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Merck

37897

Supelco

Bensulfuron-methyl

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C16H18N4O7S
Número de CAS:
Peso molecular:
410.40
Beilstein:
7447488
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24
En este momento no podemos mostrarle ni los precios ni la disponibilidad

grado

analytical standard

Nivel de calidad

Línea del producto

PESTANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
NMR: suitable
gas chromatography (GC): suitable

impurezas

≤1% water (Karl Fischer)

mp

179-184 °C

idoneidad

passes test for identity (NMR)

aplicaciones

agriculture
environmental

Formato

neat

cadena SMILES

COC(=O)c1ccccc1CS(=O)(=O)NC(=O)Nc2nc(OC)cc(OC)n2

InChI

1S/C16H18N4O7S/c1-25-12-8-13(26-2)18-15(17-12)19-16(22)20-28(23,24)9-10-6-4-5-7-11(10)14(21)27-3/h4-8H,9H2,1-3H3,(H2,17,18,19,20,22)

Clave InChI

XMQFTWRPUQYINF-UHFFFAOYSA-N

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Aplicación

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

Precaución

Sensitive, handle under argon.

Productos recomendados

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.

Información legal

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

Pictogramas

Exclamation markEnvironment

Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Aquatic Acute 1 - Aquatic Chronic 2 - Skin Sens. 1

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Certificados de análisis (COA)

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Los clientes también vieron

Lihua Yang et al.
Se pu = Chinese journal of chromatography, 30(1), 71-75 (2012-06-07)
An analytical method of high performance liquid chromatography (HPLC) was established for the simultaneous determination of bensulfuron-methyl and mefenacet residues in paddy field (paddy water, soil and rice plant). The residues in the paddy water was extracted with methylene chloride
Xiaoyan Lin et al.
Journal of environmental sciences (China), 20(12), 1494-1500 (2009-02-13)
To investigate the influence of bensulfuron-methyl (BSM) on culturable microbial quantities and unculturable microbial community structures, conventional and molecular biological methods were employed in five BSM treated soils with three replications, respectively. The results obtained with traditional culture-dependent methods showed
Weihong Wu et al.
Journal of environmental sciences (China), 21(8), 1129-1134 (2009-10-30)
The combined pollution of heavy metal Pb2+ and bensulfuron-methyl (BSM), originating from chemical herbicides, in agro-ecological environments has become commonplace in southern China. The adsorption of BSM on three paddy soils in the presence of Pb2+ was examined using high-performance
Jeannette Espinoza et al.
Environmental pollution (Barking, Essex : 1987), 157(12), 3387-3395 (2009-07-18)
Bensulfuron-methyl sorption was studied in Andisol and Ultisol soils in view of their characteristic physical and chemical properties, presenting acidic pH and variable charge. Humic and fulvic acids (HA and FA) and humin (HUM) contributions were established. Sorption was studied
Wei Luo et al.
Journal of hazardous materials, 158(1), 208-214 (2008-04-18)
The present study deals with the degradation of bensulfuron-methyl by microorganisms cultured with different sources of carbon, nitrogen and phosphorus. Addition of carbon source accelerated the degradation of bensulfuron-methyl under co-metabolism process. Sodium lactate was the best carbon source for

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