Dibenzylamine

Modify Date: 2024-01-02 07:39:44

Dibenzylamine Structure
Dibenzylamine structure
Common Name Dibenzylamine
CAS Number 103-49-1 Molecular Weight 197.28
Density 1.0±0.1 g/cm3 Boiling Point 300.0±0.0 °C at 760 mmHg
Molecular Formula C14H15N Melting Point −26 °C(lit.)
MSDS Chinese USA Flash Point 143.3±0.0 °C
Symbol GHS05 GHS07
GHS05, GHS07
Signal Word Danger

 Use of Dibenzylamine


Dibenzylamine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name Dibenzylamine
Synonym More Synonyms

 Dibenzylamine Biological Activity

Description Dibenzylamine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog
In Vitro 二苄胺是一种强大的神经生成剂的成分。

 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)

 Safety Information

Symbol GHS05 GHS07
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

 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%

 Articles24

More Articles
Spectrophotometric determination of folic acid in pharmaceutical preparations by coupling reactions with iminodibenzyl or 3-aminophenol or sodium molybdate-pyrocatechol.

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...

 Synonyms

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
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