Mutagenicity of halogenated and oxygenated three‐carbon compounds

Abstract

Four structurally related three‐carbon compounds, known for their antifertitity activity in the male, and the brominated derivatives of two of these compounds were tested for mutagenic activity by the Salmonella typhimurium test of Ames et al. In the presence of strain TA‐100, a base‐pair substitution detector strain, 1,2‐dibromo‐3‐chloropropane (DBCP), was the most active compound tested but required enzymatic conversion by S9 microsomal preparation to an active mutagen. Three of these compounds containing an epoxide group‐epichlorohydrin, epibromohydrin, and glycidol‐were highly active direct mutagens, not requiring S9 for activation, α‐Chlorohydrin was the least active compound tested; α‐bromohydrin was 40 times more active than its chlorinated analog. Epibromohydrin was only slightly more active than epichlorohydrin, but both were highly active. With both of the halogenated epoxides, S9 preparation caused a substantial decrease in mutagenic activity at every concentration tested. All six compounds showed dose‐related responsiveness for the base‐pair substitution detector strains used. However, they were relatively inactive against the frameshift detector strain of S. typhimurium, TA‐98. Glycerol, propylene glycol, and n ‐propanol, which are also three‐carbon compounds containing one or more hydroxy groups, were inactive when tested at high concentrations with strain TA‐100.