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  2. Anthraquinone - Wikipedia

    en.wikipedia.org/wiki/Anthraquinone

    Anthraquinone, also called anthracenedione or dioxoanthracene, is an aromatic organic compound with formula C 14 H 8 O 2.Several isomers exist but these terms usually refer to 9,10-anthraquinone (IUPAC: 9,10-dioxoanthracene) wherein the keto groups are located on the central ring.

  3. Anthraquinones - Wikipedia

    en.wikipedia.org/wiki/Anthraquinones

    For the parent molecule 9,10-anthraquinone, see anthraquinone. Structure proposed for the pigment carmine. Anthraquinones (also known as anthraquinonoids) are a class of naturally occurring phenolic compounds based on the 9,10-anthraquinone skeleton. They are widely used industrially and occur naturally.

  4. Anthraquinone dyes - Wikipedia

    en.wikipedia.org/wiki/Anthraquinone_dyes

    Anthraquinone itself is colourless, but red to blue dyes are obtained by introducing electron donor groups such as hydroxy or amino groups in the 1-, 4-, 5- or 8-position. [1] Anthraquinone dyestuffs are structurally related to indigo dyestuffs and are classified together with these in the group of carbonyl dyes .

  5. Quinone - Wikipedia

    en.wikipedia.org/wiki/Quinone

    Other important examples are 1,2-benzoquinone (ortho-quinone), 1,4-naphthoquinone and 9,10-anthraquinone. The name is derived from that of quinic acid (with the suffix "-one" indicating a ketone), since it is one of the compounds obtained upon oxidation of quinic acid. [4]

  6. 2-Ethylanthraquinone - Wikipedia

    en.wikipedia.org/wiki/2-Ethylanthraquinone

    Hydrogen peroxide is produced industrially by the anthraquinone process which involves using 2-alkyl-9,10-anthraquinones for hydrogenation. Many derivatives of anthraquinone are used but 2-ethylanthraquinone is common because of its high selectivity. The hydrogenation of the unsubstituted ring can reach 90% selectivity by using 2 ...

  7. 9,10-Dihydroxyanthracene - Wikipedia

    en.wikipedia.org/wiki/9,10-dihydroxyanthracene

    9,10-Dihydroxyanthracene is an organic compound with the formula C 14 H 10 O 2.It is the hydroquinone form of 9,10-anthraquinone (AQ). It formed when AQ is hydrogenated. [1] It is easily dissolved in alkaline solutions and is often called soluble anthraquinone (SAQ).

  8. 9,10-anthraquinone - Wikipedia

    en.wikipedia.org/?title=9,10-anthraquinone&...

    Retrieved from "https://en.wikipedia.org/w/index.php?title=9,10-anthraquinone&oldid=389058817"This page was last edited on 6 October 2010, at 08:27

  9. Anthraquinone process - Wikipedia

    en.wikipedia.org/wiki/Anthraquinone_process

    The anthraquinone process, also called the Riedl–Pfleiderer process, is a process for the production of hydrogen peroxide, which was developed by IG Farben in the 1940s., [1] The industrial production of hydrogen peroxide is based on the reduction of oxygen, as in the direct synthesis from the elements.