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Bethanechol Chloride

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Identification
Molecular formula
C5H14N2O2SCl
CAS number
590-63-6
IUPAC name
2-(4-aminobenzoyl)sulfanylethyl-diethyl-ammonium;chloride
State
State

At room temperature, Bethanechol chloride exists as a solid. It is often available as a powder ready to be mixed or compressed into pharmaceutical tablets.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.15
Boiling point (Celsius)
150.00
Boiling point (Kelvin)
423.15
General information
Molecular weight
196.27g/mol
Molar mass
196.2680g/mol
Density
1.1000g/cm3
Appearence

Bethanechol chloride typically appears as a white to off-white crystalline powder. It is odorless and has a bitter taste. The compound is often used in medical settings, thus commonly encountered in pharmaceutical forms such as tablets.

Comment on solubility

Solubility of 2-(4-aminobenzoyl)sulfanylethyl-diethyl-ammonium;chloride

The solubility of 2-(4-aminobenzoyl)sulfanylethyl-diethyl-ammonium chloride can be quite interesting due to its unique molecular structure. Here are some key points to consider:

  • Solvent Compatibility: This compound is more likely to be soluble in polar solvents, such as water, due to its ionic characteristics stemming from the ammonium group and the chloride anion.
  • Temperature Effects: Like many ionic compounds, solubility may increase with temperature, which means that higher temperatures could enhance its dissolving capabilities.
  • pH Influence: The solubility may also be influenced by the pH of the solution; variations in pH can affect the ionization states of the compound, leading to potentially different solubility outcomes.

In summary, while 2-(4-aminobenzoyl)sulfanylethyl-diethyl-ammonium chloride is expected to demonstrate good solubility in polar solvents, its solubility behavior can be further influenced by both temperature and pH, making it a compound of interest in various chemical and biological applications. Understanding these factors is crucial for effective usage in laboratory settings.

Interesting facts

Interesting Facts About 2-(4-Aminobenzoyl)sulfanylethyl-diethyl-ammonium Chloride

The compound 2-(4-aminobenzoyl)sulfanylethyl-diethyl-ammonium chloride is an intriguing molecule that showcases a unique combination of functional groups and structural elements. Here are some interesting insights:

  • Biological Relevance: Compounds bearing amino groups, such as this one, often play significant roles in biological systems. They can function as intermediates in pharmaceutical development, particularly in creating drugs that target specific biological pathways.
  • Ammonium Salts: As a quaternary ammonium compound, it exhibits antibacterial properties. Quaternary ammonium compounds are widely used in disinfectants and surfactants, making this compound relevant in the field of antimicrobial agents.
  • Synthetic Applications: The sulfanyl and amino groups present in the structure make this compound useful in organic synthesis. It can serve as a building block for creating more complex molecules in both academic and industrial settings.
  • Potential in Drug Design: The specific arrangement of atoms and functional groups allows for versatility in drug design. Chemists often explore such compounds for their potential to act as inhibitors or modulators in various biological processes.
  • Research Tool: The compound can be utilized as a research tool in studying cellular interactions, offering insights into the mechanisms of drug action and cellular uptake, which is crucial for developing effective therapeutic agents.

In summary, 2-(4-aminobenzoyl)sulfanylethyl-diethyl-ammonium chloride not only presents an interesting chemical structure but also opens up avenues for research and application in pharmaceuticals and biological studies. Its diverse functionalities illustrate how chemistry can intersect with biology to solve real-world problems.

Synonyms
p-Aminothiobenzoic acid S-(2-(diethylamino)ethyl) ester hydrochloride
DTXSID60208363
Benzenecarbothioic acid, 4-amino-, S-(2-(diethylamino)ethyl) ester, monohydrochloride
BENZOIC ACID, p-AMINOTHIO-, S-(2-(DIETHYLAMINO)ETHYL) ESTER, HYDROCHLORIDE
DTXCID80130854
5967-94-2
thiocaine hydrochloride