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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 | 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. |
Applications of 2-Bromo-6-Chlorotoluene in Industrial ManufacturingWe 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 SynthesisDownstream 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
Typical usage ratio
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2. Pharmaceutical Intermediate in API SynthesisBranded 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
Typical usage ratio
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3. Electronic Chemicals: Organic Synthesis for LCD MaterialsDisplay 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
Typical usage ratio
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4. Dye and Pigment Intermediate for Performance ColorantsProducers 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
Typical usage ratio
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5. Specialty Fine Chemicals for Photoinitiator SynthesisThis 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
Typical usage ratio
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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.
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.
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.
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 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.
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.
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.
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.
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.