Inosine
| Nom du produit | Inosine |
|---|---|
| Numéro CAS | 58-63-9 |
| Autres noms | Hypoxanthine riboside; 9-β-D-Ribofuranosylhypoxanthine; Inosine-9-β-D-ribofuranoside |
| Formule moléculaire | C10H12N4O5 |
| Poids moléculaire | 268.23 g/mol |
| Apparence | Poudre cristalline blanche à blanc cassé |
| Essai (HPLC) | ≥99,01 TP3T |
| Perte au séchage | ≤ 0,51 TP3T |
| Résidu au feu | ≤ 0,11 TP3T |
| Métaux lourds | ≤ 10 ppm |
| Solubilité | Slightly soluble in water, practically insoluble in ethanol |
| Granulométrie | 98% pass 80 mesh |
| Colis | Fût en fibre de 25 kg avec double revêtement en polyéthylène |
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Synonymes : Hypoxanthine riboside, 9-β-D-Ribofuranosylhypoxanthine, Inosine-9-β-D-ribofuranoside, Inosine
Inosine is a naturally occurring purine nucleoside formed by the deamination of adenosine, consisting of a hypoxanthine base attached to a ribose sugar via a β-N9-glycosidic bond. While it appears in small quantities in animal tissues and certain plant sources, commercial material is produced through fermentation or chemical synthesis, yielding a high-purity white crystalline powder that meets stringent pharmaceutical standards.
As an intermediate in purine metabolism, inosine serves as a precursor to adenosine and guanosine nucleotides, influencing cellular energy balance and signaling pathways. This central role has made it a valuable molecule for pharmaceutical research, nutraceutical formulations, and biochemical assays. Its ability to modulate adenosine receptors and support ATP regeneration has attracted interest in areas ranging from cardiovascular health to neuroprotection.
| Paramètre | Spécifications |
|---|---|
| Essai (HPLC) | ≥99,01 TP3T |
| Apparence | Poudre cristalline blanche à blanc cassé |
| Identification | IR and HPLC conform to reference standard |
| Perte au séchage | ≤ 0,51 TP3T |
| Résidu au feu | ≤ 0,11 TP3T |
| Métaux lourds | ≤ 10 ppm |
| Solubilité | Slightly soluble in water, practically insoluble in ethanol |
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