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Merck
CN

34224

甲嘧磺隆

PESTANAL®, analytical standard

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经验公式(希尔记法):
C15H16N4O5S
化学文摘社编号:
分子量:
364.38
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
277-780-6
MDL number:
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InChI key

ZDXMLEQEMNLCQG-UHFFFAOYSA-N

InChI

1S/C15H16N4O5S/c1-9-8-10(2)17-14(16-9)18-15(21)19-25(22,23)12-7-5-4-6-11(12)13(20)24-3/h4-8H,1-3H3,(H2,16,17,18,19,21)

SMILES string

COC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc2nc(C)cc(C)n2

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

General description

Sulfometuron methyl, can be called as one of the few sulfonylurea herbicides with high herbicidal activity. It can inhibit the growth of several bacterial species including Salmonella typhimurium, found in intestinal lumen and can also suppress the growth of yeast like Saccharomyces cerevisiae by blocking acetolactate synthase enzyme.

Application

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

Legal Information

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

pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Single amino acid substitutions in the enzyme acetolactate synthase confer resistance to the herbicide sulfometuron methyl
Yadav N, et al.
Proceedings of the National Academy of Sciences of the USA, 83, 4418-4422 (1986)
Genetic analysis of mutants of Saccharomyces cerevisiae resistant to the herbicide sulfometuron methyl
Falco.C.S and Dumas.S.K
Genetics, 109, 21-35 (1985)
G Leppert et al.
Genetics, 125(1), 13-20 (1990-05-01)
Yeast DNA fragments that confer multiple drug resistance when amplified were isolated. Cells containing a yeast genomic library cloned in the high copy autonomously replicating vector, YEp24, were plated on medium containing cycloheximide. Five out of 100 cycloheximide-resistant colonies were
Yael Golda Mishael et al.
Journal of agricultural and food chemistry, 50(10), 2856-2863 (2002-05-02)
The aim of this study was to understand the interactions between alkylammonium cations present as monomers and micelles and a clay mineral, montmorillonite, to develop slow release formulations of anionic herbicides, such as sulfometuron (SFM) whose leaching in soils is
A Coly et al.
Journal of AOAC International, 84(6), 1745-1750 (2002-01-05)
First-derivative photochemically induced spectrofluorimetry (PIF-1D) is applied to the simultaneous determination of binary mixtures of 4 sulfonylurea herbicides in aqueous micellar samples. Synthetic binary mixtures of sulfometuronmethyl with chlorsulfuron, metsulfuron-methyl, and 3-rimsulfuron, respectively, are well resolved by using the zero-crossing

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