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Aloesin

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Identification
Molecular formula
C16H14O7
CAS number
30861-27-9
IUPAC name
6,7-dihydroxy-9-methoxy-1-methyl-benzo[c]chromen-3-one
State
State

At room temperature, aloesin is in a solid state, usually available in the form of powder or crystalline solid.

Melting point (Celsius)
158.50
Melting point (Kelvin)
431.65
Boiling point (Celsius)
497.80
Boiling point (Kelvin)
770.95
General information
Molecular weight
316.28g/mol
Molar mass
316.2640g/mol
Density
1.5600g/cm3
Appearence

Aloesin is typically a crystalline solid. It appears as a pale yellow to white powder. The compound is often extracted from the Aloe plant, specifically from Aloe vera, and appears as colorless or off-white needle-like crystals when purified.

Comment on solubility

Solubility of 6,7-Dihydroxy-9-methoxy-1-methyl-benzo[c]chromen-3-one

The solubility of 6,7-dihydroxy-9-methoxy-1-methyl-benzo[c]chromen-3-one can be characterized as follows:

  • Polar Solvents: This compound generally demonstrates limited solubility in polar solvents due to its bulky structure and non-polar elements.
  • Non-Polar Solvents: It may be more soluble in non-polar solvents, which can better accommodate its aromatic characteristics.
  • pH Sensitivity: The presence of hydroxyl groups hints that the solubility can be affected by pH levels; higher acidity might enhance its solubility.
  • Temperature Effect: Increasing the temperature may also significantly improve the solubility of this compound in both polar and non-polar solvents.

To summarize, the solubility behavior of 6,7-dihydroxy-9-methoxy-1-methyl-benzo[c]chromen-3-one is influenced by solvent polarity, temperature, and pH levels. Understanding these factors is essential for effectively working with this compound in various applications.

Interesting facts

Interesting Facts about 6,7-Dihydroxy-9-methoxy-1-methyl-benzo[c]chromen-3-one

This compound, often referred to as a valuable derivative of natural products, presents a rich array of features that intrigue both researchers and students in the field of chemistry. Here are some fascinating aspects to consider:

  • Natural Product Origin: This compound is structurally related to flavonoids, a diverse group of phytochemicals that are prevalent in plants. Many flavonoids are known for their potential health benefits.
  • Biological Activity: Studies have indicated that this compound possesses significant antioxidant properties. Antioxidants are vital for neutralizing free radicals in the body, which can help protect against cellular damage and reduce the risk of chronic diseases.
  • Research Applications: Due to its interesting chemical properties, this compound is a subject of interest in medicinal chemistry. Its efficacy in anti-inflammatory and antimicrobial activities has gained attention, paving the way for potential therapeutic applications.
  • Key Functional Groups: The presence of hydroxyl (-OH) groups in its structure adds to its reactivity and solubility in various solvents. This enhances its potential for interactions with biological molecules, thus influencing its bioactivity.
  • Synthetic Pathways: The synthesis of this compound often involves intricate organic reactions, showcasing the beauty of **organic synthesis**. Techniques such as **reduction**, **alkylation**, and **condensation** play crucial roles in its formation.

In summary, 6,7-dihydroxy-9-methoxy-1-methyl-benzo[c]chromen-3-one stands out as a noteworthy compound in chemical research. Its natural origin, significant biological activities, and the synthetic challenges it presents make it a captivating subject in both the academic and practical realms of chemistry.