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Guaiaverin

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Identification
Molecular formula
C16H18O9
CAS number
78915-72-9
IUPAC name
4-[1-hydroxy-2-(hydroxymethoxy)-2-(2-methoxyphenyl)ethyl]-2-methoxy-phenol
State
State

Guaiaverin is typically found in a solid state at room temperature.

Melting point (Celsius)
237.00
Melting point (Kelvin)
510.15
Boiling point (Celsius)
540.00
Boiling point (Kelvin)
813.15
General information
Molecular weight
356.33g/mol
Molar mass
356.3270g/mol
Density
1.3720g/cm3
Appearence

Guaiaverin is a pale yellow amorphous powder. It is known for its phenolic structure, characterized by the presence of multiple hydroxyl groups which contribute to its appearance.

Comment on solubility

Solubility of 4-[1-hydroxy-2-(hydroxymethoxy)-2-(2-methoxyphenyl)ethyl]-2-methoxy-phenol

The solubility of 4-[1-hydroxy-2-(hydroxymethoxy)-2-(2-methoxyphenyl)ethyl]-2-methoxy-phenol is influenced by various factors given its multi-functional structure, which includes hydroxyl and methoxy groups. Here are some key points regarding its solubility:

  • Polarity: The presence of multiple hydroxyl groups suggests that this compound is polar, which typically enhances solubility in polar solvents like water.
  • Hydrogen Bonding: The hydroxyl groups can participate in hydrogen bonding with solvents, further increasing the likelihood of solubility.
  • Methoxy Groups: The methoxy groups contribute to both hydrophobic interactions and can influence solubility in organic solvents.
  • pH Dependency: The solubility might vary with pH, as the ionization of hydroxyl groups in different pH ranges can lead to enhanced solubility in certain conditions.

In summary, the solubility of this compound can be characterized as being likely higher in polar solvents due to the presence of -OH groups, **though it may also demonstrate significant solubility characteristics in organic solvents** due to the methoxy presence. Experimental data would provide a clearer understanding of its solubility behavior in various solvents.

Interesting facts

Interesting Facts about 4-[1-hydroxy-2-(hydroxymethoxy)-2-(2-methoxyphenyl)ethyl]-2-methoxy-phenol

This fascinating compound, often associated with modern organic chemistry, showcases the intricate world of phenolic compounds. Known for its diverse applications and unique structural features, it embodies innovation in medicinal and industrial chemistry.

Structural Characteristics

The structure of this compound is remarkable because it features:

  • Multiple hydroxyl groups that enhance its reactivity and solubility.
  • Substituted methoxy groups, contributing to its stability and biological activity.
  • A complex arrangement of phenolic rings, enabling it to engage in various intermolecular interactions.

Biological Significance

4-[1-hydroxy-2-(hydroxymethoxy)-2-(2-methoxyphenyl)ethyl]-2-methoxy-phenol is known for:

  • Antioxidant Properties: Acts as a scavenger of free radicals, which is vital in preventing cell damage.
  • Anti-inflammatory Effects: May aid in reducing inflammation, thus holding potential in therapeutic applications.
  • Potential in Cancer Research: Compounds like these are often under investigation for their role in inhibiting cancer cell proliferation.

Applications and Research

This compound contributes to various fields:

  • Pharmaceutical development aimed at creating new drugs.
  • Cosmetic formulations that benefit from its skin-protective properties.
  • Food preservation, as its antioxidant nature can prolong shelf life.

In summary, the compound 4-[1-hydroxy-2-(hydroxymethoxy)-2-(2-methoxyphenyl)ethyl]-2-methoxy-phenol is not just a chemical entity but is a bridge between chemistry and practical applications, making it an invaluable subject of study in both academic and applied sciences. As someone delving into the kingdom of chemical compounds, uncovering the secrets of such fascinating structures expands your understanding of their potential influence in various domains.

Synonyms
DTXSID70994886
4-[1-hydroxy-2-(hydroxymethoxy)-2-(2-methoxyphenyl)ethyl]-2-methoxyphenol
1,3-Propanediol, 1-(4-hydroxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)-