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4-Bromo-9H-Fluoren-9-One

    • Product Name 4-Bromo-9H-Fluoren-9-One
    • Einecs 226-883-2
    • 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

    670352

    Chemical Name 4-Bromo-9H-Fluoren-9-One
    Cas Number 3096-56-8
    Molecular Formula C13H7BrO
    Molecular Weight 259.10
    Appearance Yellow to orange powder
    Melting Point 212-215°C
    Purity Typically >97%
    Solubility Insoluble in water, soluble in organic solvents
    Density 1.64 g/cm³
    Storage Temperature Store at room temperature

    As an accredited 4-Bromo-9H-Fluoren-9-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 4-Bromo-9H-Fluoren-9-One

    Applications of 4-Bromo-9H-Fluoren-9-One in Industrial Manufacturing

    Our production of 4-Bromo-9H-Fluoren-9-One serves as a key intermediate for several downstream sectors, supporting specialized uses that demand precise compliance, engineering controls, and tailored integration. Details of principal real-world applications follow for informed B2B assessment and formulation planning.

    1. OLED Display Material Synthesis

    Electronics manufacturers incorporate 4-Bromo-9H-Fluoren-9-One as a coupling component to construct advanced organic semiconductors for OLED emissions layers. Its functionalized fluorenone core participates in Suzuki–Miyaura and Buchwald–Hartwig coupling reactions to generate fluorenone-based derivatives with high quantum efficiency, controlling electron mobility and spectral purity. Downstream formulators select this raw material to fine-tune layer thickness, charge transport, and stability for panel displays used in televisions, smartphones, and automotive instrumentation.

    Industry compliance standards

    • RoHS Directive (EU 2011/65/EU)
    • IEC 62321 for hazardous substance assessment
    • REACH Regulation (EC 1907/2006)
    • Japan J-Moss (JIS C 0950)

    Typical usage ratio

    • 5%–12% by mole in organic layer precursor batch; tuned for device emission wavelength and charge carrier balance; adjusted per host-dopant system

    Downstream process integration

    • Dissolved in polar aprotic solvent with boronic acid or aromatic amine; enters palladium-catalyzed C–C/C–N coupling step under inert atmosphere; output intermediate is purified and deposited via vacuum evaporation or spin-coating

    Final product types

    • OLED emitter materials
    • Organic semiconducting dyes
    • High-resolution display panels
    • Flexible display ribbons

    2. Pharmaceutical API Intermediate Manufacturing

    Pharmaceutical chemists utilize this compound as an essential building block in the synthesis of kinase inhibitors, neuroprotective agents, and antitumor APIs containing fluorenone scaffolds. It reacts via nucleophilic substitution and catalytic amination to construct active intermediates under cGMP conditions. Accurate handling and traceable source documentation ensure the end products meet strict regulatory submission demands for small molecule drugs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide
    • US FDA 21 CFR Parts 210/211
    • European Pharmacopoeia (monograph 5.10, 10th Edition)
    • Chinese Pharmacopoeia General Rule 0631

    Typical usage ratio

    • 10%–25% by mass in precursor stage; exact ratio set by target molecule structure and yield requirements; adjusted for impurity profile control

    Downstream process integration

    • Introduced to reactor during stepwise or one-pot transformations; supports halide exchange, Suzuki coupling, or reductive amination reactions; intermediate is isolated, purified via column chromatography, then used in final API assembly

    Final product types

    • Pre-clinical and clinical kinase inhibitors
    • Small-molecule oncology agents
    • Neurotherapeutic drug intermediates
    • Specialty bulk drug substances

    3. Specialty Dye and Pigment Synthesis

    Industrial dye manufacturers employ 4-Bromo-9H-Fluoren-9-One in the creation of high-performance pigments and specialty dyes for coatings, inks, and fiber treatments. The fluorenone backbone supports targeted halogenation, azo coupling, and alkylation to yield colorants with sharp absorption peaks, photo-stability, and solvent resistance. Refined blending procedures and analytical QC help guarantee batch-to-batch chromatic consistency for end-user branding specs.

    Industry compliance standards

    • EN 71-3:2019 (Toy safety migration for colored inks and pigments)
    • ISO 105-A02 (Textiles color fastness)
    • OEKO-TEX Standard 100 (Textile safety test)
    • US EPA TSCA for new chemical substances

    Typical usage ratio

    • 2%–8% by mass relative to total pigment substrate; varies with dye structure, intended color depth, and end-use UV exposure requirements

    Downstream process integration

    • Charged during pigment core building or as side group modulator during condensation; follows with purification, milling, and dispersion into application carrier matrix

    Final product types

    • Solvent-based industrial coatings
    • Textile dyes for synthetic fabrics
    • High-purity inkjet printing inks
    • UV-resistant plastics masterbatches

    4. Photochemical Sensor and Analytical Reagent Production

    Analytical device manufacturers include this intermediate in the synthesis of indicator compounds and photochemical sensors, leveraging the fluorenone’s planar ring and bromine moiety for selective molecular recognition and signal amplification. Applied in the construction of fluorometric reagents, chemists control reactivity to fine-tune detection limits, emission ranges, and matrix compatibility for downstream life sciences research and quality control tools.

    Industry compliance standards

    • ISO 13485:2016 for medical device reagent manufacturing
    • USP <1040> Analytical Reagent standards
    • REACH Annex XVII for laboratory chemicals
    • China GB/T 6682-2008 for analytical reagent purity

    Typical usage ratio

    • 1%–5% relative to final reagent bulk; ratio refined by targeted analyte sensitivity and emission absorption characteristics

    Downstream process integration

    • Incorporated as key moiety during molecular probe formation; follows with purification, formulating with solvents or matrices; packed into analytical kits or calibration standards

    Final product types

    • Fluorescent probe kits
    • Photochemical sensors for environmental or clinical labs
    • Reference standards for HPLC/GC-MS detection
    • Colorimetric indicator agents

    5. Advanced Polymer Material Modifier

    Polymer R&D and technical plastics producers deploy this material as a functional group donor during the synthesis of performance engineering resins, especially in rigid aromatic backbone construction for specialty thermoplastics. Covalent integration by nucleophilic aromatic substitution or direct copolymerization allows precise modification of glass transition temperature, mechanical strength, and UV durability for downstream applications in automotive, aerospace, and electrical insulation materials.

    Industry compliance standards

    • UL 94 (Flammability standard for plastics)
    • ASTM D638 (Tensile properties of plastics)
    • ISO 9001:2015 (Quality Management for material suppliers)
    • REACH Article 56 authorization for monomers/additives

    Typical usage ratio

    • 0.5%–3% by mass; dosage determined by polymer matrix molecular weight, target rigidity, and planned injection/extrusion process

    Downstream process integration

    • Added during melt blending or solution polymerization; reacts under elevated temperature with base monomer units; moves on to extrusion, molding, and post-treatment sequences

    Final product types

    • High-durability fluorene-modified polyesters
    • High-gloss electrical insulator sheets
    • Precision injection-molded components
    • Specialty aerospace films

    6. Agrochemical Active Ingredient Precursor

    Agrochemical developers employ this fine chemical as a precision intermediate in the multi-step creation of select herbicide and fungicide actives, benefiting from the electron-withdrawing bromide position to direct selective ring transformations. Process engineers monitor conversions for target activity, degradation pathway study, and stability performance to meet international crop protection regulations and safety reviews from both local and export markets.

    Industry compliance standards

    • FAO/WHO JMPR pesticide quality guidelines
    • China GB 2763-2022 National Food Safety Standard for Maximum Residue Limits
    • US EPA FIFRA Toxic Substances Control Act
    • EU Regulation (EC) No 396/2005 on pesticide residues

    Typical usage ratio

    • 3%–10% by mass in active ingredient synthesis; adapted for seasonal demand, crop species, and stepwise yield optimization

    Downstream process integration

    • Added at core structure-building step during active formulation; further reacts to finalize the mode-of-action motif; followed by purification, microencapsulation, and formulation into water-dispersible or EC concentrates

    Final product types

    • Selective post-emergence herbicides
    • Field-applied fungicides
    • Pesticide intermediates registered with local ministries
    • Seed treatment actives
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    Competitive 4-Bromo-9H-Fluoren-9-One prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    Discovering 4-Bromo-9H-Fluoren-9-One: A Unique Aromatic Building Block

    The World of Organic Synthesis welcomes 4-Bromo-9H-Fluoren-9-One

    Every once in a while, a new tool emerges in the chemistry landscape that makes life a little easier for researchers and manufacturers. 4-Bromo-9H-fluoren-9-one belongs to that class of fine chemicals that stands out for both versatility and reliability. With its stylish-looking fluorenone core and a bromine atom on the fourth position, this compound takes part in several cross-coupling reactions, helping organic chemists whip up complex molecules in less time. The CAS number for 4-Bromo-9H-fluoren-9-one proves handy for those who catalog reagents or maintain inventory in the lab.

    The Nitty-Gritty: Chemical Structure and Properties

    This fluorenone derivative usually comes as a light yellow crystalline solid with a distinct aromatic smell. The fluorenone scaffold itself is well-loved in synthetic labs because of its rigid structure. Tacking on a bromine atom at the 4-position ramps up its game, letting it take part in Suzuki, Sonogashira, or Heck reactions, and expand the range of derivatives one can create. From my time in university labs, I learned that small changes to aromatic compounds deliver huge swings in their reactivity. You put a bromine on fluorenone and suddenly you unlock a set of chemical pathways unthinkable with the parent compound. The melting point lands above room temperature, so it stores as a stable powder on the shelf, which reduces issues with evaporation or decomposition.

    Why Synthetics Pros Value 4-Bromo-9H-Fluoren-9-One

    The most obvious magic of 4-bromo-9H-fluoren-9-one comes from its dual personality. It brings together the sturdy fluorenone structure—long known for optical and electronic properties—and a reactive bromine handle, which means access to a spectrum of advanced molecules. Researchers building new OLED materials turn to this compound as a precursor, since the combination of rigidity and functionalizability makes for stable, high-performing organic layers. For those pursuing medicinal chemistry, the molecule acts as a core for the attachment of various pharmacophores, thanks to the ready reactivity of the brominated position.

    People who enter the world of organic light-emitting devices and pharmaceutical intermediates soon discover that raw materials quality matters. Not just purity in the abstract, but the ability to get reproducible results in scale-ups and parallel reactions. 4-Bromo-9H-fluoren-9-one, with its recognizable structure and manageable reactivity, helps bridge the gap between research and manufacturing.

    Applications: A Backbone for Innovation

    If you walk through any research lab that works on advanced materials, you almost always see bottles of aromatic ketones like fluorenone, often modified with halogens. The 4-bromo derivative marks a favorite, not by tradition, but by trial-and-error refinement through years of experience. I remember colleagues trusting this molecule during the frantic pace of thesis project deadlines, counting on it to take part in cross-coupling reactions without fuss or unwelcome byproducts.

    Several companies focus on OLED displays and organic semiconductors, and they tend to favor fluorenone-based intermediates for their stability and documented performance. Adding a bromine on the fluorenone brings about a world of coupling possibilities. It lets chemists install aryl groups, ditto alkynes or alkenes, all with decent yields. During process optimization, the presence of the bromine atom allows for cleaner separation of products, often reducing the need for tedious purification steps. That translates to less waste, lower costs, and more sustainable workflows—things production managers fret over in daily meetings.

    Getting the Details Right: Handling and Usage

    Having spent years ordering and working with fine chemicals, I know that predictability in storage and handling eases worries for lab managers and chemists alike. 4-Bromo-9H-fluoren-9-one doesn’t require intricate safety arrangements or exotic containers. Shielded from moisture and extreme temperatures, it remains robust over long storage periods. This feature makes it popular in both academic labs and larger pilot plants that value reliability as much as performance.

    For synthetic chemists, reaction planning means estimating compatibility—what solvents, catalysts, temperatures can you use? 4-Bromo-9H-fluoren-9-one fits the script. It tolerates the conditions of Suzuki coupling, or classical substitution reactions. Those in polymer labs or drug discovery units can trust its stability through a range of methods. Over the years, benefits such as minimal off-gassing and manageable dust levels in the dry powder format have won over lab safety officers who sign off on every purchase.

    Comparing Other Halogenated Fluorenones

    Chemicals with similar backbones often share properties, yet the unique blend of reactivity and physical stability sets 4-bromo-9H-fluoren-9-one apart. For example, the chloride analog sometimes shows less reactivity in coupling reactions, while the iodo version, though more reactive, tends to cost more and degrade faster under ambient conditions. The bromine strikes a useful middle ground, offering sufficient reactivity without becoming a headache for storage.

    There’s a reason behind this sweet spot. In coupling chemistry, the carbon-bromine bond breaks efficiently enough under palladium catalysis to keep reaction times reasonable, but not so rapidly that unwanted side reactions spoil the yield. In my personal experience tweaking small-scale syntheses, the brominated version let me finish projects with fewer purification headaches compared to its cousins. This makes it a favorite in settings where both speed and cleanliness matter—like rapid prototyping or commercial batch production.

    No Substitute for Purity and Documentation

    Confidence in the results starts with confidence in the starting materials. Suppliers vying for the attention of discerning chemists focus on providing solid analytical data for each lot: NMR, HPLC, sometimes even elemental analysis as a matter of routine. In production environments that must pass regulatory scrutiny, documentation matters as much as the stuff in the bottle. Traceability, batch consistency, and third-party verifications help users trust the supply chain. Over time, I’ve seen entire research programs grind to a halt when a questionable batch enters the pipeline. One learns to value certified purity backed by reliable spectroscopic data.

    Compared with some obscure building blocks, 4-bromo-9H-fluoren-9-one enjoys popularity thanks to wide documentation in both patent and academic literature. Process chemists often check for proven scale-up runs before committing resources. Knowing that others have pushed this molecule through round-bottom flasks, up to pilot reactors, builds confidence for newcomers and repeat buyers alike.

    Modular Synthesis and Green Chemistry Trends

    Organic synthesis trends change over time, but the emphasis on modular building blocks only grows stronger. 4-Bromo-9H-fluoren-9-one features centrally in this new approach, allowing modular assembly of target compounds through predictable bond-forming reactions. For young researchers, the hands-on predictability means fewer sleepless nights before project deadlines. Those trained in process engineering like the cleaner reaction profiles and ready separation of products. In addition, the desire to follow green chemistry principles nudges chemists toward reagents that offer less hazardous waste and greater atom economy. The moderate reactivity of the brominated fluorenone, plus its ability to avoid tough-to-remove side products, fits this bill.

    Groups working on hydrogen sources, alternative energy devices, or smart materials sometimes prefer building blocks they can trust to behave the same way every time, even when switching catalyst brands or changing reaction vessels. I’ve spent days optimizing syntheses with comparative halides; more than once, the bromo-fluorenone performed more consistently and profited from reliable yield curves. These real-world benefits seep into lab culture, and eventually guide procurement policies.

    Benefits in Device and Pharmaceutical Applications

    The reach of 4-bromo-9H-fluoren-9-one extends beyond classic synthesis. In the world of electronic materials, the fluorenone unit brings photostability and improved charge-transport properties. Those working on photovoltaic cells and organic LEDs select starting materials that impart these qualities, often starting with brominated fluorenones as building blocks. Teams engineering new display technologies count on this kind of versatility, especially as companies push for brighter and more energy-efficient screens.

    On the pharmaceutical front, the bromo handle serves as a launching pad for late-stage functionalization. Medicinal chemists chase new scaffolds fast, so being able to install custom side chains late in synthesis streamlines the search for active compounds. In my own experience, fluorenone-derived cores sometimes offer advantages in metabolic stability or binding profiles. Starting from a well-characterized brominated intermediate saves time and enables parallel synthesis, leading to a broader and more efficient hunt for new drug candidates.

    Challenges, Limitations, and the Path Forward

    No chemical building block works as a panacea. 4-Bromo-9H-fluoren-9-one performs best where its reactivity matches the downstream chemistry. For ultra-sensitive reactions, issues such as minor impurities or air sensitivity in certain processes crop up, though these rarely make a difference in standard applications. Some large-scale users report headaches sourcing high-purity grades in short timeframes, especially when global supply chains get knocked off balance. As labs focus on scale and green protocols, there’s demand for sustainable bromination and minimal process waste.

    Potential solutions include backing up procurement with multiple certified sources and expanding process development to reuse or recycle solvents and reactants. Encouraging dialogue between suppliers and users can also help flag batch-to-batch inconsistencies before they wreck a production run. As universities train a new generation of chemists, emphasis on best purchasing practices and collaborative troubleshooting helps keep processes moving.

    Building Trust in Chemistry’s Core Tools

    Building blocks like 4-bromo-9H-fluoren-9-one work best when both the science and the supply chain support innovation. During my years in the lab, I watched as product managers, eager grad students, and scale-up technicians all came together over the shared goal of reliable, efficient synthesis. Community knowledge, supplier transparency, and open literature collectively inspire confidence in tools like this. In day-to-day actions—double-checking documentation, sticking to validated protocols, cross-checking reactivity profiles—real progress happens on the benches and production lines.

    If there’s one lesson from working in both academic and industrial settings, it’s that the supporting details matter far more than marketing gloss. Having reliable access to compounds like 4-bromo-9H-fluoren-9-one directly shapes the pace and reliability of discovery. Trust builds slowly, maintained by solid service, well-characterized compounds, and responsive customer support from suppliers. Labs that run on trust—as much as technical know-how—achieve better results, fewer delays, and new breakthroughs over time.

    Human Experience and Continuous Improvement

    Chemistry rides on human ingenuity, not just glassware and formulas. Mornings spent troubleshooting a stubborn reaction, afternoons comparing yields between different providers, evenings reading up on the latest literature—these experiences bond teams and sharpen methods. Each bottle of 4-bromo-9H-fluoren-9-one, with its distinctive yellow glint, carries a piece of that ongoing effort. I’ve seen the difference between lackluster and high-quality product firsthand, not in abstract testing, but in smoother days at the bench and more predictable project timelines.

    Looking ahead, the best advances come from iterative improvement. Asking suppliers for updated COAs, sharing feedback when something goes wrong, and staying alert to new synthetic routes all fit into the professional toolkit. As more groups demand greener, safer, and more effective reagents, compounds like 4-bromo-9H-fluoren-9-one will adapt, driven not just by scientific curiosity but by the lived experience of thousands of chemists worldwide.

    Final Thoughts

    Mastering the art of synthesis means choosing the right ingredients. 4-Bromo-9H-fluoren-9-one stands out, not because it’s new or flashy, but because it solves problems that real chemists care about—from reliable batch outcomes to stress-free storage. Its position in both classic and emerging commercial synthesis tells a story of a compound that earned its popularity through repeated, documented success. In an era that demands both speed and sustainability, this unassuming building block will continue powering breakthroughs by aligning with what matters on the ground: quality, trust, and shared results.