354-56-3

Usage

Uses

Used in Chemical Manufacturing Industry:
FLUOROPENTACHLOROETHANE is used as a solvent for the manufacturing of certain polymers and resins, due to its ability to dissolve a wide range of substances and facilitate chemical reactions.
Used in Cleaning Products Industry:
FLUOROPENTACHLOROETHANE is used as a solvent in cleaning products, particularly for its effectiveness in dissolving grease and oils, and its low toxicity and reactivity.
Environmental Impact:
FLUOROPENTACHLOROETHANE is recognized for its destructive impact on the ozone layer and contribution to global warming. As a result, its production and use have been phased out and are heavily regulated under the Montreal Protocol to protect the Earth's ozone layer and mitigate climate change.

InChI:InChI=1/C2Cl5F/c3-1(4,5)2(6,7)8

Upstream product

• 127-18-4 1,1,2,2-tetrachloroethylene 
• 359-28-4 1,1,2-trichloro-2-fluoroethane 
• 67-72-1 hexachloroethane 
• 27794-53-2 chlorofluoroacetylene 
• 64-17-5 ethanol 
• 141-78-6 ethyl acetate 
• 7664-39-3 hydrogen fluoride 
• 7782-50-5 chlorine 
• 75-71-8 Dichlorodifluoromethane 
• 76-13-1 1,1,2-Trichloro-1,2,2-trifluoroethane 
• 7647-18-9 antimonypentachloride 
• 7783-56-4 antimony(III) fluoride 
• 76-01-7 pentachloroethane 
• 354-58-5 1,1,1-Trichloro-2,2,2-trifluoroethane 

Downstream Products

• 359-29-5 trichlorofluoroethene 

Relevant academic research and scientific papers

Dynamic behaviour of chlorofluoroethanes at fluorinated chromia aerogels and fluorinated zinc(II) or magnesium(II) doped chromia aerogels

The preparation and characterisation of two series of fluorinated chromia aerogel materials, lightly doped with zinc(II) or magnesium(II), are described. They behave as heterogeneous catalysts for transformations of 1,1,2-trichlorotrifluoroethane under HF

Conversion of 1,1,2-trichlorotrifluoroethane to 1,1,1-trichlorotrifluoroethane and 1,1-dichlorotetrafluoroethane over aluminium-based catalysts

Conversion of CCl2FCClF2 to CCl2FCF3 is achieved in the temperature range, 593-713 K, under flow conditions by using the catalysts, β-AlF3 or γ-alumina, prefluorinated with CCl2F2/sub

Catalytic Liquid-phase Fluorination of Tetrachlorethene (PCE) with Titanium Antimony Mixed Halides

A new catalyst consisting of a TiCl4-SbCl5 mixture with a molar composition Sb : Ti = 4 : 1 makes possible the fluorination of tetrachlorethene with liquid HF at 90 deg C.

REACTIONS OF CHLORINE MONOFLUORIDE. IV. ADDITION OF CHLORINE MONOFLUORIDE TO HALOGEN-SUBSTITUTED ALKENES

The reactions of chlorine monofluoride with halogenoethylenes (1,1-dichloro-, 1,2-dichloro-, trichloro-, and tetrachloroethylenes) and halogenopropenes ( 3-bromo-, 3,3,3-trichloro-, E- and Z-1,3-dichloro-, 3-chloro-2-methyl-, and perfluoropropenes) were investigated in inert solvents in the presence of ethyl acetate as external nucleophile.In all cases chloroacyloxy adducts were isolated and identified in addition to the chlorofluorination products, and this indicates an electrophilic mechanism for the chlorofluorination of polyhalogenoalkenes.Methyl chloromaleate, chlorofumarate, chlorofluoroethylenedicarboxylate, α,β-difluoroacrylate, and perfluoromethacrylate in anhydrous hydrogen fluoride form the corresponding chlorofluoro adducts with satisfactory yields, whereas the reaction takes place with difficulty in inert solvents.