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Quaternary Ammonium Salt

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Identification
Molecular formula
C13H18Cl2NS
CAS number
: 3277-32-7
IUPAC name
(5-chlorobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride
State
State

The compound exists as a solid at room temperature, typically forming as a crystalline powder.

Melting point (Celsius)
182.00
Melting point (Kelvin)
455.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
340.28g/mol
Molar mass
340.2820g/mol
Density
1.2200g/cm3
Appearence

This compound is usually found as a crystalline solid with a distinctive light color, often appearing white or slightly yellowish due to impurities or specific formulations of the substance.

Comment on solubility

Solubility of (5-chlorobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride

The solubility characteristics of the compound (5-chlorobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride are influenced by its complex structure and the presence of both hydrophilic and hydrophobic functional groups. Understanding its solubility can provide insights into various applications, particularly in pharmacology and material science.

Key Factors Influencing Solubility:

  • Ionic Nature: As a quaternary ammonium salt, the presence of a chloride counterion typically suggests high solubility in polar solvents like water.
  • Hydrophobic Regions: The chlorinated aromatic rings may contribute to hydrophobic interactions, potentially reducing solubility in aqueous environments.
  • Temperature Dependence: Solubility may increase with temperature, as higher thermal energy can overcome the interactions within the solid state.
  • pH Effects: The pH of the solvent can also impact solubility; varying pH levels may affect ionization and, consequently, the solubility pattern.

In general, one might expect that this compound will exhibit moderate to high solubility in polar solvents, but the exact solubility will depend on specific conditions such as temperature and solvent composition. As noted, it is crucial to evaluate the solubility experimentally to obtain precise data.

Interesting facts

Interesting Facts about (5-chlorobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride

The compound (5-chlorobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride is quite intriguing, especially considering its structure and potential applications in the field of chemistry and pharmacology.

Unique Structural Features

  • Chlorobenzothiophene Framework: The presence of the chlorobenzothiophene moiety not only adds to the compound's complexity but also enhances its biological activity, making it a candidate for various medicinal applications.
  • Quaternary Ammonium Ion: This compound features a quaternary ammonium structure, which is known for its ability to interact with biological membranes, potentially leading to interesting pharmacological properties.

Potential Applications

  • Antimicrobial Activity: Quaternary ammonium compounds are typically noted for their antimicrobial properties, suggesting that this compound might exhibit similar traits.
  • Antineoplastic Research: The complex structure may also provide a basis for research into cancer treatments, particularly in targeting specific cell types.
  • Material Science: With its ionic character, this compound might find applications in material science as a surfactant or a stabilizing agent in various formulations.

Exciting Research Prospects

As a student or a research scientist, diving into the synthesis, reactivity, and biological implications of (5-chlorobenzothiophen-3-yl)methyl-(2-chloroethyl)-ethyl-ammonium;chloride can unveil exciting possibilities. Exploring its mechanisms of action, stability, and interaction with other drugs could lead to significant scientific advancements. One might say, "The magic of chemistry lies in its potential to connect seemingly disparate concepts into revolutionary ideas."

This compound exemplifies how thorough chemical exploration can lead to discoveries with profound implications, opening doors to innovative treatments and advanced materials.

Synonyms
Benzo(b)thiophene-3-methylamine, 5-chloro-N-(2-chloroethyl)-N-ethyl-, hydrochloride
7384-96-5
5-Chloro-N-(2-chloroethyl)-N-ethylbenzo(b)thiophene hydrochloride