Search results
Results from the WOW.Com Content Network
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.
Benzoyl peroxide is a chemical compound ... and many other organic solvents. Benzoyl peroxide is an oxidizer, ... forming free radicals:
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]
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 ...
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.
A widely used peroxy acid for this reaction is meta-chloroperoxybenzoic acid (m-CPBA), due to its stability and good solubility in most organic solvents. [ 1 ] [ 3 ] The reaction is performed in inert solvents ( C 6 H 14 , C 6 H 6 , CH 2 Cl 2 , CHCl 3 , CCl 4 ) between -10 and 60 °C with the yield of 60-80%.