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Methyl 3-Amino-4-Methylbenzoate

    • Product Name Methyl 3-Amino-4-Methylbenzoate
    • Alias methyl-3-amino-4-methylbenzoate
    • Einecs 629-838-7
    • 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

    691105

    Chemicalname Methyl 3-Amino-4-Methylbenzoate
    Casnumber 74116-70-4
    Molecularformula C9H11NO2
    Molecularweight 165.19
    Appearance White to off-white crystalline powder
    Boilingpoint 328.1°C at 760 mmHg
    Meltingpoint 63-66°C
    Density 1.17 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents such as ethanol and chloroform
    Smiles CC1=CC(=C(C=C1)N)C(=O)OC
    Inchi InChI=1S/C9H11NO2/c1-6-3-4-7(10)8(5-6)9(11)12-2/h3-5H,10H2,1-2H3
    Storagetemperature Store at 2-8°C

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of Methyl 3-Amino-4-Methylbenzoate, tightly sealed, labeled with chemical details and hazard symbols.
    Shipping Methyl 3-Amino-4-Methylbenzoate is shipped in tightly sealed containers to prevent moisture and contamination. Packages are clearly labeled according to regulatory requirements. It is transported under ambient conditions unless otherwise specified, and handled by trained personnel using appropriate protective equipment. Ensure compliance with local, national, and international shipping regulations for chemicals.
    Storage Methyl 3-Amino-4-Methylbenzoate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizers and strong acids. Protect it from light and moisture, and avoid exposure to extreme temperatures. Ensure the storage area is clearly labeled and access is restricted to trained personnel.
    Application of Methyl 3-Amino-4-Methylbenzoate

    Applications of Methyl 3-Amino-4-Methylbenzoate in Industrial Manufacturing

    Methyl 3-Amino-4-Methylbenzoate serves as a specialty intermediate utilized by leading manufacturers across multiple sectors. Known for its amine and ester functional groups, this material is integrated at key steps of synthesis in advanced chemical production lines. Below, we detail its core application scenarios based on verified downstream demand, industrial standards, and process-specific requirements.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers rely on this ester as a core intermediate for synthesizing several heterocyclic APIs, especially in antineoplastic and cardiovascular therapy categories. This raw material enters the initial stage of multi-step organic synthesis where ring closure and substitution reactions form the foundation for further derivatization, allowing for precise functionalization required by patent-protected molecules. Production lines incorporate in-line quality controls to monitor purity at each coupling stage. The ratio used in each formulation depends on the stoichiometry of the target API and the desired batch output, with adjustments made according to impurity profile and molar equivalency.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • USP/Ph. Eur. reference monographs for related substances
    • FDA 21 CFR Part 211 (finished pharmaceuticals)
    • ICH Q3A/B guidelines (impurity limits)

    Typical usage ratio

    • 0.8–1.1 molar equivalents relative to the core substrate; scaled based on API synthesis batch size

    Downstream process integration

    • Initial condensation or amidation stage in liquid-phase organic synthesis
    • Integrated within multi-step batch reactors utilizing controlled temperature and pH

    Final product types

    • Anticancer drug intermediates
    • Selective beta-blocker APIs
    • Specialty cardiovascular actives
    • High-purity reference standards

    2. Agrochemical Building Block

    Agrochemical producers apply this compound in the synthesis of select pyridine and benzoate-based herbicides and insecticides. Engineers add the material during the nucleophilic aromatic substitution sequence, where the aromatic amino group provides a site for further chlorination or alkoxylation. Usage levels vary depending on desired active content and final product registration requirements. Strict traceability and batch segregation are required to prevent contamination and to meet export pesticide registration standards.

    Industry compliance standards

    • FAO/WHO Specification Guidelines for Pesticides
    • ISO 9001:2015 Quality Management System
    • REACH compliance (for export to the European Union)
    • China ICAMA product registration

    Typical usage ratio

    • 5–12% by mass in crude reaction mixtures; optimized based on pesticide active potency and downstream derivatization requirements

    Downstream process integration

    • Loading into closed reactor systems during initial amination stage of agrochemical synthesis
    • Sequential chlorination or oxidation following aromatic substitution

    Final product types

    • Benzoic acid-based herbicide active ingredients
    • Pre-emergent and post-emergent weed killers
    • Custom insecticidal intermediates

    3. Specialty Pigment Intermediate

    Producers of complex organic pigments, especially those for high-end plastics and automotive coatings, incorporate this raw material to generate orange and red benzoate-based colorants that require ortho-substituted amino group frameworks. The compound typically enters the azo coupling or cyclization phase, providing a reliable precursor for dense, heat-resistant final pigments. Batch addition is carefully measured to minimize unreacted byproducts and to guarantee color strength consistency for end-users in automotive and polymer sectors.

    Industry compliance standards

    • ISO 18451-1:2019 (Pigments and Extenders Testing)
    • ASTM D5639 (Standard Specification for Organic Pigments)
    • RoHS Directive (2011/65/EU, heavy metal-free compliance for pigments used in electronic and automotive applications)

    Typical usage ratio

    • 1.5–4% by weight in pigment synthesis batches; variable based on target shade intensity and vehicle compatibility

    Downstream process integration

    • Input at the diazotization and condensation steps of pigment synthesis
    • Further processed via filtration and heat stabilization before pigment milling

    Final product types

    • Automotive-grade azo pigments
    • Industrial masterbatches for plastics
    • High-performance organic dispersions
    • Specialty inks for laminated packaging

    4. Fine Chemical Intermediate for Liquid Crystal Materials

    Manufacturers specializing in advanced liquid crystal (LC) displays and related optoelectronic applications use this material as a customizable intermediate for synthesizing key benzoate derivatives. This compound offers strong compatibility during the introduction of rigid aromatic core structures necessary for LC mixtures with tailored phase transition temperatures. Integration typically takes place during the nucleophilic aromatic substitution and subsequent esterification stages, ensuring high transmission and thermal stability in the final LC mixture. Due to strict product uniformity required by the display industry, process automation and in-process purity analysis are essential throughout production.

    Industry compliance standards

    • IEC 61249 (Material standards for display device components)
    • RoHS and REACH regulatory frameworks
    • Internal QA/QC protocols based on ISO 9001:2015

    Typical usage ratio

    • 0.5–2 molar equivalents in multi-component LC precursor synthesis, adjusted for end-stage purity and target birefringence

    Downstream process integration

    • Incorporated during the initial benzene core formation of LC precursor mixture synthesis
    • Subject to repeated purification and solvent exchange prior to downstream blending

    Final product types

    • Liquid crystal display (LCD) core mixtures
    • Polymer-dispersed LC film raw materials
    • Functional additives for high-clarity LCD screens
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    Certification & Compliance
    More Introduction

    Methyl 3-Amino-4-Methylbenzoate: From Laboratory Bench to Industrial Use

    Introduction

    Decades of observation in the chemical plant grant a different perspective on the compounds we produce daily. Methyl 3-Amino-4-Methylbenzoate, known among professionals for its reliability and versatility, has built a reputation over years of precise formulation and consistent quality. Every day spent scaling up batches, testing reactions, and troubleshooting downstream processes gives rise to insights that only hands-on practice can teach. This compound brings together careful molecular design and real-world usability, often making a difference where detail cannot be overlooked.

    Characteristics Rooted in Production Experience

    Each batch of methyl 3-amino-4-methylbenzoate follows the same route from raw material to finished product, although lessons learned over years have shaped the small adjustments improving final purity. Industry standard crystallization gives a solid material, fine and evenly distributed. Measuring the melting point remains a reliable check, but sharpness in results only comes through using quality solvents and precise temperature control in each run. Manufacturing guides stress the significance of controlling moisture during final filtration—a key step to avoid sluggish dissolution in downstream steps.

    Empirical observations show that in pure form, methyl 3-amino-4-methylbenzoate retains its pale, characteristic appearance throughout shipment and storage if sealed against environmental air. As a mid-sized intermediate in scale, this product positions itself between high-volume commodity chemicals and unique, low-run fine chemicals. Its stability profile supports long-term warehousing, provided packaging methods follow lessons that chemistry plant workers develop through necessity. Achieving high purity, verified through chromatographic analysis and stringent laboratory calibration, eliminates the guesswork common among products prepared without attention to subtle batch variations.

    Use Cases: Perspective from Factory Applications

    Over years in a plant environment, engineers and chemists often remark that methyl 3-amino-4-methylbenzoate remains the compound of choice for certain downstream transformations. In practice, it anchors many synthetic routes, especially when constructing larger molecules for pharmaceutical development or agrochemical studies. The amino group brings reactivity, essential for versatile coupling reactions and functional group manipulations that stand up to scrutiny during scale-up.

    Routine feedback from R&D teams describes the convenience of the methyl ester group in this molecule. During many workups, it resists hydrolysis and oxidation, allowing clean isolation from organic extractions and less need for modification. Our production technicians address questions regarding solubility for particular solvent systems; years of handling point to its reliable performance across polar and nonpolar environments, which simplifies planning for laboratory protocols or plant-scale operations.

    From a process engineering viewpoint, methyl 3-amino-4-methylbenzoate interacts with common reagents—acid chlorides, anhydrides, boronic acids—and the expected product consistency cuts down on both rework and waste disposal. Examples drawn from on-site discussions show that even small improvements in crystal habit or filtration time can deliver real cost savings over the course of hundreds of kilograms produced. Ultimately, these process attributes help researchers and manufacturers unify discovery chemistry with pragmatic industrial practice.

    Differences That Matter: Standing Apart from Other Benzoates

    Chemical manufacturers are used to seeing many benzoate derivatives come across the plant floor, each bearing subtle variations in their structure. Still, not all methyl amino methylbenzoates behave the same. Small changes in substitution bring out big differences in reactivity, solubility, and even stability under process stress. For methyl 3-amino-4-methylbenzoate, the unique placement of amino and methyl groups on the benzene ring shapes both the chemical reactivity and physical handling in ways that set it apart from structurally similar products.

    Repeated experience with similar compounds has shown that ortho or para substitutions often produce products with less straightforward reactivity in further steps. Purification routines for regioisomers can introduce extra layers of complexity, especially if byproducts closely resemble desired material. Methyl 3-amino-4-methylbenzoate offers clean analytical profiles and easier separation, according to analytical chemists working in the final QC laboratory. The benefit to downstream users takes shape in shorter purification sequences, yielding both time and resource savings.

    Comparing related compounds, certain analogs with different alkyl or amino positions display less stability under even mild acid or base. This can lead to unwanted decomposition or impurity carryover, an issue that observers in technical manufacturing groups cite as a chronic source of customer complaints. Trial runs with various methylbenzoates clarify that our compound’s stability window remains broader than most alternatives, and feedback from scale-up chemistry teams underscores tangible differences. Ephemeral gains from using similar benzoates rarely translate into consistent, trouble-free production outside of a tightly controlled research environment.

    Specifications with a Purpose

    Specifications grow from both national and company standards, but years of shared experience among staff taught us to refine analytical methods. In practical terms, our finished material delivers above 99% purity as analyzed by high-resolution chromatography. Trace moisture levels get checked by Karl Fischer titration, and any deviation triggers in-plant review. Visual checks, melting point verification, and random sampling uphold quality. These hard-won habits ensure shipments conform batch after batch, regardless of seasonal changes.

    Standard particle size distribution fits the most-used applications in organic synthesis, and on request, custom sizing can be arranged for specialized needs. Our analytical specialists regularly engage with customer requests for impurity profiles that reach past standard paperwork. Drawing on plant experience, we share detailed certificates of analysis, built from years of trend data, rather than static or generic reporting. This openness lets customers plan their syntheses with greater confidence.

    Consistency Built from Real-World Experience

    Ongoing feedback from the field shapes how this product is handled and improved. Production managers note that strict lot traceability shortens troubleshooting times for both ourselves and our partners. Line workers build in safeguards for every stage—charge, filtration, drying, packaging. Laboratory chemists update reference libraries regularly to correlate every batch’s fingerprint with past production runs. This discipline, accumulated from lessons during routine and trouble periods alike, becomes the backbone of reliability in practical use.

    During disruptive events such as supply chain interruptions, production leads employ dual-sourcing for critical precursors, protecting availability for allies in pharmaceuticals and other specialty synthesis markets. Operating this way requires strong documentation, advanced process control, and systematically shared updates from both the laboratory and manufacturing floor staff. These methods shape market trust: over years, the number of customer audits passed without deviation speaks to the system’s strength.

    Impact on Modern Synthesis

    Methyl 3-amino-4-methylbenzoate continues to play a crucial part in modern synthetic chemistry. In pharmaceutical intermediate production, its structure acts as a template for building drug precursors, contributing to efficiency in multi-step synthesis. Interviews with process chemists from partner companies confirm they return to this compound for building blocks that must survive challenging reaction conditions. Agrochemical researchers apply it to route scouting, citing confidence in both availability and batch-to-batch consistency.

    This product: a proven performer in amide couplings, acylations, and Suzuki-Miyaura reactions. The ester group survives most reaction conditions intact, which allows multi-step modifications before final hydrolysis—making route planning more flexible for chemists. Peptide and fragment coupling in both pharmaceutical and material development benefit from predictable yields and minimal side reactions. The fine balance between reactivity and stability, measured through years on the production line, marks a difference from less-robust analogues. Real-world chemists cite cases where switching to alternative intermediates led to lower yield or more difficult purification.

    Handling and Practical Considerations Learned on the Floor

    Production staff keep close watch on packing and transfer to avoid unnecessary exposure to air and moisture. Pallets are stacked, and shipping containers are heat-sealed, based on lessons from older shipping incidents where exposure caused clumping or mild discoloration. Inbound customer visits often involve requests for demonstration in controlled laboratory handling—a request easily met thanks to familiarity and confidence with years of batch records.

    Routine equipment cleaning after batch runs, part of plant discipline, ensures no cross-contamination with other benzoate derivatives. Given that this compound’s application may include pharmaceutical synthesis, the cleanliness protocols follow standards appropriate for regulated end-markets. Document control forms part of every step, from receiving incoming materials through to final dispatch. These practices spring not just from regulation, but from direct experience troubleshooting minor issues before they become sources of non-conformance.

    Challenges and Solutions from an Operator’s Standpoint

    No production process runs free of challenges. Over the years, teams have worked through mechanical and chemical bottlenecks, equipment breakdowns, and even isolated power outages. During scale-up, particle size control surfaced as an initial point of trouble—handled through adoption of new filtration screens and better temperature ramping. Moisture ingress happened during several rainy seasons; solutions ranged from quicker transfer into sealed drums to upgraded dehumidification inside packaging rooms.

    Some users initially struggled with dissolution rates or cloudiness in extreme pH solutions. Experienced technical staff shared procedure tweaks, such as staged addition or intermediary solvent use, leading customers to overcome such setbacks without recurring support tickets. We learned that feedback loops, bridging technical and operator staff, help reduce process variability and shorten reaction optimization cycles.

    Opportunities Through Collaboration and Transparency

    Open channels with laboratory and production customers provide an ongoing stream of improvement ideas. Company scientists engage in pre-production trials, adjusting process parameters based on customer process constraints or analytical targets. We maintain records of real-time yield, impurity drift, and user outcomes to optimize each future batch, feeding lessons learned back into the daily workflow.

    This established relationship makes a difference. Analytical chemists, working both inside our plant and within partner organizations, exchange methodologies that focus on both regulatory needs and practical workflow constraints. In practice, this means faster response times if downstream users encounter questions or rare deviations. The commitment to continuous exchange ensures that finished material reflects not only technical specification but also incorporates lessons from live use cases.

    Conclusion: Advancing Chemistry Through Practiced Manufacturing

    The industry’s reliance on methyl 3-amino-4-methylbenzoate grows from a blend of technical merit and real-world practicality. The ability to manufacture in consistent, high-quality lots comes only from years of plant-floor vigilance and chemistry-driven refinement. Every day, plant operators, process chemists, and support staff bring a depth of practical experience matched by a respect for detail and a drive to improve. While technical data provides the foundation, it’s the collective lived knowledge—from the hands that batch, test, and package—that shapes this product’s continued value throughout the chemical industry.