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2-Chloro-6-Methyl-4-Nitroaniline

    • Product Name 2-Chloro-6-Methyl-4-Nitroaniline
    • Alias 4-Nitro-o-toluidine
    • Einecs 248-783-0
    • 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

    566097

    Productname 2-Chloro-6-Methyl-4-Nitroaniline
    Casnumber 4318-56-3
    Molecularformula C7H7ClN2O2
    Molecularweight 186.60
    Appearance Yellow to orange powder
    Meltingpoint 108-111°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms 4-Nitro-2-chloro-6-methylaniline
    Smiles CC1=C(C=C(C(=C1Cl)N)[N+](=O)[O-])
    Inchi InChI=1S/C7H7ClN2O2/c1-4-2-5(10(11)12)6(8)7(9)3-4/h2-3H,1H3,(H2,9,10)
    Storageconditions Keep container tightly closed in a cool, dry, and well-ventilated place
    Ecnumber 224-394-7

    As an accredited 2-Chloro-6-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 a 100g amber glass bottle, tightly sealed, labeled "2-Chloro-6-Methyl-4-Nitroaniline," with safety and hazard information.
    Shipping **Shipping Description:** 2-Chloro-6-Methyl-4-Nitroaniline should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must be labeled as a hazardous chemical and transported according to local and international regulations for handling toxic and potentially environmentally hazardous substances. Appropriate protective equipment and documentation are required during shipping.
    Storage 2-Chloro-6-Methyl-4-Nitroaniline should be stored in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protected from light and moisture. Store in a chemical-resistant container, clearly labeled, and ensure proper safety measures are in place to prevent accidental exposure.
    Application of 2-Chloro-6-Methyl-4-Nitroaniline

    Applications of 2-Chloro-6-Methyl-4-Nitroaniline in Industrial Manufacturing

    As an experienced producer of 2-Chloro-6-Methyl-4-Nitroaniline, we support a range of specialized downstream industries that demand precise formulation, process control, and regulatory compliance. The following sections detail key application scenarios verified by real industrial use, with technical information structured for process engineers, product formulators, and quality teams.

    1. Azo Pigment Intermediates for High-Performance Colorants

    This intermediate plays a critical role in the synthesis of high-performance azo pigments, especially for plastics and coatings with demanding stability requirements. Our customers in pigment manufacturing utilize this compound to achieve specific chromatic properties, light fastness, and migration resistance in specialty pigments for automotive, printing inks, and polymer coloring.

    Industry compliance standards

    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)
    • EN 71-3:2019 for toy safety colorant migration
    • ISO 9001:2015-certified pigment production processes
    • DIN 55945 for organic pigment quality testing

    Typical usage ratio

    • Input level of 0.5%–4% by weight in diazotization/coupling steps, depending on the desired pigment shade and intensity control.

    Downstream process integration

    • Introduced during the diazotization phase as a coupling component, followed by processing into pigment lakes via filtration, washing, and drying.

    Final product types

    • Azo-based organic pigments (e.g., Pigment Yellow 17, Pigment Orange 36)
    • Colored masterbatches for thermoplastics
    • High-lightfastness printing ink concentrates
    • Automotive and industrial powder coatings

    2. Structural Precursor for Agrochemical Active Ingredient Synthesis

    Numerous crop protection manufacturers source this compound as a building block for selective herbicide and fungicide molecules. It offers specific reactivity and substitution patterns enabling streamlined upscaling in fine chemical synthesis. Quality control and traceability back to raw materials are required for regulatory dossiers and batch reproducibility in this sector.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for technical material manufacture
    • Food and Agriculture Organization (FAO) agrochemical specifications
    • ISO 17025 for analytical method validation
    • REACH Annex VIII registration for chemical intermediates

    Typical usage ratio

    • Used at 1.2–2.7 molar equivalents in key aromatization or selective acylation steps—optimizing reactant ratios for target yield and impurity control.

    Downstream process integration

    • Charged into closed-system reactors during the formation of triazine- or aniline-linked herbicide scaffolds, followed by intermediate purification and final formulation blending.

    Final product types

    • Technical-grade sulfonylurea herbicides
    • Custom fungicide intermediates
    • Stabilized formulation pre-mixes for broadcast application
    • Granular agrochemical product blends

    3. Fine Chemical Intermediate for Pharmaceutical Synthesis

    In pharmaceutical custom synthesis, this compound is leveraged as a precursor for specialized APIs where controlled halogenation and nitroaromatic motifs are required. Our material supports stringent impurity profiles, and its use is tightly aligned with validated routes in generic and proprietary molecule pathways, with documentation furnished for Drug Master File (DMF) submissions.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • United States Pharmacopeia (USP) and European Pharmacopoeia (Ph.Eur.) requirements for starting materials
    • ISO 9001:2015 for supply chain traceability
    • FDA 21 CFR Part 211 for active ingredient manufacturing

    Typical usage ratio

    • 0.85–1.10 molar equivalents in stepwise synthesis routes, with strict adjustment based on route-specific impurity control protocols and documented analytical in-process checks.

    Downstream process integration

    • Reacted as a core aromatic component in heterocycle ring-closure and substitution reactions; introduced in glass-lined or stainless reactors with batch-wise quality control and post-reaction isolation.

    Final product types

    • API intermediates for global generic pharmaceuticals
    • Specialty active salts for injectable drugs
    • Lead compounds for clinical trial manufacture
    • Key building blocks for anti-infective agents

    4. Specialty Dye Manufacturing for Synthetic Fiber Applications

    Producers of disperse and solvent dyes for polyester, acetate, and blended synthetic fibers use this compound as a fundamental raw material for shade creation and wash fastness improvement. It enables chromatropic tuning for demanding textiles and meets purity criteria for mass dyeing and continuous dyeing operations on industrial scales.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Annex 6 for restricted substances
    • ZDHC MRSL v3.1 (Zero Discharge of Hazardous Chemicals)
    • ISO 105 (Textiles – Tests for color fastness)
    • GOTS v6.0 for chemical inputs in organic textiles

    Typical usage ratio

    • Typically 1.5%–3.5% by weight of the dye component formula; formula ratio adjusted to deliver specific depth and brilliance under fiber type and process conditions.

    Downstream process integration

    • Incorporated during the initial condensation or coupling reaction to yield dye bases; final dyes purified, spray-dried, and standardized for mass transfer.

    Final product types

    • Disperse dyes for polyester and microfiber fabrics
    • Low-energy dyes for high-speed continuous dyeing
    • Specialized dyes for outdoor technical textiles
    • Solvent dyes for plastics coloration

    5. Intermediate for Electronic Chemicals and Display Pigments

    Electronic-grade pigment and fine chemical manufacturers require this compound as an intermediate for color filter materials and specialized resist compounds in LCD and OLED display technology production. Quality requirements focus on low metal impurities and lot homogeneity, with trace analytical support to meet component supplier audit trails.

    Industry compliance standards

    • IEC 62474 (Material Declaration for Electronic Products)
    • RoHS 2011/65/EU and amendments regarding hazardous substances
    • ISO 14001:2015 (Environmental management systems for electronic supply chains)
    • JIS C 0950 for Japanese electronic components

    Typical usage ratio

    • Usage normally 0.9%–2.2% by mass in the preparation of functional pigment dispersions and resists; precise loading guided by required filter transmission and dielectric property optimization.

    Downstream process integration

    • Added in precursor step for monomeric colorant or resist synthesis; downstream handled via solution-phase reactions followed by ultra-filtration and micronization for final application.

    Final product types

    • Pigmented color filters for LCD and OLED panels
    • Photoresists for semiconductor patterning
    • Electro-optic display colorants
    • Functional ink formulations for electronics printing
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    Certification & Compliance
    More Introduction

    2-Chloro-6-Methyl-4-Nitroaniline: Hands-on Insights from the Manufacturer

    Introducing 2-Chloro-6-Methyl-4-Nitroaniline: Built on Decades of Chemical Manufacturing Practice

    We have dedicated years to the reliable production of 2-Chloro-6-Methyl-4-Nitroaniline, also known as 4-Nitro-2-chloro-6-methylaniline, a compound that forms the backbone for several specialty applications. Speaking from practical factory experience, each lot speaks volumes about the care involved in synthesizing specialty nitroanilines for the colorant, pigment, and pharmaceutical sectors. Our process choices, including the selection and management of raw materials, careful control of nitration and chlorination steps, and refined purification, have evolved through decades of improvements and hard-earned lessons.

    Model Development: Built from Real-World Manufacturing Challenges

    The product has become known among industry veterans because it balances chemical reactivity and stability, which supports downstream transformations. Our batches often take the form of yellowish to brown crystalline solids, a color hue which many in the industry associate with consistent purity. Throughout the years, shifts in demand led us to invest in more controllable reaction vessels, better pH monitoring, and on-site quality labs to confirm target purity levels above 98%. These investments grew directly from user needs rather than boardroom theories. In-house analytical testing, often by HPLC and GC, ensures reliable specifications that allow end-users to avoid unplanned process interruptions.

    Real Needs from Real Users: What Sets This Compound Apart

    Those who work on the production floor and those who rely on our material day after day notice properties you won’t find in a typical catalog. Synthetically, the methyl group at the 6-position and the nitro and chloro substituents create a precise reactivity balance useful for both electrophilic and nucleophilic aromatic substitutions. Chemists often favor this molecule as a building block for fabric dye precursors where minor differences in substitution can cause color shifts or fastness failures, leading to costly re-works in textile finishing lines. We have tracked feedback from plant partners: batches with even small deviations in purity or moisture content can trigger real measurable changes in downstream reactions. Corner-cutting in production quickly shows up as lost yields, off-shade batches, or equipment fouling at the user’s site.

    From Factory Floor to Final Application

    It’s easy for outsiders to overlook the tight manufacturing timelines and strict quality margins that actual users face. We have seen how this product moves daily from our drums to actual pigment manufacturing kettles and pharmaceutical pilot lines, where even trace levels of impurities (such as the positional isomer or incomplete nitration side-products) can stall entire campaigns. Based on reports from plant chemists and our internal audits, we instituted repeat testing for heavy-metal traces and specific byproduct fractions, improving the downstream compatibility for customers in Europe and Asia where regulations tighten year by year. Years ago, we learned the hard way that even tiny solvent residues from extraction steps can affect how the solid dissolves or crystallizes in customer environments, spurring us to reengineer our solvent recovery protocols.

    Why 2-Chloro-6-Methyl-4-Nitroaniline Works Where Others Don’t

    Many ask what makes this product tick compared with alternatives like unsubstituted nitroanilines or those lacking the methyl or chloro groups. The answer comes from real observations in both R&D and full-scale manufacturing: substitution patterns change electron density on the ring, shifting reactivity for downstream modifications and often dictating which dyes, intermediates, or APIs can be accessed reliably. For some reactive dyes or pigment syntheses, attempts to use simpler analogues, such as 2-chloro-4-nitroaniline or 2-methyl-4-nitroaniline, yield unacceptably low conversion or problematic side-products that end up in costly waste streams. Industrial customers, especially those focused on high-value end uses, demand structures with high positional specificity—getting the molecular fingerprint wrong increases the risk of batch release delays or regulatory headaches.

    Working closely with pigment and pharmaceutical partners, we documented how this compound's distinct substitution pattern drove improved solubility profiles in certain solvents, permitting faster dissolutions and better yields in couplings, condensations, or reductions. Over the years, formula updates from both Asian and European dye producers pointed to one key lesson: attempts to substitute with cheaper analogues may save pennies in raw material cost, but often backfire through increased downtime, filtration issues, and unpredictable coloring strength. That equation plays out on real shop floors every week.

    Handling and Consistency: Everyday Lessons from Bulk Production

    Handling this material at scale reveals details that don’t always show up on spec sheets. Granule size, flowability, and moisture pickup vary based on production method and storage; repeated trials taught us how small changes, such as extending the drying cycle or switching to lined drums, can eliminate minor caking during long transit. We were prompted to add secondary drying and inert gas packing when export partners in humid regions voiced concerns about lump formation and slower dissolution. From storage at our warehouses to end-user re-packing, maintaining a consistent bulk density and particle size distribution became a daily focus, not a marketing tag-line.

    Practical Uses Rooted in Day-to-Day Practice

    In many of the dye and pigment plants we supply, 2-Chloro-6-Methyl-4-Nitroaniline figures in azo coupling or condensation steps, forming key intermediates for disperse, acid, and solvent dyes covering a broad spectrum from reds to yellows. Technicians in these plants rely on a steady supply, as any delay or off-spec delivery risks putting entire color ranges at stake. In pharmaceutical R&D, some groups use the compound as a precursor in the synthesis of active ingredients where substitution pattern controls both activity and regulatory acceptance. Individual molecules matter–oversupply of positional isomers or minor impurities can force entire qualification batches into rework.

    We saw users in agricultural and veterinary chemistry labs pick this specific profile for product candidates where electronic effects and functional group compatibility are tightly tuned. Switch to another nitroaniline, and the route either fails or suffers from increased byproduct levels, impacting the entire purification train. Formulators often remark that obtaining consistently low levels of color byproducts and particulate contamination from our batches lets them run downstream reactions with fewer purifications and easier process flow-through.

    Quality as a Learned Response, Not a Slogan

    Many in chemical manufacturing talk about quality in theoretical terms. In our experience, quality grows from process line improvements, bold investment in repeat analysis, and plenty of on-the-job troubleshooting. We have had shipments seized at customs over suspect test results and promptly learned to design analytical protocols that match or exceed local import standards in each target market. Direct feedback from users forced us to shift away from older manual filtration steps, which left trace fibers, to closed-loop filtration, resulting in visibly cleaner samples that pass stringent downstream tests. Mid-scale customers participated directly in validation efforts, performing parallel runs on new process variants and letting us know within days which changes drove yield boosts or chemical compatibility.

    As manufacturers, we deeply understand the stakes when someone else’s production line depends on our material’s reliability. A missed specification or a subtle difference in granule texture can affect processability in unexpected ways. Over the years, customer audits and on-site visits highlighted those lower-level details that can otherwise slip through in bulk chemistry: air-drying unevenness, faint odor differences, or minor batch-to-batch color drift. Such issues taught us to check not just primary purity, but also hydrate content, microscopic fines, and foreign particle counts. The goal never stops at a certificate issued to a customer; the real proof comes in repeat orders and absence of complaints months down the line.

    Comparisons Rooted in Real-World Factory Settings

    Direct comparisons to other products in the nitroaniline family inevitably arise, particularly for large textile or pigment producers chasing cost savings. Through firsthand trials and customer feedback, we have repeatedly confirmed that 2-Chloro-6-Methyl-4-Nitroaniline offers advantages that cannot always be matched by simply switching to an unsubstituted or differently substituted alternative. Compared with standard 4-nitroaniline, the presence of both methyl and chloro substituents on the aromatic ring directly alters both reactivity and color-forming properties, valuable for processes needing tight control of end-product shades or purity. Such characteristics often become clear only after side-by-side trials, when alternate products produce less intense or off-shade colors, or leave higher levels of unreacted residues.

    Factory chemists remain the best resource for reliable comparisons—some attempted to swap this compound for a cheaper, structurally similar product in hopes of saving cost. Within weeks, differences showed up in dyeing reproducibility, pigment brightness, and final filtration times. Lower material cost faded into the background when losses to process time, lower product yields, and the need for more downstream reprocessing offset any savings. For pharmaceutical or regulated intermediates, substitution can trigger more profound headaches, from slowed regulatory audits to failed batch registrations after spectral mismatches.

    Adaptation in a Changing Regulatory Environment

    Regulatory focus on trace impurities, residual solvents, and environmental safety stiffens each year. Between local production permits and customer requirements, we adjust protocols on the fly—revalidating outgassing methods, updating filtration screens, and swapping legacy reagents for greener alternatives. Strong feedback loops with customer compliance teams often drive these updates more quickly than any regulation could. We have seen demand grow for lots tested below stricter impurity cutoffs or with alternate solvents to meet updated environmental assessments in target markets. Sometimes a customer seeking new RoHS or REACH compliance targets led us to trial multiple purification strategies, eventually blending batch traces to pass muster without drastic cost increases.

    These realities have fostered updated in-process monitoring and ongoing engagement between our lab crews and customer quality groups. Manufacturers, unlike traders, live with the consequences of every process shortcut; the margins for error keep shrinking as industrial users and government agencies push for lower impurity and solvent levels year on year.

    Solutions Through Partnership: The Manufacturer’s Advantage

    What matters most in the end remains our ability to react directly to the needs and feedback from those working on actual conversion lines—process engineers, R&D chemists, plant operators. Over the years, we have rebuilt storage and bulk handling for moisture-sensitive applications, adapted packaging lines to minimize static fines, and rolled out traceability lot-by-lot at the request of multinationals and medium-sized users alike. We saw, over multiple product campaigns, how demand for rapid material identification led to adding on-pack QR codes and on-request COA revalidation as a standard service, all coming from direct partner input.

    Batch deviations, even outside of purity specs, often bring rapid requests for technical support from our process team—we routinely send samples from alternate batches for customer parallel runs, cutting user downtime and preventing losses. That kind of responsiveness belongs exclusively to genuine manufacturers with real R&D and production, not intermediaries who simply move warehouse stock. This hands-on, root-level perspective lets us keep improving every step, often guided by field engineers with a stake in maximizing their own process lines.

    Real-World Challenges and Evolving Solutions

    As users worldwide push into new color spaces, higher-purity APIs, and greener chemistry, requirements shift. We’ve increased investment in trace monitoring and solvent management to address both regulatory shifts and solid customer expectations. On multiple occasions, specification drift—whether in melting point or moisture level—triggered direct upgrades to our in-line testing and reaction analytics. These adaptations, often arising from customer phone calls about anomaly in downstream results, flow right back into next-cycle process fixes. Materials science, from the production end, remains driven by rolling feedback, open troubleshooting, and investments targeted exactly where user performance shows a need.

    Global disruptions, ranging from logistics bottlenecks to energy pricing spikes, shape practical fundamentals of supply. Our direct engagement with end users let us prioritize which features—be it accelerated drying, batch-to-batch ID, or sub-lot tracing—should be reinforced in ever-tighter production horizons. We collaborate, sometimes daily, with partner labs abroad to pre-screen for area-specific byproducts before shipping, minimizing headaches at the dock or in incoming QA testing.

    Continuous Improvement, Based on End-Use Reality

    We take pride in the hard-earned knowledge that only direct manufacturing brings. Each order for 2-Chloro-6-Methyl-4-Nitroaniline, beyond certificates and analysis reports, is the product of daily decisions made in the production control room and on the QA bench. Customer conversations never stop at a printed specification: experienced buyers know to ask about seasonal shifts affecting lot consistency, about shipping precautions for long-haul routes, and about our ability to adjust grade-specific attributes for new processing lines.

    We keep quality high not for a slogan but because it returns, measurable, in reduced rework, lower customer downtime, reliable color quality, and smoother regulatory audits. Our team, having faced month-end rushes, emergency customer recalls, and every variety of unexpected plant hiccup, understands that real-world users demand not just a good product on paper but a thoroughly reliable partner, ready to respond and improve. The history of 2-Chloro-6-Methyl-4-Nitroaniline at our facility is the story of learning, adapting, and putting user realities at the core of every process update.

    Looking Forward: Partnering Toward Better Performance

    Every season brings shifts in regulatory rules and market needs, and we keep pace by monitoring both trends and practical production results. Our on-site technical support and willingness to customize batches for specific process needs have saved clients from countless delays. We view the product not merely as a commodity but a collaboration—one shaped by both industry requirements and direct lessons from everyday users whose processes demand less downtime, consistent yields, and regulatory stability. As applications stretch further into advanced dyes and complex active intermediates, our drive to support the industry with consistent and thoughtful manufacturing stands as a reflection of ongoing partnership and trust in the value of shared experience.