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Oxetanium, 3-[(4-chlorophenoxy)methyl]methylammonium

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Identification
Molecular formula
C15H26ClNO1
CAS number
110429-35-1
IUPAC name
[3-[(4-chlorophenoxy)methyl]oxetan-3-yl]methyl-diethyl-methyl-ammonium
State
State

At room temperature, 3-[(4-chlorophenoxy)methyl]oxetan-3-yl]methyl-diethyl-methyl-ammonium is typically a solid. It is stable under normal conditions.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
308.84g/mol
Molar mass
308.8390g/mol
Density
1.2400g/cm3
Appearence

The compound is typically a colorless or light yellow solid. It may appear as crystalline or in powdered form. The compound has characteristic aromatic features due to its phenyl group.

Comment on solubility

Solubility of [3-[(4-chlorophenoxy)methyl]oxetan-3-yl]methyl-diethyl-methyl-ammonium

The solubility of the compound [3-[(4-chlorophenoxy)methyl]oxetan-3-yl]methyl-diethyl-methyl-ammonium is influenced by several factors that can affect its behavior in different solvents. Here are some key points to consider:

  • Polarity: This compound contains both polar and non-polar functional groups. Its quaternary ammonium structure often promotes solubility in polar solvents like water, while the alkyl chains can enhance solubility in organic solvents.
  • Hydrogen Bonding: The presence of the ether and ammonium groups may establish hydrogen bonds, which can further facilitate dissolution in compatible polar solvents.
  • pH Sensitivity: Solubility might vary with pH; under more acidic or basic conditions, the ionization state of the ammonium moiety can change, potentially increasing solubility.
  • Temperature Effects: Higher temperatures generally increase solubility for many compounds, so heating might enhance the solvation of this compound.
  • Solvent Interaction: It's critical to select appropriate solvents. Common choices include water for polar interactions and various organic solvents like ethanol or acetone for non-polar interactions.

In short, the solubility of [3-[(4-chlorophenoxy)methyl]oxetan-3-yl]methyl-diethyl-methyl-ammonium can be described as being quite versatile, dependent on the solvent used and environmental conditions. As with many chemical compounds, thorough solubility tests in different environments are recommended to fully understand its solubility characteristics.

Interesting facts

Interesting Facts about [3-[(4-chlorophenoxy)methyl]oxetan-3-yl]methyl-diethyl-methyl-ammonium

This intriguing compound showcases the fascinating intersection of organic chemistry and pharmacology. With its unique structural features, it is part of a broader class of organic compounds known for their diverse applications. Here are some interesting highlights:

  • Functional Groups: The compound features an oxetane ring, which is a four-membered cyclic ether. This unique structure often imparts interesting reactivity and stability properties.
  • Biological Significance: The presence of the 4-chlorophenoxy group hints at potential biological activities, as phenoxy compounds are frequently studied for their roles in herbicides and anti-cancer agents.
  • Ammonium Ion: The inclusion of a diethyl-methyl-ammonium moiety suggests functional applications in quaternary ammonium compounds, known for their antimicrobial properties and use in surfactants.
  • Versatile Applications: Compounds like this one may find applications in both medicinal chemistry and industrial processes, showcasing the dual ability of organic synthesis to contribute to health and technological innovations.

As an amalgamation of multiple functional groups, this compound serves as an excellent example of how careful modifications can lead to novel properties. Its study furthers our understanding of chemical interactions and opens new pathways for research and development in various fields.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." This compound certainly exemplifies that spirit of creativity and exploration in the realm of chemistry.