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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. 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. ...

  4. 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.

  5. 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

  6. Category:Acetic acids - Wikipedia

    en.wikipedia.org/wiki/Category:Acetic_acids

    Print/export Download as PDF; Printable version; In other projects Wikimedia Commons; ... 4-Chloroindole-3-acetic acid; Chloroacetic acid; Cinepazic acid; D. Daprodustat;

  7. Acid dye - Wikipedia

    en.wikipedia.org/wiki/Acid_dye

    Acid red 88 is an acid dye used to produce red woolen yarns. An acid dye is a dye that is typically applied to a textile at low pH. They are mainly used to dye wool, not cotton fabrics. [1] Some acid dyes are used as food colorants, [2] [3] and some can also be used to stain organelles in the medical field.

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  9. 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 −.