METABOLISM OF TETRAMETHRIN ISOMERS IN RAT .2. IDENTIFICATION AND QUANTITATION OF METABOLITES

1. To examine the metabolic fate of (1RS, trans)- or (1RS, cis)-tetramethrin [3, 4, 5, 6-tetrahydrophthalimidomethyl (1RS, trans)- or (1RS, cis)-chrysanthemate], rat was administered a single oral dose of trans- or cis-[alcohol-C-14]tetramethrin at dose levels of 2 or 250 mg/kg. 2. The radiocarbon was almost completely eliminated from rat within 7 days after administration in all groups. C-14-recoveries (expressed as percentages relative to the dosed C-14) in faeces and urine were 38-58 and 42-58% respectively in rat administrated trans-[alcohol-C-14] tetramethrin, and in faeces and urine were 66-91 and 9-31% respectively in rat administered cis-[alcohol-C-14]tetramethrin. 3. Fourteen metabolites found in excreta were purified by using several chromategraphic techniques and identified by spectroanalyses (nmr and MS). Five sulphonate derivatives and three dicarboxylic acid derivatives were found. 4. The main metabolites were sulphonate derivatives in the faeces, and in the urine, alcohols, dicarboxylic acid and reduced metabolites derived from the 3,4,5,6-tetrahydrophthalimide moiety.