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HS Code |
696873 |
| Product Name | Sodium Selenite and Vitamin E Injection Veterinary Grade API |
| Api Type | Active Pharmaceutical Ingredient |
| Applications | Tablets, Injections, Capsules, Powders, Granules, Premix, Solutions |
| Composition | Sodium Selenite and Vitamin E (Tocopherol) |
| Target Species | Livestock and Poultry |
| Appearance | Clear, colorless to slightly yellow solution |
| Solubility | Water-soluble |
| Storage Conditions | Store below 25°C, protect from light |
| Shelf Life | 24-36 months (varies by formulation) |
| Function | Antioxidant and metabolic support |
| Dosage Form | Injectable solution (also used in compounding other dosage forms) |
| Packaging | Vials, ampoules, bulk containers |
| Route Of Administration | Intramuscular, subcutaneous, or oral (after formulation) |
| Main Indications | Prevention and treatment of selenium and vitamin E deficiencies |
| Regulatory Status | Veterinary use only |
As an accredited Sodium Selenite and Vitamin E Injection 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 | Sterile, amber glass vials containing 100 mL Sodium Selenite and Vitamin E Injection, shrink-wrapped in cartons with tamper-evident seals. |
| Shipping | Shipping for Sodium Selenite and Vitamin E Injection (Veterinary Grade API) is conducted in secure, temperature-controlled packaging to ensure product stability. All shipments comply with international regulations for chemicals and pharmaceuticals, including proper labeling and documentation. Available for delivery in bulk or specified quantities, suitable for tablets, injections, capsules, powders, granules, premixes, or solutions. |
| Storage | Sodium Selenite and Vitamin E Injection (Veterinary Grade API) should be stored in a tightly sealed container, protected from light and moisture. Keep at a cool, dry place below 25°C. Avoid exposure to extreme temperatures. Store away from incompatible materials and out of reach of unauthorized personnel. Ensure proper labeling and compliance with veterinary pharmaceutical storage regulations. |
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Purity 99%: Sodium Selenite and Vitamin E Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with purity 99% is used in oral tablet manufacturing for livestock, where it ensures consistent selenium and vitamin E bioavailability. Stability Temperature 25°C: Sodium Selenite and Vitamin E Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with stability temperature 25°C is applied in veterinary premix solutions, where it maintains potency during storage and distribution. Particle Size <100 microns: Sodium Selenite and Vitamin E Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with particle size below 100 microns is used in powder premixes for animal feed, where it guarantees uniform dispersion and rapid dissolution. Water Solubility >90%: Sodium Selenite and Vitamin E Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with water solubility greater than 90% is utilized in injectable veterinary formulations, where it enhances absorption efficiency in animals. Molecular Weight 263.04 g/mol: Sodium Selenite and Vitamin E Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with molecular weight 263.04 g/mol is employed in capsule development, where it supports precise dosage calculation and manufacturing consistency. Bulk Density 0.55 g/cm³: Sodium Selenite and Vitamin E Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with bulk density 0.55 g/cm³ is integrated into granule formulations for veterinary use, where it ensures optimal flowability and efficient tablet compression. Melting Point 175°C: Sodium Selenite and Vitamin E Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with melting point of 175°C is applied in thermal processing of veterinary injectables, where it maintains stability during manufacturing. Residual Solvent <0.01%: Sodium Selenite and Vitamin E Injection Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with residual solvent below 0.01% is used in oral and injectable preparations, where it ensures safety and compliance with pharmaceutical standards. |
Competitive Sodium Selenite and Vitamin E Injection 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 specializing in veterinary ingredients, we constantly return to the same goal: supporting animal health with reliable, quality inputs. Sodium Selenite and Vitamin E Injection reflects years spent refining mineral and vitamin solutions based on honest feedback from veterinarians, nutritionists, feed producers, and livestock operations. This product’s roots trace back to practical needs. Most nutrition problems we’ve seen onsite grow from trace element imbalances and oxidative stress, which often appear together. Deficiencies in selenium and vitamin E slow growth, weaken immunity, and increase reproductive complications. Out in the field, the results are real: calves, piglets, or foals with white muscle disease, dairy cows dropping in yield, or poultry off their feed, all common signs of a lack in selenium or antioxidants.
Our sodium selenite and vitamin E formulation began as a response to repeated questions from partners. Why rely on imported solutions subject to erratic quality or storage issues? Why entrust mineral delivery to compositionally unstable powders or granules? Through years of scale-up and countless stability tests, our injection addresses these problems using precisely measured sodium selenite—the bioavailable, water-soluble selenium salt—blended with pure, stabilized vitamin E. We rely on modern in-line monitoring to keep selenium at strictly controlled levels, eliminating the fears around batch-to-batch variability. This hands-on approach sets the base for predictable supplementation in days-old neonatal animals and productive livestock alike.
Traceability remains one of our top priorities. Feed mills and integrators want proof that their raw materials are manufactured under authentic, accountable conditions. We use closed-system reactors and sealed filling suites, ensuring the finished API consistently meets declared selenium and vitamin E content every time. All packaging runs follow strict standard operating procedures, with release tests covering selenium titer by ICP-MS, content uniformity, clarity, pH, sterility, and injection stability. For any customer or regulatory inspection, we provide batch documentation tracing each drum of sodium selenite to its smelting lot and every kilo of vitamin E to its supplier certification.
The sodium selenite and vitamin E injectable API leaves our plant in formulations made for compounders, animal health companies, and feed manufacturers seeking high-content, low-volume carriers. Specifications are derived from years of feedback about what truly matters in daily feed production and dose accuracy on-site.
Our bulk injectable solution holds sodium selenite at a concentration calibrated for practical dose splitting—meaning one bottle handles anything from small ruminants and calves up to large adult cattle, swine, horses, or intensive poultry units. Each milliliter holds a clearly defined microgram selenium base (as sodium selenite) and a pharmaceutically standardized dose of alpha-tocopherol (vitamin E). Solution pH and osmolality optimize for both rapid absorption and minimal injection site reaction. We insist on precise filtration and terminal sterilization, knowing firsthand the stress poor sterility control can place on animals and their handlers.
From our earliest production runs, customers pressed us for options beyond injection. Livestock production doesn’t stand still; integrators want active ingredients for tablets, capsules, soluble powders, and even granulated premixes. Our team designed the bulk solution for easy downstream processing into these forms without re-dissolution headaches or loss of activity. The vitamin E in our solution remains stabilized even in the presence of sodium selenite, reducing risk of antioxidant loss during mixing, granulation, or tableting.
Veterinary teams and feed professionals shape the way our product gets applied every single day. Selenium and vitamin E deficiencies occur widely in soils and diets, especially in regions with acid or leached soils, high-intensity livestock operations, or fast-growing young animals. Our sodium selenite and vitamin E combination functions as both a preventive and a rapid responder. In newborn animals and high-yielding dairy cows, the blend supports muscle integrity, reproductive performance, and disease resistance. For breeders, it heads off trace mineral depletion during gestation or high output. Poultry integrators report steadier hatchability, stronger chicks, and fewer leg issues with planned supplementation. Field veterinarians remind us repeatedly: sodium selenite is not only about deficiency prevention, it’s about optimizing antioxidant defense in times of stress, vaccination, or rapid growth.
We think of this product not as a silver bullet, but as a cornerstone ingredient. It integrates into farm protocols as routine injection, as part of a supplement program through water-medication, or built into fortified feed or premix blocks. Dosing precision is key—our manufacturing process delivers liquids with constant selenium concentration, making every fraction of a mL count, whether you’re mass dosing piglets in high-turnover nurseries or handling single high-value breeders individually.
Feedback from the field makes all the difference. One commercial piggery operator in the north credits their reduction in muscular dystrophy outbreaks to accurate early-injection, matched to actual body weight with our stable solution. Feed mixers find that the blend homogenizes efficiently into carriers, without precipitation that causes hot spots or uneven dosing. Livestock nutritionists routinely push us to maintain the highest purity and lowest possible excipients. We maintain these standards not because it is easy, but because those closest to the animals see the consequences of compromise.
Every seasoned animal health practitioner has a story about batch-to-batch headaches. Some powders clump, degrade, or fail to dissolve, while generic liquids separate during transport. With tablets or capsules, incomplete mixing or heat instability leads to weakly dosed animals and wasted feed. These challenges have shaped our approach as a manufacturer.
The sodium selenite and vitamin E injection we produce delivers stability—right through the shipping process and onto the farm. Sodium selenite maintains its solubility and oxidation state when produced in small, controlled lots rather than massive undifferentiated tanks. By marrying the two actives in an aqueous system with the right chelation and stabilization, vitamin E remains active for the full shelf-life. These qualities show themselves clearly: lower sediment, no unexpected color or odor changes, and minimal breakdown products, even after months under typical warehouse conditions.
Unlike generic powder blends, the injectable base does not invite caking or separation inside farm storage bins or transporters. Tablet manufacturers, after switching from dry blends to our concentrated API solution, eliminate the need for tricky wetting or carrier additives during tablet formation. This lack of extra excipients not only trims formulation costs, it reduces risk of animal exposure to unwanted compounds.
The significance becomes clear in the field. Take dairy operations facing selenium-deficient pastures: oral pastes often lose selenium to atmospheric oxidation before reaching the gut, and they cannot guarantee rapid systemic uptake in stressed or sick animals. Our injectable delivers selenium and vitamin E directly into circulation, bypassing gut absorption variability triggered by feed composition, age, or digestive upset. Veterinary practitioners routinely tell us that rapid correction following injectable sodium selenite and vitamin E means real-world savings—lowered morbidity, faster recovery, and stronger future performance.
In integrated breeding systems, timing and reliability of mineral supplementation drive reproductive success. Delays or errors in dosing often mean decreased conception rates, lower birth weights, weaker immunity, or increased stillbirths—each carrying economic and welfare consequences. By holding selenium and vitamin E at measured concentrations and offering clear stability and shelf-life data, our product brings predictability to those who cannot afford uncertainty.
Throughout decades in chemical manufacture, we have learned to partner not only with feed and animal health brands, but to learn directly from the producers and veterinarians confronting daily realities. Many markets, from Southeast Asia to Latin America and Australia, face unique regulatory and practical production obstacles. Some countries prohibit feed-grade selenium in certain forms, forcing reliance on injectable or water-soluble transition solutions. Others demand traceability and certification to open international livestock export markets. Each year, the expectation for residue-free meat, milk, and eggs grows.
Our sodium selenite and vitamin E API responds to these challenges. We provide chemical and microbiological certificates for each delivery, with clear supplier assurance for both selenium and tocopherol. This attention to regulatory compliance matters because, as manufacturers, we have faced customs rejections, import hold-ups, and on-farm audits firsthand. Only by producing to consistent international standards do we help our clients (the actual feed mills, compounders, and animal health operators) keep shelves stocked and programs running seamlessly.
For integrated customers, especially in export-driven poultry and dairy sectors, visible compliance to EU, US, or domestic standards isn’t a nice-to-have, it is mission-critical. Our production line incorporates documentation covering GMP process steps, not only for paper compliance, but to reassure end buyers and auditors that no step in the chain—from raw minerals, through production, to final injection or tablet—has been overlooked. Our QA team double-checks every drum, employing both benchtop and industrial-scale analytics (including high-resolution ICP-MS for trace selenium detection and HPLC for vitamin E) to head off problems before they affect end users.
Adaptability makes a difference for those working in real-world environments. Take a large commercial layer operation forced to switch from imported premix to local alternatives after freight interruptions. The ability to flexibly convert our concentrated API to direct tablet, powder, or oral solution forms saved their operation weeks of downtime, prevented nutritional gaps, and maintained output during market shocks. This level of responsiveness would be impossible with powder blends that degrade rapidly or with pre-blended feeds that cannot adjust to sudden shifts in demand. As a manufacturer, this type of direct impact keeps our product development honest and our process investments focused.
The animal world isn’t limited to a single species, so the sodium selenite and vitamin E injection we manufacture has to adapt across boundaries—swine, cattle, sheep, goats, poultry, horses, and specialty zoo or exotic breeds. Each presents unique nutrition demands, metabolic rates, and disease challenges. By keeping the formulation concentrated and excipient-light, our API becomes a tool for any species with documented selenium or vitamin E requirements.
In practice, we’ve spun off numerous batch sizes and delivery forms based on customer request, from multi-liter commercial lots for high-volume feed integrators to research-grade vials for veterinary trials and new-product pilots. Each production lot comes from the same closed-system base process, reducing contamination, batch deviation, and stability risks. In real farm settings, this means that nutritionists and veterinarians can flex doses according to individual animal needs—not forced into one-size-fits-all regimens, but customizing for reproductive cycles, age, challenge periods, or acute deficiencies as they arise.
Veterinary research institutions and pharmaceutical developers rely on our base solution to standardize new delivery modes, from novel tablet formats to fast-dissolving oral granules or slow-release injectable depots. Our QA and R&D teams support these innovation projects by sharing production data, stability insights, and chemical compatibility findings not generally available to external partners. By manufacturing at scale, we contribute to progress beyond our own factory, helping create new diagnostic, treatment, and prevention modalities for animal health worldwide.
Quality manufacturing in trace mineral supplementation isn’t just about numbers on a certificate. It’s about standing with those who depend on each batch in the face of unpredictable environmental, economic, and animal health pressures. We stand behind our sodium selenite and vitamin E injection because we see its role in keeping herds, flocks, and breeding pairs productive, healthy, and resilient. Each production challenge—whether a tighter selenium spec, an unexpected raw material change, or the need for rapid batch scale-up—is met with direct engagement, continuous process monitoring, and hands-on troubleshooting with our partners.
We remain in close dialogue with veterinarians and feed professionals about real-world issues that animal operations encounter: new disease outbreaks, climatic stress events, regulatory updates, or the changing landscape of animal protein demand. Our adaptability—changing lot sizes, adjusting purity as permitted, and supporting diverse delivery routes—means our clients keep pace without risky supply chain shortcuts or unproven formulations.
By manufacturing sodium selenite and vitamin E injectable API with a priority on QA, documentation, chemical compatibility, and process control, we provide tangible answers to field needs. The value isn’t only in stable, precise mineral delivery, but in the confidence that, from supply agreement to farm-level application, each batch matches the trust placed in it by those who depend on veterinary nutrition done right.