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2-Bromo-3-Nitroanisole

    • Product Name 2-Bromo-3-Nitroanisole
    • Alias 2-bromo-3-methoxy-1-nitrobenzene
    • Einecs 629-288-2
    • 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
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    Specifications

    HS Code

    908384

    Chemical Name 2-Bromo-3-Nitroanisole
    Molecular Formula C7H6BrNO3
    Molecular Weight 232.03 g/mol
    Cas Number 35594-98-6
    Appearance Yellow solid
    Melting Point 53-55°C
    Solubility Soluble in organic solvents (e.g., dichloromethane, ethanol)
    Smiles COC1=C(C=CC(=C1Br)[N+](=O)[O-])
    Inchi InChI=1S/C7H6BrNO3/c1-12-6-3-2-5(9(10)11)4-7(6)8/h2-4H,1H3
    Synonyms 2-Bromo-3-nitro-1-methoxybenzene
    Safety Hazards May cause irritation to skin, eyes, and respiratory tract
    Storage Conditions Store in a cool, dry, and well-ventilated place

    As an accredited 2-Bromo-3-Nitroanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle labeled "2-Bromo-3-Nitroanisole, CAS 698-96-6," with hazard warnings and secure screw cap.
    Shipping 2-Bromo-3-Nitroanisole is shipped in tightly sealed chemical-resistant containers, labeled according to regulatory standards. It should be transported as a hazardous material, protected from light, heat, and moisture. Handle with appropriate safety precautions. Shipping must comply with relevant local and international regulations for hazardous chemicals, including UN identification and documentation.
    Storage 2-Bromo-3-nitroanisole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizers and reducing agents. Protect from light and moisture. Ensure proper labeling and keep away from food and drinking water. Use appropriate chemical storage cabinets if available.
    Application of 2-Bromo-3-Nitroanisole

    Applications of 2-Bromo-3-Nitroanisole in Industrial Manufacturing

    2-Bromo-3-Nitroanisole serves as an advanced intermediate for multiple specialized chemical synthesis routes, delivering highly consistent quality for demanding downstream applications. As a manufacturer, we provide this material with traceability and process accountability in accordance with strict industry protocols.

    1. Agrochemical Intermediate Synthesis for Herbicidal Actives

    Major agrochemical producers use 2-Bromo-3-Nitroanisole as a building block for the creation of complex herbicidal agents. The compound participates in nucleophilic aromatic substitution and further transformations to introduce functional groups critical to selectivity and crop safety. Its performance and purity profile directly affect batch output yields and impurity control in downstream formulations.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • Regulation (EC) No 1907/2006 (REACH) – European agrochemical registrations
    • FAO/WHO Specifications for Plant Protection Products
    • GB/T 19001 mandatory standards for crop protection chemicals in China

    Typical usage ratio

    • 0.3–1.2 mol equiv in active ingredient synthesis, with fine-tuning based on downstream conversion efficiency and target molecule design

    Downstream process integration

    • Introduced at the aromatic substitution step for precursor formation; further functionalized via reduction, coupling, or amination under controlled reaction conditions

    Final product types

    • Selective pre-emergent and post-emergent herbicides, e.g., substituted benzoic acid derivatives, triazole-based weed controls, and proprietary custom actives

    2. Pharmaceutical Intermediate for Nitrobenzene-Derived APIs

    Pharmaceutical companies employ 2-Bromo-3-Nitroanisole in the multi-step synthesis of active pharmaceutical ingredients containing nitroaromatic and haloaromatic motifs. Controlled input of this intermediate during scale-up determines overall purity and regioisomer selectivity in final APIs, impacting compliance with global pharmacopoeial monographs and regulatory submissions.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 for pharmaceutical manufacturing
    • USP, EP, JP compendial requirements for intermediates and APIs
    • Chemical Manufacturer’s Association Responsible Care® program

    Typical usage ratio

    • 0.8–1.1 mol equiv in key coupling steps, adjusted for stoichiometry depending on desired yield and byproduct minimization

    Downstream process integration

    • Fed into Grignard, Suzuki, or Buchwald coupling reactions as a protected aryl halide; subjected to reduction or functional group transformations en route to API core structures

    Final product types

    • Nonsteroidal anti-inflammatories, anti-microbials, nitroaromatic-based antihypertensives, and related branded or generic pharmaceutical products

    3. Dye and Pigment Manufacture for Organic Colorants

    Producers of advanced organic colorants integrate 2-Bromo-3-Nitroanisole as an intermediate for extended aromatic systems. Its reactivity supports the controlled installation of nitro and methoxy groups essential for lightfastness and color brilliancy. Accurate dosing and purification during the initial stages of dye synthesis are crucial for achieving the strictest shade reproducibility required by end-users in textiles and specialty coatings.

    Industry compliance standards

    • ZDHC Manufacturing Restricted Substances List (MRSL) for dyes and chemicals
    • Oeko-Tex Standard 100 (appendix for dyestuff purity)
    • ISO 9001 and ISO 14001 for colorant manufacturing traceability
    • REACH Annex XVII for restricted aromatic amines in EU markets

    Typical usage ratio

    • 0.5–1.0 mol equiv relative to coupling partners, tailored by chromophore target and reactivity balance

    Downstream process integration

    • Incorporated at the azo coupling, reduction, or methylation step, forming core units for further diazotization or condensation in multi-stage synthesis lines

    Final product types

    • High-performance azo and anthraquinone dyes, specialty pigments for digital printing inks, and textile colorants with complex substitution patterns

    4. Specialty Fine Chemicals: Photoresist and Liquid Crystal Material Precursors

    Manufacturers of electronic specialty chemicals use carefully purified 2-Bromo-3-Nitroanisole in the preparation of aryl ether and nitrobenzene-derived monomers, critical to advanced photoresist resin systems and liquid crystal alignments. Its defined reactivity window ensures reproducibility in proprietary synthetic routes, directly influencing the electrical and photochemical properties of the final materials.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronics manufacturing
    • ISO 14644 for controlled environment production
    • IECQ QC 080000 for hazardous substance process management
    • Supplier-specific cleanroom and solvent purity standards

    Typical usage ratio

    • 0.2–0.8 mol equiv, adjusted per resin polymerization protocol and functional density requirements

    Downstream process integration

    • Charged at the monomer assembly or substitution sequence during photoactive polymer synthesis; integrated into liquid crystal backbone structures via nucleophilic reactions

    Final product types

    • Thin-film photoresist polymers for lithography, nematic and smectic liquid crystal alignment agents, and custom electronic material blends
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    Certification & Compliance
    More Introduction

    2-Bromo-3-Nitroanisole: Pushing the Boundaries of Fine Chemical Synthesis

    Introduction: Synthesizing Value for Advanced Chemistry

    From our earliest days in chemical manufacturing, we have relied on care, detail, and patience for compounds that require precise customization. Among our flagship specialty products, 2-Bromo-3-Nitroanisole stands out for its unique profile and the value it delivers in targeted organic synthesis. As a team committed to hands-on technical refinement, our focus centers on crafting materials like this for demanding research and manufacturing pipelines.

    Molecular Overview and Identity

    2-Bromo-3-Nitroanisole, which chemists know as 1-Bromo-2-methoxy-3-nitrobenzene, anchors itself among aromatic compounds with both a bromine atom at the second position and a nitro group at the third. Our process maintains purity above 98% by HPLC, ensuring reliable consistency for laboratories and industrial users. Anisole derivatives like this play a key role in complex molecule synthesis, especially when selectivity and reactivity determine the outcome.

    We have walked through the entire journey of sourcing quality raw materials, setting up tight controls on moisture and residual solvents, and fine-tuning halogenation procedures in our reactors. Our team has learned that skip in controlling temperature profiles or slight inconsistencies in solvent grade during bromination can skew the product’s composition. This hands-on oversight tightens the batch-to-batch reproducibility that advanced research and industrial settings depend on.

    Specifications That Matter in Synthesis

    Years on the plant floor taught us that the best results for downstream chemical synthesis flow from a detailed focus on several important traits:

    While many suppliers overlook details like particle size or residual solvent content, we routinely analyze and adjust these in every run. Working directly with bench chemists and process engineers, we've heard the headaches left by even trace contaminants.

    Applications: Why Laboratories and Industry Rely on This Intermediate

    Our experience shipping to research institutes, pharmaceutical development centers, and agrochemical R&D facilities offers insight into why this particular anisole derivative stays in high demand. Its usefulness lies in two key chemical handles: the activated bromine atom provides a reactive site for cross-coupling reactions while the nitro group offers a strong electron-withdrawing presence. Together, this makes 2-Bromo-3-Nitroanisole a valuable intermediate for constructing heterocycles, advanced pharmaceutical scaffolds, and specialty dyes.

    The wide use of this compound highlights its versatility. Suzuki and Buchwald-Hartwig couplings rely on the presence of an aryl bromide for controlled C-C or C-N bond formation. Nitro-substituted aromatics like this introduce opportunities for further transformations, such as reduction to amines or conversions to other functionalities. Our direct interactions with development chemists have reinforced how a dependable supply of highly pure starting materials shortens time to market for new molecules.

    We have spent countless hours in scale-up campaigns for pharmaceutical and agrochemical projects where single-point contamination can throw off an entire project timetable. Supplying consistent, contaminant-free intermediates like 2-Bromo-3-Nitroanisole supports the fast pace and high standards demanded by these industries.

    Manufacturing Perspective: What Sets Our Material Apart

    Other brominated or nitro-substituted anisoles appear on the market, but only a few deliver both the right substitution pattern and controlled impurities profile for high-yield synthetic campaigns. We’ve fielded questions from synthesis departments frustrated by inconsistent materials that show up with out-of-range melting points or unknown byproducts. By producing this compound ourselves, we can account for every step—starting from raw material inspection, in-line reaction monitoring, and comprehensive in-house testing.

    Unlike generic importers or bulk resellers, every lot passes through our internal GC-MS, HPLC, and Karl Fischer moisture analyzers. Our team tracks not just purity, but also residual halogenated byproducts. We have colleagues dedicated to studying and refining every variable: pressure during halogenation, batch aging time, solvent residuals after crystallization. These extra layers of review reflect the years invested in chasing real-world performance over checked-box compliance.

    Comparison with other anisole derivatives reveals why the 2-bromo/3-nitro arrangement offers a different reactivity and selectivity profile than the 4-nitro or 5-bromo analogues. We field requests for custom substitution patterns—yet only the 2-Bromo-3-Nitroanisole variant balances both electron-withdrawing and halogenated effects in a way that supports both stepwise coupling and further aromatic substitution.

    Handling and Storage: Stability and Safety Come from Experience

    Safe handling stems from lived experience: every drum, bottle, or bulk bag leaves our site clearly labeled and with batch-specific documentation. We use tightly lidded, chemically resistant containers that keep the product dry and protected from light. Over the years, we've refined our storage rooms with dehumidification and temperature monitoring, after seeing even short-term humidity spikes change the flow characteristics of powder stocks.

    We always emphasize the need for clean, cool, dry storage to our partners. Nothing matches the peace of mind from seeing a product arrive with its intended melting point and crystalline texture. In practice, keeping containers at 2-8°C and away from direct sunlight guards against breakdown or clumping over time.

    From our workshops, we know that retaining technical documentation isn’t enough. Only proper, on-site quality checks and hands-on training for staff ensure safety and consistent downstream usability.

    Collaborating Directly with Synthetic Chemists

    Much of our learning comes not from the specification sheets but from conversations with researchers tackling real projects. Synthetic chemists often reach out to us looking for advice on solvent compatibility, scale-up behavior, or tweaking batch sizes to match pilot plant runs. These interactions push us to test, refine, and rework our reaction routes and purification routines.

    By listening to the problem reports from partners—whether a tricky recrystallization step or unexpected byproduct—our development teams have implemented responsive changes. Over time, we've reduced throughput bottlenecks in our proprietary bromination route. Every iterative step shapes our understanding of this intermediate’s sensitivity and expected behaviors, and our ongoing support to clients gives us insight not written in any textbook.

    This close feedback has led us to methods that improve filtration rates, lower residual solvent levels, and minimize unwanted isomers. Our commitment to direct partnership means support for custom packaging formats, special purity grades, and technical troubleshooting after delivery.

    Environmental Commitment and Regulatory Compliance

    Our long history in chemical production keeps us watchful about both regulatory updates and environmental obligations. Staff receive training in the safe management of halogenated and nitroaromatic intermediates. We continuously monitor emissions and liquid waste output through company-run programs. Integrated solvent recovery and re-use systems minimize our environmental footprint, and our leadership team stays engaged with local and international compliance bodies for current and future requirements.

    Besides internal practices, we're quick to adjust product labeling, shipping documentation, and storage recommendations to reflect updates in global transport and handling regulations. Long before rules change, we look for signals from our partners and regulatory agencies, anticipating any shift that might affect safe movement or disposal.

    These efforts come from direct experience. Our staff remember years when waste solvent management was less regulated, and the corrective projects that followed. That awareness shapes how we approach technical and social responsibility for every compound leaving our facility.

    Innovation Born From Real Production Challenges

    No synthetic intermediate reaches scale without a history of lessons learned on the production line. As a manufacturer, we face on-the-ground obstacles in every batch—reactor fouling, purity drift, unanticipated byproduct formation. Our staff tracks yield changes and process deviations in real time, sometimes pulling entire batches to preserve downstream quality. Lessons sharpen our focus on reproducibility.

    For 2-Bromo-3-Nitroanisole, the need for clean, reagent-grade material fueled many years of incremental process improvement. We engage directly with reactor engineers and bench chemists to ensure document standards match reality—not just on paper, but measurable in real-world campaigns.

    Our focus moves beyond minimum testing thresholds set by authorities. We aim for clarity and reliability that partners count on for sensitive transformations—whether that involves metal-catalyzed couplings, route scouting, or pilot-scale process validation.

    Differences That Matter: Standing Apart in a Crowded Field

    Not all anisole derivatives deliver the same reliability in high-value chemical transformations. Over years in operation, we've sampled and analyzed competitor products—some well regarded, others opportunistic. The biggest differences often show up in parameters missed by broad certificate of analysis (COA) snapshots: trace metallic impurities, polymorphic content, or micron-level particle inconsistencies.

    By managing the complete route from precursor acquisition to final distribution, we can anticipate and troubleshoot these subtle effects. Direct oversight means deviations, if any, get caught in-house with full root cause analysis. Research customers and industrial scale-up teams alike receive technical support grounded in first-hand production experience—not outsourced expertise.

    Some users assume switching to a similar halogenated nitroanisole guarantees equivalent results. Our feedback from development teams proves otherwise: even small changes in substitution pattern or impurity profile lead to different conversion rates, selectivity, yield, and safety outcomes. The advantage offered by 2-Bromo-3-Nitroanisole, from our process, comes down to consistency proven over hundreds of lots and years of careful improvement.

    Supporting Ongoing Research and Scaled Synthesis

    Across decades, our product has played a role in countless efforts in medicinal chemistry, crop protection innovation, and advanced materials research. Pharma teams leverage its reactivity in building new heterocyclic compounds, probing SAR relationships, and testing new lead series. Agrochemical developers use it as a key stepping stone for plant-protective agent frameworks.

    Close partnerships with both academic and industrial researchers challenge us to maintain and expand our technical background for this and related intermediates. We routinely review new literature and participate in technical roundtables to understand emerging modification routes, alternative synthetic pathways, and novel applications. In doing so, we not only refine our primary product but develop new variants with custom substituents and improved handling characteristics.

    Conclusions from Direct Manufacturing Involvement

    Every bottle of 2-Bromo-3-Nitroanisole leaving our facility reflects years of on-site effort, technical troubleshooting, and iterative process control. Working face-to-face with the compound at all key stages—reaction, isolation, purification, packaging—gives us the perspective to constantly improve both performance and value for advanced chemical synthesis.

    For scientists and process developers, success hinges on clear difference in product quality, impurity control, and technical support from their supplier. Our story as a manufacturer tells us that reliability grows through persistence, transparency, and a sequence of lessons paid for in labor and care. We remain engaged, responsive, and proud to support ongoing scientific and technical discovery with every lot of this specialty material.