Anhui Liwei Chemical Co., Limited
Products

Phenol, 2,3,4-Trifluoro-


    • Product Name Phenol, 2,3,4-Trifluoro-
    • Alias 2,3,4-Trifluorophenol
    • Einecs 245-645-7
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    736952

    Chemical Name Phenol, 2,3,4-Trifluoro-
    Cas Number 393-06-8
    Molecular Formula C6H3F3O
    Molecular Weight 148.08
    Appearance Colorless to pale yellow liquid
    Melting Point 4-6°C
    Boiling Point 171-174°C
    Density 1.41 g/cm³
    Solubility In Water Slightly soluble
    Flash Point 68°C
    Purity Typically ≥98%
    Synonyms 2,3,4-Trifluorophenol
    Smiles C1=CC(=C(C(=C1O)F)F)F
    Inchi InChI=1S/C6H3F3O/c7-3-1-2-4(8)6(10)5(3)9/h1-2,10H
    Refractive Index 1.484

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

    Packing & Storage
    Packing Phenol, 2,3,4-Trifluoro- is supplied in a 25g amber glass bottle with a secure screw cap and hazard labeling.
    Shipping **Shipping Description for Phenol, 2,3,4-Trifluoro-:** Phenol, 2,3,4-Trifluoro- is shipped as a hazardous chemical, typically in sealed containers compliant with UN regulations. It should be packed securely to prevent leaks and labeled with appropriate hazard warnings. Transport is governed by relevant chemical and environmental safety standards for toxic and/or flammable organic compounds.
    Storage Store Phenol, 2,3,4-Trifluoro- in a tightly sealed container, kept in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizers and bases. Protect from light and moisture. Handle under a fume hood, and ensure containers are properly labeled to prevent accidental misuse. Follow all relevant safety guidelines and regulations.
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    Tel: +8615380400285

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    Certification & Compliance
    More Introduction

    Understanding Phenol, 2,3,4-Trifluoro-: From Our Chemist’s Bench to Your Application

    A Practical Approach to a Unique Fluorinated Phenol

    Every day, our chemists handle hundreds of aromatic compounds. Through decades in the laboratory, we notice trends among requests, see new approaches in medicinal research, and answer troubleshooting calls from polymer developers. Among fluorinated phenols, one molecule keeps showing up—Phenol, 2,3,4-Trifluoro-, or as some researchers prefer to call it in shorthand, 2,3,4-Trifluorophenol. Because we manufacture it under controlled conditions, we have a straightforward understanding of its place among both classic and modern chemicals. Rather than overly technical language, let’s cover why this fluorinated phenol deserves a closer look and where it diverges from other compounds, drawn from hands-on experience making and shipping kiloliter batches to customers with tight project deadlines.

    Structure and Materials: What Stands Out

    Put simply, 2,3,4-Trifluorophenol consists of a six-carbon aromatic ring, three fluorine substitutions, and a single hydroxyl. The arrangement of the three fluorines isn’t arbitrary—it changes how the compound behaves in solvents, what it reacts with, and how smooth it passes purification. The substitutions at the 2, 3, and 4 positions on the ring create a different electronic effect compared to mono- or difluorinated analogs. That structure gives it a melting point and volatility profile distinct from other phenols. Over years in the factory, we’ve tested these parameters to optimize synthesis and monitor for side-products. Routine controls guarantee the absence of extra halogens or ring isomers, responding to feedback from both industry and academia.

    Batch Consistency and Quality Control

    From a manufacturer’s point of view, the question of quality always returns to purity and reproducibility. It isn’t only about selling fine chemicals but about enabling consistent downstream results. Purity for 2,3,4-Trifluorophenol stays above 99% in our production line, based on HPLC and NMR standards. Chromatographic traces show clear separation from potential impurities like difluoro or tetrafluorophenols. Moisture content gets constant attention, especially for clients preparing highly sensitive pharmaceutical intermediates. We don’t treat this as a sales pitch—every deviation introduces troubleshooting for an end-user. In some customer calls, samples prepared with less rigorous controls by other suppliers led to batch failures or inconsistencies in bioactive development. Our efforts on redundant checks, controlled storage, and detailed documentation stem directly from those customer case reports.

    Technical Usage and Real-World Impact

    Our shipments go into several industries, from pharma labs to electronics. In R&D environments, medicinal chemists seek precise building blocks for active molecules. For many, controlling electron density and functional group placement across the aromatic ring defines bioactivity. The 2,3,4-Trifluoro- layout sets this phenol apart from 2,4,6- or 3,4,5-trifluorophenols because minor structural changes on the phenol ring create large changes in molecular recognition by enzymes. Some customers report that a scaffold swap from 3,4,5- to 2,3,4-trifluorination can flip a candidate molecule’s polarity, impacting both solubility and metabolic stability in animal tests. That’s not a small matter—these details make the difference in advancing a lead compound or halting an entire medicinal chemistry campaign.

    The electronics field also values these differences, especially where fluorine’s electronegativity supports stability or charge control. In polymer synthesis, we receive technical requests for phenols that maintain certain glass transition temperatures or resist unwanted cross-linking. The trifluoro arrangement of our material, based on feedback, delivers reliable synthetic handles for surface modifiers or copolymers and meets demanding spectrometric requirements.

    Performance in Synthesis: A Manufacturer’s Trials

    We’ve run this chemistry thousands of times, altering oxidation states, solvent compositions, and purification routines to address real process bottlenecks. For comparison, less substituted phenols create broader impurity profiles; highly fluorinated phenols like pentafluorophenol introduce handling hazards and solubility hurdles. Our 2,3,4-trifluorinated version finds a “sweet spot.” It balances process safety, reactivity, and availability. We’ve seen customers attempt to use mono- or difluorophenols for certain coupling reactions, only to hit stumbling blocks because the resulting intermediates lacked stability or selectivity. In contrast, 2,3,4-Trifluorophenol often permits higher yields with cleaner product streams.

    During scale-up, we observe that its particular substitution pattern allows for straightforward filtration and crystallization, reducing process costs for both in-house operations and client pilot plants. We monitor for hydrolytic stability, and through repeated trial and error have settled on cold-chain storage for large volumes. Every major deviation—such as switching from glass to coated steel storage—has been prompted by a specific customer requirement or regulatory shift, never guesswork.

    Adaptation and Ongoing Feedback

    Our production staff see more than numbers; we collect actionable suggestions from chemists who push new reactions. Take resin functionalization: With certain mono- or difluorophenols, resin swelling or shrinkage in organic solvents creates reliability issues at scale. Switching to our trifluorinated phenol, the backbone chemistry offers more predictable swelling and cross-linking. It’s not just theory—feedback loops from customers drive us to keep refining post-synthesis workup and packaging, especially for those scaling reactions to pilot or manufacturing scale.

    We also troubleshoot formulation bottlenecks where side reactions with amines or alkoxides ruined syntheses in other facilities. Some research partners document that competing products—those with less stringent trace metal controls—introduce enough contamination to throw off analytical reads or create regulatory delays. That’s a hard cost, both in dollars and in lost time. All of this feeds back into our ongoing efforts to oversee reagent flow, hygiene protocols for transfer lines, and real-time quality checks. It’s not abstract—it’s a daily reality for both us and the project managers counting on ready-to-use material at 99% or above.

    Process Safety and Environmental Realities

    Generating fluorinated aromatic compounds isn’t without its hazards. In over twenty years handling phenols, we have responded to incidents potentially avoided by paying attention to stability and reaction exotherms. Our team invests in continuous airflow and remote monitoring for chlorinated waste, and we keep a detailed account of every deviation from standard safety protocols. Large installations prefer trifluorinated phenols like ours because highly fluorinated alternatives often bring extra containment headaches, increase fume output, or require specialized PPE. Onsite engineers comment on the lower volatility and manageable flash point of 2,3,4-trifluorophenol, letting them operate under less restrictive engineering controls.

    For waste management, we’re frank: any aromatic phenol means dedicated containment and neutralization. Our own experience with solvent selection and batch discharge informs best practices we share openly with partner R&D teams, including solvent swaps that reduce airborne emissions. Working shoulder to shoulder with EHS auditors, we upgrade storage and transfer every time data points to a safer standard. This isn’t a marketing stance; it keeps our line operators comfortable and keeps regulatory visits straightforward. The trifluorinated profile, as we have tracked in incident logs, presents a durability and chemical compatibility edge over less substituted phenols, especially in systems prone to oxidant exposure or atmospheric moisture.

    Supply Chain and Logistics from the Source

    We produce 2,3,4-Trifluorophenol on dedicated lines to avoid batch-to-batch contamination, particularly from other halogenated aromatics that could confuse analytical downstream users. During volatile market swings, clients look for direct access to primary manufacturing sources. We receive requests for documentation, chain of custody tracking, and certificate uploads—every touchpoint shows the value of transparency and reliability.

    Packaging isn’t an afterthought; it results from receiving customer feedback about cracked ampoules or solvent incompatibilities in transit. Our teams developed lining processes and container resins that handle both bulk scale drums and lab-scale bottles, maintaining product integrity from bench to pilot plant. We’ve shipped overland to pharmaceutical hubs and through hazardous freight channels, adjusting insulation and reporting to local regulation needs. For customers with urgent analytical deadlines, transit interruptions required us to trial new cooling packs or change freight handlers—each revision driven by real delivery failures, not a theoretical logistics model.

    Comparing to Other Market Offerings

    Ours isn’t the only trifluorophenol, but direct sourcing stands apart when meeting tight specifications. We keep detailed, archived runs to track performance differences from competitor batches seen through international markets. Academic researchers highlight the clarity of our spectra compared to generic suppliers, reporting less background in NMR and cleaner baseline in GC-MS analysis. For synthetic chemists switching from older difluorophenols, the trifluoro arrangement enables those subtle electronic effects sought for new catalytic screens.

    Over the past decade, newcomers have introduced other positional trifluorophenols—like 2,4,5- or 2,4,6-trifluorophenols—yet differences emerge quickly in grant-funded lab studies and scaled pharma projects. The specific positions of fluorines in our product shift hydrogen bonding, solubility, and reaction pathway access. Some polymer developers shared data where a positional isomer triggered unpredictable crosslinks and solubility failures, costing weeks in product reformulation. Buying direct from a manufacturer, our partners contact us if batch inconsistencies ever arise—not an option with intermediaries who may not know the synthesis route or contaminant profile. As direct stakeholders, we give practical process history rather than generic certificates, and if an unexpected spectroscopic peak appears, we can trace it back to reactor maintenance records or input changes.

    Solving Real Challenges in New Product Development

    We don’t receive only routine orders. Some calls start with, “Our process collapsed with the last shipment from our previous source—can you help us recover?” That means teams genuinely frustrated with out-of-spec materials, or with off-odors or tints not appearing in the reference spectra. On several projects, developers attempted to substitute a generic difluorophenol for our 2,3,4 system, only to see physical incompatibility in solvent systems, inconsistent reaction endpoints, or chromatic changes in one-pot steps. The subtle nature of ring fluorination pattern creates these cascading effects. We worked alongside those partners to dissect impurities, troubleshoot analytical aberrations, and optimize their extraction and purification steps, often leading to higher isolated yields and improved shelf stability of their end products.

    Pharmaceutical process scale-up in particular often reveals the stark differences between small-batch, research-grade material and large-batch, consistent production. Academic groups appreciate gram-scale reproducibility; multikilogram batch customers demand ultrapure, repeatable lots. We have overhauled both upstream raw material handling and downstream filtration as a direct response to process feedback. Where off-brand or loosely sourced trifluorophenol led to wide melting point ranges and inconsistent color, our process controls hold steady—saving weeks or months otherwise wasted on repeat purification or process troubleshooting.

    Staying Open to Change and Innovation

    It would be easy to rely on established processes or chase trends in fluorinated fine chemicals. Instead, we invite suggestions for process trials, routinely opening the floor for new synthetic approaches and improved handling or safety regimes. Our facility handles feedback directly from chemical engineers, synthetic chemists, and lab QA heads. Adjustments—whether to crystallization temperature, impurity monitoring, or shipment packaging—emerge from practical needs, not theoretical perfection.

    Complex regulatory requirements continue to evolve, and each year brings new questions from customers developing consumer products or medical devices with stricter impurity or residue tolerances. We’ve adapted tracking and reporting systems so that when lots ship across borders—whether to regulatory-heavy pharmaceutical markets in Asia or North America—full documentation, history, and analytical traceability ship with each container. This transparency grew from repeated requests and compliance hiccups faced by both our partners and our own facility staff. Our records let a new customer verify performance before ever opening a drum or flask.

    What Sets Us Apart—A Manufacturer’s Perspective

    After decades in the field, we see the difference between pushing a product spec and collaborating on a concrete outcome. Our 2,3,4-Trifluorophenol isn’t just an entry in a catalog—it’s a cumulative effort of chemists, operators, engineers, and safety staff. Day-to-day, we respond to applications that test the boundaries: from cross-coupling and linker modification to bulk modification of advanced polymers. What makes a direct, knowledgeable manufacturer invaluable is the capacity to tune, diagnose, and support every phase of your development cycle, with facts and data captured over years of dedicated experience. You don’t get that from a trading house or reseller. Our priority isn’t only moving material from A to B, but building the confidence and practical support you need for your next technical breakthrough—in whatever sector your ambition takes you.