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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:
3337-71-1
Molekulargewicht:
230.24
Beilstein:
2697523
EG-Nummer:
222-077-1
MDL-Nummer:
MFCD00055534
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329756650
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

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
GHS07

Signalwort

Warning

H-Sätze

H302

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCG9508
BCBT4896
SZBC072XV
SZB7227XV
SZE7227X

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Die Dokumentenbibliothek aufrufen

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
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
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)
Yoshihiko Matsui et al.
Environmental science & technology, 36(15), 3432-3438 (2002-08-22)
The principal objective of this study was to elucidate mechanisms by which NOM affects the adsorption of a nonpolar (simazine) and a polar (asulam) herbicide on activated carbon. Experiments were carried out in microcolumns that were continuously fed solutions containing
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