|
HS Code |
154169 |
| Cas Number | 482-38-2 |
| Molecular Formula | C27H30O14 |
| Molecular Weight | 578.52 g/mol |
| Iupac Name | 5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4′-di-O-β-D-glucopyranosylflavone |
| Synonyms | Kaempferol 3,7-dirhamnoside |
| Appearance | Yellow crystalline powder |
| Solubility | Sparingly soluble in water, soluble in methanol and DMSO |
| Melting Point | 232-235°C |
| Purity | ≥98% (HPLC) |
| Source | Primarily isolated from Bauhinia species |
| Storage Temperature | 2-8°C, protect from light |
| Bioactivity | Antioxidant, anti-inflammatory, antidiabetic |
As an accredited Kaempferitrin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Kaempferitrin is packaged in a 100 mg amber glass vial with a secure screw cap and tamper-evident seal, labeled clearly. |
| Shipping | Kaempferitrin is shipped in tightly sealed, light-resistant containers to ensure stability and prevent contamination. It is typically transported as a solid powder and labeled according to chemical safety regulations. The package includes appropriate hazard notices, and shipping conditions such as temperature control are maintained as required to preserve product integrity. |
| Storage | Kaempferitrin should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry place. Ideally, storage temperature should be at 2–8 °C (refrigerator) for long-term stability. Avoid exposure to heat, air, and strong oxidizing agents. Ensure proper labeling and keep out of reach of unauthorized personnel. |
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Over the years, our team has handled a broad range of plant-derived flavonoids. Among these natural compounds, Kaempferitrin stands out as an important specialty ingredient. Known for its unique structure—a glycosylated flavonol—Kaempferitrin has roots in the natural world, appearing prominently in plants like Kaempferia galanga and Justicia spicigera. The fine, yellow crystalline nature of pure Kaempferitrin, coupled with its reliable solubility profile, sets the groundwork for consistent application in both research and industry.
We keep our production streamlined through careful sourcing and meticulous isolation. Our product’s purity exceeds 98 percent by HPLC, which reflects our commitment to provide crystalline Kaempferitrin for sensitive research purposes and formulation work. Over the years, feedback from customers in pharmaceutical research, analytical laboratories, and product development teams has guided us to keep moisture content minimal, often under 2 percent, because even a slight rise can threaten downstream usability. Ash content gets controlled below 0.5 percent to avoid non-organic contamination.
The batch-to-batch appearance matches a pale yellow powder, sometimes tending toward off-white depending on seasonal plant harvest variations. Having worked with botanical extracts in many forms, we can confirm this color profile as a good sign: minimal browning marks clean isolation, while a bright yellow tint signals effective glycoside retention. Our team regularly checks particle size distribution via standardized methods, ensuring powders disperse easily in solvents like ethanol and DMSO. This fine powder form means researchers spend less time prepping samples, an advantage for high-throughput settings.
From the start, we saw increased demand from labs working on metabolic modulation, ethnopharmacology, and cellular antioxidant mechanisms. It did not take long to understand the draw: Kaempferitrin’s glycoside linkage distinguishes it from kaempferol alone, changing the molecule’s physical properties and its absorption in biological systems. In daily work, our clients often run side-by-side assays with kaempferol glycosides and aglycone forms. Reports sent back to us confirm an improvement in stability—dissolved glycosylated forms weather shifts in light and temperature without decomposing as quickly as aglycone standards.
Years of weekly manufacturing cycles reinforce this insight. The glycosyl group in Kaempferitrin reduces harsh solvent decomposition, which allows for broader storage and transportation tolerances. Our facility has shipped this compound across multiple continents, and repeated analytical testing post-arrival continues to show robust integrity. This stability translates into lower losses during transit and easier handling in the lab, something that pure kaempferol lacks unless strictly refrigerated.
Most requests we handle come from customers developing dietary supplements, topical formulations, and laboratory reference standards. Its history in folk medicine, especially in extracts from Bauhinia forficata, motivated several academic investigators to explore mechanisms related to blood glucose regulation and oxidative stress. Our work over the years with contract research organizations has seen Kaempferitrin included in high-throughput screening projects targeting kinases and inflammatory mediators. The compound’s consistent HPLC chromatogram and stability under moderate stress conditions make it an anchor standard for these studies.
For product developers, Kaempferitrin’s solubility and mild sweetness, which stem from the sugar group attached to its structure, permit easy suspension in aqueous and oily carriers without the solubility struggles of intensely hydrophobic flavonols. Our technical conversations with food and beverage formulators show that this feature cuts down both development time and waste, as extraction can skip extra emulsifiers. It also means that end products containing this compound as an active or marker component often gain a natural antioxidant claim, which appeals to a growing base of label-conscious consumers.
From a manufacturing perspective, keeping Kaempferitrin’s quality consistent starts at the botanical raw material. Over several seasons, our team sourced Bauhinia forficata leaves from carefully vetted cultivators, knowing from experience that stress during harvesting—such as drought or over-fertilization—affects glycoside yield. Our plant biologists work closely with growers to monitor phenolic profiles before extraction begins. Inconsistent raw material spells trouble for downstream purification, and repeated testing for both identity and content confirms starting material strength before it arrives at our facility.
Once extraction begins, we avoid harsh organic solvents. We rely on food-grade, low-impact solvents under controlled pH, balancing effective extraction with environmental and operator safety. Years back, we faced several batches with low glycoside content due to improper solvent selection by suppliers attempting to save time or cost. Since taking this process in-house, we’ve maintained extract purity that stands up to rigorous HPLC and MS fingerprinting. Specialty resin columns, used for fractionation in our plant, are periodically replaced to prevent cross-contamination—a crucial control point, because even trace phenolic residues from previous lots distort both purity and biological results.
Clients often compare Kaempferitrin directly with similar flavonol glycosides or aglycones. Early on, our technical service team prepared dozens of side-by-side tests against compounds like quercitrin, quercetin, and pure kaempferol. The two main differences that stand out are water solubility and photostability. The sugar moiety on Kaempferitrin serves as a natural stabilizer, which is immediately obvious on HPLC runs kept at ambient temperatures. Kaempferol, without the glycoside, tends to degrade unless protected from light and heat, and often clumps during sample prep in solvents.
Another prevailing difference comes from biological assays. Our discussions with academic collaborators repeatedly highlight altered cellular uptake and enzymatic activities between glycoside and aglycone forms. In practical terms, assays targeting inflammation or oxidative markers generate more reliable, repeatable results with Kaempferitrin due to its steady degradation profile and its reduced risk of interfering matrix signals. Laboratories involved in reference standard preparation prefer Kaempferitrin’s ease of quantification in multi-component mixtures—a direct result of its isolation purity and minimal natural contaminants that crop up from non-glycosylated extracts.
Commercially, Kaempferitrin is often compared with rutin or hesperidin. Our experience in large-scale purification demonstrates that Kaempferitrin requires a slightly higher extraction temperature, but this cost is offset by increased batch yields and less need for clean-up. Many in the industry chase lower-cost aglycones, but repeated customer returns and complaints about stability or unpleasant sensory profiles (such as bitterness) reinforce our decision to produce a high-purity glycoside.
Decades in chemical extraction and refinement embedded a habit of close process monitoring. Kaempferitrin’s bright color, smooth flow properties, and mild scent all contribute to ease of handling, but challenges do arise. We routinely troubleshoot scaling issues—where extract concentration in pilot vessels can drop if local pH or solvent ratios swing during longer extraction periods. Small pH deviations trigger excessive co-extraction of unrelated plant polyphenols, which reduces efficiency and quality. This led us to invest in automatic pH controllers and upgraded in-process sensors, which sharply reduce batch-to-batch deviations and secure consistent Kaempferitrin content.
Another recurring challenge is analytical purity. Our team spent years verifying and fine-tuning a robust HPLC protocol—including column type and gradient selection—to tease apart closely related glycoside impurities. Problems often come from relying on external standards not certified for trace contaminants. By now, we routinely run both in-house and third-party validation with each lot, rejecting any batch that shows atypical minor peaks, no matter how small. This discipline means customers rarely face surprises during validation or downstream product launches, and our technical service line frequently walks new clients through their first external QC runs, sharing years of experience gained from troubleshooting reference standard issues ourselves.
Moisture control remains another point of continual improvement. Early batches sometimes absorbed too much ambient humidity due to insufficient packaging, eventually causing clumping and reduced shelf life. Today, we use low-permeability triple-layered packaging, with desiccant pouches included in each unit. Storage instructions reflect lessons learned: even though Kaempferitrin can handle moderate temperature swings, tight sealing and keeping the product away from light prevent long-term degradation. Feedback loops with regular customers, especially those storing bulk product, led us to refine our packaging and logistics.
Every year brings its own raw material and regulatory surprises in the natural compounds sector. Our team makes transparency a practical habit, not an empty promise. For example, all Kaempferitrin lots include a detailed Certificate of Analysis with batch-specific purity, solvent residue, and heavy metal reports. While meeting published pharmacopeial standards is a baseline, we exceed these targets whenever field testing or new informatics suggest a potential concern. On rare occasions when we have seen divergence from specifications, we have always reached out directly to clients—sharing test results, causes, and remedial actions. This commitment to traceability and open reporting has translated into longstanding, trust-based relationships.
From early extraction in small glass columns to today’s kilogram-scale runs, we have watched scientific expectations for flavonoid standards evolve. High-performance liquid chromatography, mass spectrometry, and NMR characterization have become the backbone of our QC protocols. These tools identify and quantify trace impurities and confirm structure with high confidence. Our experience convinces us that detailed lot-by-lot profiles help customers avoid costly surprises during formulation, regulatory review, or clinical trial planning. More than once, we have supported clients reworking formulations when a competitor’s batch failed identity or purity tests, helping rebuild project timelines.
New applications and market focus often shape our manufacturing plans for Kaempferitrin. The ingredient’s role in anti-inflammatory nutritional supplements or advanced cosmetic actives appears to be growing. Cosmetic developers working on antioxidant facial serums or skin-lightening formulations have approached us with increasing frequency, looking for clean, high-purity flavonoid glycosides that perform predictably in cream and gel systems. In these discussions, our technical support points to the real-world stability data and cross-study reproducibility feedback we gather from both low- and high-volume customers.
Research teams investigating metabolic and cellular aging employ Kaempferitrin for mechanistic studies, leveraging its clean HPLC fingerprint and oxidative stress modulation properties. Our facility often receives requests for reference standards to support published clinical and preclinical work, particularly in metabolic health, cardiovascular effects, and antioxidant paradigms. Based on feedback and publication trends, we continue to expand QC capabilities for both known and emerging analytical methods, investing in upgraded instrumentation and data integrity controls. Our open collaboration with academia and industry partners gives us front-line insight into developing purity specifications or assay needs that will drive the next wave of innovative products based on Kaempferitrin.
Direct conversations with product developers, researchers, quality control staff, and regulatory consultants shape our understanding of what customers need. Our operations staff, chemists, and customer support teams work in tandem to ensure that each Kaempferitrin batch reflects both scientific rigor and practical experience. This means correcting process parameters, fine-tuning extraction temperatures, and upgrading packaging as feedback dictates—not just following a static specification but adapting to what real users require for smooth workflow and downstream results.
As a manufacturer, accountability does not stop after a shipment leaves our loading dock. Over years of technical follow-up and casework, we have traced problematic analytical results to issues that ranged from minor shipping missteps to adjustment of storage protocols on the client end. Rather than disclaiming responsibility, our approach has always been to investigate fully and provide actionable suggestions, returned goods support, and if needed, replacement batches. This grounded approach to customer partnership helps build a foundation of mutual trust and technical fluency that supports both sides.
Plant-derived compounds like Kaempferitrin continue to generate scientific interest across the globe. New publications, demand for natural antioxidants, and shifting consumer expectations point to continued growth for bioactive flavonoid products. Our history in chemical manufacturing reinforces the need for robust, transparent processes capable of scaling up without compromising quality or environmental stewardship. We see plant-source variation, analytical rigor, precise process control, and rapid adaptation to client feedback as core principles for sustained Kaempferitrin production and innovation.
Looking ahead, the research and products built with this compound will reflect not only the underlying science but the reliability of those who produce and stand behind it. Drawing on decades of first-hand experience, we remain committed to Kaempferitrin’s quality, practical application, and honest engagement with clients addressing scientific, medical, and consumer health challenges.