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2,5-Diiodothiophene

    • Product Name 2,5-Diiodothiophene
    • Alias 2,5-Diiodo-2,5-dihydrothiophene
    • Einecs 'EINECS 611-206-9'
    • 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

    553819

    Chemical Name 2,5-Diiodothiophene
    Molecular Formula C4H2I2S
    Cas Number 63861-62-9
    Appearance Pale yellow to tan solid
    Melting Point 68-71°C
    Boiling Point None (decomposes)
    Density 2.88 g/cm3
    Solubility Soluble in organic solvents (e.g., dichloromethane, chloroform)
    Smiles C1=C(SC=C1I)I
    Purity Typically >97%
    Synonyms Thiophene, 2,5-diiodo-

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

    Packing & Storage
    Packing 2,5-Diiodothiophene is supplied in a 5g amber glass bottle with a sealed cap, labeled with hazard and identification details.
    Shipping 2,5-Diiodothiophene is shipped in tightly sealed, chemical-resistant containers to prevent moisture or light exposure. It is classified as a hazardous material and must be handled and transported according to local and international regulations, including appropriate labeling and documentation. Ensure the container is upright, secure during transit, and stored in a cool, dry place.
    Storage 2,5-Diiodothiophene should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from light and moisture. Use appropriate chemically resistant containers and clearly label them. Store in accordance with local regulations for hazardous chemicals.
    Application of 2,5-Diiodothiophene

    Applications of 2,5-Diiodothiophene in Industrial Manufacturing

    As a direct manufacturer specializing in halogenated thiophene derivatives, we supply 2,5-Diiodothiophene to leading global industries that demand precise functionalization for advanced material synthesis. Below, we outline the core sectors where this material plays a critical enabling role, detailing specific compliance standards, operational formulations, integration points, and representative end uses for each downstream process channel.

    1. Organic Semiconductor Synthesis for Flexible Electronics

    2,5-Diiodothiophene serves as a fundamental coupling unit in the advancement of π-conjugated polymers for organic thin-film transistors (OTFTs) and organic photovoltaic cells. Its symmetrical diiodo pattern enables regioregular polymer growth through Stille or Suzuki cross-coupling, supporting high charge-carrier mobility required in flexible displays and wearable electronics. Major device manufacturers integrate this compound at precise stages to build low-bandgap, solution-processable semiconducting materials for emerging electronics platforms.

    Industry compliance standards

    • IEC 62899 (Printed Electronics – Quality and Performance)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances for electronic materials)
    • REACH Regulation (EC 1907/2006) concerning chemical registration and restrictions
    • IPC-4101/126 for base materials in flexible circuits

    Typical usage ratio

    • Typically 2–8 mol% in monomer feed, adjusted based on the desired molecular weight and polymer backbone design for photovoltaic or transistor applications.

    Downstream process integration

    • Incorporated as the halide donor during Suzuki, Stille, or direct arylation step-growth polymerizations under inert atmosphere following monomer purification, directly preceding polymer workup, and thin-film deposition.

    Final product types

    • Flexible organic thin-film transistors (OTFTs)
    • Bulk heterojunction solar cells
    • Printed RFID tags
    • Wearable sensor arrays

    2. Specialty Intermediate for Liquid Crystal Precursor Synthesis

    Specialty chemical companies employ 2,5-Diiodothiophene as a core building block when designing halogenated heteroaryl units in the synthesis of liquid crystal intermediates, which subsequently enhance the dielectric and refractive properties of advanced display chemicals. The fine control over substitution patterns enabled by its unique structure is key to achieving specific mesogenic behaviors, facilitating the production of high-performance display panels.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for Chemical Intermediates)
    • EN IEC 60384-14 (Electronic Components–LC safety for display chemicals)
    • Chinese National Standard GB 19855 (for display materials manufacturing)
    • JIS C 8715 (Japan Display Material Quality)

    Typical usage ratio

    • Ranging from 0.5–3.5 wt% in target mesogen assembly reaction stages, tuned depending on the specific side-chain or core extension requirements of the LC precursor route.

    Downstream process integration

    • Engaged in the iodination or cross-coupling step after initial thiophene purification, introduced prior to etherification or cyclization, yielding crucial LC functional groups for downstream distillation and blending.

    Final product types

    • Twisted nematic (TN) and vertical alignment (VA) LC mixtures
    • In-plane switching (IPS) LC blends
    • TFT-LCD active matrix precursor chemicals
    • Specialty LC materials for smart windows

    3. Advanced Dye Synthesis for Photosensitizers in DSSC Production

    Producers of dye-sensitized solar cell (DSSC) components utilize 2,5-Diiodothiophene as a selectively reactive moiety in the elaboration of thiophene-based organic dyes, where the precise installation of electron-donating or accepting units determines photon absorption and conversion efficiency. It enters the modular dye assembly for customized absorption profile engineering essential to boosting DSSC device longevity and performance.

    Industry compliance standards

    • UL 1703 (Standard for Flat-Plate Photovoltaic Modules and Panels)
    • IEC 61215 (Crystalline silicon terrestrial photovoltaic modules)
    • SGS PV Module Quality Testing (global PV material QC requirement)
    • TÜV SÜD Photovoltaic Component Certification

    Typical usage ratio

    • Used at 0.3–1.5 equivalents relative to the core skeleton in the dye framework, with the dosing determined by desired sensitizer π-system extent and solubility characteristics.

    Downstream process integration

    • Activated during key halogen-metal exchange reactions, followed by cross-coupling with donor groups, prior to dye purification and deposition into the photoanode assembly process.

    Final product types

    • Organic dye-sensitizers for DSSCs
    • Hybrid thin-film photovoltaic coatings
    • Semi-transparent BIPV modules
    • Photosensitizing agents for analytical chemistry

    4. Conductive Polymer Additive in Printed Circuit Fabrication

    In printed electronics and circuit patterning, 2,5-Diiodothiophene enables the synthesis of polythiophene derivatives required to achieve fine-tuned conductivity, flexibility, and work function alignment in printed wiring applications. This compound’s distinctive substitution supports block copolymer formation for advanced ink formulations required in next-generation circuit construction.

    Industry compliance standards

    • IPC-2221 (Generic Standard on Printed Board Design)
    • UL 796 (Printed-Wiring Boards Standard)
    • IEC 60194 (Printed Board Design Terminology)
    • ISO 14001 (Environmental management for electronics manufacturing)

    Typical usage ratio

    • Generally 1.2–4.5 wt% in polymerization feedstocks; manufacturers adjust ratio based on ink viscosity, target surface resistance, and patterning precision.

    Downstream process integration

    • Introduced after solvent and catalyst pre-mixing into the monomer stage; undergoes oxidative polymerization and subsequent ink formulation prior to inkjet or screen-print application on circuit substrates.

    Final product types

    • Conductive polythiophene inks
    • Printed flexible circuit boards
    • Wearable conductive traces
    • Low-voltage heater films for de-icing electronics
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