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Brompheniramine maleate

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Identification
Molecular formula
C21H23BrClNO2
CAS number
86-22-6
IUPAC name
(4-bromophenyl)methyl-(2-chloroethyl)-[2-(2-isopropyl-5-methyl-phenoxy)ethyl]ammonium;chloride
State
State

At room temperature, this compound is in a solid state, specifically a crystalline powder. It is stable under normal conditions but should be stored in a cool, dry place to avoid degradation.

Melting point (Celsius)
115.50
Melting point (Kelvin)
388.65
Boiling point (Celsius)
774.15
Boiling point (Kelvin)
1 047.30
General information
Molecular weight
435.83g/mol
Molar mass
435.8290g/mol
Density
1.2340g/cm3
Appearence

This compound appears as a white to off-white crystalline powder. It is typically odorless and hygroscopic, meaning it can absorb moisture from the environment.

Comment on solubility

Solubility Characteristics

The compound (4-bromophenyl)methyl-(2-chloroethyl)-[2-(2-isopropyl-5-methyl-phenoxy)ethyl]ammonium;chloride exhibits interesting solubility properties that are worth noting. As a quaternary ammonium salt, its solubility can be influenced by the following factors:

  • Polarity: The presence of both bromine and chlorine atoms enhances the compound's polarity, which generally favors solubility in polar solvents such as water.
  • Ionic Characteristics: Being a chloride salt, it typically dissolves well in aqueous solutions due to the dissociation of the ammonium ion and chloride ion.
  • Hydrophobic Interactions: The isopropyl and phenyl groups contribute to hydrophobic characteristics, which can lead to lower solubility in non-polar solvents.

Overall, the compound is expected to be soluble in water but may have reduced solubility in organic solvents. This solubility profile makes it suitable for applications in various aqueous environments, while its hydrophobic parts can contribute to interactions with lipophilic systems.

In summary, the solubility of (4-bromophenyl)methyl-(2-chloroethyl)-[2-(2-isopropyl-5-methyl-phenoxy)ethyl]ammonium;chloride can be categorized as follows:

  1. High solubility in water
  2. Moderate solubility in polar organic solvents
  3. Low solubility in non-polar solvents

These characteristics make this compound versatile for various chemical applications, particularly in biological and medicinal chemistry.

Interesting facts

Interesting Facts About (4-bromophenyl)methyl-(2-chloroethyl)-[2-(2-isopropyl-5-methyl-phenoxy)ethyl]ammonium;chloride

This compound is a fascinating example within the realm of organic chemistry, particularly due to its complex structure and its potential applications in various fields:

  • Pharmaceutical Potential: Compounds like this one are often studied for their pharmacological effects. Their unique functional groups can lead to specific interactions with biological systems, making them candidates for drug development.
  • Structural Complexity: The intricate arrangement of bromine and chlorine atoms, coupled with phenoxy groups, showcases the creativity in synthetic organic chemistry. This complexity can lead to diverse chemical properties and reactivities.
  • Ammonium Cation: The presence of the ammonium ion adds to the compound's solubility in polar solvents, potentially influencing its behavior in biological and environmental contexts.
  • Research Applications: This type of compound can be utilized in research settings, particularly in studies investigating receptor interactions, as the varying substituents can modify binding affinities and selectivities.
  • Environmental Chemistry: Understanding the degradation pathways of such compounds in the environment could yield important insights into their ecological impact, especially given the presence of halogens which often exhibit persistence.

In summary, the compound (4-bromophenyl)methyl-(2-chloroethyl)-[2-(2-isopropyl-5-methyl-phenoxy)ethyl]ammonium;chloride serves as a prime example of how complex organic molecules can intersect multiple disciplines, enhancing our understanding of both chemical properties and potential applications.

Synonyms
16793-70-7
p-Bromo-N-(2-chloroethyl)-N-(2-(p-cymene-3-yloxy)ethyl)benzylamine hydrochloride
WV 820
Benzylamine, p-bromo-N-(2-chloroethyl)-N-(2-(p-cymene-3-yloxy)ethyl)-, hydrochloride