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Ipratropium Bromide

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Identification
Molecular formula
C20H30BrNO3
CAS number
60205-81-4
IUPAC name
(5-isopropyl-2-methyl-cyclohexyl)-(pyridin-1-ium-4-carbonylamino)ammonium;dichloride
State
State

At room temperature, Ipratropium bromide is commonly found as a solid.

Melting point (Celsius)
232.50
Melting point (Kelvin)
505.65
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.15
General information
Molecular weight
430.38g/mol
Molar mass
430.3800g/mol
Density
1.2200g/cm3
Appearence

Ipratropium bromide typically appears as a white crystalline powder.

Comment on solubility

Solubility of (5-isopropyl-2-methyl-cyclohexyl)-(pyridin-1-ium-4-carbonylamino)ammonium; dichloride

The solubility of (5-isopropyl-2-methyl-cyclohexyl)-(pyridin-1-ium-4-carbonylamino)ammonium; dichloride is influenced by several factors due to its complex molecular structure. Here are some key points to consider:

  • Polarity: This compound contains polar functional groups, which can enhance its solubility in polar solvents, including water. Its pyridinium moiety contributes to such polarity.
  • Hydrogen Bonding: The presence of the carbonyl and ammonium groups provides additional opportunities for hydrogen bonding, facilitating solubility in aqueous environments.
  • Temperature Dependency: Like many salts, solubility can be temperature dependent. Higher temperatures may improve solubility in solvents.
  • Ionization: The dichloride component suggests that this compound can dissociate in solution, leading to increased solubility due to the presence of ionic species.

As a result, we can generally expect that this compound has decent solubility in polar solvents, while it may exhibit limited solubility in non-polar solvents. Understanding these solubility characteristics is essential for applications in chemical synthesis, formulation, and various related fields.

Interesting facts

Interesting Facts About (5-isopropyl-2-methyl-cyclohexyl)-(pyridin-1-ium-4-carbonylamino)ammonium; dichloride

This unique compound, often referred to in simplified terms due to its long name, exhibits fascinating characteristics that intrigue both chemists and pharmaceutical scientists alike. Here are some engaging facts about it:

  • Complex Structure: The compound features a cyclohexane ring that is substituted at specific carbon atoms, giving rise to its isopropyl and methyl groups. This resemblance to natural compounds highlights its potential relevance in organic synthesis and medicinal chemistry.
  • Pyridinium Influence: The presence of the pyridinium moiety introduces quaternary ammonium chemistry, which can enhance solubility in various solvents and may improve its biological activity, making it a subject of interest for drug development.
  • Amide Bonding: The carbonylamino group showcases an amide functionality, which is significant in protein interactions and biological systems. This feature is crucial in understanding the compound's reactivity and its possible role in biological pathways.
  • Applications in Research: With its complex structure, this compound could serve as a template for designing new pharmaceuticals or as a specialized reagent in organic reactions.
  • Chloride Coordination: The dichloride component hints at potential interactions in coordination chemistry, which could lead to insights in metal complexation and catalysis.

As a scientist, delving into this compound can reveal opportunities to explore structure-activity relationships in drug design and applications in chemical synthesis. It's a compelling example of how complex organic compounds can be synthesized to tailor specific properties for innovative uses in various fields.

Synonyms
2-p-Menth-2-ylhydrazide of isonicotinic acid dihydrochloride
15407-90-6
ISONICOTINIC ACID, 2-p-MENTH-2-YLHYDRAZIDE, DIHYDROCHLORIDE