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3-Fluoro-5-Methylbenzonitrile

    • Product Name 3-Fluoro-5-Methylbenzonitrile
    • Alias 3-Fluoro-5-methylbenzenecarbonitrile
    • Einecs 841-728-6
    • 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
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    Specifications

    HS Code

    742624

    Product Name 3-Fluoro-5-Methylbenzonitrile
    Cas Number 407-24-1
    Molecular Formula C8H6FN
    Molecular Weight 135.14
    Appearance Colorless to pale yellow liquid
    Boiling Point 213-215 °C
    Density 1.12 g/cm³ at 25 °C
    Purity Typically ≥98%
    Smiles CC1=CC(=CN=C1)F
    Inchi InChI=1S/C8H6FN/c1-6-2-3-7(9)5-8(6)10/h2-3,5H,1H3
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms 3-Fluoro-m-tolunitrile

    As an accredited 3-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 labeled "3-Fluoro-5-Methylbenzonitrile, 99%, 25g" with hazard symbols, lot number, and manufacturer information.
    Shipping 3-Fluoro-5-Methylbenzonitrile is shipped in tightly sealed, chemical-resistant containers to prevent leaks or contamination. The packaging meets regulatory standards for hazardous materials. It is transported under controlled conditions, avoiding extremes of temperature, moisture, and direct sunlight. Proper labeling, documentation, and handling instructions ensure safe delivery to authorized recipients.
    Storage 3-Fluoro-5-methylbenzonitrile should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, preferably under inert gas if moisture sensitive. Store at room temperature and protect from direct sunlight. Clearly label the container and follow all appropriate chemical storage regulations and safety protocols.
    Application of 3-Fluoro-5-Methylbenzonitrile

    Applications of 3-Fluoro-5-Methylbenzonitrile in Industrial Manufacturing

    3-Fluoro-5-Methylbenzonitrile serves as a key aromatic intermediate in a range of specialized manufacturing channels. Our direct supply chain and strict production control support precise, traceable integration in each advanced downstream process.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical producers incorporate 3-Fluoro-5-Methylbenzonitrile during the early stages of active pharmaceutical ingredient (API) synthesis, especially in complex heterocyclic compounds for anti-cancer and central nervous system drug development. Its electron-withdrawing nitrile and fluoro groups support regioselective transformations in Suzuki-Miyaura and Buchwald-Hartwig couplings. Facilities rely on this intermediate for constructing fluorinated scaffolds, satisfying strict impurity and residual solvent controls throughout multi-step synthesis routes for regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • EU GMP Part II (APIs)
    • U.S. FDA 21 CFR Part 211 (Finished Pharmaceuticals Manufacturing)
    • ChP, USP, JP pharmacopoeia impurity and residual solvent limits

    Typical usage ratio

    • 5–25% of limiting reactant molar feed in API intermediates; production chemists adjust loading by target yield and desired step economy in multi-step syntheses.

    Downstream process integration

    • Introduced in the amidation or cross-coupling stage of API intermediate assembly, prior to core ring closure or final fluorination.

    Final product types

    • Anti-cancer drug intermediates (e.g., for tyrosine kinase inhibitors)
    • Central nervous system actives intermediates
    • Fluorine-containing heterocycles for research APIs

    2. Agrochemical Active Ingredient Production

    Leading agrochemical manufacturers source 3-Fluoro-5-Methylbenzonitrile for the synthesis of selective herbicide and fungicide molecules. Its methyl and fluoride substituents contribute unique selectivity and metabolic stability in target field applications. Synthetic chemists frequently deploy it for benzamide or substituted phenylpyridine assembly, introducing the nitrile group in early backbone functionalization, thus supporting cost-effective scale-up with tight impurity profiles.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Agrochemicals
    • FAO/WHO Specifications for Plant Protection Products
    • REACH Annex XVII (Europe, for handling aromatic nitriles)
    • SIN List (ChemSec) compliance, as required by downstream customers

    Typical usage ratio

    • 8–15% by weight in intermediate agrochemical backbone synthesis; process R&D teams fine-tune the ratio based on target molecule loading for pilot and commercial scale-up.

    Downstream process integration

    • Feeds directly into nucleophilic aromatic substitution, hydrolysis, and condensation steps for herbicide and fungicide pre-cursors.

    Final product types

    • Herbicide intermediates (e.g., for selective grass and broadleaf control actives)
    • Fungicide precursors targeting resistant phytopathogens
    • Finished crop protection test batches for regulatory trials

    3. Advanced Liquid Crystal Material Manufacturing

    Specialty electronics material companies utilize this benzonitrile derivative in the synthesis of high-performance liquid crystal intermediates for LCD and OLED displays. The molecular structure contributes to the fine-tuning of dielectric anisotropy and phase transition temperatures. The compound commonly enters etherification or esterification steps tailored for high-purity, low-ion contaminants—a requirement in sensitive optical applications.

    Industry compliance standards

    • IEC 61249-2-21 for electronic assembly
    • RoHS Directive (EU) 2011/65/EU and 2015/863 amendments
    • JEITA guidelines for contamination in display substrates
    • China RoHS GB/T 26572-2011 for electronics materials

    Typical usage ratio

    • 2–7% by mole in precursor blends; R&D adjusts according to the desired birefringence and viscosity profiles in display grade liquid crystals.

    Downstream process integration

    • Charged into etherification or condensation steps; purified via chromatographic or crystallization routes before blending with final liquid crystal batch.

    Final product types

    • High-purity liquid crystal monomers
    • LCD and OLED panel intermediates
    • Custom display active mixtures

    4. Fluorinated Polymer Additive Synthesis

    Polymer manufacturers deploy 3-Fluoro-5-Methylbenzonitrile during the creation of specialty monomers and additives used to fine-tune polymer surface energy, adhesion, and weather resistance. Beyond copolymerizable monomer synthesis, this aromatic nitrile acts as a functional group donor in the post-polymerization modification of engineering plastics, supporting tailor-made performance in automotive, electronics, and industrial coatings applications.

    Industry compliance standards

    • ISO 14001 Environmental Management Systems
    • ASTM D256 and D638 for polymer performance
    • UL 94 (flammability standards for polymers)
    • EU REACH registration requirements for monomer and additive import

    Typical usage ratio

    • 0.5–5% by weight in monomer feed; technical teams vary dosage based on targeted surface properties and downstream customer requests.

    Downstream process integration

    • Introduced in the functionalization or grafting stage in monomer synthesis, or blended in the extrusion compounding line for polymer modification.

    Final product types

    • Fluorinated acrylic or styrenic copolymers
    • Engineering resin additives for automotive and electronics
    • Weather-resistant industrial coatings
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    Certification & Compliance
    More Introduction

    3-Fluoro-5-Methylbenzonitrile: A Closer Look from the Manufacturer’s Perspective

    Understanding 3-Fluoro-5-Methylbenzonitrile in the Modern Chemical Industry

    Our facility has been producing aromatic nitrile compounds for years, and few products generate as much focused interest as 3-fluoro-5-methylbenzonitrile. Its chemical structure (C8H6FN) reflects a balance between fluorination and methyl substitution, a feature synthetic chemists and pharmaceutical developers value for its role in preparative routes. We see this compound ordered most often for its influence on molecular frameworks, especially where electronic effects of the fluorine atom combine with the steric profile contributed by the methyl group.

    The material comes as a colorless to pale yellow liquid, but experienced staff recognize it in the plant by the subtle, sharp aroma that’s typical of nitrile intermediates. In our line, the model used in the catalog is 3F5MBN, always produced to a minimum chemical purity of 98%, supported by in-house HPLC and GC-MS QC results. Very few requests come back with complaints about off-spec shipment because our QA procedures are tight, run by operators trained to spot changes in both process and appearance long before packing. There’s no magic in making this molecule; it demands patience through multi-step reactions and an understanding of how fluorinated aromatics react under controlled conditions.

    Why 3-Fluoro-5-Methylbenzonitrile Matters Right Now

    Clients who buy directly from us aren’t often looking for generic nitriles. They specify 3-fluoro-5-methylbenzonitrile because it builds certain target molecules that do not tolerate substitutions elsewhere on the ring, either because of activity in medicinal screening or stability in agrochemical environments. Recent years have seen a greater need for selective substitution on benzene rings, especially where electron density and steric effects must be controlled in final products. Fluorinated aromatic nitriles have stepped up in this environment to create more robust scaffolds for drug discovery and crop protection.

    Research teams bring us challenging requests: They want customized lots, clear traceability, and on-time production. For 3F5MBN, we’ve scaled up our continuous flow production lines, allowing us to keep up with pilot and commercial scale orders. Years ago, we would not have seen kilogram-scale requests for this intermediate. The expansion came directly from the needs of end-users who discovered that even a single methyl or fluorine shift changed the behavior of their final compounds. Making these molecules on scale means strict attention to reagent sourcing and close monitoring of each production parameter, especially temperature control during the cyanation step.

    Specification and Quality Control: What Matters Most to Us

    Every batch of 3-fluoro-5-methylbenzonitrile walks through our QC lab before it ships. We’re not working for traders who mix lots from different plants; our team controls reactor charge, temperature ramp, and solvent recovery on one site. Spec sheets sometimes become copy-paste affairs in the broader distribution world, but we take pride in substantiating all advertised criteria. Purity over 98%, residual solvents below 0.1%, GC retention time matching reference samples—these are not luxuries, they’re the baseline. Because the synthetic route for this nitrile passes through a sensitive aromatic halogenation, we place extra emphasis on elemental analysis to confirm both the placement and content of fluorine and methyl substituents.

    Moisture sensitivity rarely enters the conversation but matters when users store even modest amounts. Handling in our facility follows protocols to keep atmospheric water and potential hydrolysis away from business end of the process. Glass-lined storage tanks and inert gas overlays aren’t afterthoughts—they’re requirements hard-won through years of dealing with real-world returns and customer complaints about minor degradations. Documentation, from COA to shipment logs, ties directly back to production records—a level of traceability that’s proven valuable during audit seasons and regulatory submissions for downstream applications.

    Use Cases: From Discovery Labs to Scale-Up Synthesis

    Requests from the pharmaceutical industry dominate our order book for 3-fluoro-5-methylbenzonitrile. A medicinal chemistry team might select this molecule when they aim to insert precise substitutions in the ortho or meta positions of a parent drug candidate. The fluorine atom, packed onto the aromatic ring, tweaks acidity and metabolic resistance, while the methyl group often changes the way a compound interacts with biological targets or the solvent system. Clients share feedback from screening results, making it clear that slight molecular modifications change not only the activity of the parent compound but also the route efficiency and cost structure.

    Several agrochemical producers reached out over the past year seeking tons of this product per month. For them, the value sits in the way the fluorine group blocks unwanted enzymatic breakdown in crop systems. The methyl group influences volatility, making the final formulation suitable for field use. Bringing high-purity intermediates directly into these workflows means that our products touch real-world applications: crop fields, pilot pharmaceutical plants, university R&D, and even advanced materials settings where substituted aromatics serve as ligands for catalysts. We hear from catalysts researchers interested in how unique substitution patterns allow for new metal coordination behaviors, pushing innovation in synthesis routes not considered a decade ago.

    Differences from Related Aromatic Nitriles

    In the aromatic nitriles catalogue, choices quickly become overwhelming. What separates 3-fluoro-5-methylbenzonitrile from 4-fluorobenzonitrile, 3-fluorobenzonitrile, or 3,5-dimethylbenzonitrile comes down to the position and number of ring substitutions. The presence of fluorine and methyl groups at precise positions lets chemists fine-tune electronic environments, affecting the reactivity in nucleophilic aromatic substitution or transition metal-catalyzed couplings. Unlike plain benzonitrile, our target compound resists certain kinds of oxidative degradation, a property observed in stability trials across several partner labs. The methyl group also impacts boiling point and solvent compatibility, details that scale-up chemists consider non-negotiable when translating bench results to production lots.

    Clients often ask about the relative reactivity of 3-fluoro-5-methylbenzonitrile in typical synthetic transformations. Our technical support staff draws from hundreds of production batches to guide these conversations. This molecule offers a higher selectivity for ortho-lithiation protocols compared to 4-fluorobenzonitrile, largely due to the combined electron-donating and electron-withdrawing properties of its substituents. In palladium-catalyzed couplings, users see changes in conversion rates and side-product formation which differ sharply from unsubstituted aromatic nitriles. Speaking from direct synthetic experience, these chemical nuances cut down waste streams and cut back on purification headaches—critical factors in any process that values sustainability and cost-efficiency.

    Challenges in Manufacturing: Lessons from the Plant Floor

    No batch of 3-fluoro-5-methylbenzonitrile leaves our facility without a story. Manufacturing involves more than just recipes—fluctuations in raw material supply chains, variable catalyst batch activity, and evolving EH&S standards for handling fluorinated aromatics all play key roles in final cost and availability. Personnel have learned to watch for peak exotherms during halogenation and cyanation steps; we train reactor operators to expect the unexpected, not just follow SOPs. Over time, tweaks in solvent choice and agitation speeds created safer, more robust syntheses that minimize human error and environmental load.

    Scaling up from gram to ton-level introduced new headaches: heat removal and stirring efficiency play out differently in large vessels. Early pilot runs exposed weaknesses in old reactor linings, prompting a complete overhaul of containment protocols and the adoption of new monitoring technologies. It’s one thing to make lab quantities for confirmation; supporting multinational pharmaceutical launches calls for contingency planning, backup raw material storage, and direct partnerships with tanker providers.

    Working with Customers: From Inquiry to Repeat Orders

    The level of engagement with research and production customers continues to shape how we design and operate our 3-fluoro-5-methylbenzonitrile workflow. Many customers start with written queries about impurity profiles and regulatory documentation. Quick, clear, unfiltered answers establish working trust that outlasts any single transaction. Repeat orders come from firms who remember rapid delivery in a supply pinch or clear technical explanations during their last process change.

    We spend time in joint troubleshooting when users encounter unexpected side reactions or downstream purification problems. Sometimes the solution sits upstream: a change in isomer ratio, a tweak in drying protocols, or implementing a more robust filtration step can turn an experimental setback into a process gain. The closer we work to customer challenges, the more we learn about the practical performance of our product away from our own plant. That feedback loop shapes both new SOPs and the continued training of our staff—ensuring that the experience and knowledge base in the company stay practical, not theoretical.

    Looking Forward: Keys to Improvement and Collaboration

    Several drivers will increase the importance and complexity of 3-fluoro-5-methylbenzonitrile in the coming years. Pharmaceutical R&D cycles shorten as new chemical entities race to patent and clinical milestones, and so the need for reliable intermediates keeps rising. Environmental, health, and safety regulations increase scrutiny on aromatic nitrile processing; every year brings an update to waste management laws, emissions control technology, or acceptable contaminant levels. We’ve invested in energy recovery and scrubber upgrades to address these, not because of outside pressure, but because operator safety and community relations are worth the extra margins squeezed from production costs.

    Product consistency depends on strong supplier relationships upstream and real-time production data on the shop floor. Years of experience have shown the value of redundancy in everything: raw material storage, staff training programs, and IT systems backing up batch records. In direct collaboration with customers, we regularly review technical targets and problematic production phases, aiming for improvements that stick. Open dialogue and on-site visits build working knowledge that outpaces any manual or online seminar.

    Applications in Emerging Fields

    Demand for substituted benzonitriles has spilled beyond pharmaceuticals and agrochemicals. Electronics materials utilize these building blocks to develop new classes of liquid crystals and advanced polymers. We’ve seen requests for 3-fluoro-5-methylbenzonitrile in specialty pigment manufacture, where the balance of fluorine and methyl substitutions drives both color stability and processing temperature. OLED manufacturers trial our lots for new host materials; laboratory reports underscore the way subtle changes in fluorination levels alter emission wavelengths or improve device lifetimes.

    As interest grows in sustainable chemistry, our research and manufacturing teams explore bio-based or less energy-intensive synthetic routes. Initial investments in alternative cyanation chemistry show promise, but scale-up takes time and honest assessment of yield, byproducts, and overall lifecycle safety. Here, hard-earned chemical intuition and careful data sharing with supply chain partners separate which innovations last from fleeting lab curiosities. Making meaningful environmental gains means balancing the chemistry with uptime, labor safety, and regulatory talk that often lags behind technical progress.

    Supporting Innovation and Building Confidence

    One consistent lesson from long-term manufacturing: reliability earns more trust than any marketing claim. Research teams, formulators, and process engineers expect their questions about synthesis impurities, storage conditions, and regulatory compliance to be met with real answers and data-backed recommendations. We maintain open archives of batch records, analytical chromatograms, and stability studies, available for customer review as part of any due diligence or QA audit.

    Internal conversations do not stop at process yields or weekly production targets. Every lot produced ties back to operator feedback, off-spec batch investigations, and regular reviews of customer returns or complaints. Successful long-term operations develop out of this honest, sometimes messy information exchange. The plant’s incident logs and procedural revisions capture a history of what worked and what needed to change, benefiting both staff and end-users down the line. The transparency makes it possible to adjust material specifications in pace with developing regulatory or technical standards, keeping the whole system aligned with industry direction and customer needs.

    Navigating the Regulatory Environment

    Changes in regulations for handling aromatic nitriles, fluorinated chemicals, and associated waste streams have a direct impact on daily production. Operator training, detailed documentation, and constant monitoring of emissions contribute to compliance with emerging national and international standards. Over the years, we have learned not to rely on minimal compliance; emergencies and supply shocks speak in hard numbers and real consequences. Our incident response protocols are updated from lessons gathered across the sector, cementing practices that prioritize safety, integrity, and transparency—criteria our customers and partners value as highly as price or delivery time.

    Certifications and regulatory support matter most to end-users preparing their own documentation for active pharmaceutical ingredient (API) filings or crop protection regulatory dossiers. Our team supports these submissions with original analytical reports, validated stability studies, and explicit supply chain documentation. If a user’s internal audit questions a shipment, our records provide stepwise granularity from raw material input through final container sealing. This level of documentation calls for ongoing investment in data systems and staff training, but pays off in customer confidence and repeat business.

    Final Thoughts from the Production Line

    Years spent making and refining 3-fluoro-5-methylbenzonitrile have cemented lessons that carry over to nearly all our other operations: do not rush process changes, keep technical discussions open and honest, and always seek practical feedback from people handling or using the product on the ground. This approach built the backbone of a reputation for quality and reliability among direct users in pharma, agrochemical, and advanced materials industries.

    We learn from every customer request, lab report, and field complaint, turning these into tangible changes in workflow and plant practice. The end-products made from our material might span medicine, crop protection, or electronics, but every shipment delivers not just a chemical, but the result of thousands of decisions, improvements, and hours spent shaping a safe and dependable process. That experience—earned, not assumed—remains at the core of everything we do around 3-fluoro-5-methylbenzonitrile and beyond.