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Brompheniramine maleate

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Identification
Molecular formula
C16H20BrNO.Cl
CAS number
86-22-6
IUPAC name
2-[1-(4-bromophenyl)-1-phenyl-ethoxy]ethyl-dimethyl-ammonium;chloride
State
State

At room temperature, brompheniramine maleate is typically found in a solid state, presented as a fine powder or small crystalline structures.

Melting point (Celsius)
115.00
Melting point (Kelvin)
388.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
435.79g/mol
Molar mass
435.7890g/mol
Density
1.3000g/cm3
Appearence

The compound typically appears as a white to off-white crystalline powder. It is odorless and its appearance can vary slightly based on purity and environmental conditions.

Comment on solubility

Solubility of 2-[1-(4-bromophenyl)-1-phenyl-ethoxy]ethyl-dimethyl-ammonium;chloride

The solubility of 2-[1-(4-bromophenyl)-1-phenyl-ethoxy]ethyl-dimethyl-ammonium chloride can be influenced by several factors. Here are some key points to consider:

  • Polarity: The presence of a quaternary ammonium group in this compound makes it relatively polar, suggesting a likelihood of solubility in polar solvents like water.
  • Solvent Interaction: It is essential to consider the interaction between the solvent and solute. For example, hydrogen bonding and ionic interactions can enhance solubility in aqueous environments.
  • Temperature: Generally, increasing temperature can improve solubility for ionic compounds, which may apply to this ammonium salt.
  • Hydrophobic Regions: The aromatic groups in its structure could make the compound less soluble in highly polar solvents, suggesting that it may show better solubility in organic solvents.

In practical applications, determining the solubility of this compound would involve experimentally testing it in various solvents under controlled conditions. The specific solubility behavior could be critical for its utilization in chemical processes or medicinal applications.

Interesting facts

Interesting Facts about 2-[1-(4-bromophenyl)-1-phenyl-ethoxy]ethyl-dimethyl-ammonium;chloride

This compound is a fascinating example of a quaternary ammonium compound, which distinguishes itself with a range of interesting properties and applications. Quaternary ammonium compounds like this one are typically employed in various fields, including:

  • Antimicrobial Agents: These compounds are frequently used in disinfectants due to their ability to effectively kill bacteria and fungi.
  • Surfactants: The structure allows for oil and water miscibility, making them valuable in detergents and personal care products.
  • Pharmaceuticals: They have potential use in drug formulation, increasing the solubility and bioavailability of certain medications.

One of the compelling aspects of this compound is its functionalized aromatic ring, which not only contributes to its unique properties but also illustrates the versatility of organic chemistry in manipulating molecular structures to achieve desired chemical behaviors. Furthermore, the presence of the bromophenyl group suggests interesting interactions that can be explored in medicinal chemistry.

Insights into Its Mechanism

The efficacy of quaternary ammonium compounds in antimicrobial applications is often linked to their ability to disrupt bacterial cell membranes. As they interact with positively charged areas on bacterial surfaces, they can lead to:

  • Increased membrane permeability
  • Leakage of cellular contents
  • Ultimately cell death

This mechanism highlights the critical role of chemical structure in biological activity, and studying compounds like 2-[1-(4-bromophenyl)-1-phenyl-ethoxy]ethyl-dimethyl-ammonium;chloride can lead to innovations in both health and environmental sciences.

In summary, this compound exemplifies the intersection of organic synthetic chemistry and practical applications, providing a fertile ground for both research and industrial use. As scientists continue to explore the functionalities of such compounds, new avenues for enhancing human health and environmental protection are likely to emerge.

Synonyms
Mebryl
EINECS 237-757-3
UNII-7BJ3V657VC
2-(1-(4-Bromodiphenyl)ethoxy)-N,N-dimethylethylamine hydrochloride
p-Bromo-alpha-methylbenzhydryl 2-dimethylaminoethyl ether hydrochloride
(2-(1-p-Bromophenyl-1-phenylethoxy)ethyl)dimethylethylamine hydrochloride
1-(p-Bromophenyl)-1-phenyl-1-(2-dimethylaminoethoxy)ethane hydrochloride
2-(1-(4-Bromophenyl)-1-phenylethoxy)-N,N-dimethylethanamine hydrochloride
beta-Dimethylaminoethyl p-bromo-alpha-methylbenzhydryl ether hydrochloride
Ethanamine, 2-(1-(4-bromophenyl)-1-phenylethoxy)-N,N-dimethyl-, hydrochloride
Ethylamine, 2-((p-bromo-alpha-methyl-alpha-phenylbenzyl)oxy)-N,N-dimethyl-, hydrochloride