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Sodium ioxinate

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Identification
Molecular formula
C11H8I3N2NaO4
CAS number
737-31-5
IUPAC name
sodium;3,5-diacetamido-2,4,6-triiodo-benzoate
State
State

At room temperature, sodium ioxinate is typically found in a solid state.

Melting point (Celsius)
260.00
Melting point (Kelvin)
533.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
558.95g/mol
Molar mass
558.9500g/mol
Density
2.3400g/cm3
Appearence

Sodium ioxinate appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of Sodium 3,5-Diacetamido-2,4,6-triiodo-benzoate

The solubility of sodium 3,5-diacetamido-2,4,6-triiodo-benzoate in various solvents is influenced by its unique molecular structure comprising both hydrophilic and hydrophobic characteristics. Here are some key points to understand its solubility behavior:

  • Aqueous Solubility: This compound is likely to be soluble in aqueous solutions due to the sodium ion, which enhances its affinity for water.
  • Organic Solvents: The presence of iodine substituents can hinder solubility in non-polar solvents, making it less soluble in organic solvents such as hexane or toluene.
  • Temperature Impact: As with many chemical compounds, increasing the temperature can lead to higher solubility in water. However, this may vary depending on the concentration of the sodium salt.
  • pH Effects: The solubility can also be affected by the pH of the solution; typically, an increase in pH can improve solubility for ionic compounds.

Overall, while sodium 3,5-diacetamido-2,4,6-triiodo-benzoate exhibits favorable solubility in polar solvents, its solubility profile in organic media may be limited. Therefore, understanding these nuances is essential for its applications in chemical research and industry.

Interesting facts

Interesting Facts about Sodium; 3,5-diacetamido-2,4,6-triiodo-benzoate

3,5-Diacetamido-2,4,6-triiodo-benzoate, also commonly known as a derivative of *iodobenzoic acid*, is an intriguing compound with a diverse range of applications in the field of chemistry and beyond. Here are some fascinating aspects of this compound:

  • Medical Applications: This compound acts as a radiocontrast agent in medical imaging, particularly in enhancing the visibility of organs and vessels during X-ray imaging. Its iodine content makes it particularly effective in this capacity.
  • Research Importance: In various biochemical research fields, this compound aids in studying *iodinated organic compounds*, providing insights into their behaviors and interactions within biological systems.
  • Synthesis Techniques: The synthesis of 3,5-diacetamido-2,4,6-triiodo-benzoate often involves the halogenation of benzoic acid derivatives. Understanding the intricate protocols of this synthesis can enhance a chemist’s procedural skills.
  • Structure and Properties: The unique triiodinated structure gives this compound distinct chemical properties, making it a subject of interest in organometallic and medicinal chemistry. The introduction of iodine atoms can significantly alter reactivity and solubility profiles.
  • Environmental Concerns: As iodine-containing compounds can impact marine life, understanding their environmental fate and bioaccumulation is crucial for research on sustainability and ecology.

In summary, the compound 3,5-diacetamido-2,4,6-triiodo-benzoate is not just a fascinating example of iodine chemistry; its applications range from medicine to ecological research, underscoring the profound impact that chemical compounds can have on both human health and the environment. As many chemists quote, “Every compound tells a story,” and this one is filled with potential and intrigue!