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2-Bromo-9,9-Dimethyloxanthracene

    • Product Name 2-Bromo-9,9-Dimethyloxanthracene
    • Alias 2-Bromo-9,9-dimethyl-9H-xanthen
    • Einecs EINECS 695-841-8
    • 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

    543958

    Chemical Name 2-Bromo-9,9-Dimethyloxanthracene
    Cas Number 114772-55-7
    Molecular Formula C17H13BrO
    Molecular Weight 313.19 g/mol
    Appearance Yellow solid
    Melting Point 168-170°C
    Purity Typically >98%
    Solubility Insoluble in water; soluble in organic solvents such as chloroform and dichloromethane
    Storage Temperature Store at room temperature, away from light
    Smiles CC1(C)c2ccc3c(c2Oc2ccccc12)ccc(Br)c3
    Inchi InChI=1S/C17H13BrO/c1-17(2)11-7-10-8-12(18)5-6-13(10)19-16-9-3-4-14(11)15(16)17/h3-9H,1-2H3

    As an accredited 2-Bromo-9,9-Dimethyloxanthracene 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-9,9-Dimethyloxanthracene

    Applications of 2-Bromo-9,9-Dimethyloxanthracene in Industrial Manufacturing

    As a manufacturer specializing in brominated aromatic intermediates, we supply 2-Bromo-9,9-Dimethyloxanthracene to leading companies in advanced chemical synthesis. The material supports innovation in high-value segments of electronics, display technology, specialty polymers, and organic semiconductors. Below we outline key industrial application pathways, the regulatory landscape, integration into downstream processes, recommended formulation levels, and the final commercialized product outcomes.

    1. Organic Light-Emitting Diode (OLED) Emissive Layer Synthesis

    2-Bromo-9,9-Dimethyloxanthracene enables synthesis of high-purity polycyclic aromatic precursors used in blue-emissive layer materials for OLED devices. Its molecular configuration supports precise Suzuki and Stille coupling, driving the selectivity required for deep blue emission profiles and high device efficiency. Fabricators adopt it within custom organic molecule platforms for active display and lighting applications, controlling substitution levels for device longevity and color accuracy.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive, 2011/65/EU)
    • IEC 62321 (Procedures for the determination of certain substances in electronics)
    • REACH (Regulation (EC) No 1907/2006) for SVHC registration and tracking
    • EU eco-design directives for electronic displays

    Typical usage ratio

    • 5–10 wt% within the blue-emissive organic layer formulation, adjusted by molecular weight and brightness target

    Downstream process integration

    • Enters post-oligomerization step before purification and thin-film deposition
    • Coupled under cross-coupling conditions, then isolated and recrystallized
    • Introduced into panel-scale co-evaporation or spin-coating lines
    • Supports multilayer stack-up for full OLED stack builds

    Final product types

    • AMOLED display panels for smartphones
    • OLED TVs and monitor screens
    • Flexible wearable OLED screens
    • OLED-based lighting modules

    2. Organic Semiconductor Research and Electronic Devices

    Research and fabrication facilities employ this material as a core building block in small molecule organic semiconductor platforms, harnessing its extended conjugation and bromine anchoring for controlled coupling to other functionalized aromatics. It serves in R&D of new charge-transporting materials, particularly where high energy level alignment, increased film stability, and tunable solubility are critical to the improvement of field-effect mobility and operational endurance in thin-film transistors and integrated circuits.

    Industry compliance standards

    • Regulation (EC) No 1907/2006 REACH for research-scale and pilot line import/use
    • ISO 9001:2015 quality management certification in specialty chemical manufacturing
    • TSCA compliance (US Toxic Substances Control Act) for domestic electronic materials R&D
    • IEC 60068 (Environmental testing for semiconductor reliability)

    Typical usage ratio

    • 0.5–3 mol% in functional material design libraries
    • As high as 20 wt% in batch experiments for prototype validation

    Downstream process integration

    • Fed into controlled coupling reactions with various electron donor/acceptor motifs
    • Undergoes purification (chromatography, recrystallization) for device-grade purity
    • Used directly in spin coating or inkjet printing experiments
    • Components assessed in thin-film, FET, or OPV device assembly

    Final product types

    • Organic field-effect transistors (OFETs)
    • Organic memory chips
    • Experimental flexible sensors
    • Integrated organic photodetector modules

    3. Specialty Dye Intermediates for Photonic and Optoelectronic Materials

    Fine chemical and dye manufacturers use 2-Bromo-9,9-Dimethyloxanthracene to produce advanced oxanthracene-based dyes with defined absorption and emission spectra, optimizing materials for laser marking, optical filters, and high-speed photonic signaling. This intermediate underpins synthesis of products demanding defined molecular orientation, photo-stability, and thermal resistance in demanding environments. The brominated structure facilitates high-yield coupling to electron-donating or withdrawing groups, meeting custom specification requirements for colorants in demanding optoelectronic settings.

    Industry compliance standards

    • Directive 2004/42/EC (VOC limits for dye manufacturers)
    • EN 71-3 (Safety of colorants for electronic devices and toys)
    • ISO 14001:2015 for environmental management in dye production
    • Controlled Substances List regarding aromatic bromides in EU/US

    Typical usage ratio

    • 10–18 mol% as initial coupling substrate, depending on desired chromophore density and target hue

    Downstream process integration

    • Serves as primary intermediate for palladium or copper-catalyzed arylation reactions
    • Conversion to active dye after multi-step condensation and purification cycles
    • Used in micro-purification steps to reach pigment quality
    • Integrated within pigment dispersions for ink and coating formulations

    Final product types

    • Laser marking compounds for electronics and polymers
    • Optical fiber marking dyes
    • Photonic sensor color filters
    • Specialty colored polymeric films

    4. Synthesis of High-Performance Polycyclic Building Blocks for Specialty Polymers

    Chemical processing plants and polymer houses convert this brominated aromatic compound into functionalized macromolecular building blocks. It enters targeted chain extension or crosslinking reactions, enabling polycyclic backbone formation that imparts high thermal and chemical stability to specialty engineering plastics. The precise reactivity allows control over polymer glass transition temperatures and solubility in casting solvents, addressing specified end-use requirements for advanced structural and electronic polymer systems.

    Industry compliance standards

    • UL 94 (Tests for flammability of polymeric materials)
    • ISO 10993 (Biological evaluation for electronic device enclosures, if required)
    • ASTM D638 (Standard Test Method for Tensile Properties of Plastics)
    • TSCA Inventory status for new chemical polymers in the United States

    Typical usage ratio

    • 2–5 mol% relative to total aromatic content in specialty polymer resin batches, varied for target molecular weight

    Downstream process integration

    • Initiates pre-polymer formation through cross-coupling with complementary di-boronic or di-halo monomers
    • Material incorporated via bulk or solution polymerization reactors
    • Post-polymerization, the resulting polymers undergo pelletizing and drying
    • Final resins compounded and formed into high-value engineering shapes

    Final product types

    • High-temperature-resistant polymer films
    • Specialty electrical insulation parts
    • Custom injection-molded technical components
    • Polymeric substrates for advanced microelectronics
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    Certification & Compliance
    More Introduction

    Introducing 2-Bromo-9,9-Dimethyloxanthracene: A Unique Choice for Advanced Synthesis

    Understanding What Sets 2-Bromo-9,9-Dimethyloxanthracene Apart

    Chemistry always seems to come down to small tweaks with big consequences. In the world of organic synthesis and material science, just a small change on a molecule can turn it from a common starting material into a critical component for cutting-edge applications. Take 2-Bromo-9,9-Dimethyloxanthracene, for example. This isn’t something you’ll find in a high school lab cabinet or an introductory course packet. Chemists and engineers often find themselves searching for molecules just like this when they hope to tweak optical or electronic performance, or when they’re carving out a synthetic route that needs both reactivity and stability.

    With a bromine atom in the two position and methyl groups firmly situated at the 9,9 positions, this oxanthracene derivative brings together selective reactivity and useful physical properties. Oxanthracene itself is no stranger to organic chemists, but the journey toward fine-tuned molecules for organic electronics or advanced dye synthesis often leads to its derivatives. Think about the need to attach something right where bromine sits. That’s the hook, the reactive handle, allowing engineers to couple new groups selectively and efficiently, without random additions all over the ring system.

    Why This Structure Matters in Advanced Research

    Adding methyl groups at the 9,9 position doesn’t just fatten up the molecule; it can shift everything from solubility to how the molecule packs in thin films. These changes seem subtle, but anyone who has struggled to dissolve an aromatic compound or worried about aggregation-induced quenching in optoelectronics knows real pain when the substituents aren’t ideal. Flooding a scaffold like oxanthracene with methyls and a bromine allows chemists to adjust properties with care—and the resulting product, 2-Bromo-9,9-Dimethyloxanthracene, fits into a unique niche.

    A brominated aromatic ring isn’t exactly a new trick in organic synthesis, but where you put the halogen makes a serious difference. The two-position here offers a regularly exploited spot for Kumada, Suzuki, or Stille couplings—methods that have powered material discovery for decades. In the realm of OLEDs, sensors, and advanced polymers, researchers pick and choose their building blocks for a reason. The right substitution pattern can boost charge mobility, control emission wavelengths, and calibrate stability for long-term use.

    A Closer Look at the Physical Properties

    Let’s not gloss over the nuts and bolts. 2-Bromo-9,9-Dimethyloxanthracene typically appears as a crystalline solid, and purity matters. Impurities throw off photophysical measurements and can sabotage reaction yields downstream. That’s part of why so much effort goes into careful synthesis and purification here. Color can range, but pale to yellowish seems common—another tell-tale sign for chemists tracking their product at every step.

    Stability under normal storage conditions translates to less material waste and more reliable planning for researchers. Unlike sensitive organometallics or moisture-magnetizing acids, oxanthracene derivatives, especially those bolstered with methyls, tend not to decompose quickly in air. Less time worrying about decomposition means more time spent designing new materials.

    Where Chemists Use This Compound

    In the lab, utility means more than simply being “reactive.” 2-Bromo-9,9-Dimethyloxanthracene serves as a key intermediate for further functionalization, particularly through palladium-catalyzed reactions. Anyone who has ever tried to add a bulky, sensitive group to a molecule knows the challenges—side reactions, poor regioselectivity, hours spent purifying by column. Here, bromine’s reliability as a leaving group offers a predictable target for coupling reactions. Chemists attach all sorts of side chains or aromatic units to the ring, pushing the boundaries on what these molecules can do.

    Researchers chasing brighter, longer-lasting OLEDs often reach for substituted oxanthracenes. By tuning how electrons move, how the molecule absorbs and emits light, and how strongly they resist photooxidation, scientists can actually design the brightness and color of screens and detectors. This compound’s modifications help control these features, making it a tool for experimental material engineers who care about shifting light emission across the visible range—sometimes into deep blue, which remains an enduring challenge.

    Comparing with Conventional Alternatives

    Oxanthracene on its own performs well in lots of contexts, but unmodified structures can fall short if you’re hunting for new emission profiles or improved solubility. For researchers devoted to solution processing or layer-by-layer film deposition, substituents like bromine and methyl bring the molecule out of academic obscurity and into practical context. No one wants to design a new material only to struggle getting it into solution, especially at scale. The 9,9-dimethyl groups, through their steric bulk, keep the molecules from stacking too tightly, improving solubility and light emission.

    Trying to copy these results with unsubstituted oxanthracene feels like trying to fit a square peg into a round hole—close, maybe, but not quite right. Subtlety in synthetic organic chemistry often pays off, and the functional groups in this molecule serve as reminders of how big those “small” differences can be.

    Navigating Real-World Synthesis and Scale-Up

    Anyone who’s worked in a synthetic lab knows the gulf between “you can make it” and “you can make enough of it to matter.” In personal experience, pushing from milligram to multi-gram scale stretches patience and exposes weak links in a method. 2-Bromo-9,9-Dimethyloxanthracene has tested many a chemist’s resolve, since getting those methyls in the right spots and handling bromination without overdoing it calls for careful monitoring. Though not the simplest molecule in the catalog, the effort pays off when the final product does exactly what you intended.

    Scaling up production isn’t just about mixing bigger batches. Advanced material labs often invest weeks optimizing conditions—controlling temperature, purging with inert gas, tracking purification at every step. Each time you get the methylation or bromination just right, the payoff comes in the next reaction when everything slots together. For product developers, reproducibility is priceless—it saves money, time, and aggravation.

    Environmental and Occupational Health Considerations

    Every chemist who values their health and community takes safety seriously—and especially for aromatic bromides. Personal experience shows carelessness with halogenated substances can lead to headaches inside and outside the lab. Careful handling, glove use, and proper storage all help minimize exposure. Disposal and environmental handling count too; generating less waste and backing reactions with greener solvents helps reduce impact. Material suppliers who prioritize high purity and clear documentation make everyone’s job easier and safer.

    Policies around hazardous chemicals tighten every year, and with good reason. Responsible use of compounds like this can foster trust between chemists, researchers, and the communities in which they work. Nobody wants to repeat the environmental missteps of previous eras.

    Pushing the Field Forward through Creative Use

    Excitement about a molecule rarely stops at the reaction flask. In the right hands, 2-Bromo-9,9-Dimethyloxanthracene opens the door to new devices, molecules, and tools. The underlying principle—tune your structure, tune your result—becomes obvious every time a new photophysical property or synthetic method gets published. I’ve watched research groups try to squeeze every bit of performance from their materials, often leaning toward molecules like this when nothing else does the trick.

    The field of organic electronics thrives on creativity. Sometimes the next leap is about finding just the right building block to link together, or the perfect scaffold for further elaboration. Bringing a methylated, brominated oxanthracene to the table lets engineers and synthetic chemists build on decades of progress, combining reliability with a proven record in selectivity.

    Linking New Research to Practical Outcomes

    It’s not enough to stop with “we made it,” especially when university labs and private companies alike chase better displays, more sensitive sensors, and more sustainable manufacturing. 2-Bromo-9,9-Dimethyloxanthracene’s role as a building block plays into everything from foundational chemistry to real-world hardware. Watching prototypes move from benchtop testing to flexible displays or medical imaging handhelds, the importance of each intermediate becomes clear.

    Science marches on by standing on hundreds of incremental advances. Picking a smart starting material doesn’t guarantee a breakthrough, but it sure helps. In research and in industry, time lost to retooling or troubleshooting unpredictable materials sets innovation back by months. Each bright pixel in a next-generation display, each sensitive sensor deployed in environmental monitoring, owes its existence in part to simple, specific molecules designed years before the finished product.

    The Ripple Effect of Quality and Consistency

    Consistency means more than just matching melting points or color. For those managing process chemistry or analytical work, any fluctuation in the compound’s quality introduces headaches. A poorly purified batch can doom a whole chain of reactions. In tight-knit research teams, stories abound about troubleshooting gone awry, only to trace back the issue to inlet materials—not the method or the catalyst, but something as basic as a trace impurity.

    Reliable, high-quality 2-Bromo-9,9-Dimethyloxanthracene speaks to a broader commitment: putting science and engineering on firm ground. Advances in quality assurance—from better analytical techniques to improved synthetic protocols—carry through to end products. If one batch of a starting material leads to a better OLED lifetime or more precise spectral output, the impact cascades well beyond one research group.

    Looming Challenges and Potential Solutions

    The biggest hurdles often aren’t in the chemistry itself but in how the compound fits into ecosystems of technology. As electronic devices shrink, integrate more functions, and become more disposable, the demands on their internal materials grow. Researchers eyeing new uses for 2-Bromo-9,9-Dimethyloxanthracene look for robustness, compatibility with new assembly methods, and safe disposal at the product’s end of life.

    Solving these issues might mean partnering designers with chemists earlier in the process or investing in greener reaction pathways. Real success comes not just from neat reactions but from thinking through the full lifecycle of a material. In my experience, advances tend to stick when they address both performance and responsibility—from how easily a compound can be manufactured to how safely it can be recycled or disposed of.

    Efforts to make production safer and cleaner align with broader moves in the chemical industry. Using less hazardous solvents, scaling reactions with energy efficiency in mind, and pushing for tighter supply chain transparency all matter for future generations of materials. Open, honest discussion about these choices—driven by evidence and experience—broadens trust and drives smarter research.

    Reflections from Real-World Use

    What often stands out isn’t just a molecule’s synthetic potential, but the collaboration it enables and the innovations it unlocks. In group meetings and conferences, the most memorable stories come from perseverance—tracking a stubborn side reaction, tweaking a catalyst, or watching a hard-won compound light up a test device for the first time. Research with 2-Bromo-9,9-Dimethyloxanthracene follows this familiar arc: setbacks, adjustments, and, eventually, new possibilities.

    As colleagues share both successes and failures, the collective expertise grows. Mistakes with this material—wrong solvent, rushed purification, impatient heating—teach as much as the smoothest runs. Over time, these lessons shape not just better methods but more thoughtful material choices and a deeper respect for the quirks and potential of each compound we bring into the lab.

    Looking to the Future: Opportunities in Emerging Fields

    Research keeps moving forward, and so do the demands on specialty chemicals like 2-Bromo-9,9-Dimethyloxanthracene. As wearable electronics, medical diagnostics, and sustainable energy tech keep growing, the right building blocks take on a new significance. Devices require materials that deliver performance under variable conditions, endure repeated mechanical stress, and meet safety standards from start to finish.

    Innovation from organic chemistry often flows first through a handful of well-chosen intermediates. Brominated oxanthracenes occupy one such sweet spot: not so exotic as to be unreachable, not so pedestrian as to be overlooked. Thoughtful adaptation—matching synthesis with application and purpose—will keep this compound relevant as new markets emerge and old challenges evolve. The right combination of chemical creativity and practical wisdom ensures fresh potential for research and beyond.