Poisons, Their Effects and Detection: A Manual for the Use of Analytical Chemists and ExpertsBlyth, Alexander Wynter
Science
Poisons, Their Effects and Detection: A Manual for the Use of Analytical Chemists and Experts
Blyth, Alexander Wynter
Poisons
[331] Dragendorff’s _Gerichtlich-chemische Ermittelung von Giften_, St.
Petersburg, 1876, p. 141.
I. The substance, in as finely-divided form as possible, is digested for
a few hours in water acidified with sulphuric acid, at a temperature of
40° to 50°, and this operation is repeated two or three times, with
filtering and pressing of the substances; later, the extracts are
united. This treatment (if the temperature mentioned is not exceeded)
does not decompose the majority of alkaloids or other active substances;
but there are a few (_e.g._, solanine and colchicine) which would be
altered by it; and, if such are suspected, maceration at the common
temperature is necessary, with substitution of acetic for sulphuric
acid.[332]
[332] When blood is to be examined, it is better to dry it, and then
powder and extract with water acidified with dilute sulphuric acid.
However, if the so-called volatile alkaloids are suspected, this
modification is to be omitted.
II. The extract is next evaporated until it begins to be of a syrupy
consistence; the residue mixed with three to four times its volume of
alcohol, macerated for twenty-four hours at about 34°, allowed to become
quite cool, and filtered from the foreign matters which have separated.
The residue is washed with alcohol of 70 per cent.
III. The filtrate is freed from alcohol by distillation, the watery
residue poured into a capacious flask, diluted (if necessary) with
water, and filtered. Acid as it is, it is extracted at the common
temperature, with frequent shaking, by freshly-rectified petroleum
ether; and, after the fluids have again separated, the petroleum ether
is removed, carrying with it certain impurities (colouring matter, &c.),
which are in this way advantageously displaced. By this operation
ethereal oils, carbolic acid, picric acid, &c., which have not been
distilled, besides piperin, may also be separated. The shaking up with
petroleum ether is repeated several times (as long as anything remains
to be dissolved), and the products are evaporated on several
watch-glasses.
RESIDUE OF PETROLEUM ETHER FROM THE ACID SOLUTION.
1. IT IS CRYSTALLINE. 2. IT IS AMORPHOUS. 3. IT IS VOLATILE,
with a powerful
odour;
_ethereal oil,
carbolic acid, &c._
A. _It is yellowish_, A. It is fixed.
and with difficulty
volatilised.
α. The crystals are α. Concentrated sul-
dissolved by concen- phuric acid dissolves
trated sulphuric it immediately--
acid, with the pro- violet, and later
duction of a clear greenish-blue.
yellow colour, pass- _Constituents of the
ing into brown and black hellebore._
greenish-brown.
_Piperin._
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