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  2. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    Especially when in concentrated form, organic peroxides can decompose by self-oxidation, since organic peroxides contain both an oxidizer (the O-O bond) and fuel (C-H and C-C bonds). A "self-accelerating decomposition" occurs when the rate of peroxide decomposition generates heat at a faster rate than it can be dissipated to the environment ...

  3. Hydrogen peroxide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_peroxide

    Hydrogen peroxide is a chemical compound with the formula H 2 O 2.In its pure form, it is a very pale blue [5] liquid that is slightly more viscous than water.It is used as an oxidizer, bleaching agent, and antiseptic, usually as a dilute solution (3%–6% by weight) in water for consumer use and in higher concentrations for industrial use.

  4. Peroxide - Wikipedia

    en.wikipedia.org/wiki/Peroxide

    The peroxide group is marked in blue. R, R 1 and R 2 mark hydrocarbon moieties. The most common peroxide is hydrogen peroxide (H 2 O 2), colloquially known simply as "peroxide". It is marketed as solutions in water at various concentrations. Many organic peroxides are known as well. In addition to hydrogen peroxide, some other major classes of ...

  5. Acetone peroxide - Wikipedia

    en.wikipedia.org/wiki/Acetone_peroxide

    Acetone peroxide (/ æ s ə ˈ t ə ʊ n p ɛr ˈ ɒ k s aɪ d / ⓘ also called APEX and mother of Satan [3] [4]) is an organic peroxide and a primary explosive. It is produced by the reaction of acetone and hydrogen peroxide to yield a mixture of linear monomer and cyclic dimer, trimer, and tetramer forms. The monomer is dimethyldioxirane.

  6. Fenton's reagent - Wikipedia

    en.wikipedia.org/wiki/Fenton's_reagent

    Fenton's reagent is a solution of hydrogen peroxide (H 2 O 2) and an iron catalyst (typically iron(II) sulfate, FeSO 4). [1] It is used to oxidize contaminants or waste water as part of an advanced oxidation process. Fenton's reagent can be used to destroy organic compounds such as trichloroethylene and tetrachloroethylene (perchloroethylene).

  7. Methyl ethyl ketone peroxide - Wikipedia

    en.wikipedia.org/wiki/Methyl_ethyl_ketone_peroxide

    It is derived from the reaction of methyl ethyl ketone and hydrogen peroxide under acidic conditions. Several products result from this reaction including a cyclic dimer. [4] The linear dimer, the topic of this article, is the most prevalent. [5] and this is the form that is typically quoted in the commercially available material. [6]

  8. Hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxide

    Hydroperoxides or peroxols are compounds of the form ROOH, where R stands for any group, typically organic, which contain the hydroperoxy functional group (−OOH). Hydroperoxide also refers to the hydroperoxide anion ( − OOH ) and its salts , and the neutral hydroperoxyl radical (•OOH) consist of an unbond hydroperoxy group.

  9. tert-Butyl hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_hydroperoxide

    It is normally supplied as a 69–70% aqueous solution. Compared to hydrogen peroxide and organic peracids, tert-butyl hydroperoxide is less reactive and more soluble in organic solvents. Overall, it is renowned for the convenient handling properties of its solutions. Its solutions in organic solvents are highly stable.