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224294

Sigma-Aldrich

Thiophosphoryl chloride

98%

Synonym(s):

Phosphorus sulfochloride, Phosphorus thiochloride

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About This Item

Linear Formula:
PSCl3
CAS Number:
3982-91-0
Molecular Weight:
169.40
EC Number:
223-622-6
MDL number:
MFCD00011504
UNSPSC Code:
12352100
PubChem Substance ID:
24853426
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.555 (lit.)

bp

125 °C (lit.)

mp

−35 °C (lit.)

solubility

benzene: soluble(lit.)
carbon disulfide: soluble(lit.)
carbon tetrachloride: soluble(lit.)
chloroform: soluble(lit.)

density

1.668 g/mL at 25 °C (lit.)

SMILES string

ClP(Cl)(Cl)=S

InChI

1S/Cl3PS/c1-4(2,3)5

InChI key

WQYSXVGEZYESBR-UHFFFAOYSA-N

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Application

Thiophosphoryl chloride was used in the synthesis of O-ethyl dichlorothiophosphate.

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H302,H314,H330,H335

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ5809
MKCN9464
MKCM8141
MKCK5351
SHBL0202

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D Coloşi-Esca et al.
Journal of applied toxicology : JAT, 4(5), 230-235 (1984-10-01)
The rat acute oral LD50 value of PSCl3 is 750 mg per kg body weight. A rat 90-day oral feeding study at dose levels of 7.5 mg (P1) and 37.5 mg (P5) per kg resulted in increased body weight gain.
[Hygienic substantiation of the maximum permissible level of phosphorus thiotrichloride in reservoir water].
V M Tomkiv
Gigiena i sanitariia, (11)(11), 68-70 (1988-11-01)
Sarah E Lee et al.
Chembiochem : a European journal of chemical biology, 12(4), 633-640 (2011-02-10)
The elucidation of signalling pathways relies heavily upon the identification of protein kinase substrates. Recent investigations have demonstrated the efficacy of chemical genetics using ATP analogues and modified protein kinases for specific substrate labelling. Here we combine N(6) -(cyclohexyl)ATPγS with
Wen Jun Gui et al.
Analytical biochemistry, 357(1), 9-14 (2006-08-22)
Two haptens of the insecticide triazophos (O,O-diethyl O-[1-phenyl-1H-1,2,4-triazol-3-yl] phosphorothioate) were synthesized by introducing appropriate spacers in the O-ethyl site of the analyte molecular structure. First, thiophosphoryl chloride (PSCl(3)) reacts with methanol at low temperature to give O-ethyl dichlorothiophosphate. After reacting
J T Slama et al.
Analytical biochemistry, 209(1), 143-149 (1993-02-15)
Elemental [35S]sulfur was shown to equilibrate with the sulfur of thiophosphoryl chloride when these materials are heated together. This isotopic exchange reaction is the basis of a convenient, microscale synthesis of high specific activity [35S]PSCl3. [35S]Thiophosphoryl chloride is otherwise not
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