Saxagliptin
| Parametr | Specyfikacja |
|---|---|
| Nazwa produktu | Saxagliptin |
| Numer CAS | 361442-04-8 |
| Wzór cząsteczkowy | C18H25N3O2 |
| Masa cząsteczkowa | 315.41 g/mol |
| Wygląd | Biały lub prawie biały krystaliczny proszek |
| Oznaczenie (HPLC) | ≥99,01 TP3T |
| Rozpuszczalność | Soluble in DMSO, methanol; slightly soluble in water |
| Opakowanie | 25 kg fiber drum with double polyethylene liners |
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Synonimy: (1S,3S,5S)-2-[(2S)-2-Amino-2-(3-hydroxytricyclo[3.3.1.03,7]dec-1-yl)acetyl]-2-azabicyclo[3.1.0]hexane-3-carbonitrile, BMS-477118, Onglyza, Komboglyze
Saxagliptin is a potent, orally active dipeptidyl peptidase-4 (DPP-4) inhibitor developed for the treatment of type 2 diabetes. It is a synthetic small molecule that belongs to the gliptin class and is characterized by a nitrile-pyrrolidine scaffold. Unlike some other DPP-4 inhibitors, saxagliptin is rapidly absorbed and exhibits a unique metabolic profile, forming an active metabolite (5-hydroxy saxagliptin) that retains significant inhibitory activity.
Chemically, saxagliptin is a cyclopropyl-fused pyrrolidine-carbonitrile derivative. Its structure includes a 3-hydroxyadamantyl group, which contributes to its high selectivity and prolonged duration of action. The compound is typically manufactured as the free base or as the hydrochloride salt, with the free base being the most common form for pharmaceutical formulations.
In the pharmaceutical industry, saxagliptin is primarily used as an active pharmaceutical ingredient (API) in the production of oral antidiabetic medications. It is often combined with metformin or other antidiabetic agents to improve glycemic control in patients with type 2 diabetes. The API is subject to stringent quality control measures to ensure high purity and consistent performance.
| Test Item | Specyfikacja |
|---|---|
| Identyfikacja | IR, HPLC retention time conforms to reference standard |
| Strata przy suszeniu | ≤0.5% |
| Popiół po spaleniu | ≤0,11 TP3T |
| Metale ciężkie | ≤20 ppm |
| Organic Impurities | Any individual impurity ≤0.2%; total impurities ≤0.5% |
| Pozostałości rozpuszczalników | Meets ICH Q3C requirements |
| Wartości graniczne dla mikroorganizmów | Total aerobic count ≤1000 CFU/g; yeast and mold ≤100 CFU/g; absence of E. coli and S. aureus |
Our standard MOQ is 1 kg. For smaller quantities, please contact our sales team to discuss your specific needs.
Yes, a COA is provided with every shipment. Samples are available upon request to qualified customers for evaluation purposes.
Lead time is generally 3-5 business days after order confirmation, depending on the quantity and current production schedule.
Learn more about our quality control and certifications, or send us your specification for a quotation.
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