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Oxathiolane Quaternary Ammonium Compound

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Identification
Molecular formula
C8H17NO2S
CAS number
Not available
IUPAC name
trimethyl-[(2-methyl-1,3-oxathiolan-5-yl)methyl]ammonium
State
State

At room temperature, this compound is typically a liquid.

Melting point (Celsius)
-20.50
Melting point (Kelvin)
252.65
Boiling point (Celsius)
252.80
Boiling point (Kelvin)
525.95
General information
Molecular weight
191.31g/mol
Molar mass
191.3050g/mol
Density
0.9700g/cm3
Appearence

This compound is a colorless to pale yellow liquid with a slight amine-like odor. In pure form, it is transparent and may appear slightly oily.

Comment on solubility

Solubility of Trimethyl-[(2-methyl-1,3-oxathiolan-5-yl)methyl]ammonium

Trimethyl-[(2-methyl-1,3-oxathiolan-5-yl)methyl]ammonium (C8H17NO2S) exhibits a variety of solubility properties that can be influenced by several factors. Understanding its solubility is crucial for applications in chemical processes and pharmaceuticals. Here are some key points to consider:

  • Polarity: The presence of the oxathiolane ring and the quaternary ammonium structure contribute to the compound's polarity, impacting its solubility in different solvents.
  • Solvent Interaction: Trimethyl-[(2-methyl-1,3-oxathiolan-5-yl)methyl]ammonium is likely to be more soluble in polar solvents like water and alcohols due to its ionic character, compared to nonpolar solvents.
  • Hydrogen Bonding: The compound’s ammonium group can engage in hydrogen bonding, which may enhance its solubility in polar systems, allowing better dissolution in aqueous environments.

In summary, while specific solubility limits for this compound may vary, its chemical structure suggests that it is soluble in polar solvents, which can be beneficial for applications in biological systems or as an active ingredient in formulations. As always, practical solubility assessments should be conducted to determine the exact behavior under varying conditions.

Interesting facts

Interesting Facts about Trimethyl-[(2-methyl-1,3-oxathiolan-5-yl)methyl]ammonium

Trimethyl-[(2-methyl-1,3-oxathiolan-5-yl)methyl]ammonium is a fascinating compound in the realm of organic chemistry, particularly noted for its unique structure and properties. Here are some notable points:

  • Unique Functional Group: The presence of the oxathiolane ring in its structure sets this compound apart, as oxathiolanes are known for their interesting chemical reactivity and role as intermediates in various chemical reactions.
  • Quaternary Ammonium Compound: As a quaternary ammonium salt, it plays a significant role in the field of surfactants, ion exchange resins, and even as a phase transfer catalyst. The trimethylammonium group contributes to its solubility and reactivity.
  • Potential Biological Applications: Compounds similar to this one are often evaluated for biological activity. The modification of ammonium groups can lead to enhanced antibacterial or antiviral properties, making it an exciting subject in medicinal chemistry.
  • Polyfunctional Reactivity: The functional groups present may participate in diverse reactions such as nucleophilic substitutions or hydride reductions, providing various pathways for researchers to explore synthetic applications.
  • Natural Product Mimicry: The structure resembles certain natural products, potentially allowing chemists to design molecules that mimic biological activity found in nature, paving the way for drug discovery.

As we continue to explore this compound, our understanding of its properties and potential applications will undoubtedly expand. This compound encapsulates the intersection of structure, reactivity, and biological importance, inviting chemists to delve deeper into its secrets.

Synonyms
Mdmamot
cis-Oxathiolane
1,3-Oxathiolane-5-methanaminium, N,N,N,2-tetramethyl-
103314-75-6
2-Methyl-5-((dimethylamino)methyl)-1,3-oxathiolane methiodide
CHEMBL1182266
DTXSID30908323
trimethyl-[(2-methyl-1,3-oxathiolan-5-yl)methyl]azanium
N,N,N-Trimethyl(2-methyl-1,3-oxathiolan-5-yl)methanaminium