| Identification | More | [Name]
N-OCTYLBENZENE | [CAS]
2189-60-8 | [Synonyms]
1-PHENYLOCTANE
N-OCTYLBENZENE
OCTYLBENZENE
PHENYLOCTANE
Benzene, octyl-
Octane, 1-phenyl-
octane,1-phenyl-
octyl-benzen | [EINECS(EC#)]
218-582-1 | [Molecular Formula]
C14H22 | [MDL Number]
MFCD00009564 | [Molecular Weight]
190.32 | [MOL File]
2189-60-8.mol |
| Chemical Properties | Back Directory | [Appearance]
colourless liquid | [Melting point ]
-36 °C (lit.) | [Boiling point ]
261-263 °C (lit.) | [density ]
0.858 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.484(lit.)
| [Fp ]
226 °F
| [storage temp. ]
Sealed in dry,Room Temperature | [form ]
Liquid | [color ]
Clear colorless | [Stability:]
Stable. Combustible. Incompatible with strong oxidizing agents. | [Water Solubility ]
Immiscible with water. | [BRN ]
1906253 | [InChIKey]
CDKDZKXSXLNROY-UHFFFAOYSA-N | [CAS DataBase Reference]
2189-60-8(CAS DataBase Reference) | [NIST Chemistry Reference]
n-Octylbenzene(2189-60-8) | [EPA Substance Registry System]
2189-60-8(EPA Substance) |
| Safety Data | Back Directory | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29029090 |
| Hazard Information | Back Directory | [Chemical Properties]
colourless liquid | [Uses]
1-Phenyloctane is used as a solvent to study the self-assembly of derivatives of tetrathiafulvalene (TTF) on graphite and their visualization by scanning tunnelling microscopy (STM). It is also used to study the effects of the substitution of these compounds on the interactions between them. | [Uses]
n-octylbenzene is used as a solvent to study the self-assembly of derivatives of tetrathiafulvalene (TTF) on graphite and their visualization by scanning tunnelling microscopy (STM). It is also involved in the study the effects and substitution of these compounds. It is also used to prepare charge-transfer complexes with fluoranil and 1,3,5-trinitrobenzene. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 111, p. 314, 1989 DOI: 10.1021/ja00183a048
Tetrahedron Letters, 27, p. 6369, 1986 DOI: 10.1016/S0040-4039(00)87811-9 | [General Description]
Octylbenzene (1-Phenyloctane) forms charge-transfer complexes with fluoranil and 1,3,5-trinitrobenzene. | [Synthesis]
A 100 ml four-necked flask equipped with a mechanical stirrer, thermometer, nitrogen inlet and septum was charged with CuCl2 (40 mg, 0.3 nmol, 3 mol%), octyl bromide (1.93 g, 10 nmol, 1 equiv.), benzonitrile (103 mg, 1 nmol, 10 mol%) and THF (9 mL). The r |
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