Cephalotin Sodium, identified by its Chemical Abstracts Service (CAS) number 58-71-9, represents a pivotal active pharmaceutical ingredient (API) and intermediate within the global pharmaceutical landscape. Its primary significance lies in its indispensable role in the synthesis and formulation of cephalosporin antibiotics, a class of broad-spectrum antibiotics critical for treating a wide array of bacterial infections. The consistent demand for effective antibiotic therapies underscores the importance of reliable sources for high-quality Cephalotin Sodium.
Our offering of Cephalotin Sodium is presented as a fine powder, a form highly conducive to efficient handling and processing in pharmaceutical manufacturing facilities. A cornerstone of our product's value proposition is its exceptional purity, consistently maintained at a level exceeding 99%. This high degree of purity is paramount, directly impacting the safety, efficacy, and stability of the final medicinal products manufactured using this material. Impurities in pharmaceutical raw materials can lead to unwanted side effects, reduced potency, or manufacturing challenges, making stringent purity standards non-negotiable in this sensitive sector.
The production of Cephalotin Sodium adheres to rigorous international quality standards. Our commitment to quality is reflected in certifications such as GMP (Good Manufacturing Practice), USP (United States Pharmacopeia), BP (British Pharmacopoeia), and Kosher. Adherence to GMP ensures that the product is consistently produced and controlled according to quality standards appropriate for its intended use, minimizing risks inherent in any pharmaceutical production. Meeting USP and BP pharmacopeia standards guarantees that the product conforms to established specifications for identity, strength, quality, and purity, recognized globally by regulatory bodies. The Kosher certification further signifies compliance with specific dietary laws, relevant for certain markets and applications.
Each batch of Cephalotin Sodium undergoes comprehensive quality control testing. This includes verifying its chemical composition, physical properties like melting point (approximately 240ºC as per available data for this specific form), and ensuring the absence of specified impurities. Advanced analytical techniques are employed at each stage of the manufacturing process, from raw material sourcing to the final packaged product, to uphold our quality promise. The molecular formula, C16H15N2NaO6S2, and molecular weight, 418.42 g/mol, are critical identifiers that are verified to ensure consistency and authenticity of the compound.
The product is typically supplied in 25kg drums, a standard packaging size suitable for bulk handling and transportation within the pharmaceutical supply chain. This packaging ensures the integrity and stability of the powder during transit and storage. With an established production capacity, we are equipped to meet substantial demands from pharmaceutical manufacturers globally, ensuring a stable and reliable supply chain partner for their API needs. The ability to produce significant volumes annually underscores our capability to support large-scale manufacturing operations.
Reliability and consistency are critical factors when sourcing pharmaceutical raw materials. A dependable supplier of Cephalotin Sodium is essential for manufacturers to maintain uninterrupted production schedules and ensure the consistent quality of their finished drug products. Our operational protocols are designed to minimize variability and maximize consistency, from batch to batch.
Furthermore, understanding the application nuances of Cephalotin Sodium in antibiotic synthesis is crucial. As a key intermediate or direct API in cephalosporin production, its quality directly influences the therapeutic effectiveness of widely used injectable antibiotics prescribed for serious bacterial infections, including those affecting the respiratory tract, skin, soft tissues, urinary tract, and bloodstream. The pharmacological importance of the final products derived from Cephalotin Sodium highlights the critical need for sourcing this material from manufacturers committed to the highest quality standards.
For pharmaceutical companies looking to procure high-quality Cephalotin Sodium (CAS 58-71-9), finding a trusted supplier or manufacturer is the first step. We welcome inquiries from potential partners worldwide. Details regarding the current price per kilogram or per 25kg drum, minimum order quantities, and terms for purchase or buy orders can be obtained by contacting our sales department directly. We are committed to providing competitive pricing commensurate with the high quality and certified standards of our product. Our team is ready to provide all necessary documentation and support to facilitate your sourcing and procurement process.
Choosing a certified and experienced manufacturer like NINGBO INNO PHARMCHEM CO.,LTD. ensures access to a product that meets stringent global pharmaceutical requirements, supported by robust quality assurance and reliable supply chain logistics. We are dedicated to being a key partner in your success, supplying the foundational raw materials needed to produce life-saving medications.
Written by NINGBO INNO PHARMCHEM CO.,LTD.
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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.