Tolterodine Tartrate

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Identification

Molecular formula
C22H31NO7S
CAS Number
124937-52-6
IUPAC Name
[3-carboxy-3-(1-naphthyl)butyl]-dimethyl-ammonium;chloride
Molecular Weight
475.01g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3660g/cm3
Synonyms
1-Naphthaleneacetic acid, alpha-(2-(dimethylamino)ethyl)-alpha-methyl-, hydrochloride
Interesting facts

Interesting Facts about [3-Carboxy-3-(1-naphthyl)butyl]-dimethyl-ammonium;chloride

This compound, often referred to in the context of its unique chemical structure, features a combination of ammonium and carboxylic acid functionalities that play vital roles in various chemical applications. Here are some engaging insights:

  • Structural Diversity: The presence of both a carboxylic acid and an ammonium group enables this compound to participate in hydrogen bonding, which is crucial for interactions in biological systems.
  • Biological Relevance: Compounds with similar structures are frequently studied for their pharmaceutical potential. Their ability to mimic natural products can lead to the development of new therapeutic agents.
  • Solubilizing Agent: The quaternary ammonium part of the molecule typically enhances its solubility in organic solvents, making it an essential compound in organic synthesis and extraction processes.
  • Fluorescent Properties: The 1-naphthyl group is known for its fluorescence, which could be leveraged in various optical applications, including sensing and imaging technologies.
  • Environmental Impact: Like many ammonium compounds, this compound's environmental behavior can be significant, especially in soil and water, where it may affect the bioavailability of nutrients.

In summary, [3-Carboxy-3-(1-naphthyl)butyl]-dimethyl-ammonium;chloride is a fascinating compound that bridges organic chemistry and biological applications. Its diverse functionalities make it a noteworthy subject of research, with implications ranging from medicinal chemistry to environmental science.

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