Skip to main content

Docusate Sodium

ADVERTISEMENT
Identification
Molecular formula
C20H37NaO7S
CAS number
577-11-7
IUPAC name
2-(4-amino-2-hexoxy-benzoyl)sulfanylethyl-diethyl-ammonium;chloride
State
State

Solid at room temperature.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.15
General information
Molecular weight
444.53g/mol
Molar mass
444.5320g/mol
Density
1.1000g/cm3
Appearence

Docusate sodium, commonly known as a white or off-white, wax-like solid. It may exhibit a slight odor and is typically available in fine powder form for pharmaceutical use.

Comment on solubility

Solubility of 2-(4-amino-2-hexoxy-benzoyl)sulfanylethyl-diethyl-ammonium;chloride

The solubility of the compound 2-(4-amino-2-hexoxy-benzoyl)sulfanylethyl-diethyl-ammonium;chloride is an interesting topic due to its complex structure and potential applications. This compound is an ammonium salt, which generally influences its solubility in various solvents.

Key considerations regarding its solubility include:

  • Polarity: The presence of the diethylammonium group suggests that the compound may exhibit polar characteristics, enhancing its solubility in polar solvents such as water.
  • Chain Length and Structure: The hexoxy group contributes hydrophobic characteristics, which can impact overall solubility. Compounds with both hydrophobic and hydrophilic segments often exhibit unique solubility properties.
  • Temperature Dependency: Like many salts, the solubility can vary with temperature. Typically, an increase in temperature may enhance solubility.

In summary, while the solubility of 2-(4-amino-2-hexoxy-benzoyl)sulfanylethyl-diethyl-ammonium;chloride indicates potential for dissolution in polar solvents, the interplay between its ionic and hydrophobic characteristics complicates its overall solubility behavior. Understanding these factors is essential for its practical application in various fields.

Interesting facts

Interesting Facts about 2-(4-amino-2-hexoxy-benzoyl)sulfanylethyl-diethyl-ammonium Chloride

This intriguing compound, 2-(4-amino-2-hexoxy-benzoyl)sulfanylethyl-diethyl-ammonium chloride, falls under the category of quaternary ammonium compounds, which are known for their multiple applications in both chemistry and industry. Let’s explore some fascinating aspects of this compound:

  • Quaternary Ammonium Compounds: These compounds, such as the one in question, are notable for their ability to act as surfactants. They reduce surface tension, which makes them useful in various cleaning and deodorizing products.
  • Bioactivity: The presence of the amino group in this compound suggests potential biological activity. Many amino-containing compounds are studied for their pharmacological properties, making them of interest to medicinal chemists.
  • Functional Applications: Quaternary ammonium compounds are often used as antimicrobial agents, particularly in disinfectants and antiseptics, due to their effectiveness against a range of pathogens.
  • Solubility Considerations: The inclusion of a long aliphatic chain (hexoxy) improves lipophilicity, which can enhance permeability in biological systems, a key factor in drug formulation.
  • Structure-Activity Relationship (SAR): The structural elements of this compound allow researchers to investigate how the modification of certain functional groups can lead to altered biological activity and efficacy, which is crucial in drug development.

In conclusion, the study of 2-(4-amino-2-hexoxy-benzoyl)sulfanylethyl-diethyl-ammonium chloride not only contributes to our understanding of quaternary ammonium compounds but also opens avenues for research in pharmaceuticals, environmental science, and materials engineering. As you delve deeper into its properties and applications, the potential for discovering exciting uses continues to grow. Remember, as a fundamental rule in chemistry, "the structure dictates function."

Synonyms
WIN 4510
4607-43-6
4-Amino-2-(hexyloxy)thiobenzoic acid S-(2-(diethylamino)ethyl) ester hydrochloride
Benzoic acid, 4-amino-2-(hexyloxy)thio-, S-(2-(diethylamino)ethyl)ester, monohydrochloride