Names | |
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Preferred IUPAC name
Tetracene[1] | |
Other names
Naphthacene
Benz[b]anthracene 2,3-Benzanthracene Tetracyclo[8.8.0.03,8.012,17]octadeca-1,3,5,7,9,11,13,15,17-nonaene | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.001.945 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C18H12 | |
Molar mass | 228.29 g/mol |
Appearance | Yellow to orange solid |
Melting point | 357 °C (675 °F; 630 K) |
Boiling point | 436.7 °C (818.1 °F; 709.8 K) |
Insoluble | |
-168.0·10−6 cm3/mol | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tetracene, also called naphthacene, is a polycyclic aromatic hydrocarbon. It has the appearance of a pale orange powder. Tetracene is the four-ringed member of the series of acenes.
Tetracene is a molecular organic semiconductor, used in organic field-effect transistors (OFETs) and organic light-emitting diodes (OLEDs). Tetracene can be used as a gain medium in dye lasers as a sensitiser in chemoluminescence. Napthacene is the main component of the tetracycline class of antibiotics.