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2-Bromo-4,6-Difluoroaniline Hydrobromide

    • Product Name 2-Bromo-4,6-Difluoroaniline Hydrobromide
    • Alias 2-Bromo-4,6-difluoro-1-aminobenzene hydrobromide
    • Einecs 813-379-8
    • 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

    434403

    Product Name 2-Bromo-4,6-Difluoroaniline Hydrobromide
    Cas Number 1425602-42-2
    Molecular Formula C6H3BrF2N·HBr
    Molecular Weight 287.92 g/mol
    Appearance Off-white to light yellow solid
    Solubility Soluble in water and organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protect from light and moisture
    Synonyms 2-Bromo-4,6-difluoroaniline hydrobromide salt
    Smiles Nc1c(F)cc(F)cc1Br.Br

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

    Packing & Storage
    Packing The 10g of 2-Bromo-4,6-Difluoroaniline Hydrobromide is packaged in a sealed amber glass bottle with a tamper-evident cap.
    Shipping 2-Bromo-4,6-Difluoroaniline Hydrobromide is shipped in tightly sealed containers, protected from light and moisture. It is handled as a hazardous chemical, requiring appropriate labeling and documentation. The packaging complies with international regulations, ensuring safe transportation via ground or air. Suitable personal protective equipment is recommended when handling upon receipt.
    Storage 2-Bromo-4,6-Difluoroaniline Hydrobromide should be stored in a tightly sealed container, protected from moisture and light. Keep it at room temperature in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure the storage area is clearly labeled and complies with relevant chemical safety protocols to prevent accidental exposure or contamination.
    Application of 2-Bromo-4,6-Difluoroaniline Hydrobromide

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

    As a direct manufacturer, we supply 2-Bromo-4,6-Difluoroaniline Hydrobromide primarily for high-value chemical synthesis routes in advanced intermediates production. Our product supports industrial customers operating in tightly regulated sectors where precision, batch consistency, and traceability are critical to commercial success. Below are its main downstream applications across select manufacturing industries.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical producers incorporate this material into multi-step synthesis of selective post-emergence herbicides and insecticides. Its electron-deficient aromatic ring structure, combined with halogenation, allows for targeted introduction during the key amidation or coupling stage. This step typically takes place after heterocycle formation and directly influences the biological activity profile of the end formulation, an essential requirement for crop protection compound development.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • REACH Registration (EC 1907/2006)
    • GB/T 36054-2018 (China National Standards for Pesticide Active Ingredient Purity)

    Typical usage ratio

    • Usually introduced at 0.2–2.5% w/w of total reaction mass, adjusted based on target yield and molecular conversion rates in batch or continuous synthesis lines.

    Downstream process integration

    • Charged during the penultimate step of active ingredient synthesis, as a nucleophilic aromatic substitution reactant prior to product crystallization and solvent extraction.

    Final product types

    • Commercial crop protection active ingredients
    • Technical grade herbicide concentrates
    • Seed coating treatments
    • Emulsifiable concentrate (EC) and wettable powder (WP) pesticide formulations

    2. Pharmaceutical Intermediate for Fluorinated APIs

    Innovator and generic API manufacturers use 2-Bromo-4,6-Difluoroaniline Hydrobromide as a building block in the synthesis of fluorinated aromatic drug intermediates. Its highly specific substitution pattern serves to anchor functional moieties for subsequent coupling, including core scaffolds for kinase inhibitors and CNS-target compounds, particularly in research and pilot plant settings where batch reproducibility and impurity profiling drive compliance.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) specifications for intermediates
    • cGMP FDA 21 CFR Part 210/211 (APIs and intermediates)
    • EDQM Certification of Suitability (CEP) for advanced intermediates

    Typical usage ratio

    • 0.1–0.9 equivalents relative to the nucleophilic partner, typically 1–5% of total synthetic batch weight; ratio varies according to desired purity thresholds and conversion rates.

    Downstream process integration

    • Fed as a key aromatic amine during the amidation or Suzuki coupling stage under anhydrous and controlled temperature conditions; integrated prior to chromatographic purification and intermediate isolation.

    Final product types

    • Pharmaceutical grade fluorinated intermediates
    • Intermediates for fluorinated APIs and specialty actives
    • Pilot scale oncology agents and CNS pharmaceutical actives

    3. Electronic Material Precursor (OLED and Display Chemistry)

    Electronics chemicals manufacturers utilize this compound when synthesizing custom aromatic fluorinated precursors for organic light-emitting diode (OLED) and thin-film transistor (TFT) display applications. These downstream processes demand high selectivity and batch purity, as trace side-products can significantly impact device efficiency and lifetime. Its role is critical at the halogenated aniline entry point, enabling targeted introduction of electron-transporting motifs.

    Industry compliance standards

    • SEMI C64 (Specification for Electronic Chemical Purity)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 9001:2015 (Quality Management for Electronic Chemicals)
    • JEITA Guidelines for Functional Organic Materials

    Typical usage ratio

    • Standard addition ranges from 0.5–3.0% by weight in precursor formulation mixtures; process engineers fine-tune the ratio to meet final carrier mobility and stability benchmarks.

    Downstream process integration

    • Added during the initial aryl amination or C–N coupling stage of OLED monomer or small-molecule synthesis; subsequent distillation and crystallization precede device layer deposition.

    Final product types

    • OLED emitter and electron-transport layer intermediates
    • TFT display precursor formulations
    • Photoresist and resist additive base chemicals

    4. Specialty Dye and Pigment Synthesis

    Specialty pigment producers engaged in high-performance dye intermediates formulation add this raw material when engineering advanced fluorinated azo and anthraquinone dyes for high-fastness textile or technical ink systems. It supports the creation of molecular structures that exhibit increased lightfastness and chemical resistance, which are key requirements within high-end fashion, automotive, and copying toner applications.

    Industry compliance standards

    • OEKO-TEX Eco Passport Certification (input chemicals in textile processing)
    • REACH Annex XVII (restrictions for dyes and pigments)
    • CEN EN 71-3 (Safety of toys: migration of certain elements, for pigments in graphic inks)
    • ISO 14001:2015 (Environmental Management for Dye Manufacture)

    Typical usage ratio

    • Dosage varies from 0.4–2.0% w/w relative to diazotization or coupling agents, and is process-optimized to achieve specified color shade intensity and solubility characteristics.

    Downstream process integration

    • Incorporated at the aromatic amine coupling stage—typically prior to final azo or quinone coupling—followed by filtration, drying, and quality control for colorimetric uniformity.

    Final product types

    • Lightfast azo dyes for technical textiles
    • High-purity pigments for automotive coatings
    • Specialty dyes for anti-fraud inks and security applications
    • Colorant components for laser printer toner
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    Certification & Compliance
    More Introduction

    2-Bromo-4,6-Difluoroaniline Hydrobromide: A Closer Look from the Manufacturer’s Bench

    Experience in Production

    Manufacturing 2-Bromo-4,6-Difluoroaniline Hydrobromide is not a beginners’ project. Spending years perfecting crystallization and purification for such aromatic amine salts taught our team a clear lesson: every synthesis step shapes downstream usability. At our plant, this means tight control over the halogen exchange and the bromination process, where timing, solvent ratios, and temperature shifts impact both final purity and reproducibility. Our chemists have learned to read the reaction as it unfolds—slight changes in hue, precipitate formation, or odor tell more than reaction equations. We know precision here determines how researchers and process developers will experience the product, whether in a test tube or in kilogram-scale reactors.

    Customers often ask why hydrobromide salt, and not just the free base. In many labs, the salt offers better stability, minimizes dusting, and allows direct handling without unpleasant odors or volatility. Preparing the hydrobromide on site at scale brings extra steps, but it pays off with a solid that travels well, dissolves easily in polar solvents, and meets storage requirements typical for pharmaceutical or agrochemical intermediates.

    Product Characteristics and Why They Matter

    The molecule 2-Bromo-4,6-Difluoroaniline Hydrobromide brings a distinct profile to the lab table. Each batch runs through rigorous HPLC and NMR checks. Our teams have seen how slight amounts of regioisomer or incomplete bromination throw off downstream reactions, so we maintain a sharp focus on analytical purity, not just crude isolation yields. The hydrobromide form provides a distinct melting point and consistent bulk density, which matters for automated batch dispensers and precision weighing in both kilo- and gram-scale settings. Our practical experience taught us to look beyond just numbers on a specification sheet—we examine visual appearance, note clumping or caking, and address water of hydration that can sneak in during storage or shipment.

    Our production background means we’ve run the same reactions ourselves: coupling steps where halogenated anilines get used for complex heterocycle formation or Suzuki cross-coupling. If the starting material contains unknown contaminants or polymorphic forms, the final product suffers. We have seen time saved by starting with a consistent, well-characterized salt. This gives process chemists confidence, especially under tight project timelines.

    Why Choose the Hydrobromide Form—A Manufacturer’s Perspective

    The debate often comes down to choosing hydrobromide versus hydrochloride or the free base. From countless production rounds and end-user collaborations, our support for the hydrobromide version comes from certain realities: in some couplings and substitutions, the hydrobromide proves less hygroscopic and easier to manage than the hydrochloride. This translates to better shelf life, less degradation over time, and fewer unexplained side products during scale-up. While the hydrochloride often holds its own in standard methods, our partners in medicinal chemistry and crop protection synthesis noticed fewer batch-to-batch variations with the hydrobromide—especially in humid lab conditions where salt caking becomes a real issue.

    It is not always obvious from literature search or a catalog how easy—or how tricky—it can be to work with anilinium salts. Our process chemists pointed out that dust suppression, oral toxicity limits, and regulatory pathways sometimes favor the hydrobromide forms. We design the production route to minimize residual bromide ion, control particle size, and ensure the salt is free-flowing for bulk operations.

    Applications: Everyday Realities in Industry and Research

    Research chemists and process engineers stop by or call to discuss hurdles in heterocyclic chemistry. Most use 2-Bromo-4,6-Difluoroaniline Hydrobromide as a coupling partner. In recent years, demand grew for electronic-grade intermediates, fluorinated benzene rings, and specialty agrochemical scaffolds. We’ve watched how even minor tweaks in amine salt supply ripple out through multi-step synthesis. For instance, some of our partners switched from the free base to the hydrobromide to avoid amine volatilization, which improved their worker safety and eliminated headaches during pilot-plant runs.

    The molecule’s dual fluorine groups and bromination allow direct participation in cross-coupling—saving time in medicinal chemistry discovery. The salt’s reactivity profile matches well with metal-catalyzed ligand exchange methods. Our experience shows that starting with a high-purity hydrobromide can trim two or more purification steps later. An R&D group working on novel herbicide scaffolds shared that they once faced week-long delays sourcing high-purity batches from generic suppliers overseas. After adopting our consistently manufactured salt, their cycle time dropped, and analytical headaches eased.

    Quality Control: Lessons Learned on the Shop Floor

    Early on, batches could vary: sometimes we saw faint off-white powders, other times yellowish granules. These color changes signaled differences in raw material lots or subtle process drift. Over time, we’ve implemented statistical process control. We check not just for chemical purity but for bulk properties that show up in daily use—how the salt flows, lumps, or packs. A lab worker told us a past batch from another source “turned gummy” on the shelf, contaminating their moisture-sensitive reactions. We know these issues all too well, as controlled drying and tight packaging are part of our protocol.

    No matter the client’s industry, traceability remains non-negotiable. Every drum and bottle links back to batch records, with full analytical data archived. We welcome audits, run additional stability tests, and advise customers on best storage practice to keep the salt effective for over a year under controlled conditions. More than once, we’ve caught subtle polymorph transitions emerging during transit—real-world challenges that only years of transparent manufacturing bring to light.

    Key Differences Versus Generic Alternatives

    Comparisons with other suppliers or alternative products come up in meetings. Our view is shaped by daily exposure to actual production runs. Not all 2-Bromo-4,6-Difluoroaniline Hydrobromides are alike. Some contain higher levels of starting aniline or manufacturing byproducts. Others display inconsistent color or texture, undermining lab confidence during QC of critical drug or pesticide candidates. What we see most: free base versions lose mass during storage, or absorb moisture unpredictably, throwing off stoichiometry and risking spoilage in hot climates.

    Another common distinction involves elemental bromine content and fluorine placement. The difference sounds minor, until you factor in downstream reactions sensitive to trace sodium, chloride, or sulfur contaminants. Hydrobromide salt avoids some of these pitfalls, offering a tighter analytical profile. Multiple clients have reported lower overall impurity counts, reducing scavenging or post-reaction purification steps. In practical terms, this reduces not just cost, but also resource drain in pressure-filter or chromatography columns downstream.

    There’s always a temptation––especially in tough markets––to chase lower-cost alternatives. We have worked with R&D managers and procurement teams who tried lower-grade or little-known sources, only to see product recalls after discovering off-grade batches or shipment damaged from inadequate packaging. We share these stories not as marketing but as reminders from the manufacturing trenches: invisible quality issues in early intermediates quickly turn visible, and expensive, in scaled-up process plants or in late-stage pilot projects.

    Supporting Innovation with Consistent Building Blocks

    Medicinal chemistry remains hungry for building blocks that can be trusted—in both small batch and scale-up. We keep direct lines open for custom requests, run method development work to fit unique purification or crystallization needs, and help partners solve supply chain snags. Recently, a startup group working on a new class of kinase inhibitors struggled with inconsistent downstream coupling rates. By troubleshooting their synthetic route and tweaking our grade of 2-Bromo-4,6-Difluoroaniline Hydrobromide, yields rose and processing times shrank. Such fixes happen at the manufacturing level, not at the distributor’s desk.

    Academic labs sometimes overlook just how much early-stage material variability can skew discovery runs. Our experience says: better to spend time on raw material control up front than lose months debugging obscure side reactions. By maintaining close feedback loops with end-users, we uncover subtle pain points in actual bench chemistry—informing our next production improvements.

    Environmental and Regulatory Considerations

    Manufacturing halogenated aromatics brings with it real EHS responsibilities. We have invested in closed-system handling and zero-discharge protocols for bromides and fluorides. Worker safety, regulatory compliance, and waste minimization count just as much as product yield. The growing regulatory attention around persistent organic pollutants, and specific requirements for residue limits in pharma and agrochemical sectors, motivated us to upgrade our quality controls and tracking. Agencies check for trace levels of brominated compounds all the way to the finished product, so we work with partners to deliver clear compliance documentation and analytical transparency for each lot.

    Improving Process Reliability for Customers

    Developing a robust supply of 2-Bromo-4,6-Difluoroaniline Hydrobromide took years of investment in people, reactors, and QA tracking. Our engineers emphasize the importance of quick, accurate supply, particularly for clients facing pressure to deliver in patent windows or harvest seasons. We run small pilot lots for clients needing a different particle size or a custom solvent residue specification. Our technical team fields real-world troubleshooting from clients: filter clogging, unexpected reactivity, or scaling challenges. By collaborating closely with users, we test and refine production in the context of actual application—not just a theoretical spec sheet.

    Our unmistakable lesson: reliability grows from active problem-solving and open data, not from lists of features. Hard-won process knowhow finds its way into every batch, every shipment. We know which upstream chemicals can sneak in process impurities, and how to correct for them before the batch leaves our site.

    Addressing Unforeseen Challenges

    Not all lessons come from smooth runs. Weather changes, raw material shortages, or even shipping delays force us to adapt, reevaluate cleaning or drying schedules, and seek out alternate procurement channels. During global supply chain disruptions, alternative sources from traders offered questionable quality—and feedback from multiple customers confirmed anomalous FTIR and HPLC readings. We learned quickly to communicate proactively, delivering reference spectra and impurity profiles so clients could cross-check themselves. This approach kept their projects on track, prevented wasted labor, and stopped costly reactor teardown at scale-up sites.

    The Value of Direct Manufacturing Relationships

    We built strong ties with our customers by treating each inquiry as a collaboration. Open channels for feedback help us adapt packaging, scale batches, and refine analyses to fit the latest industry demands. When a pharmaceutical partner needed regulatory data for their submission files or an agrochemical producer required rapid bulk shipment to match a short spraying window, our inside knowledge of the product’s entire lifecycle made the difference.

    Having a direct line from the manufacturer offers peace of mind. There are no hidden formulation changes, no surprise excipients, no mysterious delays from downstream supply chain bottlenecks. Every gram originates at our facility, tracked by skilled hands and modern software. We believe this level of attention and transparency contributes directly to the success of research and production teams far beyond our walls.

    Conclusion: Why Manufacturing Approach Matters

    Working every day with 2-Bromo-4,6-Difluoroaniline Hydrobromide shaped our philosophy: quality, consistency, and honest communication count more than surface-level specs. Our knowledge comes not only from literature and standards—though these are essential—but from hard-earned lessons on the line. Lab results, QC logs, and first-hand user stories drive every process tweak and packaging choice. Our focus remains making each shipment one that we’d use in our own research group.

    As the landscape for specialty aromatic amines grows more demanding, we stand ready to deliver reliability supported by practical knowhow, detailed controls, and a true partnership mindset. The foundation is simple: every batch, every lot, and every package reflects who we are as manufacturers—not traders, not brokers, but direct stewards of the science and quality behind each molecule leaving our plant.