What is the Difference Between Quinoline and Isoquinoline?

🆚 Go to Comparative Table 🆚

Quinoline and isoquinoline are both heterocyclic aromatic organic compounds with the same chemical formula, C9H7N, but different ring structures. The key difference between the two is the position of the nitrogen atom in the ring structure. In quinoline, the nitrogen atom is in the first position, while in isoquinoline, the nitrogen atom is in the second position.

Some applications of quinoline include its use as a solvent for resins and terpenes, as a precursor to producing 8-hydroxyquinoline, and in the production of quinolinic acid and anti-malarial derivatives. Isoquinoline, on the other hand, is used as an anaesthetic compound, antihypertension agents, antifungal agents, disinfectants, and vasodilators.

Comparative Table: Quinoline vs Isoquinoline

The key difference between quinoline and isoquinoline lies in the position of the nitrogen atom in the ring structure. In quinoline, the nitrogen atom is in the first position, while in isoquinoline, the nitrogen atom is in the second position. Both compounds have the same chemical formula but different connectivity of atoms, making them structural isomers of each other. Here is a comparison table of quinoline and isoquinoline:

Property Quinoline Isoquinoline
Nitrogen atom position 1st position 2nd position
Chemical formula C₉H₇N C₉H₇N
Ring structure Aromatic, heterocyclic Aromatic, heterocyclic
Color Slightly yellowish Slightly yellowish
Odor Strong, unpleasant Strong, unpleasant
Hygroscopic nature Highly hygroscopic Highly hygroscopic
Solvent properties Organic synthesis, high boiling temperature Moderate basicity, low melting temperature
Biosynthesis Derived from tryptophan Derived from tyrosine

Quinoline and isoquinoline are both aromatic heterocyclic compounds with a strong odor and high hygroscopic nature. They are used in various applications, such as organic synthesis and as solvents.