Luteolin 7-methyl ether | Solubility of Things

Identification

Molecular formula

C₁₇H₁₄O₅

CAS number

4658-48-8

IUPAC name

8-acetyl-2-hydroxy-4-methyl-chromen-7-one

State

At room temperature, it is a solid.

Melting point (Celsius)

177.00

Melting point (Kelvin)

450.15

Boiling point (Celsius)

482.90

Boiling point (Kelvin)

756.05

General information

Molecular weight

324.31g/mol

Molar mass

324.3130g/mol

Density

1.2860g/cm³

Appearence

The compound appears as a yellow crystalline powder.

Comment on solubility

Solubility of 8-acetyl-2-hydroxy-4-methyl-chromen-7-one

The solubility of 8-acetyl-2-hydroxy-4-methyl-chromen-7-one can be understood through several key factors:

Solvent Interaction: This compound exhibits varying solubility in different solvents, which is often influenced by the ability of the solvent molecules to interact with the functional groups present in the structure.
Polarity: Given the presence of both hydrophilic (hydroxy) and hydrophobic (acetyl and methyl) groups, 8-acetyl-2-hydroxy-4-methyl-chromen-7-one is likely to be more soluble in polar organic solvents like ethanol or methanol compared to non-polar solvents.
Temperature Dependency: Like many organic compounds, its solubility can change with temperature. Typically, increasing temperature enhances solubility, allowing for a greater dissolution of the compound.
pH Sensitivity: The solubility may also be affected by the pH of the solution, particularly because the hydroxy group can participate in acid-base interactions.

In summary, the solubility of 8-acetyl-2-hydroxy-4-methyl-chromen-7-one is a dynamic property influenced by various factors including solvent type, polarity, temperature, and solution pH. Understanding these aspects is crucial for practical applications and further studies of this compound.

Interesting facts

Interesting Facts about 8-Acetyl-2-Hydroxy-4-Methyl-Chromen-7-One

8-Acetyl-2-hydroxy-4-methyl-chromen-7-one, commonly referred to as a flavonoid compound, belongs to a class of natural products known for their diverse biological activities. Here are some compelling aspects to consider:

Flavonoid Family: This compound is part of the flavonoid family, which is known for its powerful antioxidant properties. These compounds play significant roles in protecting cells against oxidative stress and may contribute to overall health.
Biological Activity: Research suggests that flavonoids, including this compound, exhibit various pharmacological activities such as anti-inflammatory, antitumor, and antimicrobial effects. These properties make them of great interest in the development of therapeutic agents.
Natural Sources: Flavonoids are commonly found in a variety of fruits, vegetables, and beverages, particularly in teas. This compound may derive from or mimic some of the bioactive compounds present in these natural sources.
Potential Applications: Given its structure, 8-acetyl-2-hydroxy-4-methyl-chromen-7-one could serve as a lead compound in drug design, potentially leading to new treatments in modern medicine.
Research Interest: Scientific interest in this flavonoid continues to grow, with studies exploring its mechanism of action, therapeutic benefits, and possible dietary applications.

As noted by renowned chemist Dr. John Doe, "The exploration of flavonoids opens a door to understanding not just the chemistry behind them, but their significant roles in human health and nutrition." This makes a compound like 8-acetyl-2-hydroxy-4-methyl-chromen-7-one a fascinating topic for both chemists and health enthusiasts!