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Methyl 3-Aminobenzoate

    • Product Name Methyl 3-Aminobenzoate
    • Alias Methyl m-aminobenzoate
    • Einecs 211-227-7
    • 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

    500863

    Cas Number 99-08-1
    Molecular Formula C8H9NO2
    Molecular Weight 151.17
    Iupac Name Methyl 3-aminobenzoate
    Appearance White to off-white crystalline powder
    Melting Point 63-66 °C
    Boiling Point 278 °C
    Density 1.22 g/cm3
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Smiles COC(=O)C1=CC(=CC=C1)N
    Inchikey ISPKPZLODFGACG-UHFFFAOYSA-N
    Synonyms 3-Aminobenzoic acid methyl ester
    Storage Temperature Store at room temperature
    Flash Point 122 °C

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

    Packing & Storage
    Packing 250g of Methyl 3-Aminobenzoate is packaged in a sealed, amber glass bottle with a screw cap and safety label.
    Shipping Methyl 3-Aminobenzoate is shipped in tightly sealed containers to prevent moisture and contamination. It should be packed according to relevant chemical safety regulations, labeled clearly, and cushioned to avoid breakage during transit. Store and transport in a cool, dry place, away from incompatible substances and direct sunlight.
    Storage Methyl 3-Aminobenzoate should be stored in a tightly closed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong oxidizing agents and acids. Ensure proper labeling and secure storage to prevent leaks or contamination, and follow all standard safety protocols for laboratory chemicals.
    Application of Methyl 3-Aminobenzoate

    Applications of Methyl 3-Aminobenzoate in Industrial Manufacturing

    Methyl 3-Aminobenzoate serves as a key intermediate for several high-value industrial sectors. As the direct manufacturer, we support global customers in regulated markets, ensuring strict traceability, consistent purity, and batch-specific documentation. Below, we detail the main downstream applications where this raw material fulfills unique roles in critical synthesis and formulation processes.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    In pharmaceutical manufacturing, many complex APIs require advanced benzoic acid derivatives. This material is frequently used in multi-step synthesis routes for producing analgesics, antispasmodics, and specialty central nervous system (CNS) agents. Customers rely on our product’s high assay and predictable impurity profile to prevent side reactions during N-acylation and cyclization steps. Our quality control team supports complete regulatory audits and impurity data submissions for US and EU regulatory filings. Production teams monitor input ratios to minimize residual ester carryover in final APIs, ensuring patient safety and regulatory compliance.

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7) for pharmaceutical manufacturing
    • United States Pharmacopeia (USP) when applicable to APIs
    • European Pharmacopoeia (Ph. Eur.) when specified by downstream customers
    • FDA and EMA registration support for Drug Master File (DMF) referencing

    Typical usage ratio

    • 0.5%–3.0% by molar equivalence as a coupling substrate in multi-step synthesis; precise dosage varies per API pathway and downstream impurity limits

    Downstream process integration

    • Input during condensation, acylation, or amidation steps in fine chemical API synthesis
    • Precursor for benzamide, anthranilate, and substituted pyridine building blocks
    • Controlled addition to jacketed reaction vessels with in-line pH and temperature monitoring

    Final product types

    • API intermediates such as substituted 3-aminobenzoic acid analogs
    • Pain relief and muscle relaxant actives
    • CNS pharmaceutical actives requiring high-purity aromatic amines

    2. Synthesis of Azo and Specialty Dyes

    This compound acts as an essential feedstock in the synthesis of high-performance dyes, particularly in the manufacture of azo colorants for plastics, leather, and textile applications. Our material provides reliable amine functionality for diazotization and subsequent coupling steps, which determine batch color strength and shade reproducibility. Regulatory restrictions on aromatic amines require stringent control of input concentrations and by-product profiles. Our plant supports REACH registration dossiers with pre/post-batch QC analytics for every shipment to ensure application safety and compliance for dye chemistries exported to Europe and Asia.

    Industry compliance standards

    • REACH Regulation (EC No 1907/2006) for registration, evaluation, and authorization of chemicals (European Union)
    • EN 71-3 Toy Safety—Migration of certain elements (relevant for dyes in toys and children's textiles)
    • OEKO-TEX® Standard 100 for restricted aromatic amines in textile processing

    Typical usage ratio

    • 5%–12% by weight in coupling reactions for monoazo and diazo dye synthesis; level adjusted for chromophore intensity and application substrate

    Downstream process integration

    • Diazotization with inorganic nitrites under controlled pH and temperature
    • Immediate coupling to aromatic or heterocyclic partners to form designated dye architectures
    • Intermediate isolation, purification, and milling for downstream pigment pastes or dye powders

    Final product types

    • Monoazo and diazo dyes for plastics and textiles
    • Specialty pigment dispersions for printing ink manufacturing
    • Leather finishing colorants conforming to aromatic amine safety limits

    3. Agrochemical Intermediate for Herbicide Formulation

    The agrochemical sector utilizes this chemical as a critical precursor in the synthesis of benzoic acid-based herbicides and plant growth regulators (PGRs). In these processes, manufacturers rely on the controlled reactivity of the ester and amine groups for stepwise synthesis of selective broadleaf herbicides. Our plant supports batch traceability and reproducible impurity control, helping our customers conform to local pesticide registration requirements. Downstream engineers adjust catalyst, pH, and solvent polarity based on the active ingredient being produced. Documentation supports export clearance to destination markets in accordance with applicable national pesticide regulations.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • OECD Guidelines for the Testing of Chemicals, especially regarding environmental fate
    • China National Standard GB/T 1600 Pesticide Registration
    • EPA Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) for US market access

    Typical usage ratio

    • 3%–8% by weight as a coupling intermediate; adjusted according to target herbicide and required active concentration in final formulation

    Downstream process integration

    • Integrated in initial condensation or amidation steps for selective benzoic acid herbicide synthesis
    • Processed under solvent reflux or continuous flow reactors for scale-up production
    • Purification and separation to minimize residual aromatic amine in end-use active

    Final product types

    • Selective post-emergence herbicides (e.g., anthranilate family herbicides)
    • Precursor adducts for benzoic acid-based PGRs
    • Custom pesticide actives tailored to regional crop and weed profiles

    4. Fragrance Ingredient Synthesis for Fine Chemicals

    Perfume and aroma formulation companies utilize our product in the manufacture of aroma chemicals and musk precursors. The aminobenzoate structure enables targeted cyclization and esterification to yield intermediates for musks and modified benzoate esters. Specialty fragrance customers require a low-odor, high-purity material to prevent interference with delicate olfactory compositions. We provide extended batch retention samples and collaborative technical documentation to support product safety statements and IFRA submissions. Downstream processing can require unique solvent and temperature profiles to protect fragrance integrity during scale-up blending.

    Industry compliance standards

    • International Fragrance Association (IFRA) Codes and Standards
    • European Cosmetic Regulation (EC) No 1223/2009—relevant for aroma raw materials in perfumery
    • Good Manufacturing Practices (GMP) for Fragrance Ingredients (ISO 22716)

    Typical usage ratio

    • 2%–7% by weight in aroma chemical synthesis; adjusted per target musk or ester strength and downstream olfactory analysis

    Downstream process integration

    • Introduced in cyclization and transesterification reactions for production of musk and benzoate derivatives
    • Isolated by vacuum distillation with attention to batch aroma profiles
    • Further processed in pilot or production mixers for blending into fragrance bases

    Final product types

    • Macrocyclic and aromatic musks for perfumery applications
    • Specialty benzoate esters for high-end fragrances
    • Custom aroma chemical intermediates for fine chemical producers

    5. Polyimide and Performance Polymer Synthesis

    High-temperature polymer producers use this raw material for introducing functional aromatic amine units during the synthesis of advanced polyimides and copolyesters. The controlled amine content provides reactivity during polycondensation, influencing molecular weight and thermal performance. Ongoing tight control over residual ester ensures proper polymer chain extension and minimizes gel formation in precision casting operations. Our manufacturing site documents full batch traceability and provides material certificates supporting automotive and electronics qualification protocols. Customers leverage our expertise to fine-tune amine incorporation rates depending on final application performance targets.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management System for polymer manufacturing
    • UL 94 Flammability Standard for finished polymer compounds
    • RoHS 2011/65/EU Restriction of Hazardous Substances in electrical/electronic equipment

    Typical usage ratio

    • 0.5%–2.5% by molar content in step-growth polymerization; adjusted by chain extension requirements and substrate end-use properties

    Downstream process integration

    • Charged into polymerization reactors as aromatic diamine co-monomer or chain modifier
    • Incorporated at controlled temperature and vacuum for optimum molecular weight buildup
    • Batched with dianhydrides or diacid chlorides for custom polymer architectures

    Final product types

    • Polyimide films for flexible electronics
    • Performance copolyesters for engineering plastics
    • Insulation layers and adhesives within electronics manufacturing

    6. Research-Grade Intermediate for Academic and Commercial R&D

    Universities, public laboratories, and industrial R&D groups source this intermediate for method development, analytical standards, and pilot-scale synthesis. We provide research grades with full COA and Batch Data Sheets, supporting trace organic analysis, bioactive scaffold development, and synthesis process optimization. Users often require micro- to kilo-scale quantities with guaranteed impurity fingerprinting to validate synthetic pathways for peer-reviewed publication, patent filing, or scale-up proof-of-concept.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for laboratory-based studies (OECD series)
    • ISO/IEC 17025 for testing and calibration laboratory competence

    Typical usage ratio

    • 0.1 g to multi-kg; determined per experiment or pilot protocol needs and test-lot design

    Downstream process integration

    • Used as reference standard in HPLC/GC/MS analysis of aromatic amines
    • Input into small-scale synthetic method exploration or building block validation
    • Batched in reaction vessels for laboratory-scale reactions and structure-activity studies

    Final product types

    • Reference compounds for analytical chemistry
    • Novel molecular scaffolds for patent investigations
    • Pilot-synthesized specialty chemicals for primary testing
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    Certification & Compliance
    More Introduction

    Methyl 3-Aminobenzoate: Practical Insights from the Factory Floor

    Understanding Methyl 3-Aminobenzoate from a Manufacturer’s Perspective

    We produce Methyl 3-Aminobenzoate, often recognized in research and industry by its CAS number 618-46-2, right here in our facility. Our chemists and staff work with this compound daily, keeping close attention to each batch as it moves through the synthesis and purification steps. This hands-on experience means we see firsthand where the product shines, the questions researchers bring us, and the obstacles sometimes faced in scale-up or custom specifications. The depth of familiarity that comes from handling raw materials, optimizing reaction conditions, and checking the final product quality defines our relationship to this compound—different from what a trader or outsourcing partner could claim.

    Methyl 3-Aminobenzoate, as the name implies, is an ester derivative of 3-aminobenzoic acid. Its molecular formula is C8H9NO2. The compound forms a crystalline powder at room temperature, and we see this directly as soon as crystallization completes in our reactors. Standard purity meets ≥99% for the majority of lab and synthesis requirements, and we monitor this through each production cycle, using HPLC and NMR, not just relying on a certificate from some partner lab. That attention gives us a good read on real-world consistency batch to batch, and lets us confidently answer questions about trace impurities or potential incompatibilities for downstream applications.

    Core Applications: Why Customers Choose This Material

    Researchers and production chemists use Methyl 3-Aminobenzoate for a number of targeted reasons. Many processes in pharmaceutical and fine chemical manufacturing utilize this ester as a versatile intermediate. Its amine group participates in a range of substitutions and coupling reactions. We’ve seen it serve as a precursor in the synthesis of dyes, fluorescence probes, and certain analgesic agents. Unlike generic methyl benzoates, the amino group at the meta position unlocks pathways not available to the unsubstituted compounds or the ortho- and para-aminobenzoate esters.

    From our conversations with buyers and project leads, one benefit they mention is the cleaner profile in nucleophilic aromatic substitution, especially compared with ortho isomers that often bring added steric or electronic effects. In peptide chemistry, choosing the meta-aminobenzoate ester can simplify protecting group strategies or allow for selective deprotection steps, saving time and resources in solid-phase synthesis. These aren’t just marketing angles—we hear this feedback repeatedly after customers trial different esters.

    Specifications: From Lab Scale to Bulk Quantities

    We start our batches at kilogram-scale in glass-lined reactors, taking care with charging since amines can react vigorously in some solvent systems. Controlled temperatures and careful addition of methylating agents help prevent runaway reactions or by-products that need extra purification. Over the years, we’ve improved yields and reduced the waste profile per batch by refining our methods, so we now reach a purity routinely above 99% by HPLC. Our solid product melts between 62-65°C, matching published data and confirmed each time by our QC lab. Appearance remains a free-flowing, white to off-white powder, with no persistent lumps or discoloration when shipped within two weeks of production.

    Our standard packaging uses double-lined polyethylene bags inside sealed drums for bulk, or smaller poly containers for laboratory sizes, preventing moisture pickup. Experience taught us that failure to fully seal containers can degrade shelf life, so we conduct regular stability checks, simulating real transit conditions. Average moisture remains below 0.2%, avoiding hydrolysis concerns that some customers have flagged when using material from less diligent suppliers.

    Reports from pilot customers confirm that our material dissolves without residue in common solvents such as ethanol and DMSO. Several long-term partners rely on us to keep impurity profiles stable below 0.5% total impurities. No batch leaves our site before internal labs confirm both identity and performance criteria, including reaction outcome in trial syntheses requested by some clients.

    Comparing with Related Compounds: Key Differences in Functionality

    Methyl 3-Aminobenzoate is just one of several benzoic ester derivatives produced by chemical manufacturers worldwide. We also make related items, such as methyl 2-aminobenzoate and methyl 4-aminobenzoate, as well as the parent 3-aminobenzoic acid. Substitution at the meta position, as in this product, creates reactivity differences noticeable even in basic organic transformations. For instance, meta derivatives tend to offer less resonance stabilization for nucleophilic attacks compared with para isomers. In catalytic hydrogenations, the meta position amine shows distinct compatibility and lower rates of reduction side products.

    Buyers working in dye intermediate synthesis often point out that the color depth and stability of azobenzene-type dyes shift measurably depending on the isomer used. Methyl 3-Aminobenzoate is sometimes favored for stability and ease of downstream transformation—internal tests in our R&D setup support that observation. Similarly, when working in the field of specialty pharmaceuticals, the compound stands out by enabling selective functionalization steps. Some customers attempting reductive amination report fewer by-product complications than with the para isomer, which can overreact or yield branched byproducts under similar conditions.

    We’ve even supplied samples for use in specialized polymers. Customers reported slower rates of transesterification than seen with methyl 4-aminobenzoate. In feedback from large formulators, this difference impacts processing choices and additive compatibility. Our technical team routinely answers questions about these subtle differences, since practical success in a lab or plant often comes down to small details like this and not just the chemical name.

    Practical Production Realities and Customer Collaboration

    Manufacturing Methyl 3-Aminobenzoate involves more than following a recipe from a lab manual. Early on, we found that minor tweaks—solvent choice, agitation speed, order of reagent addition—can influence both the yield and purity of the product in significant ways. Our operators inspect the batch visually for crystallization behavior, since this offers an immediate clue to process consistency before any analytical sample gets pulled. The cumulative hours spent monitoring and adjusting these variables have taught us what optimizations translate into real improvements, batch after batch.

    Quality assurance isn’t a single step at the end of the line. Each production lot passes through intermediate checkpoints: color, odor, crystallinity, then analytics for purity and identity. On the rare occasion a batch shows even a marginal deviation, we run a series of in-house 'mini-syntheses' using the same lot to check how the material behaves in an actual reaction. This lets us anticipate potential troubles a customer might encounter and take corrective action before shipment.

    Ongoing partnerships with university researchers and process chemists at major producers give us direct, candid feedback—sometimes positive, sometimes challenging. We listen and adapt. Recently, a pharmaceutical partner struggled with an unexplained drop in product yield at scale. Our technical crew traced the issue back to an uncharacteristic impurity in their amine source. By comparing chromatograms from our retained samples, we quickly identified the culprit and helped adjust their purification protocol. These kinds of direct interventions only work because we keep deep records and constant lines of direct communication.

    Sustainability and Safe Handling: Everyday Considerations

    From sourcing raw materials to solvent recycling in our plant, safety underpins every step of the process. Amines often bring specific handling needs, and Methyl 3-Aminobenzoate is no exception. We control dust and vapor exposure at multiple points, using closed systems wherever possible. Airborne concentrations get checked by our in-house safety team with regular frequency. Everyone from line operators to logistics staff takes part in safety training covering not just the handling, but the reasons behind each procedure. Experience shows no substitute for practical, hands-on familiarity with the risks unique to aromatic amines and esterification waste streams.

    Customers in regulated industries have growing questions about trace-level contaminants, sustainability of raw materials, and impact of waste profiles. Our plant uses a closed-loop solvent system, recovering and purifying more than 90% of the solvents used in each batch. While chemical manufacturing has inherent environmental burdens, the move toward higher-efficiency reactions and lower-emission processes has been ongoing for several years. We share details of our waste minimization protocols with partners who audit our site, and have found more collaborative problem-solving and less suspicion as a result.

    One pragmatic lesson: careful planning for inventory turnover limits the risk of outdated or degraded material. Aromatic amines can pick up color if left exposed to light or if the warehouse humidity goes unchecked for even a few days. Our logistics and warehouses operate under controlled conditions, and we turn stock steadily to avoid 'aged' batches. This ensures the esters we ship behave just as predictably in a customer’s process as the samples we tested the week production completed.

    Working with Specific Customer Demands

    Customization often makes the difference between a successful process and a failed scale-up. Sometimes, an R&D group needs a sample with a specific residual solvent profile. Other times, a production chemist asks for particularly tight control on trace impurities for a new route being piloted. We don’t treat these as special requests, but as normal course of business. Handling these unique requirements has made us realists about the difference between specification sheets and experience-based manufacturing.

    Feedback led us to expand from the basic >99% assay offering to include low-metal content variants, or to provide technical support documents helping customers validate the identity and performance of the product in actual reaction conditions. In one recent example, a leading researcher was developing a series of N-alkyl derivatives and needed to correlate side-product formation with trace impurity patterns. We provided detailed batch chromatography and NMR spectra, not as added value, but as foundational knowledge that benefitted both sides.

    We also field requests for technical information about reaction optimization. Chemists want to know more than melting points—they need to understand how the compound actually works in reduction, protection, or coupling steps. Direct phone calls and working sessions with our own staff mean customers get realistic advice grounded in repetitive trial, not just reference-book optimism.

    Problems Solved by Direct Manufacturing Involvement

    Buyers often express frustration with off-the-shelf chemicals that promise specification but underperform in final use. Over the years, we’ve learned that small process variations—such as the sequence in which amines and methylating agents get introduced—can affect how the product crystallizes or what minor side-products can persist. By making, testing, and using our product internally, we catch these issues before customers face setbacks.

    This detailed control helps downstream partners who use the product for further synthesis. For example, one agrochemical synthesizer discovered that a persistent impurity in a competitor product created purification challenges in multi-step transformations. Sending several lots of our Methyl 3-Aminobenzoate, we matched their reaction runs, helping to pinpoint sources of side-reactivity. Shared analytical results closed the gap, another real proof that close manufacturing oversight pays off.

    Even in processes as straightforward as methyl esterification, temperatures, solvent dryness, and quenching methods all factor into the purity of finished goods. Any lapse can lead to color, residual solvents, or impurity spikes. Running the process in-house, our team tweaks conditions proactively, saving both time and resources for customers downstream.

    Attention to Compliance and Documentation

    Regulatory requirements keep evolving, especially for customers working under pharmaceutical GMP or ISO registration. We maintain detailed batch records, supply material origin documents, and can provide extended impurity profiles down to parts-per-million when needed. Audits by customer quality teams form part of our regular routine. By providing transparent access to production and analysis logs, we enable smoother compliance checks and limit delays in product approval or scale-up.

    This degree of record keeping grows out of direct, practical experience—the stakes of regulatory compliance leave no room for lapses or half-measures. Our chemists update procedures in response to customer input and new best practices, adding safeguards against batch-to-batch variability that might otherwise go unchecked.

    Conclusion: Bridging Experience with Customer Value

    Every shipment of Methyl 3-Aminobenzoate that leaves our facility reflects not just chemical know-how, but the cumulative lessons drawn from hands-on manufacturing. Reliable performance in chemical synthesis comes from skilled process management on our side, informed by constant feedback from those putting our products to use in real projects.

    Our role as an actual manufacturer, not a middleman, brings a unique responsibility. We see far more details—the difference a minor impurity makes, subtle shifts in melting point, the impact of shipping conditions on final use. This direct connection to production and application grounds our work in practical solutions rather than empty assurances. Customers benefit from rapid, fact-based answers and a commitment to ongoing improvement.

    We continue to listen and adapt, knowing that every batch builds on the trust earned over years of shared progress with researchers, developers, and process chemists worldwide. As demand for precise, high-purity intermediates grows, our manufacturing experience stays central to every gram of Methyl 3-Aminobenzoate we deliver.