359-58-0

Basic information

• Product Name: 1-CHLORO-1,1,2,3,3,3-HEXAFLUOROPROPANE
• Synonyms: 1-CHLORO-1,1,2,3,3,3-HEXAFLUOROPROPANE;1-Chloro-1,1,2,3,3,3-hexafluoropropane 98%;1-Chloro-1,1,2,3,3,3-hexafluoropropane98%
• CAS NO: 359-58-0
• Molecular Formula: C₃HClF₆
• Molecular Weight: 186.48
• Product Categories: refrigerants
• Mol File: 359-58-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 17.15°C
• Appearance: /
• Density: 1.2904 (estimate)
• Vapor Pressure: 943mmHg at 25°C
• Refractive Index: 1.2173 (estimate)
• CAS DataBase Reference: 1-CHLORO-1,1,2,3,3,3-HEXAFLUOROPROPANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-CHLORO-1,1,2,3,3,3-HEXAFLUOROPROPANE(359-58-0)
• EPA Substance Registry System: 1-CHLORO-1,1,2,3,3,3-HEXAFLUOROPROPANE(359-58-0)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 359-58-0(Hazardous Substances Data)

Usage

General Description

1-Chloro-1,1,2,3,3,3-hexafluoropropane, also known as HCFC-225ca, is a colorless gas commonly used as a refrigerant and foam blowing agent. It is a halogenated hydrocarbon with six fluorine atoms, providing excellent thermal and chemical stability. It is commonly used in refrigeration and air conditioning systems, as well as in the production of insulating foams and fire extinguishing agents. However, due to its ozone-depleting potential, HCFC-225ca is being phased out of use under the Montreal Protocol, and is being replaced with more environmentally friendly alternatives. It's also important to note that it is a chemical compound that should be handled with care and according to safety regulations.

InChI:InChI=1/C3HClF6/c4-2(6,7)1(5)3(8,9)10/h1H

Upstream product

• 75-34-3 1,1-dichloroethane 
• 116-15-4 perfluoropropylene 
• 71-55-6 1,1,1-trichloroethane 
• 661-97-2 1,2-dichlorohexafluoropropane 
• 431-63-0 1,1,1,2,3,3-hexafluoropropane 
• 812-30-6 1,1,2-trichloro-1,2,3,3,3-pentafluoropropane 
• 1652-80-8 2,2-dichloro-1,1,1,3,3,3-hexafluoro-propane 

Relevant articles and documents

Reaction of Hexafluoropropene with Halogenoalkanes

Insertion of hexafluoropropene under thermal and/or photochemical conditions occurs into C-H bonds of the halogenomethanes, MeCl, CH2Cl2, CHCl3, MeF, CH2CF2 and CHF2Cl and the fluoroethanes EtF, MeCHF2 and MeCF3, into C-H and C-Cl bonds of the monochloroalkanes EtCl, MeCHFCl, n-PrCl, i-PrCl, t-BuCl and i-BuCl and into C-Cl bonds of allyl chloride and the chloroalkanes CH2ClCH2Cl, MeCHCl2, CH2ClCHCl2 and MeCCl3.

1,2,3,3,3-PENTAFLUOROPROPENE PRODUCTION PROCESSES

A process is disclosed for making CF3CF=CHF. The process involves reacting CF3CCIFCCI2F with H2 in a reaction zone in the presence of a catalyst to produce a product mixture comprising CF3CF=CHF. The catalyst has a catalytically effective amount of palladium supported on a support selected from the group consisting of alumina, fluorided alumina, aluminum fluoride and mixtures thereof and the mole ratio of H2 to CF3CCIFCCI2F fed to the reaction zone is between about 1 :1 and about 5:1.. Also disclosed are azeotropic compositions of CF3CCIFCCI2F and HF and azeotropic composition of CF3CHFCH2F and HF.

PHOTOCHLORINATION AND FLUORINATION PROCESS FOR PREPARATION OF FLUORINE-CONTAINING HYDROCARBONS

A process is disclosed for increasing the fluorine content of at least one compound selected from halohydrocarbons and hydrocarbons. The process involves (a) directing light from a light source through the wall of a reactor to interact with reactants comprising chlorine and said at least one compound in said reactor, thereby producing a halogenated hydrocarbon having increased chlorine content by photochlorination, and (b) reacting said halogenated hydrocarbon produced by the photochlorination in (a) with HF; and is characterized by the light directed through the reactor wall being directed through a poly(perhaloolefin) polymer.