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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.
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.
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 ...
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.
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. Fluoranthene: Benzo[b]fluoranthene, the left most ring is the extra ring, formed by adding four carbon atoms to the parent compound.
Dibenz[a,j]anthracene or Benzo[m]tetraphene or 1,2:7,8-Dibenzanthracene is an organic compound with the chemical formula C 22 H 14.It belongs to the class of polycyclic aromatic hydrocarbons (PAHs) and is formed whenever there is incomplete combustion of organic matter.
It belongs to the class of organic compounds known as benzo-coumarins or dibenzo-α-pyrones. Its precursors – ellagic acids and ellagitannins – are ubiquitous in nature, including edible plants, such as pomegranates, strawberries, raspberries, walnuts, and others. [2] Urolithin A is not known to be found in any food source.
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.