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45307

Supelco

Fensulfothion

PESTANAL®, analytical standard

Synonym(s):

Diethyl 4-(methylthio)phenyl phosphate

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About This Item

Empirical Formula (Hill Notation):
C11H17O4PS2
CAS Number:
115-90-2
Molecular Weight:
308.35
Beilstein:
2219515
EC Number:
204-114-3
MDL number:
MFCD00055487
UNSPSC Code:
41116107
PubChem Substance ID:
329756633
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

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

InChI key

XDNBJTQLKCIJBV-UHFFFAOYSA-N

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Application

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

Legal Information

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

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H300 + H310 + H330 - H410

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC9483
BCCC0153
BCBX5664
BCBW3711
BCBV6081

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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
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Protocols

US EPA Method 8141: GC Analysis of Organophosphorus Pesticides (OP-Pest) on Equity®-5, NPD Detection

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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