Perylene
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| Names | |||
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| Preferred IUPAC name
Perylene | |||
| Other names
peri-Dinaphthalene; Perilene; Dibenz[de,kl]anthracene | |||
| Identifiers | |||
3D model (JSmol) |
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| 1911335 | |||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.005.365 | ||
| EC Number |
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| 104944 | |||
| KEGG | |||
PubChem CID |
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| RTECS number |
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| UNII | |||
CompTox Dashboard (EPA) |
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| Properties | |||
| C20H12 | |||
| Molar mass | 252.316 g·mol−1 | ||
| Appearance | Brown solid | ||
| Melting point | 276 to 279 °C (529 to 534 °F; 549 to 552 K) | ||
| −166.8·10−6 cm3/mol | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
Perylene or perilene is a polycyclic aromatic hydrocarbon with the chemical formula C20H12, occurring as a brown solid. It or its derivatives may be carcinogenic, and it is considered to be a hazardous pollutant. In cell membrane cytochemistry, perylene is used as a fluorescent lipid probe. It is the parent compound of a class of rylene dyes.