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Chlorphenesin carbamate

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Identification
Molecular formula
C17H20ClNO4
CAS number
886-74-8
IUPAC name
[(4-chlorophenyl)-phenyl-methyl]-[2-(dimethylammonio)ethyl]-methyl-ammonium;2-hydroxy-2-oxo-acetate
State
State

At room temperature, chlorphenesin carbamate is generally a solid. It is stable under normal temperatures and pressures if kept dry.

Melting point (Celsius)
107.00
Melting point (Kelvin)
380.15
Boiling point (Celsius)
180.00
Boiling point (Kelvin)
453.15
General information
Molecular weight
334.83g/mol
Molar mass
334.8270g/mol
Density
1.1200g/cm3
Appearence

Chlorphenesin carbamate typically appears as a white or almost white crystalline powder. It is somewhat hygroscopic, meaning it can absorb moisture from the air.

Comment on solubility

Solubility of [(4-chlorophenyl)-phenyl-methyl]-[2-(dimethylammonio)ethyl]-methyl-ammonium; 2-hydroxy-2-oxo-acetate

The solubility of [(4-chlorophenyl)-phenyl-methyl]-[2-(dimethylammonio)ethyl]-methyl-ammonium; 2-hydroxy-2-oxo-acetate is a multifaceted topic due to the complexity of its structure. This compound contains both hydrophobic and hydrophilic regions, influencing its behavior in various solvents.

Factors Influencing Solubility

Key points to consider when evaluating the solubility of this compound include:

  • Polarity: The presence of the dimethylammonio group increases polarity, making the compound more soluble in polar solvents like water.
  • Hydrophobic Interactions: The phenyl and chlorophenyl groups contribute hydrophobic characteristics, potentially lowering solubility in water but enhancing it in organic solvents.
  • Ionization: The ammonium component is likely to become ionized in a standard aqueous environment, which can further affect solubility depending on pH levels.
  • Temperature: Like many compounds, solubility may vary with temperature, often increasing at higher temperatures.

In summary, while the solubility of this compound in water could be moderate due to its ionic nature, it is expected to show better solubility in polar organic solvents due to the combined effects of its structural elements. This dual character is crucial in understanding how it behaves during dissolution and in various chemical reactions.

Interesting facts

Interesting Facts about [(4-chlorophenyl)-phenyl-methyl]-[2-(dimethylammonio)ethyl]-methyl-ammonium; 2-hydroxy-2-oxo-acetate

This intriguing chemical compound showcases the fascinating intersection of organic chemistry and medicinal applications. Its structure incorporates both aromatic and quaternary ammonium components, contributing to its unique properties and potential effectiveness in various domains.

Key Features:

  • Aromatic Compounds: The presence of the 4-chlorophenyl and phenyl groups enhances the electronic properties, making them interesting for studies related to electron transfer and molecular interactions.
  • Quaternary Ammonium Structure: This structure provides the compound with cationic characteristics, potentially lending it efficacy in biological systems, such as surfactancy or antimicrobial activity.
  • Applications: Compounds similar to this one have been studied for their roles in drug design, particularly as antibacterial agents or in cancer therapeutics due to their ability to permeate cell membranes.
  • Antioxidant Properties: The inclusion of the 2-hydroxy-2-oxo-acetate group suggests that this compound may exhibit oxidation-reduction properties, making it relevant in studies related to oxidative stress and cellular aging.
  • Research Potential: Scientists are continually exploring the multifaceted uses of such compounds in materials science, pharmacology, and the development of new therapeutic agents.

In summary, the intricate details of [(4-chlorophenyl)-phenyl-methyl]-[2-(dimethylammonio)ethyl]-methyl-ammonium; 2-hydroxy-2-oxo-acetate not only reveal its complexity but also highlight the ongoing synergy between chemical structure and functional application in diverse scientific fields. The dynamic nature of its components propels it into various research and industrial settings, making it a compound worthy of continued observation and exploration.

Synonyms
N-(alpha-(p-Chlorophenyl)benzyl)-N,N',N'-trimethylethylenediamine dioxalate
ETHYLENEDIAMINE, N-(alpha-(p-CHLOROPHENYL)BENZYL)-N,N',N'-TRIMETHYL-, DIOXALATE
23892-35-5
RefChem:345274