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Disodium Tauroursodeoxycholate

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Identification
Molecular formula
C15H11N2Na2O4
CAS number
2624-51-3
IUPAC name
disodium;2-amino-5-(4-amino-3-carboxylato-phenyl)benzoate
State
State

Solid at room temperature.

Melting point (Celsius)
300.00
Melting point (Kelvin)
573.15
Boiling point (Celsius)
760.00
Boiling point (Kelvin)
1 033.15
General information
Molecular weight
327.25g/mol
Molar mass
327.2490g/mol
Density
2.0200g/cm3
Appearence

A white to off-white crystalline powder.

Comment on solubility

Solubility of Disodium;2-amino-5-(4-amino-3-carboxylato-phenyl)benzoate

The solubility characteristics of disodium;2-amino-5-(4-amino-3-carboxylato-phenyl)benzoate can be understood through several key points:

  • Highly soluble in water: This compound exhibits a strong affinity for water due to its ionic nature, resulting in a high solubility.
  • Ionization: The presence of carboxylate groups allows it to ionize effectively, further enhancing solubility in polar solvents.
  • pH dependence: The solubility may be influenced by the pH of the surrounding solution, as the protonation or deprotonation of the amino and carboxyl groups can affect solubility.
  • Temperature effects: Like many ionic compounds, increasing the temperature typically leads to higher solubility as kinetic energy allows for greater interaction with water molecules.

In conclusion, the solubility of disodium;2-amino-5-(4-amino-3-carboxylato-phenyl)benzoate is a significant characteristic that enhances its applicability in various fields, making it an intriguing substance for further study and utilization.

Interesting facts

Interesting Facts about Disodium 2-Amino-5-(4-amino-3-carboxylato-phenyl)benzoate

Disodium 2-amino-5-(4-amino-3-carboxylato-phenyl)benzoate is an intriguing compound known for its role as a potential therapeutic agent. Here are some fascinating highlights about this compound:

  • Biological Significance: This compound is a derivative of amino acids, making it important in biochemical pathways. It is often explored for its potential applications in drug development.
  • Structural Features: The compound contains multiple functional groups, such as amino and carboxylate groups, which contribute to its unique properties. These groups enhance solubility in physiological conditions, making it a candidate for biological studies.
  • Potential Applications: Research has indicated that this compound may have beneficial effects in areas such as:
    • Antioxidant activity, helping to neutralize harmful free radicals in the body.
    • Anti-inflammatory properties, which could be useful in treating various inflammatory conditions.
    • As a chelating agent, it may assist in binding metal ions, which is crucial in several biochemical assays.
  • Research Avenues: Scientists continue to investigate its interactions at the molecular level, which could lead to the development of novel pharmaceuticals. Studies focus on its mechanism of action and potential synergies with other therapeutic agents.
  • Role in Nutrition: As an amino acid derivative, it could also be significant in nutritional biochemistry, particularly in understanding amino acid metabolism.

In summary, Disodium 2-amino-5-(4-amino-3-carboxylato-phenyl)benzoate presents a wealth of information for scientists interested in its biochemical implications, potential therapeutic uses, and structural characteristics. As research progresses, this compound may reveal even more fascinating properties!

Synonyms
3,3'-BIPHENYLDICARBOXYLIC ACID, 4,4'-DIAMINO-, DISODIUM SALT
16993-94-5
3,3'-Benzidine dicarboxylic acid, disodium salt
Disodium 3,3'-benzidinedicarboxylate
DTXSID40168774