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| | 5-Amino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide Basic information |
| Product Name: | 5-Amino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide | | Synonyms: | 5-AMino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenediforMaMide;5-aMino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzendicarboxaMide;Iohexol Related CoMpound B;Ioversol Related CoMpound A;5-Amino-N,N′-bis(2,3-dihydroxypropyl)-2,4,6-triiodobenzene-1,3-dicarboxamide;1,3-BenzenedicarboxaMide,5-aMino-N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-;5-AMINO-N,N'-BIS(2,3-DIHYDROXYPROPYL)-2,4,6-TRIIODO-1,3-BENZENEDICARBOXAMIDE;5-AMINO-N,N'-BIS-(2,3-DIHYDROXYPROPYL)-2,4,6-TRIIODOISOPHTHALAMIDE | | CAS: | 76801-93-9 | | MF: | C14H18I3N3O6 | | MW: | 705.02 | | EINECS: | 474-080-4 | | Product Categories: | Aromatics;Isotope Labelled Compounds;Labeling and Diagnostics Reagents;Intermediate of Ioversol | | Mol File: | 76801-93-9.mol |  |
| | 5-Amino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide Chemical Properties |
| Melting point | 195°C (dec.) | | Boiling point | 684.9±55.0 °C(Predicted) | | density | 2.386±0.06 g/cm3(Predicted) | | vapor pressure | 0Pa at 25℃ | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | solubility | DMSO (Slightly, Heated), Methanol (Slightly) | | form | neat | | pka | 11.58±0.46(Predicted) | | color | White to Off-White | | Stability: | Hygroscopic | | InChIKey | KAEGSAWWVYMWIQ-UHFFFAOYSA-N | | LogP | -1.81 at 23℃ and pH5.83 | | Surface tension | 72.85mN/m at 1g/L and 20℃ | | CAS DataBase Reference | 76801-93-9(CAS DataBase Reference) |
| | 5-Amino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide Usage And Synthesis |
| Description | 5-Amino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide
is an experimental compound that is used in the industrial preparation
of pharmaceuticals and agricultural chemicals. It has a molecular weight
of 191.14 g/mol. The crystallization process involves the use of
ethanol to create supersaturation and then cooling to induce
crystallization. This compound can be synthesized by an iodination
reaction with x-ray irradiation at low temperatures. | | Uses | Used as an intermediate in the industrial preparation of non-ionic X-ray contrast agents such as Iohexol (I729500), Ioversol (I737000), Ioxilan (I737500), Iopamidol (I735600). |
| | 5-Amino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide Preparation Products And Raw materials |
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