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Tripelennamine hydrochloride

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Identification
Molecular formula
C23H29ClN
CAS number
154-69-8
IUPAC name
3,3-diphenylpropyl(1-phenylpropyl)ammonium;chloride
State
State

Tripelennamine hydrochloride exists as a solid at room temperature. Its crystalline form ensures it remains stable under typical storage conditions, making it suitable for medicinal uses.

Melting point (Celsius)
234.00
Melting point (Kelvin)
507.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
374.96g/mol
Molar mass
374.9620g/mol
Density
1.1900g/cm3
Appearence

Tripelennamine hydrochloride typically appears as a white to off-white crystalline powder. It is often odorless and can be described as having a bitter taste. This compound may also come in a solid form suitable for handling and formulation for various pharmaceutical applications.

Comment on solubility

Solubility of 3,3-Diphenylpropyl(1-phenylpropyl)ammonium; chloride

The solubility of 3,3-diphenylpropyl(1-phenylpropyl)ammonium; chloride can be quite intriguing given its unique structure. This compound, featuring both diphenyl and phenyl groups, has a nonpolar character that can influence its solubility in various solvents.

When assessing the solubility of such a compound, several factors come into play:

  • Polar vs. Nonpolar Solvents: Due to its structural characteristics, 3,3-diphenylpropyl(1-phenylpropyl)ammonium; chloride is more likely to dissolve in organic solvents like ethanol or chloroform, rather than in water, which is a polar solvent.
  • Ionic Nature: Being a chloride salt, it may have some degree of solubility in water; however, this is often significantly lower compared to its solubility in organic media.
  • Temperature Effects: Increasing the temperature generally enhances the solubility of organic compounds in solvents; thus, slightly warmer conditions may help in achieving better dissolution.

It is often said that “like dissolves like,” and this principle holds true with 3,3-diphenylpropyl(1-phenylpropyl)ammonium; chloride. Its solubility profile showcases the balance between its ionic and non-ionic characteristics, making it a fascinating subject for further investigation!

Interesting facts

Interesting Facts about 3,3-Diphenylpropyl(1-phenylpropyl)ammonium Chloride

3,3-Diphenylpropyl(1-phenylpropyl)ammonium chloride is a fascinating quaternary ammonium compound, notable for its unique structure and versatile applications. Here are some key points that highlight its significance:

  • Structural Uniqueness: The compound features a multi-phenyl substitution pattern that contributes to its intriguing physical and chemical properties. The arrangement of the phenyl groups on the propyl chains plays a crucial role in influencing its behavior and interaction with other molecules.
  • Applications: Owing to its ammonium cation, this compound finds use in various applications, including as a surfactant and in the field of electrochemistry. It can modify surface properties and enhance stability in formulations.
  • Antimicrobial Properties: Some quaternary ammonium compounds exhibit antimicrobial activity, and research into this specific compound has indicated potential effectiveness against certain pathogens, making it an area of interest for pharmaceutical and medical applications.
  • Connectivity with Ionic Liquids: The quaternary ammonium structure ties it to the larger class of ionic liquids, which are known for their low volatility and tunable properties, broadening the potential for innovative applications in green chemistry and sustainable practices.
  • Research and Development: Ongoing studies are investigating the behavior of this compound in various environments, including its interactions in biological systems and its efficiency as a catalyst in organic transformations.

As a compound that bridges multiple fields of chemistry, 3,3-diphenylpropyl(1-phenylpropyl)ammonium chloride exemplifies the vast potential of innovative chemical structures. Its diverse applications highlight the importance of understanding the relationship between molecular structure and function, an essential concept for students and researchers alike.


Synonyms
N-(3,3-Diphenylpropyl)-alpha-ethylbenzylamine hydrochloride
13636-14-1
BENZYLAMINE, N-(3,3-DIPHENYLPROPYL)-alpha-ETHYL-, HYDROCHLORIDE