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5 G
$41.90
25 G
$120.00
100 G
$345.00
About This Item
Linear Formula:
C6H5(CH2)7CH3
CAS Number:
Molecular Weight:
190.32
Beilstein/REAXYS Number:
1906253
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
98%
refractive index
n20/D 1.484 (lit.)
bp
261-263 °C (lit.)
mp
−36 °C (lit.)
density
0.858 g/mL at 25 °C (lit.)
functional group
phenyl
SMILES string
CCCCCCCCc1ccccc1
InChI
1S/C14H22/c1-2-3-4-5-6-8-11-14-12-9-7-10-13-14/h7,9-10,12-13H,2-6,8,11H2,1H3
InChI key
CDKDZKXSXLNROY-UHFFFAOYSA-N
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General description
Octylbenzene (1-Phenyloctane) forms charge-transfer complexes with fluoranil and 1,3,5-trinitrobenzene.
Application
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[1].
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
224.6 °F - closed cup
flash_point_c
107 °C - closed cup
ppe
Eyeshields, Gloves
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The synthesis, isolation and STM imaging on graphite of the cis and trans isomers of a TTF reveal isomer-dependent packing, and constitutes a way to study the non-covalent interactions at play in these systems.
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The interface between organic semiconductor and graphene electrode, especially the structure of the first few molecular layers at the interface, is crucial for the device properties such as the charge transport in organic field effect transistors. In this work, we
Assemblies at the liquid-solid interface: chirality expression from molecular conformers.
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Selective adsorption of semiconductor nanocrystals onto an organic self-organized pattern shows a time-dependent behavior. By studying the wetting behavior of delivered solvent (1-phenyloctane) on a lipid self-organized pattern and determining the adhesion energy between semiconductor nanocrystals and substrate, we obtain
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