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  2. Dichlorophenolindophenol - Wikipedia

    en.wikipedia.org/wiki/Dichlorophenolindophenol

    2,6-Dichlorophenolindophenol (DCPIP, DCIP or DPIP) is a chemical compound used as a redox dye. When oxidized, DCPIP is blue with a maximal absorption at 600 nm; when reduced, DCPIP is colorless. DCPIP can be used to measure the rate of photosynthesis. It is part of the Hill reagents family. When exposed to light in a photosynthetic system, the ...

  3. Hill reaction - Wikipedia

    en.wikipedia.org/wiki/Hill_reaction

    These dyes permitted the finding of electron transport chains during photosynthesis. Dichlorophenolindophenol (DCPIP), an example of these dyes, is widely used by experimenters. DCPIP is a dark blue solution that becomes lighter as it is reduced. It provides experimenters with a simple visual test and easily observable light reaction. [8]

  4. Hill reagent - Wikipedia

    en.wikipedia.org/wiki/Hill_reagent

    This photosynthesis article is a stub. You can help Wikipedia by expanding it.

  5. 2,6-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,6-Dichlorophenol

    2,6-Dichlorophenol is a compound with formula C 6 H 3 Cl 2 OH. It is one of the six isomers of dichlorophenol. It is a colorless solid. Its pK a is 6.78, which is about 100x more acidic than 2-chlorophenol (8.52) and 1000x more acidic than phenol itself (9.95). [3]

  6. 2,6-Dichloroquinone-4-chloroimide - Wikipedia

    en.wikipedia.org/wiki/2,6-Dichloroquinone-4...

    2,6-Dichloroquinone-4-chloroimide (Gibbs reagent) is an organic compound used as an colorimetric indicator to detect phenolic compounds. [1] Upon reaction with phenol itself, 2,6-dichlorophenolindophenol is formed, [ 2 ] a chemical that is used as a redox indicator .

  7. Indophenol - Wikipedia

    en.wikipedia.org/wiki/Indophenol

    Indophenol is an organic compound with the formula OC 6 H 4 NC 6 H 4 OH. It is deep blue dye that is the product of the Berthelot's reaction, a common test for ammonia. [2] The indophenol group, with various substituents in place of OH and various ring substitutions, is found in many dyes used in hair coloring and textiles.

  8. Liebermann reagent - Wikipedia

    en.wikipedia.org/wiki/Liebermann_Reagent

    The Liebermann reagent named after Hungarian chemist Leo Liebermann (1852-1926) is used as a simple spot-test to presumptively identify alkaloids as well as other compounds. It is composed of a mixture of potassium nitrite and concentrated sulfuric acid. [1] [2] 1 g of potassium nitrite is used for every 10 mL of sulfuric acid. [3]

  9. Redox indicator - Wikipedia

    en.wikipedia.org/wiki/Redox_indicator

    A redox indicator (also called an oxidation-reduction indicator) is an indicator which undergoes a definite color change at a specific electrode potential.. The requirement for fast and reversible color change means that the oxidation-reduction equilibrium for an indicator redox system needs to be established very quickly.