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HS Code |
641179 |
| Chemical Name | 9-Phenanthracenylboronic Acid |
| Molecular Formula | C14H11BO2 |
| Molecular Weight | 222.05 g/mol |
| Cas Number | 851276-94-8 |
| Appearance | White to off-white solid |
| Melting Point | 250-254 °C |
| Purity | Typically >98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Storage Conditions | Store in a cool, dry place, keep container tightly closed |
| Smiles | B(C1=CC2=CC=CC=C2C3=CC=CC=C13)(O)O |
As an accredited 9-Phenanthracenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 1-gram quantity of 9-Phenanthracenylboronic Acid is supplied in a sealed amber glass vial with a secure screw cap. |
| Shipping | 9-Phenanthracenylboronic Acid is shipped in tightly sealed containers, protected from moisture and light. It is handled as a stable solid under standard conditions. Shipping complies with all chemical safety regulations, and packaging ensures minimal exposure during transit. Appropriate labeling and documentation accompany each shipment for secure and compliant delivery. |
| Storage | 9-Phenanthracenylboronic acid should be stored in a cool, dry, well-ventilated area, away from moisture, direct sunlight, and incompatible substances such as strong oxidizers. The container must be tightly sealed to prevent hydrolysis and contamination. Store the chemical at room temperature or as specified by the supplier, and always follow standard laboratory safety and chemical storage protocols. |
Applications of 9-Phenanthracenylboronic Acid in Industrial ManufacturingAs the original manufacturer of 9-Phenanthracenylboronic Acid, we focus on supporting advanced chemical synthesis applications. This compound’s unique aromatic boronic structure enables it to serve key roles across several sectors, most notably in fine chemicals, OLED intermediates, pharmaceutical research, and specialty organic materials. Each area listed below represents an established downstream industry path where large-scale consumers employ this raw material in specific, process-dependent roles under strict regulatory and quality frameworks. 1. OLED Material Synthesis for Flat Panel DisplaysLeading display manufacturers rely on 9-Phenanthracenylboronic Acid as a pivotal coupling component in the design and scale-up of blue light-emitting materials for high-performance OLED screens. The compound enters Suzuki–Miyaura cross-coupling reactions to construct rigid, extended π-conjugated systems required for emitter molecules exhibiting deep blue chromaticity, thermal stability, and high quantum efficiency. Downstream partners integrate the material within their internal development cycles for OLED display panels conforming to both television and mobile device requirements. Industry compliance standards
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2. Pharmaceutical Intermediates for API Synthesis9-Phenanthracenylboronic acid serves as a boron-source building block in the modular construction of complex polycyclic aromatic intermediates used for oncology and advanced central nervous system (CNS) active pharmaceutical ingredient research pipelines. Customers apply it in pharmaceutical facilities specializing in protected boronate derivatives for further diversification, en route to patented drug candidates under GMP conditions. Industry compliance standards
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3. Specialty Organic Semiconductors and Sensor MaterialsProducers of organic semiconductors and photonic sensor substrates incorporate 9-Phenanthracenylboronic Acid when designing conjugated frameworks that offer improved charge carrier mobility and environmental robustness. This compound is introduced during solution-processable conjugated polymer or small-molecule synthesis that targets specific photoelectronic device layers with demanding performance criteria. Industry compliance standards
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4. Dye and Fluorescent Probe Chromophore ConstructionChemical manufacturers and research labs utilize 9-Phenanthracenylboronic Acid as a key coupling partner when assembling rigid organic chromophores for analytical dyes and near-UV/visible fluorescent probes. Its unique polycyclic scaffold enables the preparation of highly emissive, photostable derivatives useful in life sciences and materials diagnostics, where strict control of purity and batch reproducibility is essential. Industry compliance standards
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