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HS Code |
598345 |
| Iupac Name | 9-[3-(1-Dibenzofuran)phenyl]-7,9-dihydro-7-phenyl-indolo[2,3-B]carbazole |
| Molecular Formula | C42H26N2O |
| Appearance | Solid |
| Color | Off-white to pale yellow |
| Solubility | Soluble in common organic solvents (e.g., chloroform, dichloromethane) |
| Cas Number | 2205594-59-4 |
| Chemical Class | Indolocarbazole derivative |
| Application | Organic electronics, OLED materials |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store in a cool, dry place, away from light |
| Smiles | c1ccc(cc1)N3c4ccccc4n2cc5c6ccccc6c7c(cccc7n25)c8cccc9ccoc9c8c3 |
As an accredited 9-[3-(1-Dibenzofuran)phenyl]-7,9-dihydro-7-phenyl-indolo[2,3-B]carbazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 1-gram amber glass vial with a secure screw cap, labeled with compound name and batch information. |
| Shipping | This chemical, **9-[3-(1-Dibenzofuran)phenyl]-7,9-dihydro-7-phenyl-indolo[2,3-B]carbazole**, is securely packaged in sealed containers, protected from light and moisture. It is shipped via tracked, regulated transport in compliance with chemical safety guidelines, ensuring stability and integrity during transit. Proper labeling and documentation accompany every shipment. |
| Storage | 9-[3-(1-Dibenzofuran)phenyl]-7,9-dihydro-7-phenyl-indolo[2,3-B]carbazole should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Avoid exposure to strong oxidizing agents and extreme temperatures. Proper labeling and handling in accordance with relevant safety guidelines is essential to maintain chemical stability and prevent degradation. |
Applications of 9-[3-(1-Dibenzofuran)phenyl]-7,9-dihydro-7-phenyl-indolo[2,3-B]carbazole in Industrial ManufacturingAs a specialized producer of advanced heterocyclic aromatic compounds, we supply 9-[3-(1-Dibenzofuran)phenyl]-7,9-dihydro-7-phenyl-indolo[2,3-B]carbazole for critical applications across key sectors. Below, we detail its main industrial routes, covering application standards, recommended ratios, required integration steps, and downstream finished goods for each sector. 1. Organic Light Emitting Diode (OLED) Emissive Layer MaterialsOLED manufacturers use this compound as an advanced emitter or dopant in multilayer device structures for display and lighting technologies. Its rigid heterocyclic structure supports high thermal stability, color purity, and charge transport when used in deep-blue emitting layers. Industrial users evaluate device stability, threshold voltage, and color coordinates under pilot and full-scale integration to meet long-term performance guarantees in consumer and professional electronics. Industry compliance standards
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2. Hole Transport Material in Organic ElectronicsElectronic device producers formulate this compound as a hole-transport intermediary in organic field-effect transistors (OFETs) and organic photovoltaic (OPV) architectures, leveraging its extended conjugation and balanced HOMO-LUMO orbital energies to support efficient charge carrier mobility. These devices require precise formulation to optimize interface compatibility with adjacent polymeric or small-molecule layers under cleanroom and industrial-scale coating environments. Industry compliance standards
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3. Sensitizers in Lanthanide-Based Luminescent DevicesProducers of phosphor-based lighting and analytic devices incorporate this compound as an energy transfer sensitizer in organic-lanthanide hybrid systems. It supports efficient excitation transfer, particularly in blue and ultraviolet-excited europium and terbium complexes, for enhanced device quantum yields. Correct matrix matching and process control enable stable complexation and reproducible emission characteristics required for high-value downstream markets. Industry compliance standards
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4. Blue Host Matrix Components for High-Energy Emission DevicesMaterials engineers and device formulators introduce this compound as a blue host in multilayer organic electroluminescent architectures. Its structural rigidity and energy alignment fit the demands for high-energy, deep-blue device fabrication, particularly for achieving long operational lifespans and strict chromaticity requirements in professional-grade devices. Production lines optimize matrix compatibility and minimize excimer formation during pilot and commercial-scale runs. Industry compliance standards
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5. Advanced Photorefractive Polymer SystemsManufacturers of photorefractive polymers rely on this material to adjust trap depth and charge carrier mobility in high-sensitivity holographic recording media. Its persistent charge transfer and deep-level trapping support prolonged refractive index modulation, enhancing volumetric data storage and dynamic imaging system performance. Accurate blending and process uniformity are essential in roll-to-roll coating and film lamination operations. Industry compliance standards
Typical usage ratio
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