Skip to main content

Deferiprone

ADVERTISEMENT
Identification
Molecular formula
C7H9NO2
CAS number
30652-11-0
IUPAC name
3-butyl-2-hydroxy-6-methyl-1H-pyridin-4-one
State
State

Deferiprone is generally a solid at room temperature.

Melting point (Celsius)
137.50
Melting point (Kelvin)
410.65
Boiling point (Celsius)
331.20
Boiling point (Kelvin)
604.35
General information
Molecular weight
139.16g/mol
Molar mass
139.1630g/mol
Density
1.2850g/cm3
Appearence

Deferiprone is a light tan to brown powder. It is a crystalline solid that may appear slightly hygroscopic.

Comment on solubility

Solubility of 3-butyl-2-hydroxy-6-methyl-1H-pyridin-4-one

The solubility of 3-butyl-2-hydroxy-6-methyl-1H-pyridin-4-one in various solvents can be quite interesting due to its unique structure. Several factors influence the solubility of this compound:

  • Polarity: The presence of both hydroxyl (-OH) and pyridinyl functional groups in its structure indicates that it may be more soluble in polar solvents such as water or alcohols.
  • Hydrophobic Effects: The butyl group tends to contribute hydrophobic characteristics, suggesting that this compound may also exhibit some solubility in organic solvents like hexane or toluene.
  • Temperature Dependence: Solubility often increases with temperature; thus, heating the solvent where this compound is dissolved may enhance its solubility.
  • Acid-Base Behavior: Given the ability of the hydroxy group to act as a donor and the pyridine nitrogen to accept protons, its solubility may vary with pH levels depending on the environment.

In summary, one can expect 3-butyl-2-hydroxy-6-methyl-1H-pyridin-4-one to possess considerable solubility in both polar and non-polar solvents, with situational variability. This adaptability makes it a compound of interest within various chemical contexts.

Interesting facts

Interesting Facts about 3-butyl-2-hydroxy-6-methyl-1H-pyridin-4-one

3-butyl-2-hydroxy-6-methyl-1H-pyridin-4-one, also known as a compound in the pyridinone class, presents a fascinating combination of structural and functional properties. Here are several intriguing points about this compound:

  • Biological Relevance: This compound has been studied for its potential biological activities, particularly in relation to its antioxidant properties. Antioxidants are crucial in defending the body against oxidative stress, which can lead to various diseases.
  • Functional Groups: The presence of both a hydroxyl group and a butyl group enhances its solubility and reactivity. The –OH group contributes to the compound's ability to interact with other molecules, making it a target for biochemical reactions.
  • Applications: This pyridinone derivative has potential applications in pharmaceuticals, especially as a lead compound for drug development aimed at conditions such as neurodegenerative diseases, where oxidative stress plays a significant role.
  • Synthesis: The synthesis of this compound involves multi-step reactions, often employing strategies like condensation and cyclization, showcasing the versatility of organic synthesis techniques.
  • Research Potential: Ongoing research is focused on uncovering new derivatives of this compound. Variations in substitution patterns can lead to enhanced pharmacological properties, making it a valuable subject for medicinal chemistry studies.

Overall, 3-butyl-2-hydroxy-6-methyl-1H-pyridin-4-one serves as an excellent model for studying the relationship between structure, function, and potential applications in medicinal chemistry. Its unique features make it a compound of interest for both researchers and students alike.