enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    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.

  3. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    aqueous ammonia; used in traditional qualitative inorganic analysis: Azobisisobutyronitrile: organic compound; often used as a foamer in plastics and rubber and as a radical initiator: Baeyer's reagent: is an alkaline solution of potassium permanganate; used in organic chemistry as a qualitative test for the presence of unsaturation, such as ...

  4. Methyl ethyl ketone peroxide - Wikipedia

    en.wikipedia.org/wiki/Methyl_ethyl_ketone_peroxide

    Methyl ethyl ketone peroxide (MEKP) is an organic peroxide with the formula [(CH 3)(C 2 H 5)C(O 2 H)] 2 O 2. MEKP is a colorless oily liquid. It is widely used in vulcanization (crosslinking) of polymers. [3] It is derived from the reaction of methyl ethyl ketone and hydrogen peroxide under acidic conditions.

  5. Hydrogen peroxide–urea - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_peroxide–urea

    Hydrogen peroxide–urea (also called Hyperol, artizone, urea hydrogen peroxide, and UHP) is a white crystalline solid chemical compound composed of equal amounts of hydrogen peroxide and urea. It contains solid and water -free hydrogen peroxide, which offers a higher stability and better controllability than liquid hydrogen peroxide when used ...

  6. Peroxy acid - Wikipedia

    en.wikipedia.org/wiki/Peroxy_acid

    The most common use of organic peroxy acids is for the conversion of alkenes to epoxides, the Prilezhaev reaction. Formation of an epoxide from an alkene and a peroxycarboxylic acid. Another common reaction is conversion of cyclic ketones to the ring-expanded esters using peracids in a Baeyer-Villiger oxidation .

  7. Hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxide

    This reaction is the basis of methods for analysis of organic peroxides. [5] Another way to evaluate the content of peracids and peroxides is the volumetric titration with alkoxides such as sodium ethoxide. [6] The phosphite esters and tertiary phosphines also effect reduction: ROOH + PR 3 → OPR 3 + ROH

  8. Category:Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Category:Organic_peroxides

    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.

  9. Peroxide - Wikipedia

    en.wikipedia.org/wiki/Peroxide

    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 ...