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1,2-Bis(Dipentafluorophenylphosphino)Ethane

    • Product Name 1,2-Bis(Dipentafluorophenylphosphino)Ethane
    • Alias dppf-F
    • Einecs 814-111-6
    • 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

    934517

    Chemical Name 1,2-Bis(Dipentafluorophenylphosphino)Ethane
    Molecular Formula C28F20P2C2H4
    Cas Number 168244-63-1
    Appearance White to off-white solid
    Purity Typically >98%
    Melting Point 126-130°C
    Solubility Soluble in common organic solvents such as dichloromethane and tetrahydrofuran
    Storage Conditions Store under inert atmosphere, in a cool and dry place
    Synonyms dppf-F10, 1,2-bis[(pentafluorophenyl)diphosphino]ethane
    Smiles C1=CC(=C(C(=C1)F)F)P(CCP(C2=C(C(=C(C(=C2)F)F)F)F)C3=C(C(=C(C(=C3)F)F)F)F)C4=C(C(=C(C(=C4)F)F)F)F
    Application Ligand in homogeneous catalysis
    Boiling Point Decomposes before boiling

    As an accredited 1,2-Bis(Dipentafluorophenylphosphino)Ethane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for **1,2-Bis(Dipentafluorophenylphosphino)Ethane, 5 grams**, consists of a sealed amber glass bottle within a protective cardboard box.
    Shipping 1,2-Bis(Dipentafluorophenylphosphino)ethane is shipped in tightly sealed containers under an inert atmosphere to prevent moisture and air exposure. The chemical is packaged in accordance with hazardous materials regulations, with clear labeling and cushioning to prevent breakage. Temperature control may be applied if required by the material safety data sheet (MSDS).
    Storage **1,2-Bis(Dipentafluorophenylphosphino)ethane** should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Keep it in a cool, dry place, away from direct sunlight, heat sources, and incompatible substances like strong oxidizers. Refrigeration at 2–8 °C is recommended for long-term stability. Handle inside a glovebox if possible.
    Application of 1,2-Bis(Dipentafluorophenylphosphino)Ethane

    Applications of 1,2-Bis(Dipentafluorophenylphosphino)Ethane in Industrial Manufacturing

    1,2-Bis(Dipentafluorophenylphosphino)ethane serves as a niche ligand in advanced organometallic and catalytic applications. Owing to its highly electron-withdrawing nature and unique steric properties, it is crucial for the formulation and enhancement of high-value catalysts, especially in fine chemical manufacturing, electronic chemical production, and pharmaceutical synthesis. As a direct manufacturer, we supply this raw material based on strict process controls and proven compatibility with leading industrial applications.

    1. Homogeneous Catalytic Synthesis for Fine Chemicals

    Leading fine chemical producers employ this compound for the ligand structure in palladium and nickel-based catalysts targeted at cross-coupling reactions, such as Suzuki, Heck, and Sonogashira couplings. The compound’s strong electron-withdrawing perfluorinated aryl groups enable increased catalyst activity and selectivity, particularly when high chemoselectivity and resistance to air/moisture degradation are required during gram-to-ton scale processes.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • IUPAC technical standards for organometallic reagents
    • ISO 9001:2015 certified production systems
    • Process-specific customer QC protocols for fine chemical intermediates

    Typical usage ratio

    • 0.5–5 mol% relative to metal catalyst complex
    • Adjustments according to substrate load and reaction conditions; higher ratios for moisture-prone or low-concentration processes

    Downstream process integration

    • Ligand pre-dissolved and complexed with transition metal salts during catalyst synthesis step
    • Fine chemical batch reactors employ the prepared catalyst-ligand complex for subsequent coupling reactions
    • Solvent filtering and catalyst recovery protocols rely on the ligand’s stability

    Final product types

    • Biaryl intermediates for agrochemical synthesis
    • Functionalized heterocycles for electronics
    • Monomers and polymer building blocks for specialty resins

    2. Pharmaceutical Active Ingredient Intermediate Synthesis

    Key pharmaceutical manufacturers select this phosphine ligand to form highly active palladium or platinum catalyst systems for application in C–C bond formation, hydrogenation, or asymmetric synthesis. The structural profile of the compound enhances reaction specificity, controlling side product formation in regulated, multi-step pharmaceutical intermediate routes where trace metal and ligand residues must meet stringent pharmacopeia thresholds.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/NF and Ph. Eur. limits on metal and organic impurities
    • 21 CFR Part 210/211 for cGMP processing
    • Customer-specific impurity profiles and elemental analysis certifications

    Typical usage ratio

    • 0.2–2.0 mol% of total substrate input per reaction step
    • Ratio defined by desired reaction conversion and purification protocol

    Downstream process integration

    • Batch or flow reactor charging during catalyst preparation, immediately prior to substrate introduction
    • Integration with automated reactor dispensing systems under nitrogen or argon atmosphere
    • Removal of spent ligand during downstream API crystallization and purification

    Final product types

    • Advanced pharmaceutical intermediates (e.g., aryl amines, biaryls)
    • Precursor compounds for anti-cancer APIs
    • Selective hydrogenation products for chiral drug manufacturing

    3. Functional Materials & Electronic Chemicals Manufacturing

    Producers of high-purity functional organic materials use this ligand in the synthesis of custom organometallic complexes for incorporation in semiconductors, OLED materials, and advanced photoresists. The high fluorine content improves solubility and volatility control, enabling repeatable electronic-grade formulations that demand ultra-low impurity levels and highly controlled molecular architectures.

    Industry compliance standards

    • SEMI C3 and C93 standards for electronic chemical purity
    • IECQ QC 080000 for hazardous substance management
    • ISO 14001:2015 for environmental management in electronics production
    • Customer-specific electronic chemical material specifications

    Typical usage ratio

    • 0.3–1.5 mol% based on transition metal center concentration
    • Ratio optimized for molecular weight control and target physical property in final material

    Downstream process integration

    • Complexation with metal precursor salts in solvent-phase synthesis under dry-box conditions
    • Solution-processing for thin-film or crystallization step of electronic chemical manufacturing
    • Integration into vacuum deposition or spin-coating processes

    Final product types

    • Palladium/phosphine-based pre-catalysts for cross-coupling in OLED synthesis
    • Controlled-molecular-weight conductive polymers
    • Photoinitiators and photoresist developer components

    4. High-Performance Polymerization Catalyst Preparation

    Specialty polymer manufacturers apply this ligand during the formulation of nickel and palladium-based catalyst systems for advanced polymerization processes, such as controlled/living polymerization. The ligand’s electron-deficient profile impacts macromolecular architecture, molecular weight distribution, and minimizes branching in specialty polymers used in high-specification engineering plastics, coatings, and membranes.

    Industry compliance standards

    • ISO 9001:2015 quality system for polymer additives
    • ROHS Directive 2011/65/EU on restricted substances
    • Customer-specific catalytic residue analysis protocols
    • Internal process validation for critical performance parameters

    Typical usage ratio

    • 1–4 mol% relative to catalytic metal content
    • Tuning guided by monomer type, desired polymer dispersity, and process temperature

    Downstream process integration

    • Addition during in situ preparation of metal catalyst complex in batch or continuous polymerization units
    • Direct dosing with bulk monomer feed, followed by homogenization and temperature ramping
    • Multiple-stage catalyst activation and stabilization during pre-polymerization

    Final product types

    • Narrow-dispersity engineering thermoplastics
    • Functionalized block copolymers for specialty membranes
    • Polyolefin grades with modified electronic properties for wire, cable, and device coatings
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