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HS Code |
531333 |
| Name | 2,2':5',2''-Terthiophene |
| Cas Number | 2973-07-9 |
| Molecular Formula | C12H8S3 |
| Molecular Weight | 248.39 |
| Appearance | Yellow powder |
| Melting Point | 155-159°C |
| Density | 1.45 g/cm3 (estimated) |
| Solubility In Water | Insoluble |
| Smiles | C1=CC(=CS1)C2=CC=CS2C3=CC=CS3 |
| Inchi | InChI=1S/C12H8S3/c1-3-9(13-5-1)11-7-12-8-2-4-10(14-12)6-8-11/h1-8H |
| Purity | Typically ≥98% |
| Storage Conditions | Store at room temperature, away from light |
| Synonyms | Terthiophene |
As an accredited 2,2':5',2''-Terthiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,2':5',2''-Terthiophene is supplied in a 5g amber glass bottle, tightly sealed, and labeled with chemical details and hazard warnings. |
| Shipping | **2,2':5',2''-Terthiophene** is securely packaged in airtight, chemical-resistant containers to prevent contamination or degradation. It is shipped in accordance with applicable regulations for organic chemicals, typically under temperature-controlled and labeled conditions, with accompanying safety data sheets and handling instructions to ensure safe and compliant delivery. |
| Storage | 2,2′:5′,2′′-Terthiophene should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. It should be kept in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent degradation. Protect the chemical from light and moisture to ensure its stability. |
Applications of 2,2':5',2''-Terthiophene in Industrial Manufacturing2,2':5',2''-Terthiophene is a highly conjugated thiophene-based compound utilized in advanced organic synthesis and material applications. Its unique electronic structure allows downstream industries to develop high-performance materials in sectors such as electronics, photovoltaic devices, sensors, electroluminescent devices, and specialty coatings. 1. Organic Photovoltaic (OPV) Cell FabricationManufacturers in the solar energy sector select this material as a building block for synthesizing π-conjugated polymers used in active layers of organic photovoltaic cells. It functions as a donor segment in bulk heterojunction architectures, where fine-tuning of molecular weight and regioregularity during polymerization ensures efficient charge transport and light harvesting. Compounding adjusts the blend with fullerene acceptors or alternative small molecule acceptors, demanding strict batch reproducibility and purity control to meet cell efficiency targets. The downstream process includes solution blending, slot-die coating, and thermal annealing for precise layer morphology control, directly impacting power conversion rates and device longevity. Industry compliance standards
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2. Organic Field-Effect Transistors (OFETs)The electronics industry employs 2,2':5',2''-Terthiophene derivatives for solution-processed organic semiconductors serving as the active layer in OFET devices. Its highly planar conjugated system enables efficient π-π stacking, which improves charge carrier mobility in patterned transistor channels. Engineers design formulations based on device architecture, matrix compatibility, and voltage threshold requirements. Downstream, spin-coating or inkjet printing produce thin, defect-free films essential for reliable switching characteristics. Quality assurance includes electronic property screening and spectroscopic verification of incorporated terthiophene motifs prior to integration in final device stacks. Industry compliance standards
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3. Organic Light Emitting Diodes (OLEDs)Terthiophene and its derivatives act as luminescent components in the emissive or as hole transporting layers for OLED displays and lighting panels. Downstream producers incorporate it in conjugated polymer backbones or as discrete dopants, tuning emission wavelength and quantum efficiency. Material experts monitor the molecular weight distribution and impurity profile to avoid quenching centers and non-uniform emission. Device assembly involves vacuum thermal evaporation or inkjet printing under inert atmosphere followed by encapsulation processes to maximize device lifetime and consistent brightness. Industry compliance standards
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4. Chemical Sensors and Biosensor Transducer LayersIn analytical and bioanalytical device manufacturing, terthiophene units boost sensitivity and selectivity in chemiresistive, amperometric, and potentiometric sensor films. Downstream R&D teams synthesize functionalized derivatives for selective molecular recognition, leveraging the molecule’s redox-active nature and ease of post-polymerization modification. Formulation protocols control surface coverage and functional group density to align with required detection limits and analyte response range. Integration with microfabricated electrodes is tightly controlled to meet reproducibility and shelf-life standards. Industry compliance standards
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5. High-Performance Antistatic and Conductive CoatingsSpecialty coating manufacturers leverage the conjugated properties of terthiophene-based oligomers for high-transparency antistatic or conductive coatings. Coating formulators blend the compound with matrix resins or co-polymers to achieve the required surface resistivity and optical clarity, especially for sensitive electronic display panels, touch screens, and packaging materials. Downstream application involves direct coating by spray, roll-to-roll, or slot-die processes, with in-line resistivity checks and curing step optimization to ensure uniform film morphology and strong substrate adhesion. Industry compliance standards
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