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HS Code |
538076 |
| Product Name | 2-Amino-3,4-Dimethylbenzoic Acid |
| Cas Number | 22854-43-7 |
| Molecular Formula | C9H11NO2 |
| Molecular Weight | 165.19 g/mol |
| Appearance | Off-white to light yellow solid |
| Melting Point | 134-138 °C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥ 98% |
| Synonyms | 2-Amino-3,4-xylobenzoic acid |
| Chemical Structure | Benzene ring with amino group at position 2, methyl groups at positions 3 and 4, and carboxylic acid group at position 1 |
| Smiles | Cc1cc(C)c(C(=O)O)c(N)c1 |
| Inchi | InChI=1S/C9H11NO2/c1-5-3-6(2)9(10)7(4-5)8(11)12/h3-4H,10H2,1-2H3,(H,11,12) |
| Storage Conditions | Store at room temperature, in a dry and ventilated place |
As an accredited 2-Amino-3,4-Dimethylbenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a secure screw cap, labeled "2-Amino-3,4-Dimethylbenzoic Acid," safety information included. |
| Shipping | 2-Amino-3,4-Dimethylbenzoic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is handled as a non-hazardous, solid organic compound, with labeling compliant with local regulations. During transit, containers are protected from extreme temperatures, direct sunlight, and physical damage to maintain product integrity. |
| Storage | 2-Amino-3,4-dimethylbenzoic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture, direct sunlight, and sources of ignition. Clearly label the container, avoid prolonged exposure to air, and store at room temperature unless otherwise specified by the manufacturer or safety data sheet. |
Applications of 2-Amino-3,4-Dimethylbenzoic Acid in Industrial ManufacturingAs a core chemical building block, 2-Amino-3,4-Dimethylbenzoic Acid finds established industrial applications in specialized synthesis processes where its specific aromatic amine and carboxyl functionalities enable precision downstream modifications. Below, we detail key manufacturing scenarios with direct end-use integration based on market demand and industry formulations. 1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug (NSAID) SynthesisWithin the active pharmaceutical ingredient sector, this molecule serves as a critical intermediate for the multi-step synthesis of select NSAIDs, notably in the preparation of substituted anthranilic acid derivatives. Manufacturers incorporate it at an early condensation stage, harnessing the positional isomerism for subsequent functionalization while meeting strict trace impurity controls. Industry compliance standards
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2. Key Component in Specialty Dye and Pigment SynthesisThe molecule’s amino and methyl groups offer reactivity for azo coupling and acylation reactions, supporting dyestuff manufacturers producing high-purity specialty azo dyes for applications requiring strong light and heat stability, including industrial coatings and technical textiles. Industry compliance standards
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3. Intermediate for Agrochemical Synthesis (Herbicide Production)As a precursor in the synthesis of certain selective herbicides, the compound’s substitution pattern supports the production of benzoic acid derivatives with target phytotoxicity profiles, particularly those requiring controlled environmental persistence. Agrochemical manufacturers integrate it for downstream transformation into active crop protection agents. Industry compliance standards
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4. Precursor for High-Purity Organic Electronic MaterialsIn the advanced materials sector, this aromatic acid forms part of the upstream supply chain for specialty monomers used in organic semiconductors, where exact substitution impacts charge mobility and deposition behavior on thin film substrates. The electronics industry applies it for custom functionalization in molecular design of organic field-effect transistors (OFETs) and related components. Industry compliance standards
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From the perspective of those who spend their days in a manufacturing facility, 2-Amino-3,4-Dimethylbenzoic Acid (CAS 19037-09-7) tells its own story. This compound emerges from carefully refined processes on our production lines, designed and engineered through years of hands-on chemical synthesis. Our version of this compound follows a transparent model: predictable quality, batch after batch. Our team monitors each stage, from sourcing raw materials to purification, so every shipment meets strict standards demanded by our partners in research and downstream synthesis.
Our production batches typically deliver the compound as an off-white to pale yellow crystalline powder, reflecting the purity of ≥98% on a dry basis. We record melting points between 164°C and 168°C, confirming structural integrity after crystallization. Moisture and residual solvent levels, checked by dedicated teams at line and lab, remain tightly controlled to ensure reliable performance. Our in-house analyses confirm identity through HPLC, NMR, and mass spectrometry, all run within our purpose-built analytical lab space. We share only what can be backed by the experience of our own trained chemists at the plant, not repackaged or sourced from outside vendors.
From years of tending to details in process controls, we see the difference between lab-scale synthesis and production-scale consistency. Impurities, even in small amounts, challenge reproducibility in complex syntheses. Each milestone we set for 2-Amino-3,4-Dimethylbenzoic Acid has roots in the day-to-day problems solved on the plant floor: controlled pH at each workup, pressure-regulated hydrogenations, and repeated distillations until we achieve the right chromatographic fingerprint. That’s where our product owes its reliability.
This compound draws steady demand from specialty synthesis in pharmaceutical and dye intermediates. Looking back on past projects, many of our customers faced ongoing delays from variability in raw materials imported from unfamiliar suppliers. By working with our teams, they skipped the trial-and-error phase, narrowing down reaction variables and establishing solid protocols faster. We have seen this compound feature as a core building block for more complex benzoic acid derivatives and heterocyclic compounds, especially when adding methyl and amino groups at precise positions. In our line of work, matching lab predictions with plant-scale outcomes does not always come easily. This molecule brings a solid starting point for amide coupling, esterification, or diazo chemistry, thanks to its reactive amino group and steric effect from the methyls.
In dye and pigment manufacture, formulation chemists leverage the unique substitution pattern on the aromatic ring, gaining access to a different color profile than typical aminobenzoic acids. From our observations, customers value the higher selectivity possible with the 3,4-dimethyl configuration, leading to new chromophores that resist photobleaching. Raw material grade and trace impurity profile weigh heavily on their process yield. Direct conversations with technical managers reveal that trace heavy metals and colored impurities—problems more common in recycled or resold lots—are virtually absent in our material, thanks to proprietary filtration and chromatography routines built into our process.
Most chemists know the general class of aminobenzoic acids, but only those who work hands-on with multiple positional isomers notice the subtle but practical differences. For instance, 4-amino-3,5-dimethylbenzoic acid, though closely related, introduces steric and electronic effects that complicate downstream reactions. Our experience shows that the 2-amino group, placed ortho to the carboxylic acid, offers unique reactivity in directed ortho metalation, facilitating the introduction of further functionalities without excessive side reactions. Experiments by our own R&D staff have consistently found better selectivity and higher yields in most nucleophilic aromatic substitution reactions, when compared with isomers lacking this arrangement.
From a production standpoint, we cross-reference every new shipment against retention samples, confirming that melting point and NMR signals remain constant, even across different years. Unlike other substitutes in the market, which sometimes show unexplained color, odor, or microcrystalline impurities, our product maintains stable storage properties when kept sealed and dry under ambient conditions. Users in the field notice less caking and fewer issues during weighing, especially in high-throughput labs.
We often get asked why narrower impurity profiles matter for this material. The practical answer lies in downstream process control. During amide bond formation, even small organic byproducts from incomplete methylation or side-chain oxidation cause color changes or inconsistent reactivity. Customers complain about delayed chromatography, poorly defined end products, or unexplained side bands on their NMR spectra. By holding residual impurities below established protocol limits, our team helps users reduce troubleshooting cycles and keep their projects moving.
Long-term partnerships in pharmaceutical research repeatedly point toward regulatory requirements that keep tightening every few years. GMP or non-GMP, many projects require us to demonstrate traceability and document every step along the way. This hands-on transparency stems from our plant operations—tagged drums, digital batch logs, and regular third-party QA audits—putting all the supporting data behind each lot. Unlike spot-buyers or traders, we rely on batch histories to resolve questions, sidestep recalls, and let users scale projects without ingredient changes.
We specialize in synthesizing this molecule from basic intermediates using a mix of classical aromatic chemistry and modern purification. Besides direct benefits to our customers’ research, this integration lets us implement modifications rapidly in response to feedback. For example, after a customer experienced filtration clogs due to minor byproducts in a prior supplier’s lots, our process engineers altered the solvent systems and reduced processing time. After the change, subsequent lots improved filtration flow rates. This adaptation reflects the direct relationship we maintain with regular buyers, who send us their pain points and expect tailored solutions based on practical plant knowledge.
Reselling or repackaging can mask deeper supply chain risks. Goods changing hands multiple times before reaching the end user can accumulate invisible costs—delays, mixed batches, uncertain origin. From our vantage point, control over synthesis and logistics helps ensure not just purity, but reliability in lead times and documentation. Larger volume purchasers, especially those running pilot or commercial production, have repeatedly cited this stability as justification for standardizing on our material.
We have been fortunate to work alongside chemists, analysts, and plant operators who openly share feedback about how the product behaves in practical application. This relationship shapes every incremental improvement in our synthesis and packaging. One example: years ago, several users reported static charge buildup during winter months, leading to losses and mess during transfer. We responded by fine-tuning the final milling and packaging humidity, reducing static and ensuring cleaner handling. These details may not show up on standard specifications, but they matter in daily lab routines.
Problems with rapid caking or clumping during summer transport led us to adopt liner materials with low water vapor transmission rates. After implementation, we tracked fewer product returns due to lumping or hardening. These changes go beyond standard catalog copy and reflect the iterative improvements only possible with a direct manufacturing relationship.
The landscape for sourcing chemicals like 2-Amino-3,4-Dimethylbenzoic Acid has shifted over the years. Access to starting materials, energy consumption, and regulatory checks at the national borders shape both availability and price. Because we keep production in-house, we weather fluctuations in upstream supply more effectively than brokers buying spot lots. We negotiate directly with bulk suppliers, vet each barrel for contamination risks, and adjust our process chemistry for new grades of starting material as environmental standards change.
Increasing regulatory focus makes documentation ever more important, especially for customers working toward active pharmaceutical ingredient (API) or medical device applications. Our operation tracks batch traceability down to each input, making the audit process smoother and faster. Facing unexpected changes—say, a change in permitted water discharge or an import certificate requirement—results in direct action at our plant. By investing in on-site environmental controls and computerized tracking, we protect both our output quality and customers’ regulatory compliance efforts.
Pharmaceutical R&D, pigment formulation, advanced materials, and academic labs have all pushed the boundaries of what can be built with 2-Amino-3,4-Dimethylbenzoic Acid. High-resolution mass spectrometry groups value clean spectra, free from high molecular weight adducts or surfactant residues. Formulation chemists developing new dyes need a compound that responds predictably under acid or base conditions, without shifting color due to instability.
Our work with specialty polymer teams exposed us to demands for absolute dryness, where even small amounts of water influence polymer properties during chain extension. Applying targeted drying and packing techniques based on user feedback helped us raise the bar for anhydrous batches. In academic settings, where budgets are tight, we discovered that reliability can free up resources—fewer failed experiments mean fewer repeats and more publishable results. Students and faculty at several research centers have commented that the well-defined melting point and reproducible solubility profile not only assist synthesis but also offer valuable teaching moments for analytical techniques.
Public focus on sustainability affects how chemistry is done, not just what gets made. We view efficient chemical manufacturing as a long-term commitment. Process improvements in solvent recovery, waste heat recapture, and chemical recycling stem from years spent optimizing batch handling to minimize lost yield. Each time we recycle solvent or recover unused raw material, overhead drops and plant waste shrinks. These operational changes lead not only to lower costs, but also fewer disposal issues for our customers. Documentation of process changes and regular auditing keep us honest and drive steady improvements, even for classic compounds like 2-Amino-3,4-Dimethylbenzoic Acid.
Industry expectations for chemical sourcing and transport have also changed due to global logistics interruptions. Rather than relying on distant intermediaries for drum packaging or bulk shipment, we invested in automated filling systems and bulk handling protocols right at the production site. We adapted to export control changes quickly, realigning product labeling and documentation to cross borders smoothly.
We frequently discuss best practices for storage and use, based on our experience supporting large-scale and small-scale users. For chemical stability, we recommend keeping containers sealed, protected from moisture, and stored at room temperature away from direct sunlight. Opened packages stored in desiccators last longer and pour more easily, avoiding caking. Operators managing multi-kilogram projects often set up secondary containment and portion out volumes as needed, which helps track usage and maintain a fresh supply for longer campaigns.
From firsthand experience, we know that attention to these housekeeping details can spell success for a synthesis. Users juggling multiple raw materials can benefit from organizing storage and reordering schedules, reducing risk of running short mid-project.
Our days revolve around meeting quality expectations while solving problems as they arise during actual chemical production and use. This work at the junction of process chemistry and practical application distinguishes our manufacturing model from that of intermediaries more focused on transaction volume than technical support.
By keeping conversations open with our customers and monitoring each batch, we chart a steady path forward—one marked by improvement, responsiveness, and reliability. Our familiarity with 2-Amino-3,4-Dimethylbenzoic Acid stems from the literal hands-on labor of production, purification, and packaging, as well as the many offline conversations with customers troubleshooting real-world issues. Through these experiences, we have learned to prioritize transparency—about composition, batch record, and process change—allowing users to confidently build outwards in their own projects and research.
We thank all the chemists, engineers, and formulators who have informed each improvement with direct commentary from the bench and the plant. We rely on their expertise and their trust. Going forward, we will continue to share what we know and keep refining our process for as long as new challenges appear in the world of 2-Amino-3,4-Dimethylbenzoic Acid chemistry.