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Merck
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Key Documents

45307

Supelco

Fensulfothion

PESTANAL®, analytical standard

Sinônimo(s):

Diethyl 4-(methylthio)phenyl phosphate

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About This Item

Fórmula empírica (Notação de Hill):
C11H17O4PS2
Número CAS:
Peso molecular:
308.35
Beilstein:
2219515
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

neat

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

CCOP(=S)(OCC)Oc1ccc(cc1)S(C)=O

InChI

1S/C11H17O4PS2/c1-4-13-16(17,14-5-2)15-10-6-8-11(9-7-10)18(3)12/h6-9H,4-5H2,1-3H3

chave InChI

XDNBJTQLKCIJBV-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Informações legais

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

Pictogramas

Skull and crossbonesEnvironment

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 1 Dermal - Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Código de classe de armazenamento

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Certificados de análise (COA)

Lot/Batch Number

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Visite a Biblioteca de Documentos

C Greenaway et al.
The Journal of emergency medicine, 14(3), 339-344 (1996-05-01)
We report a foodborne outbreak causing a cholinergic syndrome in three members of a family. The clinical presentation was characterized by nausea, vomiting, abdominal pain, and weakness. Physical examination revealed evidence of peripheral motor weakness and decreased level of consciousness
S Chandra et al.
Planta, 211(5), 736-742 (2000-11-23)
Because the H2O2 and O2- generated during a pathogen-triggered oxidative burst could either protect or destroy a besieged plant cell, their synthesis might be expected to be tightly regulated. We have examined the nature of this regulation as it is
M M Sunil Paul et al.
Chemosphere, 91(3), 295-301 (2013-01-01)
Oxidative degradation of fensulfothion, a model organophosphorus compound, has been investigated by pulse radiolysis and H2O2/UV photolysis. A nearly complete transformation of fensulfothion was observed within 4min of irradiation. Very little Total Organic Carbon (TOC) reduction was obtained at this
J E Elliott et al.
Journal of wildlife diseases, 32(3), 486-491 (1996-07-01)
During the winter of 1990 in the Fraser Delta of British Columbia, Canada, nine birds of prey were found with symptoms of anticholinesterase poisoning. Immediate surgical removal of crop contents of three birds decreased mortality and recovery time. Chemical analysis
Yi He et al.
Journal of chromatography. A, 1122(1-2), 7-12 (2006-05-24)
Continuous flow microextraction (CFME) combined with high-performance liquid chromatography-ultraviolet (HPLC-UV) detection has been applied to the analysis of five widely used pesticides, simazine, fensulfothion, etridiazole, mepronil and bensulide, present at trace levels in water samples. CFME employs a single organic

Protocolos

analytical standard; Tokuthion, technical grade, pkg of 50 mg; Crotoxyphos; Phorate; Azinphos-ethyl; Diazinon; Azinphos-methyl; Demeton-O; Dimethoate; Chlorpyrifos-methyl

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