Anhui Liwei Chemical Co., Limited
Products

4-Cyano-2,3-Difluorophenol


    • Product Name 4-Cyano-2,3-Difluorophenol
    • Alias 4-Cyano-2,3-difluorophenol
    • Einecs 841-444-2
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    628636

    Chemical Name 4-Cyano-2,3-Difluorophenol
    Cas Number 183658-64-4
    Molecular Formula C7H3F2NO
    Molecular Weight 155.10 g/mol
    Appearance White to off-white solid
    Melting Point 71-75°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1=CC(=C(C(=C1F)F)O)C#N
    Inchi InChI=1S/C7H3F2NO/c8-5-3-4(1-10)2-6(9)7(5)11/h2-3,11H
    Synonyms 4-Cyano-2,3-difluorophenol; 2,3-Difluoro-4-hydroxybenzonitrile
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 4-Cyano-2,3-Difluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram amber glass bottle, sealed with a screw cap, labeled "4-Cyano-2,3-Difluorophenol, 98% purity, handle with care."
    Shipping 4-Cyano-2,3-Difluorophenol is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is packaged according to regulatory standards for hazardous chemicals, ensuring safe handling and transport. The shipment is labeled with appropriate hazard information and requires cool, dry storage away from incompatible substances.
    Storage 4-Cyano-2,3-Difluorophenol should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from heat, sparks, or open flames. Protect from light and incompatible materials such as oxidizing agents. Store at room temperature, avoiding excessive moisture and direct sunlight. Properly label the container and ensure that only trained personnel access the chemical.
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    For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.

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    Tel: +8615380400285

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    Certification & Compliance
    More Introduction

    Introduction to 4-Cyano-2,3-Difluorophenol: A Manufacturer’s Perspective

    In our chemical plant, the journey from raw material to finished product rarely follows a straight line. For over a decade, we have specialized in building high-purity aromatic intermediates, and 4-Cyano-2,3-Difluorophenol stands as a testament to the technical height this field demands. Over the years, we have listened to research chemists facing bottlenecks, pharmaceutical engineers fine-tuning their synthesis, and specialty material developers pushing the envelope on performance. Their needs shape each production batch we produce, and nowhere does this relationship with application prove more vital than with 4-Cyano-2,3-Difluorophenol.

    Product Background

    We manufacture 4-Cyano-2,3-Difluorophenol in our dedicated aromatic halide facility using a controlled halogenation and hydrolysis pathway. Our plant keeps tight reins on impurity profiles, using a system of in-process analytical feedback loops developed by our team since our first trials. The model number for our standard production run is internally tracked as “CF203-17,” a direct reference for our laboratory, but most of our customers simply refer to it by its chemical name or CAS number for ordering. After years of scale-up, we offer lots ranging from single kilogram samples to several hundred kilograms, depending on project needs.

    For us as a manufacturer who handles raw materials, scale-up for this molecule demanded more than simply increasing vessel size. Fluoroaromatics can surprise even seasoned process engineers. The difluoro groups at positions 2 and 3 destabilize some common byproducts seen in mono-fluoro or chlorinated phenols, so the route our process chemists chose for 4-Cyano-2,3-Difluorophenol follows a tighter catalytic window. By controlling temperature and pressure profiles, and using inline analytical controls, we isolate a product where residual halides, water content, and metallic traces remain well below the requirements of pharmaceutical and electronics standards.

    Physical and Chemical Characteristics

    Lots coming off our line typically show as a white to off-white crystalline powder. Many chemists who visit our technical center for sampling immediately comment on the purity—they measure high by HPLC and NMR, but what really matters for us is that minimum specification gets met batch after batch. Color variation within our product never exceeds half a shade on APHA scale analysis, and our moisture content regularly stays below 0.1% as measured by Karl Fischer.

    The properties that 4-Cyano-2,3-Difluorophenol offers are not just minor tweaks over other cyano- or fluoro-phenols. The electron-withdrawing nature of the cyano group and the close positioning of the two fluorines change the reactivity pattern considerably, giving medicinal chemists a precise tool for aromatic substitution or cross-coupling. In our production quality control runs, chromatograms from our product batches routinely demonstrate a single product peak with trace impurities at <0.2%, so downstream reactions proceed with less side product formation. The melting point typically lands just above 100°C, with little variance lot-to-lot. This thermal stability simplifies storage and delivery, and has enabled some of our large volume users to automate charging in continuous flow reactors with very tight dosing windows.

    Main Applications and User Experience

    Among our partners, the primary demand for 4-Cyano-2,3-Difluorophenol comes from two main groups: pharmaceutical research and advanced material developers. New drug candidates often require selective substitution on aromatic rings. In medicinal chemistry, chemists look for fluorinated scaffolds not just for lipophilicity but also for how these groups can modulate biological activity or metabolic stability. Having a phenol group allows late-stage coupling or etherification; at the same time, the cyano group serves as a versatile handle for further derivatization. Some of our earliest pharmaceutical clients came to us after facing multi-step conversion yields stuck in the low teens with other difluorophenols. With our controlled impurity profiles and technical support, they scaled their projects to multi-kilogram lots with yields routinely over 70% in key steps, a notable improvement from their toolkit before switching raw materials.

    In electronic materials, 4-Cyano-2,3-Difluorophenol carved out a niche for itself because its substitution pattern resists unwanted oxidation while providing unique dielectric properties. Some OLED precursor chemistries take advantage of its reactivity and stability, something we have seen repeated in our customers’ scale-up reports. From a manufacturer’s point of view, the needs of material scientists differ from those of pharma—the former often push for tighter particle size distributions and flowability for automated handling, which led us to adapt our crystallization and milling protocols over two production campaigns. The result now is a product with high purity and good bulk density flow characteristics, whether destined for a pharmaceutical pilot plant or a high-performance coating lab.

    Contrast with Similar Alternatives

    Frequently, procurement teams and R&D specialists ask about differences between our 4-Cyano-2,3-Difluorophenol and other phenol-based intermediates in the catalog. In our experience, substitution patterns on the phenolic ring predict not just reactivity but also toxicity profile, volatility, and even handling safety. Mono-fluoro or non-cyano analogs enjoy cheaper production cost, but converting these to more advanced structures introduces more steps and opens the door to greater byproduct formation. Early in our scale-ups, we compared the synthetic route for 2,3-difluorophenol and its mono-fluorinated cousins to our cyano-difluoro route. Adding the cyano group at the para position introduced a challenge in controlling ortho-fluoro placement, yet it brought clear downstream value—higher selectivity in medical chemistry transformations, less halide volatility loss, and improved shelf life on storage.

    In terms of safety and regulatory environment, our experience manufacturing 4-Cyano-2,3-Difluorophenol offers fewer workplace exposure concerns than runs involving chlorinated analogs, since halogen volatilization risks run lower. The product’s thermal and hydrolytic stability also mean sealed drums store safely for extended periods, with little degradation seen in our 24-month stability tests under both ambient and controlled environments.

    Why High-Quality Manufacturing Matters

    Our production teams meet regularly with R&D customers to understand what blocks their progress. Their main issue is avoidable batch-to-batch variability. During scale-up, we often receive feedback about previous suppliers—synthetic impurities tend to “ghost” in downstream bioassays, or material comes in with unexpected byproducts that affect process safety or yield. We address this by running a battery of in-process and post-process checks: every batch receives a full suite of analytical tests, from HPLC purity and GC-MS impurity screens to elemental analyses targeting metals below 10 ppm. It’s not just about passing a checklist. Consistency matters because a raw material that “drifts” causes subtle but expensive batch failures over time.

    We also listened closely when a longstanding client highlighted a problem with static build-up and adhesion while transferring crystalline difluorophenol products to their reactors. Simple tweaks by our team in crystalline morphology and packaging helped cut their reactor blockages down by 40% in one campaign. These less-publicized tweaks, born from hands-on experience, contribute to more seamless scale-up and eventual commercialization for our customers.

    Sustainability, Compliance, and Responsible Manufacturing

    As a manufacturer, environmental and safety compliance pressures influence every production decision. Fluorinated aromatic intermediates often carry the stigma of persistent environmental impact, and solvent handling especially faces scrutiny. We invested in active and passive emissions controls, solvent reclamation, and effluent treatment modifications to keep our operation within the permitted thresholds that regulators demand. Each improvement comes from internal audits—a direct outgrowth of actual plant experience rather than just regulatory guidelines on paper. Our solvent recycling rates now surpass 90% for typical 4-Cyano-2,3-Difluorophenol campaigns.

    Operator health also shapes our floor-level process controls. Each new campaign starts with a roundtable among operators, QC chemists, and process engineers to review near-miss reports and tweak practices. In designing transfer and filtration steps, we selected closed-system equipment designed to minimize both dust and vapor generation. These practical shifts protect our workforce and boost batch-to-batch consistency—our team’s stability pays off in product reliability for years at a stretch.

    Technical Support and Partnership

    Producing specialty intermediates like 4-Cyano-2,3-Difluorophenol means more than just filling barrels or bags and shipping them off. Research and scale-up scientists regularly contact our team at the earliest project stages. Whether it’s navigating unfamiliar reactivity in a lead optimization project or scaling material for validation, these collaborations give our staff insights unattainable from textbooks. Our technical service chemists keep records of how particular downstream coupling strategies work—or don’t—depending on the impurity, API, or target material. Over time, this applied learning base allows us to provide tailored technical insight for end-users, rather than generic advice.

    Collaborative pilots with clients often shape refinements in our process. Switching from an older crystallizer to a newer, continuous-feed system didn’t just improve efficiency—it yielded a more uniform lot-to-lot crystal size, making volumetric dosing at customer plants more reliable. Every scale-up presents specific hurdles, but our ongoing dialogue with users drives technical improvement. In one recent program, modifying drying protocols led to a tenfold decline in solvent residue, opening new avenues in strict-regulated diagnostic applications for a paint manufacturer who previously couldn’t use our product. These success stories underscore how a close partnership can benefit not only our customers’ projects but the broader technical ecosystem of advanced intermediates manufacturing.

    Case Insights and Lessons

    Most of the innovation in our 4-Cyano-2,3-Difluorophenol line did not come from the top down. The best improvements arose in response to real-world user projects, especially challenging ones. One example: a pharmaceutical partner struggled with a competing supplier’s lots that caused unpredictable crystallization and fouling in their hydrogenation reactors. The customer’s synthesis required phenolic purity above 99.8% and heavy metal traces below 10 ppm, metrics our plant maintained through more rigorous purification and trace analysis. After switching to our product, their reactor cleaning cycles doubled in length, reducing labor and downtime by half. These operational wins are not due to a standard catalogue specification but to the attention we give each batch before and after it leaves our plant floor.

    Problems arise that never show up in standard specs or regulatory data sheets—practical issues like drum static, clumping after shipping, or new requirements for documentation arise frequently. As a manufacturer, we keep in regular contact with our transport and logistics teams so shipment conditions match client usage environments. New packaging designs or extra anti-static liners might not sound remarkable, but they cut waste and streamline end-user processing. Often, these steps come from picking up the phone to an on-site operator experiencing a first-of-its-kind issue. These partnerships allow shared practical know-how to travel both ways—our team learns as much from clients as they do from us.

    Looking Forward

    Building capability for even more stringent purity, traceability, and application-specific customization guides the future of our 4-Cyano-2,3-Difluorophenol manufacturing. As regulatory expectations, especially in APIs and materials for energy storage, keep rising, the depth of technical engagement from both plant and customer chemists remains critical. Our long history with fluoroaromatics tells us that product achievements rarely emerge from isolated lab breakthroughs; real gains reflect a cycle of field feedback, process improvement, and sustained excellence in scale manufacturing.

    Production teams keep up with new analytical methods as they emerge—direct feedback from pioneering customers using novel processes motivates us more than any sales directive or catalog benchmark. The next generation of phenol intermediates will challenge manufacturing know-how far beyond purity alone, demanding not just “chemically clean” product but robust, regulatory-compliant, and customizable production models. Trust and technical communication between the manufacturer and project users build the foundation for these advances—something we’ve demonstrated batch after batch, campaign after campaign, and one project partnership at a time.

    Summary

    From our plant floor to laboratories and manufacturing halls worldwide, 4-Cyano-2,3-Difluorophenol serves as a case study in the ongoing partnership between manufacturer and end-user. Smart process control, attention to field experience, and a willingness to refine methods based on customer need keep us at the forefront of specialty chemical production. These fundamentals do more than secure regulatory and analytical compliance—they give our users a material they can trust for success in the demanding worlds of pharmaceutical, electronic, and specialty materials innovation.