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Imazamox

PESTANAL®, analytical standard

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Synonym(s):
2-(4-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-5-methoxymethylnicotinic acid, 2-[4,5-Dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-5-(methoxymethyl)-3-pyridinecarboxylic acid
Empirical Formula (Hill Notation):
C15H19N3O4
CAS Number:
Molecular Weight:
305.33
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

COCc1cnc(C2=NC(C)(C(C)C)C(=O)N2)c(c1)C(O)=O

InChI

1S/C15H19N3O4/c1-8(2)15(3)14(21)17-12(18-15)11-10(13(19)20)5-9(6-16-11)7-22-4/h5-6,8H,7H2,1-4H3,(H,19,20)(H,17,18,21)

InChI key

NUPJIGQFXCQJBK-UHFFFAOYSA-N

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General description

Imazamox is an imidazolinone herbicide which acts by inhibiting acetohydroxyacid synthase activity.

Application

Imazamox may be used as an analytical reference standard for the determination of the analyte in environmental water samples, soil and in leaves of wheat plants 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

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Repr. 2

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Quantitative analysis of imazamox herbicide in environmental water samples by capillary electrophoresis electrospray ionization mass spectrometry.
Safarpour H, et al.
Journal of Chromatography A, 1036(2), 217-222 (2004)
Alterations induced by imazamox on acetohydroxyacid synthase activity of common bean (Phaseolus vulgaris) depend on leaf position.
Garcia-Garijo A, et al.
Pesticide Biochemistry and Physiology, 104(1), 72-76 (2012)
E Kathryn Barto et al.
PloS one, 6(11), e27195-e27195 (2011-11-24)
Allelopathy, a phenomenon where compounds produced by one plant limit the growth of surrounding plants, is a controversially discussed factor in plant-plant interactions with great significance for plant community structure. Common mycorrhizal networks (CMNs) form belowground networks that interconnect multiple
Ultrasound-assisted Extraction with LC-TOF/MS Identification and LC-UV Determination of Imazamox and its Metabolites in Leaves of Wheat Plants.
Rojano-Delgado AM, et al.
Phytochemical Analysis, 25(4), 357-363 (2014)
A simple and efficient method for imidazolinone herbicides determination in soil by ultra-high performance liquid chromatography-tandem mass spectrometry.
Kemmerich M, et al.
Journal of Chromatography A, 1412(2), 82-89 (2015)

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