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3,5-Dichloro-4-Methoxybenzoic Acid

    • Product Name 3,5-Dichloro-4-Methoxybenzoic Acid
    • Alias Benzoic acid, 3,5-dichloro-4-methoxy-
    • Einecs 242-515-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    115432

    Chemicalname 3,5-Dichloro-4-Methoxybenzoic Acid
    Casnumber 31121-97-4
    Molecularformula C8H6Cl2O3
    Molecularweight 221.04
    Appearance White to off-white crystalline powder
    Meltingpoint 183-186°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Density 1.56 g/cm3
    Smiles COC1=C(C=C(C=C1Cl)Cl)C(=O)O
    Inchi InChI=1S/C8H6Cl2O3/c1-13-8-6(9)2-4(3-5(8)10)7(11)12/h2-3H,1H3,(H,11,12)
    Storagetemperature Store at room temperature, away from light and moisture

    As an accredited 3,5-Dichloro-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 25g amber glass bottle, labeled with chemical name, purity, hazard symbols, batch number, and securely sealed to prevent contamination.
    Shipping 3,5-Dichloro-4-Methoxybenzoic Acid is shipped in tightly sealed containers to prevent moisture and contamination. Packages are clearly labeled with hazard identification and handled in accordance with safety regulations for corrosive or irritant chemicals. Transport follows regulatory guidelines, ensuring safe delivery and compliance with local and international shipping standards.
    Storage Store **3,5-Dichloro-4-Methoxybenzoic Acid** in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from moisture and direct sunlight. Use appropriate chemical-resistant containers and label clearly. Ensure storage area is equipped with spill containment and appropriate safety equipment. Avoid prolonged exposure and handle with suitable personal protective equipment.
    Application of 3,5-Dichloro-4-Methoxybenzoic Acid

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

    As a dedicated manufacturer of 3,5-dichloro-4-methoxybenzoic acid, we supply this high-purity intermediate for key transformations across several specialized chemical industries. Our technical and quality management teams collaborate closely with downstream partners to support safe handling, process implementation, and compliance with international standards in regulated manufacturing environments. Below, we detail the primary industrial applications, with focus on typical formulation ratios, integration within diverse production workflows, matched to each relevant regulatory and product outcome context.

    1. Synthesis of Agrochemical Active Ingredients

    3,5-dichloro-4-methoxybenzoic acid serves as a key intermediate in the multi-step synthesis of select herbicide and fungicide actives. Its reactivity profile enables reliable introduction of methoxy and dichlorobenzene moieties within molecular frameworks that offer improved crop protection specificity and environmental safety compared to older actives. Downstream producers typically couple, hydrolyze, and condense this intermediate to generate registered formulations, where impurity control and traceability are critical throughout validation batches.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius guidelines for pesticide ingredient purity
    • REACH registration for supply and use within the European Union
    • Chinese GB2763-2021 pesticide residue standard (as applicable to active substances)
    • ISO 9001:2015 quality management system in agrochemical manufacturing

    Typical usage ratio

    • 0.2–1.1 mole equivalents per target molecule, adjusted based on the downstream reaction yield and by-product formation

    Downstream process integration

    • Introduced after primary aromatic halogenation, often in an arylation or esterification step, commonly under controlled temperature and solvent conditions

    Final product types

    • Registered post-emergent herbicide technical concentrates
    • Broad-spectrum fungicide technical materials for pre-formulation
    • Active ingredient intermediates for further derivatization

    2. Pharmaceutical Intermediate for Antibacterial Agents

    This compound is used by pharmaceutical ingredient manufacturers as an intermediate in the synthesis of select anti-infective actives, notably compounds featuring dichloromethoxy-substituted benzoic backbones. Its low impurity profile and consistent crystallinity permit integration into GMP-regulated multi-step synthesis, with documentation and trace batches maintained for audit and regulatory review. Controlled use reduces the risk of undesired side-products that could complicate downstream purification or pharmacopoeial compliance of final actives.

    Industry compliance standards

    • Good Manufacturing Practice (ICH Q7) for active pharmaceutical ingredient synthesis
    • USP–NF, Ph. Eur., JP monograph pre-requirements for intermediate traceability
    • FDA 21 CFR Part 211 for Process Controls in medicinal chemistry supply
    • ISO 14001:2015 for waste handling in pharmaceutical chemical operations

    Typical usage ratio

    • Typically 0.8–1.2 equivalents per target core in stepwise condensation; ratio specified in process validation reports according to reaction scale

    Downstream process integration

    • Added post-nitration or prior to acylation steps in the main drug substance synthetic route; frequently dissolved in polar aprotic solvents for maximized reactivity

    Final product types

    • API intermediates for anti-staphylococcal or anti-mycobacterial drugs
    • Final crystallized API for oral or parenteral formulations

    3. Specialty Dye Manufacture—Aromatic Derivative Synthesis

    Dye manufacturers utilize this benzoic acid derivative in the preparation of high-stability azo and anthraquinone dye molecules. Adding this intermediate at the diazotization or coupling stage enhances color fastness and oxidative resistance while supporting narrow spectral properties critical to fiber, plastics, or inkjet ink applications. Downstream integration requires closed-system material handling to prevent cross-contamination between dye batches, while strict raw material traceability supports customer-specific certifications.

    Industry compliance standards

    • REACH Annex XVII restricted substances lists regarding aromatic loading
    • OEKO-TEX ECO PASSPORT for dyehouse raw chemical inputs
    • ZDHC (Zero Discharge of Hazardous Chemicals) guidelines for textile dye production
    • ISO 1833 and ISO 14040 for inventory control and life-cycle assessment

    Typical usage ratio

    • Usually 3–12% of total batch mass in precursor dye synthesis, precisely measured per color specification parameters

    Downstream process integration

    • Introduced prior to or during diazotization/coupling in high-shear reactors, sometimes as a powder or slurry depending on manufacturer preference

    Final product types

    • Sulfonated azo dyes for synthetic fiber coloration
    • High-stability inks for digital textile printing
    • Polyester and polypropylene fiber masterbatches

    4. Synthesis of UV-Absorbers for Polymer Additives

    Polymer additive and masterbatch producers require this compound as a protected benzoic acid intermediate during the manufacture of light stabilizers and UV-absorbing agents. Its substitution pattern imparts high UV absorption and thermal stability to the resulting absorber, essential for plastics used in outdoor or high-light applications. Extensive QC verifies that no unwanted impurities migrate under compounding or injection molding conditions.

    Industry compliance standards

    • FDA 21 CFR 177 for indirect food contact plastics (if applicable to end-product)
    • EU Regulation (EC) No 1907/2006 for additive ingredients in plastic articles
    • ISO 10993 for biocompatibility if used in medical device components
    • ASTM D2565 for plastic weathering and UV resistance protocols

    Typical usage ratio

    • 0.5–2.5% by weight of target UV absorber formulation, with final dosage optimized by UV transmission and accelerated weathering data

    Downstream process integration

    • Included at the early condensation step in synthesizing benzotriazole or benzophenone-based absorbers; downstream pelletizing blends concentrate for masterbatch supply

    Final product types

    • Light stabilizer masterbatches for PE, PP, and PA plastics
    • Film-grade polymer UV absorbers
    • Protective coatings for outdoor-use plastics
    Free Quote

    Competitive 3,5-Dichloro-4-Methoxybenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

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