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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. GFS Chemicals - Wikipedia

    en.wikipedia.org/wiki/GFS_Chemicals

    Frederick Smith was spurred to create many of the chemical compounds, especially perchlorates and trace metal perchloric acid, in response to the needs of his colleagues in analytical chemistry. [17] This tradition is continued here and is the most commonly associated part of the business when a chemist or researcher hears of GFS Chemicals.

  4. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    Dissolving Knorr's pyrrole in concentrated sulfuric acid, and then pouring the resulting solution into water will hydrolyze the 4-ester group selectively. The 5-methyl group can be variously oxidized to chloromethyl, aldehyde, or carboxylic acid functionality by the use of stoichiometric sulfuryl chloride in glacial acetic acid. [7]

  5. 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.

  6. 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.

  7. 6-Monoacetylmorphine - Wikipedia

    en.wikipedia.org/wiki/6-monoacetylmorphine

    The production of black tar heroin results in significant amounts of 6-MAM in the final product. [citation needed] 6-MAM is approximately 30 percent more active than diacetylmorphine itself, [citation needed] This is why despite lower heroin content, black tar heroin may be more potent than some other forms of heroin. 6-MAM can be synthesized from morphine using glacial acetic acid with an ...