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2-Bromo-4,5-Dimethoxybenzoic Acid

    • Product Name 2-Bromo-4,5-Dimethoxybenzoic Acid
    • Alias 2-Bromo-DMOBA
    • Einecs 244-689-3
    • 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

    755527

    Productname 2-Bromo-4,5-Dimethoxybenzoic Acid
    Casnumber 63470-45-3
    Molecularformula C9H9BrO4
    Molecularweight 261.07
    Appearance White to off-white solid
    Meltingpoint 173-177°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Storageconditions Store at room temperature, protected from light
    Smiles COC1=C(C=C(C(=C1OC)Br)C(=O)O)
    Inchi InChI=1S/C9H9BrO4/c1-13-7-4-5(9(11)12)3-6(10)8(7)14-2/h3-4H,1-2H3,(H,11,12)
    Synonyms 2-Bromo-4,5-dimethoxybenzoic acid

    As an accredited 2-Bromo-4,5-Dimethoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram sample of 2-Bromo-4,5-Dimethoxybenzoic Acid is supplied in a sealed amber glass vial with tamper-evident cap.
    Shipping 2-Bromo-4,5-Dimethoxybenzoic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is labeled according to hazardous chemical regulations and transported under ambient conditions unless otherwise specified. Appropriate documentation, including Safety Data Sheet (SDS), is provided, ensuring compliance with relevant shipping, storage, and handling guidelines.
    Storage 2-Bromo-4,5-Dimethoxybenzoic Acid should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Ensure it is separated from incompatible substances, such as strong oxidizing agents. Clearly label the container and follow proper laboratory safety protocols during handling and storage.
    Application of 2-Bromo-4,5-Dimethoxybenzoic Acid

    Applications of 2-Bromo-4,5-Dimethoxybenzoic Acid in Industrial Manufacturing

    Direct from our plant, 2-Bromo-4,5-Dimethoxybenzoic Acid supports specialty molecule production as a core aromatic building block. We focus on well-documented, regulated downstream sectors where this compound adds advanced value in targeted synthesis. Please review the following established industrial application scenarios, each detailed for compliance, formulation guidance, integration step, and representative end products.

    1. Pharmaceutical Intermediates for Kinase Inhibitor APIs

    Pharmaceutical manufacturers use 2-Bromo-4,5-Dimethoxybenzoic Acid as a strategic benzoic acid intermediate during the synthesis of kinase inhibitor drugs, specifically in advanced heterocycle construction. Inactive raw acid undergoes controlled halogen-lithium exchange or Suzuki-Miyaura coupling, providing high-yield access to benzene ring substitution patterns critical for bioactive compounds. The stringent documentation required for regulated drug substances governs its application, from storage and validation through to residue analysis.

    Industry compliance standards

    • ICH Q7/Q11 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 211 (U.S. FDA drug GMPs)
    • European Pharmacopoeia monographs (where applicable)
    • USP General Chapter <232> (Elemental Impurities in Pharmaceuticals)

    Typical usage ratio

    • 10–30 mol% relative to target API backbone; adjusted based on specific synthetic route and iterative halogenation steps

    Downstream process integration

    • Dissolved or suspended in polar aprotic solvents (e.g., DMF, DMSO) during palladium-catalyzed coupling at Stage 2 or 3 of multi-step synthesis
    • Reaction monitored for complete consumption before conversion to subsequent closed ring or aminated structures

    Final product types

    • Active pharmaceutical ingredients (APIs) for oncology therapeutics
    • Small-molecule kinase inhibitors (e.g., anti-tumor, immunomodulatory drugs)
    • Reference standards and GMP intermediates supplied for regulatory dossier support

    2. Advanced Liquid Crystal Intermediate Manufacturing

    Producers in the electronics value chain incorporate this substituted benzoic acid into the production of high-performance liquid crystal intermediates. Through selective etherification and halogen-metal exchange, the compound provides a modular aromatic core suited to the exacting purity requirements in display technology. Purification protocols manage trace organic and inorganic impurities at the sub-ppm level, ensuring no interference with electro-optical behavior.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IEC 61249-2-21:2017 (Halogen-free requirements in base materials)
    • ISO 9001 (Quality Management for functional material production)
    • Manufacturer-specific LCD grade impurity and purity controls >99.5%

    Typical usage ratio

    • 5–15 mol% input relative to total aromatic precursors; adjusted for target birefringence and twist angle control

    Downstream process integration

    • Reactant addition during sequential alkylation/amination to form multi-ring mesogenic compounds
    • Purification via column chromatography and repeat crystallization before blending into LC prepolymer mix

    Final product types

    • Intermediate mesogens for liquid crystal display (LCD) panels
    • Customizable LC aligners for high-resolution/contrast screens
    • Photoalignment materials for TFT/AMOLED manufacturing

    3. Agrochemical Active Ingredient Synthesis

    Major crop protection formulators employ this compound as a tailored starting point in the multi-step preparation of select benzoic acid-type herbicide and fungicide active ingredients. The molecular structure facilitates selective functional group transformations—especially O-methyl and bromo-position chemistry—that are foundational for downstream urea- and sulfonylurea-based agroactives. Process controls avoid residual halide contamination in line with global MRL mandates.

    Industry compliance standards

    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) and Codex Alimentarius MRLs
    • ISO 9001/14001 (Agrochemical manufacturing and environmental management systems)
    • REACH Regulation EC 1907/2006 (Chemical registration and hazard communication)
    • SANCO/12571/2013 (EU guidance on pesticide impurities)

    Typical usage ratio

    • 3–8% w/w in batch synthesis of specific benzoic acid-derived actives; the ratio is fine-tuned according to desired substitution and final purity profiles

    Downstream process integration

    • Integrated during condensation or coupling step with amines or isocyanates to generate core scaffold
    • Post-reaction dehalogenation for product-specific impurity clearance

    Final product types

    • Selective herbicide molecule intermediates (e.g., for rice, wheat, or fruit crops)
    • Novel fungicide scaffolds under patent protection
    • Precursor blocks for EPA-approved plant protection products

    4. Organic Synthesis of Dye and Pigment Intermediates

    Specialty dye and pigment manufacturers use this benzoic acid derivative as a controlled intermediate in the tailored synthesis of high-purity aromatic chromophores. The presence of dual methoxy groups combined with the reactive bromo function enables diversity in colorant precursor libraries, especially where deep, stable color or photo-reactive groups are required for technical textile printing or optical media dyes.

    Industry compliance standards

    • DIN EN 71-3 (Safety of toys–Migration of certain elements in colored inks and coatings)
    • Oeko-Tex Standard 100 (Textile dye residue limits)
    • ZDH/Directive 2002/61/EC (Azo dye restrictions)
    • In-house QC for photostability and color fastness

    Typical usage ratio

    • 2–6 mol% relative to full dye-forming precursor blend; modified depending on required chromophore depth and fastness trade-offs

    Downstream process integration

    • Sequential nucleophilic substitution and oxidation steps to introduce spectral tuning groups
    • Blending into pigment base after final condensation or ring closure

    Final product types

    • Technical-grade optical dyes (e.g., for CD/DVD coatings)
    • Fastness-optimized pigments for textile digital printing
    • Colorant intermediates for specialty industrial inks
    Free Quote

    Competitive 2-Bromo-4,5-Dimethoxybenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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