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34224

Supelco

Sulfometuron methyl

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H16N4O5S
CAS Number:
Molecular Weight:
364.38
EC Number:
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

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)

InChI key

ZDXMLEQEMNLCQG-UHFFFAOYSA-N

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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

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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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)
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
Barbara Dunn et al.
BMC genomics, 6, 53-53 (2005-04-19)
Genetic differences between yeast strains used in wine-making may account for some of the variation seen in their fermentation properties and may also produce differing sensory characteristics in the final wine product itself. To investigate this, we have determined genomic
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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