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4-Cyanopyridinium-1-olate

    • Product Name 4-Cyanopyridinium-1-olate
    • Alias Mukaiyama reagent
    • Einecs 629-032-1
    • 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
    VTB
    Specifications

    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 & Storage
    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.
    Application of 4-Cyanopyridinium-1-olate

    Applications of 4-Cyanopyridinium-1-olate in Industrial Manufacturing

    As 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 Synthesis

    Pharmaceutical 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) standards for API intermediates
    • European Pharmacopoeia (Ph. Eur.) monographs for precursor chemicals
    • REACH Registration (EC 1907/2006) for EU imports of key chemical substances

    Typical usage ratio

    • 5–25 mol% relative to final target molecule; adjusted for scale, route efficiency, and stoichiometry optimization

    Downstream process integration

    • Pyridine ring functionalization in stepwise multi-stage flow or batch reactors
    • Used after initial halogenation or nitration stages, prior to isolation of crystalline intermediates
    • Strict in-process QC post-reaction, including HPLC purity checks and residual solvent analysis

    Final product types

    • Key intermediate compounds for kinase inhibitors
    • Building blocks for non-steroidal anti-inflammatory agents (NSAIDs)
    • Synthetic precursors for prodrugs in oncology pipelines

    2. Agrochemical Synthesis: Herbicide Precursor Manufacturing

    4-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

    • FAO/WHO Technical Specifications for Pesticides
    • US EPA Product Chemistry Data Requirements (40 CFR Part 158)
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • ISO 9001:2015 Quality Management in agrochemical production

    Typical usage ratio

    • 15–30% w/w of total reactant mass; adjusted by desired halogenation degree and plant production capacity

    Downstream process integration

    • Added following initial methylation or acylation phases in reaction sequence
    • Used with controlled dosing pumps in automated, closed-loop reactor systems
    • Purified by fractional crystallization and vacuum distillation prior to downstream amination

    Final product types

    • Pyridine-based herbicide intermediates
    • Chlorinated agrochemical active ingredients for post-emergent crops
    • Precursors for fungicide and insecticide active molecules

    3. Specialty Dye Manufacture: Fluorescent Dye Intermediate

    In 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

    • EN 71-3:2019 regarding safety of toys (dyes and ink safety)
    • REACH Annex XVII restrictions for colorant substances
    • ISO 9001:2015 for dye synthesis process control
    • OEKO-TEX® Standard 100 for textile applications

    Typical usage ratio

    • 3–12% w/w of total dye precursor mass; modified according to fluorescence intensity specifications

    Downstream process integration

    • Incorporated after ring-closing reactions during dye skeleton assembly
    • Used in condensation steps with aromatic aldehydes for pigment core formation
    • Colorimetric and luminescence control follows integration, supporting batch release

    Final product types

    • Fluorescent dyes for analytical laboratory use
    • Security inks for banknotes and document authentication
    • Textile fluorescent colorants for athletic or safety clothing

    4. Battery and Electrochemical Material Synthesis

    Producers 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

    • IEC 62660-2 safety standards for rechargeable batteries
    • UN Manual of Tests and Criteria for Dangerous Goods (Section 38.3 - Lithium Batteries)
    • ISO 14001:2015 for environmental management in materials production
    • QC/T 743-2006 (China Automotive Battery Standards)

    Typical usage ratio

    • 1–8% w/w of organic additive blend; adjusted per battery chemistry and cycle life targets

    Downstream process integration

    • Used during the synthesis of electrolyte additive masterbatches in solvent extraction reactors
    • Blended with lithium salts and polymer carriers before cavity filling into lithium pouch cells
    • Batch testing ensures stable redox performance before module assembly

    Final product types

    • Electrolyte stabilizers for Li-ion battery electrolytes
    • Functionalized polymeric salts in battery separator films
    • Organic additives for next-generation anode/cathode formulations

    5. Chemical Catalysis: Phase-Transfer Catalyst Component

    Leading 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

    • ISO 9001:2015 Certified Quality Management System for catalyst manufacturing
    • Occupational Safety and Health Administration (OSHA) requirements for handling organic intermediates
    • EU CLP Regulation (EC No 1272/2008) for hazardous materials labeling
    • Responsible Care commitments for chemical process safety

    Typical usage ratio

    • 0.25–2 mol% per catalytic cycle; loading set by substrate reactivity and turnover requirements

    Downstream process integration

    • Introduced in catalytic reactor feedstocks for nucleophilic alkylation reactions
    • Mixed with organic and aqueous phase reactants during process startup
    • Purified by extraction and filtration after batch or continuous operation

    Final product types

    • Phase-transfer catalysts for specialty esterification
    • Active intermediates for organophosphorus chemicals
    • Recyclable catalyst formulations for green chemical processing

    6. Photochemical Reaction Promoter in Fine Chemicals

    Fine 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

    • ISO 17025 Laboratory Accreditation for chemical testing
    • EU Directive 2012/18/EU (SEVESO III) for safe use of hazardous substances
    • OSHA 29 CFR 1910.1450 - Laboratory Chemical Hygiene Plan
    • REACH Annex XIV for substances in photochemical applications

    Typical usage ratio

    • 0.5–5 mol% with respect to total reaction mixture; ratio tailored to photolysis lamp intensity and desired conversion yield

    Downstream process integration

    • Added into pre-mixed starting material at initiation of UV irradiation
    • Supports conversions in glass reactor vessels, with temperature and wavelength monitoring
    • Post-photolysis extraction and chromatography isolate pure cross-coupled compounds

    Final product types

    • Highly substituted pyridine derivatives
    • Synthetic building blocks for contract research services
    • Analytical standards for photochemical process development
    Free Quote

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    Certification & Compliance
    More Introduction

    Unlocking the Potential of 4-Cyanopyridinium-1-olate in Modern Synthesis

    The Story Behind 4-Cyanopyridinium-1-olate

    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.

    Defining True Consistency: Our Approach to Production

    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.

    Where 4-Cyanopyridinium-1-olate Excels

    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.

    Learning Through Comparison: What Sets 4-Cyanopyridinium-1-olate Apart

    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.

    Evolution in Handling and Packaging

    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.

    Feedback Loop: Bringing Customer Experience Into the Fold

    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.

    Responsible Manufacturing: Regulatory and Environmental Focus

    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.

    Supporting Innovation and Collaboration

    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.

    Meeting Tomorrow’s Demands

    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.

    Conclusion: More Than Just a Building Block

    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.