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Quaternary ammonium compound

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Identification
Molecular formula
C18H28ClN
CAS number
Relevant CAS number is not known for this specific compound.
IUPAC name
benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride
State
State

At room temperature, this compound is typically a solid.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
283.86g/mol
Molar mass
283.8550g/mol
Density
1.1200g/cm3
Appearence

Benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is a crystalline solid. It typically appears as white to off-white crystals.

Comment on solubility

Solubility of Benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Chloride

The solubility of benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is influenced by several factors, which can be summarized as follows:

  • Polarity: The presence of a quaternary ammonium group (R4N+) suggests a high degree of polarity, which generally enhances solubility in polar solvents like water.

  • Hydrophilicity: Due to its ammonium component, this compound is expected to exhibit hydrophilic characteristics, further promoting its solubility in aqueous environments.

  • Temperature Effects: Like many ionic compounds, its solubility may increase with temperature, making it more soluble in warmer conditions.

  • Ion-Solvent Interactions: Interactions between the ionic chloride ions and polar water molecules facilitate the dissolution process.

However, while it shows promising solubility in polar solvents, its behavior in non-polar solvents is likely to be vastly different, as ionic compounds typically have low solubility in such media. It is essential to visualize solubility as a complex interplay of molecular structure and solvent properties.

In conclusion, the solubility of benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is expected to be high in polar solvents, particularly water, due to strong ion-dipole interactions.

Interesting facts

Interesting Facts About Benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Chloride

Benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is a fascinating compound notable for its unique structure and potential applications. Here are several intriguing aspects of this ammonium salt:

  • Quaternary Ammonium Compound: As a quaternary ammonium salt, this compound features four organic groups attached to a nitrogen atom, which enhances its solubility and stability in various environments.
  • Role in Organocatalysis: Compounds like this are often used as catalysts in organic synthesis. Their unique properties can facilitate reactions, leading to new chemical transformations and products.
  • Biological Applications: Benzyl groups have been found to increase the biological activity of molecules, potentially allowing this compound to be explored in medicinal chemistry for drug design.
  • Ion Exchange Properties: The chloride ion in this compound can serve as a counter ion, making it useful in ion exchange processes in various chemical applications.
  • Chemical Stability: The presence of the norbornane structure contributes to the presence of a rigid framework that often lends increased stability to the compound compared to more flexible alkylamines.

As you can see, benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is a compound with a rich chemistry and a wide array of potential uses. Its distinctive structure not only enhances its reactivity but also opens pathways for further exploration in research and applications.

Synonyms
(+-)-endo-N-Benzyl-2-bornanamine hydrochloride
24652-86-6
2-BORNANAMINE, N-BENZYL-, HYDROCHLORIDE, endo-(+-)-
RefChem:256685