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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.
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 ...
When R is organic, the compounds are called organic hydroperoxides. Such compounds are a subset of organic peroxides , which have the formula ROOR. Organic hydroperoxides can either intentionally or unintentionally initiate explosive polymerisation in materials with unsaturated chemical bonds .
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− ).
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.
The radicals formed from alkenyl peroxides can be utilized in organic radical reactions. For example, they can mediate hydrogen atom abstraction reactions and thus lead to the functionalization of C-H bonds, [7] or they can be used to introduce ketone residues by addition of the alkenyloxyl radicals to alkenes. [8] [9] [10]
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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.