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5-Methyl-2-Nitroaniline

    • Product Name 5-Methyl-2-Nitroaniline
    • Alias 5-Methyl-2-nitrobenzenamine
    • Einecs 244-857-6
    • 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

    544657

    Cas Number 99-52-5
    Molecular Formula C7H8N2O2
    Molecular Weight 152.15 g/mol
    Iupac Name 5-methyl-2-nitroaniline
    Appearance Yellow crystals or powder
    Melting Point 102-105 °C
    Boiling Point N/A (decomposes)
    Density 1.28 g/cm3
    Solubility In Water Slightly soluble
    Flash Point 149 °C
    Smiles CC1=CC(N)=C([N+](=O)[O-])C=C1
    Inchi InChI=1S/C7H8N2O2/c1-5-2-3-6(8)7(4-5)9(10)11/h2-4H,8H2,1H3
    Pubchem Cid 7420
    Synonyms 2-Nitro-5-methylaniline

    As an accredited 5-Methyl-2-Nitroaniline 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 100 grams of 5-Methyl-2-Nitroaniline, with tamper-evident cap and hazard labeling for safe chemical storage.
    Shipping 5-Methyl-2-Nitroaniline is shipped in tightly sealed containers to prevent moisture and contamination. It must be packaged according to hazardous material regulations, with clear labeling and appropriate documentation. Transport typically requires temperature control and secure handling to avoid physical damage, exposure, or spills during transit. Always follow relevant local and international shipping guidelines.
    Storage 5-Methyl-2-nitroaniline should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers and acids. Keep the container tightly closed and clearly labeled. Store away from direct sunlight and moisture. Use corrosive-resistant shelves and ensure proper grounding to prevent static discharge. Handle with appropriate personal protective equipment.
    Application of 5-Methyl-2-Nitroaniline

    Applications of 5-Methyl-2-Nitroaniline in Industrial Manufacturing

    As a specialized manufacturer, we provide high-purity 5-Methyl-2-Nitroaniline primarily to downstream producers in the dyestuff, pigment, pharmaceutical intermediate, pesticide, and specialty chemicals sectors. Below we elaborate on specific application areas, compliance, formulation ratios, integration processes, and resulting finished products.

    1. Dyestuff Intermediate for Azo Dye Formulation

    5-Methyl-2-Nitroaniline operates as a key diazo component for synthesizing specialty azo dyes, particularly for the textile industry. Formulators use it during azo coupling with a wide scope of aromatic amines or phenols to produce high-brightness yellow and reddish dyes that meet rigorous wet fastness and light resistance requirements demanded by modern textile processing lines. The presence of the methyl group at the 5-position enables fine-tuning of hue and bath stability. In commercial dye formulations, manufacturers must adapt batch sizes and ratios based on targeted chromaticity and substrate affinity for cotton, nylon, or polyester fabrics.

    Industry compliance standards

    • REACH Regulation (EC) No. 1907/2006 for Substances of Very High Concern (SVHC) evaluation
    • OEKO-TEX Standard 100 for restricted chemical residues in textiles
    • ZDHC MRSL (Manufacturing Restricted Substances List) for wastewater compliance
    • ISO 9875:1999 Textiles — Dyestuff quality assessment

    Typical usage ratio

    • Ranges from 10-30% by weight relative to the total diazo base in the dye batch
    • Dosing based on desired molar equivalence for coupling efficiency (0.8–1.2:1 diazo to coupler ratio)

    Downstream process integration

    • Introduced directly into the diazotization step after prior homogenization in acidic aqueous solution
    • Used within closed reactor systems to control temperature and prevent side reactions
    • Subjected to cyanuric chloride or sulfonic acid functionalization for reactive dye variants

    Final product types

    • High-performance azo dyes for cellulosic and synthetic fiber textiles
    • Mordant dyes used for silk and wool applications
    • Reactive dyes for garment dyeing and home textiles
    • Acid dyes for leather and ink coloration

    2. Intermediate for Pigment Synthesis

    Our 5-Methyl-2-Nitroaniline supports the creation of advanced organic pigments, especially for automotive and industrial coatings. It enables the generation of high-tinctorial-strength pigments through controlled coupling with β-naphthol or acetoacetanilide, producing stable hues resistant to solvents and UV. Industrial pigment makers favor it for its role in synthesizing disazo and monoazo pigment structures, required to ensure batch-to-batch consistency and compliance with end-use regulations in paints and plastics.

    Industry compliance standards

    • EN 71-3:2019 Safety of toys — migration of certain elements (for use in colored plastics)
    • ASTM D5538-94(2021) for organic pigment composition
    • Directive 2004/42/EC (VOC content in coatings)
    • ISO 1248:2006 Pigments — General test methods

    Typical usage ratio

    • 15-25% by weight of total pigment precursor charge
    • Adjusted per chroma or hiding power requirement during production scale-up

    Downstream process integration

    • Charged at the initial pigment condensation reactor stage with other aromatic amine derivatives
    • Participates in salt formation or oxidation sequences to achieve desired crystalline properties
    • Filtration, drying, and milling follow chemical synthesis

    Final product types

    • Automotive-grade azo pigments for OEM and refinish coatings
    • High-durability industrial paint pigments
    • Masterbatch colorants for thermoplastics
    • Printing ink pigments (flexo, gravure, screen)

    3. Pharmaceutical API Intermediate (Antitubercular Drug Synthesis)

    In the pharmaceutical sector, 5-Methyl-2-Nitroaniline functions as a building block during multistep synthesis of active pharmaceutical ingredients, notably certain antitubercular drugs. Its structure allows for targeted reduction and acetylation steps, supporting preparation of complex heterocyclic compounds. API manufacturers implement comprehensive in-process controls to ensure carryover residues comply with international pharmacopeial monographs and regulatory agencies demand validated cleaning procedures to prevent cross-contamination in multipurpose facilities.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP-NF Monographs as applicable for downstream APIs
    • 21 CFR Parts 210/211 for finished pharmaceuticals
    • EU GMP Volume 4: Part II for API production

    Typical usage ratio

    • Variable: 1 molar equivalent as precursor per API batch
    • Adjusted based on API synthesis pathway (commonly 2-10 kg per 100 kg API output)

    Downstream process integration

    • Introduced during the reductive amination or nitro group reduction step
    • Followed by ring closure or further functional group derivatization
    • Integrated in purified, closed-system glass-lined reactors for contamination control

    Final product types

    • Antitubercular pharmaceutical intermediates
    • Final API compounds after further synthetic transformation
    • Reference standards for pharmaceutical QC laboratories
    • Precursor for HPLC-grade fine chemicals

    4. Pesticide Active Intermediate (Aromatic Amine Derivative)

    Crop protection chemical manufacturers employ 5-Methyl-2-Nitroaniline in syntheses of select fungicide and herbicide actives. Its capabilities in substituting or coupling as an aromatic amine facilitate production of nitroaniline-class molecules with improved activity and selectivity on key crop pests and pathogens. The integration requires hazard management measures to satisfy agrochemical production safety standards and final formulation specifications for field application or seed treatment.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO Manual)
    • ISO 9001:2015 QMS for chemical manufacturing
    • China GB/T 1603-2001 for technical pesticide materials
    • EU Regulation 1107/2009 for placing plant protection products on the market

    Typical usage ratio

    • Varies between 5–18% by mass relative to active ingredient payload
    • Final dose optimized according to synthetic yield and product toxicity profile

    Downstream process integration

    • Enters early-stage reaction sequence as an amine substrate for nitration, oxidation, or condensation
    • Blended with catalyst batches for selectivity enhancement
    • Followed by crystallization and technical grade refinement

    Final product types

    • Selective herbicide active ingredients for rice, wheat, and maize
    • Fungicide technical concentrates
    • Seed dressing compounds for crop protection
    • Formulated agrochemical emulsifiable concentrates

    5. Specialty Chemical Synthesis (Corrosion Inhibitors and Photoinitiators)

    Manufacturers supplying specialty chemicals incorporate 5-Methyl-2-Nitroaniline in the synthesis of corrosion inhibitors and selected photoinitiators. Its reactivity allows controlled functionalization to tailor molecule performance for applications in industrial water treatment and UV-curable coatings. Stringent process management ensures target purity and activity in compliance with sector-specific chemical and environmental regulations.

    Industry compliance standards

    • ISO 9001:2015 certified production process
    • OSHA requirements for chemical workplace safety (29 CFR 1910)
    • EU REACH Annex XVII for hazardous chemical control
    • EPA TSCA compliance for new chemical notification in the US market

    Typical usage ratio

    • Commonly 8–15% by mass in specialty inhibitor or main photoinitiator synthesis batches
    • Adjusted as needed for downstream molecular weight and reactivity targets

    Downstream process integration

    • Charged as the initial aromatic core in ring substitution or reduction reactions
    • Coupled or further derivatized based on application (e.g., sulfonation for solubility)
    • Isolated and formulated for end-use by blending or film-casting

    Final product types

    • Organic corrosion inhibitors for closed-loop cooling systems
    • UV photoinitiators for inkjet and offset inks
    • Additive blends for epoxy or acrylate resin curing
    • Preliminary standards for advanced materials research
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    Certification & Compliance
    More Introduction

    5-Methyl-2-Nitroaniline: Experience from the Manufacturer’s Floor

    Introduction to Our Production and Insight into the Molecule

    After decades working in fine chemicals, our team knows the difference between a reagent that’s just “available” and one that meets the real needs of synthesis professionals. 5-Methyl-2-Nitroaniline (CAS number 578-46-1) holds a unique place on our roster for its reliability and purity in demanding synthetic schemes. Chemists favor this compound for its straightforward incorporation into dyes, agricultural intermediates, pharmaceutical building blocks, and specialty polymers. We have maintained our focus on this product due to its consistent demand and diverse uses in solutions where precision and trace consistency matter.

    5-Methyl-2-Nitroaniline exists as pale yellow crystalline powder, often recognized by its characteristic melting point near 93°C. From batch to batch, our facility controls particle size and moisture levels, knowing uneven texture or hidden water content can disrupt reaction kinetics or elevate downstream impurity levels. Years of experience told us purity is never just a number—so instead of hitting minimum specs, we keep our assay standards above 99%. This lets downstream teams skip redundant purification and move straight into coupling, reduction, or diazotization steps.

    Understanding the Real-World Value

    The market treats aromatic amine derivatives as commodities, but repeated conversations with process engineers taught us how the story is different in the lab or production tank. Each technical grade or specification plays a role in cost and process efficiency. Our formulation of 5-Methyl-2-Nitroaniline has sustained both pilot and large-scale operations, not because it’s “generic,” but because it arrives ready to dissolve and react as advertised—whether in NMP, DMF, or even under less typical solvent systems. Quality control teams rely on the absence of colored byproducts or residual acids, since these introduce chromatic impurities in pigment manufacture and reduce reaction selectivity in pharmaceutical intermediates. Experience says: if our analysis reports even the faintest iron or halide contamination, the whole batch stays in-house, not in circulation.

    Production admins—often juggling delayed supply chains or shifting customer specs—need a dependable option that does not introduce wildcard variances. In most dye and pigment syntheses, the methyl group at position five of the aniline ring shifts the reactivity profile enough to access unique hues and fastness grades unavailable through the more commonplace 2-nitroaniline or plain aniline. This property drove steady customer preferences for our product in the synthesis of azo dyes, sulfur dyes, and special-purpose colorants tailored for textiles or plastics, where reproducibility translates directly into fewer rejects and less scrap.

    What Sets 5-Methyl-2-Nitroaniline Apart from Simpler Alternatives

    Some foundational knowledge helps here: aniline itself—without methyl or nitro substitution—remains one of the pillars in chemical supply. Yet pure aniline lacks regioselectivity in many reactions. Adding a methyl at the ortho position (relative to the amine) and a nitro at the neighboring carbon creates a new distribution of electron density, shifting the activity for diazotization, acylation, and coupling. In practical synthesis, this means 5-Methyl-2-Nitroaniline gives better selectivity and less tendency for unwanted side reactions compared with many unsubstituted or differently substituted analogs.

    Looking at the differences from 2-Nitroaniline, the methyl group in our product not only modifies the reactivity towards electrophilic aromatic substitution but also protects certain positions from overreaction. This extra control means project leads can push for greater process efficiency, higher dye strength, or special intermediate structures without starting from scratch in synthetic planning. In our experience, research teams trying to produce advanced organic semiconductors or custom ligands turn to 5-Methyl-2-Nitroaniline precisely because it delivers access to target molecules not feasible through simpler building blocks.

    Why Product Purity Directly Shapes Customer Outcomes

    Consistent results in demanding conditions come from more than “high purity” labels. Our in-process sampling regime includes spot testing for both organic and inorganic impurities, since even trace elements can poison catalysts or shift UV/Vis signatures in dye applications. We have built our drying and filtration systems around preventing the introduction of extraneous dust, residual metals, or crystallization issues.

    In pigment and dye manufacture, trace organic contaminants such as unreacted starting material or over-nitrated byproducts can carry color and change the hue or stability of the final product. Producers of analytical reagents and pharmaceutical intermediates told us again and again: material that fails to meet tight impurity profiles pushes entire projects off schedule, causing hidden costs through double purification and extra analytical runs. Our investment in high-gradient chromatography and fused silica filtration pays off most clearly for these customers, who can observe the reduction in purification steps and improved final yields.

    Handling and Storage: Building in Reliability from Source to Delivery

    Real certainty comes with how material is handled before it gets to a customer’s bench. Many aromatics turn out to be more sensitive to light and heat than suppliers admit. For 5-Methyl-2-Nitroaniline, this means shipping and warehouse storage in opaque, tightly sealed containers, and regular monitoring for subtle signs of degradation or caking. Years of feedback pushed us to maintain controlled environments for both production and packing. Neglecting this can result in subtle color shift or unexpected reaction profiles that are tough for customers to pin down until several batches in.

    We maintain safety and traceability by using integrated batch tracking and re-analysis samples held for post-shipment questions. This combination of technical support and documented QC makes a difference when a customer faces regulatory audit or must rapidly backtrace an unexpected result in their own synthesis.

    Specialty Applications: Bringing Customer Projects to Reality

    The most evident demand for 5-Methyl-2-Nitroaniline comes from dye and pigment manufacturers. These teams work to produce colors with strong lightfastness and specific absorption maxima, often under regulatory or application-driven purity requirements. The methyl group, precisely placed, delivers unique color value and stability not accessible through alternative starting points. End users in the plastics industry find that nitroanilines without the methyl group yield products with lower weather-fastness or altered scattering.

    Downstream, in pharmaceutical synthesis, this compound enters as a building block in the construction of antimicrobial agents, specialty intermediates for kinase inhibitors, and as an intermediate for more complex heterocyclic structures. The medical sector rarely tolerates batch-to-batch differences. Inconsistent impurity levels delay regulatory approval or, in the worst case, trigger costly recalls. 5-Methyl-2-Nitroaniline streamlines the route by supplying the core structure needed for both chemical backbone creation and further functionalization, without the risk of introducing unwanted byproducts from inconsistent feedstocks.

    Specialty polymer manufacturers also choose this molecule as a monomer or cross-linking agent, capitalizing on the unique placement of substituents to influence polymer backbone rigidity and color. Subtle shifts in the position of the methyl or nitro can mean the difference between a brittle material and a stable, flexible resin. Our team has seen project leaders skip over other nitroanilines when a precise glass transition temperature or dye compatibility matters, and instead focus on the consistency possible with the five-methyl substitution.

    Solutions for Industry-Specific Challenges

    Every major sector we supply—dyes, agrochemicals, pharmaceuticals, and polymers—shares common pain points: unexpected impurities, short shelf life, and variable reactivity. Years of feedback have confirmed that generic traders, who transship bulk material without tight quality controls, introduce risks. Manufacturers end up fighting inconsistent yields, lost man-hours, and wasted feedstock. Our approach centers on direct oversight, from raw material procurement (sourced under long-term contracts with verified suppliers) to end-point analytical checks using validated instrumentation.

    In dye and colorant work, a leading challenge remains the achievement of reliable shade and resistance in the face of ever-tightening environmental limits. The methyl and nitro groups in this molecule support access to families of dyes that display both the needed chroma and stability under acid, base, and light exposure. When combined with robust process QC, this allows users to document regulatory compliance and scale up with confidence.

    Pharmaceutical makers look for low levels of residual solvents and metals, especially when their downstream intermediates enter regulated drug APIs. Our facility maintains a documented program for solvent residual analysis and heavy metal checks, with results attached to every lot produced, because “typical” levels do not meet compliance if a single sample deviates. We work with procurement and regulatory teams to tune packaging and shipment formats, reducing risk of degradation or cross-contamination during long-haul logistics.

    Agrochemical users demand resistance to hydrolysis and oxidation when using nitroaniline derivatives as synthetic precursors. We deliver lots with guaranteed shelf life and provide storage guidelines based on real-world stability data, not just theoretical estimates. This feedback loop, linking the technical specification with genuine in-field performance, strengthens both customer loyalty and in-house expertise as new formulations emerge.

    Insights from Daily Production: Lessons Learned and Ongoing Improvements

    On the factory floor, our team investigates each batch deviation, not just to resolve single incidents, but to feed lessons back into training and process mapping. Thickness of filtering cakes, temperature shifts during nitration, and degree of mixing play outsized roles in final product color and reactivity profile. Our control systems track and log each production parameter, enabling us to anticipate and prevent recurring issues. These investments in statistical process control show up in customer satisfaction, especially when projects require multi-ton scale containment of side products or color bodies.

    Cleaning validation for our crystallization vessels and drying ovens guarantees cross-contamination risk falls below detectable limits. A residue of structurally related isomers easily enters unnoticed if corners are cut on equipment cleaning. Customers have told us horror stories of mixed products from less cautious producers—problems we work hard to avoid through rigorous SOPs and sample archiving.

    We also work directly with customer R&D teams on requests for unusual particle size ranges or alternate solvents. Where a specific project requires a granular adjustment, such as reduced particle size for increased surface reactivity, we can modify granulation regimes without compromising overall purity or stability.

    Regulatory and Environmental Responsibility

    Since 5-Methyl-2-Nitroaniline finds its way to sensitive downstream products, especially those in contact with living systems or the wider environment, compliance with global chemical regulations is not optional. Our experience demonstrates that attention to source traceability, heavy metals, and waste minimization pays long-term dividends. With every batch, we carry out TDS and SDS documentation in line with the latest REACH and country-specific requirements, and maintain internal mechanisms for reporting and managing deviations. This work builds both external trust and a culture of compliance internally.

    We have invested in waste treatment systems capable of safely handling mother liquors and byproducts. Where possible, we recover useful chemicals or treat effluents to below threshold levels before discharge. Over the years, changes in treatment protocols and investment in air- and water-scrubbing has cut down the environmental footprint, making both communities and employees safer.

    Customer Partnerships and Application Support

    Our dedication does not end at batch release. Many customers approach us not just for product, but for insight on how to streamline their own syntheses or troubleshoot scale-up. We make our technical staff available for consultations—for example, advising on optimal solvent systems or conditions for specific coupling or reduction steps. Feedback often reveals application parameters outside the standard canonical literature, so we circulate this learning among our customers to drive faster, more predictable progress.

    In recent years, we have seen a welcome shift: developers share back their yields, byproduct profiles, and even small-scale failure points. This loop lets us refine process parameters and offer genuinely informed guidance, closing the gap between generic trade product and truly application-optimized supply. Projects in specialty dyes for medical diagnostics, custom electronic materials, and next-generation agricultural compounds all benefit from this two-way flow of information.

    The Manufacturer’s Commitment to Quality and Reliable Partnership

    Every ton of 5-Methyl-2-Nitroaniline leaving our gates reflects years of accumulated expertise and a culture of continuous improvement. We know our customers—small-scale innovators and large corporates alike—depend on a supplier who will answer the phone, troubleshoot a mystery impurity, or expedite a batch during critical project phases. That’s something no data sheet or price quote alone can deliver. Whether a product will be used as-is or crafted into a regulated intermediate, customers benefit from our front-line knowledge of supply realities, process technicalities, and emerging application trends. By valuing transparency and proactive technical service, we aim to build not just a transactional relationship, but a foundation for innovation and ongoing progress in all fields unlocked by this versatile compound.