Quinolinic acid

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Identification

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
Interesting facts

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.

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