Weight | 264.999 g/mol |
---|---|
Formula | C6H11FeNO7 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 5 |
Aromatic Rings | 0 |
Rotatable Bonds | 5 |
Ammonium ferric citrate (1185-57-5)
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- Two mechanisms of iron uptake from transferrin by melanoma cells. The effect of desferrioxamine and ferric ammonium citrate. (Journal of Biological Chemistry, 1992)
- Iron accumulation, ironmediated toxicity and altered levels of ferritin and transferrin receptor in cultured astrocytes during incubation with ferric ammonium citrate (Journal of Neurochemistry, 2004)
- Mycobacteria with a growth requirement for ferric ammonium citrate, identified as Mycobacterium haemophilum. (Journal of Clinical Microbiology, 1980)
- The effect of desferrioxamine and ferric ammonium citrate on the uptake of iron by the membrane iron-binding component of human melanoma cells (Biochimica et Biophysica Acta, 1992)
- Large scale clinical evaluation of bowel contrast agent containing ferric ammonium citrate in MRI (Magnetic Resonance Imaging, 1994)
- Ferric ammonium citrate as a positive bowel contrast agent for MR imaging of the upper abdomen. Safety and diagnostic efficacy. (Acta Radiologica, 1999)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(C(=O)O)C(CC(=O)O)(C(=O)O)O.N.[Fe]
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InChIKeyPLKYGPRDCKGEJH-UHFFFAOYSA-N
- Pubchem - Ammonium ferric citrate
- Wikipedia - ammonium ferric citrate
Ammonium ferric citrate has the formula (NH4)5[Fe(C6H4O7)2]. A distinguishing feature of this compound is that it is very soluble in water, in contrast to ferric citrate which is not very soluble. In its crystal structure each citric acid moiety has lost four protons, and the deprotonated hydroxyl groups act as ligands together with four carboxylate groups; two carboxylate groups are not coordinated to the ferric ion.
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