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Merck
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45460

Supelco

Disulfoton

PESTANAL®, analytical standard

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About This Item

Formule empirique (notation de Hill):
C8H19O2PS3
Numéro CAS:
298-04-4
Poids moléculaire :
274.40
Numéro Beilstein :
1709167
Numéro CE :
206-054-3
Numéro MDL:
MFCD00036234
Code UNSPSC :
41116107
ID de substance PubChem :
329756753
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

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

Clé InChI

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.

Informations légales

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

Pictogrammes

Skull and crossbonesEnvironment
GHS06,GHS09

Mention d'avertissement

Danger

Mentions de danger

H300 + H310,H410

Classification des risques

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

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

271.4 °F

Point d'éclair (°C)

133 °C

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCB2181
BCBT8321
SZBC107XV
SZB8116XV
SZE8116X

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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
T A Johnson et al.
Journal of economic entomology, 100(4), 1328-1334 (2007-09-14)
The linden borer, Saperda vestita Say (Coleoptera: Cerambycidae), is a native insect species that is common throughout north central and northeastern North America. Over the past decade, increasing occurrence of damage associated with the linden borer has been reported on
T Zahn et al.
Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie, 48(1), 47-64 (1996-01-01)
Ultrastructural, stereological and biochemical alterations in isolated hepatocytes and the permanent fibrocyte-like cell line R1 from rainbow trout (Oncorhynchus mykiss) exposed to 0, 0.2, 2 and 20 mg/l of the phosphorodithioate pesticide disulfoton (Solvirex, O,O-diethyl S-2-ethylthioethyl phosphorodithioate) for up to
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
Qiu Gan et al.
Journal of agricultural and food chemistry, 54(20), 7753-7760 (2006-09-28)
The reactions of thiometon and its ethyl analogue, disulfoton, with reduced sulfur species [e.g., bisulfide (HS-), polysulfide (S(n)2-), thiophenolate (PhS-), and thiosulfate (S2O3(2-))] were examined in well-defined aqueous solutions under anoxic conditions. The role of reduced sulfur species was investigated
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