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2-Fluoro-5-Methoxybenzonitrile

    • Product Name 2-Fluoro-5-Methoxybenzonitrile
    • Alias 2-Fluoro-5-methoxybenzenecarbonitrile
    • Einecs 841-924-0
    • 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

    409268

    Chemical Name 2-Fluoro-5-Methoxybenzonitrile
    Cas Number 180356-25-6
    Molecular Formula C8H6FNO
    Molecular Weight 151.14 g/mol
    Appearance Solid (crystalline or powder)
    Melting Point 59-62°C
    Boiling Point 263-265°C
    Density 1.21 g/cm³ (approximate)
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98% (for laboratory reagent)
    Smiles COC1=CC(F)=C(C#N)C=C1
    Inchi InChI=1S/C8H6FNO/c1-11-8-3-2-6(4-10)7(9)5-8/h2-3,5H,1H3
    Refractive Index 1.533 (estimated)
    Storage Conditions Store at room temperature, dry and tightly sealed
    Hazard Statements May cause skin and eye irritation

    As an accredited 2-Fluoro-5-Methoxybenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Fluoro-5-Methoxybenzonitrile is packaged in a 25-gram amber glass bottle with a tamper-evident screw cap for protection.
    Shipping 2-Fluoro-5-Methoxybenzonitrile is shipped in tightly sealed containers to prevent moisture and contamination. The chemical is packed securely, following all applicable hazardous material regulations. It is labeled with appropriate hazard warnings and handled by authorized personnel to ensure safe and compliant transport. Temperature and light-sensitive precautions may apply.
    Storage 2-Fluoro-5-methoxybenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Store under inert gas (e.g., nitrogen) if prolonged storage is required. Properly label the container and follow all standard laboratory chemical storage protocols.
    Application of 2-Fluoro-5-Methoxybenzonitrile

    Applications of 2-Fluoro-5-Methoxybenzonitrile in Industrial Manufacturing

    As a direct manufacturer, we provide 2-Fluoro-5-Methoxybenzonitrile for several highly specialized chemical synthesis routes. Its consistent purity and traceable batch quality make it suited to industrial-scale use in active pharmaceutical ingredient intermediates, agrochemical actives, pigment precursors, and fine chemical R&D. Each segment below details how formulation teams integrate this raw material into production, referencing real industry controls, process phases, and downstream product categories.

    1. Pharmaceutical Intermediate Synthesis

    Process chemists incorporate this compound as a critical aromatic nitrile building block in multi-step syntheses of selective serotonin receptor modulators and emerging kinase inhibitors. It enters as a late-stage intermediate, contributing the fluorinated benzene motif essential for pharmacological activity. Every batch supports full upstream-to-finished-drug traceability and aligns with standard API development controls.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) and US Pharmacopoeia (USP) guidelines for APIs and intermediates
    • DMF (Drug Master File) submission requirements (where applicable)
    • REACH Annex VII-VIII substance registration for Europe

    Typical usage ratio

    • 0.4–1.2 molar equivalents per synthesis batch; precise ratio adjusted based on the target drug and desired yield specificity in Suzuki or nucleophilic aromatic substitution stages

    Downstream process integration

    • Added after halogen-metal exchange or as a coupling partner during late-stage introduction of nitrile group
    • Handled under controlled temperature and moisture conditions to preserve aromatic integrity
    • Monitored for conversion and purity by HPLC or GC-MS before isolation

    Final product types

    • Pharmaceutical grade serotonin receptor antagonists/intermediates
    • Lead compounds for kinase inhibition in oncology research
    • Experimental CNS drug candidates synthesized in pilot or commercial scale

    2. Agrochemical Active Ingredient Development

    Formulations laboratories employ this molecule for the construction of complex heterocyclic scaffolds integral to new-generation insecticides and selective herbicides. Its fluorine and methoxy substitution template is key for tailoring metabolic stability in crop-protection actives. Quality control teams validate every shipment against regional pesticide precursor requirements before release to synthesis units.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Active Ingredients
    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 17025 Testing Laboratory Accreditation (where exported for contract synthesis)
    • EPA PRIA Registration Support (for U.S. R&D, where relevant)

    Typical usage ratio

    • 0.5–1.5 equivalents based on overall transformation yield in cyclization or condensation reactions; optimizations performed per proprietary active structure

    Downstream process integration

    • Feeds into initial nucleophilic substitution to introduce cyanobenzene fragment
    • Enters heterocycle formation via base-catalyzed condensation, followed by post-modification steps like esterification or halogenation
    • Analyzed via LC-MS/MS for residual monomer and conversion rates

    Final product types

    • Pyridine-based systemic insecticides
    • Novel herbicide active intermediates with improved environmental fate profiles
    • Experimental fungicidal scaffolds for staple crop protection testing

    3. High-Performance Organic Pigment Manufacture

    Pigment chemists apply this benzene derivative during the condensation steps to introduce targeted aryl nitrile functionalities in the synthesis of high-tint-strength red and violet pigment molecules. The methoxy and fluorine groups ensure precise solubility and fastness required for plastics and industrial coatings. Consistent purity supports batch shade reproducibility and tailors the absorption profile of the pigments produced.

    Industry compliance standards

    • ISO 9001 Quality Management for pigment processes
    • EN 71-3 Toy Safety Standard for colorant impurities (where applicable)
    • REACH Annex XVII restrictions for aromatic amines (compliance in downstream pigment)
    • ASTM D476 Color Pigments for Coating Materials

    Typical usage ratio

    • 5–12% by weight in pigment condensation batch, depending on desired chroma and shade depth; adjusted to target spectral requirements for end-use application

    Downstream process integration

    • Introduced during the diazotization or nucleophilic aromatic coupling step
    • Seeded directly into reaction with amine or phenol derivatives under controlled temperature
    • Spectral characteristics optimized post-reaction by adjusting ratio in pilot formulation

    Final product types

    • High-heat-stable organic violet pigments for automotive plastics
    • Solvent-resistant red pigment dispersions for coil coatings
    • Specialty printing ink colorants meeting migration regulations

    4. Fine Chemical Library Synthesis for R&D

    Innovation labs and custom synthesis partners utilize this aromatic nitrile as a source fragment in the combinatorial assembly of small-molecule compound libraries. Its regioselective reactivity enables the construction of diverse building blocks for structure-activity studies. The traceable, high-purity supply supports data-driven selection in medicinal, crop science, and material research projects.

    Industry compliance standards

    • ISO 17034 Reference Material Producer Accreditation
    • OECD Good Laboratory Practice (for screening compound generation)
    • Material Safety Data Sheet (MSDS) and full hazard communication
    • RoHS Annex II directives for laboratory supply (when relevant to final application)

    Typical usage ratio

    • 0.3–1.0 equivalents per reaction, determined by stoichiometry in each unique small molecule assembly; commonly scaled in 1–10 mmol multistep synthesis runs

    Downstream process integration

    • Added during the key coupling or cyclization reaction to introduce nitrile and fluorine groups
    • Handles as weighed solid or dissolved in dry DMF or DMSO for microreactor or batch automation
    • Purity and identity confirmed through LC-MS, NMR, and IR before further derivatization

    Final product types

    • Building blocks for drug discovery collections
    • Reference standards for analytical method development
    • Diversified heterocyclic compounds for high-throughput screening assays
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    Certification & Compliance
    More Introduction

    2-Fluoro-5-Methoxybenzonitrile: A Chemist’s View from the Factory Floor

    Introduction to a Focused Intermediate

    2-Fluoro-5-Methoxybenzonitrile does not draw much attention outside specialist circles, but anyone inside a modern chemical plant has seen how targeted intermediates like this shape production lines, research programs, and customer relationships. We work with this compound daily in our facility, and our close involvement, at scale, changes the way we see its role—and its unique profile among aromatic nitriles.

    Behind the Molecule: Why Structure Matters

    Handling aromatic nitriles always requires a controlled environment, robust monitoring, and staff who understand subtle differences between materials. Adding a fluorine atom at the ortho-position and a methoxy group at the meta-position on the benzonitrile ring changes not only reactivity, but also how the compound interacts downstream, even under demanding reaction conditions. This is not just bench chemistry. Factory reactors, with throughputs that dwarf laboratory glassware, highlight unexpected points: small changes in molecular structure can alter solvent handling, filtration requirements, and purity levels in ways that textbooks rarely anticipate.

    Why 2-Fluoro-5-Methoxybenzonitrile?

    Years of feedback from pharma and agrochemical customers led us to this molecule. The fluorine atom brings increased metabolic stability to pharmaceutical candidates and improves crop protection compounds by resisting degradation in soil and sunlight. The methoxy group tunes solubility and electronic properties for precise synthetic outcomes. Combining both on a benzonitrile backbone increases versatility over simpler derivatives, such as unsubstituted benzonitrile or single-substituted analogues. It is this blend of added functional handles and predictable reactivity that keeps this intermediate moving off our lines.

    What Makes Our Process Different?

    Plenty of companies list 2-Fluoro-5-Methoxybenzonitrile in their catalogs, yet most operate as distributors, passing materials from region to region without ever watching the material condense on stainless steel trays, troubleshooting purification columns at 2 a.m., or dealing with a sudden out-of-range HPLC result on the night shift. Producing this molecule at scale demanded that we look closely at each reaction step. Every batch starts with fresh control over raw materials—the fluoro- and methoxy-substituted aromatics come from established, domestic partners. Our staff, trained in both organic synthesis and real-world plant engineering, manage strict in-process analyses until final crystallization shows tight purity profiles.

    The difference in plant-made versus trader-supplied material becomes obvious at the application stage. Formulators who buy from resellers often discover batch-to-batch variance or a stubbornly persistent impurity that did not show up in the written specs. We minimize variability by controlling temperature, solvent ratios, and draining schedules directly on our manufacturing floor and by implementing real-time feedback from every reactor. We do not believe in shuffling mediocre batches under a new label, nor do we promise things we’ve not tested ourselves.

    Specifications That Match Industry Reality

    Every customer asks about specifications—our response matches what our reactors can actually achieve. HPLC purity consistently reaches 99 percent minimum, not just “on average,” but as measured lot by lot before delivery leaves our site. Color and physical appearance reflect both process health and careful post-synthesis work-up. Chemists purchasing for a pharmaceutical R&D line prefer the off-white, free-flowing crystalline powder we produce, because it dissolves with less residue and integrates cleanly into their screening libraries.

    Moisture content, volatile impurity levels, and pack-down density influence everything from storage stability to weighing accuracy in automated dispensing systems. Our team learned through direct experience how minor differences—just a half percentage point of residual water or a faint off-odor—can prompt unexpected problems downstream, whether clogging machinery or introducing artifacts into analytical runs. We monitor every lot, using calibrated equipment and validated methods developed by chemists who also run the plant floor. We store every batch in climate-controlled storage, not in a remote warehouse, so shipment quality reflects last-minute checks, not wishful thinking.

    Handling and Application: Lessons from the Field

    Our customers use 2-Fluoro-5-Methoxybenzonitrile in stepwise syntheses for active ingredients and advanced intermediates. In one pharmaceutical campaign, researchers needed selective nucleophilic aromatic substitution at the fluorine site—they relied on our consistent halogen reactivity to generate targeted metabolites. In another, crop protection developers leveraged the methoxy group as a masking handle, later removed in downstream transformations. Each application puts unique demands on reactivity and purity.

    Our technical service staff assist with more than just delivery schedules. Early in each collaboration, we share findings from our own in-plant reactions, including optimal solvent choices and ‘real world’ mixing techniques that scale from pilot plant to production. The practical tips often differ from lab-scale procedures. This hands-on experience stabilizes processes for our customers and helps avoid costly manufacturing surprises.

    Comparing with Other Benzonitrile Derivatives

    Many chemists begin screening with simpler benzonitriles, such as the unsubstituted, 2-fluoro, or 4-methoxy versions. While these compounds show some baseline activity in chemical and biological assays, results from combinatorial studies show 2-Fluoro-5-Methoxybenzonitrile opens additional routes not accessible from single-site modification. The combined electron-withdrawing effect of nitrile and fluorine, balanced by electron-donating methoxy, shifts reactivity profiles, often leading to cleaner reactions and higher yields under milder conditions.

    Our R&D department tested several positional isomers and found significant differences during regioselective substitution reactions. Yield drops, new byproduct peaks, and purification headaches are regular complaints with some analogues. As a manufacturer, we see these issues not as distant curiosities, but as real impacts—wasted solvent, higher energy bills, longer downtime, and unhappy end users. We adapt process parameters for each isomer, yet production of 2-Fluoro-5-Methoxybenzonitrile consistently achieves cleaner separations and lower waste metrics.

    Supply Chain Experience From a Maker’s Perspective

    Logistics influence every production decision we make. We learned—to our cost—how global events, like shipping bottlenecks and raw material shortages, affect the reliability of specialty intermediates. By maintaining secure relationships with reliable raw material suppliers and holding buffer stock in-house, we protect customers from unpredictable delays. Because we oversee each stage from raw material to packaged compound, our tracking and quality assurance records move with the product, not as a jumble of third-party documents.

    Over years of regular audits and regulatory reviews, we have adapted our record-keeping to satisfy both GMP and research-grade requirements. Customers receive documentation rooted in our batch records, not abstract summaries. This transparency accelerates tech transfers and analytical method validations for clients scaling up from pilot to production. Our team’s first-hand involvement in synthesis, quality control, and packaging reduces the sort of accidental mishaps that waste weeks and drain budgets.

    Sustainability and Safety: Reality on the Production Line

    Sustainability is not an advertising slogan in a plant that runs year-round. From the first synthesis runs, waste minimization and safe handling drove our process choices. We invested in closed-loop solvent recovery, efficient scrubbers, and contained transfer systems to prevent operator exposure and environmental release. Unlike brokers or non-producing traders, we implement tight on-site controls—real valves, trained shift teams, and active incident management protocols, verified by both internal audits and third-party inspections.

    Handling fluorinated aromatics requires special respect. Our plant design separates hazardous chemistry zones from main thoroughfares. We enforce standard operating procedures for nitrile compounds at every step, not simply during disposal. Employees undergo regular safety briefings, hands-on PPE training, and necessary refresher courses tailored to changes in regulatory standards and process upgrades.

    Our environmental team drove a reduction in solvent consumption through optimization of work-up and purification steps, and by selecting eco-friendlier cleaning agents where possible. By maintaining direct physical control over purification and packaging, we catch potential hazards before they reach the shipping dock. The result is fewer regulatory surprises and safer working environments for our staff and the communities that surround our facilities.

    Continuous Improvement: Listening and Learning from Each Batch

    No two batches are identical; even seasoned operators know small process variables compound over time. In practice, we monitor color shifts, melting point deviations, and reaction exotherms that suggest changes upstream. Every customer complaint, no matter how minor, feeds into our quality meetings, where process chemists and plant engineers work together to refine reaction conditions and analytical tests. Occasionally, improvements come from outside—we remain open to customer insights and independent auditor feedback, not just to satisfy compliance, but to drive more reliable, cost-effective output.

    It took years to develop our current protocols. Early on, minor handling issues exposed weaknesses in our packaging line: powders that caked in poorly sealed drums, or containers that shed fibers into samples. Adjustments came from direct operator experience—modifying drum linings, upgrading to tamper-evident closures, and launching real-time barcode tracking on outgoing shipments. Each small change cuts rework and saves both our team and our customers significant frustration.

    Problems We’ve Seen—and How We Solved Them

    Experience with 2-Fluoro-5-Methoxybenzonitrile has not been smooth from the start. In scaling up, we encountered unanticipated residue formation in the final crystallization step, traced to trace water in a commonly used solvent. The solution did not come from outside experts, but from line chemists noting a subtle shift in batch density and collaborating with quality control analysts who devised a more sensitive drying protocol. Another case involved off-spec color caused by marginal thermal control—better jacket insulation and pre-heated solvents led to a uniform product.

    Beyond technical issues, we saw how transportation and storage could undermine our work. Material shipped through consolidators or warehoused by others arrived with compacted lumps or minor contamination. Customers cannot discern the difference from paperwork; only by controlling transport through vetted carriers and routine in-house inspections did we close this final gap. Now, our product leaves via trusted channels, and every outgoing container matches lot retention samples stored in our own facilities. If an issue arises, we track it to source, without drawn-out disputes.

    Looking Forward: Demand, Partnerships, and Expanded Use Cases

    As synthetic targets grow more complex, our plant must respond with nimble processes and flexible output. We invest in process automation and analytical instrumentation so chemists working with emerging pharmaceutical or crop protection agents receive material that matches their evolving needs. Recently, new projects in electronics applications requested derivatives of 2-Fluoro-5-Methoxybenzonitrile, putting unforeseen demands on purity, trace metal content, and particle size control. We adjusted equipment settings and introduced more detailed detection routines before scale-up, anticipating the changes required for these customers.

    Our ongoing collaborations with academic and industrial partners feed information back into our process development teams. By watching how our intermediate behaves in the hands of medicinal and process chemists far from our factory, we improve both synthesis and support. We encourage open, ongoing dialogue—problems encountered in one field often reveal opportunities elsewhere. As end use grows in complexity, our manufacturing experience becomes as valuable as the molecule itself.

    Conclusion: Value Grounded in Direct Production

    As a manufacturer with full command over every step of the production chain, our team sees 2-Fluoro-5-Methoxybenzonitrile not as a generic catalog item, but as an opportunity to deliver on real customer priorities—predictable quality, responsive service, and process insights rooted in practical know-how. Our plant demonstrates that careful production, regular investment in technology, and commitment to hands-on learning yield tangible results: fewer surprises, higher yields, and more satisfied partners worldwide. Every shipment leaving our dock reflects a process shaped by collective experience, attention to details often overlooked by others, and the confidence that comes from working with material hundreds of times before sending it on to laboratories and plants around the globe.