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Supelco

Imazamox

PESTANAL®, analytical standard

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C15H19N3O4
Número de CAS:
114311-32-9
Peso molecular:
305.33
MDL number:
MFCD03427427
UNSPSC Code:
41116107
PubChem Substance ID:
329754911
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

signalword

Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCD4338
BCCB5369
SZBF036XV
SZBD338XV
SZBA197XV

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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)
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)
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)
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
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)

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