Products

Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions

    • Product Name: Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions
    • Alias: phthalylsulfathiazole
    • Einecs: 200-043-6
    • 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

    316223

    Product Name Phthalylsulfathiazole Tablets Veterinary Grade API
    Appearance White or almost white crystalline powder
    Chemical Formula C17H13N3O5S2
    Molecular Weight 419.44 g/mol
    Purity ≥98%
    Solubility Practically insoluble in water
    Pharmacological Class Sulfonamide antibiotic
    Intended Use Treatment and prevention of bacterial infections in animals
    Dosage Forms Tablets, Injections, Capsules, Powders, Granules, Premix, Solutions
    Storage Conditions Store in a cool, dry, and well-ventilated place
    Cas Number 85-73-4

    As an accredited Phthalylsulfathiazole Tablets 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 White, high-density polyethylene bottle containing 500g Phthalylsulfathiazole Tablets, sealed with a tamper-evident cap, labeled with veterinary usage and batch details.
    Shipping Phthalylsulfathiazole Tablets (Veterinary Grade API) are securely packaged in moisture-proof, tamper-evident containers. Shipping is by air or sea, following international chemical safety standards, with temperature control if required. Clear labeling ensures regulatory compliance. Rapid dispatch and global delivery are available to guarantee product integrity and prompt supply for all dosage forms.
    Storage Phthalylsulfathiazole Tablets (Veterinary Grade API) should be stored in a tightly closed container, protected from moisture, direct sunlight, and excessive heat. Store at a controlled room temperature, generally between 15°C and 25°C (59°F–77°F). Keep away from incompatible substances and out of reach of unauthorized personnel. Ensure proper labeling and follow all veterinary safe storage regulations and guidelines.
    Application of Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions

    Purity 99%: Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Purity 99% is used in veterinary antibacterial formulations, where it ensures effective pathogen inhibition and minimizes the risk of contamination.

    Particle Size <50 µm: Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Particle Size <50 µm is used in oral veterinary powders, where it enables rapid dissolution and uniform bioavailability.

    Melting Point 195°C: Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Melting Point 195°C is used in the manufacturing of heat-stable injectable solutions, where it maintains chemical integrity during thermal processing.

    Stability Temperature up to 45°C: Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Stability Temperature up to 45°C is used in premixed feed additives, where it ensures prolonged shelf-life and potency under storage conditions.

    Moisture Content <1.5%: Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Moisture Content <1.5% is used in encapsulated veterinary drugs, where it prevents hydrolytic degradation and maintains product efficacy.

    Assay ≥98.0%: Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Assay ≥98.0% is used in compounded veterinary solutions, where it provides consistent active pharmaceutical ingredient concentration for reliable dosing.

    Residue on Ignition <0.2%: Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Residue on Ignition <0.2% is used in veterinary injectable preparations, where it results in low impurity levels and meets pharmacopeial purity requirements.

    Sulfathiazole Content ≤0.5%: Phthalylsulfathiazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Sulfathiazole Content ≤0.5% is used in granulated premixes for animal feeds, where it minimizes undesirable side effects and ensures safe administration.

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    Competitive Phthalylsulfathiazole Tablets 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

    Phthalylsulfathiazole Tablets: A Reliable Antibacterial Backbone for Veterinary Applications

    Introducing Our Veterinary Grade Phthalylsulfathiazole API

    Experience has taught us that not every active pharmaceutical ingredient stands up to the demands of modern veterinary care. After years in the chemical manufacturing sector, directly supplying veterinary pharmaceutical producers both large and small, our focus on Phthalylsulfathiazole isn't a matter of chance. We've watched it earn its place as a practical broad-spectrum antibacterial agent, especially in formulations addressing gastrointestinal infections in animals. We produce and refine this API strictly for use in tablets, injections, capsules, powders, granules, premixes, and solutions. Every stage of our process—sourcing, synthesis, granulation, and quality control—centers on what veterinarians and animal owners require: predictable, compliant, and safe anti-infective action.

    A Close-Up on Specifications That Matter

    Over years of refining, we’ve settled on a model that offers high assay purity and low moisture content. Granulometry is tightly controlled for tableting and encapsulation, so each batch flows and compresses consistently in downstream processing. Particle sizing isn’t an arbitrary product spec on our sheets: colleagues on the production lines have seen how clumping or uneven mixes can ruin a run or, worse, risk dosage inconsistencies.

    Phthalylsulfathiazole’s melting point remains stable, which keeps integrity through the high-energy steps of modern dosage manufacturing. We've ensured that every kilogram leaving our facility meets not only officially published compendial standards but also our internal requirements for microbial content and residual solvents. That’s a direct result of past recalls and the lessons learned from clients worldwide. We consult directly with technicians and quality assurance teams on every continent, iterating on testing methods and confirming results in both in-house and accredited external labs.

    The Everyday Use Cases We Serve

    Veterinary practitioners still face many of the age-old problems seen on farms, in kennels, and in wildlife facilities—acute and chronic enteric infections topping the list. We hear stories of malnourished animals, young livestock unable to gain weight, and colitis spreading quickly through herds or flocks. Each scenario led formulators back to sulfonamides like Phthalylsulfathiazole, especially in rabbits, poultry, ruminants, and species too sensitive for other classes.

    Many clients ask: Why stick with a legacy sulfonamide, given the presence of newer compounds? Stability matters just as much as spectrum of activity. Sulfonamides like Phthalylsulfathiazole pass through the stomach mostly unchanged and concentrate in the gut lumen, so they don’t disrupt systemic bacterial balance unnecessarily. Other antibiotics often disturb normal flora throughout an animal’s body, which can cause secondary infections or, worse, antimicrobial resistance in commensals. After fielding technical questions from both veterinarians and research scientists, our answer returns to this simple fact: Phthalylsulfathiazole has reliable local action.

    Different forms—tablets, powders, granules, and injectable-grade—exist because of how animals receive medication. Dogs and cats need calibrated tablets or capsules for precise dosing. Livestock respond better to medicated water or feed, so our granules disperse easily and our powders dissolve cleanly, even under the variable water qualities seen across different regions. The raw material that feeds these forms stays the same, but the realities of animal husbandry demand different delivery methods, each shaped by years of feedback from both rural veterinarians and intensive facility managers.

    Comparing With Other Veterinary APIs: What Sets Phthalylsulfathiazole Apart?

    No API can pretend to be a cure-all. Narrowing down the right antibacterial agent takes as much practical experience as textbook knowledge. Our role as a manufacturer goes beyond meeting a compendial reference standard. Our team fixes its attention on how Phthalylsulfathiazole fits into a modern therapeutic strategy.

    Sulfonamides emerge time and again as cost-effective, tolerable, and straightforward to manufacture and transport. Colleagues in procurement shared with us how global supply issues and sudden market shifts upend their production schedules. In those moments, a chemically stable product—remaining potent months after arrival—outcompetes more fragile APIs requiring cold chain or special packaging.

    Newer agents, while potent, often bring a host of baggage—cost, sensitivity to sunlight, intolerance in younger or immunosuppressed animals, unpredictable withdrawal times that complicate milk or meat production schedules. Phthalylsulfathiazole rarely causes sensitivity reactions. Decades ago, veterinarians saw how fast it calmed enteric infection without leaving animals sluggish or uninterested in food, a marked contrast to some alternatives we’ve assessed in our own animal safety studies.

    We take feedback from clients seriously. Product formulations need to work on real animals, not just in laboratory settings. Our operations director still visits the facilities of our largest customers worldwide, sharing in post-market surveillance that runs the lifespan of each animal group treated. Many of our end users seek out Phthalylsulfathiazole for outbreaks that do not respond to first-line agents, valuing how it performs even against tougher gram-positive or gram-negative pathogens when options run thin.

    What Drives Our Continuous Product Improvement

    We believe that the industry still has much to teach us. The truth is, veterinary medicine operates in diverse environments—sometimes in resource-rich labs, other times in the back corners of remote farms. Our production and QA lines have adapted. Before each batch is released, our own in-house veterinarians and animal scientists review tablets for size, friability, and appearance. Feed premix clients rely on repeatability, especially when matching doses over hundreds of kilograms in a single day. Some customers reported that their prior products caked or absorbed moisture during humid transports. After learning from these reports, we implemented improved moisture barrier packaging and added extra moisture detection points in our in-line testing.

    Years ago, questions about adulterants in the Chinese supply chain prompted us to invest in third-party mass spectrometry, not just in local regulatory testing but with periodic blind-sample audits sent to international labs. Lessons from these efforts led us to invest in a tightly integrated QC program—no statistically random tests, but batch-by-batch scrutiny, including impurity profiling, residue solvents, and even checks for heavy metals, a non-negotiable for animal and ultimately human safety.

    We use Good Manufacturing Practice (GMP) controls because we recognize what’s at stake: a compromised batch doesn’t just affect a single customer but can undermine confidence in sulfonamide therapies more widely. For injectable-grade Phthalylsulfathiazole, our facility uses stainless process lines and dedicated air filtration, regularly inspected and validated. Tablets, capsules, and granules come from segregated lines to prevent cross-contamination, especially in multipurpose facilities, an issue we know from past industry recalls can devastate trust.

    Understanding the Reality of Veterinary Medication Needs

    Modern veterinarians face increasing pressures—limited treatment options due to antimicrobial stewardship guidelines, tough restrictions on animal product withdrawal periods, and the need to contain farm-level outbreaks before they reach critical stages. As a manufacturer, our direct conversations with end users help us keep offerings relevant. When new resistance profiles appear in local field trials, our team coordinates with veterinary researchers to adjust technical sheets and develop improved test batches. These collaborations resulted in our latest extended-action formulations meant for use in water supplies and feed, reducing the frequency of dosing and ensuring more reliable intake among young or sick animals.

    We saw how, in poultry production, flock-wide dosing only succeeds if the active ingredient disperses rapidly and remains suspended long enough for consistent consumption. Our powder and granule lines include enhanced disintegration agents to avoid sediment at water tank bottoms and preserve dosage across a large group. Our technical service representatives still visit client sites in person to troubleshoot solubility or flow issues as industry conditions change—from drought to cold snaps, all forcing changes in operation.

    On the regulatory side, we continue to work with importers and state-level animal health inspection teams to keep product documentation current and clear, an absolute must for continued access in markets with stricter controls. Many of our clients in developing countries rely on our full regulatory support, leveraging years of compliance to regain access to their home country’s markets when documentation lapses or standards update.

    Practical Issues Shaping Our Product Lines

    We can trace real changes in formulation work to the input of working veterinarians and pharmaceutical processors. For example, one client in the Middle East reported issues with quick dissolution in high-humidity environments leading to rough sorting during vonveying. In response, we worked with our engineering team to adjust binder selection and rebalanced excipients, resulting in denser granules that travel through augers with far less dust. Each production run led our team to catch issues missed by standard lab conditions, solving them before they reached end users.

    For injectable use, clients want assurance about low endotoxin levels and sterile conditions. Our injectable-grade material is isolated in a separate production line and undergoes additional high-temperature sterilization steps, with vials of finished product then tracked and retained for stability observations. Each improvement owes its existence to a real-world client story: livestock vaccinated at mass scale, calves surviving severe bacterial scour, or exotic zoo animals benefiting from targeted enteric antibacterial management.

    One of our largest clients, a global feed integrator, noticed previously that premix granules received from other suppliers often absorbed atmospheric moisture, leading to inconsistent blending into feed and risked overdosing some animals. After hands-on review with their technicians, our production line adjusted ambient humidity controls and updated packaging film structure. Our experience taught us not to ignore any practical detail, from packaging configuration down to batch numbering readable even in outdoor storage.

    Current Challenges and What We're Doing to Address Them

    No manufacturer can cover up the evolving nature of bacteria or the pressure international regulators place on the sector. We've felt that pressure directly—a batch delayed by a sudden change to active ingredient standards, a shipment scrutinized and then rejected due to customs paperwork lapses, or even a recall driven by a single out-of-spec impurity marker. Each event forced us to rethink processes and remain proactive in risk management.

    Resistant bacteria, especially those circulating among livestock, worry both our own quality teams and end users. Our technical team tracks emerging resistance data and works to educate veterinarians about practical stewardship—using shorter, targeted treatment periods, and rotating APIs, supported by the stability and purity data we collect on every batch. We view these stewardship steps as the shared responsibility of everyone in the supply chain, not merely an afterthought for end users.

    Another challenge concerns increasing regulatory scrutiny on veterinary drugs—trace impurities, animal origin of excipients, and the full transparency of each supply chain step. We've opened up our doors to independent certification agencies, published digital batch traceability systems, and maintained open technical support for regulatory inspectors, not just during routine audits but whenever any question arises. Our internal teams maintain constant readiness to address emerging contaminant concerns, aligned with our commitment to mutually sustaining veterinary and human health.

    The rise in demand for traceability didn’t come from nowhere. Decades ago, poor-quality generics and untraceable chemical sources undermined trust in veterinary medications. We’ve invested in both staff capability—hiring technical specialists and compliance officers—and in system upgrades, from electronic signatures on BMRs to tamper-proof seals on every container. That investment pays back in trust, from regulators, veterinarians, and the academic community.

    Choosing the Right API: Trust, Track Record, and Responsiveness

    Hard-earned lessons shape every step of how we manufacture Phthalylsulfathiazole. For veterinarians and pharmaceutical processors, the difference between a good and a bad batch isn't philosophical—it's a matter of achieving desired animal health outcomes reliably with no surprises. Each batch we release has faced the hard lens of both technical and field testing, crafted with an eye toward solving real and observed problems in animal health.

    Our ongoing success with Phthalylsulfathiazole tablets and compounds reflects not just our commitment to high standards, but our direct relationship with the animal medicine sector. We know that as animal health challenges change, so must our products. Whether the issue is resistance, purity, granule integrity, dissolution, or compliance, our manufacturing processes continue to adapt, guided by practitioners who know the real day-to-day challenges of veterinary medicine.

    Collaboration, technical innovation, and listening to our client base determine every reformulation and improvement we undertake. Our team visits farms, clinics, production lines, and trade events—not to sell, but to understand. The resulting Phthalylsulfathiazole API is more than a commodity—it's a thoroughly tested, widely relied-upon component in the world’s veterinary arsenal, field-proven and manufacturer-backed every step of its journey from our facility to the animals that depend on it.

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