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  2. Dihydroxyanthraquinone - Wikipedia

    en.wikipedia.org/wiki/Dihydroxyanthraquinone

    A dihydroxyanthraquinone is any of several isomeric organic compounds with formula (C 12 H 6 (OH) 2)(CO) 2, formally derived from 9,10-anthraquinone by replacing two hydrogen atoms by hydroxyl groups. Dihyroxyantraquinones have been studied since the early 1900s, and include some compounds of historical and current importance.

  3. 1,4-Dihydroxyanthraquinone - Wikipedia

    en.wikipedia.org/wiki/1,4-dihydroxyanthraquinone

    1,4-Dihydroxyanthraquinone, also called quinizarin or Solvent Orange 86, is an organic compound derived from anthroquinone. Quinizarin is an orange or red-brown crystalline powder. It is formally derived from anthraquinone by replacement of two hydrogen atoms by hydroxyl (OH) groups.

  4. 1,5-Dihydroxyanthraquinone - Wikipedia

    en.wikipedia.org/wiki/1,5-Dihydroxyanthraquinone

    1,5-Dihydroxyanthraquinone is an organic compound with the formula (C 6 H 3 OH) 2 (CO) 2. It is one of several isomers of dihydroxyanthraquinone . An orange solid, it is a component of traditional Chinese medications. [ 3 ]

  5. Starvation response - Wikipedia

    en.wikipedia.org/wiki/Starvation_response

    Starvation response in animals (including humans) is a set of adaptive biochemical and physiological changes, triggered by lack of food or extreme weight loss, in which the body seeks to conserve energy by reducing metabolic rate and/or non-resting energy expenditure to prolong survival and preserve body fat and lean mass.

  6. Bohn–Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Bohn–Schmidt_reaction

    The Bohn–Schmidt reaction, a named reaction in chemistry, introduces a hydroxy group at an anthraquinone system. The anthraquinone must already have at least one hydroxy group.

  7. Overpotential - Wikipedia

    en.wikipedia.org/wiki/Overpotential

    The activation overpotential is the potential difference above the equilibrium value required to produce a current that depends on the activation energy of the redox event. While ambiguous, "activation overpotential" often refers exclusively to the activation energy necessary to transfer an electron from an electrode to an anolyte.

  8. Table of standard reduction potentials for half-reactions ...

    en.wikipedia.org/wiki/Table_of_standard...

    The formal reduction potential makes possible to more simply work with molar or molal concentrations in place of activities. Because molar and molal concentrations were once referred as formal concentrations, it could explain the origin of the adjective formal in the expression formal potential. [citation needed]

  9. 1,3-Dihydroxyanthraquinone - Wikipedia

    en.wikipedia.org/wiki/1,3-Dihydroxyanthraquinone

    1,3-Dihydroxyanthraquinone, also called purpuroxanthin or xanthopurpurin, is an organic compound with formula C 14 H 8 O 4 that occurs in the plant Rubia cordifolia (Indian madder). [1] It is one of ten dihydroxyanthraquinone isomers.