157775
Phosphorus pentachloride
reagent grade, 95%
Synonym(s):
Phosphorus(V) chloride
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About This Item
Linear Formula:
PCl5
CAS Number:
Molecular Weight:
208.24
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.21
Recommended Products
grade
reagent grade
Quality Level
vapor pressure
<1 mmHg ( 20 °C)
Assay
95%
form
powder
pH
1 (5 g/L)
mp
179-181 °C (subl.) (lit.)
SMILES string
ClP(Cl)(Cl)(Cl)Cl
InChI
1S/Cl5P/c1-6(2,3,4)5
InChI key
UHZYTMXLRWXGPK-UHFFFAOYSA-N
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General description
Phosphorus pentachloride is a light yellow colored phosphorous halide. It participates in the synthesis of thiazoline analogs.
Application
Phosphorus pentachloride may be used in the synthesis of following compounds:
Phosphorus pentachloride may be used as halogenating reagent to convert any substituted aldehyde into the corresponding vinyl halide. It can also undergo reaction with ammonium chloride to yield linear phosphazenes and cyclophosphazenes.
- benzenesulfonyl chloride
- malonic dinitrile
- aromatic sulfonyl chlorides
Phosphorus pentachloride may be used as halogenating reagent to convert any substituted aldehyde into the corresponding vinyl halide. It can also undergo reaction with ammonium chloride to yield linear phosphazenes and cyclophosphazenes.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT RE 2 Inhalation
Target Organs
Respiratory Tract
Supplementary Hazards
Storage Class Code
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 1
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Comprehensive Organic Functional Group Transformations: Synthesis: carbon with two heteroatoms, each attached by a single bond (2005)
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Phosphorus-Nitrogen Compounds: Cyclic, Linear, and High Polymeric Systems (2012)
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Concise Encyclopedia Chemistry, 120-120 (1994)
Synthetic studies of thiazoline and thiazolidine-containing natural products-1. Phosphorus pentachloride-mediated thiazoline construction reaction.
Ino A and Murabayashi A.
Tetrahedron, 55(34), 10271-10282 (1999)
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