High-performance liquid chromatographic-nuclear magnetic resonance investigation of the isomerization of alachlor-ethanesulfonic acid

Cardoza, LA; Cutak, BJ; Ketter, J; Larive, CK

HERO ID

5163868

Reference Type

Journal Article

Year

2004

Language

English

PMID

14753779

HERO ID 5163868
In Press No
Year 2004
Title High-performance liquid chromatographic-nuclear magnetic resonance investigation of the isomerization of alachlor-ethanesulfonic acid
Authors Cardoza, LA; Cutak, BJ; Ketter, J; Larive, CK
Journal Journal of Chromatography A
Volume 1022
Issue 1-2
Page Numbers 131-137
Abstract The metabolism of the acetanilide herbicide alachlor in soils leads to the formation of alachlor-ethanesulfonic acid (alachlor-ESA) as one of the major transformation products of this compound. The unique structure of alachlor and its metabolites allows the formation of two diastereomers (s-trans and s-cis) due to the hindered rotation of the amide bond connected to a rigid aromatic ring. Although these stereoisomers do interconvert by rotation about the amide bond, the rate of interconversion is slow allowing separation of the isomers on the chromatographic time scale. Once separated, the unique nuclear magnetic resonance signals of each isomer can be used to monitor the rate of isomerization. This paper reports the on-line separation and detection of the rotational diastereomers using high-performance liquid chromatography-nuclear magnetic resonance (HPLC-NMR) to efficiently measure the isomerization rate of alachlor-ESA.
Doi 10.1016/j.chroma.2003.09.034
Pmid 14753779
Wosid WOS:000187662700015
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword nuclear magnetic resonance spectrometry; kinetic studies; positional isomers; alachlor-ethanesulfonic acid; alachlor; pesticides