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Mecamylamine hydrochloride

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Identification
Molecular formula
C21H35N2OCl
CAS number
102-46-5
IUPAC name
diheptyl-(4-methoxynaphthalene-1-carboximidoyl)ammonium;chloride
State
State

At room temperature, Mecamylamine hydrochloride is in a solid state.

Melting point (Celsius)
164.00
Melting point (Kelvin)
437.15
Boiling point (Celsius)
234.00
Boiling point (Kelvin)
507.15
General information
Molecular weight
323.88g/mol
Molar mass
323.8700g/mol
Density
1.0918g/cm3
Appearence

Mecamylamine hydrochloride appears as a white crystalline powder.

Comment on solubility

Solubility of Diheptyl-(4-methoxynaphthalene-1-carboximidoyl)ammonium Chloride

Diheptyl-(4-methoxynaphthalene-1-carboximidoyl)ammonium chloride is an intriguing compound when it comes to its solubility properties. Understanding how well it dissolves can offer insights into its behavior in various environments. Here are some key points about its solubility:

  • Polar vs. Non-Polar: As a quaternary ammonium salt, this compound is likely to have moderate to good solubility in polar solvents, primarily due to the presence of the chloride ion, which aids in its dissociation.
  • Solvent Compatibility: It is hypothesized that the compound may exhibit better solubility in solvents like:
    • Water
    • Alcohols (such as ethanol or methanol)
    • Aqueous salt solutions
  • Limitations in Organic Solvents: Conversely, non-polar organic solvents (like hexane or benzene) may show poor solubility due to its molecular structure that favors interaction with polar solvent environments.
  • Effect of Temperature: As with many compounds, solubility could increase with temperature, making higher temperatures a variable to consider during experiments.

In summary, the solubility of diheptyl-(4-methoxynaphthalene-1-carboximidoyl)ammonium chloride in polar solvents coupled with potential limitations in non-polar surrounding highlights the intricate balance between molecular structure and solvent conditions. "Solubility is not just a measure of how much solute can dissolve, but also a complex interaction between solute and solvent."

Interesting facts

Interesting Facts about Diheptyl-(4-Methoxynaphthalene-1-Carboximidoyl)ammonium; Chloride

Diheptyl-(4-methoxynaphthalene-1-carboximidoyl)ammonium chloride is a fascinating compound that blends organic chemistry with unique structural properties. Here are several intriguing aspects of this compound:

  • Dual Nature: This compound showcases both quaternary ammonium characteristics and aromatic functional properties, making it useful in various applications such as surfactants and drug delivery systems.
  • Role of the Naphthalene Ring: The presence of a naphthalene moiety contributes significantly to the compound's stability and interaction with biological membranes. This stability can enhance the compound’s effectiveness in pharmaceutical applications.
  • Ammonium Ion Functionality: As a quaternary ammonium compound, diheptyl-(4-methoxynaphthalene-1-carboximidoyl)ammonium chloride can form complexes with various anions and can participate in ion-exchange processes.
  • Application in Biological Sciences: Due to its unique chemical structure, this compound may serve as a potential candidate for studies involving drug design and synthesis, particularly in targeting specific cellular receptors.
  • Environmental Considerations: The synthesis and breakdown products of quaternary ammonium compounds can sometimes impact ecosystems, thus raising the importance of studying their environmental fate and transport.

Overall, this compound exemplifies the richness of organic chemistry, blending complex structures and potential applications. Remember, as scientists seek out new compounds to test for drug effectiveness or environmental safety, compounds like diheptyl-(4-methoxynaphthalene-1-carboximidoyl)ammonium chloride may hold the key to unlocking novel solutions and advancements in various fields.

Synonyms
N,N-Diheptyl-4-methoxy-1-naphthamidine hydrochloride
NSC 24112
1-Naphthamidine, N,N-diheptyl-4-methoxy-, hydrochloride
1-NAPHTHAMIDINE, N,N-DIHEPTYL-4-METHOXY-, MONOHYDROCHLORIDE