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Ambroxol hydrobromide

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Identification
Molecular formula
C12H26N3S+Br2-
CAS number
50922-51-7
IUPAC name
3-(4,5-dihydro-1H-imidazol-1-ium-2-ylsulfanyl)propyl-trimethyl-ammonium;dibromide
State
State

At room temperature, this compound is typically found in a solid state. Its crystalline powder form makes it easy to handle for various pharmaceutical applications.

Melting point (Celsius)
232.00
Melting point (Kelvin)
505.15
Boiling point (Celsius)
268.30
Boiling point (Kelvin)
541.45
General information
Molecular weight
438.20g/mol
Molar mass
438.1990g/mol
Density
1.3000g/cm3
Appearence

This compound appears as a white, crystalline powder. It is typically odorless and may have a slightly bitter taste. Its fine crystalline nature contributes to its easy solubility in water.

Comment on solubility

Solubility of 3-(4,5-dihydro-1H-imidazol-1-ium-2-ylsulfanyl)propyl-trimethyl-ammonium;dibromide

The compound 3-(4,5-dihydro-1H-imidazol-1-ium-2-ylsulfanyl)propyl-trimethyl-ammonium;dibromide exhibits interesting solubility characteristics primarily due to its ionic nature and molecular structure. Here are some key points to consider:

  • Ionic Nature: As a dibromide, this compound features ionic bonds which typically enhance solubility in polar solvents.
  • Polar Solvents: Compounds of this type are generally soluble in water and other polar solvents, owing to the positive charge on the ammonium group and the negative charges from bromide ions. This facilitates interaction with water molecules.
  • Hydrophobic Elements: The presence of hydrocarbon chains or groups can result in reduced solubility in non-polar solvents due to hydrophobic interactions, which can limit its use in organic solvents.
  • Temperature Influences: Solubility can vary with temperature; generally, increasing temperature can lead to higher solubility for ionic compounds.

In summary, the solubility of 3-(4,5-dihydro-1H-imidazol-1-ium-2-ylsulfanyl)propyl-trimethyl-ammonium;dibromide is significantly influenced by its ionic character, with good solubility expected in aqueous environments while being less soluble in non-polar solvents. The ability to dissolve in polar solvents underscores its potential applications in various chemical processes.

Interesting facts

Interesting Facts about 3-(4,5-dihydro-1H-imidazol-1-ium-2-ylsulfanyl)propyl-trimethyl-ammonium;dibromide

This compound, whose name can be quite a mouthful, is involved in a variety of chemical and biological applications due to its distinctive structures and properties. Here are some fascinating aspects about it:

  • Dual Functionality: The presence of both ammonium and imidazolium moieties provides the compound with unique characteristics that make it a potential candidate for various applications in medicinal chemistry.
  • Electrolytic Properties: As a quaternary ammonium compound, it can act as a good electrolytic agent, enhancing its usefulness in electrochemical systems and applications such as batteries.
  • Biocompatibility: Compounds like this one are often evaluated for their biocompatibility, especially in drug delivery systems, where they may facilitate the transport of therapeutic agents across biological membranes.
  • Catalytic Roles: Its structure may also enable it to function as a catalyst in various organic reactions, potentially streamlining synthesis processes in organic chemistry.
  • Antimicrobial Potential: Many ammonium compounds exhibit antimicrobial properties, suggesting that this compound could be explored for antimicrobial and antifungal activities.

In summary, 3-(4,5-dihydro-1H-imidazol-1-ium-2-ylsulfanyl)propyl-trimethyl-ammonium;dibromide is more than just a chemical formula; it represents a bridge between synthetic chemistry and biological applications. The ongoing research into its properties and potential applications continues to excite scientists and chemists alike as they uncover its secrets.

Synonyms
USAF IN-9
2-IMIDAZOLINE, 2-(3-TRIMETHYLAMINOPROPYLTHIO)-, DIHYDROBROMIDE
6305-01-7
NSC 43175
1,3-Ethylene-2-(3-trimethylamino)propylisothiouronium dibromide
Pseudourea, 2-thio-1,3-ethylene-2-(3-trimethylamino)propyl-, dibromide
1-Propanaminium, 3-((4,5-dihydro-1H-imidazol-2-yl)thio)-N,N,N-trimethyl-, bromide, monohydrobromide
1-Propanaminium, 3-((4,5-dihydro-1H-imidazol-2-yl)thio)-N,N,N-trimethyl-, bromide, monohydrochloride