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Ioxaglic acid

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Identification
Molecular formula
C11H9I3NO4
CAS number
70261-44-0
IUPAC name
2-[3-(butanoylamino)-2,4,6-triiodo-phenoxy]acetic acid
State
State

State at room temperature: Solid under standard conditions.

Melting point (Celsius)
185.00
Melting point (Kelvin)
458.15
Boiling point (Celsius)
346.00
Boiling point (Kelvin)
619.15
General information
Molecular weight
821.94g/mol
Molar mass
821.9410g/mol
Density
2.2400g/cm3
Appearence

Appearance: Ioxaglic acid appears as a white to off-white solid.

Comment on solubility

Solubility of 2-[3-(butanoylamino)-2,4,6-triiodo-phenoxy]acetic acid

The solubility of 2-[3-(butanoylamino)-2,4,6-triiodo-phenoxy]acetic acid can be influenced by several factors, particularly its molecular structure and functional groups. This compound possesses both hydrophilic and hydrophobic regions, which can lead to a varied solubility profile in different solvents.

  • Hydrophilic Regions: The presence of the carboxylic acid group in the structure confers hydrophilic characteristics, promoting solubility in polar solvents like water.
  • Hydrophobic Interactions: Conversely, the butanoyl group and triiodo arrangements could limit solubility in water but enhance it in non-polar solvents, such as organic solvents (e.g., ethanol or acetone).
  • Temperature Effects: Solubility may increase with temperature due to increased molecular motion, allowing for better interaction between the solute and solvent.
  • pH Influence: Since 2-[3-(butanoylamino)-2,4,6-triiodo-phenoxy]acetic acid is an acid itself, changes in pH can lead to varying degrees of ionization, further affecting solubility.

In summary, the solubility of this compound is likely to be dependent on the solvent type, temperature, and pH conditions. As with many chemical compounds, it is essential to conduct empirical solubility tests for precise information.

Interesting facts

Interesting Facts about 2-[3-(butanoylamino)-2,4,6-triiodo-phenoxy]acetic acid

2-[3-(butanoylamino)-2,4,6-triiodo-phenoxy]acetic acid is a fascinating compound primarily known for its applications in various fields such as medicine and agriculture. Here are some noteworthy insights:

  • Unique Structural Features: This compound incorporates a unique triiodo group, which significantly enhances its reactivity and efficacy in biological systems. The presence of iodine atoms is notable since they can impact the compound's interactions with biological molecules.
  • Biological Activity: This compound is renowned for its role as a herbicide and plant growth regulator. Its ability to mimic natural plant hormones allows it to effectively influence plant growth and development, making it valuable in agricultural practices.
  • Environmental Impact: As with many agrochemicals, the environmental implications of using this compound warrant careful consideration. Scientists are continually studying its degradation pathways and potential effects on non-target organisms.
  • Potential Health Implications: While beneficial in agriculture, compounds like this also underscore the importance of investigating their safety for human health. Toxicological studies help ensure that any potential risks are managed appropriately.
  • Chemical Synthesis: The synthesis of this compound involves intricate chemical reactions that require a deep understanding of organic chemistry principles. Researchers often explore various synthetic routes to optimize yield and purity.

As scientists continue to explore the multifaceted applications of 2-[3-(butanoylamino)-2,4,6-triiodo-phenoxy]acetic acid, its role in promoting sustainable agricultural practices while considering environmental and health impacts remains a pivotal context for ongoing research. As stated by one researcher, "Balancing innovation and safety in chemical applications is at the heart of scientific progress."


Synonyms
BRN 2706420
ACETIC ACID, (3-BUTYRAMIDO-2,4,6-TRIIODOPHENOXY)-
(3-Butyramido-2,4,6-triiodophenoxy)acetic acid
1225-80-5
2,4,6-Trijod-3-(n)-butyrylamino-phenoxy-essigsaeure [German]
DTXSID70153633
2,4,6-Trijod-3-(n)-butyrylamino-phenoxy-essigsaeure
DTXCID0076124