185493

Sigma-Aldrich

N-Benzylaniline

≥99%

Synonym(s):
N-Phenylbenzylamine
Linear Formula:
C6H5CH2NHC6H5
CAS Number:
Molecular Weight:
183.25
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥99%

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.)

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.

Packaging

25, 100 g in glass bottle

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

UN 3335

WGK Germany

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Certificate of Analysis

Certificate of Origin

Electrochemical polymerization and characterization of N-benzylaniline.
Dong S and Li Z.
Synthetic Metals, 33(1), 93-98 (1989)
Synthesis and structure-activity relationships of a class of sodium iodide symporter function inhibitors.
Fanny Waltz et al.
ChemMedChem, 6(10), 1775-1777 (2011-07-14)
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)
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...
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...

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