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Merck
CN

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

Key Documents

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Product Name

Fomesafen, PESTANAL®, analytical standard

InChI key

BGZZWXTVIYUUEY-UHFFFAOYSA-N

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)

SMILES string

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

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental

format

neat

Quality Level

100

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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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Peroxisome proliferators: species differences in response of primary hepatocyte cultures.
C R Elcombe et al.
Annals of the New York Academy of Sciences, 804, 628-635 (1996-12-27)
S Alexandre et al.
Toxicology letters, 142(1-2), 77-87 (2003-05-27)
In order to test the hypothesis of a relationship between apoptosis and neoplastic transformation, we studied the transforming potency of zinc, known for its antiapoptotic effects. In this study, zinc chloride (100 microM) was shown to induce morphological transformation (MT)
Thierry Caquet
Environmental pollution (Barking, Essex : 1987), 141(1), 54-59 (2005-10-04)
In this study, the value of carbon (delta13C) and nitrogen (delta15N) stable isotope ratios were determined in nymphs of a top-predator, the common backswimmer (Notonecta glauca L.), collected in 18 m3 outdoor freshwater mesocosms used to assess the fate and
Bo Liang et al.
Chemosphere, 77(11), 1614-1619 (2009-10-23)
The fomesafen degrading bacterium ZB-1 was isolated from contaminated agricultural soil, and identified as Lysinibacillus sp. based on the comparative analysis of 16S rRNA gene. The strain could utilize fomesafen as the sole carbon source for growth, and the total
Qingming Zhang et al.
Environmental science and pollution research international, 20(1), 201-208 (2012-05-16)
Formesafen is a diphenyl ether herbicide that has adverse effects on non-target animals. However, knowledge about the effect of fomesafen on the antioxidant defense system in earthworms is vague. Thus, it is essential to investigate the effects of fomesafen on
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