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4-Fluoro-3-Methylbenzonitrile

    • Product Name 4-Fluoro-3-Methylbenzonitrile
    • Alias 4-Fluoro-3-methylbenzenecarbonitrile
    • Einecs 626-039-6
    • 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

    710343

    Cas Number 400-51-9
    Molecular Formula C8H6FN
    Molecular Weight 135.14
    Appearance White to off-white solid
    Melting Point 37-40 °C
    Boiling Point 222-224 °C
    Density 1.15 g/cm3
    Refractive Index 1.525
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles Cc1cc(C#N)ccc1F
    Inchi InChI=1S/C8H6FN/c1-6-3-2-7(5-10)4-8(6)9/h2-4H,1H3
    Synonyms 3-Methyl-4-fluorobenzonitrile

    As an accredited 4-Fluoro-3-Methylbenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle labeled "4-Fluoro-3-Methylbenzonitrile, 99%, 100g" with hazard symbols, lot number, and tightly sealed cap.
    Shipping 4-Fluoro-3-Methylbenzonitrile is shipped in sealed, chemical-resistant containers to prevent leakage and contamination. It is transported under ambient conditions, with proper labeling as a hazardous substance. Shipping follows international regulations, ensuring safety for handling, storage, and transit. Documentation with hazard information and handling instructions accompanies each shipment.
    Storage 4-Fluoro-3-Methylbenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure labeling is clear and follow all safety guidelines applicable to handling aromatic nitriles. Use appropriate personal protective equipment when handling.
    Application of 4-Fluoro-3-Methylbenzonitrile

    Applications of 4-Fluoro-3-Methylbenzonitrile in Industrial Manufacturing

    4-Fluoro-3-Methylbenzonitrile serves as a specialty intermediate in several advanced chemical production chains. As a direct manufacturer, we supply this compound to OEM and contract processors operating in high-value chemical sectors, focusing on quality consistency required for scale-up and regulatory compliance.

    1. Pharmaceutical Intermediate Production

    Our customers use 4-Fluoro-3-Methylbenzonitrile in the synthesis of substituted aromatic compounds that act as building blocks for active pharmaceutical ingredients (API), particularly for certain oncology and CNS drug candidates. The compound’s structure enables selective halogenation and amination steps in advanced synthetic schemes. Process development laboratories integrate this raw material during Stage 2 or Stage 3 intermediate formation, with critical impact on subsequent yields, impurity profiles, and route scalability.

    Industry compliance standards

    • ICH Q7 for GMP active pharmaceutical ingredient manufacturing
    • USP and Ph. Eur. monograph references for related substances
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • REACH Regulation (EC) No 1907/2006 for use in EU API synthesis

    Typical usage ratio

    • 0.8–1.2 molar equivalents per pharmaceutical intermediate, optimized according to the yield plateaus in pilot-scale batches and impurity control restrictions

    Downstream process integration

    • Stage 2–3 of multi-step synthesis: nucleophilic aromatic substitution or direct cyanation prior to further functionalization (e.g., amide coupling, heterocycle formation)

    Final product types

    • Advanced pharmaceutical intermediates for anti-cancer and CNS therapy compounds
    • Fine chemicals for contract API manufacture

    2. Agrochemical Synthesis

    Producers in the crop protection industry source 4-Fluoro-3-Methylbenzonitrile as a core intermediate for manufacturing fluorinated aromatic rings found in selective herbicides and fungicide actives. The unique electron-withdrawing pattern enhances downstream product stability and bioactivity. Our material enters the synthetic process at the nitrile input stage, where derivatives undergo subsequent chlorination, hydrolysis, or condensation steps to tailor the mode of action against target pests.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • ISO 9001:2015 for agrochemical intermediate production
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • GLP requirements for raw material traceability

    Typical usage ratio

    • 0.7–1.0 molar equivalents relative to final agrochemical scaffold, adjusted upwards in high-yield pilot runs to maximize downstream conversion and lower cost of goods

    Downstream process integration

    • Early-phase benzene ring assembly prior to sulfonation or carboxylation, usually via continuous-flow or batch reactors

    Final product types

    • Herbicides incorporating fluorinated aromatic moieties
    • Systemic fungicide active substances

    3. Liquid Crystal Material Manufacturing

    Major electronics chemicals enterprises depend on 4-Fluoro-3-Methylbenzonitrile for the synthesis of advanced liquid crystal intermediates. The compound’s specific substitution enables fine-tuning of dielectric anisotropy and phase transition temperatures in high-end LCD and OLED display applications. This building block enters directed ortho-metalation and etherification reactions for the creation of biphenyl or phenylpyrimidine derivatives essential for controlled optical properties.

    Industry compliance standards

    • IEC 61249-2-41 standards covering material use in electronic displays
    • RoHS Directive 2011/65/EU for restricted substances
    • ISO 14001:2015 for environmental management in electronics chemicals manufacture
    • REACH pre-registration requirements for specialty chemicals

    Typical usage ratio

    • 1.0–1.3 molar equivalents per custom-designed liquid crystal intermediate, adapted based on purity cutoff at 99.5% and end-use specification

    Downstream process integration

    • First-step coupling for mono- or di-substituted aromatic cores, followed by sequential halogenation and etherification for targeted LC material grade

    Final product types

    • Liquid crystal intermediate blends for TFT-LCD and OLED displays
    • Speciality high birefringence materials for advanced display panels

    4. Dye and Pigment Intermediate Manufacturing

    Specialty dye formulators use 4-Fluoro-3-Methylbenzonitrile in the construction of high-tone, lightfast organic pigments. The presence of fluorine and methyl substituents increases the pigment molecule’s photostability, color intensity, and resistance to chemical degradation. Our manufacturing partners introduce this raw material in the coupling and azo condensation stages, especially for automotive, plastics, and textile coloration where long-term color retention is critical.

    Industry compliance standards

    • EN 71-3:2019 for safety of toys (dye residue in pigments)
    • ISO 9001:2015 with pigment-specific QC provisions
    • REACH SVHC assessment protocols
    • Oeko-Tex Standard 100 for textile dye intermediates

    Typical usage ratio

    • 0.4–0.8 molar ratio per pigment chromophore; ratio optimized for hue strength and migration resistance

    Downstream process integration

    • Intermediate coupling during diazotization and condensation, followed by blending and milling with stabilizers and dispersants

    Final product types

    • Organic pigments for high-performance automotive and industrial coatings
    • Textile dyes with enhanced fastness properties

    5. Chemical Vapor Deposition (CVD) Precursor Preparation

    Producers in the advanced coatings and microelectronics sectors select 4-Fluoro-3-Methylbenzonitrile as a tailored precursor for specialty CVD processes. Its controlled volatility and stability allow for efficient introduction of functionalized aromatic layers in protective and dielectric coatings. Downstream processors utilize the compound during precursor synthesis, involving selective fluorination and subsequent conversion to target haloaromatics used in thin-film deposition.

    Industry compliance standards

    • SEMI S2 guidelines for semiconductor materials compatibility
    • ISO/TS 16949:2009 for automotive electronics materials
    • RoHS compliance for materials entering electronics manufacturing
    • REACH Regulation (lot batch traceability for high purity chemicals)

    Typical usage ratio

    • 0.6–1.0 molar equivalents per CVD precursor molecule, tailored per substrate coverage and volatilization efficiency

    Downstream process integration

    • Integrated as a starting point in precursor molecule assembly, then purified to sub-ppm impurity level prior to vapor phase delivery

    Final product types

    • CVD precursors for surface passivation or barrier films in microelectronics
    • Dielectric thin films for advanced semiconductor devices
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    Certification & Compliance
    More Introduction

    4-Fluoro-3-Methylbenzonitrile: A Critical Intermediate for Today’s Synthesis

    Introduction to 4-Fluoro-3-Methylbenzonitrile

    Every year in our facilities, the demand for specific aromatic nitriles continues to grow, and 4-Fluoro-3-Methylbenzonitrile stands out among them. Known to chemists as an essential building block, this compound delivers versatility and reliability that’s hard to match. In our daily work, we see it bring tangible value to labs and factories producing fine chemicals and pharmaceuticals. We manufacture this product through carefully controlled steps, where the interplay of methyl and fluoro groups on the benzonitrile core alters properties compared to similar nitriles.

    Physical and Chemical Properties Defined by Experience

    The unique combination of a methyl group at the third position and a fluoro atom at the fourth position on the benzene ring changes the behavior of the molecule. Our teams have measured its melting point, boiling point, density, and purity over many batches, refining our understanding beyond what’s listed in technical reference books. Our observations show 4-Fluoro-3-Methylbenzonitrile produces a liquid that holds stability during standard storage and handling, repelling moisture and resisting degradation under typical warehouse conditions.

    We routinely achieve high-purity products using our own developed purification protocols. Product purity, usually exceeding 99.5%, remains consistent batch after batch. Quality inspectors check spectral fingerprints for every lot, using NMR and GC-MS, and we retain these records for transparency and traceability. Our 4-Fluoro-3-Methylbenzonitrile meets high standards, free of noticeable side-products that sometimes trouble offbrand alternatives.

    Usage Forged from Industry Experience

    In daily practice, customers turn to 4-Fluoro-3-Methylbenzonitrile to build more complex molecules. Laboratory teams employ it as an intermediate in the synthesis of active pharmaceutical ingredients, where downstream modifications depend on the electronic nature of both the fluoro and methyl groups. Chemists appreciate the activating effect of fluorine and the steric profile the methyl group introduces. This dual modification encourages selectivity during further reactions, a benefit we’ve witnessed over countless proofs-of-concept.

    Process scale-ups reveal additional strengths. The compound’s manageable boiling point makes it straightforward to recover from reaction mixtures. It withstands common solvents like acetonitrile, toluene, and DMF, facilitating compatibility with established synthetic pathways. Drug discovery projects often focus on such fluorinated aromatics because they help tweak surface binding and metabolic properties of drug candidates. For agrochemical and material science researchers, this compound offers a useful platform for developing new products with tailored reactivity and stability.

    What Sets 4-Fluoro-3-Methylbenzonitrile Apart

    Chemically, the placement of the fluoro atom matters. Many clients, having tried both 4-fluorobenzonitrile and 3-methylbenzonitrile, report that neither delivers the same reactivity or product profiles as their combination in this molecule. In our own labs, we have compared reaction rates, yields, and side-product profiles when using neighboring analogues. The introduction of the fluoro atom at para to the nitrile modifies electronic distribution across the ring, increasing electrophilicity, while the meta methyl group shapes reactivity at other positions. These subtle changes result in different outcomes in catalytic couplings or nucleophilic substitutions.

    Synthetic challenges also point toward this intermediate. Some transformations work only with this particular aromatic scaffold. Over the years, customers who switched from ortho- or para-methyl or fluoro variations have confirmed that only the 4-fluoro-3-methyl combination succeeds for some target molecules. Our process team often collaborates with clients to troubleshoot their routes and finds that using this intermediate unlocks pathways previously hindered by poor yields or excessive by-products.

    Why Purity Matters in Scale-Up and Production

    From small bottles shipped to research labs to drums bound for pilot plants, every batch must meet defined analytical standards. Running kilo-scale synthesis projects in-house, we’ve encountered the consequences of impurities firsthand – from unpredictable yields to difficult downstream purification. Even seemingly minor contamination, undetected by basic tests, can amplify in a process, resulting in expensive troubleshooting later. For this reason, our focus remains on analytical rigor. We maintain full spectral data for every lot produced and can trace each drum to the specific production date, purification protocol, and analytical signature.

    Scaling up reactions highlights another fact: byproducts often become more troublesome at larger volumes. Our senior chemists have refined recrystallization and distillation techniques, sometimes running parallel developmental batches to optimize conditions for maximum isolation and minimal loss. Such efforts may not appeal to every supplier, but to us, repeatable process outcomes hinge on this type of care. Internal feedback from our production sites flows directly to our QC and R&D teams, closing the loop and sharpening our process further.

    Supporting Research and Process Innovation

    Many of our collaborations with universities and pharmaceutical companies have focused on optimizing syntheses that use 4-Fluoro-3-Methylbenzonitrile as a starting point. Students and postdocs have visited our facilities, testing reaction conditions with our guidance and sometimes returning with finished samples for further evaluation. Among recent projects, a new heterocyclic scaffold was assembled through selective substitutions enabled only by this aromatic nitrile’s combination of fluoro and methyl groups. The project produced several patent applications and opened the door to further exploration.

    Our technical support extends beyond shipping product. Occasionally, customers ask our scientists to help troubleshoot synthetic steps. In one example, a scale-up team encountered yield drops that pointed back to a previously unnoticed impurity contaminating the starting material. With our deep product knowledge and capability for detailed analysis, we tracked down the culprit and helped design a new protocol, restoring process reliability. The experience underscored the importance of both product consistency and a willingness to dig into the nuances of synthetic chemistry.

    Observations on Safety and Handling

    Work in chemical manufacturing brings firsthand awareness of the practicalities of safe handling. 4-Fluoro-3-Methylbenzonitrile, like most aromatic nitriles, releases a mild odor when open to air. In the plant, operators handle it wearing butyl gloves and splash-resistant goggles, storing containers in cool, ventilated areas away from direct sunlight. Our incident tracking highlights that leaks or spills very rarely occur – prompt cleaning with standard absorbents addresses most issues without escalation. We always make the necessary safety data sheets available, updating documentation with new risk data as it arises. Our environmental team monitors effluents carefully to prevent release of organic contaminants into water systems.

    Inside the plant, tighter containment measures and secondary enclosures have proved effective. During decanting or transfer operations, we have come to rely on closed-loop systems and in-line vapor recovery. This promotes a healthy workspace and prevents loss of valuable material. We have replaced older glassware in the kilo lab with jacketed steel and PTFE-lined systems, giving operators more control and reducing the chance of contamination or spills. Years of running this product have taught us that upfront investment in containment pays back in lower clean-up costs and smoother audits.

    Environmental Consistency

    Modern buyers ask for more than just product quality. They want to know how their ingredients are made and whether the process aligns with environmental and auditing goals. 4-Fluoro-3-Methylbenzonitrile occupies a critical position here. We avoid hazardous reagents that may generate persistent waste, preferring milder fluoride sources and employing solvents that can be recovered and recycled within our plant. At several stages, exhaust gases pass through carbon capture beds that neutralize volatile organics, preventing their escape into the environment.

    Water conservation remains important during purification. Our process design minimizes the need for wash water and captures organic residues for specialist disposal. Yearly audits track waste streams and help us focus investment on equipment upgrades that bring measurable reductions. These improvements resonate with purchasing and regulatory teams looking for resilient, transparent supply chains. Colleagues in our sustainability division work alongside production, aiming to drive further efficiency into every step.

    Comparing to Other Intermediates

    The marketplace features benzene derivatives with all kinds of substitutions: fluoro, methyl, nitrile, or combinations thereof. We see customers weigh options like 3-fluorobenzonitrile, 4-methylbenzonitrile, and 4-cyanotoluene against our product, trying to match reactivity to their own downstream needs. 4-Fluoro-3-Methylbenzonitrile offers a different reaction profile compared to these alternatives. In direct substitution, the stronger electron-withdrawing nature of the para-fluoro group shifts acidity and electrophilicity of certain ring positions. Our analytical group has published spectra and reaction outcome summaries demonstrating that small changes in ring substitution influence the selectivity of follow-up reactions such as Suzuki couplings, nucleophilic substitutions, or reductions.

    We have also worked closely with customers trying to swap starting materials, seeking cost or availability gains. More often than not, the distinctive combination found here provides an edge that is hard to replicate by blending other simple aromatics. The interplay of substitution matters for both the efficacy of the transformation and the purity of the final product in their process. This practical knowledge, built up over years of troubleshooting and optimization, shapes our recommendations for customers tackling new synthesis projects.

    Lessons from Routine Production

    Reliability emerges only from repetitive experience. Each production campaign for 4-Fluoro-3-Methylbenzonitrile starts well before the first batch – sourcing upstream reagents, validating storage conditions, running small proof runs to verify equipment tolerances. From daily operations, we have learned to keep a close eye on temperature ramp rates, mixing times, and solvent quality. An overlooked valve or a variance in raw material purity can lead to noticeable changes in yield or impurity profile. By running extensive internal training, we empower our operators to recognize and react to off-normal situations without delay.

    Our continual effort does not stop with consistency; it extends into incremental improvements. Sometimes, a critical look at a ten-year-old process reveals a chance to cut cycle times or reclaim more solvent. In the past quarter, for example, we implemented a new filtration routine after a bench-scale experiment showed it could reduce fine particulate carryover into the final product. This tweak shaved hours off drying times and sharpened product color, which our customers noted in their feedback.

    Addressing Common Challenges

    Several market shifts in recent years have impacted the sourcing and manufacture of specialty nitriles like 4-Fluoro-3-Methylbenzonitrile. Cost pressure on raw fluorinated materials, volatility in global solvents, and energy prices all introduce variability. In response, we adapt sourcing strategies annually, building contingency stocks and forming multi-source agreements with upstream suppliers. Our logistics specialists keep close watch on route disruptions and customs requirements, making sure critical shipments proceed with minimal delay.

    Inside the facility, equipment maintenance remains a non-negotiable priority. Pumps and seals that fail mid-batch risk contaminating entire runs or halt production. Our shift engineers run preventive maintenance routines, using condition monitoring sensors to flag abnormal readings before they turn into downtime. Between batches, vessels undergo full inspections, with photographic logs compiled by lead technicians for accountability. From these hard-won routines comes a steady supply that customers can count on, week after week.

    Continuous Feedback and Customer Interaction

    Dialogue with end-users shapes the way we approach both production and support. Some of our most valuable insights have come from customer pilots and scale-ups. For example, a recent project required tighter specification on moisture and residual solvents, which prompted us to revisit and strengthen our drying protocols. In other cases, early-stage customers experimenting with new routes have highlighted subtle differences in product appearance or odor, leading us to run additional stability trials.

    Technical support does not stop at delivery. Our application scientists respond readily to process queries, sharing hints on how certain solvents or catalysts affect downstream steps. We take pride in promptly shipping reference samples for method development, supporting both small research outfits and multinational manufacturers launching new projects. If a batch ever falls short of expectations, we run a thorough root-cause review, report back with findings, and take corrective action. The cumulative effect of these interactions shapes stronger internal standards and increases trust.

    Navigating Regulatory Expectations

    Requirements imposed by regulatory authorities and customer quality managers continue to grow more detailed every year. We respond by keeping documentation up to date and conducting in-house mock audits. Each product pack ships with full analytical data, including chromatograms and NMR spectra, giving receivers assurance that the shipment matches what’s described. The regulatory climate often drives updates in trace impurity thresholds, residual solvent allowances, and on-site testing frequency.

    We have invested in rapid detection instruments for on-the-fly measurement of possible contaminants. Feedback loops from auditor reports flow straight into our SOP updates. In regions requiring specific registration or notification, our regulatory team compiles documentation to speed clearances and minimize surprises at customs. For customers navigating their own inspection environments, open access to these records builds confidence and allows for smoother process validation.

    Summary: Partnering for Reliable Supply and Process Success

    Looking back on years of manufacturing and shipping 4-Fluoro-3-Methylbenzonitrile, what stands out is not just the technical challenge of producing a high-purity compound, but the relationships formed through shared process improvement. Our experience has shown that small variations in molecules lead to large differences in how they perform in downstream reactions – and direct communication with users goes further than any datasheet. As markets for specialty chemicals continue to develop, this intermediary product remains pivotal in driving scientific and technological progress for pharmaceuticals, agrochemicals, and advanced materials.

    Fundamentally, long-term success rests on a foundation of careful process control, transparent quality assurance, environmental consideration, and open technical exchange. We remain committed to supporting our partners, sharing lessons from daily plant operations, and continuously striving to deliver a product that meets demanding requirements in the real world of chemistry.