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3-Hydroxy-4,5-Dimethoxybenzoic Acid

    • Product Name 3-Hydroxy-4,5-Dimethoxybenzoic Acid
    • Alias 3-Hydroxy syringic acid
    • Einecs 254-579-8
    • 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

    553384

    Chemical Name 3-Hydroxy-4,5-Dimethoxybenzoic Acid
    Molecular Formula C9H10O5
    Molecular Weight 198.17 g/mol
    Cas Number 1163-60-6
    Appearance White to off-white solid
    Melting Point 209-211°C
    Solubility Soluble in DMSO, methanol
    Synonyms 3-Hydroxy-4,5-dimethoxybenzoic acid; 4,5-Dimethoxy-3-hydroxybenzoic acid
    Smiles COC1=C(C=C(C(=C1)C(=O)O)OC)O
    Inchi InChI=1S/C9H10O5/c1-13-7-4-5(9(11)12)6(10)8(14-2)3-7/h3-4,10H,1-2H3,(H,11,12)

    As an accredited 3-Hydroxy-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 Amber glass bottle containing 5 grams of 3-Hydroxy-4,5-Dimethoxybenzoic Acid, tightly sealed with a screw cap and labeled.
    Shipping The chemical **3-Hydroxy-4,5-Dimethoxybenzoic Acid** is shipped in a tightly sealed container, protected from light, moisture, and incompatible substances. It is packaged according to regulatory guidelines for laboratory chemicals. The package includes relevant safety documentation and is clearly labeled to ensure safe handling during transit. Temperature control may be applied if required.
    Storage 3-Hydroxy-4,5-Dimethoxybenzoic acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizing agents. Keep the container tightly closed to prevent moisture absorption. Store at room temperature and avoid heat sources. Ensure appropriate labeling and use suitable personal protective equipment when handling the chemical.
    Application of 3-Hydroxy-4,5-Dimethoxybenzoic Acid

    Applications of 3-Hydroxy-4,5-Dimethoxybenzoic Acid in Industrial Manufacturing

    3-Hydroxy-4,5-Dimethoxybenzoic Acid serves as a key intermediate in multiple specialized chemical industries. Its unique molecular structure supports targeted downstream synthesis where strict regulatory, formulation, and process control standards apply. Below outlines four focused industrial application fields supported by proven manufacturing integration and compliance practices.

    1. Pharmaceutical Intermediate for Antihypertensive APIs

    This raw material plays a critical role in producing select antihypertensive active pharmaceutical ingredients (APIs), particularly in the synthesis of methyldopa derivatives. Manufacturers utilize this compound in the multi-step reaction pathway to introduce precise hydroxy and methoxy substitutions. Purity and traceability are closely regulated, with the pathway monitored under controlled batch conditions to fulfill endpoint API quality and pharmacological activity profiles required by regulatory bodies.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters – APIs
    • European Pharmacopoeia (Ph. Eur.)
    • China Pharmacopoeia (ChP)

    Typical usage ratio

    • 5–15% weight basis per batch, depending on the desired substitution level and reaction yield. Ratio adjusted in accordance with target molecule structure and in-line QC data.

    Downstream process integration

    • Sequential introduction after protection of carboxylic group in the primary stage. Incorporated in amide coupling or condensation steps, then purified as part of the API crystallization and solvent exchange process.

    Final product types

    • Antihypertensive finished drugs (e.g., tablets, capsules containing methyldopa derivatives)
    • Bulk API substances supplied to formulators
    • Direct intermediates for further modification in cardiovascular therapies

    2. Specialty Dye and Pigment Synthesis

    Many colorant manufacturers apply this compound in advanced dye chemistry. The dual methoxy positioning imparts color fastness and improved solubility to azo, anthraquinone, and specific reactive dye classes. Feedstock selection follows strict batch identity management, and the compound enters as a building block during diazotization, coupling, and subsequent sulfonation or mordant fixation stages, supporting tailored pigment synthesis for textile and paper finishing.

    Industry compliance standards

    • OEKO-TEX Standard 100 – Restricted substances for textile dyes
    • European REACH Regulation (EC No 1907/2006) – Registration of dye intermediates
    • ZDHC MRSL – Zero Discharge of Hazardous Chemicals for colorant supply chains

    Typical usage ratio

    • 2–10% of the precursor mix, determined through pilot-scale color calibration and target chromaticity. Adjusted for specific color intensity and shade requirements in the dye formulation.

    Downstream process integration

    • Added during the electrophilic aromatic substitution or diazo coupling stage. Reaction parameters such as pH and temperature are closely monitored to achieve stable dye intermediates ready for sulfonation or halogenation steps.

    Final product types

    • Textile reactive dyes
    • Paper and pulp pigments
    • High-performance coatings colorants
    • Wood stain and filler tint additives

    3. Food Contact Resin Modifier

    Producers of specialty polyesters and epoxide-based resins for food packaging applications employ 3-Hydroxy-4,5-Dimethoxybenzoic Acid as a modification agent. Its controlled introduction improves flexibility and acid resistance of the final resin matrix. Compliance with food safety regulations is essential, with manufacturers monitoring migration limits and residual levels at each batch release. The compound enters the esterification stage, contributing to polymer structure uniformity without compromising regulatory compositional thresholds.

    Industry compliance standards

    • EU Regulation (EU) No 10/2011 – Plastics intended to come into contact with food
    • FDA CFR 21 § 177.1580 – Polyethylene phthalate polymers for food contact
    • China GB 9685 – Additive use in food contact materials

    Typical usage ratio

    • 0.5–2.5% of the monomer mix; amount set based on targeted monomer conversion and finished resin performance in final product migration tests.

    Downstream process integration

    • Pre-mixed with diol or acid feedstocks, enters step-growth polycondensation reactors. Performance checking includes molecular weight distribution and clarity, tested in pilot extrusions and panel lamination trials.

    Final product types

    • Resin coatings for beverage cans
    • Flexible food-grade packaging films
    • Polyester-based trays and containers
    • Canister and bottle linings

    4. Agrochemical Intermediate for Selective Herbicides

    Synthesis of certain selective phenoxy herbicides depends on precise aromatic substitutions achieved using this compound as an advanced intermediate. Manufacturers deploy it as a starting material for generating ether or ester-linked molecules with activity against broadleaf weeds. Stringent process documentation, effluent control, and toxicological assessment steps ensure batch-to-batch reproducibility and alignment with agrochemical safety requirements.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO)
    • US EPA 40 CFR Part 158 – Data requirements for pesticides
    • ISO 9001:2015 – Quality management in agrochemical synthesis

    Typical usage ratio

    • 7–18% depending on target active content and conversion efficiency. Manufacturers optimize for minimal byproduct generation and regulatory residue tolerances in the final herbicide formulation.

    Downstream process integration

    • Enters the etherification or esterification reactor train following halogenation of base aromatic. Inline HPLC system monitors reaction progress and impurity levels prior to formulation blending with solvents and adjuvants.

    Final product types

    • Concentrated stock solutions for crop spraying
    • Water-dispersible granules
    • Herbicidal premix powders
    • Bulk technical material for downstream formulating sites
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