Skip to main content

Carbachol

ADVERTISEMENT
Identification
Molecular formula
C6H16N2O2S
CAS number
51-83-2
IUPAC name
2-(4,5-dihydro-1H-imidazol-1-ium-2-ylsulfanyl)ethyl-trimethyl-ammonium;dibromide
State
State

At room temperature, Carbachol is typically in a solid state as a crystalline powder.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.00
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.00
General information
Molecular weight
257.26g/mol
Molar mass
257.1250g/mol
Density
1.2000g/cm3
Appearence

Carbachol typically appears as a white or off-white crystalline powder. It is a hygroscopic compound, meaning it can absorb moisture from the air.

Comment on solubility

Solubility of 2-(4,5-dihydro-1H-imidazol-1-ium-2-ylsulfanyl)ethyl-trimethyl-ammonium;dibromide

The solubility of the compound 2-(4,5-dihydro-1H-imidazol-1-ium-2-ylsulfanyl)ethyl-trimethyl-ammonium;dibromide can be characterized by its ionic nature, as indicated by the presence of dibromide (Br-) counterions. Generally, ionic compounds tend to exhibit high solubility in polar solvents, particularly water. This phenomenon results from the ability of polar solvents to stabilize the ions in solution.

Key factors influencing the solubility of this compound include:

  • Polarity: The presence of charged species often enhances solubility in aqueous environments.
  • Hydrogen bonding: Functional groups within the imidazolium ring can engage in hydrogen bonding, further promoting solubility in certain solvents.
  • Temperature: Increasing temperatures can often increase the kinetic energy of solute molecules, thus enhancing solubility.

In practical applications, the solubility of this compound may allow for effective utilization in various chemical processes where ionic interactions and solvation are essential. However, it is crucial to assess solubility under specific conditions as it can vary significantly, thus influencing its behavior in different solvent systems.

As a noteworthy quote in the realm of solubility science, "Like dissolves like," meaning that polar solvents are more likely to dissolve polar compounds, which is pertinent here in exploring the solubility phenomena of this ammonium salt.

Interesting facts

Interesting Facts about 2-(4,5-Dihydro-1H-imidazol-1-ium-2-ylsulfanyl)ethyl-trimethyl-ammonium; dibromide

This compound, a fascinating quaternary ammonium salt, showcases the intricate relationship between organic chemistry and medicinal applications. Here are some engaging facts about it:

  • Structural Diversity: The presence of a 4,5-dihydro-1H-imidazolium moiety adds unique properties to this compound, making it a potential candidate for various pharmacological applications.
  • Potential Biological Activity: Quaternary ammonium compounds often display antimicrobial properties. This could open avenues for its use in developing disinfectants or antimicrobial agents.
  • Salt Formation: As a dibromide salt, it indicates that the compound has a high stability profile, facilitating easier manipulation for synthesis. The bromide ions can also be exchanged with other ionic species, leading to variations of the compound with potentially different properties.
  • Charge Distribution: The positive charge on the nitrogen atom within the quaternary ammonium structure contributes to its solubility characteristics and interactions with biological molecules, which is crucial for drug design.
  • Applications in Synthesis: It may serve as a useful intermediate in organic synthesis, particularly in creating more complex molecules in pharmaceutical development or materials science.
  • Research Interest: Compounds like this are frequently the subject of study in advanced materials and surface chemistry due to their surface-active properties.

As research progresses, the understanding of compounds such as 2-(4,5-dihydro-1H-imidazol-1-ium-2-ylsulfanyl)ethyl-trimethyl-ammonium; dibromide continues to grow, paving the way for innovative uses in various scientific fields.

Synonyms
2-(2'-Trimethylaminoethylthio)imidazoline bromide hydrobromide
18129-32-3
(2-(2-Imidazolin-2-ylthio)ethyl)trimethylammonium bromide hydrobromide
AMMONIUM, (2-(2-IMIDAZOLIN-2-YLTHIO)ETHYL)TRIMETHYL-, BROMIDE, MONOHYDROBROMIDE
Ethanaminium, 2-((4,5-dihydro-1H-imidazol-2-yl)thio)-N,N,N-trimethyl-, bromide, hydrobromide