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1-Phenyl-2,2,2-Trifluoroethanol

    • Product Name 1-Phenyl-2,2,2-Trifluoroethanol
    • Alias TFPE
    • Einecs 220-867-7
    • 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

    255560

    Chemical Name 1-Phenyl-2,2,2-Trifluoroethanol
    Cas Number 340-58-1
    Molecular Formula C8H7F3O
    Molecular Weight 176.14 g/mol
    Appearance Colorless liquid
    Boiling Point 161-163 °C
    Melting Point -23 °C
    Density 1.271 g/cm³
    Refractive Index n20/D 1.456
    Flash Point 52 °C
    Solubility Slightly soluble in water
    Smiles C1=CC=C(C=C1)C(C(F)(F)F)O

    As an accredited 1-Phenyl-2,2,2-Trifluoroethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 mL, with secure screw cap. Label displays chemical name, hazard symbols, CAS number, and manufacturer details.
    Shipping 1-Phenyl-2,2,2-Trifluoroethanol is shipped in tightly sealed containers, protected from light and moisture. The chemical is classified as hazardous; shipping complies with regulations for flammable and toxic substances. Appropriate labeling and documentation are included. Containers are packed to prevent leaks, with cushioning material to minimize breakage during transport.
    Storage **1-Phenyl-2,2,2-trifluoroethanol** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat and sources of ignition. Keep it away from incompatible materials such as strong oxidizers and acids. Protect from moisture and direct sunlight. Ensure appropriate labeling and secure storage to prevent accidental spills or exposure.
    Application of 1-Phenyl-2,2,2-Trifluoroethanol

    Applications of 1-Phenyl-2,2,2-Trifluoroethanol in Industrial Manufacturing

    As a manufacturer of 1-Phenyl-2,2,2-Trifluoroethanol, we deliver consistent quality material for specialized chemical synthesis routes across several advanced industrial sectors. Below, we detail practical application scenarios, ensuring precise integration, process value, and regulatory confidence for downstream producers requiring rigorous performance and compliance.

    1. Agrochemical Active Ingredient Synthesis

    Formulators in the agrochemical sector incorporate our material as a critical chiral building block and reaction intermediate during the preparation of advanced herbicide and fungicide actives. The compound participates directly in enantioselective hydrogenation and fluorinated moiety introduction steps that define product bioactivity and degradation profiles suited for high-performance agrochemical portfolios.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • Global Crop Protection registration guidelines (e.g., EPA 40 CFR Part 180, Regulation (EC) No 1107/2009, GB 2763—China)
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH Regulation (EC) No 1907/2006 requirements for new substance dossiers in the EU

    Typical usage ratio

    • 5–20 mol% in multi-step synthesis, adjusted to substrate ratio based on route optimization and yield targets

    Downstream process integration

    • Charged at the intermediate coupling step following halogenation or Grignard reaction, facilitating key carbon-fluorine bond construction before eventual purification

    Final product types

    • Selective triazole fungicides
    • Phenyl-substituted herbicide actives
    • Fluorinated insecticide precursors
    • Chiral agrichemical intermediates for further functionalization

    2. Pharmaceutical API and Intermediate Manufacturing

    Our facility supplies pharmaceutical manufacturers with this compound as a specialized precursor for constructing trifluoromethyl-bearing aromatic APIs, including CNS agents and anticancer molecules. MOE-optimized processes leverage its high purity for nucleophilic and transition metal-catalyzed coupling stages, affecting chirality and metabolic resistance in the resulting APIs.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia)
    • European Pharmacopoeia (Ph.Eur.) monograph compliance for intermediates
    • FDA DMF submission protocols (21 CFR Part 314)

    Typical usage ratio

    • 0.2–3 molar equivalents in Grignard addition, Suzuki coupling, or Friedel–Crafts alkylation phases, optimized to reaction scale and final dosage form load

    Downstream process integration

    • Fed into controlled addition reactors under inert atmosphere following solvent charging, often preceding column purification or crystallization of chiral intermediates

    Final product types

    • Antipsychotic agents with enhanced CNS penetration
    • Trifluoromethyl-substituted analgesic APIs
    • Non-hydrolyzable kinase inhibitors
    • Advanced pharmaceutical intermediates for prodrug synthesis

    3. Specialty Fluorinated Polymer Modifier Production

    Producers of advanced fluoropolymer systems utilize the compound as a functional chain transfer agent and structural modifier during polymerization of heat- and solvent-resistant specialty polymers. Its introduction tailors thermal stability, dielectric properties, and surface energies for engineering plastics and high-performance coatings.

    Industry compliance standards

    • ISO 14001: Environmental Management for polymer production
    • ASTM D5630 for fluoropolymer composition
    • RoHS 3 (EU Directive 2015/863) for restricted substances in end-use electronics
    • UL 94 flame classification (for electronics applications)

    Typical usage ratio

    • 0.05–1 wt% as a chain terminator or co-monomer, with dosage set according to target copolymer ratio and finished polymer characteristics (MW, Tg, etc.)

    Downstream process integration

    • Dosed inline during solution or suspension polymerization, often immediately after catalyst initiation, followed by extrusion or post-polymerization conditioning

    Final product types

    • Fluorinated polyacrylate coatings
    • High-durability wire and cable insulation
    • Engineering plastics for automotive and aerospace
    • Electronic encapsulation resins

    4. Liquid Crystal and Advanced Electronic Material Synthesis

    Electronic material manufacturers rely on the compound for crafting liquid crystal intermediates and specialty dielectric modifiers, exploiting its rigid aromatic-fluoroethanol structure for precise orientation and alignment in display technologies. Control of polarity and anchoring results in sharply defined electro-optical switching behavior in flat panel and flexible displays.

    Industry compliance standards

    • IEC 62899: Printed electronics standards
    • IPC-4101: Base materials for printed boards
    • RoHS Directive (EU) for hazardous substances
    • ISO 9001:2015 for electronics grade production

    Typical usage ratio

    • 0.5–3 mol% in nematogenic monomer precursor solutions, set by desired viscosity and dielectric response, after lab-scale validation

    Downstream process integration

    • Blended with aromatic diacrylates or cyanobiphenyls in closed system reactors during liquid crystal compound synthesis, followed by vacuum distillation and phase purity analysis

    Final product types

    • Nematic and smectic liquid crystal mixtures
    • Alignment layer precursor chemicals
    • Intermediate electronic dielectric coatings
    • LC display-grade material blends for display panel assembly

    5. Organic Synthesis Catalyst Ligand and Modifier Applications

    Catalyst manufacturers in the fine chemicals industries incorporate this fluorinated alcohol as a key ligand modifier, particularly for transition metal-catalyzed cross-coupling and asymmetric hydrogenation reactions. The resulting catalytic systems exhibit improved selectivity, unique electronic properties, and facilitate the activation of challenging substrates for specialty monomer and building block synthesis.

    Industry compliance standards

    • IUPAC Nomenclature and InChI standardization practices
    • ISO 17025: General requirements for laboratory competence
    • Responsible Care Management System (RCMS)
    • REACH registration for catalytic intermediate applications

    Typical usage ratio

    • 0.5–10 mol% as a ligand source or molecular modifier in organometallic catalyst preparation, proportion determined during bench-to-plant upscaling

    Downstream process integration

    • Introduced during dry-box ligand assembly or under inert gas as a pre-ligation step, prior to catalyst charge into the reaction vessel for substrate coupling

    Final product types

    • Chiral phosphine or N-heterocyclic carbene ligand systems
    • Palladium- and nickel-catalyzed coupling products
    • Enantioenriched monomers for precision organic synthesis
    • Fine chemical intermediates for further downstream derivatization
    Free Quote

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    Certification & Compliance
    More Introduction

    1-Phenyl-2,2,2-Trifluoroethanol: Fine Chemicals for Modern Applications

    Understanding the Material

    Working with 1-Phenyl-2,2,2-Trifluoroethanol, which industry colleagues often call PTF-OH, brings a unique set of qualities that separates it from many other alcohol-based intermediates. With a structure that features a trifluoromethyl group next to the ethanol backbone and a phenyl ring, you get not just stability but highly targeted reactivity that synthetic chemists and process developers value. Over the years, feedback from both pharmaceutical and agrochemical manufacturers has shaped how we view and refine this product. The physical purity, reliable boiling point, and the clarity in each batch come from years of internal technical work, ongoing investment in purification, and close monitoring of each production run.

    The Science Shaping Demand

    Chemists care about more than just the name. With a molecular formula of C8H7F3O and a clear, colorless appearance, each shipment gets checked for trace moisture, acidity, and residual solvents. Our lab teams continually test incoming raw materials and finished products against high-performance liquid chromatography and gas chromatography standards. Over the last decade, advances in column technology and strict attention during distillation have allowed us to deliver 99.5%+ purity batches for customers who cannot compromise. That kind of scrutiny comes from not only regulatory pressure but also real-world conversations with research and development scientists and process engineers.

    Why This Fluoroalcohol Stands Out

    Fluoroalcohols occupy a specialized place in organic synthesis. Regular ethanol or isopropanol react differently, lacking the electron-withdrawing effect that comes from a fully fluorinated methyl group. The -CF3 group does far more than merely add weight. Product designers report improved stability to oxidation, higher resistance to hydrolysis, and in some reaction platforms, sharply tuned reactivity that basic alcohols cannot match.

    What we notice in the plant is that distilling and storing trifluoromethylated alcohols calls for different metallurgy and handling compared with standard organics. This material stays less volatile and mixes better in reaction media, so operators achieve smoother transitions from lab-scale experiments to full tonnage runs. Our equipment choices, from stainless steel grade up, and the steps needed to prevent cross-contamination, stem directly from the needs of our regular fluoroarene customers, who often mention the downstream value of batch-to-batch reliability.

    Practical Uses Across Markets

    Every chemical company faces questions about “real-world” value. Here, 1-Phenyl-2,2,2-Trifluoroethanol stands up as an intermediate in synthesis routes for active pharmaceutical ingredients, pesticide actives, specialty monomers, and even advanced materials. Medicinal chemistry groups order this compound because the combination of a phenyl ring and trifluoromethyl group brings metabolic stability that traditional benzyl alcohol derivatives cannot achieve. We hear most about its role in creating aryl ethers, chiral ligands, and as a chiral auxiliary itself.

    In the formulation lab, formulating with PTF-OH means the end-user can tailor reactivity and polarity. Agrochemical groups prize the material for new herbicide and fungicide scaffolds: the electronic profile and size let researchers construct analogues that show both improved performance and lower degradability in real-life field trials. Each batch that leaves our loading dock reflects two decades of collaborative troubleshooting as new patent filings and regulatory changes alter target markets.

    Working with PTF-OH: Lessons from the Plant

    One of the myths around specialty chemicals is that consistent batches are just a matter of buying the right raw materials. Our experience shows that PTF-OH lives or dies by the handling of fluoro feedstocks and the tightness of process controls. Even a minor variation in catalyst temperature or reflux duration can introduce subtle changes in water content or byproduct profile. Several years ago, a partner flagged an odor issue due to trace phenol—we retooled the scrubber system and started a QA checkpoint specifically for trace aromatics. From plant manager to warehouse loader, everyone involved keeps records, tracks ambient conditions, and logs any deviations. We have built a culture of accountability that feeds back into stronger technical performance, lower impurity counts, and greater trust from formulators.

    Blending, storage, and shipping require careful environmental control. The trifluoromethyl group heightens the chemical inertness but does not defend against every environmental factor. Summer shipments with prolonged heat exposure taught us to tweak drum and IBC selections, moving away from certain plastics and switching to double-sealed metal drums. Our safety team always looks for tweaks to accident response and vapor detection, answering questions from downstream users who sometimes face new regulation or audit standards.

    Comparing to Other Alcohols

    Someone running a basic acylation, alkylation, or reduction often assumes all benzylic alcohols behave similarly. In practice, the trifluoromethylated alcohol group shifts reactivity in meaningful ways. The electron-withdrawing effect modulates acidity and nucleophilicity, letting chemists fine-tune selectivity in reactions where proton transfer, hydrogen bonding, or base strength matter. While benzyl alcohol oxidizes or loses performance in harsh conditions, PTF-OH holds its structure and does not degrade as easily—key for those seeking new routes through late-stage functionalization.

    One customer, working on a multi-tonne scale process for a veterinary analgesic, reported higher isolated yield and less side-product cleanup when switching from a basic phenyl ethanol to our trifluorinated version. Years ago, a batch of product aimed for OLED material synthesis revealed that the standard methylbenzyl alcohol created colored impurities, but PTF-OH maintained optical clarity. These are not abstract promises—they come from conversations we hold with users tuning polymer properties, or exploring API impurity profiles that regulators scrutinize intensely.

    Regulatory and Safety Demands

    Working closely with downstream regulatory affairs groups, we keep up with shifting requirements around material registration, labeling, and permitted end-uses. Each ten-tonne batch that leaves the site fits compliance matrices, but we go further. Documentation for REACH status, US TSCA inventory, and Asia-Pacific standards gets updated promptly, and we flag any lot as ‘deviation’ if a single test sits outside the specification window. Handling fluoroalcohols attracts extra audit attention: worker training, emission controls, and waste management go through continuous review.

    It’s not enough just to ship a product that clears hazardous goods rules. We build partnerships with safety officers and synthesize market intelligence, whether on upcoming EU hazard statements or national health ministry documentation. Training materials keep evolving as solvent regulations tighten, and every new employee receives in-depth process safety education. That feedback loop between compliance and people on the ground impacts performance in areas competitors too often overlook.

    Real Feedback and Future Directions

    Over the years, customer requests have driven how we handle everything from minimum order quantities to drum labeling and sampling. A few years ago, process groups needed higher-resolution analytical run data—our lab shifted to full-scan mass spectrometry release documentation. As new end-uses like fluorinated surfactants and advanced coatings emerge, research and production teams work together to tweak purification loads, optimize solvent usage, and address evolving stipulations from regulators and auditing labs.

    For specialty chemical manufacturers, real-world data carries more weight than brochure claims. Recent requests from research clients led us to start batch-by-batch impurity mapping for endotoxin and extractable profile characterization, especially for pharma segment customers. This level of communication between our technical group and field chemists shrinks lead times for new project launches and reduces the risk of late-cycle issues. Internal innovation pairs with the lessons learned from every new project launch or process debottlenecking feedback session.

    Logistics, Sustainability, and Production Challenges

    Sulfur, contamination, and cross-reactivity risks occupy a big part of the real manufacturing world. Each new production batch of 1-Phenyl-2,2,2-Trifluoroethanol means reviewing everything upstream—tank cleaning records, supplier traceability, blending line wear. Our adoption of more sustainable cleaning solvents and recovery loop processes reflects a commitment to lower emissions and greener daily operation. The move also helps control costs and avoid the off-odors or color problems that used to show up in legacy supply chains.

    Sustainability in specialty chemicals has become more than a buzzword. Our plant doubled down on energy recovery in the purification line: heat integration lets us save fuel and cut electrical peak loads, translating into smaller energy bills and less environmental impact. Internal records and third-party certifications anchor these changes in the real world rather than marketing claims. Feedback from major buyers shows growing attention to solvent recovery and life cycle data for every kilogram produced.

    Partnering with Innovators

    Our regular communication channels include both direct customers and their innovation teams. Weekly calls sometimes turn to technical troubleshooting at the bench: how to de-water samples, analyze minor byproducts, or shift to continuous processing. We bring process engineers into customer pilots, and sometimes work together on new purification protocols. The shifting landscape for specialty chemicals means combining plenty of old-school care—titrating alcohol groups, checking for trace iron or potassium—with digital documentation.

    When pilot plants need thirty-liter runs, our operations group jumps in to adjust blending schedules, set isolation temperature targets, and track shipments with full digital chain-of-custody. This speed and openness stand out to buyers fed up with generic suppliers who cannot answer detailed questions. Over time, the industry’s most valuable relationships come from companies who help each other solve batch issues, adapt to regulatory curveballs, and rethink material purity levels together.

    The Bigger Picture: Global Trends and Ongoing Challenges

    Specialty organic chemicals never reach a final resting point; customer demands and regulatory targets move every year. The demand for 1-Phenyl-2,2,2-Trifluoroethanol links directly to trends like ever-tighter impurity limits, new reaction media, and push for greener footprints. Our QC staff work with universities and private labs to test catalytic alternatives, limit-waste protocols, and better solvent separation.

    Downstream markets press for answers on trace residuals, new analytical signatures, and data-backed sustainability. Handling these shifts is less about flashy new products and more about detailed communication. A chemist or process developer turning to us with a challenge expects more than an MSDS. They need history, batch data, practical troubleshooting advice, and a manufacturing partner as invested in results as they are. Over decades, those are the collaborations that move the needle in both science and business.

    Moving Forward

    No two inquiries about 1-Phenyl-2,2,2-Trifluoroethanol sound the same. Some partners focus on yield and throughput, others on purity, cost profile, or sustainability. Our task is to keep refining every step—feedstock qualification, reactor design, filtration method, final QA—taking lessons from every small win or return shipment. As the next generation of end-users in biochemistry, electronics, and agriculture chase tougher targets, we make sure our plant and people keep up. The meaning of quality in specialty chemicals arises not from what we put in a brochure, but from daily attention to every detail behind each container, railcar, and bulk tanker.