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Ytterbium(III) Trifluoromethanesulfonate Hydrate

    • Product Name Ytterbium(III) Trifluoromethanesulfonate Hydrate
    • Alias Yb(OTf)3·xH2O
    • Einecs 287-665-4
    • 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

    369084

    Chemical Name Ytterbium(III) Trifluoromethanesulfonate Hydrate
    Chemical Formula Yb(CF3SO3)3 · xH2O
    Molecular Weight 728.16 g/mol (anhydrous basis)
    Appearance White to off-white solid
    Solubility In Water Soluble
    Melting Point Decomposes before melting
    Cas Number 96493-21-1
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Purity Typically ≥99%
    Coordination Number Usually 8 or 9 for Yb(III) complexes

    As an accredited Ytterbium(III) Trifluoromethanesulfonate Hydrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed 10g amber glass bottle labeled "Ytterbium(III) Trifluoromethanesulfonate Hydrate," moisture-protected, with hazard symbols and product details.
    Shipping Ytterbium(III) Trifluoromethanesulfonate Hydrate is shipped in tightly sealed containers, protected from moisture and air. Packages comply with chemical transport regulations and are labeled appropriately. The compound is kept in a cool, dry place during transit. Handling requires appropriate safety precautions to avoid exposure or contamination.
    Storage Ytterbium(III) trifluoromethanesulfonate hydrate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong acids and bases. Protect it from light and sources of ignition. Store under an inert atmosphere if sensitive to air or humidity, and clearly label the container with appropriate hazard information.
    Application of Ytterbium(III) Trifluoromethanesulfonate Hydrate

    Applications of Ytterbium(III) Trifluoromethanesulfonate Hydrate in Industrial Manufacturing

    Ytterbium(III) Trifluoromethanesulfonate Hydrate serves as a highly specialized catalyst and functional additive in advanced chemical processing. We supply this material to sectors that demand tight process control, reliable batch uniformity, and compliance with stringent industry standards. Below, we highlight key downstream application areas and the parameters relevant for industrial use.

    1. Fine Organic Synthesis – Lewis Acid Catalysis

    In the fine chemicals sector, researchers and production facilities use Yb(OTf)3 as a Lewis acid catalyst for promoting selective Friedel-Crafts alkylations, acylations, and various cyclization reactions. Its water-tolerant nature suits conditions where other Lewis acids decompose, and allows efficient catalyst recovery. Typical operations involve multi-step synthesis of advanced pharmaceutical intermediates or specialty agrochemical actives.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • FDA 21 CFR Part 211 (if used in pharma synthesis chain)
    • REACH regulation (EC 1907/2006) registration for import and downstream use in Europe
    • IPEC-PQG GMP guidelines for excipients (when used upstream of pharma APIs)

    Typical usage ratio

    • 0.5 to 5 mol% relative to substrate, dependent on substrate reactivity, batch size, and purification protocol; higher loadings apply for less reactive systems.

    Downstream process integration

    • Introduced at the main reaction stage as a homogeneous catalyst under inert atmosphere; often recovered by aqueous extraction and recycled.

    Final product types

    • Pharmaceutical intermediates containing heterocyclic scaffolds
    • Functionalized aromatic building blocks
    • Custom specialty agrochemicals
    • Fine chemical intermediates for dye and pigment manufacturing

    2. Polymer Chemistry – Cationic Ring-Opening Polymerization

    Manufacturers use Yb(OTf)3 as a cationic initiator for ring-opening polymerizations of cyclic ethers and lactones to produce specialty polyethers and biodegradable polyesters. The material offers strong control over molecular weight distribution and end-group functionality, under mild temperature protocols. This enables the production of polymers for advanced materials and medical device applications.

    Industry compliance standards

    • ISO 13485:2016 for medical-grade polymer production
    • USP Class VI biological reactivity for downstream medical devices
    • REACH-compliant monomer sourcing
    • EU Regulation (EC) No 1935/2004 for materials in contact with food (when applicable)

    Typical usage ratio

    • 0.1 to 2 mol% relative to monomer; optimized to balance molecular weight target and catalyst removal feasibility

    Downstream process integration

    • Charged with monomer and co-initiators at the polymerization reactor loading phase, usually under dry nitrogen or argon, sometimes followed by neutralization and filtration prior to final product isolation.

    Final product types

    • Biodegradable polyesters for surgical sutures
    • Block copolymers used in drug-eluting stents
    • High-performance polyethers for fuel cell membranes
    • Specialty copolymers for dental composites

    3. Rare-Earth-Based Luminescent Materials

    Yb(OTf)3 finds a critical role in the preparation of upconversion luminescent nanoparticles and thin films. Its use as a dopant source introduces ytterbium ions without non-volatile residue, enhancing the photophysical properties of host matrices for applications in display technology, bioimaging and photonics. Synthesis generally requires controlled hydrothermal or sol-gel processing environments to regulate particle morphology and energy transfer efficiency.

    Industry compliance standards

    • IEC 62471 for photobiological safety of lamps and lamp systems (for downstream devices)
    • ISO 14644 (cleanroom production protocols, downstream)
    • RoHS Directive 2011/65/EU for electronics applications
    • ISO 9001:2015 for advanced material production

    Typical usage ratio

    • 0.5% to 10% Yb by atomic ratio in dopant precursor solution; precise levels guided by emission target and host material lattice composition

    Downstream process integration

    • Added during precursor mixing prior to hydrothermal crystallization, spray pyrolysis, or sol-gel transition; post-synthesis, nanoparticles are washed to remove excess triflates.

    Final product types

    • Upconversion phosphors for display backlights
    • Biological imaging markers
    • Security inks for anti-counterfeit labeling
    • Photonic integrated circuit components

    4. Catalysis for Stereoselective Glycosylation in Carbohydrate Chemistry

    In the area of complex carbohydrate and oligosaccharide assembly for pharmaceuticals and vaccines, Yb(OTf)3 acts as a highly efficient promoter for stereospecific glycosylation reactions. It facilitates rapid activation under mild conditions, maintaining glycosyl donor configuration and minimizing byproduct formation. Process development benefits from its compatibility with a broad range of protecting groups and solvents.

    Industry compliance standards

    • cGMP standards (ICH Q7) applied to pharmaceutical intermediate manufacturing
    • USP-NF monographs for saccharide-based drug substances
    • ISO 17025 for in-process analytical support
    • Ph. Eur. standards for injectable-grade oligosaccharides (if applicable)

    Typical usage ratio

    • 1 to 10 mol% versus glycosyl donor; selected by substrate scale and sensitivity, with further adjustments during process optimization

    Downstream process integration

    • Added at the donor-acceptor coupling stage in solution-phase synthesis workflows, followed by base wash and chromatography purification of final saccharide structures

    Final product types

    • Antibiotic oligosaccharides for API synthesis
    • Synthetic vaccine candidates
    • Sugar-based cosmetic actives
    • Diagnostic reagent carbohydrates

    5. Synthesis of Chiral Organophosphorus Compounds

    Producers of chiral ligands and organophosphorus reagents use Yb(OTf)3 to catalyze asymmetric phosphorylations. The compound’s unique activity in enantioselective activation supports strict control of stereochemical purity, which is essential for downstream catalytic and pharmaceutical applications. Pilot and commercial production confirm robust batch-to-batch reproducibility when technical QC is rigorously maintained.

    Industry compliance standards

    • ISO 9001:2015-certified chemical manufacturing
    • GMP API manufacturing protocols (for pharmaceutically relevant outputs)
    • OECD Guidelines for the Testing of Chemicals (analytical validation)
    • REACH registration for use as a reaction catalyst in Europe

    Typical usage ratio

    • 1 to 4 mol% based on phosphorus substrate; titrated to minimize residual catalyst and maximize stereocontrol

    Downstream process integration

    • Charged to reactor at reagent addition stage in batch or flow systems, under controlled temperature for optimal chiral induction;

    Final product types

    • Chiral phosphine ligands for asymmetric hydrogenation
    • Enantioenriched phosphorus-based intermediates
    • Optically active flame retardants for electronics
    • Organocatalyst precursors

    6. Synthesis of Electrolytes for Advanced Lithium Batteries

    Yb(OTf)3 is increasingly specified as an additive or precursor in the compounding of ionic liquid electrolytes and salt blends for solid-state and high-voltage lithium battery research. Its role is to improve ionic conductivity, thermal stability, and to suppress dendritic growth on lithium anodes. Formulators use it primarily in laboratory-scale and pilot plant development of next-generation battery technologies.

    Industry compliance standards

    • IEC 62660-2 for safety testing of lithium-based secondary cells
    • ISO 9001:2015 for advanced energy material production
    • UN Manual of Tests and Criteria, Section 38.3 (transport safety of batteries)
    • RoHS 2011/65/EU and REACH for electronics chemicals

    Typical usage ratio

    • 0.01 to 0.2 molar equivalents relative to total salt load; optimized based on required ionic transport behavior and cell prototype design

    Downstream process integration

    • Blended during electrolyte compounding under dry-room conditions; exact point of addition based on melting or mixing protocol, followed by in situ verification of homogeneity and electrochemical testing

    Final product types

    • Ionic liquid-based lithium electrolytes for solid-state batteries
    • Electrolyte additives for high-energy density lithium-ion cells
    • Prototype pouch cells for energy storage demonstrators
    • Battery electrolyte test kits for research institutions
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