Quinolinic acid
- Molecular formula
- C7H5NO4
- CAS Number
- 89-00-9
- IUPAC Name
- pyridine-2,3-dicarboxylic acid
- Molecular Weight
- 167.11g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.6200g/cm3
- Synonyms
- quinolinic acid
Identification
Pyridine-2,3-dicarboxylic Acid: A Versatile Compound
Pyridine-2,3-dicarboxylic acid, commonly known as quinate, is an intriguing compound that serves as an essential building block in various chemical applications. This molecule possesses a pyridine ring with two carboxylic acid groups, which not only contributes to its distinctive properties but also enhances its functional versatility.
Interesting Facts
- Biological Significance: Pyridine-2,3-dicarboxylic acid is often involved in metabolic processes in living organisms, acting as an intermediate in the biosynthesis of important biomolecules.
- Applications in Medicine: This compound has shown potential in pharmaceutical research, particularly within the realm of drug design and synthesis.
- Coordination Chemistry: The presence of the carboxylic acid groups allows for the formation of coordination complexes with various metal ions, making it a valuable ligand in organometallic chemistry.
- Regulatory Role: It contributes to the regulation of pH levels in biological systems and is essential in maintaining cellular homeostasis.
- Industrial Uses: Pyridine-2,3-dicarboxylic acid is used in agriculture as a herbicide and in the synthesis of certain dyes and polymers, illustrating its broad industrial relevance.
Furthermore, the ability of pyridine-2,3-dicarboxylic acid to engage in hydrogen bonding and other intermolecular interactions adds to its functionality, making it a versatile candidate for various research and industrial applications.
As a compound, it encompasses a rich interplay of chemistry, biology, and industry, underscoring the importance of exploring its potential in future scientific inquiries.