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Betahistine hydrochloride

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Identification
Molecular formula
C14H20NClS
CAS number
5579-84-0
IUPAC name
methyl-[2-(5-methylbenzothiophen-3-yl)ethyl]ammonium;chloride
State
State

At room temperature, Betahistine hydrochloride is in a solid state, typically presenting as a crystalline powder.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
216.50
Boiling point (Kelvin)
489.65
General information
Molecular weight
239.76g/mol
Molar mass
239.7580g/mol
Density
1.1800g/cm3
Appearence

Betahistine hydrochloride appears as a white or almost white crystalline powder. It is very soluble in water and soluble in methanol, and slightly soluble in ethanol. The crystalline structure can sometimes appear as fine and powdery or in small lumps.

Comment on solubility

Solubility of Methyl-[2-(5-methylbenzothiophen-3-yl)ethyl]ammonium Chloride

The solubility of methyl-[2-(5-methylbenzothiophen-3-yl)ethyl]ammonium chloride can be influenced by several factors, primarily due to its ionic nature and the interactions within the solvent. Here are some key points regarding its solubility:

  • Solvent Dependency: This compound is likely to be soluble in polar solvents such as water, owing to the presence of the ammonium group, which can facilitate hydrogen bonding.
  • Temperature Effects: Increasing the temperature generally increases solubility for many ionic compounds; hence, heating the solvent may enhance the solubility of this compound.
  • Concentration Considerations: Like other ammonium salts, its solubility might also depend on the concentration of the chloride ions in solution. A saturated solution could lead to precipitation at higher concentrations.
  • pH Influence: The pH of the solution may affect solubility as well, as changes in acidity can alter the ionization and interactions of the compound with water.

In summary, the solubility of methyl-[2-(5-methylbenzothiophen-3-yl)ethyl]ammonium chloride is a complex interplay of structural characteristics and environmental conditions. As a result, it is essential to empirically determine its solubility under various conditions for specific applications.

Interesting facts

Interesting Facts about Methyl-[2-(5-methylbenzothiophen-3-yl)ethyl]ammonium Chloride

Methyl-[2-(5-methylbenzothiophen-3-yl)ethyl]ammonium chloride is a fascinating compound notable for its complex structure and significant implications in various fields, particularly in biological and pharmaceutical sciences. Here are some intriguing points:

  • Unique Structure: This compound contains a benzothiophene moiety, which is a bicyclic structure known for its intriguing electronic properties. The presence of the methyl group enhances its stability and can influence its reactivity.
  • Biological Activity: Compounds like this one, featuring ammonium structures, often exhibit interesting biological activities. They may play roles as potential drug candidates, especially in the realm of neuropharmacology due to their ability to cross the blood-brain barrier.
  • Research Potential: The exploration of its physiological effects can lead to insights into *neurotransmitter mechanisms*, potentially advancing our understanding of mood disorders and cognitive functions. Notably, the study of similar compounds has increased in recent years, highlighting their importance in medicinal chemistry.
  • Ammonium Salts: Being a quaternary ammonium compound, it possesses unique properties like ionic interactions, which can enhance solubility and mobility in biological systems, making it suitable for drug formulation.
  • Interdisciplinary Applications: Researchers employ this compound in various experimental settings, including materials science and drug delivery systems, showcasing its multifaceted applicability.

In summary, Methyl-[2-(5-methylbenzothiophen-3-yl)ethyl]ammonium chloride stands as a compelling subject of study due to its structural intricacies and potential roles in medicine. As we delve deeper into its properties and effects, we may unlock new therapeutic avenues and further our understanding of complex biological interactions.

Synonyms
N,5-Dimethylbenzo(b)thiophene-3-ethylamine hydrochloride
22964-01-8
BENZO(b)THIOPHENE-3-ETHYLAMINE, N,5-DIMETHYL-, HYDROCHLORIDE
RefChem:1078826
Benzo(b)thiophene-3-ethanamine, N,5-dimethyl-, hydrochloride (1:1)