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2-(Benzylamino)ethanol

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Identification
Molecular formula
C9H13NO
CAS number
104-63-2
IUPAC name
2-(benzylamino)ethanol
State
State

At room temperature, 2-(benzylamino)ethanol is typically in a liquid state. It is stable under normal conditions and can be handled easily in laboratory settings.

Melting point (Celsius)
8.50
Melting point (Kelvin)
281.60
Boiling point (Celsius)
248.50
Boiling point (Kelvin)
521.60
General information
Molecular weight
151.21g/mol
Molar mass
151.2110g/mol
Density
1.0324g/cm3
Appearence

2-(Benzylamino)ethanol appears as a colorless to light yellow liquid. It is typically clear and free-flowing with a characteristic amine odor.

Comment on solubility

Solubility of 2-(benzylamino)ethanol

2-(benzylamino)ethanol, with the chemical formula C9H13NO, exhibits notable solubility characteristics that are of interest in various chemical contexts. This compound is primarily known for its ability to dissolve in a variety of solvents, which can be attributed to its structural properties.

Key Solubility Features:

  • Polar Nature: The presence of both an amino group and a hydroxyl group in its structure contributes to its overall polarity, enhancing its solubility in polar solvents such as water.
  • Hydrogen Bonding: The hydroxyl group allows for strong hydrogen bonding interactions with solvent molecules, further increasing its solubility in aqueous solutions.
  • Organic Solvent Compatibility: 2-(benzylamino)ethanol is also soluble in various organic solvents like ethanol, methanol, and dimethyl sulfoxide (DMSO), making it versatile for use in organic synthesis.

It is important to note, however, that the solubility can be affected by factors such as temperature and the presence of other substances in the solution. Generally, one can expect that:

  • The solubility in water significantly improves with rising temperatures.
  • Interactions with other solutes may either enhance or hinder its solubility.

In conclusion, 2-(benzylamino)ethanol is a soluble compound that displays a strong affinity for various polar and nonpolar solvents. This solubility profile makes it useful in numerous applications within the field of chemistry.

Interesting facts

Interesting Facts about 2-(Benzylamino)ethanol

2-(Benzylamino)ethanol is a fascinating compound with a variety of applications in both industrial and academic fields. Here are some notable highlights:

  • Structural Innovation: This compound features a unique structure characterized by a benzyl group attached to an aminoethanol backbone, which grants it interesting chemical reactivity.
  • Pharmaceutical Relevance: Due to its amino functional group, 2-(benzylamino)ethanol is often explored for its potential as a building block in the synthesis of various pharmaceuticals. Its properties may contribute to the development of new medications targeting central nervous system disorders.
  • Versatile Reactions: This compound can participate in a multitude of organic reactions, including nucleophilic substitutions and couplings, making it valuable in synthetic organic chemistry.
  • Biochemical Significance: 2-(Benzylamino)ethanol can serve as a chiral diamine, which is useful in asymmetric synthesis processes, highlighting its role in creating molecules with specific spatial configurations essential in drug design.
  • Research Tool: In academic settings, this compound is often used as a reagent for various chemical experiments, providing insights into reaction mechanisms and pathways in organic synthesis studies.

As you can see, 2-(benzylamino)ethanol is more than just a simple organic compound; it is a versatile tool in the realm of chemistry, linking structural innovation with practical applications in pharmaceuticals and research.

Synonyms
N-Benzylethanolamine
2-(Benzylamino)ethanol
104-63-2
2-Benzylaminoethanol
Benzylaminoethanol
Benzylethanolamine
Ethanol, 2-[(phenylmethyl)amino]-
2-(Benzylamino)Ethan-1-Ol
N-Benzylaminoethanol
Ethanol, 2-(benzylamino)-
Benzyl ethanolamine
Ethanol, 2-((phenylmethyl)amino)-
NSC 11271
2-[(phenylmethyl)amino]ethanol
2-Benzylamino-ethanol
DTXSID1044356
48121MS9JM
EINECS 203-221-2
MFCD00002840
NSC-11271
NSC-60267
AI3-26796
DTXCID9024356
NSC-177008
N-Benzyl-N-ethanolamine
UNII-48121MS9JM
2Benzylaminoethanol
N-benzyl ethanolamine
2(Benzylamino)ethanol
2-N-benzylaminoethanol
N-benzyl ethanol amine
(N-Benzylamino)ethanol
N-benzyl-2-aminoethanol
2-(benzylamino)-ethanol
Ethanol, 2(benzylamino)
2-(benzylamino)-1-ethanol
2-Benzylaminoethanol, 95%
SCHEMBL177039
N-(2-Hydroxyethyl)benzylamine
CHEMBL119890
Ethanol, 2((phenylmethyl)amino)
Ethanol, 2(benzylamino) (8CI)
Ethanol, 2-(phenylmethyl)amino-
CHEBI:194998
N-benzyl-N-(2-hydroxyethyl)amine
Ethanol, 2-(benzylamino)-(8CI)
NSC11271
NSC60267
Tox21_301199
AC7917
BBL012101
STK125900
AKOS000119869
CS-W018111
DS-3380
HY-W017395
N-Benzylethanolamine;2-Benzylaminoethanol
NCGC00248331-01
NCGC00255096-01
CAS-104-63-2
SY001172
DB-002826
B1130
NS00020558
EN300-16556
Q27259085
Z56174025
F1791-1740
OEI