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  2. Phenolphthalein - Wikipedia

    en.wikipedia.org/wiki/Phenolphthalein

    Phenolphthalein is slightly soluble in water and usually is dissolved in alcohols in experiments. It is a weak acid, which can lose H + ions in solution. The nonionized phenolphthalein molecule is colorless and the double deprotonated phenolphthalein ion is fuchsia. Further proton loss in higher pH occurs slowly and leads to a colorless form.

  3. Phthalein dye - Wikipedia

    en.wikipedia.org/wiki/Phthalein_dye

    Chemical structure of phenolphthalein, a common phthalein dye. Phthalein dyes are a class of dyes mainly used as pH indicators, due to their ability to change colors depending on pH. [1] They are formed by the reaction of phthalic anhydride with various phenols. They are a subclass of triarylmethane dyes. Common phthalein dyes include ...

  4. Chromophore - Wikipedia

    en.wikipedia.org/wiki/Chromophore

    This is a property of pH indicators, whose molecular structure changes upon certain changes in the surrounding pH. This change in structure affects a chromophore in the pH indicator molecule. For example, phenolphthalein is a pH indicator whose structure changes as pH changes as shown in the following table:

  5. Phthalide - Wikipedia

    en.wikipedia.org/wiki/Phthalide

    Phthalide is an organic chemical compound with the molecular formula C 8 H 6 O 2. It is a white solid and the simplest benzo lactone . It is prepared from hydroxymethylbenzoic acid.

  6. Kastle–Meyer test - Wikipedia

    en.wikipedia.org/wiki/Kastle–Meyer_test

    Upon reduction, the very intense pink color of the cationic form of phenolphthalein fades to a faint yellow color. It is this form of phenolphthalein that is present in Kastle–Meyer test kits. In order to generate the intense pink color indicative of a positive test, the reduced phenolphthalein must be oxidized back to its normal, colored form.

  7. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    Phenols are more acidic than typical alcohols. The acidity of the hydroxyl group in phenols is commonly intermediate between that of aliphatic alcohols and carboxylic acids (their pK a is usually between 10 and 12).

  8. Thymolphthalein - Wikipedia

    en.wikipedia.org/wiki/Thymolphthalein

    Phenolphthalein; References This page was last edited on 3 August 2023, at 02: ... This page was last edited on 3 August 2023, at 02:40 (UTC).

  9. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol is an organic compound appreciably soluble in water, with about 84.2 g dissolving in 1000 ml (0.895 M). Homogeneous mixtures of phenol and water at phenol to water mass ratios of ~2.6 and higher are possible. The sodium salt of phenol, sodium phenoxide, is far more water-soluble. It is a combustible solid (NFPA rating = 2).