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3-Chloro-4-Fluorobenzonitrile

    • Product Name 3-Chloro-4-Fluorobenzonitrile
    • Alias 3-Chloro-4-fluorobenzene carbonitrile
    • Einecs 630-807-3
    • 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

    101195

    Name 3-Chloro-4-Fluorobenzonitrile
    Synonyms 3-Chloro-4-fluorobenzenecarbonitrile
    Cas Number 57381-51-8
    Molecular Formula C7H3ClFN
    Molar Mass 155.56 g/mol
    Appearance White to off-white solid
    Melting Point 53-56°C
    Boiling Point 238-240°C
    Density 1.38 g/cm3
    Smiles C1=CC(=C(C=C1Cl)F)C#N
    Inchi InChI=1S/C7H3ClFN/c8-6-1-2-7(9)5(3-6)4-10/h1-3H
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically >98%

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

    Packing & Storage
    Packing 250g of 3-Chloro-4-Fluorobenzonitrile is packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping **Shipping Description for 3-Chloro-4-Fluorobenzonitrile:** This chemical is shipped in secure, airtight containers compliant with regulatory standards for hazardous materials. It should be transported at ambient temperature, with appropriate labeling and documentation. Handle with care to avoid spills or leaks, and follow all safety guidelines regarding toxic and irritant substances during transit.
    Storage 3-Chloro-4-fluorobenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from incompatible substances such as strong oxidizing agents. Store at room temperature and avoid moisture to prevent hydrolysis. Properly label the container and follow all relevant safety and regulatory guidelines.
    Application of 3-Chloro-4-Fluorobenzonitrile

    Applications of 3-Chloro-4-Fluorobenzonitrile in Industrial Manufacturing

    As the direct manufacturer of 3-Chloro-4-Fluorobenzonitrile, we supply this specialty intermediate to a select number of advanced chemical industries. The following application scenarios demonstrate how downstream producers integrate this product into key manufacturing workflows, with attention to practical processing, regulatory compliance, and formulation parameters based on established industrial practice.

    1. Pharmaceutical Active Ingredient Synthesis

    3-Chloro-4-Fluorobenzonitrile serves as a phenyl-nitrile precursor during the synthesis of specific fluoro- and chloro-substituted heterocycles, which form the core of a new generation of pharmaceutical active ingredients. Downstream formulators incorporate it during multi-step batch syntheses, focusing on regulated intermediate handling and stringent impurity control for API pipeline development. The compound’s reactivity at the 3 and 4 positions helps streamline the introduction of further functional groups in late-stage derivatization, reducing raw material cost and minimizing waste generation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs (international)
    • USP-NF General Chapter <1007> (Process Ingredients)
    • FDA 21 CFR Part 211 (US Drug cGMP)
    • European Pharmacopoeia (for process intermediates)

    Typical usage ratio

    • Added at 0.8–1.4 molar equivalents relative to target heterocycle, depending on required selectivity and yield; adjusted based on pathway optimization studies

    Downstream process integration

    • Third or fourth step in multi-stage synthesis, entering as an aryl nitrile partner in Suzuki or Buchwald coupling sequences; handled under closed-system, nitrogen-blanketed operations

    Final product types

    • Oral solid pharmaceutical APIs (e.g., kinase inhibitors, CNS drugs)
    • Key non-intermediate process controls for regulated drug intermediates

    2. Agrochemical Synthesis: Herbicide and Fungicide Intermediates

    Agrochemical manufacturers employ 3-Chloro-4-Fluorobenzonitrile as an intermediate for constructing fluorinated benzene scaffolds, which are embedded in weed and fungal control actives. Its unique substitution pattern enables formation of compounds with enhanced target specificity and environmental stability. Integration into the synthetic sequence requires careful ratio control to stay within regulatory impurity limits while maximizing throughput during large-scale production campaigns.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides (JMPS Guidelines)
    • ISO 9001:2015 Quality Management Systems for chemical manufacture
    • European REACH (1907/2006) chemical registration and safety
    • Chinese GB/T 19001 Quality Certification (for exported agrochemical intermediates)

    Typical usage ratio

    • Typically charged at 85–92% of stoichiometric requirement for target synthetic routes; proportion adjusted based on purity of other inputs and real-time in-process chromatographic monitoring

    Downstream process integration

    • Used as the primary aromatic nitrile during initial cyclization and halogenation sequences in continuous reactor systems, later undergoing further functionalization to dialkylamino or ester-substituted derivatives

    Final product types

    • Technical-grade herbicides (e.g., for corn, soybean applications)
    • Fungicide precursors for cereal and fruit crop protection

    3. Advanced Dye and Pigment Intermediate

    Dye and pigment producers, especially those targeting high-performance textiles and plastics, use 3-Chloro-4-Fluorobenzonitrile to create azo and anthraquinone backbones with controlled color fastness and light stability. Its fluorinated ring boosts hydrophobicity, enhancing finished pigment dispersibility and weathering resistance. Downstream plants dose the nitrile at precise points to avoid unwanted side-reactions, with calorimetric controls in place to monitor exothermic stages of dye coupling.

    Industry compliance standards

    • OEKO-TEX Standard 100, Class I/II (Textile Safety/Restricted Substances)
    • EN 71-3 Safety of Toys (applicable to colorants in plastic toys)
    • ISO 14001:2015 Environmental Management
    • ZDHC Wastewater Guidelines (zero discharge of hazardous chemicals)

    Typical usage ratio

    • Used at 3–8% by weight of total pigment synthesis batch, with ratio fine-tuned during lab color matching trials

    Downstream process integration

    • Introduced as a primary aryl nitrile reactant during the oxidative coupling or diazotization stage, preceding sulfonation or carboxylation steps based on pigment class

    Final product types

    • Azo pigments for synthetic fibers and technical textiles
    • Anthraquinone dyes for automotive plastics, coatings, and printing inks

    4. Specialty Materials: Liquid Crystal and Electronic Chemical Intermediate

    In advanced electronics, 3-Chloro-4-Fluorobenzonitrile plays a crucial role as a rigid core-building block for synthesizing liquid crystal monomers and specialty polymers. Its chloro-fluoro aromatic structure promotes high dipole moments and order parameters, enabling development of high-response nematic or smectic liquid crystal mixtures for high-definition displays. Manufacturers maintain tight control on batch quality and residual halide specification before blending into multi-component assemblies.

    Industry compliance standards

    • RoHS Directive 2011/65/EU and amendments (for electronics)
    • IEC 61249 Halogen-Free Electronic Materials (for advanced displays)
    • JEDEC JESD625B Handling of ESD Sensitive Devices (for sensitive monomer synthesis)
    • ISO 9001 Quality Management (electronics-grade materials)

    Typical usage ratio

    • Charged at 2.8–5.5% by mass relative to the total blend of monomer precursors, selected for optimizing phase transition temperature and dielectric anisotropy in final liquid crystal formulations

    Downstream process integration

    • Condensed with other halogenated or nitrile aromatics in main batch reactors under anhydrous, low-redox conditions before further polymerization into oligomeric or multi-armed mesogen units

    Final product types

    • Nematic and smectic liquid crystal mixtures for TFT-LCD and OLED displays
    • High-purity specialty polymers for thin electronic films and optical materials
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    Certification & Compliance
    More Introduction

    3-Chloro-4-Fluorobenzonitrile: Insights From the Manufacturer’s Bench

    A Closer Look at 3-Chloro-4-Fluorobenzonitrile

    Years of daily work in process chemistry have taught us that each benzonitrile derivative brings its own quirks to the production line. 3-Chloro-4-Fluorobenzonitrile, often recognized by the molecular formula C7H3ClFN, fills a definite gap between simpler halogenated aromatics and more complicated substituted benzonitriles. Our plant routinely delivers both standard and custom grades, with the most popular lots meeting assay values of 99% or better by HPLC. Standard batches maintain a melting point range around 56-58°C and offer low moisture content as measured by Karl Fischer titration. The appearance—white to slightly off-white crystalline solid—signals purity to those in the know.

    Handling routine synthesis runs, you notice that 3-Chloro-4-Fluorobenzonitrile boasts a straightforward work-up. It resists most ambient air and light exposure, which means fewer headaches with storage and transit across short or long distances. Our operators appreciate how it remains steady in both glass and steel reactors, so plant contamination checks don’t run into surprises. The manageable volatility allows us to scale up runs without the need for exotic containment measures. We package it tightly, and even on the tail end of a year-long storage, GC traces rarely show significant decomposition.

    What Sets 3-Chloro-4-Fluorobenzonitrile Apart in the Lab and On the Floor?

    Working directly in manufacturing offers a better view of how practical differences translate to results. This compound stands out from similar nitriles like 3-chlorobenzonitrile or 4-fluorobenzonitrile. You gain selectivity in downstream chemistry, particularly in nucleophilic aromatic substitution and catalytic coupling reactions. The presence of both chloro and fluoro groups on the benzene ring influences reactivity during condensation with amines or when undergoing palladium-catalyzed transformations. Routine production runs often use it as a key intermediate for creating agrochemicals and specialty pharmaceuticals.

    Practical differences go beyond lab notebooks. The combined chloro and fluoro substituents alter partition coefficients, impacting the solubility profile. In our experience, 3-Chloro-4-Fluorobenzonitrile dissolves well in polar aprotic solvents like DMF or acetonitrile, but shows far lower miscibility in aliphatic hydrocarbons. That’s not just a lab curiosity—it changes the solvent choices for scale-up, waste stream management, and work-up design, letting us recycle more solvent and cut down on environmental impact.

    Real-World Use: Where 3-Chloro-4-Fluorobenzonitrile Excels

    We started seeing demand pick up from both crop protection and drug development sectors. Most customers track this compound for its role in synthesizing target molecules with either pyrazole or pyrimidine rings. In pesticide synthesis, downstream substitution reactions hinge on the dual halogen pattern carried by 3-Chloro-4-Fluorobenzonitrile. The electron-withdrawing effect from each halogen influences the electrophilicity of the cyano group, making it a highly tunable intermediate.

    Custom synthesis teams often bring us specs demanding tight impurity control, since heterocyclic intermediates work best with clean feeds. Our process design limits trace byproducts such as dichlorinated or difluorinated regioisomers. In-house, we run preparative chromatography to verify that each lot avoids contamination by non-target isomers, which downstream users appreciate for reproducibility.

    In pharmaceuticals, project managers have told us that the combined chloro-fluoro fragment can enhance metabolic stability in lead compounds. Some research groups send us feedback showing that aromatic substitution patterns like this one slow down hepatic breakdown. That translates into longer half-lives for test compounds, which makes pharmacokinetic studies smoother—another subtle benefit of choosing this intermediate over simpler nitriles.

    Why Precision and Consistency Matter in Benzonitrile Production

    You can tell who manufactures and who packages just by looking at quality deviations between batches. In our experience, slight shifts in catalytic hydrogenation pressure or quench temperature throw off the purity profiles. Our operators calibrate equipment on every cycle and avoid batch overlaps to prevent cross-contamination. GC-MS and HPLC checks run for each lot, and we track not just assay and purity but also trace colored bodies and water content. These steps offer more than routine paperwork—they prevent headaches downstream when secondary reactions pick up trace impurities.

    Scaling up from kilo to tonne scale usually exposes where the real bottlenecks appear. With 3-Chloro-4-Fluorobenzonitrile, persistent bottlenecks tend to stem from efficient gas-liquid mixing or consistent chill in crystallization. We learned to control crystallization rates tightly: slow cooling in jacketed vessels rather than ice baths produces the best solid. Quick cooling can lead to clumping or occluded solvents, so we fine-tune the ramp rate during solidification. Our shipping team runs visual inspections on every drum before lid-sealing to catch any lumps or moisture pockets.

    Advantages over Related Intermediates

    In the field, using mixed halogenated benzonitriles provides unique levers for selectivity. The 3-chloro-4-fluoro pattern alters both steric and electronic factors during Grignard, Suzuki, or Buchwald-Hartwig coupling. Why does this matter? In multiple customer projects, we’ve watched as alternate starting materials led to over-reaction or skipped target sites. The current product gives researchers control over where and how substitutions occur.

    Compared to simpler benzonitriles like the mono-chloro or mono-fluoro variants, this compound creates a more rigid aryl ring with lower propensity for random side-reactions. Researchers interested in dehalogenation, halide exchange, or C-H activation have sent us feedback showing higher yields and cleaner isolation from using the dual-substituted system. On a practical level, we see less tar or polymerized side products building up, so cleanup on the plant floor stays manageable.

    Operational Experience and Lessons Learned

    Handling this benzene nitrile on a day-to-day basis, we seldom encounter the runaway reactions or sticky residues that sometimes arise with higher-molecular-weight analogs. Reactor fouling, a notorious trouble spot for some aromatic intermediates, doesn’t show up as often in the runs involving 3-Chloro-4-Fluorobenzonitrile. We attribute this to its balanced volatility and crystalline nature, which also means filter maintenance takes less downtime.

    Solvent washes—both methanol and ethyl acetate—pull residual traces off steel walls, so we avoid shutdowns for deep cleaning. Each time we cycle a line for a new batch, the switchover documentation rarely calls for extra precautions. These day-to-day factors lead to more on-spec shipment, with less plant hours lost to troubleshooting batch problems.

    Environmental and Safety Commitment: Not Just a Buzzword

    Manufacturing specialty chemicals brings an ongoing responsibility to minimize emissions and keep safety up. In our process, off-gas scrubbing and liquid phase neutralizations capture virtually all escaped materials, with measured VOCs in the exhaust well below permitted limits. The dual halogen structure of 3-Chloro-4-Fluorobenzonitrile prompts extra attention to effluent treatment, particularly for any halide byproducts. We upgraded our plant’s liquid effluent system to treat both chlorides and fluorides, investing in ion-exchange resins designed for halogen loads. Routinely measuring process water contamination shows our limits remain compliant.

    Spill drills bring together operators and environmental officers. The compound’s solid nature keeps spreading hazards manageable, and our plant-specific containment procedures keep any leaks isolated to single production cells. Hydration and dust generation are issues we watch, with dedicated filters on both air intakes and weigh stations. As a solid handled in closed systems, worker exposure risk is kept low, a claim supported by health records over many years of practice.

    Meeting Customer Demands for Flexibility: Batch and Custom Orders

    Big and small customers have distinct requirements, nowhere more obvious than with order sizes and packaging. The most frequent orders in our workflow range from 25 kg fiber drums up to tonne-scale totes. Researchers and pilot plant chemists sometimes need just a few kilos, so we offer smaller packs with the same full testing certificate and impurity panel. Repeat orders often request adjustments—whether that’s a specialized particle size or lower residual solvent levels for downstream hydrogenation.

    Our technical service staff provide direct input to custom projects. If a partner needs a tailored melting point fraction or a tighter halogen limit, our line can accommodate with minor reworks in the isolation scheme. Scaling a new grade for a partner starts in the kilo-lab, moves through pilot, and only then proceeds to full plant. By keeping real-time logs of what works—and what doesn’t—we limit surprises.

    Supply Chain: Navigating the Real-World Challenges

    Reliability gets tested every month. Upstream delays in halogen feedstock or temporary logistics blocks can put strain on expected delivery schedules. We keep in stock both in-process and finished lots, using additional buffer tanks to absorb swings in customer demand. Integrated scheduling on plant and warehouse systems means production never runs ahead of raw material checks.

    Our team closely monitors both domestic and international regulatory updates. Some global markets require extra documentation proving absence of regulated contaminants or banned precursor substances. Each batch can be traced back to its raw material lot, shipment date, and quality control log. This traceability proves essential during audits—nothing speaks louder to a quality-focused partner than a clear, unbroken trail from raw materials to final drum.

    Continuous Improvement: Real Feedback Yields Real Progress

    Operators on the plant floor provide weekly feedback on flow, pressure, and equipment wear during 3-Chloro-4-Fluorobenzonitrile runs. We constantly review incident data for any deviations in flow or reaction yield. Whether it’s a tweak in the charging order or realigning filtration belts, we focus on capturing incremental improvements. Over the years, these granular adjustments have allowed us to cut solvent consumption, reduce cycle times per batch, and keep customer satisfaction high.

    Plant data also tracks seasonal impacts. Lower humidity seasons support faster drying, while monsoon conditions force adjustments to storage and air filtration. Adaptive controls and modular process lines let our staff shift conditions as needed, upholding batch uniformity regardless of weather. These real-life realities mean less batch rejection and more reliable volumes delivered to customers across continents.

    Commitment to Transparency and Partnerships

    Building trust in specialty chemicals manufacturing relies on more than certificates and data sheets. We welcome customer audits, provide unfiltered plant visit logs, and offer open conversation about any process risks or improvement opportunities. This transparency has earned us long-term clients in both agrochemical and pharmaceutical sectors. Direct conversations with chemists and project leads ensure that—beyond supply—a genuine partnership grows, supporting both reliable delivery and mutual technical progress.

    Future Outlook and Potential Solutions

    Emerging market shifts stress the importance of reducing environmental impact and maximizing raw material efficiency. We explore process intensification, from continuous flow upgrades to in-line process analytics, as methods to lower waste and improve energy use on each batch. Feedback from multiple partners highlights a demand for both greener solvents and solvents with higher recovery rates in extraction and work-up.

    Regulatory landscapes tighten each year. We committed early to internal reviews of our chemical management policy, tracking any impurity or byproduct risk for downstream customers. Upcoming updates to regulatory frameworks in major markets push manufacturers to invest in even tighter process control and documentation.

    Practically, we keep lines of communication open with both customers and raw material suppliers, attending to their feedback on process variance, delivery consistency, and safety. Having both in-house and customer-driven improvement plans keeps our product at the front of specialty intermediate markets.

    Summary: Value Built on Experience

    It takes more than a standard operating sheet to consistently manufacture a reliable specialty chemical. From real-world supply challenges and daily operational improvements, to close-up work on every batch and customer feedback loops, our product—3-Chloro-4-Fluorobenzonitrile—embodies accumulated know-how. The difference isn’t just in purity numbers, but in how each process adjustment, each solution to a practical plant problem, and each customer request is woven back into how we operate. What customers receive isn’t just a drum of white crystals, but the sum total of efficient manufacturing, environmental responsibility, and a commitment to genuine technical partnership.