Only chloroform has significant applications of the haloforms. In the predominant application, chloroform is required for the production of
tetrafluoroethylene (TFE), precursor to
teflon. Chloroform is fluorinated by reaction with
hydrogen fluoride to produce
chlorodifluoromethane (R-22). Pyrolysis of chlorodifluoromethane (at 550–750 °C) yields TFE, with
difluorocarbene as an intermediate. :CHCl3 + 2 HF -> CHClF2 + 2 HCl :2 CHClF2 -> C2F4 + 2 HCl
Refrigerants and solvents Trihalomethanes released to the environment break down faster than
chlorofluorocarbons (CFCs), thereby doing much less damage to the
ozone layer.
Trifluoromethane and
chlorodifluoromethane are both used as
refrigerants. Chlorodifluoromethane is a refrigerant
HCFC, or
hydrochlorofluorocarbon, while fluoroform is an HFC, or
hydrofluorocarbon. Fluoroform is not ozone depleting. Chloroform is a common
solvent in organic chemistry. ==Occurrence and production==