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31658

Supelco

Rimsulfuron

PESTANAL®, analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C14H17N5O7S2
Numero CAS:
122931-48-0
Peso molecolare:
431.44
Beilstein:
7501778
Numero MDL:
MFCD01632305
Codice UNSPSC:
41116107
ID PubChem:
329753868
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

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)
MEFOUWRMVYJCQC-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

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).

Note legali

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

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

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCD1602
BCBZ5003
BCBT7290
SZBG020XV
SZBE308XV

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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)
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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