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  2. 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.

  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) ... [2] Acetone: 0.78 56.2 1.67 –94.8 K b [3] ... [2] K b [1] Water: 100.00 0.512 0.00

  4. Acetophenone - Wikipedia

    en.wikipedia.org/wiki/Acetophenone

    Acetophenone is formed as a byproduct of the cumene process, the industrial route for the synthesis of phenol and acetone.In the Hock rearrangement of isopropylbenzene hydroperoxide, migration of a methyl group rather than the phenyl group gives acetophenone and methanol as a result of an alternate rearrangement of the intermediate:

  5. Acetanisole - Wikipedia

    en.wikipedia.org/wiki/Acetanisole

    Melting point: 38.2 °C (100.8 °F; 311.3 K) [2] Boiling point: 254 °C (489 °F; 527 K) [2] Solubility in water. 2470 mg/L [1] Hazards Flash point:

  6. Boiling point - Wikipedia

    en.wikipedia.org/wiki/Boiling_point

    Water boiling at 99.3 °C (210.8 °F) at 215 m (705 ft) elevation. The boiling point of a substance is the temperature at which the vapor pressure of a liquid equals the pressure surrounding the liquid [1] [2] and the liquid changes into a vapor. The boiling point of a liquid varies depending upon the surrounding environmental pressure.

  7. 2-Aminoacetophenone - Wikipedia

    en.wikipedia.org/wiki/2-Aminoacetophenone

    2-Aminoacetophenone, also known as β-ketophenethylamine, α-desmethylcathinone, or phenacylamine, is a substituted phenethylamine derivative. [ 1 ] [ 2 ] It is the phenethylamine homologue of cathinone (β-ketoamphetamine) and hence is a parent compound of a large number of stimulant and entactogen drugs .

  8. Glyoxal - Wikipedia

    en.wikipedia.org/wiki/Glyoxal

    Glyoxal was first prepared and named by the German-British chemist Heinrich Debus (1824–1915) by reacting ethanol with nitric acid. [4] [5]Commercial glyoxal is prepared either by the gas-phase oxidation of ethylene glycol in the presence of a silver or copper catalyst (the Laporte process) or by the liquid-phase oxidation of acetaldehyde with nitric acid.

  9. Guaiacol - Wikipedia

    en.wikipedia.org/wiki/Guaiacol

    Boiling point: 204–206 °C (399–403 °F; 477–479 K) Solubility in water. 23.3 g/L at 25 °C Related compounds Related methoxyphenols. Mequinol 3-Methoxyphenol: