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  2. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    Organic peroxides are often sold as formulations that include one or more phlegmatizing agents. That is, for safety sake or performance benefits the properties of an organic peroxide formulation are commonly modified by the use of additives to phlegmatize (desensitize), stabilize, or otherwise enhance the organic peroxide for commercial use.

  3. HAZMAT Class 5 Oxidizing agents and organic peroxides

    en.wikipedia.org/wiki/HAZMAT_Class_5_Oxidizing...

    An organic peroxide is any organic compound containing oxygen (O) in the bivalent -O-O- structure and which may be considered a derivative of hydrogen peroxide, where one or more of the hydrogen atoms have been replaced by organic radicals, unless any of the following paragraphs applies:

  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. Benzoyl peroxide - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_peroxide

    Benzoyl peroxide is a chemical compound (specifically, an organic peroxide) with structural formula (C 6 H 5 −C(=O)O−) 2, often abbreviated as (BzO) 2. In terms of its structure, the molecule can be described as two benzoyl ( C 6 H 5 −C(=O)− , Bz) groups connected by a peroxide ( −O−O− ).

  6. Category:Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Category:Organic_peroxides

    Organic peroxide explosives (9 P) Organic peroxy acids (8 P) Pages in category "Organic peroxides" The following 45 pages are in this category, out of 45 total.

  7. Alkenyl peroxides - Wikipedia

    en.wikipedia.org/wiki/Alkenyl_peroxides

    This reasoning also applies to aryl peroxides. Both compound classes thus have significantly weaker O-O bonds than other peroxides. [2] [3] Because of this weak bond, alkenyl peroxides are generally only postulated as reactive intermediates. An exception is the case of some few heteroarylperoxides, which were long-lived enough to be characterized.

  8. Methyl ethyl ketone peroxide - Wikipedia

    en.wikipedia.org/wiki/Methyl_ethyl_ketone_peroxide

    Methyl ethyl ketone peroxide (MEKP) is an organic peroxide with the formula [(CH 3)(C 2 H 5)C(O 2 H)] 2 O 2. MEKP is a colorless oily liquid. It is widely used in vulcanization (crosslinking) of polymers. [3] It is derived from the reaction of methyl ethyl ketone and hydrogen peroxide under acidic conditions.

  9. Category:Peroxides - Wikipedia

    en.wikipedia.org/wiki/Category:Peroxides

    Organic peroxides (4 C, 45 P) P. Peroxy acids (1 C, 6 P) Pages in category "Peroxides" The following 33 pages are in this category, out of 33 total.