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Dichlorotris(Triphenylphosphine)Ruthenium(II)

    • Product Name Dichlorotris(Triphenylphosphine)Ruthenium(II)
    • Alias Ru(PPh3)3Cl2
    • Einecs 221-209-7
    • 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

    531513

    Chemical Name Dichlorotris(Triphenylphosphine)Ruthenium(II)
    Chemical Formula RuCl2(PPh3)3
    Molecular Weight 1020.92 g/mol
    Appearance Dark purple to black crystalline solid
    Cas Number 15529-49-4
    Melting Point 218-222 °C (decomposes)
    Solubility Slightly soluble in dichloromethane, chloroform, toluene, insoluble in water
    Storage Conditions Store under inert atmosphere, in a cool, dry place
    Sensitivity Air and moisture sensitive
    Coordination Geometry Octahedral
    Ru Oxidation State +2
    Hazard Statements Harmful if swallowed, causes skin and eye irritation

    As an accredited Dichlorotris(Triphenylphosphine)Ruthenium(II) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram amber glass bottle, sealed with a red cap, inner PTFE liner, and labeled with hazard and storage information.
    Shipping Dichlorotris(Triphenylphosphine)Ruthenium(II) should be shipped in tightly sealed containers, protected from moisture and light. It is typically transported as a solid under ambient temperature. Handle as a hazardous chemical; follow all local, national, and international regulations for shipping transition metal complexes, including clear labelling and documentation for safe handling.
    Storage Dichlorotris(Triphenylphosphine)Ruthenium(II) should be stored in a tightly sealed container under inert atmosphere, such as nitrogen or argon, to prevent oxidation or moisture absorption. Keep the container in a cool, dry place, away from light, heat sources, and incompatible materials like strong oxidizers. Properly label the container and store it in a chemical storage cabinet designated for transition metal complexes.
    Application of Dichlorotris(Triphenylphosphine)Ruthenium(II)

    Applications of Dichlorotris(Triphenylphosphine)Ruthenium(II) in Industrial Manufacturing

    Dichlorotris(Triphenylphosphine)Ruthenium(II) serves as a high-value catalyst in targeted chemical manufacturing sectors where advanced homogeneous catalysis, predictable selectivity, and stringent quality traceability define downstream requirements. Below, we map out in detail its primary industrial applications, highlighting sector-specific regulatory standards, formula integration protocols, process touchpoints, and final output categories as practiced by leading manufacturers worldwide.

    1. Fine Chemical Hydrogenation Catalysis

    Major producers of value-added fine chemicals employ this ruthenium complex in homogeneous hydrogenation steps to reduce aromatic, unsaturated or functionalized compounds. Owing to its predictable activity and selectivity, it fits core reduction phases where throughput, minimal residual metals, and compliance to analytical standards carry critical weight. This application demands close monitoring of ligand leaching and trace impurities, with usage rates and integration adjusted based on both substrate type and final purity objectives.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management Systems
    • ICH Q3D Guideline for Elemental Impurities (if materials are pharmaceutical intermediates)
    • Specific corporate internal specifications for homogeneous catalysis control

    Typical usage ratio

    • 0.05–0.5 mol% relative to substrate, adjusted by substrate structure, reaction scale-up kinetics, and target impurity profiles

    Downstream process integration

    • Added to batch or continuous stirred-tank reactor together with substrates and solvents at hydrogenation stage prior to downstream purification or separation

    Final product types

    • Reduced amines and alcohols
    • Hydrogenated specialty aromatics
    • Custom intermediates for agrochemical and pharmaceutical industries
    • Chiral building blocks for advanced organic synthesis

    2. Olefin Metathesis Catalysis in Polymer Intermediates Manufacturing

    Manufacturers of specialty polymer intermediates, such as functionalized olefins and cyclic compounds, integrate this ruthenium catalyst for olefin metathesis reactions, including ring-closing, cross-metathesis, and enyne metathesis. The precise activity and thermal stability of the complex allow for the production of advanced monomers and diene derivatives used further down in high-performance elastomer and plastic materials. Such syntheses often follow strictly documented batch-process protocols and require handling under controlled temperature and atmosphere to meet downstream processing targets.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for chemical production
    • Good Manufacturing Practice (cGMP) where materials target the medical device or regulated packaging sectors
    • OECD Guidelines for chemical intermediates if applicable
    • Corporate quality control standards focused on trace metals in polymers

    Typical usage ratio

    • 0.01–0.2 mol% relative to total substrate; adjusted downward for high-activity transformations and upward for sterically demanding substrates

    Downstream process integration

    • Charged to inerted reactors with monomer or diene substrates during metathesis step, prior to monomer isolation or workup

    Final product types

    • Functionalized polymer precursors
    • Cyclic olefin monomers
    • Specialty diene compounds for synthetic rubber production
    • Advanced cross-linked resins

    3. Pharmaceutical API Intermediate Synthesis

    Producers of complex pharmaceutical intermediates choose this ruthenium reagent for catalytic hydrogenation and selective reduction in multi-stage synthesis, especially where control of enantioselectivity or chemo-selectivity is essential to support downstream API manufacture. The process requires thorough metal trace analysis, adherence to pharmacopoeial impurity limits, and documentation for regulatory filings. The action plan for addition, residual removal, and critical quality assurance remains procedure-driven and batch-specific per final use authorization.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • United States Pharmacopoeia (USP) Elemental Impurities <232> and <233>
    • European Pharmacopoeia 5.20: Elemental Impurities
    • 21 CFR Part 211 for process controls

    Typical usage ratio

    • 0.01–0.1 mol% per transformation, tuned according to stage yield requirements and allowable residual catalyst as defined by target market MDD (maximum daily dose) for the end API

    Downstream process integration

    • Added during specific reduction or isomerization steps in GMP suites, followed by downstream crystallization and repeated purification steps designed for catalyst removal

    Final product types

    • Chiral API intermediates
    • Key reduced or isomerized intermediates for antihypertensive, antiviral, or CNS-active drugs
    • Non-commodity specialty building blocks for finished drug synthesis

    4. Specialty Fragrance and Aroma Compound Production

    Manufacturers of high-grade aroma chemicals utilize this ruthenium complex as a selective hydrogenation catalyst in the transformation of unsaturated aldehydes or ketones into valuable fragrance components. This step enables synthesis of odor-stable alcohols and intermediates at high purity, with process adaptation to meet precise flavor and fragrance regulatory limits. Usage depends on the substrate, allowable catalyst residuals, and the need for consistent olfactory output, with ongoing monitoring throughout batch production cycles.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • ISO 9001-certified ingredient manufacturing protocols
    • EU Regulation (EC) No 1334/2008 on Flavourings
    • FEMA GRAS guidelines for food-contact aroma chemicals

    Typical usage ratio

    • 0.02–0.1 mol% based on individual substrate reactivity and customer olfactory stability validation

    Downstream process integration

    • Integrated into batch reactors with controlled H2 addition; post-reactor workup includes liquid/liquid extraction, activated carbon filtration, and GC headspace analysis for fragrance profiling

    Final product types

    • Pheromone and muscone analogues
    • High-purity fragrance alcohols
    • Odorant intermediates employed in perfumery and flavor blend design

    5. Academic and Industrial R&D Catalyst Screening

    In both corporate and institutional research environments, this ruthenium compound is an established benchmark catalyst for mechanistic studies, new ligand evaluation, and preparative-scale synthesis of rare organometallic complexes. Research-scale integration permits wide variation in additive level and handling nuance, closely tracked for lab-grade documentation and compliance with project-specific safety and waste management rules. Typically, each screened process aligns with documented experimental parameters rather than commercial SOPs, promoting peer-reviewed reproducibility.

    Industry compliance standards

    • Institutional safety requirements (e.g., OSHA Laboratory Standard)
    • Responsible Care protocols for academic chemical handling
    • Material Transfer Agreements (MTAs) for multi-site industrial collaboration
    • Internal research chemical risk assessments adhering to international lab standards

    Typical usage ratio

    • 0.01–1 mol% or as per experimental protocol, determined by pathway screening and catalyst activity benchmarks

    Downstream process integration

    • Introduced in scale-out or discovery-stage reactors at pre-optimization; tracked through analytical, isolation or crystallization endpoints for both process development and mechanistic evaluation

    Final product types

    • Reference compounds for catalyst benchmarking
    • Screened ligand complexes
    • Organoruthenium reference standards for publication or patent use
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