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Supelco

Imazamethabenz-methyl

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C16H20N2O3
CAS Number:
Molecular Weight:
288.34
Beilstein:
8328238
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

description

mixture of isomers

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

COC(=O)c1ccc(C)cc1C2=NC(C)(C(C)C)C(=O)N2

InChI

1S/C16H20N2O3/c1-9(2)16(4)15(20)17-13(18-16)12-8-10(3)6-7-11(12)14(19)21-5/h6-9H,1-5H3,(H,17,18,20)

InChI key

FFCCBBNQPIMUJI-UHFFFAOYSA-N

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General description

Imazamethabenz-methyl is a pesticide used for selective control of grass weeds in wheat and wild oat. The mode of action involves inhibition of the enzyme activity of acetolactate synthase, involved in the synthesis of branched-chain amino acids.

Application

Imazamethabenz-methyl may be used as an analytical reference standard for the determination of the analyte in fruits and vegetables, soil and water samples by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Simultaneous enantiomeric determinations of acid and ester imidazolinone herbicides in a soil sample by two-dimensional direct chiral liquid chromatography.
Polo-Diez LM, et al.
Talanta, 144(1-2), 375-381 (2015)
Multiresidue method for the determination of pesticides in fruits and vegetables using gas chromatography-negative chemical ionization-triple quadrupole tandem mass spectrometry.
Dong J, et al.
Chromatographia, 74(1-2), 109-109 (2011)
Mechanism of wild oat (Avena fatua L.) resistance to imazamethabenz-methyl.
Nandula VK and Messersmith CG
Pesticide Biochemistry and Physiology, 68(3), 148-155 (2000)
Ultra-pressure liquid chromatography-electrospray tandem mass spectrometry for multiresidue determination of pesticides in water.
Gervais G, et al.
Journal of Chromatography A, 1202(2), 163-172 (2008)

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