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Bethanidine chloride

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Identification
Molecular formula
C16H23ClN2O2
CAS number
59-40-5
IUPAC name
diethyl-[2-(1-naphthylcarbamoyloxy)ethyl]ammonium;chloride
State
State

At room temperature, bethanidine chloride is in a solid state. It is typically stable under standard conditions.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.15
Boiling point (Celsius)
580.00
Boiling point (Kelvin)
853.15
General information
Molecular weight
292.83g/mol
Molar mass
292.8270g/mol
Density
1.1900g/cm3
Appearence

Bethanidine chloride appears as a white to off-white crystalline powder. It is typically odorless.

Comment on solubility

Solubility of Diethyl-[2-(1-naphthylcarbamoyloxy)ethyl]ammonium Chloride

Diethyl-[2-(1-naphthylcarbamoyloxy)ethyl]ammonium chloride is a fascinating compound with unique solubility characteristics. Its solubility can be impacted by various factors, which are important to consider:

  • Polarity: The presence of polar functional groups in the structure, specifically the ammonium ion and the ether-like functional group, generally enhances its solubility in polar solvents such as water.
  • Hydrophobic Interactions: The naphthyl group provides a hydrophobic region, which may lower its solubility in highly polar solvents but can make it more compatible with organic solvents.
  • pH Influence: Being a quaternary ammonium salt, the solubility might also vary significantly with changes in pH, as it can affect the ionization of the compound.
  • Concentration Impacts: At higher concentrations, precipitation might occur, which can shift the solubility equilibrium in a particular solvent system.

In practical applications, it is often noted that "the solubility of ionic compounds in water tends to be higher" due to their interactions with water molecules. Hence, diethyl-[2-(1-naphthylcarbamoyloxy)ethyl]ammonium chloride is likely to exhibit moderate to good solubility in aqueous media, while showing variable solubility in organic solvents. Understanding these solubility aspects is critical for effective utilization in chemical formulations and various applications.

Interesting facts

Interesting Facts about Diethyl-[2-(1-naphthylcarbamoyloxy)ethyl]ammonium Chloride

Diethyl-[2-(1-naphthylcarbamoyloxy)ethyl]ammonium chloride is a fascinating chemical compound that serves various roles in the field of chemistry. Here are some key insights:

  • Pharmaceutical Relevance: This compound has potential applications in medicinal chemistry and pharmacology due to its unique structure, which may contribute to biological activity.
  • Structural Composition: The presence of a naphthyl group in its structure aids in enhancing its lipophilicity, which can affect its interaction with biological membranes.
  • Research Use: It is often utilized in research settings to investigate drug delivery systems and the mechanisms of action for various biological targets.
  • Charge Characteristics: As a quaternary ammonium compound, it has a positive charge that influences its solubility and interaction with negatively charged biological molecules.
  • Versatility in Synthesis: The synthesis of this compound can be approached through various chemical pathways, providing ample opportunities for students and researchers to explore synthetic methodologies.

In addition to its practical applications, the compound's unique properties and potential for innovation within pharmaceutical chemistry emphasize the importance of continued research in this area. As the field evolves, compounds like diethyl-[2-(1-naphthylcarbamoyloxy)ethyl]ammonium chloride can lead to exciting new discoveries.

Synonyms
23379-40-0
DTXSID00946050
2-(Diethylamino)ethyl hydrogen naphthalen-1-ylcarbonimidate--hydrogen chloride (1/1)
RefChem:1061719
DTXCID501374346
1-NAPHTHALENECARBAMIC ACID, 2-DIETHYLAMINOETHYL ESTER, MONOHYDROCHLORIDE
2-Diethylaminoethyl ester of 1-naphthalenecarbamic acid hydrochloride