46325
Fomesafen
PESTANAL®, analytical standard
Synonyme(s) :
5-[2-Chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitrobenzamide
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A propos de cet article
Formule empirique (notation de Hill) :
C15H10ClF3N2O6S
Numéro CAS:
Poids moléculaire :
438.76
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
276-439-9
Beilstein/REAXYS Number:
8165046
MDL number:
Service technique
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analytical standard
Quality Level
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
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
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Hazard Classifications
Acute Tox. 4 Oral
signalword
Warning
hcodes
Classe de stockage
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
Liquid chromatography mass spectrometry tandem for multiresidue determination of selected post-emergence herbicides after soil column extraction.
Lagana A, et al.
Analytica Chimica Acta, 415(1-2), 41-56 (2000)
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
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| 46325-100MG-R | 04061832355177 |