|
HS Code |
521864 |
| Product Name | Amitraz Solution Veterinary Grade API |
| Active Ingredient | Amitraz |
| Appearance | Clear to slightly yellowish liquid |
| Concentration | Varies (typically 12.5% solution) |
| Solubility | Soluble in organic solvents, insoluble in water |
| Intended Use | Ectoparasiticide for veterinary use |
| Dosage Forms | Tablets, Injections, Capsules, Powders, Granules, Premix, Solutions |
| Storage Conditions | Store below 30°C, protect from light |
| Cas Number | 33089-61-1 |
| Molecular Formula | C19H23N3 |
| Molecular Weight | 293.41 g/mol |
| Shelf Life | 2 years under recommended storage conditions |
| Mechanism Of Action | Acts as an alpha-adrenergic agonist causing paralysis and death of parasites |
| Target Species | Cattle, dogs, sheep, goats, pigs |
| Main Indications | Control of ticks, mites, lice and mange |
As an accredited Amitraz Solution 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 | Packaged in 25 kg HDPE drums with tamper-evident seals, labeled for veterinary use, ensuring safe transport and storage. |
| Shipping | The Amitraz Solution Veterinary Grade API is securely packaged in sealed, leak-proof containers to ensure stability and integrity during transit. The shipment complies with international transport regulations, includes proper labeling and documentation, and is dispatched via reliable carriers with temperature control options as required, ensuring safe and timely delivery worldwide. |
| Storage | Amitraz Solution (Veterinary Grade API) should be stored in a tightly closed container, protected from light and moisture. Keep at a controlled room temperature (15°C to 30°C) in a well-ventilated, dry area away from incompatible substances. Ensure the storage area is secure, clearly labeled, and restricted to authorized personnel. Avoid exposure to heat, direct sunlight, and open flames. |
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Purity 98%: Amitraz Solution Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with 98% purity is used in oral and parenteral formulations for companion animals, where high purity ensures reliable acaricidal and insecticidal efficacy. Viscosity grade 150 mPa·s: Amitraz Solution Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with viscosity grade 150 mPa·s is used in injectable preparations for livestock, where optimal viscosity enables precise dosing and administration. Particle size 50 microns: Amitraz Solution Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with 50 micron particle size is incorporated into powder premixes for poultry, where fine granularity promotes homogenous blending and stable dispersion. Stability temperature 40°C: Amitraz Solution Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions stable at 40°C is applied in heat-prone storage and distribution environments, where thermal stability maintains pharmacological activity throughout shelf life. Melting point 86°C: Amitraz Solution Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with melting point 86°C is formulated into oral tablets, where proper melting point facilitates precise manufacturing and consistent tablet formation. Solubility in ethanol 15 g/L: Amitraz Solution Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with solubility 15 g/L in ethanol is used in liquid veterinary solutions, where solubility supports rapid dissolution and effective dosing. Moisture content less than 1%: Amitraz Solution Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with moisture content less than 1% is incorporated in capsule and powder forms for ruminants, where low moisture prevents caking and enhances product shelf life. Residual solvents below pharmacopeial limits: Amitraz Solution Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with residual solvents below pharmacopeial limits is utilized in sterile injection preparations, where controlled solvent levels ensure safety and regulatory compliance. |
Competitive Amitraz Solution Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions prices that fit your budget—flexible terms and customized quotes for every order.
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As a chemical manufacturer with decades in active pharmaceutical ingredient (API) production, we focus on delivering Amitraz Solution suited for modern veterinary needs. Veterinary professionals and formulation developers count on API that performs predictably batch after batch. Animals, whether in livestock operations or companion care, require exacting standards from the medicines used in their treatment. As specialists in Amitraz API manufacture, we understand what reliable supply and resilient quality mean for global health and animal welfare.
We produce Amitraz Solution specifically for direct veterinary pharmaceutical use. Our customers require APIs that deliver consistent results — there’s no room for deviation in health-critical applications. With each batch, we monitor the appearance, solubility, and concentration. Rigorous process control ensures our solution works across the full spectrum of downstream products, from oral tablets and capsules to injectable forms and premixes.
The push in veterinary medicine to reduce parasites and mange in animals like cattle, sheep, pigs, and dogs relies on antiparasitics that absorb and metabolize at expected rates. Amitraz, acting chiefly as an acaricide and insecticide, represents an essential active in combating external parasites such as ticks and mites. That pharmacological role only delivers consistently if the input API keeps impurities in check and maintains robust stability under transport and storage.
For Amitraz Solution, we focus on tight control over solvent quality, amine content, and organic residue. The specifications match international veterinary pharmacopeia standards, supporting formulation into tablets, granules, capsules, powders, oral solutions, injectables, feed premixes, and topical applications. Our standard solution model optimally balances strength — typically between 12.5% and 20% w/v, depending on customer requirement — and low-level excipients necessary for a shelf-stable, ready formulation input.
Exceeding target purity consistently requires more than simple filtration or bulk processing. Every lot gets tested for heavy metals, residual solvents, and common byproducts at our in-house lab. Each analytical certificate reflects current batch data, helping veterinarians and contract manufacturers verify input quality on their end. We share details openly with customers so they can track lot history and storage recommendations, eliminating ambiguity.
Our Amitraz Solution supports several routes of use. Veterinary professionals and drug producers develop:
We see real-world application requirements shifting as livestock herd health plans evolve, new farming regulations emerge, and owners push for more predictable outcomes without residue buildup or toxicity. Our production lines adapt to formulation feedback from global clients, ensuring the solution remains compatible with current excipient systems and delivery technologies.
Buying Amitraz Solution from a direct producer unlocks several benefits for veterinary formulators and downstream manufacturers. Trading companies typically buy in bulk, repack, and sometimes dilute or relabel. We, on the other hand, own the process from raw chemical synthesis through sterile solution preparation, packaging, and documentation.
As a manufacturer, we can trace every raw material source, identify critical control points, and quickly intervene in case of out-of-spec results. Our clients count on batch traceability and retain samples for years, which proves essential during recalls or adverse event investigations. Because we handle every stage directly, there’s no risk of adulteration or specification drift due to midstream handling or warehouse mixing — a significant issue uncovered in cases where resellers have cut corners.
Unlike resellers who might blend solution lots to extend shelf life or mask off-spec characteristics, our standard operating procedures prohibit cross-batch blending. Clients can audit our facility and review recent logs anytime. Transparency and strong records reassure the veterinary sector that the Amitraz Solution in use meets every label claim, with no dilution or substitution. Evidence points to higher success rates in clinical effectiveness and fewer pharmacovigilance flags for products built from direct-sourced API.
The manufacturing floor tells its own story. Over the years, we’ve observed how small process tweaks matter in the final product’s settling time, appearance, or downstream compatibility. Examples include solvent selection, mixing sequence, and the use of nitrogen sparging to remove oxygen — even minor slip-ups can cascade into feedstock instability or unexpected precipitation. Documentation and operating discipline let us maintain solution clarity, control particulate presence, and hit viscosity requirements, all keys to smooth manufacturing and reliable dosing.
We invested early in inline monitoring using automated spectrophotometry, which lets us detect early color shifts or contamination that visual checks cannot. Staff training focuses on changeover routines and strict line clearance, critical since cross-contact with other actives (such as ivermectin or fipronil) jeopardizes batch integrity. As a manufacturer responsible for what reaches the market, frontline technicians get the power to halt production if parameters drift, rather than being pressured to run batches at borderline conditions.
Compared to raw crystalline Amitraz or technical powder, the solution form streamlines downstream processing. For pharmaceutical manufacturing, it dissolves reliably without pre-wetting or lengthy stirring, saving setup time and minimizing unprocessed lumps. This brings the concentration within working range for a variety of veterinary dosage forms — especially important for low-viscosity oral solutions or high-clarity injectables.
Amitraz Solution reduces dust and cross-contamination risks. Crystalline powder, once handled and moved around a facility, can lose potency to air moisture or settling. With solution, dosing remains exact from vial to final container, offering predictable yields. The risk of human exposure also drops, protecting operators and reducing cleanroom turnovers. We’ve seen these operational benefits lead to fewer batch rejections and lower overall production costs for our clients.
Flexibility stands as another differentiator. Our Amitraz Solution lets development labs trial new formulations without modifying entire tableting or granulation workflows. For veterinary drug innovation or scaleups, having an easy-to-handle liquid API expedites stability trials and shortens the gap between pilot and commercial runs. Feed manufacturers, too, cite improved flow and blending compared with heavy technical powders, especially in humid regions.
Veterinary markets worldwide ask for more from their API suppliers than ever before. Consistent product isn’t just about hitting a concentration on a single certificate of analysis — long-run reliability ensures future access and fewer surprises during regulatory review or third-party testing. Through years of production, we’ve refined shipping protocols, storage guidelines, and inventory traceability. Amitraz Solution from our facility arrives with a clear history and guaranteed potency until its shelf life expires.
Regulatory compliance forms the foundation of our business model. With direct oversight and continuous improvement, we qualify each step under best manufacturing practices and respond proactively to updates from global pharmacopeias. Veterinary medicine doesn’t allow for compromise: medicines must work, batches must match, unexpected breakdowns in quality should never reach a farm, feed mill, or clinic. As direct manufacturers, we treat these as core responsibilities.
Amitraz API production brings challenges rarely seen in broader chemical commodity trades. Feedstock purity, solvent residue, and byproduct formation require systematic attention. As regulations tighten on excipient origin, metals content, and cross-contamination, responsibility for due diligence lands squarely with us. Discussions with regulatory authorities and global partners shape our process tweaks, documentation practices, and recall protocols.
Batch fails, process upsets, and supply chain interruptions are a fact of chemical manufacturing. What matters is a system robust enough to catch and fix issues before they affect pharmaceutical or veterinary formulations. That’s where our experience and systematic review help — not every batch passes the first time. Sometimes, materials never reach packaging, as we prefer to lose a batch rather than risk sending product into use with questionable quality.
Livestock management has shifted dramatically in the past decade, demanding more traceable, residue-free medicines. Amitraz’s role in topical acaricides and oral antiparasitics may face adjustments as regulations change and resistance patterns evolve. Our company invests in more sustainable process inputs and safer waste handling, shrinking the environmental footprint of veterinary pharmaceutical manufacturing.
We consult with customers on residue studies, withdrawal periods, and innovative applications — including potential synergy with other actives to prevent resistance buildup in target pests. The direct channel supports this type of joint work, compared to fragmented handoffs through multiple vendors.
Animal health depends on trust and predictability. Our Amitraz Solution’s traceability, process consistency, and technical support make a difference when veterinarians, pharmaceutical compounders, or farm managers face a disease outbreak or need to launch a new formulation. Over years of feedback and process improvements, we’ve forged strong technical partnerships with some of the world’s top animal health companies. Through rigorous data collection and openness to independent audit, our API gains trust where lives and livelihoods stand on the outcome of a single treatment.
From raw material sourcing to packaging and distribution, our impact stretches beyond the manufacturing floor. Direct manufacturing provides a level of consistency, transparency, and responsiveness that trading houses cannot match. Our team stands committed to providing exceptional Amitraz API, continually raising the standard for quality in veterinary chemical products.
As global emphasis grows on food safety, animal welfare, and responsible pharmacology, manufacturers of veterinary active ingredients carry more responsibility than ever before. From perfecting the formulation and quality control of Amitraz Solution to providing clear documentation and knowledge-sharing, our mission remains focused on supporting veterinarians, pharmaceutical developers, and the health of the animals they treat. Trust, not just transaction, defines the difference between direct manufacturing and indirect trading — and it is this commitment to transparency and reliability that underpins every lot of Amitraz Solution we ship.