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Bis(2-fluoroethyl)phenylammonium chloride

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Identification
Molecular formula
C10H14ClF2N
CAS number
198478-55-6
IUPAC name
bis(2-fluoroethyl)-phenyl-ammonium;chloride
State
State

At room temperature, Bis(2-fluoroethyl)phenylammonium chloride is usually in a solid state. It is a crystalline compound, indicating its organized and structured formation.

Melting point (Celsius)
125.00
Melting point (Kelvin)
398.00
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.00
General information
Molecular weight
221.68g/mol
Molar mass
221.6810g/mol
Density
1.1900g/cm3
Appearence

Bis(2-fluoroethyl)phenylammonium chloride typically appears as a white to off-white crystalline powder. The compound is known for its solubility in water and may form a clear solution when dissolved.

Comment on solubility

Solubility of bis(2-fluoroethyl)-phenyl-ammonium;chloride

The solubility of bis(2-fluoroethyl)-phenyl-ammonium;chloride in various solvents provides insights into its potential applications and behavior in different environments.

This compound is generally known to exhibit moderate solubility in polar solvents, particularly due to the presence of the ammonium group, which can engage in strong hydrogen bonding interactions. Its solubility can be analyzed through the following factors:

  • Polar Solvents: Soluble in water and other polar solvents such as methanol and ethanol due to favorable ion-dipole interactions.
  • Non-Polar Solvents: Limited solubility in non-polar solvents like hexane or benzene, as there is minimal interaction due to the absence of polar characteristics.
  • Concentration Dependence: Higher concentrations may lead to saturation effects, potentially decreasing relative solubility as the solution becomes more concentrated.
  • Temperature Effects: Increasing temperature typically enhances solubility in most cases, though specific studies on this compound are needed for precise evaluations.

In summary, bis(2-fluoroethyl)-phenyl-ammonium;chloride's solubility is significantly influenced by its chemical structure and the nature of the solvent. As with many ionic compounds, understanding its solubility behavior is crucial for applications in fields such as drug design, materials science, and chemical synthesis.

Interesting facts

Interesting Facts about Bis(2-Fluoroethyl)-phenyl-ammonium Chloride

Bis(2-fluoroethyl)-phenyl-ammonium chloride is a fascinating compound with several intriguing aspects worth exploring. Here are some key highlights:

  • Unique Structure: This compound features a central nitrogen atom bonded to two 2-fluoroethyl groups and a phenyl group, giving it a distinctive structure that can influence its chemical behavior dramatically.
  • Applications in Industry: Due to its unique properties, this compound has found relevance in various industries, particularly in the field of materials science and pharmaceuticals. It can serve as a useful intermediate in the synthesis of more complex molecular architectures.
  • Fluorine's Influence: The presence of fluorine atoms can significantly alter the compound's reactivity and stability. Fluorinated compounds often exhibit high lipophilicity, which can enhance their effectiveness in biological systems.
  • Potential in Drug Development: Compounds containing both quaternary ammonium and fluorine elements can exhibit interesting antimicrobial and antifungal properties, making them potential candidates for new therapeutic agents.
  • Research Insights: Scientists continue to study bis(2-fluoroethyl)-phenyl-ammonium chloride to uncover its full potential. Research often focuses on its mechanism of action, interactions with biological molecules, and overall environmental impact.

As our understanding of compounds like bis(2-fluoroethyl)-phenyl-ammonium chloride deepens, we may unlock innovative applications that could positively influence both industry and health. Its unique characteristics stand as a reminder of the endless possibilities that chemical compounds can offer.

Synonyms
N,N-Bis(2-fluoroethyl)aniline hydrochloride
1201-66-7
ANILINE, N,N-BIS(2-FLUOROETHYL)-, HYDROCHLORIDE