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2,3,4,5,6-Pentafluorobenzhydrol

    • Product Name 2,3,4,5,6-Pentafluorobenzhydrol
    • Alias Perfluorodiphenylmethanol
    • Einecs 221-048-8
    • 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
    VTB
    Specifications

    HS Code

    426249

    Name 2,3,4,5,6-Pentafluorobenzhydrol
    Molecular Formula C13H5F5O
    Molecular Weight 272.17 g/mol
    Cas Number 771-62-6
    Appearance White to off-white solid
    Melting Point 92-95 °C
    Density 1.52 g/cm³ (approximate)
    Solubility In Water Insoluble
    Smiles C1=CC=C(C=C1)C(O)C2=C(F)C(=C(F)C(=C(F)C2=O)F)F
    Inchi InChI=1S/C13H5F5O/c14-10-7(15)4-3-8(16)12(10)13(19)9-5-1-2-6-11(9)17/h1-6,13,19H
    Storage Temperature Store at 2-8 °C
    Purity Typically ≥98%

    As an accredited 2,3,4,5,6-Pentafluorobenzhydrol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 5 grams, labeled with chemical name, hazard symbols, lot number, and tightly sealed with a screw cap.
    Shipping 2,3,4,5,6-Pentafluorobenzhydrol should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be clearly labeled following hazardous material regulations. For air or sea transport, use appropriate chemical packaging per IATA/IMDG guidelines, ensuring secondary containment to prevent leaks and exposure during transit. Handle with care.
    Storage 2,3,4,5,6-Pentafluorobenzhydrol should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and avoid excessive heat. Proper labeling and containment are important to prevent leaks and exposure. Follow all relevant safety and regulatory guidelines.
    Application of 2,3,4,5,6-Pentafluorobenzhydrol

    Applications of 2,3,4,5,6-Pentafluorobenzhydrol in Industrial Manufacturing

    As a dedicated manufacturer of 2,3,4,5,6-Pentafluorobenzhydrol, we supply this specialty intermediate for high-value chemical synthesis across multiple industrial sectors. Below, we detail its recognized downstream applications, with focused context on regulations, incorporation strategies, production processes, and resulting end products.

    1. Pharmaceutical Fluorinated Intermediate Synthesis

    2,3,4,5,6-Pentafluorobenzhydrol serves as a highly activated building block in the synthesis of fluorinated pharmacophores, specifically for the production of molecular scaffolds incorporated into next-generation central nervous system (CNS) active pharmaceutical ingredients (APIs). Process chemists use it in nucleophilic aromatic substitution, facilitating late-stage fluorination in multi-step small molecule synthesis for drug candidates demanding enhanced metabolic stability and bioavailability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Guidelines – Part II for APIs
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • Pharmacopeial monographs for active ingredient impurities (USP, EP as referenced by downstream API manufacturers)

    Typical usage ratio

    • Applied at 0.5–3.5 molar equivalents relative to the coupling partner, the precise ratio adapts to the specific synthetic route and batch scale-up constraints; chemists often adjust loading based on targeted degree of fluorination and yield optimization.

    Downstream process integration

    • Charged during the key nucleophilic aromatic substitution or Grignard-type coupling stage in the multi-step API synthesis pathway, often under strictly anhydrous, inert conditions to prevent undesired side reactions.

    Final product types

    • Active pharmaceutical ingredients (e.g., fluorinated CNS drugs, oncology therapeutics)
    • Advanced pharmaceutical intermediates for contract manufacturing organizations (CMOs)

    2. Agrochemical Active Ingredient Development

    Agrochemical manufacturers utilize this pentafluorinated benzhydrol derivative as a core reagent for synthesizing phenyl-based herbicide and fungicide actives with improved environmental persistence and target binding. Its high electronegativity profile enables efficient modification of aromatic rings, central to the development of next-generation crop protection molecules emphasizing controlled degradation rates and increased efficacy against resistant species.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (e.g., Guideline 501–510, pesticide active ingredient testing)
    • ISO 9001:2015 Quality Management in Crop Protection Chemicals
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • US EPA PR Notice 2011-1 for inert ingredients in agricultural formulations

    Typical usage ratio

    • Dosage varies by downstream synthesis pathway; commonly 1.0–2.0 molar equivalents with respect to halogenated aromatic or heterocyclic coupling substrates. Usage levels adjust based on conversion rates, target compound specificity, and process yield.

    Downstream process integration

    • Introduced during the formation of the key aromatic core structure in active ingredient (AI) synthesis steps, usually before chlorination, amination, or further fluorination stages in batch or semi-continuous reactors.

    Final product types

    • Novel fungicide active substances
    • Herbicide molecules for resistant crop strains
    • Registered agrochemical intermediates for partner formulation plants

    3. Electronic Materials – Liquid Crystal Precursor Synthesis

    Producers of specialty electronic materials employ our product as a reactive intermediate in the custom synthesis of pentafluorinated biphenyls and terphenyls, which are essential for high-performance nematic and smectic liquid crystal compounds. Its perfluorinated nature imparts critical dielectric anisotropy, helping display manufacturers achieve responsive, thermally stable liquid crystal mixtures for advanced thin-film transistor and OLED display technology assembly lines.

    Industry compliance standards

    • IEC 61249-2-43: Materials for Printed Boards and Other Interconnecting Structures
    • RoHS (Restriction of Hazardous Substances Directive, EU 2015/863)
    • ISO 9001:2015 Certification in specialty electronic materials manufacturing
    • REACH Regulation (EC) No 1907/2006 for chemical registration and safe use in the EU

    Typical usage ratio

    • Typically introduced at 0.8–1.5 equivalents, calculated against the di- or multi-functional core precursors, balancing desired level of fluorination and final alignment properties of the liquid crystal composition.

    Downstream process integration

    • Integrated in controlled Suzuki or Ullmann coupling reactions conducted at early or intermediate steps in the assembly of the final liquid crystal molecule, under argon atmosphere to prevent hydrolytic defects.

    Final product types

    • Nematic and smectic liquid crystal blends for TFT-LCD panels
    • OLED alignment layer additives
    • Polymeric liquid crystal building blocks

    4. High-Performance Coating Resin Modifier

    Manufacturers of specialty coatings and advanced polymer resins select 2,3,4,5,6-Pentafluorobenzhydrol as a functional monomer for producing fluorinated polyesters and epoxy resins. Its incorporation greatly enhances hydrophobicity, chemical resistance, and weatherability—essential features for anti-corrosion coatings, non-stick applications, and optical coatings for industrial and architectural markets.

    Industry compliance standards

    • ISO 12944 (Corrosion Protection of Steel Structures by Protective Paint Systems)
    • ASTM D5201 (Standard Practice for Laboratory Testing of Coating Resistance to Chemicals)
    • REACH Annex XVII (restrictions for chemicals used in coatings in the EU)
    • GSB International “GSB-ST 663 – Requirements for Coating Materials” for architectural applications

    Typical usage ratio

    • Blended at 1–7 wt% of resin mass for polyesters or epoxies, with higher ratios used for premium anti-fouling or chemical barrier coatings; final proportion determined via accelerated aging, adhesion, and resistance benchmark testing.

    Downstream process integration

    • Charged into the pre-polymerization stage for direct reaction with acid/anhydride or epoxide functional groups, facilitating covalent integration and uniform fluorination throughout the cured coating matrix.

    Final product types

    • Industrial anti-corrosion coatings
    • Non-stick cookware and bakeware coatings
    • Protective optical films for display and architectural glass

    5. Specialty Fluorous Phase-Transfer Catalyst Synthesis

    Producers of specialty catalysts employ 2,3,4,5,6-Pentafluorobenzhydrol to prepare fluorous-tagged phase-transfer catalysts used in biphasic organic reactions. The compound’s perfluorinated aryl group enables formation of fluorous-linked ligands, which provide high recovery efficiency in catalytic cycles, facilitating greener, solvent-minimized synthesis approaches for pharmaceutical and fine chemical factories pursuing sustainable manufacturing strategies.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems in chemical manufacturing
    • Responsible Care® initiative for sustainability in specialty chemicals
    • REACH (EC) No 1907/2006 for phase-transfer and auxiliary chemicals
    • Internal validated protocols for fluorous phase-transfer catalysis (frequently referenced in proprietary GMP-supporting documentation)

    Typical usage ratio

    • Generally used at 1.0–1.2 equivalents per targeted catalyst molecule, ensuring adequate surface functionalization and effective catalyst recovery rates when recycled between process stages.

    Downstream process integration

    • Incorporated via alkylation or acylation reactions in the late-stage synthesis of the phase-transfer ligand, prior to immobilization onto fluorous silica or polymer backbones for use in column or batch operations.

    Final product types

    • Fluorous phase-transfer catalysts for pharmaceutical synthesis
    • Recyclable biphasic ligands for industrial-scale organic reactions
    • Custom fluorous auxiliaries for continuous flow chemistry systems
    Free Quote

    Competitive 2,3,4,5,6-Pentafluorobenzhydrol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,3,4,5,6-Pentafluorobenzhydrol: A Chemist’s View on Precision and Performance

    Decades in the fine chemical business teach valuable lessons about understanding both the opportunities and the quirks of specialty building blocks. At our factory, our chemists spend much of their time evaluating demanding customers’ needs, especially for specialty fluoro-organic intermediates. One product that repeatedly surfaces in their requests is 2,3,4,5,6-pentafluorobenzhydrol, a molecule whose unique chemical structure opens important doors in research and industry.

    Fluorine Changes the Rules

    Organic chemists know that replacing hydrogens with fluorines in aromatic rings transforms the behavior of those rings. Pentafluorobenzhydrol stands apart from regular benzhydrol mainly because full fluorination of the phenyl ring impacts everything from polarity to reactivity. Our customers see these properties reflected in their syntheses, where this product delivers benefits that standard benzhydrol can’t provide.

    Often, producers of functionalized aromatics overlook the complications that fluorine brings to the reactions. Fully fluorinated rings resist most forms of electrophilic aromatic substitution and lend uncommon stability. At the same time, the benzylic alcohol group present in pentafluorobenzhydrol makes it a compelling intermediate for those building more complex molecules—everything from pharmaceuticals to advanced agrochemicals. The impact of five fluorines sitting on the benzene ring is unmistakable in terms of both synthetic strategies and final application.

    Specifications that Matter on the Bench

    Quality makes all the difference when working with sensitive substrates. Our process technicians have honed protocols tailored to the nuances of this compound, emphasizing a combination of purification and rigorous in-line analysis. Each batch undergoes melting point, NMR, and elemental analysis by seasoned staff before packaging. We use only trace-free, high-purity starting materials, integrating careful distillation and low-temperature handling to maintain integrity from synthesis to shipment.

    Over the years, feedback from academic labs and major pharmaceutical companies has fine-tuned our approach. Reproducibility matters most in multi-step syntheses. The rigid quality assurance for pentafluorobenzhydrol ensures that its appearance matches specification: a high-melting, crystalline solid, free from any yellowish tint that signals decomposition or residual reactants. Particularly in fluoroaromatic chemistry, trace impurities or moisture can sabotage experiments, so our packing lines integrate sealed containers with reliable labeling and tracking for recall assurance.

    Why Researchers and Developers Choose Pentafluorobenzhydrol

    This compound stands out because fully fluorinated benzhydrol derivatives offer a platform for both nucleophilic and electrophilic manipulations. Lab researchers regularly provide feedback that fluorinated alcohols, like 2,3,4,5,6-pentafluorobenzhydrol, help build complex heterocycles and drive unique perfluoroaromatic substitution reactions. Where traditional benzhydrol can polarize too easily or react too vigorously, the pentafluoro-version brings greater predictability and increased resistance to overreactions.

    We have seen pentafluorobenzhydrol integrated into advanced liquid crystal formulations, especially in precision optical device manufacturing. In those applications, any deviation in purity can impact phase stability, birefringence, or even color fidelity. Other customers use the compound as a stepping stone to pentafluorophenyl-substituted indoles and carbazoles—key scaffolds for OLED material design. Custom synthesis teams in major multinationals have described this intermediate as a “cornerstone building block” for fine-tuning both steric and electronic effects in functional materials. Some research groups, exploring perfluorinated ligand synthesis, describe pentafluorobenzhydrol as almost irreplaceable, enabling yields and selectivity difficult to achieve with less fluorinated analogs.

    Production: Safety and Reliability Matter

    The organic synthesis of fully fluorinated aromatic compounds is both art and science. Years in the pilot plant have taught our chemists how fast mishaps and cross-contamination can spiral with sensitive intermediates. Fluorinated aromatic compounds often generate toxic and persistent byproducts if overreacted. We’ve invested in specialized fluoropolymer-lined reactors, custom gas scrubbing, and closed-system handling to ensure absolute consistency and safety.

    Our colleagues in other companies often encounter challenges when adapting their standard benzhydrol protocols to pentafluorinated variants. Direct experience has shown that simple substitution or “one size fits all” approaches don’t deliver high-purity product. Exothermicity and byproduct formation rise sharply without tight control of reaction parameters. We run under strict temperature and atmosphere controls, with full traceability for every raw material.

    Product Differences: Pentafluorination Is No Small Tweak

    It helps to look at where pentafluorobenzhydrol breaks from the pack. Standard benzhydrol, a staple intermediate in many university labs, finds its limits in modern demanding syntheses. Partial fluorination of the ring nudges reactivity but only full pentafluorination—like you see here—delivers both chemical resistance and targeted reactivity.

    Alternative benzhydrols, those with less than five fluorines, change aromatic properties only incrementally. For those seeking to introduce perfluorinated groups at a late stage, smaller fluorinated benzhydrols can’t match the level of electron-withdrawing effect. The result is greater control over nucleophilic aromatic substitution, higher purity yields in condensation, and greater downstream functional group tolerance for the user.

    Many customers comment that pentafluorobenzhydrol allows sharper melting points and improved analytical traceability—useful in regulated environments. In practice, other benzhydrols frequently leave haze or oily residuals that hamper process development. Fluorine’s dominance on the ring in our product almost always confers crystalline stability and cleaner purification.

    Addressing Industry Challenges in Fluoroaromatics

    Fluorine chemistry marches to its own tune, demanding careful waste handling, worker training, and specialized equipment. Our own factory faced plenty of hurdles before hitting dependable quality and yield. The reliability of pentafluorobenzhydrol rests on deep process understanding at every production step. Our operators gain hands-on training using real-world batch data, not just manuals. That experience pays off in better consistency and in smarter troubleshooting.

    A recurring challenge is chemical waste, especially HF and fluoride-rich effluents. We built an on-site recovery and scrubbing facility, taking care to separate organic and inorganic waste streams. Regulations tighten every year, pushing for lower emissions and stricter documentation. Meeting these standards doesn’t come from checklists, it comes from quietly integrating cleaner methods, solvent reductions, and more robust filtration.

    Labs seeking this specialty product often struggle to secure material with both technical-grade consistency and safety built into the delivery. Our client-facing scientists regularly discuss handling and application protocols before each shipment, making sure end-users know the nuances of storage, transfer, and usage. Direct communication with users often uncovers small tweaks needed in packaging or documentation. That sort of transparency helps avoid mishaps down the line and generates repeat customers.

    Sustainability Considerations: Responsible Fluorochemical Manufacturing

    Sustainability matters to anyone dealing with persistent fluorinated chemicals. We continually work to minimize waste, cut solvent consumption, and harvest useful byproducts wherever possible. Recovery systems, solvent distillation, and secondary reuse help us tighten the loop from start to finish. Broad teams, from reaction chemists to shipping staff, contribute practical improvements—whether it means switching drum liners to recyclable polymer or minimizing energy use in the crystallization step.

    The perfluorination in pentafluorobenzhydrol sometimes draws scrutiny because perfluoro-compounds resist natural breakdown. Responsible handling from synthesis through delivery sets the foundation for longer-term stewardship. Working with downstream customers to retrieve and destroy off-spec or surplus chemicals closes the sustainability loop, and we pursue partnerships to pilot greener degradation pathways for used material.

    The Role of 2,3,4,5,6-Pentafluorobenzhydrol in Next-Generation Materials

    Research teams in diverse industries look to perfluorinated intermediates like pentafluorobenzhydrol as enablers for next-generation polymers, specialty pharmaceuticals, and advanced surface coatings. Its strategic value lies in modulating both steric and electronic features of target molecules. Medicinal chemists exploit these effects to increase metabolic stability and fine-tune binding affinity, while polymer researchers take advantage of the rigidity and chemical inertness imparted by the pentafluorophenyl group.

    Experience shows that specialty monomers made with pentafluorobenzhydrol feature in specialty adhesives and resins that resist chemical and UV degradation. In electronics, proprietary blends leverage its features for moisture-resistant encapsulants and ultra-thin coatings. Our technical team collaborates with users to engineer process routes that balance performance with cost and regulatory permission. This interplay between structure and final utility makes pentafluorobenzhydrol a highlight in the toolkit of inventive laboratories.

    Application Insights from Our Team

    Over many years, our application lab fielded requests to tailor the crystal size or purity for specific projects. We see academic customers who need a handful of grams for method validation, fresh startup ventures looking for scalable kilogram lots, and multinationals requesting technical advice on downstream derivatization. Using pentafluorobenzhydrol as a precursor to oxazolines, indanes, and other heterocycles illustrates how one versatile intermediate can fit into dozens of synthetic schemes.

    Having direct conversation with bench chemists gives a sense of the common stumbling blocks—solubility in mixed solvents, thermal sensitivity, or compatibility with metal catalysts. We adjust isolation and drying procedures to factor in these parameters, helping users minimize batch failures. Institutions with unique regulatory or documentation demands benefit from secure, controlled micro-batch packaging, and we document every step with validated analytics.

    Those working in dye chemistry often pick pentafluorobenzhydrol for its clean, high-yield pathway to perfluorinated triphenylmethane dyes. In that area, even small shifts in impurity profiles can blur spectral signatures, so reliability in synthesis and analytics wins return business and research partnerships.

    Patient, Iterative Process Improvements

    Manufacturing pentafluorobenzhydrol is neither quick nor forgiving of shortcuts. Our technical crew spends hours on root-cause investigations for even marginal deviations in product performance. High-purity output depends on relentless tuning of parameters—whether it’s adjusting the temperature ramp during reduction, inspection of feedstock for micro-level contamination, or spot-testing filtration elements in the off-streams.

    Staying ahead of regulatory trends forms a critical aspect of the factory’s daily work. We scrutinize new legislation on both local and international levels. Export controls, hazardous transport guidelines, and new fluorochemical frameworks in Europe or North America influence both process and packaging. That makes continued investment in process validation and system automation worthwhile, reducing errors while demonstrating compliance on demand.

    Future Directions and Solutions for Emerging Needs

    Market demand for high-performance, specialty fluoro-organics grows every year, yet expectations for environmental stewardship and safety escalate alongside. We continually pilot new synthesis pathways aimed at lowering energy input or capturing more value from reaction side streams. Our work with industry working groups brings opportunities to standardize new handling methods and recovery systems for challenging fluorinated products.

    Partnerships with academic and industrial labs enable early feedback loops for direct R&D improvements. We see our role not only as a supplier, but as a collaborator who brings manufacturer expertise directly to bear on midstream problems. Lessons from years of routine audits and client site visits translate into flexible packaging options or technical bulletins that directly address customer troubleshooting.

    In the world of specialty chemicals, details matter—from a single point of higher melting residue right up to consistent, lot-to-lot IR and NMR spectra. Pentafluorobenzhydrol exemplifies what’s possible when manufacturers blend real-world lab feedback with disciplined process design. Through long-term investment, consistent staff development, and attention to global best practices, we see pentafluorobenzhydrol—and those using it—benefiting from hard-earned manufacturer experience and a spirit of continuous improvement.