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Monocrotaline

    • Product Name Monocrotaline
    • Alias Monocrotalin
    • Einecs 207-017-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    Specifications

    HS Code

    572625

    Cas Number 315-22-0
    Molecular Formula C16H23NO6
    Molecular Weight 325.36 g/mol
    Iupac Name 7,8-Didehydro-4,5α-epoxy-3,14-dihydroxy-2,3,4,5-tetrahydro-6-methoxy-1,2,3,4,5,6-hexahydro-15-methyl-pyrrolizidine[1,2-a]quinolizine-1-carboxylate
    Appearance White to off-white crystalline powder
    Solubility Slightly soluble in water, soluble in ethanol
    Melting Point 148-151°C
    Source Isolated from Crotalaria species (plants in the Fabaceae family)
    Toxicity Hepatotoxic, pneumotoxic, and nephrotoxic; classified as a pyrrolizidine alkaloid
    Storage Conditions Store at 2-8°C, protect from light and moisture
    Synonyms Monocrotalin, Monocrotaline free base
    Usage Commonly used in research for inducing pulmonary hypertension in animal models

    As an accredited Monocrotaline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Monocrotaline, 1 gram, is packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping Monocrotaline is shipped as a hazardous chemical, requiring packaging in tightly sealed containers to prevent leakage. It should be clearly labeled with hazard warnings and shipped in compliance with local, national, and international regulations. Transport is usually via ground or air in specialized containers, with documentation for safe handling and emergency procedures.
    Storage Monocrotaline should be stored in a tightly closed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as oxidizers. Store at room temperature (15–25°C), and ensure it is clearly labeled as toxic. Access should be limited to trained personnel using appropriate protective equipment.
    Application of Monocrotaline

    Purity 98%: Monocrotaline with purity 98% is used in pulmonary hypertension animal model studies, where consistent induction of vascular remodeling is achieved.

    Molecular weight 325.36 g/mol: Monocrotaline with molecular weight 325.36 g/mol is utilized in endothelial injury experiments, where reproducible endothelial dysfunction is observed.

    Melting point 148°C: Monocrotaline with melting point 148°C is applied in pharmaceutical research synthesis processes, where thermal stability ensures process reliability.

    Solubility 10 mg/mL (DMSO): Monocrotaline with solubility 10 mg/mL in DMSO is employed in dose-dependent cytotoxicity assays, where precise concentration control enhances experimental accuracy.

    Stability temperature 4°C: Monocrotaline with stability at 4°C is used in long-term storage protocols, where extended shelf-life supports laboratory inventory management.

    Particle size <50 µm: Monocrotaline with particle size less than 50 µm is incorporated in targeted drug delivery development, where uniform dispersion optimizes formulation homogeneity.

    UV absorbance 260 nm: Monocrotaline with UV absorbance at 260 nm is used in analytical quantification workflows, where sensitive detection facilitates compound monitoring.

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    Certification & Compliance
    More Introduction

    Monocrotaline: Our Direct Experience as a Chemical Manufacturer

    Monocrotaline crystallizes years of effort in the lab and the plant. As chemists and manufacturers, we've been drawn to monocrotaline's structure—a pyrrolizidine alkaloid found in several Crotalaria species—and we have worked to refine the process that brings high-purity material into researchers’ hands. Its molecular structure, C16H23NO6, presents not only unique chemical reactivity but a fascinating biological profile that demands careful manufacturing and handling. Delivering it with the right integrity depends on small details: solvent purity, control of reaction temperatures, and careful monitoring of all intermediates. We take these seriously because we know the applications often go well beyond the bench.

    Technical Details Born of Real Manufacturing

    Our monocrotaline comes in white to pale yellow crystalline powder, typically at a purity of 98% or higher (measured by HPLC and confirmed by NMR). From our first year synthesizing this compound, we identified the need for reliable, low-residue synthesis routes. Any byproducts or contaminants—even in the sub-percent range—cause unpredictable results in bioassays or analytical studies. This isn't about echoing supplier data; it's about long conversations on the production floor, the challenge of consistent batch crystallization, and the adjustments needed when humidity creeps up during certain seasons.

    Available forms include analytic and research grades, with the most requested lot size ranging from milligrams to multi-gram packages. We keep monocrotaline in vacuum-sealed vials, stored at low temperature to prevent hydrolysis and oxidation—finding, through trial and error, that uncontrolled storage can ruin months of production in days. In our production notes, sharp odors or visible yellowing trigger a stop.

    Monocrotaline in the Real World of Research

    End users have pushed monocrotaline into diverse domains, starting with pulmonary hypertension research, toxicology, and organ injury modeling. Academic and pharma labs turn to us expecting to see the consistency that lets their protocols succeed or fail on their terms, not ours. When your project hinges on the biochemical effects of pyrrolizidine alkaloids, batch irregularities—whether in the alkaloid itself or in simple moisture levels—can erase months of work.

    Scientists often select monocrotaline because it reliably induces pulmonary vascular and right heart changes in rodent models. The point is not just to replicate historic results but to run modern studies with higher reproducibility. The smallest contaminants complicate interpretation, so a manufacturer’s internal controls matter much more here than in a bulk commodity. We stand behind certificates that reflect our real-world QC: tightly monitored batch logs, rigorous analytical tests, and a readiness to discard any batch that doesn’t achieve our full list of criteria.

    What It Takes to Manufacture Monocrotaline Well

    Producing monocrotaline isn’t about scaling up a literature method. Each production run builds on practical learning: the purification stages require recurring adaptation to raw material variability, trace solvent carry-over, and strict temperature control. Our plant teams have learned how crucial the final crystallization conditions are. Small deviations result in changes in solubility profiles, impacting either the yield or the material’s performance in animal studies. Only hands-on operators who have spent time physically working with the compound will know that.

    We’ve focused on minimizing batch-to-batch variation. This leads us to invest in small details, such as column chromatography using precisely specified particle sizes and regular calibration of our analytical balances. Chasing these details isn’t academic—it stems from the feedback of research partners describing unexpected day-to-day drift in their results with materials from less experienced sources. Consistency starts at the drum level and moves all the way through to individually checked vials.

    Distinguishing Characteristics—Not Just Numbers on a Spec Sheet

    Having produced a wide range of alkaloids for decades, we see how monocrotaline sets itself apart. Structurally, its unsaturated necine base and the functionality of its side chains influence not just its pharmacology but its reactivity under common extraction and purification processes. We have tried standard approaches with other pyrrolizidines but quickly learned monocrotaline demands lower process temperatures and greater humidity control.

    Compared to its analogs like retrorsine and senecionine, monocrotaline’s melting point and solubility differ enough to require customized purification schedules. Retrorsine or senecionine can tolerate slightly broader pH ranges in solvent extractions; monocrotaline degrades under marginally alkaline conditions. This is not just a note in a manual—it’s an observation from failed early purifications and subsequent refinement of our process.

    Unlike larger-volume phytochemical extracts, pure monocrotaline isolates have precise requirements for container compatibility. We’ve had instances where standard plastic vials led to subvisible leaching when batches sat for several weeks. Glass vials with Teflon-lined caps proved to be the best container, something only discovered after running extended stability trials and looking at aggregate formation in analytical assays.

    Safety: Drawing from Decades of Direct Handling Experience

    Anyone preparing monocrotaline must know its hazardous nature; it's well-documented in peer-reviewed research and in practical experience. Inhaling powders or letting them contact bare skin is never acceptable. Our team puts this at the center of every workplace SOP. Not because the MSDS demands it, but because we’ve dealt with the consequences of improper handling—just one unplanned exposure incident taught the shop crew to double-layer gloves and reinforce fume hood checks. We supply every batch in double containment, and we advise against opening containers outside controlled lab spaces.

    Ours is a production environment that cannot afford slipups on toxin control. High-efficiency particulate filtration and sealed transfer are minimum standards. We hold specific training workshops for new operators, walking them through monocrotaline batch history—failures included—so they see what vigilance looks like in real-life operations, not just on paper.

    Applications: Genuine Feedback from the Field

    Many of the world’s research groups studying pulmonary hypertension come back for monocrotaline, sometimes after trying alternate suppliers. They notice lower variance in their rodent response rates with material directly from us—feedback that pushes us to keep investing in process improvements. Graduate students working on mechanism-of-action studies often share both their positive outcomes and failed experiments; both forms of feedback shape our ongoing QC routines.

    In toxicology, monocrotaline remains a key agent for studying pyrrolizidine alkaloid-induced damage, especially in hepatic and pulmonary models. A significant portion of our dialogue with users revolves around preparation of dosing solutions—stability in saline versus buffered vehicles, and challenges in dissolving precise milligram quantities. We’ve learned practical tips here: using freshly prepared solutions and handling at cool temperatures minimize degradation. These aren’t suggestions lifted from papers—they come from customers’ troubleshooting sessions and our own lab verifications.

    We also supply monocrotaline to groups investigating biotransformation pathways. Isolating and characterizing its metabolites in biological matrices show just how much storage and purity impact experimental outcomes. Seeing research halted by contaminated samples motivated us early on to test every outgoing batch with both LC-MS and NMR screening.

    Addressing Contamination and Stability: What the Manufacturer Sees

    Every season, we face contamination risks from plant-derived alkaloids as well as synthetic byproducts. For years, we used to lean on basic silica gel purification; long-term observations showed persistent trace residues that inconsistently affected bioactivity. Improved column packings and gradient protocols took years to optimize, informed by both internal failures and published analytical findings. We sometimes run parallel timeline studies to monitor degradation, confirming loss of specified chemical signatures in humidity-exposed vials. It isn’t glamorous, but it means every customer batch reflects the best of what we’ve learned—never just lab recipe replication.

    Freshness matters in monocrotaline, more so than other stable alkaloids. We gained this insight after hearing about divergent toxicity results traced back to lot age. Standard room-temperature storage caused slow but measurable breakdown over months, leading us to implement cold chain handling for both intermediate and finished goods. Shipping also features tamper-proof secondary containment, which prevents environmental shifts during long transits. These real-world fixes grew naturally from repeatedly encountering, and then fixing, problems others only mention as footnotes.

    Why Monocrotaline from a Manufacturer Matters

    Research-grade chemicals from a direct manufacturer, as opposed to a distributor, bring more than a certificate and a label. Working with monocrotaline, we have internal oversight at every step: from start-of-lot reviews to end-of-run analytical checks. If a batch shows even slight irregularities, we have the power to stop and remake it—no delays, no negotiation. Customers can speak directly to a chemist who witnessed the batch instead of reading through templated replies from a distant call center. 

    This vertical integration shows up in every step: new lot testing, real-time coordination with logistics, and a willingness to delay release rather than offer a borderline product. We routinely collaborate with principal investigators to meet unique research needs, adjusting lot size or packaging according to protocols. In certain cases, researchers have visited our facility to see the process firsthand and join risk assessments for high-hazard compounds.

    Complexities Unique to Monocrotaline—And Solutions We’ve Learned

    It is tempting to see monocrotaline as just another small molecule, but longevity in manufacturing teaches humility and careful respect. We manage potential process issues—variable yields, problematic crystallizations, heat sensitivity—by building redundancy into our QC pipeline. Double checks, duplicate analytical runs, and continuous operator training turn what could be a risky guesswork exercise into a robust, reliable routine.

    No discussion of monocrotaline makes sense without acknowledging shipment logistics. As a regulated toxin in many jurisdictions, transport requires advance planning, customs documentation, and, often, direct communication with receiving labs to coordinate safe delivery. We learned to maintain traceability on every vial, so we know exactly which batch scientist “A” in one country ends up with. Record-keeping goes well beyond compliance here: incidents of mis-shipment, thankfully rare, get full forensic review and changed protocols if needed.

    Looking Forward: Commitment Rooted in Hands-on Knowledge

    We are not bystanders in the science of monocrotaline. As manufacturers, we stay embedded in the daily challenges—not only of production but of listening to the scientific community’s evolving needs. We know many researchers expect raw, honest technical support rather than generic assurances. Our role is to make sure every batch, every shipment, and every conversation reflects the depth of experience gained over years of production, not just what appears on a product webpage. 

    Monocrotaline from our plant isn’t just a SKU—it’s the end result of persistent effort, adaptation, and respect for the challenges it brings. We understand the reasons behind purity thresholds, the science behind stability tricks, and the human stories behind every research project. This ongoing partnership with scientists worldwide creates the feedback loop that makes each run better than the last.