DESCRIPTION

General description

Benzyl thiocyanate undergoes regioselective bond dissociation during its electrochemical reduction in acetonitrile at an inert electrode[1]. It is added to stimulate the chlortetracycline biosynthesis during industrial fermentations[2]. It undergoes biotransformation into dibenzyl disulphide by Streptomyces aureofaciens[3].

Application

Benzyl thiocyanate was used to study the effects of various dietary compounds on the α-hydroxylation of N-nitrosopyrrolidine in male F344 rats in vitro[4].

Packaging

100 g in glass bottle