Skip to main content

Amiodarone

ADVERTISEMENT
Identification
Molecular formula
C10H11I3O3
CAS number
1951-25-3
IUPAC name
2-(2,4,6-triiodophenoxy)butanoic acid
State
State

At room temperature, it is typically a solid.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
315.50
Boiling point (Kelvin)
588.65
General information
Molecular weight
663.84g/mol
Molar mass
663.8390g/mol
Density
2.5300g/cm3
Appearence

The compound is usually in the form of a white or off-white crystalline powder.

Comment on solubility

Solubility of 2-(2,4,6-triiodophenoxy)butanoic acid

The solubility of 2-(2,4,6-triiodophenoxy)butanoic acid presents an intriguing profile due to its molecular structure and the presence of iodine substituents. Generally, the solubility of a compound in water can be influenced by factors such as molecular weight, polarity, and the presence of functional groups. In the case of this compound, it is essential to consider:

  • Polarity: The presence of the phenoxy group and carboxylic acid may impart some level of polarity, potentially increasing compatibility with polar solvents.
  • Iodine Substituents: The three iodine atoms attached to the phenol ring can impede solubility in water due to their large size and low polarity.
  • Hydrogen Bonding: The carboxylic acid group can participate in hydrogen bonding, which might enhance solubility in polar solvents like water, although the overall effect can be complex.

From observations, it is reasonable to conclude that 2-(2,4,6-triiodophenoxy)butanoic acid may exhibit limited solubility in water but could be more soluble in organic solvents due to its overall structure. Users should consider performing solubility tests in various solvents to establish precise solubility characteristics.

Interesting facts

Facts About 2-(2,4,6-Triiodophenoxy)butanoic Acid

2-(2,4,6-triiodophenoxy)butanoic acid is a fascinating compound with a rich background in chemistry and its applications. Here are some intriguing insights:

  • Structure and Composition: This compound features a unique structure where a phenoxy group is substituted with three iodine atoms at the ortho and para positions of the ring. This not only influences its reactivity but also enhances its biological activity.
  • Biological Significance: The iodine substitutions in the compound contribute to its high biological activity. Iodinated compounds are known for their role in medicinal chemistry, particularly in developing drugs that target specific diseases.
  • Applications: 2-(2,4,6-triiodophenoxy)butanoic acid is studied for its potential in environmental chemistry, particularly in the degradation of harmful pollutants. Its ability to interact with various biological systems also opens avenues for research in pharmaceuticals.
  • Chemical Behavior: This compound exhibits interesting chemical properties, particularly due to the electron-withdrawing effects of the iodine atoms. This alters its nucleophilicity and can influence reactions involving electrophiles.
  • Research Focus: The compound is a subject of ongoing research, especially in the fields of toxicology and environmental science. Scientists are exploring its potential impact and mechanisms of action within biological systems.

In conclusion, 2-(2,4,6-triiodophenoxy)butanoic acid is more than just a chemical entity; it embodies the intricate connection between structure and function in the realm of chemistry. Explore the world of iodinated compounds, and you will find a treasure trove of possibilities waiting for discovery!

Synonyms
Phenobutiodil
554-24-5
2-(2,4,6-Triiodophenoxy)butyric acid
2-(2,4,6-triiodophenoxy)butanoic acid
67F5J7GUUR
Baygnostil
Cholognost
Biliodyl
Felotrast
Trijobil
Vesipaque
Phenobutijodilum
Phenobutiodilum
Fenobutiodilo
Phenobutiodil [INN:BAN]
Fenobutiodilo [INN-Spanish]
Phenobutiodilum [INN-Latin]
4114 TH
EINECS 209-065-1
UNII-67F5J7GUUR
BRN 2283687
Fenobutiodil
Butanoic acid, 2-(2,4,6-triiodophenoxy)-
PHENOBUTIODIL [MI]
PHENOBUTIODIL [INN]
BUTYRIC ACID, 2-(2,4,6-TRIIODOPHENOXY)-
PHENOBUTIODIL [WHO-DD]
SCHEMBL1649852
CHEMBL2104664
DTXSID80862188
CHEBI:135828
VYAGDYWTCWDKIS-UHFFFAOYSA-N
NS00006546
Q27264123