|
HS Code |
645795 |
| Cas Number | 961-29-5 |
| Molecular Formula | C15H12O4 |
| Molecular Weight | 256.25 |
| Appearance | Yellow crystalline powder |
| Purity | ≥98% |
| Melting Point | 197-201°C |
| Solubility | Soluble in DMSO, ethanol, methanol; poorly soluble in water |
| Boiling Point | 443.4°C at 760 mmHg |
| Storage Temperature | 2-8°C |
| Iupac Name | 2',4,4'-Trihydroxychalcone |
| Synonyms | ISL, Licorice chalcone A, Isoliquiritigenine |
| Pubchem Cid | 638164 |
As an accredited Isoliquiritigenin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Isoliquiritigenin, 1g: Supplied in an amber glass vial with tamper-evident seal, labeled with chemical name, purity, and safety information. |
| Shipping | Isoliquiritigenin is shipped in compliance with all relevant safety regulations. It is securely packaged in sealed, chemical-resistant containers to prevent leakage or contamination. The package includes appropriate labeling for hazard identification and is dispatched via certified carriers to ensure safe and prompt delivery. Shipping documentation accompanies each shipment. |
| Storage | Isoliquiritigenin should be stored in a tightly sealed container, protected from light and moisture, and kept at a cool temperature, ideally at 2–8°C (refrigerator). It should be stored away from incompatible substances such as strong oxidizers. Proper storage ensures chemical stability, prevents degradation, and maintains its effective use for research or experimental purposes. Always follow standard laboratory safety protocols. |
|
Purity 98%: Isoliquiritigenin with purity 98% is used in pharmaceutical formulations, where it ensures high bioactivity and consistent therapeutic efficacy. Molecular Weight 256.25 g/mol: Isoliquiritigenin at molecular weight 256.25 g/mol is used in analytical reference standards, where it enables accurate quantification in HPLC assays. Melting Point 194–196°C: Isoliquiritigenin with a melting point of 194–196°C is used in recrystallization processes, where it allows for efficient purification and stable end products. Particle Size <10 μm: Isoliquiritigenin with particle size less than 10 μm is used in topical drug delivery systems, where it improves skin penetration and controlled release. Solubility in DMSO 100 mg/mL: Isoliquiritigenin with solubility in DMSO at 100 mg/mL is used in cell-based assays, where it provides reliable compound delivery and reproducible results. Stability Temperature ≤25°C: Isoliquiritigenin stable at temperatures up to 25°C is used in long-term storage solutions, where it preserves chemical integrity and formulation performance. HPLC Grade: Isoliquiritigenin of HPLC grade is used in chromatographic separation protocols, where it ensures contaminant-free analysis and precise peak identification. Optical Purity ≥99%: Isoliquiritigenin with optical purity of at least 99% is used in chiral drug synthesis, where it guarantees enantiomeric selectivity and minimizes side product generation. Pharmacopoeial Standard: Isoliquiritigenin conforming to pharmacopoeial standard is used in regulatory submissions, where it facilitates approval processes and supports safety documentation. Moisture Content ≤1%: Isoliquiritigenin with moisture content not exceeding 1% is used in solid dosage preparation, where it mitigates degradation and ensures uniform blending. |
Competitive Isoliquiritigenin prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
As a chemical producer focused on both the reliability and traceability of our supply chain, we’ve spent years refining the production and quality standards of Isoliquiritigenin. This chalcone compound finds recognition for its distinct yellow pigment, which comes directly from licorice roots. Its value isn’t just in color, though; in the last decade, labs and manufacturers working in fields like pharmaceuticals, nutraceuticals, and cosmetic formulations have shown growing interest in the unique molecular structure and properties of Isoliquiritigenin. Our experience has shown that high purity and consistent batch quality make all the difference when translating lab results into large-scale outcomes.
The product we offer (CAS No. 961-29-5) comes in powder form, shaped by years of hands-on feedback from researchers and industrial buyers. We produce at scale, starting from botanical extracts and moving through controlled synthesis to meet rigorous testing criteria. For routine shipments, our typical purity specification reaches 98%, confirmed by HPLC and other methods before release. Over the years, we’ve seen how color consistency, moisture control, and particle size influence process efficiency for both extraction and downstream processing. Instead of bouncing between suppliers and risking batch-to-batch variation, our partners rely on the fact we control the product from source to shipment—a critical factor for repeatability, especially with regulatory paperwork or end-use applications that demand audit-ready trail.
Unlike mixed-lot products or uncertain supplies from less transparent sources, we know where each kilo originates. We validate botanical origins, watch for contamination, and maintain separate lines for synthetic and plant-derived batches. Both options have advantages; the plant-derived grade satisfies the needs of companies prioritizing natural-source claims, while the synthetically derived Isoliquiritigenin supports applications that require precise isotopic labeling or other modifications for analytical uses. Over time, we’ve learned that formulation chemists and process engineers often benefit most from knowing not just what’s in the drum today, but that next year’s lots will match up. Variability in the supply chain can disrupt development or necessitate costly reformulation.
Consistency doesn’t just help in the lab. Process scale-up often reveals hidden weaknesses in the initial supply of raw materials. For manufacturers doing large-batch extractions or blending Isoliquiritigenin into intermediate products, the actual flow properties, solubility profiles, and trace residuals can have a real world impact. A common pitfall in the market involves incomplete removal of plant matrix components, which can introduce off-odors or affect downstream purity. Our quality system focuses on eliminating these risks and documenting every batch, making troubleshooting less of a guessing game for our partners.
We often hear from R&D clients who use Isoliquiritigenin as both starting material and functional ingredient. Its primary draw comes from biological activity. Researchers and companies targeting antioxidant properties, anti-inflammatory functions, or natural preservation often single out Isoliquiritigenin because peer-reviewed studies and centuries of herbal practice align with its reputation. In the lab, it appears as a bright yellow powder, and its safety record—when handled with standard chemical hygiene—stands on solid ground.
The model produced here supports key pharmaceutical research applications. For instance, studies on melanin synthesis inhibition, cell cycle modulation, and other physiological pathways often prefer samples that have clear analytical characterization and batch records. Biochemists and formulation experts appreciate our dataset of spectral traces, impurity profiles, and residual solvent data—which accompany every order, not just occasional shipments. This transparency grew out of feedback from clients who faced regulatory questions and found incomplete paperwork from other suppliers wasted research time.
Other sectors, from food chemists seeking natural additives to cosmetics researchers building new skin care blends, also find Isoliquiritigenin’s characteristics worth attention. Its combination of color, bioactivity, and relatively high stability, especially in the free powder form, opens the door to wide applications. The challenge of scale-up and product commercialization always ties back to the same factor—does every kilogram perform the same, across time and batch? That’s the problem we aim to solve, backed by our investment in in-house analytics and traceable records from raw input to final packaging.
After years producing flavonoid derivatives and plant extracts, we’ve seen confusion in the marketplace over different licorice compounds. Customers ask: why not use liquiritigenin, glycyrrhizin, or even crude licorice extract instead? Direct comparison shows that each has distinct chemical and physical properties that can tip the balance for different uses. Isoliquiritigenin stands apart thanks to its open-chain chalcone structure, lacking glycosidic bonds or attached sugars, which results in different solubility and reactivity profiles.
For analytical research and repeatable functional outcomes, Isoliquiritigenin offers more precise control. Chromatographic purity helps avoid background interference in biochemical assays and toxicity testing. By contrast, other licorice-derived flavonoids often bring along matrix contaminants or show variable response in testing due to plant-source variability. Customers moving from raw extracts to refined ingredients regularly justify the added spend on pure Isoliquiritigenin by citing the costs and complications introduced by inconsistent raw materials. With robust COA data and certificate traceability baked into our fulfillment process, the result isn’t just cleaner experiments but lower costs downstream in development and manufacturing.
We also educate buyers to the practical differences in storage and handling. Crude licorice extracts require careful preservation to avoid microbial growth and rapid degradation of actives. Our Isoliquiritigenin powder stores well under dry, cool conditions, retaining bioactivity for extended periods as proved by in-house accelerated aging tests. This kind of stability can shrink logistical headaches and waste, especially for companies operating across multiple facilities or global distribution channels.
Across every batch, our lab provides a full portfolio of supporting data: HPLC chromatograms, NMR spectra, residual solvent reports, and heavy metal screens. Our 98% average purity opens up uses in regulated and unregulated sectors alike. Particle size ranges from fine powder to custom-milled lots, based on the processing observations reported back by our customers. Moisture content never exceeds 1% in our shipped lots, which comes directly from maintaining controlled drying and vacuum-packaging protocols.
Many buyers look only at the chemical name and CAS number, assuming purity claims from sellers are interchangeable. But in practical terms, product performance hinges on what isn’t visible to the eye—a fact that matters more than ever in regulatory and IP environments. For example, we maintain records of residual pyridine, dichloromethane, and other processing solvents at parts-per-million levels, so our end-users gain predictable performance both in yield and in compliance reviews. These aren’t details you find in generic web listings, but they drive costs, risks, and development timelines in real-world settings.
We’ve spent resources refining packaging as well. Triple-sealed mylar and food-grade HDPE containers drop loss and protect against moisture ingress during transit. Frequent buyers operating in humid or temperature-variable locations welcome these changes, as unplanned caking or color changes slow down production and invite costly failures. Our direct shipping and clear inventory controls mean less time chasing lost shipments and more reliable incoming supplies, at quantities from R&D sample lots all the way to truckload-scale production runs.
One of the pains researchers and manufacturers share is sourcing. Broker-based supply chains breed unpredictability—unmarked drums, mixed-batch shipments, or ambiguous tracking of origin or processing routes. In busy development cycles or with increased scrutiny from regulators, gaps in paperwork or lack of clear test results have slowed even the best-run programs. After several years handling direct requests for material identity and impurity datasets, we shaped our process around full traceability. This starts with vetting licorice root sources, continues through each synthetic or isolation step, and ends with batch-level breakdowns in both digital and hardcopy formats.
Traceability brings peace of mind for both our users and regulatory reviewers. We help partners eliminate the fear of last-minute sourcing issues or the disruption caused by contaminated or nonconforming ingredients. Our factory’s inventory and document controls stand up to detailed audits from pharmaceutical partners, food safety reviewers, and cosmetics industry inspectors. This level of rigor, once considered excessive, now proves essential to sustaining long-term supply agreements and keeping costs predictable.
Counterfeiting and substitution have grown as industry-wide threats, especially for in-demand plant-derived chemicals. With every lot, we run authenticity checks—end-to-end retain samples, isotopic fingerprinting, and rigorous cross-verification with past production rolls. Our partners are welcome to tour our facility, review logs, and take part in third-party verification whenever needed.
As demand for natural-source and bioactive ingredients accelerates, we’ve had to expand both our extraction capabilities and chemical synthesis operations. The rise in demand from global nutraceutical and cosmeceutical firms shows no sign of slowing, yet each brings a distinct profile of compliance concerns and end-use specs. To anticipate future needs, we’ve partnered with analytical labs and universities to pilot new methods of Isoliquiritigenin isolation, including enzyme-assisted extraction and greener synthesis protocols. Lowering the residual solvent content, improving yield per hectare, and reducing overall carbon footprint stand as ongoing projects, not just talking points. We test their impact through real batch runs, not just demo-scale runs, because our customers demand practical solutions—not just rhetoric.
Keeping pace with shifting demands also requires rapid feedback cycles. Formulation scientists often need minor shifts in physical form, blending aids, or packaging formats. We roll out process changes only after repeatable, multi-batch validation in production. Responsive change management, supported by transparent documentation, cuts down risk and ensures uninterrupted supply even as technical specs evolve.
The post-pandemic business climate has redefined how everyone works: border closures, supply interruptions, changing regulatory environments. As a vertically integrated manufacturer, we absorb market shocks and adapt faster than brokers or speculators. That’s allowed us to offer buffer stock, expedited production for urgent cases, and fast re-shipping when customs or logistics issues crop up. The pandemic taught us lessons about planning for unknowns; today our partners benefit from that experience.
Over the years, more buyers ask us about agricultural impact, waste stream management, and broader ecological footprint. Our licorice root sourcing follows documented sustainability protocols, with local inspectors monitoring soil depletion, water usage, and community impact. As pressures mount from certifying agencies and international buyers, we’ve expanded both field-level certification and in-house treatment of waste byproducts. On the synthetic side, waste solvents go through distillation and recovery steps, with continuous investment in closed-loop systems. Environmental impact isn’t just a compliance line-item—retaining local access to licorice botanical sources hinges on good stewardship.
Our production team reports back regularly on both agronomic and industrial trends. In some years, drought or pest pressures have threatened supply. Real-time feedback lets us shift between botanical and synthetic grades efficiently, with clear batch separation so downstream uses remain unaffected. Working relationships with local growers and technical schools helps us share best practices—from crop rotation to replanting.
We also review energy usage per batch, aiming for continuous improvement year over year. Our internal audits examine water recycling rates, energy draw per kilo of output, and safe recovery of all solvents. Over the last reporting cycle, we’ve seen up to a 15% reduction in net emissions through these focused operational shifts.
Some of our earliest partners return year after year, having tried other routes and discovered the value of stable, documented, single-source supply. Their feedback has shaped both our product and our paperwork—driving improvements in both purity and service. For organizations operating in sectors where traceable, batch-specific quality is the difference between regulatory approval and expensive recalls, those relationships matter.
We help our customers not just fulfill orders, but plan R&D calendars, forecast regulatory requirements, and solve sourcing headaches. As markets grow and compliance rules stiffen, handling change and documenting process matters more than ever. Off-the-shelf solutions don’t solve these real-world complications; detailed partnership and deep supply knowledge does. We invest in these connections every year, mentoring buyers and sharing technical updates as standards and science advance.
Industry and research professionals need more than a chemical name and a purity claim—they need enduring supply, transparent origins, and answer-ready documentation. By anchoring Isoliquiritigenin production under a single, accountable roof, we take the speculation and uncertainty out of the equation. Our investments in quality, sustainability, analytics, and service reflect a commitment to moving from commodity supplier to long-term partner. The result is a product shaped by both technical expertise and the accumulated lessons of decades in the field.