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  2. Hydrogen fluoride - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_fluoride

    Hydrogen fluoride does not boil until 20 °C in contrast to the heavier hydrogen halides, which boil between −85 °C (−120 °F) and −35 °C (−30 °F). [ 6 ] [ 7 ] [ 8 ] This hydrogen bonding between HF molecules gives rise to high viscosity in the liquid phase and lower than expected pressure in the gas phase.

  3. Fluoroboric acid - Wikipedia

    en.wikipedia.org/wiki/Fluoroboric_acid

    The acidity of fluoroboric acid is complicated by the fact that its name refers to a range of different compounds, e.g. [H(CH 3 CH 2) 2 O] + [BF 4] − (dimethyloxonium tetrafluoroborate), [H 3 O] + [BF 4] − (oxonium tetrafluoroborate), and HF·BF 3 (hydrogen fluoride-boron trifluoride 1:1 adduct) – each with a different acidity.

  4. Hydrofluoric acid - Wikipedia

    en.wikipedia.org/wiki/Hydrofluoric_acid

    Hydrofluoric acid is a solution of hydrogen fluoride (HF) in water.Solutions of HF are colorless, acidic and highly corrosive.A common concentration is 49% (48–52%) but there are also stronger solutions (e.g. 70%) and pure HF has a boiling point near room temperature.

  5. Linear alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Linear_alkylbenzene

    Hydrogen fluoride (HF) and aluminium chloride (AlCl 3) are the two major catalysts for the alkylation of benzene with linear mono-olefins. The HF-based process is commercially dominant; however, the risk of releasing HF (a poisonous substance) into the environment became a concern particularly after the Clean Air Act Amendment.

  6. Hexafluorosilicic acid - Wikipedia

    en.wikipedia.org/wiki/Hexafluorosilicic_acid

    The hydrogen bonding between the fluoride and protons are indicated by dashed lines. Color code: green = F, orange = Si, red = O, gray = H. [4] Hexafluorosilicic acid has been crystallized as various hydrates. These include (H 5 O 2) 2 SiF 6, the more complicated (H 5 O 2) 2 SiF 6 ·2H 2 O, and (H 5 O 2)(H 7 O 3)SiF 6 ·4.5H 2 O.

  7. 1,1-Difluoroethane - Wikipedia

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

    1,1-Difluoroethane is a synthetic substance that is produced by the mercury-catalyzed addition of hydrogen fluoride to acetylene: [4] HCCH + 2 HF → CH 3 CHF 2. The intermediate in this process is vinyl fluoride (C 2 H 3 F), the monomeric precursor to polyvinyl fluoride.

  8. 1,1,1,2,3,3,3-Heptafluoropropane - Wikipedia

    en.wikipedia.org/wiki/1,1,1,2,3,3,3...

    At high temperatures, heptafluoropropane will decompose and produce hydrogen fluoride. The decomposition produces a sharp, pungent odour, which can be perceived in concentrations far below a dangerous level. Other decomposition products include carbonyl fluoride, carbon monoxide and carbon dioxide. Prior to re-entry of a room where HFC-227ea ...

  9. Bromotrifluoromethane - Wikipedia

    en.wikipedia.org/wiki/Bromotrifluoromethane

    Chloroform is fluorinated with hydrogen fluoride. [4] ... MSDS sheet at airliquide.com ... MSDS for bromotrifluoromethane ...