Identification of a New Sulfonic Acid Metabolite of Metolachlor in Soil

D. S. Aga,* E. M. Thurman, M. E. Yockel, L. R. Zimmerman, and T. D. Williams
U.S. Geological Survey, 4821 Quail Crest Place, Lawrence, Kansas 66049, and Mass Spectrometry Laboratory, University of Kansas, Lawrence, Kansas 66045
Environ. Sci. Technol., 1996, 30 (2), pp 592–597
DOI: 10.1021/es9503600
Publication Date (Web): January 29, 1996
Copyright © 1996 American Chemical Society
*

 Author to whom correspondence should be addressed:  e-mail address:  daga@qvarsa.er.usgs.gov; telephone:  (913) 832-3561; fax:  (913) 832-3500.

,

 U.S. Geological Survey.

,

 University of Kansas.

Abstract

An ethanesulfonic acid metabolite of metolachlor (metolachlor ESA) was identified in soil-sample extracts by negative-ion, fast-atom bombardment mass spectrometry (FAB-MS) and FAB tandem mass spectrometry (FAB-MS/MS). Product-ion fragments from MS/MS analysis of the deprotonated molecular ion of metolachlor ESA in the soil extract can be reconciled with the structure of the synthesized standard. The elemental compositions of the (M − H)- ions of the metolachlor ESA standard and the soil-sample extracts were confirmed by high-resolution mass spectrometry. A dissipation study revealed that metolachlor ESA is formed in soil under field conditions corresponding to a decrease in the concentration of the parent herbicide, metolachlor. The identification of the sulfonated metabolite of metolachlor suggests that the glutathione conjugation pathway is a common detoxification pathway shared by chloroacetanilide herbicides.

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History

  • Published In Issue January 29, 1996
  • Received for review May 26, 1995
    Revised manuscript received September 6, 1995
    Accepted September 6, 1995

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