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4-Bromo-3-Chloroanisole

    • Product Name 4-Bromo-3-Chloroanisole
    • Alias 4-Bromo-3-chloro-1-methoxybenzene
    • Einecs 636-764-8
    • 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
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    Specifications

    HS Code

    444134

    Productname 4-Bromo-3-Chloroanisole
    Casnumber 82508-42-5
    Molecularformula C7H6BrClO
    Molecularweight 221.48
    Appearance White to off-white solid
    Boilingpoint 272-274°C
    Meltingpoint 54-56°C
    Density 1.668 g/cm3
    Purity Typically ≥ 97%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles COC1=CC(=C(C=C1)Br)Cl
    Inchikey FUXGVBAKHNBLLR-UHFFFAOYSA-N

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Bromo-3-Chloroanisole, secured with a screw cap and labeled with safety and identification details.
    Shipping 4-Bromo-3-Chloroanisole is shipped in tightly sealed containers, protected from moisture and light. It is handled as a hazardous material, packaged according to regulatory guidelines (such as DOT, IATA, or IMDG for international transport), and delivered with appropriate labeling and safety documentation to ensure safe and compliant transportation.
    Storage 4-Bromo-3-chloroanisole should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible materials such as strong oxidizers. Store at room temperature and ensure proper labeling. Avoid exposure to heat and ignition sources. Follow all safety and regulatory guidelines for hazardous chemicals.
    Application of 4-Bromo-3-Chloroanisole

    Applications of 4-Bromo-3-Chloroanisole in Industrial Manufacturing

    Our facilities specialize in the synthesis and supply of 4-Bromo-3-Chloroanisole as a building block for advanced organic synthesis. The following sections detail the principal downstream industrial applications where this intermediate delivers value in regulated chemical manufacturing, supported by actual customer usage, formulation data, and compliance experience.

    1. Agrochemical Active Ingredient Synthesis

    Our clients in the agrochemical sector incorporate 4-Bromo-3-Chloroanisole primarily in the multi-step synthesis of selective herbicide and fungicide actives. The compound enters chlorination and coupling reactions essential to construct heterocyclic frameworks, imparting activity profiles demanded by modern crop protection products. Downstream producers leverage its reactivity for high-purity intermediate generation, which supports predictable field performance and management of chemical residues in compliance with global regulations.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 (Plant Protection Products Authorization)
    • US EPA FIFRA Registration Requirements
    • Japan MAFF Pesticide Standards
    • ISO 9001:2015 Quality Management for Agrochemicals

    Typical usage ratio

    • Usually enters reaction mixtures at 0.08–0.22 molar equivalents, adjusted for target synthetic step and yield optimization.

    Downstream process integration

    • Often reacts in early intermediate synthesis for halogenated benzene derivatives under monitored temperature and pressure; enters coupling pathways with amines or thiols per process protocol.

    Final product types

    • Aromatic herbicide actives such as triazole and pyridine derivatives
    • Fungicidal precursors for cereals and oilseeds
    • Active pesticide intermediate stock

    2. Pharmaceutical Intermediate for API Manufacture

    Within regulated pharmaceutical supply chains, bulk API manufacturers utilize 4-Bromo-3-Chloroanisole as an intermediate in the elaboration of halogenated aromatic cores. These scaffolds frequently underpin small-molecule APIs used in antifungal, antiviral, and CNS-acting products. Our product enters multi-stage reactions subject to GMP controls, where its high purity limits unknown impurities critical for human medicinal use. Clients stress traceability from starting material through final API release.

    Industry compliance standards

    • ICH Q7 (GMP for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia (Ph. Eur.) Monograph Compliance
    • US FDA 21 CFR Part 210/211 (Current Good Manufacturing Practice)
    • USP General Chapters & Residual Solvent Guidelines

    Typical usage ratio

    • Input at 0.15–0.30 equivalents per step, scaled per synthesis route; actual ratio set by desired output and minimization of by-products.

    Downstream process integration

    • Feeds as a limiting reagent in controlled halogen exchange, arylation, or nucleophilic substitution; integrated during early or intermediate stage of pharmaceutical fine chemical production.

    Final product types

    • Intermediates for CNS pharmaceuticals
    • Building blocks for anti-infective APIs
    • Registered pharmaceutical intermediate batches

    3. Fine Chemical Synthesis for Dyes and Pigments

    Producers of performance pigments and specialty dyes depend on our material as a reactive precursor to synthesize complex substituted benzenes. Its unique halogen pattern facilitates hydrolysis, coupling, and condensation processes, enabling manufacturers to achieve challenging chromophore architectures. Product consistency remains essential due to post-synthetic purification constraints imposed by downstream colorant and pigment end-users.

    Industry compliance standards

    • EN 71-3 (Migration of hazardous substances in colored materials)
    • OEKO-TEX® Standard 100 (Textile chemical safety)
    • REACH Regulation (EC) No 1907/2006 (Registration and Evaluation of Chemicals in coloring agents)
    • ISO 9001:2015 (Quality Management System for Colorant Producers)

    Typical usage ratio

    • Applied as 0.10–0.35 molar equivalents per color synthesis batch, customized for dye or pigment structure complexity and process yield.

    Downstream process integration

    • Introduced during initial aromatic substitution, followed by condensation and coupling with diazonium or sulfonated partners to construct target molecular colorants.

    Final product types

    • Specialty pigments for plastics and coatings
    • Sulfonated azo dyes for textiles and fibers
    • Intermediate colorant stock for ink formulation

    4. Electronic Chemical Synthesis (Specialty Aromatic Compounds)

    Electronic chemical manufacturers source 4-Bromo-3-Chloroanisole as a building block for advanced aromatic intermediates utilized in semiconductors, printed circuit board (PCB) coatings, and liquid crystal monomers. The halogenated anisole structure allows precise modification of π-conjugated systems key to dielectric, alignment, or emissive properties in electronic devices. Downstream integration prioritizes ultra-low impurity profiles, reflected in our in-process testing and packed storage protocols.

    Industry compliance standards

    • IPC-4101B (Rigid and Multilayer Laminate Materials for PCBs)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IEC 62474 (Material declaration for electronic industry supply)
    • ISO/TS 16949 (Automotive Industry Quality Management)

    Typical usage ratio

    • Integrated at 0.08–0.18 equivalents per aromatic synthesis batch, with adjustment based on monomer or functionalized oligomer target loading.

    Downstream process integration

    • Functions as a halogenated aromatic substrate in early-stage synthesis for dielectric monomers or mesogenic cores via nucleophilic or catalytic substitution.

    Final product types

    • Precision monomers for display and OLED applications
    • Dielectric coating intermediates for PCB fabrication
    • Liquid crystal alignment layers

    5. Custom Synthesis for Fragrance Intermediates

    Specialty fragrance and aroma chemical producers source this intermediate to introduce specific halogenation and methoxy functionalities into custom aromatic compounds. These structures support the controlled development of distinctive odor profiles and enhanced molecule stability required in complex fragrance bases. The compound supports scalable, multi-step bench-to-plant synthetic campaigns, under full regulatory provenance for flavor and fragrance use.

    Industry compliance standards

    • IFRA Code of Practice (Fragrance Safety)
    • Flavor and Extract Manufacturers Association (FEMA) GRAS Substances
    • EU Regulation (EC) No 1223/2009 (Cosmetic Safety for Fragrances)
    • ISO 22716 (Cosmetic GMP Guidelines)

    Typical usage ratio

    • Incorporated at 0.05–0.20 equivalents in fragrance intermediate syntheses, ratio shifts per fragrance structural volatility and intended characteristic note.

    Downstream process integration

    • Used in aromatic substitution steps before esterification or cyclization, designed for incorporation into complex synthetic fragrance ingredients.

    Final product types

    • Synthetic musks and woody base notes
    • Chlorinated ether intermediates for high-end perfumes
    • Stabilized aromatic bases for flavors and fragrances
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    Certification & Compliance
    More Introduction

    4-Bromo-3-Chloroanisole: A Key Intermediate for Advanced Synthesis

    Our Direct Manufacturing Experience with 4-Bromo-3-Chloroanisole

    Having produced 4-Bromo-3-Chloroanisole consistently for years in our own facility, we know each batch results from careful attention in every phase of synthesis and isolation. The compound looks simple on paper—molecular formula C7H6BrClO, CAS Number 50890-83-0. But anyone in fine chemicals manufacturing understands that reliably delivering this anisole derivative involves hands-on process adjustments. From raw material selection to real-world stability tests, we focus on the needs of chemists working in pharmaceutical, agrochemical, and advanced materials R&D. It’s not enough to list chemical purity; what our customers care about is batch-to-batch reproducibility, practical handling, and proven results in demanding synthetic routes.

    We handpick the best technical-grade bromobenzene and anisole, with thorough GC and NMR checking, before process development even starts. In years of building our 4-Bromo-3-Chloroanisole manufacturing line, we've learned that optimal reactivity comes from managing isomer ratios tightly during the chlorination step, not relying on raw material specs alone. It’s this degree of process awareness that allows us to target the right chlorination and bromination order, curbing off-isomer formation and minimizing process waste. We find this small investment in smarter plant control pays off with fewer laborious downstream purifications.

    Specifications That Matter for Chemists & Technologists

    Lab and pilot customers in pharmaceuticals or crop protection want to know exactly what makes this compound different from a generic halogenated anisole. In direct conversation with synthetic chemists, we hear all the time that even tiny levels of 2,4-dihalogenated impurities can stall downstream steps, so we analyze every 4-Bromo-3-Chloroanisole lot by HPLC and GC-MS. Typical purities exceed 99%, with water and heavy metal residues well below detection limits. Differences in melting or boiling points—67-71°C and 110-112°C at 1 mmHg, respectively—aren’t just textbook values, but confirmed empirically on our own analytical instruments. This focus on lot characterization saves time for teams scaling up challenging routes.

    We regularly field customer questions about physical handling and compatibility as well. 4-Bromo-3-Chloroanisole’s moderate volatility can be a benefit during stripping or distillation, letting R&D teams simplify workups. Those working with related anisole derivatives often find performance diverges sharply in nucleophilic substitution or palladium-catalyzed coupling. In synthesis campaigns where chloroanisole or bromoanisole alone fail to deliver, the halogen pattern in 4-Bromo-3-Chloroanisole unlocks new catalytic windows, especially for site-selective C–C or C–N bond formations.

    Comparisons: What Sets This Molecule Apart

    Plenty of synthetic chemists wonder why 4-Bromo-3-Chloroanisole can make or break a multistep project. From hands-on plant work, we’ve learned that choosing this anisole over standard halogenated benzenes changes the game, especially at key C–Br or C–Cl activation points. Against standard 4-bromoanisole, the extra chloro group steers the molecule toward selective reactivity at either the bromo or chloro site, depending on the catalyst and conditions. We’ve seen clear differences in reactivity profiles in Suzuki or Buchwald–Hartwig couplings, where this combination of halogens can block unwanted side reactions or open up rare cross-coupling selectivities.

    With 3-chloroanisole or 4-bromoanisole alone, we see greater byproduct formation during functionalization. Our process data show that 4-Bromo-3-Chloroanisole lets medicinal chemists build novel scaffolds with fewer separation headaches. On the industrial scale, it offers more predictable kinetics in metal-catalyzed couplings, which helps cut down on expensive precious metal loading.

    We’ve also compared shelf life and handling risks across common anisole isomers in our own storage rooms. 4-Bromo-3-Chloroanisole consistently holds up under varied humidity, staying stable and colorless over months, while some isomers show yellowing or viscosity changes that hint at silent degradation. This stability means fewer in-lab surprises and wasted inventory.

    Usage Across Diverse Sectors: Real Applications, Real Results

    This anisole derivative stands out most in the hands of synthetic organic chemists and process engineers. Nearly all of our pharma and agchem clients target late-stage intermediates requiring highly selective halogen exchange. We’ve walked through multiple pilot projects and seen that 4-Bromo-3-Chloroanisole frequently acts as a plug-and-play aryl donor in Suzuki–Miyaura couplings or as a key building block feeding into advanced kinase inhibitor synthesis. In each case, the dual halogen pattern makes orthogonal reactivity manageable, even if later steps call for selective dehalogenation or oxygenation.

    We’ve collaborated on custom reaction optimization with teams exploring macrocycle assembly and heterocycle formation. In those campaigns, 4-Bromo-3-Chloroanisole enabled smooth monoarylation or diamination reactions, outperforming both mono-halogens and non-anisole derivatives for conversion and selectivity. Tech transfer from bench to pilot took less time, since our tightly validated process kept impurity levels predictable. We see similar trends in agrochemicals, where rapid analog generation gives R&D teams the edge in screening new crop protection candidates.

    For electronics materials, this compound’s unique halogenation supports functionalization needed for OLED or liquid-crystal monomers, where off-position halogens can wreck end-product performance. Chemical buyers have shared that precise control at the bromo and chloro positions means faster downstream derivatization, tighter lot control, and more yield in high-value materials production. All these gains come from direct feedback between our manufacturing floor and user labs.

    Process Knowledge: Where Real Value Emerges

    Operating as an original manufacturer, we see the full process chain and the technical hurdles at each stage. Each batch begins with hands-on verification of all precursor solvents and reactants. We track actual impurities, not assumed specs, throughout chlorination and bromination, fine-tuning temperature ramps and hold times based on each lot’s actual behavior in reactors. We’ve invested in inline NMR and IR probes—costlier than basic monitoring, but absolutely necessary for anticipating impurities that would otherwise escape off-the-shelf analysis.

    Process safety isn’t just theory for us. Our operators experience firsthand the importance of scrubbing systems and process ventilation, especially dealing with possible HCl or Br2 emissions. By understanding laboratory-scale problems from the operator’s side, we engineer our vent handling and clean-in-place routines to keep long-term plant downtime minimal. Safer working conditions directly impact our lot consistency, as fewer contaminants form than in plants where shortcuts can creep in. These are not theoretical concerns—a single missed venting event or poorly handled exotherm can set back a whole production run.

    We run real-world accelerated stability on each batch, storing retained samples under multiple temperature and humidity conditions. Any hint of degradation triggers a root cause investigation in both our synthetic pathway and our packaging workflow. As a direct manufacturer, our decisions on packaging—choice of drum liners, barrier bags, and desiccant loading—come from firsthand data, so our product ships and stores without loss of quality or surprises to customers.

    Common Issues & Support: What Chemists Report to Us

    Customers sometimes send us feedback after their own in-lab work-up. The main issues we've seen aren’t with our material, but with solvent systems that promote unwanted isomerization or hydrolysis. For anyone doing large-scale purification, choosing a sufficiently nonpolar eluent can ease separation of structurally similar byproducts, as we’ve confirmed by trialing multiple solvent mixtures over hundreds of runs. On rare occasions, a poorly rinsed glass reactor can add trace contaminants—especially acidic residues—which raise the formation of minor impurity peaks. For this reason, we constantly remind users to run test batches and consult our technical team on in-lab troubleshooting. Our chemists are always ready to discuss real-life work-up details, solvent compatibility, and downstream step planning.

    Shipping and long-term storage posed bigger problems years ago, mainly due to interaction with container linings and fluctuating warehouse conditions. After several rounds of packaging changes—including upgraded HDPE drums and new foil-linear designs—we nearly eliminated small color changes and off-odors that some customers once reported. These improvements didn’t come from supplier suggestion or generic QA checklists, but from trial-and-error, side-by-side shelf tests, and deep process review.

    Differentiation: Why Work Directly with a Manufacturer?

    Distributors and resellers see products in catalogs; working as a direct chemical manufacturer lets us access the full technical background and lifetime data for each lot. We don’t just offer a COA—we maintain tie-back samples and create a reaction data library, so clients get both current and historical quality benchmarks. This real history matters if synthesis projects hit unexpected roadblocks, or if a client needs to revisit an older synthetic route.

    Many of our competitors source their material from intermediaries, leading to unpredictable lot differences. Our synthesis happens in-house, so we can quickly adjust processing parameters or engineer custom halogenation ratios if a client’s new project requires it. Early collaboration saves time and reduces both technical and commercial risk. For clients chasing hard-to-isolate structures or novel analogs, this responsiveness is key to beating out competitors who rely on off-the-shelf solutions.

    Direct dialogue with real-world chemists—both R&D and industrial—shapes how we maintain and improve our process. Several significant upgrades to our equipment and QA routines grew from technical calls with clients who faced previously unseen byproducts in their own downstream chemistry. Dogged attention to these technical details, and willingness to go the extra mile, drive our 4-Bromo-3-Chloroanisole reputation where performance under pressure is essential.

    Solutions for Ongoing and Future Challenges

    Supply chain turbulence remains a fact of life in chemical manufacturing. Raw material sourcing can shift with new restrictions or price swings, but close relationships with trusted suppliers keep our quality stable. We keep both process redundancy and long-term inventory on hand for key starting materials, avoiding the pitfalls seen by traders caught off-guard by logistical delays. Years of working across global markets taught us not to rely on single-source providers, and our data-driven procurement team matches internal batch analytics with supplier quality records for every input.

    Scalability also asks tough questions about environmental impact. Our ongoing efforts to green our 4-Bromo-3-Chloroanisole line focus on solvent recovery, reduced organic solvent waste, and new continuous-flow halogenation technologies. These aren’t just marketing claims—they come from our plant operators diagnosing real-world pain points, like spent solvent storage or utility costs during distillations. Some projects demand specialized grades or packaging formats, and in those cases, custom batch sizes and bespoke packaging meet regulatory or process needs directly.

    Building the Future of Fine Chemicals Together

    Producing 4-Bromo-3-Chloroanisole at scale means balancing hard science with hard-earned know-how. Every batch carries our plant’s experience—what worked, what didn’t, and what actually delivered value to project chemists and engineers. Our close work with advanced R&D labs, pharmaceutical teams, and material innovation hubs circles back to continual upgrades in our workflow. We understand that what matters most to our clients is not the lowest sticker price or most generic label, but trusting the process and product to perform at critical project junctures.

    We see 4-Bromo-3-Chloroanisole’s future growing in parallel with new cross-coupling methodologies, green production goals, and rapid analog development. As chemists push boundaries—from novel pharmaceuticals to advanced polymers—having an open channel to a direct manufacturer turns problems into partnerships. We invite our customers to continue challenging us, knowing that technical discussion and process sharing help both sides push the limits of possibility together.