| Identification | More | [Name]
N-Phenylbenzylamine | [CAS]
103-32-2 | [Synonyms]
AKOS BBS-00003909
A-TOLUYL CHLORIDE
AURORA 4803
Benzeneacetyl chloride
BENZYLANILINE
BENZYL-PHENYL-AMINE
LABOTEST-BB LT00643802
LABOTEST-BB LT00852555
N-BENZYLANILINE
N-PHENYLBENZYLAMINE
PHENACETYL CHLORIDE
PHENYLACETIC ACID CHLORIDE
PHENYLACETYL CHLORIDE
Aniline, N-benzyl-
aniline,N-benzyl-
Benzenamine, N-(phenylmethyl)-
benzeneamine,N-benzyl-
Benzylamine, N-phenyl-
N-benzylbenzeneamine
N-Benzyl-N-phenylamine | [EINECS(EC#)]
203-100-4 | [Molecular Formula]
C13H13N | [MDL Number]
MFCD00000729 | [Molecular Weight]
183.25 | [MOL File]
103-32-2.mol |
| Chemical Properties | Back Directory | [Appearance]
colorless to yellow-beige crystalline powder | [Melting point ]
35-38 °C (lit.) | [Boiling point ]
306-307 °C (lit.) | [density ]
1.061 g/mL at 25 °C(lit.) | [refractive index ]
n20/D 1.5325(lit.)
| [Fp ]
217 °F
| [storage temp. ]
0-6°C | [solubility ]
alcohol: soluble | [form ]
Crystalline Powder or Low Melting Mass | [pka]
3.89±0.10(Predicted) | [color ]
Colorless to yellow-beige | [Specific Gravity]
1.061 | [Water Solubility ]
INSOLUBLE | [Merck ]
1126 | [InChI]
1S/C13H13N/c1-3-7-12(8-4-1)11-14-13-9-5-2-6-10-13/h1-10,14H,11H2 | [InChIKey]
GTWJETSWSUWSEJ-UHFFFAOYSA-N | [SMILES]
C(Nc1ccccc1)c2ccccc2 | [CAS DataBase Reference]
103-32-2(CAS DataBase Reference) | [NIST Chemistry Reference]
Benzenemethanamine, N-phenyl-(103-32-2) | [EPA Substance Registry System]
103-32-2(EPA Substance) |
| Questions And Answer | Back Directory | [Synthesis]
N-Phenylbenzylamine can be obtained by condensation of benzyl chloride and aniline. Mix and stir sodium bicarbonate, water and aniline, heat to 90-95°C, and slowly add benzyl chloride. React at 90-95°C for 3h. Cool and filter. The filtrate was separated, and the organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. Then, under reduced pressure distillation, the 81°C (1.6kPa) fraction was collected to recover aniline, and the 170-190°C (1.6kPa) fraction was cooled and solidified to give N-Phenylbenzylamine. |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P280-P302+P352-P362+P364 | [Hazard Codes ]
C,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
UN 2577 8/PG 2
| [WGK Germany ]
3
| [F ]
21 | [TSCA ]
TSCA listed | [HS Code ]
29214980 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Chemical Properties]
colorless to yellow-beige crystalline powder | [Uses]
N-Benzylaniline was used in the separation of tervalent gallium, indium and thallium by solvent extraction method. | [Uses]
N-Benzylaniline is a major metabolite of the antihistaminic Antazoline and other N-substituted benzylanilines. | [Synthesis Reference(s)]
Chemistry Letters, 8, p. 45, 1979
Organic Syntheses, Coll. Vol. 1, p. 102, 1941
Tetrahedron Letters, 19, p. 4987, 1978 DOI: 10.1016/S0040-4039(01)85789-0 | [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. | [Purification Methods]
Crystallise the amine from pet ether (b 60-80o) (ca 0.5mL/g). The picrate has m 113o (from Et2O). [Beilstein 12 H 1023, 12 I 449, 12 II 548, 12 III 2215, 12 IV 2172.] |
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J & K SCIENTIFIC LTD.
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https://www.jkchemical.com |
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Energy Chemical
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400-0056266 |
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www.energy-chemical.com |
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Maya High Purity Chemicals
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