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Atomfair 3,4-Dihexylthiophene C16H28S

Description 3,4-Dihexylthiophene (CAS No. 122107-04-4) is a high-purity organic compound with the molecular formula C16H28S , widely utilized in advanced materials research and specialty chemical synthesis. This compound features a thiophene core symmetrically substituted with two hexyl chains at the 3- and 4-positions, offering unique electronic and solubility properties ideal for conjugated polymer systems and organic semiconductors. With a molecular weight of 252.46 g/mol, it is supplied as a clear to pale yellow liquid or low-melting solid, ensuring compatibility with solution-processing techniques. Rigorous QC protocols guarantee ??95% purity (HPLC/GC), with trace metals ??10 ppm, making it suitable for sensitive applications…

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Description

Description

3,4-Dihexylthiophene (CAS No. 122107-04-4) is a high-purity organic compound with the molecular formula C16H28S, widely utilized in advanced materials research and specialty chemical synthesis. This compound features a thiophene core symmetrically substituted with two hexyl chains at the 3- and 4-positions, offering unique electronic and solubility properties ideal for conjugated polymer systems and organic semiconductors. With a molecular weight of 252.46 g/mol, it is supplied as a clear to pale yellow liquid or low-melting solid, ensuring compatibility with solution-processing techniques. Rigorous QC protocols guarantee ??95% purity (HPLC/GC), with trace metals ??10 ppm, making it suitable for sensitive applications in optoelectronics and nanotechnology. Store under inert gas at 2-8??C to maintain stability.

  • CAS No: 122107-04-4
  • Molecular Formula: C16H28S
  • Molecular Weight: 252.5
  • Exact Mass: 252.19117207
  • Monoisotopic Mass: 252.19117207
  • IUPAC Name: 3,4-dihexylthiophene
  • SMILES: CCCCCCC1=CSC=C1CCCCCC
  • Synonyms: 3,4-dihexylthiophene, 122107-04-4, DTXSID50571972, DTXCID70522744, 878-466-7

Application

3,4-Dihexylthiophene serves as a critical building block for conducting polymers in organic field-effect transistors (OFETs) and photovoltaic devices, where its extended conjugation enhances charge carrier mobility. The hexyl side chains improve solubility for spin-coating and inkjet printing of organic electronic thin films. Researchers also employ it as a monomer for synthesizing regioregular polythiophenes with tailored bandgaps. In material science, it functions as a precursor for liquid crystalline materials and supramolecular assemblies.

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