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  2. 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.

  3. Dibenz (a,h)anthracene - Wikipedia

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

    Dibenz[a,h]anthracene, Benzo[k]tetraphene or 1,2:5,6-Dibenzanthracene is an organic compound with the chemical formula C 22 H 14. It is a polycyclic aromatic hydrocarbon (PAH) made of five fused benzene rings. It is a fused five-ringed PAH which is common as a pollutant of smoke and oils.

  4. Phenanthrene - Wikipedia

    en.wikipedia.org/wiki/Phenanthrene

    Phenanthrene is used to make dyes, plastics, pesticides, explosives, and drugs. It has also been used to make bile acids, cholesterol and steroids. [3] Phenanthrene occurs naturally and also is a man-made chemical. Commonly, humans are exposed to phenanthrene through inhalation of cigarette smoke, but there are many routes of exposure.

  5. Anthracene - Wikipedia

    en.wikipedia.org/wiki/Anthracene

    Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C 14 H 10, consisting of three fused benzene rings. It is a component of coal tar. Anthracene is used in the production of the red dye alizarin and other dyes. Anthracene is colorless but exhibits a blue (400–500 nm peak) fluorescence under ultraviolet radiation. [13]

  6. 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.

  7. DNA adduct - Wikipedia

    en.wikipedia.org/wiki/DNA_adduct

    A metabolite of benzopyrene forms an intercalated DNA adduct, at center. In molecular genetics, a DNA adduct is a segment of DNA bound to a cancer-causing chemical. This process could lead to the development of cancerous cells, or carcinogenesis. DNA adducts in scientific experiments are used as biomarkers of exposure.

  8. Diboraanthracene - Wikipedia

    en.wikipedia.org/wiki/Diboraanthracene

    Diboraanthracene is a class of boron heterocyclic compounds in which two boron atoms substitute two carbon atoms in anthracene (C₁₄H₁₀), one of the typical polycyclic aromatic hydrocarbons (PAHs). The most well-studied diboraanthracene is 9,10-disubstituted-9,10-diboraanthracene (DBA) and its doubly reduced dianion (DBA²⁻).

  9. Benz(a)anthracene - Wikipedia

    en.wikipedia.org/wiki/Benz(a)anthracene

    Benz[a]anthracene or benzo[a]anthracene is a polycyclic aromatic hydrocarbon with the chemical formula C 18 H 12. [2] It is produced during incomplete combustion of organic matter. Benz[ a ]anthracene is one of carcinogenic constituents of tobacco smoke .