|
HS Code |
594323 |
| name | Ampelopsin |
| other_names | Dihydromyricetin |
| chemical_formula | C15H12O8 |
| molecular_weight | 320.25 g/mol |
| appearance | White to light yellow crystalline powder |
| solubility | Slightly soluble in water, soluble in ethanol and methanol |
| melting_point | 256-258°C |
| source | Extracted from plants such as Ampelopsis grossedentata |
| CAS_number | 27200-12-0 |
| purity | Typically ≥ 98% (HPLC) |
| storage_conditions | Store in cool, dry place away from light |
| application | Used in research for antioxidant and hepatoprotective properties |
As an accredited Ampelopsin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ampelopsin is packaged in a 25g amber glass bottle with a secure screw cap, labeled with safety information and chemical details. |
| Shipping | Ampelopsin is shipped in tightly sealed containers to prevent contamination and degradation. It is typically packaged according to standard chemical safety protocols, accompanied by a material safety data sheet (MSDS). During transit, Ampelopsin is protected from moisture, light, and temperature extremes to ensure product integrity and compliance with regulatory guidelines. |
| Storage | Ampelopsin should be stored in a cool, dry, and well-ventilated area, away from sources of heat and direct sunlight. It must be kept in a tightly sealed container to protect it from moisture and air, preferably at 2–8°C (refrigerator temperature). Ampelopsin should be stored away from incompatible substances, and handled according to appropriate laboratory safety protocols. |
| Purity 98%: Ampelopsin with 98% purity is used in pharmaceutical synthesis, where it ensures high bioactivity and consistent therapeutic outcomes. Molecular Weight 320.25 g/mol: Ampelopsin at molecular weight 320.25 g/mol is used in analytical standard preparations, where it provides accurate quantification in HPLC analysis. Melting Point 256°C: Ampelopsin with a melting point of 256°C is used in solid dosage formulations, where it improves thermal stability during processing. Particle Size <10 µm: Ampelopsin with particle size below 10 µm is used in tablet manufacturing, where it enhances dissolution rate and bioavailability. Stability Temperature up to 80°C: Ampelopsin with stability up to 80°C is used in food supplement production, where it maintains structural integrity during heat exposure. Solubility in Ethanol 50 mg/mL: Ampelopsin with ethanol solubility of 50 mg/mL is used in liquid extract formulations, where it ensures efficient extraction and homogeneous blending. Residual Solvent <0.1%: Ampelopsin with residual solvent below 0.1% is used in injectable formulations, where it meets regulatory safety standards for parenteral use. UV Absorbance (λmax 290 nm): Ampelopsin with UV absorbance at 290 nm is used in spectrophotometric assays, where it allows sensitive detection and quantification. Assay (HPLC) ≥99%: Ampelopsin with assay value greater than or equal to 99% by HPLC is used in clinical research, where it guarantees precise dosing in experimental protocols. Water Content <1%: Ampelopsin with water content below 1% is used in lyophilized preparations, where it prevents microbial growth and enhances shelf life. |
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Ampelopsin, known by many in the plant extract world under the name dihydromyricetin, has seen its reputation rise quickly, but the path from raw source to refined product takes more than following textbook guidelines. For our team, years of batch production, monitoring reaction vessels, and working closely with source growers have proved Ampelopsin deserves its place in the landscape of botanical compounds. We handle it from root to refined powder, and that firsthand experience shapes the way we view its value in formulations and ingredient systems.
The material we produce starts with genuine Ampelopsis grossedentata, grown not in manicured glasshouses but in carefully managed fields in regions with a history of responsible wild harvesting. We have learned that leaf maturity and harvesting season change the phenolic profile, and this matters for every downstream process aimed at purifying dihydromyricetin. From extraction tanks to spray-drying lines, every step is tailored for this molecule—our core product sticks to a purity grade above 98% by HPLC, and we validate these results with outside labs regularly for full transparency. The white to pale yellow powder form does not happen by accident; precise temperature and pH management during isolation and drying stops degradation, locks in natural profile variability, and delivers material that meets our release criteria for each lot.
Chemically, Ampelopsin is a flavanonol, with a molecular model showing three rings and multiple hydroxyl groups that make it both water and ethanol soluble for common formulations. These same groups drive its use in many project applications; they invite hydrogen bonding and improve dispersion in supplements, beverage bases, and more advanced delivery systems. Solubility can look trivial on paper, but only direct process experience reveals how things go in the tank. On our production floor, we dose, hydrate, and run pilot recipes to optimize everything from initial mixing to spray concentration.
Ampelopsin stands apart not just for its chemistry, but for its resilience in challenging applications. In most manufacturing lines, products might claim to “feature” plant ingredients, but only a few ingredients endure all the pH swings, heat treatments, and long storage periods common in modern formulations. We have run Ampelopsin across a spread of pH environments with beverage developers and found it keeps its clarity, color, and organoleptic neutrality in both hot and cold drinks. Its clean taste and lack of persistent aftertaste put it in a unique place among polyphenol extracts—especially compared to other flavonoids that bring bitterness and haze.
Nutraceutical firms often seek Ampelopsin when designing liver support or anti-oxidant supplement labels. Over the last decade, its broad safety profile and published research have helped it gain traction, but stability in high-volume tableting, multi-step granulation, and liquid encapsulation really make the difference for our partners. We offer guidance drawn from years of direct processing—dosing protocol, order of addition, and interactions with other extracts like silymarin or resveratrol all play a role in finished batch quality. Ampelopsin also shows reliable physical flow: after years working with various powders, we recognize those with poor reconstitution, high clumping, or dusting risk, and address these issues batch by batch in our lot QA.
From the ground up, Ampelopsin’s real competition is rarely a single molecule; rather, it’s a long list of plant-based actives trying to offer broad oxidative or anti-inflammatory action. Green tea extracts like EGCG, grape seed proanthocyanidins, quercetin, and resveratrol each draw attention for slightly different strengths. Over years of co-formulation and competitive analysis, we have seen a few predictable differences when comparing Ampelopsin to these. For example, EGCG often leads to problematic astringency and instability above neutral pH, while proanthocyanidins can cause clouding and taste masking even in modest doses. Quercetin suffers poor water solubility and settles out in beverages and suspensions, cutting real-world utility.
Ampelopsin, by contrast, tolerates a wider process window. In direct bench and pilot trials, we repeatedly find it stable across a range of carrier matrices—whether in bulk supplement powder, stick packs, or ready-to-drink bottles. It integrates well in blends where other polyphenols struggle with haze and sediment. On the regulatory side, lengthy toxicology studies and growing scientifically-referenced awareness have improved risk profiles, helping to smooth the path for end-product launches, especially in new markets where certain natural antioxidants still face skepticism.
For functional food developers, Ampelopsin’s natural palatability simplifies sweetener and flavor masking strategies. As manufacturers, we get real feedback from production lines—not just lab reviewers—on whether a plant extract can run in a continuous process without off-flavors, downtime, or cleaning headaches. This hands-on difference brings consistent cost and quality savings, and it is one reason we see repeat business from beverage and food manufacturing clients. There’s no shortcut to this level of insight; only full-cycle production experience reveals which extracts truly outperform on the line.
Every manufacturing partner—large or small—wants reassurance that each lot of Ampelopsin delivers not just the number on the specification sheet, but the same reliable performance batch to batch. Variability in natural source inputs often throws up challenges; we don’t accept this as a fixed reality. Over years of process tweaks, validation runs, and upstream improvements, we have tightened our spec window so that finished Ampelopsin holds tight purity, color, and moisture targets. Transparency matters for us—without clear and accurate COAs, customer trust erodes. That’s why we maintain traceable batch records and keep up with third-party independent lab evaluation schedules, offering open access to results rather than just in-house claims.
During scale-up trials or introductions to new facilities, we work side-by-side with technical teams to spot possible pinch points in dust control, bulk handling, and solubility challenges early on. By sharing direct process experience and “war stories” from our own plant, improvements often surface before they turn into costly downstream issues. Ampelopsin stands up to most standard application scenarios: direct compression, granule production, reconstitution in hot or cold liquid, and extended hold times in process tanks.
Many of our biggest lessons stem from past near-misses. Ampelopsin has a low threshold for moisture pickup—exposing it to high ambient humidity during open handling leads to caking. Our solution involves upgraded decanting hoppers, rigorous environment controls, and a team ingrained with habits learned the hard way. It is these day-to-day details—not just laboratory reports—that shape whether a plant extract works in the field.
Running a synthesis or purification step on a flowchart looks easy. In actual manufacturing, temperature, humidity, upstream raw material variability, and human factors introduce a chaos that only experience can handle. Over multiple production campaigns, we found that Ampelopsin’s process robustness stands above many polyphenol peers—but only if each critical control point gets proper attention.
For extractions, temperature swings drive changes in yield and profile. Holding too hot for too long strips color and can darken the end product. We keep extraction times within proven limits, maintain gentle but effective agitation, and run mid-process TLC screening on samples from the tank. If anything veers from baseline, we adjust process in real time. This hands-on approach reflects our view that experience trumps clever instrumentation when it comes to consistency.
Purification presents its own challenges; even minor pH drift can force unwanted glycolysis or phenol oxidation. Over the years, we standardized buffer additions and started using in-line pH probes with failsafes, sidestepping the tedious guesswork and countless “trial and error” rounds typical in smaller operations. Drying and final micronization, though often overlooked, set the standard for downstream usability. For Ampelopsin, particle size affects density and flow, so we dial in milling rates and screen distributions to minimize batch-to-batch swings.
Sustainable sourcing is not a buzzword dropped for marketing—it’s tied to long-term risk in supply chain and quality. With Ampelopsin, demand can push wild populations to the edge and create a flood of adulterated supply, especially when harvesters rush to market. Over years, we have built out direct purchase networks, auditing growing operations for traceability, responsible land use, and absence of harmful chemicals. Regular field checks, not just paper audits, bring us close to the plant’s source, and these visits turn up both issues and ideas for efficiency improvements hard to see from an office.
Long-term grower partnerships keep our raw materials pipeline both predictable and rooted in transparent practice. We take samples of every new lot on intake, run spectrometry and identity checks, and track biosource markers. Whenever yield fluctuations turn up, we invest extra effort correcting with new dried mass ratios, not by swapping source or compromising on purity targets.
Encouraging best practices from our growers—mulching, organic pest control, and rotational field use—reduces shock to the environment and the risk of trace contaminants in final product. Our experience proves that a stable supply of high-quality Ampelopsin comes only from building trust at every handoff in the supply chain. Consistency begins with strong roots, both literally and figuratively.
With the rise in global interest in botanical compounds, adulteration remains a constant background noise—often undetectable to the uninitiated. We have found cases where bulk material labeled as “Ampelopsin” actually had added maltodextrin, crystalline sugars, or, worse, cheaper polyphenols passed off as pure. Rigorous incoming inspection shields our clients and our reputation. Our team runs fingerprint chromatographic analysis, checks for typical marker ratios, and looks for telltale impurities.
Over the years, we have flagged and rejected numerous shipments—rejecting subpar material costs us in the short term but preserves long-term business. Blends or “FDA-registered” third-party sources, in our experience, offer little comfort unless you can trace both the sample and the documentation to a living, ongoing relationship of trust. Whenever discrepancies arise, we prefer to suspend batch release instead of risking cascading problems for our partners who rely on our authenticity.
We provide verified batch reports to every customer, linking back to original harvest, extraction date, purity testing, and contaminant screening. This paper trail stands up to regulatory scrutiny and gives teams confidence as they pursue both existing and novel end-use claims for our Ampelopsin. As manufacturers, our value lies in this diligence—not shortcuts or half-answers.
Ampelopsin’s handling quirks have taught us more than any supplier guide or academic paper. The powder holds up well when kept in cool, dry storage with active oxygen scavengers. Operators in open-air facilities noticed clumping on damp days; we responded by tightening access time, rerouting airflow, and integrating sealed weigh rooms. Bulk totes benefit from double bags and short-run unpacking.
In supplementation applications, choosing the right carrier makes a tangible difference. Mixing with microcrystalline cellulose and low-activity blend partners minimizes dust while preserving quick dissolution. Direct granulation for effervescent use needed tweaks: Ampelopsin turned out to outperform most other flavonoids here because of its clean flavor, and it resists noticeable precipitation if pH and ionic strength of the base blend are managed carefully.
Heat and pH exposure provide little drama. Ampelopsin emerges from short pasteurization cycles or even higher-heat beverage runs with profile intact—a trait much appreciated by developers stuck dealing with other fragile plant actives. In capsule and tablet applications, we prefer direct compression using a blend of dietary fiber, avoiding coatings that can risk interaction with the polyphenol backbone.
Those working in finished product lines appreciate a powder that isn’t fussy or slow in blending silos; Ampelopsin moves quickly with limited downtime on typical gear. R&D teams value the freedom to change inclusion rates without other process headaches. These operational wins are not minor—they stem from years of hands-on troubleshooting, listening to feedback, and changing plant habits to align with what actually happens in a live manufacturing setting.
With consumer preferences evolving and regulators tightening expectations on process controls and traceability, Ampelopsin sits right at the crossroads of opportunity and responsibility. We don’t treat its increasing demand as a reason to pump up volume without caution. Every production campaign gets a postmortem: what worked, what didn’t, and where minor drifts or deviations could hint at broader supply chain or process risk.
Innovation, from our perspective, involves more than seeking process shortcuts or marketing claims; it means finding upgrades that make a real difference for bulk buyers or downstream users. On the technical side, we invest in both automation and skilled operator training, closing the knowledge gap that often opens between “lab-made” and “plant-ready” material. On the supply end, constant engagement with field teams and growers keeps us ahead of quality drift, and this close connection is what keeps Ampelopsin a trusted component for our partners.
All told, Ampelopsin occupies a clear place on the plant-derived ingredient map thanks to a production approach grounded in day-to-day reality. We stake our reputation on every bag that leaves our facilities—not just by quoting lab stats, but by owning every challenge, quirk, and win along the way. Ampelopsin has made our team better manufacturers, pushing us to learn both from process data and the stories each new batch brings.