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Fluoroethylammonium chloride

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Identification
Molecular formula
C3H9ClFNO2
CAS number
51542-52-0
IUPAC name
(2-carboxy-2-fluoro-ethyl)ammonium;chloride
State
State

At room temperature, fluoroethylammonium chloride is in a solid state.

Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
204.00
Boiling point (Kelvin)
477.15
General information
Molecular weight
115.53g/mol
Molar mass
115.5300g/mol
Density
1.2500g/cm3
Appearence

Fluoroethylammonium chloride typically appears as a white crystalline solid.

Comment on solubility

Solubility of (2-carboxy-2-fluoro-ethyl)ammonium;chloride

The solubility of (2-carboxy-2-fluoro-ethyl)ammonium chloride can be impacted by several important factors. This compound is expected to exhibit a certain degree of solubility in various solvents due to the presence of both ionic and polar functional groups.

  • Ionic Nature: The ammonium cation contributes to its solubility in polar solvents like water. Ammonium salts are generally soluble in water due to their ability to form hydrogen bonds.
  • Hydrophilicity: The carboxylic acid group can enhance solubility by promoting interactions with water molecules, thanks to its polar -COOH functional group.
  • Temperature Dependency: Solubility may increase with temperature, which is common for many ionic compounds, allowing more solute to dissolve in solvent.
  • pH Sensitivity: The solubility could vary depending on the pH of the solution, as the protonation state of the carboxylic acid group may change, affecting its interaction with water.

In summary, the solubility of (2-carboxy-2-fluoro-ethyl)ammonium chloride is likely high in polar solvents, particularly water, influenced by factors such as temperature, pH, and the ionic and polar nature of its functional groups.

Interesting facts

Interesting Facts about (2-Carboxy-2-fluoro-ethyl)ammonium Chloride

(2-carboxy-2-fluoro-ethyl)ammonium chloride is a fascinating compound with unique properties and applications. Here are some interesting aspects worth noting:

  • Fluoro-Substituent: The presence of a fluorine atom in the ethyl group enhances the compound's reactivity. Fluorinated compounds often exhibit distinctive physical and chemical properties due to the electronegativity of fluorine, making them valuable in various fields.
  • Ammonium Ion: The ammonium part of the compound lends biological significance, as ammonium ions are essential in various biochemical processes. This enhances the compound's potential use in pharmaceuticals and biochemistry.
  • Acid-Base Behavior: The carboxylic acid group (-COOH) in the compound can have important acid-base properties. This group is known for undergoing deprotonation under basic conditions, which could be significant in drug formulation and chemical synthesis.
  • Potential Applications: Compounds with similar structures are often studied for their roles in medicinal chemistry. Their ability to interact with biological molecules makes them candidates for research in antibiotic development or drug delivery systems.
  • Research Interest: Scientists are actively investigating fluorinated compounds due to their stability, lipophilicity, and bioactivity. They offer unique benefits in the design of agrochemicals and pharmaceuticals.

In conclusion, (2-carboxy-2-fluoro-ethyl)ammonium chloride is a compound that encapsulates the intersection of organic chemistry, biochemistry, and pharmacology. Its intriguing properties make it a subject of ongoing research and exploration.

Synonyms
Fluoro-beta-alanine hydrochloride
(2-carboxy-2-fluoroethyl)azanium;chloride
Propanoic acid, 3-amino-2-fluoro-, hydrochloride
3-Amino-2-fluoro-propanoic acid Hydrochloride
beta-ALANINE, 2-FLUORO-, HYDROCHLORIDE
2-carboxy-2-fluoroethanaminium chloride