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Ipratropium bromide

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Identification
Molecular formula
C20H30BrNO3
CAS number
66985-17-9
IUPAC name
quinuclidin-1-ium-3-yl N-(2-chloro-6-methyl-phenyl)carbamate;chloride
State
State

At room temperature, ipratropium bromide is typically in a solid state.

Melting point (Celsius)
231.00
Melting point (Kelvin)
504.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
430.38g/mol
Molar mass
430.3750g/mol
Density
1.3600g/cm3
Appearence

Ipratropium bromide commonly appears as a white crystalline powder. It is usually odorless and is used in its salt form for pharmaceutical purposes.

Comment on solubility

Solubility of Quinuclidin-1-ium-3-yl N-(2-chloro-6-methyl-phenyl)carbamate; Chloride

The solubility of quinuclidin-1-ium-3-yl N-(2-chloro-6-methyl-phenyl)carbamate; chloride can be influenced by several factors, including the nature of the ions, the solvent used, and the temperature. Here are some key points concerning its solubility:

  • Solvent Behavior: This compound tends to be more soluble in polar solvents due to its ionic character. Solvents like water, methanol, or ethanol may enhance dissolution.
  • Temperature Effects: Generally, higher temperatures improve solubility for many ionic compounds, potentially increasing the dissolution rates.
  • pH Sensitivity: Since this compound contains a quinuclidin-1-ium moiety, changes in pH can affect solubility. For example, increasing acidity may lead to better solubility due to protonation effects.
  • Ionic Strength: In solutions with higher ionic strength, solubility may alter because of interactions with other ions present.

It is advisable to evaluate the solubility empirically under controlled conditions as theoretical predictions might not completely capture the intricacies involved. Understanding the solubility profile is crucial for its practical applications, especially in pharmaceuticals where bioavailability is key. As one expert noted, "the solubility of a compound can determine its entire efficacy in biological systems." Therefore, precise solubility assessments can lead to significant advancements in using this compound effectively.

Interesting facts

Exploring Quinuclidin-1-ium-3-yl N-(2-chloro-6-methyl-phenyl)carbamate; Chloride

Quinuclidin-1-ium-3-yl N-(2-chloro-6-methyl-phenyl)carbamate; chloride is a fascinating compound that exhibits a unique combination of chemical functionalities, making it of great interest in the field of medicinal chemistry. Here are some intriguing facts about this compound:

  • Unique Structure: The compound features a quinuclidin-1-ium core, which is a cyclic amine structure that plays a significant role in its pharmacological properties.
  • Designed for Activity: The N-(2-chloro-6-methyl-phenyl)carbamate moiety is designed to enhance the compound's bioactivity, offering potential applications in therapeutic areas such as neurology.
  • Pest Control: Due to its structural characteristics, this compound can also be investigated for its role as an insecticide, showcasing versatility across different fields of study.
  • Chloride Ion Role: The presence of the chloride ion contributes to the ionic characteristics of the compound, affecting its reactivity and interaction with biological systems.
  • Research Potential: Ongoing research on the quinuclidinyl derivatives may yield novel insights into receptor interactions and mechanisms of action.

"The study of such compounds not only enhances our understanding of chemistry but also paves the way for innovative solutions in medicine and agriculture."

This compound exemplifies the convergence of synthetic chemistry and real-world applications, making it an exciting area for future research. Continued exploration of its properties could lead to breakthroughs in drug development and pest management strategies.

Synonyms
2-Chloro-6-methylcarbanilic acid 3-quinuclidinyl ester hydrochloride
29440-70-8
CARBANILIC ACID, 2-CHLORO-6-METHYL-, 3-QUINUCLIDINYL ESTER, MONOHYDROCHLORIDE
RefChem:332938