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Galantamine hydrobromide

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Identification
Molecular formula
C25H32ClN3O3
CAS number
1953-04-4
IUPAC name
3,7-bis(3-hydroxypropyl)-1,5-diphenyl-3,7-diazabicyclo[3.3.1]nonan-9-one;chloride
State
State

At room temperature, the compound is in a solid state. It is commonly provided as a powder for uses that require precise dosing, such as pharmaceuticals.

Melting point (Celsius)
195.00
Melting point (Kelvin)
468.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
368.86g/mol
Molar mass
368.8610g/mol
Density
1.2500g/cm3
Appearence

The compound is typically a white to off-white crystalline powder. It is commonly used in pharmaceutical formulations and appears in a highly purified form for medical use.

Comment on solubility

Solubility of 3,7-bis(3-hydroxypropyl)-1,5-diphenyl-3,7-diazabicyclo[3.3.1]nonan-9-one;chloride

The solubility of the compound 3,7-bis(3-hydroxypropyl)-1,5-diphenyl-3,7-diazabicyclo[3.3.1]nonan-9-one;chloride can be influenced by various factors. Understanding its solubility profile is crucial for applications in pharmaceuticals and chemical research. Here are some key points:

  • Polar vs Nonpolar: Given the presence of hydroxyl groups, the compound exhibits polar characteristics, which can enhance its solubility in polar solvents like water.
  • Chloride Role: The chloride ion can also improve solubility in ionic solvents, potentially allowing for better dissolution in saline solutions.
  • Temperature Dependence: Like many compounds, solubility may increase with temperature. Thus, heat can facilitate increased interaction with solvents.

While exact numerical solubility values may not be available, qualitative assessments typically indicate that such compounds dissolve more readily in polar environments compared to nonpolar ones. In practical terms, researchers and formulators should consider conducting rigorous solubility tests to assess behavior under specific conditions.

Ultimately, the solubility of 3,7-bis(3-hydroxypropyl)-1,5-diphenyl-3,7-diazabicyclo[3.3.1]nonan-9-one;chloride reflects the intricate balance of molecular interactions, making it a fascinating subject for further study.

Interesting facts

Interesting Facts about 3,7-bis(3-hydroxypropyl)-1,5-diphenyl-3,7-diazabicyclo[3.3.1]nonan-9-one; Chloride

This intriguing compound is a fascinating example of the complexity and functionality found in organic chemistry. Here are some compelling points about it:

  • Unique Structure: The compound features a bicyclic system, which contributes to its distinctive properties. The incorporation of nitrogen atoms and multiple phenyl groups enhances its potential applications in various fields.
  • Biological Relevance: Compounds with a similar diazabicyclic structure are often studied for their biological activities. They may exhibit roles as potential pharmaceuticals or agrochemicals.
  • Chemical Reactivity: The presence of hydroxyl groups makes the compound more polar and can increase its reactivity. This can lead to fascinating pathways in synthetic chemistry and drug development.
  • Chloride Ion: The chloride component is notable for its role as a counterion, which can influence both solubility and the overall stability of the compound in chemical reactions.
  • Research Potential: This compound could serve as a versatile building block for the synthesis of more complex molecules, making it valuable in materials science and medicinal chemistry.

In Summary

3,7-bis(3-hydroxypropyl)-1,5-diphenyl-3,7-diazabicyclo[3.3.1]nonan-9-one; chloride exemplifies the ever-evolving nature of chemistry. Its intricate structure and promising biological activity make it a compound of great interest to researchers. As scientists continue to explore such compounds, they pave the way for groundbreaking innovations and discoveries in various scientific domains.

Synonyms
3,7-Bis(3-hydroxypropyl)-1,5-diphenyl-3,7-diazabicyclo(3.3.1)nonan-9-one hydrochloride
4478-44-8
I.S. 3232
1,5-Difenil-3,7-di-(gamma-idrossipropil)-bispidid-9-oni cloridrato [Italian]
3,7-Diazabicyclo(3.3.1)nonan-9-one, 3,7-bis(3-hydroxypropyl)-1,5-diphenyl-, hydrochloride
1,5-Difenil-3,7-di-(gamma-idrossipropil)-bispidid-9-oni cloridrato