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  2. Acetonitrile (data page) - Wikipedia

    en.wikipedia.org/wiki/Acetonitrile_(data_page)

    1 Material Safety Data Sheet. 2 Structure and properties. ... Vapor-liquid Equilibrium for Acetonitrile/Toluene [4] P = 760 mmHg BP Temp. °C % by mole toluene liquid

  3. Acetonitrile - Wikipedia

    en.wikipedia.org/wiki/Acetonitrile

    Acetonitrile is used mainly as a solvent in the purification of butadiene in refineries. Specifically, acetonitrile is fed into the top of a distillation column filled with hydrocarbons including butadiene, and as the acetonitrile falls down through the column, it absorbs the butadiene which is then sent from the bottom of the tower to a second separating tower.

  4. Lithium chloride (data page) - Wikipedia

    en.wikipedia.org/wiki/Lithium_chloride_(data_page)

    6 Material Safety Data Sheet. 7 References. Toggle the table of contents. Lithium chloride (data page) ... Acetonitrile: 0.14 Acetone: 0.83 Formamide: 28.2 ...

  5. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  6. Acetone (data page) - Wikipedia

    en.wikipedia.org/wiki/Acetone_(data_page)

    1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. 4 Vapor pressure of liquid. 5 Distillation data. 6 Spectral data. 7 References.

  7. Tetraethylammonium bromide - Wikipedia

    en.wikipedia.org/wiki/Tetraethylammonium_bromide

    Safety data sheet (SDS) External MSDS: ... Evaporation of the water and recrystallization from acetonitrile yields a crystalline sample of TEAB. [2] Structure

  8. Chloroacetonitrile - Wikipedia

    en.wikipedia.org/wiki/Chloroacetonitrile

    A colorless liquid, it is derived from acetonitrile (CH 3 CN) by replacement of one H with Cl. In practice, it is produced by dehydration of chloroacetamide. [1] The compound is an alkylating agent, [2] and as such is handled cautiously. Chloroacetonitrile is also generated in situ by the reaction of acetonitrile with sulfur monochloride.

  9. Acrylonitrile - Wikipedia

    en.wikipedia.org/wiki/Acrylonitrile

    The aqueous solution consists of acrylonitrile, acetonitrile, hydrocyanic acid, and ammonium sulfate (from excess ammonia). A recovery column removes bulk water, and acrylonitrile and acetonitrile are separated by distillation. One of the first useful catalysts was bismuth phosphomolybdate (Bi 9 PMo 12 O 52) supported on silica. [11]

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