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HS Code |
753289 |
| Chemical Name | Arecoline |
| State | Free (base) |
| Molecular Formula | C8H13NO2 |
| Molecular Weight | 155.196 g/mol |
| Appearance | Colorless to pale yellow oily liquid |
| Boiling Point | 208-209°C |
| Solubility In Water | Moderately soluble |
| Density | 1.009 g/cm³ |
| Melting Point | Less than 0°C (liquid at room temperature) |
| Odor | Pungent, characteristic |
| Cas Number | 300-08-3 |
| Pka | 6.8 (approximate) |
| Refractive Index | 1.484 |
| Stability | May darken on exposure to air or light |
| Storage Conditions | Store in a cool, well-ventilated place away from light |
As an accredited Arecoline In Its Free State factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Arecoline in its free state is supplied in a 10g amber glass vial, securely sealed, with hazard labeling and desiccant included. |
| Shipping | Arecoline in its free state should be shipped in tightly sealed, chemical-resistant containers under controlled temperature conditions, away from light and moisture. Packaging must comply with hazardous materials regulations due to its toxic and volatile nature. Ensure labeling includes hazard warnings, and transport follows local and international chemical shipping guidelines. |
| Storage | Arecoline in its free state should be stored in a tightly sealed container, under an inert atmosphere (such as nitrogen or argon), and kept in a cool, dry place away from light and moisture. It should be isolated from incompatible substances, including strong oxidizers and acids, and stored within a designated, well-ventilated chemical storage area with secure, appropriate labeling. |
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Purity 98%: Arecoline In Its Free State with 98% purity is used in pharmacological research, where it ensures reliable neuroreceptor interaction studies. Molecular Weight 155.23 g/mol: Arecoline In Its Free State at 155.23 g/mol is used in chemical synthesis, where it provides predictable reactivity in alkaloid derivative production. Melting Point 43°C: Arecoline In Its Free State with a melting point of 43°C is used in formulation development, where it facilitates ease of handling during controlled heating processes. Stability Temperature 25°C: Arecoline In Its Free State stable at 25°C is used in storage-sensitive applications, where it maintains compound integrity in ambient laboratory conditions. Viscosity Grade Low: Arecoline In Its Free State of low viscosity grade is used in liquid phase extractions, where it enables rapid diffusion and uniform mixing. Optical Rotation +22°: Arecoline In Its Free State with optical rotation of +22° is used in chiral analysis, where it confirms enantiomeric purity for stereoselective synthesis. Particle Size Under 50 μm: Arecoline In Its Free State with particle size under 50 μm is used in microencapsulation techniques, where it improves dispersion and encapsulation efficiency. Solubility in Water 80 mg/mL: Arecoline In Its Free State soluble at 80 mg/mL in water is used in injectable formulations, where it allows for precise dosage preparation. |
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Arecoline has held the attention of chemists and researchers for its unique profile among alkaloids. We manufacture arecoline in its free state based on years of hands-on production experience in organic synthesis. Free state arecoline stands apart from its salt forms, displaying a distinct volatility, purity, and solubility profile.
Arecoline in free base form is a colourless to pale yellow liquid, known for its characteristic odor and high reactivity. It’s a naturally occurring alkaloid, originally isolated from the areca nut, but our lab process guarantees purity beyond botanical extraction, removing extraneous plant constituents and minimizing contamination with related alkaloids such as arecaidine and guvacine.
The free base is hydrophobic, readily soluble in organic solvents but only sparingly so in water. This property favors applications in research settings where precise separation, specific solvent compatibility, or subsequent derivatization is needed. Chemically, the free state makes available the tertiary amine functional group, as opposed to the protonated salt, allowing direct access in alkylation, methylation, or quaternization reactions.
In the world of alkaloids, the state of the molecule often dictates its application and shelf life. The arecoline hydrobromide and hydrochloride are the most common salts found in commercial and academic contexts; they bring water solubility but at the expense of the free amine reactivity. Many researchers initially gravitate toward the salts due to ease of handling and stability, but work involving organic synthesis or biochemical assay often pivots to the free base for its adaptability.
From a manufacturing stance, producing arecoline in its free state requires additional expertise. The compound’s volatility and hygroscopic tendencies demand strict control of environment and packaging. Our proprietary distillation and purification methods minimize exposure to air and moisture, mitigating risk of self-polymerization and hydrolysis, common pitfalls among less controlled processes. We find this discipline vital, because even trace byproducts like epoxides or N-oxides can interfere with downstream chemistry or skew experimental results.
We have spent years refining our crystallization and vacuum distillation steps. Analytical testing, including gas chromatography and NMR, verify that each batch meets or exceeds benchmarks for pharmaceutical and academic research. Purity, water content, and amine value are critical for performance in drug metabolism studies, synthetic transformations, or even entomological bioassays, where arecoline acts as a model cholinergic agonist.
Manufacturing isn't just a business; it is continual problem solving. Arecoline in its free form illustrates this truth clearly. Early in our history, we encountered persistent issues with oxidative degradation—exposure to oxygen during purification promoted the formation of tars and colored byproducts. This wasn't just a cosmetic issue; it compromised downstream syntheses and reduced trust in the product among industrial clients and researchers.
We now use inert gas blanketing throughout handling and storage. Nitrogen or argon maintains the integrity of the free base, preserving its characteristic clear, nearly colorless appearance batch after batch. Moisture control, from room environment to specialized glassware, further shields the compound during bottling. These protocols, developed through hands-on experience, keep oxidation below detectable levels and extend shelf stability—a benefit seen directly in regular third-party lab results and client feedback.
Our team’s experience runs across small gram-scale batches for academic research, up to multi-kilo production for pharmaceutical intermediates. The challenges change with scale—notables include increased risk of exothermic reactions during phase transfer, and new forms of byproduct precipitation in bulk. Scaling up without sacrificing quality takes more than following a recipe; it requires continuous vigilance, attention to thermal control, and responsive adjustments in crystallization temperature, vacuum level, and reaction time.
Supply chain traceability remains a focus. Raw materials, especially substrates derived from plant origin, can vary batch to batch. We source synthetic intermediates from closely monitored suppliers, and audit each lot through our own suite of analytical checks, including HPLC, IR, and elemental analysis. This long-view approach reduces surprises, providing our customers with consistency one can recognize in results, not just paperwork.
Arecoline’s range of uses keeps expanding as research develops tools to probe cholinergic mechanisms, neurobiology, and related pharmacological pathways. The free base’s profile makes it a preferred choice where solvent flexibility or unmodified amine character are key.
Chemical synthesis employs free state arecoline in derivatization routes, where the reactivity of the tertiary amine is preserved, allowing alkyl group extensions, conjugation to larger cores, or transition metal-catalyzed transformations. The salt forms simply lack this chemical openness; their cationic nature can block or hinder such transformations, limiting their use to situations demanding water compatibility over synthetic flexibility.
In neuroscience research, arecoline serves as a potent muscarinic acetylcholine receptor agonist. Labs testing receptor activity, either in vitro or using small animal models, cite difficulty sourcing a stable free base for DMSO or ethanol-based formulations. Our product makes experiments more reproducible and maximizes dosing precision, as quantitation does not have to back-calculate counterions that might be present in salts.
There are also veterinary and invertebrate biology applications. Certain species, including insects, display unique cholinergic profiles where arecoline triggers differential responses versus its salt or plant extract equivalent. Researchers focused on animal pharmacology or toxicology tell us that the free base gives more reliable data on receptor subtype selectivity, devoid of possible confounding effects from accompanying plant alkaloids or buffer salts.
Despite known concerns about its toxicity outside the lab, careful handling and accurate formulation make the compound indispensable in several fields. We partner closely with our customers, providing application guidance based on observed successes and hazards we've seen throughout the supply chain.
As a chemical manufacturer, product stewardship shapes our entire workflow. Arecoline’s inherent hazards—ranging from acute toxicity to potential misuse—require more than what standard chemical manufacturing delivers. Regulatory changes alter access for all actors in the supply chain. Our approach centers on transparency with both academic and industrial partners. We maintain compliance documentation including certificates of analysis, full chain-of-custody records, and hazardous goods transport validation.
We do not view compliance as box-ticking. Our plant engineers and QC supervisors train each new worker in spill, exposure, and waste handling specific to arecoline, not just generic solvents or common laboratory acids. Clean-up procedures match local and international standards. Waste streams, including aqueous and organic material, are segregated and neutralized before disposal. This detail matters: lingering traces of arecoline or its breakdown products in wastewater could pose risks to plant operators or downstream users, both inside and outside the factory fence.
Counterfeit or off-specification arecoline remains a real problem in some sourcing channels. We have seen samples purchased off-market or via third-party brokers that contain hazardous adulterants, pesticides from raw plant feedstock, or even substitution with less potent cholinergic agonists. Each batch leaving our facility carries a full analytical dataset, including spectroscopic scans, so clients know not just purity percent, but the exact composition and absence of trace contaminants. Repeat customers often comment that the reliability of our arecoline sets their research timeline, making it possible to plan with confidence.
Logistics represent another piece of the puzzle. Temperature excursions in shipping, poorly sealed containers, or extended customs holds can degrade sensitive materials like arecoline. Based on our historical delivery data, we use specialized, sealed ampoules or inerted glass bottles, packed against temperature swings and labeled for urgent transit. These practices have cut spoilage and delay to near zero on our end, and we guide buyers toward appropriate handling and storage upon receipt, with extensive handoff documentation.
Years of manufacturing has taught us that downstream success starts far upstream. Arecoline’s safety profile gets close attention; our offering includes direct advice on both laboratory-scale and industrial safety strategies. Our technical staff consults with buyers about ventilation, protective equipment, and waste management specific to free state arecoline rather than defaulting to plant extract or salt protocols.
We produce a technical bulletin with each shipment, drawing from real-world case studies and accident reports gathered over decades in the field. These resources highlight not just correct handling, but also mistakes and mishaps observed both on the production floor and in client labs. Sometimes, these are as simple as incorrect storage temperatures, leading to discoloration or increased toxicity upon degradation. In rarer cases, improper mixing with incompatible solvents has led to runaway reactions or exposure incidents. Sharing these lessons makes upstream manufacturing standards directly tangible to the end user’s daily routines.
Security and stewardship also matter more than ever. Arecoline’s regulatory status varies worldwide, and we stay informed about each market’s shifting requirements. Our compliance manager tracks export controls and proactively updates customers if local changes will affect delivery or reordering. Over time, this builds a partnership that goes beyond the shipment—it is a two-way channel for feedback, updates, and mutual improvement.
Our work with free state arecoline continues to evolve with new research directions and manufacturing technology. We are actively exploring process intensification, including flow chemistry, to further reduce impurity profiles and energy use. Even modest improvements in distillation efficiency or material yield can drive down cost per gram and further limit environmental footprint.
Feedback from research groups and industrial labs helps guide our product development. Requests for isotopically labeled arecoline, for example, have prompted us to revisit precursor availability and reaction pathway design. Each new iteration comes after pilot-scale trials and feedback cycles, not just from our internal team but from the most experienced users as well. This collaboration has led to more thermally stable packaging, improvements in shelf life, and better approaches for cold-chain shipping.
We also participate in larger industry groups shaping best practices and ethics for manufacturing alkaloids and associated intermediates. By supporting pre-competitive regulatory science, we help set safer benchmarks that improve global supply chain resilience. Adopting and adapting green chemistry principles sits high on our agenda. Current trials using bio-based solvents and more efficient phase transfer catalysts offer promise for further reducing hazardous waste and solvent footprints from each batch.
Chemically and practically, the free base and salt forms of arecoline diverge in ways that impact real-world use. The most obvious differences show up in solvent compatibility: free state arecoline moves effortlessly into organic phases, making it suitable for reactions that fail in strictly aqueous or buffered media.
Compared with arecoline hydrobromide or hydrochloride, the free base delivers higher amine reactivity, essential for downstream chemical transformation. This reactivity means greater care is necessary in transport and storage; it’s not just an academic issue but a tangible challenge every time a new batch moves from finishing line to warehouse to client.
In testing scenarios, measuring out free arecoline avoids the hidden complication of inert ion content. Laboratories looking for unambiguous dose-response or precise molecular pharmacology cite this as a real advantage. In contrast, salt forms require recalculation to adjust for the hydrobromide or chloride moiety mass, complicating titration and dilution steps.
For shelf life and handling, salts carry longer stability and less requirement for specialized containers. Yet even there, certain experiments are limited: the extra ionic species can alter reaction equilibria or interfere with probes specific to uncharged molecules. In our years working with advanced organic chemists, their move toward free base forms resulted from hard-won experience, not marketing arguments. The difference shows in the quality and reliability of their published outcomes.
Others in the industry sometimes overlook the finer points of batch traceability, comprehensive analysis, or tailored shipping conditions. We have seen too many cases where shortcuts—using commodity packaging or slipshod transport—negate the technical edge offered by the free base. Our approach keeps the chain of quality unbroken from synthesis through final application.
Over the years, our team has developed a close relationship with many leading academics, pharmaceutical R&D chemists, and specialty manufacturers. They drive innovation, and we return the favor by sharing process insights, troubleshooting unexpected results, and refining material supply. Their input challenged us to develop more robust smaller-quantity packaging for benchtop research and prompted formulation advice on solvent compatibility for new bioassay formats.
Translating field feedback into production changes takes both humility and persistence. We methodically document each customer concern or anomaly, making adjustments where patterns call for change. This feedback led to improved temperature control en route, modified stabilizer ratios in packaging, and more transparent batch reporting, with not only purity ranges but breakdowns of all detected byproducts. We also aggregate case studies on use in non-standard applications, from veterinary sensors to the development of novel insecticides.
We also make changes when scientific consensus indicates a benefit to users. Peer-reviewed literature and conference findings remain a rich source of practical insight for making production more in tune with user reality. We provide comprehensive, regularly updated technical notes drawing on that literature as well as well-documented customer trials.
Producing arecoline in its free state isn’t a matter of routine—it’s an ongoing pursuit of precision, consistency, and partnership. Each iteration of our process, every adjustment in storage, and each piece of feedback helps reinforce the trust our users place in us. For many, the distinction between a good and a great experiment, or a theory confirmed or disproven, rests on the caliber of starting material.
As researchers push toward deeper understanding of cholinergic systems, novel synthetic routes, or innovative bioassays, we remain committed to supplying arecoline in its free form with the highest integrity possible. Our facility and staff are oriented toward eliminating sources of error, amplifying what works, and supporting the most ambitious goals of today’s scientific community.