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2,3,4-Trifluorophenol

    • Product Name 2,3,4-Trifluorophenol
    • Alias 2,3,4-Trifluorophenol
    • Einecs 244-362-7
    • 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

    131801

    Chemical Name 2,3,4-Trifluorophenol
    Cas Number 1143-68-0
    Molecular Formula C6H3F3O
    Molecular Weight 148.08 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 157-159 °C
    Melting Point 8-10 °C
    Density 1.419 g/cm3
    Solubility In Water Moderately soluble
    Flash Point 61 °C (closed cup)
    Refractive Index 1.481
    Purity Typically ≥98%
    Smiles C1=CC(=C(C(=C1F)F)O)F

    As an accredited 2,3,4-Trifluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2,3,4-Trifluorophenol is packaged in a 25g amber glass bottle with a secure screw cap and chemical hazard labeling.
    Shipping 2,3,4-Trifluorophenol is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be handled in accordance with hazardous material regulations, kept away from heat sources, and clearly labeled. Ensure upright transport and provide appropriate documentation per local, national, and international shipping guidelines for hazardous chemicals.
    Storage 2,3,4-Trifluorophenol should be stored in a tightly closed container at room temperature, in a cool, dry, well-ventilated area away from sources of ignition. Keep away from incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Properly label the container and ensure only trained personnel have access to the chemical.
    Application of 2,3,4-Trifluorophenol

    Applications of 2,3,4-Trifluorophenol in Industrial Manufacturing

    2,3,4-Trifluorophenol serves as a key fluorinated aromatic intermediate across multiple advanced manufacturing fields. Its distinct substitution pattern supports complex molecule synthesis and performance materials. Below are major downstream application sectors implemented in actual industrial production worldwide.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use this trifluorinated phenol as a building block in the synthesis of advanced active pharmaceutical ingredients, especially for small-molecule drugs requiring specific regioselective fluorine substitution. This compound enters multi-step synthesis schemes for kinase inhibitors, CNS agents, and antiviral compounds, supporting late-stage diversification and improving compound metabolic stability. It participates in nucleophilic aromatic substitution and coupling reactions under controlled process conditions, with strict documentation and traceability throughout GMP-compliant manufacturing lines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II
    • 21 CFR Part 211 (FDA cGMP regulations for drug products)
    • Pharmacopoeia Monograph Compliance (USP, EP as applicable to final API)

    Typical usage ratio

    • 10–30% (by weight of key intermediates), adjusted according to target API route and required fluorine content

    Downstream process integration

    • Introduced during synthesis of advanced intermediates or as a terminal functional group in final step coupling reactions
    • Subjected to GMP-quality control sampling, identity testing, and impurity profile verification

    Final product types

    • Targeted oncology APIs (e.g., fluorinated kinase inhibitors)
    • Central nervous system drug substances
    • Antiviral and immunomodulatory drug candidates

    2. Agrochemical Active Ingredient Production

    Agrochemical producers integrate 2,3,4-Trifluorophenol into synthetic routes for novel herbicides, insecticides, and fungicides that require selective fluorination to achieve field-stable activity and optimized environmental profiles. The compound supports coupling reactions and derivatization steps, improving biological activity and metabolic resistance. Industrial synthesis lines maintain batch records, trace raw material origins, and control for residual phenol levels per regional regulatory schemes.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • FAO/WHO International Code of Conduct on Pesticide Management
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) for import and use in the EU
    • EPA 40 CFR Part 158 Data Requirements for Pesticides (US market)

    Typical usage ratio

    • 8–20% (by mass of synthetic intermediates), with adjustments for targeted fluorine atom incorporation and yield

    Downstream process integration

    • Added at key coupling or cyclization stages during technical active synthesis
    • Controlled under ISO procedures for traceability and analytical verification of batch attributes

    Final product types

    • Fluorinated herbicidal actives (e.g., aryloxyphenoxypropionate derivatives)
    • Systemic fungicidal agents
    • Insecticidal technical concentrates with UV-stable profiles

    3. Liquid Crystal Material Synthesis

    Specialty chemical companies use this compound to construct high-performance liquid crystal monomers for display panel applications. The unique arrangement of fluorine substituents enhances dielectric anisotropy and thermal stability in LCD mixtures. Synthesis requires precise stoichiometric addition and process monitoring according to quality demands for electronics. Analytical control confirms trace levels of metallic and organic impurities, ensuring purity for downstream formulation.

    Industry compliance standards

    • IEC 61249-2-21 (Material standards for electronic assemblies, halogen-free requirements)
    • JEITA ET-7304 (Standards for liquid crystal materials for electronics)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances for electrical/electronic equipment)
    • ISO 9001:2015 for quality consistency in electronic material supply

    Typical usage ratio

    • 5–15% (in targeted monomeric precursor mass); ratio varies by LC formula and desired electro-optical properties

    Downstream process integration

    • Functions as a starting phenolic precursor or coupling unit in LC monomer synthesis chain
    • Requires high-purity specifications and controlled reaction apparatus to eliminate cross-contamination

    Final product types

    • Twisted nematic and super twisted nematic LCD mixture components
    • Advanced low-voltage LC materials for high-resolution displays
    • Specialty LC blends for industrial and automotive instrumentation panels

    4. Organic Electronic and OLED Material Precursors

    Manufacturers of advanced organic electronic and OLED materials employ this raw material as a key fluorinated aromatic precursor enabling synthesis of hole-transport and emitter molecules. The trifluorinated structure delivers improved electron affinity and enables fine-tuning of device layer properties. Technology lines require narrow impurity profiles, advanced analytical verification, and detailed documentation aligned to electronics industry best practices. Integration takes place at monomer coupling and advanced functionalization steps for device-scale material supply.

    Industry compliance standards

    • IPC-4101B (Specifications for electronic grade base materials)
    • ISO 14001:2015 (Environmental management for chemical production)
    • RoHS 3 (2015/863/EU) on absence of prohibited substances in electronics
    • JEDEC industry guidelines for organic functional material purity and trace metals

    Typical usage ratio

    • 3–12% (by weight of organic molecule synthesis batch), regulated by required fluorination level for target emission or transport properties

    Downstream process integration

    • Supplied to monomer synthesis units for introduction of trifluorophenyl moieties into polymeric or small-molecule frameworks
    • Monitored for metal catalyst residues and handled in cleanroom or low-particle manufacturing spaces

    Final product types

    • OLED emitter and host molecules
    • Electron or hole transport polymers for OLED displays
    • Organic field-effect transistor (OFET) materials

    5. Advanced Polymer Modification and Specialty Resin Formulations

    Chemical processors designing fluorinated polymers and high-end resins add this compound to introduce trifluorophenyl groups, giving rise to unique thermal and chemical resistance profiles for high-performance coatings or engineering plastics. Production lines integrate this input during pre-polymerization or as a chain-end modifier. Full batch traceability and environmental compliance remain critical, with process waste subjected to fluorinated organic handling norms.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems
    • ASTM D5207-09 (Standard for Polymeric Material Performance)
    • EU REACH annex XVII for fluorinated chemical handling
    • UL 94 (Plastic flammability rating, applicable to many specialty resins)

    Typical usage ratio

    • 1–7% (based on target resin formula); adjusted according to desired thermal or chemical stability in downstream product

    Downstream process integration

    • Co-fed with base monomers in resin kettle reactions, or as a functional additive during post-polymerization blending
    • Subject to quality checks for unreacted residuals and integration into batch record management

    Final product types

    • Fluorinated epoxy and polyimide resins for aerospace or electronics
    • High-thermal-stability coatings
    • Engineered fluoropolymer components for corrosive chemical environments
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    Certification & Compliance
    More Introduction

    Introducing 2,3,4-Trifluorophenol: Practical Insights from the Chemical Manufacturer’s Floor

    Our Real-World Experience with 2,3,4-Trifluorophenol

    2,3,4-Trifluorophenol stands out among phenolic compounds. Over years in manufacturing, we’ve watched this material become more valuable for chemists seeking reliability and precision. Within our own facilities, it goes by the model name TFP-234, a product of careful process control rather than a commodity off the shelf. Handling the synthesis in-house lets us tune the purity and meet demands not just for the letter of a specification, but for dependable results in real applications.

    Production Approach and Consistent Results

    Our teams oversee each production step, from raw feedstock checks to final packaging. Chlorinated phenols can introduce unwanted byproducts. To steer clear, we use a selective fluorination sequence and control every batch with high-performance liquid chromatography and gas chromatography for trace contaminants. Through tight oversight, we regularly provide a typical purity of 99 percent or better, aiming for minimal residual solvents and nearly undetectable chlorinated or non-fluorinated phenol traces.

    For researchers and process chemists, these details matter. Impurities can lead to process upsets in fine chemicals or active pharmaceutical ingredient (API) syntheses. Over the years, several pharmaceutical clients reported that inconsistent phenol grades led to yield drops or coloring in downstream steps. A reliable batch of 2,3,4-Trifluorophenol meant more robust results and less time troubleshooting, and that lesson pushes us to keep up analytical checks and equipment maintenance.

    Specifications and What They Mean for Your Work

    We’ve shaped our product around recurring questions from customers rather than textbooks. The white to pale-yellow crystalline solid we produce comes in standard net weights—drums of 25 kilograms are common, but we always package with moisture exclusion in mind. For high-throughput labs, glass-lined steel drums with nitrogen blanketing keep the material dry and stable.

    Some clients use TFP-234 for fluorinated building blocks in pharma, others see it as a step in advanced materials or lithium battery additives. Because melting point and water content affect handling and reactivity, we routinely test these parameters. Melting points usually run between 51 and 54°C. Water content stays below 0.2 percent by Karl Fischer titration. This helps chemists accurately measure it out or dissolve it in standard solvents.

    Why focus on such details? One formulation customer in OLED development noticed trace moisture from plastic-lined bags changed their batch colors. Pre-drying protocols can resolve that, but it takes attention to detail upstream. We’ve now kept all drums lined with aluminum foil laminates and sealed with tamper-evident closures.

    Performance in Practice: Where 2,3,4-Trifluorophenol Excels

    Multiple industries draw on our TFP-234. One established market is pharmaceutical intermediate synthesis. The distinct fluorine substitution pattern helps block metabolic degradation, making it valuable for medicinal chemists designing new molecules. In laboratory hydrogenation tests, we observed selective reduction without side-reactions common in higher-chlorine phenols.

    Electronics clients use TFP-234 to produce specialty polyimides or resists for semiconductor processing. With its electron-withdrawing substituents, the phenol can help control polymer chain rigidity and resistance to high-temperature degradation. In-house, our pilot coating tests showed uniform films resistant to yellowing—crucial for optical clarity and device yield.

    Some research groups now explore this molecule for custom fluorinated monomers in battery electrolyte additives. From experience, reproducible purity ensures predictable tensile strength and electrochemical performance. Through a feedback loop with our customers, we've streamlined solvent selection and mixing protocols to minimize unwanted polymer cross-linking—a common complaint with certain multihalogenated phenols.

    Subtle Advantages Versus Other Phenol Derivatives

    The fluorination pattern matters more than a catalog entry may suggest. 2,3,4-Trifluorophenol carries its three fluorines on adjacent carbons. That arrangement tweaks both reactivity and solubility. Laboratory data reinforces that nucleophilic substitutions occur with selectivity distinct from 2,4,6- or 3,4,5-trifluorophenol. The ortho-position fluorines can induce steric hindrance, limiting unwanted para-substitution in coupling reactions.

    In our own benches, control tests show diminished attack in palladium-catalyzed couplings or oxidative protocols. Where 2,4,6-trifluorophenol might overreact or lead to broad product distributions, our TFP-234 enables cleaner isolation and easier scaling. This small difference can have a big impact on process efficiency—especially in pilot plants where troubleshooting via batch analytics becomes expensive and time-consuming.

    Fluorobenzene derivatives emerge in large selection. Some chemists try to substitute closely related phenols, hoping to cut costs or simplify supply chains. Our feedback shows the backbone substitution in TFP-234 avoids pitfalls with certain catalytic cycles—especially where small changes in electronics or sterics drive product purity down. Not every route tolerates swapping out one fluorophenol for another, especially under scale-up conditions.

    Issues That Matter in Real Operations

    Stability and safety during storage come up often. Even stable fluorinated phenols react badly to excess moisture, high temperature, or sunlight. Several years ago, one client using recycled warehouse drums saw product loss after only three months of summer storage. Organoleptic checks found browning and off-odors, tracked to UV exposure and ambient humidity. Now we use UV-blocking drums and keep inventory in climate-controlled conditions.

    We also fielded customer feedback about dusting and clumping. Small-particle solids are notorious for airborne loss during transfer. On our production line, we employ vacuum transfer systems and antistatic linings. Simple measures—slow drum filling, less powder agitation—reduced operator exposure and improved batch consistency out the door.

    Regulatory compliance also plays into outgoing shipments. Many clients need full traceability for pharmaceutical or electronics GMP audits. Because we never use recycled or mixed-intermediate streams for TFP-234 production, we maintain in-house batch records matching each lot to its raw materials and analytical results. This approach isn’t just for red tape: a couple years ago, a trace impurity flagged during a random inspection led to prompt root-cause analysis and rapid lot recall, avoiding downstream issues for a major customer.

    Applications Beyond the Lab: What End Users Report

    Pharmaceutical chemists tell us 2,3,4-Trifluorophenol gives clean conversion in Suzuki, Buchwald-Hartwig, and Ullmann-type reactions. Broader substrate scope often follows from the controlled electron density the three fluorines impart. We have received numerous reports of higher product yields and reduced byproduct formation in heterocycle synthesis, which can otherwise suffer from competitive side reactions.

    Material scientists often point to the importance of predictable melting profiles for polymer feedstocks. One OLED manufacturer compared our TFP-234 to competing lots during a scale-up trial, observing fewer prepolymerization events and more consistent downstream film properties. Feedback from that trial led us to implement stricter in-process temperature controls during crystallization—a seemingly minor tweak, but one that paid off in downstream performance.

    Formulators seeking greener or lower-toxicity methodologies often ask about byproducts from our process. We rely on non-chlorinated solvents and high-purity starting materials. Internal analytics show that unwanted aromatic halides, common in some industrial phenol products, stay well below 50 ppm in our finished lots. By working with cleaner feedstocks, we not only facilitate customer compliance with global RoHS and REACH directives, but we reduce hassles in waste management and downstream product labeling.

    Supply Chain Resilience and Manufacturer Responsibility

    Our long-term customers cite stability in lot-to-lot quality as a key factor. Volatility in raw material sourcing can shake any supply chain, especially with specialty fluorinated compounds that depend on access to high-quality anhydrous hydrogen fluoride and proprietary fluorination catalysts. Over time, we've built relationships with dedicated, audited vendors. We keep emergency buffer stock and maintain backup lines to shield customers from upstream interruptions—practices sharpened during periods of raw material shortages and transportation slowdowns.

    For urgent requests or custom packaging, we keep communication open with customers and adapt to unique logistics needs. International distribution poses challenges, so we’ve implemented GPS tracking for temperature- and humidity-sensitive shipments and guarantee pre-shipment quality analytics for any load leaving our site. Customers tell us this reassurance saves time, especially when local customs or regulatory clearance hits a delay.

    Environmental and Safety Priorities from the Manufacturer’s Viewpoint

    Producing and handling halogenated aromatic compounds calls for high environmental stewardship. We operate under strict containment, use closed-system solvents, and treat all liquid waste by incineration at licensed facilities. Reducing fugitive emissions means safer conditions for our employees and limited risk for our community. Routine air and effluent monitoring supports regulatory reporting and keeps internal standards high.

    Dust from phenol processing—commonly overlooked—poses health and cleanliness hazards. We continually update our facility to reduce points of emission, investing in automation and worker training to keep exposures within the lowest achievable limits. In-house medical monitoring ensures early detection of any workplace related health trends.

    Facing the Future: Customer-Driven Product Improvement

    Working directly with those who use our 2,3,4-Trifluorophenol teaches us what works and what falls short. Recent requests include custom micronized forms for more consistent blending in polymer batches, which we now support. New compounded drum designs allow easier transfer in glovebox environments for battery teams, based on collaboration with field users. Our QC lab has expanded rapid-release testing hours to meet urgent project timelines.

    Many industries today want to drive toward safer, greener processes. By sticking with cleaner solvents and investing in energy recovery for our reactors, we’re minimizing process waste and lowering the impact per kilogram produced. This approach pays dividends not only in regulatory and insurance terms, but in customer loyalty.

    Digital data integration also matters more each year. Some partners now request direct access to lot data, spectral records, and origin documentation before product release. We’ve invested in secure portals to address these concerns, speeding up customer R&D as their teams face tighter launch windows and compliance audits.

    Direct Contact and Technical Dialogue

    Our technical and manufacturing teams remain available for troubleshooting or discussing new applications. Occasionally, we spot process issues or special opportunities for improvement as we trade data with our partners, leading to joint process refinement or shared R&D efforts. We encourage open lines of communication and peer-to-peer knowledge-sharing. Patents and competitive strategies aside, the industry advances faster through practical dialogue rooted in chemical knowledge, analytical rigor, and a shared goal of safer, cleaner, and more reliable performance.

    Through hands-on experience and ongoing conversations with our customers, we continue to strengthen the reliability and versatility of 2,3,4-Trifluorophenol. We see every batch as more than a line item—it's the result of collaborative care, detail-driven manufacturing, and continuous improvement with a real-world impact.