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34210

Supelco

Nicosulfuron

PESTANAL®, analytical standard

Sinonimo/i:

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

Formula empirica (notazione di Hill):
C15H18N6O6S
Numero CAS:
111991-09-4
Peso molecolare:
410.41
Numero MDL:
MFCD00203303
Codice UNSPSC:
41116107
ID PubChem:
329754895
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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)
RTCOGUMHFFWOJV-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

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

Note legali

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

Pittogrammi

Environment
GHS09

Avvertenze

Warning

Indicazioni di pericolo

H410

Consigli di prudenza

P273 - P391 - P501

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCBZ7480

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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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