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Decamethonium p-toluenesulfonate

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Identification
Molecular formula
C23H36N2O7S
CAS number
65-52-5
IUPAC name
bis[2-(ethylcarbamoyloxy)ethyl]-methyl-ammonium;4-methylbenzenesulfonate
State
State

At room temperature, Decamethonium p-toluenesulfonate is in a solid state.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
502.64g/mol
Molar mass
502.6410g/mol
Density
1.2060g/cm3
Appearence

Decamethonium p-toluenesulfonate is typically found as a white to off-white crystalline solid.

Comment on solubility

Solubility of bis[2-(ethylcarbamoyloxy)ethyl]-methyl-ammonium;4-methylbenzenesulfonate

The solubility of bis[2-(ethylcarbamoyloxy)ethyl]-methyl-ammonium;4-methylbenzenesulfonate can be considered intriguing due to its unique structure and functional groups. Generally, solubility can vary widely based on factors such as temperature, pH, and the presence of other solutes.

Key Points on Solubility:

  • Polar Nature: This compound contains multiple polar functional groups, such as the carbamoyloxy and quaternary ammonium moieties, which promote solubility in polar solvents like water.
  • Hydrogen Bonding: The presence of oxygen atoms allows for extensive hydrogen bonding interactions, enhancing its potential solubility in aqueous environments.
  • Organic Solvent Solubility: While it exhibits good solubility in water, the compound may also dissolve in various organic solvents, particularly those that can engage in hydrogen bonding.
  • Salts and Derivatives: Being a salt of a sulfonic acid, it often demonstrates increased solubility in concentrated solutions, as the ionic nature of the sulfonate can further facilitate dissolution.

In summary, the solubility of bis[2-(ethylcarbamoyloxy)ethyl]-methyl-ammonium;4-methylbenzenesulfonate is significantly influenced by its chemical structure, showcasing excellent solubility in both polar and some organic solvents. Understanding these solubility characteristics is crucial for its application in various chemical processes and formulations.

Interesting facts

Interesting Facts about bis[2-(ethylcarbamoyloxy)ethyl]-methyl-ammonium; 4-methylbenzenesulfonate

This compound is a fascinating example of how modern chemistry can be applied to develop materials with specific properties and functionalities. Let's explore its intriguing aspects:

  • Dual Functionality: The combination of ethylcarbamoyloxy groups and a methylammonium unit provides this compound with unique reactivity and solubility characteristics, making it useful in various chemical applications.
  • Pharmaceutical Potential: Compounds like this are often investigated for their potential use in drug delivery systems, where controlled release and targeted delivery are paramount.
  • Surface Activity: The structure suggests that it may exhibit surfactant properties, which could be beneficial in formulations requiring emulsification or dispersion.
  • Supramolecular Chemistry: The compound's ionic character due to the sulfonate group can lead to interesting interactions in supramolecular chemistry, potentially forming complex architectures when combined with other molecules.
  • Research Applications: Scientists may explore its use in interfacial phenomena, polymer chemistry, or as a catalyst modifier due to its unique functional groups.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This principle reflects the need for continuous exploration and innovation within the field. As we delve deeper into compounds like this, we not only expand our understanding of chemistry but also open doors to new technologies and applications.

In summary, bis[2-(ethylcarbamoyloxy)ethyl]-methyl-ammonium; 4-methylbenzenesulfonate serves as a testament to the advancing frontiers of chemical research and the boundless possibilities it offers.

Synonyms
CARBAMIC ACID, ETHYL-, DIESTER with METHYLIMINODIETHANOL, TOSYLATE
27585-48-4
Ethanol, 2,2'-(methylimino)di-, bis(ethylcarbamate), tosylate
DTXSID60181985
RefChem:332437
DTXCID00104476