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  • Mercapturic acid formation in the metabolism of propachlor, CDAA, and FLUORODIFEN (cas 15457-05-3) in the rat☆
  • Add time:08/21/2019         Source:sciencedirect.com

    When [14C]F3-FLUORODIFEN (cas 15457-05-3) (2,4′-dinitro-4-trifluoromethyl diphenylether), carbonyl-[14C]CDAA (N,N-diallyl-2-chloroacetamide), and carbonyl-14C-propachlor (2-chloro-N-isopropylacetanilide) were fed to rats, 57 to 86% of the 14C was excreted via the urine within 48 hr. Although very little radioactivity was excreted in the feces of CDAA-treated rats, 15–22% of the 14C was excreted in the feces of propachlor- of fluorodifentreated rats and an average of 8% of the 14C remained in these rats 48 hr after treatment. Oxidation of the 14C label to [14C]O2 was not a major process in the metabolism of these herbicides. The only major radioactive metabolite present in the 24-h urine of fluorodifen-treated rats, 2-nitro-4-trifluoromethylphenyl mercapturic acid, accounted for 41% of the administered dose of 14C. In the metabolism of CDAA, the corresponding mercapturic acid accounted for 76% of the dose; it was the only major metabolite present in the 24-h urine. In contrast, three major metabolites were detected in the 24-h urine of propachlortreated rats, and the mercapturic acid accounted for only 20% of the dose. The mercapturic acid of each herbicide was identified by mass spectrometry.

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