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HS Code |
232750 |
| Cas Number | 110499-38-8 |
| Molecular Formula | C47H80O18 |
| Molecular Weight | 932.13 g/mol |
| Appearance | White to off-white powder |
| Solubility | Soluble in water, methanol, and ethanol |
| Purity | ≥98% (HPLC) |
| Melting Point | Approximately 210°C (decomposes) |
| Structure | Dammarane-type saponin |
| Storage Conditions | Store at -20°C, protected from light and moisture |
As an accredited Notoginsenoside R1 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Notoginsenoside R1 is packaged in a sealed amber glass vial containing 10 mg, with a clear label indicating product details and storage instructions. |
| Shipping | Notoginsenoside R1 is shipped in tightly sealed, inert containers to prevent contamination and degradation. During transport, it is kept in a cool, dry environment, away from direct sunlight and moisture. All packaging complies with regulations for shipping research chemicals, ensuring safety and product integrity throughout transit. |
| Storage | Notoginsenoside R1 should be stored in a tightly sealed container, protected from light and moisture. It is best kept at -20°C or lower to maintain stability and prevent degradation. Avoid exposure to heat, direct sunlight, and strong oxidizing agents. Store in a dry, well-ventilated area away from incompatible substances. Handle under inert atmosphere if possible for maximum preservation. |
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Purity 98%: Notoginsenoside R1 with 98% purity is used in pharmaceutical formulations, where it ensures consistent bioactivity for cardiovascular support. Molecular Weight 932.09 g/mol: Notoginsenoside R1 of molecular weight 932.09 g/mol is used in cell culture studies, where it facilitates reliable compound dosing and cellular uptake analysis. HPLC Assay ≥98%: Notoginsenoside R1 tested by HPLC assay ≥98% is used in standardized herbal extracts, where it guarantees reproducible therapeutic efficacy. Stability Temperature 25°C: Notoginsenoside R1 stable at 25°C is used in oral supplement manufacturing, where it maintains active ingredient potency during storage. Particle Size <10 μm: Notoginsenoside R1 with particle size less than 10 μm is used in nanoformulation, where it enhances dissolution rate and absorption. Melting Point 198–202°C: Notoginsenoside R1 with a melting point of 198–202°C is used in analytical reference materials, where it allows precise thermal identification. Solubility 2 mg/mL in water: Notoginsenoside R1 with solubility of 2 mg/mL in water is used in injectable preparations, where it provides optimal compound delivery. |
Competitive Notoginsenoside R1 prices that fit your budget—flexible terms and customized quotes for every order.
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In our daily operations, no production line stirs up as much anticipation as the batch runs dedicated to Notoginsenoside R1. Several years ago, isolating pure R1 from Panax notoginseng roots posed a significant challenge. Extended extraction times, frequent contamination, and unpredictable yields kept optimism low throughout the lab. Today, our facility runs hydroalcoholic extractions over a monitored temperature gradient, driving up product purity batch after batch. This hands-on evolution shapes how we approach every shipment that leaves our factory’s doors.
Looking back, the key shift came from direct investment in both infrastructure and know-how. We source Panax notoginseng roots directly from high-altitude farms in Yunnan, where cultivation practices enhance root density and saponin content. Roots enter the plant within days of harvest. After a verified cleaning and drying step, our processing teams launch a dual-phase extraction that leverages both ethanol and water. Traditional single-step soaking, still popular in some facilities, often leaves behind unwanted plant debris and derivatives, but our sequential extraction narrows the chemical profile to prioritize R1 over ginsenoside mixes. We maintain routine checks at each purification stage using HPLC, which helped us bring consistent R1 purity above 98%. Impurities, including saponin analogues, get filtered out—not stockpiled for blend fillers.
Nothing replaces first-hand vigilance. Years of troubleshooting column clogs and solvent residue have taught our chemists where short-cuts fail. Customers who have toured our site recognize that product reliability is never about a fancy lab—the real trust builds in the way our teams spot a misbehaving batch hours into the process and correct it on the spot. R1 extraction, at its core, rewards precision and persistence, not just raw material costs.
In a crowded field of botanical extracts, few compounds offer as much targeted promise as Notoginsenoside R1. Similar ginsenosides—Rb1, Rd, Re—share a common backbone but diverge sharply in how they interact with human biology. Direct feedback from formulation chemists, working either in research labs or downstream pharmaceutical shops, points out R1’s unique balance: strong anti-inflammatory activity without some of the broader hormonal effects seen with other ginsenosides. This niche value often gets overlooked by traders trading in broad-spectrum Panax extracts. We make sure our R1 leaves the factory labeled and verified by COA, so there’s no confusion across batches.
For clinical investigators and nutraceutical manufacturers, access to single-compound R1 means less guesswork in both formulation and regulatory submission. Crude saponin mixes, popular for cost reasons, bring unpredictable batch-to-batch activity. In contrast, our R1’s tightly monitored purity means published research can be repeated and verified regardless of which customer orders the material. Our R&D team often fields requests for custom isolation runs, where a customer wants to tweak the residual saponin profile for a specific trial. Most projects ask for nearly pure R1, which we produce by extending chromatography runs and adjusting solvent gradients.
Our production lines generate R1 in the form of a white to pale yellow powder, with a dense, fine texture that feels almost like corn starch between the fingers. The powder collects in shielded bins fastened with moisture barriers—direct humidity exposure triggers clumping and minor hydrolysis, a reality that pantry-level quality control simply cannot manage. We’ve learned over time that warehouse staff, not just technical team members, must watch for the faint signs of moisture seepage; any packaging breach means a full discard, not a repurpose into lower-grade blends.
Once packaged, Notoginsenoside R1 needs to stay at room temperature and away from direct UV. Our control system tracks not only storage intervals but also transport time from dock to delivery address. We’ve seen more than a few competitors try thermal stabilizers or inert gas overlays, but in practice, clear labeling and transparent communication with shipping partners outperform most high-tech fixes. As one of our logistics coordinators remarked, a properly sealed bucket survives the summer heat in Guangzhou—but only because the crew understood both the handling protocol and the stakes behind a failed batch report.
Technical-grade R1 flows mainly into research pilot runs and pharmaceutical R&D pipelines. Feedback from these end-users shaped our own quality assurance routines. For instance, customers testing R1 in injectable formulations consistently need low-endotoxin levels. Our process design now includes an additional ultrafiltration pass designed on the advice of these same partners. Nutraceutical manufacturers, especially those mixing R1 into tablets or softgels, focus more on powder flow and surface consistency. Requests for particle size adjustment often push us to rerun a micronization step, trading yield for smoother blending properties.
One significant benefit of working directly with formulators instead of third-party brokers comes through technical troubleshooting. Over the years, we’ve helped research teams resolve solubility differences by supplying tailored solubility data for specific excipient choices. Not every saponin interacts equally with solvents, and those subtle differences create real bottlenecks at the formulation bench. In many cases, a quick call between our process chemist and the customer’s lab saves weeks of trial-and-error attempts. That “open door” troubleshooting impacts both research timelines and manufacturing budgets on a daily basis.
The marketplace swarms with Panax derived saponin products, often bundled as broad-spectrum or total ginsenosides. Our direct experience with both crude and purified grades leaves us convinced: for serious R&D and premium nutritional products, single-compound R1 offers clear, documentable value that broad-spectrum extracts cannot match. Crude extracts typically hover between 30 to 60% saponins by weight, with R1 comprising less than 5% of the total. Efforts to standardize these blends often falter—natural root variability and inconsistent separation both cloud test results and, ultimately, user outcomes.
On the other hand, our customers who require robust, publishable research data rely on the isolated R1’s higher purity because it behaves predictably across different test runs. For those building consumer products, this means label claims hold up under regulatory cross-check and consumer testing alike. Trouble usually starts in projects using bulk saponin blends when unexpected inflammatory or hormonal effects crop up, tied directly to the variable content of non-R1 ginsenosides. We keep our product literature blunt and data-driven: specify the need for single-compound material where project risk demands it, or use blend extracts if budget takes priority over precision. The decision should match project needs, not supplier marketing slogans.
Our commitment to producing R1 begins on the ground in the fields. Decades of root cultivation have shown that not all notoginseng roots deliver comparable saponin yields. We select partners practicing extended crop rotation and organic soil amendments, rejecting those using synthetic chemical boosters or cutting root maturation short for volume. Our agronomists routinely assess the drying and age of inbound roots—a young, under-developed plant won’t reach the density or saponin spectrum needed.
Through regular site visits and batch testing, we help our farmers understand both root quality and expected returns. These investments upstream pay off at every step downstream, reducing both waste at the extraction stage and customer complaints after shipment. Over time, the direct relationship between our plant managers and local growers has resulted in both higher R1 yield per ton and an ongoing incentive for sustainable land management. Sustainability talk in the supply sector often sounds like a checklist, but to us, it’s part of actual batch value. High-grade R1 production never comes from shortchanging the root’s lifecycle.
The early years in our plant involved almost weekly meetings about contaminant carryover and chromatography drift. R1 extraction depends on balancing aggressive solvent stripping with precise filtering. Too fast, and you lose valuable material; too slow, and you leach out unwanted analogues. Practical lessons—such as adjusting column resin pH based on seasonal variation in root quality—rarely appear in published manuals. Our team captures these nuances through daily log sheets and post-batch review sessions.
Repeated challenges refining R1 from similar ginsenosides like Rb1 and Rd pushed our team to design a closed-loop solvent recovery system. Not only does this keep solvent footprint lower, but it also lets us track minute shifts in extract composition. Our chemists now adjust the final polishing step according to the measured R1 yield mid-process, not just on the output end. These adjustments make the difference between world-class purity figures and routine batches; our customers notice the difference both in laboratory results and in their ongoing purchase decisions.
Auditors visiting our site often focus on the full chain of custody from root input to finished R1 shipment. Regulatory standards for dietary supplements and raw pharmaceutical materials require batch purity and contaminant tracking data. Our compliance staff sees regular third-party testing as a badge of honor rather than a bureaucratic hurdle. This external feedback pushes us to maintain unbroken documentation chains and to act quickly if a batch falls outside spec.
Each R1 lot ships only with a transparent Certificate of Analysis. We never blend lower-grade powder into premium runs to stretch inventory; this honesty has turned what began as a rare, specialist product into a well-recognized industry name. Regulatory shifts, including those affecting trace heavy metals or pesticide residues, often hit us with new testing expenses or demand small process tweaks. Embracing those changes rather than “working around” them protects both our customer relationships and the real-world safety of end consumers.
Researchers working on cardiovascular and neuroprotective applications turn to our R1 for its documented anti-inflammatory properties. Direct communication with lab groups revealed demand for both gram-scale and industrial orders. Academic groups in particular need small R1 lots with stringent purity data, while commercial product makers order in bulk, aiming for reproducibility and scale. In both cases, we accept R1 returns if post-entry inspections spot issues—a net loss to us, but the best way to foster genuine trust.
Pharmaceutical-grade R1 finds use in novel delivery vehicles, including nanoparticle suspensions and advanced softgel formulations. Our facility maintains process flexibility to accommodate the unique requests of each customer, collaborating on custom-run specifications rather than forcing a one-size-fits-all approach. Ingredients as specialized as Notoginsenoside R1 rarely slot into standard recipes; successful projects start with thorough, honest dialogue between our production specialists and the end formulation team.
Raw material costs for R1 tie closely to harvest cycles and weather events in southern China. Late rains or disease outbreaks hit root supply unpredictably. Our procurement team knows each upturn or shortfall in the fields directly impacts both pricing and planned volume. We hedge our own risks by staggered contracting with partner farms, warehousing extra roots when seasonal quality aligns. This hands-on strategy beats speculative buying or inflexible, long-term big vendor contracts that sometimes leave stock short when real customer orders spike.
Short-term buyers often chase the lowest headline price, cutting corners on product verification. We’ve seen well-meaning companies burn through R1 spends only to discover off-spec material adrift in their inventory. Our pricing aims for balance: not bargain-basement, but stable and justified by batch quality and source transparency. Repeat business, not flashy underbidding, sustains both product quality and plant operations in the long run.
Manufacturing Notoginsenoside R1 at scale invites more than just technical diligence; it demands personal accountability. Several of our team members grew up in the notoginseng regions and return for the harvest each year. Their hands-on experience grounds our technical expertise in the daily realities of agricultural work, batch tracking, and shipment quality.
Partnerships with researchers and formulation experts reach beyond transactional relationships. We chase feedback on every batch, eager for both praise and critique. If a production misstep occurs—a valve malfunction, a bad chromatography run—it’s our reputation, not an abstract company name, that is at stake. By responding factually and promptly, we strengthen both industry trust and the actual value our R1 delivers to every application.
As downstream applications of Notoginsenoside R1 broaden, from clinical trials to new consumer supplements, we treat every batch as both an opportunity and a challenge. Pursuing pure, reliable R1 started as a technical hurdle and evolved into a daily practice. We continue to invest in both technology upgrades and soft skills—training plant staff, engaging with end-users, and working with growers on sustainable yield improvements.
True expertise shows up in outcomes: customer research that leads to new products, regulatory approvals supported by our documentation, and a supply chain that stands up to both scrutiny and market stress. Notoginsenoside R1, in our experience, is more than a line on a catalog—it’s a measure of our manufacturing discipline, responsiveness, and commitment to genuine partnership at every stage of use.