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Bouling Chemical Co., Limited

Feed Grade Sodium Selenite

    • Product Name: Feed Grade Sodium Selenite
    • Factroy Site: West Ujimqin Banner, Xilingol League, Inner Mongolia, China
    • Price Inquiry: sales9@bouling-chem.com
    • Manufacturer: Bouling Chemical Co., Limited
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    Specifications
    HS Code 225621
    Product Name Feed Grade Sodium Selenite
    Chemical Formula Na2SeO3
    Cas Number 10102-18-8
    Molecular Weight 172.94 g/mol
    Appearance White crystalline powder
    Odor Odorless
    Solubility Freely soluble in water; slightly soluble in ethanol
    Selenium Content ≥45.0%
    Assay Purity ≥98.0%
    Loss On Drying ≤1.0%
    Heavy Metals As Pb ≤0.001%
    Arsenic As As ≤0.0005%
    Melting Point Decomposes above 350°C
    Storage Condition Keep in tightly closed containers in a cool, dry place
    Grade Feed grade

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

    Packing & Storage
    Packing Feed Grade Sodium Selenite is packaged in 25 kg net, double-lined polyethylene bags inside woven polypropylene bags for safe transport.
    Container Loading (20′ FCL) 20′ FCL: palletized feed-grade sodium selenite packed in sealed bags, securely stowed and ventilated for safe transport.
    Shipping Ship as UN 2630 (or UN 3288 as appropriate), toxic solid, n.o.s. (sodium selenite), Hazard Class 6.1, PG II. Pack in sealed, moisture-resistant drums or bags with inner liners, clearly marked, segregated from foodstuffs. Include hazardous goods documentation and placards per IATA/IMDG/ADR regulations.
    Storage Store Feed Grade Sodium Selenite in a cool, dry, well-ventilated area, away from direct sunlight and moisture. Keep containers tightly sealed to prevent caking and contamination. Avoid contact with acids, reducing agents, food, feed, or living quarters. Use separate, labeled storage; maintain good housekeeping and follow local regulations for toxic substances.
    Shelf Life Shelf life is 24 months when stored in a cool, dry, sealed container away from sunlight.
    Application of Feed Grade Sodium Selenite

    Can Sodium Selenite Carry Through Broiler Pellet Conditioning Without Assay Loss?

    Feed-grade sodium selenite assaying 45.0–45.6% selenium is introduced into broiler complete feeds at finished selenium concentrations between 0.20 mg/kg and 0.30 mg/kg. For a target of 0.25 mg/kg selenium in mash or pelleted complete feed, the equivalent anhydrous sodium selenite addition is 0.55 g per tonne; when a 1% selenium calcium carbonate premix is used, the inclusion rate is 25 g per tonne. Under 21 CFR 573.920, the completed feed for chickens must not exceed 0.3 mg/kg added selenium, while European formulations are governed by Regulation (EC) No 1831/2003 with a maximum total selenium of 0.5 mg/kg in complete feed at 12% moisture. The addition is made through a loss-in-weight micro proportioner rather than manual bag dumping because the undiluted material flow at 0.55 g/t falls below the reliable resolution of most platform scales. In concentrated premixes, direct contact between sodium selenite and ferrous sulfate or ascorbic acid is avoided because the redox pair can reduce selenite to insoluble elemental selenium.

    On the production line, the sodium selenite is first dry-diluted with ground limestone or calcium carbonate to a 1% selenium premix, then metered into a twin-shaft paddle mixer and mixed for 120–180 seconds before steam conditioning. The conditioned meal is held at 80–85°C for 30–45 seconds and forced through a 2.5–3.0 mm die. Post-pellet liquid application of fat or heat-labile additives should not include sodium selenite; the mineral remains in the core mix. Routine assay by ICP-MS or hydride-generation atomic fluorescence spectrometry after pellet cooling should return 95–105% of the label selenium concentration. Finished product types include broiler grower pellets, crumbles, or pre-starter mini-pellets.

    Sow Lactation Rations and Selenium Partitioning into Colostrum

    Sodium selenite in sow lactation diets is formulated to deliver 0.30 mg/kg total selenium on an as-fed basis, corresponding to 0.66 g/t of anhydrous sodium selenite at 45.6% selenium or 60 g/t of a 0.5% selenium premix. The U.S. limit for swine under 21 CFR 573.920 is 0.3 mg/kg complete feed, while Regulation (EC) No 1831/2003 permits a total selenium maximum of 0.5 mg/kg in EU complete feed. Formulators reducing corn-soy diets with elevated basal selenium must subtract the selenium contribution of the grain; in Upper Great Plains corn with 0.10–0.20 mg/kg selenium, added sodium selenite is often capped at 0.15–0.20 mg/kg to avoid exceeding the legal limit. Selenium from sodium selenite is transferred into colostrum and milk through glutathione peroxidase pathways, but its transfer efficiency is lower than selenomethionine; piglet liver selenium status may therefore be lower when inorganic selenium is the sole source.

    Manufacturing uses a twin-ribbon mixer with a fill factor of 55–70% and a dry-mix time of 4–6 minutes before the addition of soybean oil or liquid methionine. If the lactation diet is pelleted, conditioning at 70–75°C and a 4.5–5.0 mm die is typical; selenium recovery after pellet cooling is not significantly reduced at these temperatures. The terminal product is a sow lactation pellet or meal with a selenium assay of 0.27–0.33 mg/kg. Because sodium selenite-containing lactation feeds can carry over into non-supplemented pig starter batches, production sequencing should include a flush of ground corn after selenium-supplemented runs in medicated lines.

    In lactating dairy total mixed rations, sodium selenite is not added as a straight powder but is pre-diluted into a mineral-vitamin premix before the TMR mixer wagon is charged. The target total selenium is 0.30 mg/kg dry matter for high-producing cows, which equals 7.5 mg selenium per day at a 25 kg dry-matter intake. The equivalent anhydrous sodium selenite addition is 0.66 g/t TMR dry matter; for a 1% selenium premix, the inclusion rate is 30 g/t. Dairy selenium feeding is constrained by 21 CFR 573.920 at 0.3 mg/kg complete feed in the U.S., and by Regulation (EC) No 1831/2003 at 0.5 mg/kg total complete feed in the EU. Dry cow rations are usually reduced to 0.20 mg/kg because lower dry-matter intake changes total selenium exposure per animal per day.

    The premix is diluted to 0.05–0.10% selenium using ground limestone or wheat middlings as a carrier and is added at the dry-commodity stage of TMR mixing. A horizontal auger mixer wagon processing 10–20 m³ feed typically receives the premix after grain and protein meals are loaded, then mixes for 3–5 minutes before silage and wet byproducts are added. Direct mixing of undiluted sodium selenite into a TMR wagon is not recommended because the addition rate of 0.66 g/t cannot be distributed below a coefficient of variation of 15% in a single auger pass. The finished TMR is delivered to feed bunks as a complete mixed ration, not a pelleted concentrate. In pre-mixed mineral packs, ferrous sulfate monohydrate is physically separated from sodium selenite because the redox pair can reduce selenite to insoluble elemental selenium during storage at 30–40°C.

    When Extrusion Parameters Are Held Above 90°C in Salmonid Grower Lines

    Salmonid grower formulations use sodium selenite at a finished selenium concentration of 0.30 mg/kg, equivalent to 0.66 g/t anhydrous sodium selenite at 45.6% selenium or 30 g/t of a 1% selenium premix. The EU maximum under Regulation (EC) No 1831/2003 is 0.5 mg/kg total selenium in complete fish feed, and the inclusion margin is narrower when fishmeal and krill meal already contribute 0.10–0.25 mg/kg basal selenium. Sodium selenite is introduced in the dry micro-ingredient phase, not in the vacuum coating oil, because its water solubility and density make it unsuitable for post-extrusion lipid suspension. The production process begins with preconditioning at 90–95°C, followed by twin-screw extrusion with a specific mechanical energy input of 18–22 Wh/kg and die diameters of 4.0–6.0 mm.

    At the extrusion line, the 1% selenium premix is metered into the preconditioner feed screw at 25–30 g/t. The specific mechanical energy input during twin-screw extrusion is adjusted to maintain bulk density at 480–520 g/L. Sodium selenite is water-soluble and partitions with the aqueous phase rather than the lipid phase; therefore, adding it in the post-extrusion vacuum coater creates uneven selenium distribution and lipid-oxidation risk. Extrudate drying at 80–90°C to 92–94% dry matter does not produce significant selenium loss in closed-line audits, but sodium selenite is less efficiently retained in salmonid muscle than selenomethionine. Terminal product types are extruded salmonid grower pellets with 30–35% lipid after vacuum coating. Process limitations include the incompatibility of concentrated selenite with ascorbic acid and ferrous sulfate in the micro-ingredient premix under pre-extrusion moisture above 15%.

    Canine dry kibble lines present a different selenium dosage envelope because AAFCO nutrient profiles apply a dry-matter ceiling that differs from the FDA complete-feed limit. For adult maintenance diets, sodium selenite is added to deliver 0.20–0.25 mg/kg selenium as-fed, corresponding to 0.44–0.55 g/t anhydrous sodium selenite or 20–25 g/t of a 1% selenium premix. The U.S. regulatory ceiling under 21 CFR 573.920 is 0.3 mg/kg complete feed for dogs, while AAFCO Dog Food Nutrient Profiles set a maximum selenium concentration of 2 mg/kg on a dry-matter basis. Because extrusion and drying remove moisture from an initial 25–30% to 8–10%, the dry-matter selenium concentration rises by approximately 30–40%; a 0.25 mg/kg as-fed formula may assay near 0.35–0.40 mg/kg dry matter, which remains well below the AAFCO ceiling.

    The kibble line receives sodium selenite through the micro-ingredient cluster before preconditioning at 90–100°C. The meal is then processed in a single-screw extruder with die temperature 120–135°C and drying at 110–120°C for 15–25 minutes. Poultry fat or fish oil is applied after drying by drum coating; sodium selenite stays in the core and is not dispersed in the lipid phase. Terminal product types include adult maintenance dry kibble and small-breed formulations. In high-moisture retort pouches or canned loaf formats, sodium selenite is not the preferred selenium source because the long sterilization cycle can accelerate selenium reduction in the presence of meat reducing agents; published data for this specific configuration is limited.

    Comparative sodium selenite inclusion rates and governing standards by downstream species
    Species and terminal feedGoverning standardTarget total seleniumEquivalent anhydrous Na₂SeO₃ at 45.6% SeEquivalent 1% Se premix
    Broiler complete feed21 CFR 573.920 / Regulation (EC) No 1831/20030.20–0.30 mg/kg0.44–0.66 g/t20–30 g/t
    Sow lactation feed21 CFR 573.920 / Regulation (EC) No 1831/20030.30 mg/kg0.66 g/t30 g/t
    Dairy TMR21 CFR 573.920 / Regulation (EC) No 1831/20030.30 mg/kg DM0.66 g/t DM30 g/t DM
    Salmonid grower pelletRegulation (EC) No 1831/20030.30 mg/kg0.66 g/t30 g/t
    Canine adult kibble21 CFR 573.920 / AAFCO Dog Food Nutrient Profiles0.20–0.25 mg/kg as-fed0.44–0.55 g/t20–25 g/t

    Assay Variance in 1% Se Calcium Carbonate Premixes Escalates Under Tropical Storage Conditions

    For premix manufacturers supplying regional feed mills, the production issue is not final-feed dosage but the uniformity of selenium in a 1% selenium calcium carbonate premix. The dilution sequence begins with feed-grade sodium selenite assaying 45.0–45.6% selenium and meeting GB 34469-2017 or equivalent cGMP feed-additive specifications. The first progressive dilution is typically 1:100 with ground limestone with 90–95% passing 75 µm in a V-cone or double-ribbon blender to produce a 0.5% selenium intermediate. This intermediate is then blended again to 1% selenium or used directly at 60 g/t in sow or dairy premixes. The final multi-element premix is usually included at 0.5–2.0 kg/t complete feed, depending on the concentration of other trace minerals and vitamins.

    Batch-to-batch assay variance escalates when sodium selenite is charged directly into a 500 kg ribbon blender at quantities below 2 g; the first geometric dilution step is executed in a separate small blender with 10–15 minutes mixing time and a 45–65% fill volume. The main blender is then run for 15–20 minutes, and the premix is assayed by ICP-MS with a target coefficient of variation below 5%. Hygroscopic choline chloride and ferrous sulfate should not share the same concentrated premix package without moisture control below 4%; otherwise the redox degradation of selenite to elemental selenium can lower recovery after 60–90 days of storage at 30°C. The terminal product is a trace-mineral and vitamin premix for poultry, swine, or dairy feed mills. Packaging in foil-lined bags and storage at <25°C and <60% relative humidity is mandatory in tropical export shipments.

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    Certification & Compliance
    More Introduction

    Feed Grade Sodium Selenite (Na2SeO3; CAS 10102-18-8; EC 233-267-9) is an inorganic selenium carrier distributed as an anhydrous or pentahydrate crystalline solid for the manufacture of complete feed and mineral supplements. The anhydrous compound has a molar mass of 172.94 g/mol and a theoretical selenium mass fraction of 45.65%. Commercial feed-grade material is normally released at a guarantee of 45.0–45.6% total selenium, with total sodium selenite not less than 98.0% on an anhydrous basis and the remainder consisting of moisture, carbonate, chloride and sulfate mineral residues. Product models are distinguished by selenium mass fraction and particle form: a 45% selenium granular grade is used for direct blending into mineral premixes, and a 1% selenium calcium-carbonate-carrier premix is used where a weighable intermediate is required on less precise dosing lines. The crystal habit and particle-size distribution are controlled because selenium segregation in a batch is governed by the interaction between particle density, particle diameter and mixer shear.

    The anhydrous salt is water-soluble and redox-sensitive. Storage in closed original packaging at 10–30°C and relative humidity below 60% prevents hydration cycling and caking. Opened containers are resealed immediately after withdrawal. Storage near volatile organic acids, strong reducing agents or ammonia is avoided because these agents can reduce selenite to elemental selenium or generate reactive atmospheres. In liquid supplement practice, a stock solution is prepared at 1–5% selenium and metered into the mix line; the solution must be buffered or used promptly if the liquid supplement also contains ascorbic acid or ferrous sulfate.

    Specification Envelope for Feed-Grade Sodium Selenite

    The release specification is defined by a certificate of analysis covering total selenium, selenium species, moisture, heavy metals, arsenic and particle-size retention. The analytical methods are selected to avoid interference from the high sodium content; ICP-MS with collision-cell technology is preferred for trace metals because the sodium matrix ionizes readily and can suppress the selenium signal when external calibration without internal standard correction is used.

    ParameterTypical limit or rangeReference method
    Total selenium45.0–45.6% w/wEN 17053:2018 or AOAC 996.16
    Sodium selenite purity98.0% anhydrous basisredox titration
    Loss on drying0.5% (105°C, 2 h)ISO 6496:1999
    Arsenic2 mg/kgEN 17053:2018
    Lead5 mg/kgEN 17053:2018
    Cadmium1 mg/kgEN 17053:2018
    Mercury0.1 mg/kgEN 17053:2018
    Particle-size retention on 250 µm sieve5%ISO 2591-1:1988
    Bulk density0.85–1.10 g/cm³cylinder method

    On production lines, the compound is transferred from 25 kg sacks through a closed vacuum receiver into a 1,000 kg ribbon mixer or paddle mixer, where it is diluted with ground limestone or wheat bran. The critical process variable is not the solubility of selenite but the particle-size difference between the 1% selenium intermediate and the mineral carrier. If the Stokes settling velocities differ by more than one order of magnitude, stratification occurs during bin discharge. Carrier moisture above 12% is controlled because water bridges cause electrostatic clumping and segregation; the resulting assay variability is usually detected only after 10-point sampling according to ISO 6497. Dust generation during sack emptying is managed by local exhaust ventilation specified for selenium compounds; operators wear P3 respirators where airborne selenium dust cannot be maintained below the applicable occupational exposure limit.

    The low inclusion rate is the central engineering constraint. To deliver 0.3 mg/kg selenium to a complete feed, the feed mill adds 30 g of a 1% selenium premix per 1 tonne of finished feed; the equivalent pure 45% selenium sodium selenite dose is approximately 0.67 g per tonne. This arithmetic explains why direct addition of the pure salt at the weigh hopper is not recommended and why a two-stage dilution is used. Cross-contamination from selenium premixes into non-target batches must be controlled by sequencing selenium-containing mineral batches before line flush or by using dedicated premix bins.

    What Limits the Use Rate in Complete Feed?

    Sodium selenite is authorized as a nutritional feed additive in the European Union under code 3b801 within Regulation (EC) No 1831/2003. The total selenium content of complete feed is limited to 0.5 mg/kg at 12% moisture, which constrains the selenite contribution because the same limit applies to all selenium sources combined. In the United States, 21 CFR 573.920 permits sodium selenite and sodium selenate as selenium supplements for approved food-producing animals at levels not to exceed 0.3 mg/kg selenium in complete feed. The regulatory ceilings reflect the narrow margin between requirement and toxicity. At dietary selenium between 2 mg/kg and 5 mg/kg, chronic selenosis in poultry and swine is characterized by reduced feed intake, hepatic and renal lesions, and hoof or feather abnormalities. Because the pure salt contains roughly 45% elemental selenium, an error of only 2.2 g of pure sodium selenite in 1 tonne of finished feed raises total selenium by 1 mg/kg, twice the EU maximum.

    The dietary requirement for selenium in poultry and swine is commonly cited in the range of 0.1–0.3 mg/kg dry matter, leaving a narrow margin to the 0.5 mg/kg EU ceiling. In ruminant operations, selenite is incorporated into loose mineral mixes, blocks, or total mixed rations at rates that account for basal forage selenium and water selenium intake. Voluntary mineral intake can vary from 10 g/day to 50 g/day in beef cows depending on season, which changes selenium exposure. Formulators therefore target a mineral concentration that assumes the upper observed intake rather than the average to prevent selenosis. Where selenium-deficient forages are common, sodium selenite is combined with vitamin E in dry mineral packs because the two nutrients have complementary antioxidant functions in the glutathione peroxidase system and lipid-membrane protection.

    When Premix Formulators Compare Sodium Selenate and Organic Selenium Sources

    Sodium selenite differs from sodium selenate in oxidation state and reduction behaviour. Sodium selenate contains selenium in the +6 oxidation state; sodium selenite contains selenium in the +4 oxidation state. Selenite is reduced by glutathione in the erythrocyte to selenide before selenoprotein synthesis, whereas selenate must first be reduced to selenite and then to selenide. Sodium selenite is more redox-reactive in acidified premixes and can be reduced to elemental selenium by ascorbic acid or ferrous sulfate; sodium selenate is thermodynamically more resistant to this non-enzymatic reduction but may be taken up via sulfate transport pathways and compete with dietary sulfate. The selection between the two inorganic salts therefore depends on whether the premix contains reducing agents and whether the target species is sensitive to sulfate interference.

    Sodium selenite differs from selenomethionine and selenium yeast in metabolic fate and selenium density. Selenomethionine can be incorporated directly into body proteins in place of methionine, creating a tissue selenium reservoir; selenite is metabolized to selenide and is used mainly for selenoenzyme synthesis with less non-specific protein mis-incorporation. Selenium yeast typically contains 2,000–3,000 mg/kg selenium, while sodium selenite contains approximately 450,000 mg/kg selenium. This difference in selenium density means that selenite requires more precise dosing and is more prone to carryover risk, but it also makes the feed-additive intermediate more compact per unit of selenium. For producers seeking egg, milk or meat selenium enrichment, organic sources may deliver higher tissue transfer; for producers seeking a predictable and cost-sensitive selenoenzyme response, selenite remains a standard reference source.

    ParameterSodium seleniteSodium selenateSelenomethionine / selenium yeast
    Chemical classInorganic salt, Se(+4)Inorganic salt, Se(+6)Organic selenoamino acid / selenoprotein
    Selenium mass fraction45.0–45.6%approx. 41.8% theoretical0.2–0.3% in yeast biomass
    Water solubilityFreely solubleFreely solubleVariable; protein-bound
    Premix incompatibilityReducing agents, acid pH, ascorbic acidLess redox-sensitiveHeat and high-shear processing may denature matrix
    Metabolic fateGlutathione reduction to selenideReduction to selenite then selenideMethionine incorporation and selenoenzyme synthesis
    Primary advantage in useHigh selenium density, low cost per unit SeStable in oxidative premix conditionsHigher tissue retention and enrichment potential
    Primary limitationNarrow therapeutic margin; carryover riskSulfate competition; fewer regulatory registrationsHigher cost; variable selenomethionine content

    In aquaculture, sodium selenite is used in extruded and pelleted diets where selenium is required for oxidative stress management in intensively farmed fish and shrimp. The low inclusion rate and high water solubility create a known loss pathway through steam condensate and post-extrusion cooling water. For high-moisture extrusion, the preferred addition point for soluble selenium sources is post-extruder coating or a carrier-bound matrix; otherwise selenium recovery in the finished pellet can decline when preconditioner moisture is high. Published data for specific extrusion configurations is limited, but process evaluations show that water-soluble selenite should not be added directly to long preconditioning barrels without a protective carrier. The physical form and carrier selection therefore determine whether the compound remains available after heat treatment, and they are specified in the product model to match the intended feed-manufacturing route.