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HS Code |
514672 |
| Cas Number | 471-53-4 |
| Molecular Formula | C30H46O4 |
| Molecular Weight | 470.68 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 290-295°C |
| Solubility In Water | Insoluble |
| Solubility In Ethanol | Slightly soluble |
| Purity | ≥98% (by HPLC) |
| Origin | Derived from licorice root (Glycyrrhiza glabra) |
| Ph | Neutral |
| Logp | 6.2 |
| Storage Temperature | 2-8°C |
| Odor | Odorless |
| Stability | Stable under normal conditions |
As an accredited Glycyrrhetinic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, opaque HDPE bottle containing 100g Glycyrrhetinic Acid; labeled with product name, batch number, purity, and safety information. |
| Shipping | Glycyrrhetinic Acid is shipped in sealed, moisture-proof containers, protected from light and heat. Labeling complies with chemical safety regulations. During transit, it is handled as a non-hazardous chemical, but care is taken to avoid contamination and physical damage. Shipping documentation includes necessary safety and handling instructions for recipients. |
| Storage | Glycyrrhetinic Acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. Keep the container tightly closed and protect it from moisture and incompatible substances, such as strong oxidizing agents. Store at room temperature, typically between 15–25°C (59–77°F), to maintain stability and prevent degradation. |
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Purity 98%: Glycyrrhetinic Acid with 98% purity is used in pharmaceutical formulations, where it ensures high anti-inflammatory efficacy and batch-to-batch consistency. Particle Size <10 μm: Glycyrrhetinic Acid with particle size below 10 micrometers is used in topical dermatological creams, where it enhances skin penetration and bioavailability. Melting Point 295°C: Glycyrrhetinic Acid with a melting point of 295°C is used in process manufacturing, where it provides thermal stability during high-temperature synthesis. Molecular Weight 470.7 g/mol: Glycyrrhetinic Acid with molecular weight of 470.7 g/mol is used in controlled drug delivery systems, where accurate dosing and predictable pharmacokinetics are required. Stability pH 4–8: Glycyrrhetinic Acid with stability between pH 4 and 8 is used in cosmetic emulsions, where it maintains compound integrity and prolonged shelf-life. Loss on Drying <1.5%: Glycyrrhetinic Acid with less than 1.5% loss on drying is used in solid dosage formulations, where it minimizes hygroscopicity and preserves product quality. Heavy Metals <10 ppm: Glycyrrhetinic Acid with heavy metals content below 10 ppm is used in oral pharmaceuticals, where it reduces toxicity risk and meets regulatory safety standards. Assay ≥99%: Glycyrrhetinic Acid with assay not less than 99% is used in active wound healing gels, where it ensures optimal potency and therapeutic performance. Residual Solvent <50 ppm: Glycyrrhetinic Acid with residual solvent content under 50 ppm is used in injectables, where it guarantees safety and compliance with international pharmacopeia. UV Absorbance 240–250 nm: Glycyrrhetinic Acid with UV absorbance range of 240–250 nm is used in analytical method validation, where it allows precise quantification and identity confirmation. |
Competitive Glycyrrhetinic Acid 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.
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Tel: +8615371019725
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In our line of work, some ingredients stand out for their history, reliability, and clear advantages in both function and performance. Glycyrrhetinic acid is one of these. Extracted and refined from licorice roots, it carries a depth that can’t be matched by synthetic knock-offs or quick substitutes. We have worked with this compound on a large scale for years, which gives us a different perspective from summaries found on sales pages or third-party catalogs. Every batch that leaves our plant has been carefully processed, with attention to factors that people outside the production cycle rarely consider—source of raw material, extraction technique, purifying steps, and storage to prevent degradation. This insight lets us separate real benefits from marketing claims, especially in a market crowded with variants.
We produce Glycyrrhetinic acid in a refined crystalline powder, reaching 98% purity or higher. The consistency of the powder’s color—light off-white, not chalky or yellowed—signals the care taken in extraction and purification, as inferior grades can’t maintain this look. The main model from our facility is known for its tight quality control on particle size, which ranges around 80-100 mesh. This is no arbitrary number. Finer powder offers a better surface area for blending in formulations, especially in pharmaceutical and cosmetic applications, while controlling dust and flow during processing. Many of the big contract manufacturers insist on this specific mesh size after running real-world blending and mixing trials. If a supplier offers only 'fine powder' as a spec, it usually means they’re not in tune with process requirements downstream—something we hear about from clients frustrated by inconsistent feedstock.
Another point where our model differs is in solvent residues. Residual solvents make a real difference to both safety and ease of use. High-end applications, from skincare to oral medicines, require extremely low levels of acetone, methanol, or ethanol—sometimes below the detection limits of ordinary lab equipment. We design every step of our process to minimize solvent carryover, employing extra vacuum-drying and post-purification steps that go beyond international regulations. Some suppliers cut this short to save on energy and time, but we have learned through client audits and internal reviews that it’s better to run a longer cycle than risk contamination or batch rejection downstream. It’s a lesson learned not from policy documents, but from costly recalls that affect both producer and customer.
No matter how many technical reports we review, the feedback from end-users shapes how we refine our Glycyrrhetinic acid. In the pharmaceutical world, this compound takes on an important role in anti-inflammatory and anti-ulcer drugs. It’s well documented that glycyrrhetinic acid inhibits certain enzymes tied to inflammation; but what’s often overlooked by outsiders is the trust researchers put in supply chain consistency. In past decades, we saw research stalled or outcomes questioned because a batch did not match the claimed purity or had hidden contaminants. Our own relationships with pharmaceutical labs have taught us the value of batch-to-batch reliability, far beyond what paperwork or audit checklists might imply. When the difference between a successful trial and a compromised one hinges on a few micrograms of an unwanted impurity, cutting corners in the production phase is just not worth it.
Cosmetics bring a different set of expectations. Marketers like to highlight natural origins and traditional use, but for chemists who actually develop new creams and gels, the focus stays on bioavailability, stability, and potential for irritation. Glycyrrhetinic acid carries the reputation of being gentle yet effective in soothing and anti-redness routines. Over several years, we worked with teams formulating sensitive-skin products and found out that purity alone doesn’t guarantee good results—particle size, excipient compatibility, and even odor control weigh heavily in prototypes. Our role as a producer is to respond with custom processing adjustments, not just standard powder. Requests for super-fine versions or versions with controlled volatility informed how we scaled up our lines. Unlike synthetic analogs, our naturally refined product absorbs into emulsions without breaking structure or clouding, which matters to formulators aiming for transparency and smooth application.
The food additives industry asks something different. Traceability and safety regulatory compliance take precedence. The demand for ‘clean label’ solutions grows each year; buyers scrutinize both process and paper trail. We set up dedicated tracking systems to cover this need, integrating every shipment with upstream batch records. Over time, our records have been critical in passing overseas inspections and customs reviews without surprises or seizures. This is an area where some lower-cost producers struggle, as good documentation is expensive and time consuming to build, and not every factory can absorb those costs into their margin. We’ve witnessed this in export delays and insurance claims navigated by some of our peers.
There is a wide price range among glycyrrhetinic acid products, and customers often ask what justifies the difference. The answer lies in both raw material source and handling. We begin with field-selected roots from recognized licorice-growing regions—mainly because soil conditions and harvesting time can shift the glycyrrhizin content and introduce unwanted residues. We’ve tested harvests from different provinces and found measurable differences in trace elements and pesticide load. Our process starts with careful sorting and thorough initial washing, which goes a long way to reducing impurities before they cause trouble in downstream processes.
Extraction comes next. Some manufacturers go for quick solvent extractions, hoping to boost output with less investment. We take a longer approach using sequential extraction and controlled pH adjustments. This not only improves the overall yield, but also minimizes formation of byproducts that can be tough to remove later. In one transition year, we switched to this technique after discovering that shortcut methods left us with more yellowish powder—an unwanted trait that customers flagged during their quality checks. Other market products may try to bleach or mask out these flaws, but subtle off-colors often reveal underlying chemical inconsistencies.
Purification is another critical point of difference. We do not simply rely on a single filtration or crystallization step. Our process cycle includes multiple rounds of activated carbon treatment and vacuum concentration. Some might argue it raises the cost, but the benefit is clear. Comparing our output to mainstream low-cost brands on the market, there are lower levels of lead and arsenic, substances that regulators now monitor more closely due to changing international standards. We find that buyers working in pharmaceutical development and food manufacturing appreciate this, and rest easier with a product that already meets high-end quality control before arrival.
Another problem with generic supply is consistency batch after batch. Unrefined methods and loose controls lead to a product that might look similar one day and fail a critical assay the next. We’ve invested in in-line analytical tools—HPLC, IR, and heavy metals screening—to catch minor shifts before shipping out. A missed anomaly can ripple through an entire production line, causing recalls and lost contracts. Customers who have switched from mass-market suppliers often mention lower complaint rates and tighter compliance records since integrating our lots.
Product solubility also shows up in day-to-day manufacturing. Glycyrrhetinic acid is known for poor water solubility, and though that’s an inherent property, we have taken steps to optimize dispersibility for different client needs. By controlling crystal morphology and surface chemistry, we minimize clumping and layering during blending, whether for solid, semi-solid, or topical applications. Users from supplement manufacturers to cosmetic chemists report easier handling compared to alternative grades; production lines move with fewer stoppages and there’s less cleaning between batches.
Manufacturers in our sector walk a tightrope between efficiency, quality, and compliance. Regulatory landscapes shift faster than policies can be printed, and we’ve seen requirements for heavy metal thresholds, pesticide residues, and allergen declarations turn on a dime. Our answer hasn’t been to simply chase documents, but to build quality from the foundation up. We keep close ties to local agricultural agents and field processors, offering incentives for cleaner, traceable farming practices. It took years, but our supply chain now has transparency that audits can verify without delay. This matters when authorities request full traceability from plot to packaged drum—a detail that can halt or clear a shipment overnight.
Technical hurdles shift with each type of end-user. Some need micronized versions for high-surface-area dispersions. Others want a highly stable, odorless powder for advanced skincare. We developed distinct post-processing lines, each tailored to a known set of use-cases drawn from actual customer projects rather than broad market hunches. A client working on a new tablet delivery system taught us the importance of maintaining flow without agglomeration, leading to adjustments in particle surface modification. Another highlighted the potential for cross-reactivity in sensitive oral products, prompting a review of chemical purity and residual solvent levels. Each time, issues in real-world use led to tangible change in our production, not generic claims or broad promises.
Environmental accountability also enters the picture more and more as standards tighten—particularly regarding waste water, solvent recovery, and air emissions. Our city’s industrial zone updates requirements every few years, and we must stay a step ahead or risk plant shutdowns. We invested heavily in closed-loop solvent systems and switched to eco-friendly washing sequences, based on the belief that long-term operation depends on preventing problems, not just responding with temporary fixes. The upfront cost is always a thorny point, but long-term relationships with clients depend on staying in business under all regulatory conditions.
Our production team doesn’t just rely on charts and certificates, but knows the texture, color, and even subtle odor transitions of Glycyrrhetinic acid at every stage. It took years to develop this collective intuition. We have learned by sharing samples with close collaborators, running side-by-side stability trials, and troubleshooting failed batches both in our lab and alongside client technicians. Whether it’s a smoother blending behavior, more predictable pH response, or consistent taste masking, there are dozens of techniques and tweaks that can only be mastered through long-term production. This lived experience shapes the advice we give to prospective clients and sets realistic expectations on performance.
We know the disappointment when a supposedly ‘pharmaceutical’ grade shipment fails to meet a client’s internal test. This hit home early in our manufacturing days, cost us a few partners, and proved that a production shortcut rarely saves money or reputation over time. Our team is organized around ongoing training in best practices—chemical handling, storage, and even sample dispatch. Rather than rotating through temporary labor, we keep skilled staff who know the downstream effects of small changes. These details, while hard to capture in a product brochure or data sheet, affect everything from flavor to compliance to yield.
Over several years, we’ve followed the impact of our Glycyrrhetinic acid batches across a range of products. Clients report lower rates of batch failure in tablet manufacturing, smoother emulsion formation in skin care, and fewer complaints over flavor masking in nutritional blends. Success rests not only in the purity or mesh size listed on a certificate, but in the depth of technical guidance that follows each sale—the lessons, phone calls, and real-time troubleshooting that come with long-term business relationships.
Market trends point toward more demanding standards and a wider set of uses. Personalized medicine and advanced nutraceuticals both place a premium on verified origins, documented purity, and readiness for integration into specialized formulas. We continue to adapt by investing in lab upgrades, staff education, and sample feedback loops. As regulations around the world tighten, we expect compliance bar to rise even higher—driving differentiation for manufacturers who have invested early in process transparency and upstream quality.
Though the market is crowded, our long-term collaboration with end-users keeps us grounded in the real barriers and breakthroughs that matter to daily production. It’s not enough to meet the letter of a standard; reliability and mature quality systems earn their place batch by batch, season by season. Much of what distinguishes our Glycyrrhetinic acid can’t be captured in a slogan or a generic certificate. It’s written in the habits of our team, the track record of consistent delivery, and the willingness to take feedback from the field.
Anyone seeking more than commodity grade solutions usually cares about full-service support—application insight, customized tweaks, and availability through both regular and extraordinary production cycles. We’ve grown alongside those expectations, and the road ahead is likely to make these skills even more essential. Glycyrrhetinic acid will keep evolving as a product, but the core values of hands-on manufacturing, technical clarity, and process reliability anchor our approach for the long haul.