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2,3,4-Trimethoxybenzoic Acid

    • Product Name 2,3,4-Trimethoxybenzoic Acid
    • Alias Eudesmic acid
    • Einecs 218-972-0
    • 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
    VTB
    Specifications

    HS Code

    991958

    Chemical Name 2,3,4-Trimethoxybenzoic Acid
    Molecular Formula C10H12O5
    Molecular Weight 212.20 g/mol
    Cas Number 490-64-2
    Appearance White to off-white solid
    Melting Point 185-188°C
    Solubility In Water Slightly soluble
    Density 1.32 g/cm³ (approximate)
    Smiles COC1=C(C=CC(=C1OC)C(=O)O)OC
    Inchi InChI=1S/C10H12O5/c1-13-7-4-3-6(10(11)12)8(14-2)9(7)15-5/h3-5H,1-2H3,(H,11,12)
    Pka 4.16 (carboxylic acid group)
    Synonyms 2,3,4-Trimethoxybenzenecarboxylic acid
    Storage Conditions Store at room temperature in a tightly closed container

    As an accredited 2,3,4-Trimethoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g of 2,3,4-Trimethoxybenzoic Acid arrives in a sealed, amber glass bottle with a secure screw cap.
    Shipping 2,3,4-Trimethoxybenzoic Acid is typically shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be transported according to standard chemical handling protocols, protected from physical damage, heat, and direct sunlight. Ensure compliance with local, national, and international regulations for the transportation of laboratory and chemical substances.
    Storage 2,3,4-Trimethoxybenzoic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure the storage location is clearly labeled and meets appropriate chemical safety regulations. Handle with gloves and eye protection to prevent direct contact.
    Application of 2,3,4-Trimethoxybenzoic Acid

    Applications of 2,3,4-Trimethoxybenzoic Acid in Industrial Manufacturing

    2,3,4-Trimethoxybenzoic Acid serves as a core intermediate in multiple industrial sectors that demand precision in synthesis and strict adherence to regulatory requirements. Our experience as a chemical manufacturer supports its adoption in the production of active pharmaceutical intermediates, specialty dyes, advanced agrochemical intermediates, and innovative polymer stabilizers. Below, we detail application segments and include industry standards, formulation guidance, critical process steps, and representative end products.

    1. Synthesis of Pharmaceutical Intermediates (Antihypertensive Drugs)

    Pharmaceutical manufacturers incorporate this aromatic acid during the synthesis of specific intermediates for classified calcium channel blocker APIs such as Diltiazem. Controlled use of the acid provides steric effects and functional group orientation necessary in multi-stage condensation and cyclization steps. It ensures batch-to-batch consistency in intermediate purity, which impacts the downstream API profile. Compliance with current Good Manufacturing Practices, trace metal levels, and synthetic residue limits becomes critical.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia–National Formulary) impurity testing
    • European Pharmacopeia (Ph. Eur.) specification for intermediates
    • 21 CFR 211 (US FDA cGMP for drug products)

    Typical usage ratio

    • Generally 0.5–1.2 molar equivalents per reaction charge, adjusted according to target intermediate chain length and process yield optimization during continuous-flow or batch synthesis.

    Downstream process integration

    • Charged during acylation and cyclization reaction stage following neutralization and solvent activation; handled under nitrogen or argon atmosphere to limit side reactions.

    Final product types

    • Diltiazem base and salts (APIs)
    • Other benzoic acid-derived pharmaceutical intermediates
    • Custom-developed small molecule actives in cardiovascular therapy

    2. Fine Dye and Pigment Intermediate Production

    In dye and advanced pigment manufacturing, this compound functions as a critical substituted benzoic acid for the construction of methoxy-substituted aromatic chromophores. Its precise introduction during azo coupling or condensation phases dictates final molecule color depth, hue stability, and resistance to photobleaching. The purity grade must comply with internationally mandated azo dye safety checks and heavy metal content benchmarks due to downstream textile and ink contact uses.

    Industry compliance standards

    • Oeko-Tex Standard 100 (textile and leather ecology)
    • EU REACH Annex XVII (restrictions on azo colorants)
    • EN 71-3: Safety of Toys—Migration of certain elements
    • ISO 9001:2015 for pigment manufacturing

    Typical usage ratio

    • Applied at 1.8–3.0% by weight of total dye reaction charge; adjustment based on the final pigment molecular structure and targeted chromophore density.

    Downstream process integration

    • Added post-nitration during diazotization or coupling stages for specialty colorant synthesis; may function as the acid donor in high-temperature closed vessel condensations.

    Final product types

    • Methoxyphenyl azo dyes for textiles or digital inks
    • Organic pigments for coatings and plastics
    • High-performance pigment pastes for industrial paints

    3. Agrochemical Intermediate for Fungicide Manufacturing

    Leading agricultural chemistry suppliers rely on this raw material for downstream synthesis of triazole and strobilurin fungicide intermediates where regulated aromatic substitution influences bioactivity spectrum. Adherence to agrochemical-specific ISO systems and environmental residue testing is required, particularly as these materials affect crops for human and livestock consumption. Hydrolysis stability and minimal by-product formation in multi-step reactions ensure clean conversion to the desired intermediate in large-scale plants.

    Industry compliance standards

    • ISO 17025:2017 (Testing and calibration laboratories)
    • FAO/WHO JMPR pesticide specification reports
    • European Regulation (EC) No. 1107/2009 (placing plant protection products on the market)
    • Chinese GB/T 16631 (Pesticide Good Manufacturing Practice)

    Typical usage ratio

    • Used at 0.7–1.5 mole equivalents in stepwise condensation reactions, often adjusted for target triazole ring yield and impurity control in final API precursor output.

    Downstream process integration

    • Introduced at the early ring-substitution or esterification stage preceding heterocycle closure, processed under monitored temperature controls with in-line HPLC verification.

    Final product types

    • Fungicide intermediates for triazole and strobilurin classes
    • Custom aromatic intermediates for agricultural actives
    • Precursors for formulation into crop protection agents

    4. Functional Additive in Polymer Stabilizer Synthesis

    Specialty polymer compounders select 2,3,4-trimethoxybenzoic acid for integration in the production of heat and light stabilizers used in engineering plastics. Its multi-methoxy substitution enhances compatibility with polyolefin and polyester resin matrices and participates as an anchor group in the synthesis of hindered phenol or benzotriazole stabilizers. Adherence to ROHS and EN ISO standards for additive content and migration is required for applications in electrical and consumer plastic products.

    Industry compliance standards

    • EN ISO 9001:2015 (Quality management for chemical additives)
    • RoHS Directive 2011/65/EU (on hazardous substances in EEE)
    • ISO 17025 (Testing plastics for additives and migration)
    • FDA 21 CFR 177 (indirect food additives: polymers, if relevant application)

    Typical usage ratio

    • Integrated at 0.3–1.0% by resin weight during additive synthesis; ratio fine-tuned for stabilizer activity targets and resin compatibility during compounding trials.

    Downstream process integration

    • Employed in the esterification or amidation step of stabilizer production, then blended into polymer melt during extrusion, monitored by FTIR for complete incorporation.

    Final product types

    • Benzotriazole light stabilizer masterbatches
    • Hindered phenol antioxidant additives
    • Modified polyolefin and polyester resin granules
    Free Quote

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