34224
Sulfometuron methyl
PESTANAL®, analytical standard
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About This Item
Empirical Formula (Hill Notation):
C15H16N4O5S
CAS Number:
Molecular Weight:
364.38
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
277-780-6
MDL number:
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
Related Categories
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
signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Acute 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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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)
George Schmitz et al.
Journal of bacteriology, 186(3), 803-810 (2004-01-20)
The YjgF/YER057c/UK114 family is a highly conserved class of proteins that is represented in the three domains of life. Thus far, a biochemical function demonstrated for these proteins in vivo or in vitro has yet to be defined. In several
Joanne M Kingsbury et al.
Microbiology (Reading, England), 150(Pt 5), 1547-1558 (2004-05-11)
Acetolactate synthase catalyses the first common step in isoleucine and valine biosynthesis and is the target of several classes of inhibitors. The Cryptococcus neoformans ILV2 gene, encoding acetolactate synthase, was identified by complementation of a Saccharomyces cerevisiae ilv2 mutant. C.
J A Wemmie et al.
The Journal of biological chemistry, 269(20), 14690-14697 (1994-05-20)
The yeast YAP1 gene encodes a transcriptional regulatory protein that utilizes a basic region-leucine zipper (bZip) DNA-binding domain to recognize its cognate DNA element. A synthetic reporter gene containing a SV40 AP-1 response element (ARE) cloned upstream of a TRP5
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