Iopromide - CAS 73334-07-3
Catalog number: B0084-301958
Category: Inhibitor
Not Intended for Therapeutic Use. For research use only.
Molecular Formula:
C18H24I3N3O8
Molecular Weight:
791.11
COA:
Inquire
Targets:
Others
Description:
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.
Ordering Information
Catalog Number Size Price Stock Quantity
B0084-301958 25 mg $168 In stock
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Purity:
98%
Appearance:
white powder
Synonyms:
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;
Solubility:
DMSO, Water
Storage:
Hygroscopic, -20℃ Freezer, Under Inert Atmosphere
MSDS:
Inquire
Application:
contrast medium
Quality Standard:
USP
Shelf Life:
2 month in rt, long time
Quantity:
Milligrams-Grams
Boiling Point:
840.9℃ at 760 mmHg
Melting Point:
145-149℃
Density:
2.173 g/cm3
InChIKey:
DGAIEPBNLOQYER-UHFFFAOYSA-N
InChI:
1S/C18H24I3N3O8/c1-24(4-9(28)6-26)18(31)12-13(19)11(17(30)22-3-8(27)5-25)14(20)16(15(12)21)23-10(29)7-32-2/h8-9,25-28H,3-7H2,1-2H3,(H,22,30)(H,23,29)
Canonical SMILES:
O=C(N(CC(O)CO)C)C1=C(I)C(C(NCC(O)CO)=O)=C(I)C(NC(COC)=O)=C1I
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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