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Chlorpheniramine

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Identification
Molecular formula
C16H19ClN2
CAS number
132-22-9
IUPAC name
N'-[(4-chlorophenyl)-phenyl-methyl]-N-propyl-ethane-1,2-diamine
State
State

At room temperature, chlorpheniramine is in a solid state.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.20
Boiling point (Celsius)
364.20
Boiling point (Kelvin)
637.40
General information
Molecular weight
274.80g/mol
Molar mass
274.8000g/mol
Density
1.1020g/cm3
Appearence

Chlorpheniramine typically appears as a white to off-white crystalline powder. It may appear in different forms such as tablets or capsules when used in pharmaceutical preparations.

Comment on solubility

Solubility Insights for N'-[(4-chlorophenyl)-phenyl-methyl]-N-propyl-ethane-1,2-diamine

The solubility of N'-[(4-chlorophenyl)-phenyl-methyl]-N-propyl-ethane-1,2-diamine can be influenced by various factors due to its complex structure. Here are some critical insights regarding its solubility:

  • Polarity: The presence of the ethane-1,2-diamine functional group introduces both polar and non-polar regions in the molecule, which can affect its solubility in different solvents.
  • Solvent Interaction: This compound is likely to dissolve in polar solvents like water and alcohols to some extent, but may show reduced solubility in non-polar solvents due to steric hindrance created by the bulky chlorophenyl groups.
  • Hydrogen Bonding: The amine group can engage in hydrogen bonding with water, which may enhance its solubility in aqueous environments. However, the aromatic rings may also hinder complete solvation.
  • Temperature Dependency: As with many organic compounds, solubility can be temperature-dependent. Increased temperatures may lead to a higher solubility due to enhanced kinetic energy and solvation dynamics.
  • Concentration Effects: At higher concentrations, you may observe a decrease in solubility due to saturation effects or the formation of aggregates.

As a result, while it's feasible to expect some level of solubility in various solvents, the specific interactions of N'-[(4-chlorophenyl)-phenyl-methyl]-N-propyl-ethane-1,2-diamine with each solvent matrix will ultimately dictate its practical solubility. Thus, experimentation is essential for accurate determination of solubility characteristics.

Interesting facts

Interesting Facts about N'-[(4-Chlorophenyl)-Phenyl-Methyl]-N-Propyl-Ethane-1,2-Diamine

N'-[(4-Chlorophenyl)-Phenyl-Methyl]-N-Propyl-Ethane-1,2-Diamine is a complex organic compound that falls under the category of amines, which are known for their rich chemistry and varied applications. Here are some intriguing aspects of this compound:

  • Structural Diversity: This compound showcases significant structural diversity, featuring a combination of aromatic rings and aliphatic amine groups. The presence of a 4-chlorophenyl moiety enhances its potential reactivity and influences its physical properties.
  • Biological Significance: Compounds with similar structural frameworks are often investigated for their biological activities. Many amines are known to exhibit pharmacological properties, making this compound a candidate for further research in medicinal chemistry.
  • Potential Applications: The unique structural features suggest various potential applications in areas such as pharmaceuticals, agrochemicals, and material science. Understanding its behavior could lead to innovations in drug design or development of new materials.
  • Amine Chemistry: As a diamine, this compound is involved in a variety of chemical reactions, such as acylation and alkylation, showcasing its reactivity. Amine derivatives are also crucial in forming polymeric materials by serving as building blocks in chain growth processes.
  • Environmental Considerations: With the growing concerns regarding environmental impact, the study of such compounds extends to their behavior in biological and ecological systems. Understanding their degradation pathways is crucial for evaluating their environmental footprint.

This compound, like many others in the world of organics, holds the promise of unveiling new scientific discoveries and insights into both chemistry and biology. Its multifaceted nature encourages researchers to explore its limits and potential applications.