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Rimsulfuron

PESTANAL®, analytical standard

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C14H17N5O7S2
Numéro CAS:
122931-48-0
Poids moléculaire :
431.44
Numéro Beilstein :
7501778
Numéro MDL:
MFCD01632305
Code UNSPSC :
41116107
ID de substance PubChem :
329753868
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

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

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)

Clé InChI

MEFOUWRMVYJCQC-UHFFFAOYSA-N

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Description générale

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.

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).

Informations légales

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Certificats d'analyse (COA)

Lot/Batch Number
BCCD1602
BCBZ5003
BCBT7290
SZBG020XV
SZBE308XV

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Basis of selectivity of the herbicide rimsulfuron in maize.
Koeppe MK, et al.
Pesticide Biochemistry and Physiology, 66(3), 170- 181 (2000)
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
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
Amit Paporisch et al.
Pesticide biochemistry and physiology, 138, 22-28 (2017-05-01)
Three sweet corn genotypes, two inbred lines (IBER001 and IBER002) and their hybrid (ER00X), differ in their phenotypic responses to several P450-metabolized herbicides, used in sweet corn, namely, foramsulfuron, iodosulfuron, rimsulfuron and tembotrione. Foramsulfuron is a sulfonylurea herbicide commonly formulated
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