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Ipratroprium bromide

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Identification
Molecular formula
C20H30NO.
Br
CAS number
1197-21-3
IUPAC name
cyanomethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride
State
State

At room temperature, ipratroripium bromide is in solid form as a crystalline powder.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
430.38g/mol
Molar mass
430.3760g/mol
Density
1.2600g/cm3
Appearence

Ipratroprium bromide appears as a white to off-white crystalline powder. It is hygroscopic and soluble in water and lower alcohols.

Comment on solubility

Solubility of Cyanomethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Chloride

The solubility of cyanomethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride can be quite intriguing. This compound, being a quaternary ammonium salt, typically exhibits properties characteristic of similar compounds:

  • Polar Nature: As a quaternary ammonium salt, the presence of the ammonium ion contributes to its polar characteristics, which generally enhances solubility in polar solvents.
  • Water Solubility: Such ammonium salts are usually soluble in water, making them useful in various aqueous applications. The chloride ion can aid in ion-dipole interactions, allowing for increased solubility.
  • Solvent Compatibility: In addition to water, the compound may also demonstrate solubility in other polar solvents such as methanol or ethanol, but its solubility in organic nonpolar solvents is often limited.

However, the solubility can vary significantly depending on factors such as temperature and concentration. It’s essential to note that while many quaternary ammonium compounds possess good solubility, each compound's unique structure, including steric factors introduced by the bulky (1,7,7-trimethylnorbornan-2-yl) moiety, can influence solubility behavior. As a result:

  • The sterically hindered structure may reduce interaction with solvent molecules, affecting solubility levels.
  • The overall molecular geometry plays a critical role in how well it dissolves in given solvents.

In conclusion, while cyanomethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is likely to exhibit notable solubility in polar solvents, a deeper exploration of its behavior in varying conditions is recommended for candidates looking to utilize this compound effectively.

Interesting facts

Interesting Facts about Cyanomethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Chloride

This compound, known as **cyanomethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride**, exemplifies the fascinating interplay between organic chemistry and materials science. Here are some intriguing details about this unique ammonium salt:

  • Quaternary Ammonium Salt: This compound is classified as a quaternary ammonium salt, which features a nitrogen atom bonded to four organic groups. This structure often imparts unique properties that can enhance solubility, reactivity, and surface activity compared to its tertiary or secondary counterparts.
  • Applications: Quaternary ammonium salts, similar to this compound, are widely utilized in a variety of fields. Their applications include:
    • As surfactants in cleaning products
    • In polymer science for modifying material properties
    • In the formulation of various pharmaceuticals
  • Synthesis Considerations: The synthesis of such complex compounds can be quite challenging, often requiring specific reagents and conditions. This may involve multi-step reactions that could incorporate various functional groups, making organic synthesis an exciting area of study.
  • Environmental Impact: Understanding the behavior and potential impact of quaternary ammonium compounds on the environment is a growing area of research. These compounds can display antimicrobial properties, but their long-term effects on ecosystems are not yet fully understood, necessitating further investigation.
  • Structural Intricacy: The presence of the norbornane structure in this compound contributes to its steric attributes, often leading to interesting conformational dynamics that can alter its chemical reactivity—an intriguing aspect for chemists.

Overall, cyanomethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride represents a significant area of study for those interested in the synthesis and application of specialty organic compounds. As highlighted by one chemist, “The potential for innovation lies in our ability to explore and manipulate these molecular frameworks.” This spirit of exploration is what drives many within the field!

Synonyms
(+-)-endo-(2-Bornylamino)acetonitrile hydrochloride
24629-60-5
ACETONITRILE, (2-BORNYLAMINO)-, HYDROCHLORIDE, endo-(+-)-
RefChem:316835