Iopromide - CAS 73334-07-3
Catalog number: B0084-301958
Category: Inhibitor
Not Intended for Therapeutic Use. For research use only.
Molecular Formula:
Molecular Weight:
Iopromide is a contrast medium produced by Bayer Healthcare. It is a low osmolar, non-ionic contrast agent for intravascular use. It can be used in radiographic studies including intravenous urograms, brain computer tomography and CT pulmonary angiograms.
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Catalog Number Size Price Stock Quantity
B0084-301958 25 mg $168 In stock
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white powder
N,N’-Bis(2,3-Dihydroxypropyl)-2,4,6-triiodo-5-[(methoxyacetyl)amino]-N-methyl-1,3-benzenedicarboxamide; Iopromidum; SHL 414C; Ultravist; Ultravist 300; Ultravist 370; ZK 35760;
DMSO, Water
Hygroscopic, -20℃ Freezer, Under Inert Atmosphere
contrast medium
Quality Standard:
Shelf Life:
2 month in rt, long time
Boiling Point:
840.9℃ at 760 mmHg
Melting Point:
2.173 g/cm3
Canonical SMILES:
Current Developer:
Bayer Healthcare
1.Immobilization of metal-humic acid complexes in anaerobic granular sludge for their application as solid-phase redox mediators in the biotransformation of iopromide in UASB reactors.
Cruz-Zavala AS1, Pat-Espadas AM1, Rangel-Mendez JR1, Chazaro-Ruiz LF1, Ascacio-Valdes JA2, Aguilar CN2, Cervantes FJ3. Bioresour Technol. 2016 May;207:39-45. doi: 10.1016/j.biortech.2016.01.125. Epub 2016 Feb 8.
Metal-humic acid complexes were synthesized and immobilized by a granulation process in anaerobic sludge for their application as solid-phase redox mediators (RM) in the biotransformation of iopromide. Characterization of Ca- and Fe-humic acid complexes revealed electron accepting capacities of 0.472 and 0.556milli-equivalentsg(-1), respectively. Once immobilized, metal-humic acid complexes significantly increased the biotransformation of iopromide in upflow anaerobic sludge blanket (UASB) reactors. Control UASB reactor (without humic material) achieved 31.6% of iopromide removal, while 80% was removed in UASB reactors supplied with each metal-humic acid complex. Further analyses indicated multiple transformation reactions taking place in iopromide including deiodination, N-dealkylation, decarboxylation and deacetylation. This is the first successful application of immobilized RM, which does not require a supporting material to maintain the solid-phase RM in long term operation of bioreactors.
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CAS 73334-07-3 Iopromide

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