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Merck
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Documenti

445177

Sigma-Aldrich

O,O-Diethyl thiophosphate potassium salt

98%

Sinonimo/i:

Potassium O,O-diethyl phosphorothioate, Potassium O,O-diethylthiophosphate, Potassium di-O-ethyl phosphorothioate, Potassium diethyl thiophosphate

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About This Item

Formula condensata:
(C2H5O)2P(O)SK
Numero CAS:
5871-17-0
Peso molecolare:
208.26
Numero MDL:
MFCD00674011
Codice UNSPSC:
12352100
ID PubChem:
24868163
NACRES:
NA.22

Saggio

98%

Forma fisica

solid

Punto di fusione

180-186 °C (lit.)

Stringa SMILE

[K+].CCOP([O-])(=S)OCC

InChI

1S/C4H11O3PS.K/c1-3-6-8(5,9)7-4-2;/h3-4H2,1-2H3,(H,5,9);/q;+1/p-1
OVJCAYMARFNMQB-UHFFFAOYSA-M

Categorie correlate

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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D Koutroulakis et al.
Reproductive toxicology (Elmsford, N.Y.), 46, 98-105 (2014-04-02)
The aim of this study was to evaluate fetal exposure to organophosphate pesticides (OPs) by measuring their non-specific dialkyl-phosphate metabolites (DAPs) in amniotic fluid (AF), and to examine the potential association between prenatal exposure and fetal growth. AF samples were
M E Mount
American journal of veterinary research, 45(4), 817-824 (1984-04-01)
Recognition of exposure to diazinon, an organophosphate insecticide, was studied in goats. Urine and milk dialkyl phosphate concentrations (DETP; O,O-diethyl phosphorothionate) and blood cholinesterase activity (ChE) and diazinon concentrations were measured. Groups (n = 3 each) given (orally) diazinon at
Jialong Jie et al.
Nucleic acids research, 47(22), 11514-11526 (2019-11-15)
Phosphorothioate (PS) modifications naturally appear in bacteria and archaea genome and are widely used as antisense strategy in gene therapy. But the chemical effects of PS introduction as a redox active site into DNA (S-DNA) is still poorly understood. Herein
J Fukal et al.
Physical chemistry chemical physics : PCCP, 21(19), 9924-9934 (2019-05-01)
Structural interpretation of the 31P NMR shifts measured in O,O-diethyl thiophosphate (PT), 5,5-dimethyl-2-mercapto-1,3,2-dioxaphosphorinane 2-oxide (cPT), diethylphosphate (P) and 5,5-dimethyl-2-hydroxy-1,3,2-dioxaphosphinane 2-oxide (cP) was obtained by means of theoretical calculations including the effects of geometry, molecular dynamics, and solvent, relativistic effects and
Z Vasilić et al.
Chemico-biological interactions, 87(1-3), 305-313 (1993-06-01)
The presence and elimination rate of phosalone and its diethylphosphorus metabolites in blood serum and urine were studied in persons who had ingested a concentrated phosalone solution. Phosalone was detected only in serum samples. As it was rapidly hydrolysed and
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