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  2. Ferric chloride test - Wikipedia

    en.wikipedia.org/wiki/Ferric_chloride_test

    The ferric chloride test is used to determine the presence of phenols in a given sample or compound (for instance natural phenols in a plant extract). Enols , hydroxamic acids , oximes, and sulfinic acids give positive results as well. [ 1 ]

  3. Iron(III) chloride - Wikipedia

    en.wikipedia.org/wiki/Iron(III)_chloride

    The affinity of iron(III) for oxygen ligands was the basis of qualitative tests for phenols. Although superseded by spectroscopic methods, the ferric chloride test is a traditional colorimetric test. [26] The affinity of iron(III) for phenols is exploited in the Trinder spot test. [27]

  4. Potassium ferricyanide - Wikipedia

    en.wikipedia.org/wiki/Potassium_ferricyanide

    Potassium ferricyanide is a component of amperometric biosensors as an electron transfer agent replacing an enzyme's natural electron transfer agent such as oxygen as with the enzyme glucose oxidase. It is an ingredient in commercially available blood glucose meters for use by diabetics .

  5. Trinder glucose activity test - Wikipedia

    en.wikipedia.org/wiki/Trinder_glucose_activity_test

    The Trinder glucose activity test is a diagnostic test used in medicine to determine the presence of glucose or glucose oxidase. The test employs the Trinder reagent, and is a colour change test resulting from the Trinder reaction. The Trinder reagent, named after P. Trinder of the Biochemistry Department of the Royal Infirmary in Sunderland ...

  6. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    Total phenols (or antioxidant effect) can be measured using the Folin-Ciocalteu reaction. Results are typically expressed as gallic acid equivalents (GAE). Ferric chloride (FeCl 3) test is also a colorimetric assay. Lamaison and Carnet have designed a test for the determination of the total flavonoid content of a sample (AlCI 3 method). After ...

  7. Prussian blue - Wikipedia

    en.wikipedia.org/wiki/Ferric_ferrocyanide

    Samples and phenolic standards are given acidic ferric chloride and ferricyanide, which is reduced to ferrocyanide by the phenols. The ferric chloride and ferrocyanide react to form Prussian blue. Comparing the absorbance at 700 nm of the samples to the standards allows for the determination of total phenols or polyphenols. [53] [54]

  8. Angeli–Rimini reaction - Wikipedia

    en.wikipedia.org/wiki/Angeli–Rimini_reaction

    The reaction is used in a chemical test for the detection of aldehydes in combination with ferric chloride. In this test a few drops of aldehyde containing specimen is dissolved in ethanol, the sulfonamide is added together with some sodium hydroxide solution and then the solution is acidified to Congo red. An added drop of ferric chloride will ...

  9. Potassium ferrocyanide - Wikipedia

    en.wikipedia.org/wiki/Potassium_ferrocyanide

    A famous reaction involves treatment with ferric salts, most commonly Iron(III) chloride, to give Prussian blue. In the reaction with Iron(III) chloride, producing Potassium chloride as a side-product: 3 K 4 [Fe(CN) 6] + 4 FeCl 3 → Fe 4 [Fe(CN) 6] 3 + 12 KCl With the composition Fe III 4 [Fe II 6]