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Ellagic acid

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Identification
Molecular formula
C14H6O8
CAS number
476-66-4
IUPAC name
3,4-dihydroxy-5-(3,4,5-trihydroxyphenoxy)carbonyl-benzoic acid
State
State

At room temperature, ellagic acid is typically in a solid state with a crystalline appearance. It is stable and does not evaporate or change state under standard conditions.

Melting point (Celsius)
350.00
Melting point (Kelvin)
623.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
302.19g/mol
Molar mass
302.1920g/mol
Density
1.7330g/cm3
Appearence

Ellagic acid is typically a yellow or light brown crystalline powder. It can be pale yellowish and forms hexagonal crystals or crystalline powder depending on its preparation.

Comment on solubility

Solubility of 3,4-Dihydroxy-5-(3,4,5-trihydroxyphenoxy)carbonyl-benzoic Acid

The solubility of 3,4-dihydroxy-5-(3,4,5-trihydroxyphenoxy)carbonyl-benzoic acid can be described as moderate to high in polar solvents due to the presence of multiple hydroxyl groups that can interact favorably with the solvent molecules. Here are some key points regarding its solubility:

  • Polarity: The numerous hydroxyl (-OH) functional groups contribute to the overall polarity of the compound, enhancing its solubility in water and other polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water molecules aids in solubilizing this compound. As a result, it is likely to dissolve well in aqueous solutions.
  • Solvent Specificity: While the compound is expected to have good solubility in water, its solubility may be reduced in non-polar solvents due to the lack of similar interaction capabilities.
  • Concentration Factor: At higher concentrations, the solubility limit may be reached and could lead to precipitation if no other solubilizing agents or methods are employed.

In conclusion, the solubility behavior of 3,4-dihydroxy-5-(3,4,5-trihydroxyphenoxy)carbonyl-benzoic acid highlights the significant role of hydroxyl groups in enhancing solubility through polar interactions. Therefore, when considering its applications, it is crucial to account for these solubility characteristics to maximize efficacy in relevant contexts.

Interesting facts

Interesting Facts about 3,4-Dihydroxy-5-(3,4,5-trihydroxyphenoxy)carbonyl-benzoic Acid

3,4-Dihydroxy-5-(3,4,5-trihydroxyphenoxy)carbonyl-benzoic acid, commonly known as a derivative of benzoic acid, has intriguing characteristics that make it a subject of interest in both **organic chemistry** and **pharmacology**. Here are some noteworthy points regarding this complex compound:

  • Structure Complexity: The compound showcases a unique structural arrangement with multiple hydroxyl groups, which greatly influences its chemical behavior and potential reactivity.
  • Natural Origins: Compounds like this are often related to flavonoids and polyphenols, which are prevalent in various plants and known for their antioxidant properties. It highlights nature's uncanny ability to produce biologically active molecules.
  • Pharmacological Potential: Research suggests that derivatives like this could exhibit anti-inflammatory and anticancer activities, making them valuable in medicinal chemistry. This connection prompts ongoing investigation into their mechanisms of action.
  • Synthesis Routes: The synthesis of such compounds often involves multiple steps, including esterification and hydroxylation, which pose challenges for chemists. Understanding the synthetic pathways can lead to the discovery of new compounds with enhanced properties.
  • Environmental Impact: As a part of studies focusing on biodegradable compounds, its role in reducing petroleum-based plastic usage could become a pivotal topic in sustainable chemistry discussions.

In summary, 3,4-Dihydroxy-5-(3,4,5-trihydroxyphenoxy)carbonyl-benzoic acid serves as a reminder of the intricate connections between nature, health, and chemistry. As researchers delve deeper into its properties and applications, this compound offers numerous avenues for exploration and innovation.