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2-Bromo-4,6-Dichloroaniline

    • Product Name 2-Bromo-4,6-Dichloroaniline
    • Alias 2-Bromo-4,6-dichlorobenzenamine
    • Einecs 218-732-6
    • 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
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    Specifications

    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 & Storage
    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.
    Application of 2-Bromo-4,6-Dichloroaniline

    Applications of 2-Bromo-4,6-Dichloroaniline in Industrial Manufacturing

    2-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 Intermediate

    Large-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

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO CODEX Alimentarius — Pesticide Residue Limits
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • US EPA TSCA (Toxic Substances Control Act) listing and data reporting

    Typical usage ratio

    • 5–25% of batch mass in precursor synthesis stage; adjusted per target molecule and reaction yield optimization

    Downstream process integration

    • Initial coupling with acid chlorides or isocyanates to form key intermediates
    • Direct input at Stage 1 of multi-step synthesis under inert atmospheres
    • Continuous monitoring for trace halide content to meet final purity

    Final product types

    • Chloro- and bromo-substituted herbicide actives for pre- and post-emergence applications
    • Weed control agents used in wheat, barley, and maize cultivation

    2. High Performance Pigments: Intermediate for Complex Azo Dyes

    Pigment 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

    • EN 71-3 (Safety of Toys — Migration of certain elements)
    • ISO 9001 quality management for pigment manufacture
    • REACH Regulation (EC) No 1907/2006 — SVHC monitoring
    • OEKO-TEX® Standard 100 for textile applications

    Typical usage ratio

    • 2–10% of overall pigment coupler formulations; ratio depends on target hue and final pigment fastness

    Downstream process integration

    • Introduced in the initial diazotization reactor under acid-controlled environments
    • Real-time monitoring for unreacted aniline and halide residues
    • Solid-liquid separation followed by purification to minimize extractables

    Final product types

    • High-fastness yellow and orange azo pigments for automotive and coil coatings
    • Colorants for technical textile fibers
    • Printing inks with migration compliance for food packaging substrates

    3. Active Pharmaceutical Ingredient (API) Intermediate

    API 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

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) Residual Solvent and Impurity Limits
    • EU GMP Annex 8 — Sampling of Starting and Packaging Materials
    • China Pharmacopoeia standards for pharmaceutical intermediates

    Typical usage ratio

    • Varies from 6–20% on process mass basis; based on target molecule structure and step yield

    Downstream process integration

    • First synthetic step to introduce halogenated aromatic amines
    • Monitored by HPLC to verify complete conversion and absence of genotoxic byproducts
    • Subsequent amidation or sulfonamidation under inert conditions

    Final product types

    • Anti-infective ingredient intermediates (e.g., for cephalosporin derivatives)
    • Anti-inflammatory agents requiring high-purity intermediates
    • Registered pharmaceutical starting materials

    4. Specialty Polymers: Reactive Monomer Additive

    Chemical 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

    • UL 94 Vertical and Horizontal Flame Test
    • RoHS Directive 2011/65/EU for halogen content
    • ISO 178 for flexural properties of plastics
    • IEC 60695 for fire hazard testing in electrical applications

    Typical usage ratio

    • Ranges from 1–8% depending on required flame retardancy and compatibility with copolymer matrix

    Downstream process integration

    • Direct addition to reactor during initial condensation polymerization
    • Controlled temperature profile to ensure even distribution and prevent premature crosslinking
    • Post-polymerization analysis for unreacted halogenated amines

    Final product types

    • Halogen-modified polyamides and polyesters for cable sheathing
    • Flame-retardant interior panels for automotive and rail vehicles
    • Printed circuit board base resins with enhanced electrical insulation
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    Certification & Compliance
    More Introduction

    2-Bromo-4,6-Dichloroaniline: A Manufacturer’s Perspective

    Understanding 2-Bromo-4,6-Dichloroaniline in Everyday Manufacturing

    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.

    Hands-On: Realities of Manufacturing 2-Bromo-4,6-Dichloroaniline

    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.

    Why Structural Substitution Matters

    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.

    Real-World Uses Straight from the Factory Floor

    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.

    Choosing 2-Bromo-4,6-Dichloroaniline Over the Alternatives

    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.

    Product Stewardship: Production Consistency and Safety

    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.

    MOQ and Scale: Serving from Grams to Bulk

    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.

    Navigating Global Regulatory Demands

    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.

    Sustainability and Waste Stream Reform

    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.

    Market Dynamics: How Direct Production Shapes Value

    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.

    Reflections from Years in the Field

    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.

    Looking Ahead: Evolution and Partnerships

    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.

    Summary Table: Why Manufacturers’ Output Makes the Difference

    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

    Closing Thoughts

    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.