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Merck

34227

Supelco

Imazamox

PESTANAL®, analytical standard

Synonym(e):

2-(4-Isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-5-methoxymethyl-nicotinsäure, 2-[4,5-Dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-5-(methoxymethyl)-3-pyridincarbonsäure

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About This Item

Empirische Formel (Hill-System):
C15H19N3O4
CAS-Nummer:
Molekulargewicht:
305.33
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

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)

InChIKey

NUPJIGQFXCQJBK-UHFFFAOYSA-N

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Allgemeine Beschreibung

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

Anwendung

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.

Rechtliche Hinweise

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

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves


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Analysenzertifikate (COA)

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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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