Synonym: 2,6-Dioxopurine; 3,7-Dihydropurine-2,6-dione; Xanthin; 2,6-Dihydroxypurine
CAS Number: 69-89-6
Empirical Formula (Hill Notation): C5H4N4O2
Molecular Weight: 152.11
EC Number: 200-718-6
MDL Number: MFCD00078453
Linear Formula: C5H4N4O2
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: X0626-25G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: X0626-10G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: X0626-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: X0626-5G
| assay |
≥99.5% (HPLC) |
| biological source |
synthetic |
| form |
powder |
| InChI |
1S/C5H4N4O2/c10-4-2-3(7-1-6-2)8-5(11)9-4/h1H,(H3,6,7,8,9,10,11) |
| InChI key |
LRFVTYWOQMYALW-UHFFFAOYSA-N |
| purified by |
recrystallization |
| Quality Level |
400  |
| SMILES string |
O=C1NC(=O)c2nc[nH]c2N1 |
| solubility |
1 M NaOH: soluble 50 mg/mL, clear, colorless to faintly yellow |
| storage temp. |
2-8°C |
| Biochem/physiol Actions: |
Xanthine participates in the catabolism of nucleic acids and nucleotides and is a precursor of uric acid. It is a versatile compound that shows therapeutic effects in several pharmacological conditions related to respiratory tract, central nervous system (CNS), kidney, stomach, smooth muscle cells, and heart. Xanthine acts as a biomarker for detecting gout. |
| General description: |
Xanthine is an important component of the various natural and synthetic medicinal active compounds. Various forms of xanthine such as caffeine, theobromine, and theophylline are found in chocolate, cocoa, tea, yeast, potatoes, animal organs, and coffee. Xanthine is a purine-based natural heterocyclic alkaloid composed of a central nitrogen atom and a pyrimidine ring that is fused with an imidazole ring. Xanthine is produced from several different precursors in the purine metabolic pathway: deamination of guanine-by-guanine deaminase and conversion of hypoxanthine by xanthine oxidoreductase. |
| Packaging: |
5, 10, 25 g in poly bottle |
| Hazard Codes |
Xi |
| Risk Statements |
36-43 |
| Safety Statements |
36/37 |
| RIDADR |
NONH for all modes of transport |
| WGK Germany |
WGK 3 |
| Purity |
≥99.5% (HPLC) |
| Storage Temp. |
2-8°C |
| UNSPSC |
41106305 |