Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

3-Bromo-9-Phenylcarbazole

    • Product Name 3-Bromo-9-Phenylcarbazole
    • Alias 3-Bromo-9-phenyl-9H-carbazole
    • Einecs 821-038-7
    • 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
    VTB
    Specifications

    HS Code

    271795

    Product Name 3-Bromo-9-Phenylcarbazole
    Cas Number 1262649-62-2
    Molecular Formula C18H12BrN
    Molecular Weight 338.20 g/mol
    Appearance Off-white to pale yellow powder
    Melting Point 120-124°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DCM, chloroform, and toluene
    Storage Conditions Store in a cool, dry place, keep tightly closed
    Smiles Brc1ccc2c(c1)c3ccccc3n2c4ccccc4
    Inchi InChI=1S/C18H12BrN/c19-15-10-11-18-17(13-15)16-9-5-2-6-12(16)20(18)14-7-3-1-4-8-14/h1-13H
    Synonyms 9-Phenyl-3-bromocarbazole

    As an accredited 3-Bromo-9-Phenylcarbazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g bottle of 3-Bromo-9-Phenylcarbazole is sealed in an amber glass container, labeled with hazard and product information.
    Shipping 3-Bromo-9-Phenylcarbazole is shipped in secure, airtight containers under ambient conditions. Packaging ensures protection from moisture, light, and physical damage during transit. All shipments comply with relevant regulations for transport of chemical substances, and include proper labeling and documentation for safe handling, storage, and regulatory clearance upon arrival.
    Storage Store 3-Bromo-9-Phenylcarbazole in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon. Keep it in a cool, well-ventilated, and dry area away from light, heat sources, and incompatible materials like strong oxidizers. Ensure proper labeling and follow standard laboratory safety protocols to prevent contamination or degradation.
    Application of 3-Bromo-9-Phenylcarbazole

    Applications of 3-Bromo-9-Phenylcarbazole in Industrial Manufacturing

    3-Bromo-9-Phenylcarbazole serves as a high-purity intermediate with unique reactivity and electronic properties, widely used in advanced industrial syntheses. As an established manufacturer, we support precise downstream integration across the performance materials sector, ensuring consistency in technical formulation and compliance for demanding end uses.

    1. OLED (Organic Light Emitting Diode) Materials Production

    Downstream electronics manufacturers incorporate this compound as a carbazole-based monomer in the production of light-emitting and charge-transport layers in OLED device fabrication. The brominated structure facilitates C–N and C–C coupling reactions, supporting synthesis of high-mobility organic semiconductors. Precision in halogenation is critical to achieve desirable electroluminescent properties, and final polymer matrices undergo extensive purity and stability validation prior to use in panel assembly lines.

    Industry compliance standards

    • IEC 62341 (OLED display device safety and performance)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IEC 61000-4 (Electromagnetic compatibility for electronic devices)
    • ISO 9001:2015 Quality Management System (for traceability and batch control)

    Typical usage ratio

    • 5–15% by molar ratio in organic synthesis feedstock for emitting or host layers, variable by desired panel brightness and charge balance targets

    Downstream process integration

    • Entry point in the Suzuki, Buchwald-Hartwig, or Ullmann-type coupling steps for dendrimer or polymer electronic material synthesis
    • Precursor for deposition-grade organic layers during vacuum thermal evaporation (VTE) or solution processing

    Final product types

    • OLED display modules (televisions, smartphones, automotive HUDs)
    • Flexible lighting panels
    • Wearable optoelectronic devices

    2. High-Performance Photorefractive Polymer Manufacturing

    Polymer formulators use this carbazole derivative as a donor-acceptor component in advanced photorefractive blends, supporting efficient charge mobility and photoinduced birefringence. Its bromine functionality enables functional group exchange to customize refractive index modulation for holographic data storage and laser beam control. Quality assessment requires batch-specific testing for photostability and trace metal content.

    Industry compliance standards

    • ASTM D883 (Standard Terminology Relating to Plastics)
    • EN ISO 178 (Determination of flexural properties in plastics)
    • ISO 10993 (Biocompatibility, for optical devices in biomedical context)
    • REACH Regulation (EC) No 1907/2006 (Registration, Evaluation, Authorisation and Restriction of Chemicals)

    Typical usage ratio

    • 2–8% by weight of total photorefractive formulation, depending on desired carrier generation efficiency and matrix composition

    Downstream process integration

    • Feeds into co-polymerization or physical blending step with polymeric backbones such as PMMA, PS, or PVK
    • Introduced before extrusion, spin-coating, or casting to ensure homogeneous dispersion

    Final product types

    • Holographic data storage films
    • Rewritable optical media
    • Beam steering components for lasers

    3. Specialty Chemical Intermediate for Advanced Dyes

    Dye manufacturers deploy this compound to build high-stability molecular scaffolds for specialty colorants, targeting applications such as organic photoconductors and NIR-absorbing materials. The carbazole unit delivers desirable chromophoric properties, while the bromine site serves as a functional handle for Suzuki-Miyaura or Stille coupling, essential for extending π-conjugation. Product quality requires stringent control of halogen purity and absence of residual starting materials before final dye formulation.

    Industry compliance standards

    • EN ISO 105 (Textile colour fastness standards, for applicable dyes)
    • OEKO-TEX Standard 100 (For dyes used in textiles)
    • NIOSH Hazard Review: Occupational Exposure to Dyes and Dye Intermediates
    • ISO 14001:2015 (Environmental management for chemical processes)

    Typical usage ratio

    • 3–10% by mass as a key coupling substrate in specialty dye synthesis, adjusted per chromophore requirements

    Downstream process integration

    • Initiates cross-coupling with aryl boronates or stannanes in the targeted dye synthesis step
    • Processed in high-temperature, inert-atmosphere reactors prior to neutralization and purification

    Final product types

    • Organic photoconductor dyes
    • NIR-absorbing dyes for security printing and sensors
    • Inkjet and textile specialty dyes

    4. Intermediate for Hole Transport Materials in Solar Cells

    Manufacturers in the photovoltaic sector utilize this brominated carbazole as an essential building block in the synthesis of hole-transporting layers for perovskite and organic solar cells. By controlling substitution pattern and electronic structure, formulators enhance charge extraction and device lifetime. Critical QC includes assessment of reaction completeness and residual metal content before integration into solar cell stack lamination.

    Industry compliance standards

    • IEC 61215 (Crystalline silicon terrestrial photovoltaic modules design qualification and type approval)
    • IEC 61730 (PV module safety qualification)
    • ISO 17025 (Laboratory testing for PV certification)
    • SEMI PV18 (Process management in PV components supply chain)

    Typical usage ratio

    • 8–20% by molarity in precursor mixtures for carbazole-type hole transport materials, based on device and layer thickness

    Downstream process integration

    • Participates in key cross-coupling or polymerization stage for hole transport active layer production
    • Forms final HTM blend before application by spin-coating or inkjet printing onto device substrate

    Final product types

    • Perovskite solar cell modules
    • Organic photovoltaic devices
    • Hybrid tandem solar panels
    Free Quote

    Competitive 3-Bromo-9-Phenylcarbazole 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.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing 3-Bromo-9-Phenylcarbazole: Developed and Produced by Professional Chemists

    Direct From the Manufacturing Line: Our Process and Commitment

    Every day in our plant, our team works at the front line of organic synthesis. The focus isn’t just on yield or chemistry—it’s on real usability and reliability for research and industrial partners. 3-Bromo-9-Phenylcarbazole has become a regular production item for us, not because it is trendy, but because our partners in OLED materials, advanced polymers, and fine chemical synthesis asked for exactly the kind of repeatable purity and solid handling that we deliver. This product doesn’t come from a catalog reseller or an office full of screens; it’s the result of batch development, purification, and quality control in our own lab facilities, with our own staff, shipped directly from us for consistent upstream results.

    There’s a clear set of reasons why labs and technical teams circle back to us instead of switching to generic sources. We’ve handled this compound from kilo-lab to multi-kilogram scale, solving crystallization and solubility bottlenecks as they arise, not just reading about them in papers. Our practical insight comes from taking 3-Bromo-9-Phenylcarbazole through freezing winters and humid summers, tracking how it stores, ships, and integrates into sensitive syntheses. This feedback shapes each batch, so you see fewer problems downstream.

    Clear Specifications, Met by Practical Experience

    Our chemists don’t rewrite specs from old datasheets. Every batch receives NMR, LC-MS, and HPLC testing—with analytical printouts attached to every lot, because the academic and industrial projects we supply require chemical clarity. Typical lots reach above 99% HPLC area, based on our own in-house methods, not theoretical values. We routinely screen for residual bromide, isomeric side-products, and trace metal contaminants, rather than relying on external claims. If a customer asks, we can walk through solvent histories, temperature logs, and purification stage notes.

    Molecular formula for 3-Bromo-9-Phenylcarbazole is C18H12BrN, with a molecular weight of roughly 322.2 g/mol. This detail isn’t just a reference—it comes up every time teams need to dissolve, weigh, or formulate the product. We keep physical appearance standardized: off-white to pale-yellow crystalline powder, because color and form can tell a trained technician about purity and storage history. Having packed, sealed, and shipped thousands of bottles, we know how small physical cues can minimize waste or signal batch consistency.

    Applications Driven by Research and Development Demands

    In our experience, this compound’s core value lies in molecular electronics and synthetic pathways. The bromo group allows for efficient coupling in C–C or C–N bond formations—essential steps for OLED emitter research, specialty polymer design, and next-gen organic semiconductors. The phenylcarbazole core ensures strong thermal stability and robust electron-rich properties, supporting new organic architectures that demand both flexibility and rigidity in their backbones. Over several years, academic groups and industrial R&D labs have switched from unreliable off-the-shelf sources to our material, after seeing how high batch purity enables better yields in Suzuki, Buchwald–Hartwig, and related catalytic reactions.

    Beyond the glamour of published research, there’s the daily grind of process development: tuning light absorption, measuring charge mobility, and testing film formation. Early-stage projects tell us that 3-Bromo-9-Phenylcarbazole supports new hole-transporting layers or main-chain modifications where impurities cut down reproducibility. Because we oversee the chemical process from crude to finished lot, we can hash out technical modifications if your formulation or step requires a minor solvent tweak, or an alternative particle sizing.

    Practical Usage: What Decades in Production Teach About Performance

    Our production staff have seen this compound in action through countless process runs, from gram-scale optimizations to trials requiring multi-kilogram lots. Many users try 3-Bromo-9-Phenylcarbazole straight in standard literature protocols with direct halogen-metal exchange, palladium catalysis, or as a precursor in cross-coupling. But subtle insights from extended production make a real difference: how long drying time affects solubility; which storage vessels to avoid static charge issues; how microtraces of residual solvent can foil high-performance applications. These issues are not in the books—they’re in the lived experience of handling and formulating carbazoles day after day.

    Customers have rolled out processes using our batches in photoactive layers, photoinitiators, or even medical intermediate research. Most report fewer filtration failures, easier chromatography, and greater batch-to-batch consistency after making the switch from imported products sourced through traders or agency supply chains. We work with direct technical contacts at end-user labs, so when a unique problem arises—be it solubility in non-standard solvents, or the need to minimize trace halides in ultra-sensitive optoelectronic devices—we can act, rather than just recommend.

    Distinctiveness in the Market: What Makes Our 3-Bromo-9-Phenylcarbazole Different

    Some suppliers move product from warehouse to shelf, relabel, and call it a day. From our angle, manufacturing means blending chemistry with hands-on troubleshooting. Direct control over every step—starting with building block sourcing, picking reagents with tight control, managing reaction parameters, optimizing purification (repeated recrystallization, dual solvent washes)—protects the integrity of the final powder. By sticking with in-house analytical feedback, each lot gains traceability and reproducibility. Our chemists shut down production lines to review contaminant spikes, and only restart when variances stabilize.

    In the wider market, most 3-Bromo-9-Phenylcarbazole comes in as a standard trade issue—often reprocessed from uncertain technical grades or passed through multiple hands. We’ve seen lots where poor drying led to lumping and color shifts, and others with unexpected side-products from oxidative storage. Our direct batches aren’t shaped by minimum margin requirements, so quality remains consistent from batch to batch—not just in moisture, but crystallinity, particle profile, and mechanical flow.

    Another aspect is response time. Our technical service team isn’t three time zones away; they run benches and manage production tanks. That means if you report a problem with an analytical parameter, shipment, or end-use interaction, real solutions start in hours, not days. Long-term partners often adapt or scale their processes based on our stability data and application bulletins, which come from trials using real product, not just theoretical assessments.

    Technical Support Built from Manufacturer Experience

    We don’t treat downstream failures as theoretical. If a process sample shows unexpected reactivity, or unusual trace signals pop up in your analysis, we dig in. Years of exposure to both routine and custom requests let us spot the weak points in typical handling: how small vial closures lead to absorption, why dense powder packing can impact sub-sampling, or where minor procedural shortcuts undermine critical measurements. 

    Support flows through practical channels—logged email advice, custom technical bulletins, coordinated video conference reviews with our chemists. Real-time solutions evolve from direct production logs, not generic templates. Some customers develop entirely new OLED device sub-units or liquid crystalline intermediates, drawing on minute updates from our application team regarding shelf life and best handling practice. Because we construct every batch in-house, our staff follow each shipment to completion, closing QC and customer service gaps that slow larger, remote supply chains.

    Enabling Precision in the Next Generation of Synthesis

    Growing sectors like high-brightness OLEDs, organic photoconductors, and advanced sensor materials all demand increasingly strict controls over building block quality. Here, 3-Bromo-9-Phenylcarbazole plays a key role in fragment-coupling, core extension, and efficient functionalization pathways. Though technical literature outlines standard routes, only hands-on batch-makers appreciate how micro-scale changes in raw input or conditions affect performance in scale-up and automated lines.

    Our R&D partners rely on us to track how minor solvent residue, peroxide traces, or trace transition metals influence their most sensitive syntheses. Multi-step organometallic assemblies or next-gen photoactive complex development don’t tolerate compromise at the gram or kilogram level—so our experienced staff maintain a feedback loop from production to application support. This approach shortens troubleshooting, minimizes downtime, and builds real confidence into pilot line and commercial deployments.

    What Our Ongoing Experience Brings to the Table

    Having supported projects spanning organic electronics, specialty chemical synthesis, and materials innovation, we see how every batch represents months of cumulative learning. Greater focus on rapid analytical turnarounds and effective, safe packaging (including tamper-proof seals and flexible lot sizes) comes from our own practice—not just client requests. By keeping core chemists plugged into both the lab and the application feedback, we channel experience from the production floor directly into the next refinement or troubleshooting cycle.

    Mistakes in manufacture—whether from overlooked solvents, shortcut crystallizations, or poorly calibrated drying ovens—don’t strike just at the margin. For teams seeking quantum leaps in device performance or molecular precision, a subpar lot means project delays, blown budgets, and missed deadlines. Our on-the-ground interactions with material scientists and synthetic chemists have shown that the real cost of low-grade material isn’t just the direct expense, but the wasted effort in lost development time and failed scale-ups.

    Batch Consistency and End-User Confidence

    Labs and R&D outfits return to us because they want dependable results with each order—they don’t want to restart or recalibrate with every bottle. Since our batches are monitored for moisture, isomeric purity, trace transition metals, and handled under established SOPs, customers often bring their syntheses from preliminary stage trials all the way through to semi-commercial runs without swapping suppliers. We’ve provided side-by-side comparisons between our lots and market standards, showing reduced need for repeat purification and fewer cases of batch-to-batch drift.

    Over years, such continuity means technical teams can tweak and optimize protocols with confidence that their foundational building blocks won’t change just because of a supplier update or unnamed formulation tweak. Research scale-ups and pilot production both benefit from knowing that any problem with a batch will be reviewed quickly, with solutions drawn from real production experience, not just a distant datasheet or low-resolution certificate.

    The Practical Differences: From Manufacturer to Application

    We see the key differences in how researchers and process engineers talk about our 3-Bromo-9-Phenylcarbazole compared to market alternatives. With direct control, we set drying parameters tailored to minimize agglomeration, pack in high-integrity containers, and ship in temperature-stable packaging to prevent sweating or clumping. Our analytical chemists calibrate against global standards yet respond quickly to project-specific requests—whether that means higher-throughput sampling, or reporting on particular trace elements absent from regular documentation.

    Our process doesn’t end at shipment. Regular communications with end users let us adjust target specifications based on field results, not just preset minimums. If a photoactive device fails threshold testing, or optical batch consistency drifts in a new pilot line, we investigate—sometimes tweaking operating temperature windows, switching out feedstocks, or adjusting storage protocols in real time. This collaboration-driven practice, forged in daily contact with working chemists, sets practical manufacturers apart from remote fulfillment operations.

    Looking Ahead: Reliable Foundation for Advanced Chemistry

    We see the landscape for 3-Bromo-9-Phenylcarbazole shifting, as more industries push for higher-purity, stricter analytical traceability, and tighter handling specs. Our deep involvement in production doesn’t just set quality; it anchors trust that what leaves our facilities matches what arrives at your bench. Years of batch notes, flagged deviations, and user-driven modifications define our product as much as the chemical formula itself.

    By staying active on both sides of the scale—from kilo-lab all the way through to high-value functional materials—we build up the resilience to handle shifting market needs, regulatory updates, and next-wave research challenges. Our team’s practical, daily engagement with the chemistry, handling, and support of 3-Bromo-9-Phenylcarbazole remains our greatest asset—and your best resource for sustained innovation in organic materials.