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  2. 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.

  3. Polar aprotic solvent - Wikipedia

    en.wikipedia.org/wiki/Polar_aprotic_solvent

    A polar aprotic solvent is a solvent that lacks an acidic proton and is polar. Such solvents lack hydroxyl and amine groups. In contrast to protic solvents, these solvents do not serve as proton donors in hydrogen bonding, although they can be proton acceptors. Many solvents, including chlorocarbons and hydrocarbons, are classifiable as aprotic ...

  4. Acetonitrile (data page) - Wikipedia

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

    log 10 of Acetonitrile vapor pressure. Uses formula log e ⁡ P m m H g = {\displaystyle \scriptstyle \log _{e}P_{mmHg}=} log e ⁡ ( 760 101.325 ) − 3.881710 log e ⁡ ( T + 273.15 ) − 4999.618 T + 273.15 + 41.05901 + 3.515956 × 10 − 06 ( T + 273.15 ) 2 {\displaystyle \scriptstyle \log _{e}({\frac {760}{101.325}})-3.881710\log _{e}(T+ ...

  5. Dichloromethane - Wikipedia

    en.wikipedia.org/wiki/Dichloromethane

    Dichloromethane (DCM, methylene chloride, or methylene bichloride) is an organochlorine compound with the formula C H 2 Cl 2. This colorless, volatile liquid with a chloroform-like, sweet odor is widely used as a solvent. Although it is not miscible with water, it is slightly polar, and miscible with many organic solvents. [12]

  6. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

  7. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    Water, being the most polar-solvent listed above, stabilizes the ionized species to a greater extent than does DMSO or Acetonitrile. Ionization - and, thus, acidity - would be greatest in water and lesser in DMSO and Acetonitrile, as seen in the table below, which shows p K a values at 25 °C for acetonitrile (ACN) [ 2 ] [ 3 ] [ 4 ] and ...

  8. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    The polarity, dipole moment, polarizability and hydrogen bonding of a solvent determines what type of compounds it is able to dissolve and with what other solvents or liquid compounds it is miscible. Generally, polar solvents dissolve polar compounds best and non-polar solvents dissolve non-polar compounds best; hence "like dissolves like".

  9. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.