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  2. Acetic acid (data page) - Wikipedia

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

    1 Material Safety Data Sheet. ... Print/export Download as PDF; ... Vapor-liquid Equilibrium for Acetic acid/Water [3] P = 760 mm Hg BP Temp.

  3. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    Acetic acid: an organic acid; is one of the simplest carboxylic acids: Acetone: an organic compound; simplest example of the ketones: Acetylene: a hydrocarbon and the simplest alkyne; widely used as a fuel and chemical building block Ammonia: inorganic; the precursor to most nitrogen-containing compounds; used to make fertilizer Ammonium hydroxide

  4. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    "Glacial acetic acid" is a name for water-free acetic acid. Similar to the German name "Eisessig" ("ice vinegar"), the name comes from the solid ice-like crystals that form with agitation, slightly below room temperature at 16.6 °C (61.9 °F). Acetic acid can never be truly water-free in an atmosphere that contains water, so the presence of 0. ...

  5. 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.

  6. Cellulose acetate - Wikipedia

    en.wikipedia.org/wiki/Cellulose_acetate

    However, acetic acid is usually also formed as a by-product of the reaction, so that the solvent is ultimately a mixture of methylene chloride, acetic anhydride and acetic acid. A very rare heterogeneous process is the fiber acetate process, which is only used for the production of cellulose triacetate as an end product.

  7. Cinnamyl acetate - Wikipedia

    en.wikipedia.org/wiki/Cinnamyl_acetate

    This synthesis requires the lipase Novozym 435, and is performed in a solvent-free system. The reaction is as follows: [12] Cinnamyl acetate 2 can also be synthesized via a non-enzymatic reaction. An example of such a reaction is one with the use of cinnamyl bromide 3 and sodium acetate as reactants.

  8. Sodium diacetate - Wikipedia

    en.wikipedia.org/wiki/Sodium_diacetate

    It can be viewed as the result of homoassociation, an effect that enhances the acidity of acetic acid in concentrated solution: 2 CH 3 CO 2 H + NaOH → Na + [(CH 3 CO 2) 2 H] − + H 2 O. Also described as the sodium acid salt of acetic acid, it is best described as the sodium salt of the hydrogen-bonded anion (CH 3 CO 2) 2 H −.

  9. Acetobacter aceti - Wikipedia

    en.wikipedia.org/wiki/Acetobacter_aceti

    A. aceti has long been used in the fermentation industry efficiently producing acetic acid from alcohol as an obligate aerobe dependent on oxygen as the terminal electron acceptor. [4] A. aceti, classified as an acidophile, able to survive in acidic environments, possesses an acidified cytoplasm, providing most proteins with acid stability. [3]