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The efficacy of pharmaceutical drugs is intrinsically linked to the precise quality and properties of their Active Pharmaceutical Ingredients (APIs). Ceftizoxime Sodium, identified by CAS number 68401-82-1, stands as a testament to this principle. As a sterile cephalosporin API powder, its chemical precision makes it an invaluable asset for pharmaceutical manufacturers engaged in sophisticated drug formulation.
Ceftizoxime Sodium is a synthetic antibiotic belonging to the third-generation cephalosporin class. Its molecular structure is carefully designed to target bacterial cell walls, inhibiting their synthesis and leading to bacterial death. The compound is produced as a solid, non-volatile powder, which ensures stability and ease of handling during the complex processes of drug formulation. The rigorous adherence to GMP standards in its manufacturing guarantees a high degree of purity and a consistent chemical profile, essential for predictable therapeutic outcomes.
The antibiotic and antimicrobial function of Ceftizoxime Sodium is well-established. It exhibits a broad spectrum of activity against various Gram-negative and Gram-positive bacteria. A key aspect of its chemical design is its resistance to degradation by many beta-lactamase enzymes, which is a significant advantage in combating antibiotic resistance. This inherent stability means that formulations containing Ceftizoxime Sodium are more likely to remain effective against bacteria that have developed defenses against other antibiotics.
For pharmaceutical companies, leveraging the precise chemical characteristics of Ceftizoxime Sodium is key to developing advanced drug formulations. Whether for injectable solutions or other delivery systems, the API’s purity, stability, and well-defined activity profile allow formulators to achieve optimal drug concentration, bioavailability, and shelf-life. This level of chemical precision ensures that the final medicinal product performs as intended.
In summary, Ceftizoxime Sodium (CAS 68401-82-1) is more than just an antibiotic; it is a product of meticulous chemical engineering. Its status as a sterile cephalosporin API powder, manufactured with exacting standards, provides the chemical precision that is fundamental to the creation of effective and reliable antibacterial drugs. Its continued use underscores the importance of high-quality APIs in safeguarding public health.
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1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;
2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;
3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).
A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.
A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.
A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.
