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4-Bromo-3,5-Difluoroaniline

    • Product Name 4-Bromo-3,5-Difluoroaniline
    • Alias 4-Bromo-3,5-difluorobenzenamine
    • Einecs 801-502-6
    • 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

    329927

    Cas Number 86404-76-8
    Molecular Formula C6H4BrF2N
    Molecular Weight 208.01 g/mol
    Appearance Off-white to light brown solid
    Melting Point 56-58 °C
    Density 1.75 g/cm³ (estimated)
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Synonyms 4-Bromo-3,5-difluoroaniline; 1-Amino-4-bromo-3,5-difluorobenzene
    Smiles Nc1cc(Br)cc(F)c1F
    Inchi InChI=1S/C6H4BrF2N/c7-3-1-4(8)6(10)5(9)2-3/h1-2H,10H2
    Ec Number None assigned
    Storage Temperature Store at 2-8 °C

    As an accredited 4-Bromo-3,5-Difluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 4-Bromo-3,5-Difluoroaniline, labeled with product details, hazard symbols, and CAS number.
    Shipping 4-Bromo-3,5-Difluoroaniline is shipped in tightly sealed containers, protected from light and moisture. It should be handled in accordance with chemical safety regulations and labeled appropriately. Transport is restricted to qualified carriers, with documentation provided. Ensure compliance with local, national, and international shipping guidelines for hazardous materials.
    Storage 4-Bromo-3,5-difluoroaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect it from light and moisture. Store at room temperature and avoid exposure to heat or open flames. Ensure proper labeling and handle following standard laboratory safety procedures.
    Application of 4-Bromo-3,5-Difluoroaniline

    Applications of 4-Bromo-3,5-Difluoroaniline in Industrial Manufacturing

    As a direct manufacturer of 4-Bromo-3,5-Difluoroaniline, we supply this high-purity aromatic intermediate to established industrial sectors with proven commercial demand. Below, we detail key downstream segments where this compound is routinely incorporated, each governed by its own technical standards, formulation parameters, and quality control benchmarks.

    1. Advanced Agrochemical Synthesis

    Major agrochemical producers incorporate this aniline derivative when constructing difluorinated phenyl urea and phenoxy herbicide molecules using nucleophilic aromatic substitution and subsequent condensation protocols. This material appears mainly in the early synthesis stages of fluorinated intermediates, chosen for its halogen pattern which enables, after suitable substitution and protection group strategies, the tailoring of active ingredients to enhance soil stability and species selectivity. Its unique substitution supports high-performance pre-emergent and selective herbicides targeting grain and oilseed crops.

    Industry compliance standards

    • OECD Test Guidelines for Chemicals (Synthesis Section for Pesticide Active Ingredients)
    • FAO/WHO Specification for Pesticide Technical Materials
    • European REACH Annex VII–X (for agrochemical intermediates)
    • ISO 9001:2015 Quality Management in chemical synthesis

    Typical usage ratio

    • Initial formulation: 0.08–0.15 molar equivalent relative to total core aromatic; batch-specific correction based on target molecule yield and side-product profile

    Downstream process integration

    • Introduced in the halogen exchange or coupling step for precursor generation, followed by multi-stage condensation with isocyanates or etherification agents

    Final product types

    • Pre-emergent phenylurea herbicides (e.g., difluoronitroanilines derivatives)
    • Specialty post-emergence broadleaf weed control agents
    • Advanced selective herbicide active intermediates

    2. Pharmaceutical Intermediate Manufacturing

    Chemical process development teams in pharma rely on precision-controlled halogenated anilines during heterocycle assembly and as coupling partners for aromatic amine-based synthetics. In high-complexity synthesis, this material’s substitution offers a handle for late-stage cross-couplings pivotal in small molecule active pharmaceutical ingredient (API) synthesis, supporting targeted oncology and CNS pharmaceutical intermediates where selectivity and minimal side-chain rearrangement are essential.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU GMP Guideline Part II (APIs)
    • USP-NF and European Pharmacopoeia monographs (for intermediates and precursors)

    Typical usage ratio

    • 0.06–0.18 molar ratio, adjusted for optimal coupling conversion as monitored by HPLC and specific to targeted heterocycle synthesis path

    Downstream process integration

    • Fed into Buchwald-Hartwig amination or Suzuki-Miyaura cross-coupling steps; used for arylation to generate biphenyl or heteroaryl cores in regulated cGMP isolators

    Final product types

    • Intermediate fragments for kinase inhibitors
    • Precursors to CNS-active small molecules
    • Building blocks for fluorinated benzodiazepine-related APIs

    3. Specialty Dye and Pigment Precursor Formulation

    Colorant and pigment specialists draw upon this compound in the synthesis of high-value difluorinated azo and triphenylmethane dye precursors, where its electronic properties modify absorption spectra and fastness. Utilized particularly in pharmaceuticals and optoelectronics-related dyes, the material is essential in coupling reactions with diazo salts or amine-functionalized chromophores, influencing the resultant hue and processability, and improving pigment performance in inks, coatings, and microelectronic imaging.

    Industry compliance standards

    • ETAD Code of Practice (Specialty Organic Dyes & Pigments)
    • REACH Regulation (EC 1907/2006) – Registration and Downstream User Obligations
    • ISO 12040:2019 Pigments – General Test Methods

    Typical usage ratio

    • 0.05–0.12 molar proportion within the aromatic amine pool; final ratio follows desired absorption λmax and pigment crystallinity benchmarks

    Downstream process integration

    • Introduced during the diazotization step or as an electrophilic coupling partner for pigment precursor construction, controlled via stepwise addition under nitrogen

    Final product types

    • Microelectronic-grade yellow and red pigments for LCD and OLED devices
    • Specialty inkjet printing dyes
    • Organic photoconductor toner pigments

    4. Custom Fluorinated Material Synthesis for Electronics

    Manufacturers in the electronics material field employ this halogenated aniline as a building block during the design of fluorinated monomers and oligomers for use in high-durability insulating layers, dielectric coatings, and photolithography resists. Its unique functionalization directs the molecular geometry and dielectric response, and it is specifically incorporated via nucleophilic aromatic substitution or palladium-catalyzed amination to prepare resin additives and crosslinking agents for demanding microelectronics assembly.

    Industry compliance standards

    • IPC-4101: Specification for Base Materials for Rigid and Multilayer Printed Boards
    • RoHS Directive 2011/65/EU (safe content of regulated substances)
    • IEC 60454 (Electrical Insulating Materials)
    • ISO 9001:2015 (Specialty Materials Quality Systems)

    Typical usage ratio

    • 0.03–0.09 mass fraction in resin precursor mixtures; optimized per required dielectric constant and solubility limits during pilot validation

    Downstream process integration

    • Charged as a functional monomer for step-growth or chain-growth polymerization in fluoropolymer or specialty epoxy resin manufacture, depending on end-use performance criteria

    Final product types

    • Photoresist resin additives for semiconductor lithography
    • Precision dielectric coatings in IC packaging
    • Specialty films for flexible display substrates

    5. Fine Chemical Intermediate for Advanced Polymer Synthesis

    Downstream fine chemical plants leverage this aromatic intermediate during the development of specialty fluorinated polyimide and polyamide resins. These high-stability polymers offer performance advantages in the aerospace and high-temperature insulation industries due to increased thermal resistance and controlled hydrophobicity, with the aniline implementing electron-withdrawing properties at precise points along the macromolecular backbone. Production often employs a multi-step imidization or polymerization sequence, introduced after initial precursor activation.

    Industry compliance standards

    • ISO 9001:2015 (Polymer Synthesis)
    • ASTM D5207 (Thermal Analysis of Polyimides)
    • UL 94 Flammability Standard (Finished Insulating Materials)

    Typical usage ratio

    • 0.04–0.10 molar ratio relative to total dicarboxylic acid/diamine system, modulated to achieve target thermal and mechanical test outcomes

    Downstream process integration

    • Reacted directly with dianhydrides or diacids during imidization and condensation, in controlled batch reactors at 150–200°C under nitrogen purge

    Final product types

    • High-temperature-resistant polyimide films and sheets
    • Low-permeability polyamide membranes
    • Coating resins for aerospace wiring harnesses
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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-3,5-Difluoroaniline: More Than a Simple Building Block

    A Fresh Perspective on an Essential Intermediate

    Chemists and formulators often stay on the lookout for new molecules that can open fresh doors in research and manufacturing. 4-Bromo-3,5-Difluoroaniline is one of those compounds that quietly steers the development of new ideas in fields like pharmaceuticals, agrochemicals, and advanced materials. Recognizing the utility of this aromatic amine sheds light on innovation behind the scenes, often unseen by those who only see the end product. Bringing this compound into focus isn’t just about listing chemical features but understanding how it shapes progress, reduces unnecessary steps in synthesis, and helps researchers push boundaries.

    What Makes 4-Bromo-3,5-Difluoroaniline Unique

    This compound carries a bromo group on the fourth position of the benzene ring with two fluorine atoms at the third and fifth positions. The presence of bromine and fluorine in these positions is more than a technical detail. Bromine can regulate reactivity for specific coupling reactions, while fluorine atoms tweak the molecule’s electronic properties and increase metabolic stability in pharmaceutical applications. Choosing an aniline backbone creates a versatile entry point for downstream transformations, which extends to fields from crop protection to medicinal chemistry.

    Its chemical formula—C6H4BrF2N—and purity above 98% reflect more than just batch consistency. High-purity versions matter for those running sensitive catalytic reactions or exploring nuances in structure-activity relationships. A single impurity can distort results or trigger side reactions. As someone who’s worked hands-on with aromatic amines, I’ve seen frustrating setbacks from trace contaminants, especially in medicinal chemistry where false positives and negatives eat up precious time and resources.

    Practical Uses Shaped by Real-World Demands

    Anyone scanning a catalog for 4-Bromo-3,5-Difluoroaniline usually isn’t just filling a shelf. They’re plotting a path to a target molecule, starting with an intermediate that offers both reactivity and selectivity. In many pharmaceutical projects, the key isn’t taking the shortest synthetic route, but one that gives flexibility to adapt to unexpected hurdles. This compound offers such flexibility by providing two handles—bromine and amine—that can be independently manipulated. Cross-coupling reactions like Suzuki or Buchwald-Hartwig amination become more accessible, giving synthetic chemists extra options.

    Agrochemical development also leans heavily on intermediates like this, where small tweaks in the core structure can mean the difference between a breakthrough and an ecological headache. Having visited labs where every molecular tweak is debated for weeks, I’ve seen how compounds like 4-Bromo-3,5-Difluoroaniline let chemists fine-tune properties like soil persistence and crop compatibility.

    Industries focused on dyes, pigments, and electronics sometimes benefit from the mix of electron-rich and electron-poor spots on the ring, adjusting the behavior of the molecule in ways a mono-substituted aniline can’t match. From OLED precursors to specialty polymers, the value lies in this combination of reactivity, stability, and tunability.

    How It Stands Apart from Similar Intermediates

    Aromatics with similar names can sometimes blur together in the mind, especially as the catalog of halogenated and fluorinated anilines keeps on growing. Yet, this compound sets itself apart because of the interplay between bromine and fluorine. Bromine sits at a position that stays open to targeted modification by palladium-catalyzed coupling, which can be hard to achieve with chlorine or iodine due to their own quirks. Fluorine atoms, present at the 3 and 5 positions, resist metabolic breakdown more than hydrogen or methyl groups, making this compound a go-to choice for medicinal projects where biological stability matters.

    I remember working with other difluoroanilines, always running into headaches from low regioselectivity or poor handling characteristics. 3,5-difluoro derivatives frequently suffer from lower solubility, but attaching bromine at the 4-position strikes a balance between activity and formulation ease. This makes scale-up in chemical plants more predictable and improvements translate directly into reduced production waste.

    Why Purity and Physical Consistency Matter

    A lot of chemists first learn about the headaches of impurities during long reaction sequences. With a melting point generally falling in the 60–64°C range, people familiar with the solid’s handling properties appreciate its predictable crystallization and controlled drying. Subtle shifts in color or clumping can signal trouble, leading to time lost in recrystallization or reanalysis. Once, I spent days hunting down a false positive in a downstream assay that all traced back to a small amount of an over-brominated impurity.

    Aromatic amines are infamous for their potential toxicity, so safety standards for 4-Bromo-3,5-Difluoroaniline need to meet more than regulatory minimums. Analytical data—NMR, HPLC, MS—should not just fill a manual, but provide clarity that lets chemists proceed with confidence. Choosing sources known for reliable testing isn’t just smart, it’s necessary, especially when work feeds directly into safety-critical products.

    Meeting Industry Expectations in 2024 and Beyond

    As global regulatory frameworks tighten their rules for chemicals entering the marketplace, the role of trusted intermediates only grows. Synthetic steps must be robust for both lab-scale optimization and pilot-plant scale-up. Inconsistent raw materials spell trouble for batch-to-batch reproducibility. Formulators targeting pharmaceutical APIs see a direct path: high-quality intermediates like 4-Bromo-3,5-Difluoroaniline mean fewer headaches and reduced risk.

    Sustainability enters every conversation right now. Reducing waste and improving yields aren’t just about cutting costs—they’re signals that chemists and engineers care about their bigger impact. Sourcing from suppliers using greener methods of halogenation or fluorination sends the right message up and down the supply chain. In my own experience, the difference between solvent-heavy bromination and a clean, solvent-free method speaks volumes, both to auditors and the next generation of lab workers.

    Real-World Challenges: Sourcing and Supply Chains

    The last few years turned supply chains upside down. Lead times for specialty chemicals stretched longer, sometimes pushing important R&D beyond practical timelines. For labs bound by grant cycles or customer deadlines, waiting months for a single intermediate stops progress cold. 4-Bromo-3,5-Difluoroaniline may not grab headlines, but getting a reliable source with transparent documentation and stock guarantees can make or break a project.

    A few years ago, an R&D project we started on tight margins relied on getting pure aromatic intermediates in two weeks flat. A delay of even a few days caused the loss of a key partner. Since then, regular audits of suppliers and working with distributors who provide up-to-the-minute inventory data have proven essential. It pays to build real relationships with vendors, not just treat them as background players.

    Navigating Cost and Value

    Halogenated and fluorinated aromatics rarely come cheap. Global prices swing with energy costs, raw material shortages, and environmental regulations affecting mining and refining of key elements. I’ve watched teams sink more cash than planned chasing down the cheapest intermediates, only to run into inconsistent batches that create more waste than they save. We found paying a little more for a reliable source actually reduced total cost, saved sanity, and kept projects moving.

    Buyers working on price alone should pause and consider more than a few decimals on a spreadsheet. Issues like shelf life, packaging quality, and response times from technical support don’t show up on an invoice, but play a huge role over months and years of operation. Good value comes from trust as much as transaction.

    Supporting Research and Development

    Just as medicinal chemistry keeps evolving to tackle diseases faster and more precisely, the starting materials for those syntheses must keep pace. 4-Bromo-3,5-Difluoroaniline offers a way to create new aryl-based frameworks, opening new ground for SAR (structure-activity relationship) studies. I’ve seen teams racing to design new kinase inhibitors, and the ability to shift one atom at a time can mean the difference between a molecule that works and one that doesn’t.

    In agricultural research, a small change to the molecule can influence how a compound degrades in soil or resists pests. Unlike more conventional anilines, the difluoro pattern here slows down microbial degradation, sometimes making the difference in selectivity and persistence. I’ve sat in project meetings where environmental compliance depended on controlling breakdown rates; the right choice of intermediate changes outcomes both in the lab and the field.

    Material science also leans hard on such intermediates, whether it’s to alter charge transport in new polymers or improve stability of electronic components. Because bromine and fluorine influence both the physical and chemical durability, targeted substitutions driven by this intermediate can transform device lifetime or performance.

    Addressing Potential Drawbacks

    No chemical intermediate is perfect. 4-Bromo-3,5-Difluoroaniline presents challenges including toxicity, handling risks, and waste streams during both production and disposal. Personal experience reminds me that aromatic amines demand respect in the lab. Proper engineering controls and PPE aren’t optional. In our lab, strict handling protocols protected both workers’ health and the integrity of sensitive assays that could otherwise get thrown off by trace contamination.

    Environmental considerations count more than ever. Waste minimization through improved reaction selectivity, recovery of spent solvents, and responsible sourcing of bromine and fluorine shouldn’t just be buzzwords passed around at conferences. In-house, we’ve piloted solvent recycling and greener bromination protocols with measurable improvements—not only in waste reduction but in staff morale. Everyone likes to know the work is heading in a positive direction.

    Opportunities for Progress

    Companies and research groups targeting process intensification can look to better catalysts for downstream transformations of 4-Bromo-3,5-Difluoroaniline. Palladium-catalyzed couplings, which are still current workhorses, benefit from new generation ligands and greener solvents. In our experience, swapping chlorinated solvents for less hazardous counterparts brought both measurable improvements and regulatory wins, without sacrificing yield or clean work-ups.

    Technology transfer for scale-up brings its own set of headaches. Laboratory procedures don’t always map neatly onto pilot plant operations. Having a robust intermediate with predictable properties, like crystalline 4-Bromo-3,5-Difluoroaniline, helps buffer against scale-related setbacks. Planning up-front for factors like heat control, batch size, and solvent throughput makes for fewer production surprises. Years working across both academic and industrial settings taught me the value of “boring” consistency—nobody wants a new problem in the middle of a scale-up.

    The Future Looks Adaptable

    Everyone involved in R&D, whether in a university, startup, or global manufacturer, wants a clear path from bench to product. Simple, robust intermediates play a bigger role in mapping out that path than most realize. The niche occupied by 4-Bromo-3,5-Difluoroaniline isn’t about buzz, but about quietly enabling the hard work of innovation, safety, and resilience in supply chains.

    I’ve learned over time that it’s these “unsung” intermediates that enable big advances, whether it’s a drug that succeeds in clinical trials, an agrochemical that improves yield with less environmental impact, or a material that shapes the next wave of electronics. Giving credit to the hidden building blocks, and recognizing where small choices ripple into big gains, keeps science moving in the right direction. 4-Bromo-3,5-Difluoroaniline doesn’t promise headlines, but it does offer opportunities to build the next thing worth reading about.