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2-Amino-3,4,5-Trimethoxybenzoic Acid

    • Product Name 2-Amino-3,4,5-Trimethoxybenzoic Acid
    • Alias ATBA
    • Einecs 242-877-9
    • 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
    VTB
    Specifications

    HS Code

    762309

    Productname 2-Amino-3,4,5-Trimethoxybenzoic Acid
    Casnumber 2140-73-8
    Molecularformula C10H13NO5
    Molecularweight 227.21 g/mol
    Appearance White to off-white solid
    Meltingpoint 172-176 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storagetemperature 2-8 °C
    Smiles COC1=CC(=C(C(=C1OC)N)C(=O)O)OC
    Inchikey WKHORBLQHOEFKI-UHFFFAOYSA-N
    Synonyms 2-Amino gallic acid trimethyl ether

    As an accredited 2-Amino-3,4,5-Trimethoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 25g amber glass bottle, featuring a white screw cap, hazard labels, and a clear chemical identification label.
    Shipping **Shipping Description for 2-Amino-3,4,5-Trimethoxybenzoic Acid:** This chemical should be shipped in a tightly sealed container, protected from moisture and direct sunlight. Handle with standard chemical precautions. Store and transport at room temperature. Ensure compliance with local, national, and international regulations for chemical transport. Not classified as hazardous for shipping under most regulations.
    Storage Store 2-Amino-3,4,5-trimethoxybenzoic acid in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Ensure storage is secure and labeled, and follow all relevant safety protocols for handling organic chemicals. Use appropriate personal protective equipment during handling.
    Application of 2-Amino-3,4,5-Trimethoxybenzoic Acid

    Applications of 2-Amino-3,4,5-Trimethoxybenzoic Acid in Industrial Manufacturing

    2-Amino-3,4,5-Trimethoxybenzoic Acid supports advanced synthesis processes in multiple industrial sectors. As a direct manufacturer, we supply this raw material for critical steps in speciality chemicals, active pharmaceutical ingredient (API) production, agrochemical intermediates, fine organic synthesis, and performance dye precursor manufacturing.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers use 2-Amino-3,4,5-Trimethoxybenzoic Acid as a key intermediate in the synthesis of several advanced active ingredients, including anti-inflammatory and cardiovascular drug molecules. The compound reacts during specific amidation, coupling, and protection-deprotection sequences. Strict impurity controls and GMP documentation remain mandatory from material intake through API isolation. Production validation often involves continuous verification of purity, heavy metal content, and residual solvents, ensuring suitability for human therapeutics.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredients
    • EU GMP (Part II) requirements
    • USP/NF monograph referencing for input quality
    • EDQM certification paths when used for European market APIs

    Typical usage ratio

    • 10–35% of step-wise batch reactant mass, adjusted by reaction pathway and target API molecule size
    • Variations depend on stoichiometry and impurity profile management during coupling reactions

    Downstream process integration

    • Introduced post-initial aromatic nitration for protected amine coupling
    • Filters through intermediate purification, then proceeds through subsequent hydrolysis or reductive steps
    • QC checkpoints after each phase; batch release contingent on analytical data

    Final product types

    • Anti-inflammatory active pharmaceutical ingredients (e.g., trimethoxybenzoic acid derivatives)
    • Antihypertensive drugs using trimethoxybenzoic acid scaffolds
    • Chemical intermediates for further API modification
    • Precursor compounds for targeted pharmaceutical research

    2. Agrochemical Intermediate Production

    Agrochemical plants use this raw material to produce selective herbicide and plant growth regulator intermediates. The trimethoxybenzoic nucleus facilitates construction of active moieties that influence plant metabolism and resilience. It enters downstream nitration or chlorination steps, leading to more complex crop protection actives. Compliance relies on consistent traceability of raw materials for environmental and occupational safety audits.

    Industry compliance standards

    • FAO/WHO specifications for pesticide ingredient quality
    • ISO 9001:2015 for production management
    • REACH registration for European Union chemical compliance
    • China National Standards (GB/T) for safe agrochemical handling

    Typical usage ratio

    • 15–25% of total reactant input in intermediate formation, customized per formulation
    • Ratio further optimized based on yield of target herbicide precursor

    Downstream process integration

    • Loaded into initial esterification reactors for benzoic acid derivative formation
    • Flows into selective halogenation channels before coupling with aliphatic amines
    • Buffer and pH adjustments performed in situ to control unwanted byproduct formation

    Final product types

    • Selective herbicide intermediates
    • Plant growth regulator building blocks
    • Key raw materials for fungicidal active compounds
    • Precursors for advanced crop protection R&D programs

    3. Organic Dyes and Pigment Precursors

    Dye and pigment manufacturers employ 2-Amino-3,4,5-Trimethoxybenzoic Acid for specialty chromophores used in textile and high-performance colorant applications. Its electron-donating methoxy groups stabilize dye intermediates and intensify color output. The material feeds into diazotization and coupling stages to produce high-purity, heat-stable pigments, with strict monitoring for color consistency and impurity levels in downstream dispersions.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (applicable for textile end use)
    • ISO 1833/ISO 105 for dye extractables
    • Global Organic Textile Standard (GOTS) where applicable
    • REACH Annex XVII as to hazardous aromatic precursors

    Typical usage ratio

    • 5–18% of precursor input molar amount in high-value specialty dye synthesis
    • Proportion tailored per target chromophore framework

    Downstream process integration

    • Feeds into the initial aromatic amination processes
    • Subjected to controlled diazotization, followed by coupling with aromatic or heterocyclic partners
    • Purification through crystallization and solvent extraction stages

    Final product types

    • High-temperature-resistant textile dyes
    • Pigment intermediates for plastics and coatings
    • Specialty colorants for printing inks
    • Building blocks for advanced functional pigments

    4. Fine Chemicals and High Value Specialty Synthesis

    The fine chemicals sector utilizes 2-Amino-3,4,5-Trimethoxybenzoic Acid in the production of advanced specialty intermediates required for fragrance, photo-initiator, and advanced material R&D. Its structure enables selectivity in heterocyclic formation and acts as a template during stepwise syntheses for high-value applications. Process engineers optimize input ratios based on reactivity and the desired physical properties of the downstream target, managing solvent, temperature, and pressure tightly for quality consistency.

    Industry compliance standards

    • ISO 9001:2015 for quality assurance of specialty chemical processing
    • Responsible Care® management system for environmental and safety protocols
    • Specific NDA/CSA requirements by leading multinationals
    • Internal specification sheets validated by major OEM customers

    Typical usage ratio

    • 7–20% of the total reactant system depending on transformation route and end-use specification
    • Exact dosing tuned for purity and target molecular architecture

    Downstream process integration

    • Introduced at the aromatic ring construction or ring-substitution step
    • Participates in condensation reactions or specific cyclization paths
    • Final purification often includes column or preparative HPLC

    Final product types

    • Heterocyclic building blocks for custom synthesis contracts
    • Fragrance intermediates with methoxy-aromatic character
    • UV curing resins or photo-initiators for coatings
    • Specialty monomers for polymer R&D
    Free Quote

    Competitive 2-Amino-3,4,5-Trimethoxybenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    2-Amino-3,4,5-Trimethoxybenzoic Acid: Reliability and Progress in Chemical Manufacturing

    Understanding the Product from a Manufacturer’s Perspective

    Over the past decade, our team has witnessed a steady climb in the demand for high-purity 2-Amino-3,4,5-trimethoxybenzoic acid. This compound, recognized by its CAS number 88967-39-1, features a structural backbone that chemists value for synthetic routes, particularly in pharmaceutical research and advanced chemical intermediates. Producing this material in-house, we have paid close attention to every process—from raw input selection to purification methods—using our direct experience to continuously improve reproducibility and minimize impurities.

    The product offers a distinctive profile: a fine, crystalline powder, typically white or slightly off-white, with an assay reaching or exceeding 99% by HPLC. Throughout our production runs, we keep moisture content below 0.5%, since traces of water can hinder subsequent reactions and affect product shelf life. Our team also reviews the melting range, usually falling between 154°C and 157°C. By monitoring this parameter for each lot, we assure consistent physical properties batch after batch.

    Why Purity and Traceability Matter in Synthetic Chemistry

    Chemists counting on 2-Amino-3,4,5-trimethoxybenzoic acid for downstream reactions know that trace-level impurities throw off results. Even changes at the parts-per-thousand scale can catalyze unwanted side products or complicate crystallization behaviors. Cross-contamination is an ever-present risk, so we maintain strict cleaning protocols and integrate real-time analytical verification to catch deviations early. Our raw material sourcing policy limits supplier variability—if a starting material shifts purity or grade from one batch to the next, we trace and flag it. This vigilance has shielded users from the kinds of batch-to-batch unpredictability that can ruin months of laboratory or pilot-scale work.

    Navigating supply chain fluctuations adds another challenge. Delivering product on time, with exacting documentation and analyses, always requires flexibility. Over the years, we’ve built in redundant quality checks, and our manufacturing site implements rigorous change control. This gives researchers complete confidence that their experimental data won’t be compromised by an off-specification lot or a mislabeled drum.

    Applications Guided by Utility and Direct Experience

    Most of our customers rely on 2-Amino-3,4,5-trimethoxybenzoic acid as a building block for pharmaceutical candidate molecules, especially where aromatic substitution patterns influence downstream biological activity. The trimethoxy substitution imparts both steric and electronic effects that chemists exploit for selectivity. In our conversations with R&D labs, it’s clear that even slight shifts in isomer distribution or unreacted starting materials create downstream purification bottlenecks—reducing overall synthesis yields and adding costs.

    We have seen its value proven in the construction of advanced heterocyclic scaffolds. In particular, this acid’s electron-rich aromatic ring offers opportunities for targeted amide coupling or as a substrate for diazotization reactions. Because of our control over the process, we regularly support contract and custom synthesis requests that demand modified salt forms or adjusted particle sizes for particular reactors or flow chemistry setups. Whether customers are conducting early-stage medicinal research, pursuing agrochemical innovation, or developing specialty dyes, this molecule presents considerable versatility.

    Clear Differences from Other Benzoic Acid Derivatives

    Not all benzoic acid derivatives behave the same, either synthetically or physically. The triple methoxy substitution pattern in 2-Amino-3,4,5-trimethoxybenzoic acid sets it apart from its mono or dimethoxy analogs. Traditional 4-amino-3-methoxybenzoic acid lacks both the electron-donating strength and the solubility profile required by many modern applications. Under standard reaction conditions, our product demonstrates improved solubility in polar aprotic solvents like DMF and DMSO, which reduces processing times for scale-up operations.

    Through side-by-side pilot batches, we watched as alternative compounds with fewer methoxy groups or different amino placements failed to perform. These analogs tended to produce more side reactions or required repeated recrystallization to reach the same purity benchmarks. As the manufacturer, we saw the direct labor and material savings realized by switching to the trimethoxy compound—fewer purification passes, shorter drying times, and reduced solvent usage.

    Safety, Handling, and Process Control: A Manufacturer’s View

    Sustained experience working with aromatic amino acids has underscored the value of internal process control and robust employee training. Dusting risks and sensitization hazards are persistent concerns—our teams use local exhaust, sealed transfer lines, and personal protective equipment designed for fine organic powders. We track exposure trends, review accident reports, and adjust shop-floor practices faster than third-party handlers typically respond. Our continuous improvement cycles draw directly from operator feedback, translating to safer, steadier operations.

    Process engineers point out that thermal stability, reactivity with common chlorinating agents, and compatibility with known protecting groups allow for tighter control in complex syntheses. On our floor, we calibrate inbound quality using FTIR and NMR fingerprinting, and some analytical staff run triplicate HPLC and GCMS assays for critical lots. The depth and transparency of these quality systems ensure that each shipment reflects stated purity, and we share this data with technical partners upon request. Both in regulatory filings and for end users in high-spec R&D, this degree of traceability has strong practical advantages.

    Supporting Sustainability and Responsible Manufacturing

    Our production methodologies have evolved based on real-world learning. A large part of that involves resource use. Early batches included higher solvent volumes and longer filtration times. Continuous tuning of crystallization protocols and solvent recovery has cut waste considerably. Direct solvent recycling, closed-vessel reactors, and in-line solid handling mean the volume of waste organics and wash water is far below local regulatory limits. Third-party audits confirm these reductions—validating our internal records and contributing data used by major buyers for life-cycle assessments.

    A broad shift in the chemical industry now places added emphasis on traceability and environmental responsibility. We share details on raw input sourcing, waste recycling, and process water volumes with stakeholders willing to engage. These conversations push us toward safer alternatives for commonly used reagents and solvents. Our investment in process intensification, including continuous flow chemistry, improves not only efficiency but also reduces the risk of batch contamination and spill events. Front-line operators play a key role, calling out improvement points, which then get scaled up plant-wide.

    Customer Collaboration Fuels Product Advancement

    Direct communication between our technical staff and the end-user chemistry teams often reveals the next round of production improvements. Researchers might request tailored screen analyses, or recommend different packaging formats for high-sensitivity environments. Our team adapts, running test batches or bespoke purifications to troubleshoot real challenges. In one example, we implemented a new particle sizing protocol that cut losses during bulk transfer at a pharmaceutical plant, reducing both handling time and material loss.

    This ongoing dialogue helped us identify the need for more robust, puncture-proof containers for shipping sensitive fine powders. What started as a series of samples ended as redesigned packaging lines and a drop in customer complaints. This feedback loop has made the product more user-friendly and reliable across varied applications, from lab-scale synthesis to multi-ton industrial projects.

    Challenges and Future Directions in Manufacturing

    Much of manufacturing focuses on consistency, but the path to reliable 2-Amino-3,4,5-trimethoxybenzoic acid at industrial scale has required tenacity and technical curiosity. Some challenges persist, such as variation in raw supply quality and occasional regulatory changes affecting import and export documentation. Our response centers on flexibility—rapid testing of new feedstocks, or rewriting documentation practices as requirements evolve. Technology upgrades, such as batch record digitization, have streamlined traceability. These investments insure continuity, especially for users in highly regulated fields.

    In research-driven supply chains, speed sometimes pushes against thorough documentation and quality oversight. We prioritize clear communication back to customers whenever a variable might impact delivery or analytical expectations. Investing in up-to-date testing instrumentation yields a detailed profile for each lot—helping chemists spot deviations long before their synthetic sequences reach the troubleshooting stage. By remaining nimble, our manufacturing site adapts when new risks emerge, such as stricter transportation controls on aromatic amines.

    The Real Value Beyond the Bottle

    Across countless kilo-scale batches, our experience manufacturing and supporting 2-Amino-3,4,5-trimethoxybenzoic acid has shaped our understanding of what matters: consistency, open information sharing, and support to advanced users. Reliable building blocks are the foundation for breakthrough research—delays, contaminations, or mislabeling quickly erode trust. Through process control, technical partnerships, and a willingness to innovate, we’ve kept pace with the changing expectations of customers working at the frontiers of chemical and pharmaceutical development.

    Looking forward, our focus remains on maintaining high standards, transparent data, and a practical understanding of how minute quality decisions on the shop floor can ripple up to the most critical moments of R&D. Serving as a direct manufacturer, we pay close attention to each variable—knowing that the pathway for innovation runs straight through the reliability of every building block we ship.