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4-Bromo-2-Chlorotoluene

    • Product Name 4-Bromo-2-Chlorotoluene
    • Alias 1-Bromo-3-chloro-4-methylbenzene
    • Einecs 871-94-9
    • 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

    362450

    Chemicalname 4-Bromo-2-Chlorotoluene
    Casnumber 30412-26-1
    Molecularformula C7H6BrCl
    Molecularweight 205.48
    Appearance Colorless to pale yellow liquid
    Meltingpoint -2 °C
    Boilingpoint 220-222 °C
    Density 1.571 g/cm3
    Refractiveindex 1.578
    Purity Typically ≥98%
    Flashpoint 97 °C
    Solubility Insoluble in water, soluble in organic solvents

    As an accredited 4-Bromo-2-Chlorotoluene 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 4-Bromo-2-Chlorotoluene, sealed with PTFE-lined cap, labeled with hazard and handling information.
    Shipping 4-Bromo-2-Chlorotoluene is shipped in tightly sealed containers, protected from heat, moisture, and incompatible substances. It is classified as a hazardous material and must be labeled according to regulatory standards. Transport is typically conducted by certified carriers, ensuring compliance with local, national, and international chemical shipping regulations to ensure safety.
    Storage 4-Bromo-2-chlorotoluene should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use and store under an inert atmosphere if possible. Avoid exposure to heat, direct sunlight, and moisture. Clearly label the storage container to prevent accidental misuse.
    Application of 4-Bromo-2-Chlorotoluene

    Applications of 4-Bromo-2-Chlorotoluene in Industrial Manufacturing

    4-Bromo-2-Chlorotoluene serves as a critical intermediate for multiple sectors such as agrochemical synthesis, pharmaceutical manufacturing, specialty dye production, liquid crystal compound preparation, and advanced polymer additives. As a chemical manufacturer, we enable integrators and formulators to achieve required specifications through proven process control and regulatory compliance.

    1. Agrochemical Intermediates for Herbicide Synthesis

    This compound acts as a fundamental building block in the synthesis of selective herbicides based on substituted aromatic structures. Manufacturers use it for key coupling reactions in sulfonylurea or aryloxyphenoxypropionate herbicide APIs. Its reactivity at the bromine and chlorine positions provides high yield in condensation or substitution steps, ensuring target molecule purity and regulatory acceptability demanded in international crop protection markets.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 on plant protection products
    • United States EPA FIFRA registration requirements
    • ISO 9001:2015 Quality Management for production traceability
    • Technical Grade Pesticide (TGP) standards for starting materials

    Typical usage ratio

    • 5–15% by mass in intermediate coupling depending on target herbicide molecule
    • Exact ratio adjusted by molecular weight difference and desired batch output

    Downstream process integration

    • Acts as first aromatic halide in nucleophilic aromatic substitution or metal-catalyzed cross-coupling
    • Precursor in diazotization and condensation for triazine or pyridine-based herbicides
    • Enters early-stage reactor cascades before final step purification and formulation

    Final product types

    • Sulfonylurea herbicides (e.g., nicosulfuron intermediates)
    • Aryloxyphenoxypropionate herbicides (e.g., clodinafop-propargyl)
    • Selective rice and wheat herbicide formulations

    2. Pharmaceutical Active Ingredient Synthesis

    4-Bromo-2-Chlorotoluene serves as a selective halogenated aromatic intermediate for anti-infective, anti-inflammatory, and CNS active pharmaceutical ingredient manufacturing. It enters key steps such as Suzuki or Buchwald-Hartwig cross-couplings to construct core pharmacophores, where substituent control enables high-purity final APIs and compliance with global pharmacopoeial standards.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP and Ph. Eur. monographs for related substances/purity controls
    • FDA DMF and EU ASMF dossier standards for intermediates
    • REACH Regulation (EC) No 1907/2006 for import and use in the EU

    Typical usage ratio

    • 8–14% by weight of API for typical aryl coupling steps
    • Adjusted as per desired scale-up batch size and functional group conversion efficiency

    Downstream process integration

    • Feeds initial aromatic halide condensation or coupling stages
    • Undergoes halide exchange or Suzuki-Miyaura cross-couplings for biaryl system elaboration
    • Integrated into route prior to chiral center installation or final API purification

    Final product types

    • Anti-infective drug intermediates (e.g., quinolone derivatives)
    • Anti-inflammatory drug intermediates
    • CNS active pharmaceutical agent intermediates

    3. Dye and Pigment Intermediate Manufacturing

    Specialty dye and pigment producers use this compound as a core halogenated toluene intermediate, delivering chromophore structures with required substitution patterns for color fastness and solubility. Efficient integration into azo and anthraquinone synthesis routes supports consistent batch-to-batch reproducibility and environmental compliance required for textile, leather, and plastic coloration.

    Industry compliance standards

    • Oeko-Tex Standard 100 for human-ecological safety
    • EN 71-3:2019 Safety of toys – migration of certain elements
    • ISO 9001 for colorant manufacturing quality assurance
    • GHS classification and labeling for handling and use

    Typical usage ratio

    • 3–10% of total batch input for dye coupling or pigment condensation
    • Varied from 5–12% depending on shade intensity and finished product requirements

    Downstream process integration

    • Precursor in diazotization, nitration, or sulfonation to form base dye structure
    • Used in Friedel-Crafts acylation or alkylation steps for pigment core creation
    • Charged during pigment milling for coating and dispersion

    Final product types

    • Azo dyes for textile applications
    • Antraquinone pigments for plastics
    • Leather dyes
    • Printing ink colorants

    4. Liquid Crystal Material Precursor

    In the electronics sector, this compound is utilized for synthesizing halogenated biphenyl and phenylpyrimidine structures critical to advanced liquid crystal mixtures. Precision in isomer and impurity control aligns with exacting purity standards for display manufacturers, supporting high-performance displays with reliable electro-optical properties.

    Industry compliance standards

    • RoHS Directive 2011/65/EU compliance for electronics materials
    • ISO 9001/ISO 14001 for display and electronics manufacturing
    • JEDEC JESD96 for materials reliability testing
    • Individual display company QPLs (Qualified Product Lists)

    Typical usage ratio

    • 2–6% by weight per precursor batch for LC material synthesis
    • Optimized according to desired molecular distortion parameter and dielectric constant

    Downstream process integration

    • Input in early aromatic halide coupling for biphenyl or terphenyl scaffolds
    • Feeds into Suzuki or Ullmann coupling reactors to build LC core segments
    • Processed prior to purity-critical distillation steps before blending into LC formulations

    Final product types

    • Low viscosity nematic liquid crystals
    • Twisted nematic and in-plane switching LC mixtures
    • TFT-LCD display active material blends

    5. High-Performance Polymer Additive Synthesis

    This intermediate plays a role in the development of specialty polymer additives and monomers, where its specific aromatic substitution supports thermal stability or flame retardant functionality in engineering plastics. Processors introduce it at the monomer synthesis stage, achieving performance advantages for downstream compounders and molders.

    Industry compliance standards

    • UL 94 testing for flame retardancy of polymeric materials
    • REACH Annex XVII for restricted substances in polymers
    • ISO 14001 for environmental process management
    • RoHS Directive for plastics in electrical/electronic equipment

    Typical usage ratio

    • 2–8% by mass in monomer or additive synthesis batch
    • Adjusted for targeted thermal property or regulatory threshold

    Downstream process integration

    • Used in aromatic halide polymerization stages
    • Feeds into Friedel-Crafts alkylation for resin backbone modification
    • Enters batch at initial additive preparation prior to compounding

    Final product types

    • High-temperature engineering plastics
    • Flame retardant masterbatches
    • Polymer additives for automotive and electronics industries
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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-2-Chlorotoluene: A Practical Perspective from the Manufacturer

    Understanding the Product and Its Core Role

    Making chemicals like 4-Bromo-2-Chlorotoluene comes with years of hands-on work in synthesis, risk management, and consistent process control. At our facility, every batch of this compound reflects thousands of hours spent understanding how halogenated toluenes respond to real production demands.

    4-Bromo-2-Chlorotoluene carries the molecular formula C7H6BrCl. It stands out for its dual halogen substitution on the toluene ring, bringing both a bromine and a chlorine atom to the table. This simple-looking switch changes the reactivity and interaction profile dramatically compared to simple mono-halogenated toluenes or non-substituted analogs.

    A strong appreciation for these subtleties does not come from reading a data sheet. Over the years, we have run reactions where the precise placement of those bromine and chlorine atoms makes the difference between a high-yield, clean process and an unreliable one that fouls lines or wastes expensive reagents. This tweak in the molecular setup delivers real performance advantages, especially where later-stage functionalization and selectivity make or break a project’s economics.

    Quality and Purity: The Frontline Priorities in Our Plant

    Assuring the purity of 4-Bromo-2-Chlorotoluene is not a checkbox exercise. Our teams have learned that trace residuals—sometimes just a few hundred parts per million of starting material, side products, or even water—can sabotage downstream couplings, oxidations, or substitutions. Every shipment out of our plant meets a strict minimum of 99% purity by GC, often outperforming this mark thanks to robust distillation and highly selective crystallization steps.

    Some manufacturers will tout high purity, but years of firsthand troubleshooting teach that broad claims mean little without the assays to back them up. Every lot we release carries full chromatographic analysis, with careful review for key impurities. If a certain application requires closer control—say, for pharmaceutical intermediate routes—we scale up the QC, include NMR referencing, and assay moisture routinely to safeguard sensitive transformations.

    We have also adapted our process to minimize byproduct formation. Traditional halogenation methods fight unpredictable ring substitution. Through a blend of reagent selection, temperature control, and practical filtration techniques, we've learned to work with less operator intervention and deliver a tighter quality band.

    Technical Hands-On: Real Use Cases and Process Learning

    4-Bromo-2-Chlorotoluene does more than fill a spot on a reagent shelf. Process chemists order this compound to anchor key steps in agrochemical synthesis, pharmaceutical building block construction, and advanced material research. Its halogenation profile stands unique: introducing both a bromine and a chlorine atom opens up regioselective cross-coupling, radical substitution, and stepwise functional group replacement.

    Our customers report particular value during Suzuki and Buchwald-Hartwig couplings. Bromine sites on the ortho position activate readily for palladium catalysis, while chloro substitution at the second carbon tempers the reactivity and confers stability during storage and handling. Unlike simple bromotoluenes, having both halogens on the ring widens the menu of available transformations, letting process chemists choose the right tool for their downstream needs.

    We’ve seen smaller companies attempt to swap out dual-halogenated toluenes in favor of less costly, mono-substituted ones, only to run into low yields or challenging separation problems. The experience, both ours and theirs, backs up the argument: there's no one-size-fits-all shortcut. The unique structure of 4-Bromo-2-Chlorotoluene earns its place because it performs predictably at scale. Its substitution pattern offers synthetic routes that, after years of process optimization, run with fewer headaches and hit project milestones faster.

    Offering Value Beyond the Commodity Model

    Some view specialty toluenes as interchangeable widgets, but this ignores the sharp difference in reliability and downstream impact. Customers with real-world process concerns—fouled columns, stuck crystallizations, runaway exotherms—know the importance of a supplier with in-depth product understanding. Over years, we have learned to treat each kilogram not just as bulk output, but as a critical step in complex value chains where a missed impurity or an unstable lot can ripple into months of lost time or failed campaigns.

    A major trend shaping today’s market is the shift towards green chemistry and minimized waste. Our shop continuously adapts, using fewer hazardous reagents and closed-loop recovery where possible. Investing in updated automation systems has paid off in tighter control and fewer off-spec batches. We also keep a close dialogue with process teams who use our 4-Bromo-2-Chlorotoluene in continuous flow or semi-batch reactors and want to cut solvent use, heat loss, or emissions. These lessons feed back directly into our production practices. Eliminating inefficiencies, reducing waste per batch, and pushing overall sustainability move our whole sector forward—and let us offer more than a simple commodity.

    Comparing With Other Halogenated Toluenes

    Among the toluene derivatives we produce, 4-Bromo-2-Chlorotoluene stands out in two primary ways: stability and specificity. Mono-chlorotoluenes, like 2-Chlorotoluene, have long served as workhorses for electrophilic substitution and nucleophilic aromatic substitution. Although they work well for some applications, their chemical reactivity does not always provide the fine control needed in multi-step syntheses. Over-halogenated versions increase cost, risk, and can introduce too much reactivity—leading to hard-to-control side reactions or downstream hazards.

    We also run batches of 2-Bromotoluene, but—unlike its dichalogenated cousin—this compound brings greater lability. It reacts faster in many couplings, but without the ability to hold up under harsher process conditions or prolonged storage. Dual halogenated compounds like 4-Bromo-2-Chlorotoluene serve customers who need both activation and protection. The bromine offers a handle for cross-couplings or substitutions; the chlorine occupies the second position, imparting a shield but also a future transformation site. Our teams often reference real case histories: reactions that worked with 4-Bromo-2-Chlorotoluene gave half the yield or worse with mono-halogenated alternatives. Those differences become obvious in plant-scale runs, not just small-scale glassware.

    By contrast, other isomers such as 2-Bromo-4-Chlorotoluene or 3-Bromo-2-Chlorotoluene show different reactivity patterns and are sometimes harder to control due to positional effects. Separating these isomers at scale is challenging, often requiring more aggressive purification or higher unit operation costs. Sticking with the well-understood 4-bromo/2-chloro configuration, with rigorous process QA, brings real consistency. Analytical results from clients confirm this advantage, especially in regulated or validated settings where deviation from spec triggers costly troubleshooting and repeated batch failures.

    Production Method Insights and Lessons Learned

    Crafting 4-Bromo-2-Chlorotoluene takes more than following recipes. Real-world scale-up shows where theoretical yields break down and where investments in better control truly pay. We source high-purity chlorotoluenes as the starting material. Introducing the bromine group happens through a carefully monitored halogen exchange, monitored by GC and temperature probes throughout. Early on, we learned that allowing reactor hot spots or over-extended reaction times generates isomeric mixtures—problems that cannot always be solved by later purification.

    Our solution has come in the form of staged addition, better agitation, and using clean, dry starting material. Working over years, the plant team optimized parameters by reading both the chemistry and the equipment’s feedback—temperatures, flows, vapor pressures, and work-up losses. Solutions often come from hands-on experimentation rather than theoretical targets on a spreadsheet. Employee insight, gathered over hundreds of batches, often flags trouble before a lab report does. Programming better checks and integrating findings from bench chemists into manufacturing brings down rework rates and strengthens reliability. This practical approach puts end-use quality at the front of every batch.

    Safety and Handling Considerations, From the Trenches

    Direct experience with halogenated aromatics like 4-Bromo-2-Chlorotoluene shapes our approach to safety. Their volatility, possibility for skin contact, and role in downstream syntheses means we don’t leave safety to assumptions or generic MSDS cut-and-paste. Employees working in charge with transfers, blending, or drumming routinely report back on vapor levels, odors, and containment setups. Plant ventilation, real-time monitoring, and rigorous PPE standards all come from these lessons. Our own logs show how sharply risk falls when awareness and setup match chemical properties rather than old routines or outdated SOPs.

    Training counts more than paperwork. We keep close watch on learning, updating procedures annually as process chemistry or equipment changes. Similarly, regular audits and “near miss” log reviews highlight where improvement prevents real-world problems—both environmental and operational. For our clients, this culture of vigilance means delivered product that meets their containment requirements and integrates smoothly into closed-plant systems, solvent recovery networks, and modern material-handling environments.

    Adapting To Market Needs, Research, and Regulation

    The customer base for 4-Bromo-2-Chlorotoluene has shifted over the years. Initial demand came from bulk chemical production for intermediates. Today’s customer, often a process chemist with tight budget and regulatory targets, brings more complex queries—trace impurity profiles, solvent residue questions, REACH and other frameworks. We maintain documentation and change protocols to match, synthesizing samples under these tightened standards so that assuring compliance is not a last-minute scramble but a systemized part of the plant operation.

    We’re also speaking more frequently with research groups using these compounds to invent new polymeric materials or advanced imaging agents. Their questions often tie directly to how reproducible a given batch will be. From the plant side, these conversations steer our upstream purchasing, process scheduling, and documentation. Meeting precise, reproducible molecular ratios becomes a technical dialogue, not only between our internal teams but also in collaboration with those pushing the research frontier.

    Sustainability and Forward Progress: Practical Moves

    The days of making halogenated toluenes with little care for environmental impact or process mass intensity have ended. As a manufacturer, we have adopted alternatives to hazardous reagents wherever practical. Closed-system halogenation and greater heat integration save energy, reduce waste, and make for safer workplaces. Reusing solvents and recycling byproduct streams cuts both cost and environmental burden. Working towards these improvements comes from ongoing investment—not simply regulatory pressure.

    Clients have noticed the difference when sustainable methods lower risk in storage and transit as well. Tighter control over impurities means less hazardous waste generated in their own plants. Building these efficiencies is part of how we stay competitive, but also a core value—producing robust specialty chemicals without trading security, well-being, or regulatory stress for profit.

    Final Word: Why Real Experience Matters

    Experience as a direct producer of 4-Bromo-2-Chlorotoluene has underscored a core lesson: quality and consistency stem from deep understanding, not surface-level metrics. Each kilogram shipped carries with it the responsibility earned from decades of plant operation, troubleshooting, close customer support, and continual adaptation. Chemical manufacturing is not static; it evolves in step with each new challenge encountered on the floor or in the lab. Products like 4-Bromo-2-Chlorotoluene serve as evidence of this commitment—an intersection of precise science, operational rigor, and honest industry experience that benefits every link of the supply chain.

    Whether you are developing a new synthetic route, scaling a production campaign, or bridging the bench to the plant, input from real manufacturing experience improves outcomes. Delivering a product that supports your process begins well before the drums leave our yard. It rests on making every step—from raw material sourcing to finished lot QA—a focused, transparent, human-centered effort. We look forward to partnering with users who value reliability, technical support, and insight built on years of direct manufacturing in halogenated toluenes.