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N,N'-dibenzylethane-1,2-diamine

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Identification
Molecular formula
C16H20N2
CAS number
6342-01-2
IUPAC name
N,N'-dibenzylethane-1,2-diamine
State
State

At room temperature, N,N'-dibenzylethane-1,2-diamine is typically in a liquid form but can solidify depending on the temperature and purity. It transforms to a solid state as it approaches its melting point.

Melting point (Celsius)
18.00
Melting point (Kelvin)
291.15
Boiling point (Celsius)
168.00
Boiling point (Kelvin)
441.15
General information
Molecular weight
240.37g/mol
Molar mass
240.3660g/mol
Density
1.0300g/cm3
Appearence

N,N'-dibenzylethane-1,2-diamine is a colorless to pale yellow liquid. It may solidify upon standing at lower temperatures.

Comment on solubility

Solubility of N,N'-dibenzylethane-1,2-diamine

N,N'-dibenzylethane-1,2-diamine, with the chemical formula C16H20N2, is an intriguing compound in terms of solubility. Understanding its solubility profile is essential for its applications in various chemical processes and synthesis. Here are some key points regarding its solubility:

  • Polar vs Nonpolar: The presence of the benzyl groups makes this compound predominantly nonpolar, which influences its solubility in solvents.
  • Solvent Compatibility: N,N'-dibenzylethane-1,2-diamine is typically soluble in organic solvents such as:
    • Benzene
    • Toluene
    • Chloroform
    • Ethanol
  • Water Solubility: Due to its large organic structure, this compound is likely to have low solubility in water, which is often characteristic of larger, nonpolar molecules.
  • Temperature Effects: Solubility may vary with temperature; generally, increasing temperature can enhance solubility in many organic solvents.

In summary, N,N'-dibenzylethane-1,2-diamine exhibits solubility predominantly in nonpolar solvents while showing limited solubility in water. This solubility behavior is critical for researchers and chemists to consider during formulation and reaction conditions.

Interesting facts

Interesting Facts About N,N'-Dibenzylethane-1,2-diamine

N,N'-Dibenzylethane-1,2-diamine is a fascinating organic compound that presents a multitude of interesting features useful in various fields of chemistry. Here are some noteworthy aspects:

  • Dual Functionality: This compound contains two amine groups which can participate in a variety of chemical reactions, such as nucleophilic substitutions and reductions. Its structure makes it valuable in the synthesis of more complex molecules.
  • Versatile Building Block: N,N'-Dibenzylethane-1,2-diamine serves as an important building block in organic synthesis, particularly in the formation of polyamines and polymers, which are crucial in materials science and pharmaceuticals.
  • Biological Relevance: Compounds featuring amine functionalities like this one often show significant biological activity. This can include properties that affect neurotransmitter function, making it a compound of interest in medicinal chemistry.
  • Reactant in Ligand Formation: The presence of two benzyl groups in the structure enhances its capability to act as a bidentate ligand in coordination chemistry, forming stable complexes with transition metals.
  • Environmental Considerations: As with many organic compounds, the pathways of N,N'-dibenzylethane-1,2-diamine in biological and environmental systems are important for understanding its impact. Studying its degradation and effects on ecosystems can lead to insights into sustainable chemistry.

As noted by chemists, "Compounds like N,N'-dibenzylethane-1,2-diamine not only advance our understanding of chemical reactivity but also pave the way for innovations in drug design and materials engineering."

With ongoing research, this compound stands out as a promising agent in many scientific applications, confirming the exciting possibilities that lie in the chemistry of amines.

Synonyms
N,N'-Dibenzylethylenediamine
140-28-3
Benzathine
DBED
Benzatin
N1,N2-Dibenzylethane-1,2-diamine
1,2-Bis(benzylamino)ethane
N,N'-dibenzylethane-1,2-diamine
1,2-Ethanediamine, N,N'-bis(phenylmethyl)-
N,N'-Dibenzyl-ethane-1,2-diamine
USAF DO-53
NSC 5632
N,N'-Dibenzyl-1,2-ethylenediamine
1,2-Ethanediamine, N1,N2-bis(phenylmethyl)-
ETHYLENEDIAMINE, N,N'-DIBENZYL-
EINECS 205-408-4
UNII-C659VZ7P7T
BRN 0786668
C659VZ7P7T
CHEBI:51344
AI3-23851
benzyl[2-(benzylamino)ethyl]amine
BENZATHINE [MI]
NSC-5632
NSC-62936
N1,N2-Bis(phenylmethyl)-1,2-ethanediamine
DTXSID4048359
n,n'-dibenzyl-1,2-diaminoethane
N,N'-Dibenzyl-1,2-ethanediamine
4-12-00-02321 (Beilstein Handbook Reference)
Ethylenediamine,N'-dibenzyl-
WLN: R1M2M1R
1, N,N'-bis(phenylmethyl)-
NCGC00166222-02
N',N-Dibenzyl-ethylenediamine
MFCD00004771
n,n'dibenzylethylenediamine
1,2Bis(benzylamino)ethane
SCHEMBL5764
MLS004800109
Ethylenediamine, N,N'dibenzyl
N,N'-dibenzylethylene diamine
N,N'-dibenzylethylene-diamine
CHEMBL193646
DTXCID9028334
NSC5632
NSC62936
STR05175
N,N'-Dibenzylethylenediamine, 97%
BBL002994
STK379515
AKOS005306729
benzyl-[2-(benzylamino)-ethyl]-amine
CCG-248022
FD37250
SB33325
N1,N2Bis(phenylmethyl)1,2ethanediamine
NCGC00166222-01
1,2Ethanediamine, N,N'bis(phenylmethyl)
AC-13104
HY-20512
SMR001547335
1,2Ethanediamine, N1,N2bis(phenylmethyl)
CS-0008847
D1807
NS00006909
EN300-207802
Q2896784
F0001-0480