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Chlortetracycline

    • Product Name Chlortetracycline
    • Alias aureomycin
    • Einecs 200-055-4
    • 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
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    VTB
    Specifications

    HS Code

    447757

    Name Chlortetracycline
    Other Names Aureomycin
    Chemical Formula C22H23ClN2O8
    Molecular Weight 478.88 g/mol
    Drug Class Tetracycline antibiotic
    Appearance Yellow crystalline powder
    Solubility Slightly soluble in water
    Melting Point 220-230°C (decomposes)
    Cas Number 57-62-5
    Mechanism Of Action Inhibits bacterial protein synthesis
    Uses Treatment of bacterial infections in animals, rarely in humans
    Administration Routes Oral, topical, ophthalmic
    Side Effects Photosensitivity, gastrointestinal upset, allergic reactions
    Storage Conditions Store in a cool, dry place, protected from light

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

    Packing & Storage
    Packing The packaging for Chlortetracycline (100g) features a sealed, amber plastic bottle with a tamper-evident cap and clear labeling.
    Shipping Chlortetracycline should be shipped in sealed, clearly labeled containers, protected from light and moisture. It must be transported under cool, dry conditions, complying with local and international regulations for pharmaceuticals. Ensure secure packaging to prevent leaks or contamination. Hazard labels and safety documentation must accompany shipments as required for laboratory chemicals.
    Storage Chlortetracycline should be stored in a tightly closed container, protected from light and moisture. It should be kept at a temperature below 30°C (86°F) and away from incompatible substances such as strong oxidizing agents. Proper storage helps prevent degradation and maintains potency. Ensure the storage area is well-ventilated, dry, and secure, complying with local regulations for pharmaceuticals.
    Application of Chlortetracycline

    Applications of Chlortetracycline in Industrial Manufacturing

    Chlortetracycline serves as a strategic raw material in multiple industrial sectors, which require strict production parameters, controlled usage ratios, and direct integration into regulated processing steps. The following sections outline distinct downstream applications, presenting compliance requirements, usage guidelines, process flows, and types of final manufactured goods.

    1. Veterinary Feed Additive Manufacturing

    Manufacturers incorporate chlortetracycline as an active ingredient in medicated animal feed premixes, focusing on optimizing livestock growth and preventing bacterial infections in intensive farming environments. Production involves strict evaluation of solubility in carrier materials, homogeneous blending to ensure batch uniformity, and in-line analytical testing to meet regulated residue levels stipulated by authorities. Continuous batch monitoring is essential to fulfill compliance and client-specific quality protocols.

    Industry compliance standards

    • U.S. FDA 21 CFR 558.128 Feed Additive Regulation
    • European Medicines Agency (EMA) Veterinary Guidance
    • Chinese Ministry of Agriculture Order No. 235
    • Good Manufacturing Practice for Medicated Feed (cGMP, EU 2022/1104)

    Typical usage ratio

    • 50-700 mg/kg in premix formulations; adjusted according to species, age, and withdrawal restrictions

    Downstream process integration

    • Direct dry blending into vitamin-mineral premix bases during pre-mix manufacturing
    • Inclusion during granulation phase for pelletized feeds
    • Inline quality control at each batch to verify uniform distribution and active content

    Final product types

    • Layer and broiler poultry feed premixes
    • Swine starter and grower rations
    • Beef and dairy cattle medicated feeds
    • Aquaculture feed premixes

    2. Animal Pharmaceutical Preparation

    Chlortetracycline is processed into finished veterinary pharmaceuticals such as soluble powders, injectable solutions, and topical ointments for bacteria-related diseases in livestock. Manufacturers must assure tight control of residual solvents, excipient compatibility, and preservation of antimicrobial activity during blending, sterilization, and filling processes. Compliance batch release testing evaluates identity, purity, microbial limits, and ensures absence of undesirable by-products.

    Industry compliance standards

    • United States Pharmacopeia (USP) monograph for chlortetracycline
    • European Pharmacopoeia (Ph. Eur.) 10.0
    • VICH GL GMP (Veterinary International Cooperation on Harmonisation)
    • China Veterinary Pharmacopoeia

    Typical usage ratio

    • 2.5–10% w/w in soluble powder formulations; 0.5%–2% w/v for injection or ointment bases
    • Adjusted for administration route, animal type, and local regulations

    Downstream process integration

    • Dissolution into sterile water or buffer for parenteral preparations
    • Direct dispersal into carrier bases for ointments and topical gels
    • Granule micronization and sieving for oral powder mixes
    • Filling and packaging under validated environmental controls

    Final product types

    • Bovine mastitis ointments
    • Swine water-soluble powder anti-infectives
    • Injectable suspensions for large animals
    • Poultry and aquaculture therapeutic mixes

    3. Surface Disinfectant and Sanitizer Intermediate

    Industrial formulation plants use chlortetracycline as a component in specialized disinfectant blends, targeting sanitation of animal housing, transportation vehicles, and equipment prone to bacterial contamination. Operations require integrated dosing controls, compatibility testing with surfactant systems, and assurance of stability during packaging and post-manufacture storage.

    Industry compliance standards

    • U.S. Environmental Protection Agency (EPA) registration for antimicrobial pesticides (FIFRA)
    • REACH (EC 1907/2006) registration for biocidal uses
    • China GB 26368-2010 Hygiene Standard
    • Good Laboratory Practice (GLP) quality systems

    Typical usage ratio

    • 0.1–1% by weight in disinfectant concentrate; adjusted for contact surface type and application method

    Downstream process integration

    • Solubilization in aqueous or alcohol-based concentrate tanks
    • Mixing with cationic or nonionic surfactant blends during final formulation step
    • Quality control by chromatography to confirm active antimicrobial level

    Final product types

    • Livestock facility disinfectant concentrates
    • Transport vehicle sanitizing fluids
    • Dairy milking equipment cleaning agents
    • Veterinary hospital surface sprays

    4. Biotechnological Diagnostic Media Production

    Chlortetracycline provides selective antibacterial action in prepared culture media for biotech labs and industrial diagnostics. Manufacturers incorporate it to suppress Gram-positive and Gram-negative contaminants, allowing for accurate identification and quantification of specific microorganisms in environmental and food testing workflows. Accurate dosing and validation ensure media selectivity and shelf-life under storage conditions.

    Industry compliance standards

    • ISO 11133:2014 (Preparation, production, storage, and performance testing of culture media)
    • AOAC International Methods
    • U.S. FDA BAM (Bacteriological Analytical Manual) guidelines
    • EN 12469 for microbiological safety standards

    Typical usage ratio

    • 5–40 mg/L in agar or broth depending on target organisms and laboratory protocols

    Downstream process integration

    • Addition to cooled sterile media post-autoclaving to preserve antibiotic potency
    • Mixing with premeasured dehydrated media bases for batch-scale production
    • Bottling and sealing in sterile environments under ISO cleanroom guidelines

    Final product types

    • Selective agar plates for Salmonella and E. coli isolation
    • Diagnostic bacterial culture broths
    • Environmental monitoring indicator media
    • Food industry microbial testing kits

    5. Bulk Active Pharmaceutical Ingredient (API) Supply for Human Drug Manufacturing (Restricted Geographies Only)

    In jurisdictions where regulation permits, bulk chlortetracycline continues as an API for human oral and topical pharmaceuticals targeting specific bacterial pathogens. Manufacturers supply material with full traceability, validated impurity profiles, and documentation aligned to regional pharmacopoeia requirements. All manufacturing, testing, and packaging occur in fully qualified, validated GMP environments to safeguard patient safety and regulatory compliance.

    Industry compliance standards

    • Pharmacopoeia of the People’s Republic of China (ChP)
    • Yaozhun Chinese Drug Standards
    • API GMP certification (NMPA/CFDA, China)
    • ICH Q7 Good Manufacturing Practice for APIs

    Typical usage ratio

    • Varies by finished dosage form: 150–500 mg/tablet or capsule; 0.5–2% for ointment base
    • Determined by final product registration and clinical protocol

    Downstream process integration

    • Wet granulation and direct compression for solid oral dosage production
    • Dissolving in pharmaceutical base solvents for topical preparations
    • Blending with stabilizers and preservatives during liquid formulation
    • Final product QC and batch release under GMP

    Final product types

    • Prescription tablets and capsules
    • Topical dermatological creams
    • Combined antibiotic oral suspensions
    • Hospital-grade wound ointments
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    Certification & Compliance
    More Introduction

    What Matters Most About Chlortetracycline in Practical Manufacturing

    Real-World Experience With Chlortetracycline

    Chlortetracycline, better known by its abbreviation CTC, has earned a strong foothold in animal health for over six decades. As a manufacturer working at the sharp end of the line, our production team understands CTC not only by its chemical structure—C22H23ClN2O8—but by the hands-on concerns farmers, veterinarians, and feed compounders face every day. Our main commercial offering is CTC 20% and 15% premix, but over the years, custom concentrations and water-soluble formulations have grown in demand, especially in markets with shifting regulations around antibiotic usage.

    Chlortetracycline stands apart for tackling a stubborn range of animal diseases, particularly in poultry, swine, and cattle operations. In practice, users count on its ability to address bacterial and mycoplasma infections—issues that can quickly escalate into production losses if left unchecked. In the real world, outbreaks rarely wait for the lab report, so convenient handling—with solid shelf life and good flow in premix form—becomes just as important as any technical index.

    Purity and Consistency: Lessons from the Production Line

    We focus our investment on purity and consistency because reliable outcomes matter most to those who use our product. CTC’s specification profile reflects not just minimum standards, but what long-term users report back: consistent coloring, low levels of process impurities, and minimal dusting—since animals notice bitter tastes and off-odors even faster than humans do. Analysis in our QC lab tracks the content of active ingredient (measured in percentage mass by validated ultraviolet spectrophotometry), moisture, pH, granule size, and residue solvent profile.

    Differences between CTC and other tetracyclines (like oxytetracycline or doxycycline) play out clearly during mixing. Chlortetracycline’s higher stability in standard mash and pelleted feeds makes it a preferred choice where storage conditions run hot or humid. For dissolved or injectable delivery, OTC or doxycycline sometimes edge ahead, but in feed-grade premixes, CTC keeps its edge for cost-efficiency and resistance suppression, as long as farm biosecurity measures keep up.

    Addressing Modern Concerns: Residue and Resistance

    A lot has changed since the early days of antibiotic use. Farmers and regulators want assurance that the use of CTC leaves behind minimal residues in meat, milk, and eggs. In manufacturing, this drives tighter controls over active ingredient uniformity and withdrawal periods. Our facilities run residue monitoring in finished feed and on-farm samples, cross-checking every batch with regulatory maximum residue limits (MRLs) worldwide. The knowledge that customers rely on the trust built by decades of safe use puts extra pressure on us never to cut corners—even when raw material costs spike.

    Resistance gets more attention with every passing year. Our team sees resistance pressure not as a far-off theoretical risk, but as a practical concern for those using the product. In regions with high antimicrobial use, we work with feedmills and animal growers, reminding them of the need for targeted prescriptions—rather than blanket administration. We direct both technical and educational resources into helping customers plan rotation and rest programs, alongside the use of culture-based diagnostics, to keep CTC working in the field for as long as possible.

    Why Formulation Choices Affect Outcomes

    Feed manufacturers, veterinary practitioners, and integration managers ask us for formulation flexibility. The classic yellow crystalline powder has been the backbone of CTC premixes, but over the years, granular and microencapsulated forms have found demand where dust handling or environmental conditions call for tighter control. For instance, in integrated poultry producers in tropical climates, compressed moisture-resistant granules prevent caking and dosage loss.

    We manufacture CTC 15% and 20% to match the realities of field blending, and we hear from feed operators daily about the value of accurate flowability and stability under thermal stress. Our investments in process control—from spray granulation to sieve fractionation—tie directly to feedback from end-users struggling with segregation or inconsistent mixing in their augers and batchers.

    Comparison with oxytetracycline reveals further differences: CTC’s palatability is better received in swine and poultry feeds, while oxytetracycline may take the lead when nutritional interactions (like calcium binding) are not a concern. For water application, our water-soluble CTC formulation proves effective where clean, rapid dispersion counts—particularly in environments where labor-saving and animal handling reductions matter.

    Logistics and Shelf Life: Getting the Details Right

    As a producer, we appreciate that a good product must stand up to real distribution pressures. Our customers range from cooperative-run feed mills in the north, facing freezing warehouse temperatures, to exporters shipping to subtropical ports with little temperature control. CTC’s primary bags undergo testing for stability under light, heat, and mechanical stress. We select packaging materials—laminated, multi-layer Kraft with moisture barriers—based on results from actual storage trials, aiming not just to pass post-manufacture testing but to show up after six months in genuine farm conditions.

    Shelf life remains a top concern. We monitor not only CTC degradation rates but also track packaging performance from our own long-term stability samples stored in simulated real-world conditions. Microbial control features in processing help guard the active substance against spoilage, so what reaches the final customer performs as expected. User feedback has shown that freshly produced CTC with a low moisture content keeps potency for at least two years under typical storage environments, as long as the bags remain undamaged and tightly sealed.

    Compatibility, Safety, and Environmental Considerations

    CTC structure gives it some unique compatibility advantages—it mixes well with most premix diluents, including soybean meal, corn gluten, and fish meal, without clumping or loss of performance. But we make it a point to warn end-users about the interaction with polyvalent salts, like iron and calcium, which can chelate tetracycline compounds and reduce absorption in animal guts. Every batch is tested for heavy metal carryover, since mineral contamination can affect both product efficacy and animal safety.

    Safety in the plant matters just as much as safety in the feedmill. Our operational experience taught us to keep dust levels as low as possible, using enclosed systems and extraction units throughout transfer points—not just because of regulatory requirements but for the health of our team. Operators receive thorough training in handling protocols. In hot climates or open batch mixing, we recommend on-site extraction and ventilation to minimize exposure.

    Environmental control measures sit at the core of our production line. Wastewater, off-spec product, and dust all undergo treatment steps to keep CTC residues out of water and soil systems. Local regulators audit discharge regularly, and internal monitoring programs keep our lines at or below permitted thresholds. As more pressure builds around responsible antibiotic production, sharing our data and improvement efforts with both authorities and customers creates transparency—a benefit in building lasting partnerships.

    The End-User’s Perspective: What We Hear and Learn From the Field

    Much of what shapes our product stems from direct talks with nutritionists, veterinarians, and end-users on site visits. Swine technicians, for example, have commented on how batch-to-batch consistency saves time and worry when culling problem pigs in high-density systems. Poultry growers frequently ask about visible dust, off-flavors in eggs, and compatibility with vitamin and trace mineral packs. In every case, direct feedback gets routed to our R&D and process adjustment teams.

    We keep our focus tight on the form in which farms actually use the product. While active ingredient content receives the lion’s share of attention, mixing characteristics and ease of incorporation into existing feeding programs are often the difference between solid performance and disappointing field results. Our application team regularly runs on-farm mixing trials, comparing CTC with competitors, adjusting particle size, and reviewing mix homogeneity to verify that label claims are being met.

    Regulatory Recognition and Traceability

    Each market expects something just slightly different, and regulatory bodies place unique demands on product ledger keeping, test results, and labeling. Our traceability system links every manufactured batch to raw material input, processing equipment, and testing logs—helping our partners demonstrate compliance for both domestic sales and export documentation. Regular external audits verify these systems, and we also run periodic internal reviews after major regulatory changes in key markets.

    One growing area of importance is rapid, electronic access to Certificates of Analysis and Material Safety Data Sheets. Many of our customers want immediate access to all supporting documents, and we have invested in digital delivery systems, integrating QR code batch tracking directly onto shipping bags for instant scan-and-view by technical and regulatory teams at customer sites.

    Adjusting To Global Trends

    Few products have ridden out the kind of shifts antibiotics have seen in recent years. Limits on routine prophylactic use in places like the EU, alongside new labeling requirements in the Americas or pushback against non-therapeutic antibiotic claims in Asia, force producers like us to stay nimble. As governments refine their stances on veterinary drug imports, our constant lines of communication with distributors, regulators, and customers matter more than ever.

    Even as some markets reduce broad-spectrum antibiotic use, interest in therapeutic-focused application keeps CTC in the conversation. Our technical support team works actively with end-users helping them understand where judicious use remains permissible, how to coordinate withdrawal periods, and what label changes mean in terms of on-farm documentation and record-keeping.

    Product Quality: Not Just a Label Claim

    We find that rigorous internal control leads to products that not only meet but tend to outstrip basic label guarantees. Real-world users don’t want paperwork—they want product that works exactly as last month’s batch did. For this reason, our lot release policy holds each production run until it passes independent verification for active content, moisture, and dust level. Retained samples, including bagged finished product, stay archived for the full stated shelf life, available for post-sale investigation if needed.

    A recurring issue for feed manufacturers is how CTC interacts with other premixed ingredients—particularly vitamins and trace minerals—which tend to degrade more rapidly in the presence of moisture and certain carriers. Our technical team performs compatibility trials, seeking to minimize caking, nutrient loss, and mutual instability, reporting findings back to customers with practical recommendations.

    Differences between CTC and competitor molecules don’t always show in basic test results. In real-world conditions, variations in dustiness, flow, and color can spell reduced end-use adoption. Regular user surveys and field visits drive our process improvement, narrowing variability in these less quantifiable but highly important user experience areas.

    Supply Chain Security in an Unpredictable World

    Market disruptions—raw material pricing spikes, sudden regulatory changes, or shipping delays—have become more frequent. Over the years, we’ve developed alternate sourcing relationships for active intermediates and invested in backup handling plants. Keeping transparent communication lines with end-users helps navigate sudden shortages, as do buffer stock agreements in regions with limited warehousing infrastructure.

    We maintain strict inventory tracking for both finished CTC and all raw materials, using a digital supply chain management platform. Lot-level barcoding enforces traceability from shipment back to raw input, and any deviation from normal trends triggers immediate internal review.

    Future Developments and Continual Improvement

    Our R&D team focuses on advances that bring direct value to end users—such as improved flow properties, better solubility for water-medication forms, and lower-dust granulation methods. These initiatives respond to field challenges and also anticipate future compliance requirements on emissions, safety, and residue. Investments in waste treatment and emission-reducing granulation reflect both evolving law and real-world expectations from customers keen to lower environmental impact.

    Collaboration with universities and animal health scientists brings clinical feedback full circle, letting us refine product profiles with field-verified outcome data. Some recent projects have focused on resistance mapping, granular dust control, and packaging performance under shipping extremes—each rooted in real use conditions.

    Closing the Gap Between Production and End-User Needs

    The task for us as a manufacturer goes beyond simply achieving chemical compliance. We remain invested in listening to field results, not just test reports. Every line upgrade, QC protocol, or packaging choice flows from daily contact with those actually using CTC across farms and feedmills worldwide. We believe that open exchange means issues get caught early and solutions take hold faster.

    As regulations tighten and animal production systems become more complex, effective and responsible CTC production stands as a collaborative effort across the entire chain—from chemistry and logistics to field troubleshooting and customer service. Direct experiences and technical improvements combine to keep CTC both effective and relevant, even as the conversation around antibiotics in animal production shifts.

    From start to finish, every batch we produce reflects decades of lessons learned—about consistency, adaptability, and responsiveness to the concerns that matter most on the ground. Customer feedback, regulatory requirements, and changing disease trends guide our programs. Chlortetracycline, in our view, remains a practical tool—one that rewards close attention to detail, open communication, and ongoing improvement at every stage of its journey.