Terphenyl
From Infogalactic: the planetary knowledge core
Names | |
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IUPAC name
1,4-Diphenylbenzene
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Other names
p-Terphenyl; 1,4-Diphenylbenzene; para-Diphenylbenzene; p-Diphenylbenzene; para-Triphenyl; p-Triphenyl
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Identifiers | |
92-94-4 (para) 92-06-8 (meta) 84-15-1 (ortho) 26140-60-3 (unspecified) |
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ChemSpider | 6848 (para) |
Jmol 3D model | Interactive image (para): Interactive image |
PubChem | 7115 |
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Properties | |
C18H14 | |
Molar mass | 230.31 g·mol−1 |
Appearance | White powder[1] |
Density | 1.24 g/cm3 |
Melting point | 212 to 214 °C (414 to 417 °F; 485 to 487 K)[1] 212-213 °C[3] |
Boiling point | 389 °C (732 °F; 662 K)[3] |
Insoluble[1] | |
Refractive index (nD)
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1.65[2] |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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verify (what is ?) | |
Infobox references | |
Terphenyls are a group of closely related aromatic hydrocarbons. Also known as diphenylbenzenes or triphenyls, they consist of a central benzene ring substituted with two phenyl groups. The three isomers are ortho-terphenyl, meta-terphenyl, and para-terphenyl. Commercial grade terphenyl is generally a mixture of the three isomers. This mixture is used in the production of polychlorinated terphenyls, which were formerly used as heat storage and transfer agents.[1]
p-Terphenyl is the most common isomer. It is used as a laser dye and a sunscreen ingredient.[1]
See also
References
- ↑ 1.0 1.1 1.2 1.3 1.4 p-Terphenyl at chemicalland21.com
- ↑ [1]
- ↑ 3.0 3.1 p-Terphenyl at Sigma-Aldrich
External links
- p-Terphenyl at the Oregon Laser Medical Center
- o-Terphenyl, m-Terphenyl, p-Terphenyl at Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health