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46325

Supelco

Fomesafen

PESTANAL®, analytical standard

Sinonimo/i:

5-[2-Chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitrobenzamide

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About This Item

Formula empirica (notazione di Hill):
C15H10ClF3N2O6S
Numero CAS:
72178-02-0
Peso molecolare:
438.76
Beilstein:
8165046
Numero CE:
276-439-9
Numero MDL:
MFCD01632756
Codice UNSPSC:
41116107
ID PubChem:
329757140
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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)
BGZZWXTVIYUUEY-UHFFFAOYSA-N

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Applicazioni

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).

Note legali

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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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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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