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3-Cyano-2-Fluoropyridine

    • Product Name 3-Cyano-2-Fluoropyridine
    • Alias 3-Fluoro-2-pyridinecarbonitrile
    • Einecs 813-449-2
    • 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

    896057

    Product Name 3-Cyano-2-Fluoropyridine
    Cas Number 126140-49-6
    Molecular Formula C6H3FN2
    Molecular Weight 122.10 g/mol
    Iupac Name 2-fluoropyridine-3-carbonitrile
    Appearance Colorless to pale yellow liquid or solid
    Boiling Point 203-205 °C
    Density 1.24 g/cm³ (estimated)
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g., DMSO, dichloromethane)
    Structure Pyridine ring with cyano at position 3 and fluoro at position 2
    Smiles C1=CC(=C(N=C1)F)C#N
    Inchi InChI=1S/C6H3FN2/c7-6-4-5(3-8)1-2-9-6/h1-2,4H
    Refractive Index 1.509 (estimated)

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

    Packing & Storage
    Packing 25g of 3-Cyano-2-Fluoropyridine is packaged in an amber glass bottle with a secure, tamper-evident cap and proper labeling.
    Shipping 3-Cyano-2-Fluoropyridine is shipped in tightly sealed containers, protected from moisture and light. It is transported according to relevant chemical shipping regulations, ensuring safety and compliance. Appropriate hazard labeling and documentation accompany the shipment, while temperature control is maintained if required. Handling and transport are carried out by trained personnel only.
    Storage 3-Cyano-2-Fluoropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Always store at room temperature and clearly label the container. Use appropriate personal protective equipment when handling or transferring the chemical.
    Application of 3-Cyano-2-Fluoropyridine

    Applications of 3-Cyano-2-Fluoropyridine in Industrial Manufacturing

    3-Cyano-2-Fluoropyridine is widely used as a key intermediate for producing complex molecules in the pharmaceutical, agrochemical, and specialty chemical sectors. Our manufacturing capability ensures consistent quality and traceability for industrial customers across these specialized applications. The following sections outline the primary industrial downstream scenarios where our material plays a pivotal role in value chain production.

    1. Pharmaceutical Active Ingredient Synthesis

    In pharmaceutical manufacturing, our 3-Cyano-2-Fluoropyridine serves as a foundational building block for anti-cancer APIs and advanced intermediates, especially for the synthesis of molecules containing pyridine-based heterocycles. Leading API makers integrate this raw material during early-route manufacture using palladium-catalyzed C–N and C–C coupling for pyridine ring functionalization, providing a platform to access target pharmaceutical scaffolds with high yield and purity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices (GMP) for Active Pharmaceutical Ingredients
    • USP General Chapter <823> and applicable USP monographs for related APIs
    • European Pharmacopoeia (Ph. Eur.) standards for intermediates
    • FDA 21 CFR Part 210/211 for control of pharmaceutical production

    Typical usage ratio

    • 5–12% w/w of total batch input, adjusted according to multi-step reaction stoichiometry and overall target molecule yield

    Downstream process integration

    • Introduced in initial coupling or condensation step to form heterocyclic intermediates before additional functional group transformations

    Final product types

    • Anti-cancer APIs (e.g., pyridine-based kinase inhibitors)
    • Central nervous system pharmaceuticals
    • Intermediate compounds for orphan drug candidates

    2. Agrochemical Intermediate Manufacturing

    Producers of modern agrochemicals deploy 3-Cyano-2-Fluoropyridine as a crucial precursor for assembling active ingredients such as herbicides, fungicides, and insecticides designed to meet crop protection needs. The pyridine core, functionalized using chlorination, nitration, or amination, allows manufacturers to access custom-tailored pesticide scaffolds displaying high selectivity and biological performance.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specifications
    • ISO 9001:2015 Quality Management Systems
    • REACH Registration, Evaluation, Authorization and Restriction of Chemicals—EU Regulation (EC) No 1907/2006
    • China GB/T 1604-2014 for crop protection chemicals

    Typical usage ratio

    • 8–18% w/w relative to the total mass of the final technical-grade active material, adjusted by synthetic pathway length and target molecule functionalization pattern

    Downstream process integration

    • Charged during the initial or mid-stage synthesis of the main active ingredient, directly participating in nucleophilic aromatic substitution or Grignard addition followed by subsequent derivatization

    Final product types

    • Selective herbicide active ingredients (e.g., substituted-pyridine herbicides)
    • Fungicide building blocks
    • Precursor intermediates for insecticidal compounds

    3. Pharmaceutical Intermediate for Cardiovascular Drugs

    Within the cardiovascular drug R&D pipeline, 3-Cyano-2-Fluoropyridine enables creation of intermediates used in synthesizing compounds such as calcium channel blockers and antihypertensive agents. By offering a handle for regioselective cyanation and halogen exchange, it streamlines the production of strictly regulated, high-purity intermediates essential for scale-up in GMP facilities.

    Industry compliance standards

    • US FDA DMF (Drug Master File) submission guidelines
    • Chinese Pharmacopoeia relevant sections for intermediates
    • EU EMA guidelines for control of starting and intermediate materials
    • ICH Q3A/B Impurities in New Drug Substances/Products

    Typical usage ratio

    • 9–16% w/w on a per-intermediate reaction scale, with adjustments based on route verification and impurity profile acceptance

    Downstream process integration

    • Reacted in the condensation or cyclization phase with substituted benzyl halides or amines, providing the cyano- and fluoro-substituted pyridine moiety for cardiovascular drug backbone construction

    Final product types

    • Key intermediates for third-generation calcium channel blockers
    • Precursor to new antihypertensive candidates
    • NCE (new chemical entity) intermediates in drug discovery

    4. Development of Specialty Pyridine-Based Catalysts

    Researchers and specialty manufacturers select 3-Cyano-2-Fluoropyridine when building custom ligands and catalysts for metal-mediated organic transformations. The unique substitution pattern of the pyridine core supports strong chelating properties and allows rational design of catalytic systems, satisfying the high-purity requirements for both academic and industrial catalyst production workflows.

    Industry compliance standards

    • ISO 17025 Laboratory Accreditation (for catalyst QC)
    • OECD Good Laboratory Practices (GLP) for analytical methods on catalyst quality
    • Sigma-Aldrich internal standards for ligand purity
    • REACH Annex VII–XIX (for specialty chemical registration and characterization in EU)

    Typical usage ratio

    • 3–7% w/w in ligand preparation, depending on target chelation geometry and final ligand load—typically calculated per mole of designed ligand backbone

    Downstream process integration

    • Involved in the first or second step of assembling chelating ligands or heterocyclic framework precursors, followed by coordination with transition metals like palladium, ruthenium, or copper

    Final product types

    • Pyridine-based phosphine ligands for homogeneous catalysis
    • Bidentate or tridentate chelating agents for metal-mediated CC and CN coupling
    • Reference ligands for catalyst screening libraries

    5. Synthesis of Fluorinated Fine Chemicals

    Manufacturers of fine chemicals use 3-Cyano-2-Fluoropyridine in developing advanced fluorinated intermediates for electronics, dyes, and imaging chemicals. Its fluorinated and cyano-substituted aromatic platform grants downstream processors direct access to new molecular motifs with improved thermal stability and electronic effects, often applied in progressive materials science projects.

    Industry compliance standards

    • ISO 9001:2015 Quality Management – Fine & Specialty Chemicals
    • Japan Chemical Industry Association (JCIA) Responsible Care Program
    • RoHS 3 (EU Directive 2015/863) for electronics applications where relevant
    • China Chemicals Industry Standard (HG/T 3755-2012) for advanced fine chemicals

    Typical usage ratio

    • 4–11% w/w based on the number of steps and the desired fluorination density in the product; batch-specific adjustment driven by downstream performance testing

    Downstream process integration

    • Charged during the fluorination or cyano-derivatization phase as a core intermediate, then further altered via nucleophilic aromatic substitution, metalation, or cross-coupling for value-added chemical synthesis

    Final product types

    • Fluorinated dye precursors
    • High-purity imaging chemical intermediates
    • Fine chemical blocks for optoelectronic and specialty materials
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    Certification & Compliance
    More Introduction

    Introducing 3-Cyano-2-Fluoropyridine: A Perspective from the Manufacturer

    Our Understanding of 3-Cyano-2-Fluoropyridine’s Place in Chemical Synthesis

    Every batch of 3-Cyano-2-Fluoropyridine tells a story about how manufacturing precision can transform fundamental chemistry into tangible applications. We have seen this molecule in action across pharmaceutical and agrochemical sectors, serving as an indispensable intermediate that brings a unique combination of nitrile and fluorine functionalities within the pyridine ring. The placement of the cyano group at the third position while introducing fluorine at the second has opened new synthetic options for our partners in R&D and production, far beyond what standard pyridine derivatives offer.

    In our experience, the shift from basic halogenated pyridines or simple cyano pyridines to 3-Cyano-2-Fluoropyridine responded to concrete challenges faced by formulators and process chemists. Many times, process yields have depended on the availability and purity of intermediates like this. The demand for higher reactivity combined with controlled selectivity led us to refine our processes, ensuring that our product maintains strict limits on residual solvents and by-products, especially those known to interfere in medicinal chemistry or in downstream coupling steps.

    What Sets Our 3-Cyano-2-Fluoropyridine Apart

    On the shop floor and in quality control, no detail is too small. We produce this compound predominantly in its crystalline form and invest considerable time in eliminating trace organics, particularly those originating from upstream halide substitutions. Our chemists favor a fluorination step using robust, reproducible reagents to afford clean reactions, minimizing unwanted tars or color bodies that sometimes plague similar fluorinated pyridines. For us, these are more than technical subtleties—they directly affect reliability in subsequent transformations, especially nucleophilic substitutions or Suzuki-type couplings.

    Some buyers once asked about differences between our 3-Cyano-2-Fluoropyridine and older variants or imported stocks of uncertain pedigree. Years of iterative process improvements taught us to stay away from recycling heavily contaminated solvent lots and to maintain strict protocol for moisture control, which can make a difference in shelf stability and reactivity. For the teams handling this product in API or crop protection active development, these differences make downstream reactions cleaner and save time on unnecessary purifications.

    Model and Specification: What Quality Means in the Factory

    On paper, our main model references a batch specification that restricts the water content to less than 0.2% and a minimum assay of 99%. Impurities like 2-fluoropyridine or 3-cyanopyridine, common side-products in less optimized processes, rarely exceed 0.3% in any lot we release. We perform routine batch certifications using validated HPLC-UV and NMR quantification, but the story does not stop at numbers. Regular in-process controls verify both starting material provenance and batch consisency, long before post-synthesis workup.

    During scale-up, chemists noticed that the intermediate formation profile could vary with minor changes in temperature—something only continuous small-batch monitoring could reveal. This feedback loop between laboratory synthesis and commercial output still shapes the way we approach each order, especially when customers require special grades for pilot or commercial runs.

    Manufacturing Insights: The Value of Real Experience

    Every seasoned plant operator recognizes the challenges of handling pyridine derivatives. In our routine practice, reactor cleaning, and containment strategies must address pyridine odor and potential for cross-contamination, since even minor carryover affects both safety and quality downstream. For 3-Cyano-2-Fluoropyridine, careful isolation after synthesis, with an emphasis on controlled crystallization and solvent stripping, ensures the material ships with minimum residual odor and a high degree of lot traceability.

    The shift toward more sustainable manufacturing has not bypassed this compound either. While classic protocols leaned hard on polar aprotic solvents, we’ve gradually adopted more benign alternatives. Our solvent recovery system catches every drop possible, pushing our process closer to closed-cycle operation and reducing the carbon footprint. This is a small victory, but it matters for buyers looking to integrate their supply chains with less environmental penalty.

    Differences from Other Pyridine Derivatives

    In practical terms, anyone who has worked with a range of pyridine intermediates will understand that 3-Cyano-2-Fluoropyridine stands out for its dual functional reactivity. The strong electron-withdrawing cyano group, coupled with fluorine’s effect at position 2, shifts both chemical behavior and physical handling. Compared to plain 2-fluoropyridine or mono-cyanopyridines, this compound offers a unique reactivity profile, especially in stepwise build-up of biaryl or heterocyclic compounds. The extra activation from the cyano moiety both enhances some coupling reactions and restrains side-product formation, often making purification less resource intensive.

    Unlike polyfluorinated pyridines, which often lead to over-activation and side reactions, the single fluorine substitution permits smoother, more predictable chemistry during nucleophilic aromatic substitution and cross-coupling. For process designers, this means better selectivity, fewer wasted reagents, and higher isolated yields. In small-scale custom synthesis, several partners have remarked on greater robustness and less troubleshooting compared to attempts with similar structural analogs.

    On another front, some generic intermediates present storage headaches—hydrolysis sensitivity, volatility, or hygroscopicity. Our product’s crystalline solid format reduces these concerns and allows extended shelf life without cold storage or elaborate packaging. In transport, samples from every shipment are routinely retested, and retained reference samples track stability and impurity growth over time. This gives downstream end-users, whether in pharma, materials, or agchem, confidence in batch-to-batch interchangeability.

    Supporting Research and Application Trends

    In talking with researchers from both pharma and agrochemical companies, the consensus points to 3-Cyano-2-Fluoropyridine’s strategic position in constructing advanced molecular scaffolds. The cyano group serves as a gateway for functional group interconversions—amidines, amides, even tetrazoles. Fluorine, on the other hand, brings metabolic stability and often increases the bioactivity of lead compounds.

    Our own routine feedback from end-users highlights this trend. Medicinal chemists value the ease with which this compound allows late-stage diversification, expanding SAR studies on novel drug candidates. Agricultural companies regularly request larger lots for new herbicide and pesticide discovery campaigns, prioritizing intermediates that offer clean transformations and robust reactivity under a range of conditions.

    Real-world input from process engineers has shaped our current process. Scale-up from gram to multi-kilogram batches exposed vulnerabilities—trace water hampering crystallization, hot spots in reactors producing localized impurity formation. These issues led to further in-line controls and right-sizing of production vessels to optimize both batch quality and process economics.

    Some customers have expressed a need for custom grade specifications—whether ultra-low metal content for catalytic reactions or extra purity for use as reference standards. Our production protocols are flexible enough to respond by adjusting purification methods, always cross-validating against both customer standards and our internal benchmarks.

    Sustainability and Regulatory Considerations

    Increasingly, we field requests for paperwork on regulatory compliance and environmental stewardship—safety data, residual solvent statements, full REACH or TSCA registration status. This reflects the broader push in industry to source intermediates with traceable supply chains that align with compliance and ESG goals.

    We partner closely with our raw material suppliers, auditing both quality and ethical sourcing wherever possible. On the factory floor, newer emissions controls keep airborne pyridine and solvent emissions below detectable thresholds, and our internal audit teams routinely review compliance with both local and international regulations on hazardous chemical handling.

    Customer audits come as par for the course, sometimes unannounced, and we welcome the opportunity to open up our processes. Transparent sharing of manufacturing practices, third-party lab certifications, and regular review of health, safety, and environmental protocols back up our commitment to providing not just compliant, but high-integrity material.

    Applications and Collaborative Problem Solving

    3-Cyano-2-Fluoropyridine has earned its spot through repeated demonstration in real-world syntheses. We have seen it open new synthetic pathways in drug discovery labs, sometimes providing unique access to once-elusive molecular targets. Crop science teams have used it to build molecules capable of selective herbicidal activity with stronger resistance to environmental breakdown.

    We consult regularly with partners during process troubleshooting. For instance, when reaction scope expands into higher complexity scaffolds, small variations in reagent grade or by-product profile suddenly matter. We listen and incorporate pragmatic feedback: a run that failed due to batch-to-batch impurity drift became a catalyst for tightening our spectral release criteria. In another case, a pharmaceutical company needed tighter particle size distribution to enhance blending in their feed process; we answered with a process tweak that increased consistency across multiple lots.

    When customizations are viable and justified, we mobilize production for pilot shipments. Some applications call for material that is more granular, some purer than the standard grade, and some customers specify exclusion of certain trace elements because of subsequent testing sensitivity. These requests get handled in real-time between our technical liaisons and plant engineers, trimming response times and increasing product value for users with constrained timelines.

    Challenges and Continuous Improvement

    Working with any multi-functional intermediate throws up surprises. 3-Cyano-2-Fluoropyridine does resist some standard drying and encapsulation operations because of its odor and potential for static accumulation. Over the years, we adapted warehouse protocols: grounding hoppers, revised extraction hood settings, and improved packaging lines to cut down off-odors and minimize operator exposure. These tweaks, often rooted in hands-on learning, pay back in smoother handling for both us and our customers.

    Another challenge involved batch reproducibility, especially during periods of raw material volatility or supply chain disruption. Sourcing high-purity pyridine and ensuring stable fluorinating agent supply remain non-trivial, especially during industry-wide shortages. We’ve responded by developing secondary supplier relationships and holding more strategic inventory, intending to buffer both our production lines and our clients’ forecasts.

    Feedback from international customers seeking regulatory filings in new regions has highlighted another area of continuous improvement: documentation. Preparing extended analytical files, impurity spectra, and stability data for regulatory review keeps us busy, but the end result justifies the effort—our material often sails through customer qualification on the first attempt.

    What the Future Holds

    In ongoing dialogue with scientists, sourcing teams, and process engineers, the future shape of 3-Cyano-2-Fluoropyridine manufacture looks set to blend tighter analytical control, increased scalability, and closer integration of green technology. We are actively developing lower-waste, lower-energy processes, including continuous flow steps and alternative fluorination routes, and keeping abreast of global shifts in both regulation and market demand.

    Collaboration remains essential. Customers share their successes and setbacks, feeding into our process of incremental upgrade and troubleshooting. Our job does not finish with shipment: post-delivery technical support, stability retesting, and process improvement suggestions keep a healthy feedback loop alive. The product originated from practical needs and keeps evolving every time a new use case or challenge arrives at our door.

    We have learned that reliably manufactured 3-Cyano-2-Fluoropyridine opens new doors for a wide range of researchers and formulators. Instead of simply supplying a molecule, we enable teams to tackle modern synthetic challenges with a tool they know they can trust. The subtle distinctions between fine chemicals are never lost on us—purity, handling, batch consistency, environmental impact, and documentation each play a part in making a compound not just available but actually useful.

    As ongoing demand shapes future directions, we continue building, testing, and refining each lot. That is the ground-level thinking guiding each run of 3-Cyano-2-Fluoropyridine—and the standard by which every lot leaves our plant.