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Mepenzolate iodide

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Identification
Molecular formula
C22H30INO3
CAS number
1649-19-2
IUPAC name
[3-(2,5-dimethoxyphenyl)-3-hydroxy-1-methyl-3-phenyl-propyl]-trimethyl-ammonium;iodide
State
State

At room temperature, mepenzolate iodide is typically in a solid state. It is often stored in tightly closed containers to protect it from light and moisture, which can degrade its quality.

Melting point (Celsius)
170.00
Melting point (Kelvin)
443.15
Boiling point (Celsius)
292.70
Boiling point (Kelvin)
565.85
General information
Molecular weight
435.39g/mol
Molar mass
337.1960g/mol
Density
1.2060g/cm3
Appearence

Mepenzolate iodide is typically found as a white or off-white crystalline powder. It is important to note that the appearance of a substance can vary with its purity and specific preparation methods.

Comment on solubility

Solubility Characteristics of [3-(2,5-dimethoxyphenyl)-3-hydroxy-1-methyl-3-phenyl-propyl]-trimethyl-ammonium;iodide

The compound [3-(2,5-dimethoxyphenyl)-3-hydroxy-1-methyl-3-phenyl-propyl]-trimethyl-ammonium;iodide is an example of a quaternary ammonium salt, which generally exhibits distinctive solubility properties due to its ionic nature.

General Solubility Trends:

  • Water Solubility: Quaternary ammonium compounds tend to be soluble in water. This is primarily due to their ionic charge, which allows them to interact favorably with water molecules.
  • Organic Solubility: Many of these compounds are also soluble in polar organic solvents but may exhibit lower solubility in nonpolar solvents.

In the case of our compound, the following points are worth noting:

  • The presence of the trimethylammonium group contributes to aqueous solubility.
  • The bulky organic substituents, such as the 2,5-dimethoxyphenyl and the hydroxy group, can affect the overall solubility profile by influencing the molecular interactions.
  • When considering solubility in a given solvent system, factors like temperature and ionic strength can significantly alter solubility; thus, it might be necessary to perform solubility tests under various conditions.

To summarize, while the general expectation for this compound’s solubility would be high in aqueous solutions due to its quaternary ammonium structure, the actual solubility may be influenced by the bulkiness and polarity of the substituent groups attached to the nitrogen atom. Therefore, one should always analyze and test solubility in the context of specific applications and conditions.

Interesting facts

Exploring [3-(2,5-dimethoxyphenyl)-3-hydroxy-1-methyl-3-phenyl-propyl]-trimethyl-ammonium;iodide

This fascinating compound stands out not only due to its intricate structure but also because of its potential applications in various fields of chemistry and pharmacology. The addition of the trimethylammonium group signifies its quaternary ammonium character, which can enhance solubility and activity in biological systems.

Key Features:

  • Pharmacological Insights: Due to its unique phenyl and hydroxy substituents, this compound can interact with biological receptors, potentially leading to significant therapeutic effects.
  • Structure-Activity Relationship: The presence of multiple functional groups makes it a prime candidate for studying how structural modifications can impact biological activity.
  • Ionic Nature: As an iodide salt, it exhibits ionic characteristics that can influence its reactivity and interaction with other compounds.

This compound also highlights the importance of chemical diversity in the field of medicinal chemistry. The incorporation of dimethoxy groups allows researchers to explore their electron-donating effects, which can modify the pharmacokinetic properties of the drug.

As a scientist or student, it’s crucial to consider not only the synthetic pathways for creating such compounds but also their potential side effects and biocompatibility. Further research could provide insights into how these compounds can be optimized for improved efficacy and safety.

Ultimately, [3-(2,5-dimethoxyphenyl)-3-hydroxy-1-methyl-3-phenyl-propyl]-trimethyl-ammonium;iodide serves as a prime example of how the molecular architecture of a compound can lead to significant advancements in therapeutic opportunities.

Synonyms
1099-73-6
YS 3643
(4-(2,5-Dimethoxyphenyl)-4-hydroxy-4-phenyl-2-butyl)trimethylammonium iodide
AMMONIUM, (4-(2,5-DIMETHOXYPHENYL)-4-HYDROXY-4-PHENYL-2-BUTYL)TRIMETHYL-, IODIDE
[4-(2,5-dimethoxyphenyl)-4-hydroxy-4-phenylbutan-2-yl]-trimethylazanium;iodide
Benzenepropanaminium, gamma-hydroxy-2,5-dimethoxy-N,N,N,alpha-tetramethyl-gamma-phenyl-, iodide (1:1)
DTXSID10911395
AKOS040754545
4-(2,5-dimethoxyphenyl)-4-hydroxy-N,N,N-trimethyl-4-phenylbutan-2-aminium iodide