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1-Bromo-2-Methoxynaphthalene

    • Product Name 1-Bromo-2-Methoxynaphthalene
    • Alias 2-Methoxy-1-naphthyl bromide
    • Einecs 217-675-7
    • 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

    679845

    Cas Number 2859-97-8
    Molecular Formula C11H9BrO
    Molecular Weight 237.09 g/mol
    Iupac Name 1-bromo-2-methoxynaphthalene
    Appearance Pale yellow to brownish crystalline solid
    Boiling Point 317-319 °C
    Melting Point 52-56 °C
    Density 1.53 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥97%

    As an accredited 1-Bromo-2-Methoxynaphthalene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with secure cap, labeled "1-Bromo-2-Methoxynaphthalene, 25g," includes hazard symbols, batch number, and handling instructions.
    Shipping 1-Bromo-2-Methoxynaphthalene should be shipped in tightly sealed containers, protected from light and moisture, and clearly labeled according to chemical shipping regulations. It is typically transported as a hazardous material, requiring proper documentation and handling in compliance with local, national, and international safety guidelines to prevent leaks, spills, or exposure.
    Storage 1-Bromo-2-Methoxynaphthalene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep it away from incompatible substances such as strong oxidizing agents. Ensure proper labeling, and store in a designated chemical storage cabinet suitable for organic compounds. Use secondary containment to prevent accidental spills or leaks.
    Application of 1-Bromo-2-Methoxynaphthalene

    Applications of 1-Bromo-2-Methoxynaphthalene in Industrial Manufacturing

    We supply high-purity 1-Bromo-2-Methoxynaphthalene for advanced chemical synthesis across specialized industrial fields. Downstream manufacturers use this intermediate to build custom molecular structures for target applications. Our technical support team collaborates directly with process engineers to meet rigorous standards, ensuring quality and reliability from formulation to scale-up production.

    1. Pharmaceutical Intermediate Synthesis

    1-Bromo-2-Methoxynaphthalene serves as a key intermediate for producing oncology, CNS, and anti-infective drug candidates. It enables direct naphthyl substitution to obtain bioactive molecules through Suzuki-Miyaura, Buchwald-Hartwig, or other cross-coupling processes. Its controlled reactivity allows chemists to access complex aromatic building blocks with high yields and regioselectivity, supporting both developmental pilot programs and commercial GMP synthesis of active pharmaceutical ingredients (APIs).

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • European Pharmacopoeia (Ph. Eur.) monographs for process intermediates
    • U.S. Food & Drug Administration (FDA) cGMP Guidelines 21 CFR Part 210/211
    • ISO 9001:2015 Quality Management System certification

    Typical usage ratio

    • 0.2 to 1.5 molar equivalents relative to target pharmaceutical intermediate or coupling partner, adjusted based on reaction conditions and scale

    Downstream process integration

    • Used as a coupling partner in palladium-catalyzed C–C or C–N bond formation for complex API side chains
    • Charged into reaction vessel at intermediate synthesis stage after initial halogen-naphthalene derivatization
    • Incorporated into continuous or batch process steps for upscaling pharmaceutical building blocks

    Final product types

    • Intermediate compounds for selective serotonin reuptake inhibitor (SSRI) APIs
    • Precursors for anticancer drugs targeting kinase and topoisomerase pathways
    • Building blocks for custom heterocyclic pharmaceuticals in R&D pipelines
    • High-value starting materials for custom contract manufacturing of regulated APIs

    2. Agrochemical Active Ingredient Formulation

    Our product enables synthesis of organic molecules with enhanced activity for modern crop protection solutions. It serves as a selectively reactive halogenated aromatic for herbicide and fungicide intermediate manufacturing via Grignard reactions and C–C coupling. Precise conversion and purification deliver critical intermediates for downstream formulation of patented agrochemical products subjected to international regulatory review.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides (FAO/WHO)
    • REACH Regulation (EC 1907/2006) for manufacturing and downstream use in the EU
    • US EPA (40 CFR Part 174, 180) registration requirements for crop protection chemicals
    • ISO 9001:2015 and Responsible Care® Global Charter

    Typical usage ratio

    • 0.8 to 1.2 molar equivalents as nucleophile or electrophile, depending on process for herbicide precursor formation; specific amount adjusted per process yield and impurity profile targets

    Downstream process integration

    • Introduced during key aromatic group formation and sidechain elaboration in proprietary active ingredient synthesis
    • Reacted under inert atmosphere with magnesium or transition metal catalysts in closed-system reactors
    • QC tested post-synthesis to meet minimum purity and residual bromine thresholds for downstream blending

    Final product types

    • Precursors for triazole and strobilurin fungicide active ingredients
    • Intermediates for phenoxy-substituted herbicide molecules
    • Building blocks for neonicotinoid insecticide synthesis
    • Functional group donors for selective seed-treatment actives

    3. Liquid Crystal Material Development

    Manufacturers use this compound to access high-purity, halogenated naphthalene derivatives essential for custom liquid crystal monomer synthesis. Its methoxy and bromo substituents enable introduction of lateral or terminal groups, improving the dielectric and photonic properties required in advanced liquid crystal display (LCD), OLED, and related optoelectronic device applications. Specialist process controls ensure repeatable material characteristics to meet demanding display manufacturing requirements.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for restriction of hazardous substances
    • IEC 61249-2-21 for halogen-free materials in electronics
    • China RoHS 2 Certification
    • ISO 14001 Environmental Management Systems

    Typical usage ratio

    • Varies from 0.05 to 0.3 molar equivalents as a functional precursor per batch, adjusted based on target mesogen structure and performance in test cells

    Downstream process integration

    • Added at naphthalene ring modification stage for mesogen backbone tailoring
    • Enters advanced coupling or etherification reactions for fine adjustment of birefringence and viscosity
    • QC-checked for residual halide and color prior to monomer polymerization

    Final product types

    • Custom nematic and smectic liquid crystal monomers
    • Reactive mesogen intermediates for high-performance display materials
    • Specialty additives for OLED and flexible display coatings
    • Optical compensation film ingredients

    4. Specialty Dye and Pigment Precursor

    Chemical manufacturers select 1-Bromo-2-Methoxynaphthalene as a halogenated aromatic starting material to create high-stability, high-color-depth specialty naphthyl dyes and pigments. Its profile enables fine electron-donating or -withdrawing functionalization, allowing downstream partners to synthesize colorants for technical textiles, printing inks, and imaging applications requiring extreme lightfastness and heat resistance. Purity and controlled reaction consistency support industrial pigment production systems.

    Industry compliance standards

    • REACH Annex XVII – restrictions on specific aromatic compounds in colorants
    • OEKO-TEX® Standard 100 for textile chemical safety
    • ISO 9001:2015 Quality Assurance in dye manufacturing
    • GHS (Globally Harmonized System) labeling and handling requirements

    Typical usage ratio

    • 0.3 to 1.2 molar equivalents per pigment molecule, based on desired color intensity and downstream reactivity in azo, anthraquinone, or metal complex pigment synthesis

    Downstream process integration

    • Used in electrophilic aromatic substitution or halogen exchange reactions during chromophore construction
    • Added post-initial diazotization step for directional naphthyl group introduction
    • Filtered and purified prior to dispersion and finishing in pigment powder or liquid form

    Final product types

    • Technical naphthyl dyes for digital textile printing
    • High-stability pigments for automotive and industrial coatings
    • Photoresist colorants for circuit board manufacturing
    • Heat-resistant inks for security and flexible packaging

    5. Advanced Polymer Additive Manufacturing

    Producers of specialty plastics use this compound as a functional modifier to synthesize naphthyl-containing monomers and oligomers that enhance polymer material thermal behavior and UV resistance. Controlled integration in the aromatic backbone ensures optimal interaction within formulation blends for engineering plastics, enabling production of materials suitable for electronic housings and advanced construction composites with robust physical and optical properties.

    Industry compliance standards

    • UL 94 Flammability Standard for plastics
    • ISO 10993 Biological Evaluation of Medical Devices (for relevant applications)
    • EN 71-3 Safety of Toys (chemical migration in polymers for children’s products)
    • ISO 14001 for environmental management in polymer processing

    Typical usage ratio

    • 0.02 to 0.5 molar equivalents, mixture adjusted according to targeted polymer chain properties, end-use requirements, and required final performance metrics

    Downstream process integration

    • Introduced during pre-polymerization of naphthyl monomers in melt-phase or solution-phase synthesis
    • Integrated with catalysts and co-monomers at compounding stage for performance plastics
    • Tested after copolymerization for migration and dispersibility in finished plastic matrix

    Final product types

    • Engineering polymers for electronic component housings
    • Heat-resistant construction resin systems
    • Specialty copolymers for 3D printing filaments
    • UV-stabilized plastics for outdoor infrastructure
    Free Quote

    Competitive 1-Bromo-2-Methoxynaphthalene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1-Bromo-2-Methoxynaphthalene: Proven Value from the Manufacturer’s Perspective

    Understanding 1-Bromo-2-Methoxynaphthalene from Start to Finish

    In our years of manufacturing specialty aromatics, we have seen how 1-Bromo-2-Methoxynaphthalene stands apart when you look at the landscape of substituted naphthalenes. We synthesize this compound with a focus on consistency, starting with carefully procured raw naphthalene and stringent in-house quality checks across each step. This compound bears the CAS number 573-98-8, and chemists will recognize its formula as C11H9BrO. The compound forms as a pale yellow crystalline solid at room temperature, offering distinct handling and stability advantages, particularly for those working in downstream synthesis or chromatographic separations.

    Our facility produces 1-Bromo-2-Methoxynaphthalene in batches that focus on maintaining high purity, commonly exceeding 98% by GC, since even tiny side-product contamination can derail downstream reactions. Each batch receives rigorous QC using both GC and NMR. Year after year, this level of scrutiny pays off in real-world reactions, where reactivity, selectivity, and isolated yields depend on starting materials behaving the same way every time. The standard model we supply moves through a sequence of controlled bromination and methylation steps, followed by careful, solvent-free purification. We have invested effort in making the work-up scalable and easy to clean, reducing process waste and improving product brightness.

    Real-World Applications: Strong Track Record in Synthesis

    One of the most robust uses of 1-Bromo-2-Methoxynaphthalene is as an intermediate for custom pharmaceutical and agrochemical building blocks. For instance, the electron-rich ring system and the ortho substitution pattern make this compound a useful starting point for cross-coupling and functionalization reactions. We have seen medicinal chemists leverage its reactivity for Suzuki-Miyaura couplings, especially when constructing larger, more complex aromatic scaffolds. In our customers’ hands, the bromo group provides a handle for further transformations, while the methoxy substitution tempers electronic effects and helps direct selectivities.

    We also field frequent requests to provide this material for research in material sciences, where its naphthalene backbone lends rigidity and electron delocalization to specialty molecules, including OLED emitters and advanced dyes. The demand from optical material customers often focuses on batch-to-batch consistency in color and melting point, both of which our current process parameters address directly. From feedback, we have learned that inconsistent suppliers, often trading through brokers, rarely match these requirements, leaving project chemists troubleshooting unexpected side products or re-running reactions. As the manufacturer, closing this loop not only controls output quality—it allows our own team to tweak and optimize, since we actually see where small changes in the process impact final product feel and function.

    Distinguishing Features Versus Other Aromatic Bromides

    1-Bromo-2-Methoxynaphthalene often draws comparisons to more common mono-bromo naphthalenes or to methoxy-substituted aromatics lacking the bromo handle. From our laboratory evaluations, we see several key differences. The unique location of both the bromo substituent and the methoxy oxygen—which sits ortho to the bromine—affects the compound’s electron density and reactivity. In cross-coupling settings, this substitution precisely tunes the balance between activation and stability; our chemists get predictable, cleaner reactions compared to unsubstituted bromo-naphthalenes, which can lead to complex mixtures or overreactions.

    Practical separation and purification steps benefit as well. The methoxy group adds polarity, making column workups more straightforward and less prone to streaking or tailing—something synthetic labs appreciate, especially in multistep synthesis where every gram counts. The crystalline nature of the pure product makes isolation easier than for many liquid or oily analogs, keeping losses lower and post-processing simpler. Years in the field and customer trials have reinforced that even small improvements here save significant time and cost for downstream users.

    Supporting the Evolving Needs of Our Customers

    Chemical manufacturers see the inside view of challenges faced by researchers and pilot production teams. Sourcing 1-Bromo-2-Methoxynaphthalene direct from a manufacturer has real advantages. We can guarantee full traceability of starting materials and intermediates—no guesswork due to uncertain chain of custody. This matters for regulatory submissions, intellectual property, and routine scale-up, where unpredictability can waste months and eventually derail programs.

    Feedback from process chemists shapes our manufacturing approach as well. Years ago, we adjusted filtration and crystallization steps based on feedback from a customer who saw unexpected impurities. By adjusting solvent ratios and cooling rates, we not only improved yield but reduced levels of certain known side-products below 0.1%, which was key for an API project entering scale-up. These are changes that traders cannot make. As a manufacturer, every change passes through our own R&D pilot lines, not a phone call to an external source.

    Ongoing Commitment to Environmental and Workplace Safety

    Long-term credibility in specialty chemicals demands attention to stewardship and safety. We have implemented closed-batch handling for bromine reagents, automated vent scrubbing, and solvent recycling. This control reduces exposure for operators and the community, and keeps operational costs in check. The final product is filtered and packaged in a controlled environment, minimizing any environmental release or user exposure. Packing in tightly sealed drums or bottles prevents degradation—critical for naphthalene derivatives, which may yellow or lose reactivity if exposed to air over long periods.

    Our training and regular safety reviews address every stage, from bromination to purification. This has led to a strong safety record and smooth regulatory inspections. Customers tell us they value our history of transparent auditing and willingness to provide full Manufacturing and Compliance Statements, not just product data sheets. We also offer advice on handling brominated aromatics safely, from PPE selection to waste disposal, demonstrating the depth of experience only a manufacturer develops.

    Addressing Common Challenges in Sourcing and Utilization

    One of the biggest frustrations reported from research and production buyers comes from inconsistent sourcing of specialty intermediates. Many labs order from distributors who may change sources from batch to batch, sometimes even within a single lot code. This unpredictability leads to variable melting points, strange off-colors, or unexpected chromatographic behavior. These headaches slow down discovery and waste resources. As the original manufacturer, we control each batch from start to finish. Documentation comes direct, not filtered through middlemen, so there are no unwelcome surprises.

    Lifecycle management of 1-Bromo-2-Methoxynaphthalene also matters. Some products have long lead times or unpredictable shipping windows due to reliance on overseas third parties or poorly understood regulatory regimes. Manufacturing in-house means lead times stay short and reliable. We plan production based on real demand and historical consumption, not speculative overstocking, so users get appropriately fresh material. When unforeseen challenges arise—like a precursor shortage or new regulatory concern—our technical and production teams can explain exactly where processes stand, offering alternate supply timelines or suggested workarounds.

    Direct Support for Process Development and Scale-Up

    Many buyers underestimate the benefit of manufacturer support when they begin moving a reaction from milligram scale to kilograms. Small impurities or changes in crystalline form, which barely matter for high-throughput screening, can cause bottlenecks in pilot plants or GMP production runs. We regularly consult with our partners to provide kilogram or larger samples representative of full-scale production runs, maintaining the same purification process. Scaling up is never just about making more—it is about making sure each gram is built the same way, each time.

    We have seen examples where a project switched sources and saw their target yield fall by half, all due to impurities from lower-grade intermediates. These impacts ripple through entire development cycles. Our QC labs track each lot, storing retention samples for comparison and troubleshooting. Any time a question comes up, we trace back to the exact conditions on the day of manufacture, adjusting if needed for future runs. This is only possible because we own the process from end to end.

    Specific Feedback from Field Chemists

    Chemists rarely comment on a product when everything runs smoothly. Not long ago, a customer switching suppliers for cost reasons returned to us after a run of inconsistent results and lost time. Their feedback confirmed something we see all too often: Highly substituted naphthalenes are particularly sensitive to raw material purity and storage conditions. Even a small impurity can introduce ghost peaks in analytical HPLC, or carry through to final compounds as identifiable defects. We use desiccant control and inert atmosphere storage through every step, and it shows in the absence of these issues down the line.

    Process chemists from larger enterprises often bring up the benefit of consistent physical attributes—melting point, powder bulk density, and crystal habit—especially when manufacturing involves inline filtration or transfer. Our actual experience has taught us to tune the crystallization conditions, not just reaction chemistry, which results in a more manageable, dust-free solid. This might sound trivial, but when you’re transferring barrels in a pilot plant, clumpy or staticky powders slow everything down and even create inhalation hazards. These are working realities many generic suppliers overlook.

    Experience-Driven Quality and Accountability

    Manufacturing means living with every batch decision and learning from each cycle. Simple problems, like drum liner failures or inconsistent labeling, teach lessons about traceability. Every return or complaint is reviewed by a cross-functional team, and solutions—like new liner bio-materials or updated drum coding—are implemented plant-wide. On the chemical side, tweaking reaction reflux times based on seasonal temperature swings has reduced off-spec production, cutting waste and keeping quality tighter. None of this happens in a trading office. We build it into our process because we understand how these factors affect real-world research and production.

    We have kept our product as a crystalline solid, instead of the more commonly traded syrupy or oily variants available from some suppliers. This approach not only helps researchers by providing a consistent, storable material, but cuts down on container failures and transport leaks. Our standard packaging and storage protocols directly reflect feedback from customers who previously lost time and money due to poorly chosen packaging or transport issues. The difference becomes clear with every delivered order.

    Support for Stringent Regulatory Environments

    Custom intermediates like 1-Bromo-2-Methoxynaphthalene often feed directly into regulated environments—pharmaceutical filings, agrochemical registration dossiers, or specialty polymer QC submissions. We provide full, timely documentation of synthetic route, impurity profile, and storage conditions. This isn’t just a box to check; it is a necessity for customer compliance teams facing rising standards from regulators. As a direct manufacturer, our compliance department interfaces with regulatory review boards, incorporating their technical questions and providing supporting evidence. This experience, built from years of submissions and audits, ensures our customers can submit authentic, traceable documents.

    Sometimes delays or failed filings occur simply because a distributor cannot explain which plant or what country actually made the lot in question. We remove this from the equation. Every certificate comes with transparent data, and if further questions arise, we can dig into laboratory notebooks, batch records, and even plant instrument logs to satisfy regulatory scrutiny. This level of transparency is demanded more and more at every stage—beyond just final APIs and into every step of the value chain.

    Continuous Improvement Built on Customer Partnerships

    Our production process for 1-Bromo-2-Methoxynaphthalene has benefited from a feedback loop with our user base for years. Every time a new process or synthetic challenge comes up, we work alongside research groups or pilot plants to understand root causes and opportunities for improvement. Sometimes this means switching to a higher purity bromine source, modifying crystallization seeding patterns, or adjusting packaging to suit local environmental requirements.

    Last year, after reviewing transport vibration data, we adopted a more robust inner lining and tighter sealing drum heads. This change reduced transit breakage by 80%. The decision to drop a problematic supplier of an upstream raw material occurred after we traced a recurring minor impurity to a single shipment. These shifts come directly from seeing the intermediate’s full journey, from our own drums into research labs and industrial kettles worldwide.

    Looking Ahead: Evolving Together with End Users

    Advanced materials, custom pharmaceuticals, agrochemicals, and emerging electronic applications all push for higher quality and more predictable intermediates. 1-Bromo-2-Methoxynaphthalene, with its highly controlled bromine and methoxy placement, stays in focus for new synthetic applications. Our ongoing R&D efforts seek cleaner, greener bromination and methylation methods, not just to meet current needs, but in anticipation of future environmental legislation.

    Open lines of direct communication with scientists, process chemists, and regulatory experts means new use cases reach our ears quickly. By keeping production, documentation, and support under one roof, we help accelerate not just individual research efforts, but entire segments of the specialty and fine chemicals industry. As needs change and new applications for the molecule arise, our goal remains the same: maintain quality, reliability, and deep technical partnership for all downstream users.

    Summary: Why Direct Manufacture Matters

    Our long-standing practice making 1-Bromo-2-Methoxynaphthalene springs from a clear-eyed view of what researchers, manufacturers, and new product developers actually experience. By controlling each phase—from raw material to packaged batch—we deliver certainty and security while adapting to each customer’s reality. That is the value of sourcing from a manufacturer who actually stands behind every container, every lot, and every new technical challenge. The difference shows up in less troubleshooting, faster scale-up, and ultimately, in more successful products launched on time and in spec.