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Phenindamine

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Identification
Molecular formula
C24H27ClN2O
CAS number
82-88-2
IUPAC name
diethyl-[2-[4-(2-phenyl-1H-indol-3-yl)phenoxy]ethyl]ammonium;chloride
State
State

At room temperature, Phenindamine is typically found in a solid state.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
338.89g/mol
Molar mass
338.8680g/mol
Density
1.1560g/cm3
Appearence

Phenindamine appears as a white to off-white crystalline solid. It is often encountered in its hydrochloride salt form, which enhances its solubility in water. The solid has a characteristic crystalline structure typical for many organic ammonium salts.

Comment on solubility

Solubility of Diethyl-[2-[4-(2-phenyl-1H-indol-3-yl)phenoxy]ethyl]ammonium Chloride

Diethyl-[2-[4-(2-phenyl-1H-indol-3-yl)phenoxy]ethyl]ammonium chloride, commonly referred to as a quaternary ammonium salt, exhibits distinctive solubility characteristics dependent on various factors. The solubility of this compound can be analyzed through:

  • Polarity: Quaternary ammonium compounds tend to be polar, thus showing good solubility in polar solvents such as water, due to the ionic nature of the ammonium group.
  • Hydrogen Bonding: The presence of phenyl and indole groups may facilitate interactions with solvents that can form hydrogen bonds, enhancing solubility in organic solvents.
  • Temperature Effects: As with many organic salts, solubility can increase with temperature, indicating that higher temperatures may dissolve larger amounts of the compound.
  • pH Impact: The solubility may vary with pH since the ionization of the ammonium group can affect how well it interacts with the solvent.

In summary, the solubility of diethyl-[2-[4-(2-phenyl-1H-indol-3-yl)phenoxy]ethyl]ammonium chloride is significantly influenced by its molecular structure and the environmental conditions. Understanding these factors is crucial for effective utilization in various applications. As stated, *"the right conditions can enhance solubility, revealing the versatility of chemical compounds."*

Interesting facts

Interesting Facts about Diethyl-[2-[4-(2-phenyl-1H-indol-3-yl)phenoxy]ethyl]ammonium Chloride

Diethyl-[2-[4-(2-phenyl-1H-indol-3-yl)phenoxy]ethyl]ammonium chloride is a fascinating compound that showcases the intricate interplay between structure and function within chemical compounds. Here are some noteworthy points about this compound:

  • Versatile Uses: This compound belongs to the class of ammonium salts and is often explored for its potential applications in drug development and pharmaceutical sciences.
  • Indole Derivative: At the heart of this compound is a phenyl-indole moiety, which is well-known for its presence in many biologically active molecules. Indoles have garnered attention for various activities, including anti-cancer and anti-inflammatory properties.
  • Structure-Activity Relationship: The presence of the diethylammonium group at one end of the molecule contributes to its solubility and chemical reactivity, allowing scientists to investigate how structural tweaks can impact biological activity.
  • Receptor Targeting: The unique design of the compound may allow it to interact with specific biological receptors, making it a subject of interest in medicinal chemistry studies.
  • Research Significance: As a synthetic derivative, it can serve as a valuable tool in research aimed at understanding the pharmacodynamics of related compounds and their mechanisms of action.

This compound exemplifies the creativity inherent in the field of chemistry, where the exploration of complex structures can lead to significant advancements in therapeutic discoveries. As we delve deeper into its properties, the potential for novel applications continues to expand.