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Berberine chloride

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Identification
Molecular formula
C20H18ClNO4
CAS number
633-65-8
IUPAC name
6,7-dimethoxy-3,4-dihydroisoquinolin-2-ium;chloride
State
State

Berberine chloride is commonly found in a solid state at room temperature, characterized by its crystalline powder form.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.15
Boiling point (Celsius)
525.00
Boiling point (Kelvin)
798.15
General information
Molecular weight
372.81g/mol
Molar mass
372.8100g/mol
Density
1.3800g/cm3
Appearence

Berberine chloride typically appears as a yellow crystalline powder. It is known for its vibrant color and crystal clarity.

Comment on solubility

Solubility of 6,7-dimethoxy-3,4-dihydroisoquinolin-2-ium;chloride

The solubility of 6,7-dimethoxy-3,4-dihydroisoquinolin-2-ium;chloride can be characterized by several key factors:

  • Polarity: The presence of ionic chloride contributes to its solubility in polar solvents, particularly in water.
  • Solvent Interaction: Due to the quaternary ammonium structure, it exhibits enhanced solubility in protic solvents compared to non-polar solvents.
  • Temperature Dependency: Higher temperatures typically increase the solubility of such compounds, enabling better dissolution in solvents.
  • Concentration Effect: As the concentration of the solution increases, the saturation point must be considered, where solubility rates may plateau.

In general, ions tend to exhibit greater solubility in aqueous environments, allowing for effective interactions:

  1. Hydration of ions enhances their solubility.
  2. The molecular structure plays a significant role in how well the compound dissolves.

As such, for laboratory applications, 6,7-dimethoxy-3,4-dihydroisoquinolin-2-ium;chloride shows promise for solubility in various protic solvents, making it a candidate for numerous chemical processes and reactions.

Interesting facts

Interesting Facts about 6,7-Dimethoxy-3,4-dihydroisoquinolin-2-ium Chloride

This fascinating compound, known as 6,7-dimethoxy-3,4-dihydroisoquinolin-2-ium chloride, belongs to the isoquinoline family, which is notable for its wide array of biological activities. Researchers often investigate isoquinolines for their potential therapeutic applications due to their complex interactions with biological systems.

Key Points of Interest

  • Biological Significance: Isoquinoline derivatives, including this compound, have been found to exhibit a range of pharmacological properties such as anti-inflammatory, neuroprotective, and anticancer effects.
  • Structure and Function: The unique structure of 6,7-dimethoxy-3,4-dihydroisoquinolin-2-ium places it in a special category where the presence of methoxy groups significantly influences its chemical reactivity and biological activity.
  • Research Potential: This compound is a subject of ongoing research, particularly in the fields of medicinal chemistry and drug development, highlighting its potential for novel therapeutic agents.
  • Electrochemical Properties: Due to its charge as an ion, it may exhibit distinctive electrochemical characteristics, relevant for understanding electron transfer processes in biological systems.

As noted by researchers in the field, "The exploration of isoquinoline derivatives such as 6,7-dimethoxy-3,4-dihydroisoquinolin-2-ium chloride is crucial for unraveling new mechanisms of action in drug design." This quote underscores the importance of continuous exploration in the area of synthetic and natural products.

In summary, the study of 6,7-dimethoxy-3,4-dihydroisoquinolin-2-ium chloride not only opens a window into its potential medicinal properties but also enhances our understanding of isoquinoline chemistry, paving the way for innovative solutions to complex health challenges.

Synonyms
6,7-dimethoxy-3,4-dihydroisoquinolin-2-ium;chloride
UNII-WGL5C66P4J
AKOS015918403