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Merck

45329

Supelco

Asulam

PESTANAL®, analytical standard

Synonym(e):

Methyl-N-(4-aminophenylsulfonyl)-carbamat

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About This Item

Empirische Formel (Hill-System):
C8H10N2O4S
CAS-Nummer:
Molekulargewicht:
230.24
Beilstein:
2697523
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24
Preise und Verfügbarkeit sind derzeit nicht verfügbar.

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

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)

InChIKey

VGPYEHKOIGNJKV-UHFFFAOYSA-N

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Anwendung

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

Empfohlene Produkte

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Rechtliche Hinweise

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

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

13 - Non Combustible Solids

WGK

WGK 3

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

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
J K Rowntree et al.
Annals of botany, 92(4), 547-556 (2003-08-23)
Asulox is a herbicide used to control bracken. Its effects on mosses were investigated to ascertain whether exposure proved as detrimental as found in parallel studies on pteridophytes. Mature gametophytes of 18 mosses were exposed to a range of concentrations
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)
Direct analysis of the wild oat herbicide, asulam, in wheat samples by reversed-phase liquid chromatography at selected ultraviolet wavelengths.
J F Lawrence et al.
Journal of agricultural and food chemistry, 28(6), 1323-1325 (1980-11-01)
Julia A Spoors et al.
Journal of environmental monitoring : JEM, 4(6), 917-921 (2003-01-02)
To date, no ligand binding assay has been described for the carbamate herbicide asulam, although a variety of physical methods, dependent on pre-concentration of water samples, have been documented for its assessment. However, asulam is increasingly used in sensitive agricultural

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