Enantioselective degradation of tebuconazole in cabbage, cucumber, and soils

Chirality. 2012 Feb;24(2):104-11. doi: 10.1002/chir.21030. Epub 2011 Dec 27.

Abstract

The enantioselective degradation of tebuconazole has been investigated to elucidate the behaviors in agricultural soils, cabbage, and cucumber fruit. Rac-tebuconazole was fortified into three types of agricultural soils and sprayed foliage of cabbage and cucumber, respectively. The degradation kinetics, enantiomer fraction and enantiomeric selectivity were determined by reverse-phase high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS) on a Lux amylose-2 chiral column. The process of the degradation of tebuconazole enantiomers followed first-order kinetic in the test soils and vegetables. It has been shown that the degradation of tebuconazole was enantioselective. The results indicated that the (+)-S-tebuconazole showed a faster degradation in cabbage, while the (-)-R-tebuconazole dissipated faster than (+)-S-form in cucumber fruit and the test soils.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biodegradation, Environmental
  • Brassica / metabolism*
  • Chromatography, High Pressure Liquid / methods
  • Cucumis sativus / metabolism*
  • Fungicides, Industrial / analysis
  • Fungicides, Industrial / metabolism
  • Fungicides, Industrial / pharmacokinetics
  • Kinetics
  • Reproducibility of Results
  • Soil Pollutants / analysis
  • Soil Pollutants / metabolism
  • Soil*
  • Stereoisomerism
  • Tandem Mass Spectrometry
  • Triazoles / analysis*
  • Triazoles / metabolism*
  • Triazoles / pharmacokinetics

Substances

  • Fungicides, Industrial
  • Soil
  • Soil Pollutants
  • Triazoles
  • tebuconazole