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Iopanoic acid

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Identification
Molecular formula
C11H12I3NO2
CAS number
96-83-3
IUPAC name
2-(3-amino-2,4,6-triiodo-phenyl)butanoic acid
State
State

At room temperature, iopanoic acid is a solid. It is typically handled in its solid powder form in both laboratory and industrial contexts.

Melting point (Celsius)
263.00
Melting point (Kelvin)
536.15
Boiling point (Celsius)
341.00
Boiling point (Kelvin)
614.15
General information
Molecular weight
597.88g/mol
Molar mass
597.8810g/mol
Density
2.7800g/cm3
Appearence

Iopanoic acid appears as a white or off-white crystalline powder. The compound may exhibit variations in appearance depending on its purity and the presence of any impurities, but it is generally recognized by its powder form in laboratory and pharmaceutical settings.

Comment on solubility

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

2-(3-amino-2,4,6-triiodo-phenyl)butanoic acid is a fascinating compound with distinct solubility properties.

Typically, this compound is expected to exhibit the following solubility characteristics:

  • Polar Nature: Due to the presence of the amino group (-NH2) and carboxylic acid group (-COOH), this compound is likely soluble in polar solvents such as water.
  • Intramolecular Hydrogen Bonding: The potential for hydrogen bonding can enhance solubility in water, making the compound more amenable to dissolution.
  • Iodine Substituents: The triiodo substitution may introduce some hydrophobic characteristics; however, the balance between the hydrophilic groups and the hydrophobic regions plays a crucial role in determining the overall solubility.
  • Temperature Dependence: Like many organic compounds, the solubility might vary with temperature. Increased temperatures often promote greater solubility for such amphipathic structures.

In summary, the solubility profile of 2-(3-amino-2,4,6-triiodo-phenyl)butanoic acid is influenced by its functional groups and structural features, leading to solubility in polar environments while showcasing some limitations due to hydrophobic characteristics from the iodine substituents. Understanding these factors can aid in predicting its behavior in various chemical contexts.

Interesting facts

Interesting Facts about 2-(3-amino-2,4,6-triiodo-phenyl)butanoic acid

2-(3-amino-2,4,6-triiodo-phenyl)butanoic acid, often referred to for its intriguing chemical structure and diverse applications, is noteworthy for several reasons:

  • Biological Significance: This compound has shown potential as a pharmaceutical intermediate. Its unique functional groups allow it to interact effectively with various biological pathways, making it a candidate in drug development.
  • X-ray Contrast Agent: The presence of tri-iodo substitutions in the phenyl ring endows this compound with vibrant X-ray attenuation properties. As such, it can play a crucial role in medical imaging, particularly in enhancing the visibility of structures in the body during diagnostic procedures.
  • Environmental Considerations: Due to its iodine content, the environmental impact of this compound is an essential factor for researchers and chemists. Understanding its degradation pathways and potential bioaccumulation in the environment is key for sustainable usage.
  • Research Applications: Chemists engage this compound in studies related to organic synthesis and medicinal chemistry, examining its structure-activity relationship (SAR) which can illuminate how variations in structure influence its biological efficacy.
  • Versatile Synthesis: The synthesis of this compound often involves multi-step organic reactions, showcasing the creative ingenuity of chemists. From amino acid precursors to halogenation processes, the pathways leading to its formulation are complex and fascinating.

In summary, 2-(3-amino-2,4,6-triiodo-phenyl)butanoic acid serves as a reminder of the intricate relationship between chemical structure and application. Its properties not only make it a significant candidate in medicinal chemistry but also underline the implications of chemical science in both healthcare and environmental stewardship.

Synonyms
21762-25-4
BUTYRIC ACID, 2-(3-AMINO-2,4,6-TRIIODOPHENYL)-
2-(3-Amino-2,4,6-triiodophenyl)butyric acid
BRN 3034938
2-(3-amino-2,4,6-triiodophenyl)butanoic acid
RefChem:1080456
DTXSID60944375