Terphenyl

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para-Terphenyl
Skeletal formula of para-terphenyl
Ball-and-stick model of para-terphenyl
Identifiers
CAS number 92-94-4 YesY, (para)
92-06-8 (meta)
84-15-1 (ortho)
26140-60-3 (unspec.)
PubChem 7115
Jmol-3D images Image 1
Properties
Molecular formula C18H14
Molar mass 230.30 g mol−1
Appearance White powder[1]
Density 1.24 g/cm^3
Melting point 212-214 °C[1]
212-213 °C[2]
Boiling point 389 °C[2]
Solubility in water Insoluble[1]
Hazards
R-phrases R36/37/38 R50/53
S-phrases S26 S60 S61
Main hazards Iritant (Xi)
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oil Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point 207 °C[2]
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY (verify) (what is: YesY/N?)
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[edit]

References[edit]

  1. ^ a b c d e p-Terphenyl at chemicalland21.com
  2. ^ a b c p-Terphenyl at Sigma-Aldrich

External links[edit]