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  2. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    Glacial acetic acid is used in analytical chemistry for the estimation of weakly alkaline substances such as organic amides. Glacial acetic acid is a much weaker base than water, so the amide behaves as a strong base in this medium. It then can be titrated using a solution in glacial acetic acid of a very strong acid, such as perchloric acid. [52]

  3. TAE buffer - Wikipedia

    en.wikipedia.org/wiki/TAE_buffer

    TAE buffer is commonly prepared as a 50× stock solution for laboratory use. A 50× stock solution can be prepared by dissolving 242 g Tris base in water, adding 57.1 ml glacial acetic acid, and 100 ml of 500 mM EDTA (pH 8.0) solution, and bringing the final volume up to 1 litre.

  4. Zenker's fixative - Wikipedia

    en.wikipedia.org/wiki/Zenker's_fixative

    If the glacial acetic acid is replaced by 5 ml of formalin (37–40% formaldehyde), the resulting solution is Helly's fixative, also sometimes called "formol-Zenker".Helly is stable for only a few hours because the formaldehyde and dichromate components react, producing formic acid and chromium(III) ions; the orange solution becomes greenish.

  5. Keller's reagent (organic) - Wikipedia

    en.wikipedia.org/wiki/Keller's_reagent_(organic)

    In organic chemistry, Keller's reagent is a mixture of anhydrous (glacial) acetic acid, concentrated sulfuric acid, and small amounts of ferric chloride, used to detect alkaloids. Keller's reagent can also be used to detect other kinds of alkaloids via reactions in which it produces products with a wide range of colors.

  6. Carnoy's solution - Wikipedia

    en.wikipedia.org/wiki/Carnoy's_solution

    Carnoy's solution is a fixative composed of 60% ethanol, 30% chloroform and 10% glacial acetic acid, 1 gram of ferric chloride. [1] [2]Carnoy's solution is also the name of a different fixation composed of ethanol and glacial acetic acid (3:1).

  7. Glacial acetic acid - Wikipedia

    en.wikipedia.org/?title=Glacial_acetic_acid&...

    This page was last edited on 14 September 2019, at 22:01 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.