Dibenzylamine
Names
[ CAS No. ]:
103-49-1
[ Name ]:
Dibenzylamine
[Synonym ]:
bis-benzylamine
Dibenzylamine
Bibenzylamine
dibenzyl-amine
PhCH2NHCH2Ph
Benzenemethanamine, N-(phenylmethyl)-
DIBAM
Benzenemethanamine, N- (phenylmethyl)-
forLabetalol
(N-Benzylaminomethyl)benzene
MFCD00004770
EINECS 203-117-7
N-Benzylbenzylamine
di-benzylamine
Vulcaid 28
N,n-dibenzylamine
N-Benzyl-1-phenylmethanamine
DBZA
N-(Phenylmethyl)benzenemethanamine
Accelerator DBA
Biological Activity
[Description]:
[Related Catalog]:
[In Vitro]
Chemical & Physical Properties
[ Density]:
1.0±0.1 g/cm3
[ Boiling Point ]:
300.0±0.0 °C at 760 mmHg
[ Melting Point ]:
−26 °C(lit.)
[ Molecular Formula ]:
C14H15N
[ Molecular Weight ]:
197.28
[ Flash Point ]:
143.3±0.0 °C
[ Exact Mass ]:
197.120453
[ PSA ]:
12.03000
[ LogP ]:
3.42
[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C
[ Index of Refraction ]:
1.581
[ Stability ]:
Stable. Incompatible with oxidizing agents, acid anhydrides, acids, acid chlorides, chloroformates.
[ Water Solubility ]:
0.05 g/L (20 ºC)
MSDS
Safety Information
[ Symbol ]:
GHS05, GHS07
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H302-H314
[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
C:Corrosive
[ Risk Phrases ]:
R22;R34;R52/53
[ Safety Phrases ]:
S26-S61-S45-S36/37/39
[ RIDADR ]:
2810
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
8
[ HS Code ]:
2921499090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2921499090
[ Summary ]:
2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
Articles
Anal. Biochem. 307(2) , 316-21, (2002)
Novel coupling reagents are used for the simple and sensitive spectrophotometric determination of folic acid either in pure form or in its pharmaceutical preparations. The methods are based on the pro...
Diastereoselective construction of syn-α-oxyamines via three-component α-oxyaldehyde-dibenzylamine-alkyne coupling reaction: application in the synthesis of (+)-β-conhydrine and its analogues.Org. Biomol. Chem. 10(37) , 7536-44, (2012)
A Cu(I)-catalyzed α-oxyaldehyde-dibenzylamine-alkyne coupling reaction was delineated for the construction of α-oxyamines with excellent yields and diastereoselectivity. Crystal structure analysis and...
Kinetic study on the nitrosation of dibenzylamine in a model system.Food Chem. Toxicol. 32(11) , 1015-9, (1994)
A kinetic study of the formation of N-nitrosodibenzylamine (NDBzA), from the nitrosation of dibenzylamine (DBzA) by sodium nitrite, was performed in a model system under conditions (temperature, pH) t...