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HS Code |
974989 |
| Name | Imidocarb |
| Cas Number | 55750-06-6 |
| Molecular Formula | C12H13N6O |
| Molecular Weight | 257.27 g/mol |
| Appearance | White to off-white powder |
| Solubility | Freely soluble in water |
| Usage | Antiprotozoal agent |
| Mechanism Of Action | Inhibits nucleic acid synthesis in protozoa |
| Route Of Administration | Injection (intramuscular or subcutaneous) |
| Target Species | Cattle, dogs, horses |
| Storage Conditions | Store below 25°C, protect from light |
| Synonyms | Imidocarb dipropionate, Imizol |
As an accredited Imidocarb factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Imidocarb is packaged in a 100 mL amber glass vial with a secure rubber stopper and labeled with usage instructions and safety warnings. |
| Shipping | Imidocarb should be shipped in tightly sealed, labeled containers, protected from light, moisture, and extreme temperatures. It must comply with relevant hazardous materials regulations. Use insulated or temperature-controlled packaging as required, ensuring secondary containment to prevent leaks. Include appropriate documentation, handling instructions, and emergency contact information during transport. |
| Storage | Imidocarb should be stored in a tightly closed container at a controlled room temperature, typically between 15°C and 30°C (59°F and 86°F). Protect it from light, moisture, and incompatible substances. Keep away from food, drink, and animal feed. Store in a secure, well-ventilated area, out of reach of unauthorized personnel, following local regulations for hazardous chemicals. |
Applications of Imidocarb in Industrial ManufacturingImidocarb, as an established chemical intermediate with targeted anti-protozoal activity, supplies a critical input for veterinary pharmaceutical production and animal health management. Below we detail its primary downstream industrial applications, focusing on its integration into real-world manufacturing of value-added veterinary products. 1. Veterinary Injectable Antiprotozoal Drugs (Bovine and Equine Babesiosis Treatment)Downstream manufacturers in the veterinary pharmaceutical sector utilize imidocarb as the key API for formulating injectable antiprotozoal therapeutics targeting bovine and equine babesiosis. Compliance with veterinary drug regulations and strict GMP oversight forms the backbone of the industry, as product safety for livestock interventions remains paramount. Formulators adjust active concentration in the injectable solutions based on weight ranges and clinical severity, following precise titration to ensure effectiveness and safety. Typically, the manufacturing process starts with aqueous dissolution, controlled pH adjustment, followed by sterile filtration and aseptic vial filling, with batch-released injectables destined for distribution to animal health providers and clinics. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Oral Veterinary Tablet Production (Canine and Feline Antiprotozoal Treatment)Veterinary medicine manufacturers formulate imidocarb-based oral tablets for use in companion animal protozoal infections, such as canine babesiosis and feliforme cases. The downstream production process relies on a blend of precise milling, granulation, and direct compression, ensuring content uniformity. Regulatory approval depends on rigorous bioequivalence and batch purity documentation. Dosing flexibility is achieved through the production of scored tablets in multiple strengths, meeting prescription regimens for small animal clinics and veterinary hospitals. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Livestock Premix Formulations for Large-Scale Farm UseFeed additive and livestock pharmaceutical factories employ imidocarb for medicated premixes, intended for in-feed administration to cattle in endemic zones. Stringent compliance to veterinary feed additive regulations ensures residue management and food chain safety. Dosage per ton of finished feed must balance efficacy against risk of residues in animal-derived foods, with adjustment based on feed formulation density and species treated. The manufacturing flow integrates precision micro-dosing systems, guaranteeing consistent dispersion throughout large feed batches and supporting traceability for downstream users. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Bulk API Supply for Contract Veterinary Formulation ManufacturersImidocarb also fulfills industry demand as a bulk API supplied directly to GMP-certified contract manufacturing organizations (CMOs) specializing in global animal health products. These CMOs handle multi-format secondary production, including reprocessing, granulation for sachets, or formation of customized dose forms as required by international marketing authorizations. Each project imposes unique analytical and documentation requirements reflecting the final market’s regulatory architecture, as well as tailored API packaging solutions engineered for process compatibility at the receiving factory. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Imidocarb has carried a reputation for decades among those who work in veterinary medicine, large-scale animal husbandry, and specialized research. Our team has manufactured imidocarb since before the turn of the millennium, and we understand better than most that every lot needs precise control and full traceability from raw material to packaged vial. The soul of our process centers on chemical consistency, repeatable yields, and clear supply-chain documentation. Here in our plant, every batch gets tracked back to its source, down to which vessel, operator, and even the batch of solvents used. Why? Because livestock owners and veterinarians rely on it, not only to treat disease but to safeguard investment, animal welfare, and regional biosecurity.
At its core, imidocarb stands apart from broad-spectrum agents by targeting protozoan parasites that attack red blood cells. Unlike antibiotics, which address bacteria, or macrocyclic lactones, which address nematodes and arthropods, imidocarb has always held a narrow purpose: control of babesiosis and similar infections in cattle, horses, and occasionally dogs in endemic regions. Its chemistry, built around the diamidine scaffold, leaves most non-target organisms untouched. This targeted mechanism provides a margin of safety and supports antiresistance stewardship—something we learned through years of feedback from the field and regulatory inspection.
Many talk about “high purity,” but laboratories do not treat this as a metric you wave away on a spec sheet. Every delivery gets tested, but no one sees the daily difficulty in holding purity above 98.5%, measured by HPLC. Even impurities drifting a fraction into the wrong range can interfere with efficacy or put tissues at risk. We build every production cycle around validated reference standards, and our quality analytics confirm no single lot drifts outside set limits for residual solvents, pH, appearance, or dissolution time. For our crystalline imidocarb dipropionate, users get a free-flowing white powder, soluble in sterile saline, ready for immediate reconstitution.
Each batch leaves the factory accompanied by its full QC protocol printouts—not just a certificate of analysis summary, but the real curves, raw data sheets, and photographic evidence of absence of extraneous matter. Over time, pharmacies and veterinary buyers have asked for more granular details, including batch-to-batch consistency and storage stability profiles. By collaborating with expert toxicologists and pharmacologists, we’ve published real-time stability studies showing that imidocarb stays stable for years in cool, dry conditions, even in the furthest supply chains where logistics tend to run hot.
There’s no room for errors when farms may house thousands of high-value animals, or when export markets base clearance on a single test for residues. Today, we manufacture imidocarb mainly in two regards. The first is as crystalline dipropionate for compounding and final formulation. The second is as a formulated injectable, sterile and already dissolved in isotonic solution, for use in clinics or at scale in agricultural medicine. Some regions prefer the pure active for custom compounding, while others take final-use injectables that require only standard aseptic administration by a trained hand.
Users often ask why not ship as a ready dry suspension, but we realized early that only true injectable solutions guarantee predictable absorption and full solubility. Any shortcut in reconstitution threatens uneven dosing, especially across large batches of livestock or when field conditions challenge the patience of the most experienced technician. Pharmacies and clinics that use our bulk active consistently report ease of preparation, with no visible particulate after dissolving at proper concentration. Our careful process removes every trace of fibrillation, stray crystals, or clumpy agglomerates—problems that plagued generic attempts manufactured without the right environmental controls.
Years ago, the market saw a rush of lookalike compounds produced in uncontrolled workshops, sometimes outside regulatory view. These alternatives brought a wave of issues—unexpected residues, off-flavors in milk and meat, and unpredictable animal reactions. What most fail to capture is the tight margin for error in veterinary drugs. Additives, substitute solvents, or improper salt forms shift solubility or absorption, sometimes turning safe medicine into a source of chronic tissue inflammation or acute stress. Our factory never trades off those health margins for a quick win. Every raw input gets documented and batch-tested, every solvent gets recycled within closed systems, and our final containers endure freeze-thaw and photostability tests to match real-life conditions.
Compared with old-guard treatments such as diminazene and quinapyramine, imidocarb achieves better tissue distribution, targeting parasites in both acute and carrier states. The structure was designed to retain strong activity even in older animals, where lipid solubility helps it penetrate deep into infected tissues. Our collaborators in university trials remarked on prolonged protection compared with legacy agents, with fewer relapses when used at recommended intervals. Importantly, withdrawal times for edible tissue and milk remain within clear, manageable periods—something other formulations struggle to guarantee because of batch variability and off-label excipients. If a batch drifts even slightly outside these data-driven windows, we scrap it instead of trying to “process into spec.” Responsible oversight means putting animal and consumer safety before output volume.
Field veterinarians rarely work under laboratory conditions. The job usually unfolds among restless cattle, shifting weather, and tight timeframes. Imidocarb needs to dissolve quickly and fully, and it must remain stable for several hours during dosing runs. That’s why our freeze-dried intermediates and final solutions get stress-tested under farm conditions, with outdoor temperature swings and real world handling. We ship in containers with durable seals, dark-tinted to shield from light, and always print manufacturing and expiry data with indelible ink—so nothing wears away in a muddy treatment shed, a sunlit barn, or a harshly lit truck cab.
Most of our clients report using imidocarb for the prevention and treatment of bovine and equine babesiosis, where tick vectors spread the disease through herds rapidly. Our data show a single full dose can reduce Babesia count to undetectable in carrier animals, preventing the hidden incubators that later cause devastating outbreaks. Resellers asked us at trade meetings why we avoid certain coloring agents or stabilizers found in other brands. The reason—every additive risks unpredictable interactions with field-use water sources or syringe lubricants, both common sources of residue buildup seen in competitive samples collected during national surveillance.
Some users treat imidocarb as a curative, but the real value comes in stopping reemergence during stress or transport. The longest-standing farms in our network use the product in herd-wide protocols prior to shipping animals between auction, pasture, or market. This prevents so-called recrudescence events, which often evade detection until new outbreaks cost far more than a course of treatment. This importance surfaced during one district’s summer tick invasion, when rapid intervention kept averted economic losses in the millions. Our ongoing, direct relationship with herd managers and their consulting veterinarians ensures our QC follows more than just health ministry checklists. We adapt based on the problems encountered by the people actually applying the solution.
Global regulations for veterinary pharmaceuticals tighten every year, especially for products with potential to enter the food chain. Imidocarb carries strict monitoring for active content, absence of toxic metabolites, and adherence to withdrawal periods for both milk and meat. In our facility, production lines routinely undergo independent audits from both state and private organizations. Instead of just “passing” a certificate, we log and respond to every finding, using errors as an occasion to reinforce our training protocols and record-keeping systems.
Residue monitoring in finished products and animal tissues sits at the core of international trade compliance. For this reason, all release data comes packaged with the analytical method traceability, from sample digestion to HPLC quantification and confirmation by LC-MS when required. Our non-negotiable policy means no shipment leaves the plant until residue testing and impurity profiling close within the strictest margin of error allowed by authorities. This level of oversight attracts partners who ship animals internationally, meeting both local and export standards. After all, a veterinary pharmaceutical serves no one if it endangers the farmer’s business or erodes the safety of food for the final consumer.
Making imidocarb isn’t about optimizing for speed or squeezing every penny from inputs. Chemical engineering at this level involves precise raw material selection, strict air and water quality controls, and full digital tracking from warehouse to loading dock. During times when upstream shortages challenge basic supplies—such as specialty amines or high-purity solvents—our long-grown relationships with base chemical producers prove their value. By refusing to shortcut on raw input validation or lot release protocols, we shield users from receiving substandard or variable product, even if it means some months pass with delayed output in the pursuit of guaranteed consistency.
We’ve seen the harm caused by counterfeit, cut, or bootleg “imidocarb” alternatives pulled from failed operations or re-imported outside authorized channels. Not only are these unreliable in effect, they regularly breach residue limits and founder on the smallest stress in field conditions. Our full serialization and data integration means any vial or packet can be traced through our system and linked to shipping, invoice, and end-user data. In the rare event of a problem, this allows for pinpoint rapid response—pulling and investigating exactly the lots involved. True supply security comes from this chain of control, not just from batch testing. With our real-time inventory and logistics partnerships running from dock to field, hospital, or wholesaler, customers rarely face surprise outages or mysterious gaps in their treatment protocols.
Imidocarb treatment often goes unnoticed by anyone outside livestock, equine, and animal health circles. Yet this single compound underpins the health and marketability of entire herds and keeps tick-borne epizootics in check. Farmers and ranchers call, sometimes in the early hours, seeking confirmation an urgent shipment will actually arrive before herd losses mount. Veterinarian specialists depend on us through difficult cases, facing imported parasites or government disease-control mandates that leave no margin for error. What many miss is that these end-users teach us as much about our own product as we ever learn from laboratory records. Reports of rare injection reactions or slow resolutions become data we fold back into every refinement—tightening controls on particle size, solubility kinetics, and packaging durability.
Over decades, our technical support teams compiled substantial archives from customer-provided treatment data, tissue testing after slaughter, or milk residue surveys. These real-world cases contradicted some established dogma and taught us to listen to those applying the science in muddy, unpredictable conditions. This feedback prompted real manufacturing changes—such as adopting nitrogen flush seals, adding visual flagging to packaging for faster verification, and improving batch differentiation for high-volume users treating hundreds of animals daily. Feedback loops with practitioners help us root out even subtle trends, then close the cycle by updating our protocols, documentation, and user support resources.
Chemical production at the scale and consistency required for imidocarb demands engineers and production staff to storm through myriad small, persistent challenges. Every day, our crew runs pilot tests, watches for reaction drift, confirms glassware sterility, and logs temperatures. Deviations are a call to recalibrate, not a chance to “make it work” and push through a questionable batch. We keep full traceability logs and submit authentic samples to world reference laboratories. If any partner laboratory or veterinary authority reports an unexplained anomaly, we shut down the applicable vessel, trace every variable, and re-run controls until the source emerges—then re-educate the involved staff, all of whom have years in the field and full understanding of the stakes.
Professional pride in this work lies not in flashy advertising or chasing trends but in zeroing in on root causes and providing consistent results no matter what production season throws at us. This isn’t a theoretical exercise. A bad batch could cause mass losses or trigger national-level investigations. Our staff meets monthly with regulatory liaisons and international partners to discuss compliance and interpret rule changes ahead of enforcement deadlines. This close dialogue means we never take shortcuts or rely on legal loopholes; our finished product stands up to scrutiny in any lab, at any checkpoint, across any trading border.
Many veterinary drugs compete for attention in the antiparasitic space. Each brings its strengths and limits. Imidocarb occupies a unique place by focusing on protozoal blood parasites, especially Babesia and related organisms—pathogens unresponsive to macrolide or classic worming medicines. Diminazene covers some of the same ground, but its safety profile and residue behavior are not as favorable. Issues with acute reactions and regulatory withdrawal times persist. Meanwhile, some novel antiparasitics lack stability for field use, or carry unclear residue status across ambient shipping, storage, and rapid administration cycles.
Here, imidocarb’s stability, well-documented pharmacokinetics, and broad market experience render it the mainstay in many countries. Because it does not cross-react with antibiotics, clinics can treat simultaneously for different infections without sacrificing outcome. Years of documented use outline a clear, predictable timeline for both tissue and milk withdrawal, documented in studies feeding into national residue monitoring programs. This supports routine veterinary protocols and links field safety to consumer protection at scale.
End users sometimes request a breakdown of why our imidocarb outperforms generic equivalents. The difference does not begin in the lab—it starts in supply. Our continuous checks on intermediate purity, batch scalability, drying technique, and solvent recovery reduce unwanted byproducts and guarantee the tightest possible range on chemical content per unit. Most low-cost or “gray market” products attempt to shortcut these steps, passing on the risk to animals and end consumers. We maintain a strict rejection threshold: even a fractional drift in detectable impurities, unusually high endotoxin levels, or delayed dissolution in reconstitution triggers full batch discard. This may cost us output, but it preserves what truly matters in sustained, safe livestock health management.
We enter each production year with a sober view of the changing landscape: evolving parasite epidemiology, rising regulatory checks, new competition, but also deeper appreciation from frontline users who realize cheap imitations cost more in lost output, crisis management, and long-term animal harm. Our mission aligns with that of the veterinarians, farmers, and public health authorities who deploy our product—a bond based on reliability, shared evidence, and constant dialog.
As disease patterns shift from climate, transport, and international trade, procurement specialists in animal health increasingly request provenance, process transparency, and extensive documentation for every shipment. We respond with full lifecycle archives, forward compatibility with new residue assays, and direct lines to scientific consulting. More than a supplier, we become a technical ally—dedicated to adapting each batch, shipment, and protocol for the realities of the field.
By staying committed to true continuous improvement, strict self-accountability, and open, respectful collaboration with the animal health community, we aim to secure both the safety of those who use our product and the reliability of supply that underpins regional and global veterinary protocols. Imidocarb, manufactured with this depth of purpose and discipline, remains one standard that owner's, veterinarians and public health officials can rely on—direct from source, traceable to its origin, and always open to scrutiny by anyone committed to the same values of safety, consistency, and progress in animal health.