46325
氟磺胺草醚
PESTANAL®, analytical standard
别名:
5-[2-氯-4-(三氟甲基)苯氧基]-N-(甲磺酰基)-2-硝基苯甲酰胺
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关于此项目
经验公式（希尔记法）:
C15H10ClF3N2O6S
化学文摘社编号:
分子量:
438.76
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
276-439-9
Beilstein/REAXYS Number:
8165046
MDL number:
产品名称
氟磺胺草醚, 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
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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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
农药列管产品
此项目有
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
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
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
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