Skip to main content

X-ray contrast media

ADVERTISEMENT
Identification
Molecular formula
C7H6I3NO
CAS number
552-08-5
IUPAC name
(3-amino-2,4,6-triiodo-phenyl)methanol
State
State

At room temperature, (3-amino-2,4,6-triiodo-phenyl)methanol is in a solid state. It is stable under normal conditions and should be stored in a cool, dry place.

Melting point (Celsius)
163.50
Melting point (Kelvin)
436.65
Boiling point (Celsius)
407.60
Boiling point (Kelvin)
680.75
General information
Molecular weight
437.94g/mol
Molar mass
437.9400g/mol
Density
3.3000g/cm3
Appearence

(3-amino-2,4,6-triiodo-phenyl)methanol typically appears as a white to off-white crystalline powder. The compound is often used in applications where high atomic number and corresponding electron density are desirable, particularly in X-ray imaging.

Comment on solubility

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

The solubility of (3-amino-2,4,6-triiodo-phenyl)methanol can be a fascinating topic due to its unique chemical structure influenced by the presence of multiple iodine substituents. This compound exhibits varying solubility characteristics based on the solvent used:

  • Water: The solubility in water is typically low, primarily due to the bulky iodinated groups that hinder interactions with water molecules.
  • Organic solvents: (3-amino-2,4,6-triiodo-phenyl)methanol is more likely to be soluble in organic solvents such as ethanol or chloroform, where its nonpolar characteristics can be better accommodated.
  • Polar vs. Nonpolar: The presence of both polar (amino group) and nonpolar (iodine groups) characteristics can lead to complicated solubility behaviors, often requiring a compromise in solvent selection.

In summary, the solubility of (3-amino-2,4,6-triiodo-phenyl)methanol illustrates the crucial balance between hydrophobic and hydrophilic forces, revealing insights into how substituents impact the physical properties of organic compounds. Experimentation with various solvents remains key in understanding its full solubility profile.

Interesting facts

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

(3-amino-2,4,6-triiodo-phenyl)methanol, often abbreviated as AMT, is a fascinating compound that falls within the category of aryl alcohols with notable iodine substitutions. Here are some engaging aspects of this compound:

  • **Medical Relevance**: The presence of iodine atoms makes AMT of interest in the field of medicine, particularly in imaging and radiotherapy, due to the radioactive isotopes of iodine that are used in medical diagnostics.
  • **Protein Interaction**: The amino group in the structure can participate in hydrogen bonding, potentially allowing AMT to interact with biological macromolecules like proteins, influencing their function and stability.
  • **Synthesis**: The synthesis of AMT typically involves the iodination of phenol derivatives, showcasing interesting organic chemistry techniques such as electrophilic aromatic substitution.
  • **Antimicrobial Properties**: Some studies suggest that compounds with extensive iodine substitutions exhibit antimicrobial activity, making AMT a potential candidate for further research in antibacterial applications.

As a student or scientist delving into organic chemistry, exploring compounds like (3-amino-2,4,6-triiodo-phenyl)methanol can reveal a myriad of applications and functions, expanding your understanding of both inorganic and organic interactions in pharmacology and materials science. As we can see, the combination of traditional functional groups with halogen substitutions can lead to exciting new chemical properties and biological activities!

Synonyms
(3-amino-2,4,6-triiodophenyl)methanol
1460-43-1
BENZYL ALCOHOL, 3-AMINO-2,4,6-TRIIODO-
3-Amino-2,4,6-triiodobenzyl alcohol
BRN 2723293
Benzenemethanol, 3-amino-2,4,6-triiodo-
DTXSID70163257
DB-344655