Flavanone | Solubility of Things

Identification

Molecular formula

C₁₅H₁₂O₂

CAS number

487-26-3

IUPAC name

2-hydroxy-3-(3-hydroxy-1-phenyl-butyl)chromen-4-one

State

Flavanone is typically solid at room temperature.

Melting point (Celsius)

96.00

Melting point (Kelvin)

369.15

Boiling point (Celsius)

432.50

Boiling point (Kelvin)

705.70

General information

Molecular weight

224.24g/mol

Molar mass

224.2430g/mol

Density

1.2980g/cm³

Appearence

Flavanone is a pale yellow solid.

Comment on solubility

Solubility of 2-hydroxy-3-(3-hydroxy-1-phenyl-butyl)chromen-4-one

The solubility of the compound 2-hydroxy-3-(3-hydroxy-1-phenyl-butyl)chromen-4-one, with the chemical formula C₁₅H₁₂O₂, is influenced by several factors. Its significant structure, featuring both hydroxyl (-OH) groups and a phenyl ring, plays a crucial role in its solubility characteristics:

Hydrophilicity: The presence of the hydroxyl groups enhances the compound's ability to interact with polar solvents like water, increasing its hydrophilicity.
Hydrophobicity: Conversely, the phenyl group's non-polar nature introduces a degree of hydrophobicity, which can limit solubility in highly polar solvents.
Solvent Compatibility: This compound may be more soluble in organic solvents such as ethanol and methanol compared to water, due to its mixed polar and non-polar characteristics.

In practice, one might observe variable solubility depending on the solvent system used. As a general rule, **"like dissolves like,"** meaning that this compound would likely dissolve better in solvents that share similar polarity profiles.

In conclusion, the solubility of 2-hydroxy-3-(3-hydroxy-1-phenyl-butyl)chromen-4-one is a complex interplay of its functional groups, necessitating careful consideration of solvent choice for optimal dissolution.

Interesting facts

Interesting Facts about 2-Hydroxy-3-(3-Hydroxy-1-phenyl-butyl)chromen-4-one

2-Hydroxy-3-(3-hydroxy-1-phenyl-butyl)chromen-4-one is a member of the flavonoid family, which includes a wide range of plant-based compounds known for their various biological activities. Here are some intriguing aspects of this compound that showcase its significance and potential:

Bioactivity: This compound exhibits promising antioxidant properties, which can protect cells from oxidative stress. Antioxidants are crucial in combating free radicals that may lead to cellular damage and various diseases.
Potential Health Benefits: Research has indicated that flavonoids, including this compound, may possess anti-inflammatory and anti-cancer effects. Their ability to modulate biological pathways could contribute to therapeutic strategies.
Natural Occurrence: Many flavonoids are found in fruits, vegetables, and beverages such as tea and red wine. This connection to dietary sources highlights the potential for enhancing health through nutrition.
Pharmacological Interest: The structural complexity of this compound makes it a subject of interest in medicinal chemistry, paving the way for the synthesis of new drugs with enhanced efficacy against various ailments.
Chemical Structure: The unique structure of 2-hydroxy-3-(3-hydroxy-1-phenyl-butyl)chromen-4-one enables it to participate in a variety of chemical reactions. The presence of hydroxyl groups increases its reactivity and solubility, which is essential for biological activity.

In summary, the exploration of 2-hydroxy-3-(3-hydroxy-1-phenyl-butyl)chromen-4-one not only highlights its role as a bioactive compound but also opens doors to potential applications in pharmacology and nutrition. As a part of ongoing research into natural products, this flavonoid could very well contribute to our understanding of disease mechanisms and the development of new therapeutic agents.