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Tri(1-Naphthyl)Phosphine

    • Product Name Tri(1-Naphthyl)Phosphine
    • Alias TNPhos
    • Einecs 246-384-0
    • 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
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    Specifications

    HS Code

    633745

    Chemical Name Tri(1-naphthyl)phosphine
    Chemical Formula C30H21P
    Molecular Weight 412.46 g/mol
    Cas Number 1312-74-3
    Appearance White to off-white solid
    Melting Point 204-208 °C
    Boiling Point Decomposes before boiling
    Solubility Soluble in organic solvents such as chloroform and toluene
    Density 1.22 g/cm³
    Refractive Index n20/D 1.697
    Storage Conditions Store under inert atmosphere, protect from moisture and light
    Purity Typically ≥98%
    Synonyms Tris(1-naphthyl)phosphine
    Smiles c1ccc2c(c1)cccc2P(c3cccc4c3cccc4)c5cccc6c5cccc6
    Inchikey KWMVDJFHWFWGSX-UHFFFAOYSA-N

    As an accredited Tri(1-Naphthyl)Phosphine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g Tri(1-Naphthyl)Phosphine is supplied in an amber glass bottle with a secure, tamper-evident cap and hazard labeling.
    Shipping Tri(1-Naphthyl)Phosphine is shipped in tightly sealed containers under an inert atmosphere, such as nitrogen or argon, to prevent oxidation and moisture exposure. Packages comply with chemical safety regulations, are clearly labeled, and cushioned to avoid breakage during transit. Storage and transport typically require cool, dry conditions away from incompatible substances.
    Storage Tri(1-Naphthyl)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 sources of moisture, light, and incompatible substances such as strong oxidizing agents. Ideally, store it in a desiccator or glove box for optimal stability and safety.
    Application of Tri(1-Naphthyl)Phosphine

    Applications of Tri(1-Naphthyl)Phosphine in Industrial Manufacturing

    Tri(1-Naphthyl)Phosphine serves as a functional intermediate in several demanding downstream manufacturing environments, particularly where advanced organic electronics, fine chemicals, and performance materials require exclusive phosphine ligand properties. As the original manufacturer, we deliver consistent, tightly specified material to support advanced process needs, giving downstream producers the confidence to meet system requirements and market expectations. Below are key application areas where this material plays a critical technical role.

    1. OLED Materials Synthesis

    OLED producers rely on tri(1-naphthyl)phosphine as an electronic ligand for iridium- and platinum-based phosphorescent dopant precursors. Its bulky aromatic structure provides enhanced solubility and improved photophysical characteristics in the synthesis of high-performance emitter complexes. The material is integrated into ligand exchange or direct complexation reactions for color-tuning and brightness optimization in display and lighting panels.

    Industry compliance standards

    • ISO 9001:2015 certified production sites
    • IEC 62341 organic electroluminescent device standards
    • RoHS Directive (2011/65/EU) regarding restricted substances in electronics
    • REACH (EC) No 1907/2006 substance registration

    Typical usage ratio

    • 0.5–3.0 molar equivalents per metal center, adjusting by tuning dopant photoluminescent yield and device emission requirements

    Downstream process integration

    • Directly added during iridium or platinum complex precursor formation; usually introduced during the ligand coordination step under inert atmosphere in anhydrous solvents

    Final product types

    • Red, green, and blue phosphorescent OLED emitter materials
    • High-brightness OLED display subpixel dopants
    • OLED lighting panel emitters

    2. Homogeneous Catalysis Ligand in Fine Chemical Synthesis

    Leading fine chemical manufacturers specify tri(1-naphthyl)phosphine as an ancillary ligand for palladium- and nickel-catalyzed coupling reactions, including Suzuki and Stille processes. The aromaticity and steric profile facilitate tailored selectivity and improve catalytic turnover frequencies versus standard triphenylphosphine derivatives, supporting the scalable synthesis of performance aryl compounds and specialty building blocks.

    Industry compliance standards

    • ISO 9001:2015–certified batch tracking and quality control
    • GMP (Good Manufacturing Practice; ICH Q7) for pharmaceutical intermediates
    • Chemicals manufactured in accordance with EPA TSCA regulations for industrial chemicals
    • European Pharmacopoeia 11.0 for relevant pharmaceutical intermediates

    Typical usage ratio

    • 5–15 mol% relative to metal catalyst, variable based on substrate reactivity and desired turnover number in scale-up

    Downstream process integration

    • Charged during initial catalyst preformation or in situ complex generation prior to substrate metering in batch or flow reactors

    Final product types

    • Biaryl fine chemicals
    • Active pharmaceutical ingredient (API) intermediates
    • Agrochemical base structures

    3. Precursor Ligand for Metal-Organic Frameworks (MOFs)

    Advanced materials companies select tri(1-naphthyl)phosphine as a precision ligand in the bottom-up assembly of metal-organic frameworks with defined pore architectures. It promotes unique Naphthyl-substituted phosphine node environments, supporting high-affinity sorbent and separation materials production for gas storage or purification markets. The ligand is vital in hydrothermal or solvothermal MOF synthesis protocols.

    Industry compliance standards

    • ISO 14001:2015 for environmental management during specialty material production
    • OECD Guidelines for the Testing of Chemicals (for safety and performance studies)
    • REACH (EC) No 1907/2006 registration and extended safety data sheet communication
    • ASTM D3574 for structural testing of porous materials where applicable

    Typical usage ratio

    • Ligand-to-metal ratios typically between 1.0–2.0, set by the targeted framework topology; excess sometimes used to drive complete coordination

    Downstream process integration

    • Introduced at the precursor formulation stage; mixed with metal salts under controlled temperature and pressure in closed reactors for MOF growth

    Final product types

    • Adsorptive MOF granules for gas separation
    • Storage materials for hydrogen or carbon dioxide capture
    • Catalytic MOF specimens for chemical conversion processes

    4. Electronic-Grade Coordination Compound Manufacture

    Semiconductor and photonic industries use tri(1-naphthyl)phosphine in the production of tailored metal coordination compounds that serve as processable precursors for functional thin films and nano-structured coatings. Its aromatic-based structure supports vapor-phase deposition or solution-processable strategies, where consistent ligand-metal assembly is key for precise layer morphology and electronic performance.

    Industry compliance standards

    • SEMATECH semiconductor material guidelines
    • IEC 60747 discrete semiconductor device standards
    • UL 94 V-0 for flammability where electronic encapsulation is involved
    • RoHS compliance for restricted substance management

    Typical usage ratio

    • Stoichiometry typically controlled to 1:1 to 1:3 phosphine to metal center, fine-tuned for volatilization and film-forming requirements

    Downstream process integration

    • Fed into precursor solution blending or gas-phase precursor delivery prior to CVD or ALD (chemical/vapor deposition) unit operations

    Final product types

    • Organometallic precursors for microelectronic thin films
    • Functional coatings for photovoltaic or optoelectronic layers
    • Specialty compounds for next-generation transistor fabrication
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