|
HS Code |
689886 |
| Cas Number | 486-89-5 |
| Molecular Formula | C12H18N2O |
| Molecular Weight | 206.28 |
| Iupac Name | 1,2,3,4,5,6-hexahydro-5-methyl-2,3-methanobenzo[g][1,6]naphthyridin-7(1H)-one |
| Synonyms | N-Methylcytisin, Methylcytisine |
| Appearance | White to off-white crystalline powder |
| Melting Point | 151-153°C |
| Solubility | Soluble in water and ethanol |
| Pubchem Cid | 73962 |
As an accredited N-Methylcytisine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | N-Methylcytisine, 10g, is packaged in a sealed amber glass bottle with a tamper-evident cap and clear labeling. |
| Shipping | N-Methylcytisine should be shipped in tightly sealed containers, protected from light and moisture. It must be packaged according to applicable chemical transport regulations, ensuring clear labeling of hazards. Use secondary containment to prevent leaks, and include relevant safety data sheets (SDS) with the shipment. Handle with care to avoid breakage or spillage. |
| Storage | **N-Methylcytisine** should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed when not in use, and avoid exposure to moisture. Store separately from strong oxidizing agents and acids. Use appropriate chemical-resistant containers, and clearly label storage vessels to prevent accidental misuse or contamination. |
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N-Methylcytisine has its roots in nature, originally isolated from Laburnum and related plants, but reaching its full chemical potential inside a controlled manufacturing environment. After working with cytisine and its analogs for nearly two decades, the unique profile of N-Methylcytisine continues to intrigue both chemists and product developers. Its molecular backbone – C12H16N2O – features a fused bicyclic structure with a methyl group replacing hydrogen on the nitrogen atom, making it more than just a minor chemical tweak.
The story behind N-Methylcytisine starts with alkaloid research. Natural cytisine saw early study as a smoking cessation aid. By methylating the molecule at the nitrogen, we adjust its chemical behavior: the compound’s basicity, solubility, and interaction with biological targets change. This difference isn’t just theoretical – applications show measurable results, both in the lab and in the field.
We manufacture N-Methylcytisine in batches to ensure consistency. A typical batch follows a route beginning with plant-based cytisine, subjected to selective methylation using mild reagents to avoid over-alkylation. Over the years, improvements to this process have driven purity to levels exceeding 98% by HPLC – a point of pride and the outcome of relentless tweaking, not just a typical outcome. By keeping side reaction conditions controlled, we avoid generating excessive byproducts or residual solvents, which can be tough to separate by traditional means. Each lot gets full analytical work-up: NMR, MS, and HPLC profiles are compared against in-house standards rather than generic references. That means any shift in purity gets caught before a drum even leaves the warehouse.
Water content remains below 0.5%, confirmed by Karl Fischer titration, so our customers avoid surprises in downstream reactions. Because even minor levels of organic impurities matter in active pharmaceutical ingredient development, we routinely exceed the specification call-outs many formularies adopt. Anyone working on scale-up or regulatory submissions can see the difference between a product batch prepared to these standards versus a more commodity-grade material.
Having seen both types of molecules through from kilo to ton scale, the differences aren't minor. Cytisine, the parent compound, displays higher polarity and tends to crystallize differently. This affects not just formulation choices but also how researchers design synthetic routes, especially those working on derivatives or structure-activity relationship studies in neuropharmacology. N-Methylcytisine, with its methylated nitrogen, exhibits improved membrane permeability and modified receptor binding. Unlike nicotine itself, which carries additional toxicity and is regulated more restrictively, N-Methylcytisine enables researchers to explore nicotinic acetylcholine receptor (nAChR) selectivity without the burden of heightened handling restrictions and hazardous storage.
Some customers compare our product to synthetic analogues imported from overseas. We document the full chain of custody for every parameter, unlike many competing analogs that carry uncertainty in their provenance. Synthesizing at scale means we test every phase, from solvent residues to crystallization solvents, and that translates to replicable performance batch after batch.
The utility of N-Methylcytisine owes a lot to its clean pharmacological profile. In our observation, the bulk of interest lies in two arenas: research into central nervous system stimulants and plant-derived insecticidal agents. Universities and biotech firms often approach us for material intended for receptor binding assays, preclinical pharmacokinetics, or as a reference compound in high-throughput screening campaigns. Synthesizing reference libraries of nAChR agonists has worked best with our high-purity N-Methylcytisine, as impurities otherwise distort analytical and biological results.
Beyond pharma, agricultural chemical developers study its impact as a model for selective insect control. Many botanical insecticides suffer from variable content and batch inconsistency. Synthetic N-Methylcytisine, with its defined structure and purity, provides the reproducibility required for proper data comparison in field studies. We have supplied gram and kilogram lots for such efforts spanning multiple continents, adapting to project needs as protocols evolve.
Working hands-on with N-Methylcytisine sets expectations straight. It arrives as a white to off-white crystalline solid with a melting point in the range of 146°C to 148°C. Our drying and packaging processes cut down the potential for clumping seen with less refined alkaloid extracts. The compound carries a mild, non-pungent odor, which helps in day-to-day laboratory handling. We pack material in polyethylene-lined drums or glass bottles depending on order size and customer requirements for trace metal avoidance.
Transport and long-term storage have proven uneventful, thanks to the molecule’s stability under ambient conditions. No special refrigeration needed, just a cool, dry spot away from direct sunlight, which aligns with practical workflows at most R&D and manufacturing sites. N-Methylcytisine dissolves well in water, ethanol, and most organic solvents commonly encountered in downstream chemical transformations. Our documentation details recommended work-up protocols, but over the years, our partners have shared their own experiences in solid-phase extractions and column chromatography, giving further weight to its practical adaptability.
Our journey toward sustainable production started at the roots – literally. Sourcing cytisine from responsibly harvested plant biomass remains challenging, as wild stands fluctuate in yield, and overharvesting threatens ecological stability. That prompted us, years ago, to invest in cultivated plantations working with regional agricultural cooperatives. Tracking plant growth cycles and controlling harvest intervals, we help ensure raw plant availability year after year. Each consignment comes with documentation confirming its origin and compliance with biodiversity and conservation guidelines, so that every customer can trace the story back to living soil, not an anonymous bulk supply.
Following raw material through the chemical synthesis and purification steps, we recapture solvents and minimize waste streams. By finding secondary uses for spent plant matter and using closed-loop solvent recycling, we have steadily reduced the footprint of our overall operation. These changes arose from small stepwise adjustments to equipment and workflow rather than a one-size-fits-all manufacturing overhaul – the kind of progress slow and steady chemical work encourages.
No raw material is infinite. Shifts in harvest yield, changes in international export regulations for plant alkaloids, and supply chain disruption impact every production cycle. We maintain a supply pipeline that blends inventory management with forward contracting among partner growers in different regions. Regular dialogue with farming communities reduces the risk of bottlenecked supply just as effectively as technological advances in extraction processes.
N-Methylcytisine’s market faces its own regulatory scrutiny. With increased attention paid to plant alkaloids and their derivatives, staying ahead of compliance isn’t about checking boxes. Our in-house regulatory staff track changing requirements, preparing documentation ahead of announced legislation to help customers move through import-clearance procedures. The scientific case for N-Methylcytisine as a lower-toxicity alternative to nicotine carries weight with regulators and supports wider adoption among corporate buyers seeking less hazardous nAChR models.
For years, customers asked us to push batch sizes higher without sacrificing the clarity and analytical sharpness found in gram-scale runs. That challenge led us to replace some classical purification steps by adopting new solid-support adsorbents and high-throughput liquid chromatography. This switch reduced the need for large solvent volumes and shaved time from large-scale runs. The data coming off these processes offer better impurity profiling, which lends assurance both to our QC team and to end users trusting a single run for their next phase of synthesis.
Our relationship with N-Methylcytisine’s users doesn’t end at shipping. Technical feedback from researchers, pharmaceutical formulators, and agrochemical developers cycles directly into product improvements. On multiple occasions, customer trial results exposed a trace impurity that standard QC methods picked up only after we reviewed GC-MS profiles together. In each such case, refining our batch-testing criteria and introducing targeted clean-up steps helped not only resolve the issue but prevented recurrence further down the line.
Open dialogue about synthetic modifications has also produced a handful of route optimizations with measurable industrial impact. For one group working with radiolabelled analogs for imaging, we modified the synthetic order and achieved cleaner incorporation of isotopic methyl groups. That change reduced the time and cost per dose for the end-user’s imaging kits while making post-synthetic clean-up far simpler. These sorts of adaptations happen less frequently with less transparent supply chains, and they illustrate the advantages of dealing directly with a manufacturer.
No set of written specifications fully substitutes for lived production experience. Any deviation—be it a missed pH adjustment or a wrong batch temperature—can introduce variation that goes undetected by anyone not monitoring the process closely. In our shop, process engineers and QC staff talk through run details after each shift, corroborating findings to ensure no anomalies slip through. In one memorable case, a subtle seasonal change in plant cytisine content shifted reaction yields. Close communication along the line allowed us to adjust starting material load, which kept end-product quality uniform through the rest of the season.
Traceability matters not only for regulatory compliance but because it builds confidence. Every N-Methylcytisine consignment comes tagged to raw plant input, intermediate lots, work-ups, and finished drum weights. Internal audits do more than check paper trails; they uncover minor variations in drying efficiency or packing improvements that, once addressed, reduce caking and improve redissolution rates for all future deliveries.
Chemical manufacturers today face pressure from evolving guidelines in pharmaceutical and agrochemical sectors. N-Methylcytisine, sitting between legacy cytisine analogs and custom-synthesized nAChR models, falls under review in several destination countries as both a research chemical and a reference substance. Supporting customer submissions under these different regulatory umbrellas takes time and coordination, but clear documentation and openness about every batch’s provenance accelerate the process.
Years of export experience have given our logistics team a healthy skepticism of shipping documentation from unvetted suppliers. Each international shipment includes the analytical data package, origins documentation, and shipping declaration, so customers avoid delays based on incomplete paperwork. In some countries, importers needed less than a week to process their clearance thanks to this level of preparation. These are small successes, but they matter for buyers operating on fixed project timelines.
Every chemical presents a profile of risk and reward. N-Methylcytisine, while less toxic than nicotine, requires careful handling to avoid accidental ingestion or chronic exposure. Our in-house health and safety protocols, refined through countless campaign runs, recommend standard laboratory PPE, local exhaust ventilation, and avoidance of open handling in high-traffic spaces. Those working pilot-plant scale runs prefer closed-transfer systems to further reduce the risk of operator exposure. The crystalline solid’s modest volatility helps, but routine glove and goggle use keeps long-term exposure minimal.
We routinely cross-reference published toxicology data with real-world incident reporting from industrial and academic partners. Customers find that our documentation of oral and dermal LD50 values, plus case-specific guidance for clean-up and accidental exposure, saves time during internal hazard reviews and improves research planning. Our production staff undergoes routine medical checkups and training on changes in recommended exposure limits, incorporating best practices as new evidence emerges.
N-Methylcytisine’s end-users span departments from discovery chemistry and molecular biology to field trial teams and pilot formulators. Not every scale or application fits the same mold. We have tailored our customer service to deliver both small research pack sizes and repeated large-volume replenishments, without drop-off in documentation or responsiveness. Bulk buyers appreciate advance scheduling for recurring deliveries, while academic teams often need single-use bottles packaged free of trace metals for sensitive assay work.
At times we field urgent requests from organizations encountering process bottlenecks—a shipment delayed, a competing supplier unable to provide batch-level data, or the need for a certificate of analysis matching a unique regulatory demand. These circumstances direct us to treat every inquiry as a partnership, not a transaction, bringing what we know about synthesis, compliance, and technical support to bear.
N-Methylcytisine stands apart from mass-market fine chemicals due to the hands-on knowledge built into each production run. From deliberate raw material selection and methodical purification to constant dialogue with those actually putting the product to use, a manufacturer’s eye adds clarity that trickles into every shipment. Our path, built over years of refining both plant extraction and laboratory processing, reflects both problem-solving tenacity and collaboration with scientific partners around the world. Each lot shipped carries not just a set of analytical results but a commitment born from decades of behind-the-scenes work in alkaloid chemistry. For the customers pushing the boundaries of pharmaceutical and agricultural science, N-Methylcytisine remains more than just a commodity molecule. It is the distilled result of applied experience—science done at plant, bench, and pilot scale, ready for the next phase of discovery.