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46325

Supelco

Fomesafen

PESTANAL®, analytical standard

Synonym(e):

5-[2-Chlor-4-(trifluormethyl)-phenoxy]-N-(methylsulfonyl)-2-nitrobenzamid

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About This Item

Empirische Formel (Hill-System):
C15H10ClF3N2O6S
CAS-Nummer:
72178-02-0
Molekulargewicht:
438.76
Beilstein:
8165046
EG-Nummer:
276-439-9
MDL-Nummer:
MFCD01632756
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329757140
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Anwendung(en)

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)

InChIKey

BGZZWXTVIYUUEY-UHFFFAOYSA-N

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Anwendung

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).

Rechtliche Hinweise

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

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H302

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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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
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
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)
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