Heparin sodium
| Parametro | Specifiche |
|---|---|
| Nome del prodotto | Heparin sodium |
| Numero CAS | 9041-08-1 |
| Formula molecolare | Variable (glycosaminoglycan polymer) |
| Aspetto | Polvere di colore da bianco a bianco sporco |
| Analisi | ≥ 180 IU/mg (USP) |
| Solubilità | Freely soluble in water; practically insoluble in ethanol and acetone |
| Confezione | 100 g, 1 kg, 5 kg |
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Sinonimi: Heparin sodium salt, Sodium heparin, Heparin sodium injection, Heparin sodium USP, Heparin sodium EP, Heparin sodium JP, Sodium heparinate
Heparin sodium is the sodium salt of a sulfated glycosaminoglycan obtained from porcine intestinal mucosa or bovine lung tissue. It is a highly sulfated polymer of alternating uronic acid and glucosamine residues, supplied as a white to off-white powder that is freely soluble in water. The material is standardized by its anticoagulant activity, expressed in International Units (IU) per milligram, and is typically available in potency grades suitable for pharmaceutical compounding and research applications.
As a bulk raw material, heparin sodium is purchased by formulators for its well-characterized anticoagulant properties. The product is supplied with a Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS) to support regulatory submissions and quality control. Orders are typically fulfilled from stock within 3-5 business days, with documentation provided for each lot.
Heparin sodium is offered as a USP/EP/JP grade powder, standardized to a minimum of 180 IU/mg on a dried basis. The powder is hygroscopic and should be stored in tightly sealed containers at controlled room temperature. It is available in small-scale packaging for research and development, as well as in bulk quantities for commercial production.
In pharmaceutical manufacturing, heparin sodium is used as an anticoagulant in injectable solutions, catheter lock solutions, and blood collection tubes. It also finds application in the preparation of anticoagulant coatings for medical devices and in diagnostic reagents. Formulators incorporate it into sterile injectables where its rapid onset and predictable dose-response are required.
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