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  2. Dibenzopyrenes - Wikipedia

    en.wikipedia.org/wiki/Dibenzopyrenes

    Dibenzopyrenes are a group of high molecular weight polycyclic aromatic hydrocarbons with the molecular formula C 24 H 14.There are five isomers of dibenzopyrene which differ by the arrangement of aromatic rings: dibenzo[a,e]pyrene, dibenzo[a,h]pyrene, dibenzo[a,i]pyrene, dibenzo[a,l]pyrene, and dibenzo[e,l]pyrene.

  3. Benzo (a)pyrene - Wikipedia

    en.wikipedia.org/wiki/Benzo(a)pyrene

    Benzo[a]pyrene (BaP or B[a]P) is a polycyclic aromatic hydrocarbon and the result of incomplete combustion of organic matter at temperatures between 300 °C (572 °F) and 600 °C (1,112 °F). The ubiquitous compound can be found in coal tar, tobacco smoke and many foods, especially grilled meats.

  4. Benzopyrene - Wikipedia

    en.wikipedia.org/wiki/Benzopyrene

    Chemical structure of benzo[a]pyrene Chemical structure of benzo[e]pyrene. A benzopyrene is an organic compound with the formula C 20 H 12.Structurally speaking, the colorless isomers of benzopyrene are pentacyclic hydrocarbons and are fusion products of pyrene and a phenylene group.

  5. Polycyclic aromatic hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Polycyclic_aromatic...

    A Polycyclic aromatic hydrocarbon (PAH) is a class of organic compounds that is composed of multiple aromatic rings.Most are produced by the incomplete combustion of organic matter— by engine exhaust fumes, tobacco, incinerators, in roasted meats and cereals, [1] or when biomass burns at lower temperatures as in forest fires.

  6. Benzo (a)pyrene-7,8-dihydrodiol-9,10-epoxide - Wikipedia

    en.wikipedia.org/wiki/(+)-Benzo(a)pyrene-7,8...

    Benzo[a]pyrene-7,8-dihydrodiol-9,10-epoxide is a metabolite of benzo[a]pyrene formed by the introduction of vicinal hydroxyl and epoxide functional groups to the fifth benzene ring. [7] These oxidations are stereoselective , producing the pair of enantiomers with the hydroxyl groups on opposite sides of the pyrene plane and with the epoxide on ...

  7. Pyrene - Wikipedia

    en.wikipedia.org/wiki/Pyrene

    Pyrene is a polycyclic aromatic hydrocarbon (PAH) consisting of four fused benzene rings, resulting in a flat aromatic system. The chemical formula is C 16 H 10. This yellow-green solid is the smallest peri-fused PAH (one where the rings are fused through more than one face). Pyrene forms during incomplete combustion of organic compounds. [10]

  8. Indeno (1,2,3-cd)pyrene - Wikipedia

    en.wikipedia.org/wiki/Indeno(1,2,3-cd)pyrene

    Indeno(1,2,3-cd)pyrene is a polycyclic aromatic hydrocarbon (PAH), one of 16 PAHs generally measured in studies of environmental exposure and air pollution.Many compounds of this class are formed when burning coal, oil, gas, wood, household waste and tobacco, and can bind to or form small particles in the air.

  9. Pyrena - Wikipedia

    en.wikipedia.org/wiki/Pyrena

    A pyrena or pyrene (commonly called a "pit" or "stone") is the fruitstone within a drupe or drupelet produced by the ossification of the endocarp or lining of the fruit. [1] It consists of a hard endocarp tissue surrounding one or more seeds (also called the "kernel").