Skip to main content

Ferrioxamine B

ADVERTISEMENT
Identification
Molecular formula
C25H45N6O8Fe
CAS number
16938-64-4
IUPAC name
ferric;3-[7,13,17-tris(2-carboxyethyl)-3,8,12,18-tetrakis(carboxymethyl)-12,18-dimethyl-2,3,8,9,13,17-hexahydro-1H-porphyrin-21,22,24-triid-2-yl]propanoic acid
State
State

At room temperature, ferrioxamine B is typically in a solid state, appearing as crystalline powder. It has a characteristic violet color due to its iron complexation.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
636.76g/mol
Molar mass
636.7630g/mol
Density
0.0500g/cm3
Appearence

Ferrioxamine B is a red-violet crystalline powder. It appears as deep violet crystals when viewed in transmitted light and is soluble in water, producing a violet solution.

Comment on solubility

Solubility of Ferric 3-[7,13,17-tris(2-carboxyethyl)-3,8,12,18-tetrakis(carboxymethyl)-12,18-dimethyl-2,3,8,9,13,17-hexahydro-1H-porphyrin-21,22,24-triid-2-yl]propanoic acid

The solubility of this complex iron compound, ferric 3-[7,13,17-tris(2-carboxyethyl)-3,8,12,18-tetrakis(carboxymethyl)-12,18-dimethyl-2,3,8,9,13,17-hexahydro-1H-porphyrin-21,22,24-triid-2-yl]propanoic acid, represented by the chemical formula C25H45N6O8Fe, exhibits noteworthy solubility characteristics that can be highlighted as follows:

  • Water Solubility: The presence of multiple carboxylic acid groups contributes to the compound's ability to dissolve in water, as these polar functional groups can effectively interact with water molecules.
  • Solvent Dependence: The solubility may vary significantly depending on the solvent; for instance, it might exhibit higher solubility in aqueous solutions compared to organic solvents due to the affinity of the carboxylic groups for hydrogen bonding.
  • pH Sensitivity: The solubility of this compound might also be sensitive to pH levels, as changes in acidity can affect the ionization of the carboxyl groups, potentially enhancing solubility at higher pH values through deprotonation.
  • Concentration Effects: At elevated concentrations, self-aggregation might occur, which could lead to decreased solubility due to the formation of larger complex structures.

In summary, while ferric 3-[7,13,17-tris(2-carboxyethyl)-3,8,12,18-tetrakis(carboxymethyl)-12,18-dimethyl-2,3,8,9,13,17-hexahydro-1H-porphyrin-21,22,24-triid-2-yl]propanoic acid shows promise for substantial solubility in appropriate conditions, factors such as solvent choice, pH, and concentration play significant roles in defining its behavior in solution.

Interesting facts

Exploring Ferric 3-[7,13,17-tris(2-carboxyethyl)-3,8,12,18-tetrakis(carboxymethyl)-12,18-dimethyl-2,3,8,9,13,17-hexahydro-1H-porphyrin-21,22,24-triid-2-yl]propanoic Acid

Ferric 3-[7,13,17-tris(2-carboxyethyl)-3,8,12,18-tetrakis(carboxymethyl)-12,18-dimethyl-2,3,8,9,13,17-hexahydro-1H-porphyrin-21,22,24-triid-2-yl]propanoic acid represents a fascinating intersection of organic chemistry and biochemistry due to its intricate structure and potential applications.

Key Features

  • Transition Metal Complex: Ferric indicates the presence of iron in its +3 oxidation state, which is vital in various biological processes, especially in oxygen transport and storage.
  • Porphyrin Derivative: The compound incorporates a porphyrin framework, renowned for its involvement in heme and chlorophyll, indicating potential applications in photodynamic therapy and catalysis.
  • Carboxylic Acids: The numerous carboxyethyl and carboxymethyl groups suggest solubility and ionic interactions in aqueous environments, enhancing the compound's biological compatibility.

As a scientist delving into this compound, one might consider its roles in biochemical systems or its application in drug delivery mechanisms, where the iron center could facilitate targeted therapy. Researchers might also explore its potential as a **chelator**, binding various metal ions in environmental or biological contexts. Moreover, the structural complexity gives rise to intriguing questions about synthesis and properties.

In summary, ferric 3-[7,13,17-tris(2-carboxyethyl)-3,8,12,18-tetrakis(carboxymethyl)-12,18-dimethyl-2,3,8,9,13,17-hexahydro-1H-porphyrin-21,22,24-triid-2-yl]propanoic acid is not just a chemical entity but a potential key player in advanced material science and bioengineering, making it a rich subject for further exploration.