Products

Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions

    • Product Name: Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions
    • Alias: SCPS
    • Einecs: 242-011-3
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    355417

    Product Name Sulfachloropyrazine Sodium Soluble Powder
    Purpose Veterinary Grade API
    Appearance White or almost white crystalline powder
    Solubility Freely soluble in water
    Molecular Formula C10H8ClN4NaO3S
    Molecular Weight 322.71 g/mol
    Application Forms Tablets, injections, capsules, powders, granules, premix, solutions
    Assay Purity ≥98%
    Main Use Treatment of coccidiosis and bacterial infections in animals
    Storage Condition Keep in a cool, dry place, protected from light
    Shelf Life Two years if properly stored
    Cas Number 23282-55-5

    As an accredited Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaging: Sealed aluminum foil bag, labeled, moisture-proof, 1 kg net weight, veterinary grade, for professional use—API Sulfachloropyrazine Sodium.
    Shipping **Shipping Description:** Sulfachloropyrazine Sodium Soluble Powder (Veterinary Grade API) is securely packaged in sealed, moisture-proof containers and shipped via air, sea, or express courier. Shipments maintain original labeling and Certificate of Analysis, with careful handling to prevent damage. Delivery is prompt, with full documentation and regulatory compliance for veterinary pharmaceutical products.
    Storage Store Sulfachloropyrazine Sodium Soluble Powder (Veterinary Grade API) in a tightly sealed container, protected from light and moisture. Keep in a cool, dry place below 25°C (77°F). Avoid exposure to heat, humidity, and direct sunlight. Ensure storage areas are well-ventilated and inaccessible to unauthorized personnel, children, or animals. Follow all relevant safety and handling guidelines for veterinary pharmaceuticals.
    Application of Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions

    Purity 99%: Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with 99% purity is used in veterinary tablet formulation, where it ensures optimal antimicrobial efficacy against coccidiosis.

    Particle Size <50 µm: Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with particle size below 50 µm is used in injectable preparations, where it enables rapid dissolution and consistent bioavailability.

    Stability at 25°C: Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with confirmed stability at 25°C is used in premix manufacturing, where it maintains potency throughout shelf life.

    Water Solubility ≥95%: Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with water solubility over 95% is used in oral solution preparations, where it guarantees homogenous drug dispersion.

    Molecular Weight 350.76 g/mol: Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions at molecular weight 350.76 g/mol is used in veterinary capsule development, where it provides precise dosage control and uniformity.

    Melting Point 220°C: Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with a melting point of 220°C is used in powder premix applications, where it ensures thermal integrity during processing.

    Heavy Metal Content ≤10 ppm: Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with heavy metal content under 10 ppm is used in granule production, where it meets strict safety and regulatory standards for animal use.

    Loss on Drying ≤1.5%: Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with loss on drying below 1.5% is used in veterinary injection systems, where it assures chemical stability and efficient reconstitution.

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    Competitive Sulfachloropyrazine Sodium Soluble Powder Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.

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    Tel: +8615365186327

    Email: admin@ascent-chem.com

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    Certification & Compliance
    More Introduction

    Sulfachloropyrazine Sodium Soluble Powder: Supporting Livestock Health Through Reliable Chemistry

    Experience from the Manufacturer's Perspective

    Working closely with veterinarians, feed factories, and formulators over the years, we've seen how livestock operations rely on products that meet real-world requirements under demanding conditions. Sulfachloropyrazine Sodium Soluble Powder, veterinary grade and produced at our facility, addresses these needs by offering a stable, high-quality active pharmaceutical ingredient for manufacturers of tablets, injections, capsules, powders, granules, premixes, and solutions.

    Understanding the Product and Its Model

    From the outset, the decision to produce Sulfachloropyrazine Sodium in a soluble powder form centered on versatility and practicality. The powder flows freely, mixes evenly in feed and water, and dissolves quickly—results achieved by controlled particle size and precisely managed drying steps during production. The model we supply is a highly pure API, designed for easy formulation and consistent results. Years of continuous process improvements, guided by feedback from users and careful monitoring, ensure batch consistency and reproducibility.

    Purity and Specification

    Through experience, we have learned the importance of purity in pharmaceutical ingredients. Our Sulfachloropyrazine Sodium regularly tests above industry benchmarks for purity and solubility. With every production run, analysts employ validated chromatographic and titration methods to confirm chemical identity and exclude detectable contaminants. Specifications are set not only to meet pharmacopoeial standards where they apply but to address the concerns raised by formulation experts about carryover, dissolution rates, and shelf stability. The powder passes microbial, heavy metal, and moisture checks, tracked by fully traceable batch records. These steps protect the efficacy and shelf life of finished products, reflected in the feedback we receive from major users.

    Applications and Daily Practice

    Sulfachloropyrazine Sodium Soluble Powder remains central to the manufacture of veterinary medicines for poultry, swine, rabbits, and other food animals. It functions as a key sulfonamide antibiotic active ingredient. End-use forms include water-soluble powders for drinking water medication, tablets to treat individual animals, injectable solutions for rapid intervention, and premixes for feed manufacturing. Our technical team works with formulators to adapt powder particle size and bulk density, supporting dose accuracy and efficient dispersion. Manufacturers have no need to contend with excessive dust, caking, or undissolved residues: extensive experience in granulating, sieving, and microtracing each lot eliminates these typical processing headaches.

    Why Users Choose Our Sulfachloropyrazine Sodium Sodium

    Veterinary medicine producers have their pick of sulfonamide APIs from a wide range of sources. In our discussions with long-term customers, several points keep resurging:

    Real-World Differences From Alternative Sulfonamides

    Not all manufacturers follow equivalent processes—and outcomes reflect this reality. Compared with some domestic and regional producers, differences become clear:

    What Sets Our Process Apart

    Stories from the field continually drive home the importance of robust API production. Our teams refine every production stage based on lessons learned in real farms and factories. We select raw materials from suppliers who provide traceable origin data and test each incoming batch for heavy metals and related impurities—assembly lines grind, sift, and dry the product in tightly regulated humidity and temperature environments. On the production floor, digital sensors and human operators check every step. Periodic audits, both internal and from customers and authorities, scrutinize our records and physical product. These operational routines create a stable, reliable foundation from manufacturing through to usage in the field.

    Why Particle Size and Purity Support Tableting and Capsule Production

    In the tableting area, formulators have pointed out that excessive fines or random particle size distributions cause serious technical challenges: variable weight, poor compressibility, and sticking on machinery. Our experience with micronization tells us that consistently-sized powder saves valuable hours during blending and compression steps. The finished granulate avoids segregation, and high purity rules out unpredictable reactions with excipients. For capsule and sachet lines, this translates into dose consistency and reduced operator interventions. Mixes made with our Sulfachloropyrazine Sodium reach homogeneity targets rapidly, supporting stringent regulatory testing and documentation.

    Engineering Solutions for Injections and Solutions

    Veterinary injectable solutions present a demanding test for any sulfonamide API. No notorious undissolved particles can persist when solutions require sterile filtration or autoclaving. Our soluble powder dissolves thoroughly in water for injection with controlled agitation, revealing any insoluble traces during routine QC. Decades of experience demonstrate that low-endotoxin, low particulate batches reduce the risk of solution rejection and batch failures. By focusing on solubility, clarity, and chemical purity, our powder allows formulation teams to create trusted injectable drugs—supporting reliable therapeutic outcomes.

    Supporting Comprehensive Product Innovation

    Product development rarely follows a straight line. Our role as a manufacturer involves providing both chemical knowledge and advice on practical issues: interactions with other actives in premix, compatibility checks for excipients in suspension and granule formulations, and assistance with regulatory dossiers. These services address issues raised by customers dealing with ever-changing livestock production systems—ranging from shifts in animal genetics, farm management, or consumer demands. Through collaboration with those on the front lines, we respond to the real world, not theory.

    Dedicated Approach to Stability and Packaging

    Key details around moisture, light, and air exposure can make or break the effectiveness of a veterinary API in actual use. Recognizing this, we have invested in packaging systems that cater to the rigors of bulk export and local storage. The powder receives protection from strong foil laminates inside strong drums, and desiccant packs maintain dryness in shipment. Each packaging improvement comes from customer reports concerning unopened but compromised containers or powders that clumped on arrival. By upgrading barriers and refining sealing methods, we cut down on losses and customer complaints—not just for international buyers but for hot, humid, or variable environments at home.

    Addressing Regulatory and Compliance Realities

    Whether producing for highly regulated national programs or contract manufacturers addressing emerging markets, regulatory hurdles define daily work. Our team tracks changing animal health guidelines, antibiotic stewardship developments, and residue restrictions both locally and abroad. Each batch is produced under GMP conditions and comes with a full analytical profile, residue and contaminant status, and clear COA, helping customers navigate audits and submissions with confidence. Inspectors and customers alike can access our full documentation trail, from starting chemicals to shipped lot, reducing future risks and inquiries.

    Feedback-Driven Process Improvement

    Direct communication with users leads to improvements that static lab testing never reveals. Hearing from feed millers about off-odors or out-of-date labeling prompted us to invest in new labeling systems and upgraded air handling. Noting customer complaints about dust exposure resulted in a shift to more robust mechanical conveying, reducing powder loss and improving plant worker safety. Specification tweaks, such as adjusting particle size windows, fit real factory needs, and new product grades emerge in answer to field trials or documented failures. This iterative feedback cycle forms the backbone of our continuous improvement culture.

    Environmental and Occupational Focus

    Manufacturing responsible chemical products involves more than batch numbers and QC passes. We work to reduce occupational exposure for our own staff and downstream handlers by keeping dust and volatile residues at safe levels. Wastewater and wash residues undergo controlled treatment before discharge, and staff follow clear handling protocols. Throughout processing, routine air and surface measurements prevent contamination and safeguard operator health. These investments, tested over many years, enhance product safety profiles by reducing the risk of unintended workplace exposures and subsequent environmental impact.

    Industry Trends and the Role of Sulfachloropyrazine Sodium

    Animal health stakeholders face shifting pressures from changing disease patterns, heightened regulation on antibiotics, and increasing consumer sensitivity about drug residues in food products. Sulfonamides have earned their place in treating coccidiosis and certain bacterial infections, long recognized by veterinarians worldwide. Despite competition from newer molecules, demand for tried-and-true compounds with long-established safety profiles remains strong, particularly for markets focused on food safety and antibiotic residue control. Our experience shows that sound production and transparent supply chains outweigh mere cost advantages. Regulatory auditors and large-scale purchasing groups increasingly demand that manufacturers provide not just a substance, but a fully substantiated, well-documented supply backed by traceable records and accessible technical support.

    Solutions for Persistent Field Issues

    Coccidiosis and associated infections cost livestock producers billions in lost productivity every year. Veterinarians need consistent, shelf-stable powders that retain potency until use. From our perspective, supplying soluble Sulfachloropyrazine Sodium that maintains its properties through months of warehouse storage and across seasonal climate shifts is essential. We constantly analyze stability samples and accelerate stress tests, making packaging and formulation recommendations to producers before launch. By intervening early—helping buyers adjust mixing instructions for hard or soft water, or matching powder grades to local feed systems—we help them avoid wasted batches, regulatory setbacks, and overdoses.

    Building Trust Through Direct Experience

    As a chemical manufacturer involved in API production for decades, we deal daily with the challenges of keeping large, complex operations running smoothly. Direct relationships with customers bring another layer of understanding, letting us see how product traits—such as the speed of solubility or the accuracy of bulk density calibration—affect dosing and compliance. This approach fosters trust, as end-users know we will not walk away once the product leaves our gate. We dedicate staff to troubleshoot alongside customers, whether working through water chemistry problems on a poultry farm or meeting regulatory requirements for a new market launch.

    Why Our Sulfachloropyrazine Sodium Soluble Powder Makes a Difference

    Many animal drug manufacturers have learned the hard way that unreliable sources can cause failed mixes, weak dosing, or residue problems that damage reputation and sales. Choosing a trusted production source for Sulfachloropyrazine Sodium Soluble Powder gives veterinary drug producers, feed premixers, and distributors a dependable foundation. With documented purity, stability data, and robust support, our product stands up to the unpredictable realities of veterinary practice and animal husbandry—saving time, money, and protecting animal welfare.

    Looking Forward: Supporting Future Veterinary Needs

    As antibiotic regulations evolve, production practices will see new expectations on documentation, stewardship, and transparency—this requires not only clean product, but open lines of communication and rapid response to industry change. Every improvement in the cleanliness, stability, or solubility of Sulfachloropyrazine Sodium Soluble Powder brings practical benefits to users. With an eye on end-user experience, regulatory shifts, and evolving livestock farming practices, we continue refining our manufacturing and support to ensure our partners remain equipped to meet the dynamic needs of the industry.

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