|
HS Code |
172155 |
| Chemicalname | Dehydrated Andrographolide |
| Molecularformula | C20H28O4 |
| Molecularweight | 332.44 g/mol |
| Appearance | White to off-white powder |
| Solubility | Slightly soluble in water, soluble in ethanol and DMSO |
| Meltingpoint | 222-224°C |
| Purity | ≥98% (HPLC) |
| Casnumber | 62010-37-9 |
| Source | Andrographis paniculata (plant extract) |
| Storageconditions | Store in a cool, dry place at 2-8°C |
| Stability | Stable under recommended storage conditions |
As an accredited Dehydrated Andrographolide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Dehydrated Andrographolide, 100 grams, packaged in a sealed amber glass bottle with tamper-evident cap, labeled with handling instructions. |
| Shipping | Dehydrated Andrographolide is shipped in tightly sealed, airtight containers to prevent moisture absorption and degradation. Packages are clearly labeled and cushioned for protection during transit. Shipping complies with safety and regulatory guidelines, ensuring secure handling at controlled temperatures, away from direct sunlight, and delivered promptly to maintain product integrity. |
| Storage | Dehydrated Andrographolide should be stored in a tightly closed container, away from moisture and direct sunlight. Keep the chemical at a controlled room temperature, ideally between 2–8°C (refrigerated), in a dry and well-ventilated area. Avoid exposure to heat, oxidizing agents, and strong acids or bases to maintain stability and prevent degradation. |
Competitive Dehydrated Andrographolide prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615365186327
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As a dedicated producer working directly with botanical extracts, talking about dehydrated andrographolide means drawing on real operational experience, not just quoting lists and figures. Many years of refining extraction techniques have shown that this compound, with its marked bitterness, stands apart from typical herbal fractions. It’s recognizable to most plant chemists by the sharp crystalline structure left behind after dehydration, a signature feature we see every time we check a finished batch under the microscope. Andrographolide, isolated from Andrographis paniculata, transforms through careful control of solvent polarity and temperature. Dehydration offers distinct advantages in shipping, storage, and downstream compatibility with solid oral formulations.
In our daily practice, the shift from conventional andrographolide to its dehydrated counterpart marks more than just a water content difference. Hydrated forms, due to their molecular water, show variable bulk density and disrupt tablet production lines with unexpected sticking. By drying the compound precisely, we deliver a robust powder that flows reliably in filling machines and mixes freely with excipients. It’s not uncommon for R&D partners to comment on the smoother granule appearance and the predictable reactivity of this material during formulation. Dehydrated andrographolide resists caking, maintains purity well under ambient warehouse climates, and minimizes the risk of microbe growth, all outcomes stemming from deliberate moisture removal at the post-extraction stage.
Harvest timing matters immensely. Field partners harvest Andrographis paniculata at a defined growth phase to maximize andrographolide content. Once received, the fresh plant undergoes air-drying in ventilated sheds at a controlled humidity, never exceeding 40°C, to preserve glycoside integrity. Extraction follows a water-ethanol protocol honed over repeated campaigns, stripping out non-essential fractions before concentration. We’ve learned the hard way how temperature gradients during solvent removal influence aglycone retention – overheating can cost both yield and purity, a lesson reinforced by every full-batch loss we rescued only through reprocessing and aggressive filter polishing.
Isolated andrographolide, still bearing trace hydration, enters a vacuum drying stage. Here, we use jacketed dryers set on a pressure curve tailored to the crystalline matrix of the product. Our technicians monitor batch temperature hourly and sample product moisture gravimetrically until readings align below 3%. Colleagues across the sector agree that this threshold sharply distinguishes dehydrated product from semi-hydrated commercial lots, the latter often sold at a discount with warnings for storage risk. By adhering to process discipline developed on our shop floor, we avoid the telltale clumps and off-white streaks found in competitors’ powders suffering from residual moisture.
Observational feedback matters as much as lab results. Production staff note a perceptible increase in compressibility once true dehydration is achieved. Downstream, this translates to less dusting and less jamming, traits appreciated by contract formulators and brand owners alike who visit our facilities for in-person audits.
Over years of continuous production, we gravitate toward a specification framework that prioritizes practicality over rigid theoretical maximums. Finished lots of dehydrated andrographolide regularly reach assay values between 98% and 99% by HPLC against certified reference standards. Color ranges from a brilliant white to faint cream, a function of trace terpene retention, without drifting into the grayish tinge seen in over-dried or oxidized product. Granule size, determined through vibro-sieving, stays within a median 60-120 mesh, knowingly chosen to support direct compressibility in tableting blends without excessive fines which cause product loss.
We supply the compound in food-grade HDPE drums, nitrogen-purged where long-term stability demands, and capped with tamper-evident seals. Each drum batch receives a laboratory certificate matching it to its production campaign, showing full traceability from field to packaging. For niche users with special requirements – and these do arise, particularly in pilot formulation labs at universities attempting new drug delivery systems – we regularly prepare custom micronized lots as the machinery on-site allows. Bulk density, solubility in pharma-grade ethanol, and confirmed absence of carrier solvents are all standard requests we address with testing built directly into our weekly process control schedule.
Standards alone don’t matter if the product doesn’t behave consistently in use. Early on, we shipped a few experimental batches of semi-dried andrographolide to a multinational nutraceutical firm. Within weeks, we received field reports describing settling, diminished potency after a summer in transit, and failed attempts to disperse the product in standard mixers. The team’s decision to shift entirely to the dehydration protocol grew out of that harsh feedback. Since then, every process improvement cycle starts with data on customer returns and in-house stability mock-ups. Dehydrated andrographolide subjected to analytical stress shows stable active content for over 18 months at 25°C/60%RH, outlasting hydrated and spray-dried versions by a margin.
Filtration step upgrades brought about better physical texture, another lesson we only accepted after repeated user criticism about needle-like fragments jamming machinery. Modern micronizing mills, run after moisture has been completely driven off, avoid the static charging and product loss that plagued older generations of semi-wet grinding. Process changes like these keep the end product competitive and reliable in the face of variable raw material harvests and shifting demands from regulatory-inspected tablet manufacturers.
In pharmaceutical and nutraceutical settings, most buyers introduce dehydrated andrographolide directly into tablet or capsule formulations. The powder’s high purity and consistent flow make it suitable for low-dose, high-potency actives. The lack of moisture reduces the risk of interaction with hygroscopic excipients, a common cause of shelf-life complaints. Leading research labs work with our material not only in standard delivery forms, but also in pilot batches of transdermal patches and innovative liquid carriers. With stability data in hand, we’ve collaborated on beverage fortification studies, where only the dehydrated variant resists precipitation after extended shelf periods and thermal cycling.
Veterinary and agricultural supplement producers report similar ease when blending dehydrated andrographolide with plant-based carriers for animal health products. Moisture-sensitive feed additives benefit from stability under warehouse conditions widely encountered outside of strict climate control. Our ongoing collaboration with academic teams has yielded a deeper understanding of how the physical state conferred by dehydration directly affects bioavailability and long-term safety in living systems.
Comparing dehydration-processed andrographolide with other forms on the market always lands us in practical realities. Hydrated types, whether produced through simple air drying or incomplete vacuum runs, consistently show short shelf lives. They tend to clump and discolor, especially under tropical transit conditions. Some suppliers opt for solution-based forms, holding the active in glycerol or alcohol. While this can ease suspension in beverages, our clients in tablet production quickly report massive issues: excess solvent interfering with dry-blending setups, and product instability setting in well before labeled expiry.
Spray-dried andrographolide deserves a mention. This method, more common among broad herbal extract suppliers, results in a fine, slightly sticky powder with broader particle size distribution. Spray drying can trap solvent residues and minor plant fibers, introducing variability neither we nor high-standard pharmaceutical clients tolerate. Dehydration by controlled vacuum, in contrast, strips the material down to its essence, giving certainty on batch repeatability and compliance with purity limits set by both international pharmacopoeias and local inspection arms.
Dehydrated products, as we’ve proven through an evolving in-house protocol, remain chemically consistent through multiple downstream processes. Blending, granulation, compaction, and direct filling show stable results without need for special handling. This capability limits product wastage and machine downtime in high-volume operations, facts often overlooked in purely academic reviews of andrographolide’s chemical nature.
Years in the sector teach that trust grows from proof and transparency. Our field-to-factory program enables contract tracing for every batch, linking finished lots with planting dates, weather records, and agronomic practices. In some years, exceptional rainfall changes the phytochemical profile of harvested plants, pushing us to adjust extraction solvent ratios or tweak drying ramp rates. These adjustments come out of long days in the process lab, recalibrating tanks and reviewing chromatographies, not marketing brochures.
Buyers increasingly request not just purity but proof: pesticide analyses, heavy metal content, and solvent residuals. Dehydrated andrographolide produced at our facility routinely passes heavy metal and pesticide screens below permissible limits set by the major export markets. Auditors walk our production floor and view records in real time, something possible only with direct manufacturer oversight. This level of accountability distinguishes genuine manufacturers from trading houses that collect material from unrelated processors and attempt re-labeling at distribution hubs.
No manufacturing process escapes challenges. Some seasons, variable alkaloid content in incoming herb complicates extraction, producing lower than projected yields. Other times, a global shortage of pharma-grade solvents disrupts supply lines. In-house solutions to these issues depend on adaptability and accumulated process knowledge. We’ve implemented parallel lines for solvent preparation, stockpiling reserves during off-peak factory periods, and training partner farmers about environmental factors critical to plant chemistry, minimizing year-on-year swings.
Cross-contamination remains a constant concern in multi-product facilities. Physical separation of dehydrated andrographolide lines, with dedicated crews and exclusive cleaning protocols, prevents unwanted mixing with similar bitter-tasting actives such as swertiamarin or silymarin. Residual solvent checks after drying, verified through batch GC-MS runs, ensure that every outgoing lot meets export requirements. Regulatory tightening abroad only reinforces the importance of front-line quality control, directly addressing both traceability and integrity.
Demand for dehydrated andrographolide tracks closely with trends in herbal supplementation, especially seasonal spikes driven by acute respiratory wellness concerns. We watch competitors export blended or diluted product to capitalize on price swings. Our direct-from-source model avoids those pitfalls by clearing only full-strength lots. Innovation on the buyer side keeps us on our toes, too. Several major clients in North America and Europe develop variable-release capsules demanding a consistently dry and highly pure starting material. Only direct manufacturer-buyer communication makes adjustments and new batch customizations possible, keeping speculation out of the process.
Emerging applications, from plant-derived immunomodulators in animal feed to skin care actives, push us to test our product with a broader array of excipients and delivery forms. Heat stability and resistance to oxidative color change both challenge formulators and shape our batch improvement cycles. Working alongside application chemists at partner firms, we routinely gather and interpret data describing final product behavior, channeling that feedback back into our process line and QC standards.
The role of a manufacturer in botanical actives never ends once drums leave the plant. Real expertise means understanding not only instrumentation and process dynamics but also the shifting landscape of science and usage. Regular collaboration with university pharmacognosy labs and formulation scientists lets us look beyond routine batch testing and invest in stability trials, interaction studies, and delivery innovation.
Continuous improvement keeps operations aligned with Good Manufacturing Practice, but it also grows from a willingness to listen. Listening to on-the-ground reports, testing batches under harsh conditions clients actually encounter, and integrating findings into our protocols shape product evolution. These habits set apart genuinely reliable dehydrated andrographolide from generic commodity products with short shelf lives and uncertain origins.
In our line of work, reliability counts for more than novelty. The best results arise from controlled dehydration, careful tracking, open communication with users, and relentless focus on both process details and market demands. Dehydrated andrographolide represents more than a chemical specification – it’s the visible outcome of years of troubleshooting, refinement, and partnership with buyers whose needs continually push us to do better. As supply chains tighten, regulations grow, and application fields widen, direct manufacturing remains the surest path to consistent, trusted botanical active supplies, built to perform as intended in real-world usage.