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Merck

42206

Supelco

Flumetsulam

PESTANAL®, analytical standard

Sinónimos:

2′,6′-Difluoro-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-sulfonanilide, N-(2,6-Difluorophenyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-sulfonamide

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About This Item

Fórmula empírica (notación de Hill):
C12H9F2N5O2S
Número de CAS:
Peso molecular:
325.29
Beilstein/REAXYS Number:
8155688
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

composition

carbon content, 43.4-45.2 wt. %
nitrogen content, 21.1-22.0 wt. %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

Cc1ccn2nc(nc2n1)S(=O)(=O)Nc3c(F)cccc3F

InChI

1S/C12H9F2N5O2S/c1-7-5-6-19-11(15-7)16-12(17-19)22(20,21)18-10-8(13)3-2-4-9(10)14/h2-6,18H,1H3

InChI key

RXCPQSJAVKGONC-UHFFFAOYSA-N

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General description

Flumetsulam is postemergence, triazolopyrimidine sulfonanilide herbicide, which can find applications in agriculture, for under-sown wheat and certain legume crops and pastures. Its mode of action involves the suppression of acetolactate synthase, thereby inhibiting the amino acid synthesis in plants.

Application

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

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Legal Information

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

pictograms

Environment

signalword

Warning

hcodes

pcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3


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Certificados de análisis (COA)

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Visite la Librería de documentos

Adsorption isotherm modeling of carbendazim and flumetsulam onto homoionic-montmorillonite clays: comparison of linear and nonlinear models
Maataoui EY, et al.
Turkish Journal of Chemistry (2017)
Alkoxy base-mediated selective synthesis and new rearrangements of 1, 2, 4-triazolodipyrimidinones
Pyatakov.AD, et al.
Tetrahedron Letters, 58, 748-754 (2017)

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