Cooley's Cyclopædia of Practical Receipts and Collateral Information in the Arts, Manufactures, Professions, and Trades..., Sixth Edition, Volume ICooley, Arnold James
Science
Cooley's Cyclopædia of Practical Receipts and Collateral Information in the Arts, Manufactures, Professions, and Trades..., Sixth Edition, Volume I
Cooley, Arnold James
Formulas, recipes, etc.; Industrial arts -- Dictionaries; Technology -- Dictionaries
Sublime. Melt.
/----------\ /----------\
Sublime, melt and Fahr. Cent. Fahr. Cent.
MORPHINE } yield carbonaceous { 330° 165° 340° 171°
STRYCHNINE} residue. { 345° 174° 430° 224°
Melt. Sublime.
/----------\ /----------\
Fahr. Cent. Fahr. Cent.
ACONITINE } { 140° 60° 400° 204°
ATROPINE } Melt, change { 150° 66° 280° 138°
VERATRINE } colour, sublime, { 200° 93° 360° 182°
BRUCINE } and { 240° 116° 400° 204°
DIGITALIN } deposit carbon. { 310° 154° 310° 154°
PICROTOXIN} { 320° 160° 320° 160°
SOLANINE } { 420° 215° 420° 216°
_Selmi’s method of extracting poisonous alkaloids in forensic
investigations._ The alcoholic extract of the viscera, acidified and
filtered, is evaporated at 65° C., the residue taken up with water,
filtered to separate fatty matters, and decoloured by means of basic
acetate of lead, leaving the solution in contact with the air for 24
hours. It is then filtered, the lead precipitated by means of sulphuretted
hydrogen, and the solution after concentration repeatedly extracted with
ether. The ethereal solution is then saturated with dry carbonic
anhydride, which generally causes a precipitate of minute drops adhering
to the sides of the vessel, and containing some of the alkaloids. The
ethereal solution is then poured into a clean vessel, mixed with about
half its volume of water, and a current of carbonic anhydride passed for
about twenty minutes, which may cause the precipitation of other alkaloids
not precipitated by dry carbonic anhydride. Usually the whole of the
alkaloids present in the ether are thrown down by these means, but if not,
the solution is dehydrated by agitation with Barium oxide, and then a
solution of tartaric acid in ether added to the clear liquid, taking great
care not to employ excess of acid. This throws down any alkaloid that may
remain. In order to extract any alkaloids that may still remain in the
viscera, they are mixed with Barium hydrate and a little water, and then
agitated with purified amylic alcohol; the alkaloids may subsequently be
extracted from the alcohol by agitation with very dilute sulphuric acid.
A knowledge of the different solubilities of the alkaloids will be found
an important auxiliary in their analysis. The following is a summary of
the relative solubility of the most important of them. The figures denote
the number of parts of the liquid required for their solution:——
_Absolute alcohol._——Strychnine insoluble; brucine soluble.
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