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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. 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]

  4. Winkler titration - Wikipedia

    en.wikipedia.org/wiki/Winkler_titration

    The second part of the Winkler test reduces (acidifies) the solution. The precipitate will dissolve back into solution as the H + reacts with the O 2− and OH − to form water. MnO(OH) 2 (s) + 4 H + (aq) → Mn 4+ (aq) + 3 H 2 O(l) The acid facilitates the conversion by the brown, Manganese-containing precipitate of the Iodide ion into ...

  5. 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.

  6. Schiff test - Wikipedia

    en.wikipedia.org/wiki/Schiff_test

    The structure of the fuchsin dye. The Schiff test is an early organic chemistry named reaction developed by Hugo Schiff, [1] and is a relatively general chemical test for detection of many organic aldehydes that has also found use in the staining of biological tissues. [2]

  7. 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 .

  8. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  9. Barfoed's test - Wikipedia

    en.wikipedia.org/wiki/Barfoed's_test

    Barfoed's test is a chemical test used for detecting the presence of monosaccharides. It is based on the reduction of copper(II) acetate to copper(I) oxide (Cu 2 O), which forms a brick-red precipitate. [1] [2] RCHO + 2Cu 2+ + 2H 2 O → RCOOH + Cu 2 O↓ + 4H + (Disaccharides may also react, but the reaction is much slower.)