|
HS Code |
557007 |
| Name | Evodiamine |
| Cas Number | 518-17-2 |
| Molecular Formula | C19H17N3O |
| Molecular Weight | 303.36 g/mol |
| Appearance | Yellow crystalline powder |
| Solubility | Slightly soluble in water, soluble in DMSO and ethanol |
| Source | Extracted from the fruit of Evodia rutaecarpa |
| Melting Point | 271-273°C |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protect from light |
| Chemical Class | Quinolone alkaloid |
| Uses | Pharmaceutical research, traditional medicine |
| Synonyms | Wu-Chu-Yu alkaloid, Evodiamine (INN) |
| Structure | Contains indoloquinazoline skeleton |
| Stability | Stable under recommended storage conditions |
As an accredited Evodiamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Evodiamine, 5g, supplied in a sealed amber glass vial with tamper-evident cap, labeled with product details and safety information. |
| Shipping | Evodiamine is shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. It is packed according to hazardous chemical regulations, with appropriate labeling and documentation. Transport complies with international and local safety guidelines to ensure the compound's integrity and the safety of handlers during transit. |
| Storage | Evodiamine should be stored in a tightly sealed container, away from direct sunlight, moisture, and heat. Keep it at room temperature (15–25 °C) in a cool, dry, and well-ventilated area. Avoid exposure to strong oxidizing agents. For long-term storage, refrigeration (2–8 °C) is recommended to maintain its stability and prevent degradation. Always follow relevant safety and handling guidelines. |
Competitive Evodiamine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to sales3@ascent-chem.com.
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Tel: +8615365186327
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From years on the shop floor and in the lab, we know a molecule earns its reputation not only from its chemical structure but from performance and consistency. Evodiamine, a quinazolinocarboline alkaloid, stands out for both its scientific profile and the many roles it serves in finished products. We talk about Evodiamine with the confidence that only comes from hands-on manufacturing and R&D. We control the entire process, from raw botanical extraction through multiple purification cycles, so we are not simply passing along what we are told — this is based on what our chemists and technicians see day after day.
Precision matters most once you work at the milligram scale with sensitive compounds. Maintaining purity levels above 98% for Evodiamine, model EVO-99, is a task our plant chemists attack from batch consistency to final filtration. What we have discovered over years is that Evodiamine’s natural complexity demands strict environmental control. Temperature swings, minor solvent deviations, or trace metal contamination show up in the final analytical results. We watch for that, and this vigilance results in a material with a clearly defined melting point, no visible residue, and no variability from batch to batch.
Standardized testing with HPLC and LC-MS allows us to spot even trace impurities down to parts per million. This isn’t about chasing abstract standards — it is about customer trust. End users see just white to off-white powder, but we see the hours of extraction, filtration, and every fractionation step. Our product’s quality, EVO-99, reflects these investments of time and experience, not just the luck of a good batch.
Customers often ask about plant alkaloids for heat sensation, metabolic support, research, or specialized formulations. In the lab, we have worked with many — berberine, caffeine, even capsaicin for comparison. Evodiamine, chemically unique as a quinazolinocarboline, does not mimic the pungency of capsaicin. It produces a distinct warming sensation without the harshness or risk of skin burns. We have tested it in various simulated conditions, and it remains much less irritant at equivalent concentrations. This lends greater flexibility for topical, dietary, and pharmaceutical developers who want bioactive function without the liabilities of extreme irritancy.
In analytical comparison, Evodiamine maintains higher thermal stability than compounds such as piperine or gingerol. During formulation, we do not see the same degree of degradation at moderately elevated temperatures. This stability supports a longer shelf life and less need for formulator compensation.
We hear a lot of creative approaches from our clients, and from field work, we notice a few areas where Evodiamine gets the most attention. The molecule’s ability to stimulate TRPV1 and TRPA1, two ion channels linked to thermal sensation, underpins its main uses. This underlies its inclusion in topical creams for muscle warming, pre-workout and weight management supplements, and, increasingly, in advanced pharmacological research.
From our perspective as manufacturers, we get involved well before any product labeling. Our technical team focuses on solubility in various vehicles, especially since Evodiamine dissolves poorly in water but blends well into select organic solvents. In ethanol and DMSO, we consistently achieve concentrations suitable for controlled dosing. For customers wishing to push new delivery formats, we recommend using lipid-based carriers. Repeated tests reveal that nanoemulsions and microencapsulation enhance bioavailability, reflecting research from published pharmacokinetic studies.
Bulk buyers — from nutraceutical companies to specialty pharma developers — often ask about particle size. Our production lines allow reliable micronization down to D90 < 10 μm, supporting fast and homogeneous dispersion in creams or liquids. We invest in particle-size monitoring on every large batch, not because it reads well in specs, but because finished formulation quality depends on this level of detail.
Every chemical presents its own occupational hazards, and Evodiamine is no exception. During active processing, inhalation and skin contact present manageable risks if staff act with care. Our facility has adopted closed-system transfer and local exhaust ventilation at critical steps. Our operators have seen that proper PPE — gloves rated for permeation, face shields, suitable respirators — lets us avoid incidents even over extended shifts.
Waste management for alkaloid-rich streams involves activated carbon and multi-stage solvent recovery. We have found over the years that strict adherence to waste protocols not only keeps us compliant but makes the whole process more efficient. Spill control, fire prevention, and staff training combine to minimize risks — not theoretical best practices, but how we get through hundreds of production runs with zero lost-time accidents.
As a chemical manufacturer, trust always comes back to transparency and proof. Our Evodiamine, EVO-99, undergoes tiered quality control that includes not just HPLC and mass spectrometry, but also heavy metal and residual solvent analysis by third-party laboratories. The industry landscape shifted after stricter enforcement of key regulatory frameworks, particularly for botanically derived actives. Our batches consistently record total heavy metal content <1 ppm, and we only release material to market after securing current certificates of analysis traceable from lot to lot.
Over the years, our documentation standards have evolved to anticipate not just current needs but upcoming regulatory demand. Early in the lifecycle of Evodiamine as an ingredient, only academic papers cared about full structural elucidation or biological contaminants. Now, customers expect — and regulators enforce — full disclosure of process, storage, and distribution data. Our in-house compliance team keeps auditing procedures current, and as new regulations emerge in major markets, we document chain of custody and sample retention for every outgoing kilogram.
The story of Evodiamine, as we have lived it, is not one of static, unchanging procedures. Every year brings fresh scientific reports — some highlighting novel pharmacological mechanisms, others flagging risks or calling for improved analytical rigor. Our R&D group reads these papers closely, and that reading steers our process improvements. It was through tracking research out of major Asian university labs that we first began optimizing for higher polymorph selectivity; crystalline form influences both solubility and long-term stability.
Field feedback pushes us further. Sometimes, a customer (whether academic or manufacturer) reports solubility issues in their final blend, and our chemists dig into why: usually particle morphology, sometimes scale-up impurities, rarely but importantly, a new degradation product under unique stress conditions. Each time, adjustments follow. We swap filtration media, test alternate vacuum drying parameters, and occasionally overhaul extraction conditions. The collective benefit is not only in troubleshooting but in pushing broader process efficiency.
In many conversations with technical buyers, we hear a question: can synthetic quinazoline alkaloids substitute for Evodiamine? In practice, our hands-on experience shows that they fall short in at least two areas. Natural extraction, when properly controlled, brings a unique impurity profile that synthetic analogs neither mimic nor always improve upon — some minor plant co-metabolites in our extracts actually enhance target receptor interaction, or avoid unanticipated byproducts.
Comparisons with other plant actives highlight more differences. For end users interested in metabolic research, Evodiamine sits apart from yohimbine or synephrine both in safety profile and breadth of biological activity. Human and in vivo animal studies, published across Asia and Europe, link Evodiamine to phase-specific thermogenic and anti-inflammatory action. Our manufacturing recipes allow us to fractionate and capture these nuances, so our product does not simply replicate a single activity, but preserves a fuller range of bioactivity as found in the original Evodia fruit.
Capsaicin-based blends carry a notorious reputation for skin irritation and regulatory hurdles. End formulations using our Evodiamine, in contrast, receive fewer consumer complaints for adverse reactions at matched dosages. Sports nutrition companies lean on this feature when launching topical or ingestible products targeted for regular use.
Lab customers and specialty pharma groups count on the availability of high-purity, traceable material. We supply analytical reference standards upon request, produced and characterized under the same scrutiny as commercial quantities. Having dealt with both GLP and exploratory research needs, our technical team understands the fine difference between a compound that reads pure and one that demonstrates full traceability.
Academic collaborators often require small pilot-scale runs, and this has become an important feedback loop for our R&D operation. Issue reports from pilot developers help us spot long-term storage instabilities or offer insights into alternative excipient compatibility. We have validated stability under both refrigerated and ambient storage over six months, enabling formulation projects with both standard and extended shelf-life requirements.
Raw material selection starts far upstream from the factory floor. Years of sourcing experience have taught us that Evodia rutaecarpa, the source plant, varies in alkaloid profile by harvest cycle and microclimate. Our agronomy team, working directly with traditional growers, conducts alkaloid assays in the field before any commitment to a bulk purchase. When a source shows substandard content, we simply reject it, regardless of market pressure. This approach means our customers never face the disappointment of underperforming product when their lot arrives.
Back at the manufacturing site, crude extract undergoes sequential solvent partitioning and column chromatography to separate Evodiamine from co-extracted oils, fatty acids, and related alkaloids like rutaecarpine. Each fraction is monitored, sample by sample, with results shared internally in real time. Combined with our internal stability testing, this strategy lets us keep each lot tightly within spec, so finished goods maintain the same high alkaloid content year after year.
Customers who blend Evodiamine into dietary supplements, creams, or research mixtures notice one simple fact: the raw ingredient sets the ceiling on product performance. If the initial material contains uneven particle size, surplus solvent, or elevated heavy metal content, every step downstream becomes a patch job. By staying on top of upstream and final QC, we eliminate many headaches for finished-product manufacturers.
The feedback loop is direct. In one instance, a supplement maker cited separation in a capsule blend. Our technical team traced it to solvent residues just within legal limits, but high enough to disrupt miscibility in that customer’s specific blend. The next batch, immediately, included adjusted drying times — separating us from competitors who may not even hear about post-sale issues. This is the sort of continuous improvement we have built into our process not for marketing, but for the practical reason that our customers rely on stability and repeatable performance.
We recognize that industry trends are raising the bar for ingredient manufacturers. Evodiamine, with its complex plant sourcing and limited global supply, can wind up the target of adulteration or substitution with inferior extracts. Our in-house and third-party spectroscopic fingerprinting eliminates doubts at the batch level. Year after year, we build supplier relationships, audit fields, and run chemical identity testing on every incoming raw material lot. End users rarely glimpse this side of the business, but it underpins the reliability of every kilogram we ship.
For formulation groups aiming to launch new products, the next challenge often becomes regulatory clearance. We have navigated ingredient registration in dozens of markets and know from experience how critical it is to document every aspect — from genetic authentication of the source plant to full synthetic route mapping where applicable. Customers who need assistance with regional documentation, even label guidance, can work with our technical affairs group who draw from direct regulation-facing experience, not generic consultancy.
Longer term, sustainability and environmental compliance grow more important each year. Our manufacturing facility operates a closed-loop recycling system for key solvents and water. This approach keeps us well within discharge limits and reduces costs at the same time. As the world shifts toward greater environmental scrutiny, we continue to invest in cleaner, safer processes that align with both current regulations and expected future requirements.
For anyone seeking Evodiamine, there are many options these days — intermediaries, resellers, offshore brokers. As the manufacturer, we offer direct access to every stage of production, with every kilo backed by traceable history and in-house technical support. We have seen how direct communication with the factory, rather than through an anonymous network, makes a difference to the people formulating, blending, and researching with these materials.
Evodiamine’s reputation as a high-value bioactive is well earned, but its real benefits emerge through careful manufacturing, quality control, and a willingness to adapt alongside scientific progress. Our story with Evodiamine keeps evolving, shaped by advances in chemistry and steered by conversations with customers intent on reliable solutions. We view each batch as another opportunity to deliver value — not just in the molecule, but in the partnership and knowledge we bring to every project.
For those working on next-generation formulations, or seeking a dependable source of high-purity Evodiamine, we stand by our product with the long-term experience and proven traceability that only a true manufacturer can demonstrate.