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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Environmental fate & pathways

Endpoint summary

Administrative data

Description of key information

No biodegradation studies were conducted with1,2-dichloro-1-[difluoro(trifluoromethoxy)methoxy]-1,2,2-trifluoroethane. However, basing on the molecular structure no significant biodegradation is expected in the environment because of the fluorinated structure.

Fluorochemical products can resist degradation by acids, bases, oxidising and reducing agents, photolytic processes, microbes, and metabolic processes (Schultz et al. 2003), as the carbon–fluorine bond is the strongest existing covalent bond (450 kJ/mol) in organic chemistry (O’Hagan, 2008). Moreover, the presence of three pairs of nonbonding electrons around each fluorine atom and the effective shielding of carbon by the fluorine atoms prevents any significant attack (Kissa 2001).

Additional information