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HS Code |
843819 |
| Chemical Name | Tris(4-Methoxyphenyl)Phosphine |
| Cas Number | 855-38-9 |
| Molecular Formula | C21H21O3P |
| Molecular Weight | 352.36 |
| Appearance | white to off-white powder |
| Melting Point | 98-101°C |
| Solubility | soluble in organic solvents such as dichloromethane, toluene, and THF |
| Boiling Point | decomposes before boiling |
| Density | 1.16 g/cm3 |
| Smiles | COc1ccc(P(c2ccc(OC)cc2)c3ccc(OC)cc3)cc1 |
| Inchi | InChI=1S/C21H21O3P/c1-23-19-13-7-16(8-14-19)25(17-9-15-20(24-2)11-5-18(21(15)24-2)23-1)12-6-10-21(23-1,24-2)22/h7-14H,1-6H3 |
| Refractive Index | n20/D 1.597 |
| Storage Conditions | Store under inert atmosphere in a cool, dry place |
| Uses | Ligand for homogeneous catalysis |
As an accredited Tris(4-Methoxyphenyl)Phosphine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g Tris(4-Methoxyphenyl)Phosphine is packaged in a sealed amber glass bottle with a secure screw cap for protection. |
| Shipping | Tris(4-Methoxyphenyl)phosphine is shipped in tightly sealed containers under an inert atmosphere to prevent oxidation. It should be kept away from moisture, heat, and direct sunlight. Shipping complies with local and international regulations for chemical transport, ensuring safety and stability during transit. Appropriate hazard labeling is applied to all packaging. |
| Storage | Tris(4-Methoxyphenyl)phosphine should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry place, away from moisture, heat, and direct sunlight. Store separately from strong oxidizing agents and acids. Refrigeration (2–8°C) is recommended for prolonged storage to maintain compound stability. |
Applications of Tris(4-Methoxyphenyl)Phosphine in Industrial ManufacturingTris(4-Methoxyphenyl)Phosphine is a specialty organophosphorus compound produced to support advanced synthesis in selected sectors. As a manufacturer, we supply this phosphine ligand to downstream users that require strict adherence to formulation, reaction reliability, and regulatory integrity. Below are the principal industrial applications with detailed usage background. 1. Palladium-Catalyzed Cross Coupling in Pharmaceutical SynthesisMany major pharmaceutical companies depend on our material as a ligand of choice for applications in Suzuki, Heck, and Buchwald–Hartwig cross-coupling reactions. Its strong electron-donating character and steric bulk enhance selectivity and yield for complex active pharmaceutical ingredient (API) intermediates. Production plants use this ligand to support efficient arylation and amination, minimizing byproducts. Compliance, handling, and purification steps follow international pharmaceutical requirements at each stage of the synthesis route. Industry compliance standards
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2. OLED Material Manufacturing for Display TechnologiesMajor electronic material manufacturers use our phosphine derivative in the synthesis of organometallic complexes necessary for blue and green OLED emitters. The compound acts as an ancillary ligand, tuning emission wavelength and device efficiency. Its defined purity assures batch-to-batch consistency required by downstream device assembly. Process lines run under cleanroom standards and trace organometallic carryover undergoes strict control at every production node. Industry compliance standards
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3. Ligand Synthesis for Homogeneous Catalysis in Fine ChemicalsLeading fine chemicals producers employ this raw material for the preparation of custom phosphine ligand systems, especially where high electron density and meta-directing effects improve reaction rates and product distribution. These applications appear in chiral ligand pools, precious metal catalysts, and process intermediates that withstand harsh reaction conditions. Quality control is crucial to prevent trace contaminant interference in catalytic cycles. Industry compliance standards
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4. Synthesis of Electronic-Grade Organophosphorus IntermediatesProducers of semiconductors and specialty resins rely on this compound as a building block for electronic-grade phosphine derivatives, focusing on purity thresholds below 99.9%. The methoxy substitution pattern allows for further transformation to fine-tune reactivity in photoresist and dielectric manufacturing workflows. Customers demand detailed lot traceability and analytical backup for every shipment in accordance with downstream device safety requirements. Industry compliance standards
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5. Production of Ligand Precursors for Agricultural ChemistryFormulators in the crop protection sector utilize this phosphine derivative in the multistep synthesis of tailored ligand scaffolds. These ligands enable the formation of key metal complexes that facilitate targeted fungicide activation and controlled release mechanisms. Strict traceability and impurity controls must be maintained to comply with regulatory toxicology and environmental exposure limits throughout the formulation and packaging lines. Industry compliance standards
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