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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 | 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. |
Applications of 2,5-Diiodothiophene in Industrial ManufacturingAs 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 Electronics2,5-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
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2. Specialty Intermediate for Liquid Crystal Precursor SynthesisSpecialty 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
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3. Advanced Dye Synthesis for Photosensitizers in DSSC ProductionProducers 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
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4. Conductive Polymer Additive in Printed Circuit FabricationIn 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
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