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D91683

Sigma-Aldrich

O,O′-Diethyl chlorothiophosphate

97%

Sinonimo/i:

O,O′-Diethylthiophosphoric chloride, Diethyl phosphorochloridothionate

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About This Item

Formula condensata:
(CH3CH2O)2P=(S)Cl
Numero CAS:
2524-04-1
Peso molecolare:
188.61
Numero CE:
219-755-4
Numero MDL:
MFCD00009088
Codice UNSPSC:
12352100
ID PubChem:
24894270
NACRES:
NA.22

Tensione di vapore

1.4 mmHg ( 50 °C)

Saggio

97%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.472 (lit.)

P. eboll.

45 °C/3 mmHg (lit.)

Densità

1.2 g/mL at 25 °C (lit.)

Stringa SMILE

CCOP(Cl)(=S)OCC

InChI

1S/C4H10ClO2PS/c1-3-6-8(5,9)7-4-2/h3-4H2,1-2H3
KMJJJTCKNZYTEY-UHFFFAOYSA-N

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Avvertenze

Danger

Indicazioni di pericolo

H302,H311 + H331,H314,H411

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

197.6 °F - closed cup

Punto d’infiammabilità (°C)

92 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

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H Kataoka et al.
Journal of chromatography. A, 723(1), 93-99 (1996-02-02)
A selective and sensitive method was developed for the determination of volatile N-nitrosamines by gas chromatography (GC). After denitrosation of N-nitrosamines with hydrobromic acid, the resulting secondary amines were converted into their N-diethylthiophosphoryl derivatives and then measured by GC using
Mateusz Daśko et al.
Drug development research, 80(6), 857-866 (2019-07-14)
In the present work, we described convenient methods for the synthesis of N-thiophosphorylated 3-(4-aminophenyl)-coumarin-7-O-sulfamates as steroid sulfatase (STS) inhibitors. To design the structures of the potential STS inhibitors, molecular modeling techniques were used. A computational docking method was used to
H Kataoka et al.
Biomedical chromatography : BMC, 7(3), 129-133 (1993-05-01)
A selective and sensitive method has been developed for the determination of secondary amines by gas chromatography (GC). After removal of primary amines by the reaction with o-phthaldialdehyde, secondary amines were converted into their N-diethylthiophosphoryl derivatives and then measured by

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