gone through that paper you found on evaporation of the nic salts a few times. great info!
a couple point's to elaborate on later.... the paper is about measuring the effective release of nicotine 'real time' with a gas chromatograph online monitoring. what happens to the constituents once things cool down?
also found this. (I like the old texts!)
I won't state the obvious.
Microchemical Identification of Harmine and Harmaline. J. F. H.
Amelink. (Pharm. Weekbl., 1931, 68, 221-229.)-The properties and reactions
of Merck’s preparations, (‘ Harmine ” and Harmaline,” are described. “ Harmine ”
is identical with banisterine hydrochloride, Cl,H1,0N,HCl.2H,0. The alkaloid
melts at 263” C. without decomposing. Harmine (the hydrochloric acid salt) is a
white crystalline powder; the solubility in water at 20” C. is 1 :40 and the solution
is slightly fluorescent. With sulphuric acid the solution is yellow with a green
fluorescence. With Frohde’s reagent it gives a yellow-brown colour, turning
green on heating; with Erdmann’s reagent a green colour, turning blue-green on
warming; with Marquis’ reagent a red-brown colour, turning violet on warming;
and with Wasicky’s reagent a yellow-brown colour which disappears on heating,
and, on standing, becomes red-brown again, then red, and, finally, purple. When
0.05 mgrm. of harmine per grm. weight of the animal to be tested is injected intravenously,
the first result is violent trembling, followed by cramp and death.
Harmaline gives the same result when 0.005 mgrm. per grm. body weight is administered.
The alkaloids can thus be identified physiologically. Chemical
identification is carried out, using the 8 reagents described in the previous paper
(abstract above). Harmaline, which is dihydro-harmine, melts (without decomposition)
at 238” C.