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HS Code |
911787 |
| Product Name | Aminophenazone Injection Veterinary Grade API |
| Chemical Name | 4-Dimethylaminoantipyrine |
| Molecular Formula | C13H17N3O |
| Appearance | Clear, colorless to pale yellow solution |
| Intended Use | Veterinary pharmaceutical manufacturing |
| Dosage Forms Supported | Tablets, Injections, Capsules, Powders, Granules, Premix, Solutions |
| Solubility | Soluble in water and alcohol |
| Storage Conditions | Store in a cool, dry place away from light |
| Purity | Typically ≥98% |
| Pharmacological Action | Antipyretic and analgesic |
| Cas Number | 58-15-1 |
| Route Of Administration | Oral or parenteral |
| Manufacturing Grade | Veterinary |
| Expiry Period | 24-36 months depending on storage |
| Packaging | Customized according to client requirements |
As an accredited Aminophenazone Injection 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 | Sealed 1 kg aluminum foil bag, double-layered, labeled for veterinary use; suitable for tablets, injections, powders, or premixes. |
| Shipping | The Aminophenazone Injection (Veterinary Grade API) is securely packed in sterile, tamper-evident containers suitable for tablets, injections, capsules, powders, granules, premix, or solutions. Shipments are handled under controlled temperature conditions, complying with international chemical transport standards, and accompanied by all necessary documentation for safe and prompt delivery. |
| Storage | Aminophenazone Injection Veterinary Grade API should be stored in a tightly sealed container, protected from light and moisture. Keep at a controlled room temperature, ideally between 15°C and 30°C, away from direct sunlight, heat sources, and incompatible substances. Ensure it is stored in a well-ventilated, dry area and kept out of reach of unauthorized personnel, children, and animals. |
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Purity 99%: Aminophenazone Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with purity 99% is used in veterinary anti-inflammatory formulations, where it ensures rapid onset of action and reliable symptom relief. Particle Size <10 microns: Aminophenazone Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with particle size less than 10 microns is used in oral and injectable dosage forms, where it provides enhanced absorption and uniform distribution. Melting Point 110-112°C: Aminophenazone Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with melting point 110-112°C is used in thermal processing applications for granules and powders, where it maintains chemical stability during manufacturing. Stability at 25°C: Aminophenazone Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with stability at 25°C is used in premix solutions for livestock, where it enables long-term storage and consistent potency. pH Range 6.5-7.5: Aminophenazone Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with pH range 6.5-7.5 is used in injectable veterinary medicines, where it minimizes local irritation and improves animal tolerance. Moisture Content <0.5%: Aminophenazone Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with moisture content less than 0.5% is used in solid oral dosage forms, where it prevents degradation and enhances shelf-life. Solubility in Water >90%: Aminophenazone Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with solubility in water over 90% is used in solution-based formulations, where it ensures complete dissolution and uniform dosing. Low Endotoxin Level: Aminophenazone Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with low endotoxin level is used in parenteral veterinary injectables, where it reduces the risk of adverse immune responses. |
Competitive Aminophenazone Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions prices that fit your budget—flexible terms and customized quotes for every order.
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Aminophenazone stands as a trusted non-narcotic antipyretic and analgesic agent for animal health. Watching trends in veterinary medicine shape global livestock care over decades, our manufacturing teams have made it a cornerstone of custom animal pharmaceutical projects. We've invested in tight control over each step in the synthesis and purification process. This fine control over crystal morphology, particle size, and water content doesn’t just meet industry standards—our partners in animal health production see the impact in every batch: easier compounding, smoother dissolution, and reliable clinical outcomes.
In-house research drives our process engineering. We focus on producing aminophenazone in sterile, injection-grade API, purpose-built for veterinary tablet pressing, injectable solutions, capsules, powders, granules, premixes, and oral solutions. Each batch reflects the purity and stability required for sensitive active pharmaceutical ingredients. Veterinary practitioners and pharmaceutical technicians often encounter wide variability from other manufacturers: controlling residual solvents, pyrogen content, and achieving real sterility in bulk APIs can challenge even seasoned teams. Years of continuous scale-up and process validation, using high-grade reagents and controlled environments, create a material with consistent assay values and predictable performance during downstream formulation. Granular and fine powder forms support immediate dissolution for injectables. Our granules suit sustained-release or multi-ingredient premix applications, handling the grind of industrial-scale mixing and compounding without breaking down or caking.
Livestock operations and veterinary clinics expect products that fit multiple dosing strategies. With aminophenazone API, some clients formulate oral boluses to tackle heat stress in dairy cows, while others prioritize rapid-onset injectables for managing fever in herds. Experiences from field support show that our material disperses well in water-based injectables, which saves both production time and frustration during the filtration process. In tablet applications, our controlled particle sizing means fewer capping problems during high-speed pressing. Those in powder and granule blending report the material flows well, limiting demixing and ensuring each dose delivers consistent activity. Veterinarians using custom capsule and granule blends highlight stable active concentrations, vital for ensuring reliable dosing across flocks and herds. We also support manufacturers crafting premixes aiming for uniform distribution in bulk feed for pigs or poultry—here, poor API flow or dusting can ruin feed handling. With our API’s optimized particle morphology, granules move evenly, blend smoothly, and keep dust generation to a minimum.
Working directly with veterinary drug makers and integration teams, we've fielded requests for alternate particle sizes, adjusted flow properties, and special packaging designed for high-humidity environments on-site. These adaptations ensure material reaches production managers and veterinarians in the form best suited for their daily needs. Regulatory expectations have evolved, with greater scrutiny on residual impurity profiles and sterility assurance. Anticipating these trends keeps our quality control teams vigilant. Our process involves aggressive tracking for heavy metals and related substances, and always aims for microbiological purity. Partnering with third-party labs and our own internal QC staff, the standard protocol covers identity, purity, endotoxin, and residual solvent testing. Veterinarians administering aminophenazone injections see the benefit: low pyrogen levels protect animals from adverse reactions. Drug manufacturers know that fewer batch rejects keep schedules predictable and regulatory filings on track.
Not all aminophenazone APIs behave the same during formulation or storage. Some vendors might pass registration with average material, but the real difference appears in the production room or during animal treatment. Our experience with downstream formulation in both hot and humid climates, as well as cold storage shipping, has taught us the weaknesses of less stable grades—caking, degraded actives, or microbial contamination. In contrast, a batch from our lines can stand up to months of storage and survive long transit to the most remote veterinary sites. Veterinarians working in challenging climates report that solution clarity and stability remain high, simplifying administration and limiting the need to re-mix or discard cloudy vials. Pharmaceutical manufacturing partners say that stable, dust-free powder keeps compounding lines productive and clean, even when shifting between batch sizes or multiple product SKUs in a day.
The livestock and animal health industry relies on dependable product performance. Our own field teams have traced batch recalls, inconsistent onset time, and even false-negative routine analytics back to poorly made aminophenazone from other suppliers. With inferior grades, filtration systems clog, finished products fail shelf life specifications, and veterinary clients receive treatments that don’t match labeled potency. Down the line, this erodes trust and exposes operations to regulatory scrutiny. Our experience underlines the costs of cutting corners—manufacturers forced to halt production, animals suffering due to unpredictable dosing, and unnecessary veterinary callouts to address adverse reactions. Farmers and veterinarians invest in treatments expecting results that justify every dose. We keep quality high because we’ve seen first-hand the impact on animal safety, public trust, and our partners’ businesses.
Every year, veterinary regulations tighten. Our development teams maintain up-to-date profiles of regulatory requirements from North America, Europe, and major animal health markets in Asia and Latin America. We keep close contact with registration experts and field technical managers to head off compliance issues before they arise. This attitude toward compliance means our products move through import checks with fewer surprises. We pay attention to trace metals and decomposition products since these are now firmly in the spotlight from oversight bodies. Specifications are updated, but our underlying manufacturing process remains standardized and repeatable. We invite both government inspectors and third-party auditors to validate controls, because trust matters to the partners who place our products in livestock health supply chains.
Manufacturers today look beyond a single finished dosage form. Demands from veterinarians change with disease trends, animal age, and production environments. Some require a fine, rapid-dissolving API for water-soluble oral solutions, popular on large poultry farms for ease of bulk administration. Others seek free-flowing granules for controlled-release powder blends, especially useful in ruminant dosing. Capsule and tablet producers seek consistent bulk density and compressibility, which affect both production yields and breakdown during digestion. Our aminophenazone API adapts to each requirement due to rigorous in-process checks and committed attention during production scale-up. Variable dosage forms don’t catch us off-guard—we’ve walked the floors of feed mills, tablet shops, and veterinary compounding labs to observe real-world needs. In doing so, we see the unique stresses each form puts on an API: susceptibility to oxidation, grinding pressure, exposure to atmospheric moisture, or mixing stress in prep lines. Field experience keeps our engineers one step ahead, so each product supports varied strategies for animal health.
For animal health manufacturers, technical issues often arise in the interplay between ingredient properties and plant equipment. We talk weekly with production leaders in both large-scale industrial operations and smaller, specialized pharmaceutical labs. Reports often include issues with caking, flow problems, or material sticking during tablet compression or capsule filling. Our technical team applies lessons learned from years of troubleshooting: adjustments in drying parameters, post-milling treatments, or anti-caking blends applied as needed. A manufacturer not ready to address these nuances will ship a product that costs time and money in the plant—downtime, residue build-ups, and even machine damage. We continuously refine the physical and chemical characteristics in our aminophenazone API, working hand-in-hand with maintenance and compounding staff downstream. A stable formulation process, enabled by predictable materials, frees both operators and QC teams to work to their full potential.
Animal health technicians often face hostile environments: extreme temperatures, humidity, and inconsistent water quality. In these field settings, details in raw material can make or break success. A poorly granulated API resists proper dissolution, risks underdosing, and adds another headache to already challenging animal care jobs. On the other hand, tablets that crumble in storage cost time and breed cynicism among staff tasked with administration and monitoring for treatment efficacy. Our site visits and manufacturing partnerships developed a clear goal: keep quality consistent, make reconstitution simple, and ensure every gram lives up to its intended use. Our R&D and scale-up teams regularly incorporate operator feedback—to resolve clumping in tropical storage warehouses or revise packaging for moisture resistance during deep field deployments. These collaborations pay off in productivity and treatment reliability. We owe improvements not to abstract standards alone but to the real feedback from animal health workers on farms, in clinics, and out in the field.
No manufacturer gets far trying to hide their production floor from scrutiny. We routinely open our quality system to client audits and conduct internal “post-mortems” on any lot that doesn’t meet our strict internal criteria. Some years ago, a minor shift in a raw chemical supplier’s purification route caused out-of-spec color in a small number of aminophenazone batches. Internal controls caught it before shipment, but it illustrated how minor upstream changes cascade through to finished goods. In response, we improved our supplier qualification processes, increased in-process controls, and deployed redundant assays for key impurity markers. Real, repeated field feedback from clients reduced the cycle time for problem-solving. Improvements in our aminophenazone production followed: better color and purity control, higher throughput for sterile formulation, and higher satisfaction scores reported in client surveys. Transparency, coupled with accountability, brings our product from good to best-in-class—lessons only learned through the lived experience of a manufacturer on the shop floor and in partnership with the people who use, administer, and trust these APIs.
Our technical team works on fine-tuning key characteristics that influence not just product stability, but also field performance. Projects over the years have targeted everything from improved flowability without appreciable dust, to developing granules that handle high-speed mixing without breaking into fines. For sterile injectable APIs, we maintain validated aseptic procedures to minimize microbial risks—a major win for injectable product manufacturers who face the burden of sterility failures. Our operation benefits from close dialogue with academic partners and pharmaceutical scientists who test new delivery systems or challenge material limits. These relationships produce feedback loops that drive faster problem solving and spur technical upgrades. By manufacturing and testing under diverse global conditions, we routinely benchmark against both regulatory standards and real animal health outcomes. This way, every lot reflects more than just a chemical formula. It represents the input of those who formulate, dispense, administer, and study aminophenazone in the field and in the lab.
Animal production and veterinary medicine both depend on visibility along the entire supply chain. From the day-to-day work on our manufacturing lines to shipment that lands in a busy veterinary pharmacy, we keep records and open communication with customers, regulators, and technical auditors. Building trust means maintaining data integrity, batch traceability, and open dialogue with partners should a concern appear. Our focus on documentation—each shipment traceable by lot, with full history through production and QC—mirrors what progressive veterinary operations demand and what regulatory authorities expect. This approach limits surprises and empowers partners to keep operations safe, predictable, and defensible under inspection. Our team’s approach reflects a long-term investment in animal care outcomes, responsible stewardship, and pride in medicine well made.
Animal health needs shift over time. Endemic diseases, resistance trends, and demand for sustainable livestock practices bring new challenges each year. Our research and production teams respond by tailoring strategies for better API handling, environmental safety, and economic performance in a variety of settings. With ongoing field studies and technical partnerships, we enable animal health companies to meet today’s needs and anticipate tomorrow’s. The goal remains constant: provide a material that allows formulators and veterinarians to do their best work, whatever the dosage form or application. Built on experience, technical know-how, and honest feedback from end users, our aminophenazone injection-grade API reflects a manufacturer’s promise—constant vigilance, continual learning, and hard-earned results for real-world animal care.