Metabolism of the methoxychlor isostere, dianisylneopentane, in mouse, insects, and a model ecosystem

Dianisylneopentane or 1,1-bis(p-methoxyphenyl)-2,2-dimethylpropane was metabolized largely by O-demethylation to form mono- and diphenol derivatives. Only a small percentage was degraded by α-hydroxylation and rearrangement. In the model ecosystem, dianisylneopentane reacted very similarly to methoxychlor, accumulating in fish to about the same extent and yielding a slightly higher ratio of polar to nonpolar metabolites. The neopentyl group proved to be approximately as stable in biological systems as the isosterically equivalent trichloromethyl group.