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2,3-Dimethoxybenzamide

    • Product Name 2,3-Dimethoxybenzamide
    • Alias Anthranilamide, 2,3-dimethoxy-
    • Einecs 212-677-4
    • 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

    195358

    Chemical Name 2,3-Dimethoxybenzamide
    Cas Number 6642-31-5
    Molecular Formula C9H11NO3
    Molecular Weight 181.19 g/mol
    Appearance White to off-white solid
    Melting Point 138-142 °C
    Boiling Point Unknown
    Solubility Slightly soluble in water
    Density Unknown
    Smiles COC1=CC=CC(=C1N(C)C=O)OC
    Inchi InChI=1S/C9H11NO3/c1-12-7-4-3-5-8(13-2)9(7)10-6-11/h3-5H,1-2H3,(H,10,11)
    Synonyms Benzamide, 2,3-dimethoxy-
    Pubchem Cid 120570
    Refractive Index Unknown

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with a white screw cap, labeled "2,3-Dimethoxybenzamide," hazard symbols, and safety information.
    Shipping 2,3-Dimethoxybenzamide is typically shipped in sealed, airtight containers to protect it from moisture and contamination. Ensure packaging complies with local and international regulations for handling chemicals. The container should be clearly labeled, and the shipment accompanied by a safety data sheet (SDS) outlining proper handling, storage, and emergency procedures.
    Storage 2,3-Dimethoxybenzamide should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. It should be kept separate from incompatible substances such as strong oxidizing agents. Store at room temperature, avoiding excessive heat and moisture to prevent decomposition or degradation of the chemical.
    Application of 2,3-Dimethoxybenzamide

    Applications of 2,3-Dimethoxybenzamide in Industrial Manufacturing

    As a direct manufacturer specializing in fine chemicals, we supply 2,3-Dimethoxybenzamide to a select range of industries where its chemical structure enables advanced transformations. Below, we outline the verified industrial downstream applications, accompanied by specific regulatory, formulation, process, and finished product information for each scenario.

    1. Pharmaceutical Intermediate for API Synthesis

    Leading pharmaceutical firms utilize 2,3-Dimethoxybenzamide as a key intermediate in the multi-step synthesis of benzamide-based drug molecules. It participates in amide coupling, aromatic substitution, and deprotection reactions required to construct target active pharmaceutical ingredients, including antipsychotics and CNS therapeutic agents. Customers source this material for use in regulated manufacturing plants, where traceability and quality consistency throughout the batch record remain primary concerns.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for Active Pharmaceutical Intermediates
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • EU EudraLex Volume 4 (GMP for medicinal products)
    • Relevant monographs in USP/NF and EP (for downstream APIs)

    Typical usage ratio

    • Varies from 0.15–0.35 molar equivalents relative to the final API target, with adjustment based on reaction efficiency, stage purity, and required isolation yield.

    Downstream process integration

    • Material addition at initial or mid-stage intermediate coupling reactions.
    • Often followed by N-alkylation, selective demethylation, or acylation as per synthetic sequence.
    • Intermediate subjected to in-process testing for identity and purity prior to telescoping or isolation.
    • QC batch sampling performed before transfer to the next GMP critical step.

    Final product types

    • Antipsychotic drug APIs (e.g., benzamide-class CNS agents based on substituted benzamide frameworks)
    • Niche antiemetic pharmaceutical actives
    • Other psychiatric and neurological small molecule APIs produced in regulated facilities

    2. Intermediate for Agricultural Chemical Synthesis

    This raw material serves as an intermediate for the synthesis of certain benzamide-based herbicides and fungicides in the agrochemical sector. Direct manufacturers of crop protection chemicals employ the compound as a coupling reagent to build the aromatic core of selective plant growth regulators and disease control agents. Each batch undergoes in-house screening for residual solvents and trace impurities prior to integration into scalable production.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for agrochemical manufacturing
    • OECD Good Laboratory Practice (GLP) for test submissions
    • CropLife International traceability standards
    • Regional technical requirements for active substance dossiers (e.g., EU Regulation (EC) No 1107/2009 for crop protection products)

    Typical usage ratio

    • Ranges from 10–28% by weight in the coupling reaction, calculated against the target herbicide or fungicide core to ensure selectivity and conversion. Formulators adjust ratio following route optimization, waste minimization, and cost-performance assessment.

    Downstream process integration

    • Charged during the condensation or catalytic aromatic substitution step in the agrochemical actives manufacturing line.
    • Batchwise addition in jacketed reactors equipped for solvent recovery and temperature control.
    • Subsequent process may include further functionalization or granulation depending on the formulation target.
    • Routine in-process control for starting material depletion and byproduct signature.

    Final product types

    • Benzamide-structured herbicidal actives for selective weed control
    • Intermediate base compounds for fungicide actives
    • Non-food crop plant growth regulators based on substituted benzamides

    3. Chemical Building Block for Fine Chemical Synthesis

    In fine chemical manufacturing, our clients employ this product as a versatile building block for custom synthesis of specialized molecules. Applications include preparation of advanced intermediates for dyestuffs, UV absorbers, and specialty aromatic compounds. Its dual methoxy functionalization offers routes for downstream substitution and cyclization, supporting varied molecular frameworks beyond commodity chemicals.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for fine chemical manufacturing
    • REACH (Registration, Evaluation, Authorisation, and Restriction of Chemicals) for European markets
    • Customer-specified impurity and trace element control per project specification sheet
    • Certificate of Analysis (CoA) with defined purity, water content, and melt point testing

    Typical usage ratio

    • From 5–20% molar equivalent in multi-component reactions, dependent on downline transformation demands. Adjusted in accordance with stoichiometry, reaction time, and minimizing waste byproduct.

    Downstream process integration

    • Stage-input in aromatic amide synthesis or nucleophilic substitution protocols.
    • May be introduced via manual batch addition or automated feed systems based on project scale.
    • Integrated with closed-loop QC for intermediate assay and profile confirmation.
    • Possible recapture of byproduct streams for waste minimization and sustainability targets.

    Final product types

    • Custom dyestuff intermediates for pigment formulation
    • Precursors for UV absorber molecules in plastics or coatings
    • Substituted benzamide derivatives for specialty chemical applications

    4. Research and Development Intermediate for Novel Molecule Discovery

    Research organizations, discovery labs, and pilot-scale chemical producers select this compound as an enabling intermediate for molecular innovation. Its structural features allow late-stage diversification during lead optimization in both pharmaceutical and specialty material research. We supply research-grade material with full characterization for those contexts where experimental flexibility and high analytical transparency are required.

    Industry compliance standards

    • ISO 17025:2017 for calibration and testing laboratories
    • GLP (Good Laboratory Practice) for research reporting
    • Custom customer directives for critical raw materials (including full traceability and impurity profile disclosure)
    • Standard research material register (RM) documentation for cross-laboratory reference

    Typical usage ratio

    • No standard industrial ratio—experimental chemists adjust equivalence from 0.1 to 1.2 equivalents as dictated by target molecule structure, route optimization, and desired sidechain diversity.

    Downstream process integration

    • Material weighed and charged into test or pilot batch reactors.
    • Parallel reaction screening to compare new processing routes.
    • Close analyst review following reaction monitoring by HPLC, NMR, or LC-MS.
    • Samples archived with full audit trail for later route scale-up studies.

    Final product types

    • Novel benzamide scaffolds for preclinical drug or agrochemical exploration
    • Candidate intermediates for specialty polymer research
    • Functionalized model compounds for structure-activity and property-activity relationship studies
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    Certification & Compliance
    More Introduction

    2,3-Dimethoxybenzamide: Practical Insights from a Chemical Manufacturer

    Introduction to 2,3-Dimethoxybenzamide

    Our facility has spent years refining the production process of 2,3-Dimethoxybenzamide, known in laboratories for its role as a trusted intermediate. Its chemical structure offers functional groups favored in a range of syntheses, especially within pharmaceutical development and advanced material applications. Producing this molecule takes more than textbook chemistry. It calls for reliable technique, painstaking quality control, and a deep understanding of customer expectations. We stand behind its purity and consistency not only because certificates demand it, but because repeated requests for this compound follow evidence of proven results in the field.

    Understanding Its Place Among Benzamide Derivatives

    Direct experience shows that not all benzamide derivatives respond the same way in synthesis. Tweaking a molecule as modest as benzamide by shifting a methoxy group or adjusting the rings’ substitution pattern can shift reactivity, solubility, and downstream processing. 2,3-Dimethoxybenzamide, with its methoxy groups at the ortho and meta positions, differs noticeably from the more common 3,4- or 2,4-dimethoxy variants. This specific pattern brings out selectivity prized in targeted synthesis—something that blanket chemistry fails to achieve.

    Having run comparative batches using both 2,3- and 3,4-dimethoxy versions, we have observed changes in both physical and chemical behavior. The 2,3-derivative often demonstrates better solubility in select solvents, particularly in polar organic systems. That influences how clients choose reagents for coupling or acylation reactions, impacting overall yield and purification steps.

    Purity and Consistency: What It Means for Downstream Applications

    Supplying 2,3-Dimethoxybenzamide isn’t just about hitting a purity number on a certificate. Our chemists routinely review trace impurity profiles, as subtle differences in byproduct content can impact further functionalization or catalytic steps. In the past, even trace amounts of starting materials like 2,3-dimethoxyaniline or reaction-side esters have caused headaches during scale-up. Frequent troubleshooting with clients has shown that over-relying on basic melting point or thin-layer chromatography isn’t enough for routine quality assurance. Instead, our laboratory runs NMR and HPLC analysis for every batch, making sure no unseen contaminants skew catalytic steps or sulfonation yields.

    Common Specifications and Batch Control

    Factory output rarely meets rigid targets on its own. For our 2,3-Dimethoxybenzamide, production lines run with target purity no less than 99%, measured by HPLC. Each batch passes checks for drying loss and residual solvent—moisture and residual DMF, for example, each show up in downstream steps if not vigilantly removed. Grain size distribution also gets monitored, as caking during storage makes re-dispersion difficult when handling large orders. Our operators keep careful logs and blend samples to minimize lot-to-lot variation, giving project leaders peace of mind on tight syntheses.

    Batch to batch, we deal with the same core impurities: unreacted aniline precursors, methylated byproducts, or minor aldehyde residues from raw material streams. By tailoring reaction parameters—stirring rates, addition speeds, temperature steps—we’ve learned to push selectivity upward, avoiding tail ends that complicate post-purification. Years ago, this level of attention was uncommon in the specialty chemical trade, but rising clinical and industrial expectations have made this standard operating practice.

    Production Realities vs Laboratory Scale

    Bench reactions tell only a part of the story. Scaling 2,3-Dimethoxybenzamide from hundred-gram lots to hundred-kilo drums sets a new set of demands. At scale, choices matter: solvent load, order of addition, and especially temperature control, since side reactions trend differently in bigger vessels. Early on, scale-up revealed points where product crystallization behaves unexpectedly, or where dissolution efficiency drops as concentration increases.

    Through continuous improvement cycles and by staying close to those who actually run the reactors, we’ve learned which variables matter for process stability. One example—by tweaking the duration of methylation or using a stabilized acid catalyst, we gained nearly five points in assay purity over our earlier protocol. These aren’t tweaks pulled from a manual; they’re born from repeated cycles of feedback and hands-on adjustment.

    Practical Applications and Industrial Demand

    We know 2,3-Dimethoxybenzamide does not command the broad volumes of base chemicals, but its usage is strategic. The molecule finds itself vital as a building block in pharmaceutical manufacturing, especially for research organizations pushing into novel heterocyclic scaffolds or looking to mask key amide positions in drug candidates. Because both methoxy groups alter electron density and reactivity, synthetic chemists reach for this compound to direct forthcoming reactions—often aiming at targeted kinase inhibitors or other therapeutic leads.

    Outside pharma, advanced material researchers come calling. Organic electronics and specialty polymer groups value benzamides as functional additives or intermediates. More recently, demand for purity and traceability rose as electronics companies scrutinized every contaminant that might impact device performance. To answer this, we have opened our doors to audits and shared analytical data, helping customers justify their supply chain claims.

    Technical Handling: Hands-On Reflections

    During processing and packaging, physical properties become as crucial as chemical traits. 2,3-Dimethoxybenzamide can clump under fluctuating humidity. Our plant faced this firsthand years back, when an unfiltered air vent in one section let microdroplets creep into sealed drums, turning an evening’s output into sticky aggregates by morning. We overhauled our storage ventilation and switched to nitrogen purging for certain runs. Since then, complaints over lumping dwindled, and fewer clients spend time scraping product from the sides of drums.

    Our packing methods—from double-bagged liners to tamper-evident seals—grew out of customer feedback, not regulation. For some buyers handling fine reagents in cleanrooms, even micro-contamination from packaging glue could spoil an experiment. Through iterative design and robust packaging controls, we’ve reduced such risks and made these details standard practice.

    Distinctiveness from Other Dimethoxybenzamides

    Comparison with other dimethoxybenzamides is more than academic. While several positional isomers line the lab shelves, the reactivity profile of the 2,3 variant distinguishes it. In trials with 2,4- or 3,4-dimethoxybenzamide, performance often stumbles where directed hydrogenation or selective halogenation steps call for precise electron distribution. Our own staff experimented with both isomers in amidation and coupling reactions. Results repeatedly showed that the ortho/meta placement of the methoxy groups confers a reactivity edge for certain substitution patterns, including optimized yields in Suzuki and Buchwald-Hartwig couplings.

    Clients also talk about crystal habit—the ease with which they handle, weigh, dissolve, and recrystallize. The subtle differences influence not only chemical results but productivity on the plant floor. Lab-scale solubility comparisons in various alcohols, esters, and polar aprotic solvents have consistently placed 2,3-Dimethoxybenzamide as a preferred choice for those requiring reliable dissolution.

    Addressing Production Challenges and Solutions

    Manufacturing experience teaches patience and adaptability. We’ve watched suppliers of starting materials falter, leading to disruptions and urgent fixes. To cushion against these bumps, we strengthened relationships with reliable, audited suppliers, often sourcing from multiple regions and conducting incoming inspections that go beyond industry average. Keeping a lean but flexible stock of critical raw materials helps us weather rough patches and keeps promises to customers.

    From time to time, an unexpected impurity spikes. Our analytical group runs cause-and-effect checks: Did a raw material change? Did a subtle shift in reaction temperature allow a side product to creep in? We cross-train production chemists and lab analysts to spot patterns early, using their ground-level knowledge to identify and correct issues before they escalate.

    Years of feedback loops shape the continuous improvement process. Newer tools—real-time process analytics, modular production lines, better training—now drive yields up, costs down, and reduce the guesswork of older production cycles. Our team invests time in root-cause investigations so we don’t repeat mistakes. That builds long-term trust.

    Supporting the Next Generation of Research

    The team inside our lab often fields calls from graduate students and process engineers alike, all probing the quirks and subtleties of 2,3-Dimethoxybenzamide. We share what we know: optimal solvent choices, recrystallization tricks, tips for dissolving stubborn aggregates, cautions on shelf-life under moist conditions. Collaborative problem solving with research teams closes the loop between industrial practice and academic curiosity.

    We’ve seen more projects seek greener chemistry, driving interest in solvent recovery, waste minimization, and energy-efficient protocols. 2,3-Dimethoxybenzamide’s relative stability and moderate reactivity help project teams plan multi-step syntheses without excessive loss or dangerous off-target reactions. Through sharing technical bulletins, and in some cases, tailoring properties upon request, we aim to push collective progress forward.

    Market Developments and Regulatory Environment

    Global supply chains have become more complex. Regulatory shifts increase demand for traceability, safety, and transparent sourcing. Some countries require declaration of specific intermediates; others flag benzamide derivatives for acute toxicity or environmental persistence. Within our plant, we address this through documentation, robust analytical records, and regular compliance audits.

    We play an active role in discussions shaping handling protocols and safe-use standards. Open lines of communication with both upstream and downstream partners help anticipate changes and share best practices. It’s not only about ticking boxes; it’s about real responsibility to workers, customers, and communities affected by our products.

    Serving a Diverse Clientele

    Over years of supplying 2,3-Dimethoxybenzamide, we’ve supported both established multinationals and resourceful startups. Each brings its own set of technical hurdles. Early-stage companies sometimes need tailored lots or just-in-time shipments because storage space is tight or projects pivot overnight. For them, flexibility and shared technical dialogue prove as important as price.

    Seasoned buyers, such as pharmaceutical majors and specialty chemicals manufacturers, tend to expect the unspoken: precision in quality, absolute consistency in every drum, and instant support if something goes awry. To meet those expectations, our teams coordinate forecasting, reserve safety stock, and scramble technical staff to the phone at odd hours. These close partnerships demystify the supply chain, which often drags on too long when decision makers sit too far from the process floor.

    Ongoing Innovation and Forward Thinking

    Our R&D group never stands still. Researchers press forward, exploiting 2,3-Dimethoxybenzamide’s potential as a core for next-generation ligands or as a masked intermediate in solid-phase synthesis. We allocate a portion of our annual budget for experimental pilot runs, guided by new project leads and trial feedback. Sometimes innovation surfaces from failed experiments—a run that produced an offbeat crystalline impurity led us to identify a new approach for forming custom derivatives now used in research protocols.

    Close engagement with end users propels us beyond transactional supply. Every suggestion—whether it’s for a smaller particle size, less dust in packaging, or a hint on a chromatographic quirk—feeds back into process optimization. Such ongoing collaboration keeps us competitive and relevant against a background of shifting market demands.

    Conclusion: Commitment to Quality and Practical Impact

    Our ongoing work with 2,3-Dimethoxybenzamide stands as a product of deliberate refinement, informed by hands-on chemical processing and practical problem-solving. While the molecule itself draws attention for its reactivity and versatility in building complex structures, it’s our investment in consistency, traceability, and technical support that truly makes a difference for users.

    Each batch leaving our facility embodies lessons learned from years of troubleshooting, process adjustments, and customer feedback. This approach yields reliability, helps clients avoid unnecessary process delays, and supports both predictable outcomes in research and robust scale-up in industry.

    Satisfying the real needs of users—across pharmaceutical, specialty chemical, and research domains—demands more than just supplying a chemical. It takes ongoing dialogue, sustained attention to detail, and continuous reinvestment in both people and infrastructure. With these principles guiding our work with 2,3-Dimethoxybenzamide, we intend to remain a trusted partner in practical chemistry for years to come.