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  2. 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.

  3. 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.

  4. Benzo (e)pyrene - Wikipedia

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

    Benzo[e]pyrene is a polycyclic aromatic hydrocarbon with the chemical formula C 20 H 12. It is listed as a Group 3 carcinogen by the IARC. [1] See also. Benzopyrene;

  5. List of benzo compounds - Wikipedia

    en.wikipedia.org/wiki/List_of_benzo_compounds

    (like numbers place letters first are omitted while indexing compounds, later on they are added again if necessary) the proper name for this compound is Benzo[a]anthracene. Pyrene: Benzo[a]pyrene, by adding 4 carbon atoms to pyrene the left most ring is the extra one. Benzo[e]pyrene, by adding 4 carbon atoms to the pyrene along its short axis.

  6. Cellulosimicrobium cellulans - Wikipedia

    en.wikipedia.org/wiki/Cellulosimicrobium_cellulans

    One significant compound the bacteria can biodegrade is benzo(a)pyrene (BaP). [13] BaP is a polycyclic aromatic hydrocarbon (PAH), well-known organic pollutant associated with properties of teratogenicity, mutagenicity, and carcinogenicity. BaP is a degradation-resistant compound; thus, it is more inclined to accumulate in the environment. [14]

  7. 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 ...

  8. Tobacco smoke - Wikipedia

    en.wikipedia.org/wiki/Tobacco_smoke

    Benzo(b)fluoranthene 4–22 ng sufficient Benzo(j)fluoranthene 6–21 ng sufficient Benzo(k)fluoranthene 6–12 ng sufficient Benzo(a)pyrene: 0.1–90 ng 20–40 ng sufficient probable Chrysene 40–60 ng sufficient Dibenz(a,h)anthracene 4 ng sufficient Dibenzo(a,i)pyrene 1.7–3.2 ng sufficient Dibenzo(a,l)pyrene present sufficient

  9. 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).