8-azaxanthine

3H-1,2,3-triazolo[4,5-d]pyrimidine-5,7-diol

CAS: 1468-26-4 C4 H3 N5 O2 MW: 153.10131000

Identification

Name8-azaxanthine
IUPAC2,3-dihydrotriazolo[4,5-d]pyrimidine-5,7-dione
CAS Number1468-26-4
EINECS215-992-2
FDA UNII97MRZ3ZY2U
Molecular FormulaC4 H3 N5 O2
Molecular Weight153.10131000
MDL NumberMFCD00150528
Nikkaji NumberJ13.128H
Beilstein0010424

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 SDSView
Oral/Parenteral Toxicityintraperitoneal-mouse LD50 200 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorypharmaceuticals / chemical synthisis
Recommendation for 8-azaxanthine usage levels up tonot for fragrance use.
Recommendation for 8-azaxanthine flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

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.