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4-Fluoro-2-Methylbenzonitrile

    • Product Name 4-Fluoro-2-Methylbenzonitrile
    • Alias 4-Fluoro-o-tolunitrile
    • Einecs 624-211-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    353786

    Product Name 4-Fluoro-2-Methylbenzonitrile
    Cas Number 112898-08-7
    Molecular Formula C8H6FN
    Molecular Weight 135.14
    Appearance Colorless to pale yellow liquid
    Boiling Point 211-214 °C
    Density 1.102 g/cm³
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Flash Point 89 °C
    Synonyms 2-Methyl-4-fluorobenzonitrile
    Smiles CC1=CC(=CC=C1F)C#N
    Inchi InChI=1S/C8H6FN/c1-6-4-7(5-10)2-3-8(6)9/h2-4H,1H3
    Refractive Index 1.527

    As an accredited 4-Fluoro-2-Methylbenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100g amber glass bottle with a secure screw cap, labeled "4-Fluoro-2-Methylbenzonitrile" and hazard symbols clearly displayed.
    Shipping 4-Fluoro-2-Methylbenzonitrile should be shipped in tightly sealed, labeled containers, protected from moisture and light. It must comply with chemical transport regulations, typically via ground or air using UN-approved packaging. Ensure appropriate hazard labeling (flammable, irritant), shipping documentation, and, if required, Safety Data Sheet (SDS) accompany the shipment to guarantee safe handling and transport.
    Storage Store 4-Fluoro-2-Methylbenzonitrile in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture, direct sunlight, and excessive heat. Clearly label the container and ensure proper secondary containment to prevent leaks or spills. Follow appropriate chemical safety protocols and local regulations for hazardous materials.
    Application of 4-Fluoro-2-Methylbenzonitrile

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

    As a core manufacturer committed to specialty chemical innovation, we supply 4-Fluoro-2-Methylbenzonitrile for selected high-impact sectors with validated downstream utility. The following sections showcase major industrial applications, focusing on specialized usage aligned with strict compliance standards and robust process integration. Each scenario details the prevailing regulatory framework, precise formulation parameters, insertion into downstream operations, and the typical end products delivered by our direct customers.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Multinational API producers employ this raw material in the preparation of advanced pharmaceutical intermediates, particularly in the synthesis chains for certain CNS-active agents and antineoplastic drug candidates. As a key nitrile building block, it integrates at early-to-mid-stage processes where aromatic ring substitution is essential for target molecule bioactivity. API production environments demand strict batch traceability, regulatory adherence, and continuous process validation to satisfy regulatory review during both development and commercial manufacture.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – 21 CFR Parts 210/211 (US FDA)
    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs relevant to target APIs
    • Validated impurity profile assessment per ICH Q3A/B

    Typical usage ratio

    • Input concentration in reaction mixture: 0.8–1.5 molar equivalents per molecular target unit
    • Ratio varies by target API structure and stoichiometric requirements; adjusted to minimize waste and maximize conversion yield

    Downstream process integration

    • Used in multi-step synthesis post-halogenation and pre-amidation or further derivatization steps
    • Charged to hydrogenation or Grignard coupling reactors following standard charge-in protocols
    • QC release on entry for residual solvent and isomer content

    Final product types

    • CNS-active pharmaceutical intermediates
    • Anticancer drug precursors
    • Aryl nitrile-derived custom molecule building blocks for R&D

    2. Agrochemical Intermediate for Pyridine-based Herbicides

    Leading crop protection companies utilize this ingredient in the synthesis of selective herbicide actives where fluoroaromatic functionalities enhance biological activity and selectivity. Its controlled incorporation enables yield-efficient, chlorination-resistant pyridine compound synthesis. The addition parameters are tightly managed for consistent lot quality, especially as the chemical participates at the core ring formation stage in multi-hectare production environments operating under agrochemical Good Laboratory Practices (GLP).

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • EPA pesticide registration dossier standards (40 CFR Part 158)
    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for agrochemical production

    Typical usage ratio

    • Added at 1.0–2.0 molar equivalents relative to ring formation limiting reactant
    • Exact ratio calculated based on final yield targets and reactivity of substituted aromatic systems

    Downstream process integration

    • Charged during the initial condensation or nucleophilic aromatic substitution (SNAr) stage
    • Incorporated in batch or continuous-flow setups, depending on plant scale
    • Raw material is filtered and purity-verified before addition

    Final product types

    • Pyridine-based pre-emergent herbicides
    • Selective weed control actives for cereals and legumes
    • Herbicide intermediate concentrates for formulation in SCs, WDGs, and ECs

    3. Intermediate for High-Performance Dye and Pigment Synthesis

    Specialty dye manufacturers leverage this fluoroaromatic intermediate for designing colorants where precise electron density modulation of aromatic rings enables fine hue tuning and fastness attributes. Its addition directly determines chromophore formation during key condensation or cyclization steps, especially in the production of cationic, disperse, and solvent dyes. Early-stage process design focuses on analytical purity, as downstream performance heavily depends on the profile of trace organic residues.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical substance registration
    • Eco Passport by OEKO-TEX® certification for dyestuff inputs
    • GHS (Globally Harmonized System) classification and labeling
    • ISO 9001:2015 for dye manufacturing process control

    Typical usage ratio

    • Formulation addition: 5–12% weight basis depending on the target chromophore structure
    • Adjusted within the formulation to achieve specific absorption and colorfastness parameters

    Downstream process integration

    • Introduced during primary condensation or step-growth polymerization for dye base creation
    • Strict pre-mixing with stabilizers for dispersion uniformity in continuous reactors
    • Subjected to inline HPLC purity monitoring before pigment isolation

    Final product types

    • Cationic dyes for acrylic fabrics
    • High-performance solvent dyes used in plastics, fibers, and paints
    • Specialized colorants for inkjet and industrial coatings

    4. Electronic Chemicals: Intermediate for Liquid Crystal and OLED Materials

    Manufacturers of advanced electronic materials employ this compound as a critical intermediate in the preparation of functional liquid crystal monomers and OLED light-emitting compounds, taking advantage of its stable fluoroaromatic framework and tunable electronic properties. Precise dosage and high-purity requirements are vital, as any contamination or structural inconsistency translates directly into device performance parameters such as contrast, brightness, and environmental resistance.

    Industry compliance standards

    • IEC 61249-2-21: Halogen Free Requirements for Electronic Materials
    • RoHS Directive (2011/65/EU) restriction of hazardous substances
    • JEITA industry guidelines for advanced display materials
    • ISO 9001:2015 for electronic chemical manufacturing

    Typical usage ratio

    • Reactant input: 3–10 mol% relative to other monomer feedstocks in display material synthesis
    • Adjusted lower for high-purity LC monomer production, higher for charge-transport molecule synthesis

    Downstream process integration

    • Fed into aromatic coupling or Suzuki-Miyaura cross-coupling stages
    • In-line purification prior to use in monomer synthesis for LC cells
    • Process includes end-point monitoring for fluoro impurities

    Final product types

    • Liquid crystal monomers for TFT-LCDs and OLED panels
    • P-type and n-type organic semiconductors
    • Light-emitting layer compounds for display backplanes
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    Certification & Compliance
    More Introduction

    Introducing 4-Fluoro-2-Methylbenzonitrile: Meeting the Demands of Modern Synthesis

    The story of 4-Fluoro-2-Methylbenzonitrile begins in the laboratory, but its influence stretches far beyond benchwork. As a factory rooted in the daily routines of chemical manufacturing, we know the difference fine details can make when it comes to specialty intermediates. We deal with the production, the handling, and the problem-solving that follow each batch. There is no substitute for "good enough" here; close enough often spells trouble in downstream synthesis. Over years in aromatic nitrile preparation, this molecule, known by its chemical formula C8H6FN and CAS number 455-86-7, earns a spot as a distinct and reliable building block for numerous applications.

    Why 4-Fluoro-2-Methylbenzonitrile Matters on the Factory Floor

    Some molecules step into a reaction as generic tools, while others, like 4-Fluoro-2-Methylbenzonitrile, take on far more specific roles. Fluorinated aromatic nitriles have grown in demand from pharma and agrochemical sectors due to their unique combination of a reactive cyano group and the subtle electronic influence of fluorine on the ortho position. Over the years, our staff sees repeat requests from both established and startup R&D teams looking for this unique combo. Stability remains reliable in this compound, sidestepping many of the hydrolysis concerns that plague less robust nitrile derivatives.

    Internally, our production teams weld their expertise around the preparation: controlled aromatic substitution, robust purification, careful distillation routines. The result shows up as a clear, pale liquid or low-melting solid, depending on storage and ambient conditions. Purity speaks for itself, measured down to ppm levels using modern GC and NMR. Our operations staff remembers times with older, less stable analogs — some like 2-methylbenzonitrile or 2-fluorobenzonitrile alone — that would introduce unexpected side reactions downstream. The addition of both methyl and fluoro gives better selectivity in modern coupling steps, especially when metal catalysts join the mix.

    Consistency in Production Yields Fewer Headaches Downstream

    Each kilogram comes off the line as a testament to years of upgraded plant design, not just a number on a batch sheet. We invest as much in the reproducibility of 4-Fluoro-2-Methylbenzonitrile as the obvious parameters like melting point or solubility. Chemists in other plants will know: sharpness in spectral fingerprints and a tight boiling range mean less trouble finding byproducts at later stages. Several pharmaceutical teams share stories with our technical support about how tiny inconsistencies in earlier generations of benzonitriles would force entire reworks, costing not just time but credibility. Fine-tuning batch management, solvent recovery, and temperature control forms part of our day-to-day work precisely to dodge such pitfalls.

    The physical parameters rarely deviate: good density control, dependable refractive index, and an unmistakable faint aromatic odor. No single step stands out as glamorous, yet each phase — from raw material inspections to routine Karl Fischer titrations for trace moisture — holds back major issues that could snowball in API production or crop protection pipelines.

    Factory Experience: Nuances Beyond Brochure Specifications

    Specification sheets tell part of the story, but reality cuts sharper. The most feedback we receive from customers revolves around ease of handling and chemical compatibility. While aromatic nitriles can sometimes impart biting or acrid odors, 4-Fluoro-2-Methylbenzonitrile carries a faint, less intrusive scent. In the warehouse, this means less need for additional air scrubbing compared with compounds like 4-chlorobenzonitrile. Our handling crews consistently mention this as key during transfers and repackaging.

    From a production perspective, the margin for error is narrower when scaling new syntheses. Thermal stability and low volatility come with both the methyl and fluoro substitutions, reducing evaporative loss during open handling and maintaining batch concentrations for more predictable reaction yields. Competing nitriles without this structure tend to show inconsistent recoveries in large runs, creating frustration and unnecessary root cause analyses for engineers. As a producer, chasing batch-to-batch uniformity becomes a marathon, not a sprint.

    Solving for Synthesis: Practical Use Cases from Our Customers’ Labs

    The real test of 4-Fluoro-2-Methylbenzonitrile comes when it leaves our gate. Over time, we've seen it take on essential roles as an intermediate in synthesis pathways leading to active pharmaceutical ingredients, advanced agrochemicals, and specialty polymers. One frequent use shows up in coupling reactions: the combination of a highly activating fluoro on the ring and the position-selective methyl group allows for more targeted transformations. Medicinal chemists aiming for fluorinated aromatics in drug candidates note how these substitutions help tune the molecule’s lipophilicity and metabolic stability, two parameters that occupy their minds day and night. In these labs, minor impurities have outsized effects. We work closely with process engineers to tweak purification and drying stages, delivering an end product that stands out against generic nitrile stock commonly sourced from less regulated producers.

    Polymer researchers also turn to this intermediate for introducing fluoro-capped monomer units into specialty plastics. The cyano group opens doors for further functionalization, while the relative ease of handling and the manageable hazard profile fit well in both small pilot setups and full-scale production. In contrast, more hazardous or unstable nitriles demand stricter containment and slower runs, sapping time and energy from the schedule.

    Comparing with Other Benzonitriles: Lessons from Production

    Working with various analogs across the years, clear differences come into focus. Standard benzonitrile offers less versatility in site-selective coupling, leading to more byproduct formation, inconsistent yields, and higher purification costs. Adding a methyl group to the ortho position alone, as in 2-methylbenzonitrile, alters reactivity but does not offer the same resonance effects or selectivity in electrophilic aromatic substitution that fluorine imparts. Meanwhile, singly fluorinated benzonitriles, such as 2-fluorobenzonitrile, miss out on the blocking advantage of the methyl group, leaving the ring open to more unpredictable substitution.

    The most compelling difference sets in during scale-up. 4-Fluoro-2-Methylbenzonitrile’s dual substitutions give it enough stability to withstand shipping and storage better than many single substituent compounds. Unsubstituted or mono-substituted analogs degrade or polymerize more quickly, especially under warm or humid conditions. We listen to feedback from both overseas and local customers: shipments of the dual-substituted grade land consistently with no hint of discoloration or hydrolysis. This consistency carries through to the last vial, a factor that cannot be overvalued by anyone who has dealt with material fallout or sudden specification drifts mid-campaign.

    Challenges and Solutions: Meeting Rising Regulation and Market Demands

    Compliance expectations shift faster each year. Several customers in regulated industries, notably those facing active pharmaceutical ingredient (API) regulatory audits, require full traceability, batch documentation, and validated analytical results. Over the last decade, we built digital systems for batch tracking and auditing. Data transparency and reproducibility improve customer trust and ease their own compliance efforts. Precursors and reaction steps are backed with thorough COA (Certificate of Analysis) reporting, inline documentation, and sample retention.

    On the logistics front, we've picked up plenty of lessons. We've seen how fluctuations in raw material pricing or delays in critical reagents throw off older, less agile manufacturers. Integration of alternative sourcing and strategic stockpiling limit the impact of such turbulence. Our raw material auditing runs year-round, with regular quality spot checks on every drum. This vigilance pays dividends during turbulent supply cycles. While some stray from such routine for cost savings, we have learned that stabilization of supply chains secures our facility, and, by extension, our customers’ timelines.

    Sustainability in Specialty Chemical Manufacturing

    As sustainable chemistry becomes a central request from partners, we've adapted both synthesis and energy usage around site-wide audits, solvent recycling, and waste minimization. Conventional nitrile synthesis routes often generate byproducts that pose environmental concerns, but years of fine-tuning, investment in high-efficiency scrubbers, and process control keeps emissions safely within guidelines. Our staff spends regular time retraining for new methods, reflecting the growing importance of green chemistry even within what might seem a small, specialty product.

    Continuous improvement also impacts worker and community safety. Exposure mitigation strategies, proper containment, and up-to-date personal protective equipment remain routine. We take feedback from everyone actively involved with daily operations; small insights on valve upgrades or operator shifts have often reduced near-misses and minor accidents. This bottom-up system for safety bolsters the consistency and trustworthiness of the product as well.

    Supporting Innovation: Future Directions for 4-Fluoro-2-Methylbenzonitrile

    Market trends indicate increasing incorporation of fluorine atoms within pharmaceuticals and specialty materials. The unique properties of the 4-Fluoro-2-Methylbenzonitrile scaffold place it in an ideal position for researchers chasing next-generation leads. The dual substituents prove particularly helpful for late-stage modification strategies. Because medicinal chemistry programs continue to demand ever cleaner starting points, our QC protocols and SOPs evolve along with those needs. Every month, we evaluate new analytical techniques for improved impurity detection and push timelines on method validation so our customers have less waiting.

    Technical support also evolves. Queries range from the basics of solvent choice and reaction temperature profiles to deep dives on catalyst compatibility. By keeping lines open between our floor managers and end-user chemists, we help dodge missteps that cause delays or unexpected costs. What works in a hundred-gram flask doesn't always succeed in a five-hundred-kilogram reactor. Only broad, hands-on manufacturing experience bridges this divide. We focus on that gap relentlessly—it's where shortcutting can prove disastrous, and thoughtful planning delivers savings in every measurable category.

    What It Means to Work with Real Manufacturers

    In a world where resellers, brokers, and endless intermediaries stand between the source and the lab, engaging with a true manufacturer makes real differences. Our experience spans far beyond batch paperwork; the learning comes from every maintenance round, every unscheduled troubleshooting session, every customer audit. This daily grind—scaling up, scaling down, tempering surprises—forms our credibility. We own the outcomes of every lot that leaves our facility, whether bound for a three-person research team or a full-scale production plant. The discipline built here, from investment in analytical tools to worker training, stays with every product, especially a nuanced molecule such as 4-Fluoro-2-Methylbenzonitrile.

    Looking Ahead with Confidence

    Wholesale changes in global chemistry priorities won’t diminish the role of well-characterized intermediates. The clarity, selectivity, and stability of 4-Fluoro-2-Methylbenzonitrile reflect the persistent needs of real-world manufacturing. Our ongoing investments in quality management, traceability, and environmental responsibility form part of a continuous improvement process—one that our longest-standing customers count on and new partners seek out for their toughest synthesis challenges. The result is a molecule whose consistency and reliability speak to well-honed factory practice. We will keep listening, learning, and refining—the same way we have since the start—knowing that each detail matters, because every day on the line teaches what a specification sheet alone never tells.