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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 | 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. |
Applications of 2-Amino-3,4,5-Trimethoxybenzoic Acid in Industrial Manufacturing2-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 SynthesisPharmaceutical 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
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2. Agrochemical Intermediate ProductionAgrochemical 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
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3. Organic Dyes and Pigment PrecursorsDye 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
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4. Fine Chemicals and High Value Specialty SynthesisThe 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.