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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 ...
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.
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 ...
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− ).
In chemistry, main group peroxides are peroxide derivatives of the main group elements. Many compounds of the main group elements form peroxides (R−O−O−R'), and a few are of commercial significance. [1]
Peroxide formation is not a significant problem when fresh solvents are used up quickly; they are more of a problem in laboratories which may take years to finish a single bottle. Low-volume users should acquire only small amounts of peroxide-prone solvents, and dispose of old solvents on a regular periodic schedule.
Diethyl ether hydroperoxide forms polymers known as diethyl ether peroxide, or ethylidene peroxide: The peroxide is a colorless oil that is an extremely brisant and friction sensitive explosive material , however the polymeric materials are solid making them more dangerous as evaporation of the volatile diethyl ether can leave thin films of ...
Piranha solution should never be disposed of with organic solvents (e.g. in waste-solvent carboys), as this will cause a violent reaction and a substantial explosion, and any aqueous waste container containing even a weak or depleted piranha solution should be labelled appropriately to prevent this.