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HS Code |
276393 |
| Chemical Name | 2,6-Dibromo-4-Chloroaniline |
| Molecular Formula | C6H4Br2ClN |
| Molar Mass | 285.36 g/mol |
| Appearance | Light yellow to beige crystalline solid |
| Melting Point | 147-150 °C |
| Boiling Point | N/A (decomposes before boiling) |
| Cas Number | 6336-92-1 |
| Solubility In Water | Insoluble |
| Density | 2.16 g/cm³ (approximate) |
| Purity | Typically ≥98% |
As an accredited 2,6-Dibromo-4-Chloroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,6-Dibromo-4-Chloroaniline is supplied in a 25g amber glass bottle with a secure screw cap and chemical hazard labeling. |
| Shipping | **Shipping Description for 2,6-Dibromo-4-Chloroaniline:** Ship in tightly sealed containers, protected from physical damage, moisture, and incompatible substances. Comply with hazardous material regulations. Use appropriate labeling and documentation. Store and transport at room temperature, away from heat and strong oxidizers. Ensure personnel use gloves and eye protection. Consult SDS for further handling and shipping details. |
| Storage | 2,6-Dibromo-4-chloroaniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. It should be kept separate from strong oxidizers and acids. Store under inert atmosphere if possible, and ensure containers are clearly labeled. Handle with appropriate personal protective equipment (PPE). |
Applications of 2,6-Dibromo-4-Chloroaniline in Industrial Manufacturing2,6-Dibromo-4-Chloroaniline supports several key sectors as a specialty intermediate, driving value through its specific reactivity profile. Below, we detail its established downstream applications, relevant standards, process roles, composition ranges, and ultimate product forms, grounded in the realities of industrial practice. 1. Synthesis of Agricultural Fungicide IntermediatesThe compound functions as a designated building block for certain systemic fungicides used in crop protection. Its halogenated aniline structure supports targeted coupling and acylation reactions in the synthesis of fungicidal active ingredients, where purity must be consistently maintained to prevent formation of undesired isomers in the final agrochemical. Only certified facilities handle this step, with careful monitoring of trace impurities and batch reproducibility. Industry compliance standards
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2. Manufacturing of Specialty Dyes for High-Performance TextilesThe compound serves as an intermediate in production of disperse and reactive dye molecules designed for polyester and polyamide textile fibers. Its unique halogenation pattern enhances washfastness and dye uptake control in coloration chemistries. QC protocols require precise isomer ratios and minimal halide contaminants to ensure reproducible color qualities across long production runs. Industry compliance standards
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3. Pharmaceutical Intermediate for API Synthesis (Non-Direct Medicinal Use)Chemical producers use this compound as an advanced intermediate to construct specific regulatory-approved pharmaceutical actives, especially where controlled halogenation is required for subsequent coupling and dehalogenation chemistries. All processes must maintain stringent traceability and batch hygiene, with validated analytical procedures to exclude genotoxic or residual solvents per pharmacopeial demands. Industry compliance standards
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4. Polymer Modifier for Specialty Engineering Resin ProductionProducers use 2,6-dibromo-4-chloroaniline as a functionalizing agent during formulation of engineering polymers where flame retardancy and tailored mechanical properties are required. Its selective halogen loading enables controlled incorporation into the polymer backbone, which is critical to achieving both industry-mandated fire standards and maintaining extrusion or molding performance needed for functional components. Industry compliance standards
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5. Intermediate for Veterinary Active Ingredient ManufactureWith protocols mirroring pharmaceutical synthesis but adapted for veterinary product requirements, this compound enters as a synthesis intermediate for select antiparasitic or antimicrobial actives. Batch and route records must remain auditable, while all input materials comply with veterinary-specific monographs and residue guidelines to support final product licensing. Industry compliance standards
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In our years of manufacturing complex aromatic amines, we found that 2,6-Dibromo-4-Chloroaniline stands out for the unique performance it delivers in specialty synthesis. This compound, recognized by its precise arrangement of two bromines and a chlorine on the aniline core, bridges fundamental chemistry with industrial innovation. Its molecular composition is straightforward: two bromine atoms at the 2 and 6 positions, one chlorine at the 4 position, anchored to an aniline backbone. From hands-on production experience, managing these halogenation steps requires fine-tuned conditions and dependable batch consistency—no shortcuts. Achieving reproducibility in purity, typically above 98% by HPLC, keeps downstream processes on schedule and prevents costly setbacks.
Rolling out this compound on a regular basis has taught us how subtle variations can ruin a whole production campaign. This is not just a commodity: a minor impurity, shift in melting point, or deviation in particle size distribution can send synthesis routes spinning off target. We set up in-process checks and real-time analytical support to keep each batch tightly controlled. Any time a chemist requests technical data for a new project—dye intermediate, photoresist precursor, crop protection active—we know purity and lot integrity will make or break the chemistry. The slightest batch-to-batch fluctuation can sabotage scale-up.
2,6-Dibromo-4-Chloroaniline’s model is built for reliability in demanding synthesis. The typical specifications we adhere to include a melting range from 105 to 108 degrees Celsius, hardly deviating from the literature. Solubility leans toward low levels in water yet compatible with many common organic solvents, an asset when integrating with other aromatic substrates. By keeping chloride and bromide starting materials ultra-clean, and stringently managing temperature ramps, we reached low residual halide levels in our finished batches—details that matter when running chromatography or high-selectivity reactions. Every drum and bag we deliver is packed with robust moisture barriers because this compound likes to cake and clump if stored carelessly, a headache experienced chemists remember well.
Our continuous improvement process drove us to refine crystallization controls and post-filtering—resulting in uniform particle flow, saving customers hours of regrinding or sieving. Any odd color hints at yet-undetected impurities, so we implemented colorimetric inspection on finished goods. We’ve had cases where an off-white tint signaled residual bromide, leading us to rethink a filtration step. This attention to physical and analytical detail builds confidence with industrial clients, especially those in high-purity arenas like electronic chemicals and pigment intermediates.
The successes of our clients tell the full value story of 2,6-Dibromo-4-Chloroaniline in manufacturing pipelines. Specialty dye makers value its structure as a cornerstone for bright, lightfast pigments. Crop protection chemists appreciate its reactivity, particularly as a nucleus for further halogenation—giving a launch point for active ingredient synthesis. The pharma and specialty chemical segments push its limits in the search for robust, selective intermediates. By working directly with technical users, our process development team responds to unique flow rates, handling, and downstream requirements without diluting chemical integrity.
Process safety gets real with halogenated aromatics. Our plant operators never cut corners with ventilation in halogenation steps. Years back we learned, during a site visit with a major dye manufacturer, that downstream sulfonation worked best only with ultra-low inorganic halide residue, well below industry “standard.” That lesson steers our process design. Each industry brings a different set of demands: pigment customers flagged trace amines; pharmaceutical partners demanded exceptional batch-to-batch reproducibility; agrochemical firms monitored for reactive byproducts. Consistently meeting those demands requires short communication loops, rigorous traceability, and a plant culture where no contamination is ever “acceptable.”
Markets often consider products like 2,4-Dibromoaniline, 2,6-Dichloro-4-Bromoaniline, and their lower-halogen analogs as possible substitutes. Through direct testing and field feedback, we've documented how 2,6-Dibromo-4-Chloroaniline’s halogen pattern produces sharper reactivity and greater selectivity in cross-coupling reactions and halogen-exchange strategies than its mono- or dihalogenated cousins.
Catalytic downstream processes, such as Buchwald-Hartwig aminations and Suzuki couplings, frequently benefit from the steric arrangement in 2,6-Dibromo-4-Chloroaniline. Less-substituted anilines often drift into unpredictable byproduct profiles or incomplete conversions. During an in-depth collaboration with a pigment manufacturer, the difference in endpoint yield and purity led them to standardize on our product after a comparative trial. Less-substituted analogs produced unacceptable red-shifted impurities. Choosing the right halogen topology impacts more than yield: it prevents production bottlenecks, improves color fastness, and minimizes regulatory headaches from trace contaminants.
Furthermore, our clients have run side-by-side experiments with resorcinol-based or singly halogenated anilines, searching for a drop-in solution to cost or regulatory pressures. They came back favoring 2,6-Dibromo-4-Chloroaniline for its precise reactivity, easier purification, and reliability in process scale-up. In large-scale dye and pigment production, a shift in precursor chemistry ripples all the way through quality, reprocessing rates, and environmental emissions. These are not abstract outcomes—repeatable successes with 2,6-Dibromo-4-Chloroaniline have real operational impact.
Nothing tests a product like the transition from kilo lab to manufacturing tons. 2,6-Dibromo-4-Chloroaniline isn’t spared from challenges. Maintaining purity while scaling up halogenation calls for advanced reactor controls and careful vent handling. Our engineers notice that even small interruptions in temperature programming can spike impurity levels or create residual reaction intermediates, requiring costly reworks. Persistent moisture absorption challenges prompted us to invest in specialized packing lines, including nitrogen-flushed, double-lined sacks, both to lock in purity and to prevent caking—all stemming from lessons learned with large shipments to humid ports in Asia.
For exporters, there’s the hazard profile. Strict compliance with international rules for shipping halogenated aromatics means that logistics planning starts early. Delays on the dock can trigger off-spec conditions or deteriorate physical properties. Trace level documentation—COAs, residual solvent analyses, detailed batch records—have become as essential as the drum itself. We have first-hand experience with customs queries and regulatory audits. Only thorough preparation, direct manufacturer knowledge, and a cooperative logistics network keep the supply chain moving. We learned the hard way: relying on a third party introduces risks not worth the savings. Decades of experience—chemists, operators, and technical teams on the shop floor—stands behind each kilogram produced.
Markets don’t stand still. A decade ago, basic compliance and high assay were enough. Now, regulatory changes in Europe and Asia ask for precise traceability, details on any known contaminants, and robust ecological data across all materials. Customers value transparency: we open up process details—right down to reagent sources or analytical methods—so nobody is left guessing about their supply chain risks. Proactive dialogue with industry leaders taught us that legacy practices no longer pass muster; the new normal expects real data on every performance attribute relevant to end-use, particularly for products heading into highly regulated or consumer-facing applications.
Any time a formulator updates their systems or a government tightens rules on halogenated intermediates, our team revisits control steps, looking for overlooked byproduct risk or documentation gaps. Engaging with environmental and workplace regulators—rather than seeing them as adversaries—helped us anticipate stricter discharge, labeling, and packaging standards. Our plant invested heavily in closed-loop controls, advanced monitoring, and independent audits to ensure every shipment stands up to scrutiny both domestically and overseas. Tighter specification sheets, batch certificate protocols and integrated digitally traceable workflow systems emerged directly from years of dialogue, not generic market pressure.
The only way to keep top clients is to enable their innovation. Research teams from fine chemical blenders and electronic material suppliers lean on our ability to supply consistent lots, on spec and on time. Many research groups have built multi-year projects around our batches of 2,6-Dibromo-4-Chloroaniline, trusting that every gram from pilot plant to commercial tonnage matches their published method. Failures due to incoming raw material variance can waste months. Our technical staff maintains a feedback loop that identifies trends and tweaks—if there’s ever a question from bench scientists or scale-up engineers, we track down the source fast, not just blame the process.
One research group, developing a novel polymer additive, hit an unexpected hurdle with another supplier: batch color drifted, melting point scattered, and purification steps failed. Their trial with our material ran smooth, and our support staff walked through every test method, result, and stability check. We encouraged them to stress test different particle sizes and explore new solvent systems, and we adjusted our protocols so their process ran at maximum yield. Integrating feedback rather than dictating specs transformed that partnership into a long-term advantage, leading to new commercial applications and process improvements.
Manufacturing halogenated aromatics brings inherent environmental and safety considerations. We have seen, over time, that prioritizing closed handling systems, glovebox sample draws, routine air monitoring, and batch contaminant checks not only protects our staff but prevents environmental releases. Our active role in local chemical management networks brought stronger controls and upgraded disposal protocols, grounded in real-world incidents of improper storage and transport vulnerabilities.
Eco-conscious customers, and those facing stricter REACH and TSCA regulations, routinely ask for detailed disclosure on hazardous byproduct management, spill history, and our plans for minimizing emissions. We handle these requests openly, providing comprehensive breakdowns of our abatement systems, historical data on emissions, and changes made after internal audits flagged improvement areas. Staff training on emergency response, container integrity, and regulatory documentation is ongoing. Our facility maintains an evolving risk register, updated with every new learning—transparency nurtures confidence with every client discussion, no matter how technical.
It is tempting to see specialized halogenated aromatics as interchangeable commodities. Experience proves that the story never ends at molecular weight or purity percent. The true value lies in robust process controls, technical expertise embedded in every shipment, and direct accountability for supply, quality, and stewardship. The operational headaches disappear only when the supply partner demonstrates real depth—across chemistry, logistics, documentation, and sustainable practice.
Our commitment has concrete impact—carefully engineered drum liners mean product arrives in optimal condition in hot, humid climates; real-time analytical insights give process engineers confidence in batch-to-batch repeatability; end-use troubleshooting is grounded in hands-on experience, not just theory. We believe the relationship grows not from overpromising miracle performance, but by consistently delivering above expectations in challenging situations.
Aromatic amines with well-calibrated halogen substitution remain vital in the evolution of dyes, pharmaceuticals, agrochemicals, and advanced materials. The real-world experience from our team—chemists who solve nagging yield or impurity puzzles, logistics staff who prevent transit damage, and regulatory stewards who keep shipments safe—elevates 2,6-Dibromo-4-Chloroaniline from a mere raw material to an essential tool for industry progress.
Only by marrying product reliability with open, technical partnership can manufacturers empower clients to meet their goals: whether that means tighter color tolerance, better crop protection, or safer, more sustainable finished goods. Our everyday decisions, rigorous process reviews, and long-term partnerships build more than just a chemical supply—they contribute to the innovation and responsibility that today’s markets, regulators, and communities expect.