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2-(4-Bromobiphenyl-4-yl)benzo[b]thiophene

    • Product Name 2-(4-Bromobiphenyl-4-yl)benzo[b]thiophene
    • Alias BBT
    • Einecs NA
    • 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

    934894

    Chemical Name 2-(4-Bromobiphenyl-4-yl)benzo[b]thiophene
    Molecular Formula C20H13BrS
    Cas Number 154204-26-9
    Appearance white to off-white solid
    Melting Point 186-190°C
    Solubility soluble in organic solvents such as dichloromethane and chloroform
    Purity ≥98%
    Storage Conditions store at 2-8°C, protected from light
    Smiles Brc1ccc(cc1)c2ccc(cc2)c3ccc4sccc4c3
    Synonyms 4'-Bromo-[1,1'-biphenyl]-4-ylbenzo[b]thiophene

    As an accredited 2-(4-Bromobiphenyl-4-yl)benzo[b]thiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical 2-(4-Bromobiphenyl-4-yl)benzo[b]thiophene is packaged in a 1-gram amber glass vial with a secure screw cap.
    Shipping **Shipping Description:** 2-(4-Bromobiphenyl-4-yl)benzo[b]thiophene is shipped in a tightly sealed container, protected from light and moisture. It is handled according to standard protocols for organic compounds, with proper labeling, MSDS documentation, and secure packaging to prevent leaks or contamination during transit. Transport complies with all applicable chemical regulations.
    Storage Store **2-(4-Bromobiphenyl-4-yl)benzo[b]thiophene** in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep the container tightly closed and protected from moisture. Store separately from incompatible substances such as strong oxidizing agents. Use appropriate labeling and ensure access is restricted to trained personnel. Always follow safety regulations and institutional guidelines.
    Application of 2-(4-Bromobiphenyl-4-yl)benzo[b]thiophene

    Applications of 2-(4-Bromobiphenyl-4-yl)benzo[b]thiophene in Industrial Manufacturing

    2-(4-Bromobiphenyl-4-yl)benzo[b]thiophene enables high-value molecular innovation across advanced materials, electronics, and specialty organic synthesis. As a specialist producer, we focus on downstream sectors where this intermediate offers strong functional distinctness, integrating securely into existing supply chains that demand high chemical precision and purity. Below, we present verified industrial fields and their matched deployment details.

    1. Organic Electronics: OLED Emitter Material Synthesis

    Downstream OLED manufacturers use this compound as a key intermediate during the synthesis of small-molecule emitter materials for high-performance organic light-emitting diodes. Its biaryl-thiophene framework contributes rigidity and electron-transporting properties critical for efficient device architectures. Material grade and purity significantly affect device stability and emission performance, so production must strictly align with semiconductor and display industry requirements.

    Industry compliance standards

    • IEC 62341 for OLED display devices
    • RoHS Directive (2011/65/EU) on hazardous substances in electronics
    • JEITA quality guidelines for functional organic materials
    • ISO 9001:2015 for production process control

    Typical usage ratio

    • 1–5 mol% as a building block within emitter molecule synthesis; adjusted based on target molecular weight and structure

    Downstream process integration

    • Introduced during Suzuki or Stille coupling steps for construction of polyaromatic emitter backbones, prior to purification and device doping

    Final product types

    • Active emitting layer materials for AMOLED display panels
    • Emitter molecules for OLED lighting modules
    • Custom organic semiconductors for research applications

    2. Advanced Photovoltaic Material Precursors

    Photovoltaic material developers leverage this compound to assemble small-molecule or polymer donor/acceptor units in next-generation organic solar cell layers. Its extended conjugation enhances photo-absorption and stability, improving conversion efficiency. Accuracy during the coupling reactions and purification is crucial to avoid side-product formation, which can limit photovoltaic performance and reproducibility.

    Industry compliance standards

    • IEC 61215 for thin-film photovoltaic performance
    • REACH Registration (EC 1907/2006) as applicable for raw chemical management within the EU
    • UL 1703 for photovoltaic module safety
    • ISO 14001:2015 for environmental management throughout the product life cycle

    Typical usage ratio

    • 0.5–3.0 mol% as a structural motif in donor-acceptor copolymer synthesis; determined by electronic design targets

    Downstream process integration

    • Used as a halogenated cross-coupling partner in the main chain polymerization or in precursor stages of small-molecule synthesis before film casting

    Final product types

    • Photoactive layers in organic photovoltaic (OPV) modules
    • Donor–acceptor blend materials for flexible solar panels
    • Polymer solar cell research samples and prototypes

    3. Specialty Liquid Crystal Intermediate

    Manufacturers in the display liquid crystal sector employ this compound to synthesize advanced mesogenic monomers with rigid core units favorable for high birefringence and thermal stability. The biphenyl-thiophene scaffold introduced at controlled stages determines phase behavior and viscosity, which are critical for fast-switching liquid crystal displays.

    Industry compliance standards

    • IEC 61747 for liquid crystal device product quality
    • ISO 9001:2015 for production traceability and QC
    • Specific customer and panel maker acceptance criteria (e.g., Samsung, LG Display)

    Typical usage ratio

    • 2–6 mol% as feedstock for core mesogen units; proportion optimized to balance birefringence and viscosity for the application

    Downstream process integration

    • Micro-reactor scale batch introduction during monomer core unit synthesis via palladium-catalyzed coupling, followed by purification for subsequent LC formulation blending

    Final product types

    • Nematic liquid crystal mixtures for TFT-LCD panels
    • Specialty LC mixtures for fast-response and high-contrast display technologies
    • Prototype high-stability LC materials for advanced visualization

    4. Pharmaceutical Intermediate for Heterocyclic Drug Candidates

    A select group of pharmaceutical R&D labs use this compound to construct complex, rigid heterocyclic cores within the early-stage development of kinase inhibitors and receptor modulator scaffolds. The compound enters at the coupling stage to introduce a unique biphenyl-thiophene element into drug-like molecules, where reversibility and selectivity are critical. High-purity, trace metal control, and full documentation are mandatory.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP <232> Elemental Impurities—Limits
    • FDA 21 CFR Part 211 for manufacturing practice
    • EU GMP for Investigational Medicinal Products

    Typical usage ratio

    • 0.5–2.0 molar equiv. as a coupling partner in heterocycle formation, based on stoichiometric demands of the synthetic route

    Downstream process integration

    • Engaged at Suzuki, Buchwald–Hartwig, or Stille cross-coupling stage for scaffold construction; followed by isolation, purification, and further derivatization

    Final product types

    • Advanced pharmaceutical intermediates (preclinical research)
    • Lead candidate molecules for targeted solid tumor therapies
    • Heterocyclic small molecule library entries for structure–activity relationship studies

    5. High-Performance Organic Field-Effect Transistor (OFET) Material Intermediate

    Developers of next-generation OFETs utilize this raw material in the synthesis of conjugated backbones that enable charge-carrier mobility and environmental stability in organic transistors. Its incorporation in the main structural framework delivers planar geometry and precise functionalization points, dictating thin-film microstructure and device consistency. Stringent analytical documentation and reproducibility are essential for electronics applications.

    Industry compliance standards

    • SEMATECH guidelines for organic electronics reliability
    • IEC 62899 (Printed electronics standards)
    • RoHS for restriction of hazardous substances
    • ISO 17025 for analytical laboratory method validation (QC step)

    Typical usage ratio

    • 1–4 mol% in the monomer feed; modified according to desired OFET channel properties and end-device specifications

    Downstream process integration

    • Used during key cross-coupling polymerization stages to develop the backbone prior to thin-film deposition step

    Final product types

    • P-type and ambipolar organic field-effect transistors
    • Flexible display driving circuitry modules
    • Analytical OFET sensor chips
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