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HS Code |
836059 |
| Cas Number | 937659-57-9 |
| Molecular Formula | C14H22Br2S |
| Molecular Weight | 394.20 |
| Appearance | Off-white to light yellow solid |
| Solubility | Soluble in organic solvents such as chloroform and dichloromethane |
| Purity | Typically >98% |
| Smiles | CCCCCCCCCCc1[s]c(Br)cc1Br |
| Inchi | InChI=1S/C14H22Br2S/c1-2-3-4-5-6-7-8-9-10-12-11-13(15)17-14(12)16/h11H,2-10H2,1H3 |
| Storage Temperature | Store at 2-8°C |
As an accredited 2,5-Dibromo-3-Decylthiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 10-gram bottle of 2,5-Dibromo-3-Decylthiophene comes in a sealed amber glass vial with a screw cap and hazard labeling. |
| Shipping | 2,5-Dibromo-3-Decylthiophene is shipped in sealed, airtight containers to prevent contamination and moisture uptake. The packaging complies with relevant chemical transport regulations, including UN classification if applicable. Containers are clearly labeled with hazard information and handled according to safety guidelines. Temperature control is recommended to maintain product stability during transit. |
| Storage | 2,5-Dibromo-3-Decylthiophene should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect the chemical from light and moisture. Proper labeling is essential, and access should be restricted to trained personnel following standard laboratory safety procedures. |
Applications of 2,5-Dibromo-3-Decylthiophene in Industrial ManufacturingAs a specialized manufacturer of 2,5-Dibromo-3-Decylthiophene, we directly support key innovative sectors where advanced thiophene derivatives drive materials development. Below, we outline established downstream applications that our customers implement globally, each application reflecting actual industrial manufacturing needs, compliant processing, and differentiated formulation practices. 1. Organic Photovoltaic (OPV) Active Layer MaterialPhotovoltaic module producers utilize this thiophene derivative as a monomeric building block for low-bandgap conjugated polymers in organic solar cell active layers. Its electron-rich structure and tailored alkyl chain enable processability in solvent-based coating lines, while the dibromo groups facilitate polymer chain construction via Stille or Suzuki coupling chemistry. Manufacturers select this compound to produce photoactive layers balancing light absorption and charge mobility for flexible solar devices. Industry compliance standards
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2. Organic Field-Effect Transistor (OFET) Semiconductor LayerProducers of printed electronics and flexible display backplanes rely on our thiophene derivative as a high-purity intermediate for synthesizing π-conjugated polymers and small molecules. These are subsequently used in the active semiconductor layer of OFETs. The molecular structure, featuring decyl chains and bromine substituents, promotes solubility and controlled self-assembly, resulting in stable film formation on roll-to-roll printed circuits. Industry compliance standards
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3. Polymer Light Emitting Diode (PLED) Host Polymer SynthesisManufacturers producing specialty polymers for use in emissive layers of PLEDs employ this compound for its dual bromination, which facilitates site-selective cross-coupling during the production of well-defined copolymers. The long alkyl chain enhances polymer solubility, film uniformity, and emission quantum yield, supporting commercial-grade device reproducibility in both rigid and flexible display architectures. Industry compliance standards
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4. Organic Photodetector (OPD) Active Polymer PrecursorIn the specialty imaging sector, manufacturers leverage this raw material for constructing polymer backbones in near-infrared (NIR) or visible light photodetector arrays. The molecular flexibility and controlled bromination are critical for tailoring absorption edge and charge transport properties demanded by industrial sensing arrays and large-area detectors. Industry compliance standards
Typical usage ratio
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