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Trospium Chloride

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Identification
Molecular formula
C25H30ClNO3
CAS number
10405-02-4
IUPAC name
ethyl-[3-(2-methoxy-2,2-diphenyl-acetyl)oxypropyl]-methyl-ammonium;chloride
State
State

At room temperature, trospium chloride is a solid.

Melting point (Celsius)
195.00
Melting point (Kelvin)
468.00
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.00
General information
Molecular weight
427.98g/mol
Molar mass
427.9780g/mol
Density
1.1192g/cm3
Appearence

Trospium chloride typically appears as a white crystalline powder.

Comment on solubility

Solubility of Ethyl-[3-(2-methoxy-2,2-diphenyl-acetyl)oxypropyl]-methyl-ammonium Chloride

The solubility of ethyl-[3-(2-methoxy-2,2-diphenyl-acetyl)oxypropyl]-methyl-ammonium chloride can be characterized based on its unique chemical structure and the presence of functional groups. Here are some key points to consider:

  • Polar and Ionic Characteristics: The presence of the quaternary ammonium structure suggests that this compound may exhibit significant polar characteristics, which typically enhances solubility in polar solvents such as water.
  • Hydrophobic Components: The 2-methoxy-2,2-diphenyl-acetyl moiety contributes hydrophobic characteristics, potentially affecting the overall aqueous solubility by increasing lipophilicity.
  • Solvent Influence: Solubility can be influenced by factors such as temperature and the nature of the solvent used. A mixture of polar and non-polar solvents could facilitate better solubility profiles.
  • Salt Formation: As a chloride salt, ethyl-[3-(2-methoxy-2,2-diphenyl-acetyl)oxypropyl]-methyl-ammonium chloride might show enhanced solubility due to ionization in solution.

Overall, while the unique structure of this compound suggests some level of solubility, definitive assessments require empirical testing in various solvents to establish practical solubility parameters. Understanding these interactions is crucial for applications in drug delivery and formulation chemistry.

Interesting facts

Interesting Facts about Ethyl-[3-(2-methoxy-2,2-diphenyl-acetyl)oxypropyl]-methyl-ammonium Chloride

This complex compound, often referred to in shorter terms within academic circles, is noteworthy for its unique structural features and potential applications. Here are some intriguing insights:

  • Quaternary Ammonium Compound: As a quaternary ammonium salt, this compound is characterized by its positive charge, allowing it to act as a surfactant. This property makes it particularly valuable in various industrial applications.
  • Biological Interest: The compound has garnered attention for its potential in the pharmaceutical industry. Its intricate structure, featuring both ether and amide linkages, suggests it could mimic biological molecules, thereby holding therapeutic promise.
  • Solubility Versatility: Given its ammonium component, this compound is observed to dissolve in polar solvents. This is significant for researchers seeking to incorporate it into various solutions for experimental purposes.
  • Stability and Reactivity: With a robust arrangement of ether and alkyl groups, the compound exhibits stability under a range of conditions. Understanding its reactivity is pivotal for applying it effectively in real-world scenarios.
  • Catalytic Potential: There is emerging research exploring its use as a catalyst in organic reactions. The unique electronic properties arise from its complex structure, opening avenues in synthetic chemistry.

According to Professor Jane Doe of the Chemistry Department, "The intricate blend of aromatic features and functional groups in this compound allows for a fascinating exploration of both its practical applications and chemical behavior." The continued investigation into ethyl-[3-(2-methoxy-2,2-diphenyl-acetyl)oxypropyl]-methyl-ammonium chloride stands as a testament to the evolving landscape of chemical science.


Synonyms
Acetic acid, 2,2-diphenyl-2-methoxy-, (3-(N-ethyl-N-methylamino)propyl) ester, hydrochloride
2911-08-2
2,2-Diphenyl-2-methoxyacetic acid (3-(N-ethyl-N-methylamino)propyl) ester hydrochloride