113190
1-Phenyloctane
98%
Synonym(s):
Octylbenzene
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About This Item
Linear Formula:
C6H5(CH2)7CH3
CAS Number:
Molecular Weight:
190.32
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-582-1
Beilstein/REAXYS Number:
1906253
MDL number:
Product Name
1-Phenyloctane, 98%
InChI key
CDKDZKXSXLNROY-UHFFFAOYSA-N
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
SMILES string
CCCCCCCCc1ccccc1
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
Quality Level
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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.
General description
Octylbenzene (1-Phenyloctane) forms charge-transfer complexes with fluoranil and 1,3,5-trinitrobenzene.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
224.6 °F - closed cup
flash_point_c
107 °C - closed cup
ppe
Eyeshields, Gloves
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Yan Yang et al.
Langmuir : the ACS journal of surfaces and colloids, 31(45), 12408-12416 (2015-10-29)
Side chains containing two diacetylene units spaced by an odd number of methylene units exhibit pronounced “bumps” composed of 0.3 nm steps, in opposite directions, at odd and even side-chain positions. In densely packed self-assembled monolayers, the bis-diacetylene bumps stack
Elba Gomar-Nadal et al.
Chemical communications (Cambridge, England), (7)(7), 906-907 (2003-05-13)
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.
Assemblies at the liquid-solid interface: chirality expression from molecular conformers.
Yong-Tao Shen et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 14(1), 92-95 (2012-11-13)
Yanqiu Jiang et al.
Scientific reports, 5, 17720-17720 (2015-12-05)
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
Xiaodong Chen et al.
Nano letters, 7(11), 3483-3488 (2007-10-05)
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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