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2-Bromo-4-Chloro-6-Methylaniline

    • Product Name 2-Bromo-4-Chloro-6-Methylaniline
    • Alias 2-Bromo-6-chloro-p-toluidine
    • Einecs 253-950-1
    • 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
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    Specifications

    HS Code

    921784

    Chemical Name 2-Bromo-4-Chloro-6-Methylaniline
    Molecular Formula C7H7BrClN
    Molecular Weight 236.50 g/mol
    Cas Number 89389-87-9
    Appearance Light brown to beige solid
    Melting Point 68-72°C
    Purity Typically ≥97%
    Solubility Slightly soluble in organic solvents
    Smiles Cc1cc(Cl)cc(N)c1Br
    Inchi InChI=1S/C7H7BrClN/c1-4-2-6(9)3-5(8)7(4)10/h2-3H,10H2,1H3
    Storage Conditions Store in a cool, dry, and well-ventilated place
    Synonyms 2-Bromo-4-chloro-6-methylbenzenamine

    As an accredited 2-Bromo-4-Chloro-6-Methylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 2-Bromo-4-Chloro-6-Methylaniline

    Applications of 2-Bromo-4-Chloro-6-Methylaniline in Industrial Manufacturing

    Our facilities supply 2-Bromo-4-Chloro-6-Methylaniline into highly regulated and precisely engineered chemical synthesis chains across several specialized sectors. Below, we provide detailed application insights based on direct manufacturing expertise and on-site QC integration with real downstream production partners.

    1. Agricultural Chemical Synthesis: Herbicide Intermediate

    Formulators in advanced agrochemical manufacturing use this compound as a crucial intermediate for producing selective herbicides, especially for complex aromatic synthesis. Control over halogen substitution at specific positions enables downstream partners to build molecules with targeted herbicidal activity and tailored field residual profiles. Our technical service teams coordinate closely with agrochemical producers to adjust impurity thresholds and address minor batch-to-batch differentiation based on crop-specific or territory-specific application requirements. This integration ensures compliance with global and local regulatory restrictions on precursor purity, cross-contamination, and environmental disposal routes, protecting both operators and end users.

    Industry compliance standards

    • EPA FIFRA (USA)
    • REACH (EU) for agricultural intermediates
    • China GB/T 1604 for pesticide intermediates
    • Standard operating procedures for trace contaminant management outlined by major agrochemical consortia

    Typical usage ratio

    • 5–15% by mass in the synthesis step for key phenyl ring constructs, ratio varies with target herbicide structure and downstream yield optimization cycles

    Downstream process integration

    • Introduced post-nitration and before coupling reactions in multi-stage batch reactors, typically inline with chlorination/halogen exchange apparatus

    Final product types

    • Phenylurea herbicides
    • Substituted aniline herbicide actives
    • Graminicide pre-mixtures

    2. Pharmaceutical API Synthesis: Building Block for Active Ingredients

    Contract pharmaceutical manufacturers rely on this compound as a key halogenated aromatic intermediate in API synthetic routes where strict control over mono-substitution patterns is critical. Its integration allows high-yield amide or sulfonamide coupling, especially in CNS and anti-infective drug precursor pipelines. We coordinate directly with process engineers and QA specialists to ensure each lot meets stringent ICH Q7 GMP standards and validation parameters for impurity profiles relevant to direct human use. Our staff support validation of cleaning, traceability, and, where required, comprehensive analytical documentation for regulatory filings in major global markets.

    Industry compliance standards

    • ICH Q7 cGMP for API intermediates
    • US FDA 21 CFR Part 211 applicable to intermediates
    • European Pharmacopoeia specifications for precursor purity
    • Indian Schedule M API manufacturing codes

    Typical usage ratio

    • 4–10% w/w in specific amide and sulfonamide formation steps; adjusted based on required stoichiometry and residual impurity cut-off in isolation and recrystallization

    Downstream process integration

    • Charged to dedicated synthesis reactors post-halogenation or methylation stage; frequently involved in closed-loop reaction systems to minimize cross-contamination risks

    Final product types

    • Intermediate-stage CNS pharmaceuticals
    • Chlorinated aniline-based anti-infectives
    • Sulfonamide precursor compounds
    • Pyridine derivative bulk APIs

    3. Dyestuff and Pigment Manufacturing: Azo and Diaryl Pigment Precursor

    Producers of high-performance organic pigments and dyes utilize our compound for controlled halogenation during mono- or bis-azo pigment synthesis. The methyl and halogen pattern supports consistent shade, dispersibility, and fastness attributes required in textile, ink, and plastics coloration. Our technical experts assist plant managers in achieving optimal reaction color yield through real-time QC adjustments, and we offer customized packaging and shipment protocols to control trace element contamination which may impair color development in pigment dispersions.

    Industry compliance standards

    • OEKO-TEX® Eco Passport compliance for dyestuff ingredients
    • EN 71-3:2019 for toy and textile pigment safety
    • ZDHC MRSL for restricted chemicals in dyeing applications
    • ISO 9001 QA and ISO 14001 environmental controls for pigment processing

    Typical usage ratio

    • 3–8% by total pigment mass in coupling reactions, with tighter range for automotive-grade and plastic-use pigments due to long-term stability considerations

    Downstream process integration

    • Injected during initial diazotization stage or subsequent coupling, often under temperature-controlled, inert conditions to safeguard color quality

    Final product types

    • Mono-azo textile dyes
    • High-lightfast organic pigments for inks
    • Plastisol color masterbatches
    • Heat-stable diaryl pigments

    4. Specialty Chemical Synthesis: Halogenated Aroma Compounds and Fine Chemicals

    Manufacturers of sophisticated halogenated fine chemicals integrate this intermediate for specific aromatic frameworks involved in aroma chemicals, electronic material precursors, and industrial antioxidants. Our highly controlled halogen content allows for selective functionalization in aromatic substitution, supporting downstream partners focused on high-performance polymers and electronics-grade additives. The compound’s defined substitution pattern helps in minimizing side-reactivity and facilitating high-yield purification for specialty end-uses where performance attributes hinge on molecular uniformity.

    Industry compliance standards

    • ISO 9001:2015 process control for fine chemical manufacturing
    • Electronic Industry Code of Conduct (EICC) for all raw materials
    • Japan Chemical Industry Association standards on fine chemical processing
    • GHS hazard communication for global market shipments

    Typical usage ratio

    • 2–6% as an input in multi-step syntheses, adjusted based on targeted functional group placement and final purity criteria of downstream reactors

    Downstream process integration

    • Feeds into specific halogen exchange or metal-catalyzed cross-coupling processes, typically controlled via automated dosing systems in continuous or semi-batch setups

    Final product types

    • Halogenated aroma intermediates
    • Polymer additive building blocks
    • Specialty antioxidants for lubricants and plastics
    • Electronic-grade monomers
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    More Introduction

    Understanding 2-Bromo-4-Chloro-6-Methylaniline: What Makes It Stand Out in Chemical Synthesis

    Introduction to a Unique Building Block

    Among the many options for aromatic amines, one product that has gained notable traction is 2-Bromo-4-Chloro-6-Methylaniline. This chemical stands out not simply for its molecular structure, but for the practical advantages it brings to both research and scalable synthesis in pharmaceuticals, agrochemicals, and dye intermediates. As someone who has spent years in both academic laboratories and production-level settings, it’s clear how slight tweaks in substitution patterns on the benzene ring can lead to big changes in downstream chemistry. In comparison with plain aniline or simple chloroaniline variants, the addition of both bromine and chlorine along with a methyl group creates a compound with unique reactivity and selectivity, driving innovation in synthetic routes.

    The Details: Specifications and Structure

    2-Bromo-4-Chloro-6-Methylaniline is typically supplied as a crystalline solid, with a molecular formula of C7H7BrClN. Each of these atoms serves a role—not just in the shelf life or appearance of the product, but in its behavior during coupling reactions, substitutions, and protection steps. A methyl group at the 6-position gives increased electron density, sometimes shifting the reactivity in ways that simpler amines can’t match. In solution, this translates to a predictable interaction with standard solvents and reagents, delivering cleaner results instead of muddy byproducts.

    Quality matters. From my own experience, impurities in aromatic amines tend to creep forward in a synthesis pathway, leading to hard-to-remove contaminants at the final step. Well-prepared 2-Bromo-4-Chloro-6-Methylaniline, with a high purity level confirmed by HPLC and NMR, shaves hours off purification work. Instead of endless column runs, users see sharp TLC spots and good yields with less waste. This makes a difference in both small-scale laboratory work and multi-kilogram batches.

    Where 2-Bromo-4-Chloro-6-Methylaniline Fits in Synthesis

    This compound doesn’t only fill a gap left by more basic starting materials. In multi-step synthesis schemes, specialists often look for ways to introduce diverse functional groups on a single aromatic core. The bromo and chloro atoms allow for stepwise cross-coupling—such as Suzuki-Miyaura or Buchwald-Hartwig reactions—to introduce various substituents while retaining a high degree of control. Compared with similar anilines containing just one halogen, this dual-halogen version offers greater flexibility.

    Agrochemical and pharmaceutical innovators often seek to build libraries of molecules by combining different electron-donating and electron-withdrawing groups. 2-Bromo-4-Chloro-6-Methylaniline can access those targets more efficiently thanks to the position and nature of its substitutions. I recall one project developing herbicidal compounds, where this aniline scaffold allowed chemists to implement late-stage diversification. Instead of retracing steps or restarting, the team used this product to snap in new fragments via palladium-catalyzed reactions, avoiding both wasted time and costly raw materials.

    Making Choices: Comparing with Other Aromatic Amines

    The chemical industry presents an almost overwhelming lineup of aniline derivatives. Still, not all serve the same purposes. Simpler options, like aniline itself or 4-chloroaniline, can feel appealing for their price and widespread availability. Their lack of structural complexity reduces cost, but often forces researchers to build more steps into a synthetic route or risk producing less-selective reactions. Adding bromine and a methyl group, as seen in 2-Bromo-4-Chloro-6-Methylaniline, addresses certain bottlenecks.

    Some chemists stick with cheaper, unsubstituted intermediates hoping to cut costs, but this strategy sometimes backfires. When reactions require selective functionalization or reliable downstream coupling, using a more sophisticated scaffold can reduce overall project timelines and lower total expenses by streamlining purification and minimizing failed batches. In real-world terms, this means moving from gram-scale to kilogram-scale with far fewer headaches—a point anyone who has managed a process scale-up will appreciate.

    Impact on Research and Innovation

    Few people outside advanced chemistry realize how much time is spent troubleshooting unclear reaction pathways when using less functionalized starting materials. Over the years, I’ve seen both students and senior researchers wrangle with inconsistent results, varying between reactions. Once 2-Bromo-4-Chloro-6-Methylaniline entered the lab’s regular inventory, many of those uncertainties dropped. Its defined structure adds predictability, which matters both for yields and for the reproducibility demanded in regulated industries.

    In drug discovery, rapidly creating analogs often decides which company or team crosses the finish line first. Time lost in the synthesis phase directly eats into any competitive edge. Leveraging arylamines with optimal groups pre-installed enables high-throughput screening without lengthy detours into protecting group chemistry or multiple-step halogenations. Libraries broaden, options open up, and the likelihood of breakthrough candidates rises. Choosing a starting material like 2-Bromo-4-Chloro-6-Methylaniline changes the pace at which new molecules are born.

    Downward Pressure on Production Timelines

    Scaling up any chemical process brings a unique set of hurdles. Product consistency drifts, yields can wobble, and minor impurities at the beginning magnify as the path continues. Going through scale-up exercises with various aniline derivatives, sharp contrasts always emerge in how easily a synthetic protocol transfers from milligram to multi-kilogram levels. With 2-Bromo-4-Chloro-6-Methylaniline, those transitions feel smoother.

    Process chemists benefit from high-purity, well-characterized materials. The solid crystalline nature of this compound aids in efficient charging and measuring during manufacturing runs. Instead of dealing with sticky oils or volatile materials, operators can rely on manageable, doseable batches. Workflow interruptions drop, with less need for costly rework, and engineered control over reaction chemistry increases. The bottom line: fewer delays and more reliable outputs.

    Managing Environmental and Safety Considerations

    The chemical sector faces strong scrutiny around waste streams and worker exposure, which keeps everyone on their toes. Compared to other aromatic amines requiring aggressive treatment or producing difficult-to-treat byproducts, working with a well-understood and reasonably stable compound like 2-Bromo-4-Chloro-6-Methylaniline can reduce hazards, provided proper protocols are followed.

    Disposal of halogenated intermediates always deserves attention. Facilities with existing acetone, methanol, and organic waste streams find that the compound integrates smoothly with existing protocols. Experience in both university and industry has shown that adopting reagents requiring less aggressive post-process cleanup wins favor from both environmental auditors and practicality-focused engineers. Instead of days spent neutralizing or treating unexpected side-products, reliable input materials set the stage for safer workflows.

    Advancing Green Chemistry Goals

    With increasing focus on reducing the environmental footprint of chemical processes, chemists now consider both the overall step count and the atom economy of each transformation. Whereas some fallback aromatic amines generate mountains of waste by requiring unnecessary protection and deprotection stages, the intelligent substitution pattern in 2-Bromo-4-Chloro-6-Methylaniline helps chemists skip entire classes of auxiliary reactions. Streamlined synthesis means not just shorter project timelines, but reduced solvent use and lower emissions.

    Green chemistry isn’t just a catchphrase—it’s an operational reality for many modern producers. By selecting intermediates that minimize the generation of hazardous side-products, manufacturers build safer plants. Personal experience has shown that processes running with this aniline require fewer emergency workarounds, resulting in more stable regulatory compliance, improved worker safety, and lower insurance premiums. Stakeholders see a real difference on both the spreadsheet and the operating floor.

    Bridging Basic Research with Real-World Production

    There’s a gulf between making a few milligrams for research and producing tons for industry. Early in my career, I watched as promising research molecules stumbled during transfer to commercial plants due to impractical or dangerous intermediates. Sometimes, the issue wasn’t poor science but a poorly chosen starting material: something too reactive, challenging to isolate, or prone to decomposition. 2-Bromo-4-Chloro-6-Methylaniline bridges this gap by providing a versatile and manageable platform for both rapid screening and robust scale-up.

    Pilot facilities appreciate feedstocks that stand up to storage, temperature changes, and varied humidity. As someone who has spent long nights in both university labs and plant control rooms, I know reliability means fewer surprises, lower storage costs, and more predictable process controls. This aniline has a track record of stability not matched by more volatile or less crystalline options. As a result, scheduling isn’t constantly threatened by delays from material recalls or re-qualification tests.

    International Supply Chains and Accessibility

    The modern chemical marketplace often brings together suppliers from Asia, Europe, and North America. Ensuring a steady pipeline of raw materials causes real headaches for both procurement managers and scientists. A starting material like 2-Bromo-4-Chloro-6-Methylaniline becomes attractive partly for the predictable synthesis methods and partly for global accessibility.

    During pandemic years and periods of volatility in international shipping, I’ve seen firsthand how easy-to-produce intermediates like this one kept projects alive, while less common or patent-locked compounds led to weeks-long wait times. A robust supply network supporting this chemical, whether refined for GMP compliance or not, ensures that research programs, pilot projects, and commercial launches maintain their timelines.

    Navigating Patent Landscapes and Intellectual Property

    Competition among pharma and agrochemical developers isn’t limited to the lab bench. Patent claims often hinge on the specific substitutions brought to an aromatic core, influencing both freedom to operate and the strategic direction of new research programs. The unique combination of bromine, chlorine, and methyl groups on this aniline offers an entry point for designing novel molecules less likely to infringe on crowded technology spaces.

    Selecting differentiated starting materials helps teams innovate without constant fear of litigation or last-minute reformulation. By embedding hard-to-replicate structural elements early in the synthesis, companies gain strategic advantages and reduce both risk and uncertainty. This has been a consistent lesson throughout both consultancy projects and in-house roles: distinguish your chemistry at the input stage, and downstream hurdles shrink in number and height.

    Improving Outcomes in Medicinal Chemistry and Agrochemicals

    Few chemical components find a spot at the intersection of fine chemical research and industrial production as frequently as substituted aromatic amines. In medicinal chemistry, projects pivot quickly. Days matter. Medicinal chemists prize building blocks that accommodate a wide variety of final targets, from kinase inhibitors to novel herbicides.

    In my experience, 2-Bromo-4-Chloro-6-Methylaniline lands among those rare intermediates with tangible upstream and downstream advantages. Researchers can introduce polar or nonpolar groups on the benzene core with pinpoint control, yielding novel structures efficiently. Whether the goal is to create a new class of antifungal agents or tweak a known structure to skirt resistance, this product simplifies problem-solving at the bench and at scale.

    Lessons from the Lab and Factory Floor

    Over years working alongside experienced synthetic chemists and operators, certain truths emerge. Reliability in feedstocks translates directly to reliability in projects. 2-Bromo-4-Chloro-6-Methylaniline shows up not just as a number on a material list, but as a trusted member of a formulation arsenal. It handles laboratory mishaps well: easy to recover from, with a low tendency toward mysterious decomposition that can tank weeks of effort.

    As chemists shift projects from R&D to pilot plant, new priorities emerge: dust control, metering accuracy, regulatory documentation, and batch traceability. This compound supports those needs through its manageable physical state and well-understood analytical profile. I’ve watched projects speed through validation, hitting regulatory metrics and customer requirements without cavernous re-testing expenses.

    Potential Solutions to Current Industry Challenges

    Many of the industry’s biggest pain points stem from inconsistent input material, unpredictable supply chains, and brittle regulatory compliance. Streamlining synthetic routes with robust intermediates like 2-Bromo-4-Chloro-6-Methylaniline helps address all three. For supply chain resilience, wide international availability and the use of common synthesis methods shield projects against shortages. For regulatory compliance, well-documented spectral data and batch certificates remove many last-minute doubts. For synthetic challenges, built-in functional handles empower creative chemistry with less need for late-stage troubleshooting.

    Looking forward, adoption of such intermediates—driven by quality-first thinking and anchored in practicality—pushes the entire sector closer to dependable, scalable, and safer innovation.

    Conclusion: Why This Compound Deserves a Closer Look

    Stepping back, the lessons aren’t just about molecules, costs, or timelines. Whether developing new medicines, crop protectants, or pigments, success comes from making smart choices early. In the toolkit of modern synthetic chemistry, 2-Bromo-4-Chloro-6-Methylaniline stands as more than just another name on a list. It’s a tool that brings together efficiency, versatility, and safety, carrying advantages into research, production, and market strategies. Those seeking to advance in the fast-evolving landscape of customized chemicals would do well to consider what this unique building block offers—not in abstraction, but in lived, day-to-day results where outcomes matter.