1,1,2,2-tetrachloro-1,2-difluoroethane

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Structural formula
Structural formula of tetrachloro-1,2-difluoroethane
General
Surname 1,1,2,2-tetrachloro-1,2-difluoroethane
other names
  • 1,1,2,2-tetrachloro-1,2-difluoroethane ( IUPAC )
  • Tetrachloro-1,2-difluoroethane
  • R 112
  • Freon 112
  • CFC-112
Molecular formula C 2 Cl 4 F 2
Brief description

colorless solid

External identifiers / databases
CAS number 76-12-0
EC number 200-935-6
ECHA InfoCard 100,000,851
PubChem 6427
Wikidata Q2806548
properties
Molar mass 203.83 g mol −1
Physical state

firmly

density

1.6447 g cm −3

Melting point

26 ° C

boiling point

93 ° C

Vapor pressure

67.3 hPa (25 ° C)

solubility

practically insoluble in water

safety instructions
GHS labeling of hazardous substances
07 - Warning

Caution

H and P phrases H: 420
P: 273-502
MAK
  • DFG : 200 ml m −3 or 1700 mg m −3
  • Switzerland: 200 ml m −3 or 1690 mg m −3
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

1,1,2,2-Tetrachloro-1,2-difluoroethane is a chemical compound from the group of saturated halogenated hydrocarbons .

Extraction and presentation

Tetrachloro-1,2-difluoroethane can be obtained by reacting perchlorethylene and hydrogen fluoride in the presence of a catalyst . The most important commercial process for CFC and HCFC production is the successive replacement of chlorine with fluorine using hydrogen fluoride or antimony pentafluoride . The extent of the chlorine exchange can be controlled by varying the concentration of hydrogen fluoride, the contact time or the reaction temperature.

properties

Tetrachloro-1,2-difluoroethane is a colorless, odorless to sweet-smelling solid that is practically insoluble in water. It has an ozone depletion potential of 1.

use

Tetrachloro-1,2-difluoroethane has been used as a dry cleaning agent for wool , cotton and leather materials in combination with other solvents . It was also used as a cleaning agent in electronics and as a propellant in the plastics industry. After the Montreal Protocol came into force , the connection is practically no longer used today.

Individual evidence

  1. a b c d e f g h i j k Entry on tetrachloro-1,2-difluoroethane in the GESTIS substance database of the IFA , accessed on May 12, 2020(JavaScript required) .
  2. Swiss Accident Insurance Fund (Suva): Limits - Current MAK and BAT values (search for 76-12-0 or 1,1,2,2-tetrachloro-1,2-difluoroethane ), accessed on May 12, 2020.
  3. a b Entry on 1,1,2,2-TETRACHLORO-1,2-DIFLUOROETHANE in the Hazardous Substances Data Bank , accessed April 6, 2016.