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Nicosulfuron

PESTANAL®, analytical standard

Synonym(s):

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

Empirical Formula (Hill Notation):
C15H18N6O6S
CAS Number:
111991-09-4
Molecular Weight:
410.41
MDL number:
MFCD00203303
UNSPSC Code:
41116107
PubChem Substance ID:
329754895
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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
GHS09

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL1335
BCCH4420
BCBZ7480
SZBE279XV
SZBE022XV

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Rui Zhao et al.
International journal of environmental research and public health, 16(3) (2019-01-30)
The widely used sulfonylurea herbicides have caused negative effects on the environment and human beings. Electrochemical degradation has attracted much attention in the treatment of refractory organic compounds due to its advantage of producing no secondary pollution. Three kinds of
David M G Anderson et al.
Rapid communications in mass spectrometry : RCM, 23(9), 1321-1327 (2009-04-02)
Matrix-assisted laser desorption/ionisation mass spectrometry imaging (MALDI-MSI) has been used to image the distribution of the pesticide nicosulfuron (2-[[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-N,N-dimethyl-3-pyridinecarboxamide) in plant tissue using direct tissue imaging following root and foliar uptake. Sunflower plants inoculated with nicosulfuron were horizontally sectioned at
Cheryl Ashburn Poppell et al.
Journal of agricultural and food chemistry, 50(16), 4581-4585 (2002-07-26)
Field and soil fortification studies were conducted to evaluate the half-lives (DT(50)) of nicosulfuron and rimsulfuron in a Sequatchie silt loam surface soil. The dissipation of each herbicide was also evaluated with the two compounds applied simultaneously, which is a
Qingxiang Zhou et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 23(2), 189-192 (2007-02-14)
Recently, multiwalled carbon nanotubes (MWCNTs) have been at the center of attention because of their applications in many fields. Efforts to investigate the possibility of MWCNTs as SPE absorbents for the enrichment of environmental pollutants yielded positive results. The goal
S Bretaud et al.
Ecotoxicology and environmental safety, 47(2), 117-124 (2000-10-12)
Juvenile goldfish (Carassius auratus) were exposed to three widely used pesticides; carbofuran, diuron, and nicosulfuron. Acetylcholinesterase (AChE) activity and molecular forms of AChE were first characterized in brain and skeletal muscle of unexposed fish. Skeletal muscle had higher AChE activity
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