Dibenz(a,j)anthracene
From Wikipedia, the free encyclopedia
anthracene.svg) | |
| Names | |
|---|---|
| Preferred IUPAC name
Benzo[m]tetraphene | |
| Other names
1,2:7,8-Dibenzanthracene[1] | |
| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.005.390 |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C22H14 | |
| Molar mass | 278.3466 |
| Appearance | colorless crystals |
| Melting point | 196 °C (385 °F; 469 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Dibenz[a,j]anthracene (also known as benzo[m]tetraphene or 1,2:7,8-dibenzanthracene) is an organic compound with the chemical formula C22H14. It belongs to the class of polycyclic aromatic hydrocarbons (PAHs) and is formed whenever there is incomplete combustion of organic matter. The International Agency for Research on Cancer (IARC) has classified it as possibly carcinogenic to humans, grouped into IARC group 2B.
Dibenz[a,j]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, bound to particulates in polluted air, soil, or sediment. [2]
Occurrence
Dibenz[a,j]anthracene is generated whenever organic matter or fuel is incompletely burnt or combusted. Examples include industrial emissions such as coke oven operations in the coal and steel industry, coal tar distillation, or within engine exhaust. On a personal level it is produced with high temperature cooking like frying, grilling, broiling, roasting and baking, but also when cigarette smoking or marijuana smoking.[3]
Health effects
As of 2010, the International Agency for Research on Cancer (IARC) 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. PAHs all have a similar mechanism of causing cancer in both humans and experimental animals whereby they are metabolically converted to oxides and dihydrodiols, and then oxidized to diol epoxides, which react with DNA, inducing mutations.[2]