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46325

Fomesafen

PESTANAL®, analytical standard

Synonym(s):

5-[2-Chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitrobenzamide

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About This Item

Empirical Formula (Hill Notation):
C15H10ClF3N2O6S
CAS Number:
72178-02-0
Molecular Weight:
438.76
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757140
EC Number:
276-439-9
Beilstein/REAXYS Number:
8165046
MDL number:
MFCD01632756
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grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental

format

neat

SMILES string

CS(=O)(=O)NC(=O)c1cc(Oc2ccc(cc2Cl)C(F)(F)F)ccc1[N+]([O-])=O

InChI

1S/C15H10ClF3N2O6S/c1-28(25,26)20-14(22)10-7-9(3-4-12(10)21(23)24)27-13-5-2-8(6-11(13)16)15(17,18)19/h2-7H,1H3,(H,20,22)

InChI key

BGZZWXTVIYUUEY-UHFFFAOYSA-N

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Application

Fomesafen may be used as a reference standard in the determination of fomesafen in soil samples using liquid chromatography coupled with tandem mass spectrometry (LC-MS-MS).

Legal Information

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

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK5937
BCCH5438
BCBW2751

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Jan Krijt et al.
Toxicology and applied pharmacology, 189(1), 28-38 (2003-05-22)
Hepatic uroporphyria can be readily induced by a variety of treatments in mice of the C57BL strains, whereas DBA/2 mice are almost completely resistant. However, feeding of the protoporphyrinogen oxidase-inhibiting herbicide fomesafen (0.25% in the diet for 18 weeks) induced
Zhao-zhong Feng et al.
Journal of agricultural and food chemistry, 60(29), 7104-7110 (2012-07-05)
Fomesafen is a diphenyl ether herbicide used to control the growth of broadleaf weeds in bean fields. Although the degradation of fomesafen in soils was thought to occur primarily by microbial activity, little was known about the kinetic and metabolic
Jacqueline Russo et al.
Cell and tissue research, 333(1), 147-158 (2008-04-24)
The disturbance of plasma membrane carbohydrates and of lipopolysaccharide (LPS) ligands in relation to cytoskeletal transformations of haemocytes has been investigated after chronic exposure of pond snails (Lymnaea stagnalis) to the peroxidizing toxicant fomesafen. Neither of the two lectins used
A Chlumská et al.
Ceskoslovenska patologie, 34(2), 67-71 (1998-06-13)
Administration of herbicide fomesafen and of fomesafen combined with one dose of iron to 44 mice during 3 to 14 months caused hyperplastic and preneoplastic changes in the liver tissue which had been described in experimental carcinogenesis* small groups of
Thierry Caquet et al.
Environmental toxicology and chemistry, 24(5), 1116-1124 (2005-08-23)
Ecotoxicological effects of the diphenyl ether herbicide fomesafen, applied alone or in combination with the adjuvant Agral 90 (mixture of polyethoxylated derivatives of nonylphenol), were assessed on planktonic communities in 18-m3 outdoor mesocosms during a nine-month study. Four mesocosms were
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Global Trade Item Number

SKUGTIN
46325-100MG-R04061832355177

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