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Berberine

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Identification
Molecular formula
C20H18N4
CAS number
2086-83-1
IUPAC name
trimethyl-[3-[4-[2-(1-methylindol-3-yl)ethyl]pyridin-1-ium-1-yl]propyl]ammonium
State
State

At room temperature, Berberine is typically found in a solid state, specifically as a crystalline powder.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
336.42g/mol
Molar mass
336.4200g/mol
Density
1.3198g/cm3
Appearence

Berberine is a bright yellow color and often appears as a crystalline powder.

Comment on solubility

Solubility Overview

The solubility of trimethyl-[3-[4-[2-(1-methylindol-3-yl)ethyl]pyridin-1-ium-1-yl]propyl]ammonium is influenced by several factors due to its complex structure.


Factors Affecting Solubility

  • Polarity: As a quaternary ammonium compound, it possesses a polar head and hydrophobic tail, which can lead to different solubility behaviors in various solvents.
  • Temperature: Generally, higher temperatures tend to increase solubility in solvents, although the extent can vary based on the solvent used.
  • pH Levels: The ionic nature of the compound may also affect solubility in aqueous solutions, especially with changes in pH.

In summary, while trimethyl-[3-[4-[2-(1-methylindol-3-yl)ethyl]pyridin-1-ium-1-yl]propyl]ammonium has the potential to be soluble in polar solvents, its unique characteristics can lead to varying degrees of solubility depending on the conditions. As always, experimentation is key in determining the precise solubility profile.

Interesting facts

Interesting Facts about Trimethyl-[3-[4-[2-(1-methylindol-3-yl)ethyl]pyridin-1-ium-1-yl]propyl]ammonium

Trimethyl-[3-[4-[2-(1-methylindol-3-yl)ethyl]pyridin-1-ium-1-yl]propyl]ammonium is a fascinating compound that showcases the complexity of organic chemistry and the role of ionic compounds in various applications. Here are some intriguing aspects of this compound:

  • Structure Complexity: The compound features a unique structure that includes a pyridin-1-ium moiety and an indole derivative. This combination is significant because indole derivatives are known for their biological activity and potential pharmaceutical applications.
  • Ion Mobility: As a quaternary ammonium compound, it possesses a positive charge. This characteristic enhances its solubility in polar solvents and improves ion mobility, making it a candidate for electrochemical applications.
  • Biological Activity: The indole component in its structure is observed in many bioactive compounds, suggesting potential roles in drug design and discovery. Indoles are often linked to various forms of biological activity, including anticancer properties.
  • Applications in Materials Science: Compounds like this one can be significant in the development of ionic liquids, which are known for their low volatility and high thermal stability. This feature makes them suitable for use in sustainable chemistry processes.
  • Research Potential: Given its complex structure and unique properties, trimethyl-[3-[4-[2-(1-methylindol-3-yl)ethyl]pyridin-1-ium-1-yl]propyl]ammonium can be a subject of interest for researchers exploring new drug candidates or materials for advanced technologies.

In summary, Trimethyl-[3-[4-[2-(1-methylindol-3-yl)ethyl]pyridin-1-ium-1-yl]propyl]ammonium is not just a chemical compound; it opens doors to various fields, from medicinal chemistry to materials science. As research progresses, it may yield new insights into its mechanisms of action and broaden its applications in different industries.

Synonyms
Methindethyrium ion
Methindethyrium cation
UNII-5ZB71W73QJ
5ZB71W73QJ
793603-48-2
Pyridinium, 4-(2-(1-methyl-1H-indol-3-yl)ethyl)-1-(3-(trimethylammonio)propyl)-
Q27263096