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HS Code |
827388 |
| Cas Number | 518-43-0 |
| Molecular Formula | C15H12O4 |
| Molecular Weight | 256.25 g/mol |
| Iupac Name | 7,4′-Dihydroxyflavanone |
| Synonyms | Liquiritin aglycone, Glycyrmetin |
| Appearance | White to yellowish powder |
| Solubility | Slightly soluble in water, soluble in ethanol and DMSO |
| Melting Point | 197-198 °C |
| Purity | ≥98% (HPLC) |
| Source | Isolated from Glycyrrhiza uralensis (Licorice root) |
| Chemical Class | Flavanone |
| Uv Absorption λmax | 289 nm |
| Storage Conditions | Store at 2-8°C, protect from light |
| Smiles | C1=CC(=CC=C1C2C(CO2)C3=CC=C(C=C3)O)O |
As an accredited Liquiritigenin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Liquiritigenin, 100 mg, supplied in a clear, labeled glass vial with screw cap, packaged in a protective, sealed box. |
| Shipping | Liquiritigenin is shipped in secure, chemically resistant containers to prevent contamination and degradation. It is typically transported at room temperature, but may require cool or dry conditions based on safety guidelines. All shipments comply with relevant chemical transport regulations, including appropriate labeling and documentation to ensure safe and legal delivery. |
| Storage | Liquiritigenin should be stored in a cool, dry place, protected from light and moisture. Keep the container tightly closed, ideally at 2–8°C (refrigerator) for short-term storage, or at −20°C for long-term preservation. Use a desiccator if available. Proper storage ensures chemical stability and prevents degradation of liquiritigenin. Avoid repeated freeze-thaw cycles to maintain sample integrity. |
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Purity 98%: Liquiritigenin with purity 98% is used in pharmaceutical formulations, where it enhances anti-inflammatory efficacy in clinical applications. Molecular weight 256.25 g/mol: Liquiritigenin with molecular weight 256.25 g/mol is used in analytical research, where it ensures precise quantification in HPLC assays. Particle size <10 µm: Liquiritigenin with particle size <10 µm is used in tablet manufacturing, where it promotes uniform dispersion in solid dosage forms. Melting point 196°C: Liquiritigenin with a melting point of 196°C is used in thermally processed nutraceuticals, where it maintains compound stability during production. Solubility in ethanol 25 mg/mL: Liquiritigenin with solubility in ethanol 25 mg/mL is used in botanical extracts, where it improves extraction yield and compound bioavailability. Stability temperature up to 60°C: Liquiritigenin stable up to 60°C is used in cosmetic formulations, where it preserves antioxidant activity during storage. HPLC purity ≥99%: Liquiritigenin with HPLC purity ≥99% is used in reference standards for quality control, where it delivers reliable calibration and validation results. Residual solvent <0.5%: Liquiritigenin with residual solvent <0.5% is used in injectable drug development, where it minimizes toxicity risks in parenteral solutions. |
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Spending years in chemical manufacturing, our team has come across our share of rare natural flavonoids, but liquiritigenin stands out. This compound carries a clean, pale-yellow crystalline form, with each batch produced at a minimum purity of 98% as verified by HPLC. We learned early that keeping tight control over extraction and crystallization conditions helps us avoid the inconsistency often found in commercially sourced botanical ingredients. Such a strict approach has pushed us to fine-tune our process batch by batch, resulting in a reproducible quality that research and industrial partners have come to rely on.
The lot-to-lot difference in color, moisture, or residual solvents used to trouble early adopters. We tackled these issues head-on, updating our filtration systems, testing for residual solvents well beneath pharmacopeia limits, and running consistent Karl Fischer titration to make sure each sample matches our published moisture content of under 1%. Our liquiritigenin comes as a fine powder to ensure good mixing and optimal dissolution, no matter the end use. The product’s molecular formula, C15H12O4, and structure remain true, isolated from Glycyrrhiza species roots, not synthesized from less regulated sources.
Part of what makes liquiritigenin appealing is how readily it integrates into traditional and modern product formulations. Our direct line to pharmaceutical and nutraceutical partners has kept us grounded in what users actually want: batch integrity, clear documentation, and full analytical transparency. Our supply mostly serves R&D labs, oral supplement blenders, and some innovative food and beverage developers who want specific polyphenolic actions without the baggage of contaminants or unpredictable sourcing.
In pharmaceuticals, liquiritigenin’s known bioactivities stem from published data: estrogenic modulation, antioxidant capability, and mild anti-inflammatory effects. Our role is to guarantee a well-characterized, contaminant-free source so research delivers solid data rather than chasing around impurity artifacts. Scientists appreciate that each container ships with a COA indicating heavy metal screening (arsenic, lead, cadmium, mercury), and a full impurity profile. We pack evidence into our documentation, supporting claims with third-party audits and in-house HPLC-UV-MS runs. For supplements, the powder disperses in solution with only light stirring due to careful micronization – details matter for processing.
A few customers ask about topical applications—cosmeceutical brands in particular. Our liquiritigenin meets microbial limits appropriate for dermal formulations, and with low odor and high clarity it doesn’t muddle the end product. As production scale increases, stability in shipping and storage has come up. We use double-layered containers and confirm no decline in purity over twelve months at room temperature in a humidity-controlled warehouse. Partners aiming for extended shelf lives see the difference in powder flowability and minimal yellowing compared to other suppliers.
Some manufacturers settle for similar compounds hoping for the same activity. Isoliquiritigenin is one such compound often misrepresented by traders and resellers, but it exhibits a sharply different profile. From a chemical engineering perspective, the difference between a flavanone and a chalcone holds real consequences for biological activity and solubility in finished formulations. Our facility has invested in both thin-layer chromatography and advanced mass spec to confirm absence of these adulterants, after repeated reports of customers receiving ambiguous mixtures from other sources. We guarantee less than 0.5% isoliquiritigenin by HPLC, greatly lowering ambiguity in dosing and pharmacological results.
Digitonin, liquiritin, and a handful of other licorice-derived polyphenols often appear on product labels. Older extraction techniques failed to separate them completely, muddying the literature and making it difficult to draw clear links between ingredient and effect. By taking slow, careful steps during partitioning and crystallization, our team managed to strip the matrix down to pure liquiritigenin, without the support of cheap solvents or unreliable column resins. The resulting powder dissolves faster in aqueous base and shows low residue even after repeated redissolution, which is not something you’ll find with loosely regulated products from unknown fields.
Feedback from partners points out greater consistency in color and performance when switching from supplier blends to our pure version. This helps laboratories and commercial formulating teams avoid guesswork or recalibration in the middle of a production batch. We keep a long-term log of stability and impurity data—drawn from real-time and accelerated storage studies—so we’re ready when someone needs hard evidence to meet regulatory or academic scrutiny.
We source licorice root from agricultural cooperatives that can demonstrate traceability back to the field, supported by soil and heavy metal reports. Pesticide residues are another concern; we demand documentation for every batch of raw material before it ever reaches our doors. Early in our experience, partners flagged inconsistent performance in third-party lots due to environmental contaminants. In response, we introduced comprehensive LC-MS residue scans in our intake QC process.
Rather than relying on bulk solvent systems, our extraction line uses sequential, carefully temperature-controlled extractions, monitored for active compound yield in real time. This ensures that seasonal changes in root chemistry due to rainfall or stress do not creep into the final product. It also avoids the generic, grayish powder that flooded the market before controlled extraction caught on.
Equipment calibration, operator training, and regular process audits translate to real-world benefits: powder color that stays bright, and a powder texture that flows from container to beaker without caking or clumping. For a manufacturer creating finished products in the next stage, avoiding these headaches reduces reprocessing and waste, and feedback confirms these details cut costs on the ground.
Safety standards and international compliance come up often in conversation with our clients. Regional regulations differ – some want to see detailed documentation about solvent residuals, others are stricter about product origin and heavy metal content. Our team spends significant energy keeping technical files updated for all major regions where our customers operate, building in the flexibility so we don’t ship a product that will cause downstream compliance problems. More than a few of our partners switched to our line after failed audits on imports from traders with little real process control. We’ve learned that a straight line from root to finished powder, with documentation at every stage, avoids technical and legal headaches. Our transparency builds trust with customers and regulators alike.
A handful of issues crop up most often in feedback from industry – source verification, purity assurance, traceability, and reliable physical properties. We address these with a robust internal tracking system. Every kilogram of liquiritigenin gets a unique batch ID tied back to both the lot of licorice root and the full manufacturing record. We track environmental data at every step, so each jar can be traced to the region and even month of harvest for the original crop. Lab results are tied to this chain, ensuring that if an issue arises, investigations don’t need to start from scratch.
Purity has been both a regulatory and a practical hurdle. While many suppliers claim high purity, inconsistencies in measurement technique or careless blending can mislead buyers. Our laboratory employs both HPLC-UV and HRMS methods. Each release to the market is supported by a full spectrum assignment and impurity profile, not just summary numbers. On request, our team provides full analytical results, including spectral overlays and retention time charts for those who want to cross-verify with their own equipment. Our transparency here strengthens confidence and helps buyers avoid costly, time-consuming double checking.
Manufacturing scale brings its own challenges. As demand for clean-label supplements, natural actives, and functional ingredients increases, production needs to respond without losing detail. Our team has built redundancy into key process steps: triple-checking extraction efficiency, calibrating each crystallization run, and segmenting batches to isolate any irregularities. Process automation software tracks pressures, temperatures, and times to within a narrow error interval, which allows us to maintain consistency even as throughput ramps up during peak order cycles.
Buyers looking to integrate liquiritigenin into their own bottling or encapsulation lines want to avoid filler or processing aids unless absolutely necessary. Our powder has a tight particle-size distribution that avoids the dust or clumping issues seen in competitor products, rooted in a slow, well-controlled drying phase. This simple but critical step cuts down on flow agents or unnecessary excipients, which aligns with market movement towards minimal-ingredient formulas.
Collaboration sits at the core of building reliable supply chains. On more than one occasion, partners approached us after frustration with unexplained delays or undisclosed ingredient switches from brokers. Responding with real process data and transparent documentation, our team gets involved before problems grow out of control. For example, when customers in Europe raised questions about possible allergen contamination, we opened up our handling protocols and provided full records of cleaning and cross-contamination risk management. When a brewery partner wanted to guarantee TSE and BSE-free sourcing, we mapped the full agricultural supply chain for them, adding an extra layer of confidence for their product claims.
Environmental and social impact cannot be ignored, even for technical ingredients. Increasingly, customers in food and beverage and large-scale supplement brands expect details about cultivation practices. By engaging directly with contracted farms, we can ensure not only supply stability but also that cultivation minimizes soil erosion and improper chemical use.
Audits are welcome on-site for partners needing direct verification. We keep a culture of openness – nothing replaces the insight of seeing real equipment in motion, warehouses managed by long-serving operators, and QC laboratories running full panels. Years of direct experience have taught us that third-party certifications have more value when supported by visible, tangible process discipline.
Both the science and the market for liquiritigenin keep moving. New research into bioavailability, alternate delivery forms, and health outcomes drives us to keep refining our process. Customers developing next-generation health or cosmetic products want consistent, unimpeachable quality, not vague promises or “proprietary blends” that hide the true source or purity. By investing in process analytics, technical staff training, and active participation in scientific conferences, our manufacturing adapts as new requirements or opportunities emerge.
Emerging toxicological data encourages us to chase the lowest possible levels of residual contaminants, dictated not just by existing legislation but by the likely direction of future regulations or consumer expectations. Taking a proactive stance saves headaches later, and reassures everyone along the supply chain – from R&D scientist to end consumer – that what’s written on the analytical records truly matches what’s inside the drum.
End users, especially those in specialized industries, often need custom batch sizes, modified formats, or unique documentation. Our flexibility comes from years spent balancing machinery, personnel, and scheduling challenges. Unlike traders or third-party copywriters, we convert raw plant matter to pure liquiritigenin under our own roof, so adjustments fit seamlessly into routine production. Every tweak in process or documentation is supported by hands-on experience, not theory or outsourcing.
Crowded supplier directories and digital marketplaces have made shopping for chemical ingredients fast, but risky. It’s common to see rebranded products, overstated claims, and inconsistencies between lots. Many laboratories and production lines were forced to run repeated identity and purity assays, erasing any supposed savings from unstable sources. Our direct manufacturing feedback loops help prevent these pitfalls. Customers know our supply comes only from our own controlled plant, not from cobbled-together third-party lots. Our transparency goes beyond what is often legally required, and it grows out of a manufacturing mindset built on reliability.
Reputation takes years to build. Our factory teams work side by side with lab staff, and raise the alarm whenever a result looks off-spec, even before analytical confirmation. These built-in checks allow real-world challenges to be addressed quickly, before finished products ever leave the dock. Technical improvements—sometimes small and sometimes substantial—arise directly from hands-on problem solving, not from abstract management initiatives. This simple approach to quality assurance keeps the product’s reputation strong with those who actually use it.
Not every order goes smoothly. Machinery wears out, raw materials surprise us, regulatory questions arise, or priorities shift. Years in the business have convinced us that the foundation for success isn’t the absence of problems, but the speed and honesty of response. We aim to fix and communicate issues directly—partners appreciate truthful updates and practical solutions more than canned explanations or empty apologies.
Demand for liquiritigenin shows no signs of slowing down. As natural, plant-derived chemicals increasingly intersect with food, cosmetic, pharmaceutical, and research markets, expectations rise. Buyers do not settle for generic powders or paper-thin verification. Hands-on, evidence-backed manufacturing, supported by continuous improvement and transparent records, lets our product support new applications and scientific discoveries.
Technology keeps raising the bar—new sensors, advanced analytical methods, and data management tools let us monitor every batch at a granular level. Traceability, real purity, and reliable supply start on the production floor. Years of practical experience and close collaboration with end users keep us focused on improving with each batch. We see every new challenge as an opportunity to refine the way we approach plant extraction, chemical isolation, and documentation.
Whether a customer’s order is destined for a research publication, a finished consumer product, or a new application just emerging, our commitment to careful, hands-on, and honest production helps ensure successful outcomes. Our goal is not just to deliver a box of powder, but to support each customer’s purpose, whatever form it might take, with the kind of quality and integrity that can only come from direct manufacturer experience.