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HS Code |
347112 |
| Productname | 2-Amino-3-Methylbenzoic Acid |
| Casnumber | 585-91-5 |
| Molecularformula | C8H9NO2 |
| Molecularweight | 151.17 g/mol |
| Appearance | Off-white to beige crystalline powder |
| Meltingpoint | 164-168°C |
| Solubility | Slightly soluble in water |
| Synonyms | 2-Amino-m-toluic acid; o-Amino-3-methylbenzoic acid |
| Smiles | Cc1cccc(N)c1C(=O)O |
| Inchi | InChI=1S/C8H9NO2/c1-5-3-2-4-6(9)7(5)8(10)11/h2-4H,9H2,1H3,(H,10,11) |
| Ecnumber | 209-564-6 |
As an accredited 2-Amino-3-Methylbenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g package of 2-Amino-3-Methylbenzoic Acid comes in an amber glass bottle with a secure, tamper-evident screw cap. |
| Shipping | 2-Amino-3-Methylbenzoic Acid should be shipped in a tightly sealed container, protected from moisture and light. It is typically packed in appropriate chemical-resistant materials and labeled according to hazardous materials regulations. Ensure compliance with local, national, and international shipping guidelines for chemicals, including documentation and safety data sheet inclusion. |
| Storage | **2-Amino-3-Methylbenzoic Acid** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Use appropriate personal protective equipment when handling. Ensure that storage areas are clearly labeled and comply with all safety regulations. |
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Purity 99%: 2-Amino-3-Methylbenzoic Acid with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and reduced by-product formation. Melting Point 178°C: 2-Amino-3-Methylbenzoic Acid with a melting point of 178°C is used in the preparation of temperature-sensitive dyes, where thermal stability is maintained during processing. Molecular Weight 151.16 g/mol: 2-Amino-3-Methylbenzoic Acid of 151.16 g/mol is used in polymer modification applications, where precise molecular incorporation enhances polymer characteristics. Particle Size <50 µm: 2-Amino-3-Methylbenzoic Acid with particle size below 50 µm is used in fine chemical formulations, where rapid dissolution and homogeneity are achieved. Stability Temperature 120°C: 2-Amino-3-Methylbenzoic Acid stable up to 120°C is used in catalytic reaction development, where product integrity is preserved under moderate heat. Solubility 12 g/L (water): 2-Amino-3-Methylbenzoic Acid with water solubility of 12 g/L is used in aqueous synthesis protocols, where efficient dispersion produces consistent reaction rates. HPLC Assay ≥98%: 2-Amino-3-Methylbenzoic Acid featuring an HPLC assay of ≥98% is used in analytical reference standards, where quantification accuracy is improved. UV Absorbance (λmax 280 nm): 2-Amino-3-Methylbenzoic Acid with UV absorbance at 280 nm is used in spectrophotometric calibration, where precise measurement of aromatic compounds is facilitated. Low Heavy Metal Content (<10 ppm): 2-Amino-3-Methylbenzoic Acid with heavy metals below 10 ppm is used in electronic material synthesis, where high purity minimizes contamination risk. Bulk Density 0.65 g/cm³: 2-Amino-3-Methylbenzoic Acid with a bulk density of 0.65 g/cm³ is used in tablet formulation, where predictable packing characteristics ensure consistent dosage forms. |
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In any discussion of specialty chemicals used across various scientific fields, 2-Amino-3-Methylbenzoic Acid stands out for its reliability and adaptability. The name might sound complex, but this compound has carved out a reputation thanks to its balanced structure and precise chemical behavior. Known by its chemical formula C8H9NO2, it finds a place in everything from pharmaceutical precursors to advanced chemical synthesis. Over years of experience in laboratory settings, it's always clear—having access to such a well-behaved, pure compound can make life easier for everyone from bench chemists to industrial formulators.
2-Amino-3-Methylbenzoic Acid features a benzene ring substituted with both an amino group and a methyl group, alongside a carboxylic acid. What sets it apart structurally lies in the arrangement of these groups, where the amino is in the ortho position to the acid and the methyl group sits next to it. In practice, this means the molecule tends to form stable, reproducible results during experiments. From years handling aromatic acids and their derivatives, I have noticed how some structures just behave more predictably. Unlike similar chemicals where side reactions can complicate things quickly, this compound generally supports robust synthesis and straightforward purification.
Lab work quickly reveals who gets shortchanged by subpar chemical quality. Reliable 2-Amino-3-Methylbenzoic Acid commonly appears as an off-white crystalline solid, with a melting point in the expected range for aromatic acids. High purity grades often hit upwards of 98%, and I’ve always found that attention to trace contaminants in supply sources pays off in the long run. In my early years, I made the mistake of using generic, low-purity grades in a reaction pathway and ended up with inconsistent product yields. Consistent particle size and confirmed melting points help mitigate these risks. Acid solubility and stability at ambient temperature offer further practical benefits, making storage and weighing straightforward for most lab techs.
Few aromatic carboxylic acids bridge so many research areas. In pharmaceuticals, 2-Amino-3-Methylbenzoic Acid often helps synthesize more complex intermediates. Many medicinal chemists I’ve worked alongside prefer its directness—reactivity that doesn’t introduce unnecessary steps. Working in process chemistry, it’s rewarding to source a single precursor that feeds neatly into larger, more intricate syntheses without hidden pitfalls. Its amino group remains reactive for further substitution, making this compound a stepping stone toward dyes, agrochemicals, and specialty polymers.
Educators appreciate it as well. Students, especially those just starting with organic synthesis, need compounds that demonstrate key reactions without confusing side products. I recall supervising undergraduate labs where newcomers could see amide or ester formation firsthand, gaining confidence thanks to the predictable behavior of this compound. Reliability in basic organic reactions helps foster better understanding of broader chemical principles—and prepping these labs, you truly value reagents that deliver on their promise each time.
Every compound comes with quirks, and this one is no exception. Excess moisture can cause gradual degradation in the long term, so dry, sealed storage delivers better shelf life for both small-scale and bulk users. In my experience, transferring small crystalline batches works best using non-stick spatulas, and static charge almost never poses a problem thanks to robust crystalline structure. Odor is barely noticeable compared to sulfur- or amine-heavy alternatives—those who have spent years in the lab develop a sixth sense for problematic volatiles, and this compound causes few raised eyebrows. Minor skin or respiratory irritation may occur during heavy-scale work, so wearing gloves and using fume hoods keeps work safe without excessive hassle. Responsible chemists keep MSDS info handy, but routine handling rarely presents surprises. Compared to strong-smelling amines or volatile esters, it makes life simpler for anyone sharing lab space.
Laboratory time is precious. Reliable output saves significant frustration. Early on, I learned the hard way that compromised chemicals sabotage not only productivity but also scientific confidence. 2-Amino-3-Methylbenzoic Acid, at higher grades, tracks well with supplier claims. Analysts in QC labs running HPLC or NMR regularly see a clean peak—rarely do ghost impurities show up in experienced hands. Reliable materials help not only with yield, but also reproducibility. If a reaction fails, you want to be sure the issue lies in the process, not in the building blocks. This builds trust between purchasing departments and hands-on chemists.
In industrial plants where hundred-kilo batches move through the process pipeline, even trace contamination can echo downstream, damaging costly equipment or derailing timelines. Colleagues from these environments regularly comment: “Spend up front on quality, save down the line on repairs.” My experiences match this wisdom. High-grade 2-Amino-3-Methylbenzoic Acid provides peace of mind—everyone down the chain knows what’s going into their synthesis.
Chemistry offers plenty of similar-sounding options, such as 2-Aminobenzoic Acid or 3-Methylbenzoic Acid, but their behaviors can diverge in subtle ways. While the core skeleton remains aromatic, the placement of methyl and amino groups determines electronic density and possible hydrogen bonding. Colleagues in the pharma industry often point out that selectivity matters—a minor change can shift how intermediates connect or how downstream reactions proceed.
On paper, 2-Amino-3-Methylbenzoic Acid might resemble related structures, but even a small difference in chemical reactivity can mean needing to change catalysts or solvents. I’ve seen projects grind to a halt because someone grabbed the wrong substituted benzoic acid off the shelf—one misplaced functional group and hours disappear. This subtlety matters not just in bench chemistry but for scale-up, too. Specifications sheet alone can’t reveal everything; experience with the compound builds the necessary intuition. Over time, trusted molecules like this become familiar tools in the chemist’s toolkit.
Several practical applications make regular use of 2-Amino-3-Methylbenzoic Acid. Manufacturing sectors employ it for active pharmaceutical ingredients, advanced intermediates, dyes, and pigments. Its stability under a range of conditions means it holds up well during long multistep syntheses. Based on chemical supply records and project involvement, its popularity in both Western and Asian markets continues to grow, helped by reliable global sourcing chains and solid track records in process chemistry.
In research settings, its dual functional groups allow classroom demonstrations of coupling, amidation, and cyclization. I’ve watched students light up after seeing clear color changes and efficient product isolation using this compound—it drives home those “aha!” moments in organic chemistry. Graduate researchers often use it as a tool for mechanistic studies, learning how minor modifications to its structure influence reactivity patterns, yields, and reaction times.
As with most specialty chemicals today, sustainability and ethical sourcing have become genuine concerns. I remember early career days when few questioned the origins of precursors; today, questions about responsible chemical sourcing come up all the time. Large buyers, especially in pharmaceuticals and fine chemicals, want transparency—knowing suppliers adhere to safe labor practices, correct documentation, and responsible waste disposal.
While 2-Amino-3-Methylbenzoic Acid production doesn’t involve rare metals or especially hazardous reagents, manufacturing with green chemistry principles leads to less waste and lower environmental footprints. At conferences, process chemists share case studies demonstrating solvent recycling improvements or cleaner intermediate isolation. Labs looking to minimize hazardous waste have begun adopting new purification steps to limit effluent and maximize product recovery. A compound that’s easy to recover and repurpose naturally gains favor among sustainability-focused teams. I get frequent questions about whether supply sources are REACH compliant, offering a clear trace from raw materials to finished batches.
Lab veterans know shortcuts with chemical safety never pay off. Although handling 2-Amino-3-Methylbenzoic Acid rarely introduces major hazards, reckless use creates unnecessary problems. Proper ventilation, standard PPE, and storage outside of extreme heat or humidity suffice in almost every context. Regulatory compliance remains central—institutions that ignore these basics eventually confront audits, fines, or worse.
Tighter regulation across the globe encourages suppliers to share more extensive documentation on purity, trace contaminants, and physical properties. In high-end labs I’ve worked with, detailed COAs remain standard expectation. Regulatory scrutiny also brings new certification requirements—some clients check each lot for residual solvents and specific heavy metals. Over time, this sets higher bars for all stakeholders, creating a culture of shared responsibility. Reliability in both safety and documentation helps everyone focus on actual research and innovation.
Continuous improvement doesn’t end with better raw materials. From a practical view, researchers and manufacturers now ask even more from their reagents: better lot-to-lot consistency, environmentally friendly processing, and support for ever-diversifying end uses. I often hear about automation systems calling for improved data integration—tracking every outgoing batch with barcode systems and digital logs. The next generation expects smart labels and integrated digital tracking linking every container back to its origin. 2-Amino-3-Methylbenzoic Acid sits at this intersection, showing that even traditional chemicals can adapt to new demands—whether supplying a pilot plant in Europe or a university lab in Asia.
As applications expand, from new catalytic systems to specialized performance polymers, demands on chemical suppliers only increase. A few years ago, 2-Amino-3-Methylbenzoic Acid mostly fueled classic organic research and pharmaceutical scale-up. Now, its role has grown to include newer materials science projects—everything from novel sensors to energy storage. Cross-disciplinary teams working at today's research frontiers appreciate proven chemicals that don’t require constant troubleshooting.
Over time, a few simple principles come up again and again. Source high-purity 2-Amino-3-Methylbenzoic Acid from trusted partners to support success on the first pass. Store it in sealed, dry containers away from splashes, caustic vapors, or light. Train staff to recognize and report off-spec color, odor, or texture. Invest in regular GC/MS or NMR snapshots to guarantee ongoing purity—catching early signs of contamination prevents larger downstream headaches.
In my own lab experience, keeping accurate records and batch histories proves invaluable, especially if multiple teams rotate through shared reagents. Label every bottle with receipt date, lot number, and expiration—inventory management isn’t glamorous, but it saves projects when timelines slip or staff turns over. Don’t wait until something goes wrong to run confirmatory checks. Reliable communication with suppliers smooths ordering and troubleshooting.
Chemistry remains a collaborative journey. Chemists in both research and manufacturing rely on community knowledge, trusted methods, and shared troubleshooting to refine protocols. 2-Amino-3-Methylbenzoic Acid finds repeat use not only for its utility, but also because teams across the world report successes, failures, and best practices. Online forums, published papers, and informal lab meetings all play a part—each bit of experience helps refine collective understanding.
Mentorship keeps the discipline advancing. Newcomers benefit from learning not just reaction mechanisms, but also reagent quirks and optimal storage methods. Veterans remind junior staff to log critical observations and share even minor irregularities. This spirit of open sharing builds a foundation where common challenges—solubility hiccups, storage failures, supply chain interruptions—get addressed collaboratively rather than solo.
Looking ahead, scientific progress relies on both the reliability of classic tools and the willingness to adapt to new constraints. Experience shows that 2-Amino-3-Methylbenzoic Acid remains a steadfast choice for teams pushing the boundaries of organic synthesis. Yet, evolving standards in sustainability, verification, and digital traceability shape its future use. Chemists, educators, and industrial engineers all want certainty in their reagents, not surprises.
Engagement with sustainable practices helps ensure ongoing access to high-quality precursors without exhausting resources or putting workers at risk. People involved in the field have begun to recognize the importance of transparent supply lines and certification. This shift—toward accountability, quality, and efficiency—provides peace of mind to all stakeholders, from the undergraduate student to the director of pharmaceutical synthesis.
By focusing on reliable sourcing, safe handling, and collaboration, every team stands to benefit. Whether producing a new medicine, developing next-generation dyes, or training tomorrow’s scientists, the foundation remains the same: rigorous attention to quality, clear communication, and an eye toward both present challenges and future needs. My own experience drives home the point—trusted reagents like 2-Amino-3-Methylbenzoic Acid underpin scientific progress, and ongoing diligence ensures they continue delivering value for everyone who relies on them.