Linagliptin
| Tham số | Thông số kỹ thuật |
|---|---|
| Tên sản phẩm | Linagliptin |
| Số CAS | 668270-12-0 |
| Công thức phân tử | C25H28N8O2 |
| Trọng lượng phân tử | 472.54 g/mol |
| Hình thức | Bột tinh thể màu trắng đến trắng ngà |
| Phương pháp phân tích (HPLC) | ≥ 99,01 TP3T |
| Độ hòa tan | Soluble in DMSO, methanol; slightly soluble in water |
| Gói | 25 kg fiber drum, inner double polyethylene bags |
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Từ đồng nghĩa: 2-[[(3R)-3-Amino-1-piperidinyl]-3,4-dihydro-3-oxo-1(2H)-isoquinolinyl]methyl]-4-methyl-1H-isoindole-1,3(2H)-dione, Tradjenta, Glyxambi, Jentadueto, BI 1356
Linagliptin has become a go-to DPP-4 inhibitor for formulators targeting type 2 diabetes, particularly in combination products where metformin or empagliflozin is the partner. Demand is steady from generic and specialty pharma companies alike, driven by its once-daily dosing, no renal dose adjustment, and minimal drug-drug interaction profile.
Chemically, linagliptin is a xanthine-based small molecule with a (R)-3-aminopiperidine side chain. It works by binding reversibly to the DPP-4 enzyme, slowing the breakdown of incretin hormones GLP-1 and GIP. This mechanism is well understood across the class, but linagliptin’s distinguishing feature is its predominantly biliary excretion—less than 5% renal—which sets it apart for patients with impaired kidney function.
Commercial material is held to tight purity specs, typically ≥99.0% by HPLC. Our production follows cGMP, with full traceability from API batch to final drum. Whether you are scaling a generic launch or running clinical batches, the documentation and consistency are there to support your filing.
Linagliptin is a synthetic small molecule, not a biological or botanical extract. It is manufactured through a multi-step chemical synthesis, starting from isoindoline-1,3-dione derivatives and piperidine building blocks. The final API is isolated as a crystalline free base, which offers good stability under normal storage conditions.
Each batch is characterized for identity, assay, and impurity profile. Residual solvents and elemental impurities are controlled according to ICH Q3C and Q3D guidelines. The material is micronized to a consistent particle size to support blend uniformity in solid dosage forms.
| Test Item | Thông số kỹ thuật |
|---|---|
| Xác định | IR, HPLC retention time conforms to reference |
| Mất mát khi sấy khô | ≤ 0,5% |
| Kim loại nặng | ≤ 20 ppm |
| Chất dung môi còn lại | Meets ICH Q3C limits |
| Giới hạn vi sinh vật | Total aerobic count ≤ 1000 CFU/g; absence of specified pathogens |
| Organic Impurities | Any unspecified impurity ≤ 0.10%; total impurities ≤ 0.50% |
We can supply from 1 kg for development work, but commercial pricing applies from 25 kg.
Stock material ships within 3-5 business days. Custom packaging may take 3-5 business days.
Yes, a COA is issued for every batch, and samples up to 100 g are available for evaluation.
Learn more about our quality control and certifications, or send us your specification for a quotation.
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