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  2. Naphtholphthalein - Wikipedia

    en.wikipedia.org/wiki/Naphtholphthalein

    α-Naphtholphthalein (C 28 H 18 O 4) is a phthalein dye used as a pH indicator with a visual transition from colorless/reddish to greenish blue at pH 7.3–8.7. Naphtholphthalein ( pH indicator ) below pH 7.3

  3. 1-Naphthol - Wikipedia

    en.wikipedia.org/wiki/1-naphthol

    1-Naphthol, or α-naphthol, is an organic compound with the formula C 10 H 7 OH. It is a fluorescent white solid. 1-Naphthol differs from its isomer 2-naphthol by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol. Both isomers are soluble in simple organic solvents. They are ...

  4. Universal indicator - Wikipedia

    en.wikipedia.org/wiki/Universal_indicator

    A roll of universal indicator paper Colors of universal indicator. A universal indicator is a pH indicator made of a solution of several compounds that exhibit various smooth colour changes over a wide range pH values to indicate the acidity or alkalinity of solutions. A universal indicator can be in paper form or present in a form of a ...

  5. Benedict's reagent - Wikipedia

    en.wikipedia.org/wiki/Benedict's_reagent

    Benedict's reagent (often called Benedict's qualitative solution or Benedict's solution) is a chemical reagent and complex mixture of sodium carbonate, sodium citrate, and copper(II) sulfate pentahydrate. [1] It is often used in place of Fehling's solution to detect the presence of reducing sugars and other reducing substances. [2]

  6. Folin's reagent - Wikipedia

    en.wikipedia.org/wiki/Folin's_reagent

    Folin's reagent or sodium 1,2-naphthoquinone-4-sulfonate is a chemical reagent used as a derivatizing agent to measure levels of amines and amino acids. [1] The reagent reacts with them in alkaline solution to produce a fluorescent material that can be easily detected.

  7. Diphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphine

    The preparation of phosphine ligands, Wittig-Horner reagents, and phosphonium salts are commonly accomplished by alkylating diphenylphosphine. The hydrogen atom connected to phosphorus undergoes Michael-like addition to activated alkenes, providing products with which to produce phosphine ligands such as 1,2-bis(diphenylphosphino)ethane (Ph 2 ...

  8. N-(1-Naphthyl)ethylenediamine - Wikipedia

    en.wikipedia.org/wiki/N-(1-Naphthyl)ethylenediamine

    N-(1-Naphthyl)ethylenediamine is an organic compound. It is commercially available as part of Griess reagents, which find application in quantitative inorganic analysis of nitrates , nitrite and sulfonamide in blood, using the Griess test .

  9. Marquis reagent - Wikipedia

    en.wikipedia.org/wiki/Marquis_reagent

    Marquis reagent was first discovered in 1896 [2] and described by the Russian (Estonian) pharmacologist, Eduard Markus (1871–1944) (Russian: Эдуард Маркус) [3] in his magister dissertation in 1896; [4] and named after him, [5] and was tested for the first time at the University of Dorpat.