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Ipratropium bromide

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Identification
Molecular formula
C20H30NO3Br
CAS number
22254-24-6
IUPAC name
ethyl-dimethyl-[4-methyl-3-(methylcarbamoyloxy)phenyl]ammonium;iodide
State
State

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

Melting point (Celsius)
233.00
Melting point (Kelvin)
506.15
Boiling point (Celsius)
327.00
Boiling point (Kelvin)
600.15
General information
Molecular weight
430.38g/mol
Molar mass
430.3760g/mol
Density
1.4950g/cm3
Appearence

Ipratropium bromide is typically a white to off-white crystalline powder.

Comment on solubility

Solubility of Ethyl-dimethyl-[4-methyl-3-(methylcarbamoyloxy)phenyl]ammonium Iodide

The solubility of ethyl-dimethyl-[4-methyl-3-(methylcarbamoyloxy)phenyl]ammonium iodide can be influenced by its unique structural characteristics. Several factors play a vital role in determining its solubility:

  • Polarity: The presence of the methylcarbamoyloxy functional group may enhance solubility in polar solvents.
  • Ionic interactions: Being an iodide salt, it is likely to have higher solubility in water due to ion-dipole interactions.
  • Temperature: Increased temperature generally raises the solubility of many salts, thus, this compound might exhibit better solubility at elevated temperatures.
  • pH of the solvent: The solubility can also vary with changes in pH, due to acid-base interactions with the ammonium group.

In summary, while the iodide form suggests a reasonable expectation for solubility in aqueous solutions, the exact solubility may depend on several interplaying factors including:

  1. Nature of the solvent
  2. Temperature conditions
  3. Concentration of other ions

Understanding these aspects helps provide a comprehensive view of the compound's behavior in various environments. Therefore, experimentation is crucial for precise solubility data.

Interesting facts

Interesting Facts about Ethyl-Dimethyl-[4-Methyl-3-(Methylcarbamoyloxy)Phenyl]Ammonium Iodide

Ethyl-dimethyl-[4-methyl-3-(methylcarbamoyloxy)phenyl]ammonium iodide is an intriguing compound notable for its unique structure and potential applications. Below are some fascinating insights:

Chemical Structure and Functionality

  • The compound features a quaternary ammonium cation due to the presence of a positively charged nitrogen atom that is bonded to three methyl groups and one ethyl group.
  • Its core structure includes a phenyl ring substituted with a methyl group and a methylcarbamoyloxy functional group, enhancing its solubility and reactivity in biological systems.

Potential Applications

  • This compound is often studied for its use as a biocidal agent, showing effectiveness against various microbial strains.
  • Due to its ammonium cation, it may function as a surfactant, potentially useful in formulations for personal care products or pharmaceuticals.
  • Ongoing research is exploring its role in drug delivery systems, particularly for targeted therapy in cancer treatment.

Interesting Characteristics

Quaternary ammonium compounds, like this one, are known for their ability to disrupt microbial membranes, which is why they are often investigated for disinfectant properties.

The unique methylcarbamoyloxy substitution could offer insights into the interactions between the compound and various biological systems, paving the way for innovative therapeutic strategies.

Research Implications

As researchers continue to explore the applications of this compound, potential innovations in drug formulation could emerge, aiming to maximize efficacy and minimize side effects.

In summary, ethyl-dimethyl-[4-methyl-3-(methylcarbamoyloxy)phenyl]ammonium iodide is a compound rich in promise, with diverse applications in medicine and beyond.

Synonyms
TL-1340
5464-66-4
Ammonium, (3-(methylcarbamoyloxy)-p-tolyl)dimethylethyl-, iodide
NSC 15409
AMMONIUM, (3-HYDROXY-p-TOLYL)DIMETHYLETHYL-, IODIDE, METHYLCARBAMATE
Carbamic acid, methyl-, (5-(dimethylethylammonio)-o-tolyl) ester, iodide
Carbamic acid, N-methyl-, 2-methyl-5-dimethylaminophenyl ester, ethiodide
NSC15409
NSC-15409
Benzenaminium, N-ethyl-N,N,4-trimethyl-3-(((methylamino)carbonyl)oxy)-, iodide
WLN: 2K1&1&R D1 COVM1 &Q &I
Benzenaminium,N,4-trimethyl-3-[[(methylamino)carbonyl]oxy]-, iodide
Carbamic acid, [5-(dimethylethylammonio)-o-tolyl] ester, iodide
Carbamic acid, 2-methyl-5-(dimethylamino)phenyl ester, ethiodide