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37923

Supelco

Imazethapyr

PESTANAL®, analytical standard

Sinonimo/i:

2-(4,5-Dihydro-4-isopropyl-4-methyl-5-oxo-1H-imidazol-2-yl)-5-ethyl-3-pyridinecarboxylic acid

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120,00 €

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100 MG
120,00 €

About This Item

Formula empirica (notazione di Hill):
C15H19N3O3
Numero CAS:
Peso molecolare:
289.33
Beilstein:
7437150
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

120,00 €


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Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

CCc1cnc(C2=NC(C)(C(C)C)C(=O)N2)c(c1)C(O)=O

InChI

1S/C15H19N3O3/c1-5-9-6-10(13(19)20)11(16-7-9)12-17-14(21)15(4,18-12)8(2)3/h6-8H,5H2,1-4H3,(H,19,20)(H,17,18,21)
XVOKUMIPKHGGTN-UHFFFAOYSA-N

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Descrizione generale

Imazethapyr is an imidazolinone derivative[1] and a herbicide, which is selectively used on crops for weed control management.[2]

Applicazioni

Imazethapyr may be used as a reference standard in the determination of imazethapyr in soil samples using high performance liquid chromatography coupled with ultraviolet detector (HPLC-UV).[3]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Prodotti consigliati

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Note legali

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


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Certificati d'analisi (COA)

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Acephate

Weed control in pinto beans (Phaseolus vulgaris) with imazethapyr combinations.
Arnold NR, et al.
Weed Technology, 7(2), 361-364 (1993)
Effects of the herbicide imazethapyr on soil microbial biomass and various soil enzyme activities
Perucci P and Scarponi L.
Biology and Fertility of Soils, 17(3), 237-240 (1994)
Jacob S Montgomery et al.
Genome biology and evolution, 12(11), 1988-1993 (2020-08-25)
Amaranthus tuberculatus, Amaranthus hybridus, and Amaranthus palmeri are agronomically important weed species. Here, we present the most contiguous draft assemblies of these three species to date. We utilized a combination of Pacific Biosciences long-read sequencing and chromatin contact mapping information
Haifeng Qian et al.
Environmental science & technology, 45(16), 7036-7043 (2011-07-14)
Imazethapyr (IM) is a chiral herbicide and a widely used racemic mixture. This report investigated the enantioselectivity between R- and S-IM in rice and explored its causative mechanism at the physiological and molecular levels. The results suggested that R-IM inhibited
Da-Wei Fu et al.
Dalton transactions (Cambridge, England : 2003), (30)(30), 3946-3948 (2008-07-24)
Hydrothermal reaction of H-Imazethapyr (2-(4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl)-5-ethyl-3-pyridinecarboxylic acid) with Cd(ClO4)2.6H2O offers a diamond-like MOF Cd(Imazethapyr)2 in which it crystallizes in a non-centrosymmetric space group (Fdd2) belonging to polar point group (C2v). MOF displays a strong SHG response, and good ferroelectric and piezoelectric

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