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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. Thymolphthalein - Wikipedia

    en.wikipedia.org/wiki/Thymolphthalein

    PubChem CID. 31316; UNII: ... Phenolphthalein; References This page was last edited on 3 August 2023, at 02:40 (UTC). Text is available under the Creative ...

  4. 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 ...

  5. Phthalide - Wikipedia

    en.wikipedia.org/wiki/Phthalide

    The phthalide core is found a variety of more complex chemical compounds including dyes (such as phenolphthalein), fungicides (such as tetrachlorophthalide, often referred to simply as "phthalide"), and natural oils (such as butylphthalide).

  6. o-Cresolphthalein - Wikipedia

    en.wikipedia.org/wiki/O-Cresolphthalein

    To be produced, the method generally used to synthesize phthalein dyes is effective. This method is used to synthesize phenolphthalein and thymolphthalein. To begin, a 2M equivalent of a phenol or a substituted phenol should be combined with a 1M equivalent of a phthalic anhydride. [1]

  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. Phthalic anhydride - Wikipedia

    en.wikipedia.org/wiki/Phthalic_anhydride

    Phthalic anhydride is the organic compound with the formula C 6 H 4 (CO) 2 O. It is the anhydride of phthalic acid.Phthalic anhydride is a principal commercial form of phthalic acid.

  9. 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.