Tetrachloro-1,2-difluoroethane
chemical compound

Tetrachloro-1,2-difluoroethane is a chlorofluorocarbon known as Freon 112, CFC-112 or R-112. It has a symmetrical structure CCl2FCCl2F and so can be called symmetrical tetrachlorodifluoroethane. "Symmetrical" may also be abbreviated to "s-" or "sym-". In contrast an asymmetrical isomer has formula CCl3CClF2.
Production
CFC-112 can be made in a reaction of hexachloroethane or tetrachloroethane with hydrogen fluoride and extra chlorine. This reaction is catalysed by aluminium fluoride with some extra iron, nickel and chromium at 400°C. The extra metal in the catalyst yields can be 98% compared with the unsymmetrical isomer.
Mixed with perfluorooctane, it is a solvent for polydimethylsiloxane.
CFC-112 can be prepared as a mixture with other hydrochlorofluorocarbons from trichloroethylene and anhydrous hydrogen fluoride when electric current is passed through.
Another method involves addition of fluorine to the double bond in tetrachloroethylene by lead tetrafluoride:
CCl2=CCl2 + PbF4 → CCl2F−CCl2F + PbF2
When CFC-11 is packaged with alcohol in a metal container, a free radical reaction can result in production of CFC-112.
Properties
Critical properties are critical temperature 278°C, critical pressure 4.83 MPa at a density of 0.754 g/cc.
“Tetrachloro-1,2-difluoroethane” enters the record as chemical compound. Crown Archives preserves that source wording while asking what Tetrachloro-1, 2-difluoroethane and chemical can confirm, complicate or overturn.
Why this record matters
“Tetrachloro-1,2-difluoroethane” is worth following because a concise public description often conceals a longer documentary argument. Here, Tetrachloro-1, 2-difluoroethane and chemical provides the most credible route into that argument.
The date and method of observation matter as much as the stated conclusion, especially where classification or consensus has changed. The source revision retrieved here is dated Sep 17, 2026. The linked authority identifier is Q2806548. None of the 0 selected statements returned an explicit reference.
Scientific names, classifications and consensus can change while older terminology persists in catalogues and historical literature. The source lead contains qualifying language; that uncertainty should survive quotation, summary and reuse. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.
How to read it
Check terminology, classification and the date of the cited evidence. Scientific names and technical consensus can change while older records retain historical value.
- Current terminology
- Classification context
- Finding cited technical literature
Primary datasets, specimen catalogues, standards bodies and the most recent peer-reviewed literature.
Three-step research path
- Establish the record: confirm the title “Tetrachloro-1,2-difluoroethane”, its source revision and the description used here.
- Expand the search: follow Tetrachloro-1,2-difluoroethane primary sources, Tetrachloro-1,2-difluoroethane archive and Tetrachloro-1 research across catalogues and specialist indexes.
- Test the account: compare the strongest cited source with the responsible institution’s current record and note any disagreement.
Questions for further research
- Which source most directly establishes the central claim about “Tetrachloro-1,2-difluoroethane”?
- Is the terminology current, historical or disputed?
- Has classification or technical consensus changed since the cited source?
Search terms from this dossier
This entry incorporates text from “Tetrachloro-1,2-difluoroethane” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.