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4-Bromo-3-Chloro-2-Fluoroaniline

    • Product Name 4-Bromo-3-Chloro-2-Fluoroaniline
    • Alias 4-Bromo-3-chloro-2-fluoro-1-aminobenzene
    • Einecs 816-425-6
    • 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

    668189

    Chemical Name 4-Bromo-3-Chloro-2-Fluoroaniline
    Cas Number 886372-34-1
    Molecular Formula C6H4BrClFN
    Molecular Weight 224.46 g/mol
    Appearance Light brown to beige solid
    Melting Point 66-69°C
    Purity Typically ≥ 97%
    Solubility Insoluble in water; soluble in organic solvents
    Smiles Nc1c(F)cc(Cl)cc1Br
    Inchi InChI=1S/C6H4BrClFN/c7-3-1-2-4(9)6(10)5(3)8/h1-2H,10H2
    Storage Conditions Store at room temperature, dry and away from light

    As an accredited 4-Bromo-3-Chloro-2-Fluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical 4-Bromo-3-Chloro-2-Fluoroaniline, 25 grams, comes in a tightly sealed amber glass bottle with a hazard warning label.
    Shipping 4-Bromo-3-Chloro-2-Fluoroaniline is shipped in tightly sealed containers, protected from moisture and light. It should be transported according to local, national, and international regulations for hazardous chemicals, including labeling and documentation. Use secondary containment and ensure compatibility with other transported materials. Handle and store in a cool, well-ventilated area away from incompatible substances.
    Storage 4-Bromo-3-chloro-2-fluoroaniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Store at room temperature and avoid excessive heat. Proper labeling and secondary containment are recommended to prevent leaks and accidental exposure. Use personal protective equipment when handling.
    Application of 4-Bromo-3-Chloro-2-Fluoroaniline

    Applications of 4-Bromo-3-Chloro-2-Fluoroaniline in Industrial Manufacturing

    4-Bromo-3-Chloro-2-Fluoroaniline is widely used as a high-purity intermediate in several regulated and specialized industries. Below, we outline key downstream applications, focusing on technical compliance, processing practices, and end products as handled in manufacturing environments.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers use this material as a core building block in complex small molecule synthesis, especially within anti-infectives and oncology-related compounds. The aniline structure supports selective halogenation, ensuring positional specificity required for active pharmaceutical ingredient frameworks. Facilities monitor stringent impurity profiles, implement controlled atmospheric conditions, and execute stepwise synthesis reactions for batch consistency.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • USP & EP monographs for process-related impurities control
    • US FDA 21 CFR Part 210/211 (if exporting US-bound APIs)
    • ISO 9001:2015 quality management system certification

    Typical usage ratio

    • Applied at 0.3 – 0.6 molar equivalents per synthesis route, variable by specific API target and halogen exchange requirements
    • Ratio determined by target yield, desired selectivity, and impurity minimization in multi-step reactions

    Downstream process integration

    • Charged into primary aromatic amination or amidation steps after precision weighing and inert gas purging
    • Tightly controlled addition during coupling or cyclization for advanced intermediates
    • Isolated post-reaction by preparative chromatography or crystallization before proceeding to final API synthesis

    Final product types

    • Anti-infective API intermediates
    • Oncology-targeted heterocyclic core structures
    • High-purity pharmaceutical reference standards

    2. Agrochemical Synthesis (Herbicide & Insecticide Intermediates)

    Leading agrochemical processors incorporate this halogenated aniline variant in the synthesis of advanced herbicides and insecticides, utilizing its chemical stability for downstream chlorofluorination and aromatic amide formation. Strict formulation practices are followed to ensure field application safety and adherence to residue level requirements. Manufacturing lines often feature closed reactors and multi-filtration stages to protect both product integrity and operator safety.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius for pesticide formulation standards
    • REACH registration (EU Regulation No 1907/2006)
    • ISO 17025 (testing and traceability of process contaminants)
    • National Environmental and Safety Guidelines (country-specific)

    Typical usage ratio

    • Used at 5 – 25% w/w (weight percent) in multi-component intermediate synthesis batches
    • Proportion varies by herbicide or insecticide molecule specifications and required aromatic substitution patterns

    Downstream process integration

    • Dosed in jacketed reactors with catalytic agents for stepwise halogen exchange or amidation reactions
    • Further processed into active ingredient cores after purification and residue testing
    • Monitored by in-process HPLC for compliance with specification sheets

    Final product types

    • Triazine-based herbicides
    • Fluorinated agricultural insecticide actives
    • Plant growth regulator intermediates

    3. Specialty Dye and Pigment Intermediate Manufacturing

    Dye and pigment producers utilize this compound for its ability to introduce multiple halogen functional groups, achieving improved light fastness and chemical resistance in finished colorants. The intermediate features in diazotization and coupling reactions that demand strict color purity and batch reproducibility. Operators employ closed-system handling and continuous monitoring to ensure precise incorporation and minimize undesirable by-products.

    Industry compliance standards

    • EN 71-3 Safety of Toys – Migration of certain elements (for pigments in toys or child contact)
    • OEKO-TEX Standard 100 (for textile dye safety)
    • ISO 9001:2015 for pigment manufacturing QC
    • TSCA (Toxic Substances Control Act, US)

    Typical usage ratio

    • Introduced at 10 – 20% as a fraction of total raw material charge by weight for coupling and condensation reactions
    • Adjusted by chromophore desired and solvent system employed

    Downstream process integration

    • Added after initial coupling in azo- and anthraquinone dye syntheses
    • Retained in batch reactors under controlled temperature for pigment core formation
    • Resulting intermediates purified before blending or finishing steps

    Final product types

    • Acid dyes for textile applications
    • Industrial pigment intermediates
    • Specialty colorants for plastics, inks, and coatings

    4. Electronic Chemical Synthesis (OLED and Display Materials)

    Electronic materials manufacturers select this compound for its positional halogenation, providing tailored reactivity for aromatic coupling in organic semiconductors and light-emitting compounds. Advanced purification and handling practices are required to minimize trace contamination, as electronic-grade manufacturing tolerates only low-ppb impurity levels. Automated feed systems may be used for batch and continuous flow setups.

    Industry compliance standards

    • IATF 16949:2016 for electronic chemicals handling (automotive electronics)
    • JIS C 61000-1 (Japanese industrial standard for electronic materials)
    • RoHS Directive (2011/65/EU) for hazardous substances
    • SEMATECH purity guidelines for flat-panel and microelectronic chemicals

    Typical usage ratio

    • Formulated at 1 – 8% w/w in precursor charge for coupling or substitution reactions
    • Material input depends on target molecular weight and device layer requirements

    Downstream process integration

    • Fed into Suzuki or Buchwald–Hartwig coupling for aryl amine and arylene ether formation
    • Handled under inert nitrogen atmosphere to avoid degradation or side reactions
    • Purified through multi-stage distillation or recrystallization before device fabrication

    Final product types

    • OLED fluorescent emitter precursors
    • Field-effect transistor (FET) material intermediates
    • Advanced display driver chemical cores

    5. Fine Chemical Synthesis for Research and Analytical Standards

    Chemical research laboratories and fine chemical suppliers employ this intermediate to support small-scale synthesis and analytical method development. Its precise halogenation pattern is valuable for structure-activity relationship evaluation and internal calibration standards. Manufacturers provide high-purity, batch-controlled material in compliance with analytical testing protocols to support data reproducibility for downstream users.

    Industry compliance standards

    • ISO 17034:2016 for reference material producers
    • GLP (Good Laboratory Practice) guidelines for research synthesis
    • NIST reference material protocols for analytical standards
    • Sigma-Aldrich quality grade specifications for analytical use

    Typical usage ratio

    • Applied at 0.1 – 2 mmol/sample in pilot-scale synthesis or calibration batches
    • Usage tailored to analytical method sensitivity and experimental design

    Downstream process integration

    • Dissolved or weighed directly into reaction flasks for method validation, SAR, or impurity spiking
    • Retained as stock solution for repeated calibration use
    • Sample material stored under inert conditions to prevent hydrolysis or oxidation

    Final product types

    • Analytical reference standards
    • Research-use only (RUO) chemical libraries
    • Small-scale API validation samples
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    Certification & Compliance
    More Introduction

    4-Bromo-3-Chloro-2-Fluoroaniline: A Manufacturer’s Reflection on Its Production and Unique Value

    Introduction

    Working every day inside a chemical plant shapes my view of specialty chemicals in ways that no datasheet can describe. 4-Bromo-3-chloro-2-fluoroaniline is one of those compounds that consistently brings challenge, precision, and accomplishment to our operations. From raw material sourcing to packaging, each batch feels less like simple routine and more like a demonstration of what careful manufacturing actually means.

    Structure and Specifications

    Chemists know this molecule by more than its IUPAC name. Its molecular formula—C6H4BrClFN—matches a specific arrangement, giving the finished compound a set of physical traits that prove useful in many syntheses. What sets it apart is not just the combination of bromine, chlorine, and fluorine on the aromatic ring. Instead, the trick lies in arranging those atoms at the right spots, keeping the aniline core stable, and delivering a product where every lot passes the same high standard.

    In our plant, we keep a close eye on purity because even small traces of impurities can disrupt downstream reactions. HPLC and GC checkpoints show us what the eye cannot see. When we talk about specifications, numbers matter—purity above 98%, controlled moisture content, single-compound consistency. These are not empty figures. They reflect the patience and diligence of our technicians working through the night shifts.

    Not Just Another Aniline Derivative

    Ask a dozen chemists about anilines, and you’ll hear about how common the family is in organic chemistry. Yet, only a handful of aniline derivatives earn a spot on the bench of a medicinal or agrochemical researcher. 4-Bromo-3-chloro-2-fluoroaniline stands out for three reasons. Arranging three halogens on one ring in these exact positions opens up selectivity options in cross-coupling and further functionalization—routes that single-halogen or two-halogen analogues just cannot offer.

    The challenge begins with sourcing bromine, chlorine, and fluorine-bearing intermediates that are both stable and reactive enough. Our process does not just aim to add each group; it aims to minimize by-products that might haunt a medicinal chemistry campaign months later. Some producers focus on scale, but for us, reproducibility matters more. The academic papers rarely discuss how a jump in reactor volume introduces subtle changes: edge effects, mixing rates, and the quirks of scale-up. We have faced each of these in kind, learning that faithful scale-up depends on the operator’s understanding as much as on the recipe.

    Applications Backed by Real Experience

    This compound most often ends up as a key intermediate in pharmaceutical and agrochemical R&D. Even though we never see the drug or crop-protection agent emerge from our facility, the feedback loops with our clients tell us exactly what problems chemists face. Unlike more basic anilines—where ortho-para directors and simple syntheses dominate—the presence of three electron-withdrawing groups directs reactivity with rare specificity.

    The fluorine atom, at position 2, subtly changes electronic density across the ring, influencing how the molecule participates in nucleophilic aromatic substitution. Our customers’ reactions proceed with higher regioselectivity because of this feature, saving time and precious starting material. The bromine and chlorine atoms act almost like chess pieces: guiding palladium-catalyzed couplings toward challenging yet desired connections. We have seen two separate pharmaceutical clients choose our product over a simpler dichloroaniline, thanks to the increased selectivity in their Suzuki–Miyaura and Buchwald–Hartwig couplings.

    Those advances have nothing to do with theoretical promise and everything to do with days and weeks of trial and error at the bench. Sometimes, our technical support team gets a panicked call—someone’s test reaction produced a by-product, and they need to know how our process handles trace impurities. We go back through records, share batch data, and even rerun analytical screens to pinpoint what’s going on. It’s these regular interactions that reinforce the need to keep processes tight and transparency high.

    Why Specification Consistency Drives Progress

    Anyone who’s tried scale-up outside the comforts of a laboratory appreciates how small process variations ripple out into big problems. We’ve set up our manufacturing line so that each control point, from intermediate addition to temperature ramp, can be traced and justified. Consistency at this level is not just about regulatory confidence. It directly enables downstream chemists to batch larger amounts of finished drug intermediate without worry that an impurity profile will suddenly change.

    On more than one occasion, we have seen a single degree temperature swing alter the main impurity. This sharpens our dedication to precise monitoring. We calibrate instruments against certified standards, double-check retention times, and regularly communicate with end users if there is any process shift. Rather than issuing broad product bulletins, we welcome customer-specific technical discussions. Because we make the compound ourselves—no chain of repackagers—our lab and QA teams have the authority and information to speak candidly about the strengths and limits of each batch.

    Comparing to Related Products

    From a synthesis point of view, the crowded aniline ring in 4-bromo-3-chloro-2-fluoroaniline creates both opportunities and problems that non-fluorinated or mono-halogen analogues don’t present. Some clients initially request a mixture of halogenated anilines to “cover their bases” during lead optimization. They come back for specifically this compound when they realize standard dichloroanilines or bromo-chloroanilines either cannot handle their planned cross-coupling or lead to poor yields.

    We have produced standard anilines with single or double halogenation for years. They possess their own uses but lack the selectivity profile that fluorine imparts. The cost inputs are higher for the trifunctional molecule, mostly due to raw material price and additional purification steps. Where it shines is in selectivity for catalyst-enabled transformations, giving medicinal and process chemists options at stages where alternative approaches have stalled. Such flexibility, combined with reliable supply, keeps our customers developing drugs or pesticides with more confidence in their molecular frameworks.

    Serving the Research and Pilot Plant Communities

    In R&D labs, time and certainty are the two currencies that matter most. An unreliable supply or a batch that deviates from the previous one can stop a critical proof-of-concept, wasting weeks and budget. That’s one of the reasons we have invested heavily in in-house analytics and flexible-scale production. Our facility can deliver from grams to kilograms, with the same care at either level.

    Researchers want to see clear, up-to-date batch records before they commit to a scale-up campaign. We share those records, right down to the trace impurity analysis and moisture content measurements. This saves back-and-forth and builds trust—especially for those who have experienced the frustration of a research failure tied to reagent inconsistency.

    We also see our compound enter pilot scale campaigns aimed at evaluating active candidates before commercial manufacture. These stages tend to be under severe time pressure. Delays triggered by shipping, customs, or last-minute QA hold-ups can sink projects. Our experience with export documentation and rapid batch release is not window dressing, but a response to hard lessons learned in the field. We keep a responsive stock on hand, and we work directly with shipping partners to avoid issues that might keep a key research project waiting on our product.

    Quality Oversight Beyond the Certificate of Analysis

    Every manufacturer claims to offer high purity. Our view is that frequent, transparent, and specific communication makes more difference than the printed number on the certificate of analysis. Clients occasionally share concerns about lot variation or subtle new impurities surfacing after multiple synthesis cycles. Rather than hide behind documentation, our technical team works side-by-side with the customer, reviewing batch process logs and—when needed—running additional analytical checks to track the problem to source.

    Quality extends past our plant gates. We test how long the product keeps its purity under different storage conditions and push for feedback on how packaging performs after shipping. For example, we switched to a new high-barrier bottle after tracking moisture-related shifts in a handful of shipments to a humid region. Noticing a color change in the field doesn’t prompt us to document and move on. It pushes us back to the process, to test stability, and to adapt.

    Handling and Practical Points

    Anyone who’s opened a bottle of 4-bromo-3-chloro-2-fluoroaniline knows the dust potential. Gloves, goggles, and careful weighing—these aren’t afterthoughts but daily routines, enforced not only by regulation but by experience. The risk profile is higher than for non-halogenated compounds. We respond with secondary containment, pre-weighed pack sizes, and clear labeling that actually survives transit and bench storage.

    Our team has spent hours training new staff and sharing insights learned after a dropped bottle or clog in a feeding system. This is the type of institutional knowledge that R&D formulators may not see on arrival, but it shapes how easily a lab team can scale up their experiments. Simple operational tweaks—such as anti-static packaging or pack sizing tailored to common batch scales—come from direct experience, not theory.

    Sustainability and Process Responsibility

    Halogenated intermediates inevitably prompt questions about sustainability and waste handling. We do not take this topic lightly. Our waste-stream tracking systems trace everything from spent solvents to filtrate. Rather than ship mixed waste off-site, we neutralize acidic residues and reclaim solvents where possible, closing upstream loops on multiple streams. Dust collection and air emission controls get checked not by policy but as a direct outcome of having to keep workers safe and neighbors informed.

    Some clients ask about lifecycle impact. While fluorine, bromine, and chlorine atoms contribute significant performance at the molecular level, their presence means extra oversight is needed on effluent and solid waste. We build handling procedures for both our facility and for customers further down the line, adapting our recommendations when we learn of new regulatory or end-user requirements.

    We also buy more raw materials from audited sources with strong environmental controls. This is not simply about ticking a compliance box. Over the years, unannounced changes in upstream chemistry—sometimes triggered by a change in a supplier’s country of origin—have shown us how easily unexpected impurities can enter a supply chain. We respond by keeping our own suppliers close, regularly testing input streams, and sharing relevant findings with downstream users before, not after, it matters to their process integrity.

    Supporting Innovation Through Secure Supply

    We see the tension between global R&D pushes and the unpredictability of raw material markets every quarter. Demand for advanced intermediates like 4-bromo-3-chloro-2-fluoroaniline may spike unpredictably, driven by a promising biological screen or regulatory approval of a related molecule. Lead times for specialized starting materials stretch, tariffs rise, and logistics become a moving target. We have learned to maintain a buffer stock of critical raw materials and anticipate customers’ needs with buy-in programs rather than “just-in-time” risk.

    By engaging researchers in scheduled forecast planning, we avoid many of the supply droughts that can kill a promising project in the early phase. Our own forecasting team has grown from a single planner to a small group that coordinates across plant operations, raw material logistics, and export documentation. This team keeps production both flexible and responsive, shipping out what is needed without tying up budgets with stagnant inventory.

    What It Means to Work with a Direct Manufacturer

    Every interaction with our customers reflects the depth of understanding that comes only from hands-on production experience. Questions about shelf stability, compatibility with specific synthetic routes, or impurity carryover are not theoretical for us. Our technical team pulls from real production records and hands-on analytical work, not templated FAQ texts.

    Clients regularly share details about their next project, patterns they are exploring, or particular hurdles in scaling a synthetic route. They choose to work with us instead of intermediaries because our insights help head off avoidable pitfalls. Sometimes this takes the form of a custom-packaged lot, a special analytical assay request, or simply acting as a sounding board for an untested reaction route. Each new product or process we help launch becomes part of the collective expertise we share back with everyone who chooses our compounds.

    In our industry, reputation travels fast. Stories of impurities that sank a project, delays caused by cold supply chains, or time wasted tracking down quality documents all shape the decisions that research and manufacturing partners make. Our continuing goal is to remain not just a supplier, but a true contributor to every customer’s progress—measured not in units shipped, but in successful experiments and discoveries advanced by the work we put in, lot after lot, year after year.

    The Value of Detailed Dialogue

    Unlike bulk commodity chemicals, specialty intermediates like 4-bromo-3-chloro-2-fluoroaniline thrive when there are real conversations between producer and user. An initial inquiry often grows into an ongoing relationship. We share advance notice of process changes, regulatory updates, and analytical innovations. Customers help us improve every batch, catching what no standard inspection would flag.

    Every question from a research chemist or production manager is a sign of genuine engagement. We treat each as an opportunity to sharpen the clarity and usefulness of what we produce. Constant dialogue, grounded in the realities of chemical manufacturing, keeps the compound at its highest and best use—serving as a platform for discovery, not a point of failure.

    Looking Forward

    Each time we run a batch of 4-bromo-3-chloro-2-fluoroaniline, we bring together years of process tweaks, analytical advances, and customer-driven insights. The molecule’s complexity is a reminder of the care and attention that every specialty chemical deserves. Our experience as a manufacturer, not just a packager or broker, gives us a unique responsibility: to do more than deliver a bottle—supporting research, improving processes, and meeting the changing needs of those who innovate at the molecular level.

    Across the world, new chemistries promise better medicines, safer crops, and more advanced materials. They depend on building blocks that arrive on time, at spec, with support that goes far beyond the minimum. As we look ahead, we remain dedicated to this approach—genuine partnership, technical rigor, and the tireless pursuit of chemical quality that moves science from the bench to impact.