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Calcium iodothyronate

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Identification
Molecular formula
C9H9INO3Ca
CAS number
10556-31-7
IUPAC name
calcium;2-amino-2-(4-hydroxy-3-iodo-phenyl)acetate
State
State

Calcium iodothyronate is typically found in a solid state at room temperature. It is stable under normal storage conditions but should be kept in a sealed container to prevent moisture from affecting its structure.

Melting point (Celsius)
236.00
Melting point (Kelvin)
509.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
321.06g/mol
Molar mass
321.0600g/mol
Density
2.3000g/cm3
Appearence

Calcium iodothyronate, also known as calcium 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetate, appears as a white to off-white crystalline powder. It is odorless and can absorb moisture when exposed to air. The powder is generally fine, but sometimes presents as slightly coarser granules depending on the method of preparation and storage conditions.

Comment on solubility

Solubility of Calcium; 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetate

The solubility of calcium; 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetate can be influenced by several factors, due to its unique structure and composition. Here are some important points to consider:

  • Water Solubility: This compound is expected to have moderate solubility in water due to the presence of both ionic and polar functional groups.
  • pH Dependence: The solubility may vary with changes in pH, as the ionization state of the amino acid can affect its interaction with water.
  • Temperature Effects: Higher temperatures typically increase the solubility of solid compounds in a solvent, so heating may enhance solubility.
  • Solvent Polarity: The presence of polar groups may lead to greater solubility in polar solvents compared to non-polar solvents.

As a rule of thumb, compounds with ionic or polar characteristics tend to be more soluble in polar solvents such as water. It can also be said that, as General Chemistry elucidates, the “like dissolves like” principle is a key determinant in solubility behavior.


Understanding the solubility of calcium; 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetate is crucial for its applications and uses in various fields, including pharmaceuticals and biochemistry.

Interesting facts

Interesting Facts about Calcium 2-Amino-2-(4-hydroxy-3-iodo-phenyl)acetate

Calcium 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetate, often referred to by its systematic name, is a fascinating compound that demonstrates the intricate interplay between calcium and amino acids. Here are some remarkable aspects of this compound:

  • Biochemical Significance: The compound showcases the role of calcium in biological systems, particularly in neurotransmitter release and muscle contraction.
  • Amino Acid Derivative: As an amino acid derivative, this compound can play crucial roles in metabolic processes, enhancing our understanding of amino acid chemistry.
  • Iodine Presence: The presence of iodine in its structure points to potential applications in medicinal chemistry, particularly in developing contrast agents for medical imaging.
  • Hydroxyl Group Impact: The hydroxy group in this compound may enhance hydrogen bonding, influencing its biological activity and solubility.
  • Research Implications: Studying compounds like calcium 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetate can lead to advancements in drug design, particularly for conditions involving calcium signaling and neurotransmission.

As noted in research, "The intersection of calcium and amino acids leads to a myriad of biological interactions, each more complex than the last." This compound epitomizes this complexity, inviting further investigation into its properties and potential applications.


Overall, calcium 2-amino-2-(4-hydroxy-3-iodo-phenyl)acetate not only contributes to our understanding of biochemical systems, but it also paves the way for innovative research in various scientific fields.

Synonyms
7681-60-9
3-Iodo-L-tyrosine calcium
L-Tyrosine, 3-iodo-, calcium salt
Tyrosine, 3-iodo-, calcium salt, L-
UNII-FFG5D2B36E
FFG5D2B36E