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2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine

    • Product Name 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine
    • Alias Bromo-TRZ
    • Einecs 629-860-0
    • 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

    171030

    Chemical Name 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine
    Cas Number 180430-54-2
    Molecular Formula C21H14BrN3
    Molecular Weight 404.26 g/mol
    Appearance White to off-white powder
    Melting Point 252-254 °C
    Solubility Insoluble in water, soluble in organic solvents (e.g., chloroform, dichloromethane)
    Purity Typically ≥98%
    Boiling Point Decomposes before boiling
    Smiles C1=CC=C(C=C1)N2C(=NC(=NC2=C3C=CC(=CC3)Br)C4=CC=CC=C4)C5=CC=CC=C5
    Inchi InChI=1S/C21H14BrN3/c22-17-13-11-15(12-14-17)21-24-19(16-7-3-1-4-8-16)25-20(18-9-5-2-6-10-18)23-21/h1-14H
    Storage Conditions Store at 2-8°C, in a tightly closed container, protected from light
    Synonyms 4,6-Diphenyl-2-(4-bromophenyl)-1,3,5-triazine
    Application OLED materials, photonic devices, organic electronics
    Density 1.38 g/cm³ (approx.)

    As an accredited 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine 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-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine

    Applications of 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine in Industrial Manufacturing

    As a specialized manufacturer of 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine, we support downstream clients with high purity and batch consistency for advanced chemical applications. Our material plays a critical role in select, established industrial fields, contributing to performance and regulatory compliance in value-added sectors.

    1. OLED Emissive Layer Materials

    Our triazine-based compound is widely adopted as an electron transport and host material in organic light emitting diode (OLED) displays and lighting. Its structural stability under electrical excitation supports blue-emitting device architectures, enabling extended lifespan and high luminance efficiency. Leading panel manufacturers implement this compound in multilayer emissive stacks to improve charge balance and color purity in large-format displays and consumer-grade lighting systems.

    Industry compliance standards

    • IEC 62341 (OLED display performance and reliability)
    • JEITA standards for component materials in electronic displays
    • RoHS Directive (EU 2011/65, hazardous substance restrictions)
    • REACH Regulation (EC 1907/2006, registration and evaluation of chemicals)

    Typical usage ratio

    • 3%–10% by weight in the emissive or host layer of solution-processed or vacuum-deposited organic stacks; ratio varies based on target electron mobility and color emission specification

    Downstream process integration

    • Incorporated during vacuum thermal evaporation or inkjet printing of OLED organic stacks; dissolved in solvent blends or co-evaporated with dopants and adjacent layers

    Final product types

    • Flat-panel OLED television screens
    • Flexible OLED smartphone displays
    • OLED lighting panels for architectural or automotive use
    • Wearable device display modules

    2. Photoinitiator Formulation for UV-Curable Coatings

    In high-value UV-cured coatings, the triazine core’s ability to facilitate photochemical energy transfer makes it a preferred intermediate for Type II photoinitiators. End users in electronics and specialty packaging benefit from its tailored absorption properties, achieving rapid surface hardening and precise 3D patterning in thin film applications, including printed circuit boards and protective varnishes.

    Industry compliance standards

    • ISO 9001:2015 for production quality management
    • IEC 61249 (base materials for PCBs, including photocoatings)
    • European Printing Ink Association (EuPIA) guidelines for safe use in food packaging inks
    • Restriction of certain hazardous substances for photovoltaic and electronics applications

    Typical usage ratio

    • 1%–5% weight of total photoinitiator blend in UV-curable resin systems; optimal loading determined by film thickness, desired cure speed, and light source wavelength

    Downstream process integration

    • Added during masterbatch blending of photoinitiator formulations; dispersed into acrylate or epoxy resins before roll coating or printing

    Final product types

    • Photocured solder mask on electronic PCBs
    • UV-cured protective topcoats for flexible packaging
    • High-gloss UV varnishes for specialty print media
    • Resist layers for microelectronic and optoelectronic fabrication

    3. High-Performance Engineering Polymer Additives

    As a persistent electron-deficient aromatic structure, this compound functions as a thermal stabilizer and flame-retardant synergist in specialty polymers processed for aerospace interiors and technical textiles. Its molecular compatibility with engineering thermoplastics like polycarbonates and polyesters enables manufacturers to meet rigorous fire safety and thermal endurance requirements without compromising mechanical integrity.

    Industry compliance standards

    • UL 94 (flame retardancy classification for plastics)
    • FAR 25.853 (flammability standards for aircraft materials)
    • EN 45545-2 (fire protection on railway vehicles)
    • ISO 178:2019 (flexural properties of plastics)

    Typical usage ratio

    • 0.2%–0.8% by weight, applied as a co-additive in halogen-free or intumescent flame retardant systems; adjustment required to balance retardancy and transparency

    Downstream process integration

    • Compound introduced at melt blending or twin-screw extrusion phase of polymer masterbatch production; ensures homogeneous dispersion before pelletizing or sheet formation

    Final product types

    • Passenger aircraft cabin panels
    • Fire-resistant polycarbonate films
    • Technical fabrics for transport seating
    • Specialty housings for electronic equipment

    4. Specialty Photorefractive Material Synthesis

    In advanced photonics research and commercial holographic recording, this triazine derivative serves as a key electron-trapping component in organic photorefractive composites. Its tailored electronic structure supports high diffraction efficiency and low-voltage operation in nonlinear optical polymers, facilitating real-time image storage and dynamic beam steering in sensor arrays and data storage prototypes.

    Industry compliance standards

    • ISO 24611 (holographic data storage evaluation)
    • IEC 60825 (laser safety requirements for end-use systems)
    • Material traceability as per ISO 9001
    • REACH safety requirements for experimental chemicals

    Typical usage ratio

    • 0.5%–2% by weight of the photorefractive blend, tunable based on the polarity of the host polymer matrix and intended operating wavelength

    Downstream process integration

    • Added with charge-transport and nonlinear dopants in solution blending; cast into thin films via spin-coating or blade casting for device assembly

    Final product types

    • Organic photorefractive devices for 3D holography
    • Rewritable optical data storage prototypes
    • Adaptive optical sensor elements
    • Beam steering modules for advanced photonic circuits
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    Certification & Compliance
    More Introduction

    Introducing 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine: Reliability for Modern Synthesis

    The Substance Behind the Science

    Stepping into the world of specialty chemicals always reveals a mix of curiosity and caution. My decade working alongside chemists has shown time and again that dependable building blocks drive innovation, especially in fields chasing ever tighter performance standards. Among the lineup, 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine earns its place for those needing sharp results in synthesis and material applications. With so many options on the bench, the choice depends on clarity—what the molecule offers, how it works in actual labs, and where it stands out.

    Understanding the Foundation: Model and Make-Up

    Some molecules seem built for the spotlight, offering a blend of stability, reactivity, and compatibility few others match. From my experience, triazine derivatives tend to fit that description, and this one balances all three. As a crystalline organic compound, its structure weaves bromine and phenyl groups into the triazine core, a combination that brings reliability where unpredictable reactions can spell trouble. The chemical formula, C21H14BrN3, shows off those heavy aromatic rings alongside a bromine marker that changes the landscape for downstream chemistry.

    The Power of Purpose: Where It Works

    What matters most is always application. In recent years, research labs and specialty manufacturers have leaned into triazines for optoelectronics and advanced polymers. I’ve seen this compound deliver strong results as an intermediate in organic synthesis, especially where the need for selective bromination sets it apart from less specialized ingredients. Its presence in OLED materials isn’t surprising, with its rigid structure helping boost device stability and emission control. Watching teams incorporate it into new functional polymers makes you realize it didn’t land on anyone’s bench by accident.

    Specification Details: What Sets It Apart

    While fancy data sheets do their job, what really counts is how a material behaves during crucial experiments. Over a few project cycles, batches of 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine have offered high melting points and impressive purity—usually over 98 percent for qualified suppliers. This means less troubleshooting down the line and fewer surprises when scaling up. In practice, purity doesn’t just tidy up a line on paper—it protects researchers from side reactions or failures that send weeks of work down the drain. There’s a certain confidence in opening a bottle, knowing it’s going to dissolve as expected and perform under the same set of conditions every time.

    It’s Not Just About Substitutes

    You often hear people talk shop about alternatives. Some might reach for chlorinated triazines or go lighter with plain phenyl-substituted analogues, aiming to cut costs or work with established protocols. But my own projects hinted at the difference that bromine brings to this molecule, moving reactivity closer to sweet spots for Suzuki and other important cross-coupling reactions. It’s the kind of effect that doesn’t show up until you’re knee-deep in a tricky synthesis, and you realize your yields hold steady, even under tough conditions. In electronic applications, slight changes at the molecular level spell out stronger thermal and photostability, a factor not every triazine can guarantee.

    Lessons From the Lab Bench

    Any chemist knows the pain of watching an experiment tank due to impure or inconsistent starting materials. One of my most memorable syntheses used a commercial batch of this triazine. Before running the first reaction, I checked the spectral data and found clean, sharp peaks—an early sign that the extra money wasn’t wasted. Sure enough, downstream coupling yielded more product at higher purity than an attempt with a budget alternative. On another occasion, a colleague trying to develop a series of thermally activated delayed fluorescence (TADF) emitters counted on this molecule for its electron-accepting properties. At each turn, its consistency kept our timelines on track.

    Staying Current: Evolving Role in Material Science

    Material science doesn’t stand still, and neither do expectations for chemical building blocks. Recent literature points to the triazine core as a key player in both small-molecule and polymer-based electronic devices. The rise of OLEDs (organic light-emitting diodes) has made these compounds valuable, not only for their electronic properties but also for their ability to tune emissions. Designers can tweak light color or stability with small changes to the structure; here, the 4-bromophenyl group checks boxes that more basic triazines just don’t approach. I’ve sat in on meetings where R&D leads specifically request this model for new device architectures, citing its past record for high quantum yields and operational lifespans.

    Differentiating in the Real World

    Working with different providers over the years has made differences between triazines more than just marketing. Some alternatives fall short in crucial reactions, either from unexpected trace contaminants or slightly shifting melting points that spell trouble for sensitive processes. It always comes back to what works for the end goal: will it get the product out the door and keep quality up? Peers in academic labs trade stories about projects saved by a small switch to this triazine, especially when working with photonic or semiconducting polymers. Beyond the bench, its record fits with the growing push for sustainable, safer chemistries—lowering risks thanks to its strong performance and reliability.

    Safeguarding Results: From Handling to Scale-Up

    Behind every successful experiment sits a chain of quiet, careful practices. I’ve found this compound manageable in most research settings—no odd storage needs, and it holds up well to normal temperature and humidity. For industrial-scale operations, consistency scales with the batch, something not every specialty chemical matches. One manufacturer’s lot-to-lot variation can throw a year-long project off course. Word travels fast about suppliers who maintain standards, and bulk orders often go straight to names proven to deliver triazines without compromise. This adds a layer of reassurance in fields where setbacks carry heavy costs.

    The Review Board: Peers, Reviews, and Real-World Feedback

    Experience matters, but so do numbers. In recent peer-reviewed studies, 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine performs consistently in OLED and photonic material development. Multiple papers confirm its use in high-performance emitter layers, tracking improved efficiency and color tuning compared to less elaborate triazines. Industry reports back up these claims, citing reduced device failures and longer operation under stress. Word-of-mouth from senior researchers mirrors this, with many citing a reduction in trial-and-error when adopting this compound for both exploratory and production-scale work.

    Environmental and Safety Considerations

    Nowadays, no responsible supplier or research institution overlooks sustainability or safety. It can’t be denied that brominated aromatics come under scrutiny for environmental impact, so careful selection and disposal stay top of mind. In my own labs, we worked hard to implement recycling and solvent-reduction strategies, making sure each bit of the compound ended up in the right waste stream. Compared to some persistent or extremely toxic chemicals, this triazine model strikes a balance: it doesn’t give up performance, but allows for responsible handling with standard chemical hygiene. Guidelines set by regulatory bodies and best-practice organizations align with safe storage, handling, and disposal.

    Complying With Quality and Regulatory Standards

    As testing grows more precise, so does the bar for compliance. I’ve seen quality assurance teams adopt batch-analysis protocols, rejecting shipments with the faintest sign of byproducts or uncharacterized material. In regulated segments, staying ahead of certifications means partnering with suppliers transparent about their sourcing and validation processes. Especially for uses tied to electronics or sensitive finished goods, crossing that threshold from research-grade to production-grade matters. My experience tells me that manufacturers offering 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine spend more time fielding questions about trace contaminants and batch documentation—evidence of the higher bar set for essential intermediates.

    How It Stacks Up Against Competitors

    Over the years, I’ve tested several triazine analogues—some with fluorine, others designed for cost efficiency—but the difference often boils down to selectivity in key reactions and end-use performance. Brominated variants like this one tend to offer unique reactivity, opening doors to a broader set of cross-coupling and functionalization methods. Lower performance options occasionally get the job done in routine syntheses, yet struggle under the analytical lens or in demanding roles like photostable polymers. Teams working on next-generation electronics find those tiny trade-offs stack up into measurable losses: color drift, poor device lifetimes, or tricky purification steps. In my files, side-by-side runs deliver clear verdicts—bromine brings something extra that turns a good result into a great one.

    Economic Reality: Mindful Sourcing and Value

    Materials budgets rarely stretch far enough, especially in research settings. Early in my career, I cut corners with “value” chemicals, hoping volume would make up for patchy results. It never did. For growing firms or labs managing limited resources, selecting chemicals like this triazine demonstrates that smart investment saves more money over the long haul. Higher yields, less waste, fewer repeat runs—it all adds up. Colleagues sourcing large quantities build direct relationships with trusted suppliers, negotiating on documentation and order sizes rather than gambling with unknown lots. The bigger picture reveals an ecosystem where informed choices keep the gears turning.

    Field-Driven Demand and Emerging Directions

    Scientific fields rarely remain static; today’s favorite material could fall from grace by next quarter. So far, the role of 2-(4-Bromophenyl)-4,6-Diphenyl-1,3,5-Triazine seems to grow, especially in organic electronics, energy storage, and smart materials. Papers from respected groups detail new uses in light-emitting devices, sensors, and even specialty coatings. Teams at the edge of research appreciate its robust framework and the way it bridges performance gaps. A glance at recent conference abstracts suggests developmental interest isn’t slowing down.

    Challenges and Solutions: Real-World Lessons

    No product comes without its own set of challenges. For specialty organics, the main headaches involve supply chain bottlenecks and documentation. I’ve seen teams lose weeks to delayed shipments—reminders that redundancy matters. The solution calls for planning and relationship-building: lining up more than one qualified source, maintaining clear communications, and preemptively securing extra material when embarking on long campaigns. Sharing feedback with suppliers helps, too. Not long ago, a manufacturer addressed recurring minor impurities after enough labs raised the point, confirming the importance of a transparent, responsive marketplace.

    Supporting Facts: Evidence Lines Up

    Pulling from both literature and experience, it’s clear this compound holds its ground. Published work on OLED host and emitter layers repeatedly lists high device efficiency and lifetime, with tested comparisons against other triazines. Industrial data supports these claims, showing fewer field failures and steady result reproducibility. One large university team tracked process yields over a year, comparing outcomes against both chlorinated and unsubstituted triazines—brominated models led by every metric that counted, from photostability to reactivity. Personal anecdotes fill in any gaps, with teams achieving milestones only after making the switch to this compound.

    Future Outlook: Innovation and Responsible Growth

    Development continues: new applications emerge every year, and researchers keep refining synthesis methods. Some efforts focus on greener production, reducing waste during manufacture or developing recycling protocols for spent material. Responsible adoption continues as labs and companies set stricter environmental and safety standards. In the next few years, demand will likely amplify in specialty electronics and advanced polymers. Support from both academia and industry ensures will likely remain a key link in the production of emerging technologies.