185493
N-Benzylaniline
≥99%
Synonym(s):
N-Phenylbenzylamine
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About This Item
Linear Formula:
C6H5CH2NHC6H5
CAS Number:
Molecular Weight:
183.25
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
≥99%
form
solid
bp
306-307 °C (lit.)
mp
35-38 °C (lit.)
solubility
alcohol: soluble
chloroform: soluble
diethyl ether: soluble
water: insoluble
density
1.061 g/mL at 25 °C (lit.)
functional group
amine
phenyl
SMILES string
C(Nc1ccccc1)c2ccccc2
InChI
1S/C13H13N/c1-3-7-12(8-4-1)11-14-13-9-5-2-6-10-13/h1-10,14H,11H2
InChI key
GTWJETSWSUWSEJ-UHFFFAOYSA-N
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General description
The electropolymerisation of N-benzylaniline at transparent Indium Tin Oxide glass electrodes has been investigated by UV-visible spectroelectrochemistry. N-Benzylaniline on electrochemical oxidation in aqueous sulfuric acid solution produces an adherent conducting polymer film at the platinum electrode.
Application
N-Benzylaniline was used in the separation of tervalent gallium, indium and thallium by solvent extraction method.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Electrochemical polymerization and characterization of N-benzylaniline.
Dong S and Li Z.
Synthetic Metals, 33(1), 93-98 (1989)
M M Khosla et al.
Talanta, 21(6), 411-415 (1974-06-01)
A simple and rapid method is proposed for the separation of tervalent gallium, indium and thallium by solvent extraction with N-benzylaniline in chloroform from different concentrations of hydrochloric acid. Thallium and gallium are extracted from 1M and 7.0-7.5M hydrochloric acid
A UV-visible spectroelectrochemical study of the electropolymerisation of N-benzylaniline.
Malinauskas A and Holze R.
Journal of Solid State Electrochemistry, 3(7-8), 429-436 (1999)
J W Gorrod et al.
Xenobiotica; the fate of foreign compounds in biological systems, 15(12), 1021-1031 (1985-12-01)
Using direct specific analytical techniques microsomal metabolism of N-benzyl-4-substituted anilines has been investigated and found to include both N- and C-oxidation. N-Debenzylation was observed with all substrates and species examined. N-Oxidation usually yielded aryl nitrones, although the N-hydroxy derivative of
Masaharu Uno et al.
Organic & biomolecular chemistry, 6(6), 979-981 (2008-03-11)
N-Benzylanilines were designed and synthesized as vascular endothelial growth factor (VEGF)-2 inhibitors using de novo drug design systems based on the X-ray structure of VEGFR-2 kinase domain. Among compounds synthesized, compound showed the most potent inhibitory activity toward VEGFR-2 (KDR)
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