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Brimonidine tartrate

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Identification
Molecular formula
C15H21BrClN2
CAS number
79517-01-4
IUPAC name
2-[(4-bromophenyl)methyl-(2-pyridyl)amino]ethyl-dimethyl-ammonium;chloride
State
State

Under standard conditions, this compound is typically encountered as a crystalline solid.

Melting point (Celsius)
257.00
Melting point (Kelvin)
530.15
Boiling point (Celsius)
174.20
Boiling point (Kelvin)
447.35
General information
Molecular weight
442.24g/mol
Molar mass
442.2400g/mol
Density
0.1771g/cm3
Appearence

The compound appears as a crystalline solid, often white to off-white in color.

Comment on solubility

Solubility of 2-[(4-bromophenyl)methyl-(2-pyridyl)amino]ethyl-dimethyl-ammonium;chloride

The solubility of 2-[(4-bromophenyl)methyl-(2-pyridyl)amino]ethyl-dimethyl-ammonium;chloride can be influenced by several factors. Typically, ammonium-based compounds like this one exhibit notable solubility characteristics in polar solvents due to their ionic nature.

Key Points on Solubility:

  • Solvent Influence: This compound is likely quite soluble in water and other polar solvents because of its ionic quaternary ammonium structure.
  • Temperature: Increased temperatures can enhance solubility by providing the necessary energy to break intermolecular interactions.
  • pH Levels: The solubility may also change with varying pH levels, especially if any protonation states influence the compound's stability in solution.
  • Concentration: At higher concentrations, solubility limits may be reached, leading to precipitate formation.

As a general observation, compounds of this structure commonly exhibit good aqueous solubility, which can be advantageous for various applications in medicinal and industrial chemistry. Understanding these solubility properties ensures proper formulation and utilization in practical scenarios.

Interesting facts

Interesting Facts About 2-[(4-bromophenyl)methyl-(2-pyridyl)amino]ethyl-dimethyl-ammonium Chloride

This intriguing compound, often referred to as a quaternary ammonium salt, exhibits interesting properties and applications within the realms of chemistry and pharmacology. Here are some notable highlights:

  • Quaternary Ammonium Compounds: This compound belongs to a class of quaternary ammonium salts, which are known for their surfactant and anti-microbial properties. They are commonly used in disinfectants and antiseptics.
  • Potential Biological Activity: The presence of the 4-bromophenyl group suggests potential interactions with biological systems. Research indicates that brominated compounds can exhibit varied pharmacological activities, making this compound a candidate for drug development.
  • Structure-Activity Relationship: The combination of the 2-pyridyl moiety and the dimethylammonium functionality may influence its binding affinity and selectivity towards certain biological targets. Understanding these relationships is vital in medicinal chemistry.
  • Electrostatic Properties: The positively charged nitrogen in the dimethylammonium unit is significant for interaction with negatively charged biological membranes and biomolecules, helping in drug delivery applications.

As a chemist or a student exploring this compound, one could examine its synthesis and reactivity further:

  • Synthesis Techniques: Various synthetic routes can lead to the formation of this compound, involving nucleophilic substitution reactions that highlight the importance of functional group transformations.
  • Analytical Methods: Techniques such as NMR spectroscopy and mass spectrometry can be utilized to confirm the structure and purity of this compound during synthesis and application studies.

In conclusion, 2-[(4-bromophenyl)methyl-(2-pyridyl)amino]ethyl-dimethyl-ammonium chloride is not just a curious chemical entity but also a point of interest in ongoing research related to pharmacology and material science. This compound exemplifies the fusion of organic chemistry and biological applications, opening avenues for innovative discoveries.

Synonyms
Hibernon hydrochloride
Bromobenzyl D.P.E. hydrochloride
14612-92-1
N-p-Bromobenzyl-N',N'-dimethyl-N-2-pyridylethylenediamine hydrochloride
N,N-Dimethyl-N'-(p-bromobenzyl)-N'-(2-pyridyl)ethylenediamine hydrochloride
Pyridine, 2-((p-bromobenzyl)(2-(dimethylamino)ethyl)amino)-, hydrochloride
ETHYLENEDIAMINE, N-(p-BROMOBENZYL)-N',N'-DIMETHYL-N-(2-PYRIDYL)-, HYDROCHLORIDE
N-p-Brombenzyl-N-alpha-pyridyl-N',N'-dimethyl-aethylendiamin-hydrochloride [German]
N-p-Brombenzyl-N-alpha-pyridyl-N',N'-dimethyl-aethylendiamin-hydrochloride