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Benzyldiphenylamine

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Identification
Molecular formula
C14H15N
CAS number
101-81-5
IUPAC name
N-benzyl-1-phenyl-methanamine
State
State

Benzyldiphenylamine is typically found in a liquid state at room temperature.

Melting point (Celsius)
-13.00
Melting point (Kelvin)
260.15
Boiling point (Celsius)
337.00
Boiling point (Kelvin)
610.15
General information
Molecular weight
197.29g/mol
Molar mass
197.2910g/mol
Density
1.0300g/cm3
Appearence

Benzyldiphenylamine appears as a colorless to pale yellow liquid with a characteristic aromatic amine odor.

Comment on solubility

Solubility of N-benzyl-1-phenyl-methanamine

N-benzyl-1-phenyl-methanamine, with the formula C15H16N, exhibits notable solubility characteristics that can be intriguing to study.

General Solubility Traits

As a tertiary amine, N-benzyl-1-phenyl-methanamine typically demonstrates:

  • Moderate solubility in organic solvents such as ethanol, methanol, and acetone.
  • Limited solubility in water due to its non-polar benzyl and phenyl groups that hinder hydration.

Factors Affecting Solubility

The solubility of this compound can be influenced by several factors:

  • Temperature: Increased temperature often enhances the solubility of organic compounds.
  • pH: As an amine, the solubility can change in different pH conditions due to protonation states.
  • Solvent Polarity: The choice of solvent can greatly impact solubility due to the "like dissolves like" principle.

In conclusion, the solubility characteristics of N-benzyl-1-phenyl-methanamine make it a compound of interest, especially in applications where solvent interactions are critical. Understanding these solubility properties is essential for its effective use in various chemical processes.

Interesting facts

Interesting Facts About N-benzyl-1-phenyl-methanamine

N-benzyl-1-phenyl-methanamine, commonly known as a member of the class of compounds known as tertiary amines, has garnered interest within the fields of organic and medicinal chemistry. This compound is notable for its unique structural features and applications. Below are some engaging details:

  • Chemical Structure: With its distinctive benzyl and phenyl groups, this amine exhibits interesting steric and electronic properties, which can have significant implications on its reactivity and interactions with other molecules.
  • Applications: N-benzyl-1-phenyl-methanamine is frequently utilized in synthetic organic chemistry as a reagent or intermediate to produce various pharmaceuticals and agrochemicals. Its ability to act as a building block for more complex structures is invaluable.
  • Biological Activity: Research has shown that compounds related to N-benzyl-1-phenyl-methanamine can exhibit various biological activities. As a result, they have been explored for potential therapeutic uses, including their role in influencing neurotransmitter levels.
  • Reactivity: The amine functional group in N-benzyl-1-phenyl-methanamine can participate in a variety of chemical reactions. It can engage in nucleophilic substitutions, and the compound can be easily modified to synthesize derivatives with tailored properties.
  • Synthesis: This compound can be synthesized through several methods, with one of the more common approaches involving the reaction of benzyl chloride with an appropriate amine. The study of its synthesis methods can provide valuable insights into reaction mechanisms and compound stability.

In the world of chemistry, N-benzyl-1-phenyl-methanamine represents a fascinating intersection of structural complexity and practical application. As a chemist or student, delving into the properties and potential uses of this compound can uncover exciting opportunities for innovation and discovery in the scientific community.

Synonyms
Dibenzylamine
103-49-1
Benzenemethanamine, N-(phenylmethyl)-
N-benzyl-1-phenylmethanamine
N-Benzylbenzylamine
Bibenzylamine
DIBENZYL-AMINE
N,N-Dibenzylamine
N,N-Dibenylamine
N-(Phenylmethyl)benzenemethanamine
(N-Benzylaminomethyl)benzene
Accelerator DBA
NSC 4811
UNII-3G0YFX01C6
Vulcaid 28
3G0YFX01C6
DTXSID6044355
NSC-4811
EINECS 203-117-7
DIBENZYLAMINE [MI]
AI3-15327
DTXCID4024355
EC 203-117-7
NORADRENALINE TARTRATE IMPURITY F [EP IMPURITY]
bisbenzylamine
DIBENZYL AMINE
MFCD00004770
NORADRENALINE TARTRATE IMPURITY F (EP IMPURITY)
DBA (VAN)
N,NDibenzylamine
benzyl benzylamine
NBenzylbenzylamine
N-(phenylmethyl)benzenemethanamine; Dibenzylamine; Noradrenaline Imp. F (EP)
Dibenzylamine, 97%
Bn2NH
benzylamine, N-benzyl-
(NBenzylaminomethyl)benzene
(PhCH2)2NH
NH(CH2Ph)2
N-Benzyl(phenyl)methanamine
SCHEMBL1654
Oprea1_559431
N-Benzyl(phenyl)methanamine #
CHEMBL3182419
N(Phenylmethyl)benzenemethanamine
1PhenylN(phenylmethyl)methanamine
NSC4811
CHEBI:189125
Benzenemethanamine, N(phenylmethyl)
BCP22185
HY-Y1067
YLB28209
Tox21_301089
BBL027475
MSK001862
STK397784
AKOS000119097
CS-W020085
FD36412
NCGC00248284-01
NCGC00254989-01
AS-14038
CAS-103-49-1
1ST001862
MSK001862-1000
D0152
NS00007138
Dibenzylamine, Vetec(TM) reagent grade, 97%
EN300-17949
10.14272/BWLUMTFWVZZZND-UHFFFAOYSA-N
D77870
Dibenzylamine Solution in Methanol, 1000?g/mL
Dibenzylamine Solution in Methanol, 1000mug/mL
1ST001862-1000
doi:10.14272/BWLUMTFWVZZZND-UHFFFAOYSA-N
N-(Phenylmethyl)-benzenemethanamine; N,N-Dibenzylamine
Q27257174
Z57127894
F2190-0321
203-117-7