![]() N-Phenylbenzylamine structure
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Common Name | N-Phenylbenzylamine | ||
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CAS Number | 103-32-2 | Molecular Weight | 183.24900 | |
Density | 1.169 g/mL at 25 °C(lit.) | Boiling Point | 94-95 °C12 mm Hg(lit.) | |
Molecular Formula | C13H13N | Melting Point | 35-38 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 217 °F | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Use of N-PhenylbenzylamineN-Benzylaniline (N-Phenylbenzylamine) is an N-alkylated derivative of aniline. N-benzyl aniline also is a major metabolite of the antihistamine antazoline and other N-substituted benzyl anilines. N-Benzylaniline can be used for the research of various biochemical studies[1]. |
Name | N-Benzylaniline |
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Synonym | More Synonyms |
Description | N-Benzylaniline (N-Phenylbenzylamine) is an N-alkylated derivative of aniline. N-benzyl aniline also is a major metabolite of the antihistamine antazoline and other N-substituted benzyl anilines. N-Benzylaniline can be used for the research of various biochemical studies[1]. |
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Related Catalog | |
References |
[1]. R Betz, et al. N-Benzylaniline. Acta Cryst. (2011). E67, o1195 |
Density | 1.169 g/mL at 25 °C(lit.) |
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Boiling Point | 94-95 °C12 mm Hg(lit.) |
Melting Point | 35-38 °C(lit.) |
Molecular Formula | C13H13N |
Molecular Weight | 183.24900 |
Flash Point | 217 °F |
Exact Mass | 183.10500 |
PSA | 12.03000 |
LogP | 3.37170 |
Vapour Pressure | 0.000743mmHg at 25°C |
Index of Refraction | n20/D 1.5325(lit.) |
Storage condition | 0-6°C |
Water Solubility | INSOLUBLE |
Symbol |
![]() GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi:Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S37/39 |
RIDADR | UN 2577 8/PG 2 |
WGK Germany | 3 |
HS Code | 29214980 |
HS Code | 2921420090 |
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Summary | HS:2921420090 aniline derivatives and their salts VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0% |
Solvent extraction and separation of gallium, indium and thallium with N-benzylaniline.
Talanta 21(6) , 411-5, (1974) 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 hydrochlori... |
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Synthesis, characterization and catalytic activity of saturated and unsaturated N-heterocyclic carbene iridium(i) complexes.
Dalton Trans. (5) , 861-7, (2009) Both saturated and unsaturated N-benzyl substituted heterocyclic carbene (NHC) iridum(i) complexes were synthesized. The unsaturated carbene complex [(un-NHC-Bn)Ir(CO)(2)Cl] in the cis form was prepar... |
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Identification of a new metabolite after incubation of N-benzylaniline with rabbit liver microsomes.
J. Chromatogr. A. 202(2) , 287-93, (1980)
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N-benzylaniline |
EINECS 203-100-4 |
N-PhenylbenzylaMine |
MFCD00000729 |