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Iopanoic acid

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Identification
Molecular formula
C11H12I3NO2Na
CAS number
96-83-3
IUPAC name
sodium;2-[[3-(butanoylamino)-2,4,6-triiodo-phenyl]methyl]butanoate
State
State

At room temperature, Iopanoic acid is typically a solid.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.15
Boiling point (Celsius)
975.00
Boiling point (Kelvin)
1 248.15
General information
Molecular weight
821.93g/mol
Molar mass
821.9270g/mol
Density
2.3400g/cm3
Appearence

Iopanoic acid appears as a white or off-white crystalline powder.

Comment on solubility

Solubility of Sodium 2-[[3-(butanoylamino)-2,4,6-triiodo-phenyl]methyl]butanoate

The compound Sodium 2-[[3-(butanoylamino)-2,4,6-triiodo-phenyl]methyl]butanoate exhibits intriguing solubility properties, primarily influenced by its unique molecular structure. Here are some key points regarding its solubility:

  • Polar Nature: The presence of a sodium ion and polar functional groups in the compound suggests a tendency towards solubility in polar solvents like water.
  • Iodine Substituents: With the incorporation of tri-iodinated phenyl groups, solubility might be modified due to their hydrophobic characteristics, potentially decreasing aqueous solubility.
  • Amine Group: The butanoylamino group can contribute to solubility as it can interact with water through hydrogen bonding, enhancing miscibility in aqueous solutions.

Overall, the solubility of this compound is expected to be a balance of hydrophilic and hydrophobic interactions. Consequently, it may show a higher solubility in organic solvents compared to pure water, although its sodium salt form generally favors solubility in aqueous environments. Understanding these solubility dynamics is crucial in applications ranging from pharmaceuticals to environmental chemistry.

Interesting facts

Exploring Sodium 2-[[3-(butanoylamino)-2,4,6-triiodo-phenyl]methyl]butanoate

Sodium 2-[[3-(butanoylamino)-2,4,6-triiodo-phenyl]methyl]butanoate, commonly referred to in scientific circles for its complex structure and potential applications, is a fascinating compound that intersects various fields of chemistry, including medicinal and analytical chemistry. Here are some intriguing aspects of this chemical:

  • Structure Madness: This compound features a triiodo-substituted phenyl group, yielding three iodine atoms attached to the aromatic ring. This unique characteristic enhances its *intermolecular interactions*, making it an interesting target for research.

  • Bioactive Potential: Compounds with iodine-bearing groups often demonstrate enhanced biological activity. This aspect sparks interest in its potential use as an *antimicrobial agent* or in *cancer therapy*, highlighting the ongoing quest for effective pharmaceuticals.

  • Drug Delivery Capabilities: The butanoylamino moiety in this compound may facilitate drug delivery due to its lipophilicity. The ability to traverse cell membranes is crucial in designing new therapeutic agents.

  • Radiological Applications: With iodine playing a pivotal role in imaging techniques, the *triiodo* arrangement opens avenues in *medical imaging*. It could potentially be used as a contrast agent for various diagnostic procedures.

  • Research Noteworthiness: Compounds like sodium 2-[[3-(butanoylamino)-2,4,6-triiodo-phenyl]methyl]butanoate represent the forefront of *synthetic organic chemistry*. They help scientists explore novel pathways for creating complex molecules, pushing the boundaries of what's possible in chemical synthesis.

In summary, sodium 2-[[3-(butanoylamino)-2,4,6-triiodo-phenyl]methyl]butanoate is not just a compound; it encapsulates the *intricacies of chemical innovation*, reminding us of the *endless possibilities* within the realm of chemistry. As research progresses, this molecule could unveil even more secrets, paving the way for groundbreaking applications.