45329
Asulam
PESTANAL®, analytical standard
Synonym(s):
Methyl N-(4-aminophenylsulfonyl)carbamate
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About This Item
Empirical Formula (Hill Notation):
C8H10N2O4S
CAS Number:
Molecular Weight:
230.24
Beilstein/REAXYS Number:
2697523
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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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)NS(=O)(=O)c1ccc(N)cc1
InChI
1S/C8H10N2O4S/c1-14-8(11)10-15(12,13)7-4-2-6(9)3-5-7/h2-5H,9H2,1H3,(H,10,11)
InChI key
VGPYEHKOIGNJKV-UHFFFAOYSA-N
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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Identification and determination of asulam and related degradation products in soil.
M Franci et al.
Bulletin of environmental contamination and toxicology, 26(1), 102-107 (1981-01-01)
F García Sánchez et al.
Talanta, 77(1), 294-297 (2008-09-23)
An efficient, sensitive and fast stopped-flow method has been developed to determine asulam in water, based on its inhibition effect on the horseradish peroxidase-luminol-hydrogen peroxide chemiluminescence reaction, (HRP-luminol-H(2)O(2)). Ultra fast data acquisition (0.20s) facilitates excellent selectivity because no interferences from
R T Kon et al.
Food additives and contaminants, 1(1), 67-71 (1984-01-01)
An analytical method has been developed for the determination of the herbicide, asulam [methyl(4-aminobenzenesulphonyl)carbamate] and two metabolites, sulphanilamide and acetylasulam individually, in peaches. Asulam and acetylasulam were partitioned from an aqueous phase with ethyl ether, leaving behind more polar components
Effects of asulam on some microbial activities of three soils.
J A Marsh
Bulletin of environmental contamination and toxicology, 25(1), 15-22 (1980-07-01)
Carole Catastini et al.
The Science of the total environment, 298(1-3), 219-228 (2002-11-27)
The degradation of the herbicide asulam (4-amino-benzosulfonyl-methylcarbamate) was studied by excitation of iron (III) aquacomplexes in aqueous solutions at 365 nm as well as by exposition to solar light. Sulfanilamide was also studied as a model molecule. The initial step
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