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Hepatic microsomal metabolism of 1,3-butadiene.

Xenobiotica; the fate of foreign compounds in biological systems (1982-02-01)
E Malvoisin, M Roberfroid
RÉSUMÉ

1. In rat liver microsomes, 1,3-butadiene was metabolized to butadiene monoxide, which was subsequently transformed into 3-butene-1,2-diol by microsomal epoxide hydrolase. 2. In the metabolism of butadiene oxide in microsomes, four metabolites were detected, namely two stereoisomers of DL-diepoxybutane, and two stereoisomers of 3,4-epoxy-1,2-butanediol. No meso-diepoxybutane was detected.

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Sigma-Aldrich
3,4-Dihydroxy-1-butene, ≥99%