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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. 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.

  5. Dibenz (a,h)anthracene - Wikipedia

    en.wikipedia.org/wiki/Dibenz(a,h)anthracene

    Dibenz(a,h)anthracene is a polycyclic aromatic hydrocarbon with five benzene rings. It has low water solubility and low volatility and therefore occurs predominantly in solid form, white to light yellow crystalline, bound to particulates in polluted air, soil, or sediment. [2]

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

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

    A DNA adduct (at center) of a metabolite of benzo[a]pyrene. (+)-Benzo[a]pyrene-7,8-dihydrodiol-9,10-epoxide has been shown to bind to an N2 atom of a guanine nucleobase in DNA, [2] [3] distorting the double helix structure [4] by intercalation of the pyrene moiety between base pairs through π-stacking. [5]

  7. Dibenz (a,j)anthracene - Wikipedia

    en.wikipedia.org/wiki/Dibenz(a,j)anthracene

    As of 2010, the IARC (International Agency for Research on Cancer) has classified dibenz(a,j)anthracene as possibly carcinogenic to humans, grouped into IARC group 2B.No epidemiological studies on human exposure to dibenz(a,j)anthracene as an individual PAH exist, because PAHs always occur as components of complex chemical mixtures and never occur in isolation in the environment.

  8. 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]

  9. File:Dibenzo(a,e)pyrene.svg - Wikipedia

    en.wikipedia.org/wiki/File:Dibenzo(a,e)pyrene.svg

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