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Tris(2-Methoxyphenyl)Phosphine

    • Product Name Tris(2-Methoxyphenyl)Phosphine
    • Alias Phosferrox
    • Einecs 238-962-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    681377

    Cas Number 2530-87-2
    Molecular Formula C21H21O3P
    Molecular Weight 352.36
    Appearance White to off-white solid
    Melting Point 58-60 °C
    Solubility Soluble in organic solvents such as chloroform and dichloromethane
    Density 1.19 g/cm³ (estimated)
    Smiles COC1=CC=CC=C1P(C2=CC=CC=C2OC)(C3=CC=CC=C3OC)
    Purity Typically ≥97%
    Synonyms Tris(o-methoxyphenyl)phosphine
    Storage Temperature Store at 2-8 °C

    As an accredited Tris(2-Methoxyphenyl)Phosphine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g Tris(2-Methoxyphenyl)Phosphine is supplied in a sealed amber glass bottle with tamper-evident cap and detailed labeling.
    Shipping Tris(2-Methoxyphenyl)Phosphine is shipped in tightly sealed, chemical-resistant containers, protected from moisture and air. It should be handled as a hazardous material, following local and international transport regulations. Shipping includes clear hazard labeling, safety documentation (SDS), and temperature controls if necessary to ensure stability and safety during transit.
    Storage Tris(2-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 direct sunlight and sources of moisture. Store separately from strong oxidizing agents and acids. Refrigeration or storage at 2–8°C is recommended for prolonged stability.
    Application of Tris(2-Methoxyphenyl)Phosphine

    Applications of Tris(2-Methoxyphenyl)Phosphine in Industrial Manufacturing

    Tris(2-Methoxyphenyl)Phosphine supports complex transformations in specialty chemical industries and advanced material production. We manufacture this organophosphorus compound with precise purity and batch-to-batch consistency, meeting the regulatory and operational standards required by global customers integrating this raw material into innovative downstream formulations. The sections below detail key application areas, including regulatory compliance, formulation practices, industrial process integration, and examples of final product outcomes.

    1. Homogeneous Catalysis for Pharmaceuticals Synthesis

    Pharmaceutical API manufacturers rely on this phosphine as a highly specific ligand in homogeneous transition metal catalyst systems. It plays a critical role in catalytic processes such as Buchwald–Hartwig amination and asymmetric hydrogenation, enabling the efficient formation of C-N and C-C bonds in small-molecule APIs. The ligand’s electronic and steric properties facilitate high selectivity, process repeatability, and impurity control under GMP production.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU EudraLex Volume 4 (GMP Guidelines)
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Relevant local pharmacopoeias (USP, Ph. Eur., JP) as final API standards

    Typical usage ratio

    • Ligand loading ranges from 0.5–3 mol% relative to palladium (or nickel) catalysts, depending on substrate reactivity, desired catalyst turnover number, and impurity profile management.

    Downstream process integration

    • Direct addition to the reaction vessel during the pre-catalyst charging stage; employed in batch or continuous flow reactors; removed from the process stream during downstream purification before API isolation.

    Final product types

    • Small-molecule Active Pharmaceutical Ingredients (APIs)
    • Intermediates for oncology and CNS drugs
    • Chiral pharmaceutical intermediates

    2. Cross-Coupling Reactions in Fine Chemical Manufacturing

    Fine chemical producers utilize this phosphine ligand for critical cross-coupling steps—such as Suzuki-Miyaura and Sonogashira reactions—when manufacturing building blocks for agrochemicals, electronics, and dyes. Its specific structure supports reproducible yields and color stability in multi-step organic syntheses. The controlled reactivity enables downstream operators to meet process safety, traceability, and specification requirements for high-value specialty chemicals.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for chemical manufacturing)
    • REACH (EC No 1907/2006) for chemical substance registration and control in the EU
    • Agrochemical active ingredient regulations (EPA, EC PPP) when used as process intermediate
    • Specific customer quality agreements (QAA/CQAs) requiring batch traceability and residual ligand limits

    Typical usage ratio

    • Usually applied at 1–4 mol% relative to the transition metal catalyst—actual dosage balanced against product purity requirements and process cost control.

    Downstream process integration

    • Dispensed during initial catalyst preparation and solvent charging; utilized in temperature-controlled jacketed reactors; typically removed by silica column filtration or precipitation post-reaction.

    Final product types

    • Biphenyl intermediates for liquid crystal materials
    • Functionalized aromatic compounds for dye manufacturing
    • Aryl halides and boronic acids for electronics chemicals
    • Chemical intermediates for crop protection agents

    3. OLED Material Synthesis in Electronic Chemicals

    Producers of organic optoelectronic intermediates employ this ligand to synthesize emitter and host molecules for OLED panel manufacturing. The material’s steric and electronic influence permits reproducible cross-coupling and C–N bond formations, helping ensure molecular purity, precise emission characteristics, and robust process scalability. Formulators leverage its properties under strictly monitored cleanroom environments to minimize contamination risk in display-grade materials.

    Industry compliance standards

    • IEC 62471 for photobiological safety of lamps and lamp systems (relevant to OLED functional layers)
    • RoHS Directive (EU 2011/65) for restriction of hazardous substances in electrical and electronic equipment
    • Internal process quality SOPs for trace metals and phosphorus residues (OEM customer-driven)

    Typical usage ratio

    • Commonly used at 1–2 mol% for ligand-to-metal ratios, adapted based on fluorophore or host molecule complexity; adjusted to optimize quantum yields and minimize side-product formation.

    Downstream process integration

    • Added during palladium-mediated coupling reactions for polyaromatic synthesis; integrated into glovebox or inert atmosphere workflows; downstream removal by recrystallization and HPLC purification prior to OLED layer fabrication.

    Final product types

    • Emitter molecules for OLED display panels
    • Core intermediates for OLED host materials
    • Functionalized fluorophores for display and lighting applications

    4. Synthesis of Functionalized Ligands for Catalytic Research

    Academic and industrial R&D centers source this chemical as a modular building block for customized ligand development. Its methoxyphenyl framework allows further functionalization, enabling the design and scale-up of innovative ligands for catalytic screening, pilot studies, and material science projects targeting enhanced selectivity in new reactions. Specialized lab and kilo-lab facilities leverage its quality and documented impurity profile to support reproducibility and intellectual property filings.

    Industry compliance standards

    • Internal R&D quality and provenance requirements
    • GLP (Good Laboratory Practice) for traceable compound synthesis in regulated labs
    • ISO/IEC 17025 for accredited laboratory testing and analysis

    Typical usage ratio

    • Application rate varies by synthetic target, typically 1–10 mol% as the parent scaffold in combinatorial synthesis strategies.

    Downstream process integration

    • Used as a primary feedstock for ligand backbone assembly via directed ortho-metallation, cross-coupling, or further phosphine modification; processed in parallel synthesis or flow chemistry set-ups.

    Final product types

    • Custom ligands for transition metal catalysis research
    • Patented ligand libraries for chemical screening
    • Specialty phosphine-based intermediates for academic and pilot-scale studies
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