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| | 5,5-dihydroxyperhydropyrimidinetrione Basic information |
| Product Name: | 5,5-dihydroxyperhydropyrimidinetrione | | Synonyms: | 5,5-dihydroxyperhydropyrimidinetrione;5,5-Dihydroxy-2,4,6(1H,3H,5H)-pyrimidinetrione;5,5-Dihydroxybarbituric acid;5,5-Dihydroxyhexahydropyrimidine-2,4,6-trione;5,5-Dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione;5,5-dihydroxy-1,3-diazinane-2,4,6-trione;5,5-dihydroxy-pyrimidine-2,4,6-trione;2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-dihydroxy- | | CAS: | 3237-50-1 | | MF: | C4H4N2O5 | | MW: | 160.09 | | EINECS: | 221-796-8 | | Product Categories: | | | Mol File: | 3237-50-1.mol |  |
| | 5,5-dihydroxyperhydropyrimidinetrione Chemical Properties |
| Melting point | 172 °C | | Boiling point | 285.94°C (rough estimate) | | density | 1.8517 (rough estimate) | | refractive index | 1.4610 (estimate) | | pka | 6.60±0.10(Predicted) | | EPA Substance Registry System | 5,5-Dihydroxybarbituric acid (3237-50-1) |
| | 5,5-dihydroxyperhydropyrimidinetrione Usage And Synthesis |
| General Description | Triclinic piacoidal crystals. White granular solid. | | Air & Water Reactions | Soluble in water. | | Reactivity Profile | Organic imides, of which alloxan is one, react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generate mixed oxides of nitrogen. | | Fire Hazard | Flash point data for 5,5-dihydroxyperhydropyrimidinetrione are not available. 5,5-dihydroxyperhydropyrimidinetrione is probably combustible. |
| | 5,5-dihydroxyperhydropyrimidinetrione Preparation Products And Raw materials |
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