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  2. 1,1,1,2-Tetrafluoroethane (data page) - Wikipedia

    en.wikipedia.org/wiki/1,1,1,2-Tetrafluoroethane...

    This page lists chemical and physical properties of 1,1,1,2-tetrafluoroethane. [1] Physical Properties HFC-134a Boiling Point at 1 atm −15.34 °F (−26.30 °C)

  3. 1,1,2-Trichloro-1,2,2-trifluoroethane - Wikipedia

    en.wikipedia.org/wiki/1,1,2-Trichloro-1,2,2-tri...

    1,1,2-trichlorotrifluoroethane TCTFE Solvent 113. Identifiers ... Properties Chemical formula. CClF 2 CCl 2 F Molar mass: 187.37 g·mol −1 Appearance Colorless liquid

  4. 1,1,1,2-Tetrafluoroethane - Wikipedia

    en.wikipedia.org/wiki/1,1,1,2-Tetrafluoroethane

    1,1,1,2-Tetrafluoroethane (also known as norflurane (), R-134a, Klea 134a, Freon 134a, Forane 134a, Genetron 134a, Green Gas, Florasol 134a, Suva 134a, HFA-134a, or HFC-134a) is a hydrofluorocarbon (HFC) and haloalkane refrigerant with thermodynamic properties similar to R-12 (dichlorodifluoromethane) but with insignificant ozone depletion potential and a lower 100-year global warming ...

  5. 2,2-Dichloro-1,1,1-trifluoroethane - Wikipedia

    en.wikipedia.org/wiki/2,2-Dichloro-1,1,1-trifluo...

    Properties Chemical formula. C 2 H Cl 2 F 3: Molar mass: 152.93 ... 2,2-Dichloro-1,1,1-trifluoroethane or HCFC-123 is considered as an alternative to CFC-11 in low ...

  6. 1,1-Difluoroethane - Wikipedia

    en.wikipedia.org/wiki/1,1-Difluoroethane

    1,1-Difluoroethane, or DFE, is an organofluorine compound with the chemical formula C 2 H 4 F 2. This colorless gas is used as a refrigerant, where it is often listed as R-152a (refrigerant-152a) or HFC-152a (hydrofluorocarbon-152a). It is also used as a propellant for aerosol sprays and in gas duster products.

  7. 1,1,2,2-Tetrachloroethane - Wikipedia

    en.wikipedia.org/wiki/1,1,2,2-Tetrachloroethane

    1,1,2,2-tetrachloroethane was used in large amounts to produce other chemicals like trichloroethylene, tetrachloroethylene, and 1,2-dichloroethylene. [ 6 ] Because of its possible carcinogen effects on humans, the production of 1,1,2,2-tetrachloroethane has decreased significantly and is no longer widely used as an end-product. [ 7 ]

  8. Trichlorofluoromethane - Wikipedia

    en.wikipedia.org/wiki/Trichlorofluoromethane

    CCl 4 + Na 2 SiF 6 → CCl 3 F + CCl 2 F 2 + CCl 3 F + NaCl + SiF 4 CCl 4 + BrF 3 → BrF + CCl 2 F 2 + CCl 3 F. Trichlorofluoromethane was included in the production moratorium in the Montreal Protocol of 1987. It is assigned an ozone depletion potential of 1.0, and U.S. production was ended on January 1, 1996. [6]

  9. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    2 + BF 3. Although hydrogen fluoride may appear to be an unlikely nucleophile, it is the most common source of fluoride in the synthesis of organofluorine compounds. Such reactions are often catalysed by metal fluorides such as chromium trifluoride. 1,1,1,2-Tetrafluoroethane, a replacement for CFC's, is prepared industrially using this approach ...