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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. 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 ...

  5. 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.

  6. Bromophenol blue - Wikipedia

    en.wikipedia.org/wiki/Bromophenol_blue

    Bromophenol is also used as a colour marker to monitor the process of agarose gel electrophoresis and polyacrylamide gel electrophoresis.Since bromophenol blue carries a slight negative charge at moderate pH, it will migrate in the same direction as DNA or protein in a gel; the rate at which it migrates varies according to gel density and buffer composition, but in a typical 1% agarose gel in ...

  7. Kastle–Meyer test - Wikipedia

    en.wikipedia.org/wiki/Kastle–Meyer_test

    This is typically achieved by boiling an alkaline solution of phenolphthalein with powdered zinc, which reduces the phenolphthalein into phenolphthalin. 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.

  8. Bromothymol blue - Wikipedia

    en.wikipedia.org/wiki/Bromothymol_blue

    Bromothymol blue acts as a weak acid in a solution. It can thus be in protonated or deprotonated form, appearing yellow or blue, respectively. It is bright aquamarine by itself, and greenish-blue in a neutral solution. The deprotonation of the neutral form results in a highly conjugated structure, accounting for the difference in color. An ...

  9. Barium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Barium_hydroxide

    Its aqueous solution, if clear, is guaranteed to be free of carbonate, unlike those of sodium hydroxide and potassium hydroxide, as barium carbonate is insoluble in water. This allows the use of indicators such as phenolphthalein or thymolphthalein (with alkaline colour changes) without the risk of titration errors due to the presence of ...