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Gamma-aminobutyric acid ethyl ester

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Identification
Molecular formula
C10H18N2O3
CAS number
1646-75-9
IUPAC name
4-(diethylamino)-2-(ethylamino)-4-oxo-butanoic acid
State
State
Gamma-aminobutyric acid ethyl ester is typically a solid at room temperature, appearing as a white or off-white powder.
Melting point (Celsius)
125.00
Melting point (Kelvin)
398.20
Boiling point (Celsius)
375.20
Boiling point (Kelvin)
648.30
General information
Molecular weight
203.26g/mol
Molar mass
203.2790g/mol
Density
1.2434g/cm3
Appearence

The compound appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 4-(diethylamino)-2-(ethylamino)-4-oxo-butanoic acid

The solubility of 4-(diethylamino)-2-(ethylamino)-4-oxo-butanoic acid can be influenced by several factors, making it a fascinating compound to study. Generally, this compound exhibits moderate solubility in a variety of solvents due to its unique structure. Here are some key points regarding its solubility:

  • Polar solvents: The presence of amino groups and a carboxylic acid moiety suggests that this compound is likely to be soluble in polar solvents such as water and alcohols.
  • Apolar solvents: On the contrary, solubility in non-polar solvents may be limited due to the compound’s polar functional groups.
  • pH dependence: The solubility may also vary with pH; in acidic conditions, the carboxylate form can be protonated, potentially enhancing solubility.
  • Temperature effects: Like many organic compounds, increased temperature may increase solubility, promoting dissolution for this compound.

In summary, 4-(diethylamino)-2-(ethylamino)-4-oxo-butanoic acid displays varied solubility characteristics, which are crucial for its application in different fields. Understanding these solubility attributes allows scientists and researchers to manipulate conditions effectively for desired outcomes.

Interesting facts

Interesting Facts about 4-(Diethylamino)-2-(ethylamino)-4-oxo-butanoic Acid

4-(Diethylamino)-2-(ethylamino)-4-oxo-butanoic acid, often referred to as a specialized compound in the realm of organic chemistry, showcases the intriguing interplay between structure and function. Here are some fascinating aspects of this compound:

  • Molecular Diversity: The presence of multiple amino groups and a carbonyl functional group contributes to the compound's unique reactivity. This structural diversity is essential for potential biological activity.
  • Applications in Synthesis: Its functional groups make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals, aiding in the development of new therapeutic agents.
  • Biological Significance: Compounds similar to 4-(diethylamino)-2-(ethylamino)-4-oxo-butanoic acid are often explored for their potential roles as enzyme inhibitors or agents in metabolic pathways, highlighting their importance in medicinal chemistry.
  • Research and Development: Ongoing research could reveal new applications for this compound in drug design and development, particularly in the field of neurochemistry where amino acids and their derivatives play a crucial role.
  • Electrophilic Nature: The carbonyl group (C=O) makes this compound reactive towards nucleophiles, which is a fundamental trait in many organic reactions, paving the way for constructing more complex molecules.

Overall, the structural attributes and reactivity of 4-(diethylamino)-2-(ethylamino)-4-oxo-butanoic acid provide an exciting avenue for further exploration in chemical research. As you delve deeper into its properties, you may find yourself intrigued by its potential applications in various scientific fields.

Synonyms
28646-22-2
N,N,N~2~-Triethylasparagine
DTXSID50951311
RefChem:1090366
DTXCID601379432
DL-N,N,N(sup 2)-Triethylasparagine
BRN 3947559
ASPARAGINE, N,N,N(sup 2)-TRIETHYL-, DL-
N(sup 2)-Etil-N,N-dietil-beta-DL-asparagina [Italian]
N(sup 2)-Etil-N,N-dietil-beta-DL-asparagina