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3,4-Dimethoxybenzoic Acid

    • Product Name 3,4-Dimethoxybenzoic Acid
    • Alias Veratric acid
    • Einecs 220-002-6
    • 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

    213869

    Cas Number 93-07-2
    Molecular Formula C9H10O4
    Molecular Weight 182.17 g/mol
    Iupac Name 3,4-dimethoxybenzoic acid
    Appearance White to off-white crystalline powder
    Melting Point 181-184 °C
    Solubility In Water Slightly soluble
    Smiles COC1=CC(=C(C=C1)C(=O)O)OC
    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)
    Density 1.27 g/cm³
    Storage Temperature Room temperature
    Pka 4.02
    Synonyms Veratric acid

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

    Packing & Storage
    Packing The packaging for 3,4-Dimethoxybenzoic Acid (25g) is a labeled amber glass bottle with a tight-sealing screw cap for safety.
    Shipping 3,4-Dimethoxybenzoic Acid is shipped in tightly sealed containers to protect it from moisture and contamination. The packaging complies with applicable chemical safety regulations. It is typically transported as a non-hazardous solid, labeled accordingly, and accompanied by a safety data sheet (SDS). Temperature and handling guidelines are followed during shipping.
    Storage 3,4-Dimethoxybenzoic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. It should be kept away from strong oxidizing agents and incompatible materials. Store the chemical at room temperature, protecting it from moisture, heat, and sources of ignition. Clearly label the container and ensure safe, restricted access.
    Application of 3,4-Dimethoxybenzoic Acid

    Applications of 3,4-Dimethoxybenzoic Acid in Industrial Manufacturing

    3,4-Dimethoxybenzoic acid serves as a key intermediate in several advanced industrial applications, valued for its reliable chemical properties and consistent performance in demanding synthesis environments. Below we detail specific downstream sectors and usage scenarios based on current manufacturing practice and regulatory expectations.

    1. Synthesis of Pharmaceutical Intermediates (API Building Block)

    Pharmaceutical manufacturers use this compound as a building block for producing advanced intermediates in non-steroidal anti-inflammatory drugs, antihypertensive agents, and specialty APIs. The compound's methoxy substitutions allow for targeted transformations during multi-step syntheses, maintaining purity and controlling by-product levels. Production involves stepwise addition during catalyst-mediated esterification or amidation under Good Manufacturing Practice, closely monitored for trace contaminants.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • Ph. Eur. (European Pharmacopoeia) monographs for pharmaceutical intermediates
    • 21 CFR Part 211 (FDA current Good Manufacturing Practice)
    • USP <87> & <88> (Biological Reactivity Tests)

    Typical usage ratio

    • 5–15% w/w relative to total intermediate mass; exact ratios depend on targeted API structure and desired yield

    Downstream process integration

    • Charged to the reaction vessel during early-stage condensation, often after solvent charging and pH adjustment; followed by coupling or hydrogenation steps

    Final product types

    • Valsartan intermediates
    • Telmisartan side chains
    • Diclofenac analog synthons
    • Custom pharmaceutical intermediates for contract manufacturing

    2. Production of Aroma and Fragrance Esters

    Fragrance and flavor houses incorporate this acid to synthesize esters prized for sweet, balsamic notes in perfumery bases and food flavors. The manufacturing employs acid catalysis or enzymatic esterification, controlling temperature and solvent polarity to optimize yield and minimize residual solvent carryover. Strict limits on contaminant migration and olfactory profile consistency apply throughout production.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • EU Commission Regulation (EC) No 1334/2008 for flavorings
    • FEMA GRAS (Flavor and Extract Manufacturers Association)
    • ISO 9235:2013 (Aromatic Natural Raw Materials Vocabulary)

    Typical usage ratio

    • 2–8% of total esters produced per batch; varies by target ester type and blend specification

    Downstream process integration

    • Introduced during batch-run esterification with alcohols; followed by fractional distillation to ensure fragrance purity and compliance

    Final product types

    • Methyl 3,4-dimethoxybenzoate (fragrance ester)
    • Perfume base compounds for luxury brands
    • Food-grade flavoring ingredients
    • Personal care scented additives

    3. Synthesis of Liquid Crystal Materials

    Specialty electronics manufacturers employ the compound as a precursor for synthesizing anisotropic esters integrated into advanced liquid crystal displays (LCD). The process involves condensation with alkyl or aryl alcohols under inert atmosphere, with purity monitored by HPLC and Karl Fischer titration. Output must meet stringent optical isotropy and residual solvent regulations for use in panel manufacturing.

    Industry compliance standards

    • IEC 61747 (LCD standard requirements)
    • RoHS (EU Directive 2011/65/EU) for hazardous substances
    • REACH Registration (EC No 1907/2006)
    • JIS C0920-2:2022 (Japanese LCD technical standard)

    Typical usage ratio

    • 12–18% of precursor charge; precise ratio based on the optical properties and viscosity targets for the liquid crystal formulation

    Downstream process integration

    • Fed into the reactor as a functionalized benzoic acid segment in esterification step; downstream purification achieved through recrystallization and solvent washing

    Final product types

    • High-performance LCD panel mixtures
    • Temperature-sensitive display agents
    • Cholesteric liquid crystals for decorative films
    • Intermediate blanks for OLED panel development

    4. Agrochemical Intermediate Manufacturing

    Formulators in crop protection synthesize selective herbicide and fungicide intermediates using this compound due to its reactivity with aromatic amines and halogens, ensuring high conversion rates for regulated agrochemicals. Manufacturing always includes multi-stage purification and LC-MS verification of intermediate purity, with focus on minimizing environmental residue in final formulations.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for agrochemical development
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • EPA 40 CFR Part 180 (Tolerance limits for pesticide residues)
    • ISO 17025 (General requirements for testing/calibration laboratories)

    Typical usage ratio

    • 8–14% in intermediate synthesis procedures; ratio tuned for downstream halogenation and amidation efficiency

    Downstream process integration

    • Applied during the key acylation or chlorination step of herbicide precursor chain extension, before final formulation blending

    Final product types

    • Triazole fungicide intermediates
    • Benzyl-based herbicide precursors
    • Chemicals for seed treatment coating production
    • Custom crop protection formulations for regulated export

    5. Polymer Additive and Modifier Synthesis

    Advanced plastics and copolymer factories utilize this material to introduce functional groups for modifying polymer structures, especially in engineering resins requiring improved UV stability and electrical insulation. Integration occurs under controlled polymerization, with online spectroscopic monitoring to restrict residual monomer content and ensure targeted compatibility with existing thermoplastic matrices.

    Industry compliance standards

    • REACH (EC No 1907/2006) registration for polymers and additives
    • FDA 21 CFR §177.1520 for plastics in contact with food
    • UL 94 (Plastic Flammability Standard)
    • ISO 9001:2015 (Quality management for polymer production)

    Typical usage ratio

    • 0.5–3% as chain-end modifier or copolymerization component, adjusted for targeted dielectric and light stability performance

    Downstream process integration

    • Fed during melt or solution polymerization stage; reacted with polyesters, polyamides, or as comonomer for high-value copolymers

    Final product types

    • High-performance engineering plastics
    • Polyester UV-resistant fibers
    • Electronic encapsulation materials
    • Plastic films for food packaging
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    Certification & Compliance
    More Introduction

    3,4-Dimethoxybenzoic Acid: Practical Insights from the Manufacturing Floor

    Understanding 3,4-Dimethoxybenzoic Acid in Practice

    At our plant, 3,4-Dimethoxybenzoic Acid, known among chemists for its clarity in both structure and performance, stands out as a chemical with broad industrial value. With the molecular formula C9H10O4, this white to off-white crystalline powder often comes tagged with its CAS number: 93-07-2. Right from the production vessels, we see clear demand from sectors focused on pharmaceutical synthesis, advanced materials, and specialty chemicals.

    The Model We Supply

    Our model for 3,4-Dimethoxybenzoic Acid keeps things straightforward and reliable. Every batch gets tested to ensure a typical purity above 99.0%. Loss on drying stays well below the 0.5% mark. The melting point usually lands between 181°C and 183°C, and this tight range tells us a lot about process control and how effectively raw inputs translate into a defined end product. Each specification stems from daily experience with scale-up, repeated crystallization, and attentive handling through drying and milling.

    Production from a Manufacturer’s Perspective

    Lab data shows only part of the story. Behind every kilogram stands months of development—fine-tuning solvents to minimize impurities, managing filtration for consistent crystal size, and running multiple drying cycles to smash moisture levels to near zero. Operators watch each filtration and drying step since, in our experience, even a small slip can mean larger downstream headaches. Every finished lot draws from controlled raw material sourcing, practiced handling, and a crew familiar with chemical behavior at scale.

    In-process samples guide our technicians to adjust temperatures or solvent ratios in real time. When a tank of solvent misses specification, it’s pulled or corrected on the spot. There’s no shortcut here, just a daily commitment to doing things right, confirmed with precision before drums roll onto loading docks.

    Applications Driving Demand

    Several industries lean on 3,4-Dimethoxybenzoic Acid, but the pharmaceutical sector brings the steadiest pull. Many chemists select it as a starting block for nonsteroidal anti-inflammatory drugs, antihistamines, and other active intermediates. It forms part of the synthetic pathways to drugs that see real use in clinics and pharmacies. The methoxy groups at the 3 and 4 positions unlock selectivities not available in simpler benzoic acids, which is why it shows up on so many process development checklists.

    Beyond pharmaceuticals, dye manufacturing remains a key segment. The aromatic core and dual methoxy substituents allow it to serve as a precursor for specific azo and anthraquinone dyes. Fine chemical firms also value its clean conversion to specialty esters, salts, and amides. In plastics and coating research, its presence tweaks flexibility or reactivity profiles, making it a minor but meaningful ingredient in several new formulations chasing better performance in paints, fibers, or thermal stabilizers.

    Some agrochemical developers come asking for 3,4-Dimethoxybenzoic Acid to experiment with herbicide or plant growth regulator synthesis. The molecule sometimes finds a place in small-scale pilot projects where new analogs of existing active ingredients get evaluated for crop efficacy and environmental footprint.

    Real Differences from Other Isomers and Benzoic Acids

    On paper, the difference between 3,4-Dimethoxybenzoic Acid and something like 2,4-Dimethoxybenzoic Acid seems subtle, but experience shows otherwise. The way methoxy groups line up on the aromatic ring in the 3,4- positions gives distinct electronic effects. These differences shift reactivity in Friedel-Crafts alkylation, impacting yield and selectivity. In practice, process chemists notice fewer side-products and smoother purifications with the 3,4- isomer, especially in esterification and amidation reactions.

    Cost and ease of access matter on the floor. Some resins or fine chemicals can't tolerate contamination with other isomers. Customers report that even minor impurities from mislabeled isomers or poorly controlled reactions can drop product yields by several percentage points. We minimize risk by running final LC/MS checks—not just for nominal purity, but for pinpoint isomer profile—because small differences carry big economic outcomes.

    Compared with plain benzoic acid or monomethoxy derivatives like p-Anisic acid, 3,4-Dimethoxybenzoic Acid acts as a more specialized platform. Its two methoxy groups block certain ring positions, changing solubility profiles in solvents like methanol, ethanol, and acetone. This helps in selective reactions where reactivity or isolation steps matter, reducing the chance of off-target products or unreacted starting material. Time in the plant teaches us which solvent mixes and temperatures pull the best separation between product and residual starting material.

    Operator Experiences: What Matters During Scale-Up

    Day-to-day, our technicians see firsthand why attention to batch size and reaction conditions changes the outcome. During pilot batches, temperature spikes led to colored byproducts that climb purification costs. Scaling above 200 kg calls for careful agitation and heat transfer checks. We noticed that fine control over addition rates for reagents—especially methylating agents and oxidizers—keeps reaction times reasonable while cutting impurity levels. After several learning cycles, we’ve set up control loops that feedback into real-time adjustments, not just end-point checks.

    Every reaction draws on years of cumulative notes: solvent volumes logged per lot, agitation speeds mapped against crystal habits, and drying schedules optimized for different ambient humidity shifts. During rainy season, we found it necessary to extend vacuum drying since the atmospheric moisture changed baseline product hydration. The QC team keeps close watch on Karl Fischer titration data to ensure every shipment matches customer drying requirements.

    Sometimes a formula tweak for one customer mandates process changes for others. It’s not uncommon to rerun a portion of finished product through a second crystallization to deliver lower sodium ion content. Direct dialogue with users shapes in-plant protocols—much more than any standard operating procedure ever could. These feedback loops cut waste and deliver product people can actually use straight from the drum.

    Key Issues: Purity, Consistency, and Downstream Impact

    Nearly every issue in downstream use—be it synthesis blockage or formulation fallout—ties back to product consistency. Micro-level variations in purity, particle size, or residual solvent content often lead to macro-level problems for the next operator. We've seen a customer’s yield dip by 4% when particle size distribution strayed from the mean by just twenty microns. That may not sound like much unless you’re the one watching raw material bills rise.

    We’ve run small-scale tests for regular clients where we purposely shift drying endpoints or filter porosities, tracking how those modulate solubility rates and reaction kinetics. For most end-users, keeping 3,4-Dimethoxybenzoic Acid within spec on every shipment saves more than it costs in process headaches. That’s why investment in analytical method development—GC, HPLC, and particle sizing—anchors our operation. The payoff comes when the client’s own analytical team confirms results, saving endless back-and-forth.

    Supporting Sustainability Goals

    Manufacturing today means more than making high purity chemical. Every drum must meet rising sustainability standards, too. We recycle most of our process solvents, driven not just by regulation but by long-term cost savings. The plant switched to a closed-loop nitrogen system two years ago, after realizing how much inert gas was venting per cycle. This one shift dropped raw material expense while lowering environmental impact at the same time.

    The team keeps a close eye on changing legislation affecting specialty chemicals. Several countries push for the reduction of hazardous byproducts—especially nitrosamines and polyaromatic impurities. By keeping in-house analytics updated and training staff on early detection, we can deliver cleaner products that raise fewer red flags under scrutiny. This approach reflects long-term thinking—helping customers defend their supply chains against shifting compliance goalposts.

    A recent push in the EU for green chemistry means frequent requests for solvent replacement or waste minimization plans. The process development group works continuously on new crystallization and purification recovery routes. A couple of pilot runs last year replaced a halogenated extraction solvent with greener alternatives. It took several iterations, but eventually we cut halogen waste by over 40%. These changes didn’t just help meet client audit requirements—they kept the line running even as supplier lists shifted in response to new legislation.

    Solutions for End-User Challenges

    For customers struggling with batch-to-batch fluctuations, we encourage joint analysis—sharing our in-process control data so root causes can be pinpointed early. Our experience suggests that working supplier-to-customer as one team cuts troubleshooting time by half. In cases where minor impurity challenges persist, we offer to tweak drying, filtering, or milling to match intended process schemes. This flexibility means our partners spend less time requalifying material and more time running production.

    On scale-up projects, new users often underestimate how reaction temperature profiles or solvent selection swing the course of downstream steps. We've hosted multiple on-site visits for R&D chemists to watch pilot-scale runs, giving them insight into thermal characteristics and mixing efficiency. These real-world meetings have solved more process problems than any paper protocol.

    Technical support doesn’t stop with the final shipment. Whenever new analysis methods come online, we alert existing clients and offer to rerun critical tests on their next order. Collaboration around method harmonization secures reliable product performance in demanding pharmaceutical and fine chemical uses. Our team stands ready to update protocol sheets and supply batch-specific data packs—not on demand, but as a built-in service.

    Comparing 3,4-Dimethoxybenzoic Acid to Similar Chemicals: Recent Trends

    Some purchasing teams ask why they can't substitute with cheaper isomers or single-methoxy analogs. From a production standpoint, cost savings on purchase vanish when process optimization, yield, and labor are considered. For instance, in dye stuff applications, shifting to a monomethoxy acid led to slower coupling rates and unwanted tints, prompting a switch back to the 3,4- variant. Process diary notes show distinct reaction pathways depending on substitution, which can't be corrected by post-purification.

    In pharmaceutical synthesis, regulatory filings follow molecule structure to the letter. Trying to swap in even a slightly different isomer without exhaustive revalidation leads to project delays and out-of-spec batches. On our side, we’ve seen requests for modified processes to deliver tighter isomeric purities for APIs destined for Europe or North America, reflecting higher scrutiny from regulators and drug sponsors. Investment in final-product testing pays off for clients seeking streamlined compliance paperwork.

    Troubleshooting and Continuous Improvement

    Any complex synthesis experiences hiccups. On one run, our team caught a rise in ash content traced to a change in washing water source. The solution came not from upstream theory, but from deep familiarity with the installation layout and a manager who remembered a similar problem five years prior. Small things—tank cleaning schedules, valve swapouts, HVAC upgrades during pollen season—add up to bigger product consistency. Our regular cross-checks send people from one unit to another, breaking down silos between engineers and operators.

    Over the past year, we increased investment in analytical modernization. Bringing in new HPLC columns extended detection to low-level byproducts while reducing run times. This allowed us to respond quickly to customer concerns over trace impurity profiles in supplied acid. The same mindset applies to continuous operator training and setting up suggestions from the production floor. At our monthly meetings, some process tweaks suggested by operators get adopted plant-wide, after a short validation run. This adaptability roots our capability in direct feedback, not just remote R&D.

    Shaping the Future of 3,4-Dimethoxybenzoic Acid Manufacturing

    Looking forward, demand trends indicate growth in precision chemical needs—tighter impurity tolerances for pharma, tailored particle sizes for advanced materials, and fully traceable supply chains. For 3,4-Dimethoxybenzoic Acid, our plant keeps investment focused on these vectors: process automation, batch traceability, and mobile QA tools. We see our partners shifting toward direct integration of supplier data with their digital quality systems. To support this, we are digitizing more process records and exploring blockchain for traceability.

    The backbone of progress lies in people: seasoned operators, dedicated QA teams, and chemists willing to share best practices across industries. Manufacturers who invest in skills and information flow, not just hardware, hold a competitive edge. We stick close to users through regular site visits, data sharing, and technical workshops—because every chemical tells a story from molecule to market, shaped by thousands of small decisions from suppliers and users alike.

    3,4-Dimethoxybenzoic Acid remains more than a catalog item—it's a material built on experience, attention, and the daily rigors of production. By listening to end-users and adapting on the fly, we create not just a chemical, but a reliable base for progress across pharmaceuticals, dye chemistry, and specialty manufacturing, rooted in reality, not just formulas.