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Bethanechol chloride

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Identification
Molecular formula
C7H17Cl2N2O2
CAS number
590-63-6
IUPAC name
benzyl-[2-[[2-[2-[benzyl(diethyl)ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium;dichloride
State
State

At room temperature, bethanechol chloride is typically in a solid state. It appears as a stable compound in its powdered form.

Melting point (Celsius)
241.00
Melting point (Kelvin)
514.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
387.44g/mol
Molar mass
387.4400g/mol
Density
1.2096g/cm3
Appearence

Bethanechol chloride is a white, crystalline powder. Its crystalline nature makes it appear as small, white crystals when observed under a microscope.

Comment on solubility

Solubility of Benzyl-[2-[[2-[2-[Benzyl(diethyl)ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium; Dichloride

The solubility of this complex ammonium salt is influenced by several factors, including its ionic nature and the presence of various functional groups within its structure. Here are some essential insights regarding its solubility:

  • Ionic Character: As a quaternary ammonium salt, benzyl-[2-[[2-[2-[benzyl(diethyl)ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium dichloride possesses a high ionic character, which typically enhances solubility in polar solvents like water.
  • Hydrophilic and Hydrophobic Balancing: The presence of both hydrophilic (amine and carbonyl) and hydrophobic (benzyl and diethyl groups) elements in the compound can lead to varying degrees of solubility, often requiring specific conditions (such as temperature adjustments) for optimal dissolution.
  • Temperature Dependence: Like many salts, its solubility may increase with temperature. Therefore, heating can be a useful method to achieve higher solubility in solution.
  • Interaction with Medium: In a polar solvent, the interactions of the ammonium groups with the solvent molecules may improve solubility. However, in non-polar environments, the compound might face challenges in solvation.

In conclusion, while benzyl-[2-[[2-[2-[benzyl(diethyl)ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium; dichloride is generally soluble in polar solvents, its solubility may vary significantly based on environmental conditions and solvent choices. Understanding these factors is vital for the effective application and utilization of the compound in various chemical processes.

Interesting facts

Interesting Facts about Benzyl-[2-[[2-[2-[benzyl(diethyl)ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium;dichloride

Benzyl-[2-[[2-[2-[benzyl(diethyl)ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium;dichloride is a complex quaternary ammonium compound, notable for its multifaceted role in both medicinal chemistry and biochemical applications. Here are some intriguing insights:

  • Versatile Applications: This compound serves a variety of roles, including acting as a bioactive agent in pharmaceutical formulations and as a potential antimicrobial agent.
  • Structural Complexity: The intricate structure of this compound is formed by multiple functional groups, contributing to its diverse chemical behavior and allowing for interesting interactions with biological systems.
  • Ammonium Functionality: The presence of the quaternary ammonium group allows for strong ionic interactions, making it particularly relevant in the formulation of surfactants and emulsifiers.
  • Potential Therapeutic Use: Research suggests that compounds like this could have potential applications in drug delivery systems, enhancing the transport of active pharmaceutical ingredients across biological membranes.
  • Synthetic Pathways: The synthesis of this compound involves sophisticated organic reactions, underscoring the importance of understanding reaction mechanisms in the field of organic synthesis.

With its blend of structure and function, benzyl-[2-[[2-[2-[benzyl(diethyl)ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium;dichloride exemplifies the exciting interplay between chemistry and biological activity, holding promise for innovative applications in the future.

Synonyms
WIN 3286
152-25-0
AMMONIUM, (OXALYLBIS(IMINOETHYLENE))BIS(BENZYLDIETHYL-, DICHLORIDE
(Oxalylbis(iminoethylene))bis(benzyldiethylammonium chloride)