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  2. Triphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethane

    Triphenylmethane or triphenyl methane (sometimes also known as Tritan), is the hydrocarbon with the formula (C 6 H 5) 3 CH. This colorless solid is soluble in nonpolar organic solvents and not in water. Triphenylmethane is the basic skeleton of many synthetic dyes called triarylmethane dyes, many of them are pH indicators, and some display ...

  3. Patent Blue V - Wikipedia

    en.wikipedia.org/wiki/Patent_Blue_V

    Patent Blue V, also called Food Blue 5, Sulphan Blue, Acid Blue 3, L-Blau 3, C-Blau 20, Patentblau V, Sky Blue, or C.I. 42051, is a sky blue synthetic triphenylmethane dye used as a food coloring. [1] As a food additive, it has E number E131.

  4. Triphenylmethanol - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethanol

    After the German chemist August Kekulé and his Belgian student Antoine Paul Nicolas Franchimont (1844–1919) first synthesized triphenylmethane in 1872, [2] the Russian doctoral student Walerius Hemilian (1851–1914) first synthesized triphenylmethanol in 1874 by reacting triphenylmethyl bromide with water as well as by oxidizing triphenylmethane.

  5. Triarylmethane dye - Wikipedia

    en.wikipedia.org/wiki/Triarylmethane_dye

    Triarylmethane dyes can be grouped into families according to the nature of the substituents on the aryl groups. In some cases, the anions associated with the cationic dyes (say crystal violet) vary even though the name of the dye does not.

  6. Dye - Wikipedia

    en.wikipedia.org/wiki/Dye

    Because food dyes are classed as food additives, they are manufactured to a higher standard than some industrial dyes. Food dyes can be direct, mordant and vat dyes, and their use is strictly controlled by legislation. Many are azo dyes, although anthraquinone and triphenylmethane compounds are used for colors such as green and blue. Some ...

  7. Phenyl group - Wikipedia

    en.wikipedia.org/wiki/Phenyl_group

    Benzene is sometimes denoted as PhH. Phenyl groups are generally attached to other atoms or groups. For example, triphenylmethane (Ph 3 CH) has three phenyl groups attached to the same carbon center. Many or even most phenyl compounds are not described with the term "phenyl".

  8. Malachite green - Wikipedia

    en.wikipedia.org/wiki/Malachite_green

    Malachite green is also used in endospore staining, since it can directly stain endospores within bacterial cells; here a safranin counterstain is often used. Malachite green is a part of Alexander's pollen stain. Malachite green can also be used as a saturable absorber in dye lasers, or as a pH indicator between pH 0.2–1.8. However, this use ...

  9. Triphenylene - Wikipedia

    en.wikipedia.org/wiki/Triphenylene

    Triphenylene has delocalized 18-π-electron systems based on a planar structure, corresponding to the symmetry group D 3h. It is a white or colorless solid. It is a white or colorless solid. Preparation