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2-Fluoro-4-Methylbenzonitrile

    • Product Name 2-Fluoro-4-Methylbenzonitrile
    • Alias 2-Fluoro-p-tolunitrile
    • Einecs 701-384-6
    • 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

    939329

    Productname 2-Fluoro-4-Methylbenzonitrile
    Casnumber 369-40-0
    Molecularformula C8H6FN
    Molecularweight 135.14
    Appearance Colorless to pale yellow liquid
    Boilingpoint 206-208°C
    Meltingpoint N/A
    Density 1.13 g/cm³
    Refractiveindex 1.522
    Flashpoint 90°C
    Smiles CC1=CC(=C(C=C1)F)C#N
    Purity Typically >97%
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms 2-Fluoro-p-tolunitrile

    As an accredited 2-Fluoro-4-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 labeled "2-Fluoro-4-Methylbenzonitrile, 25g." Features hazard symbols, chemical name, CAS, and supplier logo.
    Shipping **Shipping Description for 2-Fluoro-4-Methylbenzonitrile:** 2-Fluoro-4-Methylbenzonitrile should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must comply with local and international regulations for hazardous chemicals. Appropriate labeling and documentation are required. Ensure handling by trained personnel and transport in accordance with UN and DOT guidelines for organic nitrile compounds.
    Storage 2-Fluoro-4-methylbenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Protect from moisture and sources of ignition. Recommended storage temperature is room temperature (15–25°C). Proper labeling and secondary containment are advised to prevent leaks or contamination. Use personal protective equipment when handling.
    Application of 2-Fluoro-4-Methylbenzonitrile

    Applications of 2-Fluoro-4-Methylbenzonitrile in Industrial Manufacturing

    As the original manufacturer supplying 2-Fluoro-4-Methylbenzonitrile, we provide this key intermediate to specialized chemical sectors that incorporate it into downstream processes focused on advanced material and active ingredient development. All application scenarios below reflect established industrial adoption, supported by production QC, formulation expertise, and regulatory standards aligned with global market requirements.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Our 2-Fluoro-4-Methylbenzonitrile serves pharmaceutical manufacturers engaged in the synthesis of fluoroaryl-based APIs, primarily within small-molecule drug pipelines targeting central nervous system (CNS) and oncological indications. The compound acts as a core scaffold introduced at the aromatic substitution stage, supporting SAR optimization for target selectivity and metabolic stability. Downstream processes utilize the nitrile’s reactivity for subsequent transformations, such as amidation or cyclization pathways, according to Route of Synthesis (RoS) requirements. QC protocols encompass residual solvent and impurity profile monitoring in alignment with ICH Q7. Custom formulations may adjust input ratios based on the complexity of step count and scale-up feasibility.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP Part II for API production
    • USP, JP, and EP monograph criteria (where relevant as intermediate)
    • FDA 21 CFR Part 211 for pharmaceutical manufacturing controls

    Typical usage ratio

    • 0.8–1.4 molar equivalents relative to the coupling partner, dependent on RoS and efficiency of secondary transformation; precise quantity adjusted following reaction yield and batch size in early- and late-stage API process development.

    Downstream process integration

    • Introduced during early or middle-stage aromatic substitution/synthetic elaboration
    • Transformation via nucleophilic aromatic substitution (SNAr), amide coupling, or palladium-catalyzed cross-coupling
    • Integration into solid- and solution-phase synthesis steps
    • Employed in multi-step intermediate isolation and purification (chromatography, crystallization, distillation)

    Final product types

    • CNS-active pharmaceutical ingredients
    • Oncology drug candidates
    • Pyridine- or benzamide-containing APIs
    • High-purity research compounds for clinical validation

    2. Agrochemical Synthesis: Herbicides and Insecticides

    Major agrochemical producers use 2-Fluoro-4-Methylbenzonitrile as a nitrile-bearing aromatic building block within the creation of active ingredients for selective herbicides and insecticides. The fluorinated aromatic system is leveraged for target-specific pesticide profiles, with the compound entering synthetic routes via urea or triazine derivatization. Quality assurance relies on detection and control of halogenated byproducts, and REACH registration supports cross-border movement for agricultural applications. The input ratio closely matches stoichiometric demand of the downstream halogenation or amination step, adjusted as scale and endpoint purity dictate.

    Industry compliance standards

    • EU REACH (Regulation (EC) No 1907/2006) registration for import and manufacture
    • FAO/WHO specifications for pesticide technical materials
    • OECD guidelines for chemical safety assessment
    • GLP (Good Laboratory Practice) for process QC and environmental release

    Typical usage ratio

    • 1.0–1.15 equivalents per crop protection active moiety formed; ratio selected to balance cost per ton and yield, with careful control of excess to minimize downstream purification demands.

    Downstream process integration

    • Entry point as an aryl nitrile in triazine, pyridine, or urea synthesis
    • Conversion via nucleophilic addition, condensation, or oxidation
    • Batchwise addition during multi-step technical material formulation
    • Used in pilot and full-scale technical-grade production

    Final product types

    • Selective herbicides for broadleaf weed control
    • Systemic insecticides with fluorinated aromatic profiles
    • Agricultural intermediates for further functionalization
    • Technical-grade crop protection actives

    3. Chemical Building Block for Liquid Crystal and Electronics Materials

    Producers of liquid crystal materials and functional electronic chemicals rely on 2-Fluoro-4-Methylbenzonitrile in the synthesis of anisotropic aromatic frameworks, where fluorinated groups contribute to desired dielectric properties and phase behaviors. The compound is introduced as a key intermediate enabling subsequent coupling via Suzuki or Heck reactions, particularly in creating high-performance aromatic esters and ethers for display technology. Downstream integration addresses thermal stability and electro-optical requirements, with close attention to impurity thresholds and trace metallic residues per industry guidelines. Customization of dosage occurs according to chain length and degree of fluorination required in the end functionalities.

    Industry compliance standards

    • RoHS (Directive 2011/65/EU) for restricted hazardous substance management
    • IEC 62321 for determination of certain substances in electrotechnical products
    • ISO 9001 and ISO 14001 for quality and environmental management in specialty chemical manufacturing
    • SEMI standards for the electronics supply chain

    Typical usage ratio

    • 0.6–1.2 molar equivalents per target mesogen unit; the precise range depends on final product structure and target functional group density; often optimized during pilot study prior to commercial scale production.

    Downstream process integration

    • Key intermediate in Suzuki, Heck, and nucleophilic aromatic substitution reactions
    • Batch-to-batch process QC for purity and trace metal content
    • Formulation with high-boiling organic solvents for thin-film deposition
    • Incorporation into custom-designed LC molecule libraries

    Final product types

    • Liquid crystal display (LCD) alignment layers
    • OLED intermediate compounds
    • Electronic-grade aromatic esters
    • Functional fluorinated resins for circuitry applications

    4. Fine Chemical Intermediate for Specialty Dye Manufacture

    Specialty dye manufacturers employ 2-Fluoro-4-Methylbenzonitrile as a cyanobenzene-based intermediate in the creation of high-stability dyes used in textile and industrial coatings. Its fluoro-methyl aromatic ring configuration facilitates targeted electrophilic substitution, supporting controlled color fastness and unique hue production. Process chemists implement rigorous tracking of unreacted starting material and conversion efficiency, as color reproducibility and purity requirements remain stringent. The dosage is tuned by matching to the number of downstream functional sites and final tint intensity specifications.

    Industry compliance standards

    • Oeko-Tex® Standard 100 for textile chemical safety
    • EN 71-3 (Safety of Toys: Migration of certain elements) if used in relevant coloration scenarios
    • ISO 105 series for colorfastness assessment in textiles
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)

    Typical usage ratio

    • 0.7–1.0 equivalents per chromophore condensation; dosage determined by batch size, extent of dilution, and target molar absorption coefficient.

    Downstream process integration

    • Introduced as a nucleophilic or electrophilic aromatic substrate in dye core synthesis
    • Participates in multi-stage diazo coupling and acylation
    • Integrated into aqueous or solvent-based dye processes
    • Subject to high-purity crystallization and colorimetric QC before downstream use

    Final product types

    • Disperse dyes for polyester textiles
    • Solvent-stable dyes for plastics and coatings
    • High-purity intermediates for speciality colorant libraries
    • Functional dyes in industrial labeling and marking applications
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    Certification & Compliance
    More Introduction

    2-Fluoro-4-Methylbenzonitrile: Manufacturing Perspective on a Reliable Chemical Building Block

    Experienced manufacturers know that subtle molecular differences shape the whole journey from lab synthesis to commercial production. 2-Fluoro-4-Methylbenzonitrile, which carries the molecular formula C8H6FN, carves out a specialized role in both research and industrial sectors. Opportunities to work with this compound—also called 4-Cyano-1-fluoro-2-methylbenzene—often come from demands in pharmaceuticals, agrochemicals, and advanced materials, and it’s our production floor where the rubber meets the road.

    Pushing Toward Precise Structure and Consistent Quality

    Production hinges on controlling the aromatic ring substitution: a nitrile (–CN) group at the para position, a fluorine atom at the ortho position, and a methyl group at the meta position. Tweaking these positions changes the molecule’s chemical reactivity and how it slots into more complex syntheses. The fluorine atom’s presence on the ring often improves thermal stability and adjusts electronic effects, compared with non-fluorinated benzonitriles, so synthetic chemistry teams can create targets otherwise out of reach. The nitrile function brings additional utility, acting as a functional handle for further transformations, frequently featuring in cross-coupling and nucleophilic addition reactions.

    Consistent delivery starts far before packaging. As a manufacturer, analytical control shapes nearly every batch. Most users, especially in drug development, expect high purity—98 percent minimum, with consistent results for melting point and minimal residual moisture. On our lines, we deploy gas chromatography (GC), nuclear magnetic resonance (NMR), and mass spectrometry (MS) to verify purity profiles. Side products and isomers must stay below strict thresholds, not only for regulatory compliance but so downstream chemists can trust the material’s behavior batch to batch. Moisture sensitivity often creeps in for nitriles, and traces of water challenge timelines and reproducibility. We tackle this with tight control of drying and packaging, using inert gas purging or sealed vials depending on shipment and customer requirements.

    Works Behind the Scenes: Usage in Synthesis

    2-Fluoro-4-Methylbenzonitrile isn’t notorious on its own, but its fingerprints show up throughout pharmaceutical and fine chemical pipelines. The ring’s substitution pattern creates a foundation for molecules that steer receptor selectivity in medicinal chemistry. A fluorine atom can drastically shift metabolic stability and lipophilicity—major headaches for medicinal chemists—so starting with this intermediate simplifies complex patent-targeted projects. Downstream, the aromatic nitrile serves as a launching pad for Suzuki–Miyaura and Buchwald–Hartwig couplings, letting teams elaborate even bulkier side chains without losing grip on purity.

    Outside pharma, some agrochemical compounds call for the toughness that fluorinated arenes provide. Hardier molecules mean longer effectiveness in the field and lower risk of off-target environmental impact. The methyl group fine-tunes physical properties—and any tweaks in crystal form, melting behavior, or solubility can mean smoother scaling for formulation scientists. We’ve seen R&D programs move from bench to kilo-scale without revisiting solvent selections, because the starting 2-Fluoro-4-Methylbenzonitrile keeps its expected behavior under pressure.

    Distinguishing Features: Against Other Benzonitriles

    The crowd of benzonitriles gets pretty busy, but position matters. Our teams handle industrial benzonitriles every day—4-methylbenzonitrile, 2-fluorobenzonitrile, even unsubstituted benzonitrile. Each brings something different to synthetic strategy. 2-Fluoro-4-Methylbenzonitrile stands apart by bridging properties: the ortho fluorine helps to guide regioselectivity in subsequent reactions, while the meta methyl protects the ring from certain unwanted electrophilic attacks. This dual substitution lets downstream customers run reactions traditional benzonitriles can’t match, guiding sterics and electronics just by flipping a substituent’s position.

    The methyl group does more than trim molecular weight. It widens solubility windows for many organic solvents, which speeds up processes in continuous reactors and cleans up tricky purifications. Some analogs, especially those with just one substituent, don’t give these processing advantages. Process chemists continually mention the reduced volatility and better handling characteristics during distillation and crystallization, comparing it to more hazardous, less predictable mono-fluorinated or mono-methylated counterparts. These real-world details help formulators and process engineers simplify production, reduce solvent losses, and confidently scale projects.

    A Manufacturer’s Production Experience

    It’s one thing to read off a database entry, but making 2-Fluoro-4-Methylbenzonitrile at scale means managing down-to-earth hurdles: handling raw materials, dialing in temperatures and reaction times, maintaining worker safety, and always hitting purity marks. Most synthesis routes trace back to halogen exchange reactions, sometimes starting with cheaper toluene derivatives and progressing through multiple steps. One key decision point—balancing economic efficiency with environmental health—happens during halogenation. The fluorination step, often a sticking point, has evolved. Past years saw hazardous fluorinating agents or harsh acids, but investment in newer reagents and improved waste treatment reduced corrosion and cut back on health risks. Experienced crews and vigilant monitoring prevent side reactions and keep impurity profiles consistent.

    After synthesis, our workflow includes versatile isolation strategies: crystallization or careful extraction, depending on solvent compatibility. Too aggressive on one front and unwanted byproducts climb; too conservative and batch yields fall, taking costs with them. Over time, we tuned the protocols to keep bottlenecks rare and still meet non-stop demand. Even in busy periods, customers need product with little downtime, which means redundancy in drying and storage, backup analytics, and tight container management. Removing trace metal impurities became a priority when our pharma clients mentioned catalysis concerns; adopting new chelation steps addressed this without sacrificing throughput.

    Shipping this intermediate takes planning, not only for compliance with chemical transport laws, but to address sensitivities like moisture or prolonged light exposure. We use amber glass and aluminum foil where necessary, and track climate during transit for sensitive batches. Pharma contractors—sometimes running compounds through patent timelines—expect the shipment to match their projected stability data, no unpleasant surprises that could derail regulatory filings. Years in this business mean we’re ready to solve questions about lot uniformity, trace contaminants, or documentation, delivering what customers need for strict quality audits.

    Real-World Challenges and Process Solutions

    It’s easy to overlook the complexities behind a stable supply of an aromatic intermediate. Every batch depends on uninterrupted access to upstream materials—fluorinated aromatics and cyanide donors don’t always flow predictably due to geopolitics or regulatory changes. Working closely with trusted upstream partners means we can respond quickly if a supplier has a disruption. During resource-constrained periods, we leverage long-term relationships and strategic stockpiles, built from experience rather than theory. By staying flexible on order quantities and storage solutions, supply reliability stays in front of shifting global circumstances.

    Process safety remains front of mind. Handling fluorination reactions requires robust containment and ventilation—not just for workers, but for the whole environment surrounding a facility. Years ago, tighter air and effluent monitoring cost more and slowed lines, but regular feedback from auditors and local authorities improved our systems. Routine training keeps personnel aware of the hazards (and why they matter), and our incident records back up that effort. Chemical manufacturing rewards steady hands and communication more than flashy intervention, a lesson sometimes learned the hard way.

    Resource efficiency—the line between waste and product—draws constant refining. Reaction optimization can cut energy needs and solvent loads, not just to please regulators but to tighten margins. Our data show that even subtle parameters like agitation speed or solid dosing rates meaningfully shift yields, and everyday production decisions reflect those hard-won lessons. Waste gas scrubbing and continuous distillation, introduced over several cycles, now cut emissions and boost yield purity. Some contracts demand a green chemistry focus, and we meet those needs thanks to incremental, data-driven process improvements built up batch by batch.

    Quality Audits and Regulatory Navigation

    Manufacturers working directly with regulated industries recognize the web of rules—and auditor expectations—that surround aromatic nitriles. Pharmaceutical customers in particular dig deep, expecting clear traceability for every batch, from incoming materials through to final warehousing. This means in-house documentation needs detail beyond basics: chain of custody, real-time batch data, water content, impurity profiles, and documented responses for any deviation or unexpected event. Third-party audits sometimes feel relentless, but we treat these as benefits, tightening our own standards each time. Feedback from recent compliance checks streamlined our record-keeping, making retrieval for regulatory filing much faster than older paper-based systems.

    New projects or expanded production draw environmental regulators to the table. Our engineering staff meet them early, sharing monitoring data, safety upgrades, and process improvements to maintain transparency and trust. This proactive approach reduces risk, keeps local communities informed, and smooths out any reactionary slowdowns during project scale-up. Ultimately, customers feel these efforts not in the paperwork, but in the reliability of their shipments and the confidence they have in sourcing from a compliant facility.

    What Direct Manufacturing Experience Can Offer Users

    Unlike brokers or distributors, those at the production level can immediately spot variability, sometimes before it appears in analytics. If a raw material shifts due to a new source, if solvent grades drift even slightly, downline products diverge. In our experience, successful support for partners means being able to answer not just “what’s in the bottle?” but “what does this mean for your process?” Chemists often ask for advice on solvent compatibility, compatibility with specific catalysts, prediction of impurity trends, or advice for changes in reaction workups. Our frequent feedback loop with users helps prevent bottlenecks and keeps projects on schedule. Recent collaborations helped drug discovery teams troubleshoot crystallization issues, tuning their procedures based on solubility and impurity profiles we could see firsthand.

    Sharing information builds trust. Every anomalies log helps laboratory and production teams refine stability estimates—no one benefits from batch-to-batch surprises when working against critical timelines. We encourage joint troubleshooting, either through conference calls or direct plant visits, since details like color, texture, or subtle odor changes can flag equipment or supply issues. This openness sets the manufacturing approach apart from standard “box-mover” operations, and reinforces commitments to repeat users looking for long-term collaboration.

    Addressing Market Evolution and Customer Needs

    While technical literature covers the synthesis and core uses of 2-Fluoro-4-Methylbenzonitrile, growth trajectories often run ahead of reporting. Demand from specialty pharma companies has increased, alongside requests for tailored impurity profiles or off-cycle delivery schedules. New clients prompt upgrades, not only in analytical depth but in how our teams communicate expected outcomes and possible risks. Every time a big launch comes for a new API route, frontline manufacturing experience helps anticipate technical support questions, expectations for documentation, and required response times.

    Requests to reduce packaging size, guarantee cold-chain custody, or provide rush testing during inbound transit forced realignment of older process assumptions. By collaborating closely with transportation and logistics partners, and with hands-on oversight, we reduced hold-ups during customs checks and port delays. Meeting evolving needs usually means more than tweaking a spec sheet—it’s about listening to process feedback, charting patterns, and introducing changes without compromising reliability.

    Emerging sustainability criteria, which sometimes remain vague in procurement documents, are forcing upgrades to solvent recovery and waste management processes. Green chemistry pushes compel smarter use of byproducts and stricter solvent selection, where secondary waste poses cost pressure and compliance headaches. Field experience shows that pursuing these goals rewards manufacturers with better control of input costs and risk management.

    Reflections From the Manufacturing Floor

    Molecules like 2-Fluoro-4-Methylbenzonitrile often remain invisible to the end user, but they power countless innovations behind the scenes. Decades in this field highlight a recurring theme: it’s not the headline molecules, but reliable intermediates, that determine the tempo of research and commercial pipelines. For production teams, the daily job relies on technical details, but also on communication, adaptability, and pride in consistent performance. Every improvement—better protocols, cleaner analytics, tighter containment—stems from feedback and the desire to support chemists running at industry pace.

    Future projects, especially those in high-impact sectors, will continue to expect more from their intermediate suppliers: better lot-to-lot uniformity, faster response on logistics, tailored technical advice, and transparent problem-solving. The trust placed in manufacturers who deliver on these fronts builds the foundation for medical, agricultural, and material breakthroughs, even when the ingredients themselves remain quietly in the background.