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3,5-Dibromo-4-Methoxybenzoic Acid

    • Product Name 3,5-Dibromo-4-Methoxybenzoic Acid
    • Alias 3,5-Dibromo-p-anisic acid
    • Einecs 251-185-4
    • 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
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    Specifications

    HS Code

    288641

    Product Name 3,5-Dibromo-4-Methoxybenzoic Acid
    Cas Number 50839-24-4
    Molecular Formula C8H6Br2O3
    Molecular Weight 325.94 g/mol
    Appearance White to off-white solid
    Melting Point 214-218°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles COC1=C(C=C(C=C1Br)Br)C(=O)O
    Inchi InChI=1S/C8H6Br2O3/c1-13-8-5(9)2-4(7(11)12)3-6(8)10/h2-3H,1H3,(H,11,12)
    Synonyms 4-Methoxy-3,5-dibromobenzoic acid
    Storage Temperature 2-8°C (Refrigerated)

    As an accredited 3,5-Dibromo-4-Methoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a white screw cap, labeled with chemical name, purity, safety symbols, and lot number.
    Shipping **Shipping Description:** 3,5-Dibromo-4-Methoxybenzoic Acid is shipped in tightly sealed containers, protected from moisture and light, and labeled according to chemical safety regulations. It is transported as a solid, non-flammable chemical, with standard documentation for laboratory use. Ensure compliance with all local, national, and international regulations for chemical transport.
    Storage 3,5-Dibromo-4-Methoxybenzoic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances (such as strong oxidizers). Protect from moisture, direct sunlight, and extreme temperatures. Properly label the container and ensure it remains sealed when not in use to prevent contamination and degradation.
    Application of 3,5-Dibromo-4-Methoxybenzoic Acid

    Applications of 3,5-Dibromo-4-Methoxybenzoic Acid in Industrial Manufacturing

    3,5-Dibromo-4-methoxybenzoic acid serves as a specialized halogenated aromatic intermediate in multiple industrial segments. As the original manufacturer, we supply this compound for critical transformations and molecule-building steps in targeted downstream fields, with each application governed by strict compliance standards and process protocols. Below, we detail main sectors utilizing this acid, outlining real-world use cases, regulatory frameworks, formulation specifics, and integration with production lines.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Major pharmaceutical companies incorporate 3,5-dibromo-4-methoxybenzoic acid as a pivotal functional group source for the synthesis of selective kinase inhibitors and other complex halogenated APIs. Its role is essential for introducing site-specific bromine and methoxy groups, enabling targeted biological activity in final drug molecules. Synthesis streams typically utilize this acid in chlorination or amide coupling stages, with batch-to-batch consistency and impurity profiling demanded by global market authorization protocol.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR 210/211 for finished pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) monograph requirements (for related substances, purity, and residual solvents)
    • USP <823> for analytical validation and impurity limits

    Typical usage ratio

    • Used at 0.07–0.22 molar equivalents depending on the target molecule; exact loading tailored based on desired site-selectivity in API core structure and desired yield in multistep synthesis.

    Downstream process integration

    • Introduced during heterocycle functionalization, halogen exchange, or amide bond-forming stages within synthesis of kinase inhibitors and CNS-active compounds.

    Final product types

    • Antineoplastic agent precursors (e.g., selective BRAF/MEK inhibitors)
    • CNS-active molecules for neurodegenerative disease trials
    • Pharmaceutical R&D intermediates for lead optimization
    • Targeted therapy candidates in clinical research pipelines

    2. Agrochemical Intermediate for Fungicide and Herbicide Synthesis

    Process formulators and agrochemical producers use 3,5-dibromo-4-methoxybenzoic acid as an advanced building block for triazole and pyrimidine-based crop protection actives. Its bromo-methoxy motif supports the introduction of hydrophobic and electron-withdrawing sites crucial for the bioactivity of downfield herbicidal and fungicidal compounds. Integration with chlorosulfonation, esterification, or heterocyclic coupling ensures consistent field performance in finished formulations.

    Industry compliance standards

    • FAO/WHO Specification for Agrochemicals
    • ISO 9001:2015 QMS for manufacturing consistency
    • REACH (EC 1907/2006) for environmental, health, and safety compliance
    • OECD Good Laboratory Practice for synthesis and analysis

    Typical usage ratio

    • Incorporated at 0.08–0.18 mole fraction depending on downstream crop protection compound and reactivity in core scaffold assembly.

    Downstream process integration

    • Inserted at the aryl halide coupling, esterification, or nucleophilic substitution steps for custom development of triazole and pyridyl fungicides/herbicides.

    Final product types

    • Proprietary triazole fungicides for grain and fruit crops
    • Pyrimidine herbicide precursors for broadleaf weed management
    • Seed treatment ingredient formulations
    • Research pipeline active ingredients for agrochemical innovation

    3. Advanced Material Precursor in Liquid Crystal Monomer Synthesis

    In the field of liquid crystal display (LCD) technology, materials specialists rely on 3,5-dibromo-4-methoxybenzoic acid for its halogenated aromatic core. Used for synthesizing high-performance liquid crystal monomers with precise optical and dielectric properties, the compound ensures structural regularity and desired phase transition temperatures. Its integration directly influences alignment layer compatibility and device response characteristics across different grades of flat-panel displays.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic and optical applications
    • ISO 9001 for traceability across specialty chemical production
    • IEC 61249-2-21 for halogenated material content in electronics
    • Internal advanced materials QC protocols (manufacturer/end-user specific)

    Typical usage ratio

    • Employed at 0.03–0.15 mole ratio depending on required birefringence and viscosity profiles in downstream liquid crystal blend formulations.

    Downstream process integration

    • Enters as a coupling reactant in Suzuki or Stille cross-coupling to construct rigid core monomers or end-groups for nematic and smectic phase material blends.

    Final product types

    • High-resolution TFT-LCD panels
    • OLED precursor patterned substrates
    • Mobile device and wearable display materials
    • Photonics-grade specialty liquid crystal blends

    4. Synthesis Intermediate for Specialty Dyes and Pigments

    Manufacturers of high-value performance dyes and specialty pigments utilize this compound for controlled introduction of bromo and methoxy substituents into anthraquinone or azo dye frameworks. The aromatic acid is central to bromination-driven color tone adjustment and fine-tuning of solubility or fastness in downstream textile and high-performance printing applications. Production chemists adjust loading based on chromophore extension needs during diazotization and coupling sequences.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for finished textile compatibility)
    • EN 71-3 for pigment content in toys and consumer goods
    • ISO 18451-1/2 for pigment chemical characterization
    • GMP guidelines for food-contact and cosmetic pigments (if applicable)

    Typical usage ratio

    • Utilized at 0.05–0.13 mole fraction, varying by pigment depth, shade requirement, or solubility specifications in downstream dye synthesis.

    Downstream process integration

    • Integrated during bromoarylation, diazotization, or coupling points for specialty colorant production in batch or continuous flow systems.

    Final product types

    • Textile disperse and vat dyes for polyesters or cellulose fibers
    • Inorganic/organic hybrid pigments for automotive coatings
    • Special effect pigments for plastics and electronics
    • Inkjet and specialty printing dyes
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    Certification & Compliance
    More Introduction

    3,5-Dibromo-4-Methoxybenzoic Acid: Bringing Precision to Chemical Synthesis

    Working with 3,5-Dibromo-4-Methoxybenzoic Acid: An Insider’s View

    Inside the lab and on the plant floor, precision doesn’t just come from good intentions—it depends on tight controls, steady hands, and pure starting materials. 3,5-Dibromo-4-Methoxybenzoic Acid stands as one of those dependable building blocks. In our facility, we've produced this compound for years, supporting teams scaling up routes for advanced intermediates, electronic materials, and pharmacological candidates. From experience, the difference between consistent purity and random variability shapes the outcome of multi-step syntheses and determines whether customers meet their own downstream targets.

    This molecule, with the systematic label 3,5-Dibromo-4-Methoxybenzoic Acid (CAS number 57210-00-7), brings together the reactivity of two ortho bromine substituents and the activating profile of a para methoxy group. Those features shape how it reacts in cross-coupling processes, nucleophilic substitutions, and regioselective transformations. Staff in both R&D and production lines appreciate how small changes in raw material quality ripple into yield losses or even unexpected contaminants in the end product. We watch for this with every synthesis run.

    Specifications and Quality from a Producer’s Perspective

    Producing 3,5-Dibromo-4-Methoxybenzoic Acid calls for careful inspection at each step: bromination, methylation, and the control of side reactions. Each batch, we use NMR, HPLC, and melting point analysis not just for compliance, but for feedback during purification. This product leaves our reactors as a white to off-white crystalline powder, with purity typically above 99%. Moisture, inorganic residues, and any remaining starting materials get tracked down to ppm levels. Solubility in common organic solvents matches the needs of most catalytic cycles and acylations; water solubility stays low, which simplifies both isolation and handling.

    Unlike some high-volume chemicals where a few percent up or down rarely matters, analytical chemists and formulators relying on this intermediate expect the same structure and performance every shipment. We watch for consistent lot-to-lot melting points, spectral signatures, and retention times. Deviations show up quickly in their applications—sometimes as off-notes in polymers, sometimes as poor conversion in Suzuki couplings, sometimes as difficulties downstream in crystallization or solvent recovery.

    What Makes 3,5-Dibromo-4-Methoxybenzoic Acid Special in Synthesis?

    Not every dibrominated aromatic acid performs the same. We’ve run comparative trials with isomeric and non-methoxy-substituted versions, and the unique placement on the ring makes this compound behave differently in cross-coupling and protection/deprotection strategies. The ortho-positioned bromines lend themselves to stepwise activation, allowing for controlled functionalization—often critical in the early stages of pharmaceutical and advanced material development. The para methoxy group modulates electron density, enhancing reactivity toward specific palladium- and copper-catalyzed reactions, while at the same time reducing chances of uncontrolled overreaction or polymerization.

    Colleagues working on synthesis planning point out that using this compound, rather than simpler dihalogenated benzoic acids, gives them a stronger handle on selectivity. As a manufacturer, we observe demand shifts as new routes in electronics, agrochemicals, and medicinal chemistry favor these distinctive structural elements. When clients look for greener synthesis or higher yields, this substrate often unlocks both.

    Understanding the Downstream Impact: From Advanced Intermediates to End Applications

    Most customers don’t just buy 3,5-Dibromo-4-Methoxybenzoic Acid as a catalog item—they use it as a launchpad for much more complex structures. Follow the supply chain and you find its fingerprints in UV-curable coatings, specialty monomers, next-generation OLED materials, and active pharmaceutical ingredient (API) scaffolding. For some, it serves as a key input in Suzuki-Miyaura or Negishi couplings, where the metabolic stability or electronic profile of the methoxy-bromide pattern delivers crucial advantages.

    Over the years, we’ve worked closely with partners who’ve scaled up from gram to multi-hundred kilogram lots, watching how reaction scale, impurity profiles, and handling requirements evolve. For high-potency or high-value product lines, every slight impurity gets flagged and every deviation traced back to a root cause. We’ve learned to document every batch with complete traceability, linking lot-level analytical data, source material info, and chain-of-custody records. These steps reduce troubleshooting time and enable regulatory compliance, especially for customers seeking audit-ready supply chains.

    The Reality of Raw Material Sourcing: Purity, Authenticity, and Transparency

    One question that comes up time and again from fellow chemists and procurement staff is: how do we know what we’re getting? With fluctuations in global markets and pressure to control costs, some buyers investigate third-party traders or unvetted suppliers. In our experience, corners cut on authentication, documentation, or storage conditions usually cost more in the long run. Lost time in analytical re-testing or batch rejection stings. With 3,5-Dibromo-4-Methoxybenzoic Acid, we’ve emphasized routine ID confirmation, from TLC spot tests to spectroscopic analysis, every step of the way.

    Instead of abstract “quality assurance,” we talk about transparency: providing a full spectrum of analytical data, showing customers typical impurity signatures and confirming that our processes avoid common cross-contamination risks. This isn’t only to satisfy regulations; it builds genuine trust with chemists and engineers scaling up. Supply chains grow more complex each year, but communication and documentation remain our strongest tools for ensuring endpoint results match starting material promises.

    Differentiating Features: What Sets Our Product Apart

    Other variants of dibromo-methoxybenzoic acids exist in the marketplace, varying by bromine placement, ring substitutions, or manufacturing route. We’ve benchmarked our material against several alternatives and noticed several practical differences that matter in the lab and in process-scale production. Some competitive materials arrive with higher levels of colored impurities, off-odors, or inconsistent solubility profiles—each an indicator of rushed reactions, incomplete purification, or inadequate packaging.

    Maintaining low residual solvent levels shapes both process safety and application success. Our packing methods and final vacuum-drying steps keep volatile organics below established thresholds. Differences in particle size seem minor until you try to charge a reactor or run solid dispensing systems—regular, free-flowing powder reduces clogging and ensures reproducible batch addition, preventing spills and exposure.

    We’ve refined our methods for crystallization and sieving based on direct field feedback. Researchers encountering caking or excessive fines request tighter particle distribution, so we run process trials to meet those needs. Not every supplier holds themselves to those adjustments—sometimes you only realize the problem after an unexpected halt in production.

    Regulatory and Environmental Considerations

    Regulatory expectations rise each year. End users in API intermediates or advanced materials face tough scrutiny around hazardous substances, residual solvents, and batch-specific traceability. We engage in regular self-audits of our own synthesis and waste management streams. Our manufacturing process avoids legacy chlorinated solvents, aiming to meet evolving guidelines and to respond to customer expectations around sustainability and safety.

    Disposal of byproducts and management of waste streams have real-world ramifications, both for operating costs and community safety. Production of 3,5-Dibromo-4-Methoxybenzoic Acid generates bromide-containing wash water and spent organic solvents. Instead of releasing these to a generic treatment process, we recover, treat, and neutralize on-site, minimizing landfill burden and regulatory exposure. These investments may not always show up in a line-item quote, but they shape the long-term relationship with both customers and our surrounding environment.

    Supporting Process Innovation in the Field

    Our front-line technical team keeps up with new trends in synthetic methodology, especially as more customers request continuous-flow synthesis, solventless processes, or more benign reaction conditions. We’ve seen 3,5-Dibromo-4-Methoxybenzoic Acid adapted into flow reactors and automated platforms in projects ranging from optoelectronics to late-stage pharmaceutical intermediates. Demands for quick product documentation or specialized packaging—for glovebox use, moisture-barrier storage, or nitrogen-flushed containers—come through on a weekly basis.

    By covering both the pilot scale and the transition to production, we understand the pain points: clumping during charging, static build-up from dry powders, or batch-to-batch differences that show up only at scale. Our own process improvements often arise directly from these customer insights—tighter particle distribution, enhanced drying protocols, or even offering antistatic packaging. The learning loop never closes.

    Partnership and Building on Experience

    Across decades as both chemists and producers, we’ve found that long-term partnerships matter far more than individual transactions. Every major client now expects deeper engagement than in the past: joint failure analysis, support during regulatory filings, and rapid response to outlier batch data. Unlike the arms-length deals seen with traders or short-term brokers, we’ve built relationships that last across multiple projects, regulatory cycles, and even leadership changes at customer companies.

    We encourage bench chemists and production managers alike to reach out with route-specific or application-specific questions. This goes beyond the minimum spec sheet or certificate of analysis. For example, during the last major scale-up of a cross-coupling process for a novel OLED material, our technical support worked through issues in impurity carry-over and established a customized package size, reducing waste and easing dosage in automated processes.

    Lessons from Troubleshooting and Continual Improvement

    Most process improvements spring from digging into bottlenecks: purification that takes longer than expected, or filtration that clogs during scale-up. During a five-year stretch producing multi-ton lots of 3,5-Dibromo-4-Methoxybenzoic Acid, our team tracked every deviation from standard quality metrics. Spotting trends—such as micron-scale fines causing weight discrepancies or trace inorganic residues triggering off-colors—helped us design better post-processing steps.

    We invest in operator training and equipment upgrades, not because specs demand it, but because unpredictability costs more in the long run. Each small gain in consistency frees up teams in quality assurance and reduces the frequency of customer site support visits. The reward for customers comes as fewer raw material headaches, smoother regulatory reviews, and savings on unplanned process rework.

    Looking Forward: Trends Shaping the Future Supply of Specialty Intermediates

    Markets shift every year with new regulations, technology, and corporate initiatives around sustainability. The demand for 3,5-Dibromo-4-Methoxybenzoic Acid continues across fine chemical synthesis, new molecule discovery, and electronics as miniaturization evolves. We expect even greater emphasis on transparency and data-driven batch verification, as well as more requests for secondary supply assurance and rapid batch release analytics.

    Artificial intelligence and machine learning models increasingly influence route selection and process scale-up, which in turn increase demand for detailed historical performance data from suppliers. We work to digitize batch records, give real-time feedback to customers, and support predictive models with the analytical depth only a manufacturer can provide.

    Through every cycle of product development — from small-lot supply for discovery teams to industrial campaigns running for months — we’ve found that personal, experienced attention to chemical detail pays dividends. 3,5-Dibromo-4-Methoxybenzoic Acid remains a product for specialists who appreciate what a well-made intermediate can do. We welcome connections with researchers, engineers, and production partners who, like us, believe that quality lies not in slogans, but in repeated, measurable performance batch after batch.