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Iopanoic acid

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Identification
Molecular formula
C11H9I3O3
CAS number
96-83-3
IUPAC name
4-(3-hydroxy-2,4,6-triiodo-phenyl)butanoic acid
State
State

At room temperature, iopanoic acid is in solid state.

Melting point (Celsius)
258.00
Melting point (Kelvin)
531.15
Boiling point (Celsius)
305.60
Boiling point (Kelvin)
578.75
General information
Molecular weight
597.94g/mol
Molar mass
597.9350g/mol
Density
2.2800g/cm3
Appearence

Iopanoic acid appears as a white or off-white crystalline powder. It is typically odorless.

Comment on solubility

Solubility of 4-(3-hydroxy-2,4,6-triiodo-phenyl)butanoic acid

4-(3-hydroxy-2,4,6-triiodo-phenyl)butanoic acid exhibits interesting solubility characteristics that are influenced by its complex structure. Being an organic acid, its solubility can be affected by several factors. Here are some notable points regarding its solubility:

  • Solvent Interaction: This compound may show varying solubility in polar versus non-polar solvents. Typically, organic acids are more soluble in polar solvents due to their ability to form hydrogen bonds.
  • pH Sensitivity: The solubility can vary depending on the pH of the solution. In acidic conditions, it is likely to remain in its undissociated form, while in basic conditions, it can dissociate to form ions, increasing solubility.
  • Temperature Dependence: Like many organic compounds, solubility usually increases with temperature. Careful heating may enhance dissolution.
  • Hydrophobic Character: Due to the presence of multiple iodine atoms, the compound may exhibit some hydrophobic properties, potentially hindering solubility in aqueous solutions.

In conclusion, the solubility of 4-(3-hydroxy-2,4,6-triiodo-phenyl)butanoic acid is a multifaceted topic, depending on the solvent type, pH, temperature, and interactions with other chemical species. As the saying goes, "Like dissolves like," which is particularly relevant when considering the chemical environment of this compound.

Interesting facts

Interesting Facts About 4-(3-Hydroxy-2,4,6-triiodo-phenyl)butanoic Acid

4-(3-Hydroxy-2,4,6-triiodo-phenyl)butanoic acid, often referred to in research contexts for its unique chemical properties, is a fascinating compound with a multitude of applications, particularly in the field of medicinal chemistry. Here are some noteworthy aspects:

  • Structural Significance: The presence of three iodine atoms in its structure makes this compound a member of the halogenated phenyl acids, introducing interesting electronic properties that can affect its reactivity and interaction with biological targets.
  • Biological Applications: Iodinated compounds have garnered attention for their potential uses in pharmaceuticals. This specific compound may influence thyroid hormone interactions due to the high iodine content, which can mimic thyroid hormone action.
  • Developmental Studies: Its role in research has sparked interest due to its potential influence on developmental biology. Studies have indicated that iodine levels play a crucial role in growth and development, especially in prenatal health.
  • Synthesis Interest: The synthesis of this compound is of particular interest within organic chemistry. The combination of phenolic hydroxyl groups with a butanoic acid moiety allows for various synthetic modifications, opening pathways for the creation of even more complex structures.
  • Environmental Impact: Research has been conducted into the environmental implications of halogenated compounds. Understanding the fate of such compounds in natural systems offers insights into their persistence and bioaccumulation potential.

In essence, 4-(3-hydroxy-2,4,6-triiodo-phenyl)butanoic acid is more than just a chemical formula; it represents a significant intersection of organic chemistry, pharmaceuticals, and environmental science. As researchers continue to explore its properties, it may reveal even more critical insights into health and the environment.