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2-Bromo-4,5-Difluoroaniline

    • Product Name 2-Bromo-4,5-Difluoroaniline
    • Alias 2-Bromo-4,5-difluorobenzenamine
    • Einecs 831-468-5
    • 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
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    Specifications

    HS Code

    878094

    Compound Name 2-Bromo-4,5-Difluoroaniline
    Molecular Formula C6H4BrF2N
    Molecular Weight 208.00 g/mol
    Cas Number 1015078-62-4
    Appearance light brown solid
    Melting Point 54-58°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g., DMSO, chloroform)
    Smiles C1=CC(=C(C(=C1F)Br)N)F
    Inchi InChI=1S/C6H4BrF2N/c7-3-2-1-4(8)5(9)6(3)10/h1-2H,10H2
    Storage Conditions Store at room temperature, in tightly closed container
    Hazard Statements May cause skin and eye irritation

    As an accredited 2-Bromo-4,5-Difluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 2-Bromo-4,5-Difluoroaniline

    Applications of 2-Bromo-4,5-Difluoroaniline in Industrial Manufacturing

    As a direct manufacturer with deep expertise in halogenated aromatic compounds, we support global enterprises by supplying 2-Bromo-4,5-Difluoroaniline to leaders in high-tech sectors. Our continuous quality monitoring and traceable production processes meet the rigorous demands of these applications, ensuring dependable integration into advanced downstream chemistries. Below, we detail the primary real-world industrial scenarios utilizing this raw material, with relevant technical, regulatory, and operational context for decision-makers and production teams.

    1. Active Pharmaceutical Ingredient Intermediate Synthesis

    Pharmaceutical industry innovators use 2-Bromo-4,5-Difluoroaniline as a key aromatic amine building block in the synthesis of advanced API intermediates, especially where selective fluorination and bromination are required in heteroaromatic rings. These intermediates participate in cross-coupling reactions and stepwise functional group modifications during multi-stage syntheses. Our GMP-grade material supports regulated manufacturing, where traceability and impurity control directly affect patient safety and compliance.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monographs for residual solvent and impurity control
    • FDA 21 CFR Part 211
    • ISO 9001:2015 Quality Management

    Typical usage ratio

    • 0.5-1.8 molar equivalents per target API intermediate batch, adjusted based on reaction stoichiometry and the downstream transformation yield.

    Downstream process integration

    • Introduced during early-stage amination, coupling, or heterocycle formation
    • Processed via Buchwald–Hartwig or Suzuki–Miyaura cross-couplings
    • Monitored for residual halogen impurity post-condensation; purification steps follow GMP requirements

    Final product types

    • Pharmaceutical intermediates for anti-cancer, anti-inflammatory, and anti-infective APIs
    • Advanced fluorinated aromatic scaffolds for medicinal chemistry programs

    2. Agrochemical Active Ingredient Intermediate

    Leading crop protection companies integrate this raw material in the synthesis of fluorinated aniline derivatives, which serve as intermediates for fungicide and herbicide actives with improved metabolic stability and selectivity. Its high purity and controlled halogen content minimize unwanted side-products in scale-up processes, facilitating reliable compliance with agrochemical registration requirements.

    Industry compliance standards

    • FAO/WHO specifications for technical active substances
    • OECD Guidelines for the Testing of Chemicals
    • ISO 17025 laboratory analytical testing validation for agrochemical raw materials

    Typical usage ratio

    • 0.7-2.0 equivalents per batch depending on the coupling partner and ring substitution pattern, determined by target product's route of synthesis.

    Downstream process integration

    • Feeds into nucleophilic aromatic substitution and amide bond-forming reactions
    • Serves in the elaboration of urea or triazine herbicide scaffolds
    • Processed in closed reactors with automated solvent recovery for environmental compliance

    Final product types

    • Fluorinated fungicide intermediates
    • Grass-selective herbicide intermediates with enhanced bioavailability
    • Lead compounds for further crop protection discovery

    3. Specialty Dye Intermediate Manufacturing

    Producers of specialty dyes and pigments employ this material to introduce both bromine and fluorine functionalities into aromatic systems, affording enhanced photostability, unique chromatic shifts, and improved solubility profiles in advanced colorant formulations. Consistent batch quality is critical, as the electronic effects imparted by the substituents impact the final dye’s absorption spectrum and processability.

    Industry compliance standards

    • REACH registration for industrial dye intermediates
    • EN 71-3:2019 Safety of Toys – migration of certain elements (for pigments in toy applications)
    • ISO 9001:2015 quality assurance

    Typical usage ratio

    • 1.0-1.4 equivalents within the aromatic substitution stage, contingent on desired chromophore structure and yield targets.

    Downstream process integration

    • Introduced during coupling or condensation steps to produce mono- or bis-azo dye intermediates
    • Utilized in direct halogenation and amination cascades
    • Feeds into sulfonation or acylation as required by target dye class

    Final product types

    • Azo dyes for high-performance textile coloring
    • Special fluorinated pigments for automotive and industrial coatings
    • Reactive dye intermediates for fiber modification

    4. Electronic Material Precursor for OLED and Display Industry

    Manufacturers in the electronics sector value this molecule as a high-purity precursor for constructing advanced organic materials used in OLED displays, semiconductor films, and specialty sensors. The presence of both bromine and fluorine enables precise fine-tuning of electronic and optical behaviors in the final polymers or small-molecule device layers, supporting product innovation in display panel production and circuit integration.

    Industry compliance standards

    • IPC-4101B standards for base materials for printed boards
    • RoHS Directive 2011/65/EU for restricted substances
    • IEC 61249-2-21 for halogen-free electronic materials
    • ISO 14001:2015 environmental management for electronic material manufacturing

    Typical usage ratio

    • 0.6-1.2 equivalents per polymer batch or per step in small-molecule precursor synthesis, tailored by molecular design demands.

    Downstream process integration

    • Undergoes coupling, polymerization, or cross-linking as a monomeric precursor
    • Feeds into vacuum deposition or wet-coating operations
    • Handled in nitrogen-blanketed systems for moisture/oxygen sensitivity

    Final product types

    • Emitter layer materials for OLEDs
    • Thin-film transistor intermediates
    • Fluorinated polymers for advanced circuit and sensor applications

    5. Fluorinated Building Block for Advanced Chemical Research

    Research laboratories and fine chemical producers utilize this compound for exploring new functionalized aromatic systems with customized halogen patterns. It enables the generation of reference materials, labeled standards, and advanced ligands for catalysis, serving as a cornerstone in chemical innovation and process development for end-users in both academia and industrial R&D.

    Industry compliance standards

    • ISO/IEC 17025:2017 accreditation for reference material producers
    • EU Chemicals Strategy for Sustainability for research substance handling
    • Hazardous Chemicals Registration (China MEE Order 12, Annex 2)

    Typical usage ratio

    • 1.0 equivalent precisely measured per reaction; small-scale use for structure–activity relationship exploration, scalable up to pilot plant research batches.

    Downstream process integration

    • Enters as a starting aromatic amine for nucleophilic aromatic substitution or borylation
    • Used in small-batch, reactor- or round-bottom flask-based synthesis
    • Applied in isotopic labeling and fluorine scan studies

    Final product types

    • Reference standards for analytical chemistry
    • New catalyst ligand libraries
    • Specialty fluorinated fragments for medicinal chemistry
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    Certification & Compliance
    More Introduction

    2-Bromo-4,5-Difluoroaniline: More Than Just a Building Block

    Chemistry often feels like putting together a puzzle, slotting the right molecule in the right place, shaping new compounds for medicine, agriculture, or advanced materials. Among these pieces, some seem simple. 2-Bromo-4,5-Difluoroaniline, a mouthful for non-chemists, sits on the shelf in glass bottles, waiting for its next purpose. It’s a small, crystalline powder, almost always white to light tan, with a structure so precise that synthetic chemists value it as a tool. Its chemical formula, C6H3BrF2N, carves out a niche in the world of custom synthesis—where precision and reliability become priorities. The satisfaction of holding a product whose fine structure pushes research forward is real, especially in an industry where margins for error get razor thin.

    What Sets 2-Bromo-4,5-Difluoroaniline Apart

    Many labs have their go-to reagents, but 2-Bromo-4,5-Difluoroaniline draws attention because of its balanced reactivity and the stable introduction of both bromine and fluorine atoms. Those two halogens, positioned on the aromatic ring along with the amine group, give the compound unique chemical leverage. Halogens can transform a molecule’s properties. The bromine atom makes it handy in cross-coupling reactions like Suzuki, Heck, or Buchwald-Hartwig; these are bread-and-butter reactions that let scientists string together complex molecules, building up from simple blocks. Meanwhile, the fluorine atoms nudge electronic properties in just the right ways for pharmaceutical or agricultural research where even a subtle tweak in polarity or metabolic stability can make the difference between a hit and a dud.

    In my early days as a junior chemist, choice of building block felt like a gamble. Cheap, generic reagents often promised speed but delivered frustration: low purity, unreliable yields, or contamination that set projects back days. Working with well-characterized specialty intermediates such as 2-Bromo-4,5-Difluoroaniline changed that for me. Its solid-state stability and straightforward handling in both batch and flow chemistry made it a welcome fixture in our fridge. Reliable characterization (using NMR, MS, and HPLC) lets everyone focus on the real work: making something new.

    Model, Purity, and Handling

    Most 2-Bromo-4,5-Difluoroaniline available comes in purities upwards of 97%, a threshold important for those striving to minimize side reactions. Solid at room temperature, the compound stores well under dry conditions, sparing chemists from the constant vigilance many sensitive reagents demand. Some products arrive as technical grades, others as high-purity chemistry intermediates suited for drug discovery or specialty polymers.

    Chemists generally find it simple to weigh and dissolve. There’s little odor, little tendency to cling to gloves or glassware, far from the sticky messes left by more volatile or oily reagents. Reproducibility in both small-scale synthesis and high-throughput parallel reactions stands out as a core reason why the compound appears in protocols worldwide. There’s reassurance knowing the same reaction will behave in Zurich, Singapore, or Boston, regardless of who’s at the bench.

    Applications That Matter

    Down in the weeds of synthesis, 2-Bromo-4,5-Difluoroaniline serves as a springboard for a surprising range of projects. Medicinal chemists love the amine group, using it to build customized anilide prodrugs, kinase inhibitors, or anti-infectives. The bromine atom slots perfectly into cross-coupling workflows—enabling modification of small molecules targeting neurotransmitter pathways or cancer targets. Fluorination isn’t just an academic exercise. Whole industries rely on the introduction of fluorine to boost the stability, bioavailability, and metabolic resistance of their lead compounds. This one intermediate weaves seamlessly into the chemical tapestry that leads to new drugs, herbicides, or even next-gen imaging agents.

    Bench chemists in materials science chase after modified polyanilines and organic semiconductors, where subtle electronic tweaks unlock performance leaps. Here, 2-Bromo-4,5-Difluoroaniline lands in the mix, its atoms contributing to the fine-tuning of conductivity or optical properties. During one project, our team tried tweaking polymer backbones with different halogenated anilines to balance conductivity and stability. Few tweaks made as big a difference as a well-placed difluoroaniline subunit.

    What’s Different Compared to Other Anilines and Halogenated Building Blocks?

    Anyone who’s sifted through endless catalogs will spot dozens of anilines and building blocks, featuring various halogens in every possible position. Not every one works as promised—some prove difficult to handle or deliver spurious side products because of unwanted reactivity. 2-Bromo-4,5-Difluoroaniline draws on a balance of options. Its ortho-positioned bromine offers cross-coupling potential while the adjacent difluoro pattern fortifies the ring, influencing reactivity toward both nucleophilic and electrophilic partners. That matters when trying to keep side-reactions at bay or introduce new groups precisely.

    Some traditional brominated anilines lack fluorine’s stabilizing effect, making them too reactive for fine-tuned pharmaceutical work. On the flip side, highly fluorinated anilines often become inert, refusing to participate in the transformations chemists crave. This intermediate finds that middle ground. Over the years, companies who specialize in fluorinated reagents have expanded options, with 2-bromo-4,5-difluoroaniline becoming a favorite for scaffold decoration—especially in structure-activity relationship studies for new molecules targeting GPCRs, kinases, or enzymes tied to metabolism.

    Reliability as a Metric

    Too many promising research directions grind to a halt from unreliable supplies. Sourcing from reputable manufacturers, ideally with certificates of analysis confirming identity and purity, is key. The compound’s performance—gauged in yield, purity, and ease of purification—means more than any marketing phrase. For one graduate thesis, I relied on a series of coupling reactions using this product as the core intermediate. Out of a dozen candidates, few matched both the chemical reactivity and the ease of downstream purification. The lesson was plain: if consistency and clarity matter to your workflow, intermediates like this one should become cornerstones, not afterthoughts.

    Shipping and storage rarely cause headaches. As a crystalline solid, it tends to withstand the indignities of travel—bouncing around in glass bottles across continents. If exposure to air occurs during weighing or transfer, few issues arise so long as long-term moisture isn’t a factor. Industrial users may scale up to kilogram batches without much change in risk profile, making the transition from benchtop experiments to pilot production relatively straightforward.

    Opportunities and Challenges in Sourcing

    Reliable sourcing sometimes determines the fate of a research program. For specialty chemicals like 2-Bromo-4,5-Difluoroaniline, the range of suppliers spans boutique firms offering micro-batches to larger players with multi-ton capacity. Traceability and transparency stand out. Certificates of analysis, batch records and shipment history matter just as much as price. Regulatory requirements now add an extra layer of diligence, especially for projects aiming for clinical or commercial production.

    While the compound itself rules out many risks associated with unstable or reactive intermediates, responsible handling shouldn’t slip. Labs with robust inventory controls and careful environmental safeguards minimize environmental impact and personal exposure. Disposal procedures, especially in higher education or agile startup labs, need attention. My own lab implemented a two-step neutralization protocol to handle halogenated byproducts—making sure that any expired stock never entered regular waste streams.

    The Future of Advanced Intermediates

    Every year brings new targets for pharmaceutical, agrochemical, or material applications. As these fields push for precision and speed, demand for reliable, multifunctional building blocks rises. 2-Bromo-4,5-Difluoroaniline fits this need, thanks to its chemical features and practical handling profile. Its moderate price, widespread supplier base, and minimal regulatory encumbrance ensure it stays in play as research pivots toward new disease targets or smarter materials.

    A common frustration mentioned at conferences or in Ph.D. defenses involves uncertainty over intermediate supply and quality. The lesson: choose reliable partners and validated products, with transparent synthesis routes and origin. More and more, companies respond by offering detailed online data for each batch—full spectral characterization, impurity profiles, or even the green credentials of their synthetic pathways. Labs gain peace of mind knowing the intermediate won’t undermine weeks of planning or hours of sensitive reactions.

    Dealing with halogenated intermediates brings some environmental challenges. Chemists now pivot toward greener processes—minimizing waste, optimizing atom economy, recycling halogen sources where possible. Suppliers who pre-empt these concerns with sustainable manufacturing gain ground. 2-Bromo-4,5-Difluoroaniline, owing to its efficiency in high-yield reactions and ease of purification, already beats older, less predictable analogs in minimizing waste and improving safety.

    Responsibility and the Human Element

    Every chemist who spent time at the bench knows that little choices echo down the line. Selecting a solid, well-characterized intermediate doesn’t just protect a project—it lightens the hidden load for everyone, from research associates to waste handlers, regulatory teams, and even the communities near manufacturing plants. As more research pivots toward complex molecules—whether for blockbuster drugs or advanced OLEDs—the need for intermediates that don’t complicate the process grows stronger.

    My own labs moved slowly at first, testing a series of intermediates, often wrestling with hard-to-remove side products or batches that looked fine but fell short in reactions. With 2-Bromo-4,5-Difluoroaniline, the sense of relief after running a clean coupling or producing a solid yield shapes real trust. There’s satisfaction in knowing you can spend more energy on designing molecules rather than troubleshooting supplier issues.

    There’s no single “best” intermediate for every project, but some, like this one, make themselves indispensable. Years of careful study, real-world results, and trusted protocols tell the story better than any glossy catalog. That knowledge—built in small increments, over years or even decades—gives chemists and business leaders alike the confidence to innovate, move fast, and aim higher.

    Supporting Innovation Through Choice

    With global supply chains and online tools, the once-exotic becomes routine. Yet, with this abundance comes responsibility: verifying provenance, weighing performance, and choosing partners who share your values—not just your price points. The days of grabbing whatever’s cheapest or quickest are fading. Today’s research environment rewards those who balance cost, safety, performance, and traceability.

    Looking back, it’s clear that our greatest advances in synthesis—whether in big pharma, tiny start-ups, or academic labs—flow from chemists making informed, thoughtful decisions. Choosing reliable, versatile intermediates like 2-Bromo-4,5-Difluoroaniline has allowed research teams to stay focused on discovering new therapies or materials, confident in the foundational chemistry.

    Many new students learn this compound’s name not from textbooks, but by running reactions in the lab—seeing clear results and linking structural intuition to tangible outcomes. This hands-on connection matters. The science isn’t abstract; it’s felt through clear NMR signals, high yields, and the confidence to tackle harder targets tomorrow. As global science races forward, small pieces like 2-Bromo-4,5-Difluoroaniline give researchers the certainty they need to keep experimenting, learning, and innovating.