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Betahistine hydrochloride

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Identification
Molecular formula
C12H19ClNO2
CAS number
5579-84-0
IUPAC name
[3-carboxy-3-(1-naphthyl)propyl]-dimethyl-ammonium;chloride
State
State

Betahistine hydrochloride is a solid at room temperature.

Melting point (Celsius)
149.00
Melting point (Kelvin)
422.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
281.82g/mol
Molar mass
281.8200g/mol
Density
1.1630g/cm3
Appearence

Betahistine hydrochloride typically appears as a white or off-white crystalline powder. It is freely soluble in water and alcohol.

Comment on solubility

Solubility of [3-carboxy-3-(1-naphthyl)propyl]-dimethyl-ammonium;chloride

The solubility of the compound [3-carboxy-3-(1-naphthyl)propyl]-dimethyl-ammonium;chloride is influenced by several factors that are essential in understanding its behavior in various solvents. This compound, characterized by its quaternary ammonium structure, typically exhibits a moderate to high solubility in polar solvents.

Key points regarding the solubility of this compound include:

  • Water Solubility: The presence of a quaternary ammonium group can enhance solubility in water due to its ionic nature, which facilitates interactions with water molecules.
  • Solvent Interaction: Its solubility may decrease in non-polar solvents, as the hydrophobic naphthyl moiety prefers a non-polar environment, leading to a balance between hydrophobic and hydrophilic interactions.
  • Temperature Effects: Increasing temperature often enhances solubility for many ionic compounds, which could also apply here.

In summary, while [3-carboxy-3-(1-naphthyl)propyl]-dimethyl-ammonium;chloride is generally soluble in polar media, the specific solubility characteristics can vary depending on the solvent environment and temperature. Understanding these parameters is crucial for effective application in chemical processes.

Interesting facts

Interesting Facts about [3-carboxy-3-(1-naphthyl)propyl]-dimethyl-ammonium;chloride

The compound [3-carboxy-3-(1-naphthyl)propyl]-dimethyl-ammonium;chloride is a fascinating quaternary ammonium compound that bridges multiple fields, including organic chemistry and biochemistry. Here are some engaging facts about this unique compound:

  • Dual Functionality: With a carboxylic acid group and a quaternary ammonium structure, this compound exhibits both ionic and polar characteristics, making it a valuable candidate in drug formulation and biological studies.
  • Biological Activity: Its structural configuration may lead to interesting interactions with biological membranes, enabling applications in cell signaling research and possibly even drug design to target specific pathways.
  • Environmental Implications: Studies on quaternary ammonium compounds like this one can provide insights into their impacts on environmental chemistry, particularly in relation to biodegradability and aquatic toxicity.
  • Versatile Applications: The compound’s unique properties make it a promising candidate for uses in surfactants, antimicrobial agents, and ionic liquids, thereby enhancing its applicability in various chemical processes.

Through its complex structure and diverse functionality, [3-carboxy-3-(1-naphthyl)propyl]-dimethyl-ammonium;chloride exemplifies the rich tapestry of chemistry, where the interplay of molecular design and practical application can lead to exciting developments in science and industry. As noted by scientists, "The beauty of chemistry lies in its ability to combine simple elements into complex functions."

Its study not only enriches our understanding of chemical interactions but also sparks curiosity among students and researchers alike, encouraging further exploration into the world of chemical compounds.

Synonyms
alpha-(2-(Dimethylamino)ethyl)-1-naphthaleneacetic acid hydrochloride
6389-71-5
1-NAPHTHALENEACETIC ACID, alpha-(2-(DIMETHYLAMINO)ETHYL)-, HYDROCHLORIDE