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Myricetin

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Identification
Molecular formula
C15H10O8
CAS number
529-44-2
IUPAC name
3,4,5-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-7-one
State
State
At room temperature, Myricetin is typically in a solid state, characterized by its distinctive yellow or yellow-green form. It is commonly encountered as a crystalline powder with low solubility in water.
Melting point (Celsius)
357.00
Melting point (Kelvin)
630.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
318.24g/mol
Molar mass
318.2360g/mol
Density
1.7900g/cm3
Appearence

Myricetin appears as a yellow or yellow-green crystalline powder. It is often found as a natural compound in various plants, contributing to their pigmentation. It can undergo structural changes when dissolved in solution, affecting its color intensity.

Comment on solubility

Solubility of 3,4,5-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-7-one

The compound 3,4,5-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-7-one, with the chemical formula C15H10O8, showcases intriguing solubility characteristics influenced by its chemical structure.

Generally, compounds that incorporate multiple hydroxyl (-OH) groups tend to exhibit high solubility in polar solvents. In the case of this chromenone:

  • Polar Solvents: It is quite soluble in water and alcohols due to the presence of hydroxyl groups that can form hydrogen bonds.
  • Non-Polar Solvents: Conversely, it is expected to have limited solubility in non-polar solvents like hexane or chloroform because the hydrophobic aromatic portions resist interaction with non-polar environments.

When considering solubility, it’s noteworthy to mention:

  • The more hydroxyl groups a compound has, the greater its potential for solubility in various solvents.
  • Changes in temperature can also alter solubility; generally, increased temperature results in enhanced solubility for solid compounds.

As such, it can be concluded that the solubility of 3,4,5-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-7-one is predominantly favored in polar environments where its functional hydroxyl groups can effectively interact with solvent molecules.

Interesting facts

Interesting Facts about 3,4,5-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-7-one

3,4,5-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-7-one, often referred to in research as a flavonoid compound, captivates the interest of chemists and biologists alike for several compelling reasons:

  • Natural Origin: This compound is commonly found in various plants, particularly in fruits, vegetables, and medicinal herbs, which highlights its significance in traditional and modern herbal medicine.
  • Health Benefits: Research has shown that compounds like this one may possess antioxidant properties, which help combat oxidative stress in the body. This functional attribute is believed to contribute to various health benefits, including anti-inflammatory, anti-cancer, and cardioprotective effects.
  • Role in Metabolism: As part of the flavonoid family, this compound plays a role in metabolic pathways, influencing the bioactivity of other bioactive components in the diet.
  • Versatile Applications: The unique structure of this compound makes it a subject of interest in pharmaceutical formulations, functional foods, and nutraceuticals, where it's studied for its potential therapeutic effects.
  • Synthesis and Modification: Chemists are exploring various synthetic methods to modify this compound for enhanced bioactivity, allowing for greater efficacy in clinical applications.

In conclusion, 3,4,5-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-7-one represents a rich intersection of nature, health, and innovative chemistry. As research continues, our understanding of the compound's benefits and applications is likely to expand, promising exciting future developments in science and medicine.