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Merck

37923

Supelco

Imazethapyr

PESTANAL®, analytical standard

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C15H19N3O3
Número de CAS:
Peso molecular:
289.33
Beilstein/REAXYS Number:
7437150
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

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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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.

Recommended products

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Certificados de análisis (COA)

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1 of 4

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
Weed control in pinto beans (Phaseolus vulgaris) with imazethapyr combinations.
Arnold NR, et al.
Weed Technology, 7(2), 361-364 (1993)
Determination of imazethapyr and imazapyr residues in soil by coupled-column liquid chromatography
Novakova O.
Chromatographia, 29(1-2), 62-66 (1994)
Qingyan Zhou et al.
Journal of agricultural and food chemistry, 57(4), 1624-1631 (2009-02-10)
Chiral compounds usually behave enantioselectively in phyto-biochemical processes. With the increasing application of chiral herbicides, their enantioselective phytotoxicity to plants merits further study, and little information is available in this area. The purpose of this study was to examine the

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