Tris(2-aminoethyl)amine
- Molecular formula
- C6H18N4
- CAS Number
- 4097-89-6
- IUPAC Name
- acetic acid;N'-[2-(2-aminoethylamino)ethyl]ethane-1,2-diamine
- Molecular Weight
- 146.23g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 0.5793g/cm3
- Synonyms
- SCHEMBL159616
Identification
Acetic Acid N'-[2-(2-aminoethylamino)ethyl]ethane-1,2-diamine
This compound is a fascinating example of an organic molecule with unique structural characteristics. Acetic acid, known for its pivotal role in various chemical reactions, is combined here with an amine derivative, creating a hybrid that showcases both acidity and potential for biological interaction.
Key Highlights:
- Biological Relevance: The presence of amino groups makes this compound potentially useful in biochemical applications, such as in drug development and as a biological buffer.
- Versatile Building Block: Given that acetic acid is a simple carboxylic acid and an important metabolic intermediate, this compound could serve as a versatile substrate in organic synthesis.
- Interaction Potential: The amino functionality may facilitate hydrogen bonding and ionic interactions, making it interesting for studies in enzyme-substrate binding.
- pH Regulation: Acetic acid can contribute to pH regulation in biochemical contexts, hence this compound might find applications in maintaining the stability of solutions in various settings.
In the world of synthetic chemistry and biochemistry, compounds like acetic acid N'-[2-(2-aminoethylamino)ethyl]ethane-1,2-diamine represent the blend of simple molecules leading to complex functionalities. As with any compound, understanding its properties can pave the way for innovative applications in medicine, agriculture, and materials science.