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  2. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    At its melting point (−96 °C) is claimed to polymerize to give a white elastic solid, soluble in acetone, stable for several hours at room temperature. To do so, a vapor of acetone is co-condensed with magnesium as a catalyst onto a very cold surface.

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

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

    Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: ... Acetone: 0.78 56.2 1.67 –94.8 K b [3] Benzene: 0.87 80.1 2. ...

  4. Acetone (data page) - Wikipedia

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

    Critical point: 508 K (235 °C), 48 bar Std enthalpy change of fusion, ... Vapor pressure of acetone based on formula, = + from ...

  5. Dibenzylideneacetone - Wikipedia

    en.wikipedia.org/wiki/Dibenzylideneacetone

    Melting point: 111 °C (232 °F; 384 K) ... Soluble in acetone and chloroform, slightly soluble in ethanol. Hazards Occupational safety and health ...

  6. 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.

  7. Acetone peroxide - Wikipedia

    en.wikipedia.org/wiki/Acetone_peroxide

    Acetone peroxide (specifically, triacetone triperoxide) was discovered in 1895 by the German chemist Richard Wolffenstein. [5] [6] [7] Wolffenstein combined acetone and hydrogen peroxide, and then he allowed the mixture to stand for a week at room temperature, during which time a small quantity of crystals precipitated, which had a melting point of 97 °C (207 °F).

  8. Benzylideneacetone - Wikipedia

    en.wikipedia.org/wiki/Benzylideneacetone

    Benzylideneacetone can be efficiently prepared by the base-induced condensation of acetone and benzaldehyde: [3]. CH 3 C(O)CH 3 + C 6 H 5 CHO → C 6 H 5 CH=CHC(O)CH 3 + H 2 O. However, the benzylideneacetone formed via this reaction can undergo another Claisen-Schmidt condensation with another molecule of benzaldehyde to form dibenzylideneacetone.

  9. Acetoin - Wikipedia

    en.wikipedia.org/wiki/Acetoin

    Acetoin is a neutral, four-carbon molecule used as an external energy store by a number of fermentative bacteria. It is produced by the decarboxylation of alpha-acetolactate, a common precursor in the biosynthesis of branched-chain amino acids.