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2-Fluoro-5-Methylbenzonitrile

    • Product Name 2-Fluoro-5-Methylbenzonitrile
    • Alias 2-Fluoro-5-methylbenzenecarbonitrile
    • Einecs 872-53-5
    • 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

    130511

    Product Name 2-Fluoro-5-Methylbenzonitrile
    Cas Number 70724-05-3
    Molecular Formula C8H6FN
    Molecular Weight 135.14 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 209-211°C
    Density 1.09 g/cm³
    Purity Typically ≥98%
    Flash Point 91°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms 2-Fluoro-5-methylbenzenecarbonitrile
    Smiles Cc1ccc(F)cc1C#N
    Refractive Index 1.527-1.531

    As an accredited 2-Fluoro-5-Methylbenzonitrile 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 grams, tightly sealed with tamper-evident cap, labeled with chemical name, CAS number, hazard symbols, and supplier.
    Shipping 2-Fluoro-5-Methylbenzonitrile is shipped in tightly sealed containers, protected from light and moisture. It should be packaged according to relevant hazardous material regulations, labeled appropriately, and transported by certified carriers. Handling requires proper protective equipment to avoid inhalation and contact, as the chemical can be harmful. Store in a cool, ventilated area.
    Storage 2-Fluoro-5-Methylbenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from strong oxidizing agents and acids. Ensure proper labeling and store at room temperature. Avoid moisture exposure and use appropriate personal protective equipment when handling the chemical.
    Application of 2-Fluoro-5-Methylbenzonitrile

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

    As a core manufacturer specializing in high-purity aromatic nitriles, we supply 2-Fluoro-5-Methylbenzonitrile to downstream clients focused on advanced material and specialized chemical synthesis. Our quality control, continuous process validation, and collaborative technical support enable customers in targeted sectors to optimize their production efficiency and meet evolving regulatory standards.

    1. Pharmaceutical Active Ingredient Synthesis

    Our clients in pharmaceutical production apply this intermediate in the synthesis of APIs, particularly for anti-inflammatory and central nervous system (CNS) drugs where selectivity and purity profiles are critical. The nitrile group and fluorine substitution pattern support precision coupling and downstream transformations during multi-step synthesis routes, enabling robust process consistency for patented molecule development and generics registration.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <232> Elemental Impurities Procedures
    • EU GMP Part II – Basic Requirements for APIs
    • 21 CFR Part 211 – US FDA cGMP for Finished Pharmaceuticals

    Typical usage ratio

    • 0.7–1.4 molar equivalents relative to target API structure; optimized via route-specific stoichiometry and impurity control

    Downstream process integration

    • Enters as a halogenated nitrile reagent for nucleophilic aromatic substitution or palladium-catalyzed coupling
    • Serves as starting material for amide, amine, or heterocycle formation steps
    • Monitored via HPLC for impurity purge and intermediate isolation

    Final product types

    • API intermediates for CNS agents, anti-inflammatory compounds, oncology molecules
    • Regulatory submission-grade bulk APIs containing fluoroaromatic moieties

    2. Crop Protection and Agrochemical Synthesis

    Commercial agrochemical formulators utilize this raw material as a selective building block in the synthesis of modern herbicides and insecticides. Its substituted nitrile structure facilitates stepwise construction of active ingredients with desirable environmental and toxicological profiles, in compliance with global agri-regulations. Analytical traceability and batch reproducibility are paramount for downstream synthesis validation and field application scale-up.

    Industry compliance standards

    • ISO 9001:2015 International Quality Management
    • European Regulation (EC) No 1107/2009 on plant protection products
    • US EPA Pesticide Registration Process (40 CFR Parts 150–180)
    • China GB 2763 Maximum Residue Limits (MRLs) on Pesticides

    Typical usage ratio

    • 0.4–1.0 molar equivalents depending on specific target actives and process step; batch size and reaction yield monitored with GC-MS profiling

    Downstream process integration

    • Incorporated in early functionalization or ring-closing reactions for heterocyclic actives
    • Taken up in coupling with aliphatic or aromatic precursors under controlled base or catalytic conditions
    • QC-supported crystalline isolation and impurity tracking for registration dossiers

    Final product types

    • Fluorinated herbicide intermediates
    • Nitrile-based insecticidal actives
    • Stabilized crop protection formulations

    3. Fine Chemical and Specialty Intermediate Production

    Manufacturers of advanced organic intermediates rely on this compound when producing custom fine chemicals for electronics, photographic, and specialty resin applications. The nitrile and fluoro functionalities offer programmable reactivity for further derivatization, ring-extension, or insertion chemistry. Custom purity and consistent particle morphology are specified for integration into multi-ton and pilot-scale operations, frequently supporting bespoke R&D and niche market demands.

    Industry compliance standards

    • ISO 9001/14001: Integrated Quality & Environmental Management
    • REACH (EC) No 1907/2006 registration for safe chemical handling
    • GHS (Globally Harmonized System of Classification and Labeling of Chemicals)
    • Customer-specific supplier qualification audits

    Typical usage ratio

    • 8–15% by mass in precursor blends for downstream substitution or cyclization steps; levels adjusted based on desired end-group conversion rates

    Downstream process integration

    • Added to sealed vessel reactors for high-pressure or elevated temperature synthesis
    • Applied in controlled addition protocols to maximize selectivity in multi-reactant systems
    • Monitored for conversion efficiency and yield maximization via in-process NMR/IR

    Final product types

    • Electronic grade intermediates for OLED and display materials
    • Photographic chemical building blocks
    • Custom monomers for specialty polyimides and engineered resins

    4. Advanced Dye and Pigment Manufacture

    Producers of specialty dyes deploy this aromatic nitrile as a core intermediate in colorant molecule synthesis where exceptional thermal and chemical stability are crucial. Its electronic properties allow for targeted diazotization, coupling, or ring-modification reactions suited for pigments in plastics, coatings, and fiber coloring. Consistent reactivity and minimized metal impurities are mandated for quality grading in high-performance dye sectors.

    Industry compliance standards

    • EN ISO 9001 Quality Systems for Dye Manufacturing
    • OEKO-TEX® Standard 100 for textile dyes
    • EU REACH Registered Substances List
    • Japan Chemical Substances Control Law (CSCL)

    Typical usage ratio

    • 5–15% by mass in pigment base formula, with final ratio determined according to color intensity, solubility, and product matrix

    Downstream process integration

    • Participates in condensation, azo-coupling, or metal complex formation during pigment synthesis
    • Integrated into continuous or batch processes with in-line HPLC color monitoring
    • Treated for residual impurity reduction before final dispersion or precipitation

    Final product types

    • High-stability textile dyes
    • Engineering plastics colorants
    • Advanced industrial pigments for coatings and fiber applications
    Free Quote

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    Certification & Compliance
    More Introduction

    2-Fluoro-5-Methylbenzonitrile – A Manufacturer’s Perspective

    Onsite Production, Genuine Understanding

    Among the building blocks we work with in our chemical plant, 2-Fluoro-5-Methylbenzonitrile stands out for the way it blends fluorinated and aromatic chemistry. Every day, technicians in our main synthesis hall move, measure, and process material by hand and instrument, not just exporting a code on a label, but controlling real flow and monitoring reaction paths. Where some see a catalog entry or a “Benzo derivative,” we see the output of batch hours, temperature controls, and purification that take skilled eyes and patience to truly master.

    Model and Key Characteristics—By Those Who Synthesize

    We're talking about a molecule that carries a benzene ring, a nitrogen triple-bonded to a carbon (nitrile), a fluorine atom, and a methyl group, all held together in a configuration that makes life easier for anyone working with halogenated aromatics. CAS number 448-52-4 might be the international reference, but for us, this is a familiar friend on the production line.

    Typical runs of our 2-Fluoro-5-Methylbenzonitrile deliver material at purities exceeding 99%, thanks to carefully staged distillation and crystallization. Residual solvents, moisture, or isomeric cross-contaminants demand constant attention. Each drum or container shares the same analytical signature, confirmed by both our onsite GC and NMR. Compared to analogs with chlorine or bromine substitutions, this compound’s volatility falls in an intermediate zone; it’s neither so hard to handle as pentafluorobenzenes, nor so stubborn as the heavier halides or biphenyls.

    Insightful Differences from Other Halobenzo Derivatives

    To build a fluorinated benzonitrile, our technicians run multi-stage reactions, watching carefully for over-fluorination or competitive methylation—troubles every bench chemist knows. The presence of the fluorine atom at position 2 (ortho to the nitrile) shapes both the reactivity and stability of the compound. We see this during synthesis: yields rise higher, purification smooths out, and color impurities tend to wash out more easily than with other halobenzonitriles.

    In the lab, the methyl group at position 5 doesn’t just make it easier to spot on a GC trace, it subtly affects both polarity and boiling point—critical for solvents and process engineers. The comparable 2-chloro-5-methylbenzonitrile or 2-bromo-5-methylbenzonitrile bring heavier atom effects; they sit heavier on a balance, carry higher boiling points, and create more issues with byproduct elimination. Our fluorinated compound, by contrast, gives a cleaner mass spectrum. Yields in follow-on reactions consistently prove easier to optimize, especially where downstream aminations or Grignard reactions become necessary.

    Where Expertise Shows: Handling and Use Cases

    In day-to-day operations, process engineers report that this molecule’s moderate boiling point (around 175–180°C at standard pressure) simplifies distillation. Handling precautions still matter—fluorinated aromatics demand closed systems and smooth seals to avoid vapor losses or operator exposure—but as manufacturers, we appreciate that the compound resists hydrolysis and photodecomposition. Warehousing and shipment don’t turn into headaches, unlike with some nitrated or peroxide-sensitive benzene derivatives. We keep stock in fluoropolymer-lined drums, and train staff on material transfer: no amateur shortcuts.

    Our main downstream customers come from pharmaceutical and agrochemical development. Synthetic chemists rely on the ortho-fluorine/methyl profile for cross-coupling reactions, nucleophilic aromatic substitutions, and as synthetic handles for custom scaffolds. Where benzonitrile itself proves too reactive or unselective, or when 2,5-disubstituted rings tune solubility or lipophilicity for bioactive compounds, our 2-Fluoro-5-Methylbenzonitrile fills that gap. For active pharmaceutical ingredient (API) discovery and registration, having high, consistent purity makes regulatory filings easier, avoiding requalification or costly retesting.

    Real Manufacturing Challenges and Why They Matter

    Competing companies sometimes cut corners with lower-purity lots, poorly managed batch records, or off-grade solvent residues. From experience, such shortcuts complicate everything downstream: catalyst poisoning, unexpected exotherms, or batch failures under process scale. Our own standard operating procedures enforce lot testing not just for assay, but for byproduct fingerprinting—a necessity confirmed by years of customer returns and support calls.

    Another lesson from the reactor bay: trace residue control must start at raw material sourcing. We caught a spike in hydrolysis byproducts once, traced it back to a contaminated toluidine source, and had to rework the cleaning protocols on every joint. Every bottle representing 2-Fluoro-5-Methylbenzonitrile carries that level of traceability, because there’s nothing abstract about a stuck reactor or a failed campaign.

    The Price of Overlooking Subtle Chemistry

    Colleagues sometimes talk about “just another benzonitrile.” That disregards how vital substitution pattern and purity are for successful end-product development. For example, even minor isomeric impurities can ruin selectivity in Suzuki couplings or Buchwald-Hartwig aminations, leading to wasted time and resources. We target isomer content below 0.1%, a figure backed by hundreds of QC runs and validated procedures, not marketing copy. Each lot release comes after both NMR integration and mass spec confirmation, so we do not ship trouble to a partner’s lab.

    Late-stage pharmaceutical synthesis often pushes small variations in ring substitution to exploit subtle differences in metabolic stability, solubility, or protein interaction. That’s where the 2-fluoro/5-methyl pattern helps medicinal chemists adjust compound properties, searching for better pharmacokinetics or cleaner toxicology. In our experience, every milligram counts, so in-process controls monitor both the main product and possible side products, including unreacted anilines or methylated isomers.

    Responsible Shipment and Regulatory Mindfulness

    Real-world production also means compliance with regulations. While the compound itself isn’t as tightly regulated as some more exotic halides or nitriles, cross-border transport still demands up-to-date SDS documents, clear purity reports, and safe containment. We never delegate regulatory paperwork to outside vendors; instead, trained compliance officers check each outgoing drum or container. Our batch paperwork lives onsite, not just scanned to a server on another continent. This minimizes border hold-ups and avoids any “open storage” snafus at customs warehouses or client warehouses.

    Global supply uncertainty hit the fine chemicals trade in 2022 and 2023. We saw delays caused by feedstock disruptions, particularly with fluoroaromatic intermediates sourced from outside Asia. Our solution grew from direct relationships with raw material producers and a policy of in-plant inventory for both key feedstocks and specialty reagents. When a competing plant suffered a half-year outage due to an upstream fluorination incident, our facility absorbed the demand thanks to flexible batch scheduling and consistent environmental controls.

    Stewardship Behind Each Shipment

    The manufacturing process for 2-Fluoro-5-Methylbenzonitrile doesn’t just yield a drum of clear, off-white solid. It represents years of accumulated knowledge on safe handling, purification, and environmental protection. Waste streams see in-line treatment and neutralization, and every reactor wash goes through chemical oxygen demand monitoring before discharge. Young chemists in our company learn from senior operators how to handle both the main product and byproducts, collecting and packaging even small “non-conforming” lots for specialized disposal—not just vented or buried as might happen in undocumented operations.

    Years in the industry taught us the importance of operator safety training—fluorinated aromatics require special respect. Splash exposure to the skin or inhalation can carry risks not always captured in basic safety manuals. Our PPE protocols, from gloves to vented hoods, stem from real incidents tracked and learned from, not just textbook recommendations. We review near-misses on a quarterly basis, making incremental improvements in hazard control: goggles for every pour, chemical suits for drum transfer, gas monitoring in storage areas.

    Downstream Performance and Customer Interaction

    As a manufacturer, watching a client build a new molecular scaffold off our 2-Fluoro-5-Methylbenzonitrile gives real satisfaction. Whether the end-use lands in a clinical candidate, a crop protection agent, or a photochemical innovation, the starting building block sets the ceiling for product success. Customers rely on technical openness: batch records are not just provided for inspection, but form the backbone of their own regulatory filings and patent submissions.

    From time to time, research partners come in with requests for custom packaging, sub-batches, or process modifications. We welcome this level of engagement, but always anchor technical adjustments in what our plant can reliably provide, not a wish list divorced from production reality. If an end-user brings up solubility tweaks or precipitation management, we share our own experience with solvent swapping and filtration—advice rooted in experimental runs, not just literature projections. Whenever a synthetic procedure throws an unforeseen side product, our technical team is available for joint troubleshooting; we’ve seen most of the common process wrinkles over a decade.

    Comparing to Non-Fluorinated Counterparts

    Handling benzonitriles lacking a fluorine often changes process economics. We finish more time cleaning up after unfluorinated or polyfluorinated aromatics, which generate larger waste volumes and greater energy input for distillation. The electron-withdrawing effect of the fluorine stabilizes the nitrile moiety, knocking down unwanted side reactions and promoting better throughput on scale-up. In our experience, fluorination at the ortho position compared to para or meta also affects solubility in typical reaction solvents such as DMSO, DMF, or toluene, giving formulators added flexibility.

    Other benzonitriles in our product line—like 4-methylbenzonitrile or 3-fluorobenzonitrile—find uses in more limited contexts where their regioisomeric profile suits specialized applications. Versatility makes 2-Fluoro-5-Methylbenzonitrile a central node for cross-couplings and protecting group strategies. Its performance as a synthon outpaces less substituted analogs, especially in cases involving heterocycle formation or selective reduction.

    Quality Above Scale: Why Purity Still Matters

    Scaling up production above 100-kilogram batches pushed us to rethink purification—chromatography for small lots, but better crystallization and filtration on the industrial reactor. Each approach takes careful temperature and stoichiometry adjustments: too fast and purity slips; too slow and energy waste follows. Yields can dip when operators lose discipline. Our own plant data showed how even five-degree temperature drift triggers impurity upticks. Quality assurance audits focus on both laboratory results and the workflow habits of our plant teams. Training reoccurs constantly, and lessons learned from pilot campaigns roll back into the next production run, keeping standards from sliding.

    Customers building APIs or regulatory submissions count on that consistency. For every kilo delivered, no matter the size of the batch, each specification—moisture content, appearance, melting point, GC purity—receives sign-off by at least two analysts. Repeated seasonal audits and anonymous spot tests throughout the year (especially during cold months when process solvent residues can linger) keep our technicians sharp.

    Tackling Global Chemical Supply Chain Hardships

    The post-pandemic world reinforced a lesson: single-point supply chains bring outsized risk. We diversified our precursor supply, keeping direct lines to at least two sources for each raw material. Storage protocols now account for potential transit interruptions, with buffer stock rotated proactively, not just filled on demand. The logistical complexity that comes with offshore sourcing—especially for fluorinated or methylated aromatics—means we stay in conversation with shipping partners and logistics planners at every step. By keeping shipment sizes manageable, with redundancy in routing, our plant maintains reliable output even when global freight faces disruption.

    Onsite production grants real-time feedback. Process runs that throw off unusual color, odor, or byproduct signals trigger immediate review before a drum leaves the plant. We update both production staff and end-users with process changes, adapting QC methods and shelf-life recommendations from empirical storage trials—real-world data, not theoretical shelf lives.

    The Future of 2-Fluoro-5-Methylbenzonitrile Production

    Trends point toward greater demand for custom-tailored fluorinated building blocks as biologically active molecules test new spaces in both pharmaceuticals and advanced materials. Our team watches patent filings and regulatory updates, adjusting product offerings and documentation in step with new legal and technological standards. As reaction methodologies evolve—shifting towards milder cross-couplings, C-H activation, or photoredox chemistry—the robustness and versatility of the 2-fluoro/5-methyl framework stays relevant.

    We anticipate tomorrow’s requests may look different from yesterday’s, requiring even tighter specs, specialized particle size, or new packaging to meet global transportation and environmental requirements. The plant’s modular production lines stand ready to accommodate such evolution, supported by trained technicians and chemists invested in seeing every process step done right.

    Summary of a Manufacturer’s Commitment

    Working with 2-Fluoro-5-Methylbenzonitrile daily reveals both the potential and challenges of handling specialty chemicals wisely. The lessons come from hands-on operations: late-night distillations, process troubleshooting, and face-to-face client feedback. Raw material quality, operator expertise, batch documentation, traceability, and technical support—these make up the core of what we deliver, not just a chemical formula. Underneath each delivered drum sits a chain of knowledge—our promise that every gram started in a plant that values reliability, safety, and collaboration.