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N-Methyl-2-Nitroaniline

    • Product Name N-Methyl-2-Nitroaniline
    • Alias 2-Methylamino-nitrobenzene
    • Einecs 202-815-1
    • 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

    334381

    Product Name N-Methyl-2-Nitroaniline
    Cas Number 612-28-2
    Molecular Formula C7H8N2O2
    Molecular Weight 152.15 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 77-80 °C
    Boiling Point 321.5 °C at 760 mmHg
    Density 1.305 g/cm³
    Solubility In Water Slightly soluble
    Flash Point 148 °C
    Purity Typically ≥98%
    Synonyms 2-Nitro-N-methylaniline
    Storage Conditions Store at room temperature, in a cool, dry place

    As an accredited N-Methyl-2-Nitroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250-gram amber glass bottle with screw cap; labeled with chemical name, formula, hazard warnings, and batch number for N-Methyl-2-Nitroaniline.
    Shipping N-Methyl-2-Nitroaniline should be shipped in tightly sealed containers, away from heat, sparks, and incompatible substances. Label packaging according to hazardous material regulations. Use appropriate hazard labeling; transport by approved couriers following local, national, and international chemical shipping laws. Ensure Material Safety Data Sheet (MSDS) accompanies the package for safe handling instructions.
    Storage N-Methyl-2-Nitroaniline should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers and acids. Protect from moisture and direct sunlight. Ensure proper labeling and store away from food and combustible substances. Use appropriate safety measures to avoid inhalation, ingestion, or skin contact.
    Application of N-Methyl-2-Nitroaniline

    Applications of N-Methyl-2-Nitroaniline in Industrial Manufacturing

    N-Methyl-2-Nitroaniline serves as a key intermediate for specialized chemical syntheses across a focused set of downstream industrial processes. Our manufacturing expertise ensures reliable supply for these real-world applications, all backed by strict adherence to compliance and quality protocols.

    1. High-Performance Dye Intermediates for Textile Manufacturing

    N-Methyl-2-Nitroaniline acts as a crucial intermediate for synthesizing azo and anthraquinone dyes, enabling textile producers to achieve targeted color fastness and thermal stability. It enters as a coupling component during diazotization and subsequent nucleophilic aromatic substitution steps. Adoption depends on batch-specific coloration needs, while the integration of our material meets sectoral processing timelines and formulation accuracy requirements to support bulk dyeing of cotton, polyester, and blended fabrics for clothing, home textiles, and technical applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 testing for restricted substances
    • ZDHC MRSL compliance for chemical input management
    • EU REACH Annex XVII for textile dyes
    • OECD Guideline 407 for toxicological assessment

    Typical usage ratio

    • 2%–6% weight by weight of final dye batch, adjusted by desired chromophore intensity and substrate affinity

    Downstream process integration

    • Added during coupling reaction at 40–70°C, typically following diazotization, then isolated before final dye blending

    Final product types

    • Reactive dyes for cellulosic fiber dyeing
    • Disperse dyes for synthetic textile spinning
    • Direct dyes for viscose and blended yarns
    • Anthraquinone-based specialty pigments for outdoor textiles

    2. API Intermediate in Pharmaceutical Synthesis

    Pharmaceutical producers employ N-Methyl-2-Nitroaniline for synthesizing active pharmaceutical ingredients in select anti-microbial and anti-tubercular drugs. The compound introduces a methyl-nitro functional group that undergoes further structural transformations, such as reduction and acylation, integral to forming the pharmacophore. Its use is tightly regulated under GMP systems, with exact ratios determined by target molecule yield and residual impurity profiles. In this domain, our GMP-audited production and transparent documentation ensure supply chain traceability and regulatory acceptance for finished formulations and generic bulk drug production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • EDQM Certificate of Suitability (CEP) framework for Europe
    • WHO TRS No. 986 Annex 2 for pharmaceutical excipients and intermediates

    Typical usage ratio

    • 0.5–1.5 molar equivalents per synthesis cycle, tailored by target API structural demands and waste minimization targets

    Downstream process integration

    • Charged into heterocyclic ring formation stage, following chlorination and prior to reduction or amide coupling

    Final product types

    • Bulk generic anti-mycobacterial drug actives
    • Specialty biocidal agents for hospital use
    • Custom contract-manufactured pharmaceutical intermediates
    • Research-grade chemical reference substances

    3. Agrochemical Precursor for Selective Herbicide Synthesis

    N-Methyl-2-Nitroaniline supports the agrochemical sector as a building block in the synthesis of selective herbicides containing nitroaniline-based substructures. Manufacturers use it for molecular frameworks requiring controlled electron density and tailored substituent positioning. Compliance with agricultural toxicology standards is critical as the material targets specific weed control mechanisms and minimizes non-target phytotoxicity. Precise molar ratios enable repeatable downstream conversions, supporting large-scale production of crop protection agents for regulated agricultural markets.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • US EPA 40 CFR Part 180 for residue analytical tolerance
    • ISO 9001:2015 production quality system
    • EU Regulation (EC) No 1107/2009 for plant protection product approval

    Typical usage ratio

    • 1.5–5% of total batch mass; varied according to molecular target and desired selectivity

    Downstream process integration

    • Introduced as a coupling reactant in the pre-condensation phase of herbicide synthesis, then reacted with acyl chloride or carbamate agents

    Final product types

    • Nitroaniline-derived pre-emergent herbicides
    • Selective broadleaf weed control agents
    • Granular and suspension concentrate pesticide formulations
    • Regulated raw materials for technical-grade agrochemicals

    4. High-Purity Intermediate for Electronic Materials

    The electronics sector adopts N-Methyl-2-Nitroaniline as a chemical precursor for specialty organic semiconductors and charge-transfer components in organic light-emitting diodes (OLEDs) and photovoltaic cell assembly. Precise molecular design demands reliable integration of methylaniline units, conferring tailored electron mobility and stability under device operation conditions. Purity and trace metal content are strictly monitored according to electronic grade standards, ensuring that downstream fabrication achieves stable crystal lattice incorporation and uniform electronic behavior in thin-film processing environments.

    Industry compliance standards

    • IPC-4101 standards for base materials in electronics
    • JEDEC JESD96 for material purity in semiconductor packaging
    • RoHS Directive 2011/65/EU for hazardous substances
    • ISO/TS 16949 for electronic component manufacturing

    Typical usage ratio

    • 0.8–2.5% by solution weight in monomer or oligomer blend processes, tuned according to device-specific bandgap and efficiency requirements

    Downstream process integration

    • Fed into coupling or cyclization step, post-metal catalysis, before solution-phase deposition onto substrates

    Final product types

    • Organic semiconductors for flexible electronics
    • OLED emissive and conductive layers
    • Photoactive organic photovoltaic compounds
    • Thin film transistors for display technologies
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    Certification & Compliance
    More Introduction

    N-Methyl-2-Nitroaniline: Precision Chemistry from the Manufacturer’s Bench

    Our Journey with N-Methyl-2-Nitroaniline

    After years in the synthesis business, one compound has consistently demanded attention in specialty chemical workshops: N-Methyl-2-Nitroaniline, sometimes labeled as 2-Nitro-N-methylaniline. Our team started working with it in the mid-90s, when regional dye producers began requesting more nuanced intermediates for their color libraries. Over time, as methods matured and applications widened, so did our expertise. Production lines underwent upgrades, filtration protocols tightened, and every step got tuned for reliability, batch after batch.

    Our plant operates day and night mixing the right raw materials—generally starting from 2-nitroaniline and methylating under careful conditions. You can’t just toss chemicals into a drum and hope for the best. Temperature, feed rates, cooling, and solvent selection decide the degree of methylation and overall yield. Our crews watch for off-coloration, handle recovery, and monitor each fraction. The solid product we draw from our reactors shows a light yellow crystalline appearance. Granular dust, dull brown hues, and stray oils reflect poor process discipline, and buyers learn quickly to tell the difference. Earning that repeat order depends on consistency.

    The Realities of Model, Specifications, and Purity

    We manufacture N-Methyl-2-Nitroaniline with an industrial-grade purity standard, typically reaching upwards of 98%. Every batch runs through gas chromatography to check for residue aniline, methylation byproducts, and any signs of over-nitration. Melt point and color give us fast clues if something went wrong, but spectral analysis remains the backbone of clear identification. Over the years, we encountered buyers seeking slightly higher or lower granularity, but most customers in colorant, pharmaceutical, and research sectors ask for the crystalline material—free-flowing and robust, with low moisture content for reliable downstream processing.

    A few years back, we had a large volume request from a pigment manufacturer seeking the compound in the form of a fine powder. After a few months fine-tuning the particle size reduction and controlling agglomeration in our mills, we landed on a form that didn’t clump during transit and blended smoothly at customer lines. That experience proved that even with a “fixed” product, small changes in granule size, color, and purity can create real headaches—or smooth things out for a client’s batch-to-batch operations.

    Where N-Methyl-2-Nitroaniline Finds Its Purpose

    Most chemists recognize the role of N-Methyl-2-Nitroaniline as a trusted intermediate in the synthesis of organic colorants—especially in the production of certain azo dyes. The compound’s methyl group blocks further unwanted reaction at the nitrogen, making its downstream behaviour much more predictable than other nitroaniline variants. It works as a starting point for coupling reactions, where other more volatile nitroaromatics just gunk up vessels or react unpredictably after the first condensation.

    Some research teams leverage this molecule when tailoring new pharmacophores, exploring the impact of the nitro and methyl arrangement on biological activities. For those working outside pigment chemistry, the compound’s physicochemical stability allows scientists to manipulate its framework, test hydrogenation or substitution protocols, and make modifications that stick. That reliability turns out to be the cornerstone for reproducible synthesis routes.

    We supply N-Methyl-2-Nitroaniline to those building advanced analytical reference standards as well. Because our product traces precisely to a reproducible melt point and clean spectral profile, researchers can count on it as a dependable check for method calibration. That becomes indispensable for quality control labs tasked with testing for trace residues or variants in final products.

    How Our Product Stands Apart from Other Nitroanilines

    Manufacturers often ask if there’s a meaningful difference between N-Methyl-2-Nitroaniline and its sibling compounds. The distinction lies in the characteristics the methyl group brings to the molecule. While 2-Nitroaniline gives a higher degree of reactivity in some conditions, unwanted oxidation, side reactions, and product variability show up more frequently. Switching to the N-methyl analog smooths out those problems, providing a more robust performance in syntheses where selectivity matters.

    Another common comparison comes with 4-nitroaniline or mixtures of substituted anilines. Those alternatives react at different positions, creating unpredictability in dye shading or pharmaceutical backbone efficiency. Our product locks the configuration: substitution remains exact, and performance shifts less from batch to batch, which is exactly what large-volume customers in the dye sector need. It’s the molecular predictability—achieved through diligent plant monitoring—that drives repeat business.

    From our operational perspective, N-Methyl-2-Nitroaniline stores without notable decomposition or agglomeration under ordinary chemical warehouse conditions. In contrast, some nitroaromatics develop color shifts or caking problems that frustrate formulation chemists. We address those by controlling drying, packing under inert gas when needed, and shipping in heavy-gauge containers to avoid ambient moisture pick-up or temperature-related degradation.

    Finally, our team tracks transport requirements closely. Some commercial nitro compounds fall under regulated categories for reactivity or toxicity, and we track hazard classes and label protocols to avoid unwanted surprises at customs or checkpoints. We document every run, not just for regulatory reasons but to keep our process improvements on a feedback loop—so trends don’t go unnoticed until they turn into full-blown production issues.

    Customer Conversations and Application Experience

    Direct conversations with clients, whether large pigment manufacturers or research teams at universities, often lead to incremental product refinements. Late last year, a specialty dye producer flagged an inconsistency in tone that appeared during their pilot batch runs. Through a collaborative audit of our manufacturing and their downstream processing, we isolated a micro-impurity in the recycled solvent—something that had gone undetected in standard purity assays. By looping our findings back into the plant’s solvent handling protocols, we corrected the issue for all subsequent batches, not only strengthening customer trust but tightening our quality systems.

    We’ve had orders from pilot-scale pharmaceutical shops looking for key intermediates with a tightly controlled spectral fingerprint. Pharmaceutical quality demands extra steps: an emphasis on batch-to-batch documentation, validation of all input chemicals, and full transparency around origin and traceability. While industrial-grade N-Methyl-2-Nitroaniline supplies most dye houses, higher scrutiny in the pharmaceutical sector means we must certify every analytical parameter before shipping. It’s the same molecule at its core, but the discipline in production and paperwork reflects the real difference.

    Some research labs bring up questions about solvent compatibility and byproduct formation at scale. The early days taught us that switching extraction solvents—even something as simple as replacing ethanol with methanol—shifts the purity and sometimes introduces trace levels of methyl ethers or altered nitro isomers. These nuances don’t always show up in generic chemical specs, but customers who scale up from 0.5 kg to 50 kg quickly chase down any change in their process outcomes. Only direct, technical exchange about those route-specific concerns solves such issues, and we keep our technical support line staffed with trained lab workers who know the chemistry firsthand.

    Production Challenges and Plant Adaptation

    The synthesis of N-Methyl-2-Nitroaniline doesn’t leave much room for improvisation. Many of our staff have seen what happens when cooling rates slip or if the methylation step exceeds target temperatures: runaway side reactions, colored residues, and diminished product yields. Production teams cross-check process conditions batch by batch, with inline temperature tracking and dedicated batches for cleanup at the end of multi-ton runs. Avoiding downtime means anticipating fouling and preemptively cleaning up process lines, valves, and crystallization vessels, long before they turn into problems.

    We found that seemingly small operational shifts—such as ambient humidity during crystallization or container lining material—can introduce variability in finished product color or flow. A few years ago, we switched to corrosion-resistant reactor linings and double-fitted drying ovens—those changes helped us keep both product and workplace compliance reliable even during high-volume campaigns. The manufacturing journey now emphasizes steady-state operation; equipment upgrades, skilled hands, and a steady feedback loop between QC and plant floors all underwrite the final product’s integrity.

    Patching Weak Points and Ensuring Safety

    As with most aromatic nitro compounds, workplace safety ranks high on our daily agenda. Adequate ventilation, strict exclusion of open flames or hot spots, and regular air monitoring form the backbone of our occupational safety program. Staff handling the powder wear personal protective equipment, even with our containment upgrades that have minimized exposure risk. We routinely test air, monitor dust levels, and code of practice guides every reactor cleanout.

    Plants outside regulatory environments sometimes take shortcuts, but we have learned from hard-won experience that one overlooked spill or under-maintained scrubber can set operations back weeks. Keeping compliance current and training rotating shifts isn’t easy, yet it pays off every time we pass an external safety audit or when a client requests proof of handling procedures before placing an order.

    Waste management has also evolved. Regulations around aromatic nitro compound effluents tightened across global markets, prompting changes to our in-plant neutralization and collection methods. Our team now manages all spent wash and filtrate streams through isolation and treatment units, separating hazardous organics before release or reuse. This closed-loop handling reduces both risk and environmental impact, reinforcing the responsibility we feel toward staff and community alike.

    Collaborative Evolution: Meeting Market and Regulatory Pressures

    Demand for N-Methyl-2-Nitroaniline fluctuates with global colorant trends, regulatory phase-ins, and innovation in molecular drug development. Our planning team keeps tabs on both historical usage patterns and fresh scientific literature to anticipate where the next growth opportunity or supply crunch might land. Market interruptions abroad—such as sudden clampdowns on upstream aniline derivatives—can spike lead times, so we keep safety stocks aligned to realistic sales forecasts.

    On the documentation side, our product ships with a full delivery certificate, spectral data, and batch origin tracking. International customers, especially those exporting to Europe or North America, often demand proof of regulatory clearances and absence of banned byproducts—especially those flagged by REACH and other chemical safety frameworks. We keep tabs on regulatory shifts that might affect acceptable nitroaromatic content, running targeted tests and updating client documentation to ensure nobody gets entangled in compliance headaches after receipt.

    The market has also shifted toward supplier transparency, with buyers increasingly requesting production histories and environmental reporting. Our facility tracks emissions, solvent usage, and overall plant energy through quarterly audits. Customers buying N-Methyl-2-Nitroaniline not only want assurances about purity and consistency, they seek a supply chain partner that backs up claims with facts. That level of openness not only strengthens our relationships but helps us iterate and improve.

    Looking Ahead: Innovation and Opportunity

    We believe that the true future of N-Methyl-2-Nitroaniline will involve collaboration at the technology and process level. We invest in R&D committed to greener methylation alternatives, aiming to scale up processes that cut waste, improve worker safety, and reduce environmental impact without sacrificing product quality. Plant teams trial emerging catalysts or new reactor designs, sharing technical learnings back with industry groups to push standards forward for everyone using this material.

    Beyond dyes and research, the world’s growing demand for specialty chemicals has opened up fresh uses: functional materials, specialty resins, and as intermediates in custom pharmaceuticals. With every ton we manufacture, there’s an opportunity to improve—not only for our bottom line, but for the quality and reliability of products passing from our hands to the hands of others downstream. Our technical support doesn’t end at shipment; we train, troubleshoot, and respond as customers face their own challenges downstream, recognizing that our reputation arrives at their loading dock alongside every drum or tote we ship.

    In a rapidly evolving chemical world, N-Methyl-2-Nitroaniline remains a reference compound—a point of stability for those seeking quality, pedigree, and a partner who knows the real stories and challenges behind every container. The work never stops, and neither does our commitment to raising standards for ourselves and everyone we supply.