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1,1'-Bis(Diisopropylphosphino)Ferrocene

    • Product Name 1,1'-Bis(Diisopropylphosphino)Ferrocene
    • Alias dippf
    • Einecs 629-611-8
    • 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

    494505

    Iupac Name 1,1'-Bis(diisopropylphosphino)ferrocene
    Cas Number 84692-07-1
    Molecular Formula C26H46FeP2
    Molar Mass 476.44 g/mol
    Appearance Orange solid
    Melting Point 108-110 °C
    Solubility Soluble in common organic solvents (e.g., toluene, THF, CH2Cl2)
    Density 1.16 g/cm³ (approximate)
    Air Sensitivity Air sensitive
    Chemical Structure Ferrocene backbone with two diisopropylphosphino groups at 1,1' positions
    Abbreviation dippf
    Application Ligand in homogeneous catalysis
    Synonyms Diisopropylphosferrocene

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

    Packing & Storage
    Packing 1,1'-Bis(Diisopropylphosphino)Ferrocene is packaged in a 5g amber glass vial with a secure screw cap, nitrogen-purged for protection.
    Shipping 1,1'-Bis(Diisopropylphosphino)Ferrocene is shipped in tightly sealed containers under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. It should be handled using chemical-resistant gloves and stored in a cool, dry place away from moisture and air. Transport complies with relevant regulations for sensitive organometallic compounds.
    Storage 1,1'-Bis(Diisopropylphosphino)ferrocene should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation and degradation. Store it in a cool, dry place, away from moisture and direct sunlight. It should be kept separate from strong oxidizers and acids and handled using appropriate personal protective equipment inside a well-ventilated fume hood.
    Application of 1,1'-Bis(Diisopropylphosphino)Ferrocene

    Applications of 1,1'-Bis(Diisopropylphosphino)Ferrocene in Industrial Manufacturing

    1,1'-Bis(Diisopropylphosphino)Ferrocene serves as an advanced phosphine ligand enabling multiple value-added transformations in organometallic catalysis, with significant adoption across several high-value manufacturing sectors. As the direct manufacturer, we provide this specialty material for downstream partners requiring stringent consistency and performance in demanding catalytic systems, strictly supporting each application’s compliance, process viability, and finished product performance requirements.

    1. Homogeneous Catalysts for Olefin Polymerization

    This compound functions as a bidentate ligand for metal complexes that catalyze olefin coordination polymerization. Its steric and electronic properties facilitate controlled polymer microstructures, enhancing product uniformity and consistency in specialized grades of polyolefins used for critical applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Manufacturing
    • ASTM D4101 (Polypropylene Materials Specification)
    • Relevant EU REACH registration and evaluation for downstream polymer use
    • FDA 21 CFR 177.1520 (For polymers indirectly contacting food, where required)

    Typical usage ratio

    • 0.1–1.5 mol% relative to transition metal centers in the catalyst system, adjusted based on comonomer identity and target polymer density/structure

    Downstream process integration

    • Ligand introduced in the initial catalyst complex synthesis stage, then immobilized or fed as part of the catalyst precursor solution for continuous or batch olefin polymerization reactors

    Final product types

    • Specialty polypropylene copolymers for automotive components
    • High-performance polyethylene elastomers for wire & cable insulation
    • Controlled tacticity polyolefins used in medical device manufacturing

    2. Cross-Coupling Catalysts for Fine Chemical Synthesis

    Chemical manufacturers leverage this ligand to form active palladium or nickel complexes that enable challenging C-C and C-N bond-forming reactions, crucial to multi-step organic intermediate production. Adoption of this ligand allows downstream users to streamline steps, enhance selectivity, and reduce byproducts in GMP-compliant fine chemical manufacturing plants.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Vol. IV Part II for API Synthesis
    • ISO 14001:2015 (Environmental considerations in fine chemical facilities)
    • Consent in accordance with national emissions controls for processing cross-coupling reagents

    Typical usage ratio

    • 0.5–3.0 mol% relative to metal center, tailored by substrate reactivity and scale (gram to multi-metric ton production)

    Downstream process integration

    • Ligand complexed with Pd or Ni salt in situ just prior to, or at, the start of aryl halide coupling reactions in multi-purpose stirred tank reactors or continuous flow units

    Final product types

    • Key pharmaceutical intermediates (e.g., substituted biphenyl derivatives, arylamines)
    • Agricultural active ingredients (herbicide/pesticide core scaffolds)
    • Customized performance chemicals for electronics industry (OLED precursors, intermediates for liquid crystal materials)

    3. Catalysts for Asymmetric Hydrogenation in Active Pharma Ingredient Production

    Process chemists utilize the ferrocene phosphine ligand structure to control enantioselectivity during chiral hydrogenation, particularly for intermediates bound for APIs that require absolute enantiopurity. By enabling high turnover numbers and stereochemical integrity, it helps pharmaceutical facilities reliably meet regulatory targets for optically pure drug substances.

    Industry compliance standards

    • USP General Chapter <467> Residual Solvents (with reference to catalyst residues)
    • ICH Q11 Development and Manufacture of Drug Substances
    • FDA cGMP (21 CFR Part 210 and 211) for pharmaceutical ingredient synthesis
    • Ph. Eur. 5.10 for control of catalysts and processing aids in APIs

    Typical usage ratio

    • 0.1–1.0 mol% relative to metal (e.g., rhodium or ruthenium) in chiral hydrogenation complexes, refined according to substrate loading and required optical purity

    Downstream process integration

    • Phosphine ligand dissolved and charged to hydrogenation vessel together with pre-catalyst, activated under hydrogen; employed in both batch and fed-batch hydrogenations of prochiral substrates

    Final product types

    • Nonracemic pharmaceutical intermediates for antihypertensive, antiviral, or anticancer APIs
    • Enantiopure building blocks integrated into specialty generics
    • Chiral auxiliaries for peptidomimetic drug synthesis

    4. Ligand Design for Advanced Materials Synthesis (Precursors for Functional Polymers)

    Materials R&D institutes and manufacturing plants employ 1,1'-Bis(Diisopropylphosphino)Ferrocene in preparing transition metal catalysts for controlled polymerization required in next-generation functional materials. Control over steric profile and electron-donating characteristics allows for fine-tuning new catalyst systems for producing polymers and copolymers with designed morphology and performance specifications.

    Industry compliance standards

    • ISO 14001:2015 for Responsible Materials Manufacturing
    • Global Automotive OEM Specifications (for specialty polymers in vehicle interiors)
    • RoHS Directive 2011/65/EU (when used in polymers for electronics)
    • Chinese GB Standards for Functional Polymer Materials

    Typical usage ratio

    • 0.2–1.2 mol% as ligand to metal center, modulated per the target polymer architecture and process scale

    Downstream process integration

    • Ligand used in the synthesis of custom metal complexes for controlled radical or ring-opening polymerization; introduced during catalyst precursor batch formulation prior to large-scale polymerization

    Final product types

    • Copolymers for high-performance membranes (e.g., in fuel cells)
    • Specialty block copolymers for medical device housings
    • Conductive polymers for flexible electronics and sensor components
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