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  2. Phosphorus trichloride - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride

    Phosphorus trichloride is an inorganic compound with the chemical formula PCl 3. A colorless liquid when pure, it is an important industrial chemical , being used for the manufacture of phosphites and other organophosphorus compounds .

  3. Phosphorus halide - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_halide

    Chemical formula CAS number Melting point Boiling point P–X bond length X–P–X bond angle Dipole moment; PF 3 Phosphorus trifluoride [7783-55-3] -151.5°C -101.8°C 156 pm 96.3° 1.03 D PCl 3 Phosphorus trichloride [7719-12-2] -93.6°C 76.1°C 204 pm 100° 0.56 D PBr 3 Phosphorus tribromide [7789-60-8] -41.5°C 173.2°C 222 pm 101°

  4. Diphosphorus tetrachloride - Wikipedia

    en.wikipedia.org/wiki/Diphosphorus_tetrachloride

    Near room temperature, the compound degrades to give phosphorus trichloride and an ill-defined phosphorus monochloride: P 2 Cl 4 → PCl 3 + 1/n [PCl] n. The compound adds to cyclohexene to give trans-C 6 H 10-1,2-(PCl 2) 2. [1]

  5. Phosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_chloride

    Phosphoryl chloride (commonly called phosphorus oxychloride) is a colourless liquid with the formula P O Cl 3. It hydrolyses in moist air releasing phosphoric acid and fumes of hydrogen chloride. It is manufactured industrially on a large scale from phosphorus trichloride and oxygen or phosphorus pentoxide. [4] It is mainly used to make ...

  6. Trichloride - Wikipedia

    en.wikipedia.org/wiki/Trichloride

    Trichloride may refer to: The trichloride ion, a polyhalogen ion; Actinium trichloride, AcCl 3; ... Osmium trichloride, OsCl 3; Phosphorus trichloride, PCl 3, a ...

  7. Phosphorus trichloride (data page) - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride...

    The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet for this chemical from a reliable source such as SIRI, and follow its directions.

  8. Phosphite ester - Wikipedia

    en.wikipedia.org/wiki/Phosphite_ester

    Phosphite esters are typically prepared by treating phosphorus trichloride with an alcohol. For alkyl alcohols the displaced chloride ion can attack the phosphite, causing dealkylation to give a dialkylphosphite and an organochlorine compound. [1] [2] The overall reaction is as follows: PCl 3 + 3 C 2 H 5 OH → (C 2 H 5 O) 2 P(O)H + 2 HCl + C 2 ...

  9. Methyldichlorophosphine - Wikipedia

    en.wikipedia.org/wiki/Methyldichlorophosphine

    Methyldichlorophosphine is produced by alkylation of phosphorus trichloride with methyl iodide followed by reduction of the resulting phosphonium salt with iron powder: [2] [3] CH 3 I + PCl 3 + AlCl 3 → [CH 3 PCl 3 ] + AlCl 3 I −