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Aminoethyl bromide

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Identification
Molecular formula
C4H11BrN
CAS number
5407-14-9
IUPAC name
amino-(2-bromoethyl)-dimethyl-ammonium
State
State

Aminoethyl bromide is typically a liquid at room temperature, with a consistency that may vary slightly depending upon environmental conditions and impurities present.

Melting point (Celsius)
-49.00
Melting point (Kelvin)
224.20
Boiling point (Celsius)
138.00
Boiling point (Kelvin)
411.20
General information
Molecular weight
153.05g/mol
Molar mass
153.0460g/mol
Density
1.6200g/cm3
Appearence

Aminoethyl bromide typically appears as a colorless to light yellow liquid that might emit a pungent odor. It may form crystals upon cooling, depending on the purity and environmental conditions.

Comment on solubility

Solubility of Amino-(2-bromoethyl)-dimethyl-ammonium

Amino-(2-bromoethyl)-dimethyl-ammonium, a quaternary ammonium compound, exhibits interesting solubility characteristics. Its solubility can generally be influenced by several key factors:

  • Polarity: Being a quaternary ammonium compound, it possesses a positively charged ammonium group. This feature enhances its solubility in polar solvents such as water, although its bromine substituent may impart some hydrophobic character.
  • Lattice Energy: The ionic interactions formed due to the charge on the ammonium group can affect solubility. A higher lattice energy may lead to lower solubility, whereas lower lattice energy typically results in greater solubility.
  • Temperature: Like many compounds, solubility may increase with temperature. Thus, heating the solvent could potentially enhance the solubility of amino-(2-bromoethyl)-dimethyl-ammonium.
  • pH Level: The solubility can also depend on the pH of the solution, as changes in pH might alter the ionization state of the compound.

It is essential to note that the presence of the bromine atom may contribute to a complex solubility profile, which could lead to significant variation in solubility depending on the solvent used. In summary, "the solubility of amino-(2-bromoethyl)-dimethyl-ammonium is primarily dictated by its structural characteristics and the interactions it forms in various solvent environments."


Interesting facts

Interesting Facts about Amino-(2-bromoethyl)-dimethyl-ammonium

Amino-(2-bromoethyl)-dimethyl-ammonium is a fascinating compound that highlights the intersection of organic chemistry and medicinal applications. With its unique structure, it serves as a versatile building block in various synthetic pathways.

Key Features

  • Quaternary Ammonium Compound: This compound belongs to a class of quaternary ammonium compounds, which are known for their antimicrobial and surfactant properties, making them valuable in the pharmaceutical and agricultural sectors.
  • Potential Applications: Its reactivity can be harnessed in the synthesis of biocides, surfactants, and as a precursor in the development of drugs, especially those targeting neurodegenerative diseases.
  • Importance in Research: Due to its bromine substitution, it acts as an electrophile, opening avenues for further derivatization and exploration in synthetic organic chemistry.

Scientific Exploration

This compound illustrates the **versatility of halogenated compounds** in organic synthesis. As scientists explore its properties, they often emphasize the following:

  • Reactivity: The presence of a bromine atom can significantly influence the compound’s reactivity, making it a subject of interest for investigations into nucleophilic substitutions.
  • Biological Interaction: Researchers are delving into how quaternary ammonium compounds interact with cellular membranes, which could lead to a better understanding of drug delivery mechanisms.
  • Synthetic Pathways: A thorough understanding of its synthetic routes can inspire innovative approaches in designing better therapeutic agents.

In summary, amino-(2-bromoethyl)-dimethyl-ammonium is not only a compound of significant chemical interest but also an essential tool for the advancement of much-needed research and applications in various fields. Its unique characteristics offer endless possibilities for chemists and researchers alike. As the field progresses, keeping an eye on such compounds can provide insight into future innovations!

Synonyms
SCHEMBL11254192