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| 3,7-DIMETHYL-2,6,8-TRIHYDROXYPURINE Basic information |
| Product Name: | 3,7-DIMETHYL-2,6,8-TRIHYDROXYPURINE | | Synonyms: | 3,7-Dimethyluric acid >=95.0% (HPLC);3,7-DIMETHYL-2,6,8-TRIHYDROXYPURINE;3,7-DIMETHYLURIC ACID;3,7-dimethyl-9H-purine-2,6,8-trione;3,7-Dimethyl-1H-purine-2,6,8(3H,7H,9H)-trione;3,7-Dimethyl-7H-purine-2,6,8(1H,3H,9H)-trione;7,9-Dihydro-3,7-dimethyl-1H-purine-2,6,8(3H)-trione;8-Hydroxy-3,7-dimethylxanthine | | CAS: | 13087-49-5 | | MF: | C7H8N4O3 | | MW: | 196.16 | | EINECS: | | Product Categories: | | Mol File: | 13087-49-5.mol |
| 3,7-DIMETHYL-2,6,8-TRIHYDROXYPURINE Chemical Properties |
| Melting point | ≥300 °C | | density | 1.63±0.1 g/cm3(Predicted) | | pka | 5.84±0.70(Predicted) | | BRN | 218966 |
| 3,7-DIMETHYL-2,6,8-TRIHYDROXYPURINE Usage And Synthesis |
| Uses | 3,7-Dimethyluric Acid is caffeine metabolite which eliminates through urine. | | Definition | ChEBI: An oxopurine that is 7,9-dihydro-1H-purine-2,6,8(3H)-trione substituted by methyl groups at N-3 and N-7. | | General Description | 3,7-Dimethyluric acid (3,7-DMU, 3,7-Dimethyl-2,6,8-trihydroxypurine), a purine derivative, is a dimethylated uric acid. It has a pyrimidine ring fused to an imidazole ring. Mechanism of the transformation of theobromine to 3,7-DMU in rat liver microsomal incubations has been investigated. |
| 3,7-DIMETHYL-2,6,8-TRIHYDROXYPURINE Preparation Products And Raw materials |
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