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Merck

37923

Supelco

イマゼタピル

PESTANAL®, analytical standard

別名:

2-(4,5-ジヒドロ-4-イソプロピル-4-メチル-5-オキソ-1H-イミダゾール-2-イル)-5-エチル-3-ピリジンカルボン酸

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About This Item

実験式(ヒル表記法):
C15H19N3O3
CAS番号:
分子量:
289.33
Beilstein:
7437150
MDL番号:
UNSPSCコード:
41116107
PubChem Substance ID:
NACRES:
NA.24

グレード

analytical standard

品質水準

製品種目

PESTANAL®

シェルフライフ

limited shelf life, expiry date on the label

テクニック

HPLC: suitable
gas chromatography (GC): suitable

アプリケーション

agriculture
environmental

フォーマット

neat

SMILES記法

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)

InChI Key

XVOKUMIPKHGGTN-UHFFFAOYSA-N

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関連するカテゴリー

詳細

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

アプリケーション

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).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

おすすめ製品

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.

法的情報

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

保管分類コード

11 - Combustible Solids

WGK

WGK 1

引火点(°F)

Not applicable

引火点(℃)

Not applicable

個人用保護具 (PPE)

Eyeshields, Gloves, type N95 (US)


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

Jan Code

37923-100MG-R:
37923-VAR-R:
37923-BULK-R:


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試験成績書(COA)

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Slide 1 of 5

1 of 5

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
HaiFeng Qian et al.
PloS one, 6(5), e19451-e19451 (2011-05-17)
The enantiomers of a chiral compound possess different biological activities, and one of the enantiomers usually shows a higher level of toxicity. Therefore, the exploration of the causative mechanism of enantioselective toxicity is regarded as one of primary goals of
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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