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Propiverine hydrochloride

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Identification
Molecular formula
C23H32ClN3O3
CAS number
54556-98-8
IUPAC name
methyl-[2-[(4-nitrophenyl)carbamoyloxy]ethyl]-(3-phenylpropyl)ammonium;chloride
State
State

At room temperature, propiverine hydrochloride is in a solid state. It is typically administered in a solid dosage form such as tablets or capsules.

Melting point (Celsius)
223.00
Melting point (Kelvin)
496.00
Boiling point (Celsius)
820.00
Boiling point (Kelvin)
1 093.15
General information
Molecular weight
448.99g/mol
Molar mass
448.9850g/mol
Density
1.2850g/cm3
Appearence

Propiverine hydrochloride appears as a white or almost white crystalline powder. It is odorless and has a slightly bitter taste. The compound is stable under normal temperatures and pressures.

Comment on solubility

Solubility of Methyl-[2-[(4-nitrophenyl)carbamoyloxy]ethyl]-(3-phenylpropyl)ammonium;chloride

The solubility of methyl-[2-[(4-nitrophenyl)carbamoyloxy]ethyl]-(3-phenylpropyl)ammonium;chloride can be quite intriguing due to its complex structure. This compound possesses both hydrophilic and hydrophobic characteristics, which can significantly influence its behavior in different solvents.

Key Factors Affecting Solubility:

  • Ionic Interaction: As a quaternary ammonium salt, its chloride ion contributes to its solubility in polar solvents, particularly water.
  • Non-Polar Regions: The presence of the phenyl and propyl groups leads to increased solubility in non-polar organic solvents.
  • Temperature Effects: Generally, solubility increases with temperature, particularly in aqueous solutions.

In summary, the solubility characteristics of this compound can be largely attributed to:

  1. Its ionic nature which favors solubility in ionic media.
  2. The presence of lipophilic groups which enhance solubility in organic solvents.
  3. The influence of temperature and possibly pH, which may alter ionic forms and enhance solubility further.

Given these factors, it can be said that this compound is likely to exhibit varying solubility depending on the solvent used, making it an intriguing subject of study in the realm of chemical solubility.

Interesting facts

Interesting Facts About Methyl-[2-[(4-nitrophenyl)carbamoyloxy]ethyl]-(3-phenylpropyl)ammonium;chloride

This compound, known for its complex structure and diverse applications, is particularly noteworthy in the field of medicinal chemistry. Here are some engaging points to consider:

  • Pharmacological Significance: The presence of the nitrophenyl group contributes to the compound's potential as a pharmaceutical agent. Nitrophenyl derivatives have been studied for their anti-inflammatory and analgesic properties.
  • Structure-Activity Relationship (SAR): Understanding how the various functional groups interact can aid in optimizing the efficacy of similar compounds. The carbamoyloxy and ammonium functionalities play crucial roles in modulating biological activity.
  • Ion Exchange: As a quaternary ammonium compound, this chlorinated version can participate in ion exchange processes, making it useful in various applications such as catalysis and water purification.
  • Research Interest: Compounds with such intricate structures may serve as models for drug design and development. Their synthesis and characterization often reveal important principles about molecular interactions and reactivity.
  • Environmental Impact: Given its potential synthetic routes, investigating the environmental implications of producing and using this compound is essential in modern chemistry to ensure sustainable practices.

Overall, the multifaceted characteristics of methyl-[2-[(4-nitrophenyl)carbamoyloxy]ethyl]-(3-phenylpropyl)ammonium;chloride make it a fascinating topic of study within organic and medicinal chemistry. As researchers continue to explore its properties and applications, this compound likely represents just a small piece of the larger puzzle in drug discovery and development.

Synonyms
p-Nitrocarbanilic acid 2-(methyl(3-phenylpropyl)amino)ethyl ester hydrochloride
17683-69-1
Carbanilic acid, p-nitro-, 2-(methyl(3-phenylpropyl)amino)ethyl ester, hydrochloride