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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.
As a result, while anthracene reacts with maleic acid, phenanthrene does not, and triphenylene is the most stable species of these three. [ 1 ] Three Clar structures with an increasing number of π-sextets: anthracene (on the left), phenanthrene (in the middle), and triphenylene (on the right).
Dibenz[a,h]anthracene or 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.
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.
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⁻).
A typical experimental design for studying DNA adducts is to induce them with known carcinogens. A scientific journal will often incorporate the name of the carcinogen with their experimental design. For example, the term "DMBA-DNA adduct" in a scientific journal refers to a piece of DNA that has DMBA (7,12-dimethylbenz(a)anthracene) attached ...
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]
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.