|
HS Code |
666348 |
| Product Name | Chinese Tetrandrine Extract |
| Source Plant | Stephania tetrandra |
| Main Active Compound | Tetrandrine |
| Appearance | White to light yellow powder |
| Solubility | Soluble in ethanol and chloroform |
| Purity | Typically ≥ 98% |
| Molecular Formula | C38H42N2O6 |
| Extraction Method | Solvent extraction |
| Part Used | Root |
| Common Use | Traditional Chinese medicine |
| Storage Conditions | Cool, dry place, away from light |
| Cas Number | 518-34-3 |
| Molecular Weight | 622.75 g/mol |
| Country Of Origin | China |
| Standardization | Based on tetrandrine content |
As an accredited Chinese Tetrandrine Extract factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The Chinese Tetrandrine Extract is packaged in a sealed, opaque 500g foil bag with clear labeling and safety instructions. |
| Shipping | Chinese Tetrandrine Extract is securely packaged in airtight, moisture-resistant containers to preserve its quality during transit. The shipment complies with international chemical transport regulations, ensuring safe and prompt delivery. All packages are labeled according to safety standards and shipped via reliable courier with tracking and documentation provided. |
| Storage | Store Chinese Tetrandrine Extract in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerated) unless otherwise specified. Avoid exposure to heat, humidity, and incompatible substances. Clearly label the container and restrict access to trained personnel. Handle in accordance with standard laboratory safety protocols. |
| Purity 98%: Chinese Tetrandrine Extract with purity 98% is used in pharmaceutical formulations, where it ensures consistent bioactivity and safety profile. Molecular Weight 622.7 g/mol: Chinese Tetrandrine Extract with molecular weight 622.7 g/mol is used in antihypertensive drug research, where precise molecular characterization improves dose calculation accuracy. Particle Size 50 μm: Chinese Tetrandrine Extract with particle size 50 μm is used in tablet manufacturing, where uniformity achieves optimal dissolution rate. Stability Temperature 25°C: Chinese Tetrandrine Extract with stability temperature 25°C is used in active ingredient storage, where product integrity is maintained over time. Melting Point 210°C: Chinese Tetrandrine Extract with melting point 210°C is used in controlled release systems, where thermal processing compatibility enables formulation flexibility. Solubility in Ethanol 10 mg/mL: Chinese Tetrandrine Extract with solubility in ethanol 10 mg/mL is used in liquid extract preparations, where enhanced solubility ensures improved absorption. Residual Solvent <0.05%: Chinese Tetrandrine Extract with residual solvent below 0.05% is used in clinical-grade injectable solutions, where low residuals guarantee patient safety. UV Absorbance (λmax 345 nm): Chinese Tetrandrine Extract with UV absorbance λmax 345 nm is used in quality control testing, where it enables precise quantitative analysis. Bulk Density 0.45 g/cm³: Chinese Tetrandrine Extract with bulk density 0.45 g/cm³ is used in capsule filling operations, where consistent flow properties optimize processing efficiency. Moisture Content <2%: Chinese Tetrandrine Extract with moisture content below 2% is used in dry powder inhaler production, where low moisture prevents clumping and ensures dosage accuracy. |
Competitive Chinese Tetrandrine Extract prices that fit your budget—flexible terms and customized quotes for every order.
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Chinese Tetrandrine Extract stands out among botanical raw materials. Working directly in extraction and purification, you see many plant-derived alkaloids and the different results they deliver when processed with purpose. Tetrandrine is an active ingredient sourced from Stephania tetrandra, known in Chinese medicine circles for centuries. Its presence varies in quality, composition, and safety, depending on how it is harvested, processed, and refined. Our factory's close monitoring starts in the soil. We contract-grow Stephania root in proven environments, avoiding areas with heavy metal risk and routinely test our incoming root batches for contaminants and alkaloid stability. Our own facilities manage every step from slicing through to dry extraction and high-precision purification. This hands-on control helps safeguard not just the yield, but also markers often lost through shortcuts or rough handling further down the supply chain.
Direct experience in the production plant adds insight not seen from behind a desk. Our Tetrandrine extract undergoes multiple filtration and crystallization phases. The process itself has evolved over years of problem-solving on the factory floor. Earlier methods produced high losses of active compound, fluctuations batch-to-batch, and stubborn residues. Shifting to solvent gradients, ultra-fine filtration, and slow-temperature crystallization, we achieved a more stable, snow-white crystalline powder, commonly 98% or higher in verified Tetrandrine content, low in insoluble residues, and showing greater shelf stability. We know this by constant in-plant HPLC, TLC, and moisture testing—not just spot checks after export. The ultimate aim is a tightly-controlled crystalline product, far from the brownish, sticky, or impurity-laden lots some may encounter in generic or bulk-processed extracts.
Manufacturing comparison deepens understanding. Over the years, the facility rotated through related roots: Fangji (Stephania japonica), Han Fangji (Aristolochia fangchi), and combined field pilot runs with some Menispermaceae relatives. Most do not yield Tetrandrine as the major alkaloid, or bring along problematic substances such as aristolochic acid, flagged for nephrotoxicity. Consistent Tetrandrine purity, as demanded by pharmaceutical partners, only comes from genuine Stephania tetrandra, cultivated under strict input controls. Inspection labs now routinely use DNA barcoding to screen for adulterants or botanical mislabeling, and our facility includes this in its QC workflow.
Tetrandrine shows a multi-ring alkaloid profile, water-insoluble but ethanol-soluble, with a melting point verifying its identity. The crystalline powder form differs from extracts sold exclusively for traditional, non-pharmaceutical purposes, which might be a sticky, viscous resin, or crude powder with a mix of minor alkaloids and polysaccharides. These physical differences matter, as even slight excess in water content or filler raises caking and clumping risks, undermining dosing reproducibility in end formulations. We aim to control moisture content under 1.0% for pharmaceutical-grade shipments, triple-sieving to de-dust and avoid aggregation.
Plant hygiene and environmental health are not slogans. The powder leaves our crystallization chambers shielded from open air, passing along positive-pressure rooms and vacuum transfer lines to limit any cross-contamination. Staff work in monitored PPE with changes at each stage, because the fine Tetrandrine dust poses hazards if inhaled, a point often glossed over by secondary handlers or those importing in bulk for contract repackaging. Noncompliance here risks residues on exterior packaging and equipment—not just loss of yield, but occupational exposure liabilities. We run quarterly reviews of worker health and airborne particle counts, while updating process flows when NIOSH or Chinese government standards evolve. Customers do not see all these steps, but a manufacturer’s credibility comes from practicing, not promising, accountability.
Tetrandrine attracts interest in drug development and supplement circles, but also faces tough questions from compliance officers and regulators worldwide. Some research investigates its calcium channel blocking potential, immune modulation, or anti-fibrotic signaling, with high purity and structural confirmation as prerequisites. In the current regulatory environment, too many promising research projects stall after realizing their starting material is substandard— contaminated, variable, or blended with non-Tetrandrine plant matter. Strict adherence to GMP, GLP, and, where necessary, ISO 9001 standards, is non-negotiable for any extract feeding into preclinical or investigational pipelines. No informally-processed product clears due diligence anymore; direct-from-manufacturer chain of custody and clear Certificates of Analysis with batch traceability are essential, and our QA office spends a good share of its time preparing tailored documentation packages for every high-spec buyer.
Direct users, including those formulating new chemical entities or herbal preparations, depend on the powder’s complete solubility profiles, consistent flow characteristics, and tight elemental impurity controls. Formulators buying from manufacturers expect technical backup. We provide solvent compatibility studies, particle size distributions, and accelerated aging data; we do not outsource these but run them in-house, blending technical service with production. This helps chemists avoid trial-and-error at their end, or dose variation due to unforeseen interactions with excipients. Bulk handlers for the food and supplement categories test for pesticide residues and aflatoxins; again, our full analytics program answers these needs, unlike secondary traders who might not verify at the granular level.
Modern markets move quickly, but the wrong shortcut in sourcing or processing Tetrandrine can cost a project its viability. Roots picked too early or dried incorrectly show weak or fragmented alkaloid yields. Lack of documentation or origin ambiguity triggers scrutiny at customs, sometimes resulting in holds or destruction. We counter these issues by transparent mapping from seed to final shipment, ceasing procurement from any field if soil tests trend above background for cadmium or lead. Partnering closely with field agronomists, our buyers know not only the GPS origin but the harvest technician for each batch. Photos, soil inputs, and drying logs come standard with our farm-sourced roots, not as afterthoughts. If downstream partners, customers, or even customs inspectors need any verification, we open our books.
Once processed, the warehouse team stores Tetrandrine powder under nitrogen where possible and in triple-laminated foil drums for export. We train logistics staff to watch for temperature excursions or any drum deformation. Every lot is barcoded. Before any shipment leaves our facility, a small sample is kept on-site for two years, allowing for future retesting if any inconsistency arises in a customer’s use. Adaptation comes not just from regulation, but from direct lessons earned through years of tracking lost shipments, reevaluating rejected batches, and sitting across the table from partners who require more than a regulatory minimum.
Quality has a cost. Bulk buyers sometimes request Tetrandrine by chemical formula, seeking a price a few dollars under the last trade—without confirming origin, moisture, or even whether it is truly Tetrandrine and not a close analogue. It often falls to us to explain the value behind a properly-sourced, properly-assayed batch. As a manufacturer, we see the wasted resources when subpar powder fails a customer’s internal tests, or when a material must be reprocessed to purity after arrival, cutting both performance and profit. More than once, we have been called to troubleshoot a failed end product, only to find the root cause traces back to a reseller who cut corners on source or handling. Drawing on decades of scaled production, our staff knows the questions that matter are not just price-per-kilogram—but stability, reproducibility, and transparency all the way through the ingredient’s journey.
The difference with a direct-manufactured Tetrandrine lies in more than lab values. It’s the consistency of every drum, the open window of inquiry into its origin, and the willingness to solve issues after sale—not just make them disappear in paperwork. We frequently reinvest production profits into better in-house training, air filtration, more rigorous on-ground grower audits, and R&D, rather than just external marketing or speculative trade. Those looking for extract to support their own research, pharmaceutical study, or product development—whether domestic or overseas—benefit from these continual process improvements, often reflected in lot-to-lot COAs, impurity profiles, and years-long partnerships.
As the upstream party in this chain, accountability starts inside our doors. Every plant, batch, and extracted lot receives a unique identifier and links to its full analytical record. No batch moves to blending, lot release, or final drying unless it clears heavy metals, microbial, and solvent residue tests—no exceptions. These controls grew from real market lessons: even a single tainted shipment or unverified origin can have ramifications across a whole sector. We do not rely on local brokers or untraceable intermediaries, nor do we purchase on the spot market. Relationships with field growers and in-plant auditors mean our Tetrandrine’s history can be retraced months or years after initial delivery.
Experienced customers often send their own QC teams for routine audits, reviewing our logs, production records, and storage. We invite such checks, knowing that comfort with these processes—and the people behind them—matters as much as the molecule itself. For every incoming order, we keep a channel open, exchanging product data, handling questions, or accommodating regulatory clarifications upon request. Over the years, feedback has led to subtle but important improvements—finer powder sieving, tighter moisture controls, modified container linings, and in some cases, supporting customers with documentation through difficult customs clearances.
Chinese Tetrandrine Extract production saw changes over time, driven by technology, compliance, and market demand. Interest from biopharmaceutical development triggered stricter demands on impurity testing, plant origin certification, and batch-by-batch stability proofs. The market for generic or crude Tetrandrine remains, but many buyers now prioritize material that holds up to independent, Western-licensed lab retesting. In response, we collaborate with outside reference labs to compare our own results, particularly in cases where material enters projects geared at FDA or EMA submission. The fact that about half our volume ships to research users, and the other half feeds into commercial productors and supplement manufacturers, brings keen pressure to avoid even a single failed batch or regulatory red flag.
Trends in downstream innovation bring new demands. There is movement towards Tetrandrine in topical delivery prototypes, nanoparticle suspensions, and as a supportive agent in combination therapies. These new uses depend on very specific powder properties: consistent particle size, low endotoxin presence, and validated absence of cross-reactive alkaloids from non-tetrandra sources. Innovations on our end—better micronization equipment, improved environmental monitoring, and real-time process analytics—help resolve these demands before they become barriers.
Years of manufacturing brought encounters with difficult supply years—unpredictable weather, crop failures, or market price spikes that lure counterfeiters. Some seasons carry stronger pesticide or heavy metal risk from upstream fields, particularly as regulations or agricultural practices shift in different provinces. We keep our own contingency stocks and dual-source root material, only drawing from approved lots that already show clear, passed lab analyses. Past experience of entire consignments failing due to upstream mismanagement prompted us to extend our own field inspection reach. Mistakes made once become non-negotiable checkpoints for future harvests. Partners know we proactively communicate if an issue surfaces, rather than passing surprise or substandard material along.
Every market approaches herbal alkaloid extracts with its own regulations. In the European Union and the US, proof of purity, correct identity, and contaminant profile is not optional. Shipments arriving without clear evidence face either high testing fees, shipment delays, or rejection. We have invested in learning these evolving frameworks, structuring our production to produce not just the molecule, but the chain of documentation behind it. Where customers request special tests—genetic barcoding, site visits, or multi-language documentation—we respond directly rather than relying on third-party certification. All exported Tetrandrine meets the testing standards of its destination before leaving the plant, reducing costly downstream surprises or rejections that would otherwise impact both us and our partners. We assist in guiding customers through the correct channels, based on direct experience moving product in both routine and emerging applications worldwide.
No extract is better than the care taken through its entire journey, from seed to packed drum. Consistency, reliability, and safety do not come about by chance, but through long-term commitment. A manufacturing background influences this approach at every step. Facility teams resolve actual production challenges; they understand the delicate balance between maximizing yield and minimizing impurity. Everyday routines—checking instruments, cross-validating lab data, rotating staff for training—form the backbone of credible product. Most customers want more than a product. They want reliability, traceability, and the ability to discuss any challenge openly, whether regulatory, technical, or commercial. Our doors remain open to discussion, partnership, and continuous process improvement. The quality delivered in every kilogram of Chinese Tetrandrine Extract reflects the real, tested experience of the people behind it.