Empagliflozin
| パラメータ | 仕様 |
|---|---|
| 製品名 | Empagliflozin |
| CAS番号 | 864070-44-0 |
| 分子式 | C23H27ClO7 |
| 分子量 | 450.91 g/mol |
| 外観 | 白色からオフホワイトの結晶性粉末 |
| 分析(HPLC) | ≥99.5% |
| 溶解度 | Soluble in DMSO, methanol; slightly soluble in water |
| パッケージ | 25 kg net fiber drum with double polyethylene liner |
お困りですか? 弊社チームまでお問い合わせください

同義語: (2S,3R,4R,5S,6R)-2-[4-Chloro-3-[[4-[(3S)-oxolan-3-yl]oxyphenyl]methyl]phenyl]-6-(hydroxymethyl)oxane-3,4,5-triol, BI 10773, Jardiance, Glyxambi, Synjardy, Empagliflozinum
Empagliflozin has quickly become a flagship molecule in the SGLT2 inhibitor class, and demand from formulators reflects that. Since its approval, it has moved well beyond type 2 diabetes into heart failure and chronic kidney disease indications, which has widened the customer base considerably. For generic and specialty manufacturers, the API is now a core line item rather than a niche addition.
Chemically, empagliflozin is a C-glucoside bearing a chlorinated biphenyl-like scaffold. It is synthesized through a multistep route that typically starts from a protected glucose derivative and a substituted benzyl halide, followed by stereoselective glycosylation and deprotection. The resulting molecule is a potent, orally active inhibitor of sodium-glucose cotransporter 2 (SGLT2), responsible for the majority of renal glucose reabsorption.
We supply empagliflozin with an assay of ≥99.5% by HPLC, produced under cGMP conditions. Each batch is tested for residual solvents, heavy metals, and related substances to meet pharmacopeial expectations. The material is micronized to a consistent particle size, which helps with blend uniformity in tablet formulations. It is available in development quantities as well as commercial-scale lots.
Empagliflozin is a single enantiomer, and enantiomeric purity is critical for activity. Our material is manufactured with a stereoselective route that minimizes the formation of the undesired enantiomer. The API is non-hygroscopic under normal storage conditions and shows good stability in the solid state.
It is practically insoluble in water but freely soluble in polar aprotic solvents like DMSO and DMF. This solubility profile is well suited to standard wet granulation and roller compaction processes. The substance does not require special handling beyond routine API precautions.
| Test Item | 仕様 |
|---|---|
| 識別 | IR, HPLC retention time conforms to reference standard |
| 乾燥減量 | ≤0.5% |
| 重金属 | ≤20 ppm |
| Microbial Limits | Total aerobic count ≤1000 CFU/g; yeast & mold ≤100 CFU/g; absence of E. coli and Salmonella |
| Organic Impurities | Any individual impurity ≤0.10%; total impurities ≤0.5% |
| 残留溶剤 | Meets ICH Q3C limits |
Our MOQ is 1 kg for development and pilot-scale needs. For commercial supply, we recommend 25 kg drums, but we can accommodate intermediate quantities.
Stock items ship within 3-5 business days. Custom synthesis or large-volume orders typically require 3-5 business days, depending on scheduling and batch size.
Yes, a COA is issued for every batch. We can provide samples (typically 10–50 g) for evaluation, along with MSDS and TDS. Sample requests are usually processed within 48 hours.
Learn more about our quality control and certifications, or send us your specification for a quotation.