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2-Bromo-6-Chloro-4-Fluoroaniline

    • Product Name 2-Bromo-6-Chloro-4-Fluoroaniline
    • Alias 2-Bromo-6-chloro-4-fluorobenzenamine
    • Einecs 629-865-4
    • 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

    810423

    Chemical Name 2-Bromo-6-Chloro-4-Fluoroaniline
    Molecular Formula C6H4BrClFN
    Molecular Weight 224.46 g/mol
    Cas Number 885276-41-7
    Appearance Solid (typically crystalline or powder)
    Purity Typically ≥98% (may vary by supplier)
    Solubility Slightly soluble in water; soluble in organic solvents (e.g., DMSO, DMF)
    Synonyms 6-Chloro-4-fluoro-2-bromoaniline
    Smiles Nc1c(F)cc(Cl)cc1Br
    Inchi InChI=1S/C6H4BrClFN/c7-4-1-3(9)2-5(10)6(4)8/h1-2H,10H2

    As an accredited 2-Bromo-6-Chloro-4-Fluoroaniline 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, tightly sealed, with hazard labeling and chemical details: 2-Bromo-6-Chloro-4-Fluoroaniline, purity, and safety information.
    Shipping 2-Bromo-6-Chloro-4-Fluoroaniline is shipped in tightly sealed containers, protected from light and moisture. Transport is made in compliance with local and international regulations for hazardous chemicals. Proper labeling and documentation are ensured, and handling instructions are provided to ensure safe delivery. Recommended storage is in a cool, dry place.
    Storage Store **2-Bromo-6-Chloro-4-Fluoroaniline** in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from sources of ignition, incompatible materials, and direct sunlight. Label the storage container clearly, and ensure it is used only by trained personnel while wearing appropriate personal protective equipment (PPE).
    Application of 2-Bromo-6-Chloro-4-Fluoroaniline

    Applications of 2-Bromo-6-Chloro-4-Fluoroaniline in Industrial Manufacturing

    As a direct manufacturer of 2-Bromo-6-Chloro-4-Fluoroaniline, we serve a focused range of advanced industrial fields. Below, we detail key downstream scenarios served by this intermediate, with specific attention to compliance, usage levels, processing stage, and final products manufactured by our customers.

    1. Pharmaceutical Intermediate Synthesis (Active Pharmaceutical Ingredients)

    This raw material is commonly employed as a building block in the synthesis of API precursors for targeted therapies, including kinase inhibitors and antiviral agents. Formulation chemists incorporate it early in multi-step heterocyclic constructions, exploiting its halogenated aniline framework for site-specific substitution and ring closure. Regulatory needs demand precision and documentation at each batch operation.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) for APIs (ICH Q7)
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia monographs for relevant APIs
    • ICH Q3A Impurities guideline

    Typical usage ratio

    • Ranges from 0.2 to 0.8 molar equivalents per target molecule, adjusted by stepwise yield and target structure complexity

    Downstream process integration

    • Introduced during early to mid-stage reaction steps for aromatic amine coupling or nucleophilic substitution in API synthesis

    Final product types

    • Small-molecule pharmaceuticals in oncology
    • Antiviral bulk actives
    • Generic API intermediates with fluorinated substituents
    • Clinical-stage development molecules

    2. Agrochemical Synthesis (Herbicide and Fungicide Building Blocks)

    Agricultural chemical manufacturers utilize this material in the development of selective herbicides and advanced fungicidal agents. It acts as a critical halogenated fragment for assembling pyridylanilide and triazole-type agrochemicals, supporting structure-activity demands in field trials.

    Industry compliance standards

    • FAO/WHO specification for pesticide technical grade
    • ISO 9001:2015 certified quality systems for agrochemical intermediates
    • REACH registration (EC) No 1907/2006 for EU supply
    • National pesticide formulation registration, as required

    Typical usage ratio

    • Applied at 0.1 to 0.4 mass fraction per batch, based on overall synthesis route and desired substitution pattern

    Downstream process integration

    • Charged into condensation or cyclization steps, following protection or deprotection of amino groups, for targeted agrochemical structures

    Final product types

    • Herbicide active ingredients (e.g., anilide-type, pyridine derivatives)
    • Fungicide intermediates for triazole class products
    • Pre-formulations for field evaluation in crop protection
    • Bulk technical concentrates

    3. Specialty Dye Intermediate Manufacturing

    Producers of functional dyes and high-performance pigments select this chemical as a key raw material for synthesizing azo and heterocyclic dye intermediates that demonstrate fastness and color intensity. Its multi-halogenated structure enriches chromophore stability and aids differentiation in final colorants.

    Industry compliance standards

    • EN 71-3 safety for coloring materials—limits for certain elements in toys and textiles
    • OEKO-TEX® Standard 100 for restricted substances in textile processing
    • REACH Annex XVII restrictions for certain aromatic amines
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) for global textile supply chains

    Typical usage ratio

    • Variable, from 0.15 to 0.5 molar proportion depending on chromophoric system design and end-use spectrum

    Downstream process integration

    • Feeds into diazotization or coupling reactions for stepwise pigment or dye assembly, often under controlled temperature and pH

    Final product types

    • Disperse and reactive dyes for textiles
    • Dye intermediates for ink manufacturing
    • Colorant precursors for electronic and imaging applications
    • Highly stable pigment dispersions

    4. Electronic Material Intermediate (OLED and Organic Semiconductors)

    Advanced electronic material suppliers use this compound in the preparation of precursors for organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and other organic photonic devices. It supports the synthesis of custom, fluorinated aniline-based monomers, enhancing electron transfer and stability in demanding environments.

    Industry compliance standards

    • International Electrotechnical Commission (IEC) 61249 for halogenated base materials
    • RoHS Directive (2011/65/EU) for electronic components
    • ISO 9001 for electronics materials manufacturing
    • JEDEC JESD Standard for materials reliability

    Typical usage ratio

    • Ranges from 0.08 to 0.25 mol/mol in target reaction, depending on the complexity of the functional layer and molecular weight requirements

    Downstream process integration

    • Used in the functionalization of organic semiconductors and conjugated systems during monomer synthesis or as a coupling fragment for extended pi-systems

    Final product types

    • OLED emitter and charge transport layer precursors
    • Organic semiconducting polymer intermediates
    • High-performance photonic materials
    • Active layer building blocks for optoelectronics

    5. Fine Chemical Research (Custom Fluorinated Aromatics)

    Custom synthesis laboratories, fine chemical producers, and R&D divisions employ this raw material as a tailored fragment for developing new fluorinated aromatic compounds. Used in pilot and small-scale route development, it enables exploration of structure-property relationships and pre-clinical candidate generation.

    Industry compliance standards

    • ISO 17025 for analytical and research laboratory competence
    • GLP (OECD Good Laboratory Practice) for pre-clinical studies
    • Internal SOP compliance for chemical documentation
    • Local chemical handling and disposal regulations

    Typical usage ratio

    • Applied at 0.05 to 1.0 molar ratio depending on the experimental design, target molecule structure, and scale (mg to kg)

    Downstream process integration

    • Charged into exploratory reactions, including cross-coupling, heterocyclic formation, or directed aromatic substitution

    Final product types

    • Novel fluorinated intermediates for proprietary research
    • Reference standards and analytical markers
    • Candidate scaffolds for bioconjugation
    • Proof-of-concept molecules for innovation pipelines
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    Certification & Compliance
    More Introduction

    2-Bromo-6-Chloro-4-Fluoroaniline: A Closer Look at a Core Chemical Building Block

    Understanding the Substance and Its Relevance

    Working in a plant brimming with flasks, reactors, and distillation columns all day, you learn that none of these setups matter without the right kind of chemicals behind them. Over the years, 2-Bromo-6-Chloro-4-Fluoroaniline has proven itself to be one of those hard workers of the fine chemical world—a small molecule, but with a presence that stretches across pharma, agrochemicals, and specialty intermediates manufacturing. Its structure draws attention: the aromatic ring forms the base, with bromine, chlorine, and fluorine arranged so that their combined influence steers a unique reactivity profile. Compared to simpler anilines, these three substituents bring a complexity that chemists look for when they demand site-selectivity or downstream functionality in synthesis.

    What Sets 2-Bromo-6-Chloro-4-Fluoroaniline Apart in Synthesis

    Every day, as raw material trucks pull up and control panels light up in the operations room, the push is on productivity and cost-effectiveness. But not every halogenated aniline can sustain these demands. The blend of bromine, chlorine, and fluorine at ortho and para positions on the aniline ring gives this compound a special status in multi-step synthesis. Bromine and chlorine activate the ring for further reactions, while the highly electronegative fluorine modulates both electronic and steric effects, often guiding selectivity that can be hard to achieve otherwise. In our own facilities, we’ve seen these properties help cut down on protecting group use and tedious purification steps that would otherwise drag down process yields and batch consistency. Side products decrease, which means less solvent, less reworking, and better time management for the team.

    Model, Appearance, and Critical Specifications

    The identity of 2-Bromo-6-Chloro-4-Fluoroaniline (CAS No. 142704-78-1) comes down to its raw, physical presence in the plant. Our typical product runs in the range of 98% to 99% confirmed by HPLC, appearing as a light yellow to off-white crystalline solid. The melting point tends to come in around 48–53°C, which enables relatively straightforward melting, filtration, and recrystallization routines on the shop floor without special handling equipment. Most batches come packed in sealed fiber drums or HDPE canisters, nitrogen-purged, because atmospheric moisture and light can over time degrade the quality, as we learned through trial and error early on. Our in-line IR and GC monitoring in production has shaved off much operator interference, keeping the batch integrity tight from the start to finish. It’s hard-earned experience—each run teaches something new about impurity profiles, and there’s a shared sense among the crew when the analysis prints reflect a clean, tight synthesis.

    Process Insights from Production

    Making this compound at industrial scale forced us to get creative with process development. Early trials with direct halogenations on standard anilines led to sluggish reactions and, at times, heavy byproduct formation. Building the halogen pattern required careful order of addition, as the relative reactivity of aryl halides can either speed up or choke a sequence. Over-reliance on harsh halogenation reagents sometimes meant extra corrosion on reactors or longer downtime between runs, which no one likes to see on the monthly report. Team brainstorming led to a two-step process—starting with fluorination of a chlorinated precursor, then using a selective NBS bromination—minimizing side reactions and solvent waste. By tuning the cooling profiles and agitation rates, we pulled out a sharp increase in conversion and maintained safe operations, especially with exothermic additions. Each time we deliver a drum to the next stage, it’s also a marker of how incremental improvements at the bench scale can ripple out in hundreds of kilos at plant scale.

    Comparing to Other Halogenated Anilines

    There’s no shortage of halogenated anilines on the market. By now, our catalog spans over a dozen structural isomers and analogs, each tweaked with different substituents for unique reactivity. But here’s the thing about 2-Bromo-6-Chloro-4-Fluoroaniline: it solves particular synthetic puzzles that others can't touch. For example, mono-substituted or di-substituted anilines tend to have broader reactivity but less selectivity, which means more byproducts. Those lacking in fluorine can lose valuable site control, especially in cross-coupling reactions such as Suzuki or Buchwald-Hartwig, where sterics and electronics balance out performance. In our hands, this specific trifunctional setup has shown sharper performance in step-growth and block co-polymerization chemistry than either 2,4,6-tribromo or dichloro-fluoroanilines. Long-term customer projects in biopharma synthesis—where purity requirements are razor thin—have come to favor this molecule because it keeps cumulative impurity levels lower run after run, especially once it’s worked into a multi-kilo process.

    Focus on Application: From Pharma to Crop Protection

    The crowded shelves in our finished goods warehouse tell an ongoing story: one day a batch heads off to a pharmaceuticals client, and next week it might supply someone in agrochemical development. The aniline core is a workhorse for chemists building out kinase inhibitors, where controlled halogenation pushes selectivity in the final step. Our partners in agrochemical development have favored this compound for building libraries of new active ingredients that need a balance of lipophilicity and metabolic resilience. The balance of halogens offers a controlled path for further elaboration—think lead diversification, analog synthesis, or late-stage functionalization.

    There’s also a practical side for polymer intermediates: with the rise of specialty electronics and advanced materials, researchers keep asking for anilines that push electronic envelopes for better dielectric or photonic performance. Quite a few collaborative projects in Europe and Asia have involved our product at early discovery stages, with feedback loops that flow into our batch process refinements. And for teams handling downstream transformations, the crystalline nature and defined melting behavior of our material reduces the need for excessive drying cycles or filtration after reconstitution.

    Impact of Quality Control and Consistency

    Any chemist who’s spent time on scale-up knows that a handful of percent in purity or a rogue trace of impurity can sneak up on you and derail a whole synthesis. Walking into the QC lab each morning, peering at the HPLC chromatograms, you get a sense of the pressure behind each batch. We have had entire runs set aside after a spike in meta-substituted byproducts during supplier material variances, underscoring the importance of stable raw materials. Solvent control matters—a whiff of DMF left in the drum can impact both process safety and downstream reactivity. These factors aren’t academic; they decide profitability and guarantee project timelines, whether supporting an API pilot run or a new herbicide lead.

    Tighter control on the specs also means less troubleshooting downstream for our partners. We’ve run side-by-side trials for long-standing clients where our 2-Bromo-6-Chloro-4-Fluoroaniline goes head-to-head with other suppliers—and we keep records on everything from solubility to flashpoint and dustiness under plant conditions. The payoff for persistent in-plant tweaks shows up in these real-world results—fewer stoppages, smoother downstream reactions, and a higher fraction of on-spec material arriving at customer sites.

    Safety Considerations and Handling Experiences

    Life in any chemical plant or research lab is shaped by vigilance around handling, storage, and logistics—especially for halogenated aromatic amines like this one. Team meetings often begin with a run-through on personal protective equipment and spill management, not just as a box-ticking compliance gesture but out of habit sharpened by the odd near-miss. We have learned to respect both the dust explosion risks and the reactivity with common acids, making sure all storage is dry, cool, and well-labeled.

    On the shipping and logistics side, regulatory expectations keep tightening—our staff works with dedicated compliance coordinators to manage paperwork and update SDS revisions, aiming for error-free export clearances every time. These operations have helped us avoid delays and keep product moving as demand rises worldwide.

    Continuous Improvement and Sustainability Pressure

    Every month brings a review of yields, waste streams, and solvent recapture rates. Large-scale synthesis produces streams of offcuts, side-products, and solvents, all of which must be minimized for both cost and environmental impact. A recurring theme in production meetings revolves around waste management and energy use. Even a single degree drop in recrystallization temperature or small tweaks of solvent ratios in extraction have cut total solvent usage by hundreds of liters over the course of a year.

    We’ve joined industry efforts on green chemistry, seeking out chlorination and bromination methods that run cleaner and less hazardous than those of the past. Shifting from batch to continuous operations, especially for the halogenation stages, holds promise for reducing thermal load and runaway risks, while maintaining close control on exothermal reaction steps. As the regulatory landscape becomes more demanding, we keep pace with third-party audits, regular process safety reviews, and new analytical toolkits to catch unknown impurities or waste emissions before they leave the site. All these lessons come directly from the realities of chemical production, not from a textbook.

    Developing Relationships with End-Users

    Direct feedback from those using our material can break or make a business. On-site visits and customer labs give us the chance to see firsthand how our product slots into their syntheses. Each client works differently—some run multiple parallel syntheses, some want larger particle sizes for easier handling, and others have continuous processing lines that demand dust-free, flowable material. We’ve adjusted filtration cutoffs and optimized drying conditions thanks to this feedback loop. The network of users extends outside of R&D; production and even regulatory affairs get drawn into the fine points of trace impurity profiles, ensuring nothing gets overlooked and that both compliance and performance are met day after day.

    Mutual trust grows when shipments consistently arrive in spec and on time, and we don’t take this for granted. Years of collaboration with fine chemical companies and research powerhouses have sharpened our process control—if we get even a hint that a downstream transformation isn’t performing as expected, our technical team is quick to run test reactions or provide analytical support. Mistakes get fixed promptly. It’s that willingness to treat each batch as the foundation for the next relationship that keeps both our team and our customers moving forward.

    Innovation: Responding to Industry Shifts

    Competition in chemical manufacturing means that standing still is as risky as rushing ahead without thinking things through. We invest a lot of time in keeping our production pipeline nimble, looking for ways to switch out hazardous reagents for safer alternatives, minimize solid waste, and streamline batch protocols. Our technology transfer team works closely with research groups and application development specialists, taking lessons learned from laboratory scale and folding them into production at hundreds-of-kilos scale. Take automation, for instance: by updating older manual dosing with mass flow controls and in-line cameras, we’ve trimmed cycle times and cut human error—a direct benefit our customers see from the first sample they receive.

    Global supply chain disruptions in recent years have further amplified the need to hold extra stock and deepen raw material supplier relationships. By qualifying more than one upstream source for key precursors and running critical input validation for each incoming delivery, we prevent single-point failures in our timelines. No amount of digital scheduling can substitute for hands-on relationships with precursor producers who understand the realities of our end-use requirements—delays at their end ripple downstream fast.

    The Road Ahead: Balancing Client Expectations and Practical Production

    Each month, new projects land in our pipeline—from advanced medicinal chemistry teams, crop science innovators, and material science labs. These teams don’t just ask for more product; they request ever-stringent impurity profiles, alternate polymorphs, or higher throughput. Every request sharpens our focus on process analytics, purification strategies, and continuous improvement initiatives. Feedback loops have become part of our daily operations, guiding where capital gets spent for upcoming process upgrades.

    In direct response to increased scrutiny over environmental performance, we’ve built in more robust analytics for emissions and waste water, seeking ways to capture, recycle, and reuse what can be saved from each run. This ongoing investment doesn’t just fulfill regulatory requirements; it keeps our plant safer and reduces operating expenses over time. As the demands shift, whether it's for higher performance materials or safer routes for old chemistry, the versatility of 2-Bromo-6-Chloro-4-Fluoroaniline continues to earn its place—shaped by both tree-top strategy sessions and boots-on-the-ground plant experience alike.

    Conclusion: The Value Created When Experience Guides Chemistry

    Every pallet moving out the warehouse is the sum of long days spent on plant optimization, countless analytical runs, and hard-won insights from decades of collective team effort. Our approach with 2-Bromo-6-Chloro-4-Fluoroaniline holds fast to one belief: focusing on process quality, environmental stewardship, and open dialogue with partners builds real value. Each batch reflects the experience and adaptability required by modern chemical manufacturing, proving that substance—both chemical and operational—matters more than abstract claims or one-size-fits-all promises. The reputation of this product in challenging domains comes not from isolated properties, but from decades of incremental growth, collective learning, and the kind of direct feedback loop that only a boots-on-the-ground manufacturer can provide.