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Sulphamerazine Sodium USP

    • Product Name Sulphamerazine Sodium USP
    • Alias Sulfadimidine Sodium
    • Einecs 200-188-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    282505

    Name Sulphamerazine Sodium USP
    Chemical Formula C11H11N4NaO2S
    Molecular Weight 286.29 g/mol
    Appearance White to off-white powder
    Solubility Freely soluble in water
    Pharmacopoeia Grade USP
    Cas Number 38280-23-6
    Storage Conditions Store in a cool, dry place, protected from light
    Usage Used as an antibacterial drug (sulfonamide antibiotic)
    Ph Of 10 Solution Between 9.5 and 10.5
    Melting Point Approximately 220°C (decomposes)
    Synonyms N1-(4-methyl-2-pyrimidinyl)sulfanilamide sodium salt
    Stability Stable under recommended storage conditions
    Packaging Typically supplied in airtight containers

    As an accredited Sulphamerazine Sodium USP factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE drum with tamper-evident seal, labelled “Sulphamerazine Sodium USP, 1 kg,” includes batch number, storage instructions, and expiry date.
    Shipping Sulphamerazine Sodium USP is shipped in tightly sealed, moisture-resistant containers to maintain product integrity. The packaging complies with regulatory standards for chemical safety. Shipping is conducted under controlled room temperature, away from direct sunlight and incompatible substances. Proper labeling and documentation are ensured for safe handling and transport.
    Storage Sulphamerazine Sodium USP should be stored in a well-closed container, protected from light and moisture. Keep it at a temperature not exceeding 30°C (86°F), away from incompatible substances. Store in a dry, cool, and well-ventilated area, clearly labeled, and out of reach of unauthorized personnel. Follow all applicable safety and regulatory guidelines for pharmaceutical substances.
    Application of Sulphamerazine Sodium USP

    Applications of Sulphamerazine Sodium USP in Industrial Manufacturing

    Sulphamerazine Sodium USP is a pharmaceutical-grade sulfonamide widely used in highly regulated industrial sectors. As a direct chemical manufacturer, we support downstream partners in veterinary pharmaceutical production, animal feed premix formulation, aquaculture therapeutics, diagnostic reagent compounding, and biopharma fermentation process control. Our material undergoes strict quality control to meet the demands of each specific segment.

    1. Veterinary Injectable Drug Manufacturing

    Veterinary formulators use this compound as an active pharmaceutical ingredient for parenteral injectable solutions targeting livestock bacterial infections. Blending takes place under aseptic manufacturing conditions, where precise solubility and impurity control are critical for GMP batch release. Each batch must align with veterinary pharmacopoeias, with end-point HPLC validation implemented for traceability. The formulation phase typically involves dissolving the API in sterile water, adjusting to isotonicity, and filtering before vial or ampoule filling via automated lines.

    Industry compliance standards

    • Pharmacopoeia: USP, BP, EP monographs for veterinary APIs
    • GMP for Veterinary Medicinal Products (EU Regulation 2019/6)
    • US FDA 21 CFR Part 514 (New Animal Drug Applications)
    • Chinese Veterinary Pharmacopoeia (for APAC production)

    Typical usage ratio

    • Concentration in finished veterinary injectables: 2% — 20% w/v, batch adjusted based on animal species and disease severity, always validated per VICH guidelines

    Downstream process integration

    • Dissolution in Water-for-Injection (WFI) during bulk compounding
    • Sterile filtration before vessel transfer
    • Final container fill and autoclave terminal sterilization

    Final product types

    • Livestock injectable drugs (cattle, swine, sheep)
    • Compounded multi-sulfonamide veterinary solutions
    • Emergency antimicrobial injectables for veterinary hospitals

    2. Medicated Feed Additives for Poultry and Livestock

    Feed manufacturers incorporate Sulphamerazine Sodium USP as an active ingredient to produce medicated premixes and complete feeds for disease prevention and growth support in poultry and ruminants. QA teams test every lot for homogeneity, with micro-dosing feeders or ribbon blenders dispersing the raw material during early mixing steps. Seasonal adjustments and species targeting require rigid ratio calculations to meet legal residue limits at the point of slaughter. Only facilities with feed GMP and specialized traceability modules may deploy this API in accordance with animal feed additive registrations.

    Industry compliance standards

    • US FDA 21 CFR Part 558 (New Animal Drugs for Use in Animal Feeds)
    • EU Feed Additive Register (Regulation (EC) No 1831/2003)
    • China GB/T 17888-2008 (Medicated Feed Additives)
    • ISO 22000-certified feed safety management

    Typical usage ratio

    • Premix dosage: 0.01% — 0.15% by weight in feed premixes, dosing calibrated to finished feed delivery rates and withdrawal periods

    Downstream process integration

    • Micro-ingredient silo dosing at pre-grinding blending stage
    • Batch blending with complete feed components pre-pelleting
    • Final lot testing with UPLC for uniform distribution

    Final product types

    • Medicated poultry mash and crumbles
    • Ruminant disease control feed blocks
    • Water-soluble medicated feed supplements

    3. Aquaculture Water Conditioning Treatments

    Sulphamerazine Sodium USP is deployed in aquaculture as a therapeutic agent to control bacterial outbreaks in intensive fish and shrimp cultivation systems. Downstream manufacturers prepare stock solutions enabling batch dosing directly into recirculating tanks or pond systems. All dosing requires careful titration to biomass weight and environmental factors, with residue monitoring routines set by regional aquaculture regulators. Repeated in-process verification adjusts for water volume, fish density, and uptake rates.

    Industry compliance standards

    • FAO Code of Conduct for Responsible Fisheries: Drug Use Guidelines
    • US FDA CVM GFI #209 (Aquaculture Drug Use)
    • Chinese GB/T 18106-2013 (Veterinary Drug Residues in Food of Animal Origin)
    • EU Directive 2006/88/EC (Aquatic Animal Health)

    Typical usage ratio

    • Treatment concentration in water: 15–80 mg/L, calculated against total system water volume and adjusted for treatment duration 3–5 days

    Downstream process integration

    • Dilution into liquid stock for tank-level dosing
    • Automated pump injection systems in recirculating aquaculture
    • On-site field mixing for pond or net pen applications

    Final product types

    • Fish disease control solutions for intensive farms
    • Shrimp larvae bath treatments
    • Emergency tank remediation kits

    4. In Vitro Diagnostic Reagent Production

    Producers of in vitro diagnostic (IVD) kits use this API as a reference inhibitor in microbiological assay controls and selective culture media. Stringent documentation is maintained to meet IVD regulatory audits, with every batch entering buffered reagent compounding lines under pharmaceutical cleanroom conditions. Dispensing, blending, and sterile filling procedures are calibrated to maintain ISO 13485 system integrity. Our material provides consistent chemical reactivity for challenging laboratory matrix tests, helping downstream partners reduce batch-to-batch assay variability.

    Industry compliance standards

    • ISO 13485:2016 Quality Management for Medical Devices
    • IVDR (EU Regulation 2017/746)
    • USP Reagent Specifications for in vitro use
    • US FDA 21 CFR Part 820 (Quality System Regulation)

    Typical usage ratio

    • 0.02% — 0.25% in media and reagent bases, validated per target microorganism and matrix

    Downstream process integration

    • Pre-weighed addition at raw material compounding
    • Buffered solution blending under HEPA filtration
    • Dispersion into agar or broth matrices for kit assembly

    Final product types

    • Microbial sensitivity testing media for clinical labs
    • Bacterial growth control sets for IVD
    • Selective agent reagent kits for environmental monitoring

    5. Bioprocess Fermentation Contaminant Control

    Biomanufacturers apply Sulphamerazine Sodium USP as a microbial contaminant control agent in high-value fermentation runs, including recombinant protein and vaccine production. Operators dose this API during fermentation setup, based on risk assessments for specific bacterial vectors. Documentation includes complete trace and disposal logs, with integration into Manufacturing Execution Systems (MES) for real-time QA compliance. The addition step is critical—too little impacts contaminant suppression, too much may interfere with host cell yield—necessitating tight real-time monitoring of API concentration and residuals pre-harvest.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR 211 (Finished Pharmaceuticals GMP)
    • EU EudraLex Volume 4 (GMP for Biologicals)
    • ISO 9001:2015 Quality Systems for Bioprocessing

    Typical usage ratio

    • 1—50 mg/L, titrated to fermentation volume and contaminant risk matrix; level confirmed with HPLC or LC-MS/MS before downstream protein harvest

    Downstream process integration

    • Batched into fermenter feedstock at culture inoculation
    • Online dosing as contamination detected by optical/biochemical sensors
    • Removal and residue monitoring during purification (ultrafiltration, diafiltration)

    Final product types

    • Recombinant protein APIs for human use
    • Biological vaccine intermediates
    • Research-grade microbial control samples
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    Certification & Compliance
    More Introduction

    Sulphamerazine Sodium USP: A Closer Look at the Details that Matter

    If you walk into a pharmaceutical lab or a veterinary supply warehouse, sooner or later, you notice a batch of white crystalline powder tucked away – Sulphamerazine Sodium USP. When I first encountered this compound years back, a senior pharmacist pointed out the row of jars with a nod and said, “These old-timers still do the heavy lifting.” Back then, I didn’t appreciate how much one simple molecule could provide when used the right way, under the right circumstances. Take a look at what makes Sulphamerazine Sodium USP stand apart and why it continues to deliver where others fall short.

    Understanding Sulphamerazine Sodium USP

    Sulphamerazine Sodium USP, known by many as a long-standing sulfonamide antibiotic, has earned its place through reliability and flexibility. As a sodium salt, it dissolves easily in water, which matters when every minute and every milligram counts. Those clear solutions lend themselves to accurate dosing and fast action, both in a dose given in a syringe and in oral administration, which gives teams in clinics a range of options when working on a difficult case. In my experience with under-resourced clinics, quick, clean solubility means the difference between a treatment that works and one that stalls out because something just didn’t mix.

    Physically, it presents as a fine, odorless powder, white as new paper. Many who work in compounding notice its texture immediately – it doesn’t clump, and it pours with little fuss, which matters when you’re setting up for a busy shift or need to prep something quickly for a sick animal or patient. The sodium form also means lower risk for certain types of irritation compared to some free acid sulfonamides, especially in parenteral solutions. This is no minor point. During long hours spent working up formulas for veterinary care, I’ve seen how minor tweaks like this can help animals tolerate treatment far better.

    Model and Specifications

    The version most often found carries the grade “USP” – meaning it meets the standards set out in the United States Pharmacopeia. These standards govern every aspect of the compound, from purity and strength to absence of harmful contaminants. Having USP on the label builds trust, especially if you’ve ever worked in a place where subpar ingredients lead to botched mixtures and frayed nerves. High purity translates to reliable results – no guesses, no unexpected interactions, just what you calculated.

    Typical packaging usually comes in moisture-tight containers. This protects against caking, which can spoil accurate dosing. A good batch meets USP criteria of at least 98% active content, with sodium compounded in to ensure high solubility. Some newer entrants in the market try to stretch those specifications. In practice, even a small compromise on purity or improper packaging can undo the hard work. If anything, I’ve learned that a transparent supply chain and rigorous adherence to standards offer peace of mind that pays dividends each time you draw up a solution.

    Uses in Health and Animal Care

    Most folks don’t encounter Sulphamerazine Sodium USP unless they’re dealing with infectious disease in animals, though it has played a role in human medicine too. This drug fits best with bacterial pathogens like E. coli or Salmonella, found in both large-scale farm outbreaks and smaller clinics. In decades past, it figured prominently on shelves as a treatment for pneumonia and gastrointestinal infections in cattle, sheep, pigs, and poultry. The sodium salt comes ready to dissolve in water, so it works well for mixing into drinking water, a common dosing method for livestock herds. During my time volunteering on midwestern farms during calving season, Sulphamerazine solutions were a mainstay whenever bacterial infections threatened a herd. Its role often came up during outbreaks of calf scours – an illness that can devastate farms in a matter of days if left unchecked.

    These experiences taught me that solid science isn’t enough without dependable treatments on hand. Sulphamerazine Sodium USP offers what field veterinarians need: rapid dissolution, stable storage, and clear dosing calculations. It doesn’t require mixing at high temperatures or extensive stirring; water at room temperature does the job. Comparing this to older, less soluble sulfonamides, I saw a clear reduction in time spent preparing solutions and less frustration during those intense, high-pressure moments. That time saved means more animals reach treatment – something that sticks with you when lives hang in the balance.

    How Sulphamerazine Sodium USP Sets Itself Apart

    These days, competition from newer antibiotics is fierce. Even so, Sulphamerazine Sodium USP continues to pull its weight for a few reasons. Resistance rates for some sulfonamides have climbed, but careful stewardship and use according to microbial susceptibility keep this molecule worthwhile. In developing countries, where cold chains break down or new drugs can’t be had, this compound keeps showing up as a reliable, affordable choice. The sodium salt improves velocity of absorption and means fewer issues with precipitation inside the animal or patient. This stands apart from older sulfas, which sometimes crash out of solution in the bloodstream or bladder, creating complications. I remember a colleague explaining that just a shift to the sodium version saw fewer complaints about kidney irritation during therapeutic regimens. Small design tweaks matter in medicine, even if they seem insignificant at first.

    Another advantage comes through simple logistics. With its high water solubility, Sulphamerazine Sodium USP allows flexible routes of administration. Mixed into feed, dissolved in water, given by injection – you get choices fit for different clinical scenarios. When we had outbreaks in barn settings with limited equipment on hand, being able to spray or mix up a bulk batch for group treatment made all the difference. That flexibility isn’t just a convenience; it’s a practical necessity where infrastructure is stretched thin or when animal numbers are high. Comparing with other drugs that require strict mixing instructions or specialized solvents, Sulphamerazine Sodium feels approachable to frontline staff.

    Differences from Other Sulfonamides

    A casual glance at a pharmacopeia might lump all sulfonamides together. This misses key distinctions. Sulphamerazine Sodium USP brings rapid onset and good bioavailability due to its solubility. For example, Sulfadiazine or Sulfamethoxazole sometimes demand more careful dissolution or create grainy residues that clog filters and lines in a busy field setup – something I’ve wrestled with more than once. Even more, certain other sulfas, like Sulfaguanidine, hardly absorb through the gut, which matters for systemic infections but less so for ones localized to the digestive tract. Those differences can mean wasted effort if you pick the wrong treatment for the wrong situation.

    Another contrast resides in regulatory acceptance. Sulphamerazine Sodium USP comes certified for its expected endpoints in both human and animal medicine, although withdrawal periods and use in food animals remain subject to local laws. Over time, pressure by regulatory agencies on prudent antibiotic use has changed prescription habits. That said, Sulphamerazine’s track record and inclusion in global essential medicine lists keep it on shelves even today. The sodium salt’s relatively gentle approach compared to other sulfonamides also means clinicians can use it with less anxiety about triggering hypersensitivity or severe local reactions, particularly where close monitoring is difficult. That kind of peace of mind adds value, which numbers on a specification sheet rarely capture.

    Handling, Storage, and Quality Control

    Having spent hours in storerooms, I’ve learned the simple rule: if the chemicals aren’t fresh, your job just got harder. Sulphamerazine Sodium USP tolerates fairly standard storage conditions – keep it cool, dry, and out of direct sunlight. If you store it well, it maintains activity and remains easy to measure and dissolve. Problems only arise when caps go missing and moisture finds its way inside, so tight seals are your friend. Compared with some newer antibiotics that degrade quickly or require refrigeration, this compound proves forgiving to operators working in the field.

    On the quality control front, USP specifications spell out permitted impurities and how to test for them. Most reliable suppliers provide a certificate of analysis with batch-specific data, something I always recommend checking before use. Without this, you risk inconsistent results or, worse, a complete treatment failure. Rigorous adherence to standards makes the difference. In settings with frequent audits or strict purchasing protocols, sticking to USP-grade protects the entire operation from avoidable setbacks. This isn’t just bureaucracy – it’s a hard-earned lesson from clinics that ran afoul of poor-quality imports in the past.

    Potential Issues and Solutions

    No product comes without challenges. Sulphamerazine Sodium USP faces resistance trends that crop up after years of overuse or misuse. In my career, I’ve seen barns where treatment after treatment dulls the drug’s edge, turning what was once reliable into just another packet on the shelf. Even so, by returning to strict diagnostic practices and tracking microbial profiles, veterinarians can determine if Sulphamerazine still fits. Incorporating rapid diagnostic tools, or at least a robust reporting system for drug failures, brings back some measure of stewardship and avoids casting aside a useful compound prematurely.

    Another hurdle involves regulatory scrutiny. Given the push to limit residues in the food supply, proper adherence to withdrawal times sits at the forefront. I remember meeting with farmers who struggled with complex timelines for different medicines. Many welcomed clearer labels and reminder systems – no one wants to see crops lost or shipments flagged because of a bureaucratic slip. Calling for improved record-keeping and digital reminders, along with clearer education outreach, offers a straightforward way to prevent most issues.

    Supply chain reliability formed the backbone of every well-run operation I witnessed. Global disruptions exposed just how fragile the chain gets. Building in redundancies – diversifying sources, maintaining larger safety stocks, or relying on established, transparent suppliers – gives clinics and producers breathing room in a crisis. Sulphamerazine Sodium USP, by virtue of its stability and wide manufacturer base, fits into this approach, but only if buyers keep up their vigilance. As practices switch to more targeted therapies, open lines of communication between clinics and suppliers enhance the continued relevance of older antibiotics. That’s a lesson from the COVID pandemic that will likely stick for years.

    Looking to the Future

    Discussing antibiotics in today’s landscape means acknowledging resistance, stewardship, and regulatory frameworks. Still, old standbys like Sulphamerazine Sodium USP remain vital, especially where budgets run tight and infrastructure is uneven. Broad access to basic antibiotics means everyday work can continue without drama or delay. Pairing their use with sensible stewardship policies ensures they stay effective longer. Trust in USP-grade supplies, transparency from manufacturers, and commitment from field teams make the difference.

    Newer therapy classes and molecular diagnostics might change the game in decades ahead, but, as someone who has watched trends rise and fall, core compounds like Sulphamerazine Sodium endure by delivering predictable results. Health systems do best when they keep a wide therapeutic toolbox, and this sodium salt holds its ground as a dependable entry in that box.

    As medicine continues its steady march forward, attention to detail in sourcing, using, and monitoring products like Sulphamerazine Sodium USP will carry more weight, not less. Those who value consistency and straightforward results know the worth of sticking with proven staples, even as flashier entrants grab the headlines. A century on, what keeps this molecule relevant isn’t marketing or nostalgia but a record of practical success in the places where it counts.

    The Human Side of Reliable Tools

    For those who spend their careers in the trenches – treating outbreaks, working late into the night with barn lights blazing, tallying records by hand – the presence of a reliable antibiotic like Sulphamerazine Sodium USP means reassurance. It frees up energy to tackle bigger problems. Every time a healthy animal walks out the door or a worried farmer finds peace of mind, that impact ripples far beyond paper specifications. Merely keeping one good tool available and effective lets caretakers focus on the people and animals in front of them, rather than scrambling for substitutions that may not work as well.

    Through storms of regulation, resistance, and evolving practice, it’s reassuring to see that some parts of medicine stand steady when the basics are honored. The world will doubtless see new breakthroughs, but the quiet efficiency of Sulphamerazine Sodium USP reminds us that established foundations deserve attention too. Every well-run farm and thoughtful clinic draws strength from these fundamentals. The smart path forward blends hard-earned experience with persistent curiosity – exactly the qualities embodied by this plain white powder that rarely steals the spotlight but proves essential all the same.