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2-Bromo-4,6-Difluoroaniline

    • Product Name 2-Bromo-4,6-Difluoroaniline
    • Alias 4,6-Difluoro-2-bromoaniline
    • Einecs 'EINECS 401-090-5'
    • 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

    101728

    Chemical Name 2-Bromo-4,6-difluoroaniline
    Molecular Formula C6H4BrF2N
    Molecular Weight 208.01 g/mol
    Cas Number 164255-97-8
    Appearance Off-white to light yellow solid
    Melting Point 56-60 °C
    Density 1.77 g/cm³ (estimated)
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=C(C=C(C(=C1F)Br)F)N
    Inchi InChI=1S/C6H4BrF2N/c7-3-1-4(8)6(10)5(9)2-3/h1-2H,10H2
    Storage Conditions Store in a cool, dry, well-ventilated place

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

    Packing & Storage
    Packing 2-Bromo-4,6-Difluoroaniline, 25g: Sealed amber glass bottle with tamper-evident cap, labeled with product details, safety, and hazard symbols.
    Shipping 2-Bromo-4,6-Difluoroaniline is packed securely in airtight containers to prevent moisture and contamination. It is shipped as a hazardous material according to international regulations, requiring labeling and appropriate documentation. The chemical should be transported in a cool, dry place, away from incompatible substances, and handled only by trained personnel.
    Storage **2-Bromo-4,6-Difluoroaniline** should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling and avoid prolonged exposure. Use suitable chemical-resistant containers and follow safety protocols for handling hazardous chemicals.
    Application of 2-Bromo-4,6-Difluoroaniline

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

    We manufacture 2-Bromo-4,6-Difluoroaniline to precise quality specifications suitable for process-scale downstream use. This intermediate finds established application in the development of active ingredients, specialty agrochemicals, and advanced materials, integrating directly into critical synthesis steps. Below we outline verified industrial application sectors, key regulatory standards, representative formulation details, incorporation within downstream operations, and end product targets.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    2-Bromo-4,6-Difluoroaniline serves as a building block in the synthesis of fluorinated pharmaceuticals including several advanced heterocyclic APIs. It participates as a key nucleophilic aromatic amine in palladium-catalyzed coupling and amidation reactions, contributing elemental bromine and fluorine at controlled substitution positions, which pharmaceutical chemists rely on for fine-tuning molecular activity and metabolic stability. Our consistent lot-to-lot quality supports rigorous pharmaceutical process requirements, batch traceability, and pre-registration development for regulated markets.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU GMP Part II and Part I requirements
    • 21 CFR Part 211 & 210 (US FDA cGMP regulations)
    • EdQM CEP/DMF submission frameworks

    Typical usage ratio

    • 0.3 – 1.5 molar equivalents relative to the core pharmacophore; process chemists optimize based on coupling efficiency and target yield

    Downstream process integration

    • Incorporated during Stage 2–4 intermediate construction, most commonly in Suzuki-Miyaura, Buchwald-Hartwig, or direct amidation steps in multi-step API synthesis routes

    Final product types

    • Small molecule APIs (oncology agents, central nervous system drugs, anti-viral intermediates)
    • Regulatory submission intermediates

    2. Agrochemical Active Ingredient Manufacturing

    Major agrochemical manufacturers use 2-Bromo-4,6-Difluoroaniline for the synthesis of halogenated triazine and phenoxy herbicides, as well as fungicide pyrazoles. Its position-specific bromine and fluorine atoms enable downstream chemistries that create actives with enhanced field persistence and target selectivity. Our strict impurity profiling and consistent purity help formulators meet market launch and re-registration requirements for major jurisdictions.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (JMPS)
    • ISO 9001 quality system requirements
    • European Regulation (EC) No 1107/2009—Plant Protection Products
    • EPA 40 CFR 158 (US pesticide regulatory guidelines)

    Typical usage ratio

    • 0.5 – 1.2 equivalents per aryl ring in final agrochemical backbone synthesis; adjustments made for substrate reactivity and sequential halogen management

    Downstream process integration

    • Deployed in the nucleophilic aromatic substitution and cyclization steps; added post-chlorination or fluorination during advanced intermediate formation

    Final product types

    • Triazine herbicide technical concentrate
    • Fungicide technical intermediates
    • Herbicidal formulation active components

    3. Specialty Dye and Pigment Intermediate Synthesis

    Leading dye and pigment manufacturers incorporate this aniline derivative to introduce bromine and multiple fluorine atoms into azo and anthraquinone scaffolds, achieving specialized absorption and color fastness profiles required in high-performance colorants. Its utilization allows for the design of pigments exhibiting resistance to light, heat, and aggressive chemical agents, which underpins premium pigment applications in automotive and electronics-grade plastics.

    Industry compliance standards

    • REACH (EC No. 1907/2006) registration compliance
    • EN ISO 9001 quality management for pigment production
    • OEKO-TEX® Standard 100 (relevant for textiles and coatings)
    • Color Index registration for dyestuff intermediates

    Typical usage ratio

    • 5–15% by weight in pigment synthesis steps; actual proportion adjusted to achieve targeted chromophore density and desired photostability

    Downstream process integration

    • Charged in initial diazotization or coupling reactions; incorporated during controlled halogenation of amine or phenol precursors

    Final product types

    • High-durability plastic colorants (e.g., for automotive parts)
    • Technical pigment pastes for electronic insulators
    • Specialty textile and inkjet dyes

    4. Advanced Polymer and Specialty Material Modifiers

    Producers of functionalized polymers use 2-Bromo-4,6-Difluoroaniline for the synthesis of monomers and oligomeric additives that enhance flame retardancy, electrical insulation, or chemical stability. It acts as an intermediate for arylated polyamides and fluorinated heterocyclic structural units, permitting fine control over new resin architectures demanded in advanced coatings and encapsulation systems. Our production control supports stringent contaminant management for sensitive downstream polymerization reactions.

    Industry compliance standards

    • ISO 14001 (environmental management for specialty polymers)
    • UL 94 (flammability standards for plastics and coatings)
    • RoHS Directive 2011/65/EU (for electronics and encapsulants)
    • REACH SVHC assessment (where applicable for advanced materials)

    Typical usage ratio

    • 0.2–2% by weight in polymer batch feed; proportion varies with final polymer design, integration method (block copolymer or graft copolymer approach), and target material performance

    Downstream process integration

    • Added during post-polymerization functionalization or as part of step-growth monomer feed for polyamide and specialty fluoropolymer backbone construction

    Final product types

    • High-grade electrical encapsulation compounds
    • Flame-retardant engineered plastics
    • Chemical-resistant industrial coatings
    Free Quote

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

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    Certification & Compliance
    More Introduction

    2-Bromo-4,6-Difluoroaniline: A Chemist’s Introduction

    Grounded Perspective on a Versatile Intermediate

    In the chemical industry, every intermediate plays a distinct role, shaping the outcome of synthesis with its reactive tendency and structural contribution. Through years of experience developing halogenated anilines, 2-Bromo-4,6-Difluoroaniline stands out for its utility across pharmaceutical, agrochemical, and materials research sectors. Its formula – C6H3BrF2N – hosts a core aniline scaffold, substituting hydrogen at the 2, 4, and 6 positions with bromine and fluorine. This unique substitution pattern gives the molecule behavior not easily replicated with its chloro- or mono-fluoro analogs.

    Details and Handling from a Plant Perspective

    In our plant, we oversee every stage, from halogenation to purification. Over time, our teams have refined the bromination and fluorination steps to limit impurities such as polybrominated byproducts and ensure the precise placement of halogens – not just for yield, but to keep downstream chemists’ work trouble-free. The result: crystalline, high-purity product, consistently delivered batch after batch. No intermediaries control this process; our technicians and engineers steer every variable.

    Specifications matter most to the folks using this compound in bench and pilot work. Our runs provide typical assay values above 99%, minimizing the need for additional purification cycles. Residual moisture is tracked with Karl Fischer and sits below 0.3%. Isomeric contaminants register below detection limits. Production aligns with green chemistry principles, recycling solvents and capturing trace halides.

    What Makes This Bromo-Difluoroaniline Different

    From long days spent scaling up anilines, we’ve seen the subtle shifts in reactivity a halogen brings. The ortho-bromo group, paired with two electron-withdrawing fluorines at 4 and 6, throws off the usual aniline behavior. Compared with its close cousin, 2-Bromo-4-Fluoroaniline, our compound shows a lower nucleophilicity at the amine – a detail synthetic chemists quickly notice. Suzuki and Buchwald reactions often show higher selectivity at the bromo site, reducing byproduct formation. These features don’t just make bench work smoother; they help teams cut down on analytical runs and surprise decompositions.

    In some cases, newcomers may ask why not stick to simpler anilines. The practicality comes into focus during multi-step routes in active pharmaceutical ingredient projects. With two fluorines, downstream arylations or amide couplings pick up predictable regioselectivity, which isn’t as reliable with mono-halogenated analogs. Chemists gain peace of mind knowing our aniline won’t drag in extra purification burdens hidden in the fine print.

    Real-World Usage in Synthesis

    Most of our daily output heads into consolidated storage, but shipments often serve research groups and production campaigns targeting kinase inhibitors, insecticides, or OLED precursors. Our compound acts as a flexible building block in these syntheses. Recipients report manageable reactivity for derivatization at the amine or bromo position. Fellow manufacturers working on fluorinated biphenyls or azaheterocycles come back with positive feedback on coupling consistency.

    We give practical attention to drying and packaging, moving each drum under nitrogen whenever possible to keep the product dry. Sensitive groups in the molecule don’t tolerate excess heat during storage, so our logistics team tracks temperature right up to handoff.

    Environmental Awareness and Worker Commitment

    Those of us working with halogenated aromatics know the stories about old-school practices—open vats and poorly controlled emissions. We’ve committed to closed reactors, real-time monitoring, and solvent recovery. Not only does this cap fugitive release; it bolsters confidence for our operators whose exposure risks drop sharply. The local water system benefits when we stick to internal neutralization protocols for acidic or brominated waste streams.

    At the dock, every drum ships with integrity labels and batch-specific documentation. This isn’t a bureaucratic hoop—we’ve handled enough calls from downstream users to know how much time gets wasted when an undefined impurity creeps into a project. Trust in the supply chain grows with every clean batch; for us, this isn’t abstract—it connects to each lab worker and technician placing their own trust in our processes.

    User Experience and Feedback Loop

    Customer labs often tell us what actually happens post-delivery. Synthetic teams jump first to routine purity checks using NMR and LC-MS. We want our 2-Bromo-4,6-Difluoroaniline to register as expected, whether an NMR comes from Boston or Bangalore. When a process stumbles—say, an unusual retention time pops up—we don’t take offense at being called in. Instead, we pull up the batch records and analytical data to check for batch-specific oddities. This feedback loop shortens the pathway to process improvement. For every complaint about particle size or filter clogging, we’ve iterated our crystallization or milling. Not all plants tune their output by listening to end users; we take pride in this collaborative mindset.

    Comparison to Other Halogenated Anilines

    On the surface, the catalog lists for anilines crowd together. To a chemist staring at a reaction scheme, the difference between 2-Bromo-4,6-Difluoroaniline and a mono-fluorinated cousin can feel minor—just another line item. In practice, those extra fluorines sharpen selectivity, reduce biological side products, and improve shelf stability. Subtle electronic effects from both fluorines draw electron density away from the aniline ring, slowing undesired oxidations and suppressing background side reactions. With the bromo anchor at C2, cross-coupling partners respond predictably. Researchers who tackle SAR studies for pharmaceutical targets appreciate these features.

    From the supply side, producing difluorinated anilines calls for additional controls and capital investment. Fluorination steps require more robust materials for wetted surfaces and stronger attention to worker safety. Our plant revisioned reactor seals and vapor containment decades ago to manage hydrofluoric acid risks, a commitment not every facility maintains. These improvements show up in the purity and reproducibility users report.

    Safe Transport and Storage Realities

    Packing and shipping halogenated compounds is never an afterthought. Product sitting on a loading dock too long draws moisture, risking caking or hydrolysis. Our crew double-checks seal integrity on drums and secondary liners. On rare occasions, customers in humid regions request additional desiccants—an accommodation we handle locally. Storage at user sites benefits from low ambient humidity and clean shelving, as with most dry aromatic amines.

    Feedback on caking or crystal bridging has prompted us to adjust sieving steps and add humidity monitors in the warehouse sections dedicated to 2-Bromo-4,6-Difluoroaniline shipments. Compared with fragile triphenylamines, this compound bears moderate stability, yet its performance hinges on simple precautions.

    Challenges and Problem-Solving

    Every product run, even with decades of experience, can throw curveballs. Impurity spikes, supply interruptions for specialized fluorinating agents, or batch-to-batch color shifts all challenge our controls. We respond by holding open weekly problem-solving sessions between QA, operations, and shipping—real meetings, not email threads. A blotchy color in a finished batch once sparked an overhaul of filtration mesh mesh, leading to improvements extending far beyond one lot.

    For customers seeking regulatory support, we offer complete traceability and rapid sample provision for unknown impurity investigation. Speed counts: pharmaceutical teams work on tight timelines, especially in scale-up or validation runs. Good upstream documentation, as built into our batch records, saves days hunting for the root cause.

    Process changes sparked by customer findings often drive broader reform. If an outside lab uncovers a new type of stability issue, we convene a process review, dissect the underlying causes, and shift our internal SOPs. Each incremental fix strengthens trust across the supply chain, benefiting every subsequent batch shipped.

    Continual Improvement and Accountability

    The bar for manufacturing intermediates rises every year. As regulatory authorities revise permissible impurity profiles or workplace exposure limits, we aren’t waiting around for citations. Instead of simply passing new documentation to customers, we funnel fresh training and capital investment into our plant. Most recently, replacing vented agitation with closed mixing cut both energy cost and operator exposure. These aren’t just investments in compliance; they add up to tighter control, higher reliability, and less waste.

    Open communication with downstream users is hard-earned. We invite feedback—praise, complaints, and technical questions—from anyone working with our 2-Bromo-4,6-Difluoroaniline. Our chemists can speak in-depth about batch history, production quirks, and improvements made, whether the request comes from a process engineer or a graduate student. This transparency helps prevent small hiccups from ballooning into lost hours at the customer site.

    Looking Ahead: Supporting Better Synthesis Outcomes

    2-Bromo-4,6-Difluoroaniline keeps its place on the synthetic chemist’s shelf not just on account of its unique substitution pattern but for the quiet reliability that comes from careful, human-led production. No shortcut replaces years of tuning process controls, listening to feedback, or learning from subtle color changes in the filtration bay.

    As research audiences shift toward new targets—more fluorinated heterocycles, high-performance polymers, or precision agricultural agents—we expect demand for exacting intermediates to stay strong. Our commitment sits with sustaining high standards, minimizing environmental footprint, and putting end-user needs at the core of our process improvement cycle.

    By focusing on quality, real transparency, and a hands-on approach to every kilo produced, we plan to serve research and production partners for decades more. We know that every gram of 2-Bromo-4,6-Difluoroaniline used in a project represents months of planning, care, and teamwork both on our end and the customer’s. Our promise remains simple: keep listening, keep learning, and deliver the best possible product, every batch, every time.