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Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine

    • Product Name Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine
    • Alias TTMPP
    • Einecs 293-911-8
    • 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

    631325

    Chemicalname Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine
    Casnumber 206917-54-4
    Molecularformula C33H15F18P
    Molecularweight 764.43
    Appearance White to off-white powder
    Meltingpoint 154-158°C
    Boilingpoint Decomposes before boiling
    Solubility Soluble in common organic solvents (e.g., dichloromethane, tetrahydrofuran)
    Density 1.57 g/cm³ (estimated)
    Purity Typically ≥98%
    Refractiveindex nD ~1.540 (estimated)
    Smiles C1=CC(=CC(=C1C(F)(F)F)P(C2=CC(=CC(=C2C(F)(F)F)C(F)(F)F)C3=CC(=CC(=C3C(F)(F)F)C(F)(F)F)C(F)(F)F)C(F)(F)F)C(F)(F)F
    Inchi InChI=1S/C33H15F18P/c34-22(35,36)13-7-19(8-14-22)52(20-9-15-23(37,38)29(41,42)17-11-31(45,46)25(39,40)33(49,50)27-21-5-3-1-2-6-21)21-5-3-1-2-6-21/h1-17H
    Synonyms Tris(3,5-bis(trifluoromethyl)phenyl)phosphine; P(3,5-(CF3)2C6H3)3
    Storage Store in a cool, dry place under inert atmosphere
    Applications Ligand in transition metal catalysis, homogeneous catalysis

    As an accredited Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in a 5-gram amber glass bottle with a tightly sealed cap, labeled with chemical name, hazard warnings, and supplier details.
    Shipping Tris[3,5-Bis(trifluoromethyl)phenyl]phosphine is shipped in tightly sealed containers to prevent moisture and air exposure. It is typically transported as a stable, solid compound at ambient temperature. The packaging follows regulations for chemicals, with appropriate hazard labeling. Ensure storage in a cool, dry, and well-ventilated area upon arrival.
    Storage **Tris[3,5-Bis(Trifluoromethyl)phenyl]phosphine** 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, and well-ventilated area, away from light, heat, and incompatible substances such as strong oxidizers. Store at room temperature unless otherwise specified by the manufacturer.
    Application of Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine

    Applications of Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine in Industrial Manufacturing

    As the original manufacturer, we supply Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine for several advanced downstream industries. The following sections describe detailed application scenarios based on established market use, industrial practice, and regulatory requirements.

    1. Catalyst Ligand for Cross-Coupling Reactions in Fine Chemical Synthesis

    Our phosphine compound acts as a high-performance ligand in palladium-catalyzed C–C and C–N cross-coupling. Pharmaceutical and agrochemical producers use this material to enhance selectivity, boost reaction rates, and improve isolated yields in Suzuki, Heck, and Buchwald–Hartwig aminations. Our production process ensures low metal impurity levels to meet process chemistry needs for gram-to-metric ton scale. The ligand supports both high-throughput screening and commercial batch reactors, offering reproducibility for process validation and CMC scale-up.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU REACH Registration and SVHC review
    • US EPA TSCA Inventory Listing
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • 0.5–4 mol% relative to metal catalyst; adjustment based on substrate and scale; palladium-to-ligand ratio typically 1:1–1:2

    Downstream process integration

    • Dissolving in dry polar aprotic solvents (e.g., DMAc, DMF) with metal precursor pre-charge prior to batch charging aryl halide and base
    • High-shear mixing or in-line metering for continuous flow reactors

    Final product types

    • Pharmaceutical intermediates (biaryls, aryl amines, heterocycles)
    • Agrochemical building blocks
    • Specialty fine chemicals
    • Functional dyes and pigments

    2. Ligand Component in OLED and Electronic Materials Manufacturing

    Producers of OLED displays and advanced semiconductors select our phosphine for its strong electron-withdrawing properties, supporting high-efficiency emitter dopants and charge-transport layers. It is introduced as a ligand with transition metals, such as iridium or gold, during pre-cursor synthesis of high-purity metal complexes used for vapor deposition or ink-jet formulation. The consistent low water and halide content ensures reproducible optical and electronic properties, critical for QMS in electronics fabrication.

    Industry compliance standards

    • Restriction of Hazardous Substances (RoHS) Directive compliance
    • IEC 62474 Declarable Substance List adherence
    • ISO 14001 Environmental Management
    • Sony SS-00259 Green Partner certification (material supplier assessment)

    Typical usage ratio

    • 0.3–1 molar equivalents per metal atom, tailored by target triplet energy and desired photoluminescence properties

    Downstream process integration

    • Thermal ligand substitution and purification of metal-ligand complexes prior to vacuum deposition or solution casting
    • Preparation of precursor solutions for micro-patterning in OLED panel fabrication

    Final product types

    • Blue and green phosphorescent emitters for OLED displays
    • Charge-transport materials in organic semiconductors
    • Electroluminescent inks for flexible displays
    • High-purity organometallic complexes for R&D electronics

    3. Catalyst Ligand in Specialty Polymer Synthesis

    Polymer companies incorporate this phosphine derivative into nickel- and palladium-catalyzed polymerizations to control molecular weight, stereoregularity, and functional group distribution in specialty fluoropolymers and demanding engineering plastics. The ligand design prevents undesired side reactions, enabling the synthesis of high-performance materials for aerospace, filtration membranes, and advanced coatings. We offer customized particle sizing and tailored packaging for high-shear polymerization environments.

    Industry compliance standards

    • ASTM International D7059 for fluoropolymer purity
    • 21 CFR 177.1550 for polymer additives in food contact (where applicable)
    • UL 94 flammability testing for final articles
    • ISO 9001 continuous improvement for manufacturing inputs

    Typical usage ratio

    • 0.2–3 wt% relative to total catalyst loading, optimized after pilot runs for chain-growth vs block-co-polymerization ratio

    Downstream process integration

    • Batch addition at catalyst charging step for bulk or solution polymerization
    • Inline dosing in reactive extrusion processes

    Final product types

    • Specialty PTFE and FEP fluoropolymers with controlled end groups
    • High-performance, flame-resistant engineering plastics
    • Membrane materials for filtration or battery separators
    • Coatings for semiconductor and aerospace uses

    4. Homogeneous Catalyst Ligand for Pharmaceutical API Manufacturing

    Multinational pharmaceutical firms apply our phosphine ligand in API synthesis campaigns involving asymmetric hydrogenation and carbon–heteroatom coupling. It ensures strict enantiopurity and impurity profile controls during late-stage GMP manufacturing, where batch traceability and raw material provenance are crucial. Our variant passes water, residual solvent, heavy metal, and chromatographic identity assays required for regulatory filings. We guarantee documented supply chain transparency and full batch QC.

    Industry compliance standards

    • ICH Q11 and Q3A/B for drug substance development
    • US FDA cGMP requirements (21 CFR Parts 210, 211)
    • European Pharmacopoeia 9th Edition Monographs for API synthesis aids
    • Mutual Recognition Agreement (MRA) traceability audit trail

    Typical usage ratio

    • 0.8–2.5 mol% versus metal catalyst; adjusted based on scalemic control and batch size; ligand excess controlled by validated methods

    Downstream process integration

    • Charge to reaction vessel with base metal precursor before substrate addition
    • Pre-mixed in pre-reactor for integrated continuous processes

    Final product types

    • Chiral pharmaceutical active pharmaceutical ingredients (APIs)
    • Advanced chiral intermediates
    • Drug substance for commercial and clinical supply
    • Catalog fine chemicals for active drug synthesis

    5. Ligand in Agrochemical Active Ingredient Synthesis

    Manufacturers of high-value crop protection compounds use our phosphine ligand in metal-catalyzed cross-coupling steps, especially when constructing trifluoromethyl- and aryl-functionalized intermediates. It enables high substrate conversion, sharp selectivity for challenging substrates, and repeatable crystallinity in downstream processing. Our technical team supports residue analysis and ensures batch-to-batch consistency for regulatory dossier submission and eco-toxicology studies.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 17025 laboratory accreditation
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • Japan Agricultural Chemicals Regulation Law (JMAFF registration)

    Typical usage ratio

    • 0.4–2.5 mol% in relation to catalyst, optimized per substrate type and reaction throughput

    Downstream process integration

    • Included in metal-ligand pre-mix before addition of aryl halides or alkyl coupling partners
    • Fed into jacketed reactors for temperature-controlled runs

    Final product types

    • Trifluoromethylated agrochemical active ingredients
    • Crop protection intermediates
    • Herbicide and pesticide building blocks
    • Seed treatment formulation actives
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    More Introduction

    Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine: A Closer Look from the Manufacturer’s Workshop

    Understanding What Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine Really Offers

    In chemical manufacturing, a compound as specialized as Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine (often called simply “BTFMPP”) stands out for specific reasons. Our team works daily with these chemicals, so any claims about performance or reliability come directly from our experiences on the shop floor and in technical development. BTFMPP’s structure sets it apart immediately: its three-dimensional framework features bulky 3,5-bis(trifluoromethyl)phenyl groups surrounding the phosphorus core. That shielding makes all the difference in both stability and reactivity.

    Many organophosphorus compounds compete for attention in fine chemical synthesis. Some come across the bench regularly: triphenylphosphine, tri(o-tolyl)phosphine, or trialkylphosphines. Each type finds its moment, but BTFMPP shows a different character due to those electron-withdrawing trifluoromethyl groups. You see fewer side reactions, more reliable product consistency, and notably higher yields in some coupling reactions when the actual work gets underway.

    The high purity we achieve with BTFMPP—usually surpassing 99%—did not happen by chance. Production crews know the strain that impurities place on catalysis and downstream filtration. Any residual metallic or organic contaminants often turn a promising reaction into a wasteful day. Tight control over raw material quality, batch conditions, and post-synthesis purification keeps the product within strict limits. Confirming specification with each lot, our team keeps downstream customers moving without the frustration of rework or unexplained batch failures.

    Why Specifics Matter: Model, Batch, and Real Use Cases

    Buyers sometimes ask for a universal phosphine and expect similar results across substrates. In our experience, Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine rises to the challenge where steric hindrance or electronic effects block other ligands from performing well. For example, in Suzuki and Buchwald-Hartwig couplings, bedrock technology guiding the construction of biaryl and aryl-amine bonds, BTFMPP repeatedly delivers elevated product yields. Turnover frequencies can show a marked improvement, especially with more challenging aryl chlorides.

    Some researchers or process chemists highlight selectivity issues with triarylphosphines lacking extra bulk or electron withdrawal. They find in side-by-side trials that BTFMPP helps stop over-reduction, keeps undesired coupling at bay, or cuts unwanted homocoupling. The distinctive electronic landscape around the phosphorus center supports palladium complexes in forming the desired intermediate, pushing the reaction forward without clogging up the pipeline with persistent byproducts.

    Every customer comes with a unique set of physical and regulatory demands. We gear our packaging and batch sizes to real-world laboratory and pilot-plant workflows. Whether a process laboratory requests 5 grams or a pilot plant draws down a full kilogram, each portion gets checked for compliance with analytical standards. Every batch passes through hands that know the stakes: reproducibility in contract manufacturing or scale-up remains make-or-break for pharmaceutical, agrochemical, and specialty materials work.

    Comparing to Other Ligands: What Actually Changes in Application

    On paper, phosphine ligands crowd textbooks by the hundreds. Scale-up histories in our facility point to patterns: triphenylphosphine remains common for simple carbon–carbon linkages, but as the chemistry gets more hindered, BTFMPP’s shape and electron-withdrawing kick start to matter. Instead of chasing after higher loading of a less selective ligand or suffering through endless purifications, you move faster to target yields with BTFMPP. That difference is more than theoretical; it plays out in reduced raw material wastage and fewer lost labor-hours at the plant.

    We have seen several customers swap BTFMPP for less expensive phosphines, searching for savings. Actual records show that overall material cost sometimes increases if side products choke up reactors or demand extra distillation cycles to isolate pure product. On the other end, those who switch from BTFMPP to exceedingly bulky or expensive custom ligands often face sharp learning curves and unpredictable outcomes. Standardization becomes impossible, and documentation balloons as variance between lots creeps up. Chemical manufacturers cannot afford that type of hidden inefficiency, especially where process validation needs airtight documentation.

    How BTFMPP Continues to Evolve with Industry Needs

    We struggle with bottlenecks like everyone: finding consistent high-grade fluorinated aromatics, ensuring minimum moisture intrusion in storage, and handling in ways that prevent loss by sublimation or slow decomposition. Over the years, we adopted extra dehumidification steps, doubled down on inert atmosphere transfer, and modeled our containers to limit UV exposure. Our feedback loop comes directly from customers, who report problems as early as possible so formulation tweaks actually translate into field reliability. No manager wants to hear the catalyst simply “didn’t work” after a shipment has traveled across the ocean.

    Demand from pharmaceutical and electronic materials clients sometimes spikes unpredictably, stressing both upstream raw material supply and batch productivity. BTFMPP’s role as a high-value, low-volume specialty means we dedicate reactors for custom syntheses, planning annual outages in line with market shifts. Our product development group remains active, running lots of off-cycle tests to confirm shelf stability, solubility in commercial-grade solvents, and performance across a range of supported catalysts.

    Technical Specifics: How the Phosphine Works in the Lab (and Factory)

    Experienced chemists notice BTFMPP’s pale solid character—typically a white to off-white powder—fairly quickly. It dissolves well in both polar aprotic solvents like DMF and nonpolar organics such as toluene or THF, an asset for solubility when formulating with stubborn transition metal salts. Its melting point hovers above room temperature, adding easy handling without the volatility trouble certain alkylphosphines create. We avoid excessive contact with air, as with most phosphines; our best results come from storing in nitrogen-filled containers, especially for long-term warehouse stints. This method also translates to hassle-free use at the bench and pilot scale.

    Technicians often focus on ligand loading. BTFMPP performs strongly at low molar percentages, especially compared to unmodified triphenyl derivatives. That translates to direct reductions in waste, with smaller absolute quantities still delivering the benefits in turnover and selectivity. Frequently, lab notebooks show faster reaction times and clearer isolations, which means scaled-up campaigns in the plant run with less equipment downtime. Reliability matters: no one wants surprises once a kilogram or more of product circulates in finished goods inventory.

    Phosphines traditionally get a reputation for “smelliness” and incompatibility with workplace safety goals. BTFMPP avoids the overwhelming odor of trialkylphosphines and withstands limited ambient handling during bench set-up. Standard lab PPE—gloves, eye protection, and disposable labware—provide enough protection for day-to-day use. Its crystalline form reduces airborne particulates, another small edge when planning workplace ergonomic safeguards.

    Real-World Feedback: What End-Users Tell Us

    A large part of our operational learning comes straight from client feedback. Researchers scaling up aryl chloride activation share unique challenges. They confirm, sometimes years after initial development, that BTFMPP helped them move from gram batch trials to kilo campaigns without changing core procedures or dealing with performance drift. Reports routinely mention the cleaner workup, easier chromatographic separation, and fewer downstream compatibility issues, especially in pharmaceutical intermediate synthesis.

    Process development chemists aiming at new ligand families occasionally ask for custom modifications. The BTFMPP backbone allows some subtle tuning by modifying ring substitutions, although each adjustment needs rigorous process control and fresh stability data. Some push the boundaries of solvent tolerance and thermal stability, testing runs up to 150°C and beyond. Our factory tracks feedback for each batch lot, cross-referencing specific runs to any unanticipated crystallization or solubility events so corrective action comes before the next shipment.

    Supply and Demand: Sourcing and Consistency Challenges

    Building a reliable supply of Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine takes more than just a well-written specification. Sourcing 3,5-bis(trifluoromethyl)phenyl intermediates depends on strict supplier qualification and yearly re-audits, especially with increasing environmental and safety regulations covering fluorinated aromatics. We maintain a second-supplier strategy, along with routine validation of raw stock to avoid sudden shortages if one producer changes yields or purity.

    Logistics bring their own set of obstacles. Even at moderate batch sizes, BTFMPP cannot simply “piggyback” with standard bulk shipments due to sensitivity and value. Dedicated packaging, climate-controlled storage, and careful international documentation reduce the risks of surface contamination or temperature-triggered instability. The team aims to get stock out rapidly but never at the expense of cross-contamination or spec slippage. This approach costs more in day-to-day overhead but consistently pays off in batch traceability, shipment acceptance rates, and downstream performance.

    Environmental and Regulatory Pressures: A Moving Target

    Industry-wide, environmental worries about fluorinated aromatics and strong phosphorus compounds grow each year. Our site retains current documentation for chemical handling, waste disposal, and emissions, regularly updating internal SOPs and equipment firmware. Auditors review our operations, but real compliance comes from hands-on unannounced checks and daily logs from the operators. We stay up-to-date on major regulatory shifts from the US, EU, and Asian bodies, making sure each material batch aligns before shipment approval.

    New environmental regulations shift allowable waste and emissions levels. In response, the factory has invested in solvent recovery, activated carbon traps, and closed transfer systems for phosphorus products. Each innovation shortens the compliance cycle and lowers out-of-pocket costs linked to regulatory reporting and fines. Continuous improvement remains a rule: every year brings another small adjustment to how BTFMPP gets made, stored, or delivered.

    What Sets BTFMPP Apart: Lessons Learned on the Line

    Those who work daily with organophosphorus chemicals know that paperwork and theory only take you so far. Reliability in catalytic activity, reactivity in tough C–N or C–C coupling systems, and compatibility with a range of substrates stack up to real results no brochure can substitute. Customers stick to BTFMPP not because of cost leadership or splashy marketing, but because it solves persistent selectivity and impurity headaches. Production schedules become predictable, with easier processing, simpler isolations, and fewer repeat analyses.

    Our team also works closely with industrial users adapting to ever-evolving process control needs. Some are pursuing continuous flow rather than batch processing, searching for phosphines that dissolve easily, do not precipitate in lines, and need minimal scrap batch purging. BTFMPP holds up in non-batch settings thanks to its solubility and limited side-product generation.

    Potential Solutions for Ongoing Challenges

    Persistent demand volatility challenges every specialty chemical operation. We keep extra capacity online with modular reactors, allowing rapid up-ramping of production when long-term clients scale up new products. Where raw material interruptions loom, our purchasing group negotiates multi-year contracts and cross-trains alternate suppliers to bridge shortfalls.

    Waste minimization and greener chemistry remain long-term goals. Our R&D efforts now focus on reclaiming unreacted phosphorus compounds, optimizing recycling of spent solvent, and exploring less energy-intensive synthesis pathways. Customer collaboration also plays a critical part here: production feedback from those actually running the chemistry helps direct investment in tweaks that save kiloliters of solvent or kilowatt-hours of energy across annual multi-ton campaigns.

    Improved digital documentation forms another pillar for future reliability, as clients demand granular batch-to-batch data for validation and tech transfer. By digitizing all logs, quality records, and shipment histories, we build a transparent supply chain that curtails delivery bottlenecks and forestalls disputes over technical compliance. Each flask, drum, or tote of BTFMPP sold links back to its entire provenance—from raw material acquisition to final drying and packaging.

    Looking Forward: Sustaining Value in Synthesis

    Producing versatile phosphine ligands like Tris[3,5-Bis(Trifluoromethyl)Phenyl]Phosphine means more than just filling a drum or weighing a bottle. It takes coordination between R&D, operations, and customer technical support. Every detail—batch-to-batch consistency, supply chain resilience, pragmatic technical advice—builds up the kind of trust that makes industrial innovation possible.

    We continue to invest in training, automation, and direct user feedback to keep quality ahead of market shifts. Tools may change, regulations may tighten, and competition may intensify, but the need for reproducible, high-performing ligands in fine chemical manufacture remains constant. Detailed knowledge, paired with hands-on craft, keeps this compound a favored choice in applications where small differences mean big rewards.

    New users and returning customers alike benefit from our experience in scaling, troubleshooting, and documentation. Whether the application calls for a single vial in advanced synthesis or multi-kilo campaigns in global supply contracts, the principles remain the same: tight process control, open communication with the end user, and an unwavering focus on what actually improves product quality where it counts—in the lab and on the line.