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1,2-Dibromotetrafluoroethane (C 2 Br 2 F 4) is a haloalkane. It is also known under codenames R-114B2 and Halon 2402. It is a colorless liquid with a boiling point of 47.2 °C. R-114B2 is occasionally used in fire suppression systems. It is highly volatile, passes through soil to air, and can be detected in the parts-per-quadrillion range.
1,2-Dibromotetrachloroethane (DBTCE) is an organohalide with the chemical formula C 2 Br 2 Cl 4. It is a crystalline solid that emits lachrymatory ( tear -producing) vapours. [ 2 ] Dibromotetrachloroethane can be used as a fungicide , [ 2 ] flame retardant [ 3 ] and a source for bromine in the laboratory. [ 4 ]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 1,1,2,2-Tetrafluoroethane (also called R-134 or HFC-134) is a hydrofluorocarbon, a fluorinated alkane. It is an isomer of the more-used 1,1,1,2-tetrafluoroethane (R-134a). It is used as a foam expansion agent and heat transfer fluid.
1,2-Dibromoethane has wider applications in the preparation of other organic compounds including those carrying modified diazocine rings [9] and vinyl bromide that is a precursor to some fire retardants. [4] In organic synthesis, 1,2-dibromoethane is used to brominate carbanions and to activate magnesium for certain Grignard reagents.
1,1,2,2-Tetrachloroethane. 1,1,2,2-tetrachloroethane (TeCA), also known by the brand names Bonoform, Cellon and Westron, is an organic compound. It is colorless liquid and has a sweet odor. It is used as an industrial solvent and as a separation agent. TeCA is toxic and it can be inhaled, consumed or absorbed through the skin.
Uses. 1,1,1,2-Tetrafluoroethane is a non-flammable gas used primarily as a "high-temperature" refrigerant for domestic refrigeration and automobile air conditioners. These devices began using 1,1,1,2-tetrafluoroethane in the early 1990s as a replacement for the more environmentally harmful R-12. Retrofit kits are available to convert units that ...
A convenient, safe method for generating TFE is the pyrolysis of the sodium salt of pentafluoropropionic acid: [6]. C 2 F 5 CO 2 Na → C 2 F 4 + CO 2 + NaF. The depolymerization reaction – vacuum pyrolysis of PTFE at 650–700 °C (1,200–1,290 °F) in a quartz vessel – is a traditional laboratory synthesis of TFE.
Tetrafluoroethane is a fluoroalkane with two isomers: 1,1,2,2-Tetrafluoroethane (R-134) 1,1,1,2-Tetrafluoroethane (R-134a) Categories: Set index articles on chemistry. Fluoroalkanes.