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Berberrubine chloride

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Identification
Molecular formula
C26H24ClNO2
CAS number
633-65-8
IUPAC name
6-benzyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride
State
State

At room temperature, Berberrubine chloride is a solid.

Melting point (Celsius)
224.00
Melting point (Kelvin)
497.15
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.15
General information
Molecular weight
467.02g/mol
Molar mass
467.0200g/mol
Density
0.9700g/cm3
Appearence

Berberrubine chloride typically appears as a crystalline yellow powder. It is often used in laboratories for various biochemical applications.

Comment on solubility

Solubility of 6-benzyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride

The solubility of 6-benzyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride can be intriguing due to its structural complexity. Here are some key insights regarding its solubility characteristics:

  • Solvent Polarity: This compound tends to exhibit higher solubility in polar solvents such as water or alcohols due to the presence of the hydroxyl groups which can form hydrogen bonds.
  • Ionization: As a chloride salt, it may dissociate in solution, which can enhance its solubility in aqueous environments.
  • Temperature Dependence: The solubility may vary significantly with temperature; generally, increasing the temperature can increase solubility for many organic compounds.
  • pH Dependency: The solubility might also be affected by the pH of the solution, given that the compound contains functional groups which can become protonated or deprotonated under different pH conditions.

In summary, while specific solubility data may be required for exact applications, understanding these factors can help predict the behavior of 6-benzyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride in various solvents. As with many compounds, experimental testing is essential for precise solubility determination.

Interesting facts

Exploring 6-benzyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride

This fascinating compound is a member of the quinoline family, which is renowned for its diverse range of biological activities. As a scientific discovery, the structure of 6-benzyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride showcases unique properties that draw interest in both synthetic chemistry and pharmacology.

Key Features:

  • Quinoline Derivative: The compound's unique architecture includes multiple fused benzene rings, characteristic of quinoline derivatives, making it intriguing for medicinal chemists.
  • Prodrug Potential: Due to its complex structure, this compound could exhibit enhanced absorption properties, suggesting potential as a prodrug in therapeutic applications.
  • Biological Activities: Many compounds in the quinoline family demonstrate antibacterial, antifungal, and anti-inflammatory activities, thus hinting at interesting pharmacological profiles for this compound as well.

This compound's dipolar character could enhance its solubility in biological environments, facilitating interactions with biomolecules. As scientists explore its functional potential, quotes from research may highlight its applicability: "Understanding the multifaceted interactions of quinoline derivatives can greatly enhance pharmaceutical innovation." With ongoing research, 6-benzyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride stands as a testament to the intricate beauty of chemical compounds and their profound significance in the world of science.