Sodium iopodate | Solubility of Things

Identification

Molecular formula

C₁₁H₁₂I₃NO₃Na

CAS number

338-67-0

IUPAC name

sodium;2-[2,4,6-triiodo-3-(3-oxomorpholin-4-yl)phenyl]butanoate

State

At room temperature, sodium iopodate is in a solid state. It is typically stable under standard conditions but should be stored in dry, well-closed containers, away from light and moisture to maintain its stability.

Melting point (Celsius)

280.00

Melting point (Kelvin)

553.15

Boiling point (Celsius)

881.85

Boiling point (Kelvin)

1 155.00

General information

Molecular weight

697.93g/mol

Molar mass

697.9270g/mol

Density

2.1000g/cm³

Appearence

Sodium iopodate typically appears as a white to off-white powder. It is crystalline in form and may be presented in pharmaceutical formulations as tablets or as an injectable solution.

Comment on solubility

Solubility of sodium 2-[2,4,6-triiodo-3-(3-oxomorpholin-4-yl)phenyl]butanoate

The solubility of sodium 2-[2,4,6-triiodo-3-(3-oxomorpholin-4-yl)phenyl]butanoate is a fascinating subject, revealing much about its potential applications and behavior in various environments. This compound typically exhibits significant solubility in polar solvents, particularly in:

Water: As a sodium salt, the compound is likely to be highly soluble due to the ionic nature of sodium ions, which can stabilize the dissolved form.
Alcohols: Solvents like ethanol may also dissolve the compound well, given the potential for hydrogen bonding between the molecules.

However, its solubility in nonpolar solvents is expected to be limited. This is primarily because:

The presence of highly polar groups with iodine and morpholine structures can create an imbalance, making it difficult for the compound to interact favorably with nonpolar environments.
Incompatibility with hydrophobic solvents can lead to precipitation or minimal dissolution.

To summarize, when considering the solubility of sodium 2-[2,4,6-triiodo-3-(3-oxomorpholin-4-yl)phenyl]butanoate, it is essential to highlight that:

High solubility in polar solvents increases its utility in biochemical applications.
A careful choice of solvent can optimize its reactivity and performance in synthetic pathways.

As always, it's crucial to conduct empirical tests to determine specific solubility limits, given the complexities of various solvent interactions.

Interesting facts

Interesting Facts about Sodium; 2-[2,4,6-triiodo-3-(3-oxomorpholin-4-yl)phenyl]butanoate

Sodium; 2-[2,4,6-triiodo-3-(3-oxomorpholin-4-yl)phenyl]butanoate is a fascinating compound with intriguing properties and potential applications. Here are some engaging insights into this chemical:

Medical Significance: This compound features a unique structure that may play a role in the development of pharmaceuticals. The presence of iodine in its structure suggests potential applications in imaging techniques, particularly in medicinal chemistry.
Molecular Complexity: The incorporation of a morpholine ring hints at its possible biological activity. Morpholines are often found in various bioactive compounds, making them valuable in drug discovery.
Structure-Activity Relationship: The combination of a phenyl ring and a butanoate moiety indicates interesting interactions that could influence the compound's effectiveness in therapeutic contexts. This diversity in structure allows for numerous variations that can be tailored for specific applications.
Therapeutic Potential: With its triiodinated structure, this compound may also exhibit properties related to thyroid function or metabolic pathways. The ability to modulate biological processes positions it as a candidate for further research in fields such as oncology or endocrinology.

In summary, sodium; 2-[2,4,6-triiodo-3-(3-oxomorpholin-4-yl)phenyl]butanoate stands out not just for its chemical structure but also for its potential implications in medicinal chemistry. This compound embodies the complexity and versatility of modern chemistry, inviting scientists and students alike to explore its myriad possibilities.