<?xml version='1.0' encoding='utf-8'?>
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>E.M. Thurman</dc:contributor>
  <dc:contributor>M.E. Yockel</dc:contributor>
  <dc:contributor>L.R. Zimmerman</dc:contributor>
  <dc:contributor>T.D. Williams</dc:contributor>
  <dc:creator>D.S. Aga</dc:creator>
  <dc:date>1996</dc:date>
  <dc:description>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). Production 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.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1021/es9503600</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>ACS</dc:publisher>
  <dc:title>Identification of a new sulfonic acid metabolite of metolachlor in soil</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>