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9-[(3-Bromo-5-methyl)phenyl]-9-phenyl-9H-fluorene

    • Product Name 9-[(3-Bromo-5-methyl)phenyl]-9-phenyl-9H-fluorene
    • Alias 3-Bromo-5-methyl Fmoc
    • 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

    179259

    Chemical Name 9-[(3-Bromo-5-methyl)phenyl]-9-phenyl-9H-fluorene
    Molecular Formula C26H19Br
    Molecular Weight 411.34 g/mol
    Cas Number 1393437-47-6
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as dichloromethane and chloroform
    Smiles Cc1cc(cc(c1)Br)C2(c3ccccc3)c4ccccc4c5c2cccc5
    Inchi InChI=1S/C26H19Br/c1-17-15-22(27)14-20(16-17)26(21-10-6-3-7-11-21)23-18-12-8-4-9-13-19(18)25(23)24-5-2-1-3-7-11-21(24)26/h1-16H
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited 9-[(3-Bromo-5-methyl)phenyl]-9-phenyl-9H-fluorene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a 10-gram amber glass bottle with tamper-evident seal, labeled with chemical name, formula, and safety information.
    Shipping This product, **9-[(3-Bromo-5-methyl)phenyl]-9-phenyl-9H-fluorene**, is shipped in specialized, tightly sealed containers to ensure stability and prevent contamination. Shipping complies with all relevant chemical handling regulations (including DOT and IATA). Material safety data sheets (MSDS) are provided, and temperature-sensitive options are available upon request.
    Storage Store 9-[(3-Bromo-5-methyl)phenyl]-9-phenyl-9H-fluorene in a tightly sealed container, protected from light and moisture, at room temperature or as specified on the material safety data sheet. Keep in a dry, cool, and well-ventilated area, away from incompatible substances such as strong oxidizers. Ensure proper labeling and restrict access to authorized personnel only.
    Application of 9-[(3-Bromo-5-methyl)phenyl]-9-phenyl-9H-fluorene

    Applications of 9-[(3-Bromo-5-methyl)phenyl]-9-phenyl-9H-fluorene in Industrial Manufacturing

    As an established manufacturer, we supply 9-[(3-Bromo-5-methyl)phenyl]-9-phenyl-9H-fluorene for advanced applications in electronics and high-performance materials. The following sections detail its real-life downstream uses, compliant with regulatory and industrial requirements.

    1. OLED Emitter Material Synthesis

    Leading organic display manufacturers rely on this fluorene derivative as a high-purity intermediate when assembling blue light-emitting layers for OLED display panels. Chemical engineers incorporate it into emitter molecule design to strengthen molecular rigidity, suppress non-radiative pathways, and tune voltage thresholds for high color purity in thin-film encapsulated devices. Compatibility with high-temperature vacuum deposition requires batch traceability and process consistency.

    Industry compliance standards

    • IEC 62341 “Organic light-emitting diode (OLED) displays”
    • RoHS Directive 2011/65/EU
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Used at 2–6 wt% relative to the host matrix, adjusted based on crystallinity control and device luminescence targets

    Downstream process integration

    • Dosed into solution or vapor-phase systems during the emitter layer precursor stage, typically purified by gradient vacuum sublimation and blended into host-dopant photoluminescent films before evaporation onto ITO/glass or flexible substrates

    Final product types

    • OLED display modules (mobile, TV, automotive panels)
    • Flexible and foldable display screens
    • Wearable device display components

    2. Organic Photovoltaic (OPV) Material Development

    9-[(3-Bromo-5-methyl)phenyl]-9-phenyl-9H-fluorene is an essential precursor in synthesizing advanced electron-donor polymers for organic solar cell absorber layers. Development groups exploit the halogenated substituents for subsequent Suzuki–Miyaura cross-coupling, yielding block copolymers that improve charge separation efficiency and environmental photostability in device fabrication. The material’s lot-to-lot homogeneity must meet rigorous electronic-grade controls to support reproducible module performance.

    Industry compliance standards

    • IEC TS 62876-2-1:2017 “Photovoltaic devices – Non-conventional thin-film PV modules”
    • ISO/TS 16085:2019 “Measurement of organic solar cell performance”
    • RoHS Directive 2011/65/EU

    Typical usage ratio

    • 1–4 mol% in co-polymer synthetic batches, direct ratio tailored by resulting molecular weight and target energy bandgap of the finished absorber

    Downstream process integration

    • Acts as a functional monomer/intermediate, entering at the monomer coupling step of polymer synthesis, followed by purification, spin-coating or slot-die application onto processed electrodes during cell assembly

    Final product types

    • Thin-film organic photovoltaic panels
    • Semi-transparent BIPV solar modules
    • Integrated energy-harvesting device components

    3. High-Refractive Index Polymer Manufacturing for Optical Devices

    Manufacturers leverage the unique aromatic backbone and brominated side-chain of this compound in creating specialty polymers exhibiting elevated refractive indices for imaging lenses, waveguides, and micro-optics. The raw material undergoes step-growth polymerization with diacid or dialdehyde comonomers to produce films and molded optics, optimizing light transmission in compact form factors. Tight control over the input molecular structure enables batch reproducibility aligned to optical tolerances.

    Industry compliance standards

    • ISO 8980-3:2022 “Ophthalmic optics - Uncut finished spectacle lenses”
    • ISO 13485:2016 “Medical Devices – Quality Management Systems” (for medical/diagnostic lenses)
    • RoHS and REACH compliance

    Typical usage ratio

    • Introduced at 5–12 wt% depending on required index and optical clarity targets for the polymer matrix—adjusted by end-use thickness and form-factor

    Downstream process integration

    • Charged during the monomer addition or co-polymerization phase, followed by solvent casting, hot-pressing, or precision injection molding for form-shaping

    Final product types

    • Smartphone and camera lenses
    • Micro-optic LED collimators
    • Wearable AR/VR lens elements

    4. Advanced Specialty Coating Material for High-Brightness Displays

    The structural rigidity and functional groups of this molecule offer high performance as a building block for crosslinkable precursors in electronic coatings, particularly protective and barrier layers on touch panels and advanced backplanes. Coating formulation chemists use it to achieve high transparency while enhancing scratch resistance and environmental protection, with strict controls over film thickness and defect density.

    Industry compliance standards

    • IEC 61076-4-110:2023 “Connectors for electronic equipment” (touch panel component requirements)
    • ISO 4582:2017 “Plastics — Determination of changes in color and variations in properties after exposure to daylight under glass, natural weathering or laboratory light sources”
    • RoHS/REACH; ISO 9001

    Typical usage ratio

    • Used at 3–7 phr (parts per hundred resin) in multi-component coating recipes, percentages adjusted based on final coating layer function—mechanical resistance versus optical enhancement layers

    Downstream process integration

    • Added into pre-polymer blend during compounding, then applied via slot-die coating or spray coating onto substrate sheets, followed by controlled thermal or UV crosslinking before device assembly

    Final product types

    • Protective coatings for high-resolution display panels
    • Touch sensor encapsulation layers
    • Anti-reflective and scratch-resistant covers

    5. LED Encapsulant Modifier for Solid-State Lighting

    Material scientists utilize this fluorene-based intermediate as a structural modifier in photostable encapsulant formulation for high-power LEDs, balancing the matrix’s transparency and heat resistance. By incorporating it during pre-polymerization, manufacturers modulate glass transition and crosslink density, enabling encapsulants that minimize yellowing under continuous ultraviolet exposure. This supports the reliability of solid-state luminaires exposed to demanding operating temperatures.

    Industry compliance standards

    • IEC 62471 “Photobiological safety of lamps and lamp systems”
    • ANSI C78.377 “Specifications for the chromaticity of solid-state lighting products”
    • RoHS 2011/65/EU; ISO 14001:2015

    Typical usage ratio

    • Loaded at 0.8–2.5 wt% in silicone or epoxy-based LED encapsulation formulations, adjusted based on encapsulant clarity and UV-stability performance validation

    Downstream process integration

    • Blended into the pre-polymer or resin masterbatch, then introduced prior to deaeration and degassing, followed by precision dispensing onto die-mounted LED chips during encapsulation molding

    Final product types

    • LED lamp encapsulant domes
    • Automotive and appliance LED module potting materials
    • Architectural solid-state lighting systems
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