Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

4-Bromo-2,6-Dichloroaniline

    • Product Name 4-Bromo-2,6-Dichloroaniline
    • Alias 4-Bromo-2,6-dichlorobenzenamine
    • Einecs 221-868-2
    • 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
    VTB
    Specifications

    HS Code

    527239

    Chemical Name 4-Bromo-2,6-dichloroaniline
    Molecular Formula C6H4BrCl2N
    Molecular Weight 240.92 g/mol
    Cas Number 6974-76-1
    Appearance Light yellow to brown solid
    Melting Point 74-78°C
    Solubility In Water Low
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Density 1.98 g/cm³ (approximate)
    Synonyms 2,6-Dichloro-4-bromoaniline
    Smiles C1=C(C=C(C(=C1N)Cl)Br)Cl
    Ec Number 230-202-7

    As an accredited 4-Bromo-2,6-Dichloroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, sealed with a screw cap, labeled "4-Bromo-2,6-Dichloroaniline, CAS 19820-43-6, for laboratory use."
    Shipping 4-Bromo-2,6-Dichloroaniline is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported in compliance with hazardous material regulations, often as a Class 9 substance. Proper labeling, documentation, and handling precautions are required to ensure safe transit and to prevent environmental or health risks.
    Storage **4-Bromo-2,6-dichloroaniline** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture, direct sunlight, and heat. Properly label the container and ensure restricted access to trained personnel. Use secondary containment to prevent spills.
    Application of 4-Bromo-2,6-Dichloroaniline

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

    4-Bromo-2,6-Dichloroaniline serves as a critical intermediate in the development of specialty chemicals, with well-established uses in several regulated downstream industries. We support customers throughout the value chain by supplying material tailored for specific transformation steps, adhering to both international and regional compliance requirements across each sector.

    1. Synthesis of Agrochemical Active Ingredients

    This material provides a halogenated aniline core vital for synthesizing select herbicidal and fungicidal actives. Agricultural chemical manufacturers introduce our product during key coupling steps, reacting it with sulfonyl chlorides or other electrophiles via Buchwald-Hartwig or nucleophilic aromatic substitution to build target molecule backbones. Dosage calibration depends on target compound structure and reaction scale, demanding purity assurance for downstream catalytic steps. Finished agrochemicals typically undergo registration in markets with distinct regulatory benchmarks.

    Industry compliance standards

    • FAO/WHO Food and Agriculture Organization pesticide specifications
    • US EPA 40 CFR Part 180 (Tolerances and food additive regulations)
    • European REACH (EC 1907/2006) and plant protection product regulation (EC 1107/2009)
    • China GB 2763-2021 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • Dosage in technical synthesis varies from 0.8 to 1.1 molar equivalents relative to the core coupling component; users adjust based on conversion efficiency, with an excess of 5-10% applied for low-yield reactions.

    Downstream process integration

    • Material enters during multi-step synthesis, specifically as starting arylamine in palladium-catalyzed amination or post-halogenation for target active building block assembly.

    Final product types

    • Selective herbicides (e.g., phenoxyacetic acids containing halogenated anilines)
    • Fungicidal actives (e.g., triazole derivatives)
    • Intermediate technical-grade pesticide active materials

    2. Production of Pharmaceutical Intermediates

    Pharmaceutical manufacturers use this compound as a key step intermediate in the construction of certain APIs and advanced intermediates, especially where halogenated aromatic cores are required for downstream cyclization, amidation, or ring substitution. Our strict QC assures minimal trace impurities that may carry through highly regulated GMP synthesis chains, making it suitable for non-direct API but core intermediate production. Usage levels depend on target scaffold complexity and subsequent purification requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR 210/211 for finished pharmaceuticals
    • European Pharmacopoeia (Ph. Eur) guidelines for raw materials and intermediates
    • China GMP for Chemical Intermediates

    Typical usage ratio

    • 0.9–1.2 equivalents relative to the aryl-substituted core structure in the key coupling or ring formation steps, with excess applied in pilot scale or when impurity carry-over must be strictly controlled.

    Downstream process integration

    • Material introduced during sequence steps preceding the construction of the API core, commonly via N-alkylation or cyclization after halogen exchange and deprotection steps.

    Final product types

    • Intermediates for antihypertensive agents (e.g., certain dihydropyridine derivatives)
    • Precursors for anti-infective and anti-inflammatory API cores
    • Advanced intermediates for final API transformations

    3. Development of Specialty Dyes and Pigments

    Dye and pigment manufacturers rely on halogenated anilines as coupling components to introduce colorfast and shade-tunable groups into advanced pigments and textile dyes, with this compound facilitating the production of high-purity specialty colorants. Downstream producers integrate it into azo-coupling or diazotization routines, where consistent reaction yields and impurity levels directly impact dye performance. Adjustments in input quantities follow the desired chroma values and application substrate requirements.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile ecotoxicity)
    • CFR Title 16, Part 1500 for consumer product colorants (North America)
    • REACH Annex XVII restrictions for aromatic amine precursors
    • GB/T 18414 Pigment Testing Methods (China)

    Typical usage ratio

    • Initial charge of 1.0 molar equivalent in diazotization or coupling reactions; variation of ±7% to control pigment hue and color strength as dictated by customer product line.

    Downstream process integration

    • Fed into the amine-to-azo-dye pathway either as the primary or co-reactant; nitrogen handling and reaction temperature must prevent byproduct color shifts.

    Final product types

    • Azo and anthraquinone dyes for textile applications
    • High-performance organic pigments for plastics and coatings
    • Pharmaceutical-grade colorants for tablet coatings

    4. Synthesis of Halogenated Polymer Modifiers

    In advanced polymer material production, downstream processors value this material for manufacturing chain-stoppers and functional monomers, especially where halogen-bearing aromatic units impart specialty flame retardancy or chemical resistance. Material enters chlorination or copolymerization processes in controlled ratios depending on the desired properties of the modified polymer. Quality control focuses on minimizing metal and byproduct residues critical for polymers applied in electronic or automotive sectors.

    Industry compliance standards

    • UL 94 (Flammability Standard for Plastic Materials)
    • RoHS 2011/65/EU Directive for restricted substances in electronics
    • ISO 1043 Plastics – symbols and abbreviations
    • REACH SVHC content control for downstream polymers

    Typical usage ratio

    • 0.5–1.5% by weight in the total monomer or polymer feed, modulated for targeted flame retardant class or chemical resistance profiles.

    Downstream process integration

    • Material reacts as an end-cap agent or functional comonomer prior to or during melt-polymerization or solution polymerization cycles, typically under inert atmosphere at elevated temperature.

    Final product types

    • Flame-retardant epoxy or polyester resins
    • High-durability engineering plastics
    • Functionalized polymers for automotive under-the-hood applications

    5. Use in Fine Chemical Synthesis for Photographic and Imaging Chemicals

    Manufacturers of specialty imaging and development agents use this compound to synthesize halogenated organic developers, color couplers, and stabilizers critical for photographic emulsions and digital imaging formulations. It supports the introduction of electron-withdrawing groups that modulate redox properties and light stability within the final application. The downstream formulation stage requires precise stoichiometry to ensure product performance in sensitive imaging technologies.

    Industry compliance standards

    • ISO 18902 (Photographic Materials – Processing Chemicals Safety)
    • REACH registration for specialty fine chemicals
    • RoHS compliance for chemicals in imaging devices
    • JCII (Japan Camera & Imaging Products Association) voluntary quality guidelines

    Typical usage ratio

    • 0.9–1.3 equivalents incorporated per developer or coupler molecule, adjusted by photochemical assay results and target emulsion composition.

    Downstream process integration

    • Introduced during early-stage organic synthesis as a haloaniline feedstock, subsequently functionalized by alkylation or cross-coupling prior to final formulation and purification steps.

    Final product types

    • Photographic color developers and stabilizers
    • Imaging agent precursors for medical X-ray films
    • Digital printer toner additive components
    Free Quote

    Competitive 4-Bromo-2,6-Dichloroaniline prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    4-Bromo-2,6-Dichloroaniline: A Reliable Building Block for Pharmaceutical and Agrochemical Synthesis

    Understanding the Role of 4-Bromo-2,6-Dichloroaniline in Chemical Synthesis

    Chemicals like 4-Bromo-2,6-Dichloroaniline do not catch much public attention, though they shape a surprising range of everyday products and industrial solutions. In our facilities, this compound—known as Model: 4-BDA-99—bridges the gap between basic raw materials and the specialty molecules in pharmaceuticals, crop protection, pigments, and performance materials. Our experience in handling and producing halogenated aniline derivatives stretches over two decades, allowing us to see firsthand how incremental changes at the molecular level can play out across entire industries. We have watched this compound rise in demand due to its unique behavior in creating more stable, bioactive, and processable intermediates.

    Production Standards and Handling Practices

    We approach production with a commitment to material purity and reproducibility. Our batches of 4-Bromo-2,6-Dichloroaniline consistently reach a minimum purity of 99.5% by HPLC, a benchmark that comes from both customer feedback and our in-lab experience. A small difference in isomeric purity or contaminant profile can throw off a reaction, especially when the final application deals with human or environmental exposure. While some manufacturers may cut corners in the chlorination or bromination steps, we bank on a multi-stage purification process, including full trace residue testing to catch even the smallest by-products. A poorly crystallized batch or a trace solvent problem can ruin downstream yields; strict temperature control during recrystallization and solvent switching keeps particle size and residuals in check.

    Bags and drums never sit on our shelf for long. Demand for this intermediate runs steady, especially from companies scaling up newly registered pesticide actives or seeking custom-modified dye molecules. Packaging options follow customer preferences—from 1 kg bottles for research to fiber drums for bulk industry partners—but the commitment to cleanroom-grade filling stands regardless of order size. Each batch receives full documentation, including NMR, IR, and GC-MS results (when requested), because a slip here can travel far down the value chain.

    Where 4-Bromo-2,6-Dichloroaniline Fits In: Real-World Applications

    We see most large-scale requests coming from pharmaceutical intermediates—especially in the synthesis of active pharmaceutical ingredients where halogen-substituted anilines enable selective functionalization. For agrochemicals, activity against certain pests or weeds often depends on having just the right halogen pattern, and 4-Bromo-2,6-Dichloroaniline lends itself to transformations like amide formation or Suzuki-Miyaura cross-coupling. Over the years, we have supplied custom lots tuned to fit unusual solvent systems, special crystal forms for better slurry handling, or even micronized grades for catalysis research.

    In the colorants sector, the electron-withdrawing effects of both bromine and chlorine at these specific positions lead to enhanced color fastness and light stability in azo and anthraquinone pigments. Our technical staff often works with pigment formulators seeking consistent tinctorial strength, since unpredictable halogen ratios can change the whole color profile of a batch.

    Comparisons to Other Aniline Derivatives

    Some buyers ask about the differences between 4-Bromo-2,6-Dichloroaniline and similar compounds—say, 2,6-dichloroaniline or 4-bromoaniline. We find that these subtle changes matter most in reactions that count on precise reactivity. For instance, the simultaneous presence of bromine and two chlorines in the 2,6 positions blocks certain side reactions and improves yields in palladium-catalyzed couplings. It also decreases the likelihood of unwanted oxidative by-products when processed under harsh reaction conditions. We have supported several clients in switching from mono- to di-chlorinated grades, watching impurity profiles drop significantly in both laboratory evaluation and plant trials.

    Solubility profiles shift with added halogen atoms. Our compound, though less soluble in polar solvents than non-halogenated analogues, resists hydrolysis and shows compatibility with a wide range of organic bases. This balance came into play in a recent partnership with a UK-based pharmaceutical company developing a new antibacterial agent. Their breakthrough relied on controlling residual halogen content—a feat accomplished in part by our reproducibility in halogen pattern and solvent impurity control.

    Quality Control and Traceability

    Traceability is no afterthought for us. Each lot of 4-Bromo-2,6-Dichloroaniline comes with a unique tracking code, tied to raw material lots and processing dates back to raw bromine and aniline deliveries. Regulatory teams and auditors, especially those prepping for eventual FDA or REACH registration, rely on this data to prepare compliance dossiers. Analytical packages include heavy metal screens, routine residual solvent analysis by GC, and halogen content by titration. Our plant follows a robust change-control protocol—any shift in equipment, personnel, or upstream sources triggers a full revalidation, not just a paper review.

    For waste streams, halogenated mother liquors undergo segregation and incineration at licensed facilities to prevent environmental trace contamination. Transparency with environmental authorities and downstream processors matters in every market—neglecting this has cost others dearly in permit delays and lost export privileges.

    Occupational Health and Hazard Mitigation

    Our technicians work directly with this compound, so in-house safety always comes ahead of production quotas. 4-Bromo-2,6-Dichloroaniline, like many such intermediates, carries both acute and chronic exposure risks. We invest in local exhaust ventilation, sealed charge/discharge operations, and mandatory PPE—simple steps that materially cut down worker exposure. In our earliest years, a temporary lapse in splash protection left us scrambling as one operator developed a mild dermatitis. Investments in automated filling and drum-sealing lines since then have nearly eliminated such events.

    Routine air and surface monitoring ensures contaminants never creep up inside or outside the synthesis area. We extend training well beyond regulatory minimums, emphasizing near-miss reporting and preventive maintenance. Nothing brings production to a halt faster than an unexpected exposure event; a predictable factory floor means fewer surprises and higher morale in the long run.

    Logistics, Shelf Life, and Customer Experience

    As a manufacturer, our job does not end at synthesis. Getting 4-Bromo-2,6-Dichloroaniline to partners worldwide means prepping for temperature swings, long storage times, and variable warehouse conditions. We learned early that batches sent in ordinary drums sometimes caked up after months of storage, especially in humid regions. Switching to moisture-resistant packaging lined with anti-static film solved most consistency issues. On request, we evaluate stability under customer-specific storage temperatures, providing extra assurance for those operating in tropical or high-humidity sites.

    Our technical team backs every order, fielding questions about crystal growth, reaction compatibility, and packaging tweaks to fit automated dispensing lines. Shipping support goes beyond mere documentation. We help secure the right export licenses and customs paperwork, ensuring no shipment lingers at a port due to code mismatches or missing certificates. We have lost count of the number of times our logistics staff stepped in to clear a delayed shipment bound for an urgent pharmaceutical pilot.

    Regulatory and Market Drivers

    The last decade has seen regulatory tightening, especially regarding halogenated intermediates. Our compliance staff routinely works with customer legal teams preparing for US EPA, EU REACH, or Asian market registrations. Thorough documentation and above-standard analytical testing win us repeat business in sectors that cannot afford to risk a recall or market rejection. We track every significant regulatory change; in one instance, a subtle shift in environmental classification for a downstream product reshaped our internal waste treatment policies and required a plant-wide audit.

    Global demand for more selective, less persistent agrochemicals and better-targeted drug candidates favors molecules built up from platforms like 4-Bromo-2,6-Dichloroaniline. Many of our customers are exploring greener synthetic methods—enzymatic transformations, continuous-flow brominations—to open new markets. Our R&D group has run dozens of pilot campaigns, testing new solvents, catalysts, and alternate reaction routes to cut both cost and environmental footprint over the years. One such effort led to a sustained reduction in both water use and halogenated by-product generation, a point of pride within our sustainability reports.

    Working Toward Sustainable and Reliable Supply Chains

    Supply chain shocks—from raw material shortages to sudden demand surges—put stress on both ends of the market. Past experience with abrupt increases in bromine costs or regulatory clampdowns in certain production hubs taught us that scaling in advance and keeping close ties with multiple feedstock suppliers reduces both delivery times and price swings. By securing long-term purchase commitments and holding strategic safety stocks, we have weathered trade disputes and shipping disruptions without missing major contract deliveries.

    On the customer side, we maintain responsive technical support to address changes in project scale, process modifications, or regulatory filing requirements. If a new European regulation raises requirements for residual bromine, we quickly adapt our QC parameters and documentation packets to match. We value transparent pricing, open communication, and practical problem-solving. Many partnerships last for years because buyers know our staff remains reachable and solution-driven even after the initial sale.

    Innovation Rooted in Experience

    We take pride in the expertise flowing through our production teams and technical support. No two production runs are ever the same—weather, raw material variations, and even small differences in reactor configuration all factor into each batch’s performance. Our operators can draw on decades of cumulative knowledge to solve challenges ranging from off-color batches to unexpected pressure spikes during synthesis. This discipline in the plant translates to fewer failed batches, less waste, and greater peace of mind for end customers.

    Occasionally, a customer will approach us with a challenging target—say, a special particle size range or a need for ultra-low residual solvents due to upcoming toxicology tests. Rather than hand off the problem to a third party, we take a hands-on approach, running lab trials side-by-side with customer technical staff. This approach delivers more than a product; it provides a solution and enduring trust.

    Long-term Reliability

    No process or product succeeds on technical merit alone. Trust and reliability—earned through consistent supply, responsive service, and transparent communication—factor just as heavily into why companies choose us as their production partner. Feedback loops between our plant and customer labs make it possible to catch small shifts before they become big losses. The most rigorous process development or plant trial counts for little if the supply drops out mid-project. This recognition—the importance of steadiness over years—has shaped our approach to every step in production, packaging, and shipment.

    4-Bromo-2,6-Dichloroaniline exemplifies how specialty chemical manufacturing can contribute to larger industry progress. Our facility welcomes challenging specifications, high-purity requirements, and project timelines that stretch over months or even years. The work is demanding, but the satisfaction of seeing new medicines, better crop protection tools, and more sustainable materials take shape—built from the molecules we craft every day—anchors our commitment. As customers face new syntheses, tighter regulations, and greater scrutiny, we aim to supply not just material, but assurance for every batch delivered.