M-Terphenyl
| Names | |
|---|---|
| IUPAC name
1,3-diphenylbenzene | |
| Other names
m-Terphenyl; 1,1'-Biphenyl, 3-phenyl-; 1,1':3',1''-Terphenyl; 1,3-Diphenylbenzene; 1,3-Terphenyl; AI3-00860; CCRIS 1656; EINECS 202–122–1; HSDB 2537; Isodiphenylbenzene; m-Diphenylbenzene; m-Triphenyl; NSC 6808; Santowax M; UNII-WOI2PSS0KX | |
| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.001.930 |
| EC Number |
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PubChem CID |
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CompTox Dashboard (EPA) |
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| Properties | |
| C18H14 | |
| Molar mass | 230.310 g·mol−1 |
| Appearance | yellow needles |
| Density | 1.23 |
| Melting point | 86–87 °C (187–189 °F; 359–360 K) |
| Boiling point | 365 |
| 1.51 mg/l | |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H410 | |
| P273, P391, P501 | |
| Flash point | 191 °C (376 °F; 464 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
m-Terphenyls (also known as meta-terphenyls, meta-diphenylbenzenes, or meta-triphenyls) are organic molecules composed of two phenyl groups bonded to a benzene ring in the one and three positions. The simplest formula is C18H14, but many different substituents can be added to create a diverse class of molecules. Due to the extensive pi-conjugated system, the molecule it has a range of optical properties and because of its size, it is used to control the sterics in reactions with metals and main group elements. This is because of the disubstituted phenyl rings, which create a pocket for molecules and elements to bond without being connected to anything else. It is a popular choice in ligand, and the most chosen amongst the terphenyls because of its benefits in regards to sterics. Although many commercial methods exist to create m-terphenyl compounds, they can also be found naturally in plants such as mulberry trees.