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Muscarine Iodide

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Identification
Molecular formula
C15H22IN2O
CAS number
6051-61-4
IUPAC name
2-(2-methoxy-1H-indol-3-yl)ethyl-trimethyl-ammonium;iodide
State
State

At room temperature, Muscarine iodide is typically in a solid state.

Melting point (Celsius)
256.00
Melting point (Kelvin)
529.15
Boiling point (Celsius)
204.50
Boiling point (Kelvin)
477.65
General information
Molecular weight
292.20g/mol
Molar mass
292.2000g/mol
Density
1.5000g/cm3
Appearence

Muscarine iodide is typically observed as either white or off-white crystalline solid.

Comment on solubility

Solubility of 2-(2-methoxy-1H-indol-3-yl)ethyl-trimethyl-ammonium iodide

The solubility of 2-(2-methoxy-1H-indol-3-yl)ethyl-trimethyl-ammonium iodide in various solvents plays a crucial role in its application in different fields, particularly in pharmaceuticals and organic synthesis. This quaternary ammonium compound tends to exhibit varying solubility based on factors such as polarity and ionic interactions.

Key Points about Solubility:

  • Water Solubility: Quaternary ammonium salts like this compound are generally soluble in water due to their ionic nature. However, specific solubility levels can depend on temperature and concentration.
  • Solvent Interaction: It is often soluble in polar organic solvents (such as methanol and ethanol) but may have limited solubility in non-polar solvents, reflecting its amphiphilic characteristics.
  • pH Effects: The solubility may also be influenced by the pH of the solution, as well as the presence of competing ions which could affect its ionic state.
  • Temperature Dependency: As with many chemical compounds, an increase in temperature generally enhances solubility, enabling better solvation of the ions.

In summary, understanding the solubility of 2-(2-methoxy-1H-indol-3-yl)ethyl-trimethyl-ammonium iodide in different solvents is essential for optimizing its usage. Proper knowledge of solubility enables chemists to tailor experimental conditions to enhance stability and reactivity, ultimately improving outcomes in chemical processes.

Interesting facts

Interesting Facts About 2-(2-Methoxy-1H-Indol-3-yl)ethyl-Trimethyl-Ammonium Iodide

This compound, which belongs to the quaternary ammonium salt family, engages the curiosity of chemists due to its unique structural features and biological activities.


Key Characteristics

  • Structural Significance: The incorporation of both an indole moiety and a trimethylammonium group forms a complex system that may influence its reactivity and interaction with biological systems.
  • Biological Relevance: Compounds containing indole substructures are often associated with a variety of biological activities, including antimicrobial, antiviral, and anticancer properties. This highlights the potential for this compound in pharmaceutical applications.
  • Quaternary Ammonium Salts: The quaternary ammonium framework imparts interesting physicochemical properties, such as cationic character, which may enhance solubility in polar solvents. This feature is particularly beneficial for drug design and delivery.

Applications

Due to its structure, 2-(2-methoxy-1H-indol-3-yl)ethyl-trimethyl-ammonium iodide has the potential for applications in several fields:

  • Medicinal Chemistry: Its unique features invite exploration as a potential therapeutic agent against various biological targets.
  • Material Science: The ionic nature may contribute to the development of advanced materials, including polymers and coatings.
  • Research Tool: Researchers may utilize this compound in laboratory studies to probe biological mechanisms due to its volatility and interaction potential.

Quote from a prominent chemist: "Exploring the unseen worlds of molecular interactions is where chemistry finds its greatest adventure." As we delve into the properties and potential of 2-(2-methoxy-1H-indol-3-yl)ethyl-trimethyl-ammonium iodide, we continue to unveil the mysteries that lie at the molecular level.

Synonyms
AMMONIUM, (2-(5-METHOXYINDOL-3-YL)ETHYL)TRIMETHYL-, IODIDE
6582-72-5
5-Methoxy-N,N-dimethyl-tryptamine methiodide
DTXSID60984312
2-(2-Methoxy-1H-indol-3-yl)-N,N,N-trimethylethan-1-aminium iodide