422-55-9

Usage

Physical State

Colorless and odorless gas

Usage

Fire extinguishing agent, blowing agent in insulation materials, and refrigerant in industrial applications

Non-toxic

Safe for use in sensitive environments like data centers, museums, and aircraft cabins

Non-corrosive

Does not cause damage to materials it comes into contact with

Environmentally Friendly

Low global warming potential and ozone depletion potential

Climate Change Concern

High potential for contributing to climate change

Ongoing Research

Efforts to find more sustainable alternatives due to its climate change impact

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

Upstream product

• 662-01-1 1,3-dichlorohexafluoropropane 
• 75-45-6 Chlorodifluoromethane 
• 422-54-8 1,1,3-trichloro-2,2,3,3-tetrafluoropropane 
• 64-17-5 ethanol 
• 116-14-3 polytetrafluoroethylene 
• 75-10-5 Difluoromethane 
• 354-25-6 2-chloro-1,1,2,2-tetrafluoroethane 
• 507-55-1 1,3-dichloro-1,1,2,2,3-pentafluoropropane 
• 128903-21-9 2,2-dichloro-1,1,1,3,3-pentafluoropropane 

Downstream Products

• 662-01-1 1,3-dichlorohexafluoropropane 
• 422-86-6 perfluoropropyl chloride 
• 116-14-3 polytetrafluoroethylene 
• 116-15-4 perfluoropropylene 
• 79-38-9 Chlorotrifluoroethylene 
• 35822-90-3 benzoyl-tert-butylnitroxyl radical 
• 29271-97-4 C₁₁H₁₅ClNO 
• 39058-86-1 C₁₁H₁₅FNO 
• 75-71-8 Dichlorodifluoromethane 
• 354-25-6 2-chloro-1,1,2,2-tetrafluoroethane 
• 115-25-3 Octafluorocyclobutane 

Relevant academic research and scientific papers

PROCESS FOR PRODUCING 1, 1-DICHLORO-2, 2, 3, 3, 3-PENTAFLUOROPROPANE

To provide a process for producing, at a high content ratio, 1,1-dichloro-2,2,3,3,3-pentafluoropropane (HCFC-225ca) which is useful as e.g. a starting material to obtain 1,1-dichloro-2,3,3,3-tetrafluoropropene (CFO1214ya). The process for producing HCFC-225ca of the present invention comprises subjecting a raw material composed of dichloropentafluoropropane (HCFC-225) including 2,2-dichloro-1,1,1,3,3-pentafluoropropane (HCFC225aa) to an isomerization reaction at a temperature of at most 290° C. in a gas phase in the presence of a metal oxide catalyst thereby to isomerize HCFC-225aa to HCFC-225ca.

Catalytical production processes for making hydrohalopropanes and hydrofluorobutanes

A process is disclosed for making hydrohalopropanes or hydrofluorobutanes. The process involves reacting a hydrofluoromethane with a fluoroolefin in the presence of an aluminum catalyst to produce a hydrohalopropane or a hydrofluorobutane. The hydrofluoromethane is CH2F2 or CH3F. The fluoroolefin is CF2═CF2, ClFC═CF2, or CF3CF═CF2.

PYROLYSIS PROCESS

The present invention relates to the pyrolysis of hydrochlorofluorocarbons to form fluoromonomers such as tetrafluoroethylene, the pyrolysis being carried out in a reaction zone lined with nickel and mechanically supported by a jacket of other corrosion resistant metal, the nickel lining providing an improved yield of valuable reaction products.

19F nuclear magnetic resonance studies of halogenated propanes

The relationship between 19F chemical shifts in halogenated propanes and their structures are elucidated using MNDO calculations to determine the population of rotamers.The pairs of atom gauche to a fluorine atom and van der Waals interaction between the two terminal substituents are responsible for the 19F chemical shifts.The differences among chemical shifts in diastereomers are also discussed in terms of the conformation of molecule.