8-azaxanthine
3H-1,2,3-triazolo[4,5-d]pyrimidine-5,7-diol
Identification
| Name | 8-azaxanthine |
| IUPAC | 2,3-dihydrotriazolo[4,5-d]pyrimidine-5,7-dione |
| CAS Number | 1468-26-4 |
| EINECS | 215-992-2 |
| FDA UNII | 97MRZ3ZY2U |
| Molecular Formula | C4 H3 N5 O2 |
| Molecular Weight | 153.10131000 |
| MDL Number | MFCD00150528 |
| Nikkaji Number | J13.128H |
| Beilstein | 0010424 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Flash Point | 32.00 °F. TCC ( 0.00 °C. ) (est) |
| logP (o/w) | -1.440 (est) |
| Soluble in | water, 3.943e+004 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | intraperitoneal-mouse LD50 200 mg/kg |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | pharmaceuticals / chemical synthisis |
| Recommendation for 8-azaxanthine usage levels up to | not for fragrance use. |
| Recommendation for 8-azaxanthine flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
2,3-
dihydrotriazolo[4,5-d]pyrimidine-5,7-dione
2,6-
dioxy-8-azapurine
1H-1,2,3-
triazolo(4,5-d)pyrimidine-5,7(4H,6H)-dione
3H-1,2,3-
triazolo[4,5-d]pyrimidine-5,7-diol
1H-[1,2,3]
triazolo[4,5-d]pyrimidine-5,7(4H,6H)-dione
xanthazol
PubMed:
Spectroscopic investigations and hydrogen bond interactions of 8-aza analogues of xanthine, theophylline and caffeine: a theoretical study.
PubMed:
Fluorescence emission properties of 8-aza analogues of caffeine, theophylline, and related N-alkyl xanthines.
PubMed:
Phosphodiesterase 4-dependent regulation of cyclic AMP levels and leukotriene B4 biosynthesis in human polymorphonuclear leukocytes.
PubMed:
8-Azaxanthine derivatives as antagonists of adenosine receptors.
PubMed:
Dissociation of lipolysis from the levels of cyclic AMP in rat epididymal fat cells.
PubMed:
Use of Escherichia coli mutants to evaluate purines, purine nucleosides, and analogues.