Skip to main content

2-[benzyl(2-hydroxyethyl)amino]ethanol

ADVERTISEMENT
Identification
Molecular formula
C11H17NO2
CAS number
50594-66-6
IUPAC name
2-[benzyl(2-hydroxyethyl)amino]ethanol
State
State

At room temperature, 2-[benzyl(2-hydroxyethyl)amino]ethanol is typically found in a liquid state. It is stable under normal conditions, but its hygroscopic nature means it can absorb moisture from the air over time, which can affect its viscosity and appearance.

Melting point (Celsius)
-22.00
Melting point (Kelvin)
251.20
Boiling point (Celsius)
356.40
Boiling point (Kelvin)
629.50
General information
Molecular weight
225.30g/mol
Molar mass
225.2960g/mol
Density
1.1129g/cm3
Appearence

2-[benzyl(2-hydroxyethyl)amino]ethanol generally appears as a clear, colorless to pale yellow liquid. It has a viscous consistency, and may also appear as a slightly oily substance. It is hygroscopic, meaning it can absorb moisture from the air.

Comment on solubility

Solubility of 2-[benzyl(2-hydroxyethyl)amino]ethanol

When discussing the solubility of 2-[benzyl(2-hydroxyethyl)amino]ethanol, several key factors contribute to its behavior in various solvents. This compound is known for its unique structure, which influences its ability to dissolve in different media.

Factors Influencing Solubility:

  • Hydrophilicity: The presence of the hydroxyl (-OH) group enhances solubility in polar solvents such as water.
  • Hydrophobic Regions: The benzyl group contributes a hydrophobic character, which can limit solubility in highly polar solvents.
  • Temperature: Increased temperatures may improve solubility, as kinetic energy allows solute molecules to overcome intermolecular forces.
  • pH Levels: The ionization of the amine group can also play a significant role; a more basic environment can increase solubility due to protonation effects.

In general, this compound exhibits a moderate to good solubility in water and organic solvents. However, it's important to note:

  1. Solubility tends to be better in slightly acidic solutions due to increased protonation of the amine.
  2. Its overall solubility profile indicates potential applications in both aqueous and non-aqueous environments.

In summary, the solubility of 2-[benzyl(2-hydroxyethyl)amino]ethanol can be described as being highly dependent on solvent properties, temperature, and pH. Understanding these interactions is crucial for effectively utilizing this compound in various chemical applications.

Interesting facts

Exploring 2-[benzyl(2-hydroxyethyl)amino]ethanol

2-[benzyl(2-hydroxyethyl)amino]ethanol is a fascinating compound with a variety of applications and properties that intrigue scientists and researchers alike. Here are some interesting facts surrounding this unique molecule:

  • Structural Complexity: The compound features a central ethylamine backbone, which is further substituted with both a benzyl group and a hydroxyl group. This intricate structure leads to diverse interactions which can influence its biological activity.
  • Biological Relevance: Compounds similar to 2-[benzyl(2-hydroxyethyl)amino]ethanol often find roles in medicinal chemistry. Research suggests that it could act as a potential ligand in neurotransmitter systems, impacting pathways in the central nervous system.
  • Amphiphilicity: Given the presence of both hydrophilic (hydroxyethyl and amino groups) and hydrophobic (benzyl group) portions in its structure, this compound may exhibit amphiphilic characteristics. This property is valuable in drug delivery systems, enhancing the solubility and bioavailability of therapeutic agents.
  • Synthesis Pathways: The synthesis of this compound can occur through various organic reactions involving amine chemistry. Understanding and optimizing these synthesis routes is crucial for scaling production and enhancing purity.
  • Potential Applications: Researchers are investigating usage in various fields, including pharmaceuticals, agrochemicals, and biochemicals. Its potential to serve as a building block for more complex biological molecules makes it an exciting target for study.

As we delve deeper into the realm of 2-[benzyl(2-hydroxyethyl)amino]ethanol, it becomes clear that its unique combination of properties and potential applications demonstrates the diverse functionalities that small molecules can offer in the field of chemistry.

Synonyms
101-32-6
N-Benzyldiethanolamine
2,2'-(benzylazanediyl)diethanol
2,2'-(Benzylimino)diethanol
Ethanol, 2,2'-[(phenylmethyl)imino]bis-
2,2-(BENZYLIMINO)DIETHANOL
Ethanol, 2,2'-(benzylimino)di-
N,N-Bis(2-hydroxyethyl)benzylamine
BENZYLDIETHANOLAMINE
2-[2-Hydroxyethyl(phenylmethyl)amino]ethanol
2-[benzyl(2-hydroxyethyl)amino]ethan-1-ol
2-[Benzyl(2-hydroxyethyl)amino]-1-ethanol
2-[benzyl(2-hydroxyethyl)amino]ethanol
2,2'-((Phenylmethyl)imino)bisethanol
MFCD00020587
Ethanol, 2,2'-((phenylmethyl)imino)bis-
2,2'-(Benzylimino)-diethanol
NSC-60297
2,2'-[(phenylmethyl)imino]bisethanol
2,2/'-(BENZYLIMINO)DIETHANOL
N-Benzyl-N,N-bis(2-hydroxyethyl)amine
2,2'-[(Phenylmethyl)imino]bis[ethanol]
2,2'-((Phenylmethyl)imino)bis(ethanol)
Benzylbis(2-hydroxyethyl)amine
EINECS 202-934-6
BRN 2211596
AI3-26798
NSC60297
N-benzyl diethanolamine
N-benzyl-diethanolamine
Cambridge id 5465378
Oprea1_215048
SCHEMBL79747
4-12-00-02200 (Beilstein Handbook Reference)
Ethanol,2'-(benzylimino)di-
Bis(2-hydroxyethyl)benzylamine
9CH4Q34B2G
CHEMBL425114
Bis-(2-hydroxyethyl)-benzylamine
DTXSID50143618
HMS1581H19
N,N-bis(2-hydroxyethyl)benzyl amine
NSC 60297
AKOS005070831
Ethanol,2'-[(phenylmethyl)imino]bis-
N-benzyl-N,N-di(2-hydroxyethyl)amine
N,N-bis(2-hydroxyethyl)-N-benzylamine
2,2'-(Benzylimino)diethanol, >=99%
benzylamine, N,N-bis(2-hydroxyethyl)-
SY050882
DB-082072
B5081
CS-0000081
NS00023051
2,2'-(BENZYLAZANEDIYL)BIS(ETHAN-1-OL)
6X-0943
2,2 inverted exclamation mark -(Benzylazanediyl)diethanol
202-934-6