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2-Bromo-4-Chloro-6-Fluoroaniline

    • Product Name 2-Bromo-4-Chloro-6-Fluoroaniline
    • Alias 2-Bromo-4-chloro-6-fluorobenzenamine
    • Einecs 629-515-6
    • 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
    VTB
    Specifications

    HS Code

    145792

    Chemicalname 2-Bromo-4-Chloro-6-Fluoroaniline
    Molecularformula C6H4BrClFN
    Molecularweight 224.46 g/mol
    Casnumber 927800-76-6
    Appearance Solid, powder
    Color Light yellow to off-white
    Meltingpoint 56-60°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles NC1=C(Br)C=C(Cl)C(F)=C1
    Inchi InChI=1S/C6H4BrClFN/c7-3-1-4(8)6(9)5(2-3)10/h1-2H,10H2
    Storagetemperature Store at 2-8°C

    As an accredited 2-Bromo-4-Chloro-6-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, labeled "2-Bromo-4-Chloro-6-Fluoroaniline", includes safety information and hazard symbols.
    Shipping 2-Bromo-4-Chloro-6-Fluoroaniline is shipped in tightly sealed containers, typically under inert gas or desiccated conditions to prevent moisture exposure. It is packed according to chemical safety regulations, labeled as a hazardous substance, and transported with appropriate documentation required for chemicals, ensuring protection against breakage and leakage during transit.
    Storage 2-Bromo-4-Chloro-6-Fluoroaniline should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep it in a tightly sealed container, clearly labeled, and protected from moisture. Use secondary containment to prevent spillage. Always follow appropriate safety protocols and local regulations for storage of hazardous chemicals.
    Application of 2-Bromo-4-Chloro-6-Fluoroaniline

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

    As a specialized producer of 2-Bromo-4-Chloro-6-Fluoroaniline, we supply this key halogenated aniline intermediate to manufacturers operating strict, regulated processes in fine chemical synthesis. Below we detail real-world downstream sectors leveraging this material’s unique substitution pattern to yield high-purity advanced ingredients and actives. Each scenario highlights established industrial compliance standards, applied dosage selections, process integration points, and ultimate finished product types as realized in commercial manufacturing.

    1. Agrochemical Intermediate Synthesis for Selective Herbicides

    Manufacturers of next-generation herbicides employ this intermediate when synthesizing substituted aniline-based active molecules, which target weed species with improved crop selectivity. The halogenation pattern achieves superior field stability and resistance management in several pre- and post-emergent products. Realized at multi-tonne scale, the compound enters reaction trains subjected to strict tolerance controls.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for chemical manufacture)
    • REACH Annex VII–IX (Registration, Evaluation, Authorization and Restriction of Chemicals in the EU)
    • Chemical Facility Anti-Terrorism Standards (CFATS, USA) for precursors
    • Chinese National Standard GB 2763 (restricted residues in agrochemicals)

    Typical usage ratio

    • Employed at 0.8–1.6 mole equivalents as acylation or substitution precursor per target API batch; formulation ratio depends on final active content and impurity profile requirements for selective herbicide actives

    Downstream process integration

    • Charged during the amination or halogen-exchange stage within multi-step synthesis—typically after halide coupling and prior to final ring closure; monitored via in-process HPLC for complete conversion

    Final product types

    • Pre-emergent and post-emergent herbicide actives (e.g., fluorinated phenoxyacetic acid derivatives, anilide-type herbicides)
    • Technical grade herbicide formulations for direct tank mix or microencapsulation

    2. Pharmaceutical Intermediate for Halogenated API Development

    This material functions as a key intermediate in the synthesis of specialty fluorinated or brominated aniline derivatives, which form the pharmacophore core in several new-generation small-molecule drug candidates. Pharmaceutical manufacturers utilize it for medicinal chemistry and in GMP-validated kilo-lab and pilot plant campaigns where regioselective functionalization is mandatory to suppress genotoxic impurities (GTIs) and meet regulatory batch release.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients)
    • Chinese Pharmacopoeia (2020 Edition, for API-quality intermediates)
    • 21 CFR Part 211 (US FDA, GMP for finished pharmaceuticals)
    • EDQM CEP Framework for pharmaceutical starting materials

    Typical usage ratio

    • Charged at 1.0–1.2 eq. relative to core scaffold in amide/formylation coupling; process chemists optimize via DoE (Design of Experiments) to minimize side reactions and maximize yield. Small changes in ratio impact both impurity profile and throughput.

    Downstream process integration

    • Added after pre-activation of scaffold; utilized in stepwise protection–deprotection, ring closure, or halogenation reactions. QC monitoring by NMR or LC-MS at key processing points ensures structural conformity for subsequent transformations.

    Final product types

    • Halogenated small-molecule APIs targeting CNS, oncology, or anti-infective indications
    • Preclinical lead compounds requiring medicinal-grade purity for clinical evaluation

    3. Advanced Dye and Pigment Intermediate Manufacturing

    Dyestuff and pigment producers integrate this material as a core-building block for synthesizing highly stable fluorinated azo, anthraquinone, and phthalocyanine compounds. Its substitution pattern enhances chroma, thermal resistance, and fastness properties in specialized technical colorants designed for fiber-reactive and engineering polymer applications, supporting strict industrial and textile standards.

    Industry compliance standards

    • OEKO-TEX® Standard 100—Annex 4 (for restricted amines in textile dyes)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, Manufacturing Restricted Substances List)
    • EN 71-3 (European Toy Safety for permissible migration of elements in pigments)
    • ISO 105-A02/A03 (Textile color fastness assessment)

    Typical usage ratio

    • In dye/pigment synthesis, employed at 0.9–1.3 eq. relative to given chromogenic substrate. Loading levels and chain extension depend on color index specifications and target granule stability.

    Downstream process integration

    • Charged post-diazo coupling or pre-oxidation stage for building triazine, azo, or phthalocyanine rings. Product undergoes filtration, milling, and dispersant blending before QC tests for purity and shade matching.

    Final product types

    • Reactive dyes for cellulosic fibers and polyamides
    • High-performance organic pigments for engineering plastics, inks, or coatings
    • Disperse dyes for polyester and acetate applications

    4. Electronic Chemicals and Liquid Crystal Monomer Preparation

    Advanced electronics manufacturers utilize this intermediate to create highly pure halogenated aromatic monomers for use in the development of liquid crystal display (LCD) materials and specialty organic thin-film devices. The unique fluorine, bromine, and chlorine substitutions impart the desired dielectric constant, thermal stability, and polarity to molecular structures crucial for modern display and semiconductor manufacturing.

    Industry compliance standards

    • SEMATECH/IEC 62474 (Reporting substances—electronics industry)
    • Japanese Chemical Substances Control Law (CSCL—Specified Chemical Substances)
    • RoHS 3 (Restriction of Hazardous Substances, for finished electronics)
    • ISO 14001 (Environmental management in electronics chemicals production)

    Typical usage ratio

    • Introduced at 0.1–0.7 eq., adjusted based on desired chain length and molecular orientation of the liquid crystal or functional monomer system; researchers optimize within pilot-scale reactors for molecular axis uniformity.

    Downstream process integration

    • Added during Friedel-Crafts acylation or halogen exchange sequences when assembling complex aromatic monomers; entered under nitrogen atmosphere, followed by extensive purification to reach <10 ppm metal/ionic residuals.

    Final product types

    • Halogenated or fluorinated liquid crystal monomers for TFT-LCD panels
    • Organic electronic materials for photonic and semiconducting applications
    • Intermediates for high-purity circuit board chemicals

    5. Veterinary Drug Intermediate Synthesis

    Veterinary active ingredient producers utilize this material as a precursor in the synthesis of complex halogen-containing aniline skeletons which exhibit enhanced bioavailability and metabolic profiles in companion and farm animal pharmaceuticals. The industry mandates strict impurity and trace element limits, with solid QC compliance enforced at each stage of the synthesis and subsequent formulation.

    Industry compliance standards

    • VICH GL 10 (Good Manufacturing Practice for APIs in veterinary drugs)
    • European Pharmacopoeia (Ph. Eur. 10.0, monographs for veterinary medicinal products)
    • US FDA CVM (Center for Veterinary Medicine) guidelines for new animal drugs
    • ISO 22716 (Good Manufacturing Practices for pharmaceutical raw materials)

    Typical usage ratio

    • Added at 0.8–1.2 eq. per synthetic sequence, adapted by process chemists to control side-chain introduction or aromatic substitution; routine in-process titration ensures full usage and absence of unreacted intermediate.

    Downstream process integration

    • Fed into early-stage amination or condensation reactions; batch released only after passing GC-MS/ICP-MS for residual halide and heavy metal levels; subsequent formulations use validated tablet or suspension processes.

    Final product types

    • Oral or injectable veterinary APIs for antiparasitic or anti-inflammatory use
    • Premix and finished pharmaceutical forms for livestock and pets
    Free Quote

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

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    Certification & Compliance
    More Introduction

    2-Bromo-4-Chloro-6-Fluoroaniline: Inside the Modern Synthesis Toolbox

    Leading with Clarity: What 2-Bromo-4-Chloro-6-Fluoroaniline Really Offers

    As manufacturers of fine chemical intermediates, our work follows the trail of continuous improvement—better reactions, purer outputs, fewer bottlenecks. 2-Bromo-4-Chloro-6-Fluoroaniline has taken a prominent place in our catalog because it solves hurdles that have stumped both process chemists and R&D teams for years. Whether you’re running multi-step syntheses for agrochemicals or building out a fragment for pharmaceutical discovery, this compound opens new pathways with fewer side issues.

    Real-World Synthesis: Model and Specifications Shaped by Demand

    This aniline derivative, with its specific 2-bromo, 4-chloro, and 6-fluoro substitutions on the aromatic ring, stands out due to the nature of its substitution pattern. Our chemists pay special attention during each batch, working with tightly controlled specifications: high assay, low water content, and strict thresholds for metals and residual solvents. Each parameter was not chosen from a standard but shaped through long discussions with formulation experts and hands-on troubleshooting at the bench.

    Quality control for this material centers on proven techniques—HPLC, GC, NMR, and titration—but the devil lies in the details. Experience shows traces of unreacted halides or off-position ring substitution slow down downstream reactivity or, in the worst case, generate novel impurities after scale-up. We continually adjust timing, solvents, and temperature controls in our reactors, fine-tuning each step to squeeze out unwanted contaminants and get the purity profile right every time.

    Application Story: How End Users Actually Harness 2-Bromo-4-Chloro-6-Fluoroaniline

    This building block isn’t just a lump of data or an obscure line in a catalog. Across a range of crop protection and drug discovery labs, people require complex aryl amines to explore new bioactivity. By offering both electron-donating and -withdrawing halogens in one molecule, this aniline variant allows for specific, predictable reactivity. The electron-poor nature brought on by the bromo, chloro, and fluoro groups makes it a popular candidate for nucleophilic aromatic substitution—demanded by many of today’s targeted syntheses.

    Reaction screening with this compound shows fewer surprises. Even newcomers find improvements when swapping to our 2-Bromo-4-Chloro-6-Fluoroaniline for Suzuki, Buchwald–Hartwig, or other palladium-catalyzed coupling strategies. Its clean leaving group profile and stable handling properties mean reactions run longer with fewer byproducts—a major boost for those running high-throughput platforms or scaling toward pilot-plant demands.

    Why Process Chemists Switch: Learning from Field Experience

    Questions often surface about switching from a mono- or di-halogenated aniline to this particular tri-halogenated derivative. Every month, formulation teams look for new scaffolds but struggle when older building blocks introduce too many variables. We’ve worked shoulder-to-shoulder with project chemists who saw increased yields by changing to our version. Early-stage adopters have pointed out how the meta and para positionings of the halogens allow them to dial in selectivity and compatibility, controlling downstream hydrolysis or oxidation steps much more easily.

    Some competitors offer materials that look similar on paper. The differences emerge in the reactor and the downstream analytics. Even a fraction of a percent of isomeric impurity or higher water carryover can force a project back to the drawing board. By drawing on years of pilot-scale operation, we have adapted our process around robust solvent recovery, custom purification cycles, and detailed impurity mapping. Clients who once struggled with inconsistent melt points, or who found prior sources left their reactors fouled, recognize the benefit of a compound shaped for consistent performance.

    Key Differences: Not All Haloanilines Behave the Same

    Chemically, 2-Bromo-4-Chloro-6-Fluoroaniline stands apart from more basic anilines and even from other halogenated derivatives. The specific 2,4,6 pattern means this compound resists unwanted ring activation, improving selectivity in metal-catalyzed couplings. Many customers started with just 4-chloro or 2-fluoro variants and spent weeks optimizing conditions—adding buffers, tweaking ligands or bases—to control for off-target reactions. In comparison, this molecule operates more predictably across a variety of catalyst/loadout combinations.

    Another practical distinction shows up during scale-up and storage. The triple halogen arrangement increases bench stability, reducing risk of oxidation on standing. Standard aromatic amines, or even less-substituted halogen derivatives, can discolor or degrade under light and air. Repeated monitoring in our own facilities and real-world customer feedback both point to lower batch-to-batch variability and longer shelf-life. For teams working against project deadlines, a stable intermediate that holds its profile saves pain later.

    Handling also proves more forgiving. People working with highly active or moisture-sensitive anilines often complain about dusting, clumping, or uneven dissolution. We invested in solutions to keep particle size surprisingly uniform—an overlooked detail that can shape the predictability of both lab and production scale reactions. Years in chemical plants taught us that small format changes alter the real usability of a product much more than glossy spec sheets imply.

    Supporting Data: Concrete Wins and Credible Results

    The actual benefit runs deeper than theoretical promise. Over the last few years, several pharmaceutical and agrochemical firms brought projects to us after running into recurrent trouble with other sources. They needed to synthesize bi-aryl structures, with yields falling short of targets even after extensive optimization. By shifting to our aniline derivative, one group improved coupling yields by over ten percent, reducing byproduct contamination at the same time. Another team, working under tight deadlines, reported zero instances of unexpected polymorph formation—a common headache with other intermediates.

    We keep records of product performance and track performance trends downstream. In several long-term collaborations, clients compared the handling, moisture retention, and lot-to-lot variability of our product to imports or internally produced samples. The lower variance allowed for tighter process windows and less time spent fighting batch rejects. Synthesizing value means more than just shipping high-assay lots; it means addressing those quiet liabilities that appear later—yield drops, clean-up time, and regulatory close calls.

    Commitment to Continuous Quality Improvement

    Producing a stable supply of such a specialized intermediate means constant vigilance and readiness to troubleshoot. The path from starting materials to finished product involves many cycles of solvent exchange, temperature swings, and purification. Decades of managing reactors—real, high-throughput, hot-batch vessels, not just theoretical spreadsheets—taught us which points of the process deserve guarded attention. We control every critical input: halide sources, purity of catalytic metals, environmental humidity, even the age of storage tanks. The pay-off is less unexpected downtime and fewer discussions with customers about troubleshooting bad outcomes post-delivery.

    Regulatory needs drive another layer of discipline. For applications in pharmaceuticals or crop protection, both residual solvent control and trace metal content carry strict requirements. We maintain documentation, implement validated analytics, and regularly update our internal thresholds to ensure compliance with evolving standards—because regulatory shifts have teeth, and a missed contaminant can derail whole programs.

    Being a Manufacturer, Not a Middleman

    Standing behind this product means sweating the details no phone-in order taker would care about. Years ago, we took the hard route and invested in process development, not just purchasing stock for resale. The insights gained—whether through raw RC1 data, customer debriefs, or digging through pilot plant troubleshooting logs—feed back into continuous improvement. If a batch shows even a hint of process drift or an unexpected impurity profile, our chemists pick up the phone, not the sales team. That level of skin in the game has built lasting trust with demanding customers working in fast-moving markets.

    Our R&D team spends as much time adapting process parameters as tracking changing client specifications. Some process tweaks look small but echo throughout downstream risk—adjusting the order of addition, testing alternate purification resins, tracking potential solid-state transitions at different storage temperatures. Each change gets vetted in both analytical and process control environments to make sure the final material doesn’t just hit a number on a certificate, but actually performs under high-stakes conditions.

    Addressing Challenges: Process, Scale, and Responsible Manufacturing

    Producing 2-Bromo-4-Chloro-6-Fluoroaniline at scale presents challenges even when recipes work perfectly on paper. Halogen management isn’t just a step in the process—it creates waste and emissions concerns that demand smart engineering. We put money into closed-loop solvent recovery, specialized scrubbers, and local air handling to remain responsible stewards both for staff and for our neighbors. The high price of missteps—whether in lost material, permit issues, or water discharge anomalies—keeps site leaders engaged with daily operations.

    Waste minimization also comes from tighter process design, not just end-of-pipe solutions. We map every kilogram in and out, tie together raw material tracking with final lot numbers, and loop in full batch genealogy. Being able to trace a single impurity spike not only saves troubleshooting time but also meets the kind of transparency requirements many large customers expect during supplier qualification.

    Raw material volatility has become a regular challenge. Securing reliable sources of halogenated aromatics while meeting increasing purity standards compounds the difficulty. We’ve moved to multi-sourcing strategies and locked in supply chain partnerships with transparent, regularly audited producers. Our advice to customers: prioritize these types of precautions before scaling new projects—your product only wins stability if your supplier actually produces, rather than just resells, the intermediate you count on.

    Looking Forward: Improving the Value Chain

    Tomorrow’s synthesis challenges won’t tolerate average building blocks. Chemists ask more from their intermediates than ever—less troubleshooting, better performance in automation, and compatibility with both classic and emerging reaction platforms. We continue to invest in both upstream and downstream capacity, so that batches don’t just match specs, but do so repeatedly under real pressure. A close relationship between manufacturing, QC, logistics, and customer projects helps both sides anticipate what’s next.

    Customers benefit most when suppliers match their dedication to project outcomes with technical know-how built from real production floors. Product excellence comes down to hard-won expertise: dialing in the right raw materials, controlling for the chemistry that actually matters, troubleshooting before issues reach the field. 2-Bromo-4-Chloro-6-Fluoroaniline has proven its worth in practice—in better batch yields, longer shelf lives, and fewer regulatory headaches.

    Concluding Thoughts from the Shop Floor

    Trust in fine chemicals comes from more than batch numbers on a certificate. It grows from production teams who learn each process variable through repeated cycles, managers who invest in the details, and long-standing relationships with customers who refuse to settle for “good enough”. Each kilogram of 2-Bromo-4-Chloro-6-Fluoroaniline underscores that dedication: a reflection of daily hands-on work, iterative improvement, and a clear view of what matters between bench and marketplace.

    Every challenge tightens our focus, from scaling exothermic steps without compromise all the way to ensuring the last drum meets the needs of tomorrow’s innovators. Delivering a halogenated aniline isn’t just the finish line—it's a checkpoint in a much larger journey, shaped by a respect for chemistry, for end users, and for every real-world application that follows.