Abstract
The main products of the metabolism of 7, 12-dimethylbenz[a]anthracene by rat-liver homogenates are the isomeric monohydroxymethyl derivatives. The syntheses of these compounds are described. Two phenolic products and 2 dihydrodihydroxy compounds were formed, but none of these appeared to have been formed by hydroxylation at the ''K region''. There was little evidence for the formation of a glutathione conjugate of the hydrocarbon. The monohydroxymethyl derivatives are products of the hydroxylation of the hydrocarbon in the ascorbic acid-Fe2+-oxygen model hydroxylating system.