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HS Code |
550927 |
| Chemical Name | Gamma-Mangostin |
| Molecular Formula | C24H26O6 |
| Molecular Weight | 410.46 g/mol |
| Appearance | Yellow crystalline powder |
| Solubility | Soluble in organic solvents such as ethanol and DMSO |
| Melting Point | 178-180°C |
| Source | Extracted from Garcinia mangostana (Mangosteen) fruit pericarp |
| Cas Number | 3473-01-8 |
| Purity | Typically ≥98% by HPLC |
| Storage Conditions | Store at -20°C, protected from light |
| Synonyms | γ-Mangostin, 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)xanthen-9-one |
As an accredited Γ- Mangostin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White HDPE bottle containing 1 gram of Γ-Mangostin, securely sealed with a tamper-evident cap and labeled for laboratory use. |
| Shipping | Γ-Mangostin is shipped in tightly sealed, chemical-resistant containers to protect against moisture and light. All packaging complies with relevant regulations for hazardous materials. Provides temperature-controlled shipping if required, accompanied by a certificate of analysis and safety data sheet. Handle with gloves and store in a cool, dry environment upon arrival. |
| Storage | Γ-Mangostin should be stored in a tightly sealed container, protected from light and moisture. Keep it at a cool, dry place, ideally at 2–8°C (refrigerated), to prevent degradation. Ensure adequate ventilation in the storage area and keep away from strong acids, bases, and oxidizing agents. Proper storage maintains its stability, purity, and prevents potential chemical hazards. |
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Purity 98%: Γ- Mangostin with purity 98% is used in pharmaceutical formulations, where it ensures high bioactive content for enhanced therapeutic efficacy. Molecular weight 410.5 g/mol: Γ- Mangostin with molecular weight 410.5 g/mol is used in analytical standards, where accurate quantification and consistency in HPLC applications are achieved. Melting point 182°C: Γ- Mangostin with melting point 182°C is used in solid dosage production, where it offers thermal stability during tablet compression. Particle size <10 μm: Γ- Mangostin with particle size below 10 μm is used in topical creams, where it provides improved skin penetration and uniform distribution. Stability temperature up to 60°C: Γ- Mangostin stable up to 60°C is used in cosmetic emulsions, where product integrity is maintained during storage and transportation. Solubility in ethanol >10 mg/mL: Γ- Mangostin with solubility in ethanol greater than 10 mg/mL is used in dietary supplement formulations, where it enables homogeneous blending for liquid suspensions. UV absorbance (λmax 245 nm): Γ- Mangostin with UV absorbance at λmax 245 nm is used in quality control assays, where it allows precise detection and purity assessment. Residual solvent <0.5%: Γ- Mangostin with residual solvent content less than 0.5% is used in food additive development, where it ensures consumer safety and regulatory compliance. Anti-oxidant activity IC50 8 µM: Γ- Mangostin with anti-oxidant activity IC50 8 µM is used in nutraceuticals, where it contributes to effective free radical scavenging. Microbial limit <100 CFU/g: Γ- Mangostin with microbial limit below 100 CFU/g is used in injectable preparations, where it supports aseptic formulation and patient safety. |
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Γ-Mangostin stands as a natural xanthone compound sourced primarily from the pericarp of Garcinia mangostana, known widely as mangosteen. Over the last fifteen years, shifts in consumer preferences and regulatory focus have pushed plant-derived actives into the research spotlight across several industries. In chemical manufacturing, developing pure, standardized γ-mangostin at commercial scale remains an ongoing project, and from the vantage point of an actual manufacturer, reaching that benchmark takes a blend of technical rigor, sourcing discipline, and transparency that few outside our field ever glimpse.
Our γ-mangostin extraction lines are engineered for reproducibility. Output batches regularly measure 98% minimum purity (HPLC basis) in the form of a yellow-to-light brown powder. Each step, from procurement of raw mangosteen shell to final drying, has seen iterative design. There’s no shortcut for consistent solubility or maintaining low water activity in a thermally sensitive product like this. The distinct molecular formula, C24H26O6, results in a substance that provides both phenolic and prenylated xanthone functional groups — a detail that makes a huge difference in reactivity and downstream versatility compared to α- or β-mangostins.
Recently, acquiring mature, disease-free mangosteen rind in quantities that meet the batch-scale requirements of food, pharmaceutical, and personal care formulators has grown challenging. Weather fluctuations, transport times, and commodity price swings add volatility to a raw material already rare on the world market. To secure our channels, we began working directly with orchard cooperatives in Southeast Asia, investing in drying equipment, and installing on-site QC labs to validate identity and pesticide residue loads. This adds cost and time, but avoids diluting the compound itself and builds confidence in long-term supply.
Within the pigment-rich inner rind, γ-mangostin sits among over thirty documented xanthones. The unique arrangement of methyl, hydroxy, and prenyl substituents separates it from α-mangostin, the dominant molecule in almost every extract. Where the methylation pattern in γ-mangostin grants a different antioxidant pathway, the presence of ortho-phenolic groups has allowed pharmaceutical developers to explore alternate biological endpoints — most notably in the areas of anti-inflammatory and neuroprotective research. These properties have been shown to engage distinct gene regulatory mechanisms, separate from the better-known antioxidant functions of the α-isomer.
We see requests for γ-mangostin’s use in both reference standards and functional ingredients. Our technical team regularly fields questions about the compound’s dose response, dissolution profile, or formulation compatibility. Unlike bulk xanthone extracts—the kind that rely on undisclosed blends and often variable potency—our batches guarantee a true single-entity profile. This is especially relevant to those aiming for precise, reproducible performance in advanced nutraceuticals, targeted delivery systems, or proprietary blends.
In pharmaceuticals, γ-mangostin has attracted attention not because of vague "plant-based" marketing, but due to robust data in cell assays and animal models. Research in recent years has focused on its impact on MAPK, NF-κB, and PI3K/Akt signaling pathways—core regulators of inflammation, apoptosis, and cell growth. We have worked with formulation scientists who are not interested in theoretical activity: they order pure γ-mangostin to verify mechanistic claims, run pilot trials, and calibrate dosing for clinical outcomes, particularly in the context of neuromodulation or metabolic support.
Cosmetic and skin care formulators see γ-mangostin as a partner for botanical actives seeking to support dermal repair, redness reduction, and oxidative balance without synthetic additives. Its distinct chemical profile means it doesn’t just overshadow polyphenols or terpene-based antioxidants; it provides a route to novel formulations where synergistic effects matter. We have seen demand for γ-mangostin in advanced, preservative-sensitive products — facial serums, under-eye gels, and spot treatments where even low mg/g inclusion can shift the performance envelope. Whether blended with traditional plant oils or actives like niacinamide, steady batch purity and known solubility parameters let developers hit their spec sheets without excessive trial runs.
In food and beverage sectors, challenges have arisen around regulatory clarity and the balance between substantiated claims and marketing language. Many nations slot xanthones, including γ-mangostin, into ‘novel food’ frameworks. Our experience shows that any brand aiming for mainstream functional beverages or fortified snacks needs traceable audit trails, analytical data sharing, and timely supply. By keeping direct control over production, documentation, and third-party verification, our operation has helped established regional brands pass regulatory audits that would sideline those using bulk xanthone powder without precise standardization.
Years of bench-scale process chemistry have taught us that designing an isolation scheme for γ-mangostin means solving one challenge after another. Ethanol extraction is widespread but brings trade-offs; co-extraction of interfering pigments, variable switching between fractionation steps, and the peptide binding challenges of certain food matrices. Our own scale-up strategy has replaced old solvent-heavy protocols with supercritical CO2 fractionation, allowing us to pull precise xanthone profiles while reducing process waste and minimizing residual solvents. This control has made batch-to-batch variation much smaller — and crucially, easy to monitor via in-line analytics.
After extraction, the hurdles aren’t over. Any product prepared for clinical or food applications faces scrutiny around elemental impurities (heavy metals, inorganics), solvent residues, and bioburden. We maintain continuous sampling through each production run. This takes more labor and time compared to third-party traders supplying blended extract, but it guarantees transparency for end users. Proving this data on every batch means less speculation and more trust — a topic impossible to ignore in regulated markets or with multinational partners.
Stability studies run across temperature, humidity, and light exposure. γ-Mangostin, without effective stabilization, sees degradation to less active forms at ordinary warehouse temperatures. We package every lot in nitrogen-flushed, light-proof packaging, storing it below 22°C. We collaborate with downstream users—especially those integrating our product into formulations with tight shelf-life targets—to conduct real-time and accelerated stability trials. This early communication helps avoid expensive recalls or reformulations.
A chemical catalog will show dozens of xanthone variants. Field data and academic research, though, point to significant differences in both the biological roles and performance characteristics among them. α-Mangostin, the most prevalent xanthone in mangosteen rind, boasts the highest concentration in raw fruit and dominates bulk extract products on the market. Yet direct comparisons show that its anti-inflammatory properties—as measured by cytokine modulation or COX-2 inhibition—often plateau where γ-mangostin continues to show activity at lower doses. The presence of extra hydroxyl and methyl groups in the latter supports unique interactions in receptor binding and free radical scavenging.
Most commercial xanthone streams use micronized powder blends, a practice that muddies efficacy and safety profiles. Past industrial suppliers might not distinguish well among α, β, and γ isomers, especially when documentation lacks batch-level analytical results. Our process yields authentic γ-mangostin with chromatographic fingerprints matching published authentic standards. This level of separation, which takes more investment and deeper analytical work, serves formulators looking to keep product claims aligned with active ingredient identity, dosage, and batch reproducibility.
Some buyers ask whether they need single-isomer γ-mangostin, as opposed to generic xanthone or crude extract products. From the manufacturer’s standpoint, the answer comes down to target application. For cellular research, structure-activity relationship studies, or targeted therapeutic formulations, batch-certified γ-mangostin eliminates the confounding variables seen with whole-rind extracts. This avoids regulatory and scientific headaches that can stall product launches or trigger post-market investigations.
Access to authentic γ-mangostin hasn’t kept pace with growing market interest. Old import-export loopholes once let bulk “mangosteen extract” enter under loose commodity codes, but regulatory audits now demand evidence for ingredient traceability, purity, and contamination safeguards. Our experience has taught us that regulators in the US, EU, and Asia keep raising the documentation bar. We run lot-specific analyses not only for γ-mangostin purity, but for known and suspected residual solvents, pesticide residues, and heavy metal levels as mandated by current harmonized frameworks (e.g., USP, EP, GB). Instead of waiting for mandates, our team has built relationships with accredited third-party labs for regular cross-validation.
Recent supply chain shocks — container shortages, port lockdowns, rising material prices — have bled into conversations about production security. Unlike finished product marketers, we bear the true cost (financial and reputational) of an interrupted supply. We work to diversify supplier arrangements, and co-invest in regionally distributed storage and processing nodes near mangosteen-producing areas. Raw material selection and first-pass screening are handled on site, minimizing surprise rejects or QA failures later. This lowers the chance of production delays and strengthens our hand when negotiating large volume contracts, where buyers expect consistent, documented quality.
In dialog with end users, the main concern is authenticity. The market has seen a rash of suppliers passing off α/β-rich blends or mislabeling xanthone content on spec sheets. Without coherent documentation and traceable QC data, formulating with such materials risks adverse event reports or uncovered liability claims. In our own workflow, we maintain audit-ready production and supply records accessible for regulatory partners and customers — not just as a compliance checkbox, but as a foundation for sustained trust.
Producing γ-mangostin on a scale equal to global demand isn't simply a matter of buying more mangosteen. Yields for γ-mangostin are significantly lower per ton of rind than for α-mangostin, partly due to biosynthetic constraints in the plant and partly because of loss in the refining process. Each step — from biological sourcing to solvent management to batch refinement — eats into total available product. In real-world terms, to secure a steady tonnage of pure γ-mangostin, we have needed to commit to multi-year contracts and invest in upstream value chains, including partial ownership in drying and pelleting capacity at source.
Increasing the efficiency of our extraction and purification processes lies at the heart of making γ-mangostin accessible for innovative end-use applications. Each year, process R&D runs through new solvent systems, adsorbent beds, and fractionation techniques. Lately, the shift toward green chemistry — such as supercritical CO2, reusable adsorbents, and energy recovery — isn’t just about regulatory optics but about keeping costs manageable while supporting the movement towards sustainable operations. In manufacturing circles, sustainability means reducing water, energy, and chemical input, not just slapping a label on a barrel. Every reduction in process waste or batch scrap not only trims bottom line expenses, it limits exposure to rising compliance standards around waste handling and cradle-to-gate life cycle analysis.
Another foreseeable challenge centers on the supply of genuine, unadulterated mangosteen rind. As global commerce pulls more agricultural raw materials into dietary supplement and functional food lanes, the risk of adulteration, pesticide drift, and mislabeling climbs. Staying ahead means maintaining strong field presence, strict lab authentication, and continuous engagement with farmer cooperatives. We've found that supporting traceable, fairly compensated sourcing can increase costs in the short run but pays back in reliability and compliance predictability over time.
Biomedical literature substantiates a diverse profile for γ-mangostin in in vitro and animal models. Direct-action antioxidant properties, enzyme inhibition (notably acetylcholinesterase and β-secretase relevant to neurodegeneration studies), and effects on cytokine expression have all motivated clinical exploration. Our engagement as a manufacturer has given us a unique window into the practical hurdles translational science faces — lot-to-lot consistency, scalable purity, and reproducibility coming up as leading issues for any group hoping to bridge lab data and patient outcomes.
In the nutrition realm, γ-mangostin features in pilot human trials addressing acute inflammation and metabolic dysfunction. Across these efforts, our team has supplied credentialed ingredient lots, documentation archives, and support for study formulation design. It’s not enough to push shiny spec sheets; building mutual trust with research teams means ongoing dialog about process controls, third-party validation, and proposing answers to any issues arising mid-trial. Results from unbiased research — including potential null findings — benefit the entire field by setting realistic expectations for next generation products.
Responsible manufacturers must walk a line between technical possibility and ethical stewardship. Pushing γ-mangostin into broader markets brings cross-pressures from marketing trends, health claim restrictions, and the unrelenting drive to differentiate products. Our approach emphasizes transparency: supporting post-market surveillance studies, continuously publishing analytics, and remaining receptive to feedback from the global scientific and regulatory community. No ingredient alone solves every problem, and communicating that reality builds durable success.
Manufacturing γ-mangostin for diverse, educated buyers involves more than delivering a high-purity powder. Whether we’re supplying pharmaceutical R&D, regulatory-compliant supplement factories, or preformulation partners, the real need is for experience-based support. Every batch comes backed by our technical know-how, accumulated from scaling tens of production runs, troubleshooting with end-users, and iterating quality assurance until it matches or exceeds published standards. We engage directly with formulating scientists, quality teams, and product managers to provide chemical, analytical, and formulation data tailored to the real issues active in their pipeline.
Workshops, technical webcasts, and ingredient briefings form another arm of our customer partnership. Not every team has in-house experience with the idiosyncrasies of γ-mangostin solubility, degradation profiles, or matrix compatibility. In one instance, collaborating with a beverage partner prevented loss by identifying pH-related precipitation at the concept phase, saving them costly downstream pivots. In another, sharing our internal process for validating isomeric purity shed light on performance issues seen in competitor-supplied xanthones. This level of dialog doesn’t suit every manufacturer, but it’s the only way to secure responsible long-term adoption.
Looking at the broader landscape, γ-mangostin’s commercial and scientific promise continues to expand as consumer demand evolves. Product developers, researchers, and regulatory agencies place increasing value on the connection between ingredient identity, documented purity, and backward-traceability to source. By investing in direct, controlled production and staying transparent with data, manufacturers can influence not only their own reputational standing but also create the stable base needed for responsible industry growth. With γ-mangostin, the opportunities in health, wellness, and functional innovation remain real — but only if we uphold rigorous scientific and ethical roots with every kilo produced. This commitment, learned over years and reinforced daily, keeps our focus grounded on what matters for our collaborators and the communities where our core ingredient begins its journey.