Carcinogenic potential of chlorinated ethylenes. Tentative molecular rules

D. Henschler, G. Bonse, H. Greim

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Chlorinated ethylenes are activated in mammalian metabolism to oxiranes. Only those with asymmetric chlorine substitution are mutagenic (trichloroethylene, vinylidine chloride and vinyl chloride) whilst the symmetric molecules (tetrachloroethylene, cis and trans 1.2 dichloroethylene) are inactive in this respect. Thus, stability of the oxiranes (higher in the symmetric molecules, lower in the asymmetric ones) seems to be the important feature for the mutagenic, and possibly carcinogenic potential.

Original languageEnglish
Pages (from-to)171-176
Number of pages6
JournalIARC scientific publications
VolumeVol 13
StatePublished - 1976
Externally publishedYes

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