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2-Bromo-6-Chlorotoluene

    • Product Name 2-Bromo-6-Chlorotoluene
    • Alias 2-Bromo-6-chloromethylbenzene
    • Einecs 249-506-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    980312

    Chemical Name 2-Bromo-6-Chlorotoluene
    Molecular Formula C7H6BrCl
    Molecular Weight 205.48 g/mol
    Cas Number 7499-12-1
    Appearance Colorless to pale yellow liquid
    Boiling Point 218-220 °C
    Density 1.53 g/cm³
    Refractive Index 1.573
    Purity Typically ≥98%
    Synonyms 2-Bromo-6-chloromethylbenzene
    Solubility In Water Insoluble
    Flash Point 96 °C
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 2-Bromo-6-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 25g of 2-Bromo-6-Chlorotoluene, sealed with a screw cap and labeled with hazard and safety information.
    Shipping 2-Bromo-6-Chlorotoluene is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. The chemical is classified as hazardous and transported following all relevant regulations. Proper labeling and documentation accompany the shipment to ensure safe handling. Use gloves and goggles when unpacking. Store at room temperature upon arrival.
    Storage 2-Bromo-6-Chlorotoluene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep it away from sources of ignition and direct sunlight. Store under nitrogen or inert atmosphere if possible, and avoid prolonged exposure to air and moisture. Ensure proper labeling and secondary containment to prevent leaks or spills.
    Application of 2-Bromo-6-Chlorotoluene

    Applications of 2-Bromo-6-Chlorotoluene in Industrial Manufacturing

    We supply 2-Bromo-6-Chlorotoluene to global manufacturers for key applications in chemical synthesis. Its unique halogenated toluene structure supports targeted downstream formulation and process performance. Below, we detail real industrial scenarios, standards, usage rates, integration steps, and final products that rely on this specialty intermediate.

    1. Agrochemical Intermediates for Herbicide Synthesis

    Downstream agrochemical producers commonly select this raw material as a structural building block for synthetic herbicides, particularly in the preparation of substituted aniline and benzimidazole derivatives. Its ortho-substituted halogen profile enables efficient stepwise reactions in multi-stage crop protection chemistries, where trace impurity control and consistent assay are critical for regulatory registration. Manufacturers scale from kilogram to multi-ton production using controlled halogen-metal exchange, nucleophilic substitution, and amination steps under batch reactor systems.

    Industry compliance standards

    • FAO/WHO Specifications (JMPR, CODEX) for pesticide active ingredients
    • REACH Regulation (EU)
    • US EPA FIFRA requirements
    • ISO 9001:2015 certified QC for chemical intermediates

    Typical usage ratio

    • 10–25% by molar ratio relative to target herbicide core, adjusted by reaction pathway and desired herbicidal structure
    • Solvent volume generally 4–8 times the mass of the intermediate

    Downstream process integration

    • Added during initial nucleophilic aromatic substitution or halogen-exchange step after primary condensation
    • Continuous in situ halogen-metal exchange in dedicated glass-lined or stainless steel reactors
    • Final isolated intermediate purified via distillation or recrystallization before downstream amination or cyclization

    Final product types

    • Triazine-based pre-emergent herbicides
    • Benzimidazole-type fungicidal actives
    • Aromatic amine intermediates for grass and broadleaf weed control
    • Finished EC/SC formulation concentrates used in field application

    2. Pharmaceutical Intermediate in API Synthesis

    Branded and generic API manufacturers employ this halogenated toluene variant in the design of key building blocks for several non-steroidal pharmaceuticals and specialty CNS agents. Its dual halogen orientation is essential for regioselective coupling and stepwise derivatization in final active pharmaceutical ingredient routes. GMP-control frameworks mandate rigorous trace metal, residual solvent, and halide specification testing at every stage, with precise batch documentation and impurity profiling. Custom routes may include palladium-catalyzed cross-coupling using this intermediate.

    Industry compliance standards

    • ICH Q7 and EU GMP (EudraLex Vol 4)
    • US FDA cGMP (21 CFR Part 211)
    • Chinese Pharmacopeia (ChP)
    • ISO 17025 for in-process laboratory analysis

    Typical usage ratio

    • 15–30% mole ratio based on synthetic target; specific ratio defined by stoichiometric requirement of halogen substitution or coupling step
    • Solvent selection (DMF, DMSO, or toluene) maintains reagent concentration 0.1–0.3 mol/L

    Downstream process integration

    • Charged at the protected aromatic coupling or halogen exchange stage in commercial batch reactors
    • Incorporated during Grignard or Suzuki-Miyaura reaction steps for pharma intermediate construction
    • Pulled for analytical release after each major transformation before API finalization

    Final product types

    • CNS-active API core intermediates
    • Non-steroidal anti-inflammatory precursors
    • Aryl-alkyl substituted pharmaceutical scaffolds
    • Custom fine chemical blocks for regulated drug synthesis

    3. Electronic Chemicals: Organic Synthesis for LCD Materials

    Display material manufacturers incorporate this compound as a backbone moiety for the synthesis of liquid crystal monomers, which serve core roles in next-generation LCD and OLED layers. Its specific bromo and chloro positioning supports controlled coupling and elimination reactions, yielding intermediates for mesogenic units and alignment layers. Material purity, halide profile, and sub-ppm impurity targets must meet stringent electronic chemical norms for particle, ionic, and metallic contaminants.

    Industry compliance standards

    • SEMI E49/E35 standards for electronic chemical purity
    • RoHS-directive for restricted substances
    • ISO 14001 (environmental management during production)
    • Customer-specific LCD/OLED chemical supply chain audits

    Typical usage ratio

    • 5–12% by mass as core building block in liquid crystal monomer synthesis
    • Ratio varies by desired chain length and final mesogen structure

    Downstream process integration

    • Condensation and aromatic coupling conducted in staged reactors under inert or anhydrous conditions
    • Raw material added at precursor stage for mesogen alignment group construction
    • Final monomer purified and fractionated before polymerization/LC mixture blending

    Final product types

    • Mono- and di-functional LC monomers
    • OLED alignment film precursors
    • Advanced photolithographic materials
    • Display-grade liquid crystal mixtures

    4. Dye and Pigment Intermediate for Performance Colorants

    Producers of specialty dyestuffs and pigments use this raw material as a fundamental aromatic nucleus for synthesizing halogenated azo and anthraquinone dyes. Its high selectivity during Friedel-Crafts acylation and subsequent coupling steps ensures batch-to-batch color uniformity and stability in final pigment dispersions. Batch control targets trace metal and halide residuals, enabling qualification for automotive and industrial coatings, plastics, and printing inks.

    Industry compliance standards

    • DIN EN 71-3 for pigment safety in consumer applications
    • REACH SVHC listing for pigment raw material input
    • ISO 9001 for pigment QC and traceability
    • ASTM D476 for classification of pigment types

    Typical usage ratio

    • 5–18% by mass in dye precursor blending; ratio determined by chromophore target
    • Adapted batchwise for targeted hue and solubility properties

    Downstream process integration

    • Precursor charge at initial acylation or diazotization followed by halogen substitution or further coupling
    • Employed in microreactor or semi-continuous dye synthesis lines
    • QC monitoring for color, residual halogen, and particle profile before dispersion or granulation

    Final product types

    • Azo and anthraquinone pigment dispersions
    • High-performance plastic colorants
    • Specialty textile dyes for technical fabrics
    • Offset and gravure printing ink concentrates

    5. Specialty Fine Chemicals for Photoinitiator Synthesis

    This compound is a key feedstock in synthesizing certain specialty photoinitiators used in UV-cured coatings and inks. Halogen substituents aid in forming desired aromatic frameworks for high-reactivity photoinitiator agents. Process manufacturers emphasize reaction cleanliness, yield optimization, and targeted impurity removal. Final photoinitiator performance relies on consistent halogen content and reactivity for industrial UV polymerization line compatibility.

    Industry compliance standards

    • ISO 22196 for antimicrobial photoinitiator components
    • REACH for industrial use and occupational exposure
    • US TSCA compliance for chemical inventory
    • ISO 9001 production and analytical documentation

    Typical usage ratio

    • 8–20% by mass input based on targeted photoinitiator core structure
    • Adjusted by resin compatibility and functionalized aromatic loading

    Downstream process integration

    • Raw material blended at core aromatic assembly for photoinitiator adduct
    • Reaction steps under controlled inert conditions to prevent side-product formation
    • Final purification by recrystallization or chromatography, meeting UV absorbance targets

    Final product types

    • UV-curable resin photoinitiators
    • LED-cure ink initiator blends
    • Silicone elastomer curing agents
    • Specialty coating photoinitiator bottles for electronics and optics
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    Certification & Compliance
    More Introduction

    2-Bromo-6-Chlorotoluene: A Closer Look at a Vital Building Block

    Understanding 2-Bromo-6-Chlorotoluene in Today’s Chemical Landscape

    Every day on our production floor, chemists and technicians find themselves handling molecules that shape everything from new pharmaceuticals to advanced materials. 2-Bromo-6-Chlorotoluene stands out as one of those raw materials that rarely gets much press, yet pulls a surprising amount of weight in specialty syntheses. Work with this halogenated aromatic has shaped many of our own proprietary processes, and brought valuable insight into where the best uses for such intermediate compounds truly lie.

    Our team encounters 2-Bromo-6-Chlorotoluene most frequently as a highly purified, colorless to pale yellow liquid, manufactured to tight specifications. Most batches reach a GC purity of at least 99.0%, generally with water content kept below 0.2%. The molecular formula (C7H6BrCl, CAS 876-95-9) connects a bromine and chlorine to a methyl-substituted benzene core. Some colleagues like to refer to its aroma as sharp and medicinal, though a well-sealed drum quickly masks its signature. Our plant found that strict management of reaction conditions—especially temperature and choice of solvent—lays the groundwork for consistent quality, crucial in scale-up.

    Day-to-Day Applications Driven by Real Needs

    In our work, most 2-Bromo-6-Chlorotoluene stocks head straight toward the synthesis of complex organic molecules. The halogen atoms at the 2 and 6 positions make it versatile in Suzuki and Heck couplings—reactions that have fundamentally reshaped how fine chemical and pharmaceutical manufacturers construct carbon frameworks. Medicinal chemistry groups at our site sometimes use this compound as a starting point for candidate molecules directed at new anti-infectives or central nervous system agents. Fine-chemical synthesis never follows a one-size-fits-all path, but we saw growing adoption of this compound as researchers sought out substitution patterns unavailable from less elaborate toluenes.

    Another avenue where this material truly shines lies in agrochemical development. By modifying the toluene core, agroscience researchers build libraries of new actives or intermediates for fungicides or insecticides. Handling dozens of similar halogenated aromatics daily, our operators notice that workflows based on 2-Bromo-6-Chlorotoluene offer consistent yields and manageable by-product profiles. These practical considerations, tested over many production cycles, convinced our team to maintain a dedicated line for its manufacture. Without this stable supply, some developmental projects would stall outright.

    From specialty dyes to advanced electronic intermediates, this compound fills its niche in larger synthetic schemes. The methyl group brings a convenient handle for further functionalization, helping specialists push reactions in the direction they want. In collaboration with academic partners, our R&D lab confirmed that the ortho arrangement of bromine and chlorine gives access to regioselective reactions, a key advantage when other isomers give lower selectivity or produce unwanted by-products. This is as much a story of the power of careful substitution as it is about scale or commodity manufacturing.

    How 2-Bromo-6-Chlorotoluene Differs from Its Relatives

    Benzene derivatives come in a bewildering variety, so it pays to look at how this compound holds up against more common alternatives. We regularly compare 2-Bromo-6-Chlorotoluene with 2-Chlorotoluene, 2-Bromotoluene, and 4-Bromo-2-Chlorotoluene in our own pilot studies and scale-up runs. The main difference comes down to the dual halogenation at specific positions. This not only provides two distinct points for further substitution, but also influences electron-withdrawing strength and reactivity across the aromatic ring. Operators who have run multiple coupling reactions often note a marked difference in product profiles when switching among these isomers, even when using the same catalyst system.

    For us as manufacturers, the ability to influence regioselectivity using small changes in substitution has real commercial consequences. For example, in Suzuki couplings, 2-Bromo-6-Chlorotoluene generally reacts cleaner than 2-Chlorotoluene, which tends toward more sluggish oxidative addition. In trying to scale-up certain pharmaceutical intermediates, we found that reactions run cleaner, with fewer side-products, when starting from the dual-halogenated toluene. A few of our industrial clients report that this simplifies purification and waste handling, directly impacting their turnaround times and environmental targets.

    To some technologists designing radar-absorbing materials or OLED components, the symmetry of 2-Bromo-6-Chlorotoluene gives access to architectures and tuning options unavailable from monosubstituted alternatives. Handling them side-by-side, our technical staff demonstrates how seemingly subtle changes in structure create major shifts in UV absorbance or reactivity—something we see play out in our lab’s review of specialized dyes for precision printing. No two chlorotoluenes behave identically, and this is a fact that shapes batch scheduling and even plant design.

    There’s also the question of cost and sourcing. Common monosubstituted toluenes cost less and see wider use in bulk manufacturing. We choose to make 2-Bromo-6-Chlorotoluene because its distinct synthetic features justify the added complexity. Small-batch custom synthesis groups in our network return again and again to this compound to solve difficult synthetic puzzles, especially when seeking unusual substitution patterns or constructing new rings. Reduced run-to-run variability and manageable purification contribute to their preference for this isomer in problem-solving scenarios.

    Manufacturing Realities and Process Experience

    Bringing 2-Bromo-6-Chlorotoluene from bench to drum-scale asks for tight process control, something our operators learned through both setbacks and routine runs. Halogenated aromatics present fire and health risks, so our production cell runs on strict containment and ventilation standards. Real-world manufacturing brings fluctuations in temperature, feedstock quality, and batch timing, so we spent years fine-tuning our reactors to sustain both selectivity and throughput. We invest in in-line analytical tools—GC, water content check, and IR fingerprinting—so irregularities show up before they reach downstream processes.

    Supply interruptions in the fine chemical space aren’t just an annoyance—they can freeze drug development, halt agrochemical pilot plants, and throw off schedules months in advance. We maintain buffer stock, dual sourcing of upstream halides, and a trained support crew that knows where to look the moment a batch trends out of specification. In more than one incident, we’ve rescued long-term projects by troubleshooting halogen substitution reactions late at night, saving critical weeks for a customer’s formulation timeline.

    Switching between isomer synthesis lines—in one shift, moving from 2-Chlorotoluene to the 2-bromo variant—forces real attention to cleaning, cross-contamination risks, and reactor jacket control. Experience taught us that suboptimal charging order, or weak solvent choices, can cut yields by double digits or produce hard-to-remove resinous residues. Some of our engineers have documented process improvements in internal knowledge bases—small tweaks that might mean nothing to an outsider, but shave precious hours or kilos off production runs.

    Waste handling isn’t glamorous, but the halide by-products from this process require careful isolation and scheduled removals, both for safety compliance and neighbor relations. Other firms in our cluster benchmarked our emissions handling as a practical example, recognizing the extra effort we put into waste minimization and solvent recovery. The upshot—continuous improvement and compliance audits are less headaches than headline material, but they protect the long-term viability of this type of chemical manufacturing.

    Quality as a Habit Shaped by Experience

    Quality assurance, especially for intermediates that bridge discovery and scale, remains a team-wide commitment here. We draw on years of analytic practice, checking every lot for color, purity, halide content, and moisture uptake before green-lighting it for final use. Some of this is routine: columns chirping, printouts stacking up beside clean glassware, quick QC sign-off before transfer to shipping drums. At the same time, custom projects sometimes demand deeper dive: batch-specific NMR, trace element mapping, even impurity profiling that anticipates downstream reactions. Our experience showed us that foreseeing purification pain points at this stage saves everyone headaches, especially when scale-ups face tighter timelines and compliance deadlines.

    Feedback loops between production, R&D, and customer support matter just as much. It’s common practice to hop on a call or shoot over sample chromatograms when a partner runs into an unexpected yield drop or reaction foul-up. Sharing insights into how certain halide ratios or odd impurity ghosts can trip up sensitive Pd catalysis leads to improvements both in our downstream partners’ processes and our own work habits.

    The opposite of quality—unpredictable feeds, variation between lots, or poor documentation—burns time and erodes trust. Most of our regular customers know to request real lot-level data, and we’ve doubled down on digital record-keeping, traceability, and rapid turnaround on new batch results. It may not grab as much attention as new product launches or process patents, but it keeps the gears of innovation moving forward at a pace that rewards everyone in the chain.

    Addressing Challenges Through Collaboration and Process Refinement

    No process in the fine chemical industry runs forever without hitches. One challenge in the 2-Bromo-6-Chlorotoluene line has always been ensuring consistent halide substitution rates over long campaigns. The organic halide sources themselves—bulk bromine, chlorinating agents—fluctuate in purity depending on their own upstream suppliers. As a manufacturer, this means always running checks, balancing costs, and keeping alternative sources on standby. What we found is that reliable supplier relationships, regular feedback, and transparent QC make more difference than arm’s-length purchasing ever could.

    Process safety gets special attention. Halogenated solvents and aromatic intermediates create risks both for people and the environment. Our operational experience led us to build redundancies in scrubber systems, start predictive maintenance routines, and integrate staff training directly into our shift cycles. Veteran operators lead walkthroughs for new team members, flagging hazards that often only show up after long hours and heavy throughput. We’ve also adjusted process steps based on post-run data, dialing in reagent dosing and pressure control to handle unexpected reactivity or temperature spikes.

    Collaborative problem-solving extends beyond the plant. Our customers sometimes ask for variant grades—lower impurity profiles, specific isomer ratios, even alternative packaging to fit their pilot plant’s needs. Far from being a hassle, these requests drive our manufacturing team to innovate, proving out new filtration methods, drum options, or trace test protocols. The reality of modern chemical manufacturing is that no two runs stay identical for long, and regular exchange between producer and user remains key to matching quality to use case.

    Environmental Responsibility from Batch to Disposal

    No chemical manufacturer can operate isolated from its neighbors or environment. Halogenated aromatics have a well-known reputation—persistent by-products, odor, emission risks—so keeping the process safe and clean protects not only workers but everyone nearby. We updated our emission control infrastructure several times to control vent streams from reactors and still columns, installing scrubbers fit for high-halogen output. In our water handling, close monitoring and rapid neutralization keeps plant discharges within tight boundaries, regularly reviewed by local inspectors. Shared responsibility means everyone in the plant knows to catch leaks fast, rethink rinse-out routines, and contribute ideas during safety briefings.

    Solvent recycling has become a regular feature on our plant tours. Beyond the cost benefit, distilling and reusing solvents slashes our haul-away waste and shrinks purchasing frequency, letting us choose higher-grade input material for selective steps like halogenations. This tighter control reduces the environmental footprint of every batch—hard-won improvements that stem from operator suggestions and hands-on engagement with the tools of the trade. When process changes cut emissions or simplify compliance filings, they begin inside the plant, not just in boardroom strategy.

    Neighbors in our industry often ask about our lifecycle assessment work—how our intermediate products impact the supply chains downstream. Our internal tracking and auditing, refined over years of compliance encounters, let us give honest answers about where risks or opportunities for improvement lie. The ongoing drive to minimize halide residue and by-product streams shapes everything from reactor choice to end-of-line filtration setups. Focusing on measurable impact, we treat environmental stewardship as an ongoing process, not a bolt-on policy.

    Fostering Innovation Through Flexibility

    Much of the value in producing 2-Bromo-6-Chlorotoluene lies in the relationships between manufacturer and application specialist. Chemists in specialty fields frequently come to us with requests that stretch the boundaries of standard operation—higher selectivity for a coupling step, variant isomer mixes, or improved packaging to fit pilot reactors. Our experience tells us that flexibility often beats rigid process design, especially as R&D cycles shorten and new synthetic routes demand custom intermediates. The workflows we maintain today evolved from past collaborative projects, and ongoing feedback equips us to pivot quickly when customer needs shift.

    Shortages, regulation updates, or feedstock quirks occasionally throw curveballs our way, but a deep bench of technical expertise and willingness to iterate keeps us moving. Teams document each improvement, capture lessons learned, and recommend process tweaks when they see upstream or downstream partners facing a challenge. Some of our most effective innovations—like low-residue purification or in-process real-time analytics—grew straight from these ongoing conversations. Partners know they can approach us early with a problem or a possible project, expecting both technical rigour and creative flexibility.

    We recognize that 2-Bromo-6-Chlorotoluene will never become a mass-market chemical, and this specialty status makes it even more vital to invest in manufacturing excellence. As downstream uses continue to diversify, so too do the demands placed on us as a supplier. We treat each new batch, each novel request, as a potential opportunity to improve both product and process. Ongoing training, technical troubleshooting, and hands-on care remain the tools that define our factory’s reputation among researchers and formulation experts alike.

    Looking Ahead with Purpose

    The role of 2-Bromo-6-Chlorotoluene in modern chemistry isn’t just about meeting today’s production quotas. Putting years of experience into every batch, we see its potential unlocked in the hands of talented chemists, formulation teams, and process engineers far beyond our site. Every improvement in our process—from handling, purification, to environmental controls—adds value both for our immediate partners and the broader innovation ecosystem.

    It’s easy to overlook the silent contributors in the supply chain, but for those of us who work every day with high-purity, precisely manufactured halogenated intermediates, the impact is obvious. Reliable performance, clean runs, and rapid problem-solving transform a specialty chemical from “just another material” into an enabler of progress up and down the value chain. That understanding—the lived reality of both the manufacturing floor and the research lab—drives our ongoing commitment to both quality and partnership. The story of 2-Bromo-6-Chlorotoluene is far from finished, and together with our peers and partners, we continue to refine and deliver the intermediates that power tomorrow’s breakthroughs.