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Sulfometuron methyl

PESTANAL®, analytical standard

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About This Item

Formule empirique (notation de Hill):
C15H16N4O5S
Numéro CAS:
Poids moléculaire :
364.38
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

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

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)

Clé InChI

ZDXMLEQEMNLCQG-UHFFFAOYSA-N

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Description générale

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.

Informations légales

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

Pictogrammes

Environment

Mention d'avertissement

Warning

Mentions de danger

Conseils de prudence

Classification des risques

Aquatic Acute 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves


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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

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)
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
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
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

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