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Mepyramine hydrochloride

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Identification
Molecular formula
C17H20ClN3O
CAS number
91-84-9
IUPAC name
2-[(4-methylpyridin-1-ium-2-yl)amino]-1-phenyl-ethanol;chloride
State
State

Mepyramine hydrochloride is typically in the solid state at room temperature.

Melting point (Celsius)
167.00
Melting point (Kelvin)
440.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
309.81g/mol
Molar mass
309.8100g/mol
Density
0.6830g/cm3
Appearence

Mepyramine hydrochloride appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-[(4-methylpyridin-1-ium-2-yl)amino]-1-phenyl-ethanol;chloride

The solubility of 2-[(4-methylpyridin-1-ium-2-yl)amino]-1-phenyl-ethanol;chloride can be influenced by various factors due to its unique structural characteristics. Being a quaternary ammonium compound, it usually exhibits a strong affinity for water.

Typically, the solubility attributes can be summarized as follows:

  • Polarity: The compound's polar functional groups promote interactions with water molecules, enhancing its aqueous solubility.
  • Charge: The presence of a positively charged pyridinium moiety increases solubility in polar solvents, especially water.
  • Temperature Dependence: Like many organic compounds, solubility may vary with temperature—generally increasing with heat.

In water, it is expected to be fairly soluble due to these factors. However, it is essential to note that the solubility may vary when introduced to different solvents or in the presence of other ionic species.

As a reminder, the solubility challenges might arise based on:

  • The ionic strength of the solution
  • Presence of competing ions

In conclusion, while 2-[(4-methylpyridin-1-ium-2-yl)amino]-1-phenyl-ethanol;chloride exhibits favorable solubility properties in water, the full range of its solubility profile is best assessed through empirical data and specific experimental conditions.

Interesting facts

Interesting Facts about 2-[(4-methylpyridin-1-ium-2-yl)amino]-1-phenyl-ethanol; chloride

This fascinating compound is known for its unique structural and functional properties, which place it at the intersection of organic chemistry and pharmaceutical research. Here are some intriguing aspects to consider:

  • Pyridinium Ion: The presence of a pyridinium structure indicates that the compound exhibits basic character due to the presence of a positively charged nitrogen atom. This can affect its reactivity and interaction with biological systems.
  • Biological Activity: Compounds like this one have been studied for their potential as pharmacological agents. The amino and hydroxyl groups are critical for biological interactions, influencing how the compound binds to various targets.
  • Development of Drug Candidates: In medicinal chemistry, derivatives of compounds similar to this one are often explored for their ability to act as enzyme inhibitors, receptor ligands, or other therapeutic agents. This compound's ability to mimic natural substrates enhances its potential in drug design.
  • Structure-Activity Relationship (SAR): Understanding how modifications in structure affect the activity can aid in creating more effective compounds, making understanding the profile of this molecule crucial for researchers.
  • Solubility and Ionization: The chloride ion associated with the compound can significantly influence its solubility in biological media, affecting its absorption and bioavailability when administered.

In summary, 2-[(4-methylpyridin-1-ium-2-yl)amino]-1-phenyl-ethanol; chloride stands as an exemplary model in the study of complex molecules within both organic synthesis and medicinal chemistry. As the research in this area continues to evolve, compounds like this one may play a pivotal role in the development of new therapeutic agents.

Synonyms
alpha-((4-Methyl-2-pyridylamino)methyl)benzyl alcohol hydrochloride
BENZYL ALCOHOL, alpha-((4-METHYL-2-PYRIDYLAMINO)METHYL)-, HYDROCHLORIDE
3372-96-1