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4-Methyl-3-Nitrobenzoic Acid Methyl Ester

    • Product Name 4-Methyl-3-Nitrobenzoic Acid Methyl Ester
    • Alias Methyl 4-methyl-3-nitrobenzoate
    • Einecs 629-616-8
    • 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
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    Specifications

    HS Code

    657693

    Product Name 4-Methyl-3-Nitrobenzoic Acid Methyl Ester
    Synonyms Methyl 4-methyl-3-nitrobenzoate
    Chemical Formula C9H9NO4
    Cas Number 83841-46-9
    Appearance Yellow crystalline solid
    Melting Point 66-70°C
    Purity Typically >98%
    Solubility Soluble in organic solvents such as ethanol and acetone
    Smiles CC1=CC(=C(C=C1)[N+](=O)[O-])C(=O)OC
    Storage Conditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled "4-Methyl-3-Nitrobenzoic Acid Methyl Ester, analytical grade."
    Shipping 4-Methyl-3-Nitrobenzoic Acid Methyl Ester is shipped in tightly sealed containers to prevent moisture and contamination. It is typically transported as a solid at ambient temperature. The package is clearly labeled with hazard warnings, and shipping complies with relevant chemical safety and regulatory guidelines, ensuring safe handling during transit.
    Storage 4-Methyl-3-Nitrobenzoic Acid Methyl Ester should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, moisture, and incompatible substances such as strong oxidizing agents. Keep the chemical at room temperature and avoid excessive heat. Ensure proper labeling and store away from food and drink to prevent accidental ingestion or contamination.
    Application of 4-Methyl-3-Nitrobenzoic Acid Methyl Ester

    Applications of 4-Methyl-3-Nitrobenzoic Acid Methyl Ester in Industrial Manufacturing

    4-Methyl-3-Nitrobenzoic Acid Methyl Ester is primarily used in specialized chemical synthesis industries where precise control of functional groups and reactivity underpin the production of advanced intermediates. Below, we detail key downstream sectors and practical integration insights.

    1. Pharmaceutical Intermediate Synthesis

    Dedicated process chemists use this ester as a critical intermediate in manufacturing selective pharmaceutical APIs, particularly for anti-inflammatory and CNS-active drugs. Its methyl and nitro substitutions facilitate regioselective transformations, including reduction, hydrolysis, and cross-coupling steps, often determining yield and purity during scale-up. Production facilities incorporate this material into protected reactions to ensure isolation of high-purity intermediates. Traceability and process validation align with core pharma manufacturing and regulatory frameworks, addressing both export and local registration standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA cGMP 21 CFR Parts 210 and 211
    • European Pharmacopoeia 11.0 monographs for chemical intermediates
    • EDQM TSE and impurity control guidance

    Typical usage ratio

    • Applied at 0.35–0.65 molar equivalents relative to final API batch, subject to specific synthesis pathway requirements and yield optimization studies

    Downstream process integration

    • Enter at Stage 2 or Stage 3 in the multi-step API synthesis, following initial acylation or nitration; subsequent demethylation or amidation steps follow, monitored through in-process HPLC or GC analysis

    Final product types

    • Pain management medications (e.g., nonsteroidal anti-inflammatory drugs)
    • Neuroactive therapeutic bulk substances
    • Specialty intermediates for research-grade compounds

    2. Agrochemical Synthesis

    Formulators in crop protection and seed care industries utilize this compound as a scaffold in the development of selective herbicide and fungicide actives. Nitrated aromatics from this ester undergo customized transformations, including reduction and methyl group manipulations, to introduce biologically active moieties. Continuous processing units featuring containment and QA controls ensure that reaction pathways remain consistent and safe, supporting downstream registration of finished agrochemical actives.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for agrochemical intermediates
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • US EPA 40 CFR Part 172 Experimental Use Permits guidance
    • OECD Guidance Document on Residues in Rotational Crops

    Typical usage ratio

    • Amounts vary by product, commonly 0.4–0.6 molar equivalents per target molecule; fine-tuned based on active-site substitution pattern dictated by field test efficacy and toxicology reports

    Downstream process integration

    • Used in the condensation and heterocyclization phase after aromatic nitration; processed in jacketed reactors with automated dosing systems

    Final product types

    • Triazine-based pre-emergence herbicides
    • Novel broadleaf crop fungicides
    • Seed coating actives for disease suppression

    3. Specialty Dye and Pigment Manufacturing

    Technical teams in specialty dye houses integrate this ester as a functionalized aromatic building block to achieve target chromophores with enhanced stability and colorfastness. The presence of methyl and nitro groups enables selective substitution reactions, critical for batch-to-batch reproducibility and spectrum control. Manufacturing is performed in closed systems to ensure minimal environmental impact and maximal process yield, with test samples analyzed for hue, brilliance, and application consistency.

    Industry compliance standards

    • REACH Registration (EC) No 1907/2006 for dye chemical import
    • ISO 9001:2015 certified pigment synthesis protocols
    • Oeko-Tex Standard 100 for restricted substances in dyes
    • EN 71-3 migration standards for pigments in toys

    Typical usage ratio

    • Formulations typically include 0.1–0.3 moles per mole of target chromophore; ratio adjusted per color intensity specifications or end-user application method (e.g., dispersion or solution dyes)

    Downstream process integration

    • Incorporated at the azo coupling or nitro reduction stage during pigment synthesis, followed by sulfonation or alkylation as needed for final pigment quality

    Final product types

    • Azo and anthraquinone textile dyes
    • High-performance printing inks
    • Color-stable coating pigments

    4. Advanced Polymer Additives Production

    Researchers and process developers in plastics and resins manufacturing deploy the ester as a specialty monomer precursor or functional additive to introduce precise aromatic structures with tailored properties. Its reactivity supports synthesis of heat-resistant and UV-stable polymers used in demanding applications such as automotive parts and high-spec films. The controlled addition process ensures that the final polymer chain structure delivers the intended performance in end-use conditions, with robust inline QC for specification adherence.

    Industry compliance standards

    • ISO 14001:2015 for polymer manufacturing environmental management
    • ASTM D638 standard for tensile properties of plastics
    • UL 94 flammability rating for plastic materials
    • FDA 21 CFR 177.1520 for resins in food contact (where applicable)

    Typical usage ratio

    • Ranges from 0.5–2.5% by weight of total monomer feed; adjusted for intended mechanical and chemical properties after pilot extrusion and molding trials

    Downstream process integration

    • Added during monomer solution blending or fed into the reactive extrusion zone, followed by copolymerization or direct compounding

    Final product types

    • Engineering-grade polyesters and polyamides
    • High-durability automotive interiors
    • UV-stabilized optical films and specialty sheets

    5. Fine Organic Chemical Manufacturing

    Specialty organic chemical producers employ this compound as a selective starting material for synthesizing rare functionalized aromatic acids, esters, and amides. Its substitution pattern permits downstream access to custom molecules used in catalyst design, specialty solvents, and biochemical probes. Production lines run flexibility batches, scaling from pilot to commercial volumes, with tight yield monitoring and impurity tracking.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for specialty chemical production
    • Responsible Care® chemical management practices
    • Custom synthesis NDA and IP protection policies
    • Applicable local chemical control regulations

    Typical usage ratio

    • Employed at 1.0–1.2 molar equivalents relative to final specialty molecule; variation based on contract synthesis specification and byproduct profile

    Downstream process integration

    • Introduced during the alkylation, esterification, or reductive amination stage, after initial aromatic functionalization loop

    Final product types

    • Custom organic intermediates for pharma research
    • Catalyst ligands for advanced synthesis
    • Functional probe molecules for analytical chemistry
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    Certification & Compliance
    More Introduction

    Introducing 4-Methyl-3-Nitrobenzoic Acid Methyl Ester: A Manufacturer’s Perspective

    A Glimpse Inside the Production Floor

    Every batch of 4-Methyl-3-Nitrobenzoic Acid Methyl Ester starts its journey from carefully sourced raw materials. From the very beginning, we understand that a chemical isn’t just a formula printed on paper. It represents years of accumulated skill, investment, and attention to process detail. The decisions we make on our floor—stirring rate, temperature control, careful monitoring of pressure—shape more than just output; they determine final product character and reliability. Our team has dealt with the quirks and nuances of this compound throughout countless cycles, so that those opening a drum or flask of our methyl ester see the snow-white to light yellow crystals they expect. Every kilogram reflects not just our method, but our long-standing dedication to getting the chemistry right for real-world application.

    Model and Batch Reference

    Inside our plant, we refer to this product under its standard chemical name, but on the shop floor it’s sometimes just called “4M3N methyl ester” out of habit. Models and codes matter more for logistics and lab tracking than for hands-on synthesis. Workers trust the color, purity, and density checks—they don’t wait for a model number to tell them what’s in the flask. In one of our earlier years, we had to overhaul a crystallization process because a small change in cooling led to lower flow and a less pure yield; that bottleneck taught us how subtle process details can ripple through all subsequent steps, ultimately impacting the downstream customer.

    Specifications: What the Numbers Mean on a Day-to-Day Basis

    Industry customers often approach us asking for “specs.” Numbers such as purity (above 98 percent GC, wherever possible), melt point, infrared spectrum data—those headlines matter. But our team knows true value shows up in hidden ways. We employ thin-layer chromatography and HPLC to catch impurities invisible to basic spot tests, and make it routine to compare spectral readings across batches. Sustainability matters too, so we minimize solvent residues and monitor energy usage, fine-tuning each cycle to get the smallest practical waste stream without sacrificing output per shift.

    Lab data for the ester shows a melting range that consistently hovers between 65 - 67°C, which indicates the careful control at each stage of crystallization and drying. Experienced workers can identify an off-spec batch at a glance—even before the instrument readout flashes a warning—by the subtle differences in crystal habit or color. Elemental analysis regularly confirms composition because our customers in pharmaceuticals, dyes, or advanced materials projects expect nothing less. If we notice abnormal readings—such as a slightly sharper yellow tint—QA steps in to find the root cause promptly. For example, a trace impurity, which might slip by in less stringent settings, triggers a review of solvent quality and reactor seals on our line.

    Why End-Users Value This Methyl Ester

    People look for this ester when they need both versatility and reliability. Most chemists haven’t forgotten long nights spent troubleshooting mystery impurities or chasing elusive by-products. That’s why this compound’s sharp, reproducible NMR signature and simple hydrolysis make it a backbone for further conversions. In our own experience, it serves as a useful building block connecting to so many downstream targets—esters, acids, or amides. The fact that it dissolves well in many common organic solvents gives it an accessibility edge over bulkier, less agile intermediates.

    A lot of research teams depend on this methyl ester as a protected acid, easing them through crucial synthesis steps while shielding sensitive positions from unwanted side reactions. Project leads have shared plenty of stories about projects derailed by difficult purifications; our product’s selective crystallization, combined with minimal colored impurities, keeps columns running cleaner and allows more rapid scale-up. These workday realities matter far more than painted-up catalog promises.

    Technical Advantages on the Bench—And On the Floor

    Comparing this product to standard methyl benzoate, the presence of both the methyl and nitro substitutions in the 4- and 3-positions provides key reactivity shifts. Experienced bench chemists exploit this for regioselective transformations or to steer catalytic aromatic substitutions. We’ve collaborated with development groups working in heterocycle synthesis or specialty pigment manufacture—areas where control over electron density can make or break a program. Years ago, a customer needed predictable nitration at a complex aromatic site; having the right substituents in place saved weeks of lab work. These are the kinds of invisible advantages built into every lot we ship.

    On the plant level, improved filterability and lower tendency to cake during drying mean faster lot turnover. Operators know that a stubborn, sticky crystal mass creates both a hazard and a timing headache; getting this methyl ester to solidify clean and free-flowing reflects daily trial, error, and optimization. The slightly lower melting point as compared with some ortho- or para- substituted analogs means less energy required on melting or melt-transfer operations—a detail that adds up to significant utility savings over a year’s production.

    Key Differences from Competing Esters

    Some customers ask us to help distinguish our 4-methyl-3-nitrobenzoic acid methyl ester from the more common, unsubstituted methyl benzoate. The answer goes beyond a single substitution. The nitro group at the meta position and the methyl at the para direct both physical character and downstream chemistry. We’ve noticed time and again that the electron-withdrawing character of the nitro unit suppresses side reactions during base-promoted hydrolysis, so customers report higher yields and purer material in their subsequent steps. The methyl group can also offer a subtle dampening effect in certain oxidation or reduction conditions.

    A less obvious distinction occurs in chromatographic separations. Techs working in our labs and at our customer’s sites often tell us that even under nearly identical conditions, our product produces less baseline noise and clearer separation from by-products. This makes scale-up and purification steps smoother, reduces solvent usage, and lessens environmental impact. Unlike heavier esters or those with bulkier side groups—often prone to dramatic shifts in solubility—this methyl ester works well in a broad range of organic conditions, which supports its popularity.

    End-Use Applications: Stories and Experience

    Our own experience in scaling up this compound gave us unique insight into its utility across sectors. Early batches supported specialty dye manufacture—where only high-purity intermediates meet demanding colorfastness and light resistance specifications. Later, we became part of a pharmaceutical client’s journey toward a new anti-inflammatory candidate. They needed consistent, impurity-free supply at a kilo scale, so we expanded capacity, upgraded filtration equipment, and implemented advanced in-line process analytics. The impact was tangible—reduced batch failures, faster registration, and fewer disruptions in downstream pilot plant work.

    Materials scientists, especially those developing advanced polymers or functional materials, value our product’s blend of low residual solvent and predictable melting point. In those settings, small compositional shifts or trace contaminants can lead to costly reprocessing or even outright product scrapping. We once fielded a call from a battery manufacturer who wanted to test aromatic esters as part of an electrolyte stabilization program. Our team moved fast, developing a custom drying protocol that slashed residual moisture and met the customer’s strictest trace metal specs. The positive relationship built from that first trial persists to this day.

    In the academic sector, graduate students lean on our product for teaching and research. The compound’s clear melting behavior and manageable handling properties allow less-experienced operators to avoid common pitfalls like oiling out or sublimation losses. Our team sometimes leads informal seminars on best practices for storage and transfer, fostering better habits and higher yields even outside the commercial world.

    Sustainability, Health, and Stewardship

    We pay more attention than ever before to the full life cycle of our methyl ester. Earlier habits from the chemical industry—dumping waste streams, ignoring air emissions—no longer cut it. A focus on controlled waste reduction and resource recovery shapes how we approach each synthesis run. On the plant floor, solvent reuse is tightly monitored; our evaporators track vapor loss rates, and maintenance logs show frequent upgrades to minimize leaks and losses. This not only preserves air and water quality but keeps costs under control through smarter resource management.

    Health and safety drive our layout and daily practice. Peer review of batch sheets, careful PPE policies, regular training, and open-door communication with supervisory chemists help set the tone. Everyone on the floor knows that preventing exposure—whether to solvent vapors, dust, or splash—is about protecting people, not just complying with a checklist. If a near-miss or hazard is detected, corrective action follows the same day. No product is produced at the cost of worker safety.

    We also communicate with transporters and downstream handlers about labeling and secure storage recommendations. Time-tested shipping containers, clear labeling and twenty-four hour access to technical information help our partners avoid mishaps not just on our site, but through every handoff.

    Traceability, Quality, and Upgrading

    Every drum and bottle of 4-methyl-3-nitrobenzoic acid methyl ester leaving our site is mapped back through detailed batch and reactor logs. Each lot number connects to raw material intake, reactor charge sequence, and operator who signed off on each critical stage. As our experience deepened, software support for traceability replaced hand-written logs alone. This means audit trails run deep and respond quickly to regulatory and customer inquiries.

    Continuous improvement isn’t just a phrase for us. As we receive customer feedback, our technical and production teams analyze, adapt, and implement. Last year, after receiving several requests for higher flowability in large-scale packaging, we worked out a new drying and anti-caking protocol. Material shipped since then meets both handling and use-site demands for faster transfer, less bridging, and easier manipulation. Energy and resource usage are calculated per batch, so we see in real time how changes affect both cost and environmental impact.

    Regulatory Standards and Global Consistency

    Regulatory compliance is part of the daily rhythm here. From raw material selection, through finished product testing, to export documentation, everything is carried out according to global, regional, and sector standards. We track and comply with REACH, US EPA, and Asian regulatory pathways as needed—never assuming that “almost compliant” is good enough. When documentation requirements shift, our teams meet early and often to develop, validate, and communicate updates to partners.

    Global shipping has shown us the importance of stability and reliable packaging. While weather conditions may fluctuate across continents, quality must hold steady. Field feedback sometimes highlights issues like clumping in high humidity or settlement after prolonged transport. Over the years, this informed changes in liner selection, vessel washing, and drum sealing before product release. The end-result is that whether the product is used in Sweden or Singapore, it performs in line with what our procedural controls intend.

    Future Directions: Listening to Customer Needs

    Each year pulls new uses and requirements into focus, whether from green chemistry advocates looking to minimize solvent use, or from fine chemicals manufacturers chasing tighter trace metal specs. Our R&D group pulls together cross-functional teams to pre-emptively test process tweaks. Through regular surveys and direct customer interviews, we stay ahead of the curve on needs for lower environmental footprint, improved selectivity in downstream transformation, or better thermal stability under demanding process conditions.

    Working closely with innovators means shorter response cycles and a constant urge to challenge our own standard operating procedures. Lessons learned from past scale-up hiccups—whether from batch batch inconsistency, crystal form, or filtration issues—continue to inform our daily operations. We share these lessons with customers through technical notes and informal visits, because mutual understanding reduces friction and speeds up innovation for both sides.

    Transparency and Collaboration—The Manufacturer’s Link

    Every batch, sample, and drum we produce reflects both what we know and how we listen. Most customers don’t just want a reagent—they look for a predictable, honest partner. Our doors are open for those who want to see the process behind the product, ask tough questions about process chemistry or root cause analysis, or push us to reach higher standards. Real experience, built up one shift and one cycle at a time, separates a consistent supply partner from a generic ingredient list.