Pazufloxaxin Methanesulfonate (CAS 163680-77-1): High Purity 99% Pharmaceutical Raw Material for API Manufacturing – Benefits, Applications & Sourcing Guide
Unlock the potential of your pharmaceutical innovations with our premium 99% Pazufloxaxin Methanesulfonate. As a critical Active Pharmaceutical Ingredient (API), it ensures superior drug efficacy and safety, empowering your development from concept to market.
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Pazufloxaxin Methanesulfonate
Pazufloxaxin Methanesulfonate (CAS 163680-77-1) is a 99% pure pharmaceutical-grade raw material, presented as a white or off-white solid powder. This Active Pharmaceutical Ingredient (API) is vital for chemical medicine manufacturing, adhering to stringent quality standards such as GMP, USP, EP, and BP. It features specific solubility properties and a melting point between 211ºC~216ºC, ensuring consistent performance in drug formulations. With high assay purity and controlled particle size, it is suitable for various pharmaceutical applications, ensuring efficacy and safety in drug formulations. This product is a key component for drug developers and manufacturers seeking reliable, high-quality active ingredients.
- Experience consistent results with our 99% Pazufloxaxin Methanesulfonate raw material, ensuring reliability in your production processes.
- Rely on our pharmaceutical grade Pazufloxaxin Methanesulfonate supplier for the highest quality and compliance with global standards.
- Our Pazufloxaxin Methanesulfonate CAS 163680-77-1 is meticulously produced, offering a melting point that meets rigorous industry specifications.
- Discover the optimal Pazufloxaxin Methanesulfonate solubility profile, critical for seamless integration into various drug formulations.
Product Benefits & Advantages
Exceptional Purity & Potency
Our Pazufloxaxin Methanesulfonate boasts high purity (99%), ensuring maximum potency and efficacy in every batch, a critical factor for any pharmaceutical grade Pazufloxaxin Methanesulfonate supplier. This allows for precise dosing and predictable therapeutic outcomes, reducing the risk of impurities affecting drug performance.
Global Standard Compliance
This API is fully GMP/USP/EP/BP compliant, reflecting our commitment to the highest quality standards in pharmaceutical manufacturing. Sourcing from a reliable Pazufloxaxin Methanesulfonate API manufacturer ensures adherence to regulatory requirements globally, streamlining your product's market entry.
Optimized Physical Characteristics
As a white or off-white powder with controlled particle size and specific melting point, our Pazufloxaxin Methanesulfonate offers excellent processability. These consistent quality characteristics are vital for efficient formulation and stability, making us a preferred 99% Pazufloxaxin Methanesulfonate raw material provider.
Key Applications
Chemical Medicine Production
Pazufloxaxin Methanesulfonate serves as a cornerstone chemical medicine raw material, essential for synthesizing effective pharmaceutical compounds. Its high purity ensures it meets the demanding standards of modern drug manufacturing, crucial for developing new therapies.
Antineoplastic Drug Development
While primarily an antibiotic, the reported function in the source material indicates potential for Antineoplastic drug development. This highlights its versatility as a high-value API, offering new avenues for research and therapeutic applications. Manufacturers seeking a 99% Pazufloxaxin Methanesulfonate raw material can explore its broader utility.
Active Pharmaceutical Ingredient (API) Manufacturing
As a core Active Pharmaceutical Ingredient (API), Pazufloxaxin Methanesulfonate is instrumental in producing a wide range of finished pharmaceutical products. This makes it a crucial component for companies engaged in API manufacturing, seeking to ensure the quality and efficacy of their end products.
Advanced Drug Formulation
Its precise physical and chemical properties, including Pazufloxaxin Methanesulfonate solubility and controlled particle size, make it ideal for complex drug formulation processes. This ensures optimal bioavailability and stability in various dosage forms, from tablets to injectable solutions, making it a valuable asset for pharmaceutical innovation.