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HS Code |
450380 |
| Name | Artemisinin |
| Chemical Formula | C15H22O5 |
| Molar Mass | 282.33 g/mol |
| Appearance | White crystalline powder |
| Solubility In Water | Insoluble |
| Melting Point | 156-157°C |
| Source | Artemisia annua (sweet wormwood) |
| Primary Use | Antimalarial drug |
| Mechanism Of Action | Produces free radicals that damage malaria parasite proteins |
| Cas Number | 63968-64-9 |
| Storage Conditions | Keep in cool, dry place, away from light |
| Synonyms | Qinghaosu |
| Stability | Stable under recommended storage conditions |
| Route Of Administration | Oral, intravenous, intramuscular |
| Side Effects | Nausea, vomiting, dizziness |
As an accredited Artemisinin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White HDPE bottle containing 50 grams of Artemisinin, sealed with a tamper-evident cap and labeled with safety and storage instructions. |
| Shipping | Artemisinin is shipped in tightly sealed, light-resistant containers to prevent degradation. It must be kept cool and dry, typically at temperatures below 25°C. All packaging complies with regulatory standards for chemical safety, ensuring protection from moisture, heat, and light during transport. Proper labeling and documentation accompany each shipment. |
| Storage | Artemisinin should be stored in a tightly sealed container, protected from light and moisture. It should be kept at a temperature between 2°C and 8°C (refrigerated conditions) and away from sources of heat and incompatible substances. Proper storage ensures stability and prevents degradation, preserving its potency and effectiveness for pharmaceutical or research applications. |
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Purity 98%: Artemisinin with purity 98% is used in pharmaceutical formulations for malaria treatment, where it ensures high efficacy and consistent therapeutic outcomes. Melting Point 156°C: Artemisinin with a melting point of 156°C is used in medicinal compound synthesis, where controlled thermal processing enhances product stability. Molecular Weight 282.33 g/mol: Artemisinin with molecular weight 282.33 g/mol is used in clinical drug research, where accurate dosing improves pharmacodynamic assessment. Stability Temperature 25°C: Artemisinin with stability at 25°C is used in storage and transportation of APIs, where shelf life extension reduces product degradation. Particle Size <10 microns: Artemisinin with particle size less than 10 microns is used in tablet formulations, where uniform dispersion enhances bioavailability. Solubility in Ethanol: Artemisinin soluble in ethanol is used in liquid extract preparations, where rapid dissolution improves formulation versatility. Optical Rotation +75°: Artemisinin with optical rotation +75° is used in chirality-sensitive synthesis, where isomer purity leads to consistent biological activity. Low Residual Solvent: Artemisinin with low residual solvent content is used in injectable drug manufacturing, where safety standards are maintained. UV Absorbance 1.2 (at 210nm): Artemisinin with UV absorbance of 1.2 at 210nm is used in quality control analysis, where detection sensitivity supports reliable quantification. Moisture Content <1%: Artemisinin with moisture content below 1% is used in lyophilized pharmaceutical applications, where reduced hydrolysis risk preserves potency. |
Competitive Artemisinin prices that fit your budget—flexible terms and customized quotes for every order.
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Artemisinin grew out of effort and observation on the factory floor. Extracted from the sweet wormwood plant (Artemisia annua), it stands as a vital compound in malaria treatment and makes its mark as a pharmaceutical raw material. Over the years, demand for artemisinin has not only reflected global health priorities, but also pressed us as manufacturers to keep scaling up quality, stability, and reliability.
Our plant managers often discuss how each lot of artemisinin begins with careful seed selection and targeted cultivation in the fields, followed by precise post-harvest handling. The dry leaf’s moisture and handling after cutting matter a great deal. Even the best processing line can't fully rescue a batch if the input material saw too much rain or careless storage. Harvest timing, drying temperatures, and pest management in the field all flow downstream, impacting purity and yield.
When preparing artemisinin on our site, we rely on extraction setups that can handle the plant’s unique chemical nature. Solvent extraction applies decades-old chemistry yet never feels routine due to constant variables—humidity, leaf grade, solvent purity, and more. Experienced technicians keep a careful watch on reaction temperatures and time curves, since over-extraction or overheating can quickly drop purity by introducing artifacts. Our best operators can spot potential issues well ahead of lab analysis, just from subtle cues in the extraction vessel’s aroma or color change.
Specification targets have grown more demanding, driven by regulatory oversight and our customers’ expectations. Typically, our artemisinin lays out with an assay above 98%, measured by HPLC. The residue solvents stay well under set regulatory limits; conscious effort in washing and post-processing minimizes those. Water content, measured by Karl Fischer titration, stays around 0.5%. These values reflect our commitments but also result from daily conversations among operators, chemists, and supervisors reviewing batch sheets together—real improvement rarely comes from top-down memos alone.
In the chemical business, artemisinin’s complexity stands out. Unlike bulk commodities such as paracetamol or ibuprofen intermediates, plant-derived artemisinin introduces far more process variability. Weather, seed strains, farming techniques—none can be dialed in with the same precision as fully synthetic molecules. Even when the process looks unchanged on paper, the yield and byproducts remind us that nature sets her own limits.
Some producers offer semi-synthetic artemisinin, built from fermentation or engineered yeast systems. We have observed differences there: synthetic approaches can help stabilize output, yet as of now, the end product may hold trace impurities distinct from those seen in pure plant extraction. Side-by-side chromatograms show those tiny differences. In pharmaceutical supply talks, buyers still look most closely at naturally derived artemisinin for products intended for sensitive therapies, especially in regions with strict pharmacopeial requirements.
Another comparison comes with related derivatives—artemether, artesunate, dihydroartemisinin. Each compound delivers a new profile of solubility, stability, or in vivo action. Artemisinin, being the parent compound, forms the bedrock, with modifications grafted on through additional steps. Our team always underscores the importance of upstream purity since every downstream transformation amplifies whatever was in the original artemisinin. Trace metals, excessive solvent residues, or byproduct peaks can persist if not captured early.
Scaling up artemisinin never involves following a fixed recipe. Equipment must be configured to deliver extraction at just the right flow rates and pressures. Anything above pilot scale challenges both hardware and experience. Our team constantly faces batch segregation, since even neighboring fields can yield quite different raw material. Keeping track of batch origin and characteristics is less about bureaucracy and more about building a practical map for troubleshooting and consistent quality. Paperwork supports the process, but the main control comes from skilled personnel catching trends quickly.
Our technical leads trade plenty of notes with peers at other plants—there is little secrecy when shared problem-solving lifts all boats. Last year’s longer-than-usual rainy season forced many to change drying protocols and even consider temporary storage to save the highest-yield leaves. In grinding the dried herb, particle uniformity—measured in microns, not vague “fine” or “coarse” terms—affects the solvent’s diffusion into the plant matrix. Here, sensors and process automation add value, but what’s in the collection barrel counts for more than digital readouts.
We regularly maintain and recalibrate our HPLC and GC instruments. Samples are pulled at almost every process step, sometimes more than strictly required by regulation. In our facility, double-checking results happens not out of mistrust, but because a bad number means wasted hours or even ruined product down the line. Our investment in skilled analytical chemists matches our spend on hardware; consistent, reliable results stem from both.
Extraction solvents—mainly petroleum ether—can create bottlenecks if off-spec material enters the system, either due to supplier shifts or storage issues. Monitoring involves more than spot checks; our warehouse team logs both lot numbers and key properties at each delivery. While most downstream processes can swallow some input variation, artemisinin’s sensitivity teaches us to avoid taking chances with incoming materials.
Pharmaceutical buyers insist not just on chemical data sheets, but also on full traceability, sustainability efforts, and consistent compliance with GMP and regional pharmacopeia requirements. We’ve passed several on-site audits in the past two years, not by hiding behind compliance paperwork but by letting inspection teams walk the entire production path, meeting operators and looking over real-time batch data. No process runs without error; what matters is how we catch, correct, and learn from mistakes in a way that keeps finished batches squarely inside specification.
Our clean rooms, extraction vessels, and filtration setups are easier to upgrade than workforce training. Regulations sometimes play catch-up to new analytical methods or impurity concerns, so we keep knowledge flow high—internally and with key supply partners. Last season, a spike in certain unidentified peaks in the HPLC traces led our head of quality to pull out obscure literature and coordinate with industry counterparts in Asia and Africa to identify and control the source.
Documenting not just the positive results, but also every deviation and fix, gives buyers more comfort in our batches. It’s not about over-engineering every aspect, but treating transparency as a guiding value. Periodic, surprise audits arrive from health ministry or big pharmaceutical clients and we know well the relief—and the extra business—that comes when everything checks out because day-to-day diligence beats last-minute fixes.
Doctors and formulation scientists have shaped our approach. In malaria-endemic countries, they count on consistent artemisinin content batch after batch. Variable strength or high impurities can mean treatment failure, not just business complaints. One batch leaving even a few percent below accepted assay runs the risk of halting medicine production at a downstream plant, with lasting impact for entire national programs.
Our commercial team has seen growing inquiries from research outfits looking at artemisinin beyond malaria use—oncology, virology, and even crop protection. Each new prospect brings up different technical and regulatory questions, driving us to keep datasets robust and our logistics responsive. In these sectors, we supply artemisinin where the pure compound counts above all, since blending or reformulation happens further down the chain.
Shipment quality matters: withstanding transit through heat, humidity, and customs scrutiny, our packaging decisions echo customer priorities. High-barrier liners, rigid drums, and clear labeling mean fewer surprises and less finger-pointing. Sometimes, a long route places more stress on material integrity than the entire manufacturing process. Packing teams have learned to expect the unexpected—broken seals, rough offloading—and our after-sales team checks in post-delivery, not for show but for operational learning.
Sustainability in artemisinin starts in the field. Years ago we partnered with agricultural cooperatives, sharing propagation material and best practices. Farmers shift each season’s planting plan around weather trends and cooperative agreements ensure steady buyback at pre-set prices. We monitor pesticide and herbicide use, not just for consumer safety but because minor residues can show up during final purification.
Waste from extraction isn’t an afterthought—solvent recovery setups reclaim much of what would once have burned away, saving money and lowering emissions. Spent plant material brings value as soil amendment for local crops. Visiting team members can easily see which fields benefit from this closed-loop strategy and which parts of the region thrive due to responsible sourcing. Our company hosts open days for local students and farmers, It’s a partnership, not charity, and one that brings pride to the factory as much as the surrounding communities.
More requests now come from conscious buyers—pharmaceutical or otherwise—who want supply chain maps and third-party sustainability verifications. Meeting these expectations takes documentation well beyond chemistry. Our workforce development programs, safety briefings, and environmental controls have convinced skeptical buyers over years, aligning technical proof with the human story behind each kilogram produced.
In recent years, worldwide fluctuations in artemisinin prices have driven instability for everyone in the chain. Oversupply, outbreaks, and shifting policies all play a role. As manufacturers, we walk a tightrope—committing to multi-year contracts with growers and chemical suppliers while absorbing shocks in the finished product market. Diversifying customer base, managing inventory tightly, and building a resilient process flow have carried us through periods of surplus and scarcity alike.
Improvements in process automation, batch tracking, and field-to-factory analytics answer some challenges while others demand hands-on troubleshooting. Our teams devote untold hours to debottlenecking every stage. Even the best process engineer can't foresee how a missed truck delivery or a reactor leak changes the day’s plan. Reaction to supply chain shocks shapes both our operational costs and our reputation among tough buyers.
Training new operators means investing in local education partnerships and welcoming apprentices who bring curiosity before expertise. Many who started sweeping the halls now run reactor vessels or lead packaging shifts—a true reflection of on-the-ground upskilling that no amount of imported managerial flair has replaced.
We opened new labs to research derivatives and new uses for artemisinin, leveraging our core chemical knowledge. Conversations with university researchers and end-use firms have opened unexplored applications, making each year’s cycle more than just a repeat of the last. While not every project pans out, sharing early results often leads to improvements in process safety or better product consistency.
Producing artemisinin at scale means balancing nature’s unpredictability with chemical rigor. Every cycle brings new lessons rooted in practical work—smelling a solvent batch, double-checking a drying line, or reviewing the graph curves from HPLC output at midnight. There’s pride in shipping drums that meet the strictest standards and comfort in knowing our process can catch errors long before delivery.
From initial cultivation through refinery processing, each step leaves a trace on the final product. Whether a kilogram heads to a malaria project in Africa or to a lab in Europe investigating new therapies, that journey reflects our team’s focus and real-world expertise. We draw on facts, experience, and teamwork to supply a product that saves lives and enables new science. In our view, the true difference in artemisinin comes from every decision upstream and every lesson learned at the practical end of chemical manufacturing.