Products

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

    • Product Name: Ichthammol Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions
    • Alias: ICHTHAMMOL-VET-API
    • Einecs: 263-279-9
    • 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

    851771

    Product Name Ichthammol Veterinary Grade API
    Chemical Formula C28H36S5O6 (approximate)
    Cas Number 8029-68-3
    Appearance Dark brown to black viscous liquid or paste
    Odor Characteristic bitumen-like smell
    Solubility Soluble in water and glycerin; insoluble in most organic solvents
    Usage Formulations Tablets, Injections, Capsules, Powders, Granules, Premix, Solutions
    Main Usage Antibacterial and anti-inflammatory agent in veterinary medicine
    Storage Conditions Store in a cool, dry place away from light
    Purity Typically ≥ 95% (veterinary grade)
    Molecular Weight Approx. 624.1 g/mol
    Ph Value Range 5.0 - 7.0 (10% aqueous solution)

    As an accredited Ichthammol 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 Ichthammol Veterinary Grade API, 25 kg net, comes in a sealed, food-grade HDPE drum with tamper-evident lid and product labeling.
    Shipping Ichthammol Veterinary Grade API is securely packed in tamper-evident, food-grade HDPE drums or fiber containers with double-layer polyethylene liners. Each container is clearly labeled with batch details and MSDS. Shipped via temperature-controlled, regulated freight, ensuring stability, integrity, and compliance with international standards for pharmaceutical ingredients.
    Storage Ichthammol Veterinary Grade API should be stored in a tightly closed container, protected from light and moisture. Store at room temperature (15–30°C), in a dry, well-ventilated area, away from incompatible substances. Ensure the storage area is secure, clean, and designed to prevent contamination and degradation. Follow all regulatory guidelines for veterinary pharmaceutical ingredients to ensure stability and efficacy.
    Application of Ichthammol Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions

    Purity 98%: Ichthammol Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Purity 98% is used in oral tablet formulations for livestock, where it ensures high efficacy against bacterial skin infections.

    Viscosity Grade 150 mPa.s: Ichthammol Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Viscosity Grade 150 mPa.s is used in injectable suspensions for companion animals, where it provides uniform dispersion for consistent dosage delivery.

    Particle Size D90 < 50 microns: Ichthammol Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Particle Size D90 < 50 microns is used in granule feed premixes for poultry, where it enables rapid solubility and enhanced bioavailability.

    Melting Point 175°C: Ichthammol Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Melting Point 175°C is used in capsule manufacturing for swine, where it maintains chemical stability during the encapsulation process.

    Stability Temperature up to 60°C: Ichthammol Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Stability Temperature up to 60°C is used in powder solutions for large animal dosing, where it retains therapeutic effectiveness under ambient storage conditions.

    Moisture Content < 2%: Ichthammol Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Moisture Content < 2% is used in premix additives for aquaculture, where it prevents clumping and ensures homogenous blending.

    Sulfated Ash < 0.5%: Ichthammol Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with Sulfated Ash < 0.5% is used in veterinary injectable solutions for cattle, where it guarantees low impurity levels for safe parenteral administration.

    pH Value 5.0–7.0 (1% solution): Ichthammol Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with pH Value 5.0–7.0 (1% solution) is used in oral powder syrups for equines, where it provides optimal mucosal tolerance and reduced gastrointestinal irritation.

    Free Quote

    Competitive Ichthammol 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.

    We will respond to you as soon as possible.

    Tel: +8615365186327

    Email: admin@ascent-chem.com

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    Certification & Compliance
    More Introduction

    Ichthammol Veterinary Grade API: Supporting Reliable Animal Health Solutions

    Delivering Consistency in Real Veterinary Practice

    Over decades in chemical manufacturing, we have learned that veterinarians and feed formulators expect ironclad quality and steady supply for their active ingredients. Ichthammol stands out as a dependable veterinary-grade API, trusted in treatment protocols for dairy herds, swine operations, and poultry production plants. Every kilogram that leaves our factory is the result of proven process controls, documentation, and a deep respect for the end users who rely on accurate, repeatable results in the field.

    Ichthammol—originating from natural bituminous shale and processed through precise sulfonation and ammoniation—has earned its role in veterinary medicine due to its high purity and rich sulfonated aromatic content. Unlike ‘light’ surface preparations sourced through generic distributors, our veterinary grade is engineered specifically for pharmaceutical and feed premix applications. We do not cut corners or alter our process to reduce costs, because any change in reactivity, solubility, or batch uniformity could alter outcomes for herds, flocks, or individual animals.

    Our Model of Ichthammol Production

    True Ichthammol requires multi-step extraction and refining to remove impurities common in standard technical grades. We use only medically-approved mineral shales with traceable batches documented from initial mining through processing. Each step, from high-temperature sulfonation to neutralization and dehydration, is monitored for color, odor, and total sulfonate content using industry-accepted assays. We do not outsource process steps, which allows us to maintain the sensitive balance between purity and therapeutic activity.

    Our Ichthammol API comes in batches tailored for pharmaceutical manufacturing: high-purity, black viscous fluid or powder with strict low ash, stable pH, and absence of heavy metals by validated analysis. Each specification sheet we release bears direct analytical results for each batch, not generic “typical” values. This practice is especially important for operators producing high-volume tablets, injectables, or capsules who cannot risk mislabeling or recall due to an inconsistent or contaminated input.

    Usage in Tablets, Injections, and More

    Veterinary professionals rely on our Ichthammol for anti-inflammatory, antiseptic, and mild analgesic functions in both topical and systemic products. On farms, injectable forms see frequent use for deep-tissue infections or abscesses where other topical treatments fail. Feed mills and integrators depend on our powder and premix grades to incorporate uniform concentrations into animal rations. In poultry, this helps manage recurring outbreaks and supports wound management in frequent handling environments. Swine practitioners use Ichthammol-based solutions for treatment of chronic dermatitis and pyogenic lesions, situations where only active grade, residue-tested product is acceptable.

    Capsules and granules manufactured with our Ichthammol allow repeatable dosing, which minimizes metabolic variability across populations. Unlike surface or food-grade preparations, our pharmaceutical batches contain no diluents, fillers, or unreacted precursors. That means operators can scale up without reformulating for each batch, and documentation always matches the critical traceability standards required by pharmaceutical and feed safety authorities.

    Standing Apart from Commodity Ichthammol

    The global market contains many forms of Ichthammol: some produced for veterinary use, others as low-grade byproducts from the paint and leather industries. We consistently hear from new customers who encounter issues with batch-to-batch changes, variable solubility, or unexplained residues when using generically sourced material. These problems often lead to rejections during GMP audits or—worse—field performance failures that hurt credibility and animal welfare.

    One major distinction lies in the choice of source shale and the monitored process. Only high-quality natural shales yield the complex mixture of sulfonated aromatic hydrocarbons with therapeutic value. Harsh or shortcut processing, which might be acceptable for industrial use, introduces unpredictable byproducts and compromises stability. In animal pharmaceuticals, such impurities can trigger abnormal tissue responses or fail qualitative release tests. We subject every batch of our Ichthammol API to full analytical screening, including HPLC profiling and microbial contamination checks, with all data retained for at least ten years.

    Pharmaceutical and veterinary-grade Ichthammol must also prove freedom from heavy metals and residual solvents. While commodity forms often retain variable traces from inconsistent processing water or untreated storage, our process employs closed reactors, pharmaceutical-grade neutralization agents, and continuous quality sampling at every step. This allows downstream users to confidently use our API in parenteral preparations, capsules, and topical solutions without facing hidden compliance risks.

    Responding to Market Challenges and Field Demand

    Trusting veterinary APIs means relying on suppliers who do not compromise to meet quotas or cut costs. Our technical team partners with both international and local regulatory authorities to guarantee that every specification on our certificate matches current pharmacopoeia requirements. This work reaches beyond internal lab testing—our batch files include raw material certificates, process operation logs, and reference controls tested against external standards.

    Health regulators worldwide demand proof that every intermediate and final batch has traceable, documented origins. In the realm of animal health, this matters as much for the peace of mind of veterinarians treating pet, sport, or food animals as it does for the multinational feed mills submitting dossiers to food safety boards. We open our production documentation for third-party verification, knowing these steps help bolster confidence at every segment of the industry chain.

    Supplier reliability gets tested most in times of market instability—fluctuating raw material prices, disrupted transport, or shifting regulatory standards. Over our years in this business, we learned to hedge raw materials, maintain buffer inventories, and implement parallel quality release checks so customers are never left exposed. Our Ichthammol API offers security through confirmed backward integration and dedicated transport networks to support uninterrupted operation for manufacturers of all sizes.

    Manufacturing Feedback Shapes What We Deliver

    As an integrated manufacturer, we never operate in a vacuum. Our partners—veterinarian-compounded medicine facilities, contract manufacturing organizations, and independent animal health manufacturers—provide direct feedback on solubility, handling, and performance in real-world environments. Based on their reports, we adjust production parameters, drying processes, and packaging designs to match the actual flow and dosing methods used in today’s practice.

    Internally, process optimization is ongoing. Each reactor run is reviewed not only for analytical conformity, but also for how the final product performs in end-user settings. Are granules dispersing effectively in feed? Do powders maintain performance in variable climatic conditions? Can veterinarians draw injectable formulations easily from common vial designs? Our technical staff works hand-in-hand with field professionals to address bottlenecks, whether it’s reducing dust in blending lines or altering moisture content to prevent clumping in coastal environments.

    Traceability That Supports Global Movement and Safety

    Stringent traceability does not stop at our gates. For multinational clients submitting veterinary dossiers or seeking import approvals, we package every batch with unique identifiers linked both backwards to source lots and forwards to specific customer shipments. In case of a rare post-market concern, recall effectiveness depends on this transparent and robust tracking. Each shipment is accompanied by a comprehensive document package, including full batch analytics, origin declarations, and real-time process logs.

    Working across countries with varying veterinary import regulations, we standardize every critical control point (CCP) and conduct mock recalls to test system readiness. This approach, born from years in regulated manufacturing, raises customer confidence and meets the expectations of modern veterinary audits. Whether shipping to North America, Europe, or Southeast Asia, we anticipate changes in documentation or deviation thresholds before they arise, guided by continuous monitoring of both local regulations and international standards.

    Sustainable Approach to Resource and Waste Management

    Responsible manufacturing means acknowledging the environmental impact of chemical processing. Our process design prioritizes closed water and solvent loops, with strict controls on sulfur and ammonia emissions. Process residues are tested for persistent organic pollutants to prevent accidental entry into agricultural watersheds. This work evolves with new knowledge as environmental agencies redefine safe thresholds, and we adapt plant protocols to match or exceed new benchmarks.

    We also invest in waste minimization through byproduct valorization where possible, using modern methods to reclaim sufur and ammonia compounds from spent process streams. Our environmental commitment extends to third-party land and water testing around our production facilities, with annual reports reviewed by independent auditors. This investment pays forward by supporting community trust and protecting the resource bases our agricultural customers rely on.

    Direct Technical Support From the Source

    Customers expect more than a Certificate of Analysis. Our technical team remains accessible to answer application questions—whether addressing unexpected precipitation in injectable forms, batch stratification in tablet compounding, or regulations for residue levels in food-producing animals. We provide field-based troubleshooting rooted in both chemical engineering experience and close contact with veterinary practitioners.

    Whether a client faces a sudden animal health emergency or begins developing a new feed supplement line, our scientists offer hands-on support to tweak formulations, share validated use cases, and connect them with other solution providers within our network. This direct approach accelerates resolution, drives innovation, and builds stronger relationships around a shared commitment to safe and effective animal health products.

    Why Quality Veterinary APIs Matter Now More Than Ever

    Animal husbandry faces unprecedented pressures; producers must keep herds productive under stricter welfare monitoring, disease surveillance, and consumer expectations for transparency. A single deviation in active ingredient quality can force batch recalls, disrupt supply for thousands of animals, and damage trust built up over years. We see frequent real-world impact when field veterinarians call seeking help after unexpected results tied to off-standard APIs—even small label differences can have ripple effects on health outcomes or market eligibility.

    Our manufacturing legacy carries responsibility: to never compromise or issue products that do not meet published specifications. Every kilo of our Ichthammol veterinary grade API reflects this commitment and serves as an assurance to integrators, formulators, and end users that consistency, transparency, and full documentation always accompany our product. Customers get more than a bulk shipment—they receive decades of quality systems expertise, direct support, and peace of mind that comes from working directly with the actual producer.

    Ongoing Collaboration with Regulatory Authorities

    Compliance in animal heath APIs means aligning with evolving pharmacopoeial standards and country-specific residue limits. We maintain active engagement with global regulatory working groups, submitting technical feedback on analysis methods and product monographs. By working hand-in-hand with authorities and sharing real production data, we help raise the standard for Ichthammol APIs everywhere, which in turn improves animal care and food safety outcomes at scale.

    Our technical and regulatory teams regularly review published guidance on acceptable impurities, extractable metals, and batch documentation practices to proactively update our quality assurance protocols. This ensures every dose compounded from our Ichthammol reflects best practices, not just minimum compliance targets. We also support customers preparing government submissions by providing detailed dossiers and responding to regulatory queries with transparency backed by full process documentation.

    Enhancing Value Through Packaging and Logistics

    Beyond chemistry, veterinary manufacturers need reliable, contamination-proof supply. Our packaging process uses pharmaceutical-grade containers, tamper-evident seals, and batch-level QR code tracking for instant traceability. Storage and handling protocols comply with global Good Distribution Practice (GDP) standards to prevent cross-contamination or degradation during transit—even in tropical or subarctic conditions.

    Flexibility in delivery volumes—drums, intermediate bulk totes, or small-batch packs—helps feed mills, compounding pharmacies, and contract manufacturers keep inventories manageable without facing expiry risk. Dedicated logistics partners move high-priority shipments directly from our facility, ensuring temperature and humidity requirements are met through every step. This integrated approach reduces needless delays and potential disruptions at the customer’s facility.

    Partnering for the Future in Animal Health

    The world’s animal production systems will only grow more complex and regulated. As new veterinary treatment protocols emerge and analytical standards tighten, manufacturers must keep advancing their skills and documentation systems or risk falling behind. By staying direct and fully accountable, we build partnerships rather than just transactional relationships with users of our Ichthammol veterinary grade API.

    Our record is built on proactive transparency, listening to the needs of formulators and end-users, and constant reinvestment in process improvement. Every batch released carries this assurance, and we aim to remain the trusted source for reliable, pharmaceutical-quality APIs that support animal welfare and safe food production long into the future.

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