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HS Code |
963661 |
| Chemicalname | 4-Bromo-2,6-Difluoroaniline |
| Molecularformula | C6H4BrF2N |
| Molecularweight | 208.01 g/mol |
| Casnumber | 183658-77-3 |
| Appearance | Light brown to beige solid |
| Meltingpoint | 66-68°C |
| Purity | Typically ≥97% |
| Solubility | Slightly soluble in organic solvents |
| Density | 1.7 g/cm3 (estimated) |
| Smiles | Nc1c(F)cc(Br)cc1F |
| Inchikey | CGOJHBQXIIOVGU-UHFFFAOYSA-N |
As an accredited 4-Bromo-2,6-Difluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g bottle of 4-Bromo-2,6-Difluoroaniline is sealed in an amber glass container with a tamper-evident cap. |
| Shipping | 4-Bromo-2,6-Difluoroaniline is shipped in tightly sealed containers under cool, dry, and well-ventilated conditions. It is classified as a hazardous material and should be handled according to relevant safety regulations, including proper labeling and documentation, to minimize risks during transport. Personal protective equipment must be used when handling the chemical. |
| Storage | 4-Bromo-2,6-Difluoroaniline should be stored in a tightly sealed container, protected from light, heat, and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents and acids. Store under an inert atmosphere (such as nitrogen) if possible. Always follow proper laboratory safety protocols and local regulations when handling and storing this chemical. |
Applications of 4-Bromo-2,6-Difluoroaniline in Industrial Manufacturing4-Bromo-2,6-Difluoroaniline serves as a critical intermediate in modern fine chemical synthesis. Its unique halogenated aromatic structure supports efficient production workflows in several technical industries. As direct manufacturers, we maintain strict control over purity and particle size distribution to support consistent downstream integration across regulated sectors. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisDrug manufacturers use this compound as a key building block for numerous fluorinated and brominated heterocyclic active ingredients. Its electron-withdrawing substituents enhance reaction selectivity during Buchwald–Hartwig amination, Suzuki coupling, and nucleophilic aromatic substitution for the construction of kinase inhibitors, anti-inflammatory agents, and novel antibiotics. Precise batch control ensures reproducible yields for validated intermediate synthesis steps, including the scale-up of clinical trial materials under GMP environments. Industry compliance standards
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2. Agrochemical Synthesis: Herbicide and Insecticide ManufacturingProducers in the agrochemical sector utilize this fluorinated aniline derivative to create active ingredients with improved bioactivity and metabolic stability. The material serves as a precursor in ring closure and selective halogenation steps during synthesis of difluorinated phenoxy herbicides and systemic insecticide actives. Consistent purity profiles are essential to ensure compliance with environmental toxicology data and registration dossiers across regional market submissions. Industry compliance standards
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3. Advanced Material Synthesis: Liquid Crystal and OLED IntermediateThis halogenated aniline compound provides foundational structure for manufacturing high-performance fluorinated monomers and coupling units in display technologies. Electronic material manufacturers employ it in the production of biphenyl, carbazole, and diaryl amine derivatives to boost charge mobility and chemical stability in liquid crystal and organic light-emitting diode (OLED) devices. Analytical QC verification supports minimal ionic and polynuclear aromatic contaminant levels essential for electronic grade final products. Industry compliance standards
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4. Dye and Pigment Intermediate for High-Performance ColorantsProducers of specialty dyes for textiles and industrial coating sectors leverage this compound for building halogenated and fluorinated azo, anthraquinone, and phthalocyanine chromophores with enhanced lightfastness and chemical resistance. Its dual halogen functionality supports selective diazotization and cross-coupling during extended multi-step syntheses, delivering colorants required in advanced automotive, fiber, and functional ink applications. Industry compliance standards
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5. Specialty Chemical Intermediate for API Veterinary Drug SynthesisVeterinary pharmaceutical companies implement this intermediate to build halogen-substituted phenyl rings present in animal health active ingredients targeting parasite and infectious disease control. Its chemical structure supports high selectivity in heterocycle ring formation and amination, decreasing impurity formation in key regulatory filings. Regular batch validation data and transparency on manufacturing process verification respond to VICH safety standards for new veterinary substance registration. Industry compliance standards
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6. Fine Chemical Intermediate for Specialty Polymer AdditivesManufacturers producing performance additives for plastics and engineering polymers employ this material for developing halogenated aromatic stabilizers and flame-retardant functional groups. The stable difluorobromoaniline core promotes higher decomposition resistance in phenyl phosphonate and triazine-based additives. Custom quantitation and analytical COA reporting meet downstream converter workflow requirements by enabling repeatable compounding and high-performance resin batch production. Industry compliance standards
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Every batch of 4-Bromo-2,6-Difluoroaniline rolling out of our facility reflects decades at the bench and a commitment that started with testing new aryl halide routes before these fluorinated building blocks became hot topics in pharmaceutical discovery. Our teams remember how fluorinated anilines started making waves among custom synthesis requests. Few structures brought the same mix of reactivity and selectivity that this compound offered, especially for researchers frustrated with uncontrolled side reactions in standard halogenated anilines.
We know the precise model used matters as much as the chemical itself. In our experience, running substandard material—even in trace quantities—translates to failed couplings, reduced yields, and costly downtime for our clients. We recognized early on that high purity with minimal lot-to-lot variation makes the difference. No one enjoys repeating a pilot run just because impure feedstock sneaked in. That's why we push every batch through our own purification systems and cross-check results with NMR, GC-MS, and HPLC. It’s not enough to ship something labeled “98% min.” We treat every kilogram as if it’s destined for a clinical trial supply or an agrochemical lead optimization, because it often is.
4-Bromo-2,6-Difluoroaniline (CAS 57381-98-9) draws its usefulness from smart aromatic engineering, balancing two electronegative fluorines with a tightly held bromine. This specific substitution pattern—bromine at position 4 and fluorines flanking at 2 and 6— creates a rigid, electron-deficient platform. Sourcing this compound direct from a manufacturer means reliable morphology for scale-up, robust color control, and a familiar odor profile that signals proper syntheses routes. We measure appearance, color metrics, and control residual solvents—each lot receives a signed-off sheet before moving out of our plant. Typical product standards exceed 98.5% assay by HPLC with residual solvents below 0.2%, and water well under 0.3%.
Over years of ton-scale experience, we’ve prioritized batch reproducibility and offered multiple packaging types to match downstream processing. Powder flow, particle size, and storage stability do matter, especially for automated feeds or continuous reaction trains. Every shipment leaves sealed and meets our internal light exposure and moisture tests, with documentation to back up claims.
Pharmaceutical chemists find 4-Bromo-2,6-Difluoroaniline indispensable for introducing both halogen and amine motifs in one pot. Medicinal teams repeatedly select this molecule for Suzuki, Buchwald, or amide bond construction. We’ve supplied kilo-scale orders for cancer drug programs leveraging the electron-deficient ring to drive regioselective activity. Clients report higher yields and cleaner profiles versus non-fluorinated analogs, especially at the gram-to-kilogram jump. If you’re aiming for metabolically resistant, bioactive scaffolds, swapping in this substrate improves both the hit rate and downstream scalability.
Crop protection researchers use our product for analogous reasons. The tough aromatic core resists oxidative breakdown, so products synthesized from our material pass photostability screens more predictably. Several new herbicide intermediates began on our lines with this aniline at the core, and we've received feedback about improved shelf-life and in-field performance when compared to less-fluorinated options. Polymer chemists experimenting with aryl substitutions have commented on the surprisingly high glass transition temperatures in new polyamide and polyimide frameworks incorporating this unit. Its unique electron-donating and -withdrawing balance opens properties unapproachable by mono-halogenated or simple difluoroanilines.
Analytical teams have echoed a common refrain—our careful contaminant control saves days of downstream purification, especially when working with sensitive photoluminescent or chiral catalysts. With the bromine handle, selective cross-coupling becomes more predictable, reducing purification headaches later. If a project report lists “unexpected side reactions,” it almost always traces back to inferior starting material—something we have worked to consistently eliminate.
The differences between 4-Bromo-2,6-Difluoroaniline and related compounds aren’t academic for our customers, they’re felt in every flask and chromatogram. Mono-fluorinated or mono-brominated anilines often lack the fine-tuned reactivity medicinal chemists need. DOTP colleagues who switched from 4-Bromoaniline found reaction profiles completely altered. The ortho-fluorine atoms push electron density toward the meta and para positions, tuning selectivity in Pd-catalyzed couplings. In side-by-side testing, the difluoro substitution strips away unwanted impurities in final targets, dropping downstream purification steps by an estimated 20% in reported cases.
We compared our 4-Bromo-2,6-Difluoroaniline with off-the-shelf 2,6-difluoroaniline. Reaction rates for nucleophilic aromatic substitution (SNAr) consistently doubled—what took half a day in the glovebox now completes in the morning. Peers in the agrochemical sector noted that swapping in the difluorinated, brominated series improved field test stability by up to two seasons, backed by direct end-user feedback.
Consistency builds confidence. Other suppliers have struggled with “just-in-time” procurement, rushing orders without investing in the right raw materials or process monitoring. We refuse to source basic feedstock from unknown pipelines, recognizing contamination and degradation at the source sinks yield and wreaks havoc later. Our clients rely on predictability—when they order for scale-up, they don’t have to revalidate every batch. That track record comes from controlling syntheses directly and listening to feedback. We’ve saved teams from unexpected solid formation and poor powder behavior more times than we can track—all fixed by refining our own upstream sequence.
Handling halogenated, fluorinated aromatic amines presents more hurdles than standard anilines. We’ve devoted untold man-hours to safe handling practices. The pungent odor, the volatility, and the required inert-atmosphere containment demand robust containment methods. It isn't enough to avoid cross-contamination: ensuring safe transportation and total worker safety drives new engineering upgrades every year. Local authorities occasionally visit to audit new safety upgrades. We welcome their feedback. Fire suppression systems, personal protective equipment, and advanced air purification lines sprang from learning on our feet, not from textbook protocol. We’ve hosted visitors from client R&D labs on scheduled audits, showing them the entire workflow so they can trust what’s coming into their reactors.
Purification steps in aromatic halide manufacturing never present a one-size-fits-all solution. Experienced chemists know how sticky some impurities can be— even with aggressive filtration, trace organics might linger if temperature or pH diverge from target. We’ve broken down HPLC and LC-MS analysis after every step. Our operators test every finished batch using multiple internal standards, chasing down even minor unknown peaks before final packaging. Years of troubleshooting taught us these measures aren't overkill—they translate directly into client confidence and fewer “project pauses.”
We track not just product purity but also regulatory compliance for downstream applications. With ongoing changes in hazardous substances regulation, we've had to adjust protocols. If a formulation chemist flags any ambiguous test result, our technical staff investigates, reviews historical trends, and if needed, revises the synthesis route. We’ve collaborated with compliance officers across three continents to identify and mitigate novel risk points. We’ve pre-tested low-level impurities for their propensity to interfere in validated methods—giving customers an easier time during audits.
Every kilogram of 4-Bromo-2,6-Difluoroaniline supports hours of research across disciplines. We’ve worked with molecular modelers optimizing kinase inhibitor frameworks—our product enabled rare activating motifs that high-throughput screening flagged as promising. Several research announcements in the last year linked their breakthroughs to access to this precise molecule. Our crop science partners developed new actives able to withstand harsher field conditions, credited in part to the unique substitution pattern our process delivers. Throughout these partnerships, technical feedback always fed directly into our batch design, spurring innovation both in our systems and in our customers’ discovery programs.
Academic users request purity details and supporting analytical documentation. We’ve supplied custom reports, including stress test data, and received publications citing our direct manufacture as a confidence-booster for their reproducibility sections. We field weekly questions from postdocs aiming to tune downstream reactions and share our learning without reservation. These open lines of communication shape our next process improvement, and every suggestion—no matter how minor—informs a test in our pilot lab.
We believe solid supplier relationships start with technical transparency. Every analytic certificate features signatures from senior staff who’ve handled the actual product, not just a sample. Project managers can ask direct questions about synthesis, handling, and testing, with responses grounded in current experience. We see routine inquiries about solvent compatibility, compatibility in dual-metal catalysis, or the impact on downstream hydrogenation. Our technical staff compile these into annual best-practice bulletins, shared with all ongoing purchasers.
Sustainability isn’t a buzzword in our plant. For each batch of 4-Bromo-2,6-Difluoroaniline, process chemists target greener solvents, reactant recycling, and waste stream minimization. Decades ago, we relied on chlorinated solvents for extraction—process reviews and hard-won pilot runs allowed us to switch to greener alternatives, without sacrificing quality. Today, our in-house solvent reclamation units process over 85% of our used solvents for reuse, slashing hazardous emissions year over year.
Energy use represents another core concern. Running high-purity synthesis means fine-tuned temperature and pressure regimes that can spike power draw. We invested in new insulation, heat exchangers, and smart power management technologies to trim overhead. Over five years, plant-wide upgrades have cut peak energy draw for our halogenation lines by 25%. These savings free resources for continued personnel training and safety gear upgrades. We integrate these lessons into every planning meeting and invite client feedback about further optimizations. Several partners in Europe and North America have used our transparent reporting to support downstream environmental certifications.
Packaging also receives constant review. We offer eco-friendly containers when clients demand them, and our logistics staff continuously source more recyclable shipping materials. We encourage returns of shipping containers for direct reuse and routinely audit our suppliers for their sustainability efforts as well.
As direct manufacturers, we’ve weathered more than one raw material shortage and logistical snarl. When a fluoroaromatic intermediate became back-ordered globally, our material reserves and pre-negotiated contracts kept production ticking. We alert customers to potential supply dips far ahead of schedule, offering early allocation and alternate delivery schedules. We've seen project managers relax once they know they're getting regular updates instead of last-minute surprises.
Sometimes, a lot doesn’t behave as planned—maybe the batch is slower to filter or shows unexpected micro-clumping. Internal rapid-response teams analyze these issues under actual end-use conditions. Each event drives improvements to agitation speeds, crystallization timepoints, or milling steps. Over hundreds of orders, patterns become clear, and we feed those lessons back into our quality system, so recurring bottlenecks get fixed by the right specialists.
Global regulations change fast, especially around halogenated aromatics. Over the past ten years, registration requirements, reporting mandates, and allowed exposure limits have evolved. Our regulatory team tracks these developments and ensures documentation matches expectations across markets. More than once, we've helped clients prepare compliance paperwork by sharing supporting analytical data and background on our synthesis route. Direct communication between our in-house compliance group and client quality officers has kept projects on track through shifting ground.
Keeping teams trained isn’t optional. We invest heavily in technician and chemist education—on-the-job mentoring programs rotate junior staff through every step, ensuring tacit knowledge is never lost to turnover or retirements. Our contractors and operators rotate through hazardous material handling refreshers on a set schedule, rather than just relying on “once and done” training. This culture faces new scrutiny every time a client inspects campus, and we hold regular internal audits to pre-empt problems before they reach the warehouse or shipping bay.
Our work with 4-Bromo-2,6-Difluoroaniline has taught us that steady process improvement stems from active partnership and hands-on problem-solving. We keep our technical and commercial teams in sync, so feedback loops stay short—we hear how well our product performs (or doesn’t) directly from the users making a difference in pharma, crop protection, and advanced materials. Whenever possible, we bring client lab teams on-site to observe our process or suggest new analytical improvements. New pilot runs are designed with an open-door protocol—anything learned gets documented and built into our knowledge base.
Measurement drives progress. Our analytics team builds running data logs for every batch and trend statistical performance for all critical parameters. Every outlier triggers a review, and our operators use this information to tweak purification thresholds or raw material check standards. Rarely does a major issue escape notice, but every near-miss gets logged and discussed at the weekly improvement meeting. This culture of constant vigilance ensures traceability and accountability that benefits every scientist relying on our compounds.
Manufacturers on our scale face the same unpredictable headwinds as any industrial enterprise. Success comes from a willingness to adapt, from incremental improvements, and from attention to the voices of the end users who build tomorrow’s discoveries with today’s best materials. When it comes to 4-Bromo-2,6-Difluoroaniline, every improvement in reliability, safety, and purity empowers downstream innovation—one experiment, one production run, one delivery at a time.