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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3D model (Jmol) |
Interactive image (para): Interactive image |
ChemSpider | 6848 (para) |
PubChem | 7115 |
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Properties | |
C18H14 | |
Molar mass | 230.31 g·mol−1 |
Appearance | White powder |
Density | 1.24 g/cm3 |
Melting point | 212 to 214 °C (414 to 417 °F; 485 to 487 K) 212-213 °C |
Boiling point | 389 °C (732 °F; 662 K) |
Insoluble | |
Refractive index (nD)
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1.65 |
Hazards | |
Main hazards | Iritant (Xi) |
R-phrases | R36/37/38 R50/53 |
S-phrases | S26 S60 S61 |
NFPA 704 | |
Flash point | 207 °C (405 °F; 480 K) |
US health exposure limits (NIOSH): | |
PEL (Permissible)
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C 9 mg/m3 (1 ppm) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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.
p-Terphenyl is the most common isomer. It is used as a laser dye and a sunscreen ingredient.
ortho-Terphenyl
meta-Terphenyl
para-Terphenyl