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Iopronic acid

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Identification
Molecular formula
C16H19I3N2O6
CAS number
42541-31-3
IUPAC name
2-[3,5-bis(ethylcarbamoyl)-2,4,6-triiodo-phenoxy]butanoic acid
State
State

At room temperature, Iopronic acid is solid. It does not exhibit any volatility under normal conditions and is stable when stored properly, away from light and moisture.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
821.96g/mol
Molar mass
821.9610g/mol
Density
2.0200g/cm3
Appearence

Iopronic acid is a white to off-white crystalline powder. It is known for its high iodine content, which contributes to its substantial density and appears quite dense in powdered form. The compound's crystals are typically shiny, reflecting its crystalline structure.

Comment on solubility

Solubility of 2-[3,5-bis(ethylcarbamoyl)-2,4,6-triiodo-phenoxy]butanoic acid

The solubility of 2-[3,5-bis(ethylcarbamoyl)-2,4,6-triiodo-phenoxy]butanoic acid is an interesting topic due to its unique chemical structure and substituents. Understanding the solubility characteristics of this compound can be summarized through the following points:

  • Polarity: The presence of the ethylcarbamoyl groups may contribute to increased polarity, which typically enhances solubility in polar solvents.
  • Hydrogen Bonding: The functional groups in this compound can also engage in hydrogen bonding with solvents, further influencing its solubility profile.
  • Solvent Compatibility: It is likely more soluble in solvents like dimethyl sulfoxide (DMSO) or methanol compared to non-polar solvents such as hexane.
  • Influence of Iodine Atoms: The presence of three iodine atoms may reduce solubility in aqueous environments due to their bulk and the overall hydrophobic character they impart.

Conclusion: Given these factors, the solubility of 2-[3,5-bis(ethylcarbamoyl)-2,4,6-triiodo-phenoxy]butanoic acid is likely to be moderate in polar organic solvents while it may exhibit low solubility in water. Further solubility experiments would be necessary to ascertain precise values.

Interesting facts

Interesting Facts about 2-[3,5-bis(ethylcarbamoyl)-2,4,6-triiodo-phenoxy]butanoic acid

This fascinating compound, known for its complex structure, offers a unique combination of biological activity and chemical stability. Here are some intriguing aspects that make it stand out in the realm of chemical science:

  • Diverse Applications: 2-[3,5-bis(ethylcarbamoyl)-2,4,6-triiodo-phenoxy]butanoic acid is noteworthy for its potential applications in pharmaceuticals, particularly in drug development targeting specific biological pathways.
  • Biological Activity: Compounds with similar substituents have shown activity against various pathogens, making this compound an interesting candidate for further research in medicinal chemistry.
  • Structural Intricacies: The presence of multiple iodinated phenoxy groups in the compound’s architecture contributes to its unique properties, influencing its reactivity and interactions with biological systems.
  • Ecological Implications: The study of such compounds may also yield insights into environmental chemistry, especially concerning their stability and degradation patterns in natural settings.
  • Research Opportunities: Given its complex structure, this compound presents an exciting opportunity for students and researchers to explore synthetic methods, reaction mechanisms, and structure-activity relationships.

In summary, 2-[3,5-bis(ethylcarbamoyl)-2,4,6-triiodo-phenoxy]butanoic acid represents a fascinating area of study in chemical research, with promising applications in both medicinal chemistry and environmental science. Its intricate structure and diverse potential make it a subject worthy of attention for those venturing into the depths of chemical compounds.