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Oxomemazine hydrochloride

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Identification
Molecular formula
C18H22ClNO
CAS number
307-04-0
IUPAC name
2-(piperidin-1-ium-1-ylmethyl)tetralin-1-one;chloride
State
State

At room temperature, oxomemazine hydrochloride is in a solid state. It is typically stable under normal conditions, which makes it suitable for formulation in medicinal products. The solid state is ideal for its storage and handling during pharmaceutical manufacturing and preparation.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
329.90g/mol
Molar mass
329.9000g/mol
Density
1.0880g/cm3
Appearence

Oxomemazine hydrochloride appears as a crystalline solid that is typically white or off-white in color. Its appearance can vary slightly depending on the purity and preparation method, but it is generally consistent with the description of many pharmaceutical compounds.

Comment on solubility

Solubility of 2-(piperidin-1-ium-1-ylmethyl)tetralin-1-one;chloride

The solubility of 2-(piperidin-1-ium-1-ylmethyl)tetralin-1-one;chloride can be understood through several key factors:

  • Polar Character: This compound features a quaternary ammonium ion, which typically enhances solubility in polar solvents due to its ionic nature.
  • Solvent Compatibility: It is generally soluble in water and other polar solvents like methanol and ethanol, but may exhibit limited solubility in non-polar solvents.
  • Temperature Effects: As with many ionic compounds, solubility may increase with elevated temperatures, allowing for more effective dissolving in suitable solvents.

To summarize, 2-(piperidin-1-ium-1-ylmethyl)tetralin-1-one;chloride is likely to be soluble in polar environments, making it usable in various applications depending on its solubility characteristics. Understanding its solubility profile can be crucial for its practical applications in chemical processes.

Interesting facts

Interesting Facts about 2-(piperidin-1-ium-1-ylmethyl)tetralin-1-one;chloride

This compound, known as 2-(piperidin-1-ium-1-ylmethyl)tetralin-1-one;chloride, is a fascinating example of a synthetic organic compound that showcases the interdisciplinary nature of chemistry. Let's explore some intriguing aspects:

  • Structural Diversity: The compound features a unique structural configuration that includes a piperidine ring, which contributes to its potential biological activity. This diversity may open the door to interesting pharmacological applications.
  • Biological Significance: Compounds containing piperidine moieties often exhibit significant biological activity, making them valuable as medicinal agents. Their interactions with neurotransmitter systems highlight their importance in the development of pharmaceuticals.
  • Ionization Dynamics: Being a quaternary ammonium compound, the piperidinium ion results from the protonation of the nitrogen in piperidine. This protonation enhances solubility in biological environments and allows for easier interaction with negatively charged cellular components.
  • Potential Applications: The combination of a tetralone framework and a piperidinium group may suggest applications in drug synthesis, particularly in developing compounds that target neurological disorders. The tetralin structure is known for its presence in various natural products.
  • Research Scope: Ongoing research into similar compounds may lead to the discovery of *novel therapeutic agents*, particularly in the fields of psychiatry and neurology. Each modification in the chemical structure can substantially alter biological outcomes.

As scientists continue to unravel the complexities of such compounds, the insights gained could pave the way for innovative treatments and deepen our understanding of chemical interactions in biological systems. “Chemistry is the blueprint for biology,” and compounds like this one exemplify that statement brilliantly.

Synonyms
NA-86
2-Piperidinomethyl-tetralone-1 hydrochloride
NU-805
2-Piperidinomethyl-alpha-tetralone hydrochloride
3,4-Dihydro-2-(piperidinomethyl)-1(2H)-naphthalenone hydrochloride
1(2H)-NAPHTHALENONE, 3,4-DIHYDRO-2-PIPERIDINOMETHYL-, HYDROCHLORIDE
7353-54-0