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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− ).
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. MSDS from Fisher Scientific (archived from SDSdata.org dead link) , which was a redirect to archived page (archived from msdssearchengine.com dead link) .
Diacetyl peroxide (concentration greater than 70%) 110-22-5 5000 Diazomethane: 334-88-3 500 Dibenzoyl peroxide: 94-36-0 7500 Diborane: 19287-45-7 100 tert-Dibutyl peroxide: 110-05-4 5000 Dichloroacetylene: 7572-29-4 250 Dichlorosilane: 4109-96-0 2500 Diethylzinc: 557-20-0 10000 Disopropyl peroxydicarbonate: 105-64-6 7500 Dilauroyl peroxide: 105 ...
Dialkyl peroxides, e.g., dicumyl peroxide, are synthesized by addition of hydrogen peroxide to alkenes or by O-alkylation of hydroperoxides. Diacyl peroxides are typically prepared by treating hydrogen peroxide with acid chlorides or acid anhydrides in the presence of base: [1] H 2 O 2 + 2 RCOCl → (RCO 2) 2 + 2 HCl H 2 O 2 + (RCO) 2 O → ...
Chemical formula Synonyms CAS number C 10 H 16 N 2 O 8: Ethylenediaminetetraacetic acid (EDTA): 6381–92–6 C 12 H 22 O 11: sucrose: 57–50–1 C 18 H 29 O 3 S: sodium dodecyl benzenesulfonate: 2155–30–0
This is a list of common chemical compounds with chemical formulae and CAS numbers, ... benzoyl peroxide: 94-36-0 C 14 H 11 Cl 3 N 2 O 3: RI-1: 415713-60-9 C 14 H 11 ...
Many chemical compounds that are potentially explosive have useful non-explosive applications. One large family of phlegmatizers are phthalate esters, which are used as solvents to minimize the explosive tendency of organic peroxides, such as dibenzoyl peroxide and MEKP, which are widely used initiators for polymerizations. [1]
The O-O σ bond in dibenzoyl peroxide is cleaved homolytically, distributing a radical to each benzoyloxy. Heat Certain intramolecular bonds, such as the O–O bond of a peroxide, are sufficiently weak to spontaneously homolytically dissociate near room temperature. Most bonds homolyse at temperatures above 200°C. [4]