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Merck

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
Beilstein:
8165046
EC Number:
276-439-9
MDL number:
MFCD01632756
UNSPSC Code:
41116107
PubChem Substance ID:
329757140
NACRES:
NA.24

Key Documents

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grade

analytical standard

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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format

neat

format

neat

format

neat

format

neat

grade

analytical standard

grade

analytical standard

grade

analytical standard

grade

analytical standard

product line

PESTANAL®

product line

PESTANAL®

product line

PESTANAL®

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental

application(s)

agriculture
environmental

application(s)

agriculture
environmental

application(s)

agriculture
environmental

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

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).[1]

Legal Information

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
Jacqueline Russo et al.
Cell and tissue research, 328(2), 431-441 (2007-01-26)
The effects of a xenobiotic on the circulating haemocytes of Lymnaea stagnalis were investigated after short-term (24 h, 96 h) and long-term (504 h) exposure of snails to environmental concentrations. Fomesafen, a pro-oxidant generator led to the activation of the
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
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
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
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