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3-Methyl-4-Nitroaniline

    • Product Name 3-Methyl-4-Nitroaniline
    • Alias 3-Methyl-4-nitroaniline
    • Einecs 221-636-1
    • 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

    567461

    Cas Number 618-90-6
    Molecular Formula C7H8N2O2
    Molecular Weight 152.15
    Appearance Yellow to orange crystalline powder
    Melting Point 133-137°C
    Boiling Point Unknown
    Solubility In Water Slightly soluble
    Density 1.263 g/cm³
    Purity Typically >98%
    Synonyms 2-Amino-5-methylnitrobenzene
    Ec Number 210-580-5
    Storage Conditions Store at room temperature, protected from light and moisture

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

    Packing & Storage
    Packing The packaging is an amber glass bottle containing 25 grams of 3-Methyl-4-Nitroaniline, labeled with hazard and identification information.
    Shipping **Shipping Description for 3-Methyl-4-Nitroaniline:** 3-Methyl-4-Nitroaniline should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be clearly labeled, handled with proper hazard precautions, and accompanied by safety documentation. Ship via ground or air in accordance with relevant chemical transport regulations, such as DOT, IATA, or IMDG guidelines.
    Storage 3-Methyl-4-nitroaniline should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. It must be kept separate from incompatible materials such as strong oxidizers and acids. Store the chemical in a clearly labeled container, following all relevant safety regulations and guidelines for handling hazardous substances.
    Application of 3-Methyl-4-Nitroaniline

    Applications of 3-Methyl-4-Nitroaniline in Industrial Manufacturing

    As a committed manufacturer of 3-Methyl-4-Nitroaniline, we focus on delivering consistently high-quality raw materials for key industrial sectors. Our product supports specialized chemical synthesis processes, providing reliable performance in downstream production lines for intermediates, dyes, pigments, and pharmaceutical raw materials. Below, we detail the major application scenarios based on direct feedback and process specifications from our industrial partners.

    1. Synthesis of Azo Dyes for Textile and Leather Processing

    Large-scale textile and leather producers formulate azo dyes using 3-Methyl-4-Nitroaniline as a diazo component. Its unique electron-donating and withdrawing groups facilitate rapid coupling reactions, improving chroma strength and wash fastness in finished fibers and hides. The material undergoes rigorous inspection to meet major market requirements for restricted aromatic amines and finished-goods purity, supporting continuous-dyeing and batch coloration lines in export operations.

    Industry compliance standards

    • EU REACH Regulation (EC 1907/2006) on aromatic amines
    • OEKO-TEX® Standard 100 for textile safety
    • ZDHC MRSL v3.1 (Zero Discharge of Hazardous Chemicals)
    • GB 18401—2010/National General Safety Technical Code for Textile Products (China)

    Typical usage ratio

    • 1.2%–3.8% w/w based on dyestuff batch mass, adjusted depending on target chromaticity and substrate compatibility

    Downstream process integration

    • Introduced in diazotization stage, followed by coupling with phenolic or naphthyl intermediates before drying and blending into granulated or paste dye formulations

    Final product types

    • Reactive dyes for cotton and viscose
    • Direct dyes for wool and silk
    • Azo pigment preparations for leather tanneries

    2. Production of High-Performance Pigments for Coatings

    Advanced pigment manufacturers use 3-Methyl-4-Nitroaniline as a critical intermediate for synthesizing durable, lightfast yellow and orange pigments, especially for automotive and industrial coatings. The compound’s molecular structure enhances pigment stability, color intensity, and dispersibility in both solvent-based and waterborne resin matrices. Consistent input purity is needed to guarantee no regulated amine byproducts persist in commercial pigment dispersions.

    Industry compliance standards

    • ASTM D3722 (Standard Specification for Pigments for Paints)
    • EN 71-3:2021 (Safety of toys – migration of certain elements, including azo compounds in pigments)
    • RoHS Directive (EU Restriction of Hazardous Substances)
    • ISO 9001:2015 certified QC protocols in pigment preparation

    Typical usage ratio

    • 2.0%–5.5% of total pigment intermediate recipe, fine-tuned according to final chroma strength and environmental durability requirements

    Downstream process integration

    • Added during synthesis of azo pigment molecules, preceding condensation and milling into micronized filter cakes or slurry dispersions

    Final product types

    • Organic pigments for automotive coatings
    • Printing ink dispersions (yellow/orange shades)
    • Industrial anti-corrosive paint colorants

    3. Pharmaceutical Intermediate in Active Compound Synthesis

    API and intermediate manufacturers select 3-Methyl-4-Nitroaniline as a site-selective building block when synthesizing specific classes of active pharmaceutical ingredients (APIs), particularly those containing aromatic nitroaniline motifs in antibacterial, antitubercular, or CNS drug scaffolds. The high reactivity of its nitro group enables precise reduction and subsequent substitution with controlled yields, serving critical GMP processes where trace level impurities are monitored under regulatory supervision.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF and EP standards for process impurities
    • Chinese Pharmacopoeia (ChP): Section for fine chemicals used in prescription intermediates
    • FDA 21 CFR Part 210/211 compliance for bulk intermediates

    Typical usage ratio

    • 1.0–1.6 equivalents relative to the primary aromatic precursor, specific to stepwise intermediate conversion yield management

    Downstream process integration

    • Charged to selective nitration or reductive substitution stage, followed by purification, crystallization, and transfer to API isolation lines

    Final product types

    • Pharmaceutical grade intermediates for antituberculars
    • Sulfonamide precursor molecules
    • Bulk intermediates for CNS or anti-infective APIs

    4. Synthesis of Agrochemical Intermediates

    Producers of crop-protection actives integrate 3-Methyl-4-Nitroaniline into synthesis routes for select herbicide and fungicide molecules. The compound’s controlled reactivity streamlines multi-step functional group transformations, necessary for constructing heterocyclic ring systems and specific azo-containing pesticide backbones. Input purity and supply chain traceability uphold regulatory registrations and environmental impact scrutiny for farm-use formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides Quality Control
    • ISO 17025 accredited laboratory analytics
    • EPA FIFRA requirements for intermediate tracking (USA)
    • REACH chemical safety assessments for downstream use

    Typical usage ratio

    • 0.8%–2.4% of total intermediate formulation volume, modulated for target molecule synthesis efficiency and cost optimization

    Downstream process integration

    • Fed into condensation or ring-formation reactors as a core substrate, with subsequent stages for functionalization, hydrolysis, and formulation concentration

    Final product types

    • Key intermediates for selective herbicides
    • Technical grade active ingredients for fungicide synthesis
    • Pesticide formulation intermediates for bulk export

    5. Color-Forming Compounds in Photographic Chemicals

    Specialty photographic chemical suppliers utilize 3-Methyl-4-Nitroaniline in formulating couplers and developers for analog film and photo processing. Its chemical stability and reactivity allow consistent performance across temperature and pH variations in developer tanks, supporting predictable image formation and tone control on high-resolution photographic films. Strict screening during incoming QC ensures compliance with purity and toxics standards for photographic use.

    Industry compliance standards

    • ISO 9001-based quality systems for fine chemical processing
    • ANSI/NAPM IT9.1 standard for photographic film processing chemicals
    • REACH Annex XVII restrictions on hazardous substances in photo chemicals (EU)
    • Japanese Chemical Substances Control Law (CSCL) for specialty imaging agents

    Typical usage ratio

    • 0.5%–1.7% in developer or coupler concentrate, calculated to balance color density with minimal byproduct formation

    Downstream process integration

    • Dispensed into color-developer concentrate mixing, followed by homogeneous blending and filtration prior to drum filling for B2B lab supply

    Final product types

    • Photographic developer concentrates
    • Color coupler premixes for film rolls
    • Photoprint processing kits for analog mini-labs
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    Certification & Compliance
    More Introduction

    3-Methyl-4-Nitroaniline: Hands-On Insights from the Manufacturer’s Floor

    Understanding 3-Methyl-4-Nitroaniline from the Viewpoint of the Producer

    For us, every batch of 3-Methyl-4-Nitroaniline speaks to the combination of chemistry, reliability, and years of refinement. In our business, consistency does not appear out of thin air; it comes from strict methodical work and attention to feedback from clients who use the compound downstream. This particular aromatic amine compound, often shortened in the lab as 3M4NA, earns its place in the world for its unmistakable orange-yellow solid form and a profile that meets diverse industry needs. We have honed both small and large-scale syntheses, ensuring customers always know what they’re getting—down to the color, melting point, and purity.

    Key Features: What Sets this Compound Apart

    As those working on our production lines will tell you, the quality of 3-Methyl-4-Nitroaniline hinges on safeguarding purity above all else. Typical specifications require purity levels exceeding 99 percent, supported by precise melting points and consistent particulate sizes. In our own lab, every single consignment faces a fluorescence spectrometer, TLC, and HPLC checks. Our internal benchmark insists on melting at 135–138°C, but sometimes subtle variations reflect the raw material or season. Such strictness in specs keeps the consistency our partners rely on.

    Not every aromatic amine in the catalog brings the same degree of applications. Some competitors focus on 4-Nitroaniline or 2-Methyl-4-Nitroaniline, both with separate properties and downstream use cases. In contrast, our 3-Methyl-4-Nitroaniline stands out for balancing both electron-rich methyl and strong nitro groups on the benzene ring. This balance allows the compound to deliver particular color-forming abilities and reactivities needed in dyes, pigments, and intermediates for more specialized syntheses.

    Sourcing Raw Materials and Chemical Identity

    Every successful batch starts with the raw aniline derivatives. Over years, we’ve tested supplies from dozens of upstream providers before settling on those who consistently deliver low-impurity feedstock. There’s no shortcut here. A byproduct-rich feed will infect subsequent stages and give unpredictable yields. We know from painstaking experience that the precise substitution pattern on the benzene ring makes a world of difference in subsequent coupling or reduction reactions.

    By sticking to classic nitration techniques, then refining purification, we keep side products minimal. On the finished product, we document appearance, odor, solubility—and above all, contaminant trace levels. Product lots might take slightly different hues if scaling up or down, but our QA team matches each batch against a library of reference samples before shipping. Our experience says even small color or solubility shifts can mark an underlying production slip.

    Applications: Seeing Beyond the Laboratory Bench

    Dye manufacturers come back to 3-Methyl-4-Nitroaniline because it doesn’t just serve as a one-dimensional intermediate. Both the methyl and nitro groups direct further substitutions into predictable patterns, giving dye formers a reliable route toward azo compounds and dispersing agents. When a pigment manufacturer asks for consistency in shade and batch-to-batch color tolerance, this is often where raw synthesis work pays dividends.

    Some research clients use the compound in the synthesis of target molecules beyond dyes—such as intermediates for agrochemical or pharmaceutical routes. In the medicinal pipeline, it goes toward reductive amination or coupling steps, particularly when a methyl group at the 3-position proves critical for molecular recognition. Rarely do generic anilines substitute here, as their activity and chemical reactivity differ. We’ve even seen customers develop new functional polymers and advanced materials using our compound.

    Clients may not see the process, but reproducibility in reactivity, solubility, and melting point translates to confidence in scaling reactions up without recurring surprises. Over several decades, stories from our own technical service team mapped out the headaches caused if just a fraction of impurities or positional isomers slip through. Such lapses can set off a cascade of dye absorption failures or slowdowns in pharma intermediate synthesis. We take repeatability as an obligation, not a luxury.

    Product Differentiation: Experience at the Core

    The chemical market can feel crowded. Several companies market aniline derivatives with subtle structural tweaks, and catalog suppliers often lump related products together. But on the floor, making a batch of 3-Methyl-4-Nitroaniline means controlling each synthesis variable. For instance, the nitration temperature window runs narrow—creep over a few degrees and a second nitration or tar forms. Spend any time in scale-up and such “minor” problems mean blocked filters, lower conversion, and a day lost in cleaning.

    We’ve compared countless purification processes. Column work gives high purity on a lab scale, but at hundreds of kilos it becomes impractical and can degrade the sample through repeated exposure to the silica or solvents. We developed a proprietary crystallization technique after trialing nearly a dozen solvents—adjusting ratios and temperatures after side-by-side comparisons. Our chemists know exactly which solvents lower trace byproducts, reduce attrition loss, and produce a stable product that handles shipping without caking or breakdown.

    In many catalog products, the presence of regioisomers—such as 2-Methyl-4-Nitroaniline or 4-Methyl-3-Nitroaniline—dilutes specificity. Downstream reactions can fail or slow unexpectedly. We track isomeric purity using both GC and NMR, and database every run. If even a hint of contamination appears, we trace the cause—without relying on hope or superficial visual checks.

    Handling, Safety, and Practical Insights

    Safety comes from respect for both material and process. Over the years, our team has logged every near-miss and handled hundreds of technical investigations. The dust and powdery nature require both local and full ventilation in weighing and packaging areas. Tight control keeps airborne particulate and skin contact minimal. Investing in closed transfer systems brought downtime rates down and reduced product loss. In early days, relying on open scooping or manual bagging left too much up to chance—those lessons keep shaping our every update.

    Packaging and shipping play their own roles. We supply the compound in HDPE-lined fiber drums or sealed, solvent-resistant bags, ensuring long-term stability during lengthy transports. Before each pallet leaves the plant, batch tracking and photographic documentation form part of the handoff. In every step, prevention trumps correction; if moisture pickup or temperature deviations show up, those drums never ship.

    We’ve acted on storage feedback too. Early on, our customers encountered agglomeration in humid environments, especially when storage temperatures fluctuated. After those reports, we began offering desiccant choices on request and improved our own warehouse climate controls. Open communication lines help here: if a customer sees even minor flow issues, we invite them to reach directly to our technical team—giving practical answers from real chemists, not call center scripts.

    Quality System: Trust Earned through Experience

    Years of manufacturing have taught us that quality control lives and dies on documentation and humility. Automated sensors log every critical parameter, but human verification still catches issues that simple numbers miss. Every batch faces both chemical and visual checkpoints, and we record every deviation—even those that seem minor and correctable on the line. This process forms the backbone for lot-to-lot records we share with returning clients.

    We’ve integrated continuous improvement as a daily, not yearly, process. Nearly all our methods bear the marks of customer audits and feedback. Dye makers pushed us to cut water content; pharma companies wanted an impurity profile not just for main peaks, but for obscure ones on the tail end. We responded by adding GC-MS and LC-MS runs to routine screening. Today’s product reflects that active engagement.

    Multiple parties have come to audit us, but the most valuable feedback usually arrives straight from chemists looking for that one missing analytical data point or from production managers who spotted a deviation only during a late-night run. Their vigilance keeps us sharp and strengthens our partnerships. Good chemistry is more than yield numbers; it depends on relationships between those who make molecules and those who transform them.

    Environmental Considerations and Process Sustainability

    Production of nitro-aromatic chemicals brings its own environmental challenges. Waste management is front-of-mind. Proper handling of nitration side-products, careful closed-systems washout, and responsible effluent treatment keep us compliant and responsible. Long before tighter laws pushed the need for careful record-keeping, we were already refining our mother liquor recycling and adjusting reaction stoichiometry to minimize excess reagents.

    The push for greener chemistry is unmistakable. We want future generations of chemists to see clean processes and improved E-factor numbers. Steps taken in our own synthesis—choosing less hazardous solvents, reducing reaction times, automating additions—reduce our carbon footprint. Every year, we revisit waste output and target reuse or treatment improvements. This keeps both the local environment and our long-term costs under control.

    Many industry partners now ask about life-cycle analyses. We provide data on raw material sourcing, energy use, and waste streams, reflecting the transparency expected in a responsible supply chain. Commitment to compliance with environmental and workplace safety standards is more than a checkbox for us; it forms the structure that keeps our operation credible worldwide.

    Facing Challenges Head-On

    Making 3-Methyl-4-Nitroaniline has never been a static affair. Every so often, raw material prices fluctuate, or a shipping lane closes down unexpectedly. Demand can spike or drop due to global forces well beyond chemistry itself. We keep alternate supplier relationships and hold buffer stocks for the most crucial precursors. Years back, a supply chain disruption in aromatic nitro compounds taught us the hard way that single-source reliance extracts heavy costs in lost production days and missed customer deadlines.

    We also face regulatory shifts. Sometimes, classification updates or transport changes force us to adjust packaging or documentation, or even tweak processes to remain compliant. Such changes demand vigilance; complacency would hand problems to customers in the form of import delays or non-conforming documentation. By staying connected with both global and regional compliance agencies, we navigate evolving requirements without disruption. Our quality and regulatory teams receive regular training and attend seminars to keep up with environmental and product safety developments. Their timely interventions mean that regulatory burdens don’t get passed on to customers in confused guidance or incomplete paperwork.

    Technical issues often change fastest. We integrate new analytical equipment, refine purification, and trial novel process controls. By keeping lines open between chemists, engineers, and production leads, new ideas get tested in pilot runs. Short feedback cycles mean adaptations happen before problems escalate.

    Looking Forward: Innovation and Commitment

    We do not stand still. The chemical market rewards those who predict, adapt, and improve persistently. That ethos extends to every batch of 3-Methyl-4-Nitroaniline leaving our plant. Our development group is constantly scanning new applications—both within the traditional dye and pigment sectors, and new directions in advanced materials, pharmaceuticals, and specialty polymers.

    The specialty chemicals world demands flexibility and an ability to deliver—regardless of economic swings, feedstock cost spikes, or new compliance demands. By maintaining direct, ongoing conversations with our customers’ technical teams, we can pivot quickly to meet changing specifications, packaging needs, or handling challenges.

    We remain deeply committed to producing 3-Methyl-4-Nitroaniline with a focus on proven performance, strict quality, and sustainable practices. Every lot speaks to hard-earned knowledge, careful adjustment, and respect for the people who rely on us every day. For those who need a trusted supply of this important compound, our record speaks through years of hands-on improvements and partnership.

    In the Words of a Manufacturer

    Years of manufacturing have made it clear that chemicals do not travel as faceless commodities. Behind every shipment lies attention to detail, troubleshooting, and the lessons learned from hundreds of customer experiences. Our 3-Methyl-4-Nitroaniline stands out because we keep learning, keep asking questions, and above all, keep working to meet real-world needs—batch after batch, year after year.