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45460

Supelco

Disulfoton

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C8H19O2PS3
CAS Number:
298-04-4
Molecular Weight:
274.40
Beilstein:
1709167
EC Number:
206-054-3
MDL number:
MFCD00036234
UNSPSC Code:
41116107
PubChem Substance ID:
329756753
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)SCCSCC

InChI

1S/C8H19O2PS3/c1-4-9-11(12,10-5-2)14-8-7-13-6-3/h4-8H2,1-3H3

InChI key

DOFZAZXDOSGAJZ-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,H410

Hazard Classifications

Acute Tox. 1 Dermal - 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

Flash Point(F)

271.4 °F

Flash Point(C)

133 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB2181
BCBT8321
SZBC107XV
SZB8116XV
SZE8116X

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Marilyn C Henderson et al.
Biochemical pharmacology, 68(5), 959-967 (2004-08-06)
Phorate and disulfoton are organophosphate insecticides containing three oxidizable sulfurs, including a thioether. Previous studies have shown that only the thioether is oxygenated by flavin-containing monooxygenase (FMO) and the sole product is the sulfoxide with no oxygenation to the sulfone.
Anthony M Lynch et al.
Mutagenesis, 23(2), 111-118 (2008-01-30)
There is considerable concern regarding the biological plausibility of the response of certain chemicals in the in vitro photoclastogenicity assay, suggesting that this assay is oversensitive and lacks specificity. To explore this further, four coded compounds (aminotriazole, propantheline bromide, cycloheximide
C Dauberschmidt et al.
Archives of environmental contamination and toxicology, 33(1), 42-46 (1997-07-01)
Subacute exposures (10 d) of the freshwater mollusc Dreissena polymorpha to disulfoton (10 mg/L), thiometon (6 mg/L), and its activated oxygen analogue demeton-S-methyl (6 mg/L) corroborate earlier findings of organophosphate resistance and accumulation in the organism. Mortality occurred not before
R D Jones et al.
Toxicology letters, 106(2-3), 181-190 (1999-07-14)
Technical grade disulfoton (DiSyston) was fed to Beagle dogs (four animals per sex and treatment level) at nominal concentrations of 0, 0.5, 4 and 12 ppm for 1 year. The purpose of this study was to characterize the potential general
B diSioudi et al.
Biochemistry, 38(10), 2866-2872 (1999-03-13)
Organophosphorus hydrolase (OPH, EC 8.1.3.1) is a dimeric, bacterial enzyme that detoxifies many organophosphorus neurotoxins by hydrolyzing a variety of phosphonate bonds. The histidinyl residues at amino acid positions 254 and 257 are located near the bimetallic active site present
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