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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− ).
The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet for this chemical from a reliable source such as eChemPortal search query 94-36-0, and follow its directions.
Benzoyl peroxide, much like azobisisobutyronitrile, is a white powder used as a photoinitiator in various commercial and industrial processes, including plastics production. Unlike AIBN, however, benzoyl peroxide produces oxygen gas upon decomposing, giving this compound a host of medical uses as well.
Benzoyl peroxide and hydrogen peroxide are used as bleaching and "maturing" agents for treating flour to make its grain release gluten more easily; the alternative is letting the flour slowly oxidize by air, which is too slow for the industrialized era. Benzoyl peroxide is an effective topical medication for treating most forms of acne.
The example shown here consists of indenylzirconium (a metallocene) and benzoyl peroxide (an initiator). Also, initiating systems containing heteroaromatic diketo carboxylic acids, such as 3,6-bis( o -carboxybenzoyl)- N -isopropylcarbazole in this example, are known to catalyze the decomposition of benzoyl peroxide.
Benzoyl peroxide is an over the counter, FDA-approved active ingredient used primarily for the treatment of acne, according to board-certified dermatologist Dr. Marguerite Germain. This ingredient ...
Benzoyl peroxide has been in the news spotlight lately — not in a good way. The compound is used in many acne treatment products, but it has recently been shown to break down into benzene, a ...
For industrial reactions a radical initiator, such as benzoyl peroxide, will be intentionally added. All of these processes lead to the generation of carbon centred radicals on the polymer chain (R•), typically by abstraction of H from labile C-H bonds.