an increase of pro-
^"^uguJt.^S?:'"-} American Medicinal Flora. 423
duction, which, in part at least, belongs to 1S96, as some of this
quantity may be sulphur stored in the mines in 1 895, and not shipped
promptly. Further, the quantity carried by rail from the stations
in the interior to the ports was larger in the fiscal year 1895-96 than
in 1894-95.
(6) Everything points to an increased production for 1897, and if
the present prices check the consumption, stocks must necessarily
increase during the year.
(7) Should Sicilian brimstone be partly replaced in the United
States by pyrites for the manufacture of sulphuric acid, this will di-
minish our imports, which have been from 100,000 to 125,000 tons
per annum, or 25 to 30 per cent, of the total production of Sicily.
(8) For the above reasons, it seems more than doubtful that the
Anglo-Sicilian sulphur trust can succeed in maintaining the prices
at the present artificial point for any length of time. Its capital is
^^750.000 ($3,649,885) and it has purchased its brimstone at about
65.?. ($1 5.80) per ton free on board Sicily, plus all the other expenses.
Chas. M. Cau(;hv,
Consul.
Messina, March 29, 1897.
STUDY OF THE AMERICAN MEDICINAL FLORA.
The Sub-Commission of the Pan-American Medical Congress,
appointed to study the medicinal plants of the United States, has
entered into an association with the Smithsonian Institution for that
purpose. The attention of our readers is called to the respective
circulars issued by these organizations, which wc print below :
Smithsonian Institution, Washington, I). C,
May 28, 1897.
Dkar Sir : —The Smithsonian Institution has undertaken to brinj; tojjether
all possible material bearinj^ on the medicinal uses of plants in the Tnitcd
States, .\rrangements have Ix^en made with a hotly representing the Pan-
American Medical Conj^ress, the Sub-Commission on Medicinal Tlora of the
United States, to elaborate a report on this subject, and the material when
received will l>c turned over to them for investijjation.
The accompanying^ detailed instructions relative to specimens and notes have
been prepared by the Sub-Commission.
All packaj^es and correspondtrnce should l)e adtlriss» ,1 i., •' r- >-:.....».. ..;^ii
Institution, Washington, I>. C, and marked on the uuti>i<Ic /f,
for the U. S. National Museum.
434 Ainericmi Medicinal Flora. {'''^d^lC^m!^■
Franks which will carry specimens, when of suitable size, together with
descriptions and notes, free of postage through the mails, will be forwarded
upon application. Should an object be too large for transmission by mail the
sender is requested, before shipping it, to notify the Institution, in order that a
proper authorization for its shipment may be made out.
Respectfully,
(Signed) S. P. Langi^ey, Secretary.
INSTRUCTIONS RELATIVE TO MEDICINAL PLANTS.
The Pan-American Medical Congress, at its meeting held in the
City of Mexico, in November, 1896, took steps to institute a system-
atic study of the American medicinal flora, through the medium of
a General Commission and of special Sub-Commissions, the latter
to be organized in the several countries. The Sub-Commission for
the United States has been formed, and consists of Dr. Valery
Havard, U. S. A., Chairman ; Mr. Frederick V. Coville, Botanist of
the U. S. Department of Agriculture ; Dr. C. F. Millspaugh, Curator
of the Botanical Department of the Field Columbian Museum,
Chicago; Dr. Charles Mohr, State Botanist of Alabama; Dr. W. P.
Wilson, Director of the Philadelphia Commercial Museums; and
Prof. H. H. Rusby, of the New York College of Pharmacy. This
Sub- Commission solicits information concerning the medicinal
plants of the United States from every one in a position to accord
it. The principal points of study are as follows :
(i) Local names.
(2) Local uses, together with historical facts.
(3) Geographical distribution and degree of abundance in the
wild state.
(4) Is the plant collected for market, and if so —
[a) At what season of the year ?
ip) To how great an extent ?
{c) How prepared for market ?
{d) What is the effect of such collection upon the wild supply?
{e) What price does it bring ?
(/) Is the industry profitable ?
(5) Is the plant, or has it ever been, cultivated, and if so, give all
information on the subject, particularly as to whether such supplies
are of superior quality, and whether the industry has proved profit-
able?
(6) If not cultivated, present facts concerning the life history of the
plant which might aid in determining methods of cultivation.
^"•ug"siT^'"} Amenca?i Medicinal Flora. 425
(7) Is the drug; subjected to substitution or adulteration, and if so,
give information as to the plants used for this purpose?
While it is not expected that many persons will be able to con-
tribute information on all these points concerning any plant, it is
hoped that a large number of persons will be willing to communicate
such partial knowledge as they possess.
It is not the important or standard drugs alone concerning which
information is sought. The Sub-Commission desires to compile a
complete list of the plants which have been used medicinally, how-
ever trivial such use may be. It also desires to collect all obtain-
able information, historical, scientific and economic, concerning our
native and naturalized plants of this class, and, to that end, ihvites
the co-operation of all persons interested. Poisonous plants of all
kinds come within the scope of our inquiry, whether producing dan-
gerous symptoms in man, or simply skin inflammation, or, as •• loco-
weeds," deleterious to horses, cattle and sheep. In this respect the
general reputation of a plant is not so much desired as the particu-
lars of cases of poisoning actually seen, or heard from reliable
observers. It is believed that much interesting knowledge can be
obtained from Indians, Mexicans and half-breeds, and that, conse-
quently, Indian agencies and reservations are particularly favorable
fields for our investigation. Such knowledge will be most acceptable
when based upon known facts or experiments.
In order to assist in the study of the habits, properties and uses
of medicinal plants, the Sub-Commission undertakes to furnish the
name of any plant specimen received, together with any desired
information available.
Owing to the diversity in the common names of many plants, it
will be necessary for reports, when not furnished by botanists or
others qualified to state the botanical names with certainty, to
accompany the same with some specimen of the plant sufficient for
its identification. While the Sub-Commission will endeavor to deter-
mine the plant from any portion of it which may be sent, it should
be appreciated that the labor of identification is very greatly
decreased, and its usefulness increased, by the possession of com-
plete material, that is, leaf, flower and fruit, and in the case of small
plants, the underground portion also. It is best to dry such speci-
mens thoroughly, in a flat condition under pressure, before mailing.
While any convenient means for accomplishing this result may be
426 American Medicinal Flora. {^'"XuJusi.^sS''"*
employed, the following procedure is recommended : Select a flower-
ing or fruiting branch, as the case may be, which, when pressed,
shall not exceed i6 inches in length by lo inches in width. If the
plant be an herb 2 or 3 feet high, it may be doubled to bring it
within these measurements. If it possess root leaves, some of
these should be included. Lay the specimen flat in a fold of news-
paper and place this in a pile of newspapers, carpet felting, or some
other form of paper which readily absorbs moisture, and place the
pile in a dry place under a pressure of about 20 to 30 pounds, suffi-
cient to keep the leaves from wrinkling as they dry. If a number
of specimens are pressed at the same time, each is to be separated
from the others by three or four folded newspapers or an equivalent
in other kinds of paper. In twelve to twenty-four hours these papers
will be found saturated with the absorbed moisture, and the fold con-
taining the specimens should be transferred to dry ones. This change
should be repeated for from two to five days, according to the state
of the weather, the place where the drying is done, the fleshiness of
the specimens, etc. The best way to secure the required pressure
is by means of a pair of strong straps, though weights will do. The
best place for drying is beside a hot kitchen range. When dry the
specimens should be mailed between cardboards or some other light
but stiff materials which will not bend in transit.
It is a most important matter that the name and address of the
sender should be attached to the package and that the specimens, if
more than one, should be numbered, the sender retaining also speci-
mens bearing the same number, to facilitate any correspondence
which may follow. The Sub-Commission requests that, so far as
practicable, all plants sent be represented by at least four specimens.
(Signed) H. H. Rusby, M.D.,
Chairman of the General Commission,
New York College of Pharmacy.
Valery Havard, M.D.,
Chairman of the Sub-Commission,
Fort Slocum, Davids Island, New York.
The death of Prof. Dr. Pieter Cornelio Plugge, of Groningeu, Netherlands,
has been announced. He held the chair of Pharmacy and Toxicology in the
University of his native town. His death occurred June 30, at the Royal
Botanical Gardens, Buitenzorg, Java, whither he had been sent by the Dutch
Government on a scientific mission.
^"Xjgrt.r^!'" } Ediloriorl. 4^7
EDITORIAL.
NOTABLE PHARMACEUTICAL GATHERINGS DLKING AUGUST.
The month of August, this year, will witness the assembling of a larger num-
ber of pharmacists in various parts of the world thau is usual during so short a
time.
Early in the month will be the British Pharmaceutical Conference at Glasgow,
Scotland. This body is noted for the large amount of scientific work it can
accomplish in a short time. The Eighth International Pharmaceutical Con-
gress will follow, at Brussels, Belgium, on the 14th. The scope of this assembly
was sufficienth' set forth in the March number of this Journ.\l, page i6r.
The American Pharmaceutical Association has appointed the following dele-
gates : Prof. Joseph P. Remington, of Philadelphia, and Mr. Louis Dohme,
of Baltimore, with Dr. Frederick B. Power, of London, and Mr. Adolph Meyer,
of New Orleans, as alternates.
Of the associations not strictly pharmaceutical, we will have the meeting of
the American Association for the Advancement of Science, at Detroit, on the
9th ; that of the American Chemical Society at the same place during the same
week ; and on the 19th the Twelfth International Medical Congress, at Moscow,
Russia. This last has issued a formidable programme of 7 1 pages, in the French
language, and containing some hundreds of titles of papers to be presented from
physicians and others, from all over the world. If i per cent, of the promises
should be redeemed, it would still scarcely be possible to have them all read
during the eight days that the fifteen sections of the Congress will be in
session. In addition to the papers, ten addresses have been promised ; these are
to be delivered before the general assembly.
Returning to the strictly pharmaceutical meetings, we will have that of the
American Pharmaceutical Association at Lake Minnetonka, Minn., from the
24th to the 31st, inclusive. The following programme has been adopted by the
Council :
Tuesday, August 24th.
Council Meeting 11.00 A.M.
First General Session 2.30 P.M.
Meeting of the Nominating Committee ... 6.(0 P.M.
Reception and Promenade Concert S 30 P.M.
Wednicsday, August 25th.
Second General Session . . 10.00 A.M.
Commercial Section ... 230 P.M.
Travellers' Entertainment . S. 30 P.M.
Thursday, -Vugust vaw.
Scientific Sertiou . 10.00 A.M.
•• 2.30 P.M.
«• S.30P.M.
i-KII> \ \ , .\UgllSl 2~\.\X.
Section on Phaiiii.iccutical Education and Lcgi»Iation iooo.\.M.
•' 2.30 P.M.
• • «• •♦ " 8.30 P.M.
428 Reviews. {'^"August 559^™
Saturday, August 28th.
Third General Session ( Final Business) . . 10.00 A.M.
Boat Ride ( " Session) 4.C0 P.M.
Lectures by President Northrup and Prof. F. J. Wulling, of
the University of Minnesota 8.00 P.M.
Sunday, August 29th.
Devoted to rest.
Monday, August 30th.
Trip to Taylor Falls and Dells of St. Croix.
Tuesday, August 31st.
Trip by cars and carriages through the Twin Cities (Minneapolis and St.
Paul).
Evening, Banquet.
The arrangements about transportation have not yet been completed. It is
understood, however, that a one-fare rate has been secured from Chicago and
St. Louis. Members desiring to start from either of those cities should address
Mr. A. E. Ebert, of Chicago, or Prof. H. M. Whelpley, of St. Louis. Professor
Caspari, of Baltimore, is arranging for a lake trip of three days from Buffalo to
Duluth ; those desiring to go by water should address him.
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
An Ii.i,ustrated Flora of the Northern United States, Canada and
THE British Possessions, from Newfoundland to the Parallel of the Southern
Boundary of Virginia, and from the Atlantic Ocean Westward to the One
Hundred and Second Meridian. By Nathaniel Lord Britton, Ph.D., and Hon.
Addison Brown. In three volumes. Vol. II. Portulacacese to Meuyanthaceae,
Portulaca to Buckbean. New York. Charles Scribner's Sons. 1897.
The first volume of this illustrated flora was reviewed in the American
Journal of Pharmacy, November, 1896, p. 630, the second volume contain-
ing the work in the sequence of the Naturliche PJianzenfaviilien, by Engler
and Prantl, to the buckbean family, has now been issued. The publishers are
to be congratulated upon the prompt publication of a work requiring so much
original labor of authors, artist, engraver and printer. This volume contains
647 pages, and the binding, typography, illustrations, descriptions, biblio-
graphical references and the other excellent features of the preceding volume
have been fully maintained.
The second volume contains figures of 1,467 species. In most instances
these are good representations, but in a few we are disappointed. The magni-
tude of the author's undertaking is such that the students of our flora will
willingly overlook these minor defects.
As was to have been expected, the adherence to the Rochester rules of
nomenclature has presented us with a number of new binomials for our old
friends, as, for example, our common apple becomes Mains mains (L. ), Britton
and American Wistaria (the erroneous spelling Wisierea'xs persisted in), be-
comes Kraunhia frutescens (L.) Greene. The rigid enforcement of the law of
priority is illustrated on page 358, where Polygala viridescens L. replaces the
familiar P. sanguinea L., both having been used by Liunaeus, on page 705,
Ail. Jour. I'iiariij. ) I?mtt/"'iie >« «^/^
Species Plantarum, 1753. It is our intent to more carefully note the changes
necessitated in the names of medicinal plants, upon the completion of Volume
III.
A cursory examination of the volume exhibits great freedom from typo-
graphical errors and comparatively little for criticism. On page 345 we are in-
formed that Oxalis acetosella "yields the druggists' salt of lemon." The
modern methods of manufacturing the oxalates have displaced such a primitive
source.
The distribution of plants is generally accurately given. The existence of
Ilicioides mucronata (L. ) Britton, (Nemopanthes fascicularis, Raf. 1, in New
Jersey, has, however, escaped attention.
The authors have aimed to incorporate the most recent contributions and
studies of the different genera and orders. Consequently some very recently
described plants are figured here. Of these may be mentioned as examples
Potentilla littoralis, R3'dberg, 1S96 ; Crataegus Vailia;, Britton, 1S96 ; Prunus
Gravesii, Small, 1897; Viola atlantica, Britton, 1S97. The treatment of many
groups show critical study on the part of the authors. Several entirely ne\s
species are described, and a very general tendency through the volume is to
elevate well-marked varieties of previous authors to specific rank, and a number
of species discarded in Gray's Manual have been revived.
Another commendable feature of the work is the introduction of many
foreign plants that have escaped from cultivation, or otherwise become distri-
buted in waste places. This renders the book especially valuable to the
botanists in our seaport cities, who collect on the ballast grounds.
It is an up-to-date book, and a most valuable contribution to the literature of
systematic botany, and we eagerly await the appearance of the final volume.
G. M. B,
Die Xkukn Arzneii)R(>(".en .\us dkm Pflanzenrhichk. Von Or, Carl
Hartwich, Professor der Pharmakognosie am Eidgenossichen Polytechnikum
in Ziirich. Verlag von Julius Springer, Berlin, 1S97. Prcis, M, 12,
During the past several years, the additions to the list of medicinal drugs
from the vegetable kingdom has been so rapid that in self-protection one is
driven to devise some kind of a system by which to keep track of them. The
author prepared for his own use an alphabetical list of such new drugs, with a
brief statement concerning each of them, and a number of references to the
literature of the subject. The result was so satisfactory that he decided to
elaborate the same and publish it. We have, in conscfjuence, a book of some
469 pages, filled with matter which is not only compactly printed, but, what is
more important, compactly stated. Any one interested in new plant drugs, if
he has only a moderate familiarity with the German language, will find ihir
book of the greatest value.
An introduction of twenty-three pages gives a general view of the subject,
and points out the rapidity and extent to which new plant drugs have l)een
recognized by the various pharmacop«Lias. Following this is the »|>ecial part
which constitutes the great bulk of the work, and which consists of short
notices of new plant <lrugs, arranged in alphal>etical order. The names and
synonyms of each are given, then follow short descriptions, habitat, use*,
chemical composition, etc , not always in the same order ; the latter feature has
I?^^.^^^r,,r i Am. Jour. Pharm.
430 KeVieWS. \ August, I897.
some advantages, since it renders this part more readable, and does away with
what would tend towards a tabular presentation of the subject. A few lines of
references are finally added, and enough is before one concerning a drug to
enable him to have an intelligent idea about it, or to prosecute his studies
further elsewhere.
An appendix of some 30 pages follows the special part, and includes some of
the very newest drugs. This is followed by a literary index of books and
journals used in the references. The author was somewhat in doubt about
arranging the subjects in alphabetical order, but he had found it best for his
own use, so he allowed it to stand ; but in order to make the work more com-
plete he added an index of the plants, arranged according to the natural
system. Finally, there is a very complete general index.
There is no doubt but this work will facilitate the study of plant drugs, and
aid in bringing some of them more prominently before the two professions of
pharmacy and medicine.
Onthk Presence of a True Manna on a *' Blue Grass," Andropogon
ANNULATUS. By R. T. Baker, F.L.S., and Henry G. Smith, F.C.S. Reprint
of paper read before the Royal Society of New South Wales, December 2,
1896.
In addition to identifying this substance as a true manna, the authors have
made quite a study of it from botanical, chemical and economic standpoints.
The paper is illustrated by two full-page plates, and a bibliography of the litera-
ture of eucalyptus manna and lerp has been appended.
Report of the Committee Appointed by the Nationai, Academy of
Sciences upon the Inauguration of a Forest Poi^icy for the Forested
Lands of the United States, to the Secretary of the Interior.
Washington. Government Printing Office, 1897.
This report is the result of the appointment of a committee by the president
of the National Academy of Sciences, on the request of the Secretary of the
Interior. The report is an exhaustive one, and after discussing the whole sub-
ject of forestry in the United States, the results are condensed into conclusions
and recommendations that are easily comprehended. A number of bills are
offered for presentation to Congress to enable the recommendations to be car-
ried out. The committee is composed of the following well-known experts :
Charles S. Sargent, Henry L. Abbott, A. Agassiz, Wm, H. Brewer, Arnold
Hague, Gifford Pinchot, Wolcott Gibbs.
UiCRKR IsoMERE Menthyi^amine und Menthene. By D. T. Werner.
Inaugural Dissertation. Gottingen, 1897.
This is the result of a careful study of the properties of dextro- and laevo-ro-
tary menthylamine.
The Nationai, Confectioners' Association of the United States.
1897. This Association has done a good work in compiling, in a neat volume
of 186 pages, all the " pure food and pure candy laws " in force in the United
vStates, April i, 1897. There is great lack of uniformity among the different
States ; many have no food or candy laws, others have both, and a number
hold that candy is a food, and therefore apply the provisions of the pure food
law to it.
"""iugu.".*;?^'™ } College Meeting.— Obituary. 43 1
Report OF THE Fifteenth Annual Procekdings OP THE Louisiana State
Pharmaceutical Association, held at New Orleans, May 11 to 13, 1897.
Two ori^iual communications were received and read at this meeting?, viz.:
" Does a College of Pharmacy Education Possess any Advantages over that
Gained by Long Practical Experience?" by Dr. T. A. Quayle; and ** How to
Increase our Membership," by Leon Barthet. A number of interesting reports
were also presented. The Association is doing a good work by endeavoring to
intro<luce the National Formulaty^ and thereby have physicians prescribe the
preparations contained in it.
MINUTES OF THE COLLEGE MEETING.
The quarterly meeting of the College was held June 28, 1S97, with President
Bullock in the chair. The minutes of the Boaru of Trustees for April. May
and June were read and adopted.
A communication from Chairman Beale, of the Section on Pharmaceutical
Education and Legislation, of the American Pharmaceutical Association, was
presented. Itconsisted of a list of interrogatories bearing upon the construction
of a uniform pharmacy law for all the States. This document was deemed al-
together too voluminous and comprehensive to be properly considered in the
limited time at the disposal of the College, and action upon it was postponed.
Mr. E. >L Boring offered a resolution, which appeared to involve a modifica-
tion of the charter, and the spirit of which resolved itself into two queries,
whioh the Secretary was directed to submit to the College Counsellors for an
opinion. These queries were as follows :
"Can the College restrict the eligibility of members to serve in the Board
of Trustees to such only as do not receive emoluments for service rendered the
College ?"
" Should the Board of Trustees deem it desirable to elect one or more of the
faculty associate members of the Board without voice unless requested, and
also without vote, can it do so ?"
The chairman appointed the following delegates to the meeting of the Ameri-
can Pharmaceutical Association: Samuel P. Sadtler, F. W. E. Stedeni, Josiah C.
Peacock.
William B. Thomp.son, Stctetaty.
OBITUARY.
I*fo/. Dr. Karl Rcmii^ius Fresen ins.— On the nth of June Profewor I tvsv-
nius, the noted chemist, <iied at Wiesbaden, (icrmany, in th'e seventy ninth
year of his age, of heart disease.
He was born at Prankfort-on-the-Main, December 28, 1818, an<l ol.ta:mil his
education for the most part in the schools of that city. In li'^ft he was appren-
ticed as an apothecary, and while pursuing this vocation attended Iccluieft on
chemistry and physics. Later he l>ecame a student at the I'niversity of Bonn,
and, in 184 1, went to (^iessen as assistant in Liel>ig's laUiratory. In 1843 he ac-
cepted a position as private instructor in chemistry at the University of Oie«-
acn, where, however, he remained only two yeara, when he was callc<l lo
the Agricultural Institute of Wiesba<len as profeasor of the natural sctcacea.
432 Notes and News. {^"ku'Slls^iS:^""
Here, in 1848, he established his famous private laboratory, to which was added,
in 1862, a pharmaceutical department.
As is well known, Professor Fresenius devoted his attention chiefly to the
subject of Analytical Chemistry, and his " Anleitung zur qualitative chemi-
schen Analyse" and "Anleitung zur quantitative chemischen Analyse " have
gone through a number of editions, and have been translated into almost every
living tongue. In addition to his other literary labors, he was editor of the
Zeiischrift fiir analytische Cheniie since 1862.
In recognition of his services as a scientist, numerous honorary titles and
orders of distinction were bestowed upon Professor Fresenius by various
societies and scientific bodies, both in Germany and in other countries, and in
1893 he was elected an honorary member of the Philadelphia College of Phar-
macy.
Prof. Julius von Sachs. — On the 29th of May Professor von Sachs, the
famous botanist, died at Wiirzburg, Germany, where he had resided since 1868.
He was born at Breslau, in 1832, and his life was enriched by labors which have
had a distinct and decided influence on the advances made in recent years in
scientific botany, particularly plant physiology and the principles of causality
as applied to plant life.
Professor Sachs was a voluminous writer, and of his works the following
maybe mentioned: "Botanical Experimental Physiology," "Text Book of
Botany," "History of Botany" (from 1600 to i860), and "Lectures on Plant
Physiology." He was not only distinguished as an author, but was an accom-
plished lecturer, and had devoted the greater part of his life to teaching. For
twenty-nine years he had been Professor of Botany at Wiirzburg, and for a time
during the early part of his scientific career was assistant to Purkinje at Prague.
NOTES AND NEWS,
Professor J. B. Nagelvoort has resigned the chair of Pharmaceutical Chemis-
try in the School of Pharmacy, Northwestern University, and is at present in
Amsterdam, Netherlands. Some of his contributions on pharmacy in the
Ijnited States have recently appeared in the Pharniaceutisch Weckblad of
Rotterdam.
The Hanbury Medal has been awarded for this year to Dr. John B. De Vrij,
of The Hague. He was born in Rotterdam in 1813. The President of the
British Pharmaceutical Society, in announcing the award, said : " It was interest-
ing to note that in this year of the Diamond Jubilee the award was made to a
gentleman who, although not an Englishman, had an order conferred by Her
Majesty, he being a Companion of the Order of the Indian Empire, that dis-
tinction having been given him for work done in connection with cinchona
cultivation in India. It was also interesting to remark that the first paper pub-
lished by Dr. De Vrij was written about four years before Her Majesty came to
the throne. Since that time he had been an indefatigable worker in original
research connected with the chemistry and natural history of drugs, partly in
connection with cinchona. He began life as a pharmacist, and had been con-
nected with pharmacy ever since."
THE AMERICAN
JOURNAL OF PHARMACY
SEPTEMBER, i8gj.
CAN NORTHERN SENEGA, SOUTHERN SENEGA, EUO-
NYMUS AND QUILLAJA HE DISTINGUISHED
FROM ONE ANOTHER IN THE POWDERED
STATE BY THE MICROSCOPE?
By L. E. Savrk,
Member of Research Committee C of the Revision Committee of the U. S. P. —
Preliminary Paper.
This is the question which the present investigation endeavors to
answer. As usual, the structural elements of the different druqs
were studied in their fixed relations by means of sections, and their
subsequent conduct and appearance after powdering observed. In
general it may be stated that while it is quite easy to recognize the
differences between the senegas and the other drugs, no point of
distinction could be established for the two senegas. This is easily
understood when it is observed that the two varieties of the one
drug have present the same elements in relatively equal propor-
tions, while each of the others possesses characteristic elements not
present, or differently represented, in the other drugs.
The sections of senega, both northern and southern, are easily
distinguished by the marked difference in the thickness of the routs
and in the arrangement of the tissues, but we are not surprised to
find the powders appearing very much the same under the micro-
scope. In passing through the mill and the sieve, characteristic
arrangements are destroyed and points of distinction obliterated.
Owing to this fact it is the author's opinion that no satisfactory
(433)
434
Senega, Euonymus and Quillaja. {t™p{Lmber,Y89™"
microscopical test can be established for distinguishing either
senega from the other.
In detail it may be observed that the No. 60 powder of senega
Fig. I. Cross-section Senega (Northern variety); a, cork cells; b, paren-
chyma ; Cy woody tissue ; d, tracheae.
shows mainly the suber and the parenchymatous tissues in tolerably
regular masses, while the woody centre is but rarely observed. The
soft parenchyma is sometimes broken longitudinally and sometimes
Fig. 2. Longitudinal section Senega (Northern variety), a, cork cells ; b,
parenchyma ; c, parenchyma ; d, woody cells ; <?, tracheae.
transversely, so that we get appearances characteristic of the sec-
tions made in these two directions.
As might be supposed from the appearance of the sections, no
difficulty exists in distinguishing apart the powders of senega and
Am, Jour. PHarm.)
September. 1897. j
Senega, Eiiaiiymus and Quillaja.
435
Fig. ^. Cross-section Senega (^Southern variety); a, cork cells; ^, paren-
chyma ; Cy woody centre ; d, trachea.-.
quillaja. In the latter druj^ are found elements not at ail repre-
sented in the senega. Attention is called to the strongly marked
medullary rays, to the sclerotic tissue, to the bast fibres, and more
--a
■
Fig. 4. Longitudinal section Senega (Southern variety
parenchyma ; f, parenchyma ; d, woody cells ; ^, trsche;u.
,/ r.irl: CClli ; b^
436 Senega, Euonyinus and Quillaja. { \™p£Sbefff897^"
particularly to the numerous and easily observed prismatic crystals
of calcium oxalate. Any or all of these clearly mark the powder of
quillaja, and would at once betray its presence in the powder of
senega.
Fig. s- Cross-section Quillaja ; a, parenchyma ; b, medullary rays ; c, bast
fibres.
Again, in the case of the powder derived from the root bark of
euonymus, we encounter elements that serve as points of distinction
between it and the other drugs here considered. In this instance
Fig. 6. Longitudinal-radial section of Quillaja ; a, sclerotic cells ; b, medul-
lary rays ; <:, bast fibres ; d, cork cells.
the most marked characteristic is the fragment of large-celled sub-
erous tissue, which so frequently exhibits a concentric arrangement.
In addition, the fragments of cortical parenchyma, crossed by the
narrow remains of medullary rays, appear numerously and distinctly
Fig. 7. Longitudinal-tangential section of Quillaja ; a, sclerotic cells ; b^ bast
fibres ; c, crystal ; d, medullary ray.
iStimS^r.'lIK'} Scjiega, Euonymiis and Quillaja.
437
before the observer. The bast cells would also serve to distinguish
euonymus from senega.
-d
Fig. 8. Euonymus bark of root ; a, suber ; b, parenchyma ; r, crystal ; t/,
medullary ray.
After having established these points of difference between senega
and its adulterants, numerous samples of powdered senega were
examined, but no adulteration was discovered. It would appear
a
m}
,'C'-
FifT. g. Senega powder magnified 75 diameters ; a, suber ; b, parenchyma ; r,
tracheie (rarely found in No. 60 powder).
from this that powdered senega is not difficult to secure m the
pure condition.
The drawings accompanying this arc supposed to be sclf-cxplana-
438
Senega, Euonymus and Qiiillaja. { "^s^pfember, isSt!
Fig. 10. Powder of Quillaja magnified 75 diameters; a, medullary ray; by
bast ; c, crystals of calcium oxalate ; d^ sclerotic tissue.
Fig. II. Powder of bark of root of Euonymus magnified 75 diameters ;
a, medullary ray ; b, bast ; c, suber.
tory, and show the appearance of the drugs under consideration in
as nearly a representative manner as possible.^
*This preliminary paper, containing the brief text to accompany the draw-
ings, is published at this time mainly to complete the record of the year's work
as a member of the Committee of Research.
Iv. E. S.
^s'^^ptembe^^fs^ } Gelseviic Acid. 439
GELSEMIC ACID.^
Bv Virgil Coblentz.
This principle was first isolated by Professor Maisch, in 1869,
later named and fully described by Professor Wormley in 1870.
The latter author restricted himself to the application of various
color tests and the deportment of this substance to different reagents,
with the view of its identification from the standpoint of a toxi-
colof^ist.
Dr. Chas. Robbins, in his work " Ueber die wesentlichen bestand-
theile von Gelsemium sempervirens"(i876), describes this principle
as occurrinfT in needle-like crystals, which separate in stellate
groups, possessing acid characters and forming salts with alkalies,
all of these salts being insoluble in water except those of the alka-
lies which are readily soluble and crystalline. As regards solubili-
ties, the same author claims that gelsemic acid is readily soluble in
chloroform and ether, and soluble I part in looo of water. A
number of color reactions given by Wormley were reviewed by Rob-
bins. These will be taken up later with criticisms and comments-
The material for the following investigations was supplied by
Professor J. U. Lloyd, who assured me of its purity and genuineness.
The crystals were white, when viewed in mass, of a slight yellowish
cast ; they were of the hexagonal system and varied in length from 5
to 10 mm.^
The melting point of gelsemic acid, which, to my knowledge, has
not been published, at least not by the above-named investigators,
is 206° C. (corrected).
When heated between 1 10° and 115^ C. for five hours in a tube,
through which a currrent of dry carbonic anhydride was passed, no
appreciable loss in weight occurred ; in the upper portion of the
tube a slight sublimate was noticeable. This may account for Dr.
Robbins' two molecules of crystal water. However, the solvent
employed in crystallizing may account for differences. When
heated in open air gelsemic acid takes on a deep lemon-yellow
color.
' Read at the im-fUii^ of the .Amcruati i'iiartu.ii ruiual A?>>m. i.iliuti, x^r, .
' Made from Gelsemium sempervircus by means of neutral solvents only,
no aciils or alkalies l>cinj? employed. Purified by repeate<l crystallizationt
from alcohol. — ^J. U. L.
440
Gelsemic Add,
SolMtUih'. — G. A. is soluble i p. in 1490 of distilled ^*ater at 30^ C.
" *« •' I p. " 415 of abs. ether " 22^ C.
" " ** I p. " 135 of chloroform " 24° C.
Readily soluble in hot alcohol and glacial acetic acid.
The above figures show the average of three careful determina-
tions each.
Coler Tests. — The reagents employed were r.rs: tested for such
impurities as might influence the color reaction.
(i) With cone. H.SO^ = pale yellow, disappears on standing.
(2) With cone. H^SO^ n-armed = deep yellow.
Professor Wormley obtains a yellow to red-brown color with
above.
(3) With cone. H.SO^ and trace of HNOj = blood red, quickly
tades.
(4) With cone. HjSO^ and K.Cr,0- = to yellow, pale violet,
changing to green.
Dr. Robbins obtains no reaction vnth 4.
(5) With cone. H^O^ and ammonium molybdate = yellow : on
standing from ten to twent}* minutes =: intense blue (hastened if
warmed).
The reaction 5 is ver\' delicate and characteristic.
(6) With cone. HNO- = yellow ; if G. A. is in excess = reddish
color; to this add NH^OH in excess = intense blood-red color.
Above test of Wormley is sensitive to 0-00002 gm.
Ri actions in Solution. — (1) G. A. is readily soluble in diluted
aqueous solutions of the caustic alkalies : the resulting solution is of
a pale yellow color when \iewed by transmitted light ; by reflected
light it exhibits an intense bluish-green fluorescence, i part in
1,000,000 being distinctly fluorescent. This is destroyed by addition
of acids.
(2) An aqueous solution of G. A. liberates iodine from iodic acid
(HIO,).
(3) An aqueous solution of G. A. on addition of ferric chloride
gives a green-colored solution.
(4) Lead acetate and mercuric chloride both produce, with aque-
ous solutions of G. A., yellowish precipitates called by Robbins
*' gelsemates." These precipitates proved to be a mixture of basic
hydroxides of the metal and unaltered gelsemic acid, the latter
being readily removed by washing with hot water or alcohol.
Am. Jour. Pharm, \ CZfiUfmir Ari^l tMt
(5) When silver nitrate is added to an aqueous solution of G. A.,
at first a yellow precipitate is produced, which quickly changes to
black. Solutions of auric and platinic chlorides are reduced at
once.
(6) Fehling's solution, or a concentrated solution of copper sul-
phate, gives a brownish-red precipitate of suboxide on standing, or
immediately on heating.
(7) The addition of freshly.prepared chlorine water to an aqueous
solution of G. A. produces a red coloration which disappears on
warming.
(8) The addition of Lugol's solution produces a brown precipi-
tate, which consists of a mixture of free iodine and gelsemic acid.
Analytical. — Dr. Robbins assumes gelsemic acid to be a gluco-
side, after boiling its aqueous solution with diluted sulphuric acid,
and heating with Fehling's solution. In the above cited reactions
we find that gelsemic acid is a strong reducing agent, reacting even
in cold solution, so this test is indeed, under the circumstances,
fallacious.
To ascertain whether this principle is a glucoside or not, samples
were boiled for twelve hours with diluted, also concentrated, hydro-
chloric acid, also with diluted sulphuric acid, finally; a sample was
heated in a sealed tube with 5 per cent, alcoholic hydrochloric acid
at iio°C. All gave negative results, the gelsemic acid remaining
unchanged, and the solution failing to give any reaction for sugar
with phenylhydrazine. Other sugar tests cannot be applied, because
of the above-mentioned reducing properties of this principle.
Robbins as well as Wormley calls attention to the acid prop)erties
of G. A. The former states that the salts, with exception of the alka-
lies, are insoluble in water, while the latter are crystalline. Robbins
assumes that the precipitate obtained by adding a salt of a metal to
solution of G. A. was a compound of the latter with a metallic base.
I have already stated that these precipitates consist of a mixture of
basic hydroxides and free acid.
I endeavored to obtain salts of G. A. with the alkalies by
cautiously neutralizing aqueous and alcoholic solutions of this princi-
ple with alkali carbonates and hydrates. The resulting solutions were
concentrated at the lowest possible temperature, and set aside for
some weeks, with the result that nothing more than amorphous
crusts could be obtained.
442 Gelsemic Acid, { ^sTpfembef.X^-
The dry sodium salt (so-called) when heated becomes very volu-
minous, a phenomenon similar to the " Pharaoh's Serpent " pro-
duced on heating mercury sulphocyanide.
I next attempted to produce a salt with the alkaline earths, by
boiling gelsemic acid with freshly-precipitated barium carbonate and
water, also magnesium carbonate and water for several hours. The
filtered solution was neutral, but upon concentrating, the carbonated
alkaline earth gradually separated and the solution assumed an acid
reaction. No crystals separated from the solution upon standing.
From the above it will be seen that this principle possesses very
feeble acid properties and that its compounds are of an exceeding
unstable character.
Attempts were made to produce salts by double decomposition
between the sodium compound of G. A. in solution, v/ith salts of the
metals, but the precipitates obtained were of the same character as
those mentioned under test 4.
Lassaigne's test for the presence of nitrogen was made with nega-
tive results, confirming Robbins' test.
Robbins, after making two combustions of gelsemic acid with cop-
per oxide in a simple bayonet tube, as was customary at that time,
and comparing his results with the older aesculin formula of Rochle-
der, comes to the conclusion that his gelsemic acid is identical with
aesculin, reinforcing his opinion by comparing the fluorescent prop-
erties of both and their reducing powers on Fehling's solution. It
is true that aesculin and gelsemic acid resemble each other in some
particulars, such as fluorescence and reducing powers, but, as will be
shown later, it will be seen that the latter is a distinctively different
principle.
Tne two combustions of Robbins resulted as follows :
I. C = 5204 per cent. H — 5-189 per cent.
II. C = 5182 per cent. H = 4-98 per cent.
The older formula of Rochleder for aesculin contains C 51*57 per
cent, and H 4-87 per cent.
The later accepted formula contains C 5294 per cent, and H
470 per cent.
The results of Robbins' analyses and the above formula corre-
spond quite closely. However, the suuthor questions the accuracy of
the (Robbins) analyses and the formula deduced therefrom.
The greatest difficulty was experienced in obtainmg concordant
Am. Jour. Phariu.) /^x'/cm »'/- J^i.-/ . . -.
September. IW. / UtlStmiC Acld. 443
results in combustions of gelsemic acid, for this principle is one of
those few organic substances which upon heating with copper oxide
or oxidizing agents tends to give up only a portion of its carbon as
carbon dioxide, the rest separating as a graphitic-like deposit on the
sides of the combustion tube, which the highest possible tempera-
ture cannot remove. Over twenty combustions were made after
various methods; in several instances, even with cupric oxide alone,
two of the combustions would correspond quite closely, but subse-
quent results did not justify that any reliance be placed upon the
figures. The various methods employed were : First, combustion
with copper oxide in a bayonet tube; second, with cupric oxide in
an open tube in a current of oxygen; in the third method, lead chro-
mate was employed ; the fourth method attempted consisted in
mixing the gelsemic acid with powdered fused potassium bichromate
in a platinum boat, and then burning in an open tube into cupric
oxide in a current of oxygen ; as fifth attempt, the method of wet
combustion with a. mixture of chromic anhydride and sulphuric acid
was attempted, passing the gases through a spiral cooler, then over
lead peroxide to remove sulphur dioxide, finally over calcium chlo-
ride, into the potash absorption apparatus (see American Journal
OF Pharmacv, May, 1897, p. 228). This method, although requiring
the greatest care to prevent the contaminating gases from passing
over, gave very good results in the analysis of some of the deriva-
tives of gelsemic acid, while with the mother-substance discordant
results were obtained. Finally, as last resort, a mixture of lead
chromate 3 parts and red lead (mennige) i part was tried, the com-
bustion being carried on in an open tube in a current of oxygen.
The two above-mentioned ingredients were reduced to a fine pow-
der, well mixed, moistened with water, granulated and sharply
dried at 150° C. This mixture was introduced into an open com-
bustion tube and heated to dull redness in a current of oxygen, then
on cooling the well-dried sample of gelsemic acid, which had pre-
viously been mi.xed with an ignited mi.xture of equal parts of pow-
dered lead chromate and lead oxide, was introduced, and the com-
bustion carried on slowly in a current of oxygen, bringing the tube
finally to a bright red heat. No traces of separated carbon could be
found on the sides of the tube after combustion.
The analyses resulted as follows :
... rZfiJ<:pi^ir Ari^ f Am. Jour. Pbarin-,
444 LreiSeiniC J-LCIU. \ September, ] 897.
I. 0*2432 gramme substance yielded 0-5582 gramme of 002=62*59 per cent. C.
0*0988 '* ** H,0= 4*51 " " H,
11.0*1140 " ** " 0*2610 '• " CO.,=62*45 " " C.
0-0470 •' " H20= 4-58 " " H.
111.0-2926 " " " 0*6739 " " C02=62-8i - " C.
" 0*1166 " " H30= 4*42 " *' H.
From the average of the above analyses the formula QgHj^Og was
deduced, the percentage of carbon would be 63-16 and of hydrogen
4-45. Thus for comparison :
Calculated.
Found = I.
II.
III.
C = 63*16
62-59
62*44
62*81
H= 4"45
4'5i
4-58
4*42
A molecular weight determination (which would be of great as-
sistance here), after the method of Beckmann (kryoscopic), was
found impossible because of the insolubility of gelsemic acid in the
cold solvents employed in these determinations, with the exception
of phenol, which, however, gave abnormal results, due probably to
molecular action between the two.
Action of Phosphorus Pentachloride. — Gelsemic acid was cau-
tiously fused with a slight excess of phosphorus pentachloride ; to
the mass water was added slowly, the tube being kept well cooled
with ice. After standing a few hours a white mass separated,,
which, after thoroughly washing, was taken up into as little hot
alcohol as possible, filtered and again precipitated in an excess of
water. This operation was repeated several times in order to re-
move a non-crystallizable impurity which was comparatively in-
soluble in alcohol ; finally the product was recrystallized twice from
alcohol. This chloro-derivative of gelsemic acid melts at 190° C. A
chlorine estimation was made after Carius. 00615 gramme of
substance yielded 00616 gramme of AgCl, which corresponds to
2476 per cent, of chlorine. The theoretical replacement of two
hydroxyl groups by chlorine would give us 25 per cent, of the lat-
ter. This proves conclusively that we have replaceable hydroxyl
groups present.
Thus,
C13H9 (OH)A = Q3H, {C\\0,,
Calculated, CI = 25 percent. Found CI = 24*76 per cent.
Action of Acetic Anhydride. — Gelsemic acid was heated with
acetic anhydride and anhydrous sodium acetate in a flask with reflux
^^pt'emb^r'Sr"} Gelsemic Acid, 445
condenser for several hours, then the reaction's product was poured
into an excess of water, the precipitate formed thoroughly washed,
<lried and crystallized from alcohol. This compound forms needle-
like anhydrous crystals, which melt at iSo° C. The number of
acetyl groups (C2H3O) entering this compound was determined by
saponifying a weighed quantity in an excess of normal alcoholic po-
tassium hydrate, and then titrating back the excess of alkali by
means of standard hydrochloric acid. Assuming that the two hy-
drogen atoms of the hydroxyl groups have been replaced by two
acetyl radicals, we have the following :
C^Hg (C2H30)o05, calculated percentage of (C2H3O V Found.
25-98 25-14
On adding bromme to a hot solution of gelsemic acid in glacial
acetic acid a voluminous white precipitate formed, which, when
crystallized from alcohol, formed yellow needles which fused at 250^
C. A further investigation of this body was postponed for lack of
material.
Thus far, from the above results, we may ascribe to gelsemic acid
the formula Ci3H9C)3 (OH)2. Considering the active reducmg char-
acter of this principle it is highly probable that either an aldehyde
or a ketone group is also present, which further investigation will
determine. That gelsemic acid is identical to a^sculin, as Robbins
and others have assumed (disputed by Wormle}-), is not possible, as
the comparisons and criticisms of the combustions already given
have shown. In addition to this, further comparisons are given
below. It may be possible that a relationship in certain groupings
exists between these two principles, which, however, cannot be set-
tled as yet.'
* "About fifteen years ago I prepared for and presented Professor Fliickiger
^ith a quantity of pure white crystalli7.c«l >»elseniic acid. Professor Pliickiger
became much interested in its chemistry and personally prepared son: ilin
to compare therewith. He determined that they were different Im>- us-
ing me of the fact by letter, stating that he would continue the investigation, in
which he was deeply interested. The subject, however, rrsts among his un-
completed works, and, so far as I know, he did not publish his results." — From
a personal letter from John Uri Lloyd, date<l August 16, 1897, after this paper
waa written.
446 Alkanet Root. {^s%feTbe?;?89":
jj?scuiiTi, Gelsemic Acid.
CHifiOg -f i>^HoO— melts at i6o° C. CiaHnOj — melts at 206° C.
Forms a penta-acetyl derivative, melts Forms a diacetyl derivative, melts at
at 203°-2o6° C. 180° C.
Splits up into sugar and sesculetin. Does not hydrolyze.
Bromine derivative melts I93°-I95° ^- Bromine derivative melts 250° C.
Chloro subst. prod, not prepared. Chloro subst. prod, melts 190° C.
The author desires to express his thanks to Prof. Dr. A. Hilger
(Munich), for valuable advice given during a portion of the above
investigations.
ALKANET ROOT.^
By E. M. Holmes, F.L.S.
Although alkanet vas known as a drug to Theophrastus, Dios^
corides, and Pliny ,2 and similar roots have been used in the East for
centuries, comparatively little is to be found concerning the drug in-
modern text-books on Materia Medica, notwithstanding the fact
that there are probably few pharmacists who do not keep the root
in stock. The plant is not described either in Pereira's " Materia
Medica," or in "Pharmacographia," nor is any figure of the plant
to be found in Bentley and Trimen's or other English works on
medicinal plants. In Woodville's " Medicinal Plants " (Vol. II, third
ed., plate 106) the drug is referred to Anchusa tinctoria, but the
figure given is that of A. officinalis, L. {vide Index Kewensts, I, p^
1 19), which does not yield a red root. The author, indeed, remarks
(/. c, p. 3 1 5) : " In this climate its roots never acquire the deep color
on which its utility depends." The only good figure that I have
seen of Alkanna tinctoria, Tausch, the plant which is the chief
source of the alkanet root of commerce, is given by Berg in •' Offizin.
Gewachse " (plate xxiv, c).
I have never seen the plant cultivated in botanic gardens in this
country, and for some years I have endeavored to obtain the plant,
which is a native of the south of Europe, through pharmacognosists
in Austria, but without result. At the commencement of this year
I saw the plant mentioned in the seed list of the Botanic Garden of
Montpellier, and, on writing for some, was informed that the demand
for the seeds had been so great that the stock was exhausted. Pro-
fessor L. Planchon, however, was good enough to send me several
' Pharmaceutical Journal, July 24, 1897. >
- " Pharmacographia Indica," Vol. II, p. 524.
Am. Jour. Pharm.)
September. l«;7. /
Alkatiet Root.
447
roots, so that I have been able to study the habits of the plant.
The Hterature on the subject being so scanty, and the plant itself
apparently so rare in cultivation, I have thought that a few observa-
tions on the plant under cultivation in this country might prove of
interest to some of the readers of this Journal. The roots, which
arrived in March, had scarcely any rootlets, and Professor Planchon
doubted whether they would grow. Hut as they had only a few
I. Whole plant. About one-third ualural size. 2, Corolla, niaijniflid, sliow-
ing relation of stamens to indentations in throat of corolla.
leafy shoots at the crown, and had scarcely started growtli, I had
some hopes of success. Having learned from him that the plant
grows in sandy fields amongst grass, fully exposed to the sun, the
sandy soil probably containing calcareous matter derived from
shells, I planted some in full exposure to sunlight, and others in a
position where they would only get the morning sun and be some-
448 Alkanet Root, {T^^l^^^S^ti^:
what sheltered from cold winds, two others being placed in pots in
a cool greenhouse. The soil used was a mixture of grassy loam
and " hassocks,"^ broken down into sandy grit by frost. The two
specimens fully exposed to the sun, although covered during windy
days and frosty nights, succumbed by reason of the dryness of the
soil. Those exposed only to the morning sun and sheltered by
stones and herbage from cold winds progressed slowly, but ulti-
mately flowered freely, vigorous growth occurring only as the air
became warmer. Those in the greenhouse quickly made a start and
flowered before those in the open ground had made flowering shoots.
i he crown of the root sends up several slender leafy shoots, which
are at first prostrate or decumbent, but become gradually ascending^
and when elongated and in flower, they are nearly erect from a
decumbent base. Besides these there are at the same time a few
shoots which do not develop flowers.
The plants evidently require a warmer atmosphere than is usual in
an English spring, and will not thrive in the open air except in shel-
tered warm situations. The flowers are about the size of those of
Anchusa sempervirens, but of a more beautiful ultramarine blue
color. They have no scales in the throat of the corolla, differing
in this particular from the genus Anchusa, but the tube of the
corolla has, on the external surface, two rows of indentations, which
cause a slight bulging of the corolla between the brown anthers.
These have very short filaments, three of the anthers being situated
above the upper row of indentations, and two above the lower row,
and the throat of the corolla is lined with minute glandular hairs.
The stigma in the flowers I have examined is on a level with the
two lower stamens. This may possibly be an arrangement to pro-
vide self-fertilization in case the flowers are not cross-fertilized, or it
may be a special adaptation to direct a particular insect to the
honey which lines the corolla tube. The leaves are of a slightly
grayish-green tint and are covered with hispid hairs and very short
stalked glands, the latter being visible only under a good lens. The
accompanying figure represents the plant of one.third the natural
size, as grown in a pot in this country, though possibly smaller than
the wild plant as occurring in the warmer climate of Montpellier.
• '• Hassocks " is a local name for the soft layers of stone found between layers
of Kentish ragstoue in the green sand formation, but which, unlike the rag-
stone, split up and become pulverized by the action of frost, forming excellent
soil for rockeries.
'sTpiS^rSr™} Alkanet Root, 449
In •• Les Drogues Simples " MM. Planchon and Collin state that
several other boraginaceous plants have red roots and can be sub-
stituted for alkanet, such asOnosma echioides, L. (S. Europe), Arne-
bia tinctoria, Vahl. (Egypt and Arabia). According to ** Pharma-
cographia Indica," II, p. 524, four kinds of alkanet are described by
Mohammedan writers, Harjuya being the Persian, and Ratanjot the
Indian name for the drug. It is also stated that the roots of Onosma
hookeri, C. B. Clarke, and of a species of Arnebia from Afghanis-
tan, are known as Rang-i-badshah {i. e., royal dye) and Ratanjot, and
that a third kind is imported from China, and consists of long,
wood}', twisted roots, like the alkanet of Europe.
In the Hanbury collection of materia medica there is a specimen
of a root resembling alkanet in color, but having a thin, laminated,
papyraceous bark like the tunic of a bulb. It was received from
Dr. Stocks, and has the native name of Maharrunga, and is referred
to Lithospermum euchroma, Royle, which is identified in the Kew
Index as Macrotomia perennis, Benth.
Specimens exist in the herbarium of the society, of Macrotomia
benthami, D. C, and of Onosma echioides, Linn., both of which
have roots of a deep purple color, and a laminated bark. In the
foimer the laminae are faintly reticulated, and in the latter wrinkled
transversely. Both would at once be recognized in commerce as
alkanet, but different from the European drug.
In Watts' " Dictionary of the Economic Products of India " (I,
p. 318), Arnebia thibetana, Kurz, is stated, on Dr. J. E. T. Aitchi-
son's authority, to have a scaly root bark, and to be used as dye.
The roots of Onosma emodi. Wall., and O. hookeri, Clarke, are also
said to yield a red dye (/. r., p. 48S). Whether any of these are
superior in tinctorial power to European alkanet or not, might per-
haps be worthy of inquiry. O. hookeri is said to yield the best
Lepcha red dye (" Elora British India," IV, p. 178) The root is
used as a red dye for wool, a vegetable acid, such as that of apricots,
being employed for the purpose of giving the desired tint. An al-
kanet root from Japan is referred to Lithospermum crythrorhizon.
The plants of which the roots are known to be used like alkanet are
therefore as follows: Alkanna tinctoria, Tausch ; Arnebia thibetana,
Kurz; Arnebia tinctoria, Vahl.; Lithospermum erythrorhizjn ;
Macrotomia benthami, D. C; Macrotomia perennis, Benth.; Onosma
emodi. Wall; and Onosma hookeri, Clarke.
450 Active Principle of Digitalis. {^sTpimberi89™'
THK ACTIVE PRINCIPLE OF DIGITALIS.^
By C. C. Kei.ler.=^
The unsatisfactory results obtained with the digitalin prepared
according to the method described by Kihani^ have again directed
attention to digitoxin, which is, according to Schmiedeberg, the
most potent constituent of digitalis leaves, and forms the chief part
of Nativelle's digitalin. On that account C. C. Kellei has devised
a method of determining the efficacy of digitalis preparations by
ascertaining the amount of digitoxin present in them.
The chief characters of digitoxin, which are of importance in
this connection, are its free solubility in alcohol and chloroform,
slight solubility in ether, and its insolubility in petroleum spirit. It
is precipitated from solutions in water or dilute alcohol by tannin
but not by basic lead acetate. From acid or alkaline water solu-
tions it can be extracted by shaking with chloroform. Although
pure digitoxin is almost insoluble in water, it is dissolved to some
extent in the presence of extractive materials, and the other gluco-
sides of digitalis. Digitonin and digitalin are almost insoluble in
chloroform.
To ascertain the amount of digitoxin in digitalis leaves they must
first be extracted with 70 per cent, alcohol, preferably by percola-
tion, which must be continued until the residue from 3 or 4 cubic
centimetres, redissolved in water with 2 drops of dilute hydro-
chloric acid, gives, after filtration, no appreciable turbidity on the
addition of tannin.
The residue of the extract, from which alcohol has been removed
by evaporation, is mixed with water, washed into a beaker of about
250 c.c. capacity, diluted to the volume of 222 c c, and mixed with
basic lead acetate. The very voluminous precipitate is separated
by filtration, and excess of lead removed from the filtrate by adding
sodium sulphate. The clear liquid is then mixed with 2 c.c. am-
monia solution (10 per cent.) and shaken four or five times with
about 30 c.c. of chloroform. The clear chloroform solution evapo-
rated gives the digitoxin mixed with some fat and other substances.
For purification the residue is dissolved in 3 c.c. chloroform, 7 c.c.
^Pharmaceutical Journal, ^\\\y 24, 1897.
'^ Derichtc deutsch. pharm. Geselhch., VII, 1.5.
'See /%ffr. yr;/^r., LV, 29.
^^pSber.^*^"} ^^i^'^ Principle of Digitalis. 45 1
ether, and 50 c.c. petroleum spirit added. The digitoxin then sep-
arates in white flocks, and on shaking, the Hquid becomes quite
clear. P'or weighing the digitoxin it may be dissolved off the
filter with hot alcohol and the solution evaporated in a suitable
vessel, or the petroleum spirit may be decanted off and the
digitoxin weighed in the state of powder.
Digitoxin thus obtained dissolves in strong hydrochloric acid
with a yellowish color, and the solution when warmed becomes
greenish, then greenish-brown ; on adding water the color becomes
greenish-yellow, and after some time flocks are separated.
A solution of digitoxin in glacial acetic acid containing ferric
chloride, gives Keller's reaction when floated on strong sulphuric
acid. At the line of contact a dark zone appears, and after a few
minutes the acetic acid liquor becomes dark blue. This reaction
takes place with one-tenth of a milligramme of digitoxin in i c.c.
of acetic acid.
The complete separation of digitalin is difficult, as it is sufficiently
soluble in chloroform for traces to be taken up, and to that circum-
stance must be ascribed the red coloration of digitoxin when mixed
with strong sulphuric acid.
The watery liquid from which digitoxin has been extracted by
shaking with chloroform has a bitter taste and contains digitonin,
which can be separated by precipitation with tannin ; but as it does
not possess the peculiar efficacy of digitalis, its separation is of liitic
importance. Keller was unable to obtain any substance correspond-
ing to the description of digitalein, and he con'^iders it is merely
digitonin mixed with traces of digitoxin and digitalin.
After separating digitonin tannate, the filtered liquid still contains
digitalin.
The general conclusion arrived at by Keller is that digitalis leaves
contain digitoxin, digitonin and digitalin identical witli the products
from digitalis seeds, but in somewhat different proportions, the
amount of digitoxin in the seeds being much smaller than that in
good leaves, but it varies very much in different samples of leaves, or
from o 26 to o 62 per cent. A still greater variation was found in the
pharmaceutical preparations of digitalis, and Keller strongly recom-
mends the adoption of means for ascertaining the medicinal value
of the drug on the basis of the amount of digitoxin it contains.
452 Botanical Garden at Buitenzorg. {\"pfembeM%?*
THE BOTANICAL GARDEN AT BUITENZORG.
The following description of the famous Buitenzorg Botanical
Garden in Java, is taken from an article entitled " Down to Java,"
by Eliza Ruhamah Scidmore, in the Century Magazine for August,
1897, and which is part of a book to be entitled "Java: the Equa-
torial Eden," to be issued by the Century Company in November.
The famous botanical garden at Buitenzorg is the great show-
place, the paradise and pride of the islands. The Dutch are admit-
ted to be the best horticulturists of Europe, and with the heat of a
tropical sun, a daily shower, and a century's well-directed efforts,
they have made Buitenzorg's garden first of its kind in the world,
despite the rival efforts of the French at Saigon, and of the British
in Singapore, Ceylon, Calcutta and Jamaica. The Governor-
General's palace is in the midst of a ninety-acre inclosure, reached
from the main gate near the hotel by what is undoubtedly the finest
avenue of trees in the world. These graceful kanari trees, arching
100 feet overhead in a great green cathedral aisle, have tall,
straight trunks, covered with stag-horn ferns, bird's-nest ferns, ratans,
creeping palms, blooming orchids, and every kind of parasite and
air-plant the climate allows ; and there is a fairy lake of lotus and
Victoria regia beside it, with pandanus and red-stemmed Banka
palms crowded in a great sheaf or bouquet on a tiny islet. When
one rides through this green avenue in the dewy freshness of the
early morning, it seems as though nature and the tropics could do
no more, until he has penetrated the tunnels of waringen trees, the
open avenues of royal palms, the great plantation of a thousand
palms, the grove of tree-fern, and the frangipani thicket, and has
reached the knoll commanding a view of the double summit of
Gedeh and Pangerango, vaporous blue volcanic heights, from one
peak of which a faint streamer of smoke perpetually floats.
There is a broad lawn at the front of the palace, shaded with great
waringen, sausage and candle trees, and trees the branches of which
are hidden in a mantle of vivid-leafed bougainvillea vines, with deer
wandering and grouping themselves in as correct park pictures as if
under branches of elm or oak, or beside the conventional ivied
trunks of the North.
It is a tropical experience to reverse an umbrella and in a few
minutes fill it with golden-hearted frangipani blossoms, or to find
nutmegs lying as thick as acorns on the ground, and break their
I
iTptimber'i*!;;"} Botanical Garden at Buttenzorg, 453
green outer shell and see the fine coral branches of mace enveloping
the dark kernel. It is a delight, too, to see mangosteens and ram-
butans growing, to find bread, sausages and candles hanging in
plenty from benevolent trees, and other fruits and strange flowers
springing from a tree's trunk instead of from its branches. There
arc thick groves and regular avenues of the waringen, a species of
Ficus, and related to the banian — and the rubber tree, a whole
family, the roots of which writhe over the ground, drop from the
branches, and generally comfort themselves in unconventional ways.
Bamboos grow in clumps and thickets, ranging from the fine
feathery-leafed canes that are really only large grasses, up to the
noble giants from Burma, the stems of which are solid trunks easily
soaring to 100 feet in air, and spreading there a solid canopy of
graceful foliage.
The creepers run from tree to tree, and writhe over the ground
like gray serpents; ratans and climbing palms 100 feet in length
are common, while uncommon ones stretch to 500 feet. There is
one creeper with a blossom like a magnified white violet, and with
all a wood-violet's fragrance ; but with only Dutch and botanical
names on the labels, one wanders ignorantly and protestingly in
this paradise of strange things. The rarer orchids are grown in
matted sheds in the shade of tall trees ; and although it was then
the end of the dry season, and few plants were in bloom, there was
an attractive orchid show, in which the strangest and most con-
spicuous bloom was a great butterfly flower, or pitcher plant, the
pale-green petals of which were veined with velvety maroon, and
half concealed the pelican pouch of a pitcher filled with water. It
was an evil-looking, ill-smelling, sticky thing, and its unusual size
and striking colors made it haunt one longest of all the vegetable
marvels. There were other more attractive butterflies fluttering on
pliant stems, strange little woolly white orchids, like edelweiss trans-
planted, and scores of delicate Java and Borneo orchids, not so well
known as the Venezuelan and Central American orchids commonly
grown in American hothouses, and so impossible to acclimate in
Java.
I^dy Raffles died while Sir Stamford was governor of Java, and
was buried in the section of the palace park that was afterward set
apart as a botanical garden, and the care of the little Greek temple
over her grave near the kanari avenue was provided for in a special
454 Botanical Garden at Buitenzorg. {''^^^l^^^S^xm:
clause in the treaty of cession. The bust of Theismann, who
founded the garden and added so much to botanical knowledge by
his studies in Java and Borneo, stands in an oval pleasance called
the rose garden ; and there one may take heart and boast of the
temperate zone, since that rare exotic, the rose, is but a spindling
bush, and its blossoming less than scanty at Buitenzorg, when one
remembers California's perennial prodigalities in showers of roses.
After the death of the learned curator, Dr. Treub, in 1895, Professor
Lotsy, of Johns Hopkins University, Baltimore, was called to the
charge of this famous garden, which provides laboratory and work-
ing space for, and invites foreign botanists freely to avail themselves
of this unique opportunity of study. Over one hundred native
gardeners tend and care for this great botanic museum of more than
nine thousand living specimens, all working under the direction of
a white head gardener. The Tjilewong River separates the botanic
garden from a culture-garden of forty acres, where seventy more
gardeners look to the economic plants — the various cinchonasi
sugar-canes, rubber, tea, coffee, gums, spices, hemp and other
growths, the introduction of which has so benefited the planters of
the colony. Experiments in acclimatization are carried on in the
culture-garden, and at a mountain garden high up on the slopes of
Salak, where the Governor-General has a third palace, and where
there is a Government hospital and sanitarium.
All Java is, in a way, as finished as little Holland itself, the whole
island being cultivated from edge to edge like a tulip garden, and
connected throughout its length with post-roads, as smooth and
perfect as park drives, all arched with waringen, kanari, tamarind
or teak trees. The rank and tangled jungle is invisible save by
long journeys, and great snakes, wild tigers and rhinoceroses are
almost unknown now. One must go to Borneo and the farther
islands to see them. All the valleys, plains and hillsides are
planted in formal rows, hedged, terraced, banked, drained and as
carefully weeded as a flower bed. The drives are of endless beauty,
whichever way one turns from Buitenzorg, and we made triumphal
progresses through the kanari- and waringen-lined streets in an
enormous " milord." The equipage measured all of 20 feet from
the tip of the pole to the footman's perch behind, and with a crack-
ing whip and at a rattling gait we dashed through shady roads, past
Dutch barracks and hospitals, over picturesque bridges, and through
"'^pt'embef.Ys^"'-} Boianical Garden at Buitenzorg. 455
villages where the native children jumped and clapped their hands
with glee as the great Juggernaut vehicle rolled by. We visited
the grave of Radin Saleh, a lonely little pavilion or temple in a
tangle of shrubbery that was once a lovely garden shaded by tall
cocoa-palms; and we drove to Batoe Toelis, *' the place of the writ-
ten stone," and in the little thatched basket of a temple saw the
sacred stone inscribed in ancient Kawi characters, the original clas-
sic language of the Javanese. In another basket of a shrine we
were shown the veritable foot-prints of Buddha, with no explanation
as to how and when he rested on the island, nor yet how
he happened to have such long, distinctively Malay toes.
Near these temples is the villa where the poor African prince of
Ashantee was so long detained in exile — an African chief whose
European education had turned his mind to geology and natural
sciences, and who led the life of a quiet student here until, by the
change of Ashantee from Dutch to British ownership, a way was
op>ened for him to return to and die in his own country. There is a
magnificent view from the Ashantee villa out over a great green
plain and a valley of palms to the peaks of Gedeh and Pangerango,
and to their volcanic neighbor, Salak, silent for 200 years. Peasants,
trooping along the valley roads far below, made use of a picturesque
bamboo bridge that is accounted one of the famous sights of the
neighborhood, and seemed but processions of ants crossing a
spider's web. All the suburban roads are so many botanical exhi-
bitions approaching that in the great garden, and one's interest is
claimed at every yard and turn.
It takes a little time for the temperate mind to accept the palm-
tree as a common, natural and inevitable object in every outlook and
landscape; to realize that the joyous, living thing with restless,
perpetually thrashing foliage is the same correct, symmetrical, mo-
tionless feather-duster on end that one knows in the still life of hot-
houses and drawing-rooms at home ; to realize that it grows in the
ground, and not in a pot or tub to be brought indoors for the
winter season. The arches of gigantic kanari trees growing over
by-lanes and village paths, although intended for triumphal avenues
and palace driveways, overpower one with the mad extravagance,
the reckless waste and the splendid luxury of nature. The poorest
may have his hedge of lantana, which, brought from the Mauritius
by Lady Kaffles, now borders roads, gardens and the railway tracks
456 KeVieWS, 1 September. I897.
from end to end of the island. The humblest dooryard may be gay
with tall poinsettia trees, and bougainvilleas may pour a torrent of
magenta leaves from every tree, wall or roof. The houses of the
rich planters about Buitenzorg are ideal homes in the tropics, and
the Tjomson and other great tea and coffee estates are like parks.
The drives through their grounds show one the most perfect lawns
and flower beds and ornamental trees, vines and palms, and such
ranks on ranks of thriving tea bushes and coffee bushes, every leaf
perfect and without flaw, every plant in line, and the warm, red earth
lying loosely on their roots, that one feels as if in some ornamental
jardin d' accLimatation, rather than among the most staple and serious
crops of commerce. Yet from end to end of the island the culti-
vation is as intense and careful, entitling Java to its distinction as
"the finest tropical island in the world." It is the gem of the
Indies, the one splendid jewel in the Netherlands' crown, and a pos-
session to which poor Cuba, although corresponding exactly to it
geographically and politically, has been vainly compared.
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
Incompatibilities in Prescriptions. For students in pharmacy and
medicine and practicing pharmacists and physicians. By Edsel A. Ruddiman,
Ph.M., M.D., Adjunct Professor of Pharmacy and Materia Medica in Vander-
bilt University. First edition, first thousand. New York : John Wiley &
Sons. London : Chapman & Hall, Ltd. 1897.
Part I treats of incompatibilities, taking up the various substances in alpha-
betical order, beginning with acacia and ending with zinc.
Each substance has its behavior towards the various pharmaceutical and
chemical reagents described briefly, and with this information the physician or
pharmacist is supposed to be able to decide on the incompatibilities of the sub-
stance he proposes to put into a prescription. In most cases of official sub-
stances, he would do better to consult the U. S. Pharmacopoeia, where he would
find tests that will almost always give a clue to the incompatibilities without
being obscured by a large number of tests and properties which are of doubtful
value when true, and which, in many cases, are not true.
It appears to us that Part I is top-heavy with quotations from Muir and
Morley's edition of Watts' Dictionary. This is just about the last authority we
should have thought of consulting on a pharmaceutical subject. For instance,
of what value is it to one compounding a prescription to know that morphine
is oxidized by an alkaline solution of potassium permanganate, forming an
acid ; or that potassium ferricyanide oxidizes morphine to pseudo-morphine,
when the conditions necessary for the reactions are such as are not liable ever
to occur in compounding prescriptions ?
The author has succeeded much better when he has quoted Allen or Prescott.
Am. Jour. Pbarm.l P^'7ti/"!nc aCT
September. 1897. / IKeVteiVS. 45/
What is needed, in a list of properties of such substances as occur in Part I, is
not a compilation of tests which are worn threadbare from having done long
service in text books, but a list of such as have been tried by the author him-
self, and which he can vouch for.
Part II is devoted to the criticism of 325 prescriptions. In it the author has
succeeded in presenting what will be of value for the student to study, but it is
scarcely possible that one would find, while compounding a prescription, an
example in the 325 that would correspond to that which he has in hand. The
information in Part II is valuable, especially that given in tabular form, show-
ing the effect of rubbing together equal weights of two solids, and for this con-
cise statement the author deserves much credit.
Accidents and Emergencies. A manual of the treatment of surgical and
medical emergencies in the absence of a physician. By Chas. W. Dulles, M. D.,
Fellow of the College of Physicians of Philadelphia and of the Academy of
Surgery, etc., etc. Fifth edition. Philadelphia: P. Blakiston, Son & Co. 1S97.
In these days, when students of pharmacy are instructed concerning emer-
gencies, a new edition of this work will be especially acceptable.
The style of the writer is so concise and attractive that one follows the sub-
ject with but little effort Every class of accident appears to be fully consid-
ered, and the text so elucidated by illustrations as to make the method of pro-
cedure in an emergency case easily learned as well as easily remembered.
The only adverse criticism we have to make is in the chapter devoted to
*' Description of Poisonous Plants," where the author appears to be out of his
element. Poke root is given as the learning common name of Veratrum viride,
and the illustration of the latter is given the title " poke root." If the author
has ever found any authority for the application of the name poke root to
Veratrum viride, he has seen an error that it is unfortunate to propagate. We
are aware that the term Indian poke has been applied to Veratrum, but not
poke root. The so-called wild parsnip, P.istinaca sativa, had better have been
omitted from the book altogether, for it has been shown time and again that the
parsnip, whether wild or cultivated, is not poisonous. The numerous cases of
poison cited in the newspapers as caused by wild parsnip, have in most instances
been caused by Cicuta maculata. Some typographical errors are noticeable in
this chapter, indicating that it did not receive quite ihe care at the hands of the
author that it should, although the subject is one of the most important of
those treated, and it might be made one of the most interesting. It is to be
hoped that it will be re-written for the next edition.
Brr.LETiN Vol. Ill, No. 3, of the College of Agriculture, Imperial rniversity,
Japan.
Although issued by a department of agriculture, many of the subjects treated
are of especial interest to pharmacists, as shown by the following list of titles
and authors contained in the current issue : "The Chemistry of Soja Sauce
Manufacture," by Y. Nishimura ; " Contributions to the Chemistry of Sake
Brewing," by J.Okumura; "On the Origin of Sake Yeast . Saccharomyces
Sake )," by K. Yabe ; " Note on a Grape Wine Fermented Ijy Sake Yeast," by
K. Negami ; "On the Behavior of Yeast at a High Temperaturc.'V by T.
Nakamura; "On Two New Kinds of Red Yeast," by K. Yal)e ; "On Bromal-
bumin and Its Behavior to Microbes," by O. Loew and S. Takaba)ashi ; "On
„ L> .^.*"^-.„... / Am.Jonr. Pharm.
458 KeVieWS, \ September. I897.
ail Iniportaut Fuuction of Leaves," by U, Suzuki ; "On the Behavior of Active
Albumin as a Reserve Material during Winter and Spring," by U. Suzuki ; "On
the Physiological Action of Neutral Sodium Sulphite upon Phaenogams," by
K. Negami ; " On the Poisonous Action of Ammonium Salts upon Plants," by
S.Takabayashi; "The State of Cane Sugar Manufacture in Formosa," by N.
Yamasaki.
The Japanese are a progressive people, and especially are they ahead of the
rest of the world in the matter of the application of ferments to the prepa-
ration of vegetable food. In the soja bean they have, by preliminary treat-
ment, made available a nitrogenous and fatty food which largely answers the
purposes of animal food. We could learn many valuable lessons from them
on this subject.
Some Common Poisonous Plants. By V. K. Chestnut. Reprint from the
Year Book of the Department of Agriculture for 1896.
The following plants have been considered : Poison Ivy, and the other poi-
sonous members of the genus Rhus ; Cicuta maculata, or the American Water
Hemlock, and the Death Cup, Amanita phalloides ; some other members of the
Amanita family have also received attention. We are pleased to note that the
author not only considers the chemistry of the poisonous principle of poison
ivv settled, but he also recommends a remedy which in his hands has pro-
duced excellent results. He agrees with Pfaff that the active principle is a
fixed oil (toxicodendrol). Acting on this foundation he considers that alka-
lies render it inert, but he has more easily obtained this result by alcoholic
solution of lead acetate. The solution of sugar of lead in strong alcohol is,
on account of the solvent, too irritating ; therefore, he proposes a saturated
solution of the lead salt in 50 to 75 per cent, alcohol. "The milky fluid should
then be well rubbed into the affected skin, and the operation repeated several
times during the course of a few days. The itching is at once relieved and
further progress of the malady is checked. The remedy has been tried in a large
number of cases and has always proved successful."
We hope the author is right and that all the superstition and mystery which
have surrounded this plant for centuries have been dissipated forever; but before
committing ourselves too fully, we want to hear from some of the numerous
victims of the plant who can produce abundant evidence that they have been
poisoned by it without contact.
The report is written in a clear, concise style, free from technicalities, and
cannot but be of service to all those who will study it carefully. The author
will do well to continue his researches and reports on this subject.
Proceedings of the Florida State Pharmaceutical Association, at
its tenth annual meeting, held at Jacksonville, Florida, May 22, 23, 1896.
Although late in appearing, this issue indicates creditable work by the phar-
macists of Florida. Two papers were read with the following suggestive titles :
" New Facts vStaring Us in the Face," by H. L. Irwin ; and "The * Drug Busi-
ness' is a Very Interesting Profession, but a Very Poor Business," by S. P. Fries.
Both papers picture the demoralization caused by cutting of prices, and recom-
mend organization of a manufacturing company by the pharmacists of the
State.
sTptimb^r.'is^T?*} British Pharmaceutical Conference. 459
BRITISH PHARMACEUTICAL CONFERENCE.
The thirty-fourth annual meeting of the British Pharmaceutical Conference
was held at Glasgow, Scotland, August 9 to 11, 1S97. P'or the following
information concerning the proceedings, we are indebted \o\\\^ Pliarmaccutical
Journal and the Chemist and Druggist in their issues of August 14th.
The sessions of the Conference proper were begun with the official address of
welcome on the part of the city authorities. The president then referred to the
presence of Prof. J. P. Remington of Philadelphia, and Mr. Champion,
President of the Pharmaceutical Society of Natal, who were introduced and
asked to make some remarks.
r'ollowing this came the address of the President, Charles Synies, Ph.D. In
opening his address Dr. Syracs said that during the celebration of the Diamond
Jubilee of the Queen retrospective views had been taken of the growth and
progress of science, art, literature, professions and commerce, during her reign.
He said that "the tendency in the present rapidly progressive age is to rush
forward at a pace which leaves little opportunity for reflection, for looking
back on the experiences of the past and endeavoring to find therein some solu-
tion of the difficulties which beset us in the present, or suggestions to assist us
in developments for the future." He, therefore, felt that the occasion was one
on which an historical account of the association would harmonize with their
environment. The origin of the society, together with the objects had in view
by the founders, was first described, after which the salient features of the
annual addresses of all the presidents were presented as best showing the
progress made since its establishment, in 1863.
Having concluded this part of his address, the President then considered
some of the questions with which British pharmacists are concerned at the
present time. In the matter of education and examination he thought that the
standard for the preliminary or arts examination was too low, while that of the
minor or qualifying examination, which cannot be taken for five or six years
after the first, was too stringent, and that an intermediate examination in two
or three years after the preliminary would be an advantage.
The new forthcoming British Pharmacopoeia was referred to and the speaker
regretted that "pharmacists have not yet been accorded the position which
justice demands that they should possess as niembers of the Pharmacopa-ia
Committee. The Pharniacop<uMa is a pharmaceutical and not a medical work
and yet no pharmacist has any legal standing or position other than that
accorde<l by courtesy."
The speaker said that the Medicine Stamp Act appeared to be an impediment
to trade in some instances, while on the whole, he thought, it would be found
to l>e a friend in disguise. His attention had been directed to some of the evils
which would follow its repeal, could this be obtained, and the exemption clauses
in one of its provisions were looked upon by him as " a distinct recognition of
our calling as a responsible profession."
The Pharmacy Act of iS6ii was a disappointment in certain respects. As a
body, pharmacists were better educated, but the titles which they thought had
been so thoroughly and completely safeguarded, whilst denied to unqualified
individuals, could l)c used by stores with impunity.
Competition. ])irncy and the practice by physicians of accepting ready-made
^6o British PJiarmaceiitical Conference, {^i^pfember!!^™*
formulie introduced to them by the agents of advertising manufacturers, each
received a share of attention from the speaker, and in concluding his remarks
on this subject he said : "Meanwhile, it is not the duty of the pharmacist to
stand still and wait, not to devote his energy and ability to pharmaceutical
quackery, but by integrity, legitimate enterprise and earnest scientific work to
raise the standard of his calling and thus facilitate the acceptance by the medi-
cal profession of a state of things in which he will reap the reward of his labors,
and both professions will be accorded an enhanced amount of confidence and
respect by the public."
The presidential address occupied just one hour in its delivery, after which
was the reception of delegates, the reports of the Executive Committee and
Treasurer, and Unofficial Formulary Committee.
The preliminary exercises having been concluded, the reading and discussion
of papers next occupied the attention of the Conference.
The first paper presented was a
NOTE ON THE WORD "ASAFETIDA."
By John Attkield.
Having been called upon to give an authoritative opinion as to the correct
spelling of this word, the author consulted eminent philologists with the result
that both the Latin and English spelling of the word should be "asafetida."
FURTHER NOTE ON THE PHARMACY OF CONIUM MACULATUM
By E. H. Farr and R. Wright.
The question which the authors undertook to solve was whether the action of
a standard solution of conine or of the mixed alkaloids of conium was similar
to that of a standardized galenical preparation of the same alkaloidal value.
The following were prepared for making physiological tests : (i) a fluid
extract of dried, unripe fruits, standardized to contain 2*5 per cent, of total
alkaloidal hydrochlorides ; (2) a corresponding solution of the mixed alkaloids
of the same fruits of the same strength ; (3) succus fruct. conii assaying 07
per cent, total alkaloidal hydrochlorides ; (4) a solution of pure conine
hydrochloride; (5) solution of conhydrine hydrochloride; (6) solution of
pseudo-conhydrine hydrochloride.
These were reported on in the following paper :
PRELIMINARY NOTE ON THE ACTION OF CERTAIN PREPARATIONS
AND ACTIVE PRINCIPLES OF CONIUM MACULATUM.
By Wm. Findlay.
The author found that conine and the mixed alkaloids were the most toxic,
the lethal dose being, for conine, 37 milligrammes per kilo body-weight ; for the
mixed alkaloids, 39 milligrammes ; for conhydrine, not less than 257 milli-
grammes, and pseudo-conhydrine above that quantity. The results obtained
with the fluid extract were not sufficiently exact for tabulation, although it was
as active on frogs as conine. The succus could not be compared with the
other preparations owing to its low percentage of alkaloids.
vSOME OBSERVATIONS ON ORGANOTHERAPY.
By J. C. McWalter.
The writer referred to the serious symptoms which sometimes follow the
administration of the tablets prepared from various animal glands, and which,
'^pimberiS?"} British Pharmaceutical Conference. 461
he believed, were due to poisonous properties developed on exposure to air He
strongly coudemned this mode of administration, and suggested a preparation
made by dialysis of aglycerin (sterilized) extractof the fresh glands as probably
being the best.
FURTHER OBSERVATIONS ON COMMERCIAL OIL OF CITRONELLA.
Bv John C. I'mnev and R. S. Swinton.
The object had in view by the authors in this investigation was to determine
whether the differences observed to exist between native-distilled citronella oil
and that distilled by English firms were due to adulteration or to the mode of
distillation. Their work showed that the latter was the cause of these differ-
ences, and, in conclusion, they stated that the native-disiilled commercial oils
differ from those distilled by English firms iu containing a highly optically active
terpene, which raises the optical rotation, and a large percentage of sesquiter-
|>ene, which raises the specific gravity, the presence of which constituents
reduces the odor value and impairs the solubility in alcohol ; and that the
products of the English firms possess much greater odor value than most
native-distilled commercial oils.
THE PHARMACEUTICAL VALUE OF SUMATRA BENZOIN.
By Thomas Dcnlop.
The author examined a number of samples of commercial Sumatra benzoin
and drew the following conclusions from his results: (i) Sumatra benzoin
contained from 8 to 30 per cent, of barky and woody matter ; (2) the price
paid for the drug was no criterion of the quality ; (3) if this variety were to be
used pharmaceutically, it should be previously estimated, so that proper allow-
ance could be made for impurities ; (4) in the forthcoming British Pharmaco-
poeia more accurate statements should be made regarding the actual "char-
acters" and solubility of this drug.
NOTE ON SOLUBLE COMPOUNDS OF ARSENIC.
By G. G. Henderson.
The writer prepare<l several compounds similar in type to tartar emetic, but
containing arsenic instead of antimony. The sodium arsenio-tartrale was re-
commended as best adapted for medicinal purposes on account of its stability
and ready solubility. It can be ma<le by boiling 100 parts of arsenious acid
with 190 parts of acid sodium tartrate.
PHARMACEUTICAL ETHICS -A RETROSPECT.
By Lko Atkinson.
This paper embodied a consideration of the evils and annoyances which have
hampered the advancement of pharmaceutical practice ; but, in closing his re-
marks, the author took an optimistic view of the situation, and indicated meas-
ures whereby a healthier slate of affairs might be hoped to 1)C attained.
NOTE ON SVRUPUS lERRI QUININ.T-: ET STRYCHNIN.^-: PHOS-
PHATIS (EASTON'S SYRUP).
By R. Hrodik.
In this paper the writer proposed to modify the B.P.C. formula for this prep-
aration by substituting hydrochloride of quinine for the phosphate at present
462 British Pharmaceutical Conference, {^l^pimberfi™'
used. He did not consider the small amount of hj'drochloric acid thus intro-
duced as objectionable, and stated that most of the commercial syrups contain-
ing phosphates contain this acid in larger proportion.
HYPOPHOSPHITBS.
By Charles T. Tyrer.
The writer experimented with the tests of both the United States and British
Pharmacopoeias, and also with several unofficial methods. Those of the U.S. P.
were found to be more definite and satisfactory than those of the B.P., particu-
larly the qualitative tests. The permanganate method was not considered re-
liable, since hypophosphites invariably contained notable quantities of phos-
phate, phosphite, sulphite and hyposulphite, and these salts apparently an-
swered the B.P. test, the cause being that they either directly or indirectly
reduced the permanganate. Details of a volumetric method, which was said to
be very accurate, for estimating hypophosphites by reduction of copper sul-
phate, were described by the author. The odor of HgS, which is sometimes
developed by hypophosphorousacid and syrup of the hypophosphites, was at-
tributed to the use of charcoal as a filtering medium, the explanation being
that hypophosphorous acid cor-tains traces of sulphuric acid, which is decom-
posed by the charcoal forming SO 2, which is acted on by the hypophosphorous
acid, forming H2S.
MEDICINAL PETROLEUM.
By F. C. J. Bird.
The fact that the medicinal petroleum oils, when emulsionized with a pure
hypophosphite as one of the ingredients, developed a strong sulphuretted odor
led the author to believe that they contained sulphur in some form, and in
order to determine the extent of the impurity he examined a number of com-
mercial sample.'', and summarized his conclusions as follows : White petroleum
oil, having a specific gravity of about o"855, could be obtained more free from
taste and odor than lighter oils, but it was evident from the results that the
bulk of the white oil found in commerce, much of which was sold as chemi-
cally pure, contained a greater or less proportion of sulphur compounds.
White petroleum jelly was frequently a mixture of cerasine and white oil, and
partook of the impurities of the latter. Very pale jellies, which were true non-
crystalline petroleum residues, generally contained sulphur, probably due to an
analogous process of bleaching. Yellow oils, although generally free from
sulphur, were in many cases so tainted with a " paraffine " flavor as to
be unfit for internal use. The yellow petroleum jellies, as far as sulphur was
concerned, were the purest. Of the liquid petroleums, those from American
oil were free from sulphur compounds, while those from Russian oils all
contained these impurities. The presence of sulphur in the bleached products
was thought to l)e due to the use of sulphuric acid.
THE SALIENT FEATURES OF THE SCOTTISH FLORA.
By G. C. Druce.
This was an extempore lecture, and the speaker stated that the British flora
contained about i,8co species, between sixty and seventy of which were con-
fined to Scotland.
^septimb^ri^""} British Pharmaceuti.al Conference. 463
NOTE ON THE STRENGTH OF COMMERCIAL SAMPLES OF
ALKALOIDAL TINCTURES.
By Clarence A. Seyler.
Seven samples of the commercial tincture of nux vomica were examined,
and in no case did the alkaloid found reach the iheoreticpl amount, which is
0229 part of alkaloids per 100 volumes, and in several the amount was consider-
ably below this. Of eleven samples of tincture of opium, five gave about the
theoretical percentage (075 per cent, part of morphine per 100). and three
samples were considerably over the maximum strength possible with >tandard-
ized opium. Tincture of belladonna was very variable, two samples containing
only about one-half the proper amount of alkaloid. Three out of four samples
of tincture of hyoscyamus were stronger than the standard suggested for this
tincture. Tincture of aconite showed great variation. Samples of tincture
(compound) of cinchona showed most variation, one sample which was over
standard being nearly five times as strong as one having the lowest percentile
of alkaloid.
PHOSPHATES AND PLATINUM.
By W. G. Stratton.
In this note attention was called to the fact that when phosphates are heated
in a platinum vessel in the presence of carbon, the platinum fuses.
LIQUOR BISMUTHI ET AMMONII CITRATIS.
By \V. G. Stratton.
The question with the author was whether a variation in the composition of
the commercial solution was the cause of the varying results obtained when
this preparation was dispensed with an alkaline bicarbonate.
An excess of ammonium citrate was found in five of eleven samples exam-
ined by the writer, and as this salt is known to prevent the precipitation of
bismuth carbonate the examination furnished an affirmative answer to tlu-
question. Nitrates were found in some of the samples and one or two were
markedly deficient in bismuth.
DISINFECTANT SOAPS.
By S. Ridbal.
The writer said it must not be forgotten that soaps themselves have some
antiseptic power. An olein base W8S considered preferable to one containing pal-
mitic or stearic acid, since the latter gives insoluble precipitates wiih hot wi-ter.
Superfatted soaps were objectionable for disinfecting purposes, as fatty bodies
impede the action of many of the germicides. A number of disinfectants were
considered with reference to their usefulness or uselessness, as the case might
be, when employed in soaps. Many of the so-called disinfectant soaps were
found to have little or no value when subjected to bacteriological tests.
OUR PRESENT KNOWLEDGE OF THE MYDRIATIC GROUP.
By (Gordon Sharp.
This was a review of the various membersof the niydiiaiir group of alkaloi<U,
and in considering the sui)posed identity of beveral of lhe«e Ihe author huni-
marized his views by stating that ( 1) the names daluriue and duboisiue should
be given up; (2) the relationship of atropine and hyoscyaiuibe can hardly be
464 Internatioual Pharmaceutical Congress. { "V^ptember.^Te?
said to be clearly understood ; (3) hyosciue is like atropine in its action ; (4)
scopolamine could hardly lay claim to being a new base.
The consideration of papers having been brought to a close, after occupying
four sessions, the question of next year's meeting was brought up, and an invi-
tation to hold the conference in Belfast in 1898 was accepted.
The following ofl5cers were elected for the ensuing year :
President, Charles Symes ; Vice-Presidents, Walter Hills, J. Laidlaw Bwing,
J. C. C. Payne, W. F. Wells ; Treasurer, John Moss ; Honorable General Secre-
taries, W. A. H. Naylor, F. Ransom ; Honorable Local Secretary, R. W.
McKnight ; Assistant Secretary, J. C. Nightingale; other members of the
Executive Committee, F. C. J. Bird, H. Collier, J. C. Umney, J. Anderson Rus-
sell, Edmund White, R. Wright ; Auditor, D. W\ Elliot ; Editor of the " Year-
Book," Louis Siebold.
EIGHTH INTERNATIONAL PHARMACEUTICAL
CONGRESS.
The following account of the meeting of the above-named Congress has been
taken largely from the Pharmaceutical Journal of August 21, 1897 :
The Eighth International Pharmaceutical Congress, organized by the Asso-
ciation General Pharmaceutique de Belgique, was formally opened on Saturday,
August 14th, in the Conference Hall of the University of Brussels, under con-
ditions which promised great success, over 600 pharmacists from Belgium and
other countries having registered themselves as members.
The chair was taken at the inaugural meeting by M. De Bruyn, the Minister
of Agriculture and Hygiene, who was accompanied by several other Govern-
ment officials and the members of the Organizing Committee. M. Ranwez,
Professor at the University of Louvain, was elected President of the Congress,
and M. Duyk, General Secretarj^. The delegates from the countries repre-
sented at the Congress were elected Vice-Presidents.
On Monday, August i6th, the first paper was presented by Professor Ranwez
on "The Proportion of Active Principle in Drugs, etc." This was in answer to
the query : " Is it not desirable in the present condition of scientific knowledge
to insist on the presence of a normal proportion of active principle in a pre-
paration ?" and, after a general review of the subject by the author, he con-
cluded by offering the following resolution : •' That the competent authorities
should require a uniform percentage of active or important principles in medi-
cinal preparations." This resolution called forth considerable discussion, /rt*
and C07i; but after the addition of the words "as far as possible," proposed by
M. Petit, delegate from France, it was adopted by a large majority.
The next paper submitted was a " Report on New Medicaments," by F. E.
Fayn, of Antwerp.
The author pointed out that the introduction of new chemical and animal
products of late years has been attended with many inconveniences, and has
placed the reputation of pharmaciens in a somewhat awkward position. Many
of the products are monopolies, and are issued under names that give no clue to
their chemical constitution. At the time they are introduced to the medical
profession there* is not sufficient information published concerning them to
■^ptembeJ!^!™'} International Pharmaceutical Congress, 465
enable thepharmacien to ascertain their strength or purity, whilst they actually
vary both in strength and purity in commercial samples bearing the same label.
He suggested, therefore, for the protection of the public, and for the safeguard-
ing of the reputation of the prescriber and dispenser, that there should be espe-
cial depots for new remedies established by pharmacists at certain centres ; that
the specially distinctive reactions of each new remedy should be published on
the label as well as in the brochure relating to the remedy ; that laboratories
should be established by pharmaciens in certain centres for the analysis of new-
remedies ; that a permanent committee for the study of new medicinal pro-
ducts should be established, the members of which should be selected by differ-
ent Governments from the members of the academies of medicine or pharma-
copceia committees ; that there should be an official verification of serums and
various glandular juices, etc. ; that the nomenclature of new medicaments
should be revised ; that there should be an annual supplement to the Pharma-
copoeia published in every country. These suggestions were offered to the
Congress for universal application, and in the discussion which followed, a reso-
lution, " that trade-mark property should not be created in medicaments," was
offered by M. Petit, and adopted by the Congress.
The discussion of Mr. Fayu's paper was resumed on Tuesday, and a resolution
to the effect that the chief pharmaceutical associations in each country should
be recommended to appoint authorized committees to carry out the work sug-
gested by the author, was also adopted.
In Section I the consideration of the subject of specialties was again taken
up. The first paper read was by Professor Remington, of Philadelphia, on
" Phamiacopoeial Revision ; Its Influence on the Relations of Pharmacists and
Physicians." The author especially advocated the endeavor to differentiate the
practice of pharmacy and that of medicine as being the most effectual means
of promoting the true intetests of pharmacy and of those engaged in its prac-
tice. On the basis of progress made in that direction by securing the respect
and co-operation of the best members of the medical profession, the jiractice of
pharmacy would attain a position more compatible with the professional nature
of the duties its followers have to perform, and they would be likely to find
themselves acknowledged as welcome co-c)])crat(irs in the work of pharmaco-
poeia revision.
Mr. Wren, Professor Tichborne and Dr. McWalter made some remarks, and
Mr. W'ootton posed as the advocate of secret remedies, supporting his argu-
ment by reference to the tradition that the only remedy from which the late
Lord Beaconsfield could obtain relief was a secret preparation. On that
ground he contended that the Congress would, in his opinion, be allow:: 1
to outrun discretion if it gave its sanction to a recommendation that 1;
men should abstain from prescribing secret remedies, and when the purport of
his remarks l)ecame known to the meeting by translation into the French lan-
guage, considerable amusement was evinced.
In replying to the several speakers, Professor Remington said he would con-
fine himself to the expression of his opinion that whatever might be Mr. Woot-
ton's faith in the virtues of secret remedies, it was important for the interests
of pharmacy throughout the world to place on record an enunciation of the prin-
ciple that if any progress was to be made, it was above all indispensable to get
away from secrecy in the preparation of medicines. To adduce the use of an
466 International Pharmaceutical Congress. {^s^pfembe^^T9^*
asthma cure by the distinguished statesman who had been mentioned, as a
ground for the prescription of secret remedies by physicians, was, he thought,
entirely illogical, for it might, with equal reason, be inferred that Lord Beacons-
field's death was due to his having taken the medicine referred to by Mr.
Wootton.
The following resolutions were carried by acclamation :
(I ) That efforts should be made to obtain larger representation of pharma-
cists in pharmacopoeia revision, including professional teachers, as well as
pharmacists in practice ; and (2) that local pharmaceutical associations should
co-operate with medical societies with the object of suppressing quackery and
the use of secret remedies.
The most interesting items in the later programmes included a comparison of
pharmaceutical legislation in different countries, by M. Idiers ; the advantages
and disadvantages of admitting women to practice pharmacy, by M. Georges
Detlian ; several papers on a universal pharmacopoeia ; and a consideration of
the appointment of a board of reference, by M. Huart. Most important of all
was the presentation of the following report :
REPORT OF THE CHICAGO COMMITTEE — PHARMACOPCEIA OF POTENT REME-
DIES.
The committee reports that progress has been made, and it is now in corre-
spondence with representatives of various nations relative to the appointment
of members of the permanent commission in these countries. The illness of
our distinguished confrere, Herr von Waldheim, of Vienna, has prevented the
presentation of a full report at this time. The delays produced by the widely-
separated locations of the correspondents in the various nations has added
greatly to the difficulties, but the committee expects to complete the work as
soon as possible. The resolutions adopted by the Seventh International Con-
gress, under which the permanent committee derives its authority, are as fol-
lows :
" Resolved^ That the Seventh International Congress appoint a committee of three, of which
the President ( Professor Remington) shall be chairman, the duty of which committee shall be
to take the necessary steps for the appointment of an International Pharmacopoeia Commission
to compile, publish and distribute an international pharmacopcjeia of potent remedies. The
International Pharmacopceial Commission shallconsistof one member from each country rep-
resented at this Congress (Chicago), and from other countries as the committee of three may
decide, the members of the Commission to be selected by the Pharmacopceia Committee of
the various countries, or to be otherwise chosen if necessary. The committee of three shall
be a permanent committee, and it shall be its duty to urge and expedite the work in every
proper way, and in the event of the death or resignation of any member of this committee of
three, the vacancy shall be filled by the other members.
*' Rrsolved, That the Congress (Chicago) accepts with thanks the proffer, by the American
Pharmaceutical Association, of the sum of $1,000 to help defray the expense of compiling,
publishing and distributing an international pharmacopoeia of potent remedies."
Respectfully submitted,
(Signed) Joseph P. Remington, Philadelphia,
MiCHAEi* Carteighe, lyondon.
August 16, 1897. Anton Von Wai^dheim, Vienna.
'B?ptimber.*i8ff7"} A?nerican Pharmaceutical Association. 467
AMERICAN PHARMACEUTICAL ASSOCIATION.
The forty-fifth annual meeting of the American Pharmaceutical Association con-
vened at Lake Minnetonka,|Minn., on Tuesday, August 24, 1897. A very cordial
reception was tendered the visiting members of the Association en route via Chi-
cago, by the Chicago Retail Druggists' Association and the Chicago Apothecaries'
Society, at the Great Northern Hotel, Chicago, on Monday, August 23, 1S97.
Luncheon was served, and after it had been partaken of, a tally-ho ride to South
Park, World's Fair site, and thence to the special train, which had been
arranged for by the Chicago members, was extended. Hotel Lafayette was the
headquarters of the Association at Lake Minnetonka. The council of the body
met at 11 a.m., on Tuesday, August 24th. At 3.25 p.m., the same day. President
Joseph v.. Morrison called the first general session to order, and introduced Sen-
ator C. K. Davis, who welcomed the visitors to the hospitality of the good people
of Minnesota and the " Twin Cities." Following him. Prof. F. J. Wulliug bade
the Association welcome on behalf of the Minnesota Pharmaceutical Associa-
tion, which had just closed its meeting on the previous morning. The members
were then extended a welcome to Minnetonka Beach, bj* its Ma3or, Mr. J. C.
Eliel. The Chair then asked Prof. Good to reply to the courtesies of the pre-
vious speakers, which he did in very expressive terms of appreciation. First
Vice-President Geo. Y. Payne was then called to the chair, while the President
read his address, which was as follows :
Ladies and Gentlemen :
For the first time in our history we meet within the confines of what may be called the
NoTthwcstem States. After going all over this vast country and into Canada, we have come
here to admire the natural wonders and beauties of this section, and to make more extended
acquaintances among our brethren. When our Minnesota brothers, a year ago, came to our
meeting and extended an invitation to us to convene "in the land of the Decotahs, where the
Falls of Minnehaha flash and gleam among the oak trees, laugh and leap into the valley," it
was gladly accepted, and we h«ve since then been living in anticipation of seeing and hearing
the water as it tumbles over the far-famed Falls of Minnehaha, and of gazing ufKan the beauties
of Lake Minnetonka, a gem set by the hands of the Almighty in the midst of this fair land ;
nor have we been disappointed; although we had been prepared for beautiful sights, the reali-
zation exceeded the anticipation, and one glance from the shores of this lake has repaid us for
the toil of our journey.
However, we do not come here to indulge in poetic flights of fancy, but to di.ncu.ss the hard
matter-of-fact interests of to day, an undertaking devoid of any tendency towards poetic
license. Unfortunately, we pharmacists l\pve not much time to cultivate the muses, as our
attention is too closely concentred on the grosser things of material earth, so we will dis-
mount from our Pegasus and stand on solid ground.
Your President was a.sked by the State Department to name delegates to represent the
I'nited States at the Dru».sels International Pharmaceutical Congress, and in accordance
therewith I named Prof. J. P. Remington and Mr. Louis Dohme as such, and Mr. Alfred
Myers, of New Orleans, and Dr. P. B. Power, now of London, Kngland, as alternates.
The reports of the variou? committees will show that the work of the Atsociation has t>een
carried on with the same enthusiasm and generally successful results as heretofore.
I desire, however, to draw attention to the very effective work done by the Committee on
National Legislation, especially as regards tax-free alcohol, which requires eternal vigilance
on the part of the committee to guard against attacks from unexpectetl quarters, as evidenced
by the proposal made in the Senate to tax wood alcohol, which, if succensful, would have had
serious results. Happily, the secretary of the committee. Mr. \. K. Kbert, Is one of those who
Is alwayii on guard and never sleeps at his post, so that as soon as the proposition was made,
Mr. Et>ert immediately telegraphed to over eighty of the Senators, protesting in the name of
this Association against any such taxation ; and we think we are justified in claiming that Mr.
Kbert' s prompt and energetic action was the main cause of the rejection of Senator Lindsay's
motion.
468 American Pharmaceutical Association, {^s?pf?mbe^^Y9™•
The first question which I desire to take up is that of membership. For several years past
our numbers have fluctuated between 1,500 and 2,000. The last report of the Membership
Committee showed that we had 1,800 enrolled in this Association, At the same time, the
Secretary of the Section on Legislation and Education, in his report, stated that there were
51,000 druggists in the United States and 2,000 in Canada, making a total of 53,000 from which
we can draw for our members. The discrepancy thus revealed between our membership and
the total number of pharmacists is indeed very striking ; and, even admitting that 53,000
represents good, bad and indifferent, and perhaps many who would or should not be deemed
desirable to be had as members, there still remains a great field for earnest work in the direc-
tion of recruiting our ranks. Five thousand is a moderate estimate to make of what our num.
bers should be before we can become, as has been suggested, a delegate organization, such as
the American Medical Association, or before we can hope to wield the influence to which our
organization is entitled by reason of the high objects which it has in view
The securing of new members is a matter which has heretofore been left solely and entirely
in the hands of the committee charged wilh this work. That committee has been unremitting
in its efforts, and I know that the chairman and members of the Auxiliary Committee have
rendered yeoman service. While, however, expressing my appreciation of the valuable work
done by these gentlemen, I will avail myself of the opportunity offered to state that on the
part of the members at large, more could and should be done towards increasing our member-
ship. Every member of the Association should constitute himself an auxiliary member of the
Auxiliary Committee, and should take advantage of every occasion which presents itself for
setting forth the benefits to be derived from this Association, or enlisting the sympathy and
active interest of fellow-pharmacists in this Association.
It has been brought to my notice that many valuable papers are presented at the annual
meetings of the State associations by members of this body, and that these papers would be
presented at our meetings if the State associations were not in existence. Among these
papers are to be found many worthy of a wide circulation, and of beiug preserved in more
permanent form than that offered by the usual volume of State association proceedings. I
would, therefore, suggest that an arrangement be entered into with the State associations by
which we would be permitted to publish these papers in our Proceedings, subject to the
approval of our Committee on Publication. We would thus secure what is best and most
worthy of preservation among these papers, and also make our Annual Proceedings a more
complete record of pharmacal progress in this countr}'.
The Treasurer's report will contain a statement of the number of members who have been
delinquent in the payment of their fees, and who will be dropped from the rolls. The num-
ber of delinquents has been increasing of late years, and it is not difficult to assign the prin-
cipal reason for this .state of affairs. It is due simply to the changed and changing conditions
of pharmacy. The pharmacist, originally a manufacturer, and a combination of chemist, bot-
anist and merchant, has allowed the last-mentioned component to greatly overshadow the
others, and has become almost entirely a dealer in patent medicines, toilet articles, soda water
and drugs. The laboratory is not to be found in connection with modern pharmacy. Every-
thing that should be made is bought from the wholesaler or manufacturer. Pharmacy as a
profession is apparently a thing of the past, and is now but a trade or mercantile pursuit. But
I believe that we are now going through one of the transition stages in the process of evolu-
tion which governs all things, and that we will find our present troubles to have been a fire of
purification in preparation for a new era, in which pharmacy will be differentiated into a pro-
fession and a trade. We see evidence of this in the pharmacal journals and the colleges. We
find the former devoting a large amount of their space to the matter of advertising and other
strictly commercial topics, showing that the mercantile feature is rapidly developing. On
the other hand, we find that the colleges are increasing the number and length of their
courses. Subjects which some years ago were thought unnecessary or useless are now
included in their curricula, and pharmacy by them is regarded as a profession alone.
Can the average individual put into practice his college instruction in chemistry, phar-
macy, pharmacognosy, microscopy, etc., and at the same time look sharply after the buying
and selling of the thousand and one items which go to make up the stock of the modern phar-
macy? Impossible, And a change must come and we must prepare for it. If we desire to
follow pharmacy as a trade, we must adopt the methods of other trades. We must buy in the
cheapest market, sell as cheaply as our neighbors, use printer's ink on every possible occa.
sion and in every po.ssible way, and, in a word, spare no effort to increase our trade.
But then we must be prepared to stand the fierce fire of commercial competition, and can-
not claim, because we are druggists, any more protection than that given other merchants.
^piimber'^isyT" } American Pharmaceutical Association. 469
As it is now. we have gone outside of our own territon,- and invaded that of every other trade,
and added their goods to our stock under the name of " side lines."
Remedies innumerable have been proposed for the present depressed condition of phar-
macy. You cannot control commerce : trade will seek its own channels in spite of laws or
obstacles ; and, as far as I can see, there is only one way out, that is to return to pharmacy
proper ; devote more attention to the laboratory, cultivate more corlial feelings with the
medical profession and strive for higher ideals The higher the standard we set up, and the
closer we approach to it, the greater will be the esteem in which we will be held by the
public.
One of the first requisites for the elevation of the profession is more stringent pharmacv
laws, and more especially as regards examinations. In this connection I would s^y that the
Section on Legislation and Education will present for our consideration a model pharmacy
law.
Now I wish to draw attention to what I consider a fault in all American pharmacal legisla-
tion. As far as education is concerned, they all begin at the wrong end. By this I mean
that no supervision is exercised over students or apprentices in drug stores. It is the almost
universal custom to take any boy applying for a position without any examination as to his
mental equipment and general fitness for the profession : and if he does his work reasonably
well, he is promoted from errand boy to clerk, and then to dispenser, and after three or four
years' service he commences to prepare for his examination, in which, by means of quiz com-
pends and other cramming de\'ices, he succeeds. Of course there are exceptions ; but I
believe tnat the number of college graduates is out of proportion to the number of young men
employed in drug stores. If pharmacy is to become a profession, we must commence with
the beginners. We must have a class of men who have acquired a .sound foundation upon
which to erect the composite structure which we call the science of pharmacy. If the law
recognized a class of app-entices and compelled all desiring to study pharmacy to pass an
examination in such subjects as arithmetic, history, geography, elementary algebra, and one
modern language besides English, either German or French, before a board named by the
Board of Pharmacy, and consisting of two or more well known high-school teachers, a super-
ior class of young men would be attracted to the study of pharmacy proper, who would almost
invariably become college graduates, and would aim at becoming proficient pharmacists
rather than merely passing the board examination. This requirement would also lessen the
number of clerks and pharmacists and decrease competition, which is one of the greatest e\'il8
of the present system.
The delegation to the American Medical Association will bring before you for consideration
a most important question, viz.: Will Spiritus Frumenti and Spiritus Vini Gallici be retained
in the next revision of the Pharmacopoeia? There is no necessity for my dilating on the evil*
of the liquor traffic, and the incalculable amount of injury it has done to American pharmacy.
The pharmacists of the United States are at present in a peculiar position: for just as long as
liquors are sold in pharmacies, even if only on presciptions, will we be in the eyes of the
Government on the same footing as saloon keepers. It is time that this condition of things
be terminated by the complete abolition of every form of dealing in fermented or spirituous
liquors. A great advance in that direction will have been taken when it will be decided to
delete all such preparations from thePharmacopicia. For my part, I believe that the sale of
liquors by pharmacists is unnecessary, and is simply a result of a bad habit into which we
have allowed the public to fall. In the Province of (Quebec, pharmacists do not deal in liquors.
The physician, when desirous of prescribing stimulants, invariably sends his patient to the
grocer; and in all my experience of twenty years ns a retail i)hannaci.st. I do not believe I
have had to sell a quart of liquor, except dining the time I was employed in this country. I
am not a temperance crank, but I l>eli^ve that the sale of liquor is degrading to the prufe.ssion
of pharmacy, and is an unmitigated evil. The only excuse which I have heard advanced for
the retention of this class of preparations in the Pharmacop<iria is that we have a standard by
which to test our goods. Now. let us examine the reliability of this ktandard Under "Spiritus
Frumenti," we find the Pharmacop<ria says : ' Its specific gr.tvity should not l»e more than
0*930 nor less than 0*917, corresponding approximately to an alcoholic strength of 4S to 5,0 |>er
cent, by weight, or 50 to .s** per cent, by volume"— a rather wide mnrgin AntI Is the test for
impuriiicK any more reliable? Under" Spiritus ViniGallici " we find thai " It»i*|>ecihc gravity
should not be more thano'cMi nor le.ssthan o 935, corresponding, approximately, to an alcoholic
strength of 39 to 47 per cent, by weight, or 46 to 55 per cent, by volume." The tests for fusel
oil, etc., are not more definite than under "Spiritus Frummti." An examiuation of the
tests for wines will show that they are not more definite. Admitting that the tests are suffi.
470 American Pharmaceutical Association. {^^^^it^\,S^im:
cientlv exact, I would like to ask, how mauy pharmacists test their liquor purchases to see if
they an>5\ver the requirements of the Pharmacopoeia? Furthermore, of what benefit is the
standard to us, when the price we have to pay for it is the levelling of the profession of phar-
macy, in the eyes of the Government and of the public, to that of the saloon-keeper ? The
price is too great to compensate for any imaginary or even possible or probable advantage.
I have only touched upon one phase of the question. The therapeutical aspect is one out-
side of our province.
Another important question which we should take up is that of patented medicinal com-
pounds. During the past ten or twelve years a number of organic compounds, principally of
German origin, have been patented and introduced into this country. One peculiarity of
these goods is the very high price charged here in comparison with that ruling elsewhere. I
give a comparative statement of prices which obtain in the United States and Canada :
U. S. A, Canada.
Phenacetine $i-oc ;^o.35
Sulphonal 1-35 .3°
Trional 1.50 i.oo
Chloralamid 90 .35
Antipyrine 1-40 1. 10
Now, why should the people of the United States be compelled to pay such exorbitant
rates as are shown here ? It is simply due to the patent laws of this country, which allow
a patentee to cover everything within his reach. Patent laws are avowedly designed for the
encouragement of inventive genius, by guaranteeing to an inventor an adequate return for the
trouble and study required for the invention of new appliances, new methods, etc., and it is
as much to the United States patent laws as to any other cause that this country owes its
proud pre-eminence in the manufacturing world.
In the matter now under consideration, I venture to say that such a contingency was never
foreseen by the framers of the law. Nor do I think it was ever intended that the law should have
any such results as have come from itsapplication to the invention or discovery of new remedial
agents. One of the objects of the law was the encouragement of inventive genius. Has it
operated in this case? No. For net a single new synthetic compound has been discovered
and brought to completion in this country since the flood of synthetics first began to pour into
the United States. The only result has been the enriching of the few at the cost of the whole
countrj', and, as a matter of fact, the American people have been paying foreigners millions
annually for taking advantage of the privileges granted by the United States patent laws.
Looked at in any light, except in that of the German patentee and his American represen-
tative, this position of affairs is intolerable ; and it is for us to draw the attention of the legisla-
tors of this country to the gross iniquity perpetrated upon the sick. Germany is the home of
these preparations, but an examination of the German patent laws shows that such prepara-
tions as those we speak of cannot be patented. The patent law of April 7, 1891, says :
" Discoveries of food-stuff or medicinal preparations, or bodies which maybe prepared by a
chemical method, cannot be patented, but that the method of preparation of these objects
may be."
Now, if German manufacturers cannot patent their products in their own country, why
should they be allowed to do so in this ?
Turning to France, we find the law of July 5, 1844, which is still in force, says :
" May not be patented : first, pharmaceutical compounds or remedies of every sort, these
articles remaining subject to the special laws and regulations on this subject, and particularly
to the law of August 18, iSio, relative to secret remedies."
Again we find in a recent report of the commission appointed by the French Minister of
Public Instruction, to prepare a new Pharmacy Act, that they propose the following clause to
be added to Article 9, which sets out that none but pharmacists shall sell remedies, either com-
pound or simple, used in human or veterinary medicines.
"These remedies and their method of preparation cannot be made the subjects of a patent.
Their scientific or commercial names fall into the public domain, and cannot become private
property, nor constitute in themselves a trade mark. Secret remedies remain prohibited."
These quotations require no comment.
If the patentees of these remedies were satisfied with a reasonable profit, we might not
complain. It may be claimed that the great expense of advertising and introducing these
preparations necessitates high prices ; but does it cost more to advertise these goods in this
country than it does in Germany or Eugland or Canada, where the prices are so much lower ?
^s^piemb^r.'iawr!'' ; American Pharmaceutical Association. 471
And is it not a fact that most of the advertising is free? Do we not see, month after month,
-communications in the medical press on the action of the new synthetics in certain affections?
This is the most effective kind of advertising, and it is impossible to imagine that the journals
in which these articles appear would receive pay for their publication. There is no reason for
the high prices charged for these goods, but the knowledge of the patentees that with the
process and product patented and the name copyrighted, they have an absolute monopoly,
and can charge j ust what they please. What we want is that the patent laws be changed on
the lines of German laws, which, while safely guarding the public from extortion, give ample
protection to the patentee. We should demand that products used in medicine should not be
patented, and that the names by which they are known in commerce should not be copy-
righted.
On this subject a resolution was presented and adopted at the last convenliou, but it did
not go far enough. I would therefore suggest that although this work would be within the
province of the Committee on National Legislation, a special committee, composed of one
member from each State and Territory and all members residing in the District of Columbia,
be appointed to undertake and carry on an agitation for the amendment of the United States
patent laws on the lines already indicated.
I would also suggest that our delegation to the American Medical Association be instructed
to bring this matter before the next convention and secure the tndorsation of that body ; that
we also secure the co operation of all the State associations through their delegates present at
this convention, and, in fa^f, employ every legitimate means to accomplish our object.
The address was received and referred to a committee composed of Messrs.
Ebert, Thompion and Whelpley, appointed by Vice-President Payne.
President Morrison then resumed the chair, and Secretary Caspari called for
the reports of the various standing and special committees. These were ready.
The selection of the Nominating Committee to elect the officers for the ensuing
year was the next business in order, and a recess of five minutes was granted
by the President in order to afford the members from the various States, Terri-
tories and Provinces an opportunity to choose their representatives. At the
end of this time the meeting was again called to order. Secretary Caspari then
called the roll for the names of the nominators. Responses were had from
Arkansas, Colorado, District of Columbia, Georgia, Illinois, Indiana, Indian
Territory, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts,
Michigan, Maine, Missouri, Nebraska, New Jersey, New York, North Carolina,
Ohio, Pennsylvania, Rhode Island, South Dakota, Texas, Virginia and Prov-
inces of Manitoba and Quebec. In addition to those representing these sec-
tions, the President appointed at large Messrs. Ivbert, Tilden, Good, Prost and
Main as members of the Nominating Committee. The committee decided to
meet immediately after the adjournment of the session. Secretary Kennedy
then read the minutes of the meeting of the Council. These comprised the
various motions which had been made in the body, and statements of such
measures as had been adopted during the past year, as well ascertain proposed
changes in by-laws. The minutes also dealt with a proposition to reinstate Mr.
Frederick Stearns to membership in the Association, from which he had been
previously expelled. The correspon<lence connected with this matter follows
here in full :
Chicago. Auj^i:-'; - , 1897.
Mr a. K. Kbbbt, City.
Dear .\fr. I'.bfrt : — \ have the pleasure to send you « letter received from Mr. Strarniin rejvly
to one from myself to him, in relation to the proposition made by several of his olil friends,
to bring al>out a reinstatement of Mr. Stearns os a member of the American Pharmaceutical
Association. You will observe he takes a very manly position, and one that can hardly fail to
create a kind feeling toward him In those who do not know him. and a feeling of respect and
confidence by the old friends who know him well. The many years which have pasaed since
472 American Pharmaceutical Association. { 's^^pfember^s™'
the event of his severance from the American Pharmaceutical Association have no doubt
caused most members to forget the cause of it, and there is little reason for reviving the his-
tory- of it now; to me it is sufficient that a former member and a gentleman has seen the error
of his hasty decision, and is willing to stand upon his more recent record for vindication of
his character and motives.
As I cannot be present at the meeting of the American Pharmaceutical Association, I would
be glad if you will present the matter to the council for their approval, and trust that our
action may be viewed favorably and receive endorsement, to the end that a worthy man may
be relieved from the odium which attaches to dismissal from membership, when he confesses
and repents of his hasty action of long ago.
Sincerely yours, E. H. SARGENT.
Mr. Stearns' reply was as follows :
Detroit, Mich., August 13, 1897.
Mr. E. H, Sargent, Chicago, 111.
Dear Sir :—\o\\r kind letter of August 7th, in which you ask my feelings and sentiments
regarding the action of the American Pharmaceutical Association in depriving me of member-
ship, as a penalty for the violation of its code of ethics, nearly thirty years ago, and your
expression of desire— having been its presiding officer at that time— to take some action now,
with a view to my reinstatement to fellowship if possible, comes to me as a pleasant and grate-
ful surprise.
The error for which I have borne the penalty for so many years would never have been
committed in the light of maturer experience and reflection, and I have accepted the verdic^
of my peers, realizing that it was just, though, perhaps, unduly severe.
I have suffered banishment from fellowship with friends and members of the Associa-
tion for nearly thirty years, depriving myself of their friendship and esteem, because I did
not take time to consider the far-reaching effects of not bowing to the will of the Association
at the time.
This I now sincerely regret ; therefore, while I have never asked to be reinstated, and
would not urge it now, yet I would gladly receive such treatment from the Association as
would show that my business career since that time justifies it in taking the action you are to
propose. Sincerely yours, FREDERICK STEARNS.
The minutes were approved as read.
Secretary Kennedy then read the names of eighty-one applicants for mem-
bership, and they were invited to become members. After this, President Mor-
rison appointed a Committee on Time and Place of Next Meeting, consisting
of Messrs. Sheppard, Dohme, Kuhn, Miller and Jacobs. This committee met
in the council chamber, after the adjournment of the Nominating Committee,
and the invitations which had been received from Richmond, Omaha, Baltimore
and Texas to hold the meeting of 1898 in these respective places, were referred
to it.
Secretary Caspari also read a communication from the Minnesota Pharma-
ceutical Association, which embodied a resolution against the present copy-
right laws, and also a proposition that a bill be drafted to revise these laws, as
they apply to certain well-known chemicals. This communication was received
and referred to the Committee on National Legislation. This was followed by
a communication from the Proprietors' Section of the National Wholesale
Druggists' Association, which was referred to the Commercial Section. A com-
munication from the chairman of the delegates to the American Medical Asso-
ciation was referred to Council.
Two communications from the national delegates to the Brussels meeting of
the International Pharmaceutical Congress were then read. A letter signed by
a dozen or more military pharmacists was next read. It expressed appreciation
of the work that has been done by the Association toward improving the status
of the apothecaries in the Government service.
^8ei>tembe^!'m7! } American Pharviaceutkal Association. 473
After this, Professor Whelpley offered a motion resolving that the mem-
bers of the Association be requested to use the metric system of weights and
measures in all the business of the Association, and in papers, reports, circulars
and communications presented to the Association.
After some discussion this was adopted. The session then adjourned until the
following morning. In the evening a reception and promenade concert, fol-
lowed by informal dancing, was tendered the visitors by the members of the
Minnesota Pharmaceutical Association. The events of the evening were much
enjo^'ed by all.
SECOND GENERAL SESSION.
The second general session convened at 10.27 a.m., Wednesday, August 25th,
with President Morrison in the chair. Secretary Caspari read the minutes of
the first general session. These were adopted as read.
The minutes of Council were then read by Secretary of Council Kennedy,
who spoke of the acknowledgment by Mr. Stearns of his error, and stated
that as the Council saw no obstacle in the way, he was reinstated to
membership. Twenty-two new applicants for membership were reported.
The minutes also stated that Professor Oldberg had reported that the Proceed-
ings of the Seventh International Pharmaceutical Congress, held in Chicago in
1893, were ready, and that the price had been fixed at 50 cents per volume. The
minutes were approved.
Secretary Payne, of the Nominating Committee, reported the following
ticket as the choice of the committee for the officers of the Association for the
ensuing year :
President, H. M. Whitney, Lawrence, Mass. ; First Vice-President, Geo. C.
Bartells, Camp Point, 111. ; Second V^ice-President, W. S. Thompson, Wash-
ington, D. C. ; Third Vice-President, J. A. Miller, Harrisburg, Pa.; Treas-
urer, S. A. D. Sheppard, Boston, Mass. ; General Secretary, Chas. Caspari, Jr.,
Baltimore, Md. ; Reporter on Progress of Pharmacy, C. Lewis Diehl, Louis-
ville, Ky. ; Members of Council for three years, W. A. Frost, C. A. Mayo
and Geo. F. Payne.
The report was received, and the Secretary was asked to cast an affirmative
ballot for the nominee for the presidency. This was followed by similar ballots
for the remaining nominees.
Secretary Caspari then announced that he liad received the credentials of
delegates from a number of State and local associations, colleges of pharmacy,
alumni associations and other bodies. On motion, these were received by the
Association.
Chairman Dohme, of the Finance Committee, reported fair prospects for the
betterment of the Association's finances.
Secretary Kennedy, of the Committee on Membership, presented his twenty-
third annual report. Of the 1 14 persons proposed for membership at the Mon-
treal meeting last year, 91, or about 80 per cent., had completed their member-
ship, and have their names on the roll as active nRinl)er8. The percentage of
those who were proposed anil invited to l>ecome n»enjl)ers, and who finally
completed their meml)ership, was much larger this year than last, and was a
little above the average of former years. The new meml»ers represented nearly
Jill sections of our country. They are credited to twenly-eighl States, the D»-
4/4 Avierican Pharmaceutical Association. { ^s'^p£"ber.^i89?*
trict of Columbia, Canada, East Africa, aud Paris, France. Every State and
Territory is now represented by membership in the Association. Mr. Kennedy
also said: "The Treasurer, Mr. S. A. D. Sheppard, reports that on July i,
1897, 241 delinquents of three or more years, were liable to be dropped from the
roll. This is a very large number, being an increase of thirty-two over the
number reported last year, when the secretary of membership made a state-
ment that the number reported on then was the largest since he has filled the
office." He also called the attention of the meeting to the excellent work
which has been performed by W. H. Huntington, apothecary of the United
States Navy, at Newport, Rhode Island, and a member of the Association, who
had secured the consent and annual fee in advance, and had endorsed forty-one
of the apothecaries of the army, navy and marine hospital service of the United
States. The following tabulated statement of membership was then read :
Active or contributing members in good standing at last report 1,448
Members elected since last report 91
Total 1,539
IvOSS IN MKMBERSHIP (active).
By resignation 35
By transfer to life membership 13
By death • • • 30
Dropped from roll for various causes . 67
Total loss 145
Number on the roll at this report i>394
I,IFE MEMBERSHIP.
Number on the roll at last report 95
Number added since last report 13
Total 108
I.OSS IN I,IFE MEMBERSHIP.
By death
Number on the roll at this report 102
HONORARY MEMBERSHIP.
Number on the roll at last report 15
Loss by death 2
Number on the roll at this report 13
TOTAI, MEMBERSHIP.
Active or contributing members 1.394
Life members 102
Honorary members 13
Total 1,509
The Secretary also reported that the mortuary record, which numbered
twenty-nine deaths, was the largest that he had yet been called upon to report.
'^ptimbe^.^issT!'} Afftericati Pharmaceutical Association. 475
Appended to his report was a memorial sketch of each of the deceased mem-
bers. The report was referred to the Committee on Publication. Secretary
Whelpley, of the Auxiliary Committee on Membership, made a motion to
extend the thanks of the Association to the Presidents of the State Associations
and to Mr. Huntington for their interest in the effort to increase the member-
ship. Prof. C. Lewis Diehl read the introduction to his Report on the Progress
of Pharmacy. The report was received and referred to the Committee on
Publication. The report of the Committee on Revision of the United vStates
Pharmacopreia was called for and read by title, but was referred to the Scien-
tific Section for reading in full and discussion. Treasurer Sheppard then
read his report, and stated that the cash balance in the treasury this year was
nearly double what it was last year. He suggested, in view of the depressed
condition of business, that the resignations of the delinquent members be
received instead of dropping them for non-payment of dues. The Auditing
Committee found the report to be correct, and it was received, and a vote of
thanks was tendered the Treasurer by the Association.
The General Secretary then read his report, which dealt with the financial
accounts in his hands, and the publication of the National Formulary. He
reported a handsome balance on hand from the sale of the National Formulary.
It was ordered that the report take the usual course. The Committee on Publi-
cation reported on last year's volume of Proceedings, and also on the stock
of the Proceedings on hand. The report was received.
Mr. Ebert moved that the General Secretary be authorized to bring to the
annual meetings a number of unbound copies of the Constitution and By-Laws,
and of lists of officers, members, places of meeting, etc., for the use of
members in attendance. Secretary Caspari then read the report of the Com-
mittee on General Prizes for pajjers presented at the meeting in Montreal.
The first prize was awarded to J. W, T. Knox and A li. Prescott, for their paper
on "The Caffeine Compound in Kola ;" the second to S. P. Sadtler, for his con-
tribution entitled "Some Results Obtained in the Destructive Distillation of
Linseed Oil, with Remarks on its Bearing on Engler's Theory of the Origin of
Petroleum ;" and the third to \V. O. Richtmann and F^lward Kremers, for their
article on " The Menthol Group." The report was adopted.
The Committee on Ebert Prize awarded it to Messrs. Knox and Prescott, for
the paper previously referred to. The Committee on President's address
recommended that the papers contributed to the meetings of the State Associa-
tions be secured for the use of the Reporter on the Progress of Pharmacy for
abstracting or printing in full, as he may see fit. They also approved of the
educational measures proposed by President Morrison, and coincided with him
on the subject of dropping liquors from the Pharmacopceia. Considerable dis-
cussion was elicited by this last proposition, and was participated in by Messrs.
Whitney, Mayo, Sheppard, F-l)ert, F)liel, Torbett and Alpr rs. The report of
the Committee was finally accepted, with the exception (»f the proposition to
eliminate liquors from the Pharmacopreia.
The twenty-two new applicants for metnbership were then invited to com-
plete their meml>ership, which they did by signing the Constitution and paying
the annual fee.
The Committee on Time and Place of Next Meeting submitted three reiwrts
in favor of Baltimore, Omaha and Richmond, respectively. The majority
476 American Pharmaceutical Association. {^s^pSeM^sg?!*
report proposed that the uext meeting take place in Baltimore, on the first
Monday in September, 1898.
The reports were received, and after some discussion a ballot was taken. Of
the ninety-one votes cast, thirty-four were for Omaha, forty-nine for Baltimore
and eight for Richmond. A unanimous vote was then cast for Baltimore. The
time of mfeeting could not be agreed upon, so the matter was referred to the
last general session. The meeting then adjourned until 3.45 p.m., when it was
again called to order, prior to the convening of the Commercial Section. The
special session then adjourned and Chairman Hopp called the Commercial
Section to order. In the absence of Secretary D'Avignon, Mr. Palton was
elected Secretary pro iem. D. R. Noyes delivered an address of welcome to
the Section. Mr. Dewoody then took the chair, while Mr. Hopp delivered his
address. He advocated the revision of the United States copyright laws, and
suggested that the co-operation of State Associations, and of the American
Medical Association be obtained. He advised standardization of drugs, and
the adjustment of the minimum and maximum limits of the standard. He
re-suggested 50 per cent, tinctures and recommended that such preparations be
advertised to the physicians as a means of combating the large manufacturers.
He asked for some form of rebate plan free from the evils of previous plans for
protecting the retailer in prices. He favored the interchange of certificates of
registration by boards of pharmacy. The address was referred to a committee
appointed by Mr. Dewoody, and consisting of Messrs. Stewart, Ebert and
Good. There were no reports of committees to be heard from, nor were there
any papers read.
Chairman Hopp read a communication from the Proprietors' Section of the
National Wholesale Druggists' Association, which suggested that a committee
on fraternal relations be appointed to confer and co-operate with similar com-
mittees from State Associations to prevent substitution. The communication
was received and its import discussed. Mr. Bbert mentioned a plan whereby
the proprietors of patent medicines could secure to the retailer the full retail
price, if they so chose. The plan mentioned was the establishment of dis-
tributing depots, which should have complete supervision of all the stock
handled in a community, both by jobbers and retailers. Under such arrange-
ments the price-cutters would soon be identified, and could be denied such
stock as they cut price on. But Mr. Ebert declared the proprietors did not
want the retailer to ask the full retail price, and both he and Mr. Whitney
cited instances where the proprietors had come to them and quoted such prices
and terms as would induce many to meet the cut rates. Much argument was
expended on the matter of this communication from the proprietors, by Messrs.
Werner, Main, Whitney, Hammel, Bobbett, Sheppard, Simmons, Hassebrock,
Dohme, Ryan, Holzhauer and Thompson. The consensus of opinion was that
the experience with the proprietors in the past did not warrant the appoint-
ment of a committee, as suggested by them, that the retailer is able to take
care of himself, and that the time had come when he should await the action
of the proprietors to protect him, and not ask their interest in his behalf. It
was also shown that the products of the various State manufacturing pharma-
ceutical associations, like those of Illinois, Minnesota and Wisconsin, were in
a large measure replacing many of the proprietary products, and it was
believed on account of this that the proprietors would be glad in the near
I
J
sS>'timbeJ!*i^7"} American Pharmaceutical Association. 477
future to adopt some means of protecting the retailer in obtaining the full
retail price set by the proprietors on their products. The Secretary was finally
instructed to acknowledge the receipt of the communication, and to state that
the Association did not see fit to appoint the committee suggested. The Com-
mittee on Chairman's Address approved the measures proposed therein. The
report was received and the recommendations adopted. The following officers
were nominated and elected for the ensuing j'ear :
Chairman, Joseph Jacobs, Atlanta, Ga. ; Secretary, J. Hal. Bobbett, Raleigh,
N. C; Associate Members, N. A. Kuhn, E. C. Bent and H. F. Hassebrock.
When he came to be installed, Mr. Jacobs was loath to accept the chairman-
ship, and told the Association he thought they were doing just the opposite of
what they had been proposing to do but a few minutes before ; that he was an
arch-cutter, and was proud of the fact, and that the Association had better
reconsider his election. Still, he said, if it was the intention of the Association
to kill the Section, they had taken the necessary means.
Messrs. Mayo, Ebert and Stewart replied to Mr. Jacobs, and assured him
that the Association had elected him in a full consciousness of his beliefs
and methods ; they acknowledged that the Section had not done in the past
what it was intended to do, and stated that was the reason for trying a chair-
man who held opoosite views.
Mr. Jacobs accepted after much hesitancy, and promised to do the best he
could in his peculiar position.
A vote of thanks was given the retiring officers, and the Section adjourned,
subject to call of the Chair.
In the evening, President Cyrus Northrup, of the University of Minnesota,
delivered an address on Education. On Thursday, August 26th, the Ladies'
Auxiliary conducted a trolley tour of Minneapolis and St. Paul, for the visit-
ing ladies and their escorts. The party left Hotel Lafayette at 8 a.m. Lakes
Harriet and Minnetonka were included in the itinerary, lunch was served on
the beautiful grounds of the State University, and in the afternoon Como and
other points of interest within the borders of the saintly city were viewed.
On account of this excursion, when Chairman Alpers called the first
session of the Scientific Section to order, at 9.40 a.m., only a dozen
members of the .Association were in attendance. Mr. Geo. B. Kaufmanu
was elected Secretary pro tcm. On account of the small attendance, the
reading of the Chairman's address was postponed until the evenifig session.
The report of the Committee on Indicators was then presented. It was as fol-
lows :
Mr. i halt nmu and Mftuhrt s of t/ir A ssfcialmn : — The tliird rfi)f)rt ol Ihe C •'
•iats principally of some results obtainrd by certain of the workers who were di ^
■ome of their data in last year's report. Trof. J. U. I.lojd and the Chaimian. ai
their result* reported at the Montreal meeting, decided to repent the work for
Its fluid extract. This it was ccmcluded should he done on about the same dute and in the
■anip iM.-ifitirr ! H.- I tiqimian prepared the material and forwarded it wii)i instrn.tint.s
FLl7It> EXTRACT OK COCA LKAK.
For assaying this preparation the directions of the committee, as reported in the Proceed-
lags for 1S96, were adhered to. employing, however, enoiinh of the flnid extract to make»!x
9r seven determinations from the same extractiuu, so that there would be no s«arce mt
error here.
- Titrations were executed only with chlorophyll-free (nearly) alkaloids, using the moat satia-
factory indicators, rix. : Urazil wood, cochineal and htcmatosylon.
478 American Pharmaceutical Association, {^s'^pfembe^^%"'
The results reported by I^loyd and Kebler last year, on fluid extract of coca, were as follows :
IvLOYD. Kebler.
Gravimetric. Volumetric. Gravimetric. Volumetric.
Brazil wood 0-48 034 0-53 035
Cochineal 0-57 029 0*55 0-40
llicmatoxylon .... 0-53 0*27 o'54 0-38
Lacmoid o-6o 0-35 0-50 0-38
While all of their other results agreed quite closely, this position was considered unsatis-
factory.
On assaying the second fluid extract, November 7th, the results were as follows :
Lloyd. Kebler.
Using Alcohol. Excluding Alcohol. Using Alcohol.
Gravimetric. Volumetric. Gravimetric. Volumetric. Gravimetric, Volumetric.
Brazil wood . 0-406 0-328 o 36 0*323 0-369 0-416 0-277 0-289
Cochineal . . . 0-37 0*290* 0-412 0*298* 0*416 0*416 0*277 0*286
H£ematoxylon,o-4o6 0-315 0*376 0-321 0384 0-370 0-290 0-293
Average . . 0*394 0*311 0-383 0-314 0-389 0-401 0-315 o 289
The average of Lloyd's gravimetric results is 0-388 ; of Kebler's gravimetric, 0*395 ; differ-
ence, 0007 per cent. The difference of the volumetric results is 0*011 per cent.
ASSAY OF POWDERED COCA LEAF.
Since the mode of procedure is contained in the report of the workers, the directions will
not be repeated here. Prof. Lloyd reported his work as follows : 50 grammes of the powdered
coca, not previously dried to constant weight, were put into a one-half gallon bottle and
covered with 500 grammes of chloroform ether (i to 3) mixture ; after five ininutes' rotating,
50 c.c. of 10 per cent, ammonia were added, and the bottle shaken for two hours, almost con-
tinuousl}-, occasionally cooling the bottle in cold water. Then 50 grammes more of 10 per
cent, ammonia were added, well shaken, and finally, seven times 50 grammes of the ethereal
fluid drawn off. Six of them were assayed, with results as follows : (Probably it was case F,
where some difficulty was experienced in pouring off 50 grammes.)
Gravimetric.
Hfematoxylon A, 1*102 per cent.
" 3 drops B, o'994 " "
Cochineal C, 1*038 " "
3 drops D, 1-096 " "
Brazil wood, 50 drops E, 1*002 " "
" " 10 " F, o'944 " "
Average 1-029 per cent.
In case D.^t was attempted to see what effect the exclusion of alcohol would have on the
results. The visible effect is that it is difficult to dissolve the alkaloid completely from the
resinous material. After volumetric results were found too low (see a), the same determin-
ation was continued by adding an equal bulk of alcohol, which caused an increase in the
results (see b).
In these experiments the titrations were carried out in the same beaker in which the
gravimetric results were obtained. The varnish-like residues were dissolved in 5 c.c. of
alcohol, 2 c.c. of N/io sulphuric acid and 10 c.c. of water were added, then the indicator,
and the excess of acid titrated back with N/ioo potassium hydroxide. In each case i c.c.
of N/ 10 was added again and the excess titrated back with centinormal potassium hydroxide.
Hicmatoxylon and cochineal gave sharp changes of tint ; also brazil wood, but the latter
indicator requires a trained eye to see the change plainly. However, the solution may have
deteriorated.
Mr. Kebler proceeded exactly as did Professor Lloyd, except that the shaking was intermit-
tent instead of almost continuous, shaking about every fifteen minutes during two hours.
His results were as follows :
•Change of color indistinct except when using more of the indicator than prescribed.
Volumetric.
1*000 per
cent.
0*957 "
0-950 •'
lb
-0-927 "
-0-982 "
0-952 "
0-897 "
<(
0-952 per
cent.
'^&?pfembe^.^^97?' } American Phar^naceiitical Association. 479
Gravimetric. Volumetric.
Brazil wood ouo o'Sy
Cochineal 0'92 o 887
Haematoxylon 0*97 o'893
Average 0*95 o"883
The differences here amounted to : gravimetric, 0*079 per cent.; volumetric. o'c69 percent.
These variations appeared too great, so it was decided to do the work in a reverse manner,
that is, Professor Lloyd apply less agitation and Mr. Kebler more. Professor Lloyd, by reduc-
ing his shaking to three-quarters of an hour, and Mr. Kebler by ajjitating two hours con-
tinuously, with the same coca leaf, obtained somewhat different results :
Lloyd. Kebler.
Gravimetric. Volumetric. Gravimetric. Volumetric.
Brazil wood i'034 o 950 1*02 091
Cochineal 1004 o"939 099 o"89
Hiematoxylon . . . . 0976 o"934 1'03 o"94
Average 1*005 0*941 i*oi 0*91
On comparing these results with those obtained above, we come to the conclusion that time
of agitation does seem to increase the percentage of yield, to some extent, and this fact
should be borne in mind when parallel assays are made. While the above data are not in
complete accord, yet they approximate one another as closely as can be expected for this
character of work, and are considered tjuite satisfactory by the workers.
Lyman V. Kebler, Chairman.
The report was received and ordered to take the usual course.
The reading of the report of the Committee on Research was deferred till the
evening session, as was also the report of the Committee on the Revision of the
United States Pharmacopoeia.
The next business was the nomination of the officers for the Section during
the coming year. Messrs. Kremers and Alpers were put in nomination for
Chairman, and Mr. Kaufmann for Secretary.
The reading of certain papers presented by members in attendance were car-
ried over to the evening session, so as to allow discussion on the subjects by a
larger audience. The following papers were then read by title :
STANDARDS FOR LINSEED AND WHITE AND BLACK MUSTARD
SEEDS.
By J. U. Lloyd.
COMPARATIVE STRUCTURE OF HYOSCYAMUS, BELLADONNA AND
STRAMONIUM LEAVES.
By J. O. SCHLOTTBRBBCK.
EXAMINATION OF POWDERED VEGETABLE DRUGS.
By Hbnry Kraemer.
SULPHUR PRECIPITATUM.
By T. D. Rked.
IS GLUCOSE OR GRAPE SUGAR OF ANY VALUE AS A PRESERVA-
TIVE IN SYRUP OF HYDRIODIC ACID AND SYRUP OF
FERROUS IODIDE?
By David Walkkr.
GELSEMIC ACID.
By Viroil Coblbktz.
This paper is printed in full on page 439.
480 American Pharmaceutical Association, {^s^pfembe?.^!™*
A CHEMICAL BIBLIOGRAPHY OF MORPHINE.
By a. B. Prescott and H. E. Brown.
By special action, a paper on
THE EFFECT OF TEMPERATURE UPON PERCOLATION.
By H. DeForrest Smith,
a non-member, was received. These papers were referred to the Publication
Committee. On motion, the meeting adjourned at 10 a.m. Immediately after
this action the
SECOND SESSION OF THE SCIENTIFIC SECTION
was convened by the Chairman. The reading of the minutes of the first session
was dispensed with. On account of the small number of members in attend-
ance, the election of officers was postponed until the evening session, and at
10.07 A.M. the second session adjourned, so the audience could overtake the
trolley party.
The
THIRD SESSION OF THE SCIENTIFIC SECTION
was called to order by Chairman Alpers at 8.30 p.m., on Thursday, August 26th.
Upon motion, the reading of the minutes of the second session was dispensed
with. Prof. Good then took the chair, while Mr. Alpers read his address. In
reply to the remark not infrequently heard, " Pharmacy has ceased to be a
science ; it is a mere trade, and a poor one at that," the author discussed the
topic: "Is there Science in Pharmacy?" He believed that the commercial
admixture in American pharmacy predominates over the scientific part to such
an extent that the latter is nearly or entirely concealed.
Driven by competition into a state of nervous agitation, often bordering on
recklessness, he thought it no wonder that pharmacists sometimes ignored their
professional standing, and plunged into the strife for mere commercial supre-
macy ; and, said the speaker, what is the worst sign of the times from the point
of view of the question — " Is there Science in Pharmacy? " — is that the men
who conduct their business on these lines are, as a rule, the most successful
ones, if the gaining of wealth is to be the sole evidence of success. He pointed
to the well-known fact that many pharmacists do not make the preparations
and chemicals which they handle, and mainly because of the capital required
for investment, and because of the protection which copyright laws provide for
so many articles in use at present. He said the time is fast approaching when
the pharmo-chemical and pharmacal manufacturing industries, with their bound-
less array of capital and superior resources, will have rendered the pharmacist's
modest laboratory, in every productive direction, not only wholly superfluous,
but, indeed, absurd.
. He said science in pharmacy is to-day like the princess in the fairy tale,
lying spellbound under noxious weeds and thorns, awaiting her delivery. He
foresaw a division of pharmacists into two classes, not hostile to each other,
but mutual coadjutors in their respective lines of work, and supplementing one
another. One class is to look after the purely commercial side of the drug
business as now conducted, and handle the so-called "side lines," while the
scientific part of pharmacy is to be conducted by those who fit themselves for
the compounding of prescriptions, the sale of drugs, the assaying and standard-
^8?ptimber isy?" ; American Pharmaceutical Assoiijiion. 481
izing of drugs, the analysis of foods, medicines, secretions, etc , and who haye
perfected themselves by higher education in the use of the microscope as a
means of diagnosis, and also in bacteriology, which is being more used every
day by physicians in order to study diseases. He said it is impossible for the
physician to charge himself with this work on account of his inability to give
it the constant attention it often needs, and that it will find its way to those
prepared to do it. He thought it a field of desirable activity, and stated that it
was still largely unclaimed, and that the pharmaci>t should enter it. Then
the analyst pharmacist would be a connecting link between the laity and the
medical profession, indispensable to both, a constant searcher for truth, a once
more truly professional man, far from priding himself on successful competition
with the "general store " in the favor of the sidewalk public. To regulate and
enforce the proposed measures, the Chairman recommended that a Department
of Health be created. He proposed that it be made national in function if the
Constitution of the United States would permit ; otherwise that funds be
appropriated by the Government for its support. He referred to the fact that
the medical press had recently suggested such a measure, and that Senator
Mallory, of Florida, had already introduced a bill in the Senate for the estab-
lishment of such a department. The speaker believed an institution of the
foregoing character would afford relief from the many disadvantages and draw-
backs caused in medicine and pharmacy by the confusing multitude of State
laws. He believed the .\merican Pharmaceutical Association should assume
leadership in such a new departure, and he recommended that a committee be
appointed either by the Scientific Section or by the Association, to whom this
matter should then first be referred, to examine the bill introduced by Senator
Mallory, and to confer witli its author for the purpose of procuring for pharmacy
and its subsidiary sciences proper recognition and representation in the pro-
po.^ed National Department of Public Health ; or, if this bill should fail, to
take steps on the introduction of a new bill. The address was received with
the thanks of the Association, and was referred to the Section on Pharma-
ceutical Kducation and I^egislation for discussion. The following paper, from
the Special Research Committee, was then presented:
THI-; CAIFEIN COMPOU.VD IN KOLA. PART II. KOI.ATANNIN.
By a. B. Prescott antj J. W. T. Knox.
Continuing the work reported on at the meeting a year ago, the authors find
all the tannin of the kola nut, that combined with caffein and that uncombined,
lobe a single chemical individual, distinct from any tannin previously repoi ted
as found in the beverage plants or elsewhere. The "free" kolatannin was
prepared as follows : Presh kola nuts were sliced into boiling alcohol (to pre-
vent the formation of the colored body which would otlurwist- appear^ removed
after a few minutes' boiling, and dried in a current of warm air, then ground
to a No. 20 powder and packed in a percolator. The alcohol so used iu
sterilizing the drug was diluted to about 50 per cent, strength, and cujployetl
as a menstruum, with addition of sufficient dilute alcohol to complete the
extraction. The highly colored extract of kola thus obtained was concentrated
by distillation in vacuo, until the alcohol was all removed. The contents of
the flask were then filtere«l, the insoluble portion being chiefly c»ffein kola*an-
nate, while the solution contained cuOein, kolatannin, cbflcin kt latanrate, glu-
482 American Pharmaceutical Association. {'Veptembef.^isgT"'
cose, traces of fatty matter, coloring matter, and more or less colored derivatives
of tannin, according to whether the sterilization by boiling alcohol has been
properly done. Common salt was then added to this filtrate to saturation and
the caffein kolatannate was completely precipitated. It was filtered out and
added to the first residue of cafFeiu kolatannate. The reddish-colored filtrate
was then transferred to a large separatory funnel and agitated with chloroform
repeatedly to remove alkaloids and the traces of fat. The dissolved chloroform
was then separated by agitation with small portions of ether. Ethyl acetate
was then added to the liquid in the funnel, and the liquid extracted with it as
long as any tannin was removed. The united solutions of tannin in ethyl ace-
tate were transferred to a distilling flask, and concentrated to dryness under
reduced pressure. The tannin residue in the flask was a porous, pinkish mass,
very friable, and easily and completely soluble in water. It was redissolved in
saturated salt solution, filtered and again shaken out with ethyl acetate, which
was distilled off in the way just described. The tannin residue was next dis-
solved in cold distilled water, and shaken out as before, this process being
repeated as often as necessary. The final tannin residue, after the ethyl acetate
had been removed as far as possible by distillation, was treated in the distilling
flask with a small quantity of ether, which, after permeating the mass, was
removed by distillation under reduced pressure, to remove the odor of ethyl
acetate. The tannin was then transferred to a vacuum desiccator and kept over
sulphuric acid for several days to remove the last traces of ethyl acetate. The
kolatannin from cafifein kolatannate was prepared by decomposing the purified
salt with lead hydroxide. Freshly precipitated lead hydroxide, triturated to a
smooth paste with warm alcohol, was added in excess to a warm solution of
the caffein kolatannate in dilute alcohol. The mixture was warmed on a water
bath for a few minutes, with stirring. The precipitate of lead kolatannate,
mixed with the excess of lead hydroxide, was allowed to subside, the superna-
tant liquid removed and the precipitate washed repeatedly with dilute alcohol
until all cafl"ein was removed. The precipitate was then suspended in dilute
alcohol and treated with hydrogen sulphide until the tannin was all liberated.
The lead sulphide was removed by filtration, and the filtrate concentrated by
distillation in vacuo to small volume. Eight or ten volumes of water were then
added. This precipitated a reddish mass, a mixture of certain anhydrides of
kolatannin, which was filtered out and set aside.
The filtrate containing tannin, together with dissolved anhydrides, was now
shaken with ether once or twice, which was thrown away. Then ethyl acetate
was added and the tannin separated and purified in the way already described
under the method of preparation of free kolatannin. Kolatannin is a cream-col-
ored powder, with a slight pinkish tinge. It is freely and completely soluble
in water, alcohol, acetone and ethyl acetate, sparingly soluble in ether, insolu-
ble in chloroform and m benzene. In properties and reactions with ferric salts,
bromine and calcium hydroxide, it agrees with the "oak tannin group," not
with the "gall tannin group." It precipitates metallic salts, alkaloids and
albumen, and produces, with solution of formaldehyde in the presence of
a condensing agent, as hydrochloric acid, a pink precipitate which
becomes red. In empirical atomic composition it is homologous with
the caff't tannic acid of Hlasiwetz. It purifies to perfect constancy of com-
position, C, gH^i.O^, as found in repeated preparations. The results which
^pt'embef.'isPT^' / Avierican Pharmaceutical Association. 483
were obtained by the authors last year seemed to indicate that kolatannin was
a glucosidal body; but after repeated experiments, in which .the glucose of the
plant was entirely elitninated from the tannin, negative results were obtained
for glucose resulticg from decomposition of the kolatannin, and the inter-
pretation was made that kolatannin is not a glucoside. The authors said it is
significant that this result places kolatannin in a category and gives it a char-
acter essentially different from the character of caffetannic acid as understood
by the chemical world from the report o*" Hlasiwetz. In every case kolatannin
yields at once a pentacetyl derivative ; it readily admits successively three,
four and five atoms of bromine in substitution for hydrogen, and these several
bromine and acetyl substitutions are obtained just the same, whether the
bromine substitution or the acetyl substitution be made first in order. A sixth
atom of bromine can, with more difficulty, be introduced, but this product will
at most receive only four groups of acetyl, forming tetracetylhexabromkola-
tannin. In analysis of the acetyl derivatives, the figures from combustion were
confirmed by a method of saponification,
Kolatannin itself forms a first, a third and a fourth anhydride, and, like
anhydrides, are formed by the several bromine derivatives, all these purifying
intact, sojis to give, on combustion, figures quite close to the theoretical ones.
By boiling kolatannin with dilute acids, an insoluble "red" is obtained, in
place of the " kola-red " of Knebel, and corresponding to the oak-red, and the
phlobaphene of Grabowski, Etti and others, but with utmost efforts this body
could not be prepared of constant composition.
The figures from six preparations ranged C, 50*45, 53"6o, 56'38 per cent.,
etc. The authors believe it to be a mixture of two or more compounds. The
report of Knebel and of Hilger that sugar is formed coincident with the red
body was not confirmed by the present experiments. Kolatannin, underaction
of fused potassium hydroxide, was found to yield protocatechuic acid, as well
as phloroglucin, indicating both di- and trihydroxy benzoic constitution. Pro-
tocatechuic acid was also obtained by heating with glycerine. The authors
stated their desire to make further detenninations of decomposition ] roiucts of
kolatannin, and proposed, for further studies, the following constitutional for-
mula, which they think is consistent with the results so far obtained :
C,.H,(CH,UOin,C() „ .> „ o
QH. CHJ(OCH,)(OH),0 " '-le^^o'^"
The authors also discussed the two processes for the assay of kola which
have been proposed in the past year by Jean and Carles. They gave the essen-
tial points of these methods as follows : Afethod of Jtau. — This author boils the
dried and powdered drug with milk of lime, dries the whole in an oven and
powders it again. This powder is exhausted with chloroform, which removes
the free alkaloids. The chloroform is evajwrated to dryness, the residue dis-
solved in hot water and filtered. The filtraie is evaporated to dryness and
weighed as caffein. For "kolanin:" the drug, after treatment with chloro-
form, is extracted with alcohol, the alcohol evaporated from the |>ercolate, and
the soft extract remaining is di.ssolvcd in boiling water, which solution, after
cooling, is filtered. The insoluble matter remaining in the filter is dried iu an
oven and weighed as " kolanin."
The authors, in criticising the foregoing nielho is, stale that the most serious
484 American Pharmaceutical Association. ; ^^'eptember/TsMT^'
defects are: (i) the boiling with milk of lime, (2) prolonged heating necessary
to dry the drug after that treatment, (3) weighing the caffein instead of esti-
mating it with Wagner's reagent volumetrically, (4) the means emplo}ed to
separate the so-called "kolanin," (5) estimating caffein kolatannate, "kola-
nin," by weight as such instead of by its caffein content, (i) Boiling with
milk of lime or other aqueous alkalies tends to decompose caffein itself and to
liberate caffein from its tannate, and thus prevent an exact determination of the
proportion of "free " to combined alkaloids that originally existed in the drug.
The starch of kola, amounting to nearly 40 per cent., causes the drug to
become of a jelly-like consistency when boiled with aqueous liquids, and when
dried the mass is very difficult to powder, and even when powdered the condition
of it is well calculated to resist the penetrating action of the solvent, and thus
cause incomplete extraction. (2) The gelatinous condition of the drug after
boiling with lime water renders it hard to dry completely, and as very pro-
longed heating is necessary, there is danger of loss of caffein by sublimation.
(3) We do not consider that the alkaloids of kola are sufficiently pure
when removed in this manner to be weighed as such. Gomberg's volu-
metric method gives more accurate results, (4) If any caffein kolatannate
escapes decomposition during the first part of the assay, which will occa-
sionalh' happen, it is removed by the extraction with alcohol. But as
it is somewhat soluble in water and more soluble in aqueous solutions contain-
ing tannin, the directions to collect and weigh the portion left undissolved by
water will generally be found superfluous, for the small amount of it present
will generally pass into and remain in solution. Dieterich had this experience
and met with nothing but disappointment in trying to estimate caffein kolatan-
nate by this method. (5) Caffein kolatannate has been shown to be a body of
somewhat variable composition, with a caffein content ranging from 19 to 25
per cent. Inasmuch as the value of kola as a stimulant depends primarily on
its percentage of caffein, and as the weight of its caffein compound indicates
only approximately the amount of its combined caffein, there would not seem
to be any reason for attaching much importance to the weight of this compound
if a very precise valuation of the drug is desired. We hold that a direct esti-
mation of the caffein of this compound is preferable, and, at least, as expedi-
tious.
Method of Carles. — Ten grammes of kola, i gramme of calcium hydroxide,
and 20 grammes of 80 per cent, alcohol, are mixed together and dried on the
water-bath until the weight is reduced to 14 grammes. The mixture is then
powdered and transferred to a 100 c.c. flask containing 35 c.c. of a mixture of
100 parts of chloroform and 20 parts of alcohol, and heated for one hour on a
water-bath. After filtration, the residue is extracted next with 20 c.c. of the
same solvent, and finally with 10 c.c. The united extracts are evaporated to
dryness and the residue taken up with 10 c.c. of boiling water, containing four
or five drops of i per cent, sulphuric acid, then with 6 c.c, and finally with 5 c.c.
The solutions are united, filtered, evaporated to constant weight and weighed
as caffein. For "kolanin," which the author recognizes as caffein kolatan-
nate, another sample of ihe drug is taken and extracted with water to remove
the caffein and other soluble constituents. The drug is next extracted with
70 per cent, alcohol, the extract evaporated to dryness, transferred to a filter,
waslied with cold water, iheu dried by a gentle heat and weighed. If it is
I
iTptimbefl^sS-^'} American Pharmaceutical Association, 485
desired to estimate the alkaloids of this compound, i gramme of "kolaniu,"
I gramme of calcium hydroxide, and 3 grammes of chalk, with a little 70 per
cent, alcohol, are mixed together, and evaporated on the water-bath to about 6
grammes and extracted with alcoholic chloroform in the manner already
described. The objections to this method are in part among those already
mentioned in the discussion of Jean's method. The use of lime or other alka-
lies in the assay of a caffein-beariug drug is to be deprecated. The solvent
used is not a proper one, for the reason that sufficient alcohol is present to
extract other constituents, in addition to the alkaloids, which are not removed
from caffein during the subsequent treatment of the residue, and which when
weighed with the caffein lead to erroneous results. Moreover, the manner of
applying the menstruum is inconvenient, does not insure complete extrac-
tion, and is in no way preferable to the ordinary extraction by the use of
Soxhlet's apparatus. The addition of the sulphuric acid is unneces-
sary, and does noi add to the purity of the final product, which is dark-colored
and very plainly impure. The objection to weighing a final residue as caffein
finds especial application in this method. As the properties of caffein kola-
tannate had not been made known very generally at the time of publication of
these methods, there is some excuse for the assumption of both these writers,
that it is wholly insoluble. Carles has proceeded on this hypothesis, in direct-
ing the drug to be extracted with cold water, to remove the water-soluble con-
stituents before exhausting it with alcohol to remove the caffein compound;
but inasmuch as caffein kolatannate is not onlj- somewhat soluble in water, but
considerably more soluble in solutions of caffein and of tannin, the extraction
of kola by water will remove a considerable amount of it. The same is to be
said of the final washing of the caffein compound with water, which is quite
inadmissible in quantitative work. Carles seems to have recognized the uncer-
tain value of gravimetric determinations of caffein kolatannate, and is to be
commended for offering an alternate method providing for its valuation
according to the amount of its alkaloids. Both methods give very low results
as compared with those obtained by the nitthcd proposed at the meeting last
year by the authors. The paper was received and referred to the Publication
Committee. During the discussion that followed, Prof. Kremers referred to
a late contribution to the knowledge of the tannin of coffee by Kuntz-Krause,
in which caffetannic acid is said to be a glucoside.
The subject of the next paper was :
WHY A PHARMACIST SHOULD BE A BACTERIOLOGIST.
By O. W. Kki'Kgkr
He said because physicians are employing bacteriology more and more as a
means in determining the nature of diseases and the selection of proper reme-
dies, and because they do not possess the required laboratories and apparatus
which the pharmacist should always have ; therefore, and in order to be an
up-to-date co-worker with an up-to-date physician, a pharmacist should be a
bacteriologist.
The paper was discussed by Messrs. Whelpley, Alpcrs, Prescott and Hall-
l>erg. It was received and referred to the Publication Committee. Then fol-
lowed the report of Professor Kremers, a member of the Si>ecial Kesearcii
Committee, on the volatile oils which were considered last year in the report
486 American Pharmaceutical Association. { 'september^^?.''
of the Committee on Revision of the U. S. Pharmacopceia. He mentioned the
ambiguity of the term "volatile oil," and spoke of the care that should be
used in deciding on the particular constituent by the estimation of which it is
sought to value the oil. The report was received and referred to the Publica-
tion Committee. The second annual report of the Research Committee was
then presented by Chairman Prescott. It considered the pharmaceutical assay
of and the limitations of the percentage of essential constituents of volatile oils
at large. The Chairman also reported that the constitution of commercial oil
of bay was under investigation by a member of the committee. The following
subjects were also reported by him as under investigation : Standards for Lin-
seed and White and Black Mustard Seed ; (he reported that Professor Lloyd
had accepted this subject so far as the mustard seed were concerned ;) stand-
ardization of Powdered Acacia and Gamboge, giving Limitations for the Amount
of Starch Allowable ; Investigation of Syrups Made with Cane Sugar, and a
report on the desirability of using glycerin in place of cane sugar in syrups \
(the chairman of the committee had done something toward working this sub-
ject;) the Chemistry of Cascara Sagrada ; (Dr. Dohme is investigating this
matter;) Chemistry of Taraxacum ; (Professor Sayre has this subject;) the
Perhalides of Alkaloids in Relation to their Volumetric Estimation ; (the
chairman has this;) Toxic Action of Phenol on Living Plants; (under the
supervision of Professor Kremers; ) Comparative Structure of Hyoscyamus,
Belladonna and Stramonium Leaves; (assigned to J. O. Schlotterbeck ;) A
Chemical Bibliography of Morphine from 1875 to 1896 ; (compiled by H. E.
Brown.) The report was received and approved. The thanks of the Section
were extended the committee. The Secretary was then asked to cast an affirma-
tive ballot in order to elect Messrs. Kremers and Dohme members of the
Special Research Committee for a term of two years and to fill the vacancies
of Messrs. Kremers and Coblentz, whose terms had expired. Professor Good
moved that the chairman of the committee be empowered to fill any vacancy in
the committee until the next meeting, should one occur in the intervals of the
meetings. The following two papers from the Special Research Committee
were then read in abstract, received and referred to the Publication Committee:
ALKYL BISMUTH IODIDES.
By a. B. Prkscott.
The paper dealt with the theories of the structure of this class of compounds
and with work upon bismuth iodides of nitrogen bases, both of fatty alkyls and
those of pyridine and pyridine-derived alkaloids. The interest attached to
pharmacy in the paper laid in the fact that the alkaloidal bismuth iodides were
shown not to be quantitatively uniform enough to be entirely satisfactory for
alkaloidal assay, but were shown to be more stable and uniform than the alka-
loid mercuric iodides formed by Mayer's reagent. On the other hand, they
are more bulky, less easy to gather into compact mass, and less manageable
in filtration. On the whole, the author believed that the use of Dragen-
dorfPs reagent (potassium bismuth iodide) for alkaloidal assay affords no
general advantages over that of Mayer, which is well known to be unsatis-
factory.
Following this paper came one on
A'li.Juiir Pharni )
September. l8i*7. .
American Pharmaceutical Association.
487
ARAI.IA XUDICAULIS.
By William C. Alpers ani> Benjamin L Mi.rray.
The botany of the entire plant, and the microscopy, chemistry and pharma-
ceutical preparations of the rhizome were treate<l. Drawings of a cross-section
of the corky layer of the old bark, a longitudinal section of the outer bark, also
one of the wood from pith to bark, and a segmentary cross-section of the entire
root showing pitted vessels, lignified cells, cork cells, medullary rays, medullary
rays prolonged in»^o bark, cambium layer, resin and oil cells, phellogen, bark,
wood and p th, accompanied the paper.
As a summary of the systematic analysis and estimation of the constituents,
the following table was presented :
Extract with
Pf rcentage of
Dry Drug.
Chloroform
Alcohol, 80 percent.
Water
Acid I, water \ . .
Alkaline solution
(By subtraction) . .
338
875
358
56- 10
6-89
21 30
Containing
Resin, 305 per cent.; oil, 0*33 per cent.
Tannin ; organic acid ; acid resin (neutral resin?)
Albuminous bodi? s ; coloring matter.
Mucilaginous matter.
Crude fibres, etc.
Cellulose.
Regarding the pharmaceutical preparations, the authors said a quantity of the
fresh rhizome gathered in the fall was digested with alcohol, according to the
directions of the Pharmacopoeia for making fresh tinctures. This tincture,
after standing nearly a year, exposed to the varying temperatures of winter
and summer, showed no precipitate, and possessed the odor and taste of the plant.
Mixed with water it formed a milky precipitate, indicating the presence of oil
and resin. It had a beautiful gold-yellow color, which seems to be permanent.
A fluid extract was prepared from the rhizome gathered in the spring. A men-
struum of four parts of alcohol and one of water was used, and the general
directions of the Pharmacopoeia for making fluid extracts were followed. The
evaporization of the second percolate was performed at a very low temperature,
in order not to drive ofl^ oily or resinous parts. The fluid extract resembled
the tincture, but is darker, owing to the solution of the coloring matter of the
plant, and more aromatic.
Although this fluid extract appears to be an elegant and highly concentrated
preparation, and to possess all the properties of the <lrug, it is doubtful, in the
writers' minds, if therajjeulically it would be the most desirable form of admin-
istering the drug. The virtues of the drug depend, they believe, on the oil and
resins. The properties of the drug, judging from some crude experiment.^.
seemed to be .stimulant, diaphoretic and probably neurotic.
Professors Sayre and Lloyd spok** of the compound syrup of arali.i bring
used as an alterative by the Eclectics, instead of the compound syrup of sary.i-
parilla.
Mr. Alpers said he had been unable to procure Aralia nudicaulis in the
market, but that each time he had ordered it another <lrug liad been sent. In
488 American Pliarniaccutical Association. { '"s^pimbe^S"-
explanation of this, Prof. Lloyd said that what Mr. Alpers had received when
he ordered Aralia uudicanlis was probably Aralia hispida ; and he also said that
the Eclectics have carefully distinguished between the two, and that they
refuse to accept spikenard for the plant under consideration.
By a special action the report of the Committee on Revision of the United
States Pharmacopoeia was presented at this stage by Chairman Eliel, who said
in effect :
Podophyllum.— k.% podophyllin is the active principle, a podophyllin require-
ment should be established. As the process of assaying the drug and obtain-
ing the purified Podophyllin, U.S P., is a simple one, it should be adopted as
such, or in a modified form. Four per cent, of purified U.S P. podophyllin
appears to be an average good yield from resinous prime root.
Prunus Virgifiiana. — It has been established that wild cherry bark can
readily be assayed and its value be determined A process of assay should
therefore be adopted and a standard hydrocyanic acid requirement be
established.
Sajigui naria. —'Q\oo^ root has an active principle, sanguinarine, and as this
can readily be determined, a process of assay should be adopted, and a sangui-
narine requirement established.
Sarsaparilla, Quillaja and Senega have similar properties, and their active
principles are similar and allied. These principles should be investigated and
closely compared. Methods of assay and standard requirements should be
established so as to give pharmacists a means of determining their merits and
value independently of the crude microscopical methods now necessarily and
onl}' employed, and which can have no real value. If, as has been maintained,
soap bark and senega root have the same therapeutic value, and can be inter-
changed, the more valuable one should be determined and adopted, and the
less valuable one droppe d .
Slrophanthus. — The most valuable variety of this drug should be adopted and
the less valuable varieties excluded by the Pharmacopoeia, and a method of
assay for determining the strophauthin adopted, as well as a minimum content
of the same.
Syrupus Acidi Hydriodici is not a stable preparation, and it is doubtful if it
can be made such. A concentrated solution of hydriodic acid can be made
that is stable, and from which the syrup can be made as wanted for dispensing.
Such a solution should be substituted for the syrup. Prof. Ryan suggested, if
the syrup be continued, that its strength be increased.
Syrup of Garlic. — This syrup is practically obsolete, as far as usefulness is
concerned, and should be dropped; but if retained in the Pharmacopoeia, the
quantity of dilute acetic acid should be reduced, for if made with a good quality
of garlic, the finished product, according to quantities now directed to be used,
will yield about looc.c. more than the looo c.c. that the Pharmacopoeia directs.
Vanillin has been recognized as the odoriferous and valuable principle of
vanilla beans, and is a definite chemical compound whose purity can readily be
determined. It should be made official, especially as its use is becoming gen-
eral among pharmacists.
Mucilago Acacice may be kept for an indefinite time if 25 per cent, of the
■water directed to be used is replaced with liquor calcis, and we recommend its
adoption in the Pharmacopoeia.
^'J^t'^mberiao™} American Pharmaceutical Association. 489
Tinctura Moschi. — The pharmacoprcial requirement of 5 per cent, stren^^th
is too great and wasteful, as this amount of musk will not be exhausted by the
process now directed. The strength should be reduced to 2 per cent, and
100 c.c. of the water replaced by liquor calcis.
Methyl Alcohol may now be obtained of a high degree of purity, and the use
of such purified wood alcohol should be sanctioned in the manufacture of such
preparations as linimentum saponis, linimentum saponis mollis, linimentum
sinapis compositum, spiritus myrcice, tinctura arnicae florum, tinctura benzoini,
tinctura cantharidis and tinctura iodi. Samples of these preparations made with
purified wood alcohol were submitted for inspection by Mr. Eliel.
It was the intention to submit at this meeting aline of samples of fluid and
solid extracts of alkaloidal drugs with wood alcohol as a solvent, but in order
to obtain trustworthy results, the committee found that individual experiments
have to be repeated a great many times. The practicability of using methyl
alcohol in the manufacture of alkaloidal solid extracts was tested on the follow-
ing drugs :
Aconite, belladonna, cinchona, henbane and stramonium. Methyl alcohol
does wholly extract the alkaloids of these drugs.
In the cases of aconite, belladonna and nux vomica, the volume of menstruum
for complete exhaustion was ascertained. Two portions of the drug (100 gm.
each) were packed in separate percolators and were exhausted under the same
conditions and at the same rate of flow, one portion being exhausted with
official menstruum, the other with a menstruum differing from the otTicial in
containing purified methyl alcohol in place of official ethyl alcohol.
The percolation was conducted with ordinary percolators, and in the manner
ordinarily employed in retiiil stores, who follow the specifications of the
U.S. P.
The results were as follows :
Volume of menstruum required for complete exhaustiuu.
Htbyl Methyl
Drugf. Alcohol Menstruum. Alcohol Menstruum.
Aconite 450 c.c. 550 c.c.
Belladonna 695 c.c. 700 c.c.
Nux vomica 950 c.c. 1060 c.c.
The first and the second 100 c.c. of percolate were assayed for total alkaloids,
with the following results :
First 100 c.c. of Fir«t too c.c. of
Kthyl Methyl
Drug. .Alcohol Percolate. Alcohol Percolate.
Aconite 0*49 gm. 043 gm.
Belladonna 0*437 gra. 0458 gm.
Nux vomica 1437 gra. i'437 gm.
Second 100 c c. of Second lOo c c. of
Ethyl Methyl
DruK. Alcohol Percolate. Alcohol Percolate.
.\conite 0135 gm. 0135 gm.
Belladonna '0578 gm. '048i4gm.
Nux vomica '733 gm. '668 gm.
490 American Pharmaceutical Association. { ^sTp/emberfsg"*
The solvent power of methyl alcohol for non-alkaloidal plant constituents is
not identical with the so vent power of ethyl alcohol. As a consequence, the
mass of extract obtained from a given quantity of drug is not the same as that
obtained from the same quantity of drug by means of an ethyl alcohol men-
struum. The dose of the extract would, therefore, have to be ascertained and,
perhaps, changed if methyl alcohol be adopted as the solvent.
The weights of extract, calculated as pilidar extract, obtained from loo gm.
of drug by completely exhausting loo gm. of drug with the ethyl alcohol men-,
struutn and with the methyl alcohol menstruum, were :
Drug, Ethyl Alcohol Extract. Methyl Alcohol Extract.
Aconite 7'57gai. 14 gm.
Belladonna 54 gm. 25708 gm.
Nux vomica 12-55 gm. 20*4 gm.
Cinchona ...... . 54-62 gm. 53-134 gm.
The Committee stated they had made arrangements for further work on this
subject.
The toxicity of methyl alcohol was discussed by several of the members.
Mr. Puckner reported having taken 30 c.c. of a purified methyl alcohol, with a
slight increase in pulse and temperature as the only results. On other occa-
sions he took 15 c.c. every three hours with the same effect. He believed
methyl, ethyl and propyl alcohols are all about alike in their physiological
effects. Prof. Kremers pointed out that it had been determined that the toxi-
city of alcohols of the paraffin series increases with the number of carbon
atoms ; and he said, if this was true, methyl alcohol must be less toxic than
ethyl alcohol. Contrary to all this, Prof. Hallberg reported a case where two
persons had died from the drinking of 10 ounces of commercial methyl alcohol.
It was the opinion of some present that the same amount of ethyl alcohol
might have caused the same result. The members differed in their experience
with the so-called " Columbian Spirit." Some had found it to contain acetone,
while others had not. Prof. Hallberg said that tincture of iodine made with
purified methyl alcohol became colorless, or nearly so, on standing, while Mr.
Ebert said he had a sample of that tincture made in January, and that it had
not lost color. The report was received and referred to the Publication Com-
mittee. A paper on
PEANUT OIL.
By S, p. Sadtler,
was then read.
The author dealt with the source and preparation of the oil. He stated the
results of his analysis of the oil of Virginia peanuts in tabular form, and also
placed alongside for comparison some partial analyses of peanut oil from for-
eign sources, as follows :
Am. Joar. Pbann.
!:ieptember. IRW.
} American Pliartnaceutical Association.
491
Specific gravity at I5°C
Saponification value
Iodine value
Hehner value . . .
(Percentage of insoluble acids)
Reichert-Meissl vnlue
Percentage of free acid as oleic .
Cold test of the oil
Maumen^ Test
Melting point of fatty acids . .
Solidifying point of fatty acids .
Oil from Oil from Oil from
Virjfinia Spanish African
Nuts. Nuts. Nuts.
Oil from Commer-
Puducheri. ; cial Oil.
o'93r9
1921
98-4
95-86
6ao
+ 10° C.
45 5° C.
25° C.
He also said the production of peanut oil in this country has hitherto been,
unless secretly, only carried on in a desultory way, and it has not been much
known as a commercial article. However, as the chemical composition of the
peanut has become better known, attention has been drawn to the food value
of the peanut meal and the peanut grits. It has been found that they are
richer in nitrogenous principles than any of the vegetable seed cakes, and a
demand has sprung up for them. So the expression of the oil has now been
undertaken on a larger scale and with more suitably designed presses.
The sample which was shown was cold-pressed oil from Virginia peanuts,
and about 38 per cent, by weight is obtained in the first cold-pressing. By a
second hot-pressing nearly 10 per cent, more can be obtained. The cold-
pressed oil is, as seen, of a pale yellow color, and of pleasant flavor and o<lor. A
very slight refining makes from it a very agreeable table oil for salads and general
culinary purposes. It has already been noted with the European peanut oil
(and the author said he could confirm it from his experiments with the Amer-
ican oil) that, when once freed from the free acid found in the raw state, it
does not tend to l)ecome rancid as easily as olive oil. The author said he had
exposed samples to strong sunlight for weeks without developing the slightest
rancidity.
Now, asked the author, as this is an abundant American product 1 the annual
product of Virginia and North Carolina peanuts is over two million bushels),
why should the oil not be used in pharmacy where olive oil is now used ? The
investigator had prepared, in an experimental way, a soda soap from this oil, a
sample of which was shown, and a sample of lead plaster from the same.
With this latter for comparison was put lead plaster, made from a sample of
pure California olive oil. He thought these showed that the p)€anut oil will
make at least as good products as the official olive oil.
As regards the soap, it is an open secret that the bulk of the castile soap
made in Marseilles to-day is made from .\frican peanut oil.
The author said, in conclusion, that when he a^kcd permission of the com-
pany, who arc now starting iu to tiianufaclure this oil in this country, lo
492 American PharmacetUical Association. {^^^^^.t^^f^xl^:
present an account of his examination of the oil before the Association, he was
told that they would cheerfully send samples of the oil in response to
inquiries Irom any one interested. He stated the cost of peanut oil is much
below that of olive oil.
The paper was followed by some
PRACTICAL NOTES.
By Joseph Feil.
A series of experiments indicated to the author that under the ordinary con-
ditions of most drug stores, tincture of iodine will remain of U.S. P. strength for
about one month — that is to say, if the bottle is opened once or twice a day, and
if kept on a shelf exposed to diffused daylight ; if, however, the container is
kept in a dark closet, exposed to the same conditions of occasionally being
opened, it remains unchanged for two months. The author suggested that the
Pharmacopoeia require the preparation to be kept in a dark place.
In regard to the variation in strength of tincture of opium, he stated that
inquiry seemed to clearly indicate careless manipulation in the preparation of
the tincture as almost the only reason for this condition of affairs.
The author stated that powdered cinchona of a quality far exceeding U.S. P.
requirements is readily obtainable at a moderate price, yet the ordinary article
is only 50 to 70 per cent, of what it should be in alkaloidal strength. He
believed a possible cure for this condition of affairs would be a shorter method
of assay for the drug, if it is possible to devise one, even if it does not give
absolute results.
The writer said although the U.S. P. recommends excellent wines, such as
California Reisling and Ohio catawba, from which to prepare the vina, yet the
favorite article used extensively to-day is sherry wine, an article notoriously
impure. He found pharmacists consider the preparations made by the latter as
better. He considered this doubtful, and added that he had failed to find any
proof that the newer wines make better preparations ; undoubtedly they are
purer, but this does not prove that for medicinal purposes they are better, unless
clinical evidence can be shown to this effect.
In the discussion that followed the reading of the paper, Mr. Payne referred
to the frequent habit of some druggists making the tincture of opium from the
gum opium instead of from an equal weight of the powdered drug, as the prob-
able cause of the varying strength. Professor Hemm stated that he had obtained
the strongest tincture by using maceration instead of percolation. He believed
that the calcium phosphate of the official method was often a disturbing feature
that prevented solution of the morphine, possibly through being alkaline in
reaction, and therefore causing the alkaloid to be liberated from its salts and
remain undissolved. He said if this did not account for the deficiency in
strength the official process of percolation must yield an incomplete extraction.
Professor Hallberg spoke of the use of granulated opium with the omission of
calcium phosphate in the process of maceration with water as having been
reported on favorably by many pharmacists. Regarding Mr. Feil's note on
wines, Dr. A. \\. Lyons spoke of the necessity of using wines containing 16
per cent, of alcohol instead of 12 per cent , if permanent preparations were
desired.
'^si'ptlmber^rjwr } ^tfterican Pharmaceutical Association. 493
CHEMICAL COMPOSITION OF COMMERCIAL EXTRACT OF WITCH-
HAZEL.
Bv Joseph Feil. Ph.O.
The author gave the tests by which he found what was believed to be pro-
tocatechuic acid, and he considered that substance to represent the peculiar
properties of extract of witch-hazel. The extractive matter found averaged
about I part in 3,000 parts of the liquid.
These papers were referred to the Publication Committee.
A paper entitled
BOILER-SHOP PHARMACY.
Bv C. S. N. Hallberg,
was then read. The author had tabulated the percentage of disintegration and
solution in acid and alkaline aqueous liquids of mass-made pills and friable pills.
The results were in favor of the former kind. After considerable discussion by
Messrs. Caspari, Werner, Kuhn, Payne, Sayre.Whelpley, Hallbeig, Lyons, Good
and Prescott, as to the propriety of the title and contents of the paper, it was
referred to the Publication Committee and business again proceeded.
SOME MEDICINES OF THE SWAMPY CREE INDIANS OF THE
NORTH.
Bv C. Flf.xon,
was then presented. The paper gave some particulars furnished l)y Mr.
Strath, Medical Officer at Norway House, which is located about 400 miles
north of Winnepeg, Manitoba. These Indians administer most of iheir medi-
cines in the form of infusions. A combination of malefern. senna and wild
indigo is used for worms. Wild indigo is also use<l as an antiseptic. Cala-
mus is used as a specific in all throat troubles, except diphtheria, which,
however, is not known to them. The calamus is chewed and the saliva swal-
lowed. The Indians are not easily induced to gargle. Great difficulty is also ex-
perienced in getting them to take the salts. Pills, however, are swallowed with
a relish. Podophyllum, spearmint, sarsaparilla and dandelion are used by
them. Caraway is used as a remedy for colic. Hlue cohosh is used in obste-
trics and female complaints, also for the production of abortion, in which case
it is mixed with an unknown powder ; an oil from a mixture of hemlock
spruce, poj)lar and black birch is used for the same purpose. Cypripedium is
used for rheumatism ; the Indians will not take salicin or salicylates. He-
deoma is given as an aromatic stimulant and to produce abortion. Plantain is
chewed and applied by the doctor in the form of paste as a hitrtnostatic ; willow
bark is used for the same purpose. Juniper berries are used as a diuTetic ; the
leaves are drie<l and dusted over indolent sores ; the root is infused and given
for gravel. The rotten interior of the hemlock spruce '\% used as an agreeable
al>sorbent toilet powder. The Crees believe that fever can only be cure<l by
vomiting it up, and the powdered rhizome and rootlets of Veratruni viride arc
used to produce vomiting to relieve fever. The same medicine is used as a
snnfF to reduce hernia ; to do this the naked patient is elevate*! to a horizontal
position ; he then takes a pinch of the snuff and during the intense snec/ing
which follows, R companion standing ready at the side plunges back the rupture
with his fist. It is said that if it l)e not a strangulated case, the treatment b
sufficient. Gunpowder and lanl in equal quantities arc used for skin diMafre^.
494 American Pharmaceutical Association. {^Si'^^ZhS^S^
Sturgeon oil is used in i -ounce doses as a cathartic. Wild raspberry and
willow bark are used for cholera infantum. Rumex is used as a laxative and
for poultices. The Crees look upon wild carrot as their most fatal poison.
A paper entitled the
PREPARATION OF FLUID EXTRACT OF WILD CHERRY FOR
SYRUP.
By J. M. Good,
was read by title.
THE IMPORTANT CONSTITUENTS OF TARAXACUM ROOT.
By Iv. E. Sayre,
was then read by the author. This work of Prof. Sayre on taraxacum has been
that of several years past ; but during the last two years he has connected this
investigation with the work of the Special Research Committee of the Associa-
tion. The author has come nearer crystallizing the bitter principle taraxacin than
ever before. He does this from a solution m acetone, but the crystals are
unstable; the presence of the least particle of moisture breaks them down into
oleoresinous globules. He crystallized the fatty substance known as taraxa-
ceriu in the pure state and submitted it to ultimate analysis, which indicated
the substance to have the empirical formula (CgHijOx ).
THE PREPARATION OF SOLUBLE FERRIC PHOSPHATE.
By W. a. Puckner.
The following formula, aiming at the production of a preparation of less
variable composition, as well as a simplification of the process, was submitted
for trial and criticism :
SOLUBLE FERRIC PHOSPHATE.
Ferrous sulphate, in clear crystals 156 gm.
Sulphuric acid 20 c.c.
Potassium chlorate 12 gm.
Ammonia water 34° c.c.
Citric acid 120 gm.
Sodium phosphate, uueffloresced 200 gm.
Water A sufficient quantity.
Add the sulphuric acid to 240 c.c. of water, contained in a glass or porcelain
vessel, to this add the ferrous sulphate, warm gently until all is dissolved, then
add the potassium chlorate and continue the heat for one-half hour, or until a
drop of the solution added to potassium ferricyanide test solution no longer
produces a distinct green or bluish-green color. Add this solution, slowly and
with constant agitation, to the ammonia water contained in a suitable vessel ;
to this mixture add hot water 4,000 c.c, and allow to subside and, after one-half
hour, decant or siphon off the clear supernatant liquid. To the residue add
2,000 c.c. hot water, allow to subside and decant ; repeat this washing with six
portions of hot water, allowing the last portion to subside for at least six hours
or over night. Decant or siphon off the clear liquid as closely as possible, then
add to the remaining magma the citric acid and the sodium phosphate, warm
geatly until solution results, and then evaporate on a water-bath at a tempera-
ture not exceeding 60° C, until the solution weighs 500 grammes, and spread it
on plates of glass, so that, when dry, the salt may be obtained in scales.
'^'ept^e^mberf'^ } Aviericafi Pharmaceutical Association. 495
To obtain a solution of which 2 c.c. are equivalent to i gramme of soluble
ferric phosphate, U.S. P., 1890, evaporate on a water-bath at a temperature not
exceeding 60° C. until the solution measures 500 c.c.
SELENIUM IN COMMERCIAL SULPHUR.
Bv T. D. Reei>. M.D..
and
SULPHUR PRECIPITATUM.
Bv T. D. Reed, M.D.
were then read by title, received and referred to the Publication Committee.
It was then moved to proceed with the election of officers for the Section
during the coming year. Mr. Alpers withdrew his name, and the Secretary was
ordered to cast a unanimous ballot for Prof. Kremers, of Madison, Wisconsin,
as Chairman. Dr. A. B. Lyons, of Chicago, 111., was then nominated for Secre-
tary ; nominations were closed, and the Secretary* asked to ballot affirmatively
for Dr. Lyons, who was thereafter declared elected. The election of Prof.
Kremers to the Chairmanship having caused a vacancy in the Special Research
Committee previously elected at the session (for the Chairman of the Section
is an ex officio member of the said committee 1, Dr. A. B. Lyons was substituted.
There beiug no reports of committees, the newly elected officers were installed,
and a vote of thanks was given the retiring officers. It was moved and carried
that the Chairman of the Scientific vSection make such arrangements with the
Chairman of the Section on Pharmaceutical Education and Legislation as to
obtain time to deal with the unfinished business of the Scientific Section. The
reading of the minutes was dispensed with, and on motion the Section
adjourned.
SECTION ON PHARMACEUTICAL LEGISLATION AND EDUCATION.
Chairman Hallberg called the section to order at 9.45 a.m., on Friday,
August 27th. Professor Whelpley then took the chair while Professor Hallberg
delivered his address. The speaker recommended that the Slate Hoards of
Pharmacy be again requested to send the Section one or more sets of the ques-
tions which they have asked applicants ; that the orthography and pronuncia-
tion of chemical terms as adopted by the American Association for the
Advancement of Science be reported on at the next meeting ; that the feasi-
bility of establishini; a memorial to Hager l>e considered ; that rules in detail
for the conduction and working of the Section on Pharmaceutical Education
and Legislation be presented at the next meeting for consi<leration and adop-
tion. The atldress was received and referre<i to a committee composed of
Messrs. Prescott, Parisen and Purkner. The Secretary of the Section then
read his report, which gave the changes that have taken place in pharmacy
laws during the past year, as well as other measures uhich hav.- been pro-
posed in the legislation of the affairs of pharmacy. Statistics rega ding the
number of registered and unregistere<l pharmacists in the United States i»ere
also presented. These showe<l that fewer applicants are registere<l on dipl ma
every year. The author said there was a lack of interest in the work of
gathering this information by some V>oards of pharmacy. Mr. El>ert propo«cd
that, in order to obtain the ntcessary information, a circular letter be i»e» I to
the secretary of each board of pharmacy early in the year. The report was
496 American Pharmaceutical Association. { IsTptimbe^iSg™*
received and referred to the Publication Committee, and Professor Beal was
given a vote of thanks for his laborious work.
The report of the Committee on the Preliminary Education of Apprentices
was referred back to the Committee on the Revision of Pharmacy Laws.
A SUMMARY OF ANSWERS TO MAIN QUESTIONS OF THE COM-
MITTEE'S CIRCULAR OF INTERROGATORIES.
Compiled by C. S. N. Hallberg,
was read by that gentleman. This consisted of a tabulated statement of
responses to questions regarding pharmacy laws, boards of pharmacy, require-
ments for registration, methods of registration, examinations, examination
fees, registration of licenses, revocations, titles and privileges, poison laws and
label provisions, adulteratioa, limited license and exemptions. Thirty-one
replies expressing opinions were received from various boards, associations and
schools of pharmacy. The paper was received and referred to the Publica-
tion Committee. Messrs. Hallberg and Beal were then nominated for the
chairmanship of the Section for the ensuing year, while Messrs. Oldberg, Hall-
berg, Hereth, Beal, Whelpley, Puckner, Kaufmann, Mason and Webster were
named for the secretaryship, and these names were posted until the second
session of the Section.
The next business was the reading of a paper entitled
SHOULD A PHARMACY LAW BE UNIFORM TERRITORIALLY?
By Edw. S. Dawson, Jr.
This paper was in answer to the query : " Should a pharmacy law be uniform
in its application throughout the State, or should a distinction be made for
smaller towns?"
The author gave his reasons for and against such applications, and concluded
by saying : " I am of the opinion that a pharmacy law should be framed so as
to secure greater protection to public health, and afford protection to the legiti-
mate druggist up to a point where the cry of ' monopoly for the drug business '
cannot be set up ; but care should be taken that the druggist who receives the
least benefit from the operation of the law should not have his hands legally
fettered."
Following this was another, called
SHOULD PHARMACISTS OR THE STATE SUPPORT THE PHARMACY
LAW AND THE BOARD?
By H. M. Whitney.
The writer maintained that all examinations to secure a personal State certifi-
cate of registration, conveying a special and legalized position, with its rights
and privileges, should be paid for by the applicant. But he believed that the
enforcement of the pharmacy law, poison law, or any other special duty placed
by the vState upon the board should be supported and paid from the State
treasury.
Professor Kremers suggested that the applicant be not allowed more than
three opportunities to pass the examination. Mr. Ebert was opposed to
pharmacists supporting the board unless the latter did more to enforce the law
and detect adulteration. Mr. Mason believed two opportunities sufficient for
an applicant to show his fitness for registration, Mr. Whitney said measures
^ptimbef^iS^} American Pharviaccutical Association. 497
would be taken in Massachusetts to limit the number of opportunities allowed
the applicant. Messrs. Bartells and Webster also spoke on the subject.
A paper on
PROVISIONS OF A POISON LAW, AND MEASURES FOR ITS
ENFORCEMENT.
By Albert B. Prescott,
was then read. The author said the registration of sale of poisons is upon
about the same footing that it was before the advent of State boards of phar-
macy. It depends largely upon the will of the pharmacist. In this situation
it seemed to the writer the better way, y^ri/, to propose, as a general State law
upon this subject, one that is simple and moderate in its demands, and second^
to undertake vigorous measures for the enforcement of registration laws.
In the provisions of the law, as to rules of registration of a given poison, the
writer said he would adopt those of Number 79 of the Legislation Committee
circular. He said it is of the first importance to the business interests of phar-
macy that local druggists should all act alike in registration, and as to what
articles to register. He suggested that the druggists of a town or city, if not
organized into a society, might well call a meeting and confer upon what shall
be the list of medicines to be always registered as poisons when sold without a
prescription. Such an agreement gives a most satisfactory explanation to the
purchaser, who may ask: "Why do I have to answer these questions here
when I have not been asked the same at other places ? "
As to the second named undertaking, that of vigorous measures for the
enforcement of registration laws, it seemed to the author certain thai this should
be the duty of the State Board of Pharmacy.
The next paper presented was on
UNIFORM PHARMACY LAW— AS TO PLACE OF REGISTRATION.
By Jos. Jacobs.
The author thought it desirable that every licentiate should be required
to register at the county seat of the county of his residence. This would
be a wise provision, because it would make it clear to the licentiates
themselves who were their legitimate co workers, and the public at large could
easily ascertain whether they were dealing with a pharmacist duly qualified or
with an impostor. He suggested that the place of registration be designated
in a clause similar to the following:
" All persons qualified by law to practice pharmacy in this State shall, before
entering upon such practice, cause their names to be entered upon a book to
be kept for that purpose in the office of the clerk of that court in which wills
arc filed for probate and record, in the county of the residence of such licen-
tiate, and of the county in which he does business as a pharmacist." Then
follow with appropriate penalty for violation.
Mr. I\bert said this suggestion should be taken into consideration by the
Committee who are to draft the uniform pharmacy law, and he believed it
should l)e aflopted, and that the secretaries of the l>oards should Ik* instrucle<i
to send the names of the registere<l pharmacists to the clerk of the court.
Prof. Oldberg then moved that the discussion of these papers be postponed
498 American Pharmaceutical Association. { ^s^pimbef.^sg?!'"
till the report on the revision of the pharmacy laws and the presentation of
the model pharmacy law had been submitted.
The next paper presented was in answer to the query :
SHALL A COMPULSORY CURRICULUM BE ESTABLISHED IN LIEU
OF REGISTRATION BY DIPLOMA?
By I^. K. Sayre.
The author said he interpreted the term curriculum to be a systematic course
of training under competent instructors in pharmacy, materia medica, chemis-
try, toxicology, and such allied branches as are taught in the reputable col-
leges of pharmacy. The author's ideal method was that the candidate for
recognition as registered pharmacist by the State Board of Pharmacy must first
have a systematic course of training in a reputable school of a certain stand-
ard and must possess a diploma certifying to this fact, and then be examined.
Following the last paper was one on
PRACTICE AND OWNERSHIP IN PHARMACY.
By Joseph Jacobs.
The author defined what constitutes the practice of pharmacy, and also
defined and distinguished between to own, open, operate, manage, conduct,
direct or supervise a pharmacy. In reply to the question : " Which, if any, of
these provisions should be enjoyed by non -pharmacists ?" he answered : none
but ownership.
The next paper read was :
CONCERNING THE QUESTIONS GIVEN IN STATE BOARD OF PHAR-
MACY EXAMINATIONS.
By Harry B. Mason,
The author discussed the character of the oral and written questions asked by
boards, and then said: "Such questions should be asked as require the use,
first, of trained pharmaceutical faculties, and next, of such knowledge only as
is likely to be retained in the mind by its constant application. Questions dealing
with memory alone should be subjugated instead of given precedence. Then an
examination would demand of a pharmacist just what practice does, and if
really competent he would be able any minute to step from behind his prescrip-
tion desk and pass it. He would be put to no necessity of acquiring the diffi-
cult art of preparing for an examination, and would be relieved of the injustice
of going through a special ' cramming ' process for months. And the quiz
compend student, skilled in the art of preparing for the examination, but woe-
fully deficient in the art of preparing for practice, would find himself wallow-
ing beyond his depth."
The foregoing papers were received and referred to the Publication Committee
and then discussed. Dr. Lyons thought it might be well to ascertain the ability
of the candidate to consult books, by allowing him to refer to a library, and
thereafter write a short dissertation on a given subject. Mr. Feil thought like-
wise, Mr, Helfman referred to a paper on the subject of examinations by Peter
T. Austen, and published in the Chemical News about a year or so ago. Prof.
Oldberg said more practical examinations should be given and less questions
re<juiring the mere act of memorizing ; he also suggested that the examinations
'^sepfember^»7! } American Pharfnaceutical Association. 4199
be held at places, say colleges, where facilities for practical work are accessible.
Prof. Whelpley thought it would be well iu all cases to ascertain the qualifica-
tions of the board to examine. Mr. Ford thought one of the main troubles is
that some boards have too many applicants at a time to examine them properly.
Messrs. Hammel, Flexon and Parisen also spoke on the matter. It was finally
suggested that a set of instructions be prepared by the Association and furnished
the persons who appoint the members of the boards. The Committee on Chair-
man's Address reported their approval of the recommendations made therein,
with the exception of the one regarding the orthography and pronunciation of
the American Association for the Advancement of Science. They suggested that
this one be reported on at the next yearly meeting. This action was approved
and the report was adopted. The Section then adjourned. The second session
of the Section convened on the same day at 2.50 p.m. Chairman Hallberg pre-
sided and read the report of the committee on a model pharmacj' law. A num-
ber of propositions for a model pharmacy law were made. The chairman pro-
posed a division or separation of the drug business into two classes, the persons
conducting these classes of business to be known as pharmacists and druggists,
and their places of business to be designated pharmacies and drug stores
respectively. The report was received. It was moved that the report be not
acted on at once, but that the Section request the Association to have 500 copies
of the report printed, and that the officers of the Section be instructed to send
them to all the State Boards and Associations, to all colleges of pharmacy, and
to supply them to members and others desiring them for study and thought;
that such recipients be asked for their opinions ; also that the matter be taken
up at the next meeting. The motion prevailed, and the Association, at a subse-
quent meeting, granted the foregoing request. The session then adjourned.
In the afternoon, a steamer ride, including the upper and lower lakes, was
enjoyed by the Association, and in the evening, a concert in the hotel parlors,
under the direction of the Ladies' Auxiliary, was listened to by a large and
appreciative audience.
Chairman Hallberg called the third session on Saturday at 10.25 A.M. The
reading of the minutes of the previous session was dispensed with. A paper
entitled
A STATISTICAL RKPORT OF THK USK OF THE MFTRIC SYSTEM IN
233,000 PRESCRIPTIONS.
By H. M. Whf.i.plev,
was read. Reports had been received from 233 drug stores, and each dealt with
the last 1,000 prescriptions on its file. These stores were located in lyi cities
and towns of thirty States and Territories. Gypsum City, Kansas, led the
list with 100 per cent, of prescriptions written in the metric system. The
average use of the system during the past year amounted to 6*27 per cent.
The report also contained the expressions of opinions of many pharmacists on
the clesirability and feasibility of adopting the system as the official one. The
report indicated that the druggists generally arc ready and prepared to fill
prescriptions written in the metric system, but that the system is not, as n.
rule, used by physicians. Mr. liartells said that in his experience the younger
graduates in medicine uaed the system to a greater extent than the older
practitioners. Prof. Hallberg referred to the fact that the system is the more
500 American Pharmaceutical Association, {UptimbeKT"'
popular among students of pharmacy. The paper was received and referred to
the Publication Committee.
The next paper was entitled
SHALL PHARMACISTS PRESCRIBE OVER THE COUNTER?
By F. E. Stewart.
He " advocated that the druggist shall be educated in medicine and taught
to prescribe intelligently over the counter in minor ailments, for which the
public now consult the apothecary, not charging for his advice, but receiving
his pay in the medicines he has for sale ; this he will be obliged to do if the
times demand it, and this is virtually what he is doing every time he recom-
mends a medicinal preparation of any kind to his customers. "
Following this came a paper entitled
A DISTINGUISHED PHYSICIAN-PHARMACIST— HIS GREAT DISCOV-
ERY, ETHER-ANESTHESIA.
By Joseph Jacobs.
He concluded by saying : " Whatever credit may be due Jackson and Morton
and Wells for their researches and their use of anaesthetics, and whatever honor
may attach to the eminent surgeons of the Massachusetts General Hospital for
publishing the facts at home and abroad, the real glory of the first discovery
and proof of the efficacy of ether for the prevention of pain in surgery must
be finally awarded to Crawford W. Long, the eminent Georgian and lamented
physician-pharmacist. ' '
The paper was received and a special vote of thanks was extended to the
author. It was also moved that the Association be requested to have 500 copies
of the paper printed, and that a copy, properly inscribed, be sent to each of
the domestic and thereafter to foreign medical journals by the General Secre-
tary, in order to give it wide distribution. This request was subsequently
granted.
A paper entitled
IS IT ETHICAL FOP. MEDICAL MEN TO PATENT MEDICAL
INVENTIONS ?
By F. E- Stewart,
was then read by title.
The Committee on the Revision of Pharmacy Laws then reported. Prof.
Oldberg moved that the report be referred to a sub-committee, to be appointed
by the incoming Chairman of the Section, and whose duty it should be to con-
tinue the work during the coming year. It was so ordered.
The attention of the Association was then called in a note on the
REAL RELATIONS OF THE PHARMACIST TO THE PHARMACY LAW.
By J. H. Beal,
to the fact that the required registration of poisons and keeping of qualified
clerks are not legal persecutions, as many pharmacists seem to think, but are
really in the first instance a legal protection, and in the second instance to the
best interest of the pharmacist, because it makes the public recognize and
appreciate the responsibility of his occupation. Some business remaining over
from the Scientific Section was then allowed to be brought up, and Mr. Alpers,
of New York City, explained in detail the system of filing and checking of
prescriptions which he uses. It was regarded by many as the best system ever
I
^?ptimbef.^i897°} American Pharmaceutical Association. 501
proposed. Mr. Ebert,of Chicago, explained his method, which was also considered
a good one. The minutes of the second and third sessions were then read and
approved. Mr. Thompson suggested that in the model pharmacy law the
exemption of poisons dispensed on physicians' prescriptions from the list of
articles required to be registered, should be qualified to read in such a manner
that the prescription is specified to be intended for a patient. Mr. Thompson
also suggested that the law be constructed so as to restrict the use of narcotics,
like opium and cocaine. The suggestions were referred to the Committees on
the Revision of Pharmacy Laws and on a Model Pharmacy Law. Prof, Hallberg
then withdrew his name as nominee for Chairman. The Secretary was then
instructed to cast a ballot for Prof. Beal as Chairman. Messrs. Oldberg, Hall-
berg, Puckner, Whelpley, Beal, Mason, Hereth and Kaufmann withdrew their
names, and Mr. Webster, of Minnesota, was declared unanimously elected for
Secretary. The newly elected officers were then installed, and the retiring
officers were given a vote of thanks. Adjournment was then ordered. Presi-
dent Morrison called the
THIRD AND FIXAI. GENERAI, SESSION OF THE ASSOCIATION
to order at 2.55 r.M., on Saturday, August 28th. Secretary Caspari read the
minutes of the second general session, and they were approve<l. Secretary
Kennedy, of the Council, followed with the minutes of the sessions of that body.
He reported that a communication had been received from IL L. Palmer and
E. L. Ruddy in regard to publishing a history of the Association. Prof. Hall-
berg had proposed that a semi-centennial of the organization of the Association
be held in I9fj2. A Committee on Semi-Centennial Celebration was appointed
and these matters were referred to it. Mr. H. P. Hynson, of Haltimore, Md.,
was then elected Local Secretary for 1898. An appropriation was made for
the support of the bills of the Committee on the Status of Pharmacists in the
United States Army and Navy. Secretary Kennedy also reported the names of
27 new applicants for membership. The total new applicants at the meeting
numbered 130, and over 100 had paid their first annual dues.
The following gentlemen were elected officers of the Council for the coming
year: Chairman, \V. S. Thompson, Washington, D. C; Vice-Chairman, J. M.
Good, St Louis, Mo.; Secretary, Geo. W. Kennedy, Pottsville, Pa. The Com-
mittee on Transportation then made its report. Following this the Committee
on Tax-Free .\lcohol reported that Congress had attempted no legislation on
the question except to impose a tax on wood alcohol, and that this measure
was defeated. The committee had no recommendations to make, but it men-
tioned the various methods that are adopted in European countries to prepare
alcohol in such a way as to render it unfit for internal use, but still retain it in
a condition fit for use in the arts. It was also pointed out that tax-free alcohol
would render wood alcohol (|uite unnecessary, as it costs about three times aa
much to produce wooti alcohol, and l>esides, the latter is not so useful as ethyl
alcohol. The report was referred to the Publication Committee. The Com-
mittee on National Legislation reported that the matters which had engaged
its attention during the past year were the tax on alcohol, the retention of
alcoholic beverages in the I'nited States Phannacopeeia, and the question of
patents and trade-marks as applied to me<licincs. The report was received and
referred for publication. It was moved and carried to continue the Special
502 American Pharmaceutical Association, {^^^l^^^i^xm:
Committee on National Ivegislation, that its personnel be increased to seven,
and that this be appointed by the President.
The report of the Committee on Beneficiary Features was then presented.
The committee had collected information concerning such features as are carried
on in foreign countries. The committee recommended that a committee be
appointed to present a working plan at the next meeting, and that an appro-
priation of $50 be made to permit them to engage an expert insurance agent to
formulate this plan. The report was received and referred to the Publication
Committee. There was objection to making the appropriation, and after some
discussion as to whether the committee could not devise its own plan, the
motion to make the appropriation was tabled. The Committee on Meeting in
1900 reported that they had made inquiry in regard to the proposed meeting on
board of a steamer en route to Paris, but that they had no plan to submit, for
none of the steamship lines are ready to arrange for it so far in advance. They
had learned that prices will not be higher than at present, that a steamship
will be able to accommodate 300 persons, that the expense of going and return-
ing will not exceed |ioo, and that the Hamburg- American Steamship Com-
pany's line would probably be the best to take.
The Special Committee on Weights and Measures then reported as follows :
The report presented by this committee, at the meeting held in Montreal,
expressed a hope that some substantial progress might be made in the adoption
of the metric system of weights and measures in this country during the year
to come.
Those who have followed the proceedings of Congress for the past year will
readily understand why this work has not been accomplished, or any material
advancement made in it.
At the first session of the Fifty-fourth Congress, the Metric Bill was passed
by a very small majority, but, upon reconsideration of the vote, the Bill was
referred back to the Committee on Coinage, Weights and Measures, where it
still remains.
The^second and short session of the same Congress was occupied with the
consideration of subjects of greater interest to the members, and it was not
thought wise to bring the matter forward.
At the special session of the Fifty-fifth Congress, recently closed, the consid-
eration of such a measure would have been impossible, consequently the past
year has been one altogether unfavorable to securing any definite action upon
the bill in question.
Hon. C. W. Stone, Chairman of the House Committee on Coinage, Weights
and Measures, of the Fifty-fourth Congress, has been continued in the same
position in the present Congress, and the Chairman of the reporting commit-
tee is informed that this gentleman will take the first available opportunity to
bring the matter forward for consideration.
During the past year a number of interesting reports have been made by
consuls representing the United States in foreign countries now using the
metric system, as to the methods employed and inconvenience experienced
in the change from their customary systems. These reports will be used as
additional arguments for the adoption of the metric system in this country.
On account of the large number of changes in the membership of both the
Senate and House of Representatives, caused by the elections of last year, it
\™ptimber,*i88^} American Pharmaceutical Association. 503
will be necessary- for the members of the reportinj^ committee, and all others
interested, to do active work whenever it is thought wise to brinj^ the subject
forward for consideration.
Many of the new members, as well as some of the old, will have to be con-
vinced of the advantages to be gained by making the metric system the legal
system in this country.
Although there has been very little that the committee could do during the
past year, the members thereof are ready to take active interest in the matter
whenever there appears to be an opportunity for securing favorable consider-
ation of the subject.
The report was received and referred to the Publication Committee.
The report of the Committee on the Status of Pharmacists in the Army and Navy
was next presented. Chairman Payne reported that there were three bills bearing
on the subject in the House of Representatives, and that the outlook is far more
encouraging than ever before. The report was received and referred to the
Publication Committee ; the reporting committee was ordered to be continued,
and a vote of thanks was given it. The Chairman of Council reported that
there had been no change in the investment of the funds of the Associa-
tion, and that the present funds were invested in 4 per cent, trust companies'
del>enture bonds. Mr. Kennedy moved that the Local Secretary of next year's
meeting be made Chairman of the Committee of Arrangements, with authority
to apjxjint the other members of the committee. The motion was carried.
The delegates to the National Wholesale Druggists' Association were ordered
to report in writing to the General Secretary. The delegates to the American
Medical Association then made their report through their Chairman, Dr. F. E.
Stewart. The following subjects were referred to the Section on Materia
Medica, Pharmacy and Therapeutics of the American Medical Association by
the American Pharmaceutical Association at its last annual meeting, held in the
city of Montreal : I.iquor-selling in drug stores ; dismissal of Spiritus I'rumenti
and Spiritus Vini Crallici from the United States Pharmacopccia ; dismissal of
Vinum Rubrum and Vinum Album from the United States Pharmacop(L'ia ;
dismissal of all tinctures having a fluid extract of the same drug official, and
all fluid extracts having a tincture of the same drug official, and substitute
for such tinctures and fluid extracts 50 per cent, tinctures under a distinctive
title ; and the return to potassium sulphate as a diluent in making Dover
Powder, in place of sugar of milk, used since 1880. The Section concurred in
the dropping of licjuors from the Pharmacopcuia, and in the restoration of
potassium sulphate, but did not agree to the other changes.
The report was received, accepted and referred to the Publicuiun v^onimiiiee.
The Committee on Time and Place of Next Meeting reported that the .\ssmMa-
tion would convene on the last Monday of August, 1898, in Haltimore, Md. Sec-
retary Caspari then read a communication from the South Carolina Pharmaceuti-
cal Association, in the form of a telegram, expressing the best wishes of that Asso-
ciation. He also read invitations from Galveston, Tex., and lUiflfalo, N. Y., for
the Association to hold its meetings in these respective places. The Sccrctju-y
was authorized to reply to all of these courtesies. An acknowledgment by
Prof. J. U. Lloyd, on behalf of the Lloyd Library, of the receipt of the various
books from the libraries of the Association, and from some of its members, was
read, received and referred to the Publication Committee. Mr. Alpers then
presented the following resolution :
504 American Pharmaceutical Association. {i^ptimbe^^ss^T"
Resolved, That in accordance with the recommendatioji of the Chairman of
the Scientific Section, a committee of five be appointed during the coming
year by the President-elect of the Association, for the purpose of taking
action to give pharmacy its due recognition and representation in the
proposed National Department of Health ; and that the President of the
Association and the Chairman of the Section on Legislation be members
of this committee ex officio. It was adopted. Mr. Sheppard moved that
Local Secretary Shumpik be empowered to call meetings and act as presiding
officer during the social week following the regulat business of the Associa-
tion. Secretary Kennedy then invited the applicants for membership whose
names had been posted during the session to complete their membership and
become active members of the Association. A preamble and accompanying
resolutions which had been drafted by the American Medical Association were
then presented to the session by the delegates to the American Medical Asso-
ciation. This document had been considered by the Council of the American
Pharmaceutical Association, but not being disposed to act on it, that body had
referred it to the Association proper for discussion. The preamble explained
that the intention of the resolutions was the formation of a code of ethics
which should govern physicians and pharmacists alike in the matters considered
in the resolutions. These resolutions dealt with the subjects of the relation of
physicians and pharmacists to each other and to the public at large ; the pre-
vention of secrecy and monopoly in the manufacture and use of medicines ;
the granting of patents on medicines, machinery and methods of preparation ;
a commission of medical men to regulate the publication of certain trade
secrets ; the sanctioning of the specification by ph^'sicians on prescription of
the products of those pharmacists who conform to the code of ethics ; the
teaching of sufficient pharmacy in colleges of medicine to enable the graduates
thereof to distinguish between legitimate pharmacy and pharmaco-quackery ;
and the use of the United States Pharmacopoeia as a text book in both
colleges of medicine and pharmacy. After discussing the resolutions, certain
of them were amended and then adopted ; others were stricken out as impractic-
able or antagonistic to certain efforts of the Association, while still others were
adopted as presented. The adopted resolutions were then referred to the Amer-
ican Medical Association, and Dr. Stewart, the chairman, was given a special
vote of thanks. It was moved and adopted that a delegation of five members
be appointed by the President to visit the National Wholesale Druggists' Asso-
ciation, and carry the fraternal greetings of the American Pharmaceutical Asso-
ciation. On motion of Mr. Thompson, a resolution of appreciation was offered
to the Local Committee of Arrangements, the Ladies' Auxiliary Committee, and
all others who had taken part in providing the hospitable entertainment which
the Association had received during the meeting. Mr. Frost replied to the reso-
lution in some well-chosen words. A recess of five minutes was then granted
by the Chair. The first business, when the session was thereafter called to
order, was the installation of the officers-elect. President Whitney now occu-
pied the chair, and Mr. Main moved that a vote of thanks be tendered the retir-
ing officers for the able manner in which they had carried out their duties.
This action was heartily approved by the session. The meeting then adjourned,
subject to the call of the Chair, on September 6, 1897.
THE AMERICAN
JOURNAL OF PHARMACY
OCTOBER, iSgy.
thp: tannin of ceriops candolleana.
By Henry Trimble.
Contribution from the Chemical Laboratory of the Philadelphia College of
Pharmacy. No. 170.
Havinf^ received two samples of the bark from this member of
the mangrove group, which had been collected in widely separated
localities in India, it was thought that an investigation of the princi-
pal constituent, tannin, might prove of interest.
One sample was received from A. E. Wild, Conservator of Forests,
Bengal ; it was collected in that locality in February. The other
sample was sent from Singapore, and was collected there in Novem-
ber; it was forwarded to me by M. N. Ridley, of the Botanic
Gardens at that place.''
Ceriops Candolleana, like many other members of the Rhizo-
poraceai, is found in nearly all the low muddy shores of India, and
the Andaman Islands. It is known under the vernacular names of
Kirrari, Goran, Mada and Tcngah, according to the locality in
which it grows. It is a small, evergreen tree, with dark red hark
and hard red wood. The pores of the wood are very small, and
the medullary rays very fine, slightly wavy and equidistant. Pores
jo ned by fine, wavy, interrupted, concentric bands.
The bark is of a deep reddish-brown color, and is covered on the
outer surface with numerous conspicuous lentircls. U yields a
' To both Mr. Wild .lud .Mr. Kuilev the author is under obln;.itionb for other
valu;il)U* samples.
(505)
5o6 Tannin of Ceriops Candolleana. {^"o/tSerfisgy."''
deep port wine coloring to water, and contains large quantities of
both coloring matter and tannin. On these two substances depends
the use of the bark for both dyeing and tanning. It is by far the
most valuable one of the mangrove barks for tanning. The claim
is made- that it imparts a fine red color to leather. It may be said,
in regard to this, however, that tanners usually object to a reddish
color imparted by tanning materials, and the objection heretofore to
all mangrove barks has been the tendency they have to produce a
red color and a soft leather. Another real objection to the man-
grove extract sent from a tropical climate has been noted by Mr.
Ridley, who says the stuff has generally been so abominably pre-
pared that no one will look at it. At the present time attempts
are being made to manufacture a good quality of extract in southern
India and Borneo for export.^
The wood is used in the province of Sind for the knees of boats
and several other purposes, and in Lower Bengal for house posts
and for firewood.
Each of the two samples yielded the following percentages of
moisture, ash and tannin :
Ash in Tannin in Tannin in
absolutely original absolutely
Moisture. dry sample. sample. dry sample.
Sample from Bengal . , .1370 5*83 27-24 31*56
Sample from Singapore . .13*34 io*6o 20*00 23*07
It will be seen from the tannin percentages that Ceriops well de-
serves the reputation it has for being the most valuable one of the
mangroves. The per cent, of tannin is more than is usually found
in barks, and is perhaps only equalled by the wattle barks of Aus-
tralia. The differences of both tannin and ash in the above
samples are considerable, but not more than is found in our oaks
when collected at different seasons of the year.
A quantity of tannin was prepared from the Bengal sample. It
was thoroughly purified and submitted to elementary analysis,
yielding the following percentage results :
Carbou 61*13
Hydrogen 5*29
These figures, with the reactions towards iron salts, bromine
water and calcium hydrate, prove it to belong in the class of oak
bark tannins.
' Watt, Dictionary of the Economic Products of India, Vol. II, p. 261.
' Kciu Bulletin for February and March, 1897, contains a report by Professor
Hummel on the value of Ceriops bark for dyeing purposes.
^"cS.V^^"-} Camphor Tree. 507
thp: camphor tree.^
{^Cinnamomum camphora, Nees & Eberm.)
By Lyster H. Dewey.
DESCRIPTION.
The camphor tree is a broad-leaved evergreen, related to the red
bay and to the sassafras of the United States. In its native habitat
it attains a height of 60 to 100 feet, with wide-spreading branches
and a trunk 20 to 40 inches in diameter. Its general habit is simi-
lar to that of the basswood. The leaves are broadly lanceolate in
Fig. I. — Camphor tree : a, young, lealy shoot, scale one-third ; ^, flower
cluster, life size ; c, fruit, life size.
form, with acuminate points at both base and apex, of a light green
color, smooth and shining above and whitish, or glaucous, on the
under surface. The lower pair of lateral veins arc more prominent
than the others, but the leaves are not as distinctly thrce-ncrved as
^ United Sutes Department of Agriculture, Division of Botany. Circular
No. 12.
5o8 Camphor Tree. {'^''l^i^.r^^^r'
those of the cinnamon and many other species of the genus. The
small white or greenish- white flowers {Fig. i, b) are borne in axillary-
racemes from February to April, on shoots of the previous season,
and are followed in October by berry-like, one-seeded fruits about
^ inch in diameter {Fig. /, c). The fruiting pedicels terminate in
a saucer-shaped disk, persisting after the mature fruit has fallen.
NATIVE RANGE.
The camphor tree is native in the coast countries of Eastern Asia
from Cochin China nearly to the mouth of the Yang-tse-kiang, and
on the adjacent islands from the southern part of the Japanese Em-
pire, including Formosa and the Ryukyu Islands, to Hainan, off the
coast of Cochin China. Its range also extends into the interior of
China as far as the province of Hupeh, about 500 miles from the
coast on the Yang-tse-kiang, in latitude 30° north. This area, ex-
tending from 10° to 34° north latitude, and from 105° to 130° east
longitude, is all embraced in the eastern monsoon region, which is
remarkable for abundant rains in summer.
The camphor trees growing wild in the native range are usually
most abundant on hillsides and in mountain valleys, where there is
good atmospheric as well as soil drainage. The temperature in the
greater part of this region, which is partly within the tropics and
partly subtropical, rarely falls below freezing. The tree is an ever-
green, changing its leaves generally in April, and therefore the
winter temperature is a factor of more importance than would be
the case with a deciduous tree.
RANGE UNDER CULTIVATION.
Notwithstanding the comparatively narrow limits of its natural
environment, the camphor tree grows well in cultivation under
widely different conditions. It has become abundantly naturalized
in Madagascar. It flourishes at Buenos Ayres. It thrives in Egypt,
in the Canary Islands, in southeastern France, and in the San Joaquin
Valley, in California, where the summers are hot and dry. Large
trees, at least 200 years old, are growing in the temple courts at
Tokyo, where they are subject to a winter of seventy to eighty
nights of frost, with an occasional minimum temperature as low as
12° to 16° F. The most northern localities in the United States,
so far as known at this Department, where the camphor tree has
Am. Jour. Pharm.
October. 1897.
CampJior Tree.
509
been grown successfully out of doors, are Charleston and Summer,
ville, in South Carolina, Augusta, Ga., and Oakland, Cal.
At Charleston, Summerville and Augusta the trees have with-
stood a minimum temperature of 15° F., but they have been pro-
tected by surrounding trees and buildings. At Mobile, Ala., the
trees have grown and fruited in protected situations, while in ex-
posed places they have been repeatedly destroyed by frosts. While
the camphor tree will grow on almost any soil that is not too wet,
it does best on a well-drained sandy or loamy soil, and it responds
remarkably well to the application of fertilizers. Its growth is com-
paratively slow on sterile soils, but under favorable conditions it
Fif[. 2. — Map showing approximate areas where the camphor tree may be
grown in the United States. In the dotted area protection from cold will be
require<l. In the line-shaded area protection will not often be required, except
in exposed situations and on the mountains of California.
sometimes grows very rapidly. An instance is recorded of a cam-
phor tree in Italy a foot in diameter and 90 feet high, eight years
from the seed. Under ordinary conditions, however, such a girth
is not often attained in less than twenty-five years, and such a height
is rarely attained in a century. Under favorable conditions an aver-
*^gc of 30 '^cet in height, with trunks 6 to 8 inches in diameter at the
base, may be expected in trees ten years from the seed.
510 Camphor Tree, { ^"ocSr .^im"'
USES OF THE TREE AND ITS PRODUCTS.
The principal commercial uses of the camphor tree are for the
production of camphor gum and camphor oil. Camphor gum is
employed extensively in medicine. It enters into the composition
of many kinds of liniments for external application. For liniment
it is used especially in combination with olive oil. It is taken inter-
nally for hysteria, nervousness, nervous headaches, diarrhoea and
diseases affecting the alimentary canal. It is a specific in cases of
typhoid fever and cholera. Camphor fumes have been used with
success in cases of asthma. It has been used very extensively to
keep insects out of furs, woollens, etc. In Japan camphor and cam.
phor oil are used in lacquer work. The oil is somewhat similar to
turpentine, and could doubtless be used to advantage in varnishes
and shellacs. It is now used in the manufacture of toilet soaps. In
Japan and China it has been used for illuminating purposes, but it
produces a smoky flame.
Among the secondary uses of the camphor tree the most im-
portant is for ornamental planting. Its bright evergreen leaves,
rapid growth and long life make it valuable for this purpose. In
Japan and China it has been the principal tree planted in the temple
courts for many centuries, and in those countries it takes the place
of the historic oaks of England. It has been extensively introduced
into Southern Europe and South America for ornamental purposes.
The wood, with its close grain, yellow color, and susceptibility to
polish, taking a kind of satin-like finish, is exceedingly valuable in
cabinetwork, especially for making drawers, chests and cupboards
proof against insects. The leaves and young branches, although
they have but a slight odor of camphor, are packed with clothing
or scattered about unused rooms to guard against insects.
The tree produces an abundance of berry-like fruits, which are
used in Japan and China to make a kind of tallow. The fruits are
greedily eaten by chickens and birds, especially mocking birds,
which often select camphor trees for nesting places.
CONDITIONS OF SUCCESSFUL CULTIVATION.
For most of the secondary purposes, the camphor tree may well
be cultivated wherever it can be made to live ; but for the distilla-
tion of gum and oil with a commercial view, and for the production
of wood for cabinet purposes, it must be grown under the most
-""ocrXr^^T-} Camphor Tree, 511
favorable conditions. The minimum winter temperature should not
be below 20° F., and this minimum should be of rare occurrence.
The soil, preferably sandy and well drained, should be irrigated
unless there are abundant rains. Fifty inches of water during the
warm growing season is desirable, and much more may well be used
where the air is very dry.
An abundance of plant food, rich in nitrogen, is required for rapid
growth ; but the kind of fertilizer that can be most profitably applied
will vary according to the character of the soil in each locality. In
the absence of definite information in this regard, the kind of fertilizer
producing most rapid growth of wood in the orange or in other
fruit trees may be taken as an index.
The northern boundary of the dotted area on the accompanying
map i^Fig. 2) marks, approximately, the limit within which the cam-
phor tree may be grown in situations protected by buildings or by
other trees, while the northern limit of the area shaded by lines
marks the approximate boundary of the area within which it may
be grown without protection. Further experiments in planting the
camphor tree will doubtless modify both of these lines somewhat.
It is hoped that by continued selection of seeds from the most hardy
trees plants may be bred up to endure more cold.
PROPAGATION.
Camphor trees may be grown either from seed or from cuttings.
They are usually grown from seed, as the trees fruit abundantly, and
seedlings can be grown more easily than cuttings. The seeds are
collected at maturity in October and November, and, after drying,
are packed in sharp white sand or some similar material to keej)
them fresh until the time of planting in spring. About the last of
March they are sown in drills in the seed bed.
The soil of the seed bed should be a good sandy loam mixed with
about one-third leaf mould. The seed bed should be kept moist,
but not too wet, and should be shaded from the direct rays of the
sun if the weather is warm. The best soil temperature for germi-
nating camphor seeds is from 70° to 75° F. The temperature of
the atmosphere may be 10 degrees higher. The seedlings will
grow well at higher temperatures, but are likely to lack vigor and
hardiness.
The seedlings may be grown in pots, which will facilitate trans-
512 Camphor Tree. {^"^cfober.^sQr'
planting at any time, or they may be transplanted in nursery rows
early in April when one year old. Plants two years old are gene-
rally regarded as best for final planting. At this age they vary from
20 to 40 inches in height.
PLANTING AND CULTIVATION.
When set out for ornamental purposes, the camphor tree may be
expected to grow, in favorable situations, about as rapidly as a Le
Conte pear, and to require about as much room. In Japan, where
the law requires that a new tree shall be set out for every one cut,
they are not generally set in straight orchard rows, but cultivation
there is performed almost exclusively by hand labor. There are no
records showing results of regular orchard planting, hence the dis-
tances at which trees should be planted must be determined by the
size and form of the trees and the methods of cultivation, and of pro-
curing the gum. They may be set closely in rows about 10 feet
apart, and alternate rows cut and reset every five years, thus pro-
ducing bush-like plants of ten years' growth. They may be planted
in checks 10 feet square, and alternate trees cut every ten or twelve
years, or they may be planted in larger checks, and all of the trees
be cut at the age of fifteen or twenty years.
There are not sufficient data obtainable upon which to base
definite statements as to the best methods of planting or the
age at which the trees may be cut with greatest profit for
the production of gum. A recent English consular report from
Japan states that " although hitherto the youngest wood from which
camphor was extracted was about seventy to eighty years old, it is
expected that under the present scientific management the trees will
give equally good results after twenty-five or thirty years." Cam-
phor of good quality has been produced in Florida from the leaves
and twigs of trees less than twenty years old, I pound of crude
gum being obtained from seventy-seven pounds of leaves and twigs.
The trees will endure severe pruning with little apparent injury.
One-third of the leaves and young shoots may be removed at one
time without materially checking the growth of the tree. The
largest proportion of camphor is contained in the older, larger roots;
the trunk, limbs, twigs and leaves containing successively a decreas-
ing proportion. When the camphor tree is killed nearly to the
ground by frost it sends up vigorous shoots from the base. It may
""^cforr.*;^'"} Camphor Tree, 513
be expected to do the same when cut, especially if cut late in the
fall. Experiments are needed to determine whether this growth
may be depended upon, or whether it will be more profitable to dig
out the larger roots and set out new seedlings.
DISTILLATION OF CAMPHOR IN JAPAN.
In the native forests in Formosa, Fukien and Japan camphor is
distilled almost exclusively from the wood of the trunks, roots and
larger branches. The work is performed by hand labor, and the
methods employed seem rather crude. Different methods of distilla-
tion are employed in different districts, but those in use in the prov-
ince of Tosa, in Japan, appear to be the most skilful. The camphor
trees are felled, and the trunk, larger limbs, and sometimes the roots,
are cut into chips by hand labor with a sharp concave adz.
The fresh chips are placed in a wooden tub about 40 inches high
and 20 inches in diameter at the base, tapering toward the top like
an old-fashioned churn. The perforated bottom of the tub fits tightly
over an iron pan of water on a furnace of masonry. The tub has a
tight-fitting cover, which may be removed to put in the chips. It is
surrounded by a layer of earth about 6 inches thick to aid in retain-
ing a uniform temperature. A bamboo tube extends from near the
top of the tub into the condenser. This consists of two wooden tubs
of different sizes, the larger one right side up, kept about two-thirds
full of water from a continuous stream which runs out of a hole in
one side. The smaller one is inverted with its edges below the
water, forming an air-tight chamber. This air chamber is kept cool
by the water falling on the top and running down over the sides.
The upper part of the air chamber is sometimes filled with clean
rice straw, on which the camphor crystallizes, while the oil drips
down and collects on the surface of the water. In some cases the
camphor gum and oil are allowed to collect together on the surface
of the water, and are afterward separated by filtration through rice
straw or by pressure.
About twelve hours are required for distilling a tubful by this
method. Then the chips are removed and dried for use in the fur-
nace, and a new charge is put in. At the same time the camphor
and oil arc removed from the condenser. By this method 20
to 40 pounds of chips are required for I pound of crude camphor
gum.
514
Camphor Tree.
/Am. Jour. Pharm.
1 October, 1897.
The principles orenerally held to be essential in distilling camphor
of good quality are : (i) The heat must be uniform and not too
great, producing a steady supply of steam ; (2) the steam, after
liberating the camphor, must not come in contact with metal, that is,
the tub and condensing apparatus must be of wood.
SUGGESTED IMPROVEMENTS.
Many improvements upon the methods described can doubtless
be made, tending both to a reduction in cost and an increase in the
proportion of crude gum obtained. Instead of an adz wielded by
hand labor a machine similar to the •* hog " used for grinding up
waste slabs in saw-mills may be used to reduce camphor limbs to
the requisite fineness for distillation. Better distilling apparatus can
probably be devised. Thermometers may be introduced to deter-
mine the heat in the distilling tub, and the furnace may be so arranged
as to permit better control and greater economy in fuel. Camphor
and camphor oil are both slightly soluble in water, and the con-
densing chamber should be improved so as to recover the product
that is being constantly carried off in the running stream which
cools the chamber.
OUTLOOK FOR FUTURE MARKET.
The consumption of camphor in this country, as measured by the
importations, has been decreasing during the past ten years, while
the price has been increasing, as indicated by the following table:
IMPORTS, VAI.UES AND APPROXIMATE; VAI^UES P^R POUND OF CAMPHOR FOR
YEARS ENDED JUNE 30, 1887-1896, AND FOR NINE
MONTHS ENDED MARCH 31, 1897.
Crude Camphor— Duty Free.
Years.
Quantities.
Pounds.
1887 2,873,184
1888 2,779,719
1889 I 1,974,500
'890 2,061,370
'891 1,666,074
'^92 1,955,787
1893 1,723,425
'894 1,323,932
*°95 1,509,713
*^6 943,205
For 9 months, March,
31. 1897 (latest re-
ports obtainable) . 855,284
•Ten per cent, ad valorem.
j Value
Values. [ per
pound.
$352,861.00
304,460.00
293,031.44
421,385.00
468,025.00
447,634.00
446,548.00
309,407.00
284,958.00
328,457.00
207,137-77
$0.12
• II
.15
.20
.28
• 23
.26
.23
•19
•35
.24
Refined Camphor— Dutiable.
Quantities,
Pounds.
307
61
72
87
63
56,820
156,291
137,882
271,164
1.53,912
155.027
Value
Values.
per
pound.
$45.00
$0.15
7-77
-13
10.50
• 15
37-75
-43
21.23
•33
17,361.00
.31
51,229.33
•33
44-233.00
.32
8^,382.00
.31
68,785.00
•45
52,811.00
.34
Rates of
Duty.
Per lb,
5 cents.
do
do
do
4 cents.
do
do
do
(*)
(*)
(*)
^"dctXr.^^^"} Camphor Tree. 515
The Tariff Act approved July 27, 1S97, imposes a duty of 6 cents
per pound on refined camphor and leaves crude camphor on the free
list, as heretofore.
There has been an increase in importations of refined camphor,
due to improved methods of refinin^r and packing in Japan and to
changes in the tariff; but this increase has been much more than
counter-balanced by the decrease in importations of crude camphor.
The decrease may be attributed to the following causes: (i) The
exhaustion of the supply oi the available camphor trees near the
shipping ports ; (2) the governmental restrictions on the trade in
camphor in Formosa : (3) government taxes on the exportation of
camphor from Formosa ; (4) hostilities and wanton destruction of
camphor stills by the natives in Formosa; (5) disturbances in the
camphor-producing district of China ; (6) the China-Japan war ;
(7) attempts by speculators to corner the market.
These causes have increased the price of camphor, and this in
turn has led to the introduction of substitutes. Menthol and other
peppermint derivatives or compounds, carbolic acid and its deriva-
tives, naphthalin, formalin and insect powder are now used for various
purposes where camphor was former!)' employed. Camphor has
been manufactured artificially at a cost leaving a margin of profit at
present prices. It is, therefore, apparent that if the production of
camphor from the trees is to be carried on with profit in this
country, and the industry increased to any considerable extent, the
price of camphor must be reduced to compete with the prices of
substitutes now taking its place.
Camphor has been obtained from several other plants not at all
related to the ordinary camphor tree; but only two kinds, Borneo
camphor and Hlumea camphor, are of any importance commer-
cially.
Borneo camphor is obtained from the camphor tree of Horneo
and Sumatra, Dryobalanops aromatica. It is deposited in clefts and
hollows in the wood, and has simply to be taken out. This cam-
phor is comparatively rare and the supply is consumed almost ex-
clusively in China, where it is valued at from thirty t(i ninct\' times
as much as ordinary camphor.
Blumea camphor is obtained by distillation from Blumea balsami-
fera, a shrub growing in Hurmah and the Malay Peninsula. This
is usually refined in Canton, whence about 10,000 pounds are ex-
5i6 Therapeutic Properties of Alcohol, { ^'^.cioberasg/"-
ported annually. The source of this supply is abundant, and as the
industry develops it is likely to enter more into competition with
ordinary camphor. Neither of these plants can be grown in the
United States, except possibly in southern Florida, without protec-
tion against cold.
Approved :
James Wilson,
Secretary of Agriculture.
Washington, D. C, August 12, 1897.
ON THE THERAPEUTIC PROPERTIES OF ALCOHOL
AND THE REASONS WHY THE FERMENTED AND
DISTILLED LIQUORS USED AS BEVERAGES
SHOULD NOT BE RECOGNIZED IN THE
PHARMACOPCEIA AS MEDICINAL
AGENTS.i
ByN. S. Davis, A.M., M.D., LL.D.
Pure ethyl alcohol, undiluted, is regarded by all chemists and in-
telligent physicians as an active poison, rapidly destructive of both
vegetable and animal life whenever brought into contact with either.
The presence of absolute alcohol in contact with any living tissue
immediately arrests all natural metabolic and vital processes in such
tissue, and causes it to become corrugated or shrunken and dead.
Swallowing absolute alcohol, undiluted, as quickly destroys the
vitality of the membranes of the mouth, throat and stomach, and
kills the individual, as does pure carbolic acid. Consequently, alco-
hol, in its pure and undiluted state, is not capable of being used as
a medicine, but when largely diluted with water, as it is in all the
fermented and distilled beverages, its direct corrosive or corrugating
effect upon the membranes it comes in contact with is so much
diminished that it is capable of being absorbed and conveyed in the
blood to all parts of living body. In this diluted condition, there-
fore, it early began to be used both as a medicine and as a popular
drink; and as the most readily appreciable effect was to diminish the
^ Presented to the Section on Materia Medica, Pharmacy and Therapeutics at
the Forty-eighth Annual Meeting of the American Medical Association, held
at Philadelphia, June 1-4, 1897, and taken from \he Journal of the American
Medical Association, o{ August 21, 1897.
^°octXr!'f^.'"' } Therapeutic Properties of Alcohol. 517
individual's consciousness oi impressions, not only from without, but
also from within, it soon came to be regarded as a universal tonic
and restorative. Its supposed tonic and restorative effects were
based wholly on the sensations and movements of patients or indi-
viduals under the influence of moderate doses, for it was soon demon-
strated that large doses directly diminished strength, sensibility and
action. But when, under the influence of moderate doses, the
patient said he felt less weak or weary, felt the sensation of cold or
heat as painless, felt lighter or more buoyant, and his heart was
found to beat faster, it was perfectly natural for both physician and
patient to think the alcohol was acting as a tonic or stimulant and
general restorative. It was not until the advancement in analytic
chemistry and the physiology ot all parts of the nerve structures of
man, coupled with the researches in physics and biology of the last
half century, that we have had it in our power to prove the incor-
rectness of these conclusions founded on the sensations and actions
of the patient under its influence. The more recent chemico physi-
ologic researches have shown more clearly the composition of the
blood and the various tissues of the body, and especially the exist-
ence and functions of the haemoglobin, leucocytes and other corpus-
cular elements of both blood and tissues, and the part each plays in
the reception and internal distribution of oxygen, with its effects on
all the metabolic changes in living bodies. By the same class of re-
searches it is shown that alcohol, diluted with water and taken into
the stomach, is rapidly absorbed by the capillaries and is conveyed
in the blood to every tissue in the body, and by its presence retards
the natural metabolic changes, lessens the processes of oxidation and
elimination, diminishes nerve sensibility and, when repeated from
day to day, induces cell and tissue degeneration. By the more re-
cent studies in the anatomy and physiology of the several parts of
the nervous system, it has been shown not onh' that the action of the
heart and the movement of the blood in the vessels are directly
under the control of the cardiac and vasomotor nerves, some of the
fibres of which are exciters of action, while others are inhibitors, by
which uniformity and harmony is maintained in the circulation of
the blood, but also that our voluntary movements and sensations are
manifested by the cerebro-spinal nerves, having their exciters and
inhibitors by which we are enabled to co-ordinate muscular contrac-
tions and relaxations in executing all complex movements, and
5i8 riurapeutic Properties of Alcohol. {^^ctoberS™''
equally so it is that our mental actions, manifested through the con-
volutions of the brain, are regulated by exciters and inhibitors.
Every individual whose brain is in its normal condition has fre-
quent sensations, impulses or exciters of mental actions which he
promptly inhibits or disregards. Indeed, it is on the proper devel-
opment of this mental inhibition that every person's self-control and
sense of propriety depends.
If it is true, as has been already stated, that alcohol, when taken
into the living system in large doses, is an active poison, quickly
destroying animal life, and in smaller doses is an anaesthetic, directly
diminishing cerebral sensibility and mental consciousness and retard-
ing all metabolic changes, both in the blood and tissues, it follows as
a logical and necessary inference that, if administered as medicine, it
should be done with the same care and exactness in regard to purity,
dose and time that we exercise in prescribing morphine, quinine,
aconite, arsenic or any other active drug. This cannot be done by
using any of the various fermented and distilled liquors ordered
either from drug stores or liquor dealers, since they are kept at no
uniform standard of either strength or purity. The present Pharma-
copoeia recognizes as medicines, vinum or wine, spiritus frumenti or
whiskey, and spiritus vini gallici or brandy, but does not give a defi-
nite official standard of alcoholic strength for either of them. Neither
does it give any reliable and readily available tests by which the
strength and purity of the articles can be determined by the ordinary
practitioner of medicine. Repeated analyses have shown that the
amount of alcohol in difierent samples of wine varies from 6 to 25
per cent.; in whiskey, from 35 to 50 per cent., and in brandy, from
40 to 60 per cent. Such variations in the strength of any other medi.
cine would quickly cause its standard to be corrected, or its exclusion
from the official list of drugs. As alcohol is the only important
therapeutic agent in all these liquors, why not let pure alcohol
of fixed strength be officially recognized to the exclusion of all the
varieties of both fermented and distilled drinks? Then every practi-
tioner desiring to give alcohol as a remedy could order it with any
desired degree of dilution with water, and he would know what his
patient was getting and how much, and the pharmacist would no
longer need to pay for a license to sell liquors, or to be classed with
the ordinary dealers in such beverages. One of the most important
improvements in modern pharmacology consists in the separation of
'^'ocfoberriSS-'"''} Therapeutic Properties of AlcoJwl. 519
the active therapeutic agents from the more complex or crude drugs,
and thereby enables the physician to administer them with far
greater convenience and certainty. Very few intelligent physicians
of the present day would think of prescribing crude opium when
they desired to produce only the anodyne effects of the morphine it
contained, certainly not without knowing what per cent, of morphine
would be in the crude drug. Why, then, should he prescribe the
uncertain mixtures called beer, wine, whiskey or brandy, when his
sole object is to obtain the therapeutic effects of alcohol? If it is
claimed that these several fermented and distilled liquors contain
other therapeutic agents in addition to the alcohol, we answer that,
so far as any such agents exist, their proportionate quantity and
quality are far more variable and uncertain than is their per cent, of
alcohol. Almost the only constituents found in whiskey and brandy,
besides the alcohol and water, are very variable quantities of fusel
oil, tannin and, in very old specimens, a trace of some ethereal sub-
stance to which connoisseurs attribute the special bouquet. So far
from adding to the therapeutic value, the first two substances are
regarded as very undesirable impurities, and the last named has
never been isolated in sufficient quantity to have its medical quali-
ties tried. Much has been said and written concerning valuable
nutritive constituents in the different varieties of wine, but the
numerous analyses on record show onl\' very variable quantities of
fecula, saccharine matter, tannin, some vegetable acids and potassium
salts, in addition to the alcohol and water. Of these extra ingred-
ients the fecula and saccharine matter are the only ones that could be
classed as nutritive or capable of being converted into any natural
element of the blood or tissues of the body.
The quantity of these in any variety of wine is so limited that it
would require several barrels of the wine to furnish the equivalent
of a pound of bread. Consequently, it would be far more economic,
as well as more scientifically accurate, for every physician to pre-
scribe such doses of pure alcohol and water to be given witli such
quantity of sugar, milk or meat broth, as he thought his patient
might need. The physician who cannot do this, and thereby accu-
rately adjust the proportion of all the elements his patient may need,
has certainly received a very defective professional education. It
would be a long and very important step in advance, both in the
interests of .scientific accuracy and of humanity, if all physicians,
520 Strophanthus Nicholsonu {^"oiobeA^r'
when they thought alcohol was needed, would prescribe it in the
manner just indicated, and if in the next revision of the Pharma-
copoeia, only alcohol of standard strength was retained to the exclu-
sion of all fermented and distilled liquors. If these changes were
adopted and carried into general practice, the result would be a
more complete separation of both pharmacist and physician from
connection with, or responsibility for, the general traffic in and uses
of the various alcoholic liquors in popular use.
STROPHANTHUS NICHOLSONI— A NEW SPECIES.^
By B. M. Hoi^mes.
For some years past I have been endeavoring to obtain herbarium
specimens in flower and fruit of the species yielding the kombe
seed of commerce, and the •• white woolly " strophanthus seeds im-
ported from the same district, but hitherto without success. Dr. T»
G. Nicholson, who has lately returned from Central Africa, kindly
promised to endeavor to obtain specimens, and has brought back
flowers and fruit of a strophanthus, the seeds of which appear to be
identical with those of the " white woolly" strophanthus. The plant
proves to be a new species hitherto undescribed. Dr. Nicholson
has given me the following description of the plant : It is a small
bush or shrub, about 3 or 4 feet high, having the habit of
growth of the flowering currant (Ribes sanguineum, Pursh.), but the
main branches curve slightly outwards, and the slender twigs are
patent at an obtuse angle.
It grows in alluvial plains at the base of granite hills, intersected
by quartz veins. These plains are at an altitude of about 2,200 feet
above sea- level. The ground is sodden from the middle of Novem-
ber until the beginning of April. It is sparsely covered with bush,
and there is very little shade where the strophanthus grows. The
temperature averages about 105*^ F. in the sun and 50° F. in the
night. The specimens in flower were gathered at the end of Octo-
ber. There are the pods of the previous year opening on the bush
at the same time that the flowers are in blossom, and in December
the flowers are over and the seeds scattered. At the time the plant
flowers there are no leaves formed, or they are only very slightly
developed.
Pharmaceutical Journal, September 4, 1897.
Am. Jour. Phartn.
October, 1897.
StrophantJius Nicholsoni.
21
The general color of the flowers is of a pink hue, with a tinj^e of
dusky fawn. The throat of the corolla is yellow, with dark purple
lines and spots. The thread-like corolla segments or " streamers "
are of a pinkish purple. The whole corolla in withering fades to
yellow, but does not readily fall off. The fruit is of a purplish plum
Strophanthus Nicholsoni, n. sp. — a, leafy twig with leaves undeveloped ; ^,
leafless inflorescence ; r, unopened flower ; d, calyx ; e, corolla, with tails re-
moved ; y, anthers ; g^ seed ; a, b^ r, g^ about two-thirds natural size ; d, e, /,
enlarged.
color, and marked with linear oval lenticcls, S(^me of which are
nearly i centimeter long. The district in which he found the plant
extends from Lusengasia, in the Senega country, in a southwest
direction to the Loangwa River.
The Ozimba natives would not admit that they used it as an
522 Strophanthus Nicholsoni. {^'octobeVisw.'"-
arrow poison, but stated that it was so used by the Chipeta people.
The plant is most nearly allied to S. schuchardti, Pax., and may be
characterized by the following description :
Strophanthus Nicholsoni, n. sp. — Frutex dumosus, ramis griseofuscis, vetustis
glabris, novellis dense tomentosio ; folia (juuiora solum visa, ad i centimeter
longa), brevissime petrolata, crassa, ovata, basi cordata, obtusa, utraque facie
velutina, grisea, nervis in conspicuis ; cymae secus ramos denudatos, ramulum
abbreviatum terminantes, abortu 1-3 floras, pedunculo calycem subsequante,
bracteis augiiste linearibus ; calycis segmenta erecta, linearia, ijiequalia, acuta
duo latiora, diametro millimetrum aequantes, corollse tubo paulo breviora ;
corolla tola pubescens, fauce interno tenuissime pubescente, tubo inferne cylin-
drico, fauce dilatato, lobis lanceolatis ad 15 millimeters, in caudam elongatam
6-10 centimeters, productis ; faucis squatnce tenuissime pubescentes, parvae, ad
2 millimeters longae, lauceolatae, obtusae, antherse sagittatae filamentis glabris;
ovarium hirsutum ; fructus purpureus lenticellosus, 14-27 centimeters longus ;
semina i j^ centimeters longa 5 millimeters lata, dense velutina, pallide brun-
neo alba, aristae parte nuda 4>^ centimeters, comosa 6 centimeters longa.
The main branches are about i^ centimeters thick, with slightly
swollen internodes, at a distance of about 4-7 centimeters, dull pur-
plish-brown with a glaucous surface, but strongly marked with elon-
gated brownish, narrow lenticels. The young leafy twigs and the
pedicels and bracts are densely velvety. The anthers have a pro-
jecting appendage or rib at the back near the base.
This species resembles S. sarmentosus in flowering before the
leaves appear, but differs in its erect, bushy habit, small flowers and
more slender flowering branches. From S. schuchardti it differs in
the lateral leafless inflorescence, the linear bracts and unequal calyx
segments, in the latter nearly equalling the corolla tube, in the
whole of the corolla being pubescent, in the much longer tails to the
segments of the corolla, and in the pubescent glands. With sul-
phuric acid the section of the seeds gives the same rose color as the
" white woolly" strophanthus seed of commerce. The velvety coat-
ing of the seeds hides the base of the awn, and, like that of the
" white woolly " strophanthus seeds, the hairs look white when their
bases are presented to the light, and brownish-fawn color when
their apices are turned to the light. The average measurements of
the seeds are the same.
An adulteration of magnesium sulphate with zinc sulphate has been observed
by P. A. Ivamanna, Boll. Chim. Farm., 36, 198. The zinc salt maybe detected
by the addition of one drop of solution of potassium ferricyanide to a solution
of the suspected salt, when, if zinc is present, a brownish-yellow precipitate is
produced.
^"ociobe/lltr} Powdered Vegetable Drugs. 523
EXAMINATION OF POWDERED VEGETABLE DRUGS.
By Henry Kr^,mer.
Powdered drugs and " pressed herbs " will, no doubt, at a not
very distant day, be the form in which most of the vegetable drugs
will be bought and sold by the apothecary. It seems reasonable to
suppose, however, that a few drugs, as licorice root, slippery elm
bark, chamomile flowers, rhubarb, orris root, Canada snake root,
senna leaves, manna, etc., will always be obtainable in a more or less
crude condition, as most of these require that they be broken as
little as possible for some of the purposes for which they are used.
But even these may be ground and compressed into forms, as " rhu-
barb fingers," that may be in keeping with more elegant pharmacy.
Some of the manufacturers, at least, of powdered vegetable drugs and
*♦ pressed herbs " have overcome probably nearly every objection
that might be raised against their products. They have done,
moreover, the art of healing an immense amount of good, inasmuch
as their products are sold in proper containers or are wrapped so as
to insure against the maximum amount of deterioration.
It is well known that the average pharmacist pays very little
attention to the preservation of all his stock of crude vegetable
drugs. The number of suitable containers are generally few, and
the stock is necessarily in much greater excess of these. Those
that have no proper receptacles, as well as the over-abundance of
drugs purchased for which no suitable containers are provided, are
wrapped in what is by no means impervious paper and stored away
either on top of each other or side by side, or both, in an •• out-of-
the-way " place.
Some of the advantages in the buying of powdered drugs are :
(1) That they are ground by the manufacturer of pharmaceutical
products to the fineness specified by the U. S. Pharmacopo-Ma, or,
when the drug is not official, to that which is generally used.
(2) The pharmacist is saved the expense for apparatus, as a drug-
mill, sieves, etc.
(3) He furthermore saves time in grinding the crude drugs or
attending to the same.
(4) The powdered drugs which he purchases are in impervious
containers, and of such a form that he does not hesitate to place
them on his shelves or his " out-of-the-way" place, be it the hottest
part of his store (over the cases) or the most humid part.
524 Powdered Vegetable Drugs. {^"^/tXerf'^sir-
(5) No additional expense may be felt by the pharmacist for secur-
ing other containers than those in which his products come to him.
Some of the disadvantages in the purchasing of powdered drugs
are :
(i) That the drug in this condition costs from 5 to 50 per cent,
more.
(2) The apprentice does not obtain the kind of practical experi-
ence in grinding drugs that will be always of inestimable value to
him in determining either their identity or quality.
(3) The product which has been ground by someone else is likely
to be more uncertain than one ground by the pharmacist himself
from crude drugs of which he can so readily test the quality.
(4) There is at present no easy method for the average pharma-
cist to determine the purity of the powdered drugs he purchases.
Now, some pharmacists have the idea that a large sum of money
must be expended in order to be able to grind one's own drugs —
that, for instance, steam-power is necessary, an expensive mill must
be provided and a special room set apart for doing this kind of
work. The fact of the matter is that such an expensive and elabo-
rate plant is impracticable as well as unnecessary. Comparatively
little money need be expended to purchase a good hand-mill and
the necessary sieves. With but very little outlay, the retail pharma-
cist can grind his own drugs and overcome the disadvantages above
noted. It is not the object of this paper, however, to discourage
the buying of powdered drugs or even to compare the expense of
grinding either commercial drugs or those of one's own collecting
with that of commercial powdered products, but to consider the
qualitative and quantitative investigation of powdered drugs.
QUALITATIVE EXAMINATION.
We are indebted particularly to the labors of Pliickiger, Wigand,
Vogl, Arthur Meyer, Moeller, Tschirch, Schrenck and others, who,
during the past ten years, chiefly have given to us in their publica-
tions the characteristic structures of many of our crude drugs. All
this has been necessary and is a preparation for the study of pow-
dered drugs. While much has been done, even in the study of
powdered products, there still remains much to be done in the study
of both crude (particularly American) and powdered drugs. Sev-
eral things are necessary for the study of powdered drugs:
'"'ocfober.'i'slr'.'" } Powdered Vegetable Drugs. 525
(i) Suitable methods for the rapid discrimination and study of
the characteristic tissues and contents of the powder. While sec
tions of the fine particles can be made (by holding the particle be-
tween the forefinger and thumb and drawing the razor through the
specimen), still this is laborious and requires considerable practice,
time and confidence. It is, therefore, necessary to devise means and
employ reagents which shall make the specimen transparent and not
destroy either the tissues or contents that need to be seen. The
most satisfactory reagent for general purposes in the hands of the
writer has been the employment of the following solution :
CHLOR.AL-GLVCERIN SOLUTION.
Glycerin (C. P.) l.^q^^lp^^
Distilled water >
Chloral — sufficient to saturate the solution.
A few drops of this solution are placed on the slide and from
0002 to o 008 gramme of the powder added. The cover-glass is
put on the specimen and the preparation is heated gently over either
a spirit lamp, gas flame or oil lamp until it begins to boil. This is
then allowed to cool and e.xamined. If not sufficiently transparent
it is heated again. This is generally not necessary, as with but one
heating the tissues are transparent and contents may be examined.
It is true that this treatment causes a slight swelling of the cell-
wall, and is not applicable in testing for starch ; but this reagent
has the advantages of clearing the specimen and preventing it,
without further treatment, from drying out.
When examining specimens containing starch another solution is
used, as follows :
CHLORAL-GLYCERIN SOLUTION + IODINE.
Chloral-glycerin solution — any con^enient quantity.
Iodine — a sufficient quantity is added to saturate the solution. '
This .solution is placed on the slide and the same quantity of
powder used as before, but heat is not applied. The starch grains,
with all of the characteristic markings, will be brought out and may
be studied.
When lignified cells are sought, the powder must first be
moistened with a drop or two of the following solution of anilin
hydrochloride, and then after a few minutes a few drops of the
chloral-glycerin solution may be added :
526 Pimdered Vegetable Drugs. {^^^'i^^^
ANTLEN' HYDROCHLORIDE SOLUTTOX.
Anilin hjrdrochloride - • 5 g""-
Hydrochloric addi C- P.) 25 cc.
Alcohol i 95 per cent.) -- 25 cc.
Distilled water . . 50 cc.
The anilin hydrochloride is diss-z.vcd in :he alcohol, and to this
solution the water containing the hydrochloric acid is added. When
this solution is used, of course, cn.-stals of calcium oxalate or
calcium carbonate are destroyed.
The author is at present at work upon other solutions ha^-in^
the same principle in their coniposition as the above : but those
mentioned are all that are necessary' gener ;. .-- \ — :
with success.
(2) All investigators should record the sa& of the tissues or their
contents in microns. The lengtii of bast or wood fibres, size of
pores, cr>'stals, starch grains, stone cells, etc, arc all more or less
characteristic for the drugs we have to consider. It is not suflBdent
to say that drawings were made by the use of a ^indi objective
and a i-inch ocular. The objectives and oculars of the various
makes of microscopes not only magnify difierently, but the question
of tube length is also important in this connection. But even if all
of these data were given, it must be conceded as beii^ tedious to the
reader to calculate the size of the elements, which might be so
easily done by the author. Even for an investigator to say that his
drawings are magnified so many diameters <ioes not give us tihe true
and scientific idea of the elements which the author has seen and
we are to use in the study of powdered drugs. We need records
in microns of the size of tissues and constituents of drugs from
many sources for comparison, so that another investigator may
readily get at the facts. This is the only scientific method for the
prosecution of this kind of work, and must be rigidly pursued bjr
alL
(3) A scheme for the logical quaiitatiYe determination of a
powder is necessary. It will be somewhat difficult to work out a
scheme that will be of practical benefit, because it is necessary to
begin with the consideration of the characteristics of all dn^s and
adulterants that may be used. It will not be possiUe, for instance,
to separate the leaves from roots, etc., as is done in the study of
crude drugs. Many points, such as color, taste, odor, as well as con-
^'october.?8^':'"} Powdered Vegetable Drugs. 527
stituents and structural characteristics must be considered. The author
is at present engaged in a work having for its object the identifi-
cation of a powder and quahty of it, and hopes to have it completed
during the coming year.
(4) Furthermore, it is necessary for all those who have to do with
the training of the apprentice, and buying and selling of powdered
drugs, to engage in the study of the same until the most satisfactory
methods for determining the identification and quality be ascertained.
In our educational institutions there is little or nothing being done,
apparently, in this direction. It seems that the time is ripe for
some time to be given to the study of powdered drugs in connection
with that of crude drugs. This will undoubtedly be of the most
practical benefit, as powdered drugs are already handled by most
pharmacists to some extent at least.
This subject of the investigation of powdered drugs is one of great
importance to-day. The older method of teaching pharmacognosy
in this country must be supplanted by the new, having for its object
the study of the powdered commercial drugs. This knowledge
ought to be demanded by our State boards of pharmacy. It is in
keeping, too, with the desires of the professional pharmacist, as it
will tend to keep out the competing ^'merchant" and "grocer." Our
♦' pure food laws " will require the pharmacist to know the value
of the drugs and foods he sells. This may be required also of the
grocer, but he can buy and sell in original packages. The pharma-
cist is hardly in the same position, as he cannot always dispense in
original packages, and he is responsible for the purity of the goods
that he possesses and sells. The conscientious pharmacist wants
this knowledge, desires stringent examinations and just laws, and
will in his everyday dealings live up to what he knows. He has
nothing to lose; it is only the incompetent or dishonest dealer in
drugs and foods who will suffer.
QUANTITATIVE EX AMI. NATION.
In a paper presented to the A. Ph. A. in 1894, a preliminary notice
of a method for securing appro.ximatc quantitative results of the
examination of a powder by means of the microscope was given. After
a few years of deliberation and some practice the principles of the
process are somewhat more satisfactorily developed and the results
will be given. Since 1894 the results of several workers — Day
528 Powdered Vegetable Drugs, {
A.m. Jour. Pharm.
October, 1897.
(A.Ph.A. Proc, i896)andKebler(AMER. Jour. Pharm., 1897, p. 244) —
as well as the labors of some students during the past year, indicate
that the principle of the process suggested is satisfactory, whatever
the modifications recommended. The following are the important
points embracing the principles of the process as developed thus
far:
(i) The same reagents and mounting media are employed in doing
quantitative work as were considered in the qualitative examination
of the powder. In quantitative work, not only some, but all of the
important characteristic tissues and contents are to be rendered
visible.
(2) The quantity of powder to be examined by means of the
microscope must represent the sample in every particular ; in other
words, the sampling must be done properly and in accordance with
the methods used in the assay of ores. While the quantity to be
examined may consist of but a few grammes, it must thoroughly
represent the lot of powder on which value is to be given.
(3) The standard powders, with which the powder under investi-
gation is to be compared, must thoroughly represent the drug in the
various ways in which it may be treated. The degree of fineness
must especially be carefully borne in mind. A sample of a drug of
No. 40 powder cannot be compared with one of No. 60. If the sam-
ple of a drug to be examined is of a No. 40 powder, the standards
must also be of the same degree of fineness. If extraction of active
principles is suspected in the powder, it must be compared with a
standard that has been extracted. In fact, every treatment that is
possible in a sample to be analyzed must be given to a standard, if pos-
sible, with which the comparison is made.
(4) The amount of powder used in the examination is generally
about ^^^ gramme (== 0-0039 gramme = 006 grain). In
some cases twice this quantity (y^^ gramme) or but one-half this
amount {^\^ gramme) may be used to greater advantage. The
quantity of powder may be weighed out, or, what is more conven-
ient, with practice a gramme is weighed out and divided with a
spatula with the eye, as follows :
Am. Jour. Pharm,
October. 1S97.
} Powdered Vegetable Drugs,
529
\
i
i
1-
ife
il
h
jt 01
^ = o"5oo gramme,
X=-- 0-250
>^ = o-i2S
tV = o-c62S ••
,ij = 0-03125 "
yiy = 0-0078 "
ik = o'oo39 "
(5) The cover-glasses used, whether round or square, should be
uniform in size and tJiickness for comparison of the mounts of the
standard with those of the specimen to be tested.
(6) The amount of rfr7^i7// employed in making a mount must be
just sufficient to float the cover-glass, and as few air-bubbles as pos-
sible are permitted to be formed.
(7) A homogeneous mixture of powder with reagent must be formed
before the cover-glass is put down. This is best done by taking the
edge of the cover-glass in a pair of forceps and distributing the
powder in the mounting media or reagent
(8) After the mount has been made and the powder examined
previously qualitatively, the quantitative estimation of the powder is
determined. This is based on one or more of the structures or con-
stituents that are characteristic of the drug or drugs that may be
present. A few examples may be given :
In Cinchona, the bast fibres are best selected.
In Quillaja, the monoclinic calcium oxalate crystals are most
characteristic.
In Belladonnce folia, the pieces of tissues, with some cells contain-
ing the characteristic grayish sand.like crystals of calcium oxalate,
are selected.
In Hyoscyami folia, the pieces of tissues, with some cells con-
taining the characteristic cubical or tetragonal crystals of calcium
oxalate, are used.
In Stramonii folia, XhQ pieces of tissues, with some cells containing
the characteristic " rosette-shaped " crystals of calcium oxalate, are
most characteristic.
In Zingiber, the estimation is based on the starch grains, or better,
the oil-secreting cells.
530
Powdered Vegetable Drugs.
Am. Jour. Pharm.
October, 1897.
In Scilla, the number of cells with groups of acicular crystals
are best selected.
In Bcllado7incB radix, the starch grains are most easily used, but it
must be borne in mind that there are several kinds of Belladonna
root in the market.
In JSlux Vomica, the lignified hairs are most characteristic.
In Rheum, the large ''rosette-shaped " crystals of calcium oxalate
are best selected.
In Caryophyllus, the oil-secreting reservoirs are used.
In Cinnainomum, the groups of stone cells or starch grains are
characteristic, taken in connection with the presence or absence of
cork cells.
In Sarsapanlla, the starch grains are considered after the kind of
root has been ascertained.
X X
X
X X
Fig. 2.
In Glycyrrhiza, the characteristic fibres with calcium oxalate crys-
tals adjoining them, or the starch grains, are employed.
(9) The method consists in counting the number of characteristic
elements in several portions of the slide, and may be performed in
several ways :
{a) By the use of an ocular micrometer ruled in lOO square milli.
meters, as proposed in 1894. Five portions, at least, of the mount
are examined, as in the places marked X (Fig. 2).
The number of characteristic elements that appear in each of
these places in certain portions of the ocular micrometer are counted,
as, for instance, those that appear in the square millimeters marked
X (Fig J).
The low power (>^ to ^-inch objective) is used in some cases, as
in the estimation of rheum, scilla, etc.; but in most instances, espe-
cially when starch grains are to be counted, a higher power (}( to
^-mch objective) is preferred, as in Belladonnae radix. Zingiber, etc.
Am. J oar. Pharm.
October. 1897.
} Powdered Vegetable Drugs.
531
(b) While these ocular micrometers ruled in square milhmeters
are easily made, still the makers of microscopical accessories charge
such a very high price for the same that it has been found desira-
ble to devise another way for doing the same kind of work. An
ordinary ocular micrometer divided into tenths of millimeters is
taken, and the number of elements between the outer portions, ruled
to a less number of divisions (as those marked X, Fig. ^), are
counted.
It is better, when using this ocular micrometer, to turn the latter
around i8o° after counting in the one direction, and counting again.
In other words, an additional count is made, i. c, ten are made upon
each mount.
(r) There are some cases when it is not desirable to use either (^)
or {o), as when the elements or tissues are so large that it is more
practicable to exclude the ocular micrometers, and to count all of the
tissues or constituents as they appear in the whole field of view of
X in Fig. I.
The low power (-^ to ^A inch) ma)- be used sometimes, as in the
—
r-
X
X
X
X
X
X,
y,
x*
,x
X
X
x;
•^
>
X
fi
X
X
X
X
_,
_j
Fig. 3.
estimation of cinchona, quillaja, glycyrrhiza, etc., while in other
drugs, as Hyoscyami folia, Bclladonn;u folia, etc., a higher power
(i ^^ i) *^ used.
(10) The number of mounts \o be made of the standard and the
powder under examination should generally not be less than twelve
each. But as two to three mounts can be made upon the same slide,
from four to six slides only are necessary for each powder.
(11) If the powder is found to be a mixture, a similar compound,
representing the proportions found, should be made up, and the
powder under investigation be compared with it.
(12) It is apparent that the quantitative results are purely com-
parisons of an unknown with a known powder. The conditions
must be nearly the same in both. The sampling must be done
similarly ; the same amount of powder must be used in both, and
532 Poivdered Vegetable Drugs, { ^"^ctoberasQ/"'
no more reagent or mounting media should be used than is neces-
sary to hold the cover-glass without any air being impinged. The
same microscope and powers, as well as other conditions, must be
employed to secure even approximate results, as this is all that can
be expected at present.
It would be useless for the author to record some of his standards
and results; but it no doubt will be profitable to give the records of
one or two instances where a number have worked upon the same
powder.
STANDARD OF NUX VOMICA.
No. Hairs.
1. Mean of lo readings 12
2. " 8 " 12'^
3. "10 " io*9
X
X
X
X
X
X
Fig. 4.
A sample of cinchona, that contained 75 per cent, of cinchona
and 25 per cent, of wheat starch, was assayed by the process given
under 9 (b) for starch and 9 (c) for bast fibres, and gave the follow-
ing results to nine different workers :
No
I
2
3
4
5
6
7
Cinchona.
Per Cent.
Mean of 20 readings 74
9-
Total
10
20
12
16
12
II
20
28
149
67
82
77
66
77
69
80
75
Starch.
Per Cent.
23
25
28
35
27
23
30
22
74-11
26-66
Conclusion. — We need more effective work in the qualitative study
of powdered drugs, and we have some recent evidences that this
will be done in this country.
Am. Jour. Pharru.) I^itt^e .. ^ *
October. 1897. / KftlOS. 533
Approximate quantitative results may be obtained in the exami-
nation of unknown powders b\' the methods j^iven. There are some
cases, at least, where the quantitative determinations of admixtures
and adulterations, if they are to be determined at all, can be done
so only by means of a microscopical method.
It is possible that a microscopical separation of active principles
may be effected of both drugs as well as their preparations. This
would be the desideratum in quantitative microscopical work. Thus
far, the work of the author has been unsatisfactory in this direction,
because, while at times results come, still the products disappear as
quickly, owing no doubt to microscopic conditions of heat and
moisture altering the products formed.
KINOS.^
By Joseph Bosisto, C.M.G.
The question whether the place of the official variety of kino,
which is now almost unobtainable, can be effectively supplied by
others met with in commerce (B.P.C. Blue List, No. 49), is answered
from Victoria, Australia, to the following extent. Although the
Pterocarpus marsupium, and other species of the natural order Legu-
minosai yielding kino, are not known to exist in Australia, yet the
natural order Myrtaceae, which exists throughout Australia, contains
many species which exude kinos and some catechus. Those have
not, so far (save and except one), been found of commercial value,
owing to their sparse solubility in water, and in all other known
cheap solvents. This arises from the gum kino not being collected
within a few days after its appearance on the outer bark. The
extreme bright sunlight of Australia, together with the warm ther-
mal lines existing both night and day, causes it rapidly to degenerate
into a degraded bassorin, which is insoluble.
Quantities of such kinos exist throughout Australia, obtainable
chiefly from Eucalyptus marginata, K. amygdalina, E. sideroxylon,
E. fissilis, and many others. The one I have already indicated is
Eucalyptus rostrata, from which is exported annually about two
tons of its gum; this is almost entirely soluble in water, and is a true
kino. It is mentioned in Scjuire's "Companion to the H.r.," 1882,
and in Martindale's •• Extra Pharmacopceia," as gummi rubrum from
Eucalyptus rostrata.
^ Pharmaceutical Journal , August 28, 1897.
534 ^^^^^'^ NudlCaulis. {^^cSer.'isyT'.""
Eucalyptus rostrata is one of the leading trees in many of the
forests of Victoria, and is productive of this kinic substance, which,
being unable to force its way through the hard, tough outer bark,
lodges itself in treacly form in large orifices or carbuncles between
the wood and the bark in such quantities that I have known one
and two bucketfuls of the liquid to be obtained by boring a small
orifice in the swollen part. This liquid kino, when evaporated in a
vacuum pan, is obtained as beautiful ruby-red gum kino entirely
soluble in water or spirit. The supply from Australia would be very
great if only a remunerative market opened.
ARALIA NUDICAULIS.^
By William C. Alpkrs and Benjamin L. Murray.
Aralia nudicaulis grows abundantly in the New England and
Middle States, extending north into Canada, south as far as North
Carolina, and west to the Mississippi Valley, selecting principally
rich hilly woods. It is indigenous to the United States, not being
mentioned in European text-books, and has a number of synonyms,
as wild licorice, shotbush, small spikenard, false sarsaparilla, Vir-
ginia sarsaparilla, and wild sarsaparilla, the latter being the term
more commonly used. While country people know this aromatic
herb well under the name of wild sarsaparilla, or simply sarsaparilla,
and use it " to purify the blood and cleanse the skin," it has attracted
but little attention by the medical profession ; its only use in medi-
cine seems to be to serve as an adulterant of the official sarsaparilla,
in several lots of which, purchased in the New York market, the
writers have discovered it.
The late Professor Bastin examined Aralia nudicaulis microscopi-
cally, and published the results of his examination in The Western
Druggist, Vol. VII, 1885, P- SM- This is the only literature that
the writers were able to find on this interesting plant, and a chemi-
cal examination of its rhizome was probably never made before.
There is a slight difference in the description of the leaves and the
rhizome between Bastin's paper and ours, which suggests the idea
that possibly the Western species varies from the Eastern, Bastin
having collected his specimens in the vicinity of Chicago, while
^ Read at the annual meeting of the American Pharmaceutical Association,
August, 1897.
^"'/toTr.';^':"} ^ralia Nudicaulis, 535
ours were gathered near New York. Bastin, for instance, says that
the rhizome will reach a length of from 3 to 5 feet, and Gray, in
his text-books, makes the same statement, while we have hardly
found any rhizome shorter than 5 feet, and have a specimen here of
29 feet. The description of the leaves also shows some points of
difference, the leaves of our specimens being more divided than the
ones that Bastin describes. This latter observation was also made
by Professor A. C. Apgar, who proposed the name of Aralia mtdu
caidis prolifera i^BulL Torr. Bot. CL, 14: 166, 1887) for the species
found in New Jersey, while Professor N. Britton, in his ♦' Illustrated
Flora," calls this kind •' a mere form."
BOTANY.
Aralia nudicaulis belongs to the order Araliacec-e, and shares with
the other members of the order the warm, aromatic, almost pun-
gent, taste of some parts, principally the rhizome. Early in the
spring a petiole and a scape grow near each other from the rhizome,
which lies from i to 4 inches under the ground, and only rises
occasionally a little above the soil. The straight petiole, swollen at
the base, rises from 8 to 18 inches high and divides into three
Fig. I. — Corky layer of old hark, cross-section.
divisions, which at this point of divergence thicken like the base of
the main petiole ; each division bears a compound leaf of from three
to five leaflets. Occasionally one of the lower leaflets is again com-
pound. The leaflets are from 2 to 5 inches long, and from i to 2^
inches wide, pinnate with one terminal one, the lower pair on short
petioles, the upper one mostly sessile, oblung-ovate, one of the
lower ones occasionally almost round, acuminate, finely serrate,
smooth on both surfaces. The scape is a few inches shorter than
the petiole, and therefore, together with the flower, or later, the
fruit, hidden under the spreading leaves. It has neither leaf nor
bract, hence the name nudicaulis, and bears from three to seven
536
Aralia Nudicaulis.
/Am. Jour. Pharm.
\ October, 1897.
small, simple umbels, each consisting of from five to twenty-five
crreenish flowers. Occasionally there is one or more odd flowers,
with rather long stalks growing at right angles out of the scape
below or between the umbels. The flowers are perfect or poly-
gamous, with both fertile and sterile ones on the same plant. The
calyx is destitute of lobes or teeth ; the petals, stamens, and styles
are five in number. During the summer a dark purple, nearly
black, drupe develops about one-fourth of an inch in diameter. This
fruit is probably a welcome food for birds, as it disappears soon after
ripening, and can only seldom be found on the ground under the
Fig. 2. — Outer bark, longitudinal section.
leaves. It does not seem to serve for the propagation of the plant,
the creeping root-stock performing this function.
The most interesting part in which the peculiar aroma of the
plant is best noticeable is the rhizome. It grows horizontally and
spreads very quickly over a large area, reaching a length of more
than 25 feet, branching abundantly and producing small hairy root-
lets rather sparingly. The parts of the rhizome that rise out of
the soil harden and afterwards die off, producing by their decadence
two new growing plants in place of one. The rhizome is nearly
^"^ociTeJi^"^-} Ara/m Nudicaulis. 537
cylindrical, with many concave leaf-scars, corresponding in shape to
the swollen end of the petioles. The outer, very thin, grayish,
somewhat glossy layer of the bark is easily detachable, and the
lower, thick, fibrous layer can readily be peeled off the white or
slightly yellowish wood, as long as the rhizome is fresh and moist.
A white and spongy pith forms the interior of the wood. On drying,
the rhizome becomes wrinkled and brittle, and is from y^ to |< inch
in diameter. The taste of the fresh rhizome is peculiarly aromatic,
similar to that of ginseng, leaving no bad after-taste.
MICROSCOPY.
A cross-section of a segment of the rhizome shows under the
microscope three distinct parts, the pith, the wood and the bark.
The pith consists of rather large, granular cells, containing starch
with occasional crystals of oxalate of calcium.
The pith is surrounded by a wood zone which varies in thickness
according to the age of the specimen. In old rhizomes the wood is
about twice as thick as the bark, while in very young specimens a
cross-section shows a large pith, a thick bark, and very little wood.
The thick-walled woody edges of irregular size are separated by
medullary rays of one or two rows of cells. Sometimes these rays
are prolonged into the bark. A layer of cambium cells in a double
row surrounds the wood.
The bark consists of a fibrous layer, a corky layer and an epidermis.
The parenchyma cells are rich in starch anc* contain, like the pith,
crystals of calcium oxalate. The characteristic part of the fibrous
layer of the bark is the great number of oil or resin cells, the largest
cells of the plant, resembling tubes that can often be traced quite a
distance in longitudinal sections. They are intrenched by a wall of
small cells that undoubtedly secrete oil and resin, while the large
inner cells serve as reservoirs. The medullary rays often extend
into this layer, taking an irregular, somewhat tortuous course, and
sometimes their two rows ot cells separate and encase one of these
large oil cells. The resin is probably held in solution by the oil.
Between the fibrous and corky layers of the bark, a double row of
peculiarly shaped cells are observable, probably a layer of
phellogen.
The corky cells are empty and rather large, presenting no points
of particular interest. A thin epidermis covers the corky layer,
easily detachable and often wanting.
538
A ra Ha Nu die a u lis.
Am. Jour. Pharm.
October. 1897.
CHEMISTRY.
Samples of Aralia nudicaulis were gathered in the fall in the hilly
woods in Bergen County, N. J., and most of the chemical exami-
nations were made on these samples. A further supply was collected
in the following spring, when the flowers of the plant were in
bloom.
The general plan of the work was :
(i) To determine the presence or absence of alkaloids or gluco-
sides.
(2) To determine the presence of other important constituents.
O0o0o<^n^^0°p^^^''n000n toU
o o OOqOoO (^n^ Of)L
Fig. J. — Wood, from pith to bark, longitudinal section.
(3) To undertake a systematic analysis and estimation of the
constituents.
For the first part of the work, testing for alkaloids and glucosides,
samples of the drug gathered in the fall as well as in the spring
were finely ground and digested for three days in a closely stoppered
flask with Prollius' fluid. After filtering, the liquid was treated with
acidulated water (sulphuric acid i part, water 5 parts) and the aque-
ous liquid submitted to examination. Wagner's reagent, tannin,
^"?JcioTr.?8«"r-} Aralia Nudicaulis. 539
picric acid, platinic chloride, sodium phospho-molydate, and Mayer's
reagent, gave no precipitate. All the tests were repeatedly verified
by using larger quantities of acidulous solutions.
For the further determination of important constituents, together
with alkaloids and glucosides, the following experiments were
made :
Large samples of the finely ground rhizome of the plant, gathered
both in spring and fall, were digested in benzene for three days.
After filtering and evaporating to dryness, a yellowish-brown, resin-
ous mass was obtained. This residue was treated with warm water,
filtered and tested for alkaloids, glucosides and organic acids. The
still insoluble residue was treated with acidulous water, and this
acidulous liquid tested like the preceding one. The reagents
applied were salts of lead and calcium, tannic acid, Wagner's
reagent, platinic chloride, gelatin solution, and Fehling's solution.
No reaction was obtained, except a slight change of color in
Fehling's solution. To still further verify the above results and
avoid the uncertain action of water upon the resinous matter, which
became soft with heating, another benzene e.xtract was made and
treated directly with water and then with acidulated water. These
aqueous solutions caused no new changes, the color of Fehling's
solution alone being affected.
Tests for tannin were then made. A finely ground sample of the
drug was digested with a good grade of absolute alcohol and the
liquid filtered. This alcoholic liquid caused a slight reduction of
P'ehling's solution, and likewise precipitated a solution of gelatine,
starch paste, and antimony and potassium tartrate. A solution of
potassium hydrate was darkened, a solution of potassium perman-
ganate reduced in about two minutes, solution of silver nitrate
reduced, and a solution of ferric chloride rendered green. Confirma-
tory tests were made on two additional samples of the drug, in both
cases with the same result. The same reagents were also applied to
the alcohol alone, used for digesting, without showing any reaction.
The presence of a small percentage of tannin was therefore
determined.
The residue of the drug left in the experiment mentioned above,
after treating the Aralia with absolute alcohol, was washed thor-
oughly with more absolute alcohol, dried, and then digested twenty-
four hours in cold water. The aqueous liquid alter filtration wa.^ of
540
A ralia Nudicaii lis.
Am. Tour, Pharm.
October, 1897.
brown color. Upon application of heat it reduced Fehling's solution
and precipitated with a solution of basic acetate of lead, with a
solution of borax, with alcohol, and with ether. With a solution of
ferric chloride in the cold it caused no precipitate. The presence
of mucilaginous matter was thus shown.
As the next experiment, a sample of coarsely cut Aralia nudi-
caulis was distilled with steam, the distillate showing the presence
of an agreeable-smelling volatile oil. The liquid comes over milky,
Fig. ^. — Entire rhizome, segment, cross-section.
A, pitted vessels ; B, lignified cells ; D, cork cells ; E, medullary rays ; E^
medullary rays, prolonged into bark ; F, cambium layer ; G, resin and oil cells ;
Hy phellogen ; D to F, bark ; Fto /, wood ; I\.o K, pith.
and oily globules soon collect, floating upon the surface. The
microscopical examination had already revealed that this oil resides
in the bark of the rhizome, and upon distilling some of the fresh
bark alone, without the wood and pith of the rhizome, quite appre-
ciable quantities of oil were found.
Whether the rhizome gathered in the fall contains more or less
^'ociXr!'m-r } ^raiia Nudicaulis. 541
volatile oil than the spring drug has not been determined ; our
impression, based on the odor and taste of the samples of various
seasons, is, however, that the oil is more abundant in the fall than
in the spring. In working with the fresh bark alone the distillate
became more milky and the oil-drops solidified at about 20° C,
showing a light yellow color. Further investigations of this oily
portion led us to believe that some of the resins present in the plant
were carried over in the distillation, though precautions were taken
against it. The odor of the oil is persistent and gives the drug its
characteristic smell, noticeable even in the air of places where the
plant grows abundantly.
After having determined the absence of alkaloids and glucosides,
and the presence of tannin, starch, volatile oil and resins m the
rhizome of Aralia nudicaulis, examinations were made for some of
the more important constituents according to Parson's scheme. At
a temperature of 98° to 100° C, the drug lost 6-50 per cent, of
moisture, and the dry sample, on which all future percentage calcu-
lations were based, contained, on incineration, 547 per cent, of ash-
This ash yielded 2482 per cent., equal to 1-36 per cent, of the
original dry sample, of soluble matter, consisting of chlorides and
sulphates of sodium and potassium. The drug yields to chloroform
3-38 per cent, of a soft, brown, resinous and oily matter. This
chloroformic extract was dried for two months over sulphuric acid
without hardening. At a temperature of 110° C, it suffered a loss
equal to 0-33 per cent, of the original dry drug, which amount
represents the volatile oil present. Subsequent estimations of this
oil were not successful.
After the treatment with chloroform, the residue was exhausted
with 80 per cent, alcohol, yielding 875 per cent, of brown resinous
matter, of which 6-66 per cent, was ash. The portion of this alco-
holic extract, soluble in absolute alcohol, and again soluble in water,
forming neutral solutions, gives tests with the following reagents
for tannin : Hasic acetate of lead — light yellowish precipitate ; gela-
tine, starch, potassium and antimony tartrate — precipitates ; potas-
sium permanganate, silver nitrate- reductions; ferric chloride —
green color. Further examination of this extract, omitting con-
fusing details, shows the presence of acid resins and indications of
neutral resins. An organic acid is also present.
After the chloroform and alcohol extractions, a water extract was
542
Aralia Nudicaulis.
Am. Jour. Pharm.
October, 1897.
made, yielding 3- 5 8 per cent, of the dry Aralia, of which 24-36 per
cent, was ash.
The next extraction, made with an acid menstruum of i part of
sulphuric acid and 5 parts of water, yielded 56-10 per cent, with
11-67 per cent, of ash.
The final extraction, with an alkaline menstruum, yielded 689
per cent.
As a summary the following table is presented :
Extract with
Chloroform . . .
Alcohol, Sopercent.
Water .
Acid I, water ^ . .
Alkaline solution .
( By subtraction ) .
Containing
Resin, 3*05 per cent.; oil, 0-33 per cent.
Tannin ; organic acid ; acid resin (neutral resin ?).
Albuminous bodies ; coloring matter.
Mucilaginous matter.
Crude fibres, etc.
Cellulose.
Further investigation will be conducted, especially on the oil and
resins in which the active medicinal properties seem to reside.
PHARMACEUTICAL PREPARATIONS.
A quantity of the fresh rhizome of Aralia nudicaulis, gathered in
the fall, was digested with alcohol, according to the directions of
the Pharmacopoeia for making fresh tinctures. This tincture, Tinc-
tura Araliae Nudicaulis Recentis, after standing nearly a year,
exposed to the varying temperatures of winter and summer, showed
no precipitate, and possessed the odor and taste of the plant in a
marked degree. Mixed with water it forms a milky precipitate indi-
cating the presence of oil and resin. It has a beautiful gold-
yellow color which seems to be permanent. A fluid extract was
prepared from the rhizome gathered in the spring. A menstruum
of 4 part s of alcohol and i of water was used, and the general
directions of the Pharmacopoeia for making fluid extracts were
followed. The evaporization of the second percolate was performed
at a very low temperature, in order not to drive off oily or resinous
parts. The fluid extract resembles the tincture, but is darker,
^"ctefober jSS!^™ } Important Constituents of Taraxacum Root. 543
owing to the solution of the coloring matter of the plant, and is
more aromatic.
Although this fluid extract appears to be an elegant and highly
concentrated preparation, and to possess all the properties of the
drug, it is doubtful, in the writers' minds, if therapeutically it would
be the most desirable form of administering the drug. If the virtues
of the drug depend, as we believe, on the oil and resins, the sepa-
ration of these constituents, if possible, seems to be the most advis-
able step. The properties of the drug, judging from some crude
experiments, seem to be stimulant, diaphoretic, and probably
neurotic.
THE IMPORTANT CONSTITUENTS OF TARAXACUM
ROOT.»
By L. E. Savre.
According to the promise made at the meeting of this Section
last year, the investigation upon Taraxacum has been continued.
It was begun, not without considerable misgiving, but with the
hope that some process for crystallizing the bitter principle would
be found, so that a more accurate study of its chemical and physical
properties could be accomplished, and that a method of accurately
standardizing this much-used drug could be furnished.
Briefly summarizing the work of which this is a continuation, it
will be seen, by referring to the papers previously published in the
Association Proceedings,' that the following constituents, among
others less important, have been identified: (i) A resin soluble in
chloroform and ether, insoluble in alcohol ; (2) A resin soluble in
alcohol ; (3) Taraxacerin, a white, waxy substance, separating from
alcoholic solution in cauliflower-like forms; (4) A bitter principle,
which, in somewhat concentrated solution, is precipitated by a
number of alkaloidal reagents. Solutions containing the seemingly
pure principle, when evaporated, produced a film which, under the
microscope, revealed oftentimes crystals of acicular form mixed
with globules of oleoresinous aj)pearance. When this mixture was
treated with oxidizing agents — even by hydrogen peroxide — it was
gradually converted into a crystalline mass, which proved to be
oxalic acid. Attempts to separate the crystals found in the unoxi-
' Presented at the meeting of the .American Pharmaceutical Aasociation. 1897.
'See Proc. A. Ph. A., 1896, p. 160.
544 Important Constituents of Taraxacum Root. { ^'oSera897.'°*
dized evaporate were unsuccessful. To decide whether these
crystals or the oily globules were the bitter principle, or whether
the one was derived from the other, was little more than a con-
jecture. Slow evaporations of chloroformic, ethereal, alcoholic and
aqueous solutions failed to produce crystals free from oleoresinous
globules. Evaporation of aqueous solution in vacuo was no more
successful.
The work was begun this year by making an ultimate analysis
of taraxacerin. Slowly evaporating its impure alcoholic solution,
the cauliflower-like crystals separated as stated in paper of last year.
The taraxacerin thus freed from extraneous matter was collected,
dried over sulphuric acid, and a number of combustions made.
The result of these combustions will be subjoined to this paper.
A quantitative analysis of the inorganic constituents of taraxacum
root will also be appended.
For the further investigation of the bitter principle an extraction
of taraxacum root was made for me by J. U. Lloyd, as follows:
Forty pounds of the powdered root were percolated with chloro-
form, and the dregs were then exhausted with alcohol. The chloro-
formic and alcoholic tinctures were separately distilled, leaving
behind in each case a residue of thick, syrupy consistence. These
syrupy extractives were used as a starting point for the further
investigation of taraxacin and other constituents.
Taraxacin, Bitter Principle. — Further efforts have been made to
bring the bitter principle to the crystalline form. Thus far these
efforts have been only partially successful ; a detailed description of
this work is unnecessary. Suffice it to say for the present, acetone
as a solvent seems to promise some aid in its isolation. An acetone
solution of the yellowish, amorphous, viscid and extremely bitter
extractive (corresponding to crude taraxacin) was made. On slowly
evaporating this solution, a thin, syrupy, transparent film was left
which contained imperfectly formed stellar crystals — tufts imbedded
in viscid media. On adding a drop of water, the film and crystals
immediately broke down into yellowish oleoresinous-like globules.
The most satisfactory method thus far employed for purifying this
principle is to dissolve the crude principle (extractive) in 20 per
cent, alcohol ; treat this with specially purified animal charcoal until
the solution loses its bitterness ; carefully wash the carbon with
water ; dry, and treat it with boiling alcohol; evaporate the alcoholic
^ oc"!ober/iS97"" [ Important Constituents of Taraxacum Root. 545
solution at a low temperature, and dry the residue over sulphuric
acid. This has, however, the disadvanta^^e of being a wasteful pro-
cess. The dried product dissolved in acetone behaves as stated above.
Althou<^h the crj'stallization of taraxacin at present seems almost
impossible, it has not been given up as hopeless.
Analysis of Taraxacerin. — The result of the combustion of this
principle may be here stated. Several combustions were made, but
only three recorded ; of these three, the second and third seemed
to be the most reliable. A tabular statement of the percentages is
as follows :
I. 2. 3.
Carbon 7736 77'i6 77*32
Hydrogen ii'SS "'13 "*^3
Oxygen 11 09 11 71 ii'55
Mean of i, 2, 3 : Mean of 2 and 3 :
C 77'28 C 77'24
H . . 11-27 H 1113
O 11*45 O 11-63
Reducing the percentages of the last table, the following amounts
appear :
77*24
C = „.9i = 64803
H=-'-'3 = n-.3
11-63
Taraxacerin would therefore correspond to the empirical formula
CjHj^O, or a multiple thereof.
The melting point of this substance was about 45° C. Its chem.
istry will probably be worked out in detail in the future. For aid
in this work in combustion I am especially indebted to Mr. W. M.
Whitten, Assistant in Chemistry of the Kansas University, who
promises in the future to aid in its further study.
Inorganic Constituents of Taraxacum Root. — Ash in dried root
(dried at 100° C). 11 13 per cent.
CONSTITUENTS Ol- ASH.
Per cenl.
SiOj and 8an<l 43**7
A1,0, »8o7
Fe,0, 080
6-4803
7324
= 885
II-I3
•7324
i5'2o
•7324
•7324
I -GO
546 Recent Literature Relating to Pharmacy. {^Vtoberfi'str*
Per cent.
CaO 575
MgO 6-6o
KoO I3"83
SO^ 4'22
P2O5 trace.
CO2 6'53
CI I'20
Total 10*027
This latter work was performed by Mr. C. M. Palmer, a senior
student of the School of Pharmacy.
The examination of the chloroformic and alcoholic extractions was
carried beyond the report made in this communication, but the
interesting work is not yet completed, and will be made the subject
of another paper at the coming meeting of the society.
RECENT LITERATURE RELATING TO PHARMACY.
SYNTHETIC REMEDIES.
Lactophenin, according to Dr. George Thompson (Universal
Medical journal, August, 1897), possesses several advantages over
phenacetin. As is well known, lactophenin is a definite chemical
compound, differing from phenacetin by containing lactic instead of
acetic acid. The substitution of lactic acid, it is claimed, overcomes
almost entirely the possibility of cardiac depression or the conver-
sion of haemoglobin into methsemoglobin, an attribute only too fre-
quently met with in antipyrin, acetanilid and phenacetin. As an
analgesic it is equal, according to the author, to the best pain reliever
in the materia medica, and it may be given with confidence in neu-
ralgia from any other cause than traumatic.
Thiol has been found by Dr. Wirz (Deut. Med. Wochenschrifly
July, 1897) to be superior to ichthyol in some hundreds of cases. It
is odorless, so that patients who could not bear the odor of ichthyol
improved under thiol. It can be used in every description of inflam-
mation, in carbuncles, erysipelas, typhilitis, furunculosis, etc. The
best results are obtained with liquid thiol as supplied by the manu-
facturers, not by that prepared from powdered thiol with an addi-
tion of water.
^"icfoTr.7^""'} Editorial. 547
EDITORIAL.
READ BY TITLE.
The custom of reading papers by titles before the sections of the American
Pharmaceutical Association is a growing one, and, at the same time, it is one
much to be deplored. For what purpose is a paper presented to a scientific
body unless it be for the discussion ? The matter of publication is a secondary
one ; for, if valuable, the paper finds its way into print rapidly enough, either
in part or in abstract. From the journals in which it appears it is copied by
foreign periodicals, and thus it becomes distributed over a large part of the
world. Except for purposes of reference, the paper has served its purpose long
before the bulky Proceedings appear. If, for any reason, the title is the only
accessible part of a paper at the meeting, and thereby the journals fail to print
it, it takes a short cut to oblivion; for neither journals nor individuals ever
attempt to do anything with papers after they appear in the Proceedings; they
are considered stale by that time, and certainly foreign journals never abstract
from such a source ; they would be pretty sure to be reprinting old matter, and
avoid it.
At the recent meeting of the American Pharmaceutical Association, over
twenty papers were presented to the Scientific Section, yet something like half
of these were read by title and passed on to obscurity. Some others were
crowded into the Section on Education and Legislation, and one has appeared in
full in at least one drug journal as having been presented, which was only read
in abstract by the author, he having decided, after reaching the meeting, to
withhold part of it for one year.
Presumably the sessions of the .\ssociation lasted a week. The work, how-
ever, was condensed into parts of five days; still there was, apparently, not time
to read and discuss the papers presented to the two sections, amounting to some-
thing over thirty. It has been said that this was due to an accident, whereby
certain social features occurred concurrent with the sessions of the Scientific
Section, but such accidents occur almost every year. Members must naturally
ask themselves whether attendance at the American Pharmaceutical .Association
is to listen to and discuss papers or to take trolley rides. In the case referred to,
the meml)ers elected in favor of the trolley, and the work which was mapped
out for three sessions was crowded into one and continued past the midnight
hour, with everybody tired out after a day of sightseeing. Naturally, the man
who travelled i.cxxjor 2,oori miles to attend the meeting was disgusted.
The fact has been deplored that the retail pharmacist is every year l)ecouiing
more conspicuous by his al)sence from the meetings. He attends the sessions
for the purpose of learning something that will be of value to him in his busi-
ness. In what part of the programme will he find it ? Certainly not in that
devote<l to social features.
The real earnest members are not utircasonablc in recjuesting that no social
features be introduced until all the business has l>een trans.icled. or else that
there be no simultaneous meetings for business and pleasure. Papers should
he in the hands of the chairman of the section to wlr are to be pre-
sented, at least ten days Ixrfore the meeting, and an . only Kbould be
read by the author ; this would help to do away with the custom of some
^ o IPi^'-iia^-cc f Aui. .)our. Pharm.
54S KeOiecVS. \ October. 1S97.
authors of writing their papers on the way to the meeting. It is safe to say-
that the author who is so terribly pushed for time as to be compelled to call in
the services of a stenographer and typewriter after he reaches the place of
meeting, is not going to produce anything that will prevent the section from
disintegrating into a trolley party, if such an opportunity occurs.
A COMPARISON.
The editor of the Pharmaceutical Journal has expressed a fear that our
remarks in the August number on the ability of the British Pharmaceutical
Conference to transact a large amount of scientific work in a short time were
sarcastic rather than complimentary, and we are desirous of assuring him that
he may interpret in favor of the Conference. The assertion was made with a
comparison in mind, which has been made during the past several years, while
the two great English-speaking pharmaceutical bodies have been holding their
annual meetings. The developments this year at Minnetonka still more empha-
sized the difference in the manner of conducting the two associations. At Glas-
gow the Conference lasted three days, the last of which was devoted to pleasure-
seeking, and seventeen papers were read and discussed. The report in the
Pharuiaceuiical Journal does not record that any were read by title ; one,
making eighteen in all, arrived from Australia too late for the meeting, but was
accepted by the Publication Committee. At Minnetonka five days were set
down for business, and two more, with Sunday, for pleasure ; about thirty
papers were disposed of, many of them being merely read by title, and dis-
cussion was much curtailed on the others. Certainly no sarcasm can be found
in our remarks after making this comparison.
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
SuR UN Strophanthus dq Congo Fran^aise. — Par MM. les professeurs
Schlagdenhauffeu et Louis Planchon. Reprint from Annates de L' Institute
Colonial, Marseilles. 1897.
The authors studied this new species because they believe that strophanthus
will be an important medicine of the future, and because every new variety
of such a valuable remedy, which appears in commerce, should have its fit-
ness for medicinal use established. From the several botanical characters
clearly shown in the beautiful illustration which accompanies the contribution,
the authors feel justified in declaring this to be a new species, which they have
designated Strophanthus d'Autran, after the botanist who collected it.
In Chapter I the fruit and seed are described, and the anatomic differences
between this and other species illustrated. Chapter II is devoted to the chemical
analysis of the fruit and seed ; and Chapter III describes the physiological
action of the several commercial species compared with the new species, and
their influence on the heart action of a frog is illustrated.
The conclusions reached are that there is a close resemblance, chemically,
between the new species and the Strophanthus hispidus, analyzed by Fraser,
and that the physiological actions of S. Kombe, hispidus, glabre, Zambese and
d'Autran are identical.
Am. Jour. I'Lianu. I J?j^"')f/y>':ie r m^
October. 1»97. ) KlcneixJS. 549
The whole is a creditable piece of research work, which, in view of the
growing popularity of the drug, is worth the while of pharmacognosists to
study.
Anniversary Address before the Royal Society of New South Wales, by
the president, J. H. Maiden, Government Botanist and Director of the Botanic
Oardens, Sydney, May 5, 1897.
This comprehensive pamphlet of sixty-nine pages is composed as follows :
" History of the Society during the past year," " Progress of Science in New
South Wales during the past year," "Some Botanical Matters," "Forestry,
etc.," "Australian Timbers," "Botanical Teaching in New South Wales,"
"A Plea for a Botanical Survey."
Under botanical matters, a fitting allusion is made to the life work of the late
Baron von Mueller. Every part of the address contains valuable information
about Australia.
Contributions from the U. S. National Herbaril m, Vol. V, No. 3
Studies of Mexican and Central American Plants. By J. N. Rose,
Washington, 1897.
The similarity in the flora between the Southwestern Inited States and the
regions covered in the above contribution makes this number of considerable
interest. The illustrations are numerous and well executed.
Age of Trees and Time of Blazing Determined by Annual Rings.
By B. K. Fernow, Chief of Division of Forestry. Circular No. 16, issued by the
U. S. Department of Agriculture, Division of Forestry.
The author is a firm believer in the method of determining the age of trees
by counting the annual rings ; indeed, it is difficult to understand how there
can be any controversy on the subject. Mr. Fernow, after a close study of the
objections, has written a clear and concise account of how to overcome the
difiiculties. The part devoted to the covering of blazes, wounds and knots is
also valuable. The circular is remarkably well illustrated.
Cider Vinegars of Pennsylvania. By Dr. William Frear, Bulletin No.
22, of the Pennsylvania Department of Agriculture.
While much of this report is especially of value to the farmer in determining
the value and ripeness of his product, still the chemist, after reading it, cannot
but be better prepared to identify a true cider.
Salicylic Acid and Calcium Sulphite as Preservatives of Cider. By
E. H. S. Bailey and Chas. M. Palmer. From the Kansas University Quarterly,
Vol. VI, No. 3, 1897.
Bulletin of the Bussey Institution, Jamaica Plain, Boston, Vol. II,
Part VI, 1897.
This numl>er is devoted to "Observations on Some of the Chemical Substances
in the Trunks of Trees." By F. H. Storer, Professor of .\gricultural Chemistry.
It is of especial interest liecause of its record of the investigation of cellulose and
closely allied bo<lies.
Medical Botany. By William Trelcasc, Sc.D.. Direclor of the Mis.<(ouri
Botanical Garden.
Coming from such a source, this contribution should l>c rcail with more than
550 y'otes and yeus. {^^JSSJ^ST'
ordinary interest bv pharmacists and physicians. The author points out that
the study of medical botany of to-day has fallen to the pharmacist to a larger
extent than to the medical student ; he, however, states that the growing
knowledge of bacteria is a necessary branch of medical botany, and that the
physician cannot ign<»e this subject. The paper was originally read before the
Section on Materia Medica and Pharmacy of the American Medical Associa-
tion, at the 1S97 meeting, in Philadelphia.
NOTES AND NEWS.
Professor Oscar Loew, who has been professor of chemistry in the Agricul-
tural Department of the Imperial University at Tokio, Japan, for the last four
years, has returned to Germany and is again engaged in teaching in the Univer-
sity at Munich. His successor in Tokio is Ihr. Bieler. fcrrrter'. v 2=;- -taut in the
Agricultural Laboratory at Halle.
The i7ic(h[grr itfJafa/ was awarded by •. . , . nz.:: r!i^r~r.:r_ ^^'^cia-
tion, during its recent meeting, to E. M. Hohnes, Curator of the 31 of
the Pharmaceutical Society of (^^eat Britain.
This medal is awarded once in fire years, for distinguished services in the
promotion of pharmaceutical research. In selecting Mr. Holmes as the subject
of this honor, the society did credit to itself, and at the same time acknowl>
edged the eminent worth of a man whose researches have been so numerous
and productive of results that if the titles alone were given they would fill some
pages of this Jourxai..
Citric acid by fermentation of carbohydrates is claimed by German patent
^o- 72,957» April 5, 1893, and species of citromyces are especially mentioned as
bringing about this fermentation. The patent is now supplemented by a new
claim German patent 91,891!!, based upon the discovery that the same result
may be obtained by means of Mucor piriformis. The latter fungus is found on
putrefying fruit, especially on pears and apples ; its spore carriers only grow in
a moist atmosphere, and form long, white filaments, terminated by brownish-
black heads. It can readily be obtained in pure culture by sowing the spcH^s
in a suitable medium, such as sugar solution, beer wort, steamed rice, starch
paste, etc, the ordinary room temperature being favorable for its growth. The
solution becomes add from the formation of citric ^xA'^.—Jour. Soc. Chem,
Industry^ June 30, 1897.
The BiU of Serpents is found by Professor Fraser to have the power of
neutralizing serpent venom, whilst ox bile has the same property in a lesser
d^ree. This neutralizing action is manifested to a wonderful degree when the
bile is injected along with the venom, and to a less extent when it is injected
after the venom. In a paper treating of this subject, read by the Professor
before the Royal Society of Edinburgh, on Monday, July 5th, he stated that he
had separated the water-soluble part of the bile from the alcohol-soluble part,
and found it quite equal to the best antivenene in its immnniTing effects with
regard to serpent venom. These are very interesting results of the investiga-
tion upon which Professor Fraser has been engaged so long, and it is to be
Am. Jour. PbATin. \ NnffK ntiii JV^iti - '• i
October. le97 ] l^Ol€S UflU IWrWS. 55 I
hoped that they may prove capable of practical application. — Phann. Journal^
July 17, 1897.
Ginseng is one of Corea's most valued products, and during 1S96 realized
ftome £30,000. For centuries past red ginseng has gone to Pekin with the
annual overland embassy, the trade in ginseng being a royal monopoly, from
which the King of Corea derived a considerable portion of his revenue, and
its export by sea was prohibited. In November, 1S95, however, an ordinance
was promulgated legalizing its export, the king receiving compensation by an
addition to his privy purse, which now stands at some £60,000 a year. The
annual crop of ginseng is limited in quantity to about 15,000 catties, upon
which an excise duty of l^io a catty is charged under the new regulations, to
which is added an import duty of 5 per cent, ad valorem, levied on its arrival
at a treaty port in China. The prescribed scale of taxation is not rigidly
adhered to, and there is reason to believe that in practice the amount raised
exceeds considerably 15,000 catties. — Pharm. Jour., August 7, 1897.
A Monument to Pelletier and Caventou has been proposed in Paris, and the
following committee has been appointed :
Honorary President, M. A. Chatin.
President, M. Planchon.
Vice-Presidents, MM. Moissan and Marty.
General Secretary-, M. Behal.
Assistant Secretary, M. de Mazieres.
Treasurer, M. Bocquillon-Limousin.
The committee feels justified in calling on all those who have been benefited
by the discovery of Pelletier and Caventou. These scientists gave to the
world, unencumbered by trade-mark, patent or any other reservation, one of
the greatest of remedies — quinine. It is proposed to erect the monument in front
of the Ecole de Pharmacie de Paris. The address of the Treasurer is 2 bis, Rue
Blanche, Paris.
The thirteenth annual meeting of the Minnesota State Pharmaceutical Asso-
ciation met at Lake Park Hotel, Lake Minnetonka, August 23d and 24th, with
thirty-five members in attendance at the opening session, and nearly 100 were
in attendance before the meeting closed.
Secretary C. T. Heller, reported 286 members on the roll ; lost by death, 5.
Treasurer H. W. Rietzke reported a balance of |i6o. Twenty-five new mem-
bers were elected at the first day's meeting, and five at an adjourned imretiii^'
held .\ugust 2Sth.
The following officers were elected for the ensuing year: Presideul, 1 red.
Scott, Stillwater; First Vice-President, H. T. Holverson, Alexandria ; Second
Vice-President, F. \V. Finch, Hastings ; Third Vice-President, Miss Jo»ie A.
Wanous, Minneapolis ; SccreUn', Charles T. Heller, St. Paul ; Treasurer, IL
W. RieUke, St. Paul ; Executive Committee, John F. Dauek, Minneapolis ; A.
T. Hall. St. Paul, and A. J. Lckstein, New Ulm.
Committee on National Legislation offered the following resolution, which
was unanimously adopted :
Whkrkas, it is customary for the Government to grant a trademark or
copyright to manufacturers of articles made in foreign countries where said
articles are not protected by trade-mark or copyright, thus restricting compe-
tition in the manufacture of said articles iu this country. Therefore, l)e it
^ _ _ nhifu/i'TM (A.in. Jour. Pharm.
552 UOUUary. \ October, isa?.
Resolved, That the members of the Minnesota State Pharmaceutical Asso-
ciation, in convention assembled at Lake Park, August 23d, do earnestly urge
the Committee on National Legislation of the A. Ph. A. to see that a bill is
drafted and presented to Congress prohibiting the future granting of such copy-
right or trade-mark for goods manufactured in foreign countries, and not thus
protected in the countries where made, and thereby remove the excessive cost
on such goods in this country, whereas as the law now stands an alien can intro-
duce articles into this country for four or five times the price in his own coun-
try, while our Government hardly receives a cent of revenue.
A committee of three was appointed to formulate a price-mark to be used in
marking copies of prescriptions, so that there will be more uniformity of prices
throughout the State on prescriptions, the Secretary to be the custodian of the
mark, and to be given only to those who will agree to use it.
Meeting adjourned to meet at Lake Minnetonka, June 14, 1898.
OBITUARY.
Professor Dr. Victor Meyer, whose brilliant discoveries in the field of chemi-
cal research won for him the esteem and admiration of his fellow-laborers in
this branch of science, died unexpectedly at his home in Heidelberg, Germany,
August 7th.
He had been suffering from nervous troubles, accompanied by insomnia,
brought on, no doubt, by excessive work, and it is sad to reflect that a man of
such energy and ability as Professor Meyer should, perhaps, during a tempor-
ary aberration of mind, end his own career, as was evidenced by the circum-
stances connected with his death.
Professor Meyer was born at Berlin, September 8, 1848. He entered the
university there in his sixteenth year, but remained only a short time, when
he went to Heidelberg, where he devoted himself to the study of chemistry
under Bunsen. After graduation at the latter institution he continued his
study of chemistry under Baeyer, at Berlin. In 1867 he became assistant to Bun-
sen, and in 187 1 was made professor of chemistry at the Polytechnic School at
Stuttgart, and in 1872 at the Polytechnic School at Ziirich. In 1855 he removed
to Gottingen, and in 1889 was appointed successor to Bunsen at Heidelberg,
the latter recommending him for the position. As an instructor he was singu-
larly gifted, and the study of chemistry at Heidelberg received a great impetus
through his teachings.
His scientific papers were numerous and covered a wide range of subjects in
the domain of chemistry, and it is only necessary to refer to a few of the
results accomplished by him to show the importance of his work. Of particu-
lar significance was his study on the subject of vapor density; for not only did
he devise a method for determining vapor density, which has largely supplanted
other methods, but the principles of pyro- chemistry were more thoroughly and
clearly established by the results obtai ed by him at high temperatures. By
his discovery of thiophene in benziy--, and the subsequent study of its properties
and derivatives, he added to organic chemistry an entirely new series of com-
pounds.
In 1893 Professor Meyer was elected an honorary member of the Philadel-
phia College of Pharmacy.
THE AMERICAN
JOURNAL OF PHARMACY.
NOVEMBER, iSgj,
INTERNATIONAL CONGRESSKS.
By Prof. Joseph P. Remington, Philadelphia.
A great deal of misconception evidently exists in the minds of
many upon the objects and aims of international congresses of
various kinds.
This is not only the case in relation to pharmaceutical conferences,
but medical and professional international gatherings of all kinds.
The absence of a universal language must always continue to be the
principal bar to effective intercourse between representatives of
mixed nationalities, and the larger the attendance at a congress the
greater becomes the babel of tongues, with its necessary confusion.
The International Medical Congress at Moscow had an immense at-
tendance, a very large number of papers were read of unequal
value and although the Russian Government provided most liberally
for the entertainment of the delegates, it was found impossible to
send invitations to each member for every official function. This
necessarily j)roduced heart burnings which even Russian diplomacy
could not entirely soothe.
The International Pharmaceutical Congress, which met at lirus-
sels, has been criticised by a German editor in America, who found
fault with it, for •• from the beginning to the end not a German word
was heard in the deliberations of ti'^'^-Congress," and " because the
subjects on the programme were princ j)ally of interest to Belgium,
and almost exclusively presented from the Belgium standpoint," and
the writer consequently argues •• that it could not be international
(553)
554 International Congresses. [%^
Am. Jour. Phartu.
ovember, 1897.
in character." Thus we have two contrasts presented. One con-
gress was too international and suffered from unwieldiness, and the
confusion incident upon the attendance of too many foreigners, and
the other could not be international because no German voice was
heard in its deliberations, and too much local flavoring was injected
into its composition.
It will always be a question for many generations to come, whether
the world would be likely to flourish better under one supreme
mundane ruler or a number of rulers governing as many separate
nations. The German nation itself is wrestling with this problem,
and many of its best citizens are asking : " Are we better off" to-day
under the Empire than we were before consolidation was effected?"
and this condition exists notwithstanding the fact that the same
language is spoken by all. Is it strange, then, that an international
gathering largely attended by men of one profession like the one
at Moscow should be criticised by some of its own members, who
have been heard to say : " I have derived more benefit from my
own County Medical Society than from the deliberations of the
great Congress which I have travelled 7,000 miles to attend ?"
The truth is, that international congresses must not be judged from
a local standpoint. The ideal congress, either pharmaceutical or
medical, would probably be one in which all civilized nations were
equally represented and equal prominence given to each, papers
read and discussed only by the most distinguished representatives
from each nation, and each one bristling with original observations
or newly discovered facts, while the decision of the congress upon
general questions should be such as would deal fairly and justly with
every nation, and accepted as final by the subordinate bodies in each
country. Finally, every member should return home, perfectly satis-
fied that he had received every attention due him as the representa-
tive of his nation, and the action which he especially desired the
congress to take was adopted, and what he did not want adopted
was rejected. No one can ever hope to see such an ideal realized.
Unfortunately, those who desire to accomplish any good, no mat-
ter how high their ideal may be, must be prepared to accept the
conditions whiclL exist, and strive earnestly to bring about the ideal.
If a congress is not international the cause should be sought for and
removed if possible. \\\ pro.dhsional gatherings, political differences
should be ignored ; " Science knows no language and no country."
iber.'^ti*:!''} International Congresses. 555
A ni. Jour. Phariu
Noven
The earnest seeker for truth is rewarded by makinf; a discovery
which will rescue many a valuable life or alleviate suffering wherever
it exists ; a liberal profession should embrace in its membership
those who are willing to labor for the benefit of all, and until such a
motive actuates the members of the pharmaceutical profession
throughout the world, and unless the true international feeling is
cultivated, the ideal can never be approached. If rejoicing is in
order and congratulations tendered, because the representatives of a
great nation decline the invitation to attend a congress, then is the
first principle sacrificed. Some one spot in the world must always
be selected as the place of meeting, and long distances travelled by
some delegates, of course, loyalty to the international spirit should
overcome personal feeling, and if members have grievances, nothing
can be gained by staying away from the meeting ; there is really
more necessity for activity and personal interest. It is deplorable
that international pharmacy, standing as it does to-day, more in need
thiii any other profession, of united effort, seems to possess a greater
proportion of iconoclasts and pessimists than any other; this is
especially the case in America ; it an organization for mutual benefit
is started, more hands seem to be at once raised to tear it to pieces,
than to build it up. Will it be thus always?
International congresses, in the writer's opinion, serve a most
valuable purpose in bringing together pharmacists of different
nations; notwithstanding the difficulties of interchanging thought
fluently, it is worth something to realize that progress in education,
in scientific research and social advancement is constantly going
forward, and if abuses and obstacles are found in one's own country,
it is some consolation to hear (even in a foreign tongue), that efforts
are made to reform the abuses and to overcome the obstacles, and
*' the fellow-feeling that makes one wondrous kind " is kindled. In
all international and national gatherings, whether professional or
otherwise, the social features are claiming more attention and rcC'>g-
nition. It is true that there are many scientists who stand aloof
from social entertainment of all kinds, others rail at them in public
and private, but nevertheless are seen always at these entertainments.
It may be assumed, however, that without social functions, con-
gresses would be very poorly attended. The pharmacist, over-
worked, confined during the day and often a large part of the night
within the walls of his dingy shop or laboratory, looks forward lo a
556 International Congresses. {^No/embeMsg"'
vacation in the heated term for a relief; if he can combine mental
and physical recreation by associating with his fellows and kindred
spirits, and thus gaining by social intercourse and rational pursuits
the much needed rest, he has enlarged his horoscope and becomes
much better qualified to deal with the perplexing problems which
threaten his existence, and has taken the preliminary steps toward
that organization and united effort which will make him a power in
the community, instead of a disorganized mass of disjointed entities.
Eight International Pharmaceutical Congresses have come and
gone, and while it can be truly said that not one has reached the
ideal, it must be remembered that great difficulties have stood in
the way. Some of these have already been noted. Such gather-
ings suffer greatly from the impossibility of organizing them com-
pletely until the first day of the meeting, for it can never be told in
advance with certainty how many foreign delegates can be present.
Necessary delays in travel and many other contingencies prevent the
local committees from arranging satisfactory programmes for each
day. There is a difficulty of finding, even in a large city, competent
interpreters who have a knowledge of the technical subjects dis-
cussed ; then again, no one person has ever been found who has a
complete knowledge of the abilities and capacities of each delegate,
and hence it must follow that committees are not always appointed
which embrace the best available material; in short, all of the
responsible organizing authorities are reduced to the necessity of
selecting those whom they know and whom they believe to possess
the necessary qualifications. Hence it will always be found that
each pharmaceutical congress must suffer from what is called " local
flavoring." In conclusion, the writer does not share in the belief
that international gatherings should be discontinued. The faults
are capable, in a large measure, of being corrected or minimized
when they are fully recognized, and greater experience will lead to
their elimination, but one valuable consideration stands out promi-
nently which overshadows the minor faults. Pharmacy is recog-
nized officially by European Governments as a profession, and, as in
the case of pharmacy laws which are admittedly imperfect, it must
be said that the steady advancement in the recognition by the peo-
ple of the important relations which the pharmacist sustains toward
them is one of the greatest value. Is it not possible we have had
too much criticism of the detail in judging such gatherings, and too
little real appreciation accorded to the greater results accomplished ?
^i?ovi';;;^er'.l!;?;'} Destruction of Tobacco. 557
THE DESTRUCTION OF TOBACCO IN VIRGINIA BY ACT
OF GENERAL ASSEMBLY, JANUARY 6, 1639, UNDER
SIR FRANCIS WYATT, GOVERNOR.^
By John Uri Li.oyd, Ph.M., Ph.D.
Query by Professor Fluckiger. — " In Alonzo Calkins (Opium and
the Opium Appetite), Philadelphia, 1871, p. 373, there is a state-
ment to the effect that in 1639, by authority of the • Virginia As-
sembly * there went out a decree that all the tobacco then standin^j
in cultivated fields should be duf;j up and exterminated. Is this
correctly abstracted from some official records ?"
Answer by John Un Lloyd. — In reply to this question, I am con-
vinced that the evidence is conclusive that only part of the tobacco
was destroyed. This was because tobacco was too abundant to
command a good price in the market, and 7iot with a view to its
extermination. By destroying a large share of the crop the remain-
der was enhanced in value. In support of my view, I offer testi-
mony which seems to me conclusive.
The subject may be traced as follows :
G. Bancroft makes only general allusion to the laws restricting
the planting of tobacco in Virginia at that time.
Robert R. Howison, A History of Virginia, 2 Vols., and
Henry Hczve, Historical Collection of Virginia, 1856, both point
to:
Hening, Statutes at Large, ist Vol., pp. 224 and 225, as a book of
reference on the records of Virginia administration. In this publi-
cation, jst Vol., pp. 22^ and 22 j, we find the following Acts by the
Grand Assembly of Virginia, January 6, 1639, under Sir Francis
Wyatt, Governor:
ACT I.
•' Tobacco, by reason of excessive quantities being made, being so
low that the planters could not subsist by it, or be enabled to raise
more staple commodities, or pay their debts:
' When Professor FliickiKer visited America (July, 1894) he hoped to obtain
historical data that would enable hini to give the records of several interesting
American productions. In this he faile<l, and he then associate*! in his Iwhalf
the services of the author of this paper. After much of the work had In-en
done, the death of Professor Pliicki>;er iuterrtipted the invesli)4atiou. This
piper on tobacco was one of the subjects consideretl. — Ivditor Am. Jour.
Ph.\km.
558 Destruction of Tobacco. {^nov
Jour. Pharm.
ember, 1897.
" Enacted, that the tobacco of that year be viewed by sworn
viewers, and the rotten and unmerchantable and half the good to be
burned."
"So the whole quantity made would come to 1,500,000 pounds
without stripping and smoothing, and the next two years 170 pounds
tobacco per poll, stripped and smoothed, was to be made, which
would make, on the whole, about 1,300,000 pounds, and all creditors
were to take 40 pounds for lOO."
ACT II.
'• No man should be obliged to perform above half his covenants
about freighting tobacco in 1639."
Adjoined to the copy of these Acts we find the following, added
by Hening, to show his authority:
"These acts are printed from a MS. which belonged to Thomas
Jefferson, President of the United States, and which is now in the
Library of Congress at Washington.
"This MS. volume is lettered 'Writings Related to Virginia' and
contains most of the old charters, instructions to the governors, etc.
At the end of the volume is an abstract of public papers, taken from
the rolls, the number and page of which are referred to, but without
regard to chronological order. The Acts of 1639 appear to be a
mere abridgement, and, from the handwriting and orthography, it
seems to have been made long posterior to their date.
" This abstract concludes with a list of the governors of Virginia
down to the year 1722, at which time, or shortly afterwards, it was
probably compiled.
" The handwriting, on comparison, appears to be that of ' R. Hick-
mann,' by whom, as ' clerk of the secretary's office,' several public
papers are attested."
In connection with the foregoing, as an evidence that " history
repeats itself," we find that the president of the Cotton Growers'
Association has recently (1897) advocated the destruction of part of
the cotton crop of the South, in order to increase the price of that
which remains. A paper headed " Signs of the Times," in the
Nation, March 4, 1897, prints the following, thus showing that the
method adopted 250 years ago has met the theorist of to-day:
'' Signs of the Times — The Southern farmers are again showing
that it is not the principle of combination to which they are opposed,
but the use of that principle by any other class of people than farmers
Vovember.?8^"} Official Lead Preparations. 559
— except * org^anized labor.* They denounce bitterly any union on the
part of those who buy their cotton to raise the price of products
manufactured from it, but they earnestly advocate the adoption of
measures to make the manufacturers pay hi^^her prices for the staple.
The president of the Cotton Growers* Association has issued an
address callinor conventions of the Texas farmers at Waco, Texas,
March 8th ; of those in the Mississippi Valley at Memphis, March
lOth, and of those east of the Mississippi at Augusta, March i 5th, to
secure ' concert of action,' as ' by a systematic and judicious market-
ing of our crops we can realize inestimable benefits that never can be
secured permanently otherwise.' The method urged upon the cot-
ton growers is that which is so bitterly complained of when applied
to the cotton manufacturers — a restriction of the output in order to
secure higher prices. ' Destroy the annual surplus of cotton ' is the
watchword. • You will be better off with a 7,000,000-bale crop sell-
ing at 10 cents, supplemented by ample food crops, than with a
10,000,000-bale crop selling at 5 cents.' "
AN EXAMINATION OF SOME OFFICIAL LEAD
PREPARATIONS.
By Frederick W. Haussmann.
Sub-Committee of Research of the United States Pharmacopceial Committee
of Revision.
The observation that certain official preparations prepared from
lead salts differed from the standard prescribed by the Pharma-
copoeia, induced the writer to inc[uire into the cause of such
variations.
Continued investigations revealed the fact that the statements of
the Pharmacopcuia, regarding the preparations under examination,
were also open to criticism, and in the course of this paper, altera-
tions and additions which may be regarded necessary will be
mentioned.
The experience of other pharmacists is invited to be rendered
for comparison either to corroborate or disprove the conclusions
arrived at by the writer.
The original researches were confined to Goulard's extract, the
liquor plumbi subacetatis of the Pharmacopcria, where the first
deviations from the official standard were noticed. It was soon
found, however, that, to determine the exact causes thereof, it was
also necessary to examine the metallic ingredients, lead acetate and
oxide.
56o Official Lead Preparations. {^^To/embeTS'
LIQUOR PLUMBI SUBACETATIS.
If it were possible to realize the idea of an international Pharma-
copoeia, this preparation deserves attention among the first to secure
uniformity in method of preparation as well as in the proportion of
basic salt.
It is unnecessary to point out the respective variations in different
pharmacopoeias, and only sufficient to call attention to varying
degrees of specific gravity, volumetric strength and method of prepa-
ration.
Even in the Pharmacopoeia of the United States the two last
revisions have been productive of deviation in strength from the pre-
vious editions.
The subject of Goulard's extract may be treated under the follow-
ing heads, viz.: preparation, specific gravity and volumetric strength.
PREPARATION.
The following are the full pharmacopceial directions :
Grammes.
Lead acetate 170
Lead oxide c 100
Distilled water to make 1,000
Dissolve the lead acetate in 800 grammes of boiling distilled
water, in a glass or porcelain vessel. Then add the lead oxide, pre-
viously passed through a fine sieve, and boil for half an hour, occa-
sionally adding hot distilled water to make up the loss by evapora-
tion. Remove the heat, allow the liquid to cool and add enough
distilled water, previously boiled and cooled, to make the product
weigh 1,000 grammes.
Finally filter the liquid in a closely covered funnel.
In these directions the amount of insoluble basic lead subacetate
is included in the final weight, and the solution is directed to be
filtered therefrom.
The filtrate weighs, according to the National Dispensatory,
approximately 950 grammes.
An inquiry among a number of pharmacists revealed that the
pharmacopceial directions are interpreted by several to read to
make the filtrate weigh 1,000 grammes. This would result in a
preparation approximately 5 per cent, weaker in strength.
The basis for this opinion is furnished by the official direction of
boiling the oxide in 800 grammes of distilled water, in which the
"^November't^"-} Official Lead Preparations, 561
acetate has previously been dissolved, and making up the loss by
evaporation by the occasional addition of hot distilled water.
The exact observation of the original volume in this manner, it is
claimed, would necessarily produce an aggregate weight of 1,070
grammes. To substantiate this claim, the specific gravity of the
solution thus prepared is advanced, which closely approximates that
stated by the Pharmacopctia.
Determinations by the writer in instances where cold maceration
was employed, with the stated increase in the amount of the water,
again where the pharmacopoeial method of preparation under like
conditions was followed, and finally in another process, to be de-
scribed subsequently, it was found that the specific gravity remained
within pharmacopoeial bounds, although a less quantity of — sul-
phuric acid was required for the complete precipitation of 13 67
grammes of the solution.
Goulard's extract may also be prepared by cold maceration, viz.:
by introducing the lead salts in a bottle with the water, with occa-
sional agitation, until the yellow color of the oxide is changed to
white.
This is the process of the Austrian Pharmacopoeia, and two to
three days are stated to be required for completion. Positive asser-
tion is made that with the disappearance of the yellow color of the
oxide no more enters into solution. The chief objection to this
method is the time it requires.
While preparing the solution by cold maceration, it occurred to
the writer to try if the substitution of hot or even boiling for the
cold water would accelerate the solution of the oxide.
This was determined to be the case, and it was found possible to
prepare Goulard's extract in a comparatively short time, avoiding
the troublesome boiling and the difficulty experienced in the pres-
ervation of a definite volume.
The following are the directions :
A strong bottle — a fruit juice bottle holding a full quart will an-
swer— is graduated to 730 c.c.
Distilled water is heated to boiling and poured into the bottle
up to the graduation mark.
170 grammes of selected crystallized lead acetate, previously
broken into small pieces, are ncnv quickly added and the bottle
corked.
562 Official Lead Preparations. { Vo v^embe^.Ysl^'
A few turns of the vessel will dissolve the salt.
lOO f^rammes of lead oxide, previously sifted, are now added in
divided portions, thoroui^hly shaking the bottle after each addition.
In from five to ten minutes, on repeated thorough agitation, the
yellow color of the oxide will have changed to white.
The mixture is allowed to stand two hours or until cold, with oc-
casional agitation, and filtered, with observation of the usual precau-
tions.
The solution thus prepared will fulfil the requirements of the
Pharmacopoeia in all particulars.
The only precautions necessary are the observation of the liability
of fracture of the bottle, unless the same is previously warmed, and
the protection of the hands with gloves or a towel to prevent
burning.
The oxide must be added in divided portions, as the full addition
is liable to be followed by caking, with consequent less rapid
solution.
The question may be raised — will this comparatively brief contact
of the lead salts sufifice to complete the solution, or, by further
prolonged maceration, will more of the oxide be not taken up ?
To determine this point, the following trial was made : The pro-
cess described was employed, preparing i,ooo grammes of the
solution.
After a contact of exactly two hours 1 00 c.c. of the solution were
filtered off and marked filtrate No. i.
The remainder of the solution was allowed to stand twenty-four
hours longer, with occasional agitation.
An additional lOO c.c. were again filtered and marked No. 2.
The remaining portion was allowed to stand forty eight hours
more, and a third portion of lOO c.c, marked No. 3, filtered off. j
The final remaining mixture was allowed to stand eight days, with I
occasional agitation, making the total time of maceration from the 1
time of preparation about twelve days, and filtered.
The solutions were each examined in turn as to specific gravity
and percentage of basic salt, according to pharmacopoeial direc-
tions.
The respective specific gravities were all found to be identical, and
the estimation with normal sulphuric acid gave little variation, in no
case being more than a fraction of a cubic centimetre, and none
"^i/e'r^berilS-:" } Official Lead Preparations. 563
were found to require less than 25 c c. for precipitation of 13-67
grammes of the solution.
Similar experiments were repeatedly performed, and it was invari-
ably found that after a contact of two hours, little or no oxide
passes into solution.
In one instance, the mixture of lead, salts and water was allowed
to stand three weeks before filtration, but no difference was found
between this and a filtrate of two hours' standing.
Various modifications of this .process, such as trituration of the
mixed lead salts in a mortar and subsequently adding boiling dis-
tilled water, were also tried, but furnished no improvement over the
method described.
OTHER METHODS OF PREPARATION.
Acetates of the alkaline earth metals also possess the power of
dissolving lead oxide.
Of these, magnesium acetate has been suggested to prepare a
modification of Goulard's extract, and particularly^ lead water.
This process, as given in the Proceedings of the American Phar-
maceutical Association of 1893, possesses no advantage. It is
tedious and does not furnish an official preparation.
Of greater importance is a process which is based on the fact
that if ammonia water is added to a solution of lead acetate in the
proper proportion, a solution of the basic salt is immediately pro-
duced.
The following is the process recommended:
Seventy-five parts of pure crystallized lead acetate are dissolved
in 165 j)arts of distilled water and 1 1 parts of water of ammonia,
20° B., sp. gr. 0923, are added.
In place of the ammonia water of this strength, 22 parts of the
official 10 per cent, water can be added, deducting 11 parts from
the amount of water employed to dissolve the acetate. The prep-
aration is stated to be immediately ready for use.
Goulard's extract, thus prepared, resembles the official prepara-
tion in appearance, has no odor of ammonia, but in point of stability
possesses no advantage, also depositing lead carbonate on prolonged
standing.
The specific gravity of the solution was found to be i'2oS.
In the volumetric estimation of Goulard's extract, prepared by
564 Official Lead Preparations, { ^^- •^«"^- ^^*^"^-
November, 1897.
the ammonia process, several conditions were noted, which, when dis-
regarded, are liable to lead to error.
Titrated with sulphuric acid, using methyl-orange as indicator,
it was found that nearly 30 c.c. were required before the orange
color was changed to crimson, while in precipitation without the
indicator, only 22 to 23 c.c. were required for 13-67 grammes of the
solution.
Both estimations were found erroneous, the ammonia probably
influencing the reaction with the indicator, while in the simple acid
estimation the fact must be considered that ammonium acetate,
which necessarily is present in the preparation, has the property of
dissolving lead sulphate.
If the lead is completely precipitated by means of sulphuric acid,
the sulphate removed by filtration and the filtrate examined, the
presence of the metal is revealed by every reagent, excepting sul-
phuric acid.
To accurately estimate an ammonia-prepared Goulard's extract
by means of volumetric analysis, it is therefore necessary to employ
a different precipitant.
Volumetric -oxalic acid solution was substituted for sulphuric
acid, and it was found that 1367 grammes of the preparation
required 23 to 24 c.c. for complete precipitation.
COMMERCIAL GOULARD's EXTRACT.
A number of specimens of Goulard's extract, procured from vari-
ous sources, were also examined as to their specific gravity and
volumetric strength.
In appearance, considerable difference was noticed, some being
clear and perfectly colorless, while one sample was of a decidedly
yellowish-brown color.
All degrees of intensity in precipitation of lead carbonate were
also observed.
The liability of the preparation to deposit the carbonate on stand-
ing must be considered when comparing commercial samples with
the pharmacopoeial standard.
This takes place even when every precaution is employed to pre-
vent the access of air.
^:?;>\Se?S} Ojgicial Lead Preparations 565
As a necessary consequence, decrease both in specific gravity and
volumetric strength will result.
This was noticed by Prof. J. U. Lloyd in a paper published in the
American Journal of Pharmacy, and in a number of observations
the writer can only record a similar experience.
SPECIFIC gravity OF GOULARD's EXTRACT.
The specific gravity of commercial Goulard's extract varies
widely.
One sample, which was stated to be of recent preparation, had a
specific gravity of 1-270, and 13-67 grammes required between 29
and 30 c.c. of sulphuric acid for precipitation.
This specimen was evidently prepared according to the Pharma-
copoeia of 1870.
On the other hand, one solution was found of the specific gravity
of ri28, which required only 15 c.c. of the normal acid for the pre-
cipitation of 1367 grammes.
This preparation was cloudy, and bore evidence of careless
preservation.
The present Pharmacopoeia states the specific gravity to be about
I- 195, while the edition of 1880 requests the same to be 1-228.
The latter employs a larger quantity of lead oxide, but both are
unanimous in the amount of basic salt, each demanding 25 per
cent.
A number of determinations have led the writer to the conclu-
sion that the specific gravity point of the present PharmacoptL-ia is
placed too low.
This was first suggested while e.xamining a commercial speci-
men, which possessed the specific gravity of 11875, but only
required 20 c.c. of normal sulphuric acid for precipitation of 1367
grammes.
Several samples, with specific gravities closely approximating the
official figure, were invariably found to require less than 25 c.c. of
the normal acid for precij^itation.
It was also found that considerable variation in specific gravity
took place if lead acetate was employed obtained from different
sources.
It was, in fact, found impossible to purchase this salt in the mar-
566 Official Lead Preparations. { ^^o/embef.X'"-
ket, to employ it with any degree of confidence for the accurate
determination of the specific gravity of Goulard's extract.
The results of the writer, pertaining to the quality of commercial
lead acetate, will be treated of subsequently.
At the suggestion of Prof. H. Trimble, the writer prepared lead
acetate from a sample of litharge, which assayed 99 per cent, of
lead oxide, crystallizing the salt from a slightly acid solution.
The air-dried salt was obtained in silky masses, considerably more
bulky than the commercial salt.
Goulard's extract was prepared from this salt.
For the accurate determination of the specific gravity maceration
was first employed, each step in the process being carefully checked
and every precaution observed.
About I litre of distilled water was heated to boiling, and, while
hot, poured into a previously sterilized bottle and allowed to cool.
730 c.c. of the water were measured out and, to determine the
exact quantity, weighed.
To further prove, the amount was calculated to troy weight, and
compared.
170 grammes of the acetate were dissolved in the water, and to
this solution lOO grammes of the 99 per cent, lead oxide were
added in divided portions.
The mixture was allowed to stand in a well-closed bottle for five
days, agitating repeatedly, at the expiration of which time the mix-
ture was again weighed and no loss noticed.
It was then filtered with the usual precautions.
The specific gravity of the finished solution was found to be
1-230, and 13 67 grammes required between 25 and 26 c.c. of -
H.SO^ for complete precipitation, using methyl-orange as indicator.
To verify the above result the solution was prepared by the phar-
macopojial process, with scrupulous observation of all details, em-
ploying the same salts as in the foregoing operation.
The specific gravity of this solution was 1-229, and 13-67 grammes
also required between 25 and 26 c.c. of the normal acid for precipi-
tation, thus obtaining almost identical results.
Various similar experiments were also made with acetates and
oxides of lower percentage than employed in the foregoing. The
results thus obtained were deemed of importance, as the lead acetate
VoVi^^beni^"-} Official Lead Preparations. 567
of commerce is usually prepared from litharge more or less impure,
and this may influence the specific gravity of lead subacetate solu-
tion prepared from such salts.
For instance, the solution was made from an acetate which the
writer prepared from a sample of litharge assaying 96 5 per cent, of
oxide, the latter being also employed.
The finished preparation had the specific gravity of 1*225, ^"^ re-
quired exactly 25 c.c. of normal sulphuric acid for the precipitation
of 13-67 grammes.
The specific gravity of lead subacetate solution will not answer
either for an identity test or a criterion as to percentage
strength.
An aqueous solution of lead acetate containing between 25 and
28 per cent, of the salt will have a specific gravity closely approxi-
mating I 195, the official figure for Goulard's extract.
A 17 per cent, solution of lead acetate was found to have the
specific gravity of 1-123, and 13-67 grammes required lor precipita-
tion about 14 c.c. of H.,SO,.
An addition of 100 grammes of lead oxide to 1,000 grammes of
this solution, allowed to stand one week with occasional agitation,
yielded a filtrate of the specific gravity 1207, which, however,
only required 23 c.c. H.^SO^ for precipitating the usual amount.
It will be seen that although the specific gravity of this solution
is in excess of the pharmacopceial figure, it fell short in the percent-
age of basic salt, while having a 10 per cent, increase in water over
the official amount.
From tJie above and other results obtained, the writer draws the
conclusion that the specific gravity^ of liquor plumbi subacetatis
must be placed as about 1-225. in'^tead of I -195, the pharmaco[:a.Mal
figure.
LIQUOR PLUMBI SUBACETATIS DILUTUS.
The official lead water is one of the preparations for which, due
to its liability to chemical change, it is alike impossible to suggest
improvement or to fix a definite standard.
When recently prepared, a clear solution is obtained. I^ut aside
fruin tlic procedure o( many pharmaci.sls to draw their distilled water
568 Official Lend Preparations. {
Am. Jour. Pharm.
November, 1897.
for this preparation from the water spigot, it still remains that the
solution cannot be kept long in a cloudless condition.
Many prefer to dispense a cloudy solution, to lessen the liability
of error in connection with lime water.
In the Aqua plumbi Goulardi, a spiritous form of lead water of
several continental pharmacopoeias, ordinary soft water is directed.
An important feature is thereby lost sight of, namely the impair-
ment of the efficacy of the preparation as a local application, the
insoluble lead sulphate and carbonate not possessing an equal value.
For the Pharmacopoeia to direct recent preparation is also imprac-
ticable and would be disregarded.
The writer attempted to estimate the percentage of basic lead sub-
acetate in samples of lead water procured from the shops, but, due to
the constantly decreasing strength of the official preparation, found
it impracticable to fix a definite standard.
It was found, however, that commercial lead water presents even
greater variations in strength than Goulard's extract.
In view of the liability of confounding the solution with liquor
calcis, it is perhaps not out of place to call attention to the direction
of the French codex to add a small quantity of vulnerary spirit, an
alcoholic solution of the oils of lavender, sage and rosemary.
In connection with the official lead solutions, the writer would
finally call attention to a preparation recently published in Diete-
rich's Manual, namely, a dried lead subacetate, plumbum aceticum
siccum. As the quantities of the ingredients are based upon the
German Pharmacopoeia, it is unnecessary to reproduce them here.
From this dried salt, both Goulard's extract and lead water may
be made extemporaneously, and as its preparation presents no diffi-
culty to the practical pharmacist, a similar compound, based on
U.S. P. quantities can easily be furnished.
The salt would solve a problem which, as long as the solutions
are official, will always confront the pharmacist, namely, rapid and
recent preparation.
THE LEAD ACETATE OF COMMERCE.
By far the greatest importance, and of paramount influence upon
Goulard's extract and similar preparations, is found in the quality of
the lead salts.
P'irst attention is claimed by the acetate.
^Novem'^K"} Officmi Lead Preparations. 569
Every pharmacist has undoubtedly observed the physical and
chemical variations in commercial su<^ar of lead. In the price lists of
wholesale drug firms we find quoted several varieties, among which
we find the white and brown. That the latter has been used in
making Goulard's extract in some instances was revealed by the
examination of commercial samples.
But not only careless selection of the salt, but the inherent phys-
ical properties, as well as the liability of chemical change, have a
material influence, and may either increase or diminish the strength
of the preparations made therefrom.
Treating first of the liability of increase, we find that lead acetate
contains 14-25 per cent, of water of crystallization.
The Pharmacopoeia states that this is lost at a temperature of 40°C.,
and Ladenburg states that the salt loses its water of crystallization
in dry air.
As in our climate the summer temperature falls but a few degrees
short of the above figure, the liability of the loss of water must be
borne in mind.
This will result in an increase in the lead strength of a salt thus
exposed, and is, in not a few instances, in consequence, the result
of keeping the salt in packages in place of well-closed vessels.
To substantiate this point, the writer made the following obser-
vation:
Goulard's extract was prepared from a specimen of lead acetate
obtained from a reputable manufacturer and labelled C.P., U S.P., put
up in paper cartoons.
The solution had the specific gravity of 1-253, and 13 67 grammes
;/
required 27 c.c. HjSO^ for precipitation.
But the prolonged exposure of the salt to air is, on the other
hand, liable to cause a decrease in the lead strength.
Lead acetate absorbs CO.^ from the atmosphere, giving the salt a
white crust of carbonate.
Prolonged exposure results in partial conversion into lead carbon-
ate, and as the latter is insoluble in water, a deficiency in the lead
strength of the salt takes place.
This is probably the cause of the diminished strength of commer-
cial Goulard's extract, and is the result of the not unusual procedure
of using the effloresced, unsalable scraps and refuse of packages in
the sugar of lead drawer.
570 Official Lead Preparations, {^Njv'Lmber.mT"-
To obtain a satisfactory lead subacetate solution, it is, therefore,
necessary to employ only crystallized lead acetate, free from efflor-
escence or carbonate, in its preparation.
The writer has examined fifteen samples of lead acetate, purchased
in open market, with avoidance of duplication of source.
In the course of these examinations the advisability of introduc-
ing some means of estimating the lead strength of the salt, either
gravimetrical or volumetric, became apparent, and a consideration
of the subject may be urged upon the Committee of Revision
of the Pharmacopoeia.
The British Pharmacopoeia has given directions for the volumetric
estimation of the salt by means of sulphuric acid.
In an examination of fifteen samples of lead acetate, the writer
found calcium in every specimen in varying amounts.
As the presence of this impurity may interfere slightly with an
accurate estimation by means of normal sulphuric acid, decinormal
potassium bichromate solution was employed as precipitant, and the
number of c.c. necessary to precipitate i gramme of the salt
determined.
This precipitant was suggested by the method of F. Lux m the
valuation of red lead.
This author directs the decinormal solution to contain 14-761
grammes to i litre, each c.c. being equivalent to -0207 gramme
of lead.
If the decinormal solution of the U. S. Pharmacopoeia, containing
14-689 grammes to the litre, be employed, each c.c. is approxi-
mately equivalent to -02064 of lead, and consequently 0378 of
lead acetate.
Before, however, giving directions for a volumetric estimation, a
standard of purity for the acetate must be fixed.
If allowance is made for impurities amounting to 2 per cent., we
•98
have the foUowinc^ calculation: = 2';-Q c.c.
Nitrate of silver is used as an indicator to determine the end
of the reaction, and as a slight excess of the bichromate solution is
necessary for the development of the red silver chromate, it may
safely be made 26 c.c.
The following addition may, therefore, be recommended to the
Pharmacopoeia :
Am. Jour. Pbarm.')
.November, 1897. /
Official Lead Preparations.
571
One gramme of lead acetate, dissolved in 15 c.c. of water and
acidulated with acetic acid, should require at least 26 c.c. of decinor-
mal potassium bichromate solution for complete precipitation (pres-
ence of 98 per cent, absolute lead acetate).
Special directions for determining the end of the reaction by
means of silver nitrate may also be added.
A number of commercial samples of lead acetate were examined
in the following manner:
4 grammes of the salt were dissolved in sufficient recently-boiled
distilled water to measure 40 c.c.
The degrees of opalescence of the solutions were noted.
10 c.c. of the solution were acidulated with acetic acid and esti-
mated by means of the bichromate solution.
10 c.c. more wtvG filtered 2t.r\d also precipitated in the same manner.
This procedure was employed with the object of determining the
difference between the acetate as found and the actual amount of
soluble acetate in the sample.
EXAMI.VATION OF COMMERCIAL LEAD ACETATE.
n
Treatment
1
Appear-
auce.
Appearan'e
of Sol. in
llaO
Precipita'n
with Pot.
Ferro-
cyanide.
10
K,Cr„0,
Titrate of
Acidulated
Un filtered
&0I.
Titration
of Filtered
Sol.
with
NH^OH
after Ppig.
with
H,SO*.
Fe. Ca.
Granular
marked
Ver>'
Flocculent
I
C. P.
opalescent
Pure white
268
265
reddish
Present Present
3
do
do
do
28 6
Vi
do
do do
3
Granular
do
do
269
265
do
do do
Slightly
1
4
Crystals opalescent
do
270 1
27S
27-2
do
do ! do
5
do
do
do
27-3
do
do 1 do
Somewhat
1
6
do
opalescent
Slightly
do
26 '9
367
do
do ' do
7
do
Mixture of
powd. and
opalescent
do
270
265
do
do do
8
crystals
Mixture «>f
opalescent
Opalescent
do
263
26'0
do
do do
9
andcryst'ls
Upnlescent
do
do
26-8
1
26s
do
do do
10
piece*
do
do
28 0
27'a
do
do do
XI
do
Marked
C. P.
U. S. P.
do
do
267
26-4
do
do do
i
12
mucbefnor
do
do
^97
29'a
do
do do
13
CryktaU
Mixtureof
powd. and
do
do
30' 1
277
do
do do
>4
crystals do
do
27-9
27- 1
do
do do
SliKhtly
IS
CrysUls
opalcscciit
do
271 ,
2^'-:
do
«!»• do
572 Official Lead Preparations. {"^W^sS^^S^xm:
In the table furnished above the results obtained are recorded.
A portion of the remaining solution was precipitated by potas-
sium ferrocyanide solution, as directed by the Pharmacopoeia.
The remaining solution, acidulated with acetic acid, was precipi-
tated by means of sulphuric acid.
The filtrate from the precipitated sulphate was examined for iron
and calcium in the usual manner.
COMMERCIAL LITHARGE.
A good quality of lead oxide is indispensable in the preparation
of Goulard's extract and similar galenicals. Among the queries
presented to the A. Ph. A., the following is found :
Commercial litharge is grossly adulterated. What are the adulter-
ants and in what quantity are they present ?
The writer examined twenty- five samples of litharge, obtained in
each case, as far as known, from a different source. Physically the
respective specimens differed little, but evident carelessness in keep-
ing the oxide, especially when procured from paint shops, was
apparent.
The color varied in few instances; several samples, however, con-
tained red lead, which was revealed by special examination.
The specimens were examined according to the pharmacopoeial
directions as to the amount insoluble in acetic acid.
A portion of the acetic solution was precipitated by means of
sulphuric acid, and the filtrate examined for copper and iron by
means of ammonia water.
Further examinations for zinc, aluminum and calcium, were also
made in the usual manner.
Every sample of litharge examined contained iron and calcium ;
aluminum was present in some, while copper and zinc were either
absent or present only in trifling amounts.
During the course of these examinations the pharmacopoeial
directions were found inadequate for complete valuation of com-
mercial litharge, and thenecessityofdirectionsforgravimetricor volu-
metric estimation became apparent. The Pharmacopoeia, for instance,
gives directions for the determination of impurities insoluble in
acetic acid, but fails to recognize the liability of the presence of I
soluble impurities or adulterants. \
The logical deduction from this omission is the necessary intro-
duction of a fixed valuation.
NSvim^n^T} Official Lead Preparations. 573
As in the case of the acetate, calcium is present in the lead oxide
of commerce, and is liable to interfere, if normal sulphuric or oxalic
acid is employed as precipitant.
A gravimetric estimation, by means of sulphuric acid and weigh-
ing the dried precipitated sulphate, from a solution of the litharge
in acetic acid, was originally employed by the writer, but was dis-
carded for the less tedious volumetric estimation with decinormal
potassium bichromate solution.
Before directing the proper precipitant, however, the Pharma-
copoeia must fix a standard and require a definite per cent, of lead
oxide in commercial litharge.
The pharmacopceial limit as to the amount of moisture and
carbonate is 2 per cent., that of insoluble impurities 15 per cent.
If, in addition to this, another allowance of 1-5 per cent, is made
for impurities soluble in acetic acid, such as zinc, calcium, iron,
aluminum, etc., an actual percentage of 95 of lead oxide can be
demanded in litharge.
If decinormal potassium bichromate solution is employed, 95
gramme of absolute lead oxide, when in solution, should require
for complete precipitation 428 c.c.
As each c.c. is equivalent to -02064 Pb, it is equivalent to 022236
of lead oxide.
We have, consequently, the following division :
'95 ^ 427
•022236
and as a slight excess of the dichromate solution is necessary, the
above amount can be demanded.
The following addition to the pharmacopceial description of lead
oxide may be introduced :
One gramme of lead oxide, dissolved in 5 c.c. of acetic acid,
diluted with 5 c.c. of water, by means of a gentle heat, should
require for complete precipitation at least 42 8 c.c. of the decinormal
potassium bichromate solution, using silver nitrate solution as
indicator.
In the following examination of twenty-five specimens of litharge,
the pharmacopoeia! directions were followed, except in the determi-
nation of carbonate and moisture.
As volumetric determinations were made, this was not deemed
necessary.
574
Official Lead Preparations.
{
Am. Jour. Pharm.
November, 1897.
In the samples of litharge examined, not one was found which
could be considered as grossly adulterated.
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^^ovSeriS^^-} Official Lead Preparations. 575
CERATUM PLUMBI SUBACETATIS.
Probably one of the most unsatisfactory official preparations used
for inunction is Goulard's cerate.
Its liability of becoming rancid in a comparatively short time is a
source of annoyance to many pharmacists who are compelled to
keep a stock of the cerate on hand.
The alkaline nature of the lead subacetate solution has the ten-
dency to saponify the fat employed, and in our older text-books on
pharmacy the statement is found that a kind of lead soap is formed.
Continental pharmacopoeias endeavor to overcome this difficulty
by the substitution of paraffin ointment bases for animal or vege-
table fats, changing the preparation from the nature of a cerate to
that of an ointment.
But in the employment of petrolatum and similar ointment bases
one of the most important objects of Goulard's cerate, its cooling
property, is impaired, and this substitution is, therefore, of doubtful
value.
The following is the official formula :
Grammes.
Solution of lead subacetate 200
Camphor cerate 8(X)
Mix them thoroughly.
This cerate should be freshly prepared when wanted for use.
The PharmacopcL'ia gives the operator no special directions how
to mix the cerate.
Mixing without melting, with the usual method of incorporation
with a spatula on an ointment slab, is doubtlessly to be understood.
It is questionable, however, if this method is exclusively followed,
especially when large quantities of the cerate are prepared.
The ease and rapidity of incorporating the subacetate solution
with the melted cerate is too tempting, particularly if the Pharma-
copoeia does not furnish prohibitory directions.
It is obvious that the stated saponification is more liable to occur
by the employment of this process than where mixture without heat
is effected.
An objectionable feature of animal fats in this preparation lies in
the production of a yellow or reddish color on standing. This is
not only likely to occur in the stock jar of the pharmacist, but in
the ointment container of the patient as well, frequently giving rise
to unpleasant suspicions.
5/6 Official Lead Preparations, {""^o'^^^S^f:
To prevent this discoloration, the addition of acetic acid to the
the fresh cerate is recommended, but it must be considered that this
addition is Hable to change the chemical character of the lead so-
lution.
The writer has employed various ointment bases for the prepara-
tion of Goulard's cerate.
Petrolatum, either yellow or white, will not answer on therapeu-
tical £^rounds.
The substitution of olive, almond, lard or cotton-seed oil in place
of lard in camphor cerate, similar to one of the 1870 Pharmacopoeia
methods, appears to furnish no improvement concerning preserva-
tion.
Some months ago the writer suggested to several physicians the
substitution of hydrated wool fat for the camphor cerate, but invari-
ably recommended recent preparation.
The results have, as far as known, been satisfactory, both from
the standpoint of preservation as well as therapeutic action.
More recently anhydrous wool fat has been substituted, with the
object of doing away with the excess of aqueous liquid.
Eighty grammes of the wool fat, commercially known as Adeps
Lanae, were melted at a low heat, and 20-0 grammes of lead sub-
acetate solution incorporated by stirring until cool.
The finished ointment closely resembles lanolin in appearance,
has a satisfactory therapeutic action, and does not show any signs
of deterioration on two months' standing. This time is, however,
too brief to draw any definite conclusions.
The disadvantage of the lanolin substitute for Goulard's cerate
may be found in the ropy consistence of the ointment base.
Unless warmed, satisfactory inunction cannot be accomplished.
Finally, the writer would suggest the following rough valuation of
the quality of Goulard's cerate :
Two grammes are introduced into a wide-mouthed vial, holding
about 15 c.c. — a half-ounce homoeopathic bottle will answer — and 10
c.c. of chloroform added.
The mixture is shaken occasionally, until the fat is dissolved by
the chloroform.
If the cerate is of recent preparation or of good quality, the
milky mixture will separate into two layers on standing, the lower
but slightly milky, and no precipitation will be found on the bottom
of the vial.
i
^^Jremhet i-^y] BalsajH Copixtha and Giirjun Balsam. 577
In an old, rancid or ropy cerate, similarly treated, a white precipi-
tate will be found, and if the cerate is discolored, the varying
degrees of intensity will be revealed in the chloroform solution.
BALSAM COPAIBA, OIL OF COPAIBA, MASS COPAIBA,
RESIN COPAIBA AND GURJUN BALSAM.
BV LVMAN F. Kebijcr.
The 1890 U.S.P. recognizes the first four of the above-named
products. These are supplied, directly or indirectly, by leguminous
shrubs and trees of the genus Copaiba, all natives of tropica)
America, excepting two African species. According to the investi-
gations of J. C. Umney,^ the African species supply a very different
product from those met with in commerce coming from tropical
America. All these varieties and the unknown composition of any
of them contribute materially to the difficulties attending a quali-
tative analysis of the oleoresins.
In 1895 I made- a careful comi)arison of the available methods for
detecting gurjun balsam in balsam copaiba. The conclusion arrived
at then was that a modification of the glacial acetic acid test gave
the most trustworthy results. Since contributing the article referred
to above, I have tested many samples of copaiba, some of which
were reported as coming to hand in original packages. In every
case the glacial acetic acid test was relied on to reveal the presence
of gurjun balsam.
Having had an opportunity for accumulating ample material, and
to make a further study of the commercial products, it was thought
tlie results and some comments might be of service for future refer-
ence. The results of this examination are tabulated below.
The articles examined two years ago, and the samples in the table,
marked copaiba, represent the commodity largely used in commerce.
Sample collected in 1S46 was kindly furnished by Prof. Remington,
from his cabinet. The Para samples were very good, except one,
which had a specific gravity of 09874 at 15° C. This was probably
not a normal Para copaiba, but a more concentrated olcoresin. The
solidifiable copaiba fairly represents the commercial article. I have
never examined a sample that had a specific gravity below 09800 at
15° C. and solidified well.
' 1891, Phann. / , Trans. (3), »a. 449. Am. Jour. Pharm., o«, 33. ii>v3,
IVtarm.J. Trans. (3), 24. 215. Am. Jour. Pharm., 03, 544.
2 Am. Jour. Pharm., «7. 394.
578
Balsam Copaiba and Gurjun Balsam. {
Am. Jour. Pharm.
November, lb97.
1
i
\
TCinrt nf
Specific
Specific
Per cent
of Oil
Distilled
Boiling
Point of
Specific
Gravity
of such
Oil at
15° c.
Specific
Gravity
of Steam-
Specific
Gravity
of Steam-
Source.
Balsam.
Gravity
at 15° C.
Gravity
at 250 C,
from
Metallic
such Oil,
C°.
Distilled
Oil at
Distilled
Oil at
Bath.
15° c.
25° c.
Carthagena .
Copaiba
0-9560
0 9506
53
250-265
0*9207
0*8997
0-8981
South America Copaiba
0'94i6
0-9372
56
253-268
0-9174
0*9014
o-gooo
Cent. America Copaiba
0-9526
0-9467
76
250-274
0-9231
09132
0*9067
Collected in
1846 Copaiba
0-9410
0-9381
62
25^-270
0*9036
08978
South America Para
0-9254
0-9200
90
258-270
0-9116
0-9079
0*9066
South America Para
0-9661
0-9583
88
254-268
0*9100
0*9093
09037
South America Para
0-9874
0-9818
54
253-265
0*9346
09019
0*9100
Sovith America Para
0-9176
0-9116
92
256-268
0-9150
0-8951
0*9043
South America Para
09146
0-9101
90
254-264
—
0*8936
0*8904
i Solidifi-
South America
able
0*9926
I -0000
23
260-269
0-9283
0*9201
0-9172
Commerce . .
Gurjun
09576
0 9516
0*9200
0*9146
Commerce . .
Gurjun
0-9796
0-9722
54
245-263
0-9202
0-9192
0-9141
Commerce . . Gurjun
09531
0-9476
66
240-260
B. P. of
Oil
0*9146
0-9093
0-9176
Commerce . . ! —
—
—
—
2:18-263
—
0-9104
0-9087
Commerce . - —
~
260-269
09133
0-9101
The samples of gurjun were all secured in New York. The two
latter items represent commercial oil of copaiba, the last is adulter-
ated with oil of gurjun and the other is pure. The specific gravi-
ties at 25° C. were sim.ply taken for data.
There is a very limited demand for solidifiable copaiba, mass
copaiba and resin copaiba. The article of which large quantities
are used is a copaiba containing from 40 to 60 per cent, of oil. The
representative of a large essential oil firm informed me that 1,000
pounds of the latter were sold to Jive pounds of the solidifiable, and
three and one-half ^^ouwds of the resin. This included the territory
from Detroit, Mich., east to the Atlantic, through Canada and south
to Philadelphia and vicinity. If the above territory is at all repre-
sentative of the country covered by the U.S.P., it would appear that
the commodity which is used more than all the other copaiba
compounds ought to have been recognized by our Pharmacopoeia.
The present requirements of the Pharmacopoeia for balsam copaiba
(properly an oleoresin of copaiba) have undoubtedly wrought hard-
ships for some well-meaning druggists. Only the solidifiable is
recognized, and practically nothing but an unofficial article is used.
From this it can readily be seen that in ninety-nine cases out of a
hundred the average druggist is violating the requirements of the
Pharmacopoeia when he dispenses copaiba, and is thus rendered cul-
pable, especially in some states.
I
^^^■vimb^J!*i8^•} Balsam Copaiba and Gurjini Balsam. 579
The requirements of the Pharmacopoeia for oleoresin of copaiba
(balsam copaiba) are also quite inadequate for the end in view. The
range of specific gravity for solidifiable is rather too low ; 0-9800-
1-0173 would be better. On removing the oil, the residue may or
may not be brittle, in the absence of any fixed oil. I have removed
90 and 92 per cent, of oil from Para copaiba, and the residue was
even then far from being brittle.
The test for detecting gurjun balsam when the article is heated to
130° C. must be in error, since none of the samples of gurjun sub-
mitted to this test by me have ever congealed, but became only
slightly more viscous. Such a test becomes worthless in mixtures.
The other test for gurjun balsam is unreliable.
The tests for oil of copaiba are fairly good. According to my
work, the range of specific gravity ought to be a little greater. A
test for oil of gurjun should be given. The specific gravity of the
latter is a little higher than that of the oil of copaiba ; gurjun oil is
also somewhat darker in color, but in mixtures these can readily be
adjusted.
Resin copaiba might well be dismissed from the Pharmacopoeia
without any inconvenience to the drug trade. If it is retained,
more stringent requirements ought to be added. As it is, almost
any resin will answer.
The therapeutical side of the copaiba compounds is an interesting
one. The various authorities are generally agreed that an oleoresin
containing from 40 to 60 per cent, of oil is the one best suited for
gonorrhceal affections and kindred diseases. Those writers who
make any comparisons between the oil and the oleoresin almost
universally concede the oil to be less efficient than the oleoresin.
One recent eminent authority says the oil distilled from the oleo-
resin is of little value. The same writer considers mass copaiba as
a useless and clumsy form of giving the pill.
In U. S. Dispensatory, 17th edition, foot-note, page 445, is the
following : "As the virtues of copaiba depend mainly on the oil,
this variety (Para) should be more efficacious than the copaiba in
common use." Here is room for more therapeutical study. It is
evident that the oleoresin containing from 40 to 60 per cent, of oil,
and the oil ought to be recognized by the U.S. P., but the other
copaiba compounds could be dismissed.
580 Fermented and Distilled Liquors. {^No/e^mberlm?!"
SHALL FERMENTED AND DISTILLED LIQUORS BE
DISMISSED FROM THE UNITED STATES
PHARMACOPOEIA ?
By Joseph W. EngIvAnd.
The recommendation of the President of the American Pharma.
ceutical Association, Mr. J. E. Morrison, in his annual address dehv-
ered before the recent meeting of that body, held at Lake Minne-
tonka, that fermented and distilled " liquors " be not recognized by
the U. S. Pharmacopoeia as medicinal agents — which recommenda-
tion, by the by, was voted down by the Association — and the paper
by N. S. Davis, A.M, M.D., LL.D., on " The Therapeutic Proper-
ties of Alcohol and the Reasons why the Fermented and Distilled
Liquors used as Beverages should not be Recognized in the Phar-
macopoeia as Medicinal Agents,"^ have both excited interest in the
medical and pharmaceutical professions.
President J. E. Morrison, of the American Pharmaceutical Asso-
ciation, takes the ground that the sale of *• liquors " by druggists
has done an incalculable amount of injury to American pharmacy,
that the Government has placed pharmacists who sell " liquors "
on the same footing as saloon-keepers ; that this condition of affairs
should be terminated by the complete abolition of every form of
dealing in fermented or spirituous liquors, and that a great advance
in this direction would be taken if it were decided to discard all
such preparations from the U. S. Pharmacopoeia.
The question as to whether fermented and distilled liquors shall be
dismissed or not from the U. S. Pharmacopoeia is, to my mind,
wholly a medical question. If these liquors have sufficient thera-
peutic worth to warrant their use in medical practice, they should
be retained. If they have not, they should be dismissed. It is not
a matter of sentiment either for or against the liquor traffic. It is
a matter of simple justice to the sick. So long as "liquors" are pre-
scribed by a majority of physicians and used by the sick, so long
should our national guide-book recognize them, and demand a cer-
tain standard of quality, the same as it does for any other drug.
The mere fact that " liquors " are recognized by the Pharmacopoeia
^ Read before the Section on Materia Medica, Pharmacy and Therapeutics of
the American Medical Association, at the meeting held June 1-4, 1897. Journal
of American Medical Association, August 21, 1897. American Journai, of
Pharmacy, October, 1897.
^^ovimber^.^^} Fermented and Distilled Liquors. 581
does not compel a druggist to keep or sell them if he does not wish;
but it does compel him, if he sells them on the orders of physi-
cians, to sell them of a certain quality, or violate official standards.
On the other hand, if " liquors " were not officially recognized, there
would be no medicinal standards, and the sick would suffer. A
•• liquor " is sold, or should be sold, by pharmacists only as a drug.
If sold for any other reason, then the liquor-dealers masquerading as
druggists should be legislated out of the business. The sick should
not be punished for needing liquors, nor denied the privilege ot ob-
taining them of standard quality.
Dr. N. S. Davis, in his paper, claims that physiological experi-
ments have shown that the presence of alcohol in human tissues
retards natural metabolic changes, lessens the processes of oxida-
tion and elimination, diminishes nerve-sensibility, and when re-
peated from day to day, induces cell and tissue degeneration. What
the changes would be in human tissues undergoing abnormal meta-
bolic changes, he does not refer to, and yet the clinical value of a drug
is an all-important factor. Physiological experiments are necessary,
and are good enough, as far as they go; but unless confirmed by
clinical results, the)' are not conclusive.
Further, Dr. Davis alleges that while the present United States
Pharmacopoeia recognizes wine, whiskey and brandy,// ''docs not
give a definite official standard of alcoholic strength for cither of
them.'' This is an error. While no fixed standard is given,
yet it is demanded that white and red wine shall contain 10
to 14 per cent., whiskey 45 to 50 per cent., and brandy 39 to 47
per cent, of alcohol. The most radical claim, however, in Dr.
Davis' paper, and the one, doubtless, that will be most disputed by
clinicians, is the assertion that alcohol is the only important thera-
peutic agent in all •' liquors," and if other therapeutic agents exist
in addition to alcohol, that their proportionate quantity and
quality is far more variable than is their per cent, of alcohol.
•• Almost the only constituents," he writes, •• found in whiskey and
brandy, besides the alcohol and water, are very variable quantities
oi fusel oil, tannin and, in very old specimens, a trace of some ethe-
real substance to which connoisseurs attribute the special bouquet.
So far from adding to the therapeutic value, the first two substances
are regarded as very undesirable impurities, and the last named
has never been isolated in sufficient quantity to have its medical
qualities tried."
582 Fermented and Distilled Liquors. { "^Novimbe^S?"
Let us first note the inaccuracies of these statements. While
fusel oil or amylic alcohol is found in recently distilled whiskeys, it
is not found in those that have been properly aged, or, if present,
it is present, as stated by the Pharmacopoeia, in traces only. The
Pharmacopoeia requires the absence of all fusel oil from the official
brandy. As to the oak tannin in whiskey and brandy, from the
casks, it is only present in traces, and it is difficult to see how it can
be regarded as a very undesirable impurity.
If " liquors " have therapeutic worth over simple mixtures of
alcohol and water in fixed strengths — and the burden of clinical
evidence is that they have — this value must be due to the extractive
matters contained in them ; and it is upon this line, with regard to
a certain constituent of whiskey, that a few words may be said.
During the past five years the writer has examined many samples
of whiskey chemically, and next to the alcoholic strength and the
absence of fusel oil, one of the most important factors in such
examinations has been the determination of the total acidity. The
importance of this factor has been generally overlooked, and was
pointed out to me by the late Prof. John M. Maisch, who said that
he had examined many barrels of whiskey during the Civil War,
tor the Government, and always found that the best whiskeys had
the highest acidity. He referred me to a paper in the American
Journal of Pharmacy (1859, p. 573), which he had translated from
the German, wherein S. J. Kappel showed the presence of valerianic
acid, and the absence of acetic acid, in potato and in rye whiskeys,
and expressed the opinion that while valerianic acid was probably
the main acid of whiskeys, this had not been positively deter-
mined. Since then, the writer has been especially observant of the
acid factor in whiskey examinations, and has found that, generally,
the oldest, fusel-oil-free, highest-priced, and most strongly alcoholic
whiskey has the highest acidity. Occasionally there is an exception.
A raw whiskey may be so refined before aging that it will
not have the usual amount of the acid-forming compounds, and
hence show a low acidity.
The Pharmacopoeia of 1890 demands a whiskey "at least two
years old," and requires that to render 100 c.c. of whiskey dis-
tinctly alkaline to litmus there should be required not more than
1-2 c.c. of normal potassium hydrate solution.
To determine the acidity, a very much better way than the official
^z^ov^emberi^"'} Fermented and Distilled Liquors. 583
method is to use a dccinormal solution of sodium hydrate, rather
than the official normal solution of potassium hydrate, and to
employ 10 c.c. of whiskey, rather than 100 c.c. Place the sample
to be examined in a flat-bottomed test tube, resting on a piece of
white paper, add a few drops of phenolphthalein solution — do not
use litmus, as it is not sufficiently delicate — and run in the soda
solution from a burette (graduated to a tenth c.c). By a little
practice, and especially by *' checking" results, the end reaction may
be very quickly and accurately determined. To measure the whis-
key the writer uses a 5 c.c. pipette, graduated to the twentieth of a
c.c. Probably one graduated to the one-tenth would answer equally
as well.
The results had, during the past five years, in determining the
total acidity of some seventy-five samples of whiskey, according
to the above method, in the number of cubic centimetres of deci-
normal sodium hydrate solution needed to neutralize 10 cubic
centimetres of a sample, were as follows :
jSgj.—i, I'l, 1-4, 1-8, 1-2, 0-6, I, i-i, 1-2, 1-3, iS, 1-5, 1-5, 1-5, 1-5, 1-5, 1-5,
7^9/ .-—I '4, 1-2, 16, 1-3, 1-3, 0-9, 0-9, 1-3, 13, 1-6, 1-6, 1-6, 17, 17, 1-6.
/Sgj.—i-j, 1-6, 1-4, 1-3, 1-3, 1-3, 1-8, 1-4, 1-5, r6, 19, v6, rS, 17, 1-4, 1-4.
J896:— 1-2, 1-2, II, 13, 17, 17, 1-2, 1-5, 1-5, 1-5, 15, 14.
/<?P7.-— 1-6, 1-3, 1-3, 17, 13, 1-2, 13, 15, 13, 04, 05, 06, 1-6, 17.
It is imi)ortant to note that the acidity of whiskey does not
increase with age beyond a certain point. In May, 1895, ^^^ writer
examined ten samples of whiskey. None of the samples were less
than three years old. The results were in cubic centimetres of
decinormal sodium hydrate solution used to neutralize 10 c.c. of
whiskey, as JoUows:
17, 1-6, 14, 1-3, 1-3, 1-8 1-4, 1-5, 1-6, 1-6.
The same samples were examined a few days since (October, 1897),
and the acidity was found to be unchanged.
If valerianic acid is the main acid in whiskey, the reaction in neu-
tralization with sodium hydrate would be as follows:
I1C,U,0, NallO = NaC.HA -: li.O
10177 39-96 12377 \7<j6
Assuming that, in good whiskey, an average of /f c.c. of dcci-
584 -^^7 Bean, {
Am. Jour. Pharm.
November, 1897.
normal sodium hydrate solution (or 1-5 c.c. of normal) was required
to neutralize 100 c c. of whiskey, this would be equal to o-o6 gramme
of NaHO. And if 39-96 grammes of NaHO neutralize 10177
grammes of valerianic acid, 006 gramme should neutralize 01 5
gramme of acid, as follows:
39-96 : o-o6 :: 10177 : 0-15.
In other words, ^2ic\\ fluid ounce of whiskey would contain nearly
3/ of a zrain of free valerianic acid.
The U.S P. (1890) standard of i-2 c.c. is, in the writer's judgment,
too low for a good whiskey. It should be at least 1*4 or 1-5, and a
three or four-year-old whiskey should be required instead of a •' not
less than two-years-old " product. The U.S P. of 1880 required
that 100 c.c. of whiskey should be rendered distinctly alkaline to
litmus by 2 c.c. of the volumetric solution of soda. What the exact
chemical changes are that take place in whiskey on aging, whether
or not any acetic acid is formed from the ethyl alcohol by oxidation
from the air during the process of fermentation, whether acetic ether
is produced with acetic acid as an ultimate product, and whether
the fusel oil or amylic alcohol present in raw whiskey is directly
oxidized by age into valerianic acid, or is first converted into valeri-
anic ether and then into acid, are all questions which have not yet
been solved by chemical science, and remain for future work.
The extractive of whiskey most probably has therapeutic worth, as
has also the extractives in wines and brandies, and before any action
is taken by the Committee on Revision of the U. S. Pharmacopoeia,
looking toward the dismissal of these products, there should be a
thorough and extended examination made of them chemically and
therapeutically.
THE SOY BEAN.
By Henry TrimbIvE.
In this Journal for June, 1896, the writer published a summary of
the literature of this bean, which bean is of especial interest to phar-
macists because of the digestive ferment said to exist in it. Recently
the U. S. Department of Agriculture has issued Farmers' Bulletin No.
58, entitled "The Soy Bean as a Forage Crop," by Thomas A. Wil-
liams, under the direction of F. Lamson-Scribner, with an appen-
dix on "Soy Beans as Food for Man," by C. Y. Langworthy, Ph.D.
Am. Jour. Pn>«rra.
November. 1897.
Sojf Bean,
585
While not addinfr anything new to the knowledge of the digestive
ferment, still there is so much valuable information in the report as
to make it desirable to reproduce it in abstract.
General Characteristics and Origin. — The Soy Bean, Glycine his-
pida, previously, but incorrectly, called soja bean, is a leguminous
Soy bean : a, flowering branch (reduced -3); b, one of the flowers
(enlarged); c, pods of soy bean (reduced ']).
plant, native of Southeastern Asia. De Candolle says that it orig-
inally occurred in the wild state in the region " from Cochin China
to the south of Japan and to Java " It has been cultivated from
very ancient times, and in some countries, notably Japan, it is a very
important food plant, an 1 its cultivation has reached such an
586 Soy Bean, {""Woil^^^^?:
advanced stage that innumerable varieties and forms have been
developed. Professor Rein says it is the most important legume in
extent of varieties, uses, and value grown in China or Japan. It is
supposed to have been used for food in China even before the time
of Confucius. Although it has been grown in China and Japan for
such an extended period, its cultivation seems to have spread very
slowly to the surrounding countries. Its introduction into India
seems to have taken place in comparatively modern times. More
recently it was brought to Europe, where it was grown in botanic
gardens for more than lOO years without attracting attention as a
plant of much economic importance. Aiton says in his Hortus
Kewensis that it v/as first brought to England in 1790. In 1875
Professor Haberlandt began an extensive series of experiments with
this plant in Austria-Hungary, and in a work published in 1878 he
gave the results of his studies and strongly urged the cultivation of
the soy bean as a food plant for both man and beast. Although he
succeeded in exciting a great deal of interest in its cultivation while
making his experiments, and distributed a considerable amount of
seed, very little seems to have come of it ; for at his death, which
occurred in 1878, the interest flagged, and the soy bean has failed
to obtain the place as a staple crop which he prophesied for it.
In our own country soy bean has been grown for a great many
years, chiefly in the South, but it is only within the last fifteen years
that it has received much attention as a forage crop. Recently it
has been the subject of considerable experimentation at a number
of the experiment stations, and its great value as a crop has been
clearly demonstrated.
The term " soy" applied to this bean is derived from a Japanese
word '' shoyu," denoting a certain preparation from the seeds which
is a favorite article of diet in that country. The term ** soja " is
often used in connection with this plant, but Professor Georgeson,
who spent some time in Japan, and who, since his return to this
country, has experimented extensively with this plant, says :
The term soja, often applied to this bean, is misleading, inasmuch as the
species named by Siebold and Zuccarini Glycine soja is not cultivated there
(Japan), or at least rarely cultivated, though wild in the South ; and later this
species was confounded with the cultivated species, G. hispida Moench.,
whence the origin of the term soja, as applied to the cultivated bean.
Recent works on Japanese botany seem to substantiate this posi-
Am. Joiir. Pharm.l C , ,, R/>nn "Rt
November. 1897. / -^^J DCaH. 557
tion, though it is still a matter of doubt as to what botanical name
properly belongs to the cultivated species.
The soy bean is an erect, annual plant, with branching hairy
stems, trifoliate, more or less hairy leaves, rather unconspicuous pale
lilac or violet-colored flowers, and broad, two to five-seeded pods
covered, like the stem, with stiff, reddish hairs. The seeds vary in
color from whitish and yellowish to green, brown and black, and
in shape from spherical to elliptical and more or less compressed.
Under favorable conditions the plant may reach a height of four feet
or more.
In Professor Haberlandt's experiments in Austria- Hungary the
plants yield about 200 pods and 450 seeds each, and though this is
probably considerably above the average, it shows them to be
remarkably prolific.
Tiie fact that the flotvers are self-pollinated makes the yield
entirely independent of insects, and renders the soy bean free from
an important obstacle in the way oi the introduction of many
legumes into new regions.
Varieties — The different varieties of soy bean are distinguished
largely according to the color, size and shape of the seed and the
time required for the plants to reach maturity. The names applied
in the United States are, for exampje, ** Early White," " Medium
Late Green," " Medium Black," etc. The early varieties generally
fruit heavier in proportion to the size of the plant than the later
ones, and hence are better to grow for seed, while the medium or
late varieties are better for forage, on account of the larger yield of
fodder that may be obtained.
Conditions of Growth. — It is believed in Japan that in northern
climates soils of a rather strong character are best adapted to the
soy bean. It is usually sown about the end of May, and when used
for hay cut early in August. In both Europe and America it has
been found to thrive best on soils of medium texture, that are well
sup[)lied with potash, phosphoric acid and lime. Fairly good results
have been obtained in Kansas on very poor soils, and under very
adverse conditions as to moisture. In South Carolina the soy bean
gives excellent crops on sandy limestone or marshy soils, and also
on drained swamps or peaty lands that are well marled. The tem-
perature should be about the same as that required for corn. The
methods of culture are such as are usually recommended for ordi-
nary field beans.
588
Soy Bean.
Ana. Jour. Pliaip .
November, 1897
Chemical Coviposition. — The following tables on the chemical
composition of the various parts of the soy bean used for feeding
purposes, have been arranged with great care, to show as far as
possible the latest and best results obtained by experimenters in the
United States during the course of their studies of this plant:
CHEMICAIv COMPOSITION OF THE VARIOUS KINDS OF FORAGE MADE FROM
THE vSOY BEAN.
Soj'-Bean Forage.
Fresh or Air-dry Substance. Water-free Substance.
Fodder (earU' bloom to
earU'seed)"^
Soy-bean hay (Japanese)
Soy-bean liaj- (Mass.)^ .
Soy-bean straw (Mass.)-
Soy-bean straw (hulls
and vines after thresh-
ing)='
Soy-bean seed*
Soy-bean meaP . . . .
So3'-bean ensilage*' . . .
Corn and so3'-bean en-
silage"
Millet and .soy-beau en-
silage'
76-5
i6'o
I2'I
11-4
57
10-8
io"4
74-2
76-0
79
3-6
16 9
I4"2
4*9
40
34'o
36-0
4" I
2-5
2-8
I"0
2'2
4*1
19
0-8
i6'9
18-9
22
o-S
I"0
O X
lO'I
23-1
412
37-8
36-0
28-8
27*0
7-0
ii'i
7-2
6-5
35 "9
21T
37-6
49 '5
4-8
2-6
97
72
7-2
2-3 I5'3
5'9 20-1
7'3
6-4
3'9
47
162
5'5
4-25
38-1
5"i : 402
2-8
2*4
2-8
157
io"4
I3"3
i)
(LI
1
<i:^
5^
V *-
t*-
c X
V.
iw
r\
^
^ 1
4"i
2-6
47
2 2
43'o 27'6 I 10. o
27"5 427
46 8 24-0
42 7 i 42-4
70
085 38-2 ! 52-6
189
210
87
3'3
4-8
32-2
30-2
27-0
5 '4
2-9
376
46*3 30'o
i
34"3 ' 34"3
5'3
5"3
57
iro
> Ninth An. Rep. Storrs Exp. Sta., pp, 281, 285 ( 1896).
2 tCighth An. Rep. Mass. Hatch. Sta., p. 87 (1896).
=> Second An. Rep. S. C. Exp. Sta., p 179 (1890).
■» Bull. 15 U. S. Dept. Agric, Office Exp. Stations, p. 390 (1S93).
° Eighth An. Rep. Storrs Exp. Sta., pp. 1S3, 186 (1895)
•^ Bull. Tenn. Exp. Sta., Vol. IX. No. 3, p. 106 ( 1896)
^ Ninth An. Rep. Mass. Hatch Sta., p. i \o (1897).
If the preceding analyses are compared with those of other legu-
minous crops, it will be seen that the soy bean ranks high from a
chemical point of view. The green fodder has much the same com-
position as red clover, being slightly lower in crude protein and
higher in crude fiber. In the two most important substances, crude
protein and fat, the soy bean is considerably richer than the cowpea.
The hay also shows a relatively high fat and protein content. The
only available analysis of soy bean ensilage shows it to agree very
closely in composition with red clover ensilage, being higher in
Am. Jour. Pharm.1 <r^^. Vi^ntt ' 9rk
November, 1897 / -^^J l:>eafl. 3J^9
crude fiber and fat, and lower in extract matter. From the analysis
of the beans it will be seen that there are about two-fifths protein
and one-sixth fat, with but very little fiber present, making them
almost as rich in crude protein as the best cotton-seed meal, with a
hic^her percentage of fat. They contain three times as much crude
protein and nearly three and a half times as much fat as oats ;
nearly three and one-half times as much protein and about three
times as much fat as corn, and almost twice as much crude protein,
and over twelve times as much fat as peas; all of which show them
to form one of the most concentrated of our feeding stuffs.
Digestibility. — The chemical analysis alone will not prove the feed-
ing value of a forage crop. Soy bean meal has a high percentage
of digestibility. It contains almost two and one-half times as much
digestible protein, and over five times as much digestible fat as the
common roller process, wheat bran, and its digestibility is decid-
edly higher in everything but the fat than that of cotton-seed meal.
The experiments which confirmed these statements were made on
cattle and sheep, chiefly the latter.
As a Soil Renciver. — One of the great advantages in growing
leguminous forage crops lies in the benefit which the soil derives
from the nitrogen and other important elements of plant food that
are left in it by the crops. Soils that have become impoverished by
continuous cropping with small grains of other nitrogen-using crops
may be restored to fertility by the use of leguminous crops, as, for
example, the clovers, cowpeas, vetches, lupines, and the soy bean.
The value of a crop as a soil restorer depends upon the amount of
available plant food which it adds to the soil, and also upon the
effect which the roots have upon the mechanical condition of the
soil. Leguminous plants, through the aid of the root tubercle
organisms, are able to add to the available nitrogen of the soil, and
hence are extensively used in restoring tho.so deficient in that
element.
The soy bean is highly valued in Japan as a nitrogen gatherer
and is extensively grown in rotation with cereal crops. When the
soy bean was first introduced into the United States it did not form
root tubercles, owing to the absence of the tubercle organism from
the soil, and it has been grown for several years in some localities
without the appearance of any tubercles. In other cases the tuber-
cles have developed in great abundance a ter a short time. At the
590 ^^J^ ^^^^^- {''November.".s;7:'-
Massachusetts (Hatch) Station the medium green soybean produces
great numbers of the tubercles. At the same station it was
found that a liberal application of nitrates interfered with the
development of the tubercles.
In experiments made at the Storrs Experiment Station soy beans
were planted in soil uninfested with the tubercle microbes, and then
later in the season (about the middle of July) a portion of the field
was inoculated with infected soil. Tubercles were produced on the
plants in the inoculated land, but owing to the lateness of the inocu-
lation, they made but little development, and no difference could be
noticed between the crops grown on the two parts of the field.
Soy Beans as Food for Man. — The soy bean has been used as a
food for man in Japan, China and neighboring countries, from the
earliest times. In more recent years it has been cultivated for this
purpose in Europe. Analyses were given in this Journal, June,
1896.
Comparatively little information is available concerning the chemi-
cal character of the different constituents of the soy bean. Accord-
ing to the Japanese investigators, the bean contains, on an average,
7-5 per cent, of nitrogen, 6.9 per cent, being albuminoid nitrogen,
exclusive of peptones, o-i per cent, amide nitrogen, and 03 per
cent, nitrogen of peptones. Osborne studied the nitrogenous con-
stituents of white or kidney beans. He found that they contained
on an average 23-5 per cent, of protein, made up of phaselin and
phaseolin. The percentage of protein in the soy bean is much
higher than this, and it is not improbable that it differs materially
in chemical character. According to Japanese authors, the soy
bean contains no starch. No statements have been found concern-
ing the character of the fat.
The fact is well recognized that beans of all kinds are valuable
food because of the large amount of protein and fat which they con-
tain. In order that the nutrients may be available, the beans must
be cooked or prepared in some way so that the cell walls may be
broken down and the contents readily acted on by the digestive
juices. What is true of beans in general, is especially true of the
soy bean. Though it is eaten more extensively in China and Japan
than in any other countries, so far as can be learned it is never eaten
there as a vegetable, but more or less complex food products are
prepared from it. At least five preparations are commonly made in
Am. Joar. Phariu
Novenibtr. I
arm. \
*'7. ;
So}' Bean.
591
Japan from the soy bean. These are natto, tofu, miso, whose prepa-
ration has already been described in this Journal, and yuba and
shoyu.
A sort of film forms on the surface of soy-bean milk which in
appearance suggests cream. This material is sometimes prepared in
quantity by evaporatinj][ the milk, and when dried it is used as an
article of food under the name oi yuba.
Shoyu is a sauce prepared from a mixture of cooked and pulver-
ized soy beans, roasted and pulverized wheat, wheat flour, salt, and
water. The mass is fermented with rice-wine ferment in casks for
from one and a half to five years, being very frequently stirred. The
resulting product is a moderately thick brown liquid. In odor and
taste it is not unlike a good quality of meat extract, though perhaps
a trifle more pungent. Under the name of soy sauce it has been
known in India, and to some extent in Europe, for many years.
The composition of each of the above-described foods is given in
the following table :
y>oy-bean food products.
Protein.
Fat.
Nitrogen-
free ex- Fiber,
tract.
Ash.
Percent., Percent Percent.] Percent.
Frc»h tofu . .... 89-00
Fresh tofu . ^9 29
Frozen tofu . . 1870
Natto 15*32
Yuba 2i"85
White miso 5070
Red miso ... 5040
Swiss miso 13*53
Shoyu . . 6329
Sbosm I 67'4a
500
4*87
3 '40
2 10
4 35
Per cent.
48*50
2850
2 -60
—
1 ''-''
23'65
1505
1*48
42 60
24*62
765
570
2440
1260
10*08
1877
825
2643
1391
I9'54
'■41
8-3.
-
5 >"
-
m
—
406
--
Per cent.
0*50
0-48
I 70
3o3
2-SS
6*60
I 2 50
I - .5
It will be noticed that most of these soy-bean products are fer-
mented ; that is, they are prepared with the aid of microorganisms
The cell walls and other carbohydrate material are broken down
and the cell-contents rendered more accessible to the digestive
juices, and at the same time peculiar and pleasant flavors are devel-
oped. The special microorganisms used m the preparation of these
foods have been studied in recent years. The manufacture of these
-„-, C^y Rpn-H f Am. Jour. Pharm,
^9^ ^^y ^'^"'^- \ November, 1897.
products is of very ancient origin, and affords an interesting practical
illustration of the use of bacteria for economic purposes.
Though these soy-bean products are prepared chiefly in Japan and
other eastern countries, their manufacture has been attempted to
some extent in Switzerland and elsewhere.
The statement is frequently made that the Japanese live almost
exclusively upon rice, eating little or no meat. It is not, however,
generally known that the deficiency of protein in the rice is made
up by the consumption of large quantities of shoyu, miso, or other
soy bean products. It is stated on good authority that these pro-
ducts actually take the place of meat and other nitrogenous animal
foods in the Japanese dietary. They are eaten in some form or
other by rich and poor at almost every meal.
A large number of dietary and digestion experiments have been
made in Japan in which soy bean preparations formed a considerable
part of the food consumed, although no experiments have been
made, so far as can be learned, in which such preparations were
eaten alone. Generally speaking, the nitrogen was well assimilated.
For instance, when 12 grammes of nitrogen were consumed daily,
the dietary consisting of soy bean cheese and rice, only OT gramme
of nitrogen was excreted in the feces. When 13-9 grammes of nitro-
gen was consumed daily in a dietary of bean cheese and barley,
only 1*4 grammes was excreted in the feces. According to one
author, in a dietary containing a large amount of bean cheese, 90
per cent, ot the protein, 899 per cent, of the fat, and 14-5 per cent,
of the crude fiber are digestible. The general opinion of Japanese
investigators and others familiar with oriental dietetics is, that the
protein in articles of food prepared from soy beans is in a very
available form, and that these preparations are most valuable foods.
Bean sausages in considerable variety are prepared in Germany,
and formed part of the ration of the German soldier in the Franco-
Prussian war. So far as can be learned, these are always made from
ordinary varieties of beans and not from soy beans.
Since soy beans contain no starch, they have been recommended
as food for persons suffering from diabetes. A soy bean bread for
this purpose is manufactured in Paris.
Under the name of coffee beans, soy beans are eaten to some ex-
tent in Switzerland as a vegetable, and dried and roasted are also
used as a coffee substitute. Their use for this latter purpose is not
^No\4mbe^.^w7^} Hyoscinc-Scopolamine Question. 593
unknown in America. The attempt has recently been made by cer-
tain dealers to place the soy bean on the market as a new substitute
for coffee, and to sell it under other names at an exorbitant price.
Bulletin No. 98, of the North Carolina Experiment Station, re-
commends soy beans as a palatable vegetable when prepared as fol-
lows : Soak the beans until the skins come off, and stir in water
until the skins rise to the surface and then remove them. Boil the
beans with bacon until soft, season with pepper, salt and butter, and
serve hot. If the beans are green the preliminary soaking may be
omitted. No other references to the use of soy beans for human
food in the United States have been found.
Several of the Bulletins issued by the College of Agriculture of
the Imperial University of Japan contain valuable articles on the
soy bean and its products.
THE PRESENT STATUS OF THE HYOSCINE-SCOPOLA-
MINE QUESTION.^
By Louis Merck, Ph.D.
Hyoscine has been an object of active controversies, more so,
probably, than any other one of the notable alkaloids. These con-
troversies, after apparently becoming dormant for a time, have again
and again sprung up and engaged scientists of note on opposite
sides.
It was from the so-called amorphous hyoscyamine, the mi.xture
of bases obtained from hyoscyamine seeds, that Ladcnburg first
isolated a substance to which he gave the name of hyoscine. The
same discoverer assigned to the newly-found base the formula
Ci^H^gNOj, thus claiming it as an isomer of atropine and hyoscya-
mine. Hesse, on the other hand, contended that the new base was
possessed of the composition C,-H^,NO^. He also declared it to be
identical with the substance which E. Schmidt had isolated from
scopolia atropoides, and which had been named scopolamine. Subse-
quently, E. Schmidt found the hyoscine hydrobromatc of the mar-
kets to consist almost exclusively of the hydrobromatc of scopola-
mine. He does not, however, consider the non-existence of a hyos-
cine Cj^H^NOg to be thereby demonstrated. He argues \t\ favor of
the possibility that a ba.se of such composition may mdecd occur in
' The Journal of the Society of L hem i cat Industry, June 30, 1897.
594 Hyoscinc-Scopolainine Question. {^'^ov^^hS^xm.'
the mixtures of alkaloids obtained from the solanacere ; that Laden-
burg had actually got hold of that base, which gave him the data
for his formula and description of what he called " hyoscine," and
that the same base has since then happened to be isolated again.
Be that as it may, the *' hyoscine " put upon the market by E.
Merck has been and is assuredly identical with scopolamine. It is
only for the purpose of obviating misunderstandings in commercial
and medical circles, where a change of name is apt to create great
confusion, that our house has retained in its trade-list the desig-
nation of " hyoscine " for the base from hyoscyamus, while apply-
ing that of '' scopolamine " to the base from Scopolia atropoides.
Since the opening of this controversy, the Merck laboratories have,
in working considerable quantities of the solanaceous drugs for
alkaloids, steadily been directed toward the object of identifying a
base C1.H03NO3, which is to possess the properties of hyoscine. So
far, however, we have not succeeded in isolating such a base.
, In the course of these labors we were indeed fortunate enough to
isolate a base Ci^H23N03, thus isomeric with hyoscyamine and atro-
pine, from Duboisia myoporoides. This base we have named
" pseudo-hyoscyamine." Its properties, however, differ essentially
from those known for hyoscine. For instance, hyoscine is an oily
liquid, while pseudo-hyoscyamine melts at about 132° to 134°. Thus,
the possibility of any confusion between these two appears wholly
excluded. The base isolated from Duboisia myoporoides by J.
Gadamer (albeit in quantity insufficient for exact determination) is
equally unlikely to represent Ladenburg's " hyoscine," inasmuch
as Gadamer, from his analytic results, concludes that it contains
but 15 atoms of carbon. Our own investigations at the works
covered these solanaceous drugs : Belladonna, duboisia, datura,
stramonium, hyoscyamus, scopolia.
On examining even very large quantities of the bases residuary
from the manufacture of atropine, we have so far encountered no
substance which would, even approximately, be capable of identifi-
cation with the "hyoscine C17H23NO3." Furthermore, repeated
efforts were made by us to isolate all the alkaloids from duboisia.
All that were obtained on such occasions were: hyoscyamine, hyos-
cine (or scopolamine) C17H21NO4, considerable quantities of amor-
phous bases, and pseudo-hyoscyamine. Never was an alkaloid met
with in this work answering to the formula given by Ladenburg for
'xovimberilg:'"} Hyoscine-Scopol amine Questiou. 595
hyoscine, and at the same time possessing its characteristic proper-
ties regarding salts and double salts — properties which would have
rendered such an alkaloid incapable of being overlooked. The
same negative result was had from investigation of the alkaloids of
stramonium seeds, which, likewise, were worked in quantities of
thousands of kilogrammes. The Merck laboratories are also con-
tinually working, for alkaloids, large quantities of hyoscyamus seeds
and scopolia roots. Also, in these lines of manufacture, we con-
stantly kept our attention directed toward isolating the alkaloids
occurring among the residuary bases. Nevertheless, the search for
the particular base here in question has proved equally fruitless on
these two drugs.
In this connection I may be pardoned the liberty of alluding to
still another interesting fact developed at our laboratories. The
statement is frequently met with in literature, that hyoscine (that is,
scopolamine) has been isolated from the residual bases obtained in
the manufacture of atropine. Therefore, it might readily be inferred
that hyoscine is a side-base to hyoscyamine or atropine in the
belladonna. We have studiously kept this issue in view during the
working of many hundreds of thousands of kilos of belladonna roots.
And still we have never been able to discover hyoscine (meaning
scopolamine) among the residual bases resulting from these exten-
sive operations. This experience of ours thus directly contradicts
the inference before mentioned. The experiences of others, as
quoted before, may be presumed to have been due to defective sort-
ing of the belladonna roots, among which may have remained roots
of other solanacea^. Or, the residues remaining from the manufac-
ture of various solanaceous alkaloids, and utilized for obtaining side-
ba.ses, may not have been kept absolutely apart.
It may be contended that, in the Merck researches, the hyoscine
or scopolamine that might have been present could have been over-
looked in consequence of its own minimal quantity. This conten-
tion, however, is met by the fact that the mixtures of residual bases
were, at the end, also subjected to splitting; whereupon the appear-
ance of scopoline among the products of this operation must have
indicated that hyoscine had been present, if such were indeed the
case. From a single batch, lor instance, of residual bases thus
treated. lOO kilos of tropme were obtained, whereas the presence
•of a hi^lier-boiling base was not demonstrable.
596 H yoscine-Scopolatnine Questmi. { ^iK;%4mber!i8}J7""
To return, after this little digression, to my main topic, I would
once more summarize our laboratories' experiences regarding the
latter, to wit: With due consideration of the various solanaceous
drugs, and with the use of very considerable quantities of them, the
results so far have failed to show the possibility of obtaining a base
possessing the properties of hyoscine and answering to Ladenburg's
formula of CJ7H23NO3. Thus, this whole question has by this time
dwindled down almost exclusively to a controversy between O. Hesse
and E. Schmidt as to the propriety of designating the surely-estab-
lished alkaloid QyHgiNO^, either as " scopolamine " or as " hyoscine."
The polemics between the two investigators named have, how-
ever, recently extended into still another chapter of the solanaceae-
alkaloid research, which bears close relations to the one I have here
discussed. O. Hesse published an observation made by him in the
scopolamine hydrobromate of commerce, to this effect : He fre-
quently found this salt to contain also notable quantities of another
base, differing from scopolamine by the absence of optical rotatory
power. This would, of course, have the result that such a mixed
salt would show a smaller arc of rotation than that due to the pure
scopolamine hydrobromate.
He succeeded in isolating this inactive base and gave it the name
ot " atroscine." Hesse argues against any supposition of identity as
between his " atroscine " and the so-called " inactive scopolamine,'*
found by E. Schmidt. His reasons herefor are two : Firstly, he did
not succeed in obtaining, by the treatment of hyoscine with alkalies^
an inactive base of equal composition. Secondly, he claimed, on the
other hand, that the decrease in optical activity resulting in hyos-
cine upon treatment with alkalies is due altogether to a splitting of
the hyoscine into a *' split-base," which he calls •' oscine," and
tropic or atropic acids. O. Hesse's " oscine " is stated as being
identical with E. Schmidt's split-base " scopoline."
E. Schmidt, again, gives the genesis of his •' inactive scopolamine "
as being likewise brought about through the action of alkalies on
scopolamine, with the additional statement that it can also be pro-
duced by using silver oxide instead of the alkalies. He states that
he never encountered any ''atroscine " in the process of isolating
alkaloids from commercial scopolia roots or hyoscyamus seeds.
Schmidt further explains that accordingly as the liquors from sco-
polia root are treated with less or more intensively-acting alkalies^
^NivimhVf.*i897°'} H yoscinc-Scopolaminc Question. 597
one may obtain at will either a normal scopolamine (rotating about
24° to 25°), or a feebly rotating one. He succeeded even in directly
obtaining, from one and the same scopolia root, a normally (that is,
strongly) rotating and a feebly rotating scopolamine. The former
was obtained by alkalinizing the liquors with sodium bicarbonate or
ammonia ; the other by employing strong bases, such as soda-lye,
concentrated solution of potassa, etc.
It is thus still an open question whether or not Hesse's •' atros-
cine " should be regarded as identical with Schmidt's *' inactive
scopolamine." Upon considering the contradictory verdicts of
medical authorities who have tested both these substances as to their
action on the eye, one might almost incline toward the second
alternative, that is, non-identity.
O. Hesse, in his treatise, quotes medical councillor Dr. Konigs-
hbfer's conclusions from physiological tests made by him with
atroscine, to the effect that its action differs in certain points from
that of scopolamine. The passage quoted reads as follows : " We
thus find that this remedy (that is atroscine) acts identically with
atropine and scopolamine, in so far as its mydriatic effect is con-
cerned ; while in the matter of paralyzing the accommodation it
considerably surpasses both these substances in promptness of
action, as well as in duration of effect, the ratio of difference rang-
ing from double to quadruple."
E. Schmidt, on the other hand, reports that Prof Dr. Uhthoff,
director of the eye clinic at the University of Marburg, in conjunc-
tion with Dr. Axenfeld, lecturer, arrived at the following important
conclusion : In comparative tests with a strongly rotating scopola-
mine hydrobromate (25-43°) and a very feebly rotating salt (662°),
"... it was found that no difference, whatever, could be
shown between the effects of these two salts."
To these contradictory reports published by Schmidt and by
Hesse, I can add the following tacts, gathered from observations
made by us at the Darmstadt Laboratory. Kver since this property
of hyoscme, of strongh' rotating the plane of polarization, has been
known, special regard has been given to this point at our labor-
atories in working the side-bases from hyoscyamus seeds for
hyoscirte. The product of each separate batch was invariably
examined for the determination o( its optical properties. In the
course of these observations it was found that wc aUvavs obtained a
598 Hyoscitie'Scopolamine Question. {"N^ov^mbefS™'
hyoscine of normal rotatory power with but very slight variations,
that is, ranging between about 24° and 25°. We have been unable
so far to discover a feebly rotating preparation obtained from
hyoscyamus seeds.
In the manufacture of scopolamine from scopolia roots, we made
the optical rotatory power a subject of special research only quite
recently, and in consequence I can give you the results only on an
aniount of scopolamine obtained from about 10,000 kilos of the
roots. The scopolamine hydrobromate from this quantity, on being
crystallized, was shown to be absolutely pure, but to possess a laevo-
rotatory power of only 13-47°.
In connection herewith I should state that, in working the sco-
polia roots and in working up the side-bases for scopolamine, exactly
the same stages were adhered to, as in working the hyoscyamus
seeds and in working up their side-bases for hyoscine. Especially
in the manner of using alkali in both series, the most punctilious
care and attention were exercised in order to make the conditions
in both exactly equal. Hence, I cannot well refrain from the con-
clusion that the alkali can hardly have caused the difference in
rotatory power in these cases of ours ; for had it done so, a more
feebly rotating product must have resulted in the isolation of the
hyoscine as well as in the other case. This experience seems to me
to argue largely in favor of O. Hesse's view, that two chemically
equal basic substances, which so far can be distinguished from one
another only by their optical activities, are contained in the ordinary
scopolamine hydrobromate, and that, quite possibly, they exist pre-
formed already in the scopolia root.
The few observations so far available cannot, of course, suffice to
settle the pending controversy ; but it affords me gratification to
be in a position to promise the early publication of further results
from considerably larger batches of scopolia roots, in which, likewL^e,
the various results will be most carefully noted, which I hope may
contribute toward the elucidation of this question.
Tonca or Tonquin Beans, according to Bulletin of Miscellafteoics Infornia-
iion, Trinidad, October, 1897, were imported from Venezuela in 1896 to the
value of €130,985. Rum to the extent of 11,000 gallons was used in curing
them ; the greater part of the product was shipped to the United States, only
£1,091 in value going to other places. See also this Journal, March, 1897,
page 157.
^."oV'e^rll^r.r^iL} Lactic Add. 599
THE MANUFACTURE AND APPLICATIONS OF LACTIC
ACID.^
By Alax a. Claflin.
Tliis paper consists of extracts from notes on observations taken
during seven years* experience in the manufacture of lactic acid on
a large scale, on lines laid down by my predecessor, Mr. Chas. E.
Avery. While some of my facts are not new, considerable vork
having been done very recently on this subject, and while none of
my investigations have been carried farther than the daily exi-
gencies of manufacture required, yet I trust that from the ex-
ceptional opportunities that I have had, they may be found of
interest.
«
The lactic acid industry dates back about twenty years, when Mr.
Avery began his investigation, which resulted in the process which he
covered from 1881 to 1885 by American and foreign patents. The
production of lactic acid on a large scale by fermentation is interest-
ing because it employs micro-organisms to split up the glucose
molecule into two molecules of ethylidene lactic acid. The micro-
organism that does this work is well known as the bacillus acidi
lactici. This bacillus has been described variously — not from any
inaccuracy of the observer, but because it is of great variety itself,
a certain variety developing most rapidly in a certain medium. The
bacillus which does the work in a highly nitrogenous saccharine
solution is a large species. Its form is a double truncated cone,
averaging in length 2 to 2^2 millimetres, and about i millimetre in
diameter. It has the tendency of all lactic bacteria to link itself
together in pairs or short chains. The most abundant lactic
bacteria in sour milk are only ^^ millimetre long, but a little
thicker in proportion than those found in my saccharine solutions.
The manufacture of lactic acid has three divisions: The prepara-
tion of the saccharine solution, the fermentation, the conversion of
the fermented liquor into commercial lactic acid. The source from
which the saccharine solution is obtained is not important. The
location of the factory determines the raw material that can furnish
a glucose liquor most cheaply. The proportional composition of
the saccharine solution is very important. For complete decompo-
sition the saccharine solution should not vary between the limit
' The Journal of th^ SocUty of Clumual Industry, June 30, 1897.
6oo Lactic Acid. { iT^^i^e^isIf '
105 to 1-075 ^P ^''•' '^''^^ technical reasons tlie hi^^her density is
preferable. A solution of that density will contain from 7^ to 11
per cent, of saccharine matter. It is not essential to have all
the saccharine matter in the form of grape sugar. In fact,
it seems to be advantageous to have 10 to 15 per cent, of it as cane-
sugar, which, becoming inverted in the process, furnishes fresh mate-
rial, as it were, for the ferment. To do its work thoroughly, the
lactic bacillus needs to be well nourished by nitrogenous matter.
The most convenient form for this nitrogenous material is as
it comes from vegetable life, as extracted, for instance, from bran
by the action of boiling water and dilute acid. At different times I
have used material obtained from animal and mineral sources. In
the laboratory it is difficult to detect material differences. On the
large scale, I prefer a vegetable source ; there seems to be a com-
plete utilization of the material. The amount of nitrogenous mate-
rial should be at least 8 per cent, of the saccharine constituents. I
assume by nitrogenous matter a body of substantially the compo-
sition of albumin, containing 15 to 20 per cent, of nitrogen in com-
plex form. Perhaps it would be more accurate to say the total
nitrogen should be nearly 2 per cent, of the saccharine material,
and preferably combined with carbon. If a mineral food is to be
employed, ammonia salts should be in larger proportion than
nitrates. A low percentage of phosphates will suffice, and the pres-
ence of such potassium does not seem to be essential.
The requisite saccharine solution made up and boiled for at least
an hour, to make sure of sterilization, is conveyed into the fermen-
tation tank. There it is rapidly cooled to 55° C. or lower, not going
below 45°, and impregnated. Impregnation takes place at a higher
temperature than observers have generally stated, a peculiarity per-
haps arising from the large scale at which the work is earned on. I
may state here, in a general way, that the modified conditions
caused by working the bacteria on a large scale give an oppor-
tunity for variation from laboratory results. A large body of fer-
mentable liquor is less susceptible to foreign spores, more energetic
in its development, and productive of more obvious results than a
solution such as is usually found in the laboratory. Consequently
I feel that the chemist, who is to investigate and utilize, to the
fullest extent, nature's great oxidizing agent, the mycoderma aceti,
and nature's great reducing agent, the bacillus butyrici, must be as
Am. Jour. Pbarni. ) T n/-iir J ^i,V ^^-w
November. IS.7. \ iMCtlC AClct. 60I
familiar with them in a 5,000-gallon vat as in the pure culture state
in a test tube.
In continuous manufacture the ferment solutions are impregnated
from a preceding ferment liquor, in which a lively fermentation is in
progress. Decided advantage is obtained by using a generous
amount of such liquor. Twenty per cent, is none too much. For an
original impregnation, lactic bacteria must be obtained from an
outside source. I prefer to use for that source milk that has been
allowed to stand at a temperature of 45"^ until slightly sour. If the
milk is allowed to sour too long, before using as an impregnating
fluid, a tendency is shown for butyric bacilli to develop. This same
objection is true if rotten cheese is used. Should the saccharine
solution be allowed to ferment spontaneously, everything may hap-
pen or nothing. A good lactic fermentation may develop, a meagre
alcoholic or a meagre viscous, a little butyric, or a little of each, and
very much butj'ric, the last of which is most probable. 1 he best
original impregnation I ever had was obtained in the following
manner : A pure culture of the lactic bacillus was obtained from the
bacteria in a ferment tank and preserved. Previously sterilized
milk was impregnated from this culture, and kept under pure cul-
ture conditions for a day, and then used with noticeable advantage
over the spontaneously soured milk.
The impregnation accomplished in the saccharine solution, which
should be neutral or faintly acid, not alkaline, the main process in
the manufacture of lactic acid is begun. The success or failure in
the manufacture depends wholly in the management of the fermen-
tation. F*or economical production, over 90 per cent, of the glucose
must be converted into lactic acid. Any unconverted glucose works
a double injury, not only being a loss of material, but also making
the resultant lactic acid liable to subsequent decompositions. In our
factory to day we have practically no residue of undecomposed glu-
cose, and the yield of lactic acid is over 98 per cent. As I have
said before, the impregnation takes place at 45^ or above, and from
that point the temperature is allowed to decrease somewhat as the
fermentation solution grows older. If it is desirable, as it usually
is, to have the fermentation proceed briskly, the temperature must
be higher than when, as is occasionally the case, it is desired to
have a slow fermentation. It should be borne in mind, however,
that a lactic fermentation of itself gives out considerable heat — the
more so if quick running.
002 I^ULCCL riLLU. I November, 1897.
As the fermentation progresses, the solution must be neutrahzed
with milk of lime, or chalk in suspension. The limits of acidity in
which lactic bacteria are healthy are rigidly confined between o 02
and 05 of I per cent. Keeping the acidity of the fermentation
between these limits is the main preventive against butyric fer-
mentation, as the regulating of the temperature is the preventive
against alcoholic fermentation. If the fermenting solution is over-
neutralized, the butyric ferment will at once begin to act, and, once
active, is very difficult to control. It is the greatest enemy to the
lactic fermentation, destroying the lactic acid that has been made,
and devouring new quantities as fast as they can be produced. In
twenty-four hours one -third of the lactic acid may be destroyed by
the butyric bacillus. Anti-ferments cannot be used with much
safety in lactic fermentation. The lactic bacillus is more susceptible
than other ferments, and is killed while others are only stagnated.
Mustard-seed oil is about the only exception that I know. This
has apparently a deadening effect on butyric fermentation, with no
serious effect on the lactic fermentation. The lactic fermentation is
best completed in from three to six days, although its life may be
prolonged up to a fortnight. Any prolongation of life is attended
with danger of butyric invasion. When the fermentation is ended,
the liquor must be heated sharply to kill all bacteria and spores
and prevent subsequent fermentation.
The fermented liquor, which is now a solution of calcium lactate,
with a multitude of dead lactic bacteria floating in it, is filtered and
evaporated. If a pure lactic acid is desired, the calcium lactate is
allowed to crystallize and purified by repeated crystallization. For
a commercial lactic acid, decomposition by sulphuric acid of the
dense uncrystallized solution of calcium lactate gives an acid of
sufficient purity. The free acid obtained from this decomposition is
further concentrated to such strength as the market demands. In
evaporating free lactic acid there is danger of forming lactic anhy-
dride. It is possible to have conditions such that the longer evapo-
ration takes place the less percentage of lactic acid is obtained. In
concentrated solutions very little lactic acid is lost by volatilization.
In dilute solutions much acid may be mechanically carried away with
steam, especially if a blast is used. A 50 per cent, solution is about
as concentrated as it is economical to manufacture. This appears
on the market as a syrupy liquid, with more or less brown color,
Am.Jour. Pharra.l T nrtic Add 60'1
November. 1897. j l^UCllL J-iLJU. UU^
and a specific gravity of r20, and contains about 7 per cent, of
lactic anhydride.
The appHcations of lactic acid to-day, while limited, are increasing.
The majority of all that is produced is used by the woollen dyer as
an assistant in mordanting with bichromate of potassium. For this
purpose I believe it has advantages which the technical world is
beginning to appreciate. Without discussing at length the compara-
tive merits of tartaric, oxalic and lactic acids, I will just mention
the advantages which are claimed for lactic acid, namely, greater
reducing power, greater solubility of itself and its salts, and less
corrosive action. The first claimed advantage, the greater reducing
power of lactic acid toward chromium salts and chromic acid, is
^^enerally admitted in comparison with oxalic acid, and also in the
case of tartaric acid, although the fact that tartaric acid reduces
chromium salts more quickly has led to some discussion. Admitted
that lactic acid has the greater reducing power, the value of this
propeity in the dye-bath is not yet absolute, as with many coloring
matters I do not find that the best results are obtained with the
chromium reduced to its lowest terms. Yet, if lactic acid does the
most economical reducing, it is but a question of correct proportion-
ing of the recipe to obtain the desired shade at the lowest cost.
The second and third advantages — greater solubility and less corro-
sive action — are unquestioned. In corroboration of my estimate of
the value of lactic acid in the woollen industry, the following
statistics of lactic acid are submitted. In 1894 the dye-houses of
the United States and Canada used about 400,000 pounds of lactic
acid, while none was used in England or Europe. In 1895 there
was a domestic consumption of 1,000,000 pounds, and a foreign
consumption of 500,000 pounds; in 1896 the domestic consumption
was 1,200,000 pounds, and the foreign 1,000,000 pounds.
Lactic acid is used to a very limited extent in the calico-printing
industry. Some discharge effects can be obtained advantageously
with it. In most instances, however, the liygroscopic nature of the
acid is injurious in its effect on colors which have to be steamed.
Next to the woollen indu.stry, the most important application for
lactic acid is in the preparation of hides for tanning. The efficiency
of the bian drench for removing the lime from the skm, and making
it porous and in good condition for receiving the tannage, is due to
the lactic acid produced by the fermentation of the bran. A dilute
6o4 A Soluble Compound of Hydrastine. {^^jfj/embe^S'
solution of lactic acid will do this work as well, and is much easier
to control in its action. The slightly higher cost is more than com-
pensated for by the prevention of waste. To the researches of Mr.
Wood and Mr. Andreasch (F. Andreasch, Der Gerber, 21, 506; 22,
513) this application is attributable. In America over 300,000
pounds of lactic acid have been consumed, mainly by a few tanneries,
during the last six months.
In the household lactic acid is used medicinally, and it is a substi-
tute for other acids and fruit juices in makmg acid beverages. The
large possible application of lactic acid for domestic use — the re-
placing of cream of tartar by the acid lactate of calcium — has not
yet been put in practical operation.
With regard to the analysis of lactic acid, I feel I can add little
to what Allen has collected in the latest volume of his Organic
Analysis (A. H. Allen, Commercial Organic Analysis, Vol. Ill, Part
III, 411, et seq). On account of the solubility of all its salts, the
direct determination of lactic acid is a long and delicate process.
Generally the indirect method — determining total acidity and per-
centage of foreign acids — gives more expeditious results. There is
not much sophistication of lactic acid. Sometimes acetic and mine-
ral acids are found in it, and now and then samples of so-called
lactic acid containing no lactic acid at all. Usually, however, com-
mercial lactic acid is pure, except from products incident to manu-
facture and not deleterious in effect. The strength varies from 20
to 50 per cent., according to the price and for what purpose the acid
is intended to be used.
OM A SOLUBLE COMPOUND OF HYDRASTINE WITH
MONOCALCIUM PHOSPHATE.^
By T. H. Norton and H. B. Newman.
The following experiments were made in connection with an
endeavor to enlarge the number of soluble salts of hydrastine,
especial interest attaching to the combination of the alkaloid with a
mineral salt of recognized value in medicine.
"^ Journal of the American Chemical Society, October, 1897.
^x^imberit^"} ^ Soluble Compound of Hydrastine, 605
As is well known, but few salts of hydrastine are readily soluble
in water. In our work we made use of monocalciuni phosphate,
which was carefully purified by prolon<:^ed washint^ with alcohol.
A saturated solution ol the salt in cold water was prepared by thor-
ough trituration, the phosphate being in excess. On triturating this
saturated solution with a large excess of pure hydrastine, a certain
amount of the latter would enter into solution, time, as was eventu-
ally found, being an important factor. In order to ascertain the
nature of the product obtained, the filtered solution was evaporated
either by heat or spontaneously, or in a vacuum. In no case was it
possible to detect any trace of crystallization. The solution invari-
ably became syrupy, and finally left an amorphous residue quite
similar to rosin in its appearance. This residue was soluble in
about 10 parts of cold water. A small amount of boiling water
would change it into a syrup. Both boiling and cold alcohol dis-
solved it easily and in about the same proportions. The melting
point was I26°-I28°. Although there was no criterion of the pur.
ity of the substance, it was submitted to analysis. No success fol-
lowed an attempt to determine the amount of hydrastine present by
the use of potassium permanganate, as no definite end reaction could
be obtained. Resort was then had to incineration, care being taken
to avoid unnecessarily high temperatures in the use of platinum
dishes for the purpose. The substance dried /;/ vacuo was heated
to 105°. The very divergent results obtained showed that there
was no fixed percentage of water held by the compound after desic-
cation ;';/ vacuo. The product of incineration was white, vitreous
calcium metaphosphate.-
It was in all cases calculated to monocalcium orthophosphate, and
the difference was assumed to be hydrastine. Analytical results
soon showed that prolonged trituration was necessary to increase
the amount of the alkaloid taken into combination by the phosphate.
From 2^ to ^ gramme was used in each analysis of the substance
dried at 105°. The following analytical data were obtained:
Monocalcium
Time of rhosphate. Hydrnstinc.
No. Trituration. Percent. I'er ccnt
1 10 minutes \\'^ 55\y
2 15 " 3'>*33 61 67
3 5 " 5570 4430
* Birnbaum : Jsb. d. Ch^m., 187 1, 281.
6o6 A Soluble Compound of Hydrastine. {Vo/emberi™'
Monocalcium
Time of Phosphate. Hydrastine.
No. Trituration. Per cent. Per cent.
4 5 minutes 5773 42*27
5 Sohours^ 29 00 71*00
6 80 " 28*03 71*97
7 40 " 31*00 69*00
8 50 " . . . . r 30*43 69*67
9 50 " . , 28-10 71*90
10 6 weeks 28*95 7i"05
^ In experiments 5 to 10 the alkaloid and the solution were placed in a corked bottle, and this
was introduced into a box provided with paddles and suspended on an axis, which was kept
in constant agitation beneath a water tap.
In order to appreciate these figures, let us note the theoretical
percentages of the simpler possible combinations of monocalcium
phosphate and hydrastine.
A. 2Ca(H,PO,)2 . C21H21NO6.
Ca(H2P04)2 = 54*10 per cent.
C21H21NO6 = 45*90 per cent.
B. Ca(H2PO,)2 . C2,H2,NOe.
Ca(H2P04)2 = 37*9 per cent.
C2iH2iNOg = 62*1 per cent.
C. 2Ca(H2PO,)2 . 3Q1H21NO6.
Ca(H2P04)2 — 289 per cent.
C2iH2iN06 = 71*1 per cent.
It will be seen at once that the apparent limit of the amount of
hydrastine which can enter into combination with the phosphate,
as shown by analyses 5 to 10, is practically identical with the percent-
age of the alkaloid present in the hypothetical salt C, where two
molecules of monocalcium phosphate are in combination with three
molecules of the alkaloid. In the picrate of hydrastine, one of the
few crystalline derivatives, we encounter a combination of equal
molecules [C6H2(N02)30H . C21H21NO6]; the amorphous sulphate
and chloride (C21H21NO6 . H2SO4) correspond, however, to the for-
mula B. While the formula C is unsupported by analogy and the
aid of crystallization is lacking, the analytical data point strongly
towards this as the correct expression for the product obtained by
the method described.
^xiNimberM^*} Recent Literature Relating to Pharmacy. 607
RECENT LITERATURE RELATING TO PHARMACY.
THE PREPARATION OF HIGHLY PHOSPHORESCENT STRONTIUM SULPHIDE.
According to J. R. Mourelo {Compt. Rend., 124, 1024), the most
satisfactory phosphorescent strontium sulphide is prepared as follows:
An intimate mixture of 285 grammes commercial strontium car-
bonate, 62 grammes flowers of sulphur, 4 grammes crystallized
sodium carbonate, 25 grammes sodium chloride and 0-4 gramme
bismuth subnitrate is placed in a crucible, covered with a layer of
coarsely powdered starch, then submitted for five hours to a bright
red heat and allowed to cool very slowly during ten or twelve hours.
A white, friable mass is thus obtained, which develops a fine
greenish-blue phosphorescence when exposed for about one second
to daylight, and so intense as to be plainly visible in a shaded situa-
tion. The mixture becomes inert when powdered, but may usually
be restored by re-ignition with starch.
PARAFORMIC ALDEHYDE AS AN ANTISEPTIC.
Dr. B. H. Paul and A. J. Cownely (Pliannaccutical Journal^ Au-
gust 7, 1897), have conceived the idea that paraformaldehyde,
which is a solid substance, volatilizable at about 100°, might be
used as a more compact antiseptic than formaldehyde, since, by
boiling with water, the para modification is converted into form-
aldehyde.
Since the latter in 40 per cent, solution is the only form that is
possible commercially, there would be a considerable saving in
transportation, both in volume and by using the para modification.
For comparative experiments the authors boiled the solid modi-
fication with water in the proportion of four to ten, connecting the
flask to an inverted condenser. The conversion was effected in
about two hours, as was also the case when the operation was con-
ducted in a sealed tube. In both cases clear solutions were obtained
with only traces of acidity. The products were assayed by the
ammonium hydrate method and found satisfactory. The conclu-
sions are that it is readily possible to convert the insoluble para-
formaldehyde into its soluble modification, formaldehyde, and that it
would seem to be more advantageous to produce paraformaldehyde
than formaldehyde for commercial use, as the former is more readily
manipulated and is easily rendered soluble to a suitable dcj^rec of
6oS Rcctnt Literature Relating to Pharmacy, {X'/embeMtsT"
strength for antiseptic purposes when required. Indeed, where an
antiseptic powder is required there is no reason why paraformalde-
hyde itself should not be of great service.
On exposure to air of an aqueous solution of formic aldehyde
until it dries up, there appears to be formed not the true para com-
pound but a mixture partaking to some extent of the characters of
the substance (CHaO).,, described by Tollens and Mayer as being
formed when formic aldehyde is evaporated over sulphuric acid.
This substance was found to melt at about 131° C, and was more
soluble in water than paraformaldehyde. The polymer produced by
adding sulphuric acid to formic aldehyde had a much higher melt-
ing point, namely, 170° C. The variation of the melting point
from 152° to 172° C, ascribed to paraformaldehyde is no doubt
due to an admixture of these two bodies.
SYNTHESIS OF CANE SUGAR.
L. Marchlewski (Rocznik Akad. Umiej. Krakowskiej., 1896) has
obtained cane sugar by the action of acetochlorhydrose upon the
potassium salt of ^-fructose. The reaction is expressed by the fol-
lowing equation :
CH2.OCOCH3 CO2.OH
(CH.OCOCH3)3 (CH.OH)3 + 4C2H5OH = 4CH3COOC2Hg -f
KCl + Ci2H220n.
CH -f COK
/ /
o o
\CH — CI \
Pure acetochlorhydrose is dissolved in alcohol, and to the solution
freshly prepared potassium levulosate is added. The mixture is left
to stand for about seven days at ordinary temperature ; to complete
the reaction it is heated for half an hour on a water bath; next, the
potassium chloride formed is filtered off, the filtrate evaporated at
80° C, and the residue dissolved in boiling water. The solution
obtained is next treated with a solution of calcium hydrate, and the
gradually formed precipitate filtered off, stirred in some water, and
decomposed with CO2. The calcium carbonate is filtered off, and
the filtrate purified by calcium hydrate in a similar manner. Finally,
^^oyimuJX'-^} I^ecent Literature Relating to Pharmacy. 609
the aqueous solution of the sugar isextracted with ether in order to
remove the saccharin, and then evaporated in vacuo. After some
days' standing the cane sugar formed, crystallizmgin the well-known
forms. All the reactions and physical properties agree with those
of natural cane sugar. — Jour. Soc. CJieni. /ndustrj', ]u\y 31, 1897.
RARE METALS IN NORTH CAROLINA.
In a recent circular of a North Carolina mining company, the
claim is made that the future supply of some of the rare metals will
come from that State.
Monajjite yic\ds 14 to 17 per cent, of cerium oxide, the metal being
worth $2,880 a pound troy. There are in commerce no less than
twenty-two preparations of cerium, of which the oxalate and nitrate
are the most important medicinally.
Cufnniitc, found in mica deposits, yields 50 per cent, uranium.
The fused metal is worth I3^j cents a grain, or $768 a pound.
Lit/iro/>/i i/ite a.nd amblygonite contain from 9 to 10 per cent, lithium
oxide. The demand for this metal has largely increased of late
years, owing to the large consumption of lithia tablets.
SURGICAL ANTISEPTICS AND DRESSINGS.
Antiseptic Crayons. — L. Adrian {^Nouveaiix Renudes, 13, 483) has
proposed a number of formulas for surgical antiseptics. The fal-
lowing is a typical formula for an antiseptic cra}'on :
Corrosive sublimate o'5oo graniiiie
Powdered talc 25CXX) "
Gum tragacanth 1.500
Distilled water ... 1--
^, . ) [la q. s.
Glycerm i *
For 10 crayons.
In place of the corrosive sublimate a number of medicinal sub-
stances may be used as antiseptics, as boric acid, iodoform, phenol,
salol, iodol, ichthyol, etc. Astringent and antiseptic crayons are
prepared by using tannin, alum, antipyrine, ergotine or ferric chlor-
ide. Resolvent crayons are made with potassium iodide, and seda-
tive crayons with belladonna, morphine, cocaine, etc.
Starch, dextrin or sugar may be employed to replace part of the
tragacanth.
Laminaircs antiseptiques. — The dried pieces of the stems of Lami-
naria digitata are employed in place of sponge tents. The iaminaria
6io Recent Literature Relating to Pharmacy. {^-^owSe^^i^'
are solid, black in color, and the size of a goose-quill, and on coming
in contact with the liquids of the economy, evenly swell to six times
their volume. Before introduction into the cavity the surface is
roughened by a grater or file, and they are then plunged for some
minutes in tepid water. They may be preserved in one of the
foMowing solutions :
a. Corrosive sublimate i part.
Absolute alcohol lOO parts.
b. Corrosive sublimate i part.
Ether loo parts.
c. Iodoform lo parts.
Ether loo parts.
Antiseptic pozvders are made with an inert base, and such sub-
stances as sulphocarbolate of zinc, iodoform, phenol, corrosive sub-
limate, salol, etc.
The following is the formula of the powder of Lucas Champion-
niere.
Grammes.
Iodoform, finely powdered ) _ _
Benzoin " " ^^ 93°
Quinine " " 960
Magnesium carbonate, finely powdered 930
Oil of eucalyptus 120
This powder has a great reputation for indolent ulcers, and par-
ticularly with sores of the sacrum.
Kiimmel has recommended common sand as a basis for antiseptic
powders. White sand is sieved and heated to redness, whereby it
is thoroughly sterilized; it is then incorporated with corrosive subli-
mate, phenol, iodoform, etc., in the proportion of 5 to 10 per cent.
Cloves and Caffeine 171 Frajice. — At the last meeting of the Paris Syndical
Chamber of Chemical Products, M. Adrian mentioned that the excise authori-
ties had given distillers facilities for preparing oil of cloves, which were formerly
not permitted. The cloves are admitted duty free, and, after having been used
for preparing the oil, are burnt in the presence of an excise officer. M. Adrian
thinks the same favor might be accorded to chemists for the preparation of
certain alkaloids, and he especially referred to caffeine as being one of the most
important on account of its increased use. — The Chemist and Druggist, October
9- 1897.
^^ivtrber'".:;?;- } EdUonaL e 1 1
EDITORIAL.
The following circular letter has been received from the Department of Agri-
culture :
United States Department of Agriculture,
Division of Chemistry.
Washington, D. C, September 17, 1S97.
Dear Sir: — Under authority of Congress, the Department of Agriculture is
investigating the extent and character of food and drug adulterations, and is
desirous of securing all the information possible on the subject. Having been
appointed special agent to inquire into and report upon this matter, the under-
signed writes to request that you kindly furnish the Department all the
information you have in regard to adulterations, together with any sugges-
tions as to the best remedy for the evil.
( I) Do you know of any new adulterant ? If yes, state what, and how used;
(2) Would a national food and drug law assist in preventing adulteration ?
(3) Would uniform food, drug and pharmaceutical laws tend to promote effi-
ciency and purity ? (4) Please suggest what would best promote the interests
of consumers and legitimate manufacturers and dealers ; (5) What is your
opinion as to the extent of damage done legitimate business by imitation of
brands, packages, etc.? (6) To what extent do sophistication, misbranding and
injurious adulteration exist? (7) Have State laws aided in preventing adul-
teration ? To what extent? (8) Would a national law assist State officials in
properly executing the local laws? (9) Have adulteration, sophistication and
misbranding increased or decreased ? Prompt replies to the above, together
with any other information or suggestions, will be highly appreciated.
Yours respectfully,
A. J. Wedderburn,
Special Agent.
Approved :
James Wilson,
Secretary.
We confess to an inability to answer some of these questions. An affirmative
reply to 2 and 3 and a correct solution of 4 would leave nothing in the way of
worldly success and happiness, but the indifference of Congress and the neglect
of that body to pass the necessary laws. No. 7 we would respectfully refer to
the people of the State of Ohio.
We predict that answers to all the queries in the letter will come in slowly*
but it is possil)le that they may lead to the compilation of a new set of questions
not quite so comprehensive. Certainly the Department of Agriculture can do
no l>etter work than collect information on the extent and character of food
and drug adulteration, and individuals may feel that they are doing a public
service in writing to the special agent, answering the (|ueslions, as far as possi-
ble, and in making suggestions as he re([uests.
6 1 2 Reviews, { VovSlLei?'^'
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
Missouri Botanical Garden. Eighth Annual Report. William
Trelease, Director. St. Louis, Mo. 1897. Pp. 236,
The Report for the 3'ear 1896 contains : Report of the Officers of the Board ;
Eighth Annual Report of the Director ; Scientific Papers ; Library Contri-
butions. The report of the Director is always interesting, but this year it is
made additionally so by short accounts of the disastrous storms which visited
the Gardens on May 21st and 27th ; the former being especially destructive on
account of the accompanying hail, and the latter being cyclonic in character.
" While the grounds were not traversed by the cyclonic funnel, but were
exposed only to the strong northwest gale which accompanied it, the violence
of the wind was such that a number of the structures on the grounds were
either unroofed or totally wrecked, while some 450 trees, many of them of
large size, were wholly or practically destroyed, and a large percentage of those
left standing were seriously broken. A more graphic view of the destruction of
the trees may be obtained from the statement that 186 cords of firewood have
been prepared from the more workable trunks and larger branches of the trees
removed." It was found necessary to expend over $4,000 in such storm repairs
as could be made, and the loss in specimen plants cannot be expressed in
money.
The herbarium, during the period of time covered by this report, has
increased from 159,046 unmounted specimens to 258,629 mounted specimens,
protected by impregnation with corrosive sublimate.
The scientific papers, which occupy the bulk of the volume are: "The
Mosses of the Azores," by J. Cordot ; " On Some Mosses Collected in Madeira,"
by William Trelease; "Botanical Observations on the Azores," by William
Trelease. The last is very interesting, includes a catalogue of the plants
occurring in the Azores, and is illustrated by fifty-five full-page plates. The
other portions of the book are beautifully illustrated.
Proceedings of the Nineteenth Annual Meeting of the Missouri
Pharmaceutical Association, June 8-12, 1897.
This is one of the first reports of this year's State meetings to reach us. It
contains a number of good original papers, among them one by G.H. Charles
Klie, on "A So-called Tasteless Quinine." He has done considerable work in
exposing the fraud of the substitution of calcium sulphate for quinine sulphate,
under the name of "Flora-China." This substance was first shown at the
Montreal meeting of the American Pharmaceutical Association in 1896 ; but
notwithstanding the publicity given to it there, it has continued to flourish in
the Southern States. Mr. Klie traced its origin to Hankins Mook Company,
Live Oak, Fla.
Annual Report of the Clerk of Forestry for the Province of
Ontario, 1897. Thomas South worth, Clerk.
The following are the chief subjects discussed in this interesting volume :
" The Crown Lands Forestry Problem ; " " Forestry on the Farm ; " " Nature
Study in the School ; " " Entomology ; " " The Manufacture of Wood Char-
coal."
Am. Jour. Pharm.) Mi^n/tfi^ (\\ 1
November, 1897. / lYllHllieS. OI3
Report of thk Board of Managers of the Pennsylvania Hospital
TO THE Contributors. Philadelphia, 1S97.
The report of a charity which has existed and flourished for a century and a
half is a matter that should attract attention, and a careful perusal of it will
convince one that this time-honored institution is one to be proud of. The
volume is elaborately illustrated with interior and exterior views of the
buildings.
Early American Chemical Societies. By H. Carrington Bolton, Ph.D.
Reprint from \y\^ Journal of the American Chemical Society, August, 1897.
The author makes out a very interesting historical account of the early efforts
of chemists to associate for mutual benefit. The Chemical Society of London,
the oldest in Europe, was founded in 1S41, forty -nine years after the first Amer-
ican society. The early American societies are summarized as follows :
I. The Chemical Society of Philadelphia, founded in 1792.
II. The Columbian Chemical Society of Philadelphia, founded in 1811,
III. The Delaware Chemical and Geological Society, founded in 1S21.
The account of the active workers in these societies constitutes the main
body of the paper.
Uhber FlechtENSTOFFE, von O. Hesse. Reprint from Berichte der
Deutschen Chcmischcn Gesellscha/t, 30, 1S93.
MINUTES OF THE PHARMACEUTICAL MEETING.
Philadelphia, October 19, 1S97.
The first of the series of pharmaceutical meetings for 1897-98 was held in the
College Museum, with J. W. England in the chair. The reading of the minutes
of the last regular meeting was omitted and they were allowed to stand as
published.
The chairman then called for the presentation of specimens. Dr. C. B. Lowe
showed some extraordinarily fine samples of asafetida which he had procured
from the Smith. Kline & French Company, of this city, they having received it
in original packages from Bombay, through London. He also showed some
samples of Japanese f)ersimmons from Florida, where they are grown to a con-
si<lerable extent by grafting the wild variety. Prof. Trimble presented, on
behalf of Mr. Charles Bullock, quite a collection of minerals and ores for the
cabinet of the College. The chairman showed a colchicum plant which had
been place<l in alcohol while in bloom and which also was intcnde<i for the
cabinet. Prof. Triml;le move<i that a vote of thanks be extended Mr. Bullock
for his valuable donation, and it was so ordered.
The reading and discussion of papers next occupietl the attention of the
meeting, and the first one presented was on " An Examination of Some Ofilicial
Lead Preparations," by F. W. Haussmnnn.
This paper gave evidence of much careful and thoughtful work on the part of
the author, and the criticisms and suggestions contained therein were of an
5 14 Minutes. {%
Am. Joiir. Pharm.
ovember, 1897.
eminently practical and useful kind. The chairman spoke in complimentary
terms of the paper, and said that suggestions whereby rapid methods could be
adopted were of great value to the pharmacist.
Prof Remington said that detailed methods, such as Mr. Haussmann described,
were very valuable to the Committee on Revision of the Pharmacopoeia, and
that he had done pharmacy a distmct service by this work.
"International Congresses" was the subject of a paper by Prof. J. P. Reming-
ton. The author took a comprehensive view of the question of international
gatherings, and while he portrayed the ideal congress, he did not lose sight of
the real difficulties which attend all such undertakings. He believed in con-
sidering conditions as they actually exist, and that by so doing, many of the
hindrances which retard the successful issue of international scientific gather-
ings could be eliminated.
A paper entitled " Balsam Copaiba, Oil of Copaiba, Mass Copaiba, Resin
Copaiba and Gurjun Balsam " was presented by Lyman F. Kebler.
This paper embodied the results of an examination of a number of samples
of the above substances. The author said that on account of the number of
varieties of copaiba and the unknown composition of them, their qualitative
analysis was attended with difficulty. The data presented by him was there-
fore intended to supply this deficiency.
In discussing the active constituents of copaiba, Dr. Lowe said that there
seemel to be some misapprehension among physicians as to the particular
effect of each of these. He said that the volatile oil has a stimulating action,
while the acid resin is a diuretic.
The last paper on the programme was presented by the chairman, J. W.
England, and was on the question, " Shall Distilled and Fermented Liquors be
Dismissed from the U. S. Pharmacopoeia?"
Notwithstanding the interpretation placed by many upon the attitude of the
Government on the subject of alcoholic liquids, the author believed that the
above question had no bearing upon the saloon question. He looked upon
these liquids as drugs, and urged retaining them in the Pharmacopoeia and
demanding them of a certain quality.
His remarks occasioned considerable applause, and the subject was freely
discussed by the members present.
Wm. B. Thompson was in favor of dismissing whiskey from the Pharmaco-
pfjeia since it entered into no official preparation. He furthermore believed
that the official wines would serve their purpose as well if made with alcohol
of the required strength.
Dr. Lowe was of the opinion that alcohol was the only therapeutic constitu-
ent of these liquids, but that the bouquet made them more palatable, which was
an argument for retaining them.
C. Carroll Meyer, referring to the sale of liquor in stores, believed that drug-
gists were honorable in this respect, and that very few of them sold it, except
in Prohibition States, without the physician's order.
Mr. Kebler took the negative side of this question, and said that he had
examined samples of wine and found many which were adulterated and others
which were artificial products colored with aniline dyes. He believed that
many victims of the alcohol habit were attracted by the so-called bouquet who
might not otherwise have persisted in the habit.
.^NovembeMX} Notcs and Nezvs. 615
MINUTES OF MEETING OF MEMBERS OF THE
COLLEGE.
The stated quarterly meeting of the members of the College was held Septem-
ber 27th, at 4 o'clock P.M., Vice-president Jenks presiding. Minute of previous
stated meeting read and adopted. Minutes of meetings of the Board of Trustees
for Jul}' and September presented and approved. The secretary referred to the
subject of a proposed uniform pharmacy law for the States, concerning which
this College was requested to send a form or draft to the Chairman of the Sec-
tion on Education and Legislation of the American Pharmaceutical Association.
The consideration of the subject having been postponed for the want of suffi-
cient time, it was again resolved to defer action until some more definite pro-
gress or report should be made by the Committee of the Association. In
obedience to the direction given the secretary, there was presented and read
the opinion of the legal counsellors of the College, upon the purpose contained
in the interrogatories submitted by Mr. Boring at the June meeting. These
questions involved the constitutionality of certain proposed by-laws which were
contemplated as an amendment to the existing code. On motion, it was
resolved to receive and file this report. Mr, Boring objected to this method of
disposing of the subject of this report, and desired that the matter should be
discussed at the present meeting. Whereupon Mr. Beringer moved, and the
motion was carried, that the chairman should appoint a committee of five inem-
l>ers who should consider the propositions, and report upon the same at the
next stated meeting. The chairman named Messrs. Beringer, Boring, Stedem,
Weidemann and Cliffe as members of this committee. Prof. vSadtler reported,
verbally, at length, on behalf of the delegates of the college to the sessions of
the American Pharmaceutical Association upon the proceedings of that bo<ly at
the recent meeting in August. The terms of Messrs. Krewson, Weidemann
and Kline, as trustees, expiring with this date, and these gentlemen being
re-nominated without opposition, the secretary was instructed to cast an affirma-
tive ballot, which, being done, all were declared to be elected. The decease of
Prof. Bastin creating a vacancy in the Board of Trustees, nominations for this
position were called for. Upon the nominations being made, and the votes of
candidates recorded, the tellers announced that Mr. C. Carroll Meyer had
received the highest number and was therefore duly elected.
The meeting, on motion, adjourned.
Wii.Li.\M B. Thompson, Secretary.
NOTES AND NEWS.
Tribuna Farmaclutica is the name of a new pharmaceutical journal in
Buenos Ayres. It is the organ of the Circulo Farmaceutico Argeutino. The
publishing co:nmittee consists of Jos^' Bonauni, Dr. Estanislao Zubieta, Victor
B. Molina, Bernardo Nespral and Lino Vifias Loureiro.
The first two numbers of eight pages each are made up partly of matters
relating to members and of professional interest, and contain original articles
on the estimation of tannin, on some incompatibilities and on the rapid and
economic preparation of hydrogen peroxide.
This new journal bids fair to publish considerable original matter.
6i6
Obituary
f Am. Jour. Pharin.
I November, 1897.
The Cinnamomums of Neiu South Wales. — A paper was read at the July
meeting of the Linnean Society by R. T. Baker, assistant curator Technical
Museum, on the Cinnamomums of New South Wales, with a special research
on the oil of C. Qliveri, Bailey.
The genus Cinnamomum, hitherto unrecorded for New South Wales, is now
showni to occur over a large area of the coastal district, being represented by
two species, C. Oliveri, Bailey, C. virens, sp. nov The former species has in
the past been mistaken in the northern colony for Beilshmiedia obtusifolia, and
has only recently been identified as a Cinnamomum ; very probably the same
confusion of species has occurred in this colony. C. virens appears to stand
somewhat alone, its affinities with known species not being very marked.
Descriptions of the timber, gall-fungus, bark and oil are given. The oil
obtained from C. Oliveri is highly aromatic, and is found to contain cinnamic
aldehyde, eugenol, together with other constituents. The bark gave nearly
one per cent of oil. It is hoped that a new commercial product may result from
these investigations. — The Pharmaceutical Jour7ial of Australasia, August
28, 1897.
OBITUARY.
Athafiase Roidot, who for forty-nine years conducted a drug store in the
vicinity of Eighth and Vine Streets, this city, died on October 9th, at his resi-
dence, 905 Buttonwood Street. He was born nearly
eighty years ago, in France, and came to this country
H^^K 'mimlmam ^^ ^^ early age.
^^^VIj^^V^^BH He learned the drug business in his native country,
I^^^^B - **^^^^ and when he came to this city he entered the employ
of Blias Durand, who at that time had a store at the
northwest corner of Sixth and Chestnut Streets. Mr.
Roidot was elected a member of the Philadelphia Col-
lege of Pharmacy in 1852.
Peter Lund Sifnjuonds, whose portrait we present
with this sketch, died in the Charterhouse, London,
October 3d, in the eightj'-third year of his age.
The deceased was formerly well known as a writer
on applied science and as having taken an active part
in the management of several of the large international
exhibitions. He was born at Aarhuus, Denmark, in
1814, but spent most of his life in England. He was an extensive writer on
agricultural and food topics and commercial matters in general, including the
subject of drugs, and was not an infrequent contributor to this Journal. He
was proprietor and editor of the Technologist, 1862-66, dM^\.\i^fournal of Applied
Science, 1870-81 . Of his other published works the following may be mentioned :
"The Commercial Products of the Vegetable Kingdom," "Waste Products and
Undeveloped Substances," "Waste Products, A New and Enlarged Edition,"
"Tropical Agriculture, New and Enlarged Edition," and "A Hand-book of
British Commerce."
Mr. Simmonds had, at different times during his life, been elected to mem-
bership in various literary and technical societies, including several representa-
tive agricultural societies and the Society of Arts, London, and in 1896 was
elected an honorary member of the Philadelphia College of Pharmacy.
QUERCUS PHELLOS, L.— WILLOW OAK.
THE AMERICAN
JOURNAL OF PHARMACY.
DECEMBER, iSgy.
THE WILLOW OAK.
By Henry Trimble.
One of the most interesting of the oaks in this vicinity is the
Quercus Phellos, L., or willow oak. While it is not of great value
from an economic standpoint, it nevertheless affords the means of
profitable study by the botanist. The casual observer, if he did not
notice the tiny acorns, would pronounce it a willow tree, and its
resemblance to the latter, especially in the matter of fohage, is very
striking. It has, therefore, always been regarded with curiosity, and
judging from the correspondence of Peter Collinson and John Bar-
tram, it is evident, from the appeals o\ the former for specimens,
that it was especially a botanical curiosity in London over a century
ago.
About thirty-five years ago the late Professor Procter visited,
with S. H. Buckley, a grove of willow oaks near Mount Holly, N. J.,
for the purpose of identifying one among them which showed some
variations in foliage. Mr. Buckley contributed a paper on this oak
to the Academy of Natural Sciences and published it with additions
in the American Journ.\l of Pharmacy, for March, 1862. Evidently
these two men decided that the peculiar member o( the group was
Bartram's oak, Quercus heterophylla, Michx.and that it was merely
a variety of the willow oak and not a hybrid. It may be said that
this opinion is held by many at the present day, although, according
to Sargent, it is a hybrid of the willow oak with Quercus vclutina,
and Britton and Brown state that it is probably a hybrid of the
(617)
5i8 Willow Oak. {
Am. Jour. Pbara
December. 1807.
willow oak with Q. rubra. Gray gives the combination as Q.
Phellos with Q. rubra or coccinea.
Some pertinent remarks on " Hybrids in Nature," by Thomas
Meehan, have recently appeared in the Proceedings of the Academy
of Natural Sciences of Philadelphia (1897, p. 194), in which, using
the oaks as an illustration, he shows that hybridization will not
account for the variations in this genus.
The willow oak is found along the coast of the Eastern United States,
from Long Island, New York, southward to Florida, and thence
westward to Missouri and Texas. It prefers low, moist ground, and
is quite common in the lowlands on both sides of the Delaware
River, south of Philadelphia. It has also become more common of
late years by cultivation as an ornamental tree.
In this latitude it is a rather small tree, rarely exceeding a height
of 40 to 50 feet, but further south it attains a maximum of 80 feet,
and a diameter of 3 feet.
The accompanying illustration shows the peculiar character of the
foliage, which is rather densely crowded at the ends of the branches.
Nearly all the illustrations of the acorns which are figured in books
on the subject are far from being true representations. Sargent's
" North American Silva " is, however, a notable exception in this
respect. In the present instance the illustration, being a photo-
graphic reproduction, differs from the natural object only by a slight
reduction in size.
As stated at the beginning of this paper, the willow oak has not
attained any great economic value, and most writers give it a poor
name. No less an authority, however, than Dr. Charles Mohr, of
Mobile, Ala., says the wood is hard, very elastic, compact, and suit-
able for railway carriages and many other purposes.
It is hoped that, ere long, something will be forthcoming from the
Chemical Laboratory of the College, on the composition of the
bark, which has been under investigation for some time. So far as
the tannin is concerned, the bark does not appear to be sufficiently
rich to warrant its use in the manufacture of leather.
For the photograph from which the illustration was made I am
indebted to my friend. Dr. Charles Schaffer.
''S^"m^r?i8^"} Laboratory Notes, 619
LABORATORY NOTES.
By Charles H. LaWall.
The question of stability in pharmaceutical preparations is one
which has received comparatively little consideration. A process
for making a tincture or a fluid extract is considered satisfactory
when little or no precipitation takes place after standing for some
time.
The methods for alkaloidal assaying, which are in use at the
present time, are of such recent origin that very few data have been
recorded as to the stability of such preparations as may be assayed.
In a few years such facts as these will have been published and a
better knowledge will have been obtained regarding the character
of the precipitate which forms in many fluid extracts and tinctures.
In the case of fluid extract of ipecac, the author has an op-
portunity of recording the alkaloidal assay of a sample which was
made by the late Prof. John M. Maisch while he was in charge
of the Government hospital laboratories during the Rebellion.
No knowledge can be obtained as to the alkaloidal strength of
the preparation as originally made, or the quality of the drug which
was used in manufacturing it; but, in view of the fact that it assays
considerably above the standard after a lapse of more than thirty
years, it is safe to conclude that fluid extract of ipecac, as made by
the process in use at that time, is a stable preparation.
The process described in the i860 Pharmacopoeia, by which this
preparation was no doubt made, is essentially as follows :
Si.xtecn troy ounces of powdered ipecac are exhausted by percola-
tion with alcohol, and the alcohol is distilled off" until a syrupy liquid
remains ; this is mixed with i fluid ounce of acetic acid and 10
fluid ounces of water, and boiled gently until it is reduced to 8 fluid
ounces (this separates resinous matter) ; the liquid is then filtered
and made up to 8 fluid ounces in volume by the addition of water,
after which it is mixed with 8 fluid ounces of alcohol.
In the 1890 Pharmacopoeia the process is very different
1,000 grammes of powdered ipecac are percolated with a men-
struum consisting of 3 parts of alcohol to I part of water; i,ooo
c.c. of fluid extract are made. This is a different drug strcngtli in
the finished preparation. The i860 preparation has about 1,055
grammes of drug to each i ,000 cc, the alcoholic strengths of the
menstrua differ, and the present official process dispenses with the
620 Laboratory Notes. { ^SlcimbenS"-
acetic acid, as formerly used. These differences indicate that it
would not be wise to conclude that a preparation made by the
present officinal process would keep as well as the one recorded
here.
The preparation is of undoubted authenticity, and was obtained
throug[hthe kindness of Mr. Frederick Sher, of the Smith, KHne &
French Company, in whose possession it has been for many years.
It bears a label stating that it was "prepared at the U. S. A. Labor-
atory, Philadelphia, Pa., 1864." The bottle has the words : " U. S. A.
Hos[). Dept.," blown in the glass, which is of a very deep blue
color. The bottle had been so carefully sealed that no apparent
evaporation of the liquid had taken place when it was received by
the author. It has a pleasant acetic odor and strong characteristic
taste, and the sides of the bottle are covered with a resinous de-
posit, the quantity of which could not be determined.
For the assay, a sample was carefully decanted so as to avoid
transferring any precipitate which might contain the alkaloids. The
process of Keller was followed, titrating the varnish-like residue by
means of decinormal sulphuric acid and centinormal potassium hy-
drate, using haematoxylin as indicator. The alkaloidal strength
was 2 76 per cent., calculated as emetine. As 2 00 per cent, is the
present standard adopted by manufacturers who assay this prepara-
tion, it has lost little or no alkaloid after a period of thirty-three
years. It speaks well for the quality of the drug, and the thor-
oughness of the manipulation used, and would compare favorably
with our present day products, made by so-called improved appara-
tus and perfected methods.
Japan Wax. — In the American Journal of Pharmacy for Janu-
ary, 1897, the author published an article on the extensive adultera-
tion of Japan wax with starch. Since that time more than 300
cases of Japan wax (aggregating 60.000 pounds) have been exam-
ined, all of which complied with the requirements of a normal pro-
duct. The melting point ranged from 50° to 54° C; the specific
gravity Irom 0965 to 0984; the acid number from 1798 to 2045,
and the saponification value from 21793 to 224-86.
In physical characters there was a slight variation; some of the
samples seemed to be more greasy than others, this being notice-
able either by pressing the wax between the fingers or by masticat-
ing a small portion. Such a slight difference, however, might be
^^emberX"} Laboratory Notes, 621
due to variations in the ap^e of the product or in the methods of
preparinfT^ it for the market
Mercurial Ointment — A nu Tiber of samples of mercurial oint-
ment, made by reputable manufacturers, were examined. The per-
centage of metallic mercury was found, in every case, to approxi-
mately a^^ree with the amount claimed upon the label.
Calcium Phosphate Precipitated — Several large consignments of
this substance were found to contain a great quantity of carbonates.
In one case the amount of calcium carbonate present reached 40 per
cent.
The use of such a product in the manufacture of tincture of opium
by the formula in the 1890 Pharmacopoeia would result in the reten-
tion of tlie morphine and the consequent worthlessness of the prep-
aration. An unsuspecting druggist, using it in this manner, might
render himself liable to prosecution for dispensing tincture of opium
below the legal standard, or the dispensing of such an inert prep-
aration upon a prescription might contribute to the death of a
patient.
The occurrence of such products, which eventually find their way
into the market, emphasizes the necessity for that personal exam-
ination of goods which it is the duty of each druggist to make.
Honest manufacturers have nothing to fear from this, while those
who are in the habit of furnishing inferior goods would either be
compelled to raise their standard or go out of business.
Beeswax. — The record of the samples of beeswax examined dur-
ing the present year was very unfavorable, notwithstanding the
number of reputable dealers who are interested in the ])urification
and sale of this product.
Sixteen (16) samples were examined. Of these but seven (7)
answered all of the requirements of a pure wax; five (5) contained
small quantities of stearic acid, indicated by an acid number of
about 2500 and verified by Fehling's test; one (i) contained a
larger amount of stearic acid (acid number, 4692), and three (3)
contained paraffin in varying quantities, the acid numbers ranging
from 453 to 1255.
Those samples which contained paraffin were of a suspicious
appearance and feel, but the presence of such small quantities of
stearic acid as indicated by an acid number of 25, does not materi-
ally alter the appearance of the wax, while it totally unfits it for
622 Coloring of Various Tannin Matters, {^^d^^l-^%^-
some purposes, among which may be mentioned its use in Htho-
graphic work.
Such a shght contamination should be looked upon as accidental,
rather than wilful adulteration, and those who buy the wax from
the producer should carefully examine it before refining, as it is pos-
sible for it to have its origin in a manner which is very well known
to those who are acquainted with the details of apiculture, namely,
in the use of artificial comb foundation, which is purchased by
many bee-keepers to save part of the labor of the colony and insure
regularity in the building of the comb.
Contaminations originating in this manner are frequent, and the
blame rests upon the manufacturer of the artificial comb foundation.
305 Cherry Street, Philadelphia.
THE YELLOW COLORING PRINCIPLES OF VARIOUS
TANNIN MATTERS.^
By a. G. Perkin,
The author continues his investigation of tanning materials, with
the object of studying the yellow coloring principle which is so
often found associated with the tannin in plants, and also for the
purpose of determining the relationship between the coloring matter
and tannin, by the character of their decomposition products.
Cape sumach, Colpoon compressum, was first examined. The
leaves (which constitute the part utilized), roughly broken, were
extracted in a Soxhlet's apparatus, first with ether to remove wax
and chlorophyll, and then with alcohol, which dissolved both color-
ing matter and tannin. The alcoholic extract, after being evaporated
to a small bulk, was poured into water, and the mixture extracted
with ether. The aqueous liquid was freed from the small amount
of alcohol remaining by distillation, and on cooling became semi-
solid, owing to the production of crystals. These were collected and
washed with ether, chloroform, and dilute alcohol until the washings
were colorless. The yellow product obtained was further purified
by crystallizations from dilute alcohol and a final crystallization
from boiling water.
Experiments showed this substance to be a glucoside, which, on
decomposition with dilute sulphuric acid, yielded a yellow coloring
^Ahsit^ci^d.iTom\h^ Journal 0/ the Chemical Society, London, October, 1897.
^Dl^eSr?^'" } Coloring of Various Tannin Matters. 623
principle as one of the products. The acetyl derivative of this
crystallized from alcohol in colorless needles melting at 189° to
191°. By fusion with alkali two crystalline decomposition products,
namely, phloroglucinol and protocatechuic acid, vere obtained. These
properties, together with an examination of its dyeing and other
properties, clearly showed the coloring principle resulting from the
decomposition of the foregoing glucoside to be quercetin.
To ascertain the nature of the sugar liberated in the above action,
the osazone derivative was prepared. This consisted of glistening
yellow needles melting at 205°, and was apparently dextrosazone.
Of the three distinct glucosides of quercetin which have been
described, the one under consideration was found to resemble
viola-quercitrin, in that it yielded quercetin and glucose on decompo-
sition. The author proved, however, that they were not identical,
and proposed to name the substance obtained by him Osyriiin from
Osyris compressa, another name for Cape sumach.
The tannin obtained from the filtrate, from which the osyritin had
been separated, was examined to determine its general characters.
It was found to be a tannin glucoside, and to closely resemble quino-
tannic acid and quinovatannic acid, which are decomposed by acid
into a sugar and an anhydride, and yield protocatechuic acid on
fusion with alkali.
A study wasmideof the coloring principles of the two varieties
of commercial catechu, namely, gambier and acacia catechus. The
identity of the coloring principle of the former variety with quercitin,
as reported by Lowe {^Zcit. anal. C/ieni., 1 874, 12, 1 2'/), was confirmed,
and while the properties of the principle from the latter variety in-
dicated that it was also identical, it was not obtained in sufficient
quantity for ultimate analysis, 4CX) grammes of catechu yielding only
005 grammes of coloring matter.
Rhus cotinus, the Venetian variety of sumach, next received at-
tention, and the coloring principle, determined to be myricetin in-
stead of quercetin, as reported by Lowe. It yielded, with dilute
alkalies, a deep green solution, and its acetyl derivative crystallized
in colorless needles, melting at 203°-204^. Owing to the excessive
adulteration which is practised with this product, the author does
not consider his results in this case as final, but, nevertheless, regards
them as extremely suggestive.
Of other tannin matters, the following fruits and seeds were ex-
624
Coloring of Various Tannin Matters. {
Am. Joor. Pharm.
December, 1897.
amined : " Valonia," the acorn of Quercus aegilops ; *' Dividivi," the
seed pods of Caesalpinia coriaria ; " Myrabolans," the unripe fruit of
Terminalia chebula ; " Algarobilla," the seed pods of Caesalpinia
brevifoha; pomegranate rind, Punica granatum; and gall nuts, Quer-
cus infectoria. An exhaustive investigation of these products by
numerous methods showed that they contained no member of the
quercetin or allied series, but all were found to depend, either directly
or indirectly, upon ellagic acid alone for their dyeing properties.
They are all very similar in this respect. Experiments were made
with woollen cloth mordanted with chromium, aluminum, tin and
iron. For the sake of comparison, some of the results were tabu-
lated, as follows :
Chromium.
Aluminum.
Tin.
Iron.
Ellagic acid . . .
Pale green-olive-
yellow
Pale olive-yellow
Scarcely dyed
Somewhat
olive -gray-black
Valonia nuts . . .
Green -olive-yellow
Faint olive
Scarcely dyed
Weak gray-black
Pomegranate rind
Yellow-olive
Faint olive
Scarcely dyed
Weak bluish-gray-
black
Gall nuts
Green-olive
Faint olive
Scarcely dyed
Purplish-black
The following table was presented to show the intimate connec-
tion between the coloring principles and the tannin matters in the
plants examined, for, on decomposition, the same acid, and, in some
cases, the same phenol was obtained from both :
Quebracho Colo-
rado
Rhus coriaria . .
Rhus cotinus , .
Gambier Catechu '
Acacia Catechu
Acacia catechu . .
Colpoon compres-
sum
Dividivi, etc. . . .
Tannin.
Quebrachotannic
acid
Gallotannic acid
Catechin
Catechin
A catechol tannin
Ellagitanuic acid
Decomposition
Products of
Tannin.
Phloroglucinol
and protocate-
chuic acid
Gallic acid
Phloroglucinol
and protocate-
chuic acid
Protocatechuic
acid
Coloring
Matter.
Fisetin
Myricetin
quercetin
Myricetin
quercetin
Quercetin
Gllag^c acid
Decomposition Pro-
ducts of Coloring
Matter.
Resorcinol and pro-
tocatechuic acid
Phloroglucinol and
gallic acid
Phloroglucinol and
protocatechuic acid
Phloroglucinol and
protocatechuic acid
^li^emlJJ'm?! } Vegetation of Yellowstone Hot Springs. 625
THE VEGETATION OF THE YELLOWSTONE HOT
SPRINGS.
By John W. Harshberger, Ph.D.
The actual discovery of the Yellowstone Wonderland, by which
is meant its full and final disclosure to the world, was the work of
three parties, who visited and explored it in the years 1869, 1870
and 1 87 1. Althouf^h, since the last date, much has been written
concerning the f^eolofj^ical and physiof^raphical features of the park
set aside by Act of Congress in the year 1872, little has been writ-
ten concerning the flora of the region, and what has been published
deals almost entirely with the plants from a systematic standpoint.
Situated in the northwestern corner of Wyoming, in the Rocky
Mountains, at an elevation ranging from 6,000 to 12,000 feet, the
region is one of high and lotty mountains, of deep caiions walled in
by precipitous sides, and of beautiful upland valleys, the natural
haunts of the timid herbivora that seek the mountain meadows for
the tender and nutritious grasses which grow there luxuriantly.
The pasturage in many of the meadows and valleys is excellent,
being formed by the growth of such grasses as alpine timothy,
Flileum alpinum,h\uQ ]o\t\X., Calamagrostis Canadensis, sheep's fescue,
Festuca ovina, Koelena, KceUria cristata. The herbaceous vegetation
is not so striking as in many other regions, but still the distribution
of such species as do occur is interestmg. In the lakes and rivers
we find the aquatic vegetation to consist of Ranunculus aquattlis,
Nupliar advena, Nupliar polycephalum, Utricularia vulgaris, Lcniua
trtsulca, Typha latijolia, Sparganium simplex, etc. Near the head
of Yellowstone Lake is found Subularia aquatica, a plant of quite a
remarkable distribution, found nowhere else in America except in
Maine and New Hampshire. Gentiana detonsa, Spraguea unibellata
are striking plants. The meadows and hillsides are spangled with
bright-colored flowers, among which may be noted the bee larkspur,
Delphinium Mcnzicsii, the columbine, Aquilegia Jlavescens, the hare-
bell, Campanula, ihc aconite, Aconitum Columbianu;n, the lupine, Lu-
pinus, the evening primrose, CEnothcra, the aster, the painted cup, Cas~
tilUia. It is a remarkable fact that scarcely a night passes through-
out the summer without frost, so that the herbaceous plants grow
and bloom under somewhat unusual conditions. The fringed gen-
tian, Gentiana dctonsa, closes its flowers as night approaches, to
open them again in the morning, and many other plants provided
626 Vegetation of Yelloivstone Hot Springs. { ^Dei^imber^^ST""*
with a hairy or woolly covering are thus secure against frost action.
The plants of the Yellowstone region, as far as observed, are well
adapted to their surroundings.
The forests are formed by one tree predominating, Pinus contorta,
var. Murrayana, which grows tall and straight, but never reaches
any considerable girth. Interspersed among the pines we find sev-
eral other arborescent species, namely, Douglass spruce, Pseiidotsuga
DoHglasii, the largest tree in the park; balsam, Abies subalpina, pine,
Pinus Engelmannii, red cedar, Juniperiis Virginiana, poplar, Popu-
lus tremuloides, and willow, Salix, of several species. These forests
are of great importance in conserving the rain which falls. Many
of the most important rivers of the western United States rise in
this region, the Missouri, the Yellowstone, the Wind, the Big Horn,
the Platte, the Green (afterward the Colorado), and the Snake,
which flows through Wyoming, Idaho and Washington, emptying
into the Columbia, and thus reaches the Pacific.
Yellowstone Park, notwithstanding its wild grandeur as a moun-
tain domain, is yet more interesting on account of the geological
wonders which are found within its boundaries, namely the geysers
and hot springs. The geysers are actively throwing up in jets at
periodic intervals, steam and boiling water ; the hot springs are
either quiescent, or are bubbling and boiling without explosive erup-
tion. They are found in four distinct areas in the Park; the geysers
and the hot springs in the Upper, Lower and Norris Geyser Basin,
hot springs only in the Mammoth Hot Spring Region. This divis-
ion also accords with the predominating chemical content of the
waters. In the Upper, Lower and Norris Geyser Basins, we have
springs and geysers which are actively depositing silicious material
(sinter); in the Mammoth Hot Spring Basin, springs which are
forming calcareous deposits, called travertine.
Much inquiry has been instituted concerning the therapeutic value
of the mineral spri ngs of the Park. Many hot spring regions through-
out Europe and America are resorted to by thousands in search of
health. The hot springs of Virginia are visited by hundreds every
year. It is said of the Yellowstone region, that the first explorers
to ascend the Gardiner River, in 1871, found numbers of invalids
encamped on the banks, where the hot waters from Mammoth Hot
Springs enter the stream ; and it is recorded that they were most
emphatic in their favorable impressions in regard to their sanitary
^D^mi!4r 'J^'" ! Vegetation of Yellowstone Hot Springs. 627
effects. No one now goes to the Park on account of its mineral
waters. It would, therefore, be premature to assume that there is
no medicinal virtue in them. Two great drawbacks are to be
encountered, and these alone are sufficient to explain why the Yel-
lowstone will probably never become a resort for invalids. Inacces-
sibility, length and severity of the winters are sufficient obstacles
to the National Park ever becoming such a resort. The open
summer season lasts only about three months.
The hot springs and geysers, on the other hand, are interesting
to the geologist, because of the remarkable phenomena connected
with their origin and activity ; to the botanist they are fascinating,
because of the low forms of vegetal life found existing in them
even at high temperatures.
As before stated, the waters which run from the hot springs and
geysers of the Yellowstone may be comprehended under two heads —
those which deposit silica, as sinter, and those which form calcium
carbonate, as travertine. The last-mentioned substance is only
found in the Mammoth Hot Spring Basin ; the latter makes up the
characteristic formations of the Norris, Lower and Upper Geyser
Basins. The question naturally arises, how are the beautiful terraces
which surround many of the hot spring centres formed ? Are they
not simply built up by the deposition of new material from the over-
flow water, as it evaporates and cools at the surface ? At first sight,
it would seem that the craters and bowls of the geysers and hot
springs were foimed in this way, because we know that boiling
water, under pressure, will dissolve and hold in solution much more
inorganic material than ordinary river or spring water at the normal
temperature, and that in many instances, when the pressure is
relieved and the temperature lowered, the water will precipitate its
mineral contents.
In the case of the richly carbonated waters of the Mammoth Hot
Springs, calcium carbonate is deposited by the relief of pressure, by
the escape of the carbon dioxide and by the evaporation of the
water ; but this physical process is not the sole cause of the varied
and beautiful terraces, which will presently be described. At th<*
Norris Geyser Basin, relief of pressure and cooling will cause a
separation of silica from the hot waters, but the waters of the other
geyser basins contain very much less silica, and, as far as has been
observed by geologists, neither relief of pressure nor cooling will
628 Vegetation of Yellowstone Hot Springs. { ^Declmber?i^"-
produce a separation of the silica. Water collected from the springs
and o^eysers of the Upper and Lower Geyser Basins was perfectly
transparent, and remained clear and without sediment after standing
for several years. Experiments showed that the silica in these
waters remained dissolved, even when the water was cooled down to
the freezing point, and it was only after the crystallization of the
water by freezing that the silica was separated and settled down as
an insoluble flocculent precipitate upon melting the ice.
How, then, are we to account for the production of the exquisite
terraces, mounds, pools and geyser cones? It has been proved, in
addition to the causes operative in the above instance, that the rapid
deposition of the sinter and travertine from both classes of water is
due to the action of vegetation in removing the carbon dioxide from
carbonated waters, thus depositing calcium carbonate, and, in the
case of the silicious waters, depositing by the activity of the proto-
plasm a gelatinous silica, which, upon exposure, finally hardens.
We know, from numerous observations, that plants are active in
rock building and disintegration.
The plants of the Carboniferous Period, by their death and con-
solidation, formed the extensive and useful coal beds. Sphagnum
and mosses compacted yield peat, and, in some cases, soft coal. Sili-
cious diatoms have given rise to extensive diatomaceous earths.
In several of the higher algae, for example, Halimeda opuntice, the
carbonate of lime deposited by the plant forms a sieve-like cover
about the tips of the algal filaments, and, in Acetabulariay it occurs
as a tube about the stalk of the plant. In the charge the lime is
separated and deposited in the cells and cell walls of the back alone,
while in the Corallines it is found only within the cells. Nor is our
knowledge of the activity of protoplasm in the deposit of mineral
substance solely confined to plants. We know that many animals
secrete silex and carbonate of lime, foraminifera, coral polyps and
molluscs generally. Before, however, we can understand the part
which vegetation has played in forming the travertine and sinter
beds of the Yellowstone Park, we must become familiar with the
general appearance and character of the deposits themselves.
First in importance among the many points of interest accessible
are the Hot Spring Terraces. These have been built one upon
another, until the present active portion constitutes a hill rising 300
feet above the site of the Mammoth Hot Springs Hotel. The for-
'^K;«m^ri*,^} Vegetation of Yellowstone Hot Springs. 629
mation about these springs, it will be remembered, is calcareous,
and to this fact is due its distinctive character, so different from the
silica formations which prevail elsewhere in the Park. •* The over-
hanging bowls which these deposits build up are among the finest
specimens of Nature's work in the world, while the water that fills
them is of that peculiar beauty to be found only in thermal springs."
Cleopatra Spring, Jupiter Terrace, Pulpit Terrace, Minerva Terrace,
are among the most interesting and beautiful of the active springs.
One of the most beautiful is a pool filled with pellucid water in vio-
lent ebullition. The sides and bottom of the basin are formed of pure
white travertine, while the varying depths cause the water to appear
all shades ot blue and green, from a deep peacock blue in the deeper
parts of the bowl, to the lightest of Nile greens in the shallow re-
cesses. In wandermg about the terraces, one is much impressed
with the brightly tinted basins about the springs, and the red and
orange colors of the slopes overflowed by the hot waters. These
colors are due to the presence of the microscopic plants, algai of
several forms and species. In the cooler springs and channels simi-
lar vegetation forms the bright green, orange or brown mem-
brane-like sheets, or masses of jelly without apparent vegetal struc-
ture. Silken yellow filaments are found in bowls and channels of
the hottest springs. Words fail to convey an adequate idea of the
massive marble-like terraces, rising tier upon tier, and the exquisite
coloring of their sides and the margins of the bowls filled with
steaming hot water of most magnificent iridescent hues.
The silicious formations are similar, although not raised in ter-
races so grand or imposing, simply because the formation of silicious
sinter is much slower than the formation of the travertine, and
because the region seems to be of later geologic age. Many of the
geyser cones are bee-hive in shape, of a white adamantine like
appearance, and are, as a rule, delicately colored by pale greens and
pinks of exquisite variation. The many hundreds of springs of the
Upper Geyser Basin, where they are seen at their best, are generally
characterized by the transparent clearness of the water, which
appears of varying shades of blue and green, according to the depth
and amount of light admitted. Morning Glory Spring is one of the
most beautiful springs of the Park, with a funnel-shaped cone sug-
gesting the flower, and with walls most delicately colored.
Black Sand Basin is, however, most interesting tor our pur-
630 Vegetation of Yellowstone Hot Springs. [^^^^:^^;£X'^-
pose. The description of Dr. Peale is interestingly comprehensive,
and is as follows : " This is one of the most beautiful springs in the
Upper Basin. It has a delicate rim, with toadstool-like masses
around it. The basin slopes rather gently toward a central aperture,
that, to the eye, appears to have no bottom. The water in the
spring has a delicate turquoise tint, and as tiie breeze sweeps across
its surface, dispelling the steam, the effect of the ripple of the water
is very beautiful. The sloping sides are covered with a light brown
crust ; sometimes it is rather a cream color. The funnel is about
40 feet in diameter, while the entire space covered by the spring
is about 55 X 60 feet, outside the rim of which is a border of pitch
stone (obsidian) sand or gravel, sloping 25 feet. From its west
side flows a considerable stream, forming a most beautiful chan-
nel, in which the coloring presents a remarkable variety of shades ;
the extremely delicate pinks are mingled with equally delicate tints
of saffron and yellow, and here and there shades of green."
The overflow from this spring spreads out over a large area, called
Specimen Lake, where absorption of the silica from the water has
destroyed many of the trees of the vicinity, the dry, lifeless trunks
adding to the attractiveness of the place by affording the appear-
ance of petrifactions.^ All of these exquisite masses of colors which
are found lining the pools, filling the overflow channels and spread-
ing out flat in the lower marshy places, are due to the growth of
vegetal organisms belonging to the bacteria and algae.
Walter H. Weed^ describes the appearance of the Black Sand
Basin and channels filled with algal growths : " As the water from
this spring flows along its channel it is rapidly chilled by contact
with the air and by evaporation, and is soon cool enough to permit
the growth of the more rudimentary forms which live at the highest
temperature. These appear first in skeins of delicate white filaments
which gradually change to pale flesh-pink farther down stream. As
the water becomes cooler, this pink becomes deeper, and a bright
orange and closely adherent fuzzy growth, rarely filamentous,
appears at the border of the stream, and finally replaces the first-
mentioned forms. This merges into yellowish-green, which shades
into a rich emerald farther down, this being the common color of
fresh-water algai. In the quiet waters of the pools fed by this stream
' Haynes-Guptill, Guide to Yellowstone Park, p. 68.
' Weed, Ninth Annual Report U. S. Geological Survey, p. 657.
^Decimberl^'" } VegetatwH of Yellowstone Hot Springs. 631
the algae present a different development, forming leathery sheets of
tough gelatinous material, with coralloid and vase-shaped forms ris-
ing to the surface, and often filling up a large part of the pool.
Sheets of brown or green, kelpy or leathery, also line the basins of
warm springs whose temperature does not exceed 140° F., but in
springs having a higher temperature the only vegetation present
forms a velvety, golden-yellow fuzz upon the bottom and sides of the
bowl. This growth is rarely noticed in springs where the water
exceeds 160° F., except at the edge of the pool. If the basin is
funnel-shaped, with flaring or saucer-shaped expansion, algae grow
in the cooler and shallower water of the margin, forming concentric
rings of yellow, old gold and orange, shading into salmon-red and
crimson, and this to brown at the border of the spring. Around
such springs the growth at the margin often forms a raised rim of
spongy, stiff jelly, sometimes almost rubber-like in consistency, and
red or brown in color. Evaporation of the water drawn up to the
top of such rims leaves a thin film of silica, which thickens to a crust
and so aids in the production of a permanent sinter rim."
Near some springs, for example near the Emerald Pool, algal
channels are formed and the waterway is floored with a sheet of
olive or emerald green, kelpy jelly. Where there is a moderate
current, this lining is nearly smooth, resembling a sheet of wet
leather, but in quieter waters this soft carpet is dotted with little
warty excrescences, and little pillars produced by the upward growth
of the algae; the pillars sometimes terminate by balloon-like caps
or globes containing bubbles of gas. When, by their upward
growth, these pillars reach the surface of the pool, they increase
rapidly in diameter, and form flat, cap-shaped formations which
sometimes merge into table-like expansions of quite peculiar form^
The continued growth of new pillars dams up the outlet, and the
water collecting forms .shallow lagoons or pools of varying degrees
of temperature. As the temperature changes, the nature of the
growth changes, the bright-colored algous jelly lorming the outer
covering of the pillars changes to light salmon-pink, and the sub-
stance itself becomes noticeably silicious, or forms a filmy web upon
the silicious centre.
It has been for some time known that the hot springs of the
world support various growths of microscopic plants. Agardh and
Corda recognized and described such in the hot .springs of ('arlsbad,
632 Vegetation of Yellowstone Hot Springs, { '^D^cimb'eri^sT'
Bohemia. Later, Cohn, in 1 862, showed that the algae of these
springs deposited travertine. Sir Wilham Hooker, in 1809, found
CONFERVACE/E at the borders of many of the hot springs there. Con-
ferva liniosa, C. flavescens, C. rivuiaris were abundant in the water.
Baring Gould, who visited the Icelandic geyser region in 1864,
found in the overflow channels of the spring, Tunguhver, a species
of the genus Hyp/ieothrix, common in hot waters all over the world.
In New Zealand, the presence of algae in hot springs has been deter-
mined. In the hot springs of the Azores, Mr. Moseley found algae
forming a pale yellowish-green layer an inch and a half thick. The
temperature of the water was 176° F. to 194° F. A thick, brilliant
green growth, consisting of Chroococcus was found at the edge of a
shallow pool of hot water, where the temperature was between
149° F. and 156° F.
In the hot springs of the Yellowstone no plant life has been found
at a temperature exceeding 185° F., some degrees below the boil-
ing point of water, which, at the altitude of the park (7,000-8,500
feet) is 198° F. The most luxuriant growth of algae is found in
water which has cooled down to a temperature of 104° F. to 122° F.
In water of a temperature ranging from 100° F. to 125° F., we
have the greatest display of color, because many green algae can
live in water of that degree of heat. In the hottest waters (185^ F.)
only white filamentous bacteria are found, which gradually become
of a sulphur-yellow color at 175° F. This yellow growth is due to
a species of Beggiatoa, a plant which may be classed with the Bac-
TERiACE^, and which, during life, deposits sulphur granules.
As the water cools down, other forms of vegetable lite appear^
give variety to the colorations and give beauty to the borders
of the hot pools and overflow channels leading from them. The
sequence of temperatures and of colors is somewhat as follows:
white, 160° F.-i85° F.; yellow, 145° F.-i6o° F.; red, 130° F; green,
110° F.-i30° F.; green-orange-brown, 95° F. There are varia-
tions, however, in the sequence of these colors, owing to various
environmental conditions. Thus, in the Black Sand Basin and
Specimen Lake, the range of color is somewhat this: White, yel-
low, flesh pink, bright pink, yellowish-green, emerald.
Studying the growths at the several temperatures, we find Lepto-
tkrix laminosa growing at 135° F..-i85° ^ \ Phormidiiim at 165° F.;
Beggiatoa at i 50° F.-i65° F» and Spirulina at a lower temperature.
^i^imber*:i?^° ; VcgetatwH of Yeilowstotte Hot Springs. 633
Gleocapsa, a blue-green alga, is found growing on the sides of gey-
ser cones, where steam is escaping, forming there a delicate olive-
green coloration. A kind of fibrous sinter is formed by the growth
of the little alga, Calothrix gypsophila, or the young form of MaUigo-
nema tkermaU, the latter olive colored, and forming the sinter of
the crater of the Excelsior Geyser.^ A coarse sinter is due to a
bright red species, Leptothrix, a finer variety to Leptothrix [Hypheo-
thrix) laminosa, ranging in color from white to flesh pink, yellow
and red to green, as the water cools. Besides the above plants,
which belong to the Bacteriace.*: and the CvANOPHYCEi*:, speak-
ing in a general way, we find that several mosses, Musci, are active
in the formation of sinter on the slopes below Hillside Spring.
These springs issue from the rhyolite slopes beneath the cliffs of
the Madison Plateau, and the waters, whose temperatures are
184° F.-I98° F., contain both silica and lime in solution, which
they deposit in their downward flow. This moss has been deter-
mined by Prof. Charles R. Barnes, of the University ol Wisconsin,
to be Hyptium aduncum, var. grasilcscens, Br. and Sch.
Besides the sinter and travertine formed by algae, which remove
in the case of the carbonated waters, containing calcium bicarbonate,
Ca (HCOj)^, in solution, the gaseous carbon dioxide, thus depositing
calcium carbonate, CaCOj, we have stalactites produced by the
growth of several algse, Gleocapsa violacca, Schizothrix calcicola,
Synechococcus (Bruginosus and Phortnidiuui [Leptothrix) laminosum.
An interesting account of the formation of these stalactites has been
given to us by Miss Jo.sephine Tilden, who visited, recently, the
Yellowstone Park.
In the tepid waters of the overflow basins, for example Speci-
men Lake, which is produced by the water from the Black Sand
Pool, we find extensive diatomaceous beds formed by the growth of
numerous diatoms. The water of these areas has encroached on
the timber, killing the trees, which stand as bare poles from the
treacherous marshes. It is known that these plants deposit silica,
as a box, test, or frustule, and it is thus by the activity of the proto-
plasm that the silicious diatomaceous earths are formed. Samples
of this material show the presence of Denticula valida, which forms
the bulk of the material, Denticula clegans, Navicula major, N. virt-
dis, Epithema, Cocconema, etc.
634 Pomegranate Rind. {^S^'imber^T
It seems likely to me, in studying the vegetation of hot springs,
notwithstanding the statements of Prof. Ernst Haeckel, of Jena,
in his interesting work, " Systematische Phylogenie der Protisten und
Pflanzen," that the early forms of life on this globe were green uni-
cellular algae, and from these by retrogression and development
other forms have sprung, animal life appearing later than plant, it
seems to me, I repeat it, that we must look to the hot springs for
the most primitive forms of life, because the temperature conditions
are such as more nearly to simulate the conditions existing when
this world of ours was in a highly heated state, when seismic phe-
nomena were the rule rather than the exception. It would be neces-
sary in order to establish this proposition to investigate compara-
tively the vegetation of all the hot springs of the globe, before it
would be safe to make such a general declaration as to the origin
of vegetal life.
The above ecological sketch sufficiently discloses the salient char-
acters of the interesting geysers and hot springs of the Yellowstone
Park. In preparing this article, the writer has endeavored to give
the results of personal observation on the spot during eight days of
August, 1897. He has been materially aided in its preparation by
the following papers and books, which give a somewhat more
detailed account of the Yellowstone Wonderland:
BIBI^IOGRAPHY.
1887-88, Weed. Ninth Annual Report U. S. Geological Survey y p. 619.
1895, Chittenden. The Yellowstone National Park, Historical and Descrip-
live.
1897, Haynes and GuptilIv. Guide to Yellowstone Park,
1897, Davis, in Scie^ice, N. S., I., p. 145 (July 30).
1897, TiLDEN, in Botanical Gazette, September, 1897.
University of Pennsylvania, November 16, 1897.
POMEGRANATE RIND.
By Henry Trimbi^e.
Contribution from the Chemical Laboratory of the Philadelphia College of
Pharmacy. No. 171.
At this season of the year pomegranate fruit is frequently seen
on the market stalls of Philadelphia and other Northern cities, and
is brought here from Spain. Small quantities ot the fruit are raised
in the Southern States and in California, but so far it has never
attained much popularity with us, partly, no doubt, on account of
^D^im^riST} Pofnegranate Rind. 635
the price, but more because we have not tried the exceedingly juicy
and slightly acid pulp.
Since the main object of this paper is to consider the constituents
of the rind or peel, it is not necessary to dwell on the history,
source, etc., of the plant and its fruit, as full descriptions of them
are to be found in several text-books.
The rind of the fruit has long enjoyed a reputation in medicine
as an astringent, especially in chronic cases; it also possesses, in
some degree, the anthelmintic properties of the root and stem
barks.
The most important constituents of the rind are the yellow color-
ing matter and the tannin ; the former has been employed consider-
ably as a dye, especially in producing yellow morocco leather. The
tannin has been used in the manufacture of leather in nearly all the
countries where the fruit is found.
The writer has always been somewhat skeptical about the high
percentages of tannin which have been reported, and has undertaken
to verify or refute them.
The fresh rind from some Spanish pomegranates purchased in the
Philadelphia market gave the following results :
Per Cent.
Moisture 56"66
Ash in absolutely dry substance 392
Tannin " " " 28-38
The figures obtained by Mr. Griffith H. Maghee, a student in the
Laboratory, confirmed these, although his estimations were made on
different lots of rind. Others have reported from 20 to 30 per cent,
of tannin.
FlLickiger found 5 90 per cent, ash in the rind dried at IOO° C, as
in the above case. A recent estimation on a new lot of rind gave
me 3 68 per cent, ash in dry substance.
A quantity of the tannin was extracted from the rind with ace-
tone, and purified according to the usual method ; on drying at 120°
it yielded, on combustion, the following results :
Per Cent.
Carbon ... 52- 11
Hydrogen 4' 17
Oxygen 4372
100 00
A portion of the tannin dissolved in water gave the following char-
acteristic reactions :
636 Digestive Power of Pepsin, { ^^ecimber*;^^"'
Ferric salts Blue-black precipitate.
Bromine water No precipitate.
Calcium hydrate Yellowish ppt. , turning brown.
These reactions correspond with those of gallotannic acid, and the
combustion results show a composition very similar to the same
acid, so it may safely be concluded that the tannin of pomegranate
rind is identical with gallotannic acid. This is in accord with the
results obtained by CuUey' on the tannin of the root bark.
' American JournaIv of Pharmacy, 1894, page 280.
THE DIGESTIVE POWER OF PEPSIN IN THE PRESENCE
OF ALCOHOL.^
By C. Symes, Ph.D.
Some years ago I conducted a series of experiments with a view
of determining the relative digestive value of the various pepsins
then on the market, and published the result of the inquiry.^ Subse-
quently I was requested to continue and extend the investigation for
publication in one of the medical journals, and in consequence I
gained some amount of experience in this kind of work. The experi-
ments were carefully conducted and, after a lapse of time, were
repeated by a French investigator, who confirmed my results. Time,
" which tries all things," also testified to their correctness, for the
pepsin, which was then mostly prescribed and relied on, has since
practically disappeared from the market, its quality having been
found by experience to be inferior to that of similar preparations by
other makers. Apart from the relative value of various pepsins, I
also experimented on the digestive power possessed by pepsin in
the presence of alcohol, and found that its activity was reduced in
proportion to the amount of alcohol present. From this I drew
deductions which I have since learned to modify, although the facts
remain. I condemned wine as a vehicle for the administration of
pepsin because of its property of retarding the activity of the medici-
nal agent it carried, and recommended in the place thereof a solu-
^ Pharmaceutical Journal, November 6, 1897.
•2 Pharmaceutical Journal (3), IV, i. See also note on "Latent Pepsin," by G
W. C. Phillips, in Pharmacist, VIII, 200, and "Year Book of Pharmacy," 1875
p. 317 ; paper on "Pepsin and Alcohol," by M. Bardet, Nouveaux Rem^aes^
1887, p. 243, and Pharmaceutical Journal (3), XVII.1,93; and paper on "Pepsin
Wine," J. Clark, Pharmaceutical Journal (3), XXII, 597.
^^"ra"^er':i^"} Digestive Powcr of Pepsin. 637
tion of fresh pepsin in raspberry vinegar. This constitutes an excel-
lent preparation, and at present I know of no better; but the public
never took very well to this " pepsin elixir," as many persons have a
decided objection to acids. It has, however, been prescribed with
satisfactory results.
The experiments referred to were conducted in glass bottles
placed in a water-bath kept at a uniform temperature of 100° F. by
means of a Reichart's thermo-regulator. The importance of adopt-
ing the same temperature on all occasions when conducting com-
parative experiments was rendered evident by increasing the tem-
perature to 1 10^ F., when digestion was found to proceed much
more vigorously than at 100° F., all other conditions being equal.
Still, the presence of alcohol had the same prejudicial effect in retard-
ing solution of the coagulated albumen used. If, however, the
bottles were replaced by wetted animal membranes, the condition of
things was materially altered. It was found that the alcohol present
in the liquid through which the coagulated albumen was distributed
soon began to diff'use through the wetted membrane, and that the
pepsin commenced to act with the same energy as in those con-
tainers where no alcohol was present, so that at the end of two
hours there was no considerable difference between the weight of
undissolved albumen in each case. The interest which this experi-
ment has for us, as pharmacists, is that it shows that an alcoholic
liquid, such as wine, may be used in preparing a solution of pepsin
for medicinal use, and that if properly made it soon becomes active
when taken into the stomach in the presence of suitable food. Recti-
fied spirit may also be used as a preservative in making essence of
rennet, because its excessive dilution and ready evaporation, when
mixed with the proper quantity of milk and warmed, overcome any
prejudicial effect the spirit may have on the f)eptic bodies present.
Glycerin is an excellent solvent of pepsin, as is well known; but
unless it is used in sufficiently large quantity to render the solution
distasteful to the patient, it is not a good preservative. A solution
of freshly prepared undried pepsin in dilute glycerin, to which 10
per cent, of rectified spirit is added, forms, when filtered, an excel-
lent medicinal preparation which may be flavored to taste.
638 Chemistry of Clove Oil. { ^SlcimbeolS*
THE CHEMISTRY OF CLOVE OIL ^
Erdmann has published some interesting results of his investi-
gation of clove oil and the oil distilled from clove stalks. In pre-
paring caryophyllene by treating clove oil with solution of caustic
alkali, the undissolved portion of the oil was always found to be
oxygenated, and only by using alcoholic potash was it obtained free
from oxygen. Oil from clove stalks shaken with dilute caustic
alkali yielded at once the sesquiterpene.
On treating the oil that is separated from clove oil by solution of
caustic alkali, with alcoholic potash, and adding some ether to dis-
solve and separate the terpene, the alkaline solution was found to
contain eugenol, which was separated on acidifying with sulphuric
acid, and on distilling the acidified liquid, acetic acid was obtained.
Hence it was evident that clove oil contains, as one of its constitu-
ents, aceteugenol, a compound which is at once saponified by alco-
holic potash, but less readily by a water solution of caustic alkali,
and thus the presence of oxygen in the oil undissolved by caustic
alkali solution was accounted for, as well as the circumstance that
neither this undissolved oil nor clove oil itself has a constant boil-
ing point. That is not due to difference in the amount of caryo-
phyllene; for though it has a somewhat higher boiling point than
eugenol, the tension of both substances is nearly the same at 123° C,
under a pressure of 13 millimetres, and the higher boiling-point,
125° to 150° C, of the oil undissolved by caustic alkali is due to
the presence of aceteugenol.
In the determination of eugenol in clove oil by Thorns' method,*
it is assumed that the whole of the eugenol is present in the free
state, and the question arose whether the presence of some portion
of it in the state of ester affected the determination. That was
found to be the case by comparative experiments with clove oil pre-
viously saponified by heating to 100° C, with caustic alkali, and
with oil which had not been so treated, the results given by three
samples being as follows :
Thorns. Total eugenol.
Clove oil, A 83*9 85*68
Clove oil, B [ 82-97
1 8277 84-84
Clove oil, C 8o*2 81*9
^Jour. Prakt. Chem., LVI., 175, through Pharmaceutical Journal, November
6, 1897.
' Pharmaceutical Journal, (3), XXII, 450.
^^eciTr.eTHl^'"-} Chemistry of Clove Oil. 639
The low specific gravity of the oil distilled from clove stalks, as
compared with the large amount of eugenol it contains, is explained
by the absence of aceteugenol, the relation between the specific
gravity and the amount of eugenol in the case of clove oil being
due to the presence of some aceteugenol, the specific gravity of
which is much greater than that of eugenol.
On saponifying clove oil with a known quantity of alcoholic
potash, and determining the residual free alkali, a result was obtained
indicating the presence of a much larger quantity of aceteugenol
than was actually present, and this was ascertained to be due to the
presence of a compound yielding salicylic acid, the occurrence of
which in clove oil was pointed out by Schenck,'* but disputed by
Wassermann/
By merely shaking clove oil with solution of caustic alkali, no
indication of salicylic acid is obtained ; but after the saponification
effected by boiling with soda solution, salicylic acid can be detected
in the aqueous liquor. It is suggested that the compound present
in clove oil, and yielding salicylic acid by saponification, may be
eugenol ester of acetyl salicylic acid.
The yellow coloration produced on treating clove oil with caustic
alkali was suggestive of the presence of an aldehyde, and a product
was obtained which proved to be furfurol. a substance which Messrs.
Schimmel have also found in clove oil, together with normal amyl-
methyl ketone, to which they attribute some influence as to the
cause of the ether-like odor of clove oil, which a mixture of eugenol,
caryophyllene and furfurol does not possess.
Erdmann also suggests that eugenol is probably not the only
phenolic constituent of clove oil, because the boiling-point of the
crude product has a wider range than is consistent with its chemical
individuality, and also because in redistilling eugenol he has obtained
a residue of phenolic character, though its resinoid character did
not invite further investigation.
^ Ann. them., 12$, 14.
* Ann. Chem., 179, 369.
640 Recent Literature Relating to Pharmacy, {^'^'J^^l;^^xS^:
RECENT LITERATURE RELATING TO PHARMACY.
ASCLEPIAS CUKASSAVICA AS AN INSECTIFUGE.
The following information concerning the uses of this plant is
taken from the Kew Bulletin, October, 1897, ^^^ which, as there
stated, appears to be unrecorded :
The plant grows everywhere, as a weed about the Isthmus of
Tehuantepec (Southern Mexico), and is used by the Indians there
to keep away vermin, especially fleas, for which latter purpose it is
reported as being most successful. They make a rough broom of
it, and sweep the floors and walls of their huts, and find that they
are not troubled with fleas for a considerable time afterwards.
They have tried brushing dogs with it when their coats are full of
vermin, and it appears to answer the same purpose with them.
The Indian name of the plant is " Chilpati."
DETERMINATION OF THE ALKALOIDS IN SOLANUM CAROLINENSE.
In a recent communication (The Journal of Pharmacology, Vol. 4,
p. 225), Charles Gundlich refers to the results obtained by G. A.
Krauss and Professor J. U. Lloyd in their investigations of Solanum
Carolinense. He then outlines the processes which he employed for
the extraction of the alkaloidal constituents of the drug. The alcoholic
liquid in which the fruit was preserved was examined by various meth-
ods, but only traces of alkaloid could be found. Then an examination
of the fruit was undertaken, but only traces of alkaloid were found
in 500 grammes of material. Next, 10 grammes of the powdered
root were examined, using various solvents for the extraction of the
alkaloid, but only traces could be found. Lastly, 1,000 grammes of
the finely-powdered root were treated with dilute acetic acid (10 per
cent.), but with no better results. At this juncture, the author
learning that Professor Lloyd had used several hundred pounds of
drug for obtaining his material, the investigation was given up.
CAFFETANNIC ACID.
Paul Cazeneuve and E. Haddon (Compt. rend., 1897, 124, 1458-
1460) have recently studied this subject. Since the investigations
of Hlasiwetz, caffetannic acid has been usually regarded as having
the formula CigHj^Og, but the authors, from a study of the behavior
of the substance towards phenylhydrazine, conclude that it has the
composition C21H28O14, and ascribe to it the constitutional formula ;
COOH . CH : CH . QH3(0 . Q,^,^0,\.
^D^mLr.T^ } Recent Literature Relating to Pharmacy. 641
The osazone of caffetannic acid, C^^H^NgOio. crystallizes in yellow
needles, very sparingly soluble in alcohol, and melts at 180° ; it is
insoluble in most media, and is so sparingly soluble in phenol and
naphthalene that no determinations of molecular weight have been
possible.
The sugar, CgHj^Og, obtained on hydrolyzing caffetannic acid, will
be described m a subsequent paper. — Journal of the Chemical
Society, London, October, 1897.
PREPAR.\TION OF HYDROGEN PEROXIDE.
Hydrogen peroxide may rapidly and economically be prepared,
according to Pedro Etchegorry {Tribuna Farmaccutico, \^ 16), by
triturating with ice a mixture of i part barium peroxide and 2 parts
(by weight) of hydrochloric acid. The following reaction takes
place.
BaO, -V 2HCI = H2O, -f BaClo.
The filtered solution is treated with a solution of silver sulphate
until no more precipitation occurs, according to the following
reaction :
BaCU + HA -t- Ag^SO, = l^aSO, -f 2AgCl -f H.O^-
On filtering, the barium sulphate and silver chloride are retained
on the filter, while the hydrogen peroxide passes into the filtrate in
a state of purity.
This process has already appeared in some text-books on chemistry
and, consequently, is not new; but it seems worthy of further
investigation.
CAFFETANNIC ACID (GLUCOSVLCAFFEIC ACID) AND ITS DECOMPOSITION
INTO CAFFEIC ACID, VINYLCATECHOL, AND CATECHOL.
Hermann Kunz-Krause (^^r., 1897,30, 1617-1622) has recently
studied this subject. Both caffetannic acid and matctannic acid,
when hydrolized, yield a syrupy sugar and caffeic acid (dihydroxy-
cinnamic acid). This acid, when heated at 200°, readily loses
carbonic anhydride, yielding vinylcatechol (3 : 4-dihydroxycinna-
mene), the decomposition at this temperature being quantitative.
A characteristic reaction for vinylcatechol is the one previously
mentioned {Arch. Pharm., 1S93, 231, 635). This reaction is also
given by Ticmann and Will's hesperetol or vinylcatechol piaranio-
642 Recent Literature Relating to Pharmacy. {"^iJ^cimbe^
Am. Jour. PbartD.
1897.
nomethyl ether (Abstr., 188 1, 739). The carmine-red coloration
with sulphuric acid therefore appears to be characteristic of 3 : 4-
dihydroxycinnauiene and its ethers. The author has only suc-
ceeded in obtaining the vinylcatechol as an amorphous powder; it
is a somewhat unstable substance, for when distilled under a pres-
sure of 12 millimetres it is decomposed, the chief product being
catechol. The author thinks it probable that caffetannic acid is
distributed throughout the vegetable kingdom in very much the
same manner as choline. — Journal of the Chemical Society, London,
October, 1897.
CHINESE BANDOLINE WOOD.
The origin of this curious product, of which a specimen has long
been in the Museum of the Royal Gardens, has always been a
puzzle.
Shavings of the wood yield a mucilage, when soaked in water,
which is used by Chinese ladies in " bandolining " their hair. Dr. E.
Bretschneider (" Notes on Some Botanical Questions Connected with
the Export Trade of China," 1880, p. 14,) mentions the shavings as
being exported from Canton to Peking, under the name of " meio
kao pao hua " {i. e., cosmetic glue shavings), and their probable
source as Sterculia plantanifolia. In 1895, G. M. H. Playfair, Esq.
H. B. M. Consul at Ningpo, sent to Kew specimens in leaf of a tree,
called " tiao chang," which he had collected in the mountains near
Ningpo, with the information that shavings of the wood were used
for the purpose described above by the women of that part of China.
These specimens were identified as Machilus Thunbergii, Sieb. et
Zucc, and flowering specimens subsequently received from the same
gentleman confirmed the identification. Mr. Playfair further adds,
on the authority of Dr. A. Henry, that the Canton shavings are
from the same tree.
The species is a native of Hong Kong and Chekiang westward
to Szechuan, in China ; also of P'ormosa, Japan, and the Corean
Archipelago. Owing to the interest attaching to the identification,
the species has been figured in Hooker's " IconesPiantarum " (t. 2538).
— Kew Bulletin, October, 1897.
FUNCTION OF TANNIN IN PLANTS AND ESPECIALLY IN FRUITS.
C. G^rh^r {Compt. Rend., 1897, 124, 1106-1109) has practically
studied this obscure but interesting subject, and reached the follow-
ing conclusions : In the respiration of soft fruits containing tannin,
^D^lmheT^"^'} Recent Literature Relating to Pharmacy. 643
the volume of the carbonic anhydride evolved is less than that of
the oxygen absorbed so long as any tannin remains unaltered. As
soon as all the tannin has disappeared, pectin is produced. If the
temperature is so low that the cellular activity is not great, the res-
piration quotient remains lower than unity; but if the temperature
is so high that the cellular activity requires more energy than is
furnished by the free oxygen, the cellules obtain the necessary
energy from the alcoholic fermentation of the sugars, the carbonic
anhydride produced by it being added to that produced by respira-
tion, and thus giving a quotient higher than unity. It follows that
one of the principal functions of tannins in fruits is to prevent pectic
transformations, and thus check the fermentation of the sugars.
Direct experiments with the fruit of Dyospyros kaki show that
the disappearance ot tannins does not involve an increase in the
amount of sugar, and experiments on the respiration of Sterigma-
tocystis nigra on a solution of nut-gall tannin lead to the same con-
clusion. In fruits containing tannins, the latter disappear as the
result of complete oxidation, without forming any carbohydrates. —
Journal of the Chemical Society, London, October, 1897.
LICORICE ROOT GROWN IN NEW SOUTH WALES.
In the Northern Star, Mr. W. F'inselbach,. Ph.D , Lismore, N. S. VV.,
mentions that at a recent local agricultural show, the Govern-
ment Experimental Farm exhibited two samples of Spanish licorice
root, the stolens or suckers, only two years old, being 12 feet long.
While a student under Professor Fllickiger, in Strassburg, and
while travelling in Italy, he had frequently examined three and four-
year-old roots, running from 9 to 10 feet long, showing that the
soil and climatic conditions of the Lismore district, at any rate, were
very favorable to the growth of the plant. He states that he has
made an analysis of the samples exhibited, and finds them to be of
first-class quality, although they have not secured full maturity.
In parts of Italy he saw the licorice cultivated on maize fields. The
plant requires three, and, in wet seasons, even four, years, to mature,
and the general custom where licorice is grown rationally is that a
crop of another kind should be found on the same field. An acre
in Europe is said to produce three or four tons of the roots, worth
on the London market \2s. to \6s. per cwt. There is a large con-
sumption of the root in the United Kingdom. Mr. Finsclbach says,
644 Recent Literature Relating to Pharmacy. {^^^i^^^^%^'
in the brewing trade as well as for medicinal uses, and we may add
in confectionery. The largest consumers, however, are the United
States. Mr. Finselbach suggests that the plant, which can be
grown from suckers, would be a remunerative crop in certain dis-
tricts.— The Pharmaceutical Journal of Australasia, August 28, 1897.
ON MORRHUOL AND THE ALLEGED IODINE AND THE BROMINE CON-
STITUENTS IN COD-LIVER OIL.
Charles Gundlich(77^^ Journal of Pharmacology, Vol. 4, pp. 223),
reports that in experimentmg with cod-liver oil for the production of
the so-called morrhuol, he first tried concentrating a pure oil in a
vacuum of 15 millimeters pressure at 100° C, he having surmised
that this substance might be the concentrated oil. The results
were negative.
A sample of crude oil, having a specific gravity of 0-923, and
Hehner value 95*15 (percentage of insoluble fatty acids), was then
treated, after ascertaining its freedom from free acids, with 80 per
cent, alcohol. The alcoholic extract was evaporated, and the product
obtained had a specific gravity of 0-900 at 19° C, and congealed at
4° C. In these respects it corresponded with samples of purchased
morrhuol (one foreign, one domestic), as well as in taste, odor and
color. The author is, therefore, of the opinion that the commercial
product is prepared in a like manner from any crude product sold as
cod-liver oil.
Tests for iodine and bromine showed that they were neither pres-
ent in the crude oil used in the preceding experiment nor in the
purchased morrhuol.
The latter appeared to be a mixture of various impure fatty oils,
for, after repeated attempts at fractional distillation, no products
could be isolated having a uniform boiling point.
An examination of the crude cod-liver oil and the morrhuol for
amine derivatives revealed their presence in each. The process for
the separation of the amines was applied to a sample of oil from
which morrhuol had been extracted by treatment with alcohol, and
the results showed that a large proportion of the alkaloids had been
removed by this treatment. The conclusion is therefore reached
that morrhuol contains a considerable quantity of amines.
A NEW ALKALOID, RETAMINE.
Battandier and Malosse (Jour, de Ph. et de Chim. [6], 6, 241)
have separated from the young branches and bark of Retama
^Deirab^J!^!?^"' / Receiit Literature Relating to Pharmacy. 645
sphaerocarpa, by the ordinary processes, a perfectly definite alkaloid,
which they have named Retamine. A kilogramme of the fresh
plant furnished some 4 grammes of alkaloid. This alkaloid is
slightly soluble in water and in ether ; alcohol and p)etroleum ether
dissolve it more readily ; and chloroform dissolves it very readily,
but not without some decomposition. It crystallizes in long needles
by chilling the saturated petroleum ether solution, and in prismatic
plates by similarly cooling the saturated alcoholic solution; the
spontaneous evaporation of its alcoholic solution yields beautiful
rectangular tables. It is dextrogyre, melts at 162° C, and decom-
poses at a higher temperature, giving a sublimate in long needles,
and other products having the odor of pyridine.
Retamine impartsa distinct color to phenolphtalein. It isa powerful
base, which combines energetically with acids, and yields clearly-de-
fined salts. It displacesammonia, especially with heat, and precipitates
the hydrates of iron, copper, etc. The caustic alkalies precipitate it
from its saline solutions. It possesses extremely energetic reducing
action — the chloride of gold and phosphomolybdic acid are instantly
reduced, the salts of silver and ferricyanide of potassium are more
slowly reduced, while the mercuric chloride is changed to the mer-
curous salt. It gives the general reactions of alkaloids and furnishes
with potassium bismuth iodide, a beautiful red precipitate. The
chloride of platinum is not precipitate, by it, but it gives feebly, with
ammonium sulphide, the reaction of sparteine.
The salts of retamine crystallize very easily and with great dis-
tinctness, except the nitrate, which has only been obtained in the
form of a varnish. The salts which have been studied contain for I
molecule of retamine, either i or 2 molecules of monobasic acid.
The solubility in absolute alcohol is 2-462 parts in 100 of solvent.
The specific rotation is [rf]j, = 43°,I5'. The elementary analysis
indicated the formula Cj-H^jgNjO. It is probably an oxysparteine,
but differs from the artificial oxysparteine known at present.
THE TREATMENT OF TUBERCULOSIS WITH CI.NNAMIC ACID.j
It is interesting to note that a remedy is reconmiended for the
treatment of tuberculosis, which is neither a new synthetic com-
pound nor a product of some manufacturing firm.
Dr. T. Heusscr, of Davos-Platz (Therapeutische Monatslujte ;
* The Nerv York Afediral Joumai, October 16. 1897.
646 Recent Literature Relating to Pharmacy. { ^December! IT'
Therapist, September 15, 1897), relates his experience with cinnamic
acid in the treatment of tuberculosis. He states that the theory
upon which the method of using cinnamic acid is based, was pro-
pounded by Landerer in 1888. The important points to be noted
in the treatment are: (i) Induction of general leucocytosis. (2)
Aseptic inflammation of the tuberculous centre, commencing with a
circumvention and permeation of the tubercles with leucocytes^
subsequently with young vessels and vascular tissue. To bring
about these conditions, Landerer used an intravenous injection of an
emulsion of cinnamic acid; but Dr. Heusser prefers to use gluteal
injections of the emulsion on account of the danger attending the
former method of administration. He uses a minim and a half
of a 5 per cent, emulsion for the beginning dose, which he
increases gradually with each injection. If the symptoms are favor-
able, these are made every second day. The maximum dose is
15 grains and is continued until the end of the treatment, which is
continued for a month after all symptoms disappear.
In summarizing his opinions with regard to his experience with
this treatment, the author stated that: (i) Cinnamic acid is a. drug
having great influence on tuberculosis. (2) The gluteal cinnamic acid
injections, if cautiously made, are absolutely innocuous. (3) The
gluteal cinnamic acid treatment is capable of curing a considerable
number of cases of pulmonary tuberculosis. (4) Cinnamic acid is
not a specific against tuberculosis.
Citric acid is, reported as manufactured in San Diego, Cal., a factory for its
manufacture, along "with oil of lemon, having been established in 1896. It
takes from four to six weeks to condense the juice from 60 to 70 pounds
of lemons into i pound of acid. The factory employs seven hands, has
steam works, and a capacity for 40,000 lemons a week ; only culls are used. —
Chem. Trade Jour. ^ October 2, 1897.
Cadmium is meeting with an increasing demand, and the shortage in the
supply still continues, notwithstanding a little more is being made in Upper
Silesia (which is, practically, the only district where cadmium is produced).
The Upper Silesian production in the first quarter of the current year was
3,326 kilos, valued at ii*844 marks per kilo, against 3,256 kilos, valued at
10-261 marks per kilo in the last quarter of 1896; and 2,436 kilos, valued at
5-380 marks per kilo in the first quarter of 1896. At present, it is said the metal
is lacking entirely, and urgent demands for it cannot be satisfied. If the new
demand proves to be permanent, however, there will be no difficulty in meet-
ing it, since most of the Upper Silesian ore is cadmium-bearing, and the metal
can be recovered without diflSculty as a by-product. — Eng. and Mining Jour.,
October 9, 1897.
^Sci^XrX"} Editorial. 647
EDITORIAL.
PURE FOOD LAWS.
Last month we printed a circular letter of inquiry from the Ajjricultural De-
partment at Washington, concerning adulteration of foods and drugs and laws
governing them. One of the questions was: " Would a national food and drug
law assist in preventing adulteration ?" In the light of some years of study of
food and drug laws, we have hesitated to attempt an answer to any of the
inquiries, for the reason that occurrences are fre(iuently taking place which
tend to weaken one's confidence in all laws which propose to regulate the qual-
ity of foods and drugs.
One of the most notable instances of this kind occurred recently in Pennsyl-
vania. A special despatch to the Public Ledger, of Philadelphia, and printed
in the issue of October 30, reports that the Pure Food Bureau of the Depart-
ment of Agriculture at Harrisburg seems to be laboring with the question, " Is
mustard a food or poison ?" We quote a part of the despatch, as follows :
A sample of ground mustard, receutly sent to the Department by one of its special a^nU.
was found to contain 70 per cent, of adulteration. Suit was brought in Monroe County, where
the sample was found, against the party who sold the goods. During the trial the adulteration
was not denied and was proven beyond all doubt, but the question was raised as to whether
mustard was a "food " within the meaning of the pure food law. A resident medical prac-
titioner testified that it was a poison, and not a food ; the chemist of the Department testified
that it was food. In giving the case to the jury the judge instructed them that the question
of food was one of fact which they must decide for themselves, and if they believed it was not
they must acquit the defendant, but if they believed that it was a " food," they must convict
him.
To make this farce more complete, the jury disagreed as to guilt, and directed
that the costs be divided between the defendant and the county. When asked
for their reasons for this verdict, the foreman stated to the court that six of the
jury thought that mustard was a food and the remaining six took the opposite
view, and, to satisfy those who thought it was a ft)od, they put one half of the
costs on the defendant, thus showing that they thought him about half guilty.
It is such cases as this that make one skeptical about all laws which have for
their object the prevention of adulteration. With such a judge and jury a
national law would not be of any more value than one enacted by the State. It
has been said that two many laws breed anarchy, and the same might be said
of the poor administration of a few laws.
DESTRUCTION AS A MEANS OK PROTECTING PRICES.
The history of the partial destruction of the tobacco crop in Virginia in 1639,
as detailed in our last issue by Professor IJoyd, finds a mo<lern parallel in the
action of the Spanish Government, In the Cosmopolitan Magazine for Novem-
ber, John Langdon Heaton, on "Some Curiosities of Farming," makes the fol-
lowing statement: ** Ihit perhaps the most phenomenal peculiarity of Spanish
agriculture is the fostering care given it by the Government. This enlightened
rule not long ago caused to l>c destroyed in a single province 6,000,000 tobacco
plants, not because of any prejudice against nicotine, but in order not to dis-
turb the tariff income from Havana imports. This is a tariff for revenue only."
648 Reviews. {''^iZl^T^-
REVIEWS AND BIBLIOGRAPHICAL NOTICES.
The Right Side of the Car. By the author of " Etidorhpa " (John Uri
Lloyd). Richard G. Badger & Co., Boston, 1897.
While this dainty volume has little in it bearing directly on pharmacy, still
we are induced to notice it in these pages, not only on account of the distinct
merit of the work, but also because of the author's well-known contributions on
pharmaceutical subjects. That it will be read and enjoyed by pharmacists more
than by any other class, we have little doubt. It is the second venture of the
author in literature, and his transition from " Etidorhpa " to this is as startling
as his first departure from scientific literature.
' ' The Right Side of the Car " is a short story of a ride across the Great Ameri -
can Desert on the Northern Pacific Railway, and of the approach to Mount
Tacoma. The author will have none of the modern name, Mount Ranier after
an obscure British admiral who never saw this continent ; it does not compare
with Tacoma, given to it by the Indians long before the British landed in
America.
Two editions of this book have been issued, one a special author's souvenir
edition, and the other for popular sale ; the former will only be sent to those
who have subscribed in advance. The profits of both will go to erect a monu-
ment to the late Professor John King.
Pharmacopceia of the American Institute of Homceopathy. Pub-
lished for the Committee on Pharmacopoeia of the American Institute of Homoe-
opathy. Otis Clapp & Son, agents, No. 10 Park Square, Boston, 1897.
In reviewing a work of this kind it is difficult to avoid drawing comparisons
between the two branches of the medical profession, as well as between the two
pharmacopoeias representing those branches. It is the intention, however, to
review this homoeopathic pharmacopoeia on its own merits and without unneces-
sary reference to other works in existence.
As long ago as 1868, the American Institute of Homoeopathy, realizing the
need of "a dispensatory which should embrace pharmacy," appointed a com-
mittee to prepare one. Reports of progress were made from time to time until
1888, when, owing to the death of the chairman some time previously, and the
loss of the original manuscript, a new committee was appointed, consisting of
twelve members, six to represent the profession of medicine and six to repre-
sent the profession of pharmacy.
The following quotation from the historical introduction is of interest, as it
indicates the extent to which recognition is accorded homoeopathic pharmacy.
It is earnestly hoped that each and every medical college will hereafter include in its curri-
culum, instruction in the principles and practice of pharmacy. The physician who dispenses
medicine should at least be qualified to supplement the work of the professional pharmacist
so thoroughly and accurately that his clinical reports will have a scientific value. Pharma-
ceutical knowledge seems to be even more important to the homoeopathic than to allopathic
practitioners, for the reason that only a portion of the former are within easy reach of the
professional pharmacist who understands the preparation of medicines for homoeopathic use.
The great bulk of the book of 674 pages is divided into three parts. Part I,
of some 30 pages, is devoted to General Pharmacy, under which the following
subjects are treated : Unit of Medicinal Strength, Menstrua, Drugs and Medi-
cinal Substances, General Treatment of Drugs, Preparations from Drugs,
Tinctures, Dilutions, Triturations, Medications, Prescriptions.
Am. Jour. Pharm. ) f?/>'7frp'-nt f\Ar\
December. 1897 ) /\e7't^tUS. O49
Part n is devoted to Si>ecial Pharmaceutics, and occupies some 545 pages.
In this section the various medicinal substances are taken up in alphal>etical
order, and considered somewhat as they are in the U. S. Pharmacopoeia, but in
some respects rather more fully, which gives the book a resemblance to a
dispensatory. For instance, the first article, Abies Canadensis, is treated under
the following heads : Natural Order, Synonyms. Description, Habitat, History,
Parts Used, Preparations. The last heading embraces the tincture and method
of preparing it.
Acidum Aceticum and other chemical substances and compounds are treated
under the following headings : Chemical Symbol, Synonyms, Description
Preparations. Many of the physiologically active metallic salts and alkaloids
have the maximum dose given.
Part in consists of some 25 pages of Select Tables for Reference, many of
which have been taken by permission from the U. S. Pharmacopceia; List of
Medicines and Pronunciation, 15 pages, and Index of over 50 pages.
The Section in Part I, on General Pharmacy of Drugs for Homoeopathic Use, is
a concise statement of the processes used in, and the principles governing
homoeopathic pharmacy, and any well-educated pharmacist would be able to
practise homoeopathic pharmacy after a careful reading of this part. A section
is devoted to cleanliness and cleaning of utensils, which contains directions con-
cerning that which has been one of the reasons for the existence of homcBO-
pathy. Every school of pharmacy and medicine should keep the subject of
cleanliness constantly before the students.
The first edition of a book having the scope of this one is sure to contain a
number of errors, and a few of these may be pointed out.
The term "chemical symbol" is used throughout the book where in most
cases "chemical formula" would be more in accordance with chemical nomen-
clature. In the German siiure, the umlaut is in nearly every instance placed over
the », making saure. The sweeping statement is made that tannic acid •* unites
with all vegetable alkaloids, forming whitish precipitates." which will not hold
true in the cases of morphine and caffeine. Petroleum ether and petroleum
benzin are given as synonyms of nitrobenzol, which is away off from the truth,
very misleading and liable to cause serious accidents.
In regard to the nomenclature in the book, it may be said to be a mixture of
ancient and modern systems; for example, in accordance with the reform spell-
ing movement, the final ^• is dropped from chloride, io<line and the alkaloids;
consequently we have in this case morphin acetate, in which the e is dropped
from morphine, where it is of use in distinguishing the alkaloid as a member
of its class, while it is retained in the acetate, where it is of no apparent us€.
We believe that this book has been compiled with a hope of removing the
veil of mystery which apparently surrounds honueopathy. but the di.sniissal
of a few substances like " Hahnemann's Causticuni " would remove both book
and school from the possible accusation of mysticism.
A Tkxt-Book OF Practical Thkrapki'TICS, with 8i)ecial reference to the
application of remedial measures to disease and their employment upon a ra-
tional basis. By Hobart Amory Hare, M.I)., H.Sc, Professor of Therapeutics
and Materia Medica in the Jefferson Me<lical College of Philadelphia. PhiU-
delphia : Lea Bros. & Co. Svo, Pp. 75S. Sixth edition.
The fourth edition of this valuable and practical work wan noticc<l in the
6E>-_,V^_.,- )' Am. Jour. Pharra.
50 KeVieWS. \ December. Ia97.
Ambric.vn JoURNAi, OK PHARMA.CY, 1894, p. 494. aud the good opinion then
expressed about it has been strengthened by a more intimate acquaintance with
it. We think that every pharmacist of the country would find it of advantage
to give it a place in his library.
An article of special interest is that on the Thyroid Gland, which is being
so extensively employed at the present time in treating myxoedema and cre-
tinism ; the statements made coincide with some of the experience of the
writer.
The statement that "Pilocarpine is so good a myotic as to be rapidly
supplanting eserine (physostigmiue) for this purpose with some clinicians,'
will be new to many.
The book is abreast of the day in treating of the newer remedies, such as
Eucaine Hydrochlorate (the synthetic substitute for cocaine), Formaldehyde,
Nuclein, Thiosinamine and Thymus Gland.
The article upon Diphtheria is a most interesting and valuable one. Profes-
sor Hare is strongly in favor of the antitoxin treatment.
It is probably an omission that in the article on Nux Vomica no reference is
made to the use of strychnine nitrate in the treatment of acute alcoholism.
C. B. U
Year-Book of Pharmacy. Comprising abstracts of papers relating to
pharmacy, materia medica and chemistry, contributed to British and Foreign
journals, from July i, 1896, to June 30, 1897, with the transactions of the British
Pharmaceutical Conference, at the thirty-fourth annual meeting, held at Glas-
gow, August, 1897. J. & A. Churchill. I^ondon. 1897.
The foregoing title sufficiently explains the scope of the Year-Book, and it
only remains to be said that this year's volume is fully up to the standard of its
predecessors. Its compactness is a valuable feature, which is obtained by the
elimination of all unnecessary matter.
Contributions from the Botanical, I^aboratory of the University
OF PennsyIvVANIA. Philadelphia. 1897.
This is the third and last number of Volume I, and contains the index to the
volume. The first number was issued in 1892. The present number consists
of about 160 pages of text and nineteen plates. The following subjects are
considered : "A Chemico-Physiological Study of Spirogyra nitida," by Mary
E. Pennington, Ph.D.; " On the Structure and Pollination of the Flowers of
Eupatorium ageratoides and Eupatorium ccelestinum," by Laura B. Cross,
Ph.D.; "Contributions to the Life-History of Amphicarpsea monoica," by
Adeline F. Schively, Ph.D. All of these give abundant evidence of creditable
research work.
L' Azote ET i.e Veg]§:tation ForestiERE. Par E. Henry, Charg^de Cours
a TEcole Forestiere. Pp.23. Nancy, France. 1897.
On the Mechanisms in Certain Lamei^libranch Boring Molluscs.
By Francis Ernest Lloyd. Pp. 17 and two plates. Reprinted from 77a7tsac-
/^«5 New York Academy of Science, August, 1897.
Semi-Annual Report of Schimmel & Co. Leipzig and New York. Oc
tober, 1897.
The novelties prepared and studied during the past six months were : Savory
^D^i^niberi^aS?!^'} Minutes. 631
oil, from Satureja hortensis, L. ; mountain savory oil, from Satureja montana,
I/.; balsam tansy oil, from Tanacetum balsamita, L.; and Xanthorrhoea j^um
oil, from Xanthorrhoea hastilis, R. B.; and some other species. There is also
much other information of value in the 88 pages that make up the pamphlet.
Index-Catalogue of the Library of the Surgeon-General's Office,
U. S. Army. Second Series. Vol. II. B to By water. Government Printing-
OflSce. Washington. 1S97.
MINUTES OF THE PHARMACEUTICAL MEETING.
Philadf.lphia, November 16, 1897.
The regular Pharmaceutical Meeting was held at 3 p.m., with J. W. England
in the chair.
The minutes of the last meeting were allowed to stand as published.
Dr. John W. Harshberger, of the University of Pennsylvania, favored the
audience with an address on the " Vegetation of the Yellowstone Hot Springs,"
which was not only highly scientiSc, but at the same time replete with vivid
descriptions of the numerous phenomena which delight the naturalist in our
National Park in Wyoming.
In closing, the speaker fittingly indulged in speculation concerning the origin
of life on the earth, and asked the question whether the facts he had presented
did not point to hot springs as the origin of primeval organisms.
In replying to a query as to the medicinal virtues of the water of the hot
springs, Dr. Harshberger said that he believed they were attributed to the inor-
ganic constituents.
The chairman remarked that he had been of the opinion for some time that
the efficacy of many of the so-called medicinal waters depends more upon their
purity than upon the amount of mineral salts, inasmuch as these are present in
very small proportion.
Dr. C. B. Lowe coincided with this view and attributed their usefulness to a
mechanical action rather than to any intrinsic (qualities.
Charles H. LaWall communicated some analytical data which he had
obtained during the year, in a paper entitled '* Laboratory Notes."
Replying to a question concerning the use of Japan wax, Mr. La Wall said
that it is used in the laundry business and also for making pomades.
Prof. Henry Trimble presented a paper on " Pomegranate Rind." In com-
menting upon the quantity of tannin present in this substance, he said that 40
percent, had l>een reported in the wild variety. A number of the Spanish
fruits were exhibited, and those who had never eaten of them were given an
opportunity of testing the merits thereof
Dr. Harshberger remarked that in Mexico the pulp of this fruit is used for
giving a red color to different kinds of drinks.
Having recently been engaged in an examination of willow oak (Qucrcui
Phcllos), Prof. Trimble called attention to the leaves and acorns of this plant,
and also to the leaves of Quercus imbricaria, to show the difference in Appear-
ance of these two species. In the course of his remarks, he alluded to the in-
terest which Prof. Procter had taken in Quercus heterophylla, Bartram's oak,
some thirty-odd years ago.
652 Notes and Neivs — Obituary. {
Am. Jour. Pharna.
December, ls97.
Some cabinet specimens were presented as follows :
Samples of monobromated camphor and salol by Mr. La Wall, and a handsome
specimen of metallic bismuth by Mr. Harry B. French.
On motion, the meeting adjourned.
T. S. WiSGAND,
Registrar.
NOTES AND NEWS.
Formaldehyde may, in the near future, become of considerable industrial
value in addition to the use it already has in medicine. Prof. C. S. Dolley has
recently secured a patent for its use in the manufacture of leather. Hides or
skins, prepared in the usual way for tanning, are subjected to the action of for-
maldehyde of a strength gradually increasing from 3 to 10 per cent. About one
hour's treatment completes the process. Or the hides are exposed in a closed
chamber to gaseous formaldehyde, either by itself or in conjunction with
aqueous or alcoholic vapors.
The Plant IVorld is a new monthly journal of popular botany. The first
number was issued October ist, and contains papers on " The Sword Moss," by
Elizabeth G. Britton ; "The Families of Flowering Plants," by Charles
Ivouis Pollard; "Sensitiveness of the Sundew," by F. H. Knowlton ;
" Ferns of the Yosemite and the Neighboring Sierras," by S. H. Burnham;
"Some Sand-Barren Plants," by Willard N. Clute ; Editorials, Notes and
News. F. H. Knowlton, Ph.D., of the U. S. National Museum, Washington,
D. C, is editor-in-chief, assisted by six associate editors, all well-kuown writers
on botanical subjects. Willard N. Clute & Co., Binghamton, N. Y., are the
publishers.
OBITUARY.
Prof. Dr. Lt. A. Buchner, who, during a long and honorable career, was identi-
fied with the sciences of medicine and pharmacy, died at Munich, October 23d,
in the eighty-fifth year of his age.
He was the son of Prof. Johann Andreas Buchner, the founder of scientific
pharmacy in Germany, and naturally followed in the footsteps of his distin-
guished father. He served his apprenticeship in Niirnberg, after which he
studied iu Munich, Paris and Giessen. In 1839 ^^ received the degree of Doctor
of Philosophy, and in 1842 graduated in medicine. Later became a member
of the Medical Faculty of the University of Munich, and in 1852 was named
Professor of Pharmacy and Conservator of the Pharmaceutical Institute. In
1871 Buchner was appointed a member of the Berlin Commission for composing
the German Pharmacopoeia, on which he wrote a very complete commentary.
In addition to much other literary work he was, after his father's death, editor
of the Repertoriumfur Pharmacie for twenty-five years.
The deceased was highly esteemed by his associates, and his kindly interest
in the welfare of his students earned for him the title of '* Vater Buchner.'»
He was the possessor of several honorary titles, and was a corresponding mem-
ber of the Philadelphia College of Pharmacy.
I
J
INDEX
TO VOLUME 69 OF THE AMERICAN JOURNAL
OF PHARMACY.
Acacia of commerce, observations on (^VrAro^i/fr) 195,223
Senegal, decline in use of 223
Acetanilid, ammoniated, formula of 152
Acetic anhydride, use of, in oil analysis 189, 222
Acetone, keeping qualities of 66
some literature on 73
volumetric estimation of ( AV^/^t) 65, 118
"Acetracts," preparation of 122
Acid, acetic, as a menstruum and solvent (/?^w/«^/£>«) 121, 164
acetic, as a preservative and solvent 253
benzoic in the preser\ation of ointments 258
boric, fungoid growths in solutions of 256
caffetannic, decomposition of 641
formula of 640
carbolic, as a preservative for hypodermic solutions . . 257
carbonic, inhibitory action of 257
cinnamic, in the treatment of tuberculosis 645
citric, by fermentation of carbohydrates 550
citric, color reactions of 215
manufacture of . . 646
gelsemic [Coblcntz) 439
gelsemic, investigation oi yCoblentz) . 228
hypophosphorous, use of, as a preservative 257
isoirachylolic, presence of, in Zanzibar copal 156
lactic, manufacture of {Claflin) 599
malic, color reactions of 215
phytolaccic, supposed constituent of fruit of Phytolacca decandra and
P. Kaempferi . 282
pyrethrotoxic, principle found in C. caucasicum 362
salicylic, use of, as an antiseptic 254
sulphurous, as a preservative . 256
tannic, percentage of, in kino of Eucalyptus rostrata 3
tartaric, color reactions of 215
trachvlolic, constituent of Zanzibar copal 155
valerianic, in whiskey 583
Alcohol as a preservative 251
in the titration of alkaloids {Caspari) 42
method for <lctermination of morphine . . 344
methyl, use of, for pharmaceutical preparations 489
question, the, common sense on 213
therapeutic properties of [Davis) .... 516
Alkaloids, mydriatic, present knowledge of 463
Alkanet root {//olnws) 446
Alkyl bismuth iodides 486
Almanac. Datent me<licine ... 5*
Alpers, William C, and B. L. Afutrav. Aralia nudicaul:^ . . 534
American Me<lical Association, annual meeting 261, 373
Pharmaceutical Association 467
(6531
f^c A fv/ffT f Am. Jour. Pharm.
t)54 inutA,, I December. 1897.
Ammonol, analysis of [Beritiger) 150, 165
Audromedotoxin, isolation of 341
Anisol, use of, for separating codeine from morphine 158
Antiseptics, surgical, and dressings 609
Aqua pura. suggestion concerning 212
Aralia nudicauiis (/4//>^;.? and i)/?(trrrtj/) . . .487, 534
Arkansas Association of Paarmacists 326
Amy, H. l\ Parthenium hysterophorous 169, 222
Arsenic, soluble compounds of 461
Artemisia tridentata, Nutt. (See sage brush) 152
Asclepias curassavica, as in insectifuge 640
Ash, estimation of, in various drugs (La Wall) 137, 165
"Asafetida," spelling of 460
Atomic weights, report on ........ 321
Aitfield, Professor, testimonial to 219
Bacilli, exhibition of slides and cultures of 53
Bacillus acidi lactici, description of 599
Bacteriology for pharmacists 485
Balance, micrometer, the 165
Balsam copaiba, requirements for 578
Bandoline, wood, Chinese 642
Barium platino cyanide, preparation of 49
Bastin, Edson Sewell, memoir of 261, 385
and H. Trimble. North American coniferae 90, 354
Bates, John P. Liquor potassse and liquor sodae 240
Benzom, Sumatra, pharmaceutical value of 461
Benzoyl-ecgonine. formation of . . . 258
Beringer, Geo. M. Analysis of ammonol 150, 165
Blumea balsamifera, camphor of 515
Bosislo, Joseph. Kinos 533
Botanical Garden at Buitenzorg 452
Botany, field, in winter 115
Breithaupt, A. P. Structure of leptandra 235
Brimstone in Sicily 420
British Pharmaceutical Conference 459
Broniwell, JVm., and J. L. Mayer. Identifying fats and oils 145
Burdock as a vegetable ( AHtobe) 416
Cadmium, demand for 646
Calomel, corrosive sublimate in (A'<?<5'/6'r) 338
Camass, food plant of Indians . 159
Camphor, Borneo, source and value of 515
production of, in China {Henry) 259
tree, the [Dewey) 507
turpentine. (See Terpin hydrate) 73
water, disadvantages of, as a preservative 256
Canaigre root, cultivated, samples of 118
Carslens, Louis P. Analysis of the bark of honey locust 40
Caspari, Chas.,Jr. Alcohol in the titration of alkaloids 42
Castanopsis, description of Indian species of 408
tannin of ( Trimble) . 406
Ceratum plumbi subacetatis, preparation of 575
CeriopsCandolleana, tannin of ( 7>zw<^/^) 505
Cerium oxide, percentage of, in monazite 609
Chemicals, C. P., purity of 352
Chemistry as applied to industrial arts 410
gradations of * 408
Cherry laurel water as a preservative for hypodermic solutions 257
Chloral hydrate as an antiseptic 257
Chloroform, analysis of ] 114
Am. Jnar. Pbaruj. ) T>t,-td>y f^" r
December. 1«^. / ITliltX. O33
Chloroform as an antiseptic for pharmaceutics! preparations
256
Chlorophyll, function of. in growth of foliage leaves iii
Cinchonacultivation in lienpal ... 47
powdered, inferior quality of . . . . . 492
Ctnchonine. alleged conversion of, into cinchonidine . . 215
Cinnamomums, the, of New South Wales 616
Clajiin, Alan A. Manufacture of lactic acid 599
Cloves, duty free in France .... 610
Cnicus altissimus, fasciated stem of . . 23
Cob/entz, Virfiil. Gelsemic acid . . 228, 439
Coffee, assay process for . . 350
Codeine, separation of, from morphine 158
Colchicum plant, specimen of 613
Cold cream, criticisms on 382
Commclinaceae, some members of. (See Yerba del Polio) 290
Compensation, professional 45
Compton, Richatd Ilal. Valuation of liquor iodi compositus 242
Congresses, international [Ronington) 553.614
Cotiium maculatum, action of active principles of 460
maculatum. pharmacy of 460
Contributions, meritorious 51
Cooley, Grace E. Official Prunus virginiana 414
Copaiba balsam and gurjun balsam {Kehler) 577, 614
Copal. Zanzibar [Stephan) 154
Copper nitrate and silver nitrate, separation of . 156
.Cork, -\lgerian, production of 41
Cownlry, A. /. and R. H. Paul. Pilocarpine hydrochloride ro8
Crayons, antiseptic 609
Crvsanthemum caucasicam and C. cinerariiefolium, value of, as insecticides 3^9
Cutch extraction 371
I>atunL' albie, fl ores, assay of ( A^7^r/r'0<?r/) 142
Davis, X. S. Therapeutic properties of alcohol 516
Designs, curious, in nature . 45
Dewar, J. si\u\ //. Afoissati. Liquefaction of fluorine 366
Dewry, Lysler H. The camphor tree 507
Digitalis, active principle of {Keller) 450
Digitoxin. estimation of 450
Dipterix o<lorata. Willd.. source of tonka beans 157
Drugs, examination of powdered vegetable ( AV^m^r) 523
proportion of active principle in • . . 464
Durrani, Gcoti^e RewoUis. Insect powders of commerce 359
Editorial 51, 115. 161. 217, 261, 323, 373, 427, 547, 611, 647
Etnanufl, Louis. Petrolatum v^. vaseline 21
England, Joseph H\ Fermented and distilled liquors . . s?o, 614
Note on red mercuric oxide 311, 328
Ointment of mercuric nitrate 209
Esters, report on 223
FHhirs, pharmaceutical 461
Kucaine. properties of J4
Eucalyptus rostrata. (See Murray red jfum) . i
Euonvnius. microscopical examination of .wj
Experience in pharmaceutical education ^SI
Extracts, fluid (' Thompson) ».S^
fluid, in the manufacture of galenicals . 98, 118
Fats an<l oils. metho<l for identifying {/iromwell and Afayrr) 145
Ferric phosphate, soluble, preparation of 494
Flora, medicinal, .'\meriran 42 ^
of Bushkill Falls, the .... 3.S0
6,/- T-nf^/r-r / Am. Jour. Piiarni.
^D inaex^ | December. 1897
Flora, Scottish 462
Fliickiger Medal, award of 550
Fluorine, liquefaction of (7J/ioma« and /^(fZi/ar) 366
Food adulteration, investigation of 611
plants, native, of the Coeur d'Alene Indians 159
Formaldehyde, applications of, as a preservative 257
detection of 180
generator, Moffatt 223, 328
industrial value of 652
Frangula and cascara barks {Sayre') 126
Frankforter, G. B. Chemical study of Phytolacca decandra 134
Siwdi F. Ramaley. Root of Phytolacca decandra 281
Fruits and juices 46
native, used by Coeur d'Alene Indians 160
Fungi, presence of, in Johore gambier 156
Gambier, Johore, assay of 156
Garlic, wild, note on 224
Gauze cloth, sample of 53
Gelsemium, analysis of (6(2y?'(?) 234, 280
rhizomes, roots and stems {Sayre) 8
Ginyer, commercial, and essence of ginger 320
Ginseng, production of, in Corea 551
Gleditschia triacanthos. (See locust) 40
Glycerin, applications of, in pharmacy 251
Glycine hispida, source of soy bean 585
Gold and silver in sea water 50
Goulard's extract, modification of 563
Guarana, assay process for 350
Gurjun balsam, detection of . 577
Ha^er, Hennann^tn^moir oi {Hoff7nann) 160, 182
Hahn, Edward T. Preparation of terpin hydrate 73, 118
Harshberger, John W. Vegetation of the Yellowstone Hot Springs . . . 625
Hanbury Medal, award of 432
Hart, J. H. Shaddock or grape fruit 181
Hiussmann, Frederick W. Examination of official lead preparations 559, 613
Heat and cold, influence of, on micro-organisms 258
Hellebore, white, estimation of alkaloids in 351
Heloderma suspectum, Cope, venom of (^(2«/<?.y5<3«) 391
Henry, Augustine. Camphor in China . 259
Herbs and simples 409
Herrera, Alfonso. Verba del Polio 290, 327
Hoffmann, Fred. Memoir of Hermann Hager 182
Holmes, E. M. Alkanetroot 446
Cultivation of sumbul in England 314
Strophanthus Nicholsoni 520
Homoquinine, reaction of 215
Hooper. David, Personal 297
Hydrastine, soluble compound of (A^(?r/(7« and 7V<?z«/wa«) 604
Hydrogen peroxide, preparation of 641
Hyoscine-scopolamine question {Merck) 593
Hypophosphiles, tests for 462
Indicators, report of committee on 477
Insect powders of commerce [Durrani) 359
International Pharmaceutical Congress, eighth > 464
Iodine manufacture in Japan 48
Iodoform reaction for acetone 65
Johnson, Charlton G. Microscopical examination of Solanum Carolinense, 76
Am. Jour. Pbarm. ) fur/^-Y- f\CT
December, ls87. / inoex. U^/
Kalmia latifolia, analysis of root {Matusow) 341
KebUr, Lyman F. Balsam copaiba and gurjun balsam 577, 614
Corrosive sublimate in calomel 338
Estimation of menthol 189, 222
Pure spermaceti 104
Volumetric estimation of acetone 65, 118
and C. //. La Wall. Presence of starch and strontium in opium, 244, 280
Keller, C. C. Active principle of digitalis 450
Kessler, Lawrence A. Assay of spirit of nitrous ether 307
Kilmer, F. B. Modern surgical dressings 24, 53
Kino of eucalyptus rostrata 2
Kinos [Bosisto) 533
Kobt'rt, R., Professor Dr. Personal 160
Kola, assay of, by method of Carles 4>^4
assay of, by method of Jean 483
assay process for . 350
caflfeine compound in 481
Kolatannin, preparation and properties of 481
Krt^fner, Henry. Kxamination of powdered vegetable drugs 523
The pharmacist and the microscope 39^
Laboratory notes (/.a /f^a//) 619,651
and processes [La Wall) 350
Lactophenin, medicinal properties of 546
L^minaria digitata, use of stems of, in surgery .... 609
La Wall, Charles H. Adulterated Japan wax 18, 54
Estimation of ash in various drugs 137, 165
Laboratory notes 619, 651
Ointment of mercuric nitrate 232, 280
Processes and laboratory notes 350
and L. F. Kcbler. Presence of starch and strontium in opium . . 244, 280
Lead acetate of commerce 568
preparations, official I //rtMi.rwa««) 559.613
Leptandra, structure of [Breithaupt) 235
Lichens used as food by Cccur d'Alene Indians 160
Licorice root, commercial sources of {Rittenhouse) 13. 54
grown in N. S. W 643
Lime, chlorinated, in zinc containers 381
Liquor bismuthi et ammonii citratis 463
iodi com positus, valuation of (0^;w^/<7w) 242
plumbi subacetatis, preparation of 560
plumbi subacetatis dilutus, preparation of 567
potassx' and li(juor sodie {Bates) ... 240
Liquors, fermented and distil le<l (Zf«^/a//^) 580,614
Litharge, commercial ... 572
Lithium oxide, percentage of, in lithrophilite and amblygonite 609
Locust, honey, analysis of bark of ( Ozri/<'«5 ) 40
Loezv, Oscar, return of, to (Germany 55©
Lloyd, John Uri. Destruction of tobacco 557
Solnine note 108
The California manna . . 329
Lucium, exit of 5'
Maghee, Griffith IL Analysis of sage brush . 152,165
Magnesium sulphate, method for detecting zinc in . 522
Maiden, J. //. Murray red gum and its kino ... it54
Afaisch, Henry C. C. Estimation of sugar in urine . 294
Manna, California, the (Lloyd) 32Q
Marrubiin and its dichlorine derivative i Afatusou 2i»i, 223
dichloride, preparation and properties of 208
Marrubium, vulgarc, source of marrubiin 201
/r _ o /"m//^-*- /Am. Jonr Pharm.
050 inuex. \ December. 1897.
Marttndale, IVilliam. Preservatives of pharmacopoeial preparations . . 250
Afatusow, Harry. Marrubiin and its dichlorine derivative 201,223
Root of Kalniia latifolia 341
Medical Congress-, Pan-American (i'?<fwz«^/^«) '5.53
Mauniene's method of identifying oils 145
Mayer, Joseph L., 3.116. Wm. BromweU. Identifying fats and oils . . , . 145
Medicaments, new, report on 464
Medicine, study of, by druggists 381
Medicines of the Swampy Cree Indians of the North 493
Menthol, estimation of (A'(?<5'/<?r) 189,222
Merck, Louis. Hyoscine-scopolamine question . 593
Mercuric oxide, red, note on (i5"«^/a«^) 311,328
Metals, rare, in North Carolina 609
Mineral products of the United States 353
statistics of the United Stales for 1896 115
Minerals, samples of 613
Minnesota State Pharmaceutical Association 551
Moerk, Frank X. Notes on opium assaying 344
Moissati, H., andy. Dewar. Liquefaction of fluorine . 366
Monocalcium phosphate in combination with hydiastine 604
Morphine, estimation of 216
estimation of, by ash and lime-water methods 344,345
Morrhuol, preparation of 644
Mucilago acaciae, permanency of 488
Murray, Benjamin L.^islXs.^ W. C. Alpers. Aralia nudicaulis 534
Murray red gum and its kino (i)/a7V/<?w) i, 54
Myrrh, botanical origin of no
Nagelvoori, J. B. Flores daturae albse 142
resignation of 432
Naphtol, reaction for distinguishing the a and (i varieties 368
Newman, H. E., and T. H. Norton. Soluble compound of hydrastine . 604
New York State Pharmaceutical Association 326
Nitobe, Inazo. Burdock as a vegetable 416
North American Coniferae [Bastin and Trimble) 90, 354
Norton, T. H., and H. E. Newman. Soluble compound of hydrastine . (04
Nostrums, the evolution of 217
Notes and news 224, 432, 550, 615
Oak, the willow (7>/wd/^) 617,651
OhxiwdLxy— Allen, John C. 166 Robbins, Alonzo 167
Buchner, L. A 652 Roidoit, Athanase 616
Bower, Henry 166 Sachs, Julius von 4^2
Fresenius, Karl Remigius 431 Schacht, George Frederick 167
Mason, Alfred Henry . . 167 Simmonds, Peter Lund . . 616
Mattern, IVilliam Kline . 224 Trecul, Aufruste 166
Meyer, Victor 552 Trimen, Henry 166
Plugge, Peter Cornelio . . 426 Wormley, Theodore George t68
Odors, avoirdupois of ... 44
Ohio Pharmaceutical Association 2r9
Oil, citronella, commercial 461
clove, chemistry of 6^8
copaiba, tests for ^70
eucalyptus c
fusel, presence of, in whiskey 582
lovage, properties of 340
peanut, source, preparation and analysis of 490
sandalwood, tests for ... 224
spruce, composition of 90
Oils, recognition of, by Hehner and MitchelPs method 145
Ointment of mercuric nitrate (^«^/a«rf) 209
Am. Jour. Pharm,» /»////•> />Crt
December, 1W7 j UlilC^. '-'59
Ointment of mercur'c nitrate (Z-a /Ka//) 232,280
Oleoresin copaiba, req uremenis for 579
Opium assaying [Moerk) . . 343
presence of starch and strontium in (AV^/^r and La IVa/l) 244, 280
Orange groves of Naples . . 112
Organotherapy, observations on . . . . 460
Orris root, proximate analysis of ( /wiT/t^r) . . 199,222
Osyritin, glucoside isolated from Cape sumach . . 623
Palms, a collection of i6
Paraffins, soft, as preservatives 258
Pardformic aldehyde as an antiseptic 607
Papawjuice, collecting of 370
Papers read by title 547
Parthenicine, supposed existence of 169
Parthenin, isolation of '77
Parthenine, supposed existence of . . . 169
Parthenium hysterophorous, study of {Amy) .... 169, 222
Passion flower in epilepsy and other neuroses 320
Piiu/. B. // , and A. J. CownUy. Pilocarpine hydrochloride loS
Peiletier SLnd Caventou. Monument to 551
Pennsylvania Pharmaceutical Association 325, 378
Pepsin, digestive power of (6^vwr5 ) 636
Peptic action, artificial, on food substances 409
Percolates, device for regulating flow of ... 165
Perkiu, A. G. Coloring principles of tannin matters 622
Persicein. acid found in C. caucasicum .361
Persimmons. Japanese, samples of 613
Persiretin. acid principle found in C. caucasicum • 361
Petrolatum vs. vaseline {Emanuel) 21
Petroleum, medicinal 462
Pharmaceutical Congress, Eighth International 161
gatherings, notable 427
legislation and education 495
Pharmacist and the microscope, the (Kramer) 398
Pharmacopreia of potent remedies, report of committee on 466
Pharmacopcjeial preparations, preservatives of (^l/tzr/zw^/rt/^) 250
revision, influence of 465
Pharmacy, boiler shop 493
literature on 48, no, 156, 215, 320, 368, 546,607, 638
rocks and shoals of 382
science in . . . 480
Phenacetine, discussion of sale of 379
Philadelphia College of Pharmacy :
.Mumni .Association 275
Classes of 1896 97 . 55. 59. 61
C'lmniencement 272
Kxaminations 262, 264, 265
(iraduates 272
Minutes of Meetings . 278,431,615
New professors in 323
Officers and trustees elected .... 279, 43 », 615
Pharmaceutical meetings . 53, 118, 164. 222, 279. 327. 613, 651
Specimens presented . -53. 54. J'^. '^4. 222, 328.613,652
Philippium, discovery of . 3W
Phospiiates and platinum . 463
Phragmiles coninumis, sugar of ,VW
Phytolacca decandra. chemical studv o^ (Frank/or ter) • >4
root of { Frank forit'r Aw\ Ramalev) ^"^J
Phytolaccin, supposed constituent of Phytolacca decandra -84
Phytolaccine. suppose*! alkaloid of I'hytolacca tiecandra . 28^
x-yc Tnrli> 1- / •A^Di- Jour. Pharm.
(j(X) mat A. ^^ December. 1897.
Pills, Blaud's I7
ferruginous [^Thompson) I7> 54
Pilocarpine hydrochloride (/52«/ and (r«9Z«/w/<?>') io8
Pineapple, ash of _ 3^9
Pinite, saccharine principle from the manna of Pinus Ivambertiana . . 331
Piuus Lambertiana, manna of 331
Plant World, The 652
Piatt, Charles. The normal urine 411
Podophyllum, Indian, origin of 75
standardization of . . 488
Pomegranate Rind (7>m<{'/^) •• -^ 634,651
Potassium platino cyanide, preparation of 49
Powders, antiseptic . 610
Proprietary preparations, ethics and economics of • • 317
Prunus Virginiana, assay requirement for 488
oflficial \Cooley) 4^4
Pseudo-hyoscyamine, properties of 594
Query, a pertinent 381
Quicksilver, export of, in Russia ■ • • 114
Quicksilver, production of, in California 49
Quillaja, microscopical examination of 436
Rimaley, Francis, and G. B Frank forter. Root of Phytolacca decandra 281
Remington, Joseph P. Acetic acid as a menstruum 121, 164
International Congresses 553, 614
Pan-American Medical Congress I5) 53
Research Committee, second annual report of . 486
Resin copaiba, inadequate tests for 579
Resinous application for trees, solvent for 328
Resume of recurrent topics ( Thompson ) 44, 408
Retamine, a new alkaloid 644
Reviews — Allen, Alfred H. Commercial organic analysis 117
Altschnl, Julius. Reagents and reactions known by the names of their
authors 324
Antitoxins 378
Bailey, E. H. S., and C. M. Palmer. Salicylic acid and calcium sul-
phite as preservatives of cider 549
Baker, R. T., and H. G. Smith. On the presence of a true manna
on a " Blue Grass," Audropogon annulatus 430
Bolton, H. Carrington. Early American chemical societies 613
British and Colonial Druggists' Diary for 1897 52
Britlon, Nathaniel Lord, and Addison Brown. An Illustrated Flora
of the Northern United States, Canada and the British Possessions . 428
Brown, Addison, and Nathaniel Lord Britten. An Illustrated Flora
of the Northern United States, Canada and the British Possessions . 428
Bulletin, Imperial University, College of Agriculture, Tokyo, Japan . 378
Bulletin of the College of Agriculture, Imperial University, Japan . . 457
Bulletin of the Bussey Institution, Jamaica Plain, Boston 549
California College of Pharmacy, prospectus of the twenty-fifth annual
session of 118
California State Board of Pharmacy, fourth and fifth annual reports of 52
Chemists' and druggists' diary for 1S97 . . 52
Chestnut, V. K Some common poisonous plants 458
Clarke, Frank Wigs^lesworth. A Recalculation of the Atomic Weights 221
Complete Price List and Catalogue of Parke, Davis & Co 222
Contributions from the Botanical Laboratory of the University of
Pennsylvania . . ... • . . . . 650
Contributions from the U. S. National Herbarium. Vol. 5. No. i . . . 164
Coville, Frederick V. Notes on the plants used by the Klamath
Indians of Oregon 376
Am. Jour. Pharm. ) ftirf^ »- fif\ i
December, 1897. / lUaeX. ^ OOl
Reviews. — Creevy, Caroline A. Flowers of field, hill and swamp . . . 375
Denaeyer, A. La Composition des Peptones de Viande 118
Dethan, Georges. Des Acanthac^es M^dicinales 163, 261
Du/aii, J/. Quelques Oxydes Doubles Cristallis^s Obtenus a Haute
Temperature 377
Dulles, Chas. IV. Accidents and emergencies 457
Electro-Germination 164
Fernow, B. E. Age of trees and time of blazing determined by
annual rings 549
Formaldehyde 324
Frear, William. Cider Vinegars of Pennsylvania 549
Friedenzvald, Julius. The action of taka-diastase in various gastric
disorders 378
Geoffroy, Emtnanuel. Rapport de Mission a la Martinique et a
Guyane . 220
Hare, Hobart Amory. A text-book of practical therapeutics .... 649
Harshberger,John W. Natural history charts and illustrations. . . 325
Hartwich , Carl. Die neuen Arzneidrogen aus dem Pflanzenreiche 429
Meckel, ^douard. Les Plantes M6dicinales et Toxiques de la Guyane
Fran^aise ... 221
Henry, E. L' Azote et le V^g^tation, Forestiere 650
Hesse, O. Ueber Flechtenstoffe . 262,613
Zur PriifungdesChinins 325
Hirsch, B., and /. Stedler. Die Fabrication der Kiinstlichen Mineral-
wasser und anderer Moussirender Getriinke 220
Hiss, A. Emil. The standard manual of soda and other beverages . 375
Hofftnann,Fr. Popular German names of domestic drugs and medicines 1 17
Jackson, C. Loring, and W. R. Lamar. On certain derivatives of
trichlordiuitrobenzol 52
Index Catalogue of the Library of the Surgeon -General's Office, U. S.
Army 651
Journal of Pharmacology, The 164
Kahlenberg, Louis, and Rodney H. True. On the toxic action of dis-
solve<l salts and their electrolytic dissociation 163
Krcgjner, Henry. Viola tricolor, L., in morphilogischer, anatomischer
und biologischer Beziehung 262
Kunz-k'rause, Hermann. Kinfiihrung in das Studium der Alkaloide,
von Dr. Icilio Guareschi ... 116, 323
Lamar, li'. A'., and C. Loring Jackson. On certain derivatives of
trichlordiuitrobenzol 52
Leffmann, Henry. Hand-book of structural formuLx- 163
Leiberg, John B. General report on a botanical survey of the Coeur
d'Alene Mountains in Idaho, during the summer of 1895 163
Lloyd, F. E. On the mechanics in certain lamellihranch boring mol-
luscs 650
Lloyd, fohn Uri. The right side of the car 648
MacMillan, Conway. Minnesota l)Otanical studies 376
Maiden, J. //. Anniversary address before the Royal Society of New
South Wales ... 549
Michael, Helen Abbott. A review of recent synthetic work in the class
of carbohydrates 377
Mill spa ugh, Charles Frederick. Contribution II to the coastal and
plain flora of Yucatan 222
North Carolina and its resources ^19
Palmer, Charles M., and E. H. S. Bailey. Salicylic acid and calcium
sulphite as preservatives of cider 549
Papain, the vegetable pepsin, its origin, properties and U8c« 37*t
Petroleum, a series of papers on the origin and chemical composition of 377
Pharmaceutical Society of Great Britain, calendar of . . 164
Pharmacologist, The ... 5I5
Pharmacopu-Ma of the American Institute of Homrpopathy . ^i
/'/'_ /m///?*- f Am. Jour. Pharm,
002 inatX. \ December, 1897.
Reviews. — Physician's vest-pocket formula book, the 164
Planch on, Louis. Le Commerce Aciuel de I'Herboristerie dans une
Region du Languedoc 117
Les Drogues Recemment Inscrites au Codex 164
Observations et Experiences sur I'ouverture des fleurs de L'Oeno-
thera laniarkiana, Ser 261
Practical Druggist and Pharmaceutical Review of Reviews 164
Proceedings :
Ameiican Pharmaceutical Association 162
Florida State Pharmaceutical Association 458
Illinois Pharmaceutical Association 378
Louisiana State Pharmaceutical Association 431
Missouri Pharmaceutical Association 612
Ndlioual Confectioners' Association of the United States 430
North Cirolina Pharmaceutical Association , 163
South Carolina State Pharmaceutical Association 325
Virginia Pharmaceutical Association 222
Renisen, Ira. The principles of theoretical chemistry 52
Report of the Board of Managers of the Pennsylvania Hospital to the
contributors 613
Report of the committee appointed by the National Academy of Sci-
ences upon the Inauguration of a Forest Policy for the Forested
Lands of the United States, to the Secretary of the Interior .... 430
Pose, J. N. Contributions from the U. S. National Herbarium, Vol.
V, No. 3 549
Puddiman, Edsel A. Incompatibilities in prescriptions 456
Sajous, Charles E. Annual of the Medical Sciences and Analytical
Index 220
Schlagdenhauffen et Louis Planchon. Sur un Strophanthus du Congo
Fran9aise 548
Semi-Annual Report of Schimmel & Co 52,325,652
Siedler, P., and B. Hitsch Die Fabrication der Kiinstlichen Mineral-
wasser und andtrer Moussirender Getranke 220
Smith, Henry G. On the constituents of the sap of the " Silky Oak,"
Grevillea Robusta, R, Br., and the presence of butyric acid therein 262 .
The dveing properties of aromadendrin and of the tannins of Euca-
lyptus kinos 262
and R. T. Baker. On the presence of a true manna on a " Blue
Grass," Andropogon annulatus 430
Southiuorth, Thomas. Annual report of the Clerk of Forestry for the
Province of Ontario 612
Tassilly, Eugenie. Sur le Dosage de la Caffeine 377
Thorp^ Erank Hall. Inorganic chemical preparations 52
Thresh, John C. A simple method of water analysis 162
Trelcase, William, Medical botany 549
Mis<Jouri botanical garden, report of 612
True, Rodney H. Native drugs of Ceylon 163
and Louis Kahlenberg. On the toxic action of dissolved salts and
their electrolytic dissociation 163
Warner's pocket medical dictionary of to-day 324
Werner, D. 7. Ueber Isomere Menthylamine und Menthene . . 430
Wilcox, Rey?iold W. Strophanthus : a clinical study 325
Wilder, Hans M. Digest of criticisms on the United vStates Pharma-
copoeia ... 221
Wiley, Harvey W. Principles and practice of agricultural analvsis . 162
Wright, John S. A guide to the organic drugs of the United States
Pharmacopoeia 52
Year-book of treatment for 1897 220
Year-book of Pharmacy 650
Rhamnus purshiana, R. frangula and R. Californica, distinction of, in pow-
r 126
Am.Jour. Pharno.) huifr fJ\i
December. 1887. / inutx. 003
Rittenhouse^ H. N. Commercial sources of licorice root 13, 54
Sage brush, analysis of {Maghce) 152, 165
Sanxuinaria, standardization of 488
Satilesson, C. C. Veuom of Helo<ierma suspectum, Cope 391
Sdrsdparilla, quillaja and senega, standard requirement for 488
SayrCy L. E. Alexandria and India senna 298
Analysis of gelsemium 234, 2:10
Consiiiueuts of taraxacum root 543
Distinction of senega, euonymus and quillaja in the powdered state . 433
Frangula and cascara barks 126
Gelsemium .... 8
Scaramony, note on a sample of {'Iliomson) 313
Schroeder, J. Henry. Observations on acacia of commerce 195
Senega, euonymus and quillaja, distinction of, in powder {Sayre) .... 433
microscopical appearance of Northern and Southern varieties .... 433
Senna, Alexandiia and India [^Sayre) 298
Serpents, action of bile of 550
Shaddock or grape fruit {Hart) 181
Shoemaker, Robert, memoir of 225
Silva of North America, tenth volume of 54
Silver in sea-water 50
Soaps, disinfectant 463
Solanum Caroliiiense, determination of alkaloids of 640
microscopical examination of {Johnson) 76
microscopical and chemical study of ( TTrrttiA) 84
Solnine note ( A/cj^ ) 108
Soy bean ( Trimble) 584
Sp>ermaceii. examination of samples 53
y\xr^ [k'ebler) 104
Spirit of nitrous ether, assay of (AVw/^r) 307
Starch, presence of, in opium 244
Stephan, A. Zanzibar copal 154
Strontium, occurrence of, in plants ( TVi'w^/^) 296,327
presence of, in opium 244
sulphide, phosphorescent 6o7
hydrate in sugar refining -^iS
Stroph inthus, assay requirement for 488
Ni'holsoni [Holmes) 520
SuV>stitutiou 217
Sugar as a preservative 253
cane, synthesis of (^
maple, protiuction of 50
milk, .American 161
Sum^ul. cultivation of. in Kneland [Holmes) 314
Surgical dressings, modern {Kilmer) 24, 53
Symes, C. Digestive power of pepsin d^b
Syrup of garlic, obsoleteness of 488
Syrupus acidi hydriodici, suggestions concerning 488
eucalypti rostrati, sample of 54
ferri quinime et strychniniL- phosphatis 461
Tannin, hemlock, properties of g«
in plants, function of 5^2
matters and coloring principles ( /^r>t/«) 522
Taraxacer in, waxy sul)stance found in taraxacum c 4 »
Taraxacum root, constituents of iSayre) 404 cj,
Terpin ludrate, preparation of {Hahn) -V 118
samples of .118
Theobromine, determination of, in cacao ii.
Thiol, advantages of, over ichthyol ^5
^^ Tyi^r,^- r Am. Joar. Pharm.
004 inaex. \ December. I897.
Thompson, Win. B. Commercial ferruginous pills 17. 54
Fluid extracts 153
Resiling of recurrent topics 44, 408
Thomson,!. W. Note on a sample of scammony 313
Thrush, M. Clayton. Microscopical and chemical study of Solanum Caro-
lineuse 84
Tiuctura moschi, preparation of 489
Tincture of iodine, keeping qualities of 492
opium, variability of strength of 492
Tinctures, alkaloidal, strength of 463
Tobacco, destruction of {Lloyd) 557
Tonca beans, exports of, from Venezuela 598
information concerning 157
Tribuna Farmacdutica, publication of 615
Trimble, Henry. Occurrence of strontium in plants 296, 327
Pomegranate rind 634, 651
Tannin of castanopsis 406
Tannin of Ceriops candoUeana 505
The soy bean 584
The willow oak 617, 651
and E. S. Basiin. North American Coniferae 90, 354
Tsuga Canadensis, chemical composition of 90
Caroliniana, general characters and composition of 358
Mertensiana, description and composition of 354
Tucker, S. Allen. Proximate analysis of orris root 199, 222
United States Pharmacopoeia, report of committee on revision of ... . 488
Uranium, percentage of, in gummite 609
platino cyanide, preparation of 49
Urine, estimation of sugar in (./l/a/j^^) 294
normal [Piatt) 411
Vanillin, admission of, to Pharmacopoeia 488
Vaseline, evolution of 22
Veratrine, formula and properties of 372
Veratrum, alkaloids of 372
Veronica Virginica, Linne, source of leptandra 235
Waters, aromatic and essential oils as preservatives 258
Wax, Japan, adulterated (Z«^<2//) 18, 54
Whalebone, artificial, preparation of 89
Wines for pharmaceutical preparations 492
Witch-hazel extract, chemical composition of 493
Yellowstone Hot Springs, vegetation of (//ar.sA/^<?r^^r) 625,651
Verba del Polio {Herrera) 290, 327
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