## Abstract 3‐Phenoxybenzyl [1R,cis]‐3–2(2,2‐dichlorovinyl)‐2,2‐dimethyl‐cyclopropanecarboxylate (I) and its [1R,trans]‐isomer (II) were labelled with carbon‐14 at C‐2 position of the dichlorovinyl side chain for metabolic studies. The stereospecific syntheses were achieved according to the reactio
Application of trans and cis isomers of p-nitrophenyl-(1R,S)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate to the assay of pyrethroid-hydrolyzing esterases
✍ Scribed by Peter W. Riddles; Herbert J. Schnitzerling; Patricia A. Davey
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 386 KB
- Volume
- 132
- Category
- Article
- ISSN
- 0003-2697
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✦ Synopsis
A continuous-rate assay for the detection of esterases which hydrolyze synthetic pyrethroids is described. The assay is based on the release of pnitrophenolate ion upon hydrolysis of the pyrethroid-like compound, trans-or cis-p-nitrophenyl-( lR,S)-3-(2,2-dichlorovinyl)-2,2dimethylcyclopropanecarboxylate, at pH 7.4 where spontaneous hydrolysis is not detected. The reagent is solubilized by 0.02% Triton X-100 in the presence of 1 .O% ethanol. A simple procedure for the synthesis and separation of the isomers is described. The application of the reagent to the assay of esterases which detoxify synthetic pyrethroids in the cattle tick Boophilus microplus is reported.
📜 SIMILAR VOLUMES
The analysis (separation and identification) of eleven C,H,, isomers is performed using coupled GC/MS with a 70 m glass capillary column containing a 2.5 pm thick film of P a 2 5 as stationary phase. Cryogenic €20, cooling improves the separations. The total analysis time is lees than 12 minutes. S