Disulfoton

Name: Disulfoton
Brand: SIAL
Price: 55.12 USD
Availability: InStock

PESTANAL^®, analytical standard

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250 MG

$55.12

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About This Item

Empirical Formula (Hill Notation):

C₈H₁₉O₂PS₃

CAS Number:

298-04-4

Molecular Weight:

274.40

Beilstein/REAXYS Number:

1709167

EC Number:

206-054-3

MDL number:

MFCD00036234

UNSPSC Code:

41116107

PubChem Substance ID:

329756753

NACRES:

NA.24

Key Documents

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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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This Item	31562	45871	32487
Supelco 45460 Disulfoton	Supelco 31562 Disulfoton-sulfoxide	Supelco 45871 Disulfoton-sulfone	Supelco 32487 Spirotetramat Metabolite BYI08330 enol-glucoside
format neat	format neat	format neat	format neat
technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable
grade analytical standard	grade analytical standard	grade analytical standard	grade analytical standard
product line PESTANAL^®	product line PESTANAL^®	product line PESTANAL^®	product line PESTANAL^®
shelf life limited shelf life, expiry date on the label	shelf life limited shelf life, expiry date on the label	shelf life limited shelf life, expiry date on the label	shelf life limited shelf life, expiry date on the label
application(s) agriculture environmental	application(s) agriculture environmental	application(s) agriculture environmental	application(s) agriculture environmental

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

GHS06,GHS09

signalword

Danger

hcodes

H300 + H310,H410

pcodes

P262 - P264 - P273 - P280 - P301 + P310 - P302 + P352 + P310

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 3

flash_point_f

271.4 °F

flash_point_c

133 °C

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number

BCCM5550

BCCB2181

BCBT8321

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S-oxygenation of the thioether organophosphate insecticides phorate and disulfoton by human lung flavin-containing monooxygenase 2.

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.

Cycloheximide and disulfoton are positive in the photoclastogencity assay but do not absorb UV irradiation: another example of pseudophotoclastogenicity?

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

Organophosphates in the zebra mussel Dreissena polymorpha: subacute exposure, body burdens, and organ concentrations.

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

Growth rate influences reductive biodegradation of the organophosphorus pesticide demeton by Corynebacterium glutamicum.

L Girbal et al.

Biodegradation, 11(6), 371-376 (2001-10-06)

The organophosphorous pesticide, demeton-S-methyl was transformed by Corynebacterium glutamicum in co-metabolism with more readily degradable substrates. Glucose, acetate and fructose were tested as growth substrates, and the highest demeton-S-methyl biotransformation average rate (0.78 mg l(-1) h(-1)) and maximum instantaneous rate

Mutant of Bungarus fasciatus acetylcholinesterase with low affinity and low hydrolase activity toward organophosphorus esters.

Thomas Poyot et al.

Biochimica et biophysica acta, 1764(9), 1470-1478 (2006-09-12)

Enzymes hydrolysing highly toxic organophosphate esters (OPs) are promising alternatives to pharmacological countermeasures against OPs poisoning. Bungarus fasciatus acetylcholinesterase (BfAChE) was engineered to acquire organophosphate hydrolase (OPase) activity by reproducing the features of the human butyrylcholinesterase G117H mutant, the first

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