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3-Chloro-4-Fluoroanisole

    • Product Name 3-Chloro-4-Fluoroanisole
    • Alias 3-Chloro-4-fluoro-1-methoxybenzene
    • Einecs 84621-85-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    877302

    Product Name 3-Chloro-4-Fluoroanisole
    Cas Number 57381-97-2
    Molecular Formula C7H6ClFO
    Molecular Weight 160.57
    Appearance Colorless to pale yellow liquid
    Boiling Point C 191-193
    Density G Per Cm3 1.281
    Purity Typically >97%
    Smiles COC1=CC(=C(C=C1)Cl)F
    Solubility Insoluble in water; soluble in organic solvents
    Flash Point C 71

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

    Packing & Storage
    Packing Amber glass bottle, 100 grams, tightly sealed with a screw cap, clearly labeled with "3-Chloro-4-Fluoroanisole," hazard symbols, and safety instructions.
    Shipping 3-Chloro-4-Fluoroanisole is shipped in tightly sealed containers, compliant with chemical safety regulations. It should be kept away from heat, sparks, and open flames. The package is clearly labeled with hazard information and handled by trained personnel. During transit, it is protected from moisture, physical damage, and extreme temperatures.
    Storage 3-Chloro-4-Fluoroanisole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep it away from sources of ignition, heat, and incompatible substances such as strong oxidizers and acids. Store at room temperature and avoid direct sunlight. Ensure proper labeling and restrict access to trained personnel to maintain safety and prevent contamination or accidental exposure.
    Application of 3-Chloro-4-Fluoroanisole

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

    As a specialized producer of 3-Chloro-4-Fluoroanisole, we supply this compound for critical synthesis steps in advanced chemical, pharmaceutical, agrochemical, and materials manufacturing. Below are authentic industry segments where this intermediate plays a defined technical role in end-product workflows.

    1. Pharmaceutical Intermediate Synthesis

    3-Chloro-4-Fluoroanisole is widely adopted by pharmaceutical manufacturers for constructing advanced intermediates critical in active pharmaceutical ingredient (API) synthesis, particularly in anti-infective, CNS-active, or oncology drug projects. Its specific substitution pattern enables targeted halogenation and methylation steps during the elaboration of complex heterocyclic scaffolds. The aryl ether group offers improved stability under coupling protocols such as Suzuki or Buchwald–Hartwig reactions, allowing for efficient introduction into the final rigid pharmacophores demanded by novel drug substances. Development and GMP production lines depend on this molecule during medicinal chemistry scale-ups, route scouting, and late-phase campaigns, including process validation runs.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for API production
    • 21 CFR Part 211: US FDA cGMP for Finished Pharmaceuticals
    • Relevant monograph references, including British and European Pharmacopoeias guidance for intermediates

    Typical usage ratio

    • Applied at 1–10% molar ratio versus overall API target yield, adjusted for route efficiency or impurity control based on synthesis design

    Downstream process integration

    • Introduced after initial ring construction as a substituent donor in C-N/C-C cross-coupling or O-demethylation sequences
    • Acts as a terminal halogenated precursor for functional group elaboration during lead optimization and pilot-scale synthesis

    Final product types

    • Small molecule drug substances (e.g., CNS, anti-cancer, anti-infective APIs)
    • Registered intermediates (KSMs and Advanced Intermediates)
    • Generic API building block inventory

    2. Agrochemical Active Compound Development

    Agrochemical companies use 3-Chloro-4-Fluoroanisole to construct core aromatic skeletons in advanced herbicide, fungicide, and insecticide research. Its dual halogen substitution and methoxy group facilitate the synthesis of diverse active ingredients through controlled electrophilic aromatic substitution, nucleophilic displacement, and downstream alkylation or sulfonation steps. Labs employ this compound for generating new molecular entities (NMEs), optimizing selectivity, and tuning environmental fate properties during regulatory trials and scale-up.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System in Agrochemical Production
    • OECD GLP Guidelines for Safety Assessment Studies
    • EPA Title 40 CFR, Part 158 Data Requirements for Pesticides

    Typical usage ratio

    • Ranges from 2–7% by mol in early-stage synthesis or 0.5–3% by mass for downstream modification, with adjustment for scale or targeted compound loading

    Downstream process integration

    • Introduced as an early-stage aryl ether donor or halogen carrier during lead compound library synthesis
    • Acts as an intermediate in selective demethoxylation or fluorine exchange, prior to coupling with bioactive moieties

    Final product types

    • Formulated crop protection active substances
    • Synthetic pesticide intermediates
    • Environmental fate study metabolites

    3. Electronic Chemicals and Specialty Polymers

    In electronics, 3-Chloro-4-Fluoroanisole integrates into specialty polymer chains, such as fluorinated aromatic polyimides and high-performance resins. These polymers deliver superior dielectric constants, flame retardancy, and thermal stability required in chip packaging, flexible circuitry, and high-frequency antenna substrate manufacturing. The anisole moiety acts as a polymerizable unit to tailor backbone rigidity or processability, while chlorinated and fluorinated sites enhance compatibility with photoresists or etch chemistries. QC teams routinely monitor raw material incorporation to ensure electrical properties meet industry benchmarks.

    Industry compliance standards

    • IPC-4101B: Base Materials for Rigid and Multilayer Printed Boards
    • UL 94: Flammability Testing of Plastic Materials
    • RoHS Directive 2011/65/EU for Hazardous Substances
    • IEC 61249: Requirements for Materials for Printed Circuit Boards

    Typical usage ratio

    • Used at 0.5–3% by weight in specialty polymer formulations, varied to achieve targeted electrical or thermal parameters

    Downstream process integration

    • Co-polymerized with dianhydrides in imidization processes for films, sheets, or coatings
    • Added in monomer blend tank before curing or extrusion

    Final product types

    • Polyimide films for circuit substrates
    • Photoresistant layers in semiconductor fabrication
    • High-frequency PCB base materials

    4. Fine Chemical Building Block for Dye and Pigment Manufacture

    Producers of high-stability Dyes and organic pigments utilize 3-Chloro-4-Fluoroanisole as a key building block in the synthesis of complex aryl-ether dyes for plastics, coatings, and specialty ink formulations. Its chemical structure introduces halogen and methoxy substituents at precise positions, facilitating nucleophilic aromatic substitution as well as subsequent metallation and coupling with diazo or anthraquinone moieties. Analytical and color quality teams monitor lot consistency throughout the process for maximum reproducibility across large colorant consignments.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for Industrial Chemicals
    • ISO 9001:2015 Quality Management in Dye Synthesis
    • EN 71-3: Safety of Toys – Migration of Certain Elements (for pigment applications)
    • ASTM D4236 Labeling of Art Materials

    Typical usage ratio

    • Varies between 3–8% by mol for specialty dye projects or 1–5% in pigment synthesis, adjusted per desired shade, solubility, and metallation rate

    Downstream process integration

    • Engaged in primary batch vessels for aromatic nucleophilic substitution and diazo coupling
    • Used in multi-step syntheses where precise halogenation is required prior to final colorant conjugation

    Final product types

    • High-purity pigments for polymer coloring
    • Solvent dyes for plastics and coatings
    • Specialty inks for industrial and security printing
    Free Quote

    Competitive 3-Chloro-4-Fluoroanisole prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 3-Chloro-4-Fluoroanisole: A Manufacturer’s Perspective on Quality, Consistency, and Application

    Understanding the Role of 3-Chloro-4-Fluoroanisole in Modern Chemistry

    Working day in and day out at the core of chemical synthesis, we gain an intuitive sense for which molecules genuinely make a difference across research, agriculture, pharmaceuticals, and specialty materials. 3-Chloro-4-Fluoroanisole stands out for its balance of reactivity, stability, and functional group compatibility. Its chemical structure, a methoxy-substituted benzene ring bearing both chlorine and fluorine atoms in specific positions, creates a backbone for downstream modifications many related compounds cannot match. This unique profile makes it indispensable for both seasoned process chemists and researchers exploring new territory in aromatic chemistry.

    In our experience, customers approach us with goals that hinge on reliability. One formulation team focuses on developing new fungicidal chemistries, needing a substrate stable enough for multi-step reactions without unwanted side products. Elsewhere, a pharmaceutical development group emphasizes purity – even trace isomers or impurities can undermine advances or delay regulatory milestones. We see 3-Chloro-4-Fluoroanisole consistently meet these demands because our production methods focus not only on yield, but on control over by-product formation through rigorous stepwise purification, in-line analytics, and experienced staff following proven protocols.

    Specifications and Models: Inside Our Approach

    The materials available on the open market vary more than most buyers realize. Our batches of 3-Chloro-4-Fluoroanisole follow a synthesis process that keeps batch-to-batch differences remarkably low. The product is typically presented as a clear to pale yellow liquid with an assay above 99.0% as confirmed by gas chromatography and NMR. Moisture content, halide levels, and residual starting materials fall below 0.1% in every lot. The melting and boiling endpoints line up with published literature, but we also keep tabs on physical data unique to each lot in our records.

    Many external labs validate reported specifications, but nothing replaces close dialogue between manufacturing and analytical teams. For each run, we hold back samples, not just for customer retention, but to continuously improve our own understanding of how subtle process tweaks affect the product’s behavior. In doing so, we’ve prevented recurring issues – such as trace impurities stemming from solvents, or side-reaction byproducts creeping in under certain climate conditions – before they could reach customer hands.

    Working closely with industrial partners, we see that what’s reported on a technical data sheet sometimes matters less than who prepared it and how. Commercial models of 3-Chloro-4-Fluoroanisole with a stated “minimum 98% purity” from bulk commodity suppliers have shown, after further analysis, to contain measurable byproduct aldehydes and unreacted anilines. Such trace content can foul up downstream catalysts, change reaction rates, or even introduce color or odor into final products. Our facilities tackle these risks by leaning on in-house distillation and crystallization techniques honed over years, not just standard per-lot testing.

    With the model we offer, large-scale manufacturing is possible without process drift. From multikilogram campaigns to small custom batches, our scale-up follows a documented process route that fixes each critical parameter – solvent loading, temperature ramp, reaction time, and, crucially, in-process monitoring for each key transformation. Many competitors automate with little oversight; we retain hands-on oversight and real-time troubleshooting, using modern analytics alongside experience earned from production runs conducted across different seasons and feedstock conditions.

    Comparing 3-Chloro-4-Fluoroanisole to Other Anisoles

    The introduction of both chlorine and fluorine on an anisole ring transforms its habits in synthesis. Our chemists have long observed that 3-chloro-4-fluoro substitution creates distinct electronic and steric effects, affecting everything from nucleophilic substitution to metal-catalyzed cross-coupling. Standard anisoles or mono-substituted variants, such as 4-fluoroanisole or 3-chloroanisole, often prove too reactive or not selective enough for certain complex coupling reactions.

    By sitting between electron-withdrawing and electron-donating forces, 3-Chloro-4-Fluoroanisole offers more predictable reactivity with fewer side reactions, especially where regioselectivity is crucial. For our manufacturing clients, this means higher yields with less purification burden downstream. Pharmaceutical innovators tell us that the difference goes well beyond chemical theory; they observe improved performance in actual medicinal syntheses, reduced unwanted rearrangements, and cleaner intermediate isolation.

    Interactions with process developers have shown that even seemingly minor differences in substitution pattern can dictate whether a project succeeds. For example, substituting with just chlorine or just fluorine at random positions tends to leave open more reactive sites prone to degradation, which increases the risk of polymer formation or discolored byproducts. Our 3-Chloro-4-Fluoroanisole presents a balance, supporting mid-stage transformations required in heterocycle construction, but resisting premature or over-reactive side processes.

    Experience-Driven Production and Why It Matters

    Decades of combined experience in aromatic halide synthesis back every drum and bottle shipped. Scale-up from gram-scale research to full commercial production often reveals pitfalls invisible in the literature. Our engineers have run pilot batches side-by-side with downstream users, allowing both parties to capture and solve unexpected problems as they first arise, rather than after market launch. Mistakes such as uncontrolled exotherms during halogenation, or solvent selection that fosters isomer contamination, have been isolated, analyzed, and eliminated from our current method.

    It’s tempting for facilities to lean on automated solutions and skip investing in skilled operators, but our success in producing 3-Chloro-4-Fluoroanisole stems from respect for hands-on oversight. For example, our facility routinely conducts in-process analytics rather than relying on post-batch analysis. Catching small signals—a slight haze, a shift in phase separation, an unexpected GC-MS spike—lets us intercept out-of-specification material long before it leaves the plant. These efforts protect not just our reputation, but our partners’ projects downstream.

    Application Scope in Industrial Settings

    End-users drive the direction for many chemicals, and we’ve seen that 3-Chloro-4-Fluoroanisole finds its best fit in finely-tuned applications. Pharmaceutical researchers pick it for cross-coupling and aromatic substitution routes in building advanced molecules, often as a key intermediate in multi-step synthesis. Fine chemical companies utilize it while seeking motifs that resist degradation during pesticide formulation or to introduce halogen signatures for regulatory tracking.

    We often discuss with formulation chemists how the molecule’s particular arrangement of groups inhibits certain unwanted reactions, such as dealkylation, which can plague less robust analogs. This reliability extends shelf-life in real-world manufacturing environments. In our experience, bulk buyers need a product with predictable melting and boiling range, non-hygroscopic nature, and a storage profile that gives months—sometimes longer—of consistent behavior, even through seasonal temperature shifts.

    We’ve also worked with labs benchmarking new catalysts who require ultra-pure starting materials to test theory in metal-catalyzed coupling. Even trace contaminants can mask or skew results in these applications. In one recent case, an academic partner noticed a dramatic drop in catalytic efficiency using similar-sounding products from alternate suppliers. Side-by-side headspace, NMR, and LC-MS studies tied the problem to trace aromatic aldehydes missed in less stringent preparations. Our material, checked rigorously, proved free of the suspect byproducts, restoring desired performance and saving several months of research time.

    Challenges and Solutions: From Sourcing to Final Use

    Consistent sourcing of raw materials has defined many of our operational puzzles. Halide feedstocks and fine-grade methoxy reagents can swing in both cost and purity. Instead of chasing the lowest priced option, we partner with vetted suppliers holding transparent quality and audit records, sacrificing volume margin in favor of steady, assured quality. In times where global supply chains wobble, our relationships support regular shipments, giving us—and our customers—greater certainty for both planned and rush orders.

    We have faced questions over solvent footprints and waste minimization, especially from multinational partners required to meet tighter environmental reporting. We answer this by running a closed-loop recovery for commonly used solvents and optimizing reaction stoichiometry to cut the need for expensive downstream purification and neutralization. Waste acid handling, particularly, has seen attention: we constructed an acid treatment section to safely neutralize spent streams, tying it to regular monitoring and sliders for throughput adjustment based on batch size.

    Regulatory Awareness, Purity, and Safety in Our Context

    Every year brings evolving standards for trace impurity thresholds, especially in products intended for active pharmaceutical or agrochemical research. Our compliance staff work directly with the analytic chemists to stay ahead of changes in regional and international guidelines. Where others release material at a base-level analysis, we supplement our lot records with expanded impurity profiles drawn from 2D NMR, GC-MS, and high-res LC—identifying not just what’s “expected,” but capturing low-level signature contaminants others might miss.

    Batch records tell the story of every adjustment, whether a process change causes a ripple in impurity profiles or a specific batch faces higher-than-normal ambient humidity, affecting both production yield and downstream usability. We treat these logs as living documents, revisiting them before starting each large campaign, especially when planning for downstream medicinal chemistry. In turn, when questions arise from clients, we reference this archive directly, offering more than just a certificate of analysis—real answers grounded in actual experience.

    We also maintain a focus on transport and handling safety. Neither casual nor cavalier about the risks, we package 3-Chloro-4-Fluoroanisole in containers rated for both chemical compatibility and vapor retention, label each with detailed hazard information, and advise storage away from oxidative or moisture sources.

    Comparing Ourselves to Outsourced and Brokered Material

    Too often, buyers who’ve sourced intermediates from brokers or regional traders come to us with tales of frustration—weeks of delays, unclear product origins, composition that proves unpredictable when challenged by in-house analytic labs. What appears to be a bargain can turn costly when a process fails or valuable time is lost chasing impurities through downstream syntheses. We’ve carved a different path. As direct manufacturers, our commitment goes deeper than technical compliance.

    We’re open about plant location, equipment specification, and traceability of the feedstock supply chain. Our analytic records go back years, available for review upon request, with real samples held in archive for comparison or problem-solving. Instead of responding to issues with stock replies, we assign experienced technical staff to discuss details—often running or replicating key steps in the lab. Our ability to troubleshoot stems from holding practical understanding of synthesis history, not just paperwork.

    Chemicals are no commodity when specific performance counts. In one instance, a customer sourcing bulk from a multi-level supplier chain encountered a recurring phase separation problem, which, after weeks of delay, we traced to a difference in solvent residue from regional distillation protocols not present in our own processes. Transitioning to our direct supply resolved the matter, offering both a technical fix and greater confidence in scaling up to commercial volume. These stories show that a manufacturer’s deeper process knowledge, transparency, and willingness to take responsibility really matter when timelines and compliance are tight.

    Meeting Industry Demands for Versatility and Dependability

    While the world of fine chemicals evolves quickly with new catalysts, synthetic routes, and regulatory frameworks, our guiding principles hold steady. Process predictability, root-cause troubleshooting, and advanced analytics ensure that 3-Chloro-4-Fluoroanisole keeps meeting the needs of chemists and product developers. Our modular production setup enables both small bespoke runs for academic clients and large manufacturing orders for industry partners scaling up pilot projects. These systems proved their worth as supply chain strains increased—and customers appreciated our agility and responsiveness.

    Researchers tackling new methodology feed back insights, helping us fine-tune the properties and packaging options. Demand fluctuates by sector, and our experience has built a network to ship and store material safely across climates and regulatory zones, making sure spec and stability carry through to actual use.

    Improvement doesn’t stop with synthesis, either. Regular technical forums, open conversations with downstream applications teams, and direct review of any reported oddities ensure that our processes don’t stagnate but reflect the needs of chemists pushing the boundaries.

    Why 3-Chloro-4-Fluoroanisole Remains a Reliable Intermediate

    Reliability rests on a foundation of many small decisions: careful sourcing, commitment to in-process analytic oversight, and technical staff willing to step into the details. Through hands-on interaction with both the molecule and the chemists depending on it, 3-Chloro-4-Fluoroanisole remains more than a catalog item—it becomes a trusted link in the chain of industrial and research progress.

    The chemistry, structure, and reactivity of 3-Chloro-4-Fluoroanisole carve a niche for it as a platform intermediate, especially where precision and purity demand more than theoretical minimums. Years of manufacturing experience have proven the molecule’s ability to withstand tough protocols and expand what’s possible in both the discovery laboratory and the scale-up plant. While new challenges will always arise, persistent attention to detail keeps the product ready for next-generation uses.

    Each bottle and drum leaving our facilities carries the weight of collective experience, continuous improvement, and a willingness to tackle the subtle problems that never quite make it into the academic papers. This is our edge as a manufacturer—and why 3-Chloro-4-Fluoroanisole plays its crucial role in so many avenues of modern chemical advancement.