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2,5-Dibromo-3-Octylthiophene

    • Product Name 2,5-Dibromo-3-Octylthiophene
    • Alias 3-Octyl-2,5-dibromothiophene
    • Einecs 410-790-4
    • 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

    274742

    Cas Number 312616-04-9
    Molecular Formula C12H18Br2S
    Molecular Weight 370.15
    Appearance Yellow to orange solid
    Purity Typically ≥ 95%
    Solubility Soluble in organic solvents such as chloroform and dichloromethane
    Smiles CCCCCCCCc1c(Br)cs(Br)c1
    Inchi InChI=1S/C12H18Br2S/c1-2-3-4-5-6-7-8-10-9-12(14)15-11(10)13/h9H,2-8H2,1H3
    Storage Condition Store at room temperature, protected from light and moisture

    As an accredited 2,5-Dibromo-3-Octylthiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical comes in a 5-gram amber glass vial, tightly sealed, with a white security cap and clear labeling for identification.
    Shipping **Shipping Description:** 2,5-Dibromo-3-Octylthiophene is shipped in securely sealed, clearly labeled containers to prevent leakage or contamination. It is protected from light, heat, and moisture, and transported in compliance with chemical safety regulations. Appropriate documentation, including the Safety Data Sheet (SDS), accompanies each shipment to ensure safe handling and delivery.
    Storage 2,5-Dibromo-3-octylthiophene should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and moisture. Keep the container tightly closed and protected from light. Store separately from strong oxidizing agents and acids. Use appropriate chemical storage containers, typically amber glass bottles. Always follow local regulations and the manufacturer’s guidelines for safe chemical storage.
    Application of 2,5-Dibromo-3-Octylthiophene

    Applications of 2,5-Dibromo-3-Octylthiophene in Industrial Manufacturing

    2,5-Dibromo-3-Octylthiophene serves as a specialty intermediate in the development of advanced organic materials, playing a crucial role in performance-critical niche markets. Below, we detail its practical integration in downstream industrial applications where quality control, formulation expertise, and compliance with international standards are essential.

    1. Organic Photovoltaic (OPV) Materials

    Manufacturers of organic solar cells source 2,5-Dibromo-3-Octylthiophene as an essential building block for polymer donor and acceptor materials in OPV active layers. This monomer offers increased solubility and controlled electronic properties for high-mobility copolymers, directly influencing power conversion efficiencies in flexible photovoltaic modules. Its use demands strict quality protocols, consistent batch purity, and formal process documentation from polymerization through device encapsulation.

    Industry compliance standards

    • IEC 61215: Crystalline silicon terrestrial photovoltaic (PV) modules – Design qualification and type approval
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 9001: Quality management systems for photovoltaic supply chains
    • REACH (EC 1907/2006): Registration, Evaluation, Authorisation and Restriction of Chemicals

    Typical usage ratio

    • 5–15 mol% of total monomer input in copolymer synthesis; the proportion adjusts based on target bandgap, molecular weight, and device structure

    Downstream process integration

    • Engages in Stille or Suzuki coupling during conjugated polymer backbone synthesis, followed by precipitation, purification, and solution blending into thin-film ink formulations for roll-to-roll printing of PV layers

    Final product types

    • Flexible photovoltaic sheets for building-integrated photovoltaics (BIPV)
    • Printed organic solar panels for wearable electronics and off-grid power
    • Lightweight modules for portable and emergency solar chargers

    2. Organic Thin Film Transistor (OTFT) Arrays

    This speciality thiophene derivative acts as a functional monomer for synthesizing high-mobility semiconducting polymers used in large-area OTFT backplanes. By controlling its feed composition and ensuring tightly regulated residual bromine content, device makers achieve uniform film morphology, necessary for stable switching characteristics in active-matrix displays and sensor arrays. Consistent batch traceability and documentary control throughout conversion and blend preparation are mandatory for reliable electrical performance.

    Industry compliance standards

    • JEITA ED-5001: Standard for organic semiconductor raw materials evaluation
    • ISO 14001: Environmental management for electronic materials processing
    • IEC 62047-3: Mechanical engineering of thin film devices
    • RoHS Directive 2011/65/EU

    Typical usage ratio

    • 8–13 mol% as precursor in donor-acceptor copolymer backbone construction; variation depends on required carrier mobility and ink viscosity for printing

    Downstream process integration

    • Introduced in controlled-polymerization phases, followed by multi-stage purification, blending with high-boiling-point solvents, and slot-die or inkjet deposition onto patterned substrates prior to encapsulation

    Final product types

    • Backplane circuits for E-paper displays
    • Flexible sensors for industrial and biomedical diagnostics
    • Transparent logic circuits for next-generation touch panels

    3. Hole Transport Layer (HTL) Components for OLEDs

    The compound provides a backbone monomer for developing solution-processable HTL polymers, which enable low-voltage, high-luminance OLED devices. Reliability, reproducible reactivity during coupling reactions, and strict exclusion of heavy-metal contaminants are vital for display manufacturers integrating these materials into mass production. Low impurity profiles directly impact operational lifetime in commercial OLED lighting and display panels.

    Industry compliance standards

    • IEC 62341: OLED panels performance and safety requirements
    • ISO 14644: Cleanroom standards for optoelectronics production
    • RoHS Directive 2011/65/EU
    • REACH compliance registration for supply chain transparency

    Typical usage ratio

    • 10–18 mol% in HTL copolymer synthesis; optimized according to desired film thickness, glass transition temperature, and device voltage requirements

    Downstream process integration

    • Utilized in cross-coupling polymerizations, followed by solution casting onto transparent anodes in continuous web coating or inkjet processes; subsequent annealing and vacuum treatment before OLED stack assembly

    Final product types

    • High-brightness OLED lighting panels
    • Flexible AMOLED display modules
    • Wearable and automotive-grade organic light-emitting displays

    4. Precursor for π-Conjugated Molecular Wires in Nanoelectronics

    Research-intensive and commercial labs utilize 2,5-Dibromo-3-Octylthiophene to synthesize molecular wires that facilitate charge and spin transport in molecular-scale logic circuits and memory devices. Stringent documentation during precursor transformation and meticulous records for chain length distribution remain essential for advanced device prototyping and IP-sensitive manufacturing, ensuring reliability in percolation pathways and device switching uniformity.

    Industry compliance standards

    • ISO/TS 80004-8: Nanotechnologies – Terms and definitions for nano-enabled electrical materials
    • IPC-6012: Qualification and performance specification for rigid printed boards (applied for characterization standards)
    • IEC 62607-4-4: Measurement of electrical properties for nanomaterials

    Typical usage ratio

    • 12–20 mol% in oligomer chains; ratio adjusted according to target wire length and electronic property tuning

    Downstream process integration

    • Enters as starting unit in iterative coupling–deprotection polymerizations, undergoes end-group modification, then incorporated into Langmuir–Blodgett films or spin-coated onto nanolithography-prepared substrates

    Final product types

    • Molecular interconnects for nanoelectronic testbeds
    • Experimental memory elements for neuromorphic computing devices
    • Functionalized substrates for quantum computing research
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