Pyrene: Difference between revisions

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== Pyrene ==
<gallery>
File:Pyrene.svg|Pyrene structure
File:Br4Py_self-assembly_on_Au.jpg|Br4Py self-assembly on gold
File:Br4Py_self-assembly_on_Au_2.jpg|Br4Py self-assembly on gold (second image)
File:Pyrene-numbering.svg|Pyrene numbering
</gallery>

Latest revision as of 04:53, 18 February 2025

Pyrene is a polycyclic aromatic hydrocarbon (PAH) consisting of four fused benzene rings, resulting in a flat aromatic system. The chemical formula is C16H10. This yellow crystalline solid is the smallest peri-fused PAH (one where the rings are fused through more than one face). Pyrene forms during incomplete combustion of organic compounds.

Properties[edit]

Pyrene is a flat molecule that can intercalate into DNA, while it is not a particularly potent mutagen, it is quite toxic and teratogenic. Pyrene is also used as a probe to determine the polarity of a solvent. It also has a high quantum yield of fluorescence, and because of this it is used in biochemistry experiments as a fluorescent probe, particularly when studying lipids.

Occurrence[edit]

Pyrene and its derivatives are products of combustion and are produced by fossil fuel burning for heat and power, making them common air pollutants. Pyrene is not a major constituent of tar, but it is a component of soot, which is a byproduct of the combustion of diesel and other fuels.

Uses[edit]

Pyrene is used commercially to make dyes and dye precursors, and it is also used in research as a reference standard for the spectroscopic quantification of polycyclic aromatic hydrocarbons.

Health effects[edit]

Exposure to pyrene can cause skin irritation and inflammation. Long-term or repeated exposures can lead to more serious health effects, including cancer.

See also[edit]

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Pyrene[edit]