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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
State
State

At room temperature, tolterodine tartrate is in a solid state, specifically as a crystalline powder. It is stable under normal conditions of storage and handling, given that it is kept in a dry environment to prevent the absorption of moisture.

Melting point (Celsius)
242.00
Melting point (Kelvin)
515.15
Boiling point (Celsius)
349.15
Boiling point (Kelvin)
622.30
General information
Molecular weight
475.01g/mol
Molar mass
475.0100g/mol
Density
1.3660g/cm3
Appearence

Tolterodine tartrate typically appears as a white to off-white crystalline powder. It is known for its hygroscopic nature, meaning it can absorb moisture from the environment. The substance is odorless and has a bitter taste.

Comment on solubility

Solubility of [3-carboxy-3-(1-naphthyl)butyl]-dimethyl-ammonium;chloride

The solubility of the compound [3-carboxy-3-(1-naphthyl)butyl]-dimethyl-ammonium;chloride is an interesting topic due to its unique structural characteristics. This compound is a quaternary ammonium salt, which typically exhibits notable solubility in polar solvents.

Generally, the solubility of this compound can be discussed in the following points:

  • Highly soluble in water: The presence of the charged +N(CH3)2 group contributes to its affinity for water, allowing it to interact favorably with water molecules.
  • Influence of the carboxylic group: The carboxylic acid functional group -COOH enhances solubility because it can form hydrogen bonds with water, further stabilizing the molecule in solution.
  • Solubility in organic solvents: While it is soluble in polar solvents, the large aromatic naphthyl group may also provide some degree of solubility in less polar organic solvents, albeit to a lesser extent.
  • Temperature dependence: As with many salts, solubility may increase with temperature, allowing for a greater dissolution as the kinetic energy of the solvent molecules rises.

Overall, the solubility of [3-carboxy-3-(1-naphthyl)butyl]-dimethyl-ammonium;chloride highlights the intricate balance between its ionic and hydrophobic interactions, making it a fascinating subject of study in the realm of chemical compounds.

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.

Synonyms
1-Naphthaleneacetic acid, alpha-(2-(dimethylamino)ethyl)-alpha-methyl-, hydrochloride
6680-33-7
alpha-(2-(Dimethylamino)ethyl)-alpha-methyl-1-naphthaleneacetic acid hydrochloride