|
HS Code |
561510 |
| CAS_number | 61281-37-6 |
| Molecular_formula | C23H28O6 |
| Molecular_weight | 400.47 g/mol |
| Appearance | White to off-white crystalline powder |
| Purity | ≥98% (HPLC) |
| Melting_point | 129-131°C |
| Solubility | Slightly soluble in water, soluble in ethanol and DMSO |
| Storage_temperature | -20°C |
| Synonyms | Schisandrol B, Gomisin N |
| IUPAC_name | 3,4,5,14,15,16-Hexamethoxy-6,7-dimethyl-4H-dibenzo[a,c]cycloocten-1(2H)-one |
| Source | Schisandra chinensis (plant) |
As an accredited Schisandrin B factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Schisandrin B, 100 mg, is packaged in a sealed amber glass vial with tamper-evident cap and clear labeling for identification. |
| Shipping | Schisandrin B is shipped in secure, airtight containers to maintain stability and prevent contamination. It is packaged in compliance with safety regulations for chemicals, including proper labeling. Shipments are typically sent via specialized carriers, with temperature control and tracking available for sensitive research-use-only materials. Delivery times depend on destination and local regulations. |
| Storage | Schisandrin B should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep it tightly sealed in its original container, preferably under an inert atmosphere like nitrogen or argon. Store at 2-8°C (refrigerator) for optimal stability. Avoid exposure to strong acids, bases, and oxidizing agents. Handle with appropriate safety precautions. |
| Purity 98%: Schisandrin B with purity 98% is used in pharmaceutical formulations, where it ensures consistent bioactivity and enhanced therapeutic efficacy.Molecular weight 432.5 Da: Schisandrin B at a molecular weight of 432.5 Da is used in metabolic research studies, where it facilitates accurate compound quantification and metabolic pathway analysis.Melting point 189°C: Schisandrin B with a melting point of 189°C is used in solid dosage preparations, where it provides superior thermal stability during manufacturing.Particle size <10 µm: Schisandrin B with particle size below 10 µm is used in oral tablet production, where it offers improved dissolution rates and higher bioavailability.Stability temperature up to 80°C: Schisandrin B stable up to 80°C is used in controlled-release formulations, where it maintains structural integrity during processing and storage.HPLC grade: Schisandrin B of HPLC grade is used in analytical laboratory analysis, where it delivers precise and reproducible chromatographic results.Solubility in ethanol >50 mg/mL: Schisandrin B with solubility in ethanol over 50 mg/mL is used in injectable solution development, where it allows high-concentration formulations and efficient drug delivery.Optical rotation +17°: Schisandrin B with optical rotation of +17° is used in stereochemical research, where it facilitates chiral purity assessments and enantiomeric separation studies.Moisture content <1%: Schisandrin B with moisture content less than 1% is used in dry powder inhalation systems, where it enhances product shelf-life and minimizes degradation. |
Competitive Schisandrin B prices that fit your budget—flexible terms and customized quotes for every order.
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Our production of Schisandrin B hinges on over a decade of hands-on experience with natural product extraction. Each year, new buyers ask what sets our raw material apart from what drifts into the market through resellers. The answer always comes back to extraction method and control over raw herb sourcing. We select ripe, ethically grown Schisandra chinensis berries—never over-processed, never from unknown plantations. That guarantees traceability and lets us avoid pesticide residue issues, which too often compromise quality from batch suppliers using mass commodity inputs.
Our Schisandrin B emerges from our facility in crystalline powder form, with content above 98% as confirmed by HPLC. Production relies on a solvent system that preserves the integrity of the lignan structure. We understand that harsh solvents or excessive heat can damage this sensitive molecule—so our protocol uses only food-grade ethanol and a precise temperature curve. This kind of care in extraction earns us repeat orders from research groups and high-end supplement brands looking for reliability in every delivery.
From the start, we noticed inconsistent results in trials using off-the-shelf extracts from wholesalers. Customers explained they’d experienced this too—batch-to-batch variation in less controlled products led to unpredictable purity and occasional off-notes in finished applications. Using in-house wet chemistry and third-party HPLC, we tightly track every outflow. Our Schisandrin B batches hold a narrow specification window. Sharp, clean appearance and a neutral taste make our material straightforward for both tablet and capsule formulations.
On the supplement line, Schisandrin B draws research interest because it supports liver function, cellular protection, and stress adaptation, as described in peer-reviewed studies. In these applications, precision matters. Even a small jump in content value or trace solvent out of range threatens both compliance and bioactivity. By locking down inputs and process, we protect our customers from failures during incoming inspection or final product QC.
Several times, end users have shown us chromatograms from poorly regulated extracts. Peaks for residues, extra lignans, or unknown contaminants caused headaches on their QC bench. Some traders dilute authenticated Schisandrin B with low-grade Schisandrin A or other related lignans, chasing a cheaper price point. Our direct manufacturing eliminates this issue. We publish lab results with every lot, including full HPLC and GC-MS profiles. This transparency earns trust—no mystery peaks, no ambiguous “total lignans.” Our process generates one main peak, tight and clean, signaling authenticity and consistency.
Occasionally, newcomers push for “ultra-high purity”—over 99.5%. What they often find is that excessive purification steps damage yield and drive up cost without measurable benefits. In our view, a reliable 98% purity hits the right balance between extraction efficiency and practical application needs. Our customers get this level with every batch, without seasonal variations.
We make only industrial and research-grade Schisandrin B, not “blended Schisandra extract”—a critical distinction. Blended extracts sound appealing but seldom contain a consistent dose of pure Schisandrin B. Pure material gives formulators control over dosing, labeling, and repeat activity in clinical or consumer settings. That’s why supplement brands sourcing from our plant report fewer returns due to color, taste, or labeling inconsistencies. Product managers avoid costly reformulation later.
We pack each batch in double-layer high-barrier bags to keep oxygen and moisture at bay. Schisandrin B’s structure resists breakdown under normal temperature, but even so, high humidity environments can lead to clumping or slow oxidation. Our team ships directly from controlled storage. Before any outbound shipment, in-house product managers test for stability—every time.
Raw material intermediaries lean on cost efficiency, blending lower-purity fractions from different suppliers to meet volume. We take a slower path—contract farming, traceable harvest dates, and in-situ drying right at the field. Year after year, this keeps pesticide risk low and batch variation in check. Shorter supply chains let us audit at every step, and catch issues before they reach the main extractor line.
Some industries think a powder’s just a powder—until trials fail or regulatory agencies request documentation. Major research groups often visit our plant for audit—walking through herb validation stations, extraction tanks, and post-processing air filtration. They see firsthand the absence of foreign matter, and the consistent batch outcomes from start to finish. This accountability gives them assurance in both published research and commercial production.
Experienced buyers know that “Schisandra extracts” and true “Schisandrin B” differ sharply in cost and quality. Generic extracts, even if tested for “total lignans,” often combine Schisandrin A, B, and C without disclosing content breakdown. Market-testing shows supplement users experience more predictable results with clear, high-content products. Many commercial blends hover below 5% actual Schisandrin B content—ours never falls below 98%. That purity allows companies to dose accurately for capsule or tablet manufacturing lines.
On a practical level, pure Schisandrin B dissolves steadily and offers better bioavailability profiles. Unrefined extracts generate more sediment, inconsistent color, and often interfere with capsule filling due to sticky byproducts. High-purity Schisandrin B avoids these headaches, as it resists agglomeration and handles smoothly on automated equipment.
Beyond supplements, several research labs use our Schisandrin B for animal trials, liver enzyme assays, and cellular studies. Every customer receives the full QC report, plus a digital certificate of analysis—detailing not just purity but also loss-on-drying and identification spectra. Researchers save time—no need to requalify or “clean up” unknown extracts on-site.
In the last three years, global ingredient supply chains have faced sudden disruption—border rules, crop failures, and pandemic slowdowns. Many suppliers dropped grades or switched to cheaper raw herbs. We invested in stable farming contracts and storage upgrades instead. That decision paid off in customer retention. Essential for pharmaceutical and nutraceutical brands, ingredient reliability influences every link in their quality chain. Our engineering team and plant managers meet weekly to review supply status and adjust production schedules well before the market feels the pinch.
Traceability marks another gap between direct manufacturers and multi-level intermediaries. When regulatory agencies ask about our batches, details run all the way to field harvest, drying protocol, and extraction date. We log every pallet, photo-documenting the herb’s journey from field to drum. Auditors like that kind of record-keeping—not just for compliance, but for the assurance that every order matches specification.
Feedback drives much of our workflow improvement. Several supplement companies report smoother tableting and encapsulation since switching to our high-purity material. Our powder’s tight particle size range allows even flow and dosing accuracy—a big jump from variable blends that clog machines or create dose scatter. We mill and sieve batches on request to suit customer manufacturing needs, always scanning for foreign matter before release.
Veteran product managers judge a supplier by response time and documentation, not only price. They stay loyal to our process for two reasons—QC is always ready (with immediate COA download), and shipments leave on time, every time. By avoiding shortcuts and blend dilution, we protect brand reputation downstream. Customers say they sleep better knowing what’s in their capsule, and that’s a fact we’re proud of.
Working directly with pharmacology groups, we answer requests for customized specifications. While some suppliers send generic lots, we listen to target requirements for purity, solvent limits, and batch size. In research, re-order consistency trumps price—nobody wants to restart a clinical study over raw material drift. For several university-led projects, our team executed on zero-tolerance residue specs, confirmed with independent third-party certificates. Experience shows this extra layer prevents delays, regulatory trouble, and compliance headaches.
Collaboration also sparks innovation. Customers sometimes request scale-up from pilot to kilo lots for pre-clinical work. Our QA and engineering teams review each step, ensuring process holds stable even as volumes increase. Open lines with buyers and researchers give us firsthand insight into shifting needs and future product development areas.
In the lab, every processing change starts with small-scale tests. Our analysts monitor yield, solvent recovery, temperature hold times, and impurity drift across each production trial. Over the years, we’ve refined our SOPs to limit loss, capture maximum actives, and keep energy costs in check. By focusing on continual optimization, we’ve managed to hold pricing more stable—even through turbulent global energy cycles. Reliable vendors and well-trained staff make all the difference. We invest heavily in annual retraining, sending QA and lab managers for third-party workshops and compliance certification.
Customer feedback steers process upgrades as well. Several clients in the past five years pushed for non-GMO status and tighter solvent limits. We responded by converting all upstream fields to GMO-free status and capping ethanol residues far below EU limits. Independent labs confirm levels ahead of each delivery. By acting on direct feedback, we build trust and adapt smoothly to new regulatory demands.
Not every production run goes smoothly. Equipment malfunctions or unexpected yield drops occasionally surface. Because we keep extraction on-site, problems get flagged at source. We call buyers immediately if a batch looks off spec, and document every change in process. This open communication helps prevent costly surprises downstream. Relying on resellers, on the other hand, means slow response and traceability gaps. Direct dialogue builds relationships—customers know who to contact and trust us to resolve any issue quickly.
Raw material volatility remains an ongoing reality in herb-based ingredient markets. Lower-yield growing seasons or increased demand for Schisandra berries can pressure raw input costs. To manage this, we lock in forward purchase agreements and store buffer stock. A steady supply means downstream brands avoid market shocks and production shutdowns during peak demand. These behind-the-scenes choices insulate buyers from disruption—a critical factor for those tied to long-term contracts.
Buyers face a maze of options—extracts “standardized to lignans,” variable powder lots, and cheaper inputs from shifting origins. Our own experience shows that chasing the lowest-cost source may guarantee disappointment in sensitive application areas. Research users, supplement formulators, and pharmaceutical buyers repeatedly return to quality and documentation as their top selection drivers.
Independent purity analysis stands as the final judge. Chromatograms from all batches, paired with GC-MS, validate our output well above 98%. By investing in robust internal QC and external verification, we sidestep the reputation risk tied to every commodity trader or short-cut blend in the field. Consistency wins contracts; erratic supply does not.
Beyond technical quality, ethical sourcing holds real weight. Our field teams train local growers to avoid prohibited pesticides and meet environmental standards. Sourcing from audited fields, we set harvest calendars for optimal berry content—no forced early pick, and no exploitation of hillside land that risks soil leaching. Grower partnerships benefit both the land and our long-range supply curve. That benefits our team, our environment, and every brand built on our raw material.
Waste minimization matters too. We re-purpose extracted marc as compost, returning nutrients to contracted farms. Sludge management, solvent recovery, and rigorous water recycling form part of our environmental stewardship program. This cycle closes the loop, limiting environmental impact and setting a baseline for industry accountability.
Staff experience counts. Our process managers average 12 years in botanical extractions and track every kilo from receipt to outgoing batch. Plant operators spot color or texture variance and intervene before QC needs to step in. By retaining trained staff and rewarding attention to detail, we maintain lower error rates per batch—delivering steady product quality year after year.
Upstream, our long partnerships with growers secure honest product—the right species, mature fruit, handled with care. Downstream, staying small enough for direct control but big enough for global reach, we offer tailored shipment sizes and direct technical support. These real-world, boots-on-the-ground differences turn technical claims into measurable quality improvements that every batch delivers.
Schisandrin B extraction and purification demands attention, accountability, and proven experience. Our business stays focused on technical quality, process transparency, and hands-on supply chain control. Production starts at the field, moves through well-audited extraction and lab testing, and finishes with reliable delivery. Customers return because the product matches claim, the documentation backs every lot, and process improvements come directly from years of feedback and learning. As a manufacturer, we know trust grows batch by batch, built on results, not words.