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Phthalein dye information


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:

  • Bromothymol blue
  • Bromocresol green
  • Bromocresol purple
  • Cresol Red
  • o-Cresolphthalein
  • Chlorophenol red
  • Dixylenolphthalein
  • Guaiacolphthalein
  • α-Naphtholphthalein
  • Phenolphthalein
  • Phenolsulfonphthalein
  • Tetrabromophenolphthalein
  • Thymol blue
  • Thymolphthalein
  • Xylenolphthalein
  1. ^ Sabnis, Ram W. (2010). "Phthalein Dyes". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.phthsabn.a01. ISBN 978-0471238966.

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Phthalein dye

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Phthalein dyes are a class of dyes mainly used as pH indicators, due to their ability to change colors depending on pH. They are formed by the reaction...

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Triarylmethane dye

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dominant use as dyes, many of these dyes react reversibly with acid and base, and thus serve as pH indicators. Zelyonka attack Phthalein dye Wikimedia Commons...

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Thymolphthalein

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Thymolphthalein is a phthalein dye used as an acid–base (pH) indicator. Its transition range is around pH 9.3–10.5. Below this pH, it is colorless; above...

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Phenolphthalein

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solutions and pink in basic solutions. It belongs to the class of dyes known as phthalein dyes. Phenolphthalein is slightly soluble in water and usually is...

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Bromsulfthalein

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bromosulfophthalein, and BSP) is a phthalein dye used in liver function tests. Determining the rate of removal of the dye from the blood stream gives a measure...

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Naphtholphthalein

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α-Naphtholphthalein (C28H18O4) is a phthalein dye used as a pH indicator with a visual transition from colorless/reddish to greenish blue at pH 7.3–8...

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Adolf von Baeyer

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include the synthesis and description of the plant dye indigo, the discovery of the phthalein dyes, and the investigation of polyacetylenes, oxonium salts...

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Bromothymol blue

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Bromothymol blue (also known as bromothymol sulfone phthalein and BTB) is a pH indicator. It is mostly used in applications that require measuring substances...

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List of German inventors and discoverers

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console. Adolf von Baeyer: Chemist. Synthesized indigo, discovered the phthalein dyes, and investigated polyacetylenes, oxonium salts, nitroso compounds (1869)...

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Phenazine

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yellowish-green fluorescence. The rhodamines, which are closely related to the phthaleins, are formed by the condensation of the alkyl metaaminophenols with phthalic...

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List of Heidelberg University people

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(1835–1917) Chemist ~around 1852–1858 Synthesized indigo; discovered the phthalein dyes; proposed the correct formula for indole; introduced the strain theory...

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Phenol red

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Beilstein 5-19-03-00457 Tamura, Z.; Maeda M. (1997). "Differences between phthaleins and sulfonphthaleins". Yakugaku Zasshi (in Japanese). 117 (10–11): 764–770...

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Leonard Rowntree

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with John J. Abel, a prominent pharmacologist. Abel introduced him to phthalein, from which he and J. T. Geraghty developed the Rowntree test of renal...

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Emil Fischer

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earned his doctorate in 1874 under Adolf von Baeyer with his study of phthaleins. Fischer remained with Baeyer in Strassburg as an independent research...

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Chemical sensor array

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Brønsted-Lowry acid-base functionality have been developed such azo dyes, nitrophenols, phthaleins, and sulfonphthaleins. The Brønsted-Lowry acid-base functionality...

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