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Tetrachloroethylene

Tetrachloroethylene
Tetrachloroethylene
Tetrachloroethylene
Names
IUPAC name
Tetrachloroethene
Other names
Perchloroethene; Perchloroethylene; Perc; PCE
Identifiers
3D model (Jmol)
ChEBI
ChemSpider
ECHA InfoCard 100.004.388
EC Number 204-825-9
KEGG
RTECS number KX3850000
UNII
UN number 1897
Properties
C2Cl4
Molar mass 165.82 g·mol−1
Appearance Clear, colorless liquid
Odor mild, chloroform-like
Density 1.622 g/cm3
Melting point −19 °C (−2 °F; 254 K)
Boiling point 121.1 °C (250.0 °F; 394.2 K)
0.15 g/L (25 °C)
Vapor pressure 14 mmHg (20°C)
-81.6·10−6 cm3/mol
Viscosity 0.89 cP at 25 °C
Hazards
Main hazards Harmful (Xn),
Dangerous for
the environment (N)
Safety data sheet See: data page
External MSDS
R-phrases R40 R51/53
S-phrases S23 S36/37 S61
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point Not flammable
Lethal dose or concentration (LD, LC):
4000 ppm (rat, 4 hr)
5200 ppm (mouse, 4 hr)
4964 ppm (rat, 8 hr)
US health exposure limits (NIOSH):
PEL (Permissible)
TWA 100 ppm
C 200 ppm (for 5 minutes in any 3-hour period), with a maximum peak of 300 ppm
REL (Recommended)
Ca Minimize workplace exposure concentrations.
IDLH (Immediate danger)
Ca [150 ppm]
Related compounds
Related Related organohalides
Tetrabromoethylene
Tetraiodoethylene
Related compounds
Trichloroethylene
Dichloroethene
Tetrachloroethane
Supplementary data page
Refractive index (n),
Dielectric constantr), etc.
Thermodynamic
data
Phase behaviour
solid–liquid–gas
UV, IR, NMR, MS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YesYN ?)
Infobox references

Tetrachloroethylene, also known under the systematic name tetrachloroethene, or perchloroethylene ("perc" or "PERC"), and many other names, is a chlorocarbon with the formula Cl2C=CCl2. It is a colorless liquid widely used for dry cleaning of fabrics, hence it is sometimes called "dry-cleaning fluid." It has a sweet odor detectable by most people at a concentration of 1 part per million (1 ppm). Worldwide production was about 1 million metric tons (980,000 long tons; 1,100,000 short tons) in 1985.

Michael Faraday first synthesized tetrachloroethylene in 1821 by thermal decomposition of hexachloroethane.

Most tetrachloroethylene is produced by high temperature chlorinolysis of light hydrocarbons. The method is related to Faraday's discovery since hexachloroethane is generated and thermally decomposes. Side products include carbon tetrachloride, hydrogen chloride, and hexachlorobutadiene.

Several other methods have been developed. When 1,2-dichloroethane is heated to 400 °C with chlorine, tetrachloroethylene is produced by the chemical reaction:

This reaction can be catalyzed by a mixture of potassium chloride and aluminium chloride or by activated carbon. Trichloroethylene is a major byproduct, which is separated by distillation.

According to a United States Environmental Protection Agency (EPA) report of 1976, the quantity of tetrachloroethylene produced in the United States in 1973 totaled 320,000 metric tons (706 million lb). By 1993, the volume produced in the United States had dropped to 123,000 metric tons (271 million lb).


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