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
§ 306. =Colour Tests.=--=Fröhde’s reagent= is made by dissolving 1 part
of sodic molybdate in 10 parts of strong sulphuric acid; it strikes
distinctive colours with many alkaloids.
=Mandelin’s reagent= is a solution of meta-vanadate of ammonia in mono-
or dihydrated sulphuric acid. The strength should be 1 part of the salt
to 200 of the acid. This reagent strikes a colour with many alkaloids,
and aids to their identification. It is specially useful to supplement
and correct other tests. The following table gives the chief colour
reactions, with the alkaloids. (See also p. 55 for the spectroscopic
appearances of certain of the colour tests.)
METHODS OF SEPARATION.
§ 307. =Stas’s Process.=--The original method of Stas[325] (afterwards
modified by Otto)[326] consisted in extraction of the organic matters by
strong alcohol, with the addition of tartaric acid; the filtered
solution was then carefully neutralised with soda, and shaken up with
ether, the ethereal solution being separated by a pipette. Subsequent
chemists proposed chloroform instead of ether,[327] the additional use
of amyl-alcohol,[328] and the substitution of acetic, hydrochloric, and
sulphuric for tartaric acid.
[325] _Annal d. Chem. u. Pharm._, 84, 379.
[326] _Ib._, 100, 44. _Anleitung zur Ausmittel. d. Gifte._
[327] Rodgers and Girwood, _Pharm. Journ. and Trans._, xvi. 497;
Prollin’s _Chem. Centralb._, 1857, 231; Thomas, _Zeitschr. für analyt.
Chem._, i. 517, &c.
[328] Erdmann and v. Ushlar, _Ann. Chem. Pharm._, cxx. pp. 121-360.
COLOUR REACTIONS[329] OF CERTAIN ALKALOIDS.
[329] Caustic potash also gives characteristic colours with certain
alkaloids. Out of seventy-two alkaloids (using 0·5 mgrm.), the following
alone gave characteristic colours when fused with KHO:--Quinine,
grass-green, and peculiar odour; quinidine, becoming yellower and
finally brown; cinchonine, at first brownish-red to violet, with green
edges, later, bluish-green; cinchonidine, blue passing into grey;
cocaine, greenish-yellow, turning to blue, and then dirty red on strong
heating.--W. Lenz, _Zeit. f. anal. Chem._, 25, 29-32.
Public-domain text, read in full here on John Shaqi.
Reviews
Reviews
No reviews yet
Be the first to share your thoughts on this work.
Elsewhere in the archive
Join the Discussion
Join the discussion
Sign in to leave a comment or review.
Sign InorCreate an account