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Quaternary ammonium compound

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Identification
Molecular formula
C12H24ClN
CAS number
8265-39-4
IUPAC name
dimethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride
State
State

At room temperature, the compound exists in a solid state, typically as a powder or crystalline form.

Melting point (Celsius)
242.00
Melting point (Kelvin)
515.20
Boiling point (Celsius)
225.50
Boiling point (Kelvin)
498.70
General information
Molecular weight
215.79g/mol
Molar mass
215.7890g/mol
Density
0.9473g/cm3
Appearence

The compound appears as a white crystalline solid. It is generally available in powder or crystal form.

Comment on solubility

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

The solubility of dimethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride, a quaternary ammonium compound, can be characterized as follows:

  • Solvent Interaction: This compound is likely to exhibit good solubility in polar solvents like water due to its ionic nature from the +1 charge of the ammonium group.
  • Temperature Dependence: Increased temperature often enhances solubility for ionic compounds, which may contribute to greater dissolution rates in heated solutions.
  • Hydrophilic vs. Hydrophobic Balance: The presence of the bulky 1,7,7-trimethylnorbornan-2-yl moiety introduces hydrophobic characteristics that may limit solubility in non-polar solvents.
  • Concentration Effects: At higher concentrations, precipitation may occur as the solution approaches saturation, leading to a complex interplay of solubility behaviors.

In conclusion, while dimethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride demonstrates reasonable solubility in polar solvents, its solubility can be intricately influenced by various factors including temperature, concentration, and solvent choice. Experimentation and characterization in specific environments are essential for a comprehensive understanding of its solubility properties.

Interesting facts

Interesting Facts about Dimethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Chloride

Dimethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is a fascinating compound, primarily due to its unique structure and diverse applications in organic and medicinal chemistry. Here are some notable aspects:

  • Quaternary Ammonium Compound: This compound belongs to a class of chemicals known as quaternary ammonium compounds, commonly used for their surfactant properties. They play crucial roles in various industrial and biochemical applications!
  • Chiral Center: The structure of this compound includes a chiral center, which means it exists in multiple mirror-image forms (enantiomers). This feature makes it a subject of interest in studies related to stereochemistry and its influence on biological activity.
  • Versatile Application: Its derivatives can be used in several fields, including pharmaceuticals, where they can aid in drug delivery systems and improve the solubility of active pharmaceutical ingredients (APIs).
  • Biological Interaction: Compounds like this one have shown potential in modulating neurotransmitter receptors and ion channels, suggesting applications in neuropharmacology and the development of new therapeutic agents!
  • Environmental Impact: Research into the environmental effects of quaternary ammonium compounds is ongoing, particularly focusing on their biodegradability and potential toxicity, crucial aspects for sustainable chemistry.
  • Research Potential: The ongoing studies into its structural properties and biological implications have made it an important topic in the current chemical research landscape.

This compound's unique combination of structural characteristics and functional properties makes it a compelling subject of study for both chemists and students alike. Understanding its mechanisms and applications can contribute significantly to advancements in science and technology.

Synonyms
(+-)-endo-N,N-Dimethyl-2-bornanamine hydrochloride
2-BORNANAMINE, N,N-DIMETHYL-, HYDROCHLORIDE, endo-(+-)-
22243-55-6
RefChem:256671