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2-Fluoro-3-Methylpyridine

    • Product Name 2-Fluoro-3-Methylpyridine
    • Alias 2-Fluoro-3-picoline
    • Einecs 826-787-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    701267

    Productname 2-Fluoro-3-Methylpyridine
    Casnumber 28983-56-4
    Molecularformula C6H6FN
    Molecularweight 111.12
    Appearance Colorless to pale yellow liquid
    Boilingpoint 145-147°C
    Meltingpoint -30°C (approximate)
    Density 1.066 g/mL at 25°C
    Purity Typically ≥98%
    Synonyms 3-Methyl-2-fluoropyridine
    Smiles CC1=CN=CC=C1F
    Refractiveindex 1.505-1.509
    Solubility Slightly soluble in water; soluble in organic solvents
    Flashpoint 46°C
    Storagetemperature Store at room temperature

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

    Packing & Storage
    Packing Amber glass bottle, 100 mL, with tamper-evident cap; labeled with chemical name, CAS number, hazard warnings, and manufacturer details.
    Shipping 2-Fluoro-3-Methylpyridine is shipped in tightly sealed containers, protected from light, heat, and moisture. It is classified as a hazardous material, requiring appropriate labeling and handling under applicable transport regulations. During shipping, sturdy packaging minimizes the risk of leaks or spills, and safety data sheets accompany the product for safe transit and handling.
    Storage 2-Fluoro-3-methylpyridine should be stored in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from moisture. Store in a chemical storage cabinet, preferably under an inert atmosphere if possible, and clearly label the container to prevent accidental misuse.
    Application of 2-Fluoro-3-Methylpyridine

    Applications of 2-Fluoro-3-Methylpyridine in Industrial Manufacturing

    2-Fluoro-3-Methylpyridine is a high-value pyridine derivative produced in-house to demanding quality control standards. It plays a crucial role as an intermediate in several downstream sectors with strict compliance and technical requirements. Below, we outline dedicated use cases matched to on-the-ground industrial processing, detailing regulatory, formulation, operational, and end-product considerations for manufacturers across each field.

    1. Pharmaceutical Synthesis – API Intermediate for Antiviral Compounds

    Our material is valued for integration as a building block in synthesis of antiviral active pharmaceutical ingredients (APIs), particularly within pyrazine and pyridine-based small molecule drugs. Manufacturers deploy it during multi-step synthesis routes, exploiting its fluorinated structure to enhance target molecule properties. Its production batch documentation and traceability support downstream GMP and regulatory reviews.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for APIs
    • US FDA 21 CFR Part 211 requirements for finished pharmaceuticals
    • China Pharmacopeia (ChP) for domestic submission

    Typical usage ratio

    • 0.5–3.0 mol equivalents relative to subsequent reactants, adjusted by specific synthetic route design and yield optimization requirements

    Downstream process integration

    • Charged in condensation or substitution reactions to introduce the fluoro-methylpyridine moiety in Step 2 or Step 3 of multi-stage API synthesis
    • Undergoes further derivatization, alkylation, or cross-coupling before isolation and purification of the active compound

    Final product types

    • Antiviral APIs used in oral solid dose medications
    • Prescription drugs for respiratory viral infections
    • New chemical entities in clinical trial supply chains

    2. Agrochemical Ingredient Manufacturing – Herbicide Intermediate

    Downstream agrochemical producers source this raw material for formulating selective herbicides. The presence of the fluorine atom is leveraged for metabolic stability in formulated actives. The intermediate enters reaction trains leading to heterocyclic key structures used in crop protection, and its handling observes regional registration and residue compliance frameworks.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • REACH (EC No 1907/2006) registration for Europe
    • China ICAMA pesticide registration
    • EPA 40 CFR Part 180 (tolerances for pesticide residues)

    Typical usage ratio

    • 1.0–2.2 molar equivalents in key cyclization or substitution reactions, adjusted per target molecule and crop chemistry requirements

    Downstream process integration

    • Reacted in the synthesis step forming the pyridine-based core of post-emergent herbicidal actives
    • Serves as a fluoro-methyl controller in subsequent functional group additions

    Final product types

    • Selective herbicide actives for cereals and broadacre crops
    • Formulated pesticide EC (emulsifiable concentrate) and SC (suspension concentrate)
    • Bulk pesticide technical grade ingredients

    3. Fine Chemical Synthesis – Pyridine-Modified Ligand Production

    Chemical plants manufacture specialty ligands and catalysts, introducing the material as a core substrate. Its precise substitution pattern enables the design of fine-tuned chelating ligands for transition metal complexation, especially for catalysis in polymerization, reduction, or cross-coupling reactions.

    Industry compliance standards

    • ISO 9001:2015 for chemical manufacturing
    • Custom specification and lot traceability according to downstream QC protocols
    • Documentation for purity (HPLC, GC) and residual solvent analyses

    Typical usage ratio

    • 0.8–1.5 equivalents per ligand design batch, adjusted according to chelate stoichiometry and catalyst loading targets

    Downstream process integration

    • Employed in core functionalization or cross-coupling to introduce the fluorinated methylpyridine ring at key ligand positions
    • Integrated prior to final ligand purification and metal coordination steps

    Final product types

    • Custom ligand molecules for homogeneous catalysis
    • Organometallic complex pre-catalysts supplied to fine chemical and polymer industries
    • Polymerization catalyst activators

    4. Electronic Chemical Raw Material – Precursor for OLED Emitting Materials

    Manufacturers specializing in functional materials for electronics utilize this compound as a precursor for the synthesis of specific pyridine-based small molecules in organic light-emitting diode (OLED) materials. Its molecular architecture supports downstream functionalization steps, directly influencing charge transport and emission properties in display technologies.

    Industry compliance standards

    • ISO 9001:2015-certified production and quality documentation systems
    • RoHS (Restriction of Hazardous Substances Directive) conformity for electronic chemicals
    • Internal corporate specifications for impurity profiles, ash, and heavy metals

    Typical usage ratio

    • 0.6–1.3 equivalents incorporated into target intermediates, scaled according to batch size and photophysical property optimization

    Downstream process integration

    • Introduced during N-functionalization or cross-coupling to generate the emitting core of OLED material
    • Treated under anhydrous, inert conditions to protect the fluoro-methyl structure throughout multi-step organic synthesis

    Final product types

    • Pyridine-containing emitting material precursors
    • Small molecule blue or green emitters for OLED displays
    • Electronic grade fine chemical intermediates

    5. Veterinary Drug Intermediate Manufacturing

    Producers of veterinary active substances rely on this material as a precursor in the assembly of fluorinated pyridine scaffolds, integral to ensuring metabolic target compatibility and stability in livestock medications. Batch consistency and low impurity content are stipulated for interface with GMP-compliant veterinary API synthesis.

    Industry compliance standards

    • VICH GL40: Good Manufacturing Practice for Active Pharmaceutical Ingredients Used in Veterinary Medicinal Products
    • EU Regulation (EC) No 470/2009 on veterinary pharmaceuticals
    • US FDA CVM (Center for Veterinary Medicine) guidance for sponsors

    Typical usage ratio

    • 1.1–2.0 accounting for yield adjustment and specific veterinary drug molecular structure requirements

    Downstream process integration

    • Added during carbon–carbon bond forming steps of the veterinary API assembly
    • Subjected to stringent intermediate cleaning before final step condensation and crystallization

    Final product types

    • Active pharmaceutical substances for veterinary therapeutics
    • Ready-for-formulation veterinary premixes
    • Intermediates for animal health feed additive manufacture
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    Certification & Compliance
    More Introduction

    2-Fluoro-3-Methylpyridine: Practical Insights from Our Factory Floor

    Understanding the Real Product: Roots in Consistent Manufacturing

    After more than a decade handling pyridine derivatives, we know that 2-Fluoro-3-Methylpyridine, with CAS number 349-61-9, keeps surfacing in demand for very good reasons. This compound, C6H6FN, distinguishes itself through a blend of subtle reactivity and resilient structure, often opening pathways that simple pyridine or methylpyridine can’t support. We pour resources into exacting production steps and raw material vetting so each batch leaves the facility without the trace contaminants or performance inconsistencies that tend to trip up downstream synthesis.

    Concretely, our reactors handle the careful introduction of selective fluorination directly into the pyridine core. The positioning of the fluorine and methyl groups on the ring does more than tweak performance on paper—it drives sharper selectivity in pharmaceutical and agrochemical intermediates. We’ve fielded questions from chemists who tried broad-spectrum methylfluoropyridines from bulk retailers and wound up with variable conversion rates and trace impurities. Years refining our process led to a reliable method that cuts down on byproducts and ramps up reproducibility, especially for those manufacturing active ingredients or high-purity catalysts.

    Purity Matters: The Difference Factory Methods Deliver

    Chemists watch for small differences in purity because even minor deviation disrupts reaction chains or bioactivity screens. We consistently deliver content exceeding 99%, monitored by multiple analytical techniques at every batch stage. We maintain state-of-the-art chromatography and NMR systems to ensure the product aligns with strictest specifications. Some buyers discount impurities, but—when you scale trials—a single co-eluting impurity from a poorly managed precursor affects not just the immediate process but analytics, registrations, and even final product toxicity testing.

    By producing 2-Fluoro-3-Methylpyridine from carefully sourced 3-methylpyridine, ensuring full traceability, and running tailored fluorination, we guarantee a tighter control over the isomer distribution. This matters a lot to downstream users seeking to synthesize fine chemicals or advanced heterocyclic compounds, where a misplaced substituent leads to waste, or worse, failed regulatory filings. Avoiding mixed isomers from less careful sources reduces headaches and cost for anyone pushing towards high-value end uses.

    Why 2-Fluoro-3-Methylpyridine Shapes Multiple Industries

    Across our customer base—especially in pharmaceutical research and agrochemical innovation—demand has steadily risen for this particular pyridine. The dual presence of the electronegative fluorine and the electron-donating methyl group on the aromatic ring shifts reactivity compared to plain 3-methylpyridine or its non-fluorinated cousins. This means downstream reactions can proceed with greater predictability, saving time during multi-step synthesis.

    We see biologists and medicinal chemists preferring this compound in lead development for its ability to adjust metabolic stability and bioavailability of new drug candidates. Small changes at the molecular level alter binding affinity or resistance to metabolic degradation, and 2-Fluoro-3-Methylpyridine often fits the bill better than beefier or more heavily halogenated structures. Several clients have leveraged our high-purity output to advance kinase inhibitor programs, noting cleaner conversion rates and far fewer column purifications during optimization.

    Application Cases: Real Stories from Chemical Production

    One notable situation involved a European pharma partner who needed reliable 2-Fluoro-3-Methylpyridine to advance a novel cardiovascular agent. Before working with us, their route would stop dead at scale-up due to a persistent high-boiling impurity traced to low-quality material from bulk resellers. Our product, made with precision in atmosphere-controlled reactors and stripped of all side products, ran cleanly into their subsequent Suzuki coupling. Months that would have gone into re-optimization instead accelerated straight into pilot plant runs.

    In the agrochemical field, a mid-size firm faced batch-to-batch inconsistency using generic sources, with variable yields in the synthesis of a pre-emergent herbicide intermediate. After switching to our 2-Fluoro-3-Methylpyridine, yield and product consistency climbed, backed by full CoA and stability profile, reducing both scrap waste and analytical retesting. We have plenty more stories, but the pattern holds: exact, repeatable production at the molecular level saves effort in process validation and final product registration.

    Stability, Storage, and Practical Insights from Years of Handling

    Let’s get down to brass tacks. We don’t merely ship bottles but store and handle metric tons of pyridine derivatives throughout the year. 2-Fluoro-3-Methylpyridine stands up well under standard warehouse conditions, with volatility and odor contained through sealed processes and proper venting. The methyl group nudges boiling point a notch higher than some lighter fluoropyridines, but the compound does not call for exotic containment or controlled substance management, simplifying international logistics.

    Our own packaging, developed after moderate trial and error, focuses on fluoropolymer-lined drums and amber glass containers for R&D scale. Customers using automated dispensing lines have reported zero compatibility issues, and bulk handlers see no clumping or unexpected volatility. Storing this material year-round in mixed chemical warehouses delivers no surprises, even with routine shuttling between warm and cold seasons—far better than the fussier di- or trifluoro analogues.

    Comparing with Related Pyridines: More than a Simple Substitution

    Chemists often ask us about differences between 2-Fluoro-3-Methylpyridine and its close relatives in both structure and application. The parent 3-methylpyridine, widely used and easy to source, doesn’t deliver the same electronic tweaks as a strategically placed fluorine. Such changes open the door for new coupling reactions, smoother halogen exchanges, and improved metabolic profiles. We have tracked comparative performance data: where 2-fluoro substitution is present, yields in certain oxidative and cross-coupling reactions improve by double digits.

    In contrast, other mono-fluoropyridine isomers show less pronounced impact in some pharmaceutical settings. The combination of methyl and fluorine provides better blocking of oxidative metabolism—an effect well-documented in medicinal chemistry literature and corroborated by our own internal data. For plant protection agents, introducing this specific isomer into pyridine derivatives has led to upticks in stability in both ambient storage and after application, a boon when shelf life and field resilience matter.

    The Manufacturing Challenge: Realities of Clean Room and Scale

    There is always a temptation in the market to blend batches or overlook a single outlier tank that just meets threshold assay. We stick close to narrow specifications, refusing to dilute or disguise any deviation. Our fluorination steps run in closed systems with tight monitoring because open batch fluorination can introduce not only environmental hazards but trace moisture, which shows up as difficult-to-remove high-boiling residues. Through extensive investments in ventilation, containment, and rigorous worker protection, we support not only continuity of supply but also a safer working environment—this discipline shines through in the product itself.

    Scaling up from lab to plant often exposes hidden pitfalls. We’ve learned the hard way that modest impurities or slightly elevated moisture, trivial in gram-scale flaskwork, start to ruin kilo-scale syntheses. Each campaign, we validate inputs from solvents to metals. We’ve tested alternate fluorine sources and batch timings, but nothing replaces stable, experienced operators and in-line reality checks on density, color, and GC traces. Some competitors lose sight of this, chasing speed instead of methodical production. Our choice is to keep production output within a range that ensures inspections at every step, not just at the end.

    Regulation and Transparency: Ensuring Market Confidence

    Demand for 2-Fluoro-3-Methylpyridine especially sharpens during registration of new pharmaceutical or agrochemical actives, which attracts increased scrutiny from authorities. Each batch is fully traceable, and our documentation includes not just a Certificate of Analysis but a chain-of-custody for raw materials, solvent lots, and environmental data. We proactively share impurity profiles and residual solvent checks with every shipment, so there are no surprises in later regulatory filing or customer QA audits.

    In our experience, the difference between a smooth regulatory review and a series of delays comes down to transparent, comprehensive data. We maintain open channels with customers’ quality departments, quickly providing any additional batch details or analytical validation—reducing friction when proof of purity or method validation is required. This attention to detail removes bottlenecks and also strengthens trust over years, making us a preferred partner rather than just a supplier.

    Continuous Improvement: What Decades in Fine Chemical Production Have Taught Us

    We regularly review market feedback, production yields, and in-field performance data. Process tweaks or equipment upgrades flow from direct dialogue with users facing real-world challenges. One major upgrade in fluorine delivery hardware was directly inspired by a client’s inability to pass a certain toxicity threshold—minor equipment changes made a measurable impact on impurity spectra. Keeping equipment modern and operator training current ensures we don’t lag behind evolving industry requirements.

    It’s not about just cranking out more product or squeezing costs. Each campaign informs improvements for the next. Over two decades, we moved from multi-step purification with large solvent footprints to cleaner, lower-impact routes. These changes also cut down on emissions, providing better conditions for workers and reducing environmental loading, which matters to us as much as to our customers’ compliance teams.

    Customer-Focused Solutions: Beyond the Drum or Drum Label

    Purchasing decisions are driven by performance at the bench and on the line, not just price per kilo. We welcome on-site visits, supply audit trails, and offer split-lot validation samples for new customers eager to trial before full commitment. Our technical team provides practical support, from process scouting to impurity characterization, helping users get more value per batch. Returning customers routinely report improved throughput and reduced downtime caused by material anomalies.

    Production isn’t just pushing molecule out the door. For us, it means walking the line between exact chemistry and hands-on accountability. We take pride in seeing our 2-Fluoro-3-Methylpyridine contribute directly to advances in therapy, crop protection, and fine chemical innovation around the world.

    Addressing Market Challenges: Security of Supply and Logistics

    Recent shifts in transport and supply chain reliability forced us to rethink and diversify raw material sourcing. We balance multiple regional supply partners for key precursors, keeping a healthy inventory buffer. Airlifting emergency orders or shifting production to satellite lines helps neutralize disruptions, so users see no gap in availability.

    Our warehousing plays a big role—modern facilities reduce climate-induced degradation and let us manage larger call-off contracts without shipping delays. Each shipment leaves with tamper-evident seals and full QC sheets available electronically, which cuts out confusion and cements our supply reliability, even during spikes in demand.

    Future Directions: Building on Real Scientific and User Experience

    As researchers push for greener synthesis or targeted environmental controls, we keep adapting production systems and analytical practices. We’re experimenting with continuous-flow fluorination, aiming for even greater selectivity and lower byproduct rates. Product portfolio expansion pairs closely with the needs of our industrial partners—when clients identify a desired impurity profile or physical property, we explore new formulation or package sizes. Our goal stays the same: making sure each drum or vial empowers innovation at the user’s bench.

    Conclusion: What Choosing Manufacturer-Grade 2-Fluoro-3-Methylpyridine Offers

    Choosing 2-Fluoro-3-Methylpyridine from a dedicated manufacturer means more than securing a raw chemical. It’s the result of hard-won experience, focused process control, and an unbroken chain from raw input to finished material. Over the years, we’ve seen this care save time and trouble for both smaller research groups and large-scale manufacturers who understand every gram counts.

    The right choice in chemical procurement starts with understanding more than just the name on a label or a purity spec. Each shipment carries with it a guarantee of repeatable performance, open data, and responsive support—all learned through years operating at the sharp end of pyridine chemistry. As research and industry needs grow, we remain ready to adapt, improve, and deliver not just a molecule, but a promise of partnership.