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2,4-Dichloro-5-Fluorobenzonitrile

    • Product Name 2,4-Dichloro-5-Fluorobenzonitrile
    • Alias 2,4-DCFN
    • Einecs 629-031-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    575104

    Chemical Name 2,4-Dichloro-5-Fluorobenzonitrile
    Molecular Formula C7H2Cl2FN
    Molecular Weight 190.00 g/mol
    Cas Number 161957-61-1
    Appearance White to off-white solid
    Melting Point 51-55°C
    Purity Typically >98%
    Solubility Insoluble in water, soluble in organic solvents
    Storage Conditions Store in a cool, dry place
    Smiles N#Cc1cc(Cl)c(F)cc1Cl
    Inchi InChI=1S/C7H2Cl2FN/c8-5-1-4(3-11)2-6(10)7(5)9

    As an accredited 2,4-Dichloro-5-Fluorobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g amber glass bottle with screw cap, white hazardous label, chemical name and CAS number printed; sealed for safety and compliance.
    Shipping 2,4-Dichloro-5-Fluorobenzonitrile is typically shipped in sealed, chemical-resistant containers to prevent moisture and contamination. It should be packed according to relevant hazardous materials regulations, with clear labeling and documentation. Ensure transportation is in compliance with local, national, and international safety standards for chemicals. Store in a cool, dry, and well-ventilated area.
    Storage Store 2,4-Dichloro-5-Fluorobenzonitrile in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Handle with appropriate personal protective equipment and avoid inhalation or prolonged contact. Clearly label containers and ensure emergency procedures are in place for accidental spills or exposure.
    Application of 2,4-Dichloro-5-Fluorobenzonitrile

    Applications of 2,4-Dichloro-5-Fluorobenzonitrile in Industrial Manufacturing

    2,4-Dichloro-5-Fluorobenzonitrile is a specialized intermediate relied upon by manufacturers in several chemical synthesis sectors. We supply to regulated production lines requiring consistent performance for advanced organic molecules, contributing directly to final product yield and regulatory compliance. Below, we detail major, validated downstream applications, each with scenario-specific standards, integration methods, dosage ranges, and final goods.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical producers select this compound as a nitrile building block for the synthesis of next-generation herbicide and fungicide actives. Its halogen arrangement enables targeted coupling or condensation reactions essential for manufacturing broadleaf weed inhibitors and disease control agents, entering the synthesis route at the formation of critical heterocyclic scaffolds and post-chlorination steps for selectivity enhancement.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides
    • EPA 40 CFR Part 180 Residue Tolerances
    • ISO 9001:2015 for chemical manufacturing
    • EU Regulation (EC) No 1107/2009 for plant protection products

    Typical usage ratio

    • 0.5–2.5 molar equivalents per batch, adjusted based on required active yield and reaction step; multi-kilogram scale in bulk synthesis

    Downstream process integration

    • Charged after initial aromatic compound halogenation, reacts with amines or acid chlorides to build core molecules; sometimes introduced at cyclization step if intermediate reactivity is needed

    Final product types

    • Broadleaf and grass weed herbicides (e.g., triazine, pyridine derivatives)
    • Systemic fungicides for grains and vegetables
    • Pre- and post-emergence formulations for field crops

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

    Pharmaceutical manufacturers purchase this benzonitrile for use in multi-step synthetic routes, particularly for creating fluorinated aromatic amine APIs and key heterocyclic pharmaceuticals. The controlled introduction of both chloro- and fluoro- groups facilitates downstream palladium-catalyzed coupling, amination, or reduction processes, often determining both the safety profile and patent position of the drug substance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP-NF, Ph. Eur., JP pharmacopoeial monographs (for finished APIs)
    • REACH Registration (EC) 1907/2006 for intermediate substances
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.2–1.0 molar equivalents per API synthesis cycle; ratio finalized after yield and impurity profile QC in pilot scale runs

    Downstream process integration

    • Fed into the sequence post-halogen exchange, typically as a nucleophile/reactant in amide or imine formation, or as a leaving group source in cross-coupling processes

    Final product types

    • Fluorinated antidepressants
    • Pyridine-containing anti-inflammatory APIs
    • Halogenated kinase inhibitors and oncology scaffolds

    3. High-Performance Liquid Crystal Monomer Production

    Select LCD panel component and advanced material manufacturers introduce this specialty benzonitrile as a functionalized aromatic core in the step-growth polymerization for novel liquid crystal monomer production. Its specific electronic and steric configuration enables precise alignment and switching behavior in displays and optical shutter devices, impacting end-use device clarity and color purity.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronics components
    • ISO 14001:2015 Environmental Management
    • IEC 61249 series for base materials in printed boards
    • JIS C5016 for liquid crystal device performance

    Typical usage ratio

    • 5–12% by weight of total aromatic monomer feed; varies to modulate birefringence and phase transition thresholds

    Downstream process integration

    • Dosed into the polycondensation or esterification vessel after catalyst activation; position and concentration set according to the desired nematic or smectic LCM structure

    Final product types

    • Twisted nematic and in-plane switching liquid crystal mixtures
    • Optical compensator film polymers (LC polymers)
    • Specialty LCDs for instrumentation and automotive panels

    4. Agrochemical Intermediate for Insecticide Synthesis

    Producers in crop protection markets integrate this aromatic nitrile into the synthesis of specific neonicotinoid and pyrazole insecticides. The compound acts as a tailored reactant in nucleophilic aromatic substitution and cyclization reactions, helping achieve the proper substitution pattern crucial for pest selectivity and chemical stability in the agricultural field.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • OECD Guidelines for Testing of Chemicals
    • ISO 17025-certified lab batch records
    • Chinese GB/T 1604-2016 standards for pesticide raw materials

    Typical usage ratio

    • 1.0–3.0 molar equivalents per intermediate synthesis, set after impurity profiles are validated in scale-up trials

    Downstream process integration

    • Added following amination or etherification pre-steps, typically handles halogen exchange or forms part of final heterocycle prior to purification and isomer separation

    Final product types

    • Neonicotinoid granules and concentrates for row crops
    • Pyrazole-based contact insecticides for orchards
    • Seed coating formulations for pests such as aphids and beetles

    5. Biocide Intermediate for Industrial Water Treatment

    Chemical formulators for industrial water treatment plants select this benzonitrile derivative in the synthesis of advanced biocide actives, where halogenation profile is critical to effectiveness and regulatory acceptability. Integrated after the formation of core aromatic frameworks, it ensures both broad-spectrum microbial inhibition and compliance with discharge regulations for treated water applications.

    Industry compliance standards

    • EU Biocidal Products Regulation (BPR, Regulation (EU) 528/2012)
    • US EPA FIFRA guidelines for antimicrobials
    • DIN EN 14885 for disinfectant validation
    • ISO 9001:2015 and ISO 14001:2015 for specialty chemical manufacturing

    Typical usage ratio

    • 0.8–2.2 molar equivalents per biocide batch, rate tailored by target molecule and required broad-spectrum activity level

    Downstream process integration

    • Added mid-stage after aromatic ring halogenation, preceding imination or amide coupling steps for biocidal molecule formation

    Final product types

    • Batch biocides for paper and pulp mills
    • Closed-cycle cooling water microbicides
    • Industrial and institutional disinfectant actives

    6. Intermediate for Specialty Dyestuff and Pigment Manufacture

    Manufacturers of high-purity dyes and pigments incorporate this aromatic nitrile during the synthesis of specialty fluorinated and chlorinated azo dyestuffs. Its introduction at early condensation or coupling phases allows tuning of color fastness, fluorescence, and solvent compatibility in end-use markets demanding both stability and eco-profile certifications.

    Industry compliance standards

    • REACH (EC 1907/2006) for dyestuff intermediates
    • OEKO-TEX Standard 100 for textile use
    • EN 71-3 Safety of Toys (for pigments in plastics/paints)
    • ZAH/Blue Angel Ecolabels (for reduced hazardous ingredients)

    Typical usage ratio

    • 3–15% by weight depending on required shade intensity and dispersion in final matrix

    Downstream process integration

    • Mixed into diazotization or metal-complexation reactors after initial auxiliary group introduction, serving as electronic modifier or coupling agent

    Final product types

    • Fluorescent textile dyes for polyester or nylon
    • Special-effect pigments for inks and coatings
    • Stable colorants for engineering plastics and high-end paints
    Free Quote

    Competitive 2,4-Dichloro-5-Fluorobenzonitrile prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,4-Dichloro-5-Fluorobenzonitrile: A Key Intermediate for Modern Chemical Synthesis

    Direct from the Manufacturer: Our Deep Experience with 2,4-Dichloro-5-Fluorobenzonitrile

    At our plant, we’ve worked with halogenated aromatic compounds for years. The demand for 2,4-Dichloro-5-Fluorobenzonitrile (model DCFBN-01, purity standard >99%) has grown as the fine chemical and agrochemical markets evolve. Production crews in our facility see it every day: precise batch records, careful temperature controls, high-purity washing procedures—we know the ins and outs from the reactor itself to the final packaging drum. This product’s reputation in industry circles isn’t just due to its chemical structure, but to the reliability and scalability of its manufacture as well as its adaptability for custom molecules.

    Our team realized early on that 2,4-Dichloro-5-Fluorobenzonitrile brings unique benefits compared to standard benzonitriles. The placement of chlorine on the 2 and 4 positions and fluorine on the 5 position makes this compound especially useful for further reactions. It stands apart from other nitriles because the dual halogenation and the addition of fluorine create versatile reactivity. Our chemists appreciate how the electronic effects influence selectivity and yields. Reliable sourcing of high-purity DCFBN lets clients stretch beyond commodity intermediates, tackling next-generation active ingredients and high-value material science projects.

    The Craft of Manufacturing High-Purity DCFBN

    The synthesis process for 2,4-Dichloro-5-Fluorobenzonitrile is more-than-a-simple halogenation. Operators at our site handle raw materials with care—chlorinated anilines and fluorinated benzenes show their quirks in the reactor when you push parameters too hard. We learned to respect the differences between this route and other aromatic nitrile syntheses. Proper agitation, exact solvent quantities, and containment of off-gassing fluorides are routine but critical for a repeatable process. Our QC team uses HPLC, GC-MS, and titration for every batch because even small deviations in halogen content or trace impurities can throw off downstream chemistry.

    Seasoned staff comment on the smell of freshly drawn DCFBN, the appearance of crystals under good lighting, and the difference it makes to unload 25kg drums with consistent color and crystal size. Customers have told us more than once: batches with the right appearance match the analytical purity every time. Any fluctuation in the manufacturing process becomes plain before a product leaves our gates.

    Why Formulation Scientists and Process Chemists Seek DCFBN

    In our conversations with research chemists, the demand for 2,4-Dichloro-5-Fluorobenzonitrile has never been a passing trend. It’s a building block for synthesis routes that othwerwise stall without electron-withdrawing halogens and a para-fluoro group. Agchem specialists point to its use in constructing modern herbicides and pesticides, thanks to the molecule’s solid chemical stability and the selectivity for follow-up chloro-fluorobenzene couplings. Where single-halide nitriles risk uncontrolled branching, DCFBN’s trio of substituents offers control and pattern-specific reactivity.

    Pharmaceutical route-scouting teams use it as a “handle” for further substitutions, sometimes adjusting the fluorine position to fine-tune activity in pipeline molecules. Both pilot plant and production-scale users rely on a consistent melting point and solubility range—they tell us it matters in each scale-up trial. Too many inconsistencies in crystal form or hydrate content lead to delays, and a missed window on a multistep route can set a project back months. Over the years, we’ve responded by investing in new drying and screening equipment, simply because the direct feedback from bench chemists showed a tighter need for uniformity batch-to-batch.

    What Makes DCFBN Distinct from Other Benzonitriles?

    From raw material sourcing to fractionation, 2,4-Dichloro-5-Fluorobenzonitrile behaves differently from comparable intermediates like 2,4-dichlorobenzonitrile or 4-fluorobenzonitrile. Those who work in formulation scale-ups notice the way DCFBN crystallizes—techs report fewer filter cake losses and cleaner filtrates. These differences start with subtle shifts in molecular polarity and the interplay between chlorine and fluorine across the benzene ring.

    Reactivity profiles differ too: coupling reactions with DCFBN as a substrate run faster, with less side-product formation, especially in SNAr and palladium-catalyzed cross-couplings. For teams troubleshooting bottlenecks, this is more than a theoretical advantage. One of our customers shared how their previous supplier’s inconsistent halogen ratios led to incomplete conversions in pilot trials. Our material, tested upfront for the right balance, improved their yields on scale. We’ve seen that tight controls over elemental halogen content and water content distinguish our material’s performance.

    End-Use Applications: The Role of DCFBN in Modern Industries

    Chemical industries demand a reliable intermediate for innovating in both established and developing markets. Over time, the use of 2,4-Dichloro-5-Fluorobenzonitrile spread from agri-chemistry to broader life sciences. Large manufacturers of active plant protection molecules draw on DCFBN for halogenated ring systems, especially ones hard to assemble by any other method. Our technical support team frequently helps customers unravel downstream process questions—whether in nucleophilic aromatic substitutions, or fine-tuning the production of quinolone-based structures.

    Emerging materials science companies approach us too. In polymers, specialty coatings, and resin technologies, they investigate new performance properties by integrating DCFBN-derived units. Here, not just reactivity but batch-to-batch appearance and handling properties mean the difference between laboratory investigation and scalable commercialization.

    Reliability, Traceability, and Trusted Relationships

    As manufacturers, direct control over the supply chain carries weight—controlling everything from raw material audits, to finished-goods certification, to logistics documentation. Auditors from multinational clients walk our shop floors, examine the solvent tanks, inspect drum seals, and review chromatograph records. Our operators and QA analysts work hand-in-glove. Any shift in the intended outcome shows up first in their records and gets discussed on the floor. The value of transparency and open reporting matters—customers trust our lot records because their credibility and our reputation follow directly from the discipline of transparent process management.

    We make it a point to maintain certificates of analysis with detailed impurity profiles—not just ticking a regulatory box, but because our own engineers and our clients want to trace every input. Many DCFBN users tell us about hidden impurities from lower-tier vendors causing glitches at the critical stages of downstream synthesis. By tracking halide content, solvent residues, and particle size, we reduce the unknowns our users face. Trust is reinforced every time a shipment matches expectations by technical readout, not just by outward label.

    Economic and Regulatory Factors in Global Supply

    Halogenated intermediates like DCFBN have shifted in cost as production locates nearer to feedstock supplies and dedicated chlorination capacity. Rising regulatory standards place demands on tracking every lot from factory intake to the export dock. Audits from regulatory agencies focus especially on the safe handling of chlorine and fluorine sources as well as the treatment of waste streams. We go beyond minimal compliance—dedicated containment and neutralization plants built on-site let us recycle and detoxify byproducts before shipment or disposal. These investments keep costs predictable and compliance records clean, both of which matter for ongoing partnerships with demanding multinational companies.

    Our regulatory experts keep current on restrictions concerning persistent, bioaccumulative substances—especially because both chlorine and fluorine draw extra scrutiny in many countries. Customers benefit from this vigilance: shipments accompanied by the right compliance documents clear customs with fewer questions, and production schedules run with greater certainty. This comes back as positive feedback not just from regulatory affairs teams, but from process engineers and procurement managers who recall the time lost to customs holdups or reactive paperwork from less meticulous vendors.

    Technical Support and On-Site Solutions

    “Real-world support matters.” This is the message we hear from development chemists and process managers around the world. We staff our technical team with individuals who have run reactors and filled drums themselves, not just read data sheets. When a client calls about unexpected solubility changes in a winter shipment, or a shift in melting point in a large batch scale-up, it’s a person with years of hands-on DCFBN experience who answers.

    One example from last spring sticks out. An outfit in central Europe struggled with mixing and filtering a DCFBN-related suspension, causing hours of downtime. Our support crew worked through their data, reviewed local process conditions, and recommended subtle tweaks in temperature and agitation—something we know from direct manufacturing experience, not formulaic troubleshooting. Problems got solved, production restarted, and everyone kept to their timelines.

    Providing drum size flexibility, bulk container options, and guidance on optimal storage conditions all stem from direct user feedback. Our field engineers have spent time on customer factory floors, reviewing transfer lines and storage practices, not just providing shipping advice from afar. This keeps our partnerships grounded in practical know-how where it matters.

    Solving Problems That Reach Beyond the Lab

    Improvement in the supply and handling of 2,4-Dichloro-5-Fluorobenzonitrile requires more than tweaking a recipe. Downstream incidents involving dust hazard or skin exposure don’t just spark paperwork, they spark hard-won improvements. We implemented a closed charging system for DCFBN after a batch operator outlined issues with fine dust during drum transfers. In response, our engineers worked with them to design and install a transfer hopper that minimized operator contact and improved plant air quality—simple in theory, but revolutionary for daily working life. That practical feedback loop benefits every user.

    At the warehouse level, controlling humidity spares customers from receiving lumpy product during transport in monsoon conditions. We adjusted liner selection after a season’s worth of feedback. A simple switch from a single-ply plastic liner to a multi-layer, anti-static bag helped retain flowability and quality across long transit times. These small manufacturing-level solutions show up as savings in productivity and fewer customer complaints.

    On the environmental protection front, minimizing production waste is not just a balancing act with cost, but a moral commitment. We invested in recovery of halogenated solvent streams, reducing hazardous output. This lets us offer “greener” product alternatives to clients who face tougher audits or internal sustainability quotas.

    Continuous Improvement and Industry Evolution

    Experience in this sector teaches patience—small savings in time or purity today pan out as competitive edges by year’s end. Feedback from our clients, whether they request a new drum size, better flow under cold conditions, or tighter impurity targets, drives direct technological progress. Our process development team sits with both analytical chemists and operations staff every quarter to review the last run and look for ways to shave off handling variances or purity deviations. Analytical method improvements still pay dividends: investing in more sensitive detection of halogen contaminants lowered reorder rates and built further confidence among the most demanding R&D customers.

    Researchers exploring new synthetic applications relay their needs to use specific halogen ratios for a custom active molecule. Our laboratory can provide not only off-the-shelf DCFBN, but support for custom syntheses and analytical documentation to demonstrate suitability for novel processes. As application expansion continues—into smart materials, advanced crop science, or specialty dyestuff production—manufacturers who tie product quality, handling, and support to real-world results will maintain their place at the center of the chemical innovation chain.

    Conclusion: Grounded Value in Consistent Quality and Relationships

    Every kilogram of 2,4-Dichloro-5-Fluorobenzonitrile from our reactors reflects the sum total of experience, feedback, and iterative improvement. The difference between our product and generic alternatives does not rest only in purity statistics, but in the day-to-day reliability experienced at the customer’s own kettle, filter, or warehouse. By listening to process bottlenecks, regulatory challenges, technical requests, and end-use demands, we offer not just a molecule, but a partnership that helps clients reach their innovation targets. The ongoing investment in product quality, traceability, safety, and direct support is our answer to the growing complexity and opportunity across the fine and specialty chemical landscape.