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HS Code |
862810 |
| Name | Vitamin A |
| Type | Fat-soluble vitamin |
| Chemical Form | Retinol |
| Molecular Formula | C20H30O |
| Primary Sources | Liver, dairy products, fish, and orange-colored vegetables |
| Daily Requirement Adult Men | 900 mcg |
| Daily Requirement Adult Women | 700 mcg |
| Major Functions | Vision, immune function, reproduction, and cellular communication |
| Deficiency Risks | Night blindness, increased infection risk |
| Overdose Symptoms | Liver damage, headache, blurred vision, bone pain |
| Storage Site | Liver |
| Stability | Stable in dry, cool conditions but degrades with light or air exposure |
As an accredited Vitamin A factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of Vitamin A powder, sealed with a screw cap, labeled with safety and usage information. |
| Shipping | Vitamin A should be shipped in tightly sealed containers, protected from light and moisture. Store at controlled room temperature. Label packages clearly with “Keep Away from Light” and “Dry Place.” Follow all applicable regulations regarding chemical handling, including safe packaging and transit documentation to ensure stable and secure delivery. |
| Storage | Vitamin A should be stored in a tightly closed container, away from light, heat, and moisture to prevent degradation. It should be kept at room temperature, typically between 15°C and 25°C (59°F–77°F), in a dry and well-ventilated area. Avoid exposure to oxidizing agents and acids, and ensure the storage area is secure and labeled to avoid accidental misuse. |
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Purity 99%: Vitamin A Purity 99% is used in pharmaceutical tablet manufacturing, where it ensures consistent bioavailability and potency in finished products. Molecular weight 286.45 g/mol: Vitamin A molecular weight 286.45 g/mol is used in injectable formulations, where it allows precise dosing and predictable pharmacokinetics. Stability temperature 25°C: Vitamin A stability temperature 25°C is used in cosmetic creams, where it maintains efficacy throughout shelf life under standard storage conditions. Oil-soluble grade: Vitamin A oil-soluble grade is used in fortified edible oils, where it enables homogeneous dispersion and nutritional fortification efficacy. Micronized particle size 10 µm: Vitamin A micronized particle size 10 µm is used in soft gel capsules, where it enhances absorption and uniformity. Retinol content 95%: Vitamin A retinol content 95% is used in dermatological serums, where it provides targeted skin rejuvenation with high activity. Encapsulated form: Vitamin A encapsulated form is used in animal feed premixes, where it improves stability against oxidation and enhances shelf life. USP grade: Vitamin A USP grade is used in pediatric syrup formulations, where it ensures compliance with pharmacopoeial quality standards for safety and purity. Melting point 62°C: Vitamin A melting point 62°C is used in nutritional supplement granulation, where it supports controlled processing without degradation. Light protection packaging: Vitamin A light protection packaging is used in over-the-counter multivitamin products, where it prevents photo-oxidation and preserves potency. |
Competitive Vitamin A prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
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Tel: +8615371019725
Email: admin@sinochem-nanjing.com
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For over thirty years in chemical manufacturing, we've witnessed firsthand how small changes in production can ripple through the industries that rely on us. Vitamin A ranks among those rare products where purity, stability, and consistency matter—not just for formulating supplements, but for keeping people healthy worldwide. Every batch reaches hospitals, food fortification programs, livestock feed operations, and households. We feel responsible not only for supplying a compound but also for ensuring it meets the real demands of end-users, whether in tablet presses, premix facilities, or injection lines.
Our Vitamin A comes in several models, but the most widely demanded is the stabilized retinyl acetate and retinyl palmitate. These forms have earned their place through stability, solubility, and established safety in food and pharmaceutical applications. No-one wants a vitamin powder that breaks down in sunlight, so our models use antioxidant systems—typically a blend of tocopherols and ascorbyl palmitate—to guard against oxidation. This is not a laboratory luxury; oxidation leads to potency loss, and wherever clinics and food processors are located, especially in places where temperature control isn’t perfect, resilience matters more than ideal conditions.
We typically supply Vitamin A in both oil and beadlet form. Oil forms (concentrated up to 1.7 million IU per gram) fit well into softgel capsules, liquid blends, and pharmaceutical suspensions; customers need smooth, filterable solutions, so particle size and viscosity get constant attention. Our experience shows that controlling free fatty acid content improves oil stability, and we tailor antioxidant levels specifically for each customer’s shelf-life and environmental requirements.
Beadlets, often ranging from 500,000 to 1 million IU per gram, are chosen when ease of handling and blendability count—nutrition bars, dry premixes, and feed pellets require free-flowing particles. We design our beadlets to resist dusting and caking, especially in humid environments, which isn’t just a convenience for production technicians: it reduces product loss and improves dosing precision throughout the supply chain.
Trust in our Vitamin A products depends on full traceability—including documentation of every raw material batch, blending step, and analytical readout. Our GMP-certified facility doesn’t cut corners. We trace problems, wherever they arise, to their root cause, whether a slight variation in raw ester content or a change in shipment packaging. We keep detailed records readily available for customers who want to confirm origin or ask questions about our supply chain. From the solvent recovery process to the final packaging, we enforce rigorous controls, validated by regular third-party audits and in-house quality teams who’ve worked decades with us.
Vitamin A isn’t a product that leaves much room for error—overdosing can cause toxicity, underdosing wastes resources and misses nutritional targets. We use HPLC to ensure every lot consistently matches label claims and monitor isomer ratios, minimizing unwanted byproducts. Experience taught us long ago not to rely solely on theoretical process yields. We analyze and release each batch only when we see documented compliance with strict reference standards.
Choosing a Vitamin A product is rarely about searching for the highest IU claim. Each process has its own quirks. For example, our beadlets differ in their dispersants and coatings, based on whether they go into a water-based infant nutrition formula, a baked product, or animal feed. In direct compression tablets, flow and compressibility matter. Feed applications require stability against high humidity and heat during pelleting. Some customers need non-GMO or allergen-free options, so we design our systems accordingly, even sourcing different excipients or tweaking powder profiles for specific needs.
We’ve supplied fortification programs in countries with no cold chain and high humidity, where other products failed to maintain activity. Adjusting the balance of carriers, binders, and antioxidants to local processing realities became one of our core skills. In high-fat matrices like margarine, oil-based models blend seamlessly. Where dry mixing is needed, beadlets avoid clumping and dust.
Comparing our Vitamin A to market alternatives, we see big differences in uniformity, handling, and stability under stress. Some producers focus on synthetic purity but overlook storage realities in warehouses or field clinics. Uncoated powders or those without robust antioxidant protection break down fast. Our blend of hands-on factory experience and ongoing dialogue with customers lets us catch issues early, adjust formulations, and speed up troubleshooting. We also listen closely to feedback from end-users who notice changes in performance, even when the paperwork looks perfect.
Global vitamin markets don’t operate in a vacuum. Harvest failures and logistics bottlenecks affect not just the price of Vitamin A, but its availability. Years ago, we learned to diversify raw material sources and keep safety stocks ready to buffer against unforeseen events, like droughts affecting plant oil feedstocks or shipping container shortages. We never treat Vitamin A as a purely commodity process—too many lives depend on reliable dosing—so we maintain near-real-time inventory updates and backup logistics partners, fully aware that a missed shipment may disrupt both small clinics and major food producers.
Covid and geopolitical conflicts added new layers of complexity, turning packaging supplies and raw chemical transport into serious bottlenecks. Our crisis teams stay in daily contact with global suppliers and freight partners. Drawing from long-term relationships in the supply chain, we adapted faster, reduced lead times, and put extra checks on any alternate source materials. Customers benefit from faster time-to-resolution, and our transparency means clients can pivot if plans or regulations change.
Vitamin A connects directly to regulatory oversight—food-grade and pharmaceutical customers both operate under strict rules on content, purity, contaminants, non-nutritive additives, and label claims. Decades of audit experience taught us to work one step ahead of new requirements, keeping thorough master files up to date and training new staff in evolving standards, whether for USP, FCC, CFR 172.375, EU regulations, or other international protocols. Allergen statements, kosher/halal certification, residual solvent profiles, and packaging contamination prevention feature in every batch record, and we proactively communicate with regulatory authorities for approvals and renewals.
We’ve seen what happens when rushed production or documentation shortcuts threaten compliance—stocks get held at customs, deliveries for fortification programs stall, and entire product lines may be recalled. By building batch-level document control and integrated lab analyses into our in-house ERP system, we avoid the drama of last-minute compliance checks or missing paperwork. There are no substitutes for this kind of transparency, and customers can audit us at any time.
While some view Vitamin A as an established, mature molecule, the pace of customer feedback and regulatory change pushes us to keep improving. Our R&D and process engineering teams study how particle morphology, microencapsulation, and excipient selection impact everything from tablet hardness to shelf-life in tropical ports. Over the past decade, advances in carrier technology—starches, gums, and phospholipids—let us offer non-GMO, vegan, and allergen-reduced beadlets without giving up protection against oxidation.
We invest heavily in pilot batches and real-world application testing, running parallel stability studies under various temperature and humidity conditions. It’s one thing for a product to pass a six-month shelf-life claim in ideal lab settings; replicating that performance in a rural warehouse is another matter. Our long-standing partnerships with local food companies and fortification NGOs give us the feedback loops needed to identify where formulation changes make a difference.
During one recent round of customer site visits, new concerns emerged around microplastics in coating excipients. We responded quickly by trialing natural and bio-based alternatives, now a standard in certain beadlet models. R&D is no longer just about making what’s required—it’s about anticipating what end-users, regulators, and advocacy groups care about next.
Clinicians depend on accurate Vitamin A content for treating deficiency in children and at-risk adults. For some applications, stability in suspension makes all the difference; in others, controlled release is critical—for example, in animal feeds, where Vitamin A must release in the right section of the digestive tract. We’ve helped scale programs that improved public health outcomes—reducing rates of blindness, boosting immunity, and supporting healthy growth among children—by delivering exactly the forms needed by local food manufacturers and supplement companies.
Pharmaceutical clients require stringent impurity and residual solvent control. We keep our trace internal process contaminants well below required limits and communicate test results straight from our chromatograph files. Each lot ships with a full certificate of analysis, including detailed impurity profiles.
Food supplement producers often prioritize rapid blending and stability in flavored matrices. Experience showed us that high oil-based retinyl esters need special attention to flavor-masking and interaction with other functional ingredients. In vivid, complex health food blends, we’ve worked side by side with formulators to fine-tune Vitamin A additions so that activity persists through shelf-life and exposure conditions—constant improvements, informed by both lab stability curves and real-world taste tests.
Feed and veterinary sectors push us to innovate around shelf-life, tolerance for pelletizing temperatures, and even color. Our beadlets are custom-formulated so they deliver on farms as intended. We track how product moves through the system, from arrival in bulk tanks to blending into final rations, so animals receive the intended dose. Any deviation—caking, clumping, or segregation—can cut effectiveness, so field feedback keeps our production and R&D grounded in solving real problems.
We believe customer trust starts with open communication. We don’t hide problems: we address them directly, explain root causes, and offer solutions, even if it means extra cost or schedule changes for us. Traceability includes not just compliance documents but also sharing details about our antioxidant systems or excipient sources, tailored to needs across nutrition, food, and pharma sectors.
Any time a client reports an unexpected issue—a change in color, a drop in potency, or ship container packaging trouble—our technical staff respond directly, drawing on both the batch record and personal knowledge of our people who ran the lines that day. By putting experienced technicians on calls, most issues resolve before they escalate, and process changes don’t get buried in bureaucracy.
Feedback from staff on the filling lines or powder blenders sometimes matters as much as any lab value. We draw on this internal expertise to adjust blends, improve flow properties for bulk powders, and calibrate antioxidant levels to real transportation schedules and packaging needs. Many of our updates originate from hands-on experience, not management mandates.
Customers increasingly ask about our environmental footprint—from the palm or soy oil origin in our retinyl palmitate to energy use in our reactors. We’ve invested in green chemistry solutions, using supercritical CO2 extraction, recycling side streams, and minimizing solvent usage. Our carriers and antioxidants are sourced with responsible practices in mind, and we track waste generation closely.
During the transition to palm oil with internationally recognized sustainability certification, we self-audited every step, from plantation sourcing to shipment. We work with NGOs and certification bodies, opening our doors to show exactly how our raw materials reach the factory floor. These efforts have helped reduce overall impact and meet the rising expectations of customers—both large-scale multinationals and smaller, purpose-driven companies.
Managing energy demand is as much about cost savings as environmental responsibility. Reactor heat recovery, optimized drying cycles, and continuous process monitoring keep us agile, cutting down energy consumption per unit. These efforts have reduced emissions and let us keep costs competitive, while providing long-term environmental security that increasingly factors into partnership decisions.
Vitamin A manufacturing requires more than technical expertise. It demands close listening to evolving customer, regulatory, and environmental expectations. Over three decades, our production methods, product models, and quality systems have shifted, bringing new tools, better analytics, and a deeper field focus to every operation. By staying true to fundamentals—attention to detail, transparency, hands-on problem-solving—we’ve become a trusted source for Vitamin A across industries.
Each new challenge, from raw material volatility to packaging innovations, opens the door to further product improvements. Field results, customer stories, and ongoing bench research guide us toward better products for tomorrow’s health and nutrition needs. The result: Vitamin A supply that adapts, performs, and delivers—consistently, batch after batch, wherever it’s needed most.