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Merck
CN

31658

Rimsulfuron

PESTANAL®, analytical standard

Synonym(s):

1-(4,6-Dimethoxy-2-pyrimidinyl)-3-[3-(ethylsulfonyl)-2-pyridylsulfonyl]urea

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About This Item

Empirical Formula (Hill Notation):
C14H17N5O7S2
CAS Number:
122931-48-0
Molecular Weight:
431.44
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753868
MDL number:
MFCD01632305
Beilstein/REAXYS Number:
7501778

Key Documents

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Product Name

Rimsulfuron, PESTANAL®, analytical standard

InChI

1S/C14H17N5O7S2/c1-4-27(21,22)9-6-5-7-15-12(9)28(23,24)19-14(20)18-13-16-10(25-2)8-11(17-13)26-3/h5-8H,4H2,1-3H3,(H2,16,17,18,19,20)

SMILES string

CCS(=O)(=O)c1cccnc1S(=O)(=O)NC(=O)Nc2nc(OC)cc(OC)n2

InChI key

MEFOUWRMVYJCQC-UHFFFAOYSA-N

grade

analytical standard

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

Quality Level

100

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Rimsulfuron may be used as a reference standard for the determination of the analyte:
  • In honey samples using a method based on an on-column liquid-liquid extraction (OCLLE) using diatomaceous earth as inert solid support and liquid chromatography (LC) coupled to mass spectrometry (MS) operating in tandem mode (MS/MS).

General description

Rimsulfuron is a sulfonylurea herbicide primarily used to control a wide variety of perennial and annual grasses and some broadleaf weeds. The mode of action of rimsulfuron involves inhibition of acetolactate synthase (ALS), a key enzyme in the biosynthetic pathway of branched-chain amino acids.

Legal Information

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

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCD1602
BCBZ5003
BCBT7290

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Basis of selectivity of the herbicide rimsulfuron in maize.
Koeppe MK, et al.
Pesticide Biochemistry and Physiology, 66(3), 170- 181 (2000)
Development and validation of a multi-residue method for pesticide determination in honey using on-column liquid- liquid extraction and liquid chromatography- tandem mass spectrometry.
Pirard C, et al.
Journal of Chromatography A, 1152(1-2), 116- 123 (2007)
Shuo Wang et al.
Bulletin of environmental contamination and toxicology, 105(4), 602-606 (2020-09-27)
A method for simultaneous quantitation of rimsulfuron, quizalofop-P-ethyl and quizalofop-P in potato plant, soil and potato tuber samples was established. The mean recoveries of rimsulfuron, quizalofop-P-ethyl and quizalofop-P in different matrices spiked with them were 81.4%-101.1%, 76.1%-99.0% and 77.4%-106.4% with
Paola Ganugi et al.
Plant science : an international journal of experimental plant biology, 303, 110727-110727 (2021-01-26)
Herbicide application is a common procedure in agriculture, whose potentially adverse effects are assessed mainly with respect to weeds or in terms of residues and environmental impact. However, recent evidence has highlighted possible effects of pesticide treatments on plant metabolism
Joanna Płonka et al.
Chemosphere, 245, 125616-125616 (2019-12-22)
The influence of pesticides on the metabolism of edible plants has not been fully investigated. Moreover, once introduced into the environment, pesticides are degraded to many compounds with undefined bioactivity. In presented work, under experimental conditions, model edible plant (Raphanus
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