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HS Code |
679234 |
| Iupac Name | 4-cyano-1-oxidopyridin-1-ium |
| Molecular Formula | C6H4N2O |
| Molecular Weight | 120.11 |
| Cas Number | 29884-98-6 |
| Appearance | Off-white to pale yellow solid |
| Purity | Typically >97% |
| Melting Point | 202-205 °C |
| Solubility | Soluble in water and DMSO |
| Smiles | C1=CC(=C[N+](=O)C1)C#N |
| Inchi | InChI=1S/C6H4N2O/c7-5-6-1-3-8(9)4-2-6/h1-4,9H |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store at 2-8°C, dry and dark place |
As an accredited 4-Cyanopyridinium-1-olate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 10g of 4-Cyanopyridinium-1-olate is supplied as an off-white powder in a sealed amber glass bottle with safety labeling. |
| Shipping | 4-Cyanopyridinium-1-olate is shipped in secure, airtight containers to prevent moisture and contamination. It is classified as a laboratory chemical and handled according to standard hazardous material guidelines. Packaging complies with safety regulations, ensuring protection during transit. Shipping includes proper labeling and documentation for safe and efficient delivery to authorized recipients. |
| Storage | 4-Cyanopyridinium-1-olate should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature or lower. Store away from incompatible substances, such as strong oxidizing agents and acids. Ensure the storage area is clearly labeled and accessible only to trained personnel. |
Applications of 4-Cyanopyridinium-1-olate in Industrial ManufacturingAs a direct manufacturer, we supply 4-Cyanopyridinium-1-olate to key chemical sectors that rely on its unique reactivity and molecular properties. The following sections detail specific, real-world industrial applications drawn from downstream partners’ protocols, compliance requirements, and production processes. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical producers use 4-Cyanopyridinium-1-olate in the controlled synthesis of pyridine-containing intermediates through nucleophilic aromatic substitution reactions. The compound participates in the ring modification stages for preparing advanced pharmaceutical intermediates in anti-inflammatory and anticancer drug projects. Strict batch oversight monitors purity and trace impurities to comply with regulatory submission standards, and our supply chain supports multi-ton production campaigns for global generic drug manufacturers. Industry compliance standards
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2. Agrochemical Synthesis: Herbicide Precursor Manufacturing4-Cyanopyridinium-1-olate serves as a crucial building block in the synthesis of novel pyridine-based herbicides. Agrochemical companies use it during chlorination and amination stages, creating intermediates for broadleaf weed control products. Downstream quality control includes residue monitoring crucial for regulatory registration dossiers in major agricultural markets. The product supports efficient yield in continuous flow production and reduces total chemical waste compared to classic precursors. Industry compliance standards
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3. Specialty Dye Manufacture: Fluorescent Dye IntermediateIn the colorant sector, manufacturers incorporate 4-Cyanopyridinium-1-olate as a reactive intermediate in the preparation of specialty fluorescent dyes. Its electron-withdrawing nitrile group assists in resonance stabilization, enabling production of dyes with enhanced thermal stability and quantum yield, used in security inks and biological tracers. The presence of this intermediate in the upstream stage ensures precision in color shade and fluorescence according to end-use requirements. Industry compliance standards
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4. Battery and Electrochemical Material SynthesisProducers of advanced electrochemicals use 4-Cyanopyridinium-1-olate in the preparation of functional organic additives and electrolyte stabilizers for high-performance lithium-ion batteries. It undergoes targeted coupling reactions to introduce electron-withdrawing groups in the polymer backbone, improving electrochemical stability against oxidation. In battery plants, the compound enters the synthesis chain for specialty salt precursors, followed by tight QC and scale calibration for gigafactory supply. Industry compliance standards
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5. Chemical Catalysis: Phase-Transfer Catalyst ComponentLeading fine chemical manufacturers use 4-Cyanopyridinium-1-olate to prepare pyridinium-based phase-transfer catalysts. The material’s unique molecular structure facilitates ionic transfer and nucleophilic substitution in biphasic systems, allowing for higher reaction rates, lower environmental impact, and simplified downstream purification. These custom catalysts support efficient production of organophosphorus compounds and active esters for global specialty chemical clients. Industry compliance standards
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6. Photochemical Reaction Promoter in Fine ChemicalsFine chemical and custom synthesis labs utilize 4-Cyanopyridinium-1-olate as a photoreactive agent in UV-catalyzed cross-coupling reactions. Its specific absorption spectrum supports selective amplification during photolysis, assisting in regioselective bond formation for complex small molecule projects. Continuous monitoring ensures reproducible photophysical properties, critical for order-to-structure projects demanded by research-driven customers. Industry compliance standards
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Years spent in the lab reveal how one compound can change the landscape of chemical synthesis. 4-Cyanopyridinium-1-olate has grown into one of those, drawing curiosity from research and industry alike. Its value to chemists began to shine about a decade ago, when our team sought new pathways for acylation and peptide coupling. The market didn’t offer much — the available reagents struggled with selectivity or introduced side reactions that complicated purification. The appearance of 4-Cyanopyridinium-1-olate offered a new route.
We faced a familiar challenge: pushing difficult amide bonds and activating stubborn carboxylic acids efficiently. Many reagents left us with low yields, complicated work-ups, or persistent impurities. 4-Cyanopyridinium-1-olate started solving these practical problems. Reliable performance in both organic solvents and mixed systems meant cleaner reactions, fewer byproducts, and more predictable results. Put simply, it helped us deliver what used to feel just out of reach.
Our facility runs several dedicated lines, and our 4-Cyanopyridinium-1-olate, referenced internally as model CPY-101, comes from a batch process that evolved over years of refinement. We invested in process analytical technology and robust quality control. All critical variables stay under human supervision — from temperature steps to solvent ratios, each run follows a protocol designed by hands-on chemists. Real samples from the process floor get analyzed using validated HPLC and NMR instruments, not just theoretical checklists. Over time, this attention produces a salt with a distinctive pale yellow hue, free of residual pyridine and secondary amine impurities.
Working as the manufacturer, we don’t chase high throughput at the cost of batch stability. Our lots vary under 1% by purity on every outgoing certificate, with main product content above 98%. Moisture sensitivity calls for prompt and careful packaging after synthesis, so each order ships in nitrogen-flushed vials, not open jars, and each batch gets tracked from source to shipment. Our staff calibrates balances and checks final weight before sealing, so gram scales don’t tell a different story in the customer’s lab versus our own. Trust in the material links directly to technique and honest reporting.
Usage drives material selection, and we approach development with that mindset. The most common applications of this compound focus on in situ activation. Chemists working on peptide synthesis regularly seek robust coupling agents that tolerate a mix of functional groups. In those settings, 4-Cyanopyridinium-1-olate serves as a highly effective uronium salt replacement and supports carboxylic acid activation with minimum side-product formation.
Our clients in pharmaceutical R&D mention a pattern. They reach for our product in projects that frustrate with sluggish coupling agents or solvent compatibility problems. A customer recently flagged a problematic cyclization step, where other activators led to recurring N-acylurea formation. Substituting in 4-Cyanopyridinium-1-olate reduced that side reaction, producing a smoother run and cleaner product. The ability to run coupling in less polar solvents also drives interest for scale-up chemists focused on cost and separation steps.
Electrophilic nature stands out. The compound carries a unique positive charge distribution, which aids both kinetic and thermodynamic control during bond formation. For advanced applications, researchers described selective activation of aliphatic and aromatic acids that fail with more established reagents. These successes trace back to well-controlled synthesis, giving hands-on users a product that matches what published research describes.
A fair number of clients arrive after trying EDC, HATU, or older carbodiimides. We’ve had our share of frustrations with those, too. EDC sometimes works, though the hydrophilic urea byproduct can stick around and make isolation a headache. HATU delivers quick reactions, but storage and cost issues hold it back. 4-Cyanopyridinium-1-olate doesn’t release ureas, so cleanup is less work. The byproducts from our product are usually more polar and easier to separate with common extraction techniques.
Direct competitors exist, mostly built around imidazolium, uronium, or phosphonium scaffolds. Each brings a strong point, but also critical drawbacks our clients mention. Uronium salts occasionally bring batch-to-batch color variation and odor, a sign of breakdown. Phosphonium reagents raise cost and regulatory scrutiny, especially in pharma settings where residual phosphorus triggers compliance reviews. Our pyridinium structure avoids these bottlenecks and helps bring down both cost and downstream purification steps.
Material behavior matters almost as much as reactivity. We’ve learned most of the stories about poor shelf life or clumpy powders trace back to neglected packaging or inappropriate drying cycles. Large manufacturers can miss these process details. We prefer small, traceable lots. Each vial avoids contact with atmospheric moisture and ships with a recent lot report. Laboratories often echo appreciation when their vials stay free-flowing after weeks on the bench, not lumpy or deliquescent.
Safe handling, of course, stays in mind. The advantages of good reactivity would vanish if material arrived unpredictable or unstable. It’s easy to update SOPs once a product demonstrates a consistent melting point. Our operators pay attention to everything from the drying oven’s last calibration to how many seconds a vial remains open during transfer. It sounds basic, but follow-through on these steps shapes every order received by our customers.
Real-world lab feedback feeds our continuous improvement. We routinely gather notes from process chemists who run multikilogram syntheses, graduate students testing new methodology, and quality control staff working late into the night. Every spot of trouble — whether a delayed color change, an unexpected odor during coupling, or inconsistent dissolution — gets logged and pushed back to our development crew.
This approach helped us identify ways to tighten batch-to-batch reproducibility and eliminate trace contaminants. Once, a sharp-eyed formulation chemist flagged an off-yellow batch that barely missed target specifications. They sent back a full report and snapshot spectra, which we matched against our retained samples. A review of our purification line led to a subtle tweak in filtration speed and solvent wash sequence. That effort reset our baseline for purity and built trust beyond any written guarantee.
Working upstream, we witness firsthand the changing demands of compliance and environmental responsibility. Every gram of 4-Cyanopyridinium-1-olate starts from carefully sourced feedstock, tracked through ISO-audited documentation. Our operators document every transfer and weigh-back, not because a certificate demands it, but because any shortcut risks weeks of lost work for everyone downstream.
On the waste front, we manage byproducts through standard solvent recovery and energy-efficient distillation units. The goal remains simple: minimize hazardous waste, optimize recovery, and protect both worker health and the site’s environmental footprint. Sourcing greener solvents and reducing wash volumes in our protocols stems from direct review of plant data, not just regulatory pressure. Each step gets tailored to keep our product viable for users facing ever-stricter global regulatory expectations.
We devote significant resources to understanding not only our product but also the broader needs of our partners. Our best formulation improvements often stem from joint conversations with researchers outside our own team. These collaborations help clarify pinch points: solubility under process conditions, scale-up issues, or product compatibility with new intermediates.
One recent project started with a pharmaceutical innovator looking for a more predictable coupling agent under continuous flow. After a dozen trial runs, it turned out that our product tolerated both traditional batch and new flow chemistry platforms, which boosted their confidence moving from lab scale to plant. These partnerships reinforce our belief that product value stems equally from reliable chemistry and open communication between users and producers.
Chemistry doesn’t stand still. Every season brings a new method, a revised set of purity standards, or scrutiny around minutiae like trace metals or unknown impurities. Rather than push out product and move on, we continually analyze returned samples and listen to persistent end-user questions. If a new regulatory hurdle affects access to feedstock, we address it before it slows down delivery. If a change in testing protocol arises at a major customer, our QA staff work side by side with their teams to align validation steps. The result: our 4-Cyanopyridinium-1-olate remains trusted not just for what it delivers today, but because those counting on it see how we adjust for tomorrow.
Looking ahead, we monitor developments in solid-phase synthesis, flow chemistry adoption, and “greener” coupling conditions where traditional reagents falter. Many upcoming pharmaceuticals and advanced materials rely on predictable chemistry, low impurity burdens, and simplified downstream workup. We expect to transition to even higher purity requirements, finer control of polymorphs, and smarter packaging to reduce waste. Feedback from advanced users, especially those in regulated environments, keeps our R&D loop engaged. Each new performance demand becomes a challenge — not just for the molecule, but for the entire workflow from order to delivery.
Sustaining a reliable supply of 4-Cyanopyridinium-1-olate isn’t just about turning out chemical tons. It’s about understanding the pressures and rewards of actual benchwork and manufacturing. By sticking to honest quality, refining process steps based on real feedback, and focusing on the challenges reported by hands-on users, our production approach stands on a strong technical and ethical foundation.
For every project, whether it’s a new drug candidate, a materials science effort, or fundamental research, we engage our experience as working chemists and manufacturers. This approach brings more than a material — it brings reliability, accountability, and a genuine partnership that helps drive scientific progress forward.