37923
咪草烟
PESTANAL®, analytical standard
别名:
2-[4,5-二氢-4-甲基-4-(1-甲基乙基)-5-氧代-1H-咪唑-2-基]-5-乙基-3-吡啶羧酸
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选择尺寸
关于此项目
经验公式（希尔记法）:
C15H19N3O3
化学文摘社编号:
分子量:
289.33
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
7437150
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)
SMILES string
CCc1cnc(C2=NC(C)(C(C)C)C(=O)N2)c(c1)C(O)=O
InChI key
XVOKUMIPKHGGTN-UHFFFAOYSA-N
grade
analytical standard
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
Quality Level
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General description
Imazethapyr is an imidazolinone derivative and a herbicide, which is selectively used on crops for weed control management.
Application
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.
Other Notes
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.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
农药列管产品
此项目有
Weed control in pinto beans (Phaseolus vulgaris) with imazethapyr combinations.
Arnold NR, et al.
Weed Technology, 7(2), 361-364 (1993)
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
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)
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
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