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2,6-Dimethoxybenzoic Acid

    • Product Name 2,6-Dimethoxybenzoic Acid
    • Alias veratric acid
    • Einecs 219-054-9
    • 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

    590208

    Name 2,6-Dimethoxybenzoic Acid
    Cas Number 4030-10-4
    Molecular Formula C9H10O4
    Molecular Weight 182.17 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 156-159°C
    Solubility In Water Slightly soluble
    Density 1.32 g/cm³
    Smiles COC1=CC=CC(C(=O)O)=C1OC
    Inchi InChI=1S/C9H10O4/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5H,1-2H3,(H,10,11)
    Pubchem Cid 10818
    Synonyms 2,6-Dimethoxybenzoate; Benzoic acid, 2,6-dimethoxy-

    As an accredited 2,6-Dimethoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package of 2,6-Dimethoxybenzoic acid comes in a sealed amber glass bottle with a tamper-evident cap.
    Shipping 2,6-Dimethoxybenzoic Acid is shipped in sealed, chemical-resistant containers to ensure safety and prevent contamination. Packaging complies with regulatory standards for chemical transport. The product is labeled with hazard and handling information, and shipped via ground or air freight, depending on destination and customer requirements. Safety Data Sheet is included.
    Storage 2,6-Dimethoxybenzoic acid should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizing agents. Keep it in a cool, dry, and well-ventilated area, protected from direct sunlight. Ensure the storage area is labeled and access is limited to trained personnel. Regularly check for signs of degradation or contamination.
    Application of 2,6-Dimethoxybenzoic Acid

    Applications of 2,6-Dimethoxybenzoic Acid in Industrial Manufacturing

    2,6-Dimethoxybenzoic acid is an important fine chemical intermediate across several industrial sectors. Our direct manufacturing approach ensures tailored material quality for precise downstream use. Below, we outline authentic industrial application areas, detailing the regulatory, process, and product end-points served by this acid.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredients (APIs)

    Many pharmaceutical production routes employ 2,6-dimethoxybenzoic acid as a building block in the synthesis of complex APIs, especially for non-steroidal anti-inflammatory drugs and selective central nervous system agents. Manufacturers rely on its consistent purity to minimize downstream purification steps and avoid formation of undesirable side-products, especially when constructing substituted anthranilic acid derivatives via esterification or amidation. Systems operate under heavily validated, traceable conditions in full compliance with global pharmaceutical regulations governing intermediates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • EU GMP Guidelines Parts I & II (EudraLex Volume 4)
    • US FDA 21 CFR Part 210/211 for finished pharmaceuticals
    • Pharmacopeia monograph reference when applicable (USP, EP, JP)

    Typical usage ratio

    • Intermediate concentrations of 5–15% by mole in target API synthesis, with exact amounts adjusted based on API side chain complexity, synthesis route, and intended API batch scale

    Downstream process integration

    • Enters at the condensation or coupling reaction stage, typically following protection or activation steps
    • Integrated within multi-step batch synthesis, with in-process quality monitoring before further transformations

    Final product types

    • NSAIDs (e.g., Mefenamic acid class)
    • Antidepressants and antipsychotic agents (biphenyl derivatives synthesis)
    • Pharmaceutical chemical intermediates

    2. Specialty Liquid Crystal Material Synthesis

    Producers of liquid crystal substances for LCD and OLED displays use this raw material in the controlled introduction of methoxy-substituted aromatic groups, ensuring high-purity mesogenic compounds for display panel manufacturing. The acid’s structural features impart desirable thermal and dielectric properties, which downstream users harness through careful mono- or diesterification steps.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for fine chemicals
    • RoHS Directive (2011/65/EU) for substance restrictions in electronics
    • IEC 61249 lead, mercury, and halide content restrictions for electronics
    • RSL (Restricted Substance Lists) of major panel and device manufacturers

    Typical usage ratio

    • Blend concentrations typically between 6–12% by mass in downstream esterification reactions depending on target mesogen structure and clearing point requirements

    Downstream process integration

    • Introduced at early-phase organic synthesis, often in mixed solvent esterification followed by purification, then used directly in LC compound mixture formulation

    Final product types

    • Twisted nematic (TN) and super twisted nematic (STN) liquid crystal mixtures
    • Cholesteric phase display fluids
    • Precursor chemicals for matrix and active-matrix LCD panels

    3. Organic Synthesis for Dye and Pigment Manufacturing

    The methoxybenzoic framework serves as a foundational aromatic core in making advanced organic pigments, particularly soluble dyes and specialized pigments used in high-performance inks, textile dyeing, and lightfast coatings. Production recipes employ the acid for its reactivity profile under Friedel-Crafts acylation and nucleophilic substitution, helping pigment manufacturers achieve desired chromophore stability.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for pre-registration and registration of dye intermediates in EMEA
    • Oeko-Tex Standard 100 limits on regulated aromatic amines in textile applications
    • EN 71-3 heavy metal and aromatic compound content for toys and children’s products
    • ISO 9001:2015 for pigment production quality

    Typical usage ratio

    • Generally dosed at 8–25% of the aromatic raw material blend, with final proportion contingent on dye class (azo, anthraquinone, etc.) and application fastness demands

    Downstream process integration

    • Charged into the reactor during the colorant backbone construction; undergoes coupling, sulfonation, or acylation in solvent or melt phases before fine purification and blending

    Final product types

    • Solvent-soluble dyes for printing inks
    • Disperse dyes for synthetic fiber coloration
    • Organic pigments for plastics and coatings

    4. Agrochemical Intermediate for Herbicide Synthesis

    Manufacturers in the agrochemical sector utilize this compound as a key intermediate in the assembly of certain herbicide active ingredients, especially benzoylurea or methoxybenzoate derivatives. The rigid aromatic structure and methoxy functionalization enable process routes with higher selectivity for target crop applications, aiding in development of novel active substances under specific regulatory guidance.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides (FAO/WHO 2010)
    • ISO 17025:2017 for chemical testing and certification
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act) guidelines
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market

    Typical usage ratio

    • Loaded at 3–8% of total precursor weight in key condensation or substitution reactions, depending on end-use herbicide and route specificity

    Downstream process integration

    • Enters synthesis sequence after initial activation or chlorination steps, followed by condensation with urea or carbamate moieties
    • Incorporated prior to final purification and formulation into active ingredient concentrates

    Final product types

    • Benzoylurea class herbicide technicals
    • Cereal and paddy herbicide intermediates
    • Ready-to-use agricultural active ingredient formulations

    5. Polymer Additives and Functional Resin Modifiers

    Producers of engineered plastics and advanced resins use 2,6-dimethoxybenzoic acid as a functional modifier to introduce flexibility or toughness in specialty polymers. The acid participates in copolymerization or as a chain stopper in the production of polyesters or polyamides, conferring improved thermal resistance and altered solubility characteristics required for electronics and automotive components.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Standard
    • UL 94 flammability standards for polymer materials
    • REACH SVHC (Substances of Very High Concern) compliance
    • RoHS II Directive (EU) 2015/863 on hazardous substances

    Typical usage ratio

    • Typically 2–12% by weight in specialty polyester and resin formulations, customized based on polymer backbone and desired thermal/mechanical properties

    Downstream process integration

    • Introduced during melt-polycondensation or solution-phase polymerization, followed by direct blending and extrusion as granules or pre-polymers

    Final product types

    • High-performance polyesters for electrical insulation
    • Modified polyamides for automotive molding
    • Functional resins for electronic and LED encapsulation
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    Certification & Compliance
    More Introduction

    Introducing 2,6-Dimethoxybenzoic Acid: A Chemist's Perspective

    Experience in the Lab: What Sets 2,6-Dimethoxybenzoic Acid Apart

    Plenty of chemists get used to reaching for standard benzoic acids. Substitution patterns might look minor on paper, but working hands-on with 2,6-dimethoxybenzoic acid, you soon see subtle changes turn into significant results right on the benchtop. Our experience with synthesis and quality control has taught us that this compound’s properties make it a tool of real value, not just another reagent to keep in the storeroom. Consistency in purity, reliable handling, and chemical behavior you can count on—these lay the foundation for its regular use across research and manufacturing.

    Product Overview and Key Specifications

    The chemical structure, with its two methoxy groups at the ortho positions, pushes 2,6-dimethoxybenzoic acid (CAS 93-08-3) into a category of its own. Unlike most simple benzoic acids, this configuration blocks certain electrophilic substitutions while opening up pathways for targeted synthesis of advanced molecules. We supply it primarily as a high-purity, crystalline powder—free-flowing, moisture-stable, and easy to weigh by hand or with automated dispensers. Rigorous analytical protocols keep impurities below practical detection limits, using proven techniques such as NMR, HPLC, and GC. Typical melting points range from 175°C to 180°C, a direct result of its symmetrical, methoxy-capped structure.

    Handling and Storage: Trust Through Experience

    Many small-lot reagents come with promises about stability, but years in the manufacturing workflow have shown that 2,6-dimethoxybenzoic acid holds up well during storage. Standard packaging keeps contamination at bay, and the compound’s low volatility means you don’t lose mass between measurements. Users can expect ease of transfer, minimal dust generation, and robust compatibility with glass and common plastics. It resists hydrolysis under normal humidity, so long-term bench stock rarely gives surprises.

    Why the Ortho-Substitution Matters in Application

    Placing methoxy groups at positions 2 and 6 of the benzene ring shields the carboxylic acid group, reducing its participation in hydrogen bonding compared to meta or para-substituted analogs. This unique substitution influences solubility: 2,6-dimethoxybenzoic acid dissolves well in polar organic solvents, allowing reaction setups that can struggle with less substituted benzoic acids. Researchers who need selective functionalization find that these steric and electronic effects tune reactivity for applications like ligand synthesis, cross-coupling studies, and pharmaceutical intermediate preparation.

    Building Blocks for Modern Chemistry

    Decades of direct synthesis work have shown that this molecule serves as a gateway to advanced aromatic compounds. Its predictable reactivity streamlines esterifications, amidations, and other modifications—processes that falter with less precisely substituted benzoic acids. Chiral auxiliaries, transition metal complexes, and stable conjugates rely on these properties for reliable assembly. Many pharmaceutical and materials science innovations trace roots to the careful, reproducible chemistry made possible by such well-defined building blocks.

    Scientific Rigor in Manufacturing

    Repeated batches and continuous feedback from downstream reactions highlight how reproducibility starts at the manufacturing step. We monitor reaction temperature profiles, optimize solvent selection, and test lot-to-lot consistency using both in-line and final product assays. Delicate crystallization and drying preserve the characteristic flake or powder morphology that users expect, ensuring each container performs predictably whether you’re preparing a single-spout flask for screening or ramping up to a pilot-scale batch. Continuous improvement cycles are driven by bench data, not just spec sheets.

    Comparisons with Other Benzoic Acids

    The world of substituted benzoic acids stretches wide, but subtle details shift outcomes in the lab. Simple benzoic acid serves as an entry-level precursor, useful for standard aromatic chemistry and preservation, but it falls short in selective synthesis where sterics or electron donation must be tightly controlled. Meta- or para-methoxybenzoic acids, for example, show different solubility and reactivity, often leading to unwanted side-products or sluggish conversions when specificity is needed. The 2,6-dimethoxy pattern renders the molecule less accessible to certain oxidizing agents, which finds favor in multi-step synthetic plans where protecting groups and functional group interconversions play a central role.

    Applications: Not Just a Supporting Player

    Many compounds slip quietly through the supply chain, rarely noticed except by the most detail-oriented chemists. 2,6-dimethoxybenzoic acid stands out in several research and manufacturing contexts. Medicinal chemists rely on its substitution pattern to develop lead compounds resistant to metabolic breakdown, since the ortho-methoxy groups often slow enzymatic oxidation. Material scientists incorporate it into advanced polymers and functional materials, counting on its electron-rich, rigid aromatic core to transmit properties into the final product. Analytical chemists appreciate the clean background it gives in derivative formation for instrument calibration and standards.

    Role in Pharmaceuticals and Agrochemicals

    The trend toward greater safety and specificity in pharmaceuticals makes building blocks like 2,6-dimethoxybenzoic acid more valuable each year. Its electronic properties help tune binding affinity to biological targets, making it a stepping stone for compounds that must thread the needle of potency, selectivity, and safety. Agrochemical formulators also use derivatives to design active ingredients with favorable environmental profiles, improving fate and transport behavior in soil and water.

    Quality Assurance: Tangible Commitment

    Quality boils down to careful attention at every processing stage, not just the final certificate. Our laboratory teams don’t just run automated instruments; they scrutinize chromatograms for unexpected byproducts and examine powder texture under magnification. Packing procedures include double-sealed containers and desiccant packs where requested, based on actual climate and shipping demands. Repeat customers value being able to run syntheses without troubleshooting solubility or contamination issues, letting focus stay on chemistry, not logistics.

    Environmental and Safety Practices

    Working hands-on with chemical manufacture means accepting responsibility for every output. We developed waste minimization strategies during scale-up, targeting reduced solvent use and recycling streams as far as possible. All wash and mother liquors run through established treatment processes before discharge, and standard operating procedures keep raw and finished materials well segregated to avoid cross-contamination. Our teams wear and maintain adequate PPE, monitor air quality, and train for safe handling from the plant floor to the analytical lab. Periodic site audits and ongoing risk assessments mean new hazards don’t slip under the radar.

    Challenges and Adaptive Solutions

    Manufacturing 2,6-dimethoxybenzoic acid at scale presents unique hurdles—trace byproducts from incomplete methylation, managing alkali residues after workup, and handling the strong, sometimes irritating odor of methylated aromatics. Early on, we trialed several filtration media before settling on a method that removed colored impurities without stripping product yield. Temperature control during methylation prevents runaway side reactions, while solvent recycling reduces overall environmental impact. Experienced operators track subtle shifts in batch color and odor, nipping problems in the bud before batches progress downstream.

    Insights from Collaborative Research

    Chemists at research institutes regularly approach us looking for modifications—extra purification, tailored particle size, or alternate solvent washes. These requests don’t just keep customers happy; they feed back into improving our process and help identify new application frontiers. Through direct supply to academic and industrial labs, we see protocols take shape for high-throughput catalyst screening or scale-up for pilot pharma plants. Decades of close dialogue with innovators have fine-tuned our quality metrics, analytical standards, and packaging choices.

    Sustainability in Practice

    Long-term availability of specialty chemicals depends on prudent resource management. We work at reducing waste generation, optimizing solvent cycles, and searching for lower-impact precursors without sacrificing quality. Batch water use gets tracked closely and evaporated solvents are recovered wherever possible, so production stays both sustainable and cost-effective. These improvements emerged not from distant policy but from day-to-day plant experience and a persistent effort to trim inefficiency.

    Supporting Innovation in the Field

    The best moments come when researchers turn out novel molecules using our 2,6-dimethoxybenzoic acid as the key starting point. We’ve supported customers through failed runs and process redesigns, supplying insight based on previous experiences or pointing out hidden pitfalls in untested transformations. Countless feedback loops refine our protocols and inventory management, letting us respond quickly to shifting demands in the field.

    Packaging Options Based on Real Lab Use

    Early feedback showed small labs needed manageable packs—clean, moisture-resistant, easy to open without waste. Bulk users found value in larger drums fitted with optional liners, simplifying both transfer and storage. We standardized threading and sealing to keep bench handling simple, responding to user reports about clumping, static, or loss during weighing. Each revision drew on phone calls, surveys, and visits to both research and production sites.

    Lessons Learned in Supply Chain Reliability

    Global events and transport bottlenecks have tested every specialty chemical supply chain. Building resilient logistic channels means holding buffer stock, working with reliable carriers, and forecasting demand by season and project cycle. We share updates with customers regarding delays, origin changes, or documentation shifts—clear, direct communication earned through years of partnership. The team steps up to resolve customs issues and avoids shipping in extreme weather that could affect product condition.

    Smart Data Management, Not Just Paperwork

    Digital traceability covers every lot, but real trust comes from matching data with hands-on inspection. Retention samples, redundant balances, and cross-checks in our physical archive mean that every shipment traces back to actual process runs, not just numbers on a screen. Researchers know they can call and clarify any detail, and we welcome direct reporting of outlier results, so future batches can only improve.

    Trends in Downstream Chemistry

    The future holds new opportunities for compounds like 2,6-dimethoxybenzoic acid. Demand for greener pharmaceuticals pushes the need for more selective synthetic routes, which favor well-characterized, reproducible intermediates. New catalyst systems and enzyme-based processes regularly integrate advanced building blocks to streamline transformations, and our production insights ensure chemists don’t need to worry about unexpected reactivity as they innovate.

    Ongoing R&D and Product Support

    We reinvest a portion of every year’s revenue into analytical research, process safety, and synthesis optimization. Internal groups review published literature and coordinate with cooperative labs to refine test methods, solvent options, and materials handling for this compound. Continuous dialogue with bench chemists, scale-up engineers, and quality managers keeps our production line responsive—adapting to new purity demands, changing regulatory standards, or development of novel applications in real time.

    Conclusion: Chemical Manufacturing Rooted in Real Practice

    Decades of hands-on work with 2,6-dimethoxybenzoic acid have forged deep understanding of what matters in both small and large-scale chemistry. Regular interaction with users, rigorous attention to upstream and downstream processes, and persistent product refinement define our approach. This compound offers more than just a reaction partner; it provides dependable performance and supports progress in research and manufacturing. Researchers, engineers, and procurement specialists find value in solid, direct experience—not just the promise of quality, but its delivery in every container.