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3-Bromo-4-Chloroanisole

    • Product Name 3-Bromo-4-Chloroanisole
    • Alias 3-Bromo-4-chloro-1-methoxybenzene
    • Einecs 629-523-4
    • 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

    518452

    Chemical Name 3-Bromo-4-Chloroanisole
    Cas Number 7745-89-7
    Molecular Formula C7H6BrClO
    Molecular Weight 221.48
    Appearance White to light yellow crystalline solid
    Melting Point 47-50°C
    Boiling Point 252-254°C
    Density 1.61 g/cm3
    Solubility Insoluble in water, soluble in organic solvents
    Purity Typically >97%
    Smiles COC1=CC(=C(C=C1)Br)Cl
    Inchi InChI=1S/C7H6BrClO/c1-11-7-3-2-5(8)6(9)4-7/h2-4H,1H3
    Refractive Index 1.584 (estimated)
    Storage Temperature Store at room temperature, keep container tightly closed

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

    Packing & Storage
    Packing The chemical 3-Bromo-4-Chloroanisole is packaged in a 25g amber glass bottle, tightly sealed with a screw cap, and labeled clearly.
    Shipping 3-Bromo-4-Chloroanisole is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transport adheres to local and international regulations for hazardous chemicals. Appropriate labeling, safety documentation, and protective packaging are used to prevent leaks and ensure safe handling during shipment. Store in a cool, dry, well-ventilated area upon arrival.
    Storage **3-Bromo-4-chloroanisole** should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong oxidizing agents. Keep the container clearly labeled and protected from moisture. Store at room temperature, following standard laboratory chemical storage guidelines, and ensure appropriate precautions to prevent spills and accidental exposure.
    Application of 3-Bromo-4-Chloroanisole

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

    As the direct manufacturer of 3-Bromo-4-Chloroanisole, we support industrial partners in key synthesis routes for pharmaceuticals, agrochemicals, specialty dyes, and advanced materials. Below, we outline major downstream applications with regulatory, technical, and end-use details for each distinct sector.

    1. Pharmaceutical Intermediates Synthesis

    Pharmaceutical process engineers select 3-Bromo-4-Chloroanisole as a halogenated aromatic building block during API intermediate synthesis, particularly in routes requiring molecular diversification via electrophilic substitution. This compound offers controlled reactivity for coupling reactions and facilitates the introduction of complex functional groups under GMP-compliant synthesis environments. End-stage purification typically includes chromatographic steps and rigorous batch testing against pharmacopeial standards before moving to API or finished drug manufacture.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP; ICH Q7 guidelines)
    • USP and EP specifications for intermediates
    • FDA 21 CFR Part 210/211 for pharmaceutical processing
    • ISO 9001:2015 certified QC systems

    Typical usage ratio

    • Batch loading: 5–15% w/w of core synthesis batch depending on the target intermediate structure and yield optimization.

    Downstream process integration

    • Reaction input during halogenation or anisole-coupling steps in core pharmaceutical intermediate sequence
    • Integrated into solvent-based or solid-phase synthesis streams
    • Post-reaction washing, extraction, and purification ahead of next step

    Final product types

    • Quinolone derivatives
    • Chlorinated benzene-substituted drug intermediates
    • Anti-infective and anti-inflammatory API precursors
    • Specialty small molecule therapeutics

    2. Agrochemical Active Ingredient Customization

    Many agrochemical R&D and industrial divisions employ 3-Bromo-4-Chloroanisole as a core intermediate for synthesizing selective fungicide and herbicide molecules. Its dual halogen substitutions enable precise electronic effect modulation, critical for structure-activity optimization in active ingredient development. Formulators often leverage this intermediate for direct coupling or further halogen-exchange reactions before downstream formulation into biological or environmental test batches.

    Industry compliance standards

    • FAO/WHO specifications for technical material
    • EU Regulation (EC) No 1107/2009 on plant protection products
    • ISO 17025-certified quality management
    • REACH registration (EC 1907/2006) for chemical safety

    Typical usage ratio

    • Initial input: 8–18% by weight in the synthesis of key benzoic acid or phenoxy-related active ingredients. The level depends on the complexity and planned yield per stage.

    Downstream process integration

    • Intake for Suzuki or Ullmann coupling in seed molecule functionalization
    • Used directly in methylation or etherification steps
    • Purification via crystallization prior to downstream blending

    Final product types

    • Triazole-based fungicides
    • Selective pre-emergence herbicides
    • Custom agricultural intermediate molecules
    • Crop protection product building blocks

    3. Specialty Dye and Pigment Manufacture

    Industrial dye syntheses, especially for high-stain resistance and persistent chromophores, utilize 3-Bromo-4-Chloroanisole as a redesigned aromatic input to create advanced azo or anthraquinone systems. Its anisole ether group can be selectively cleaved or retained based on the specific absorption profile desired. Dye chemists often employ this building block in coupling or ring-substitution reactions during controlled batch manufacturing for technical textiles and high-performance coatings.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances
    • EN 71-3 concerning toy and pigment safety
    • ISO 14001 for pigment environmental management
    • REACH (SVHC) alert for aromatic amines

    Typical usage ratio

    • Input ratios: 6–17% of aromatic substrate batch, adjusted for target hue intensity and shade performance.

    Downstream process integration

    • Reacted at the diazotization or coupling stage in dye backbones
    • Introduced to reactors under temperature-controlled conditions for monochlorinated or monobrominated pigment lines
    • Solution purification and spray-drying before final dispersion formulation

    Final product types

    • Reactive azo dyes for cellulosic fibers
    • High-stability anthraquinone pigments
    • Technical colorants for engineering plastics
    • Special effect textile and inkjet dyes

    4. Advanced Performance Polymer Additive Synthesis

    Researchers and production lines in advanced materials employ 3-Bromo-4-Chloroanisole as an initiator or functionalization agent for the synthesis and modification of specialty polymers and resins. Its well-defined electron-donating and withdrawing groups enable controlled polymer branching or crosslinking. It is particularly important in aromatic polyether sulfone (PES) and high-performance resin synthesis, where it participates in nucleophilic aromatic substitution and end-capping reactions in precision polymer engineering.

    Industry compliance standards

    • ASTM D4066 polymer standards for engineering thermoplastics
    • ISO 11357 for polymer DSC testing
    • RoHS Directive 2011/65/EU for electronic and electrical equipment
    • UL 94 flammability standard for polymeric materials

    Typical usage ratio

    • Addition range: 3–10 mol% as initiator or chain-terminating agent, depending on the desired molecular weight and glass transition temperature

    Downstream process integration

    • Introduced at oligomerization or monomer charging step
    • Used in solvent or melt polymerization cycles
    • Purification and post-synthesis stability testing prior to compounding

    Final product types

    • Engineering thermoplastic resins (PES, PEEK blends)
    • Electronic encapsulating polymers
    • High-clarity, halogenated specialty adhesives
    • Crosslinked composite matrix materials
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    Certification & Compliance
    More Introduction

    3-Bromo-4-Chloroanisole: A Closer Look from the Manufacturer’s Bench

    Creating reliable organic intermediates often means paying attention to the smallest details, especially when precision drives downstream results. Over years in the factory, we’ve learned some fine distinctions matter more than they seem at first. 3-Bromo-4-chloroanisole stands out as a specialty chemical where such nuances count. We’ve seen it become a mainstay for customers in fine chemicals, pharmaceuticals, and advanced materials development. Our hands-on experience with this compound has shaped the way we approach both synthesis and quality management, so let’s walk through its real properties and uses, based on our direct manufacturing practice.

    Appearance, Handling, and Storage Insights

    Every batch of 3-Bromo-4-chloroanisole we produce typically appears as a white to off-white crystalline powder. We keep a close eye on color and consistency, as subtle changes signal impurities or undesired side products. The chemical’s stability under ordinary conditions makes it resilient for standard lab handling, though we always remind technicians to prevent unnecessary exposure to air and moisture, especially for storage over months. In our production lines, final packaging often happens under inert gas, minimizing degradation and safeguarding your product quality all the way to your site.

    Specifications That Matter in the Lab and On the Line

    The compound’s structural formula brings together a methoxy group, bromine, and chlorine on the aromatic ring. With a molecular weight of 235.49 g/mol and the CAS number 6940-78-9, our team focuses on keeping purity above 98% on a dry basis, according to HPLC and GC standards. We target low residual solvents, often far below the accepted industry limits, as many of our customers work in regulated pharmaceutical and agrochemical research.

    Physical properties—such as melting point range, which generally sits between 37–41°C—tell you more than numbers on a sheet. From our experience, minor variations in melting behavior often relate to microimpurities or small differences in synthesis route. We track these differences across production batches to support repeatable performance for scale-up or formulation work downstream.

    Applications: Where It Proves Its Value

    What we’ve seen in our factory is that 3-Bromo-4-chloroanisole consistently earns its place as a solid intermediate for making more complex organic compounds. Medicinal chemists use it to anchor halogenated aryl motifs into pharma candidates; it’s also essential for research into specialty building blocks, advanced polymers, and agrochemical leads. Some customers come to us after facing supply issues with polyhalogenated aromatics; this molecule bridges many of those needs, providing both reactivity and selectivity in cross-coupling and electrophilic substitution reactions.

    The real difference for a synthetic chemist or process engineer comes from 3-Bromo-4-chloroanisole’s substitution pattern—having bromine and chlorine on the same ring with a methoxy group. This arrangement opens several synthetic doors not easily accessed with mono-halogenated anisoles or unprotected phenols. The bromine tends to be more reactive in Suzuki and Stille coupling protocols, whereas the chlorine allows further diversification down the line. This double-halide functionality turns a single intermediate into a versatile platform. In our conversations with project leads and bench chemists, the ability to run tandem reactions saves precious development time, especially under demanding deadlines.

    Manufacturing Approach: Building in Reliability

    True confidence in a synthetic intermediate comes from spending years at the reactor, learning its quirks. Our process begins with stringent selection of starting materials—halobenzenes and anisole derivatives with traceable, consistent quality. Batch-by-batch QA checks include spectral matches (NMR, IR, and MS) against reference standards that we prepare in our own QA/QC labs. Small mistakes at early steps, such as moisture in the bromination stage or unfiltered precursors, show up later as hard-to-fix impurities, so we target very tight in-process specifications.

    Scaling up from lab to pilot and then to commercial scale always brings surprises—be it solvent compatibility, phase separation, or heat management during bromination or chlorination. Our manufacturing team constantly reviews these parameters. Controlling reaction temperature and agitation, for instance, helps reduce formation of unwanted di-brominated or tri-halogenated byproducts. The difference between 98% and 95% purity may not read as much on paper, but product applications in pharma and materials science demand minimal trace contaminants. One of our longtime partners noted substantial improvements in downstream yields after switching to our grade versus other suppliers, specifically due to our focus on byproduct control in the halogenation step.

    Comparative Advantages: How It Stands Out

    Comparing 3-Bromo-4-chloroanisole to classic mono-halogenated anisoles like 4-bromoanisole or 3-chloroanisole, real advantages emerge in multi-step syntheses. The presence of both bromine and chlorine groups brings site-selective functionalization, minimizing the need for protection–deprotection cycles. Chemists working on high-value compounds appreciate this selectability, as it directly impacts their resource use and project timelines. Mono-halogenated analogs might provide a simpler route for single coupling, but every extra synthetic step increases cumulative process risk and cost.

    We also see fewer compatibility issues with many common palladium and nickel-catalyzed protocols when using our product compared to other halogenated aromatics. That’s not luck; it comes from shared R&D with our partners, optimizing for solvent regimes and catalyst loads. Many process chemists turn to 3-Bromo-4-chloroanisole to cut the total number of synthetic steps and avoid problematic, unreactive byproducts that can linger from less pure or differently-substituted intermediates.

    Solubility in organic solvents runs close to other anisole derivatives, making it straightforward for bench and pilot scale operations. We’ve handled bulk orders where dissolved compound stability was critical. Through careful solvent selection (matching toluene, THF, or DMF, for instance), we’ve minimized crystallization in transit and on storage. That reduces headaches for technicians further along the value chain and keeps our product easy to dose, purify, or react without loss in yield.

    Environmental Considerations

    Regulated sectors demand traceability and transparency. We regularly support customer audits, providing full histories on raw material sourcing and handling protocols. Per our internal records, 3-Bromo-4-chloroanisole production brings minimal aqueous and organic waste compared to some multi-step halogenation pathways. We recycle compatible solvents in closed-loop systems and neutralize process streams before environmental disposal.

    Some of the more stringent buyers ask about worker safety and emissions control. Our manufacturing lines feature local exhaust and real-time monitoring where halogenation reactions take place. By reducing fugitive emissions and capturing vent gases, we meet—and often beat—local regulatory guidelines. Every modification to the plant layout or recipe gets reviewed by both safety and environmental teams, keeping both end users and our community protected. Project managers working under strict audit regimes don’t face unknowns when tracing our intermediates.

    Consistent Quality Through Decades of Experience

    The practical difference between a good and a great supplier lies in batch-to-batch reliability. Some intermediates are forgiving; this one is not. Missed specs on melting point, residual solvents, or halide content show up as poor yields, unpredictable impurity profiles, or analytical headaches in final products. We approach every production campaign with a mindset formed by decades at the bench—treating bulk manufacturing as a scaled-up extension of research chemistry, not a separate, distant process.

    Our technical team tracks long-term stability data, identifying not just measurable degradation but also subtle shifts that might not show until the compound is in your hands. That lens on both acute QC and real-world, long-term performance is why many of our customers have stayed through multiple project cycles and regulatory reviews. One practical lesson from our production floor is the value of analytical redundancy: every finished lot gets double-reviewed by different analysts, using independent calibration sets. In regulated sectors, that attention to detail prevents both regulatory setbacks and practical, day-to-day lab frustrations.

    Helping Chemists Adapt and Innovate

    A consistent theme from partners and repeat clients: 3-Bromo-4-chloroanisole unlocks flexibility for both exploratory and late-stage synthesis. For those building combinatorial libraries, the dual-halogen system supports rapid SAR studies—multiple derivatives from a single starting material, with fewer purification headaches. Customers developing process chemistry often report smoother transitions from milligram to kilogram scale because our material maintains physical and chemical behaviors across lots. Some chemists shift to this compound after repeated column chromatography headaches with mono-halogenated analogs, finding our product leads to narrower impurity windows and less material loss on isolation.

    Field feedback also drives our internal R&D. Several years ago, a customer working with emerging fluorination protocols pointed out minor cross-reactivity between traces of dibrominated byproducts and their reagents. Tweaking our bromination step to reduce dibromo anisole below 0.1% not only addressed their problem but also improved downstream yields for other clients. Manufacturing isn’t static; it grows by listening and adapting—not just scaling.

    Transparent Communication and Support

    As a manufacturer, we know real-world hurdles can appear after the product leaves our site, not just at our QC release. Our technical support keeps lines open for everything from interpreting spectral data to troubleshooting formulation challenges. Customers running into bottlenecks with scale-up often find our shared production notes, troubleshooting logs, and suggested tweaks useful—those practical insights come straight from our own process teams, not from a distributor’s manual or a recycled spec sheet.

    We also value in-person and online discussions about formulation strategies. Small, detail-oriented feedback—on filtration rates, solvent swaps, or stability under stress testing—often reveals the production realities no catalog or datasheet can cover. A comment about stir time, for example, can pinpoint a subtle difference in product flow or ease of transfer, helping both us and our partners adjust procedures for efficiency.

    Challenges, Solutions, and the Path Forward

    Every intermediate brings potential roadblocks. Recrystallization can expose batch variability, and downstream reactions may reveal unexpected impurity signals under more sensitive analytical methods. Over the years, we’ve refined our QA checkpoints specifically for 3-Bromo-4-chloroanisole after early feedback showed peak shoulder artifacts in certain GC traces. Shifting to extra purification loops eliminated these signals, and retesting with wider-area NMR screening allowed us to assure downstream compatibility for even the most demanding pharmaceutical applications.

    Another lesson emerged around mixing and packaging. Bulk transport sometimes led to compaction and caking, so we reviewed our granulation and sieving protocols. By optimizing crystal size and moisture conditioning, we ensure better flow in both semi-automated and manual dispensing systems. This adjustment, suggested by a customer handling multiple kilogram lots, now defines our shipment specifications for this compound.

    Quality isn’t just about purity. Trace inorganic residues from reagents also matter. Routinely, we test for residual copper and iron, both of which could poison sensitive catalysts used in cross-coupling reactions. Our raw material auditing goes beyond standard supplier certificates—we test in-house and monitor for lot-to-lot shifts, as even a small error in halide content can cascade into bigger problems later.

    Supply security has grown in importance. Global disruptions taught us the value of localizing parts of our raw material procurement. Direct relationships with primary suppliers, not trading agents, allow for faster response and clearer traceability, which many pharmaceutical customers require before even placing an order. Our proactive inventory system lessens the risk of out-of-stock situations for critical intermediates.

    A Commitment Built on Real Manufacturing Practice

    Nothing replaces deep, hands-on manufacturing experience. 3-Bromo-4-chloroanisole provides a direct example of how thoughtful process control impacts every step downstream, from small research labs to large-scale active pharmaceutical ingredient synthesis. We never see this compound as “just another intermediate”—we watch for the fine details and maintain flexibility to support innovation by our customers. Every improvement in purity, consistency, or packaging starts on our production floor, often inspired by open conversations with those working at the lab benches and reactors.

    Those searching for an organic intermediate ready to support complex synthesis will find practical advantages with our 3-Bromo-4-chloroanisole. Years spent refining every step, from sourcing to packaging, show up in every flask and reactor where our product plays a role. We invite developers, process chemists, and technical specialists to reach out with observations or requests. Progress isn’t just a function of equipment or technology—it grows from accumulated experience, direct feedback, and a shared commitment to quality. Every batch we dispatch carries the fingerprints of the manufacturing team, evidence of hard-earned expertise, and readiness to support the most challenging advances in chemistry.