High Purity Cefazolin Sodium CAS 27164461 China Factory and Suppliers
Looking for premium Cefazolin Sodium? As leading China suppliers and a certified factory, we provide high-purity API for sterile injectable antibiotics. Our Cefazolin Sodium ensures broad-spectrum efficacy against Gram-positive organisms, ideal for surgical prophylaxis and clinical use.
About this product
Product information from the supplier.
Cefazolin Sodium is a premium-grade sodium salt form of Cefazolin, a potent β-lactam antibiotic within the cephalosporin class. Specifically engineered for high antibacterial efficacy, it demonstrates exceptional activity against staphylococci and streptococci, positioning it as a critical pharmaceutical component for preoperative prophylaxis and the treatment of moderate bacterial infections.
Designed for stability and rapid therapeutic action, our Cefazolin Sodium is a mainstay in emergency and surgical medicine. It serves as the primary active pharmaceutical ingredient (API) for sterile injectable formulations, ensuring reliable performance in treating infections of the skin, bone, urinary tract, and respiratory system while maintaining a favorable safety profile.
Detailed Parameters
| Product Name | Cefazolin Sodium | CAS Number | 27164-46-1 |
|---|---|---|---|
| Chemical Class | Cephalosporin / β-lactam | Form | Sodium Salt Powder |
| Primary Use | Antibiotic API | Target Pathogens | Staphylococci & Streptococci |
| Packaging Options | Fiber Drums / Sterile Vials | Standard Weight | 10 kg to 25 kg per drum |
| Storage Condition | Cool, Dry, Ventilated | Sensitivity | Moisture & Light Sensitive |
Key Advantages
Broad Spectrum Efficacy
Excellent antibacterial activity against key Gram-positive pathogens, ensuring superior clinical outcomes.
Fast-Acting Response
Known for rapid therapeutic onset, making it ideal for urgent surgical and emergency medical interventions.
High Purity API
Manufactured under strict pharmaceutical standards to ensure maximum potency and minimal impurity levels.
Proven Safety Profile
A dependable safety record when administered according to pharmacopeial guidelines by medical professionals.
Excellent Stability
Maintains high chemical stability in solution, facilitating precise dosing for injectable formulations.
Flexible Packaging
Available in customized pharmaceutical-grade containers to meet diverse global manufacturing needs.
Product Gallery
Management Platforms
Quality Control
Rigorous batch testing ensures every shipment meets global pharmacopeia standards.
Sterile Processing
Handled under sterile manufacturing conditions to prevent contamination.
Supply Chain Sync
Real-time tracking and logistics management for time-sensitive pharmaceutical delivery.
Compliance Audit
Full documentation and traceability for regulatory submissions and audits.
Inventory Optima
Strategic stockpiling to ensure uninterrupted supply for critical medical needs.
Custom Formulation
Technical support for reconstitution and solvent integration guidelines.
Investment Return Comparison
| Metric | Standard Grade API | Our Premium Cefazolin Sodium |
|---|---|---|
| Purity Level | Standard Pharma | Ultra-High Pharmaceutical Grade |
| Stability Period | Moderate | Extended Shelf-life Stability |
| Solubility Rate | Variable | Optimized Rapid Solubility |
| Regulatory Ease | Basic Docs | Full Compliance Documentation |
| Yield Efficiency | Average | High Conversion in Formulation |
Frequently Asked Questions
Cefazolin Sodium is used as a primary Active Pharmaceutical Ingredient (API) to manufacture sterile injectable antibiotics used for perioperative prophylaxis and bacterial infection treatment.
It must be stored in a cool, dry, and well-ventilated area, strictly protected from moisture and light to ensure chemical stability and potency.
Standard bulk packaging consists of double polyethylene bags inside fiber drums, typically in 10 kg to 25 kg sizes, though customized sterile glass vials are available.
It exhibits excellent antibacterial activity particularly against staphylococci and streptococci, making it ideal for skin and bone infection prophylaxis.
It is generally reconstituted using sterile water for injection or other suitable solvents in accordance with specific pharmacopeial guidelines.
Yes, our product is manufactured under strict pharmaceutical-grade conditions to meet the rigorous requirements of the chemical reagents and additives industry.