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HS Code |
187852 |
| Chemicalname | 2-Bromo-4,6-Dichloroaniline |
| Casnumber | 70153-39-0 |
| Molecularformula | C6H4BrCl2N |
| Molecularweight | 256.92 g/mol |
| Appearance | Light brown to beige solid |
| Meltingpoint | 95-98 °C |
| Solubility | Slightly soluble in organic solvents |
| Density | 1.86 g/cm3 (estimated) |
| Purity | Typically ≥98% |
| Synonyms | 2-Bromo-4,6-dichlorobenzenamine |
| Smiles | Nc1cc(Cl)cc(Cl)c1Br |
| Storagetemperature | Store at 2-8 °C |
As an accredited 2-Bromo-4,6-Dichloroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed with screw cap, labeled with hazard symbols; contains 25 grams of 2-Bromo-4,6-Dichloroaniline. |
| Shipping | 2-Bromo-4,6-Dichloroaniline is shipped as a hazardous chemical, typically in sealed, chemical-resistant containers to prevent leaks and contamination. It must be accompanied by appropriate safety documentation and labeling in compliance with regulations, transported by trained personnel, and stored securely away from incompatible substances, heat, and moisture during transit. |
| Storage | 2-Bromo-4,6-Dichloroaniline should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep the storage area clearly labeled and restrict access to trained personnel. Avoid moisture and sources of ignition. Use secondary containment to prevent accidental spills or leaks. |
Applications of 2-Bromo-4,6-Dichloroaniline in Industrial Manufacturing2-Bromo-4,6-dichloroaniline serves as a critical intermediate in several high-value chemical production chains. Its unique halogenation pattern supports advanced synthesis routes in the agrochemical, pigment, specialty polymer, and pharmaceutical sectors. As a direct manufacturer, we supply consistent quality material suited for demanding downstream integrations. 1. Agrochemical Synthesis: Herbicide IntermediateLarge-scale herbicide producers use this compound as a core building block in selective weed control formulations. Its electron-withdrawing characteristics allow stable coupling in aromatic substitution, favoring synthesis of chloro- and bromo-substituted herbicidal actives. Regulatory compliance requires detailed tracking of raw material origins and consistent halogenation ratios. Major processing steps include amide formation and further halogen exchange under controlled conditions. Finished herbicides based on this intermediate demonstrate controlled soil degradation rates and selectivity for broadleaf weed management in cereal crops. Industry compliance standards
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2. High Performance Pigments: Intermediate for Complex Azo DyesPigment manufacturers employ this chemical as a halogenated aniline precursor for synthesis of fastness-critical yellow and orange azo pigments. Its controlled reactivity supports diazotization reactions, producing stable pigment couplers with enhanced light and weathering resistance. Stringent purity and absence of metal contaminants are essential, as off-color generation and migration properties directly impact industrial coatings and textile applications. Implementation requires strict batch reporting and raw material segregation to comply with banned amine directives. Industry compliance standards
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3. Active Pharmaceutical Ingredient (API) IntermediateAPI manufacturers utilize this compound as a highly controlled intermediate in the synthesis of specific anti-infective and anti-inflammatory drug candidates. The dual halogen functionality allows regioselective amide or sulfonamide formation under GMP conditions. This step demands traceability, dedicated equipment, and validated cleaning protocols. Residual levels and potential impurities are tightly regulated under pharmacopoeial specifications. Downstream processing involves further functional group transformations and salt formation to meet clinical quality controls. Industry compliance standards
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4. Specialty Polymers: Reactive Monomer AdditiveChemical processors in the specialty polymer sector incorporate this material for introducing halogen sites into custom-engineered aromatic resins and high-performance plastics with enhanced flame retardancy. The compound enters condensation polymerization steps, contributing to controlled crosslink density and polymer backbone modification. Compliance requires adherence to polymer-grade specification limits on residual monomers and extractables. Producers adjust feed ratios to meet required mechanical and fire safety properties, especially in electronics and automotive interior components. Industry compliance standards
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The chemical industry lives by its molecules. Each building block on our production floor carries its own signature, both in reactivity and influence downstream. 2-Bromo-4,6-Dichloroaniline—known across research benches and synthesis pipelines—shows what consistent quality and purity bring to process efficiency. Its structure, with bromo and two chloro groups bracketed on the aniline ring, provides a unique combination of electronic effects. Consistency is king in synthesis, and one recurring lesson from years working with this fine chemical is simple: true reliability springs directly from each batch’s identity and integrity as we ship material to our partners.
Daily production starts long before a single drum leaves our doors. Raw material scrutiny determines batch outcomes; incoming halogenated aromatics undergo layered analysis using gas chromatography and NMR. People sometimes ask, “What separates manufacturer-produced chemicals from brokered lots?” The answer is felt on the shop floor and confirmed in the customer’s reactor. Sourcing is about more than price—it means tracking purity to the decimal and understanding where every atom comes from.
2-Bromo-4,6-Dichloroaniline arrives as a tan to light brown crystalline powder. In-house methodologies shape its properties tightly around key analytical targets. HPLC consistently meets or surpasses 99% area purity. This work takes real attention to detail during every synthesis, work-up, and purification stage. We do not outsource core processing, and every lot’s journey through crystallization, filtration, and drying brings with it years of hands-on refinement. Each stage is recorded in data logs—not for compliance, but to preempt potential downstream reactivity issues regularly encountered by end users.
Aniline derivatives are a crowded field, with minute changes affecting how these molecules behave in reactions. The bromo and dichloro pattern on the aromatic ring in 2-Bromo-4,6-Dichloroaniline tips a balance of steric hindrance and electron withdrawal unique among specialty intermediates. Many customers working in the agrochemical or pharmaceutical sphere use analogs like 4,6-Dichloroaniline or 2-Bromo-6-Chloroaniline, but side-by-side bench trials often highlight differences that are only obvious when you live with the chemistry day-in day-out.
With two chloros and a bromine, 2-Bromo-4,6-Dichloroaniline gives reduced electron density compared to mono-substituted anilines, meaning it moves slower in certain nucleophilic aromatic substitutions. This matters for scaling up couplings or targeted diazotization. Our partners rely on this predictability not just for one-off pilot runs, but integrated multi-step syntheses feeding full-scale production. Where analogs could open unwanted side pathways or form by-products, this compound’s profile allows for cleaner product slates in many APIs and crop protection active ingredients.
We manufacture for an audience that takes synthesis seriously—teams who measure process time in seconds and yields in fractions of a kilogram against budget. The most important uses for 2-Bromo-4,6-Dichloroaniline trace to its role as a synthetic intermediate. As a coupling partner, it gets engaged directly in Buchwald–Hartwig and related amination reactions, and for certain pyrimidine and benzimidazole scaffolds, process scientists prefer this particular substitution pattern for consistent selectivity.
This material finds a ready path into industrial dye manufacture, acting as a precursor for pigments used in specialty applications where weather resistance and color fastness take precedence. Years of feedback from dyes and pigments customers made it clear: minute contamination in the aniline itself can ruin entire batches, leading us to double down on purity benchmarks—every single drum is qualified against highly specific trace impurity criteria, not just general purity.
On the crop-protection side, several actives rely on the dichloro-bromo motif. We support customers formulating fungicides and insecticides—molecules that stay active in the field, withstanding sunlight and moisture thanks to halogen-bolstered stability. Development teams have worked closely with us to nail down grade specifications tuned for carryover in multi-hectare application scales.
The market shows no shortage of chlorinated or brominated anilines. Each has its champions: 4,6-Dichloroaniline sports moderate electron withdrawal, 2-Bromoaniline brings high reactivity, but the twin-chloro/twin-bromo motif offers a signature fit for specialists. Change one group, and reactivity profiles shift. In-house teams learned this through hard-won experience during process development, especially when side-by-side comparison runs exposed subtle but critical shifts in yields, selectivity, or crystallization profiles.
For projects where only a specific reactivity window is tolerated, 2-Bromo-4,6-Dichloroaniline stands apart. The difference shows up in the number of purification steps needed and the nature of by-products. In the pesticide industry, for example, the wrong isomer drives up costs down the line in formulation and leads to waste streams that are more difficult to validate for ecological safety. This is more than theoretical: major agricultural clients who switched from lower-purity, mismatched analogs to tightly-controlled lots from our lines reported measurable improvements in final product shelf life and application strength.
Taking care with hazardous intermediates amounts to more than regulatory box-checking. Teams on our floor handle 2-Bromo-4,6-Dichloroaniline with understood protocols. Its synthesis brings hydrobromic and hydrochloric acid by-products, which we recycle and neutralize in closed-loop waste treatment setups. The end product itself does not present volatile hazard risk under standard storage, yet the dust calls for standard NIOSH filtration precautions.
Some users have struggled with batch variability from third-party traders, especially when off-spec isomer ratios or higher levels of residual halogenated impurities slip past basic inspections. Direct-from-manufacturer relationships close that gap. Technical support teams work both on remote calls and on-site, walking client teams through scale-up or troubleshooting off-line analytics to make sure what ships performs as promised with every lot.
Distribution models shape how customers interact with the chemical supply ecosystem. By manufacturing at scale, we can offer true lot-to-lot traceability, something less concrete with intermediate traders. Starting from gram samples for bench trials, contract clients frequently scale up to multiple-metric-ton offers for long-term partnerships. This reach into consistent batch delivery reduces changeover costs and bottlenecks traced to inconsistent characteristics—qualities that make or break high-throughput production in pharmaceuticals and agrochemicals.
End users remark on the difference between small pilot batches sourced from labs and the reliable performance seen in commercial, production-scale lots straight off a consistent synthesis line. Those working with sensitive catalytic couplings or step-economy synthesis processes saw dramatic improvements in time to qualification and scale-up when shifting away from poorly-documented intermediates to those built and tracked under a single manufacturing roof. This feedback loop, passing from our plant floor back to the customer, drives improvements every single quarter.
Cross-border shipments of halogenated aromatics face a thicket of paperwork and oversight. Product identity certification, safety documentation, and tailored certificates of analysis keep every lot above-board. Regulatory frameworks in the US, EU, and Asia evolve year by year, often in response to misuse or environmental legacy concerns. Manufacturers track these changes closely, sometimes amending process flows to cut trace impurities not for immediate reactivity, but for compliance and reputational trust.
Direct producers act as partners through this maze. Documentation collected and maintained over years means customers find easier customs clearances and less downtime stuck at ports. For those deploying final products in regulated markets—crop protection firms, API manufacturers—the peace of mind comes from lot-specific documentation that proves compliance with evolving environmental and product safety standards.
Aniline derivatives invite scrutiny due to their environmental persistence and potential toxicity. As a manufacturer, we’ve had to confront the impact of our own off-gas streams, halogenated residues, and parent chemical run-off. Improvements built into modern plants include on-site solvent recovery, real-time emissions monitoring, and staged aqueous waste treatment selected for halogen load.
Feedback from downstream users—especially large-scale formulators—led to the adoption of returnable containers and recapture programs for residual solids. A constant push exists within facilities to reduce overall process intensity, both to trim operational costs and to meet tightening legal caps on discharge. Innovation flourishes under pressure, and some of the biggest steps forward come from collaboration between technical teams and end users: recoverable synthetic intermediates and closed-cycle routines cropped up out of brainstorming with major partners, not regulatory dictates.
Markets for specialty intermediates move with regulatory cycles, patent churn, and seasonal shifts in agricultural demand. Direct manufacturing ropes in a suite of risks and opportunities. As raw material prices fluctuate—bromine sourcing is notorious for its volatility—production schedules flex not just to meet short-term orders, but to lock in year-long frameworks supporting both small, research-driven firms and high-volume formulators.
Having control over the continuous synthesis pipelines shields us from many supply chain jolts. Sudden shortages affecting brokers ripple less, as built-in inventory schemes and trusted raw providers support on-time shipment even during disruptions. Long-term partnerships developed with core clients allow for collaborative scheduling, smoothing both forecasts and the fulfillment rate. Feedback, positive or troubleshooting, routes right back to our in-house chemists, not traders.
Nothing replaces the insights gained from repeated hands-on synthesis and close contact with users. Time spent troubleshooting a slow amination, or finding the root cause behind an off-color pigment batch, underlines every improvement in how 2-Bromo-4,6-Dichloroaniline gets prepared, packaged, and supported. The demands of the manufacturing sector mean every mistake costs—lost time, scrapped material, or regulatory delay. Direct feedback taught us early that upstream diligence, on-site analytics, and full process transparency matter more than buzzwords or corporate gloss.
The relationships we build, shipment by shipment, hold together through thick and thin. Producers see their product downstream—in vibrant textile dyes, in effective crop protectants, and in targeted drug syntheses—knowing the batch history not as a digital file, but as real, testable quality, shaped by hands, machines, and disciplined routines. Every ton shipped is rooted in deeply local accountability and the shared stories of researchers, engineers, and operators whose work is measured not in platitudes, but in consistent results.
Chemical intermediates like 2-Bromo-4,6-Dichloroaniline bridge laboratory dreams with industrial realities. The future leans on agile manufacturing—new process analytics, ongoing purity improvements, and even cleaner waste treatment. We listen to partners looking to meet tighter residue limits or boost throughput with improved intermediates. As research advances—new green syntheses, bio-based aromatics—downstream expectations rise, and so do standards on the production floor.
This spirit of collaboration drives change from within. More open channels between manufacturers and end users promote process tweaks felt not just at one site, but across product lifecycles. The role of the direct producer is less middleman, more strategic partner; reliability transcends any single drum or order sheet. Processes evolve, but the heart of manufacturing remains tied to the hands-on, unglamorous discipline that built the industry—a daily, practical pursuit of the perfect batch.
| Aspect | Impact on Users |
|---|---|
| Production Traceability | Ensures consistent performance, supports regulatory and process troubleshooting |
| Purity Analytics | Reduces by-product risk, improves downstream yield and efficiency |
| Direct Feedback Loops | Enables rapid response to batch or application challenges |
| Sustainability Practices | Reduces environmental footprint, helps meet downstream compliance |
| On-Demand Scale | Supports both research and industrial demand without quality drift |
Manufacturing 2-Bromo-4,6-Dichloroaniline becomes more than an exercise in chemical synthesis. The day-to-day experience informs a practical, results-driven mindset shaped by customer feedback, hands-on process optimization, and a firm stand on transparency. Refining each batch to meet tough standards is a shared achievement, connecting the manufacturer directly to the breakthroughs and products that shape industries and improve lives.