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1-Phenylpropylammonium chloride

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Identification
Molecular formula
C9H14ClN
CAS number
5651-38-7
IUPAC name
1-phenylpropylammonium;chloride
State
State
At room temperature, it is in a solid state appearing as a crystalline powder.
Melting point (Celsius)
220.00
Melting point (Kelvin)
493.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
185.69g/mol
Molar mass
185.6940g/mol
Density
1.0640g/cm3
Appearence

1-Phenylpropylammonium chloride typically appears as a white crystalline powder. It is often odorless and has a solid structure.

Comment on solubility

Solubility of 1-phenylpropylammonium chloride

1-phenylpropylammonium chloride (C10H14ClN) presents interesting solubility properties that exemplify the behavior of quaternary ammonium compounds. As a salt formed from a quaternary ammonium base, its solubility is heavily influenced by several factors:

  • Polarity: Due to the presence of the ammonium group, the compound is generally polar, allowing it to dissolve well in polar solvents.
  • Solvent Compatibility: 1-phenylpropylammonium chloride demonstrates good solubility in water and other polar solvents. This is largely due to ionic interactions with water molecules.
  • Temperature Effects: Like many ionic compounds, its solubility can increase with temperature, exhibiting typical behavior of salts.
  • Hydrophobic Interactions: The phenyl group, being hydrophobic, can affect the overall solubility in mixed solvents, introducing unique solubility dynamics.

In conclusion, the solubility behavior of this compound is characterized by a delicate balance of ionic and hydrophobic interactions, making it an interesting subject for studies in chemistry and material science. As with many ionic solids, it is essential to consider the solvent environment to understand the solubility potential of 1-phenylpropylammonium chloride. This compound stands as a prime example of the intersection between organic and inorganic chemistry in solubility phenomena.

Interesting facts

Interesting Facts About 1-Phenylpropylammonium Chloride

1-Phenylpropylammonium chloride is an intriguing compound that belongs to the class of ammonium salts. It is noteworthy for several reasons that highlight its chemical significance and potential applications:

  • Ammonium Salt Properties: Being an ammonium salt, it plays a vital role in various chemical reactions and biological processes. These compounds are known for their ability to participate in ion exchange and are commonly used in different industrial applications.
  • Optical Isomerism: This compound is of interest in the field of stereochemistry due to its potential for optical isomerism. The presence of chiral centers in its structure may lead to different enantiomers, which can exhibit distinct biological activities.
  • Applications in Organic Synthesis: 1-Phenylpropylammonium chloride is often utilized as a reagent in organic synthesis. It can serve as a precursor for various chemical transformations, thus making it an important compound for chemists.
  • Role in Pharmaceuticals: Compounds of this nature are extensively researched in pharmaceutical chemistry. Their ability to form stable complexes with other molecules opens avenues for drug formulation and delivery systems, enhancing the efficacy of therapeutic agents.
  • Behavior in Solution: The interaction of this compound with solvents can lead to unique behaviors in aqueous environments, which is crucial for applications involving biological systems, such as drug solubility and stability.

As a versatile compound, the study of 1-phenylpropylammonium chloride not only enhances our understanding of ammonium salts but also paves the way for advancements in synthetic chemistry and drug development. Its properties and interactions make it a significant subject of interest in both academic research and industrial applications.

Synonyms
alpha-Ethylbenzylamine hydrochloride
1-phenylpropylazanium;chloride
(alpha-Ethylbenzyl)ammonium chloride
Phenyl-1-amino-1-propane hydrochloride
Propane, 1-phenyl-1-amino-, hydrochloride
H 1672
Benzenemethanamine, alpha-ethyl-, hydrochloride
BENZYLAMINE, alpha-ETHYL-, HYDROCHLORIDE