“Benzyl bromide” was also used during the early part of the war, usually mixed with bromoacetone. The material was not pure benzyl bromide, but the reaction product of bromine upon xylene, and should perhaps be referred to as “xylyl bromide.”
Pure benzyl bromide is a colorless liquid, boiling at 198-199° C., and having an odor reminiscent of water cress and then of mustard oil. The war gas is probably a mixture of mono- and dibromo derivatives, boiling at 210-220° C., and having a density at 20° C. of 1.3. The mixture of benzyl and xylyl bromides used by the Germans was known as “T-Stoff,” while the mixture of 88 per cent xylyl bromide and 12 per cent bromoacetone was called “Green T-Stoff.”
As in the case of the halogenated acetones, it is necessary to use lead lined shell for these compounds. Enamel and glass lined shell may be used and give good results. While they are difficult of manufacture, satisfactory methods were being developed at the close of the war.
“T-Stoff” may be detected by the nose in concentrations of one part in one hundred million of air, and will cause profuse lachrymation with one part in a million. It is a highly persistent material and may last, under favorable circumstances, for several days. While it is relatively non-toxic, French troops were rendered unconscious by it during certain bombardments in the Argonne in the summer of 1915.
A number of derivatives of the benzyl halides have been tested and some have proven to be very good lachrymators. The difficulty of their preparation on a commercial scale has made it inadvisable to use them, and especially inasmuch as bromobenzyl cyanide has proven to be such a valuable compound.
Bromobenzyl Cyanide
Bromobenzyl cyanide is, chemically, α-bromo-α-tolunitrile, or phenyl-bromo-acetonitrile, C₆H₅CHBrCN. It is prepared by the action of bromine upon benzyl cyanide.
Benzyl cyanide is prepared by the action of sodium cyanide upon a mixture of equal parts of 95 per cent alcohol and benzyl chloride. The benzyl chloride in turn is obtained by the chlorination of toluene at 100°. The material must be fairly pure in order that the benzyl cyanide reaction may proceed smoothly. The cyanide is subjected to a fractional distillation and that part boiling within 3 degrees (the pure product boils at 231.7° C.) is treated with bromine vapor mixed with air. It has been found necessary to catalyze the reaction by sunlight, artificial light or the addition of a small amount of bromobenzyl cyanide.
The product obtained from this reaction, if the hydrobromic acid which is formed is carefully removed by a stream of air, is sufficiently pure for use as a lachrymator. It melts from 16 to 22° C., while the pure product melts at 29° C. It cannot be distilled, even in a high vacuum. It has a low vapor pressure and thus is a highly persistent lachrymator.
Bromobenzyl cyanide is about as toxic as chlorine, but is many times as effective a lachrymator as any of the halogenated ketones or aromatic halides studied. It has a pleasant odor and produces a burning sensation on the mucous membrane.