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MilliporeSigma

34210

Supelco

Nicosulfuron

PESTANAL®, analytical standard

Sinónimos:

1-(4,6-Dimethoxy-2-pyrimidinyl)-3-[3-(dimethylcarbamoyl)-2-pyridylsulfonyl]urea, 2-[(4,6-Dimethoxypyrimidin-2-ylcarbamoyl)sulfamoyl]-N,N-dimethylnicotinamide

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About This Item

Fórmula empírica (notación de Hill):
C15H18N6O6S
Número de CAS:
Peso molecular:
410.41
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

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

COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2ncccc2C(=O)N(C)C)n1

InChI

1S/C15H18N6O6S/c1-21(2)13(22)9-6-5-7-16-12(9)28(24,25)20-15(23)19-14-17-10(26-3)8-11(18-14)27-4/h5-8H,1-4H3,(H2,17,18,19,20,23)

InChI key

RTCOGUMHFFWOJV-UHFFFAOYSA-N

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General description

Nicosulfuron belongs to the group of sulfonylurea herbicides, which can be largely used to control grasses and broad leaved weed species in crop protection like in corn.

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

pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Certificados de análisis (COA)

Lot/Batch Number

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Los clientes también vieron

P Saglio et al.
Archives of environmental contamination and toxicology, 41(2), 192-200 (2001-07-20)
The immediate behavioral responses of goldfish (Carassius auratus) to pesticide-contaminated flows were recorded in a countercurrent olfactometer. In addition, electro-olfactograms were recorded from the epithelial surface of the olfactory rosette as a preliminary check for the olfactory sensitivity of the
Adsorption and desorption of nicosulfuron in soils
Gonzalez.MJ and Ukrainczyk L
Journal of Environmental Quality, 25, 1186-1192 (1996)
Jean Sabadie
Journal of agricultural and food chemistry, 50(3), 526-531 (2002-01-24)
Alcoholysis (methanol or ethanol) and hydrolysis (pH ranging from 4 to 11) of the herbicide nicosulfuron at 30 degrees C principally involves the breakdown of the urea part of the molecule. A high yield of the corresponding carbamate was obtained
Lieqing Yang et al.
Analytica chimica acta, 670(1-2), 72-77 (2010-08-06)
A new molecularly imprinted stir bar was prepared using nicosulfuron, a sulfonylurea herbicide, as a template. To achieve the selective and direct extraction of a target analyte from aqueous samples, several main parameters, including extraction time, pH value and contents
Eunsoo Choe et al.
Pest management science, 76(9), 3012-3019 (2020-04-06)
Nicosulfuron, a sulfonylurea herbicide widely used for grass weed control in corn production, injures some sweet corn hybrids and inbreds. A specific cytochrome P450 (P450), CYP81A9, is suggested to be responsible for sensitivity to nicosulfuron and other P450-metabolized herbicides. Corn

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