|
HS Code |
757321 |
| Name | Isosteviol |
| Molecular Formula | C20H30O3 |
| Molecular Weight | 318.45 g/mol |
| CAS Number | 27975-19-5 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 205-207°C |
| Solubility | Slightly soluble in water, soluble in DMSO and ethanol |
| Purity | Typically >98% |
| Storage Temperature | 2-8°C |
| IUPAC Name | ent-16-oxobeyeran-19-oic acid |
| Synonyms | Steviol isomer, ent-16-Ketobeyeran-19-oic acid |
| Origin | Derived from hydrolysis of stevioside (Stevia rebaudiana) |
| Usage | Pharmaceutical intermediate, sweetener precursor, research chemical |
| Stability | Stable under recommended storage conditions |
As an accredited Isosteviol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Isosteviol, 25g, is supplied in a sealed amber glass bottle with a secure cap, labeled with product and safety information. |
| Shipping | Isosteviol is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture intrusion. The packaging complies with local and international regulations for safe handling and transport. Proper labeling and documentation accompany each shipment, ensuring traceability and safe delivery. Store in a cool, dry place during transit. |
| Storage | Isosteviol should be stored in a tightly sealed container, away from direct sunlight and moisture. Keep at room temperature (15-25°C) in a dry, well-ventilated area, and avoid exposure to strong oxidizing agents. Ensure the storage area is clearly labeled and complies with local regulations for chemical safety. Proper storage helps preserve isosteviol's stability and prevents contamination or degradation. |
| Purity 98%: Isosteviol Purity 98% is used in pharmaceutical formulations, where it ensures batch-to-batch consistency and high therapeutic efficacy.Particle size 10 µm: Isosteviol Particle size 10 µm is used in oral tablet manufacturing, where it supports rapid dissolution and uniform bioavailability.Melting point 205°C: Isosteviol Melting point 205°C is used in high-temperature processing for food additives, where it maintains structural integrity under thermal stress.Stability temperature 70°C: Isosteviol Stability temperature 70°C is used in beverage sweetener formulations, where it retains sweetness profile during pasteurization.Molecular weight 318.45 g/mol: Isosteviol Molecular weight 318.45 g/mol is used in controlled-release drug delivery systems, where it enables predictable pharmacokinetic properties.Solubility 0.01 g/100 mL (water): Isosteviol Solubility 0.01 g/100 mL (water) is used in powdered beverage mixes, where it provides low caloric content while minimizing off-taste.Residual solvent <0.1%: Isosteviol Residual solvent <0.1% is used in nutraceutical blends, where it guarantees product safety and compliance with regulatory standards.Optical rotation -127°: Isosteviol Optical rotation -127° is used in chiral separation techniques, where it aids in enantiomeric purity assessment for analytical applications. |
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Stepping into the field of natural sweeteners and high-value plant extracts, Isosteviol stands apart as a unique and versatile ingredient. Our production site has seen steady growth in requests for Isosteviol over the past decade, and we’ve watched both scientific and commercial interest blossom as a result. Extracted from the leaves of Stevia rebaudiana after the enzymatic transformation of stevioside, Isosteviol brings together the worlds of food technology, nutrition, and specialty chemical manufacturing. As a direct manufacturer, we've experienced firsthand the stringent requirements for traceability, purity, and batch consistency that everyone from food processors to researchers demand. Unlike basic steviols or crude extracts, our Isosteviol reaches high standards seen in pharmaceutical, cosmetic, and food additive applications.
Every kilogram of Isosteviol leaving our facility reflects layers of careful work, beginning with sourcing properly identified Stevia leaves and concluding with multi-step purification. Over years of optimizing extraction and hydrolysis protocols, we have standardized a series of Isosteviol types. Our most widely produced product, Isosteviol Model ISO-97, features purity greater than 97% as determined by HPLC testing, and that purity has proven essential for precise formulations. Granular white to off-white powder, almost odorless, with a faintly sweet aftertaste—this is what quality looks like from a manufacturer's lens. We target moisture levels below 1%, with ash content limited to below 0.1%. In-house research teams regularly assess each batch for heavy metals and pesticide residues, setting strict maximums well under prevailing legal thresholds. Stereochemistry and residual solvent analysis using GC and NMR increase our confidence in both purity and safety.
Our facility’s core philosophy is providing a product that meets not only objective measures but also the less tangible standards developed through open dialogue with customers. Custom batches with tailored characteristics for specific end uses, such as higher solubility or finer mesh size, are regularly produced at customer request.
Manufacturing Isosteviol requires a strong focus on consistency. Engineers at our site manage carefully controlled fermentation and hydrolysis units that break down stevioside into Isosteviol through a cascade of natural enzymatic and acid-catalyzed reactions. Over time, we’ve invested in better reactor monitoring, enabling tighter control over temperature gradients and pH swings. Experienced technicians monitor the entire conversion, knowing from experience how raw material variation by harvest season can alter yields or impurity profiles. Each batch is sampled not just at the start and finish, but at key points throughout the process—monitoring for color shifts, clarity, and any physical signs of deviation.
Quality control is more than lab numbers for us. Years spent talking with formulators and R&D teams worldwide has taught us that real-world product performance trumps theoretical specs. This practical philosophy translates into rigorous batch records, real-time process analytics, and exhaustive documentation—available for audit, whenever needed. From raw material certificates of origin to detailed chromatograms, we believe that openness strengthens trust between manufacturer and client. We regularly allow onsite audits for supply partners, opening our records and letting them track the product from sourced leaf to finished powder.
Over two decades, our Isosteviol has moved far beyond the lab bench. The food ingredient sector remains a pillar of demand, with beverage, bakery, and confectionary brands keen to leverage the sweetening power and metabolic stability of Isosteviol. Its relatively clean flavor profile means it offers a subtle, lingering sweetness without the harsh licorice tail many encounter with crude stevia extracts. Our process removes bitter byproducts early, inspired by direct feedback from flavor chemists who value a neutral base for blending into complex food systems.
Pharmaceutical and nutraceutical sectors have also taken a keen interest, both as researchers and as formulators. The compound’s recognized role in modulating glucose levels, combined with its resilience in formulation, opens pathways for new health-focused products. Our collaborations with academic and clinical research centers keep us in tune with the science, allowing us to adapt the product to new requirements as evidence develops.
We have supplied Isosteviol to cosmetics manufacturers seeking mild antioxidative or skin-conditioning effects, and feedback from this sector has shaped our approaches to purification, microbiological controls, and packaging options. Not every ingredient makes a smooth leap from the food to cosmetic sectors—but Isosteviol, with its multi-functionality and absence of major allergen risks, fits right in.
To most people, the distinctions between different Stevia-derived compounds blur together. In a production setting, these differences stand at the center of every technical discussion. Isosteviol comes from the hydrolysis of steviosides and rebaudiosides, resulting in a unique structure—a diterpenoid core with distinct carboxylic groups. This subtle shift changes how it interacts with both human sensory receptors and the digestive system. Many food formulators have struggled with the lingering bitterness typical of basic steviosides. Through our process, Isosteviol generates a cleaner, less polar molecule, dropping most of the bitterness and improving solubility in aqueous mixtures. This shift doesn’t just help the end consumer—it eases blending at the mixing tank, reducing risk of clumping or undissolved particles.
Compared to pure Steviol or crude Stevia extracts, Isosteviol brings greater batch-to-batch chemical uniformity. Crude extracts may hit a general sweet note, but they are mixture by nature—fluctuating ratios of different glycosides, coloring agents, and plant matrix remnants. That inconsistency forces downstream processors to test and filter each load, increasing both cost and uncertainty. Isosteviol, once purified and standardized, behaves predictably. This reliability gives formulators space to develop products with longer shelf lives, fixed sensory properties, and stable regulatory filings.
Synthetic or semi-synthetic sweeteners often differ in both their metabolic pathways and legal status. While they usually pass through manufacturing lines with fewer microbial concerns, they lack the “natural” tag so vital in clean-label product development. Our customers consistently tell us that consumers are looking for natural origins and recognizable processes. The fact that Isosteviol arises from plant leaves, with only minimal chemical intervention, lines up well with both regulatory frameworks and marketing needs.
Each new production cycle brings risks and troubleshooting opportunities. Isosteviol synthesis depends on the quality of each input, from water purity to the specific strain of Stevia grown. As a manufacturer, we’ve lived through disrupted supply chains, poor harvests, and regulatory reclassification of botanical ingredients. In one year where excessive rainfall damaged leaf quality throughout several provinces, we had to work with growers to stagger harvests, test additional contaminant panels, and adjust extraction parameters for different impurity profiles.
Purification, especially solvent removal and crystallization, can make or break the process economics. Years of experience have taught our team that temperature ramps must be paced tightly, and batch records tracked in real-time to anticipate scale-up complications. Investing in automated monitoring tech has reduced losses and strengthened our resource efficiency. Training staff to recognize subtle changes—like a shift in the aroma or the settling pattern during filtration—has kept our highest-purity batches repeatable.
Documenting every production run for traceability turned into an unexpected strength. Food safety authorities ramped up regulatory scrutiny over plant-derived ingredients, asking for multi-year supply chain provenance and exacting records on every lot. Our multi-department project to digitalize documentation paid off, shortening audit prep from weeks to hours and earning us smoother regulatory acceptance.
Experience shows that customers expect full transparency for every ingredient. We’ve shared batch certificates, audit reports, and even traceability down to the fertilizer records at particular Stevia fields. Scandals in other sectors have driven this, and the only response is greater openness. Our relationships with growers go back years. Some of our partner farms have sent their quality managers to witness extractions directly, fostering a spirit of mutual accountability.
We keep documentation chains intact from leaf to isosteviol shipment. Every batch comes with a data package showing the growing, harvesting, drying, and processing history. Electronic batch records have replaced paper logs, and periodic spot-checks by international verification bodies keep the quality assurance robust. Our clients—whether in Japan, the EU, or North America—get exactly the same documentation language, and any update in compliance or technical spec is shared without delay.
Our operation has gone through a transformation, shifting toward greener chemistry and more responsible resource use. Early on, water consumption and solvent recovery were our main headaches. Repeated cycles of process improvement have halved water use relative to output. On-site solvent recovery has become a technical centerpiece, driving down emissions and waste outputs. Authorities now demand life-cycle assessments and annual sustainability reports for large-scale producers, and our investments in water effluent treatment and photovoltaic energy reflect this push.
We send byproducts—including leaf fibers and minor glycoside fractions—to animal feed and biogas plants, reflecting the principle that manufacturing footprints stretch far beyond the main product. Employee health and chemical handling training have cut workplace incidents dramatically, and our relationship with local authorities improves as site visits show tangible improvements. These moves aren’t just about compliance—they stem from direct dialogue with downstream partners who sell to sustainability-conscious businesses. Demand for responsible supply is only growing, and as a manufacturer, we see this trend shaping every major investment decision.
Real growth comes from solving problems together. Our R&D and tech support teams work with clients throughout product development, not just the early sample-testing phase. For example, customers in the dairy sector faced stability issues when adding Isosteviol to probiotic yogurt lines. The finished products risked separation or lost sweetness during storage. By tweaking mesh granularity and monitoring for reactive impurities, our engineers helped stabilize flavor profiles for six months in the fridge—a breakthrough reached only by sharing technical data and running joint pilot trials.
We’ve seen pharmaceutical partners call for the highest purity specifications, demanding undetectable levels of certain trace contaminants. Food partners, meanwhile, routinely urge us to create new packaging systems compatible with automated bulk blending lines. Listening, adapting, and reporting back on test results keeps everyone moving forward. Our team tracks new patents, regulatory changes, and large-scale projects in this field, so we stay a step ahead on technical upgrades. Being in the trenches means knowing what questions to ask.
Years of regulatory compliance efforts have built up our institutional expertise. Authorities in major markets view Isosteviol as a distinct ingredient, with approvals sometimes following separate tracks from whole-leaf Stevia or traditional sweeteners. Every market has different residue limits, labeling standards, and traceability expectations. Our documentation processes and legal review practices grow out of past audit experience; the European Union, United States, and Japan each shaped our reporting approaches.
Recent years have seen market demand move sharply toward “natural” and “clean label” ingredients. Our production choices—selecting botanically-derived starting materials and limiting synthetic intervention—line up well with these trends. Business partners tell us the ability to document these steps aids their product launches in restrictive markets. Further, as more consumers scrutinize product sourcing, our investment in digital traceability and transparent packaging keep our clients out in front.
We treat every batch of Isosteviol as a chance to learn, drawing lessons from customer feedback, supply challenges, and emerging technical literature. Investments in analytical equipment, process automation, and staff training have delivered tangible gains. Our continuous improvement program encourages employees to flag process inefficiencies and suggest new ideas, even outside their roles. Improvements in filtration speed, better residue monitoring, or upgraded packaging lines all grew from incremental steps rather than one-time fixes.
Sustained success rests on a culture of openness—admitting mistakes, celebrating small victories, and remembering that customer needs evolve constantly. Our customers challenge us, and in turn, we drive innovation by offering deeper technical support and new formulations. Only by listening to the real-world needs—taste, shelf-stability, label claims—can we keep pace with not just regulation, but with rising standards in taste and transparency.
Looking back across the years, the story of Isosteviol has been one of adaptation and commitment to quality. We have grown from basic batch processes to highly controlled, technically advanced manufacturing capable of serving global markets. Side by side with our partners, we’ve refined every aspect—selection of raw materials, process control, purification, testing, and product support. Every shipment that leaves our gates reflects a shared understanding of quality, accountability, and service earned through hands-on experience.
From the early days of manual extraction to today’s digitalized, continuous quality monitoring, our Isosteviol remains a testament to what focused, open, and responsible manufacturing can achieve. We’ve shaped our product in conversation with a global community of formulators, food scientists, and innovators. Reliability, traceability, and readiness to adapt remain our driving forces. As the world of natural ingredients pushes forward, so do we—committed to collaboration and quality, batch after batch.