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2,3,5,6-Tetrafluorotoluene

    • Product Name 2,3,5,6-Tetrafluorotoluene
    • Alias 1,2,4,5-Tetrafluorotoluene
    • Einecs 206-210-1
    • 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

    328167

    Name 2,3,5,6-Tetrafluorotoluene
    Chemical Formula C7H4F4
    Cas Number 2454-66-6
    Appearance Colorless liquid
    Boiling Point 102-104 °C
    Melting Point -31 °C
    Density 1.387 g/cm3
    Refractive Index 1.436
    Flash Point 19 °C
    Solubility In Water Insoluble
    Vapor Pressure 20 mmHg (at 25 °C)

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

    Packing & Storage
    Packing Amber glass bottle, 500 mL, with screw cap; labeled with chemical name, hazard symbols, and handling instructions; securely sealed.
    Shipping 2,3,5,6-Tetrafluorotoluene is typically shipped in sealed, chemical-resistant containers to prevent leakage and contamination. It should be transported according to applicable regulations for hazardous materials, stored in a cool, well-ventilated area away from heat, ignition sources, and incompatible substances. Handle with appropriate personal protective equipment and safety precautions.
    Storage 2,3,5,6-Tetrafluorotoluene 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, heat, and direct sunlight. Ensure proper labeling and keep away from sources of ignition. Store in accordance with local regulations for hazardous chemicals. Personal protective equipment should be used when handling.
    Application of 2,3,5,6-Tetrafluorotoluene

    Applications of 2,3,5,6-Tetrafluorotoluene in Industrial Manufacturing

    2,3,5,6-Tetrafluorotoluene serves as a critical intermediate in various industrial production chains. Its distinctive aromatic structure and compatibility with halogenation and substitution reactions make it a preferred choice in multiple specialty chemical and pharmaceutical workflows. The following sections outline its concrete applications in established downstream manufacturing sectors.

    1. Agrochemical Intermediate Synthesis

    Major agrochemical producers incorporate this compound in the development of selective herbicide and fungicide actives, benefiting from its stability under chlorination and alkylation conditions. It enters the synthesis route as a fluorinated aromatic building block, where producers leverage its ortho/para-directing effects for subsequent functionalization. Users typically calibrate concentrations to ensure reactivity balance and eco-toxicological compliance in the final crop protection agent.

    Industry compliance standards

    • OECD Test Guidelines for Chemicals
    • REACH Regulation (EC) No 1907/2006
    • FAO/WHO Specifications for Agricultural Pesticides
    • ECHA CLP Regulation (EC) No 1272/2008

    Typical usage ratio

    • 10–35% by mol in total aromatic substrate load, adjusted by specific active ingredient target and downstream functionalization route

    Downstream process integration

    • Stage 1 or 2 of active ingredient synthesis, input as aryl fluoride core during halogen exchange, Grignard, or metal-catalyzed coupling reactions

    Final product types

    • Selective herbicides (e.g., fluorinated triazines, pyridine-carboxylates)
    • Advanced fungicides with enhanced resistance profiles

    2. Active Pharmaceutical Ingredient (API) Building Block

    Original pharmaceutical manufacturers leverage this tetrafluorinated aromatic as a precursor in medicinal chemistry programs, mainly for anti-infective and anti-inflammatory compounds. It provides key electronic modulation in benzyl moieties, which is essential for pharmacophore tuning. API process development teams integrate this building block during targeted halogenation and cross-coupling steps, with rigorous batch traceability and impurity control according to global GMP.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.)
    • United States Pharmacopeia (USP)
    • China Pharmacopoeia (ChP)

    Typical usage ratio

    • 5–15% by mol in stepwise syntheses, with specific proportion determined by target heterocycle attachment and downstream API route

    Downstream process integration

    • Introduced as key aromatic intermediate during Suzuki or Stille coupling, nucleophilic aromatic substitution, or halogen-lithiation protocols

    Final product types

    • Benzyl-fluorinated pharmaceuticals (e.g., anti-inflammatory and antimicrobial APIs)
    • Research reagents for medicinal chemistry screening

    3. Liquid Crystal Monomer Precursor

    Producers of advanced display technology and specialty polymers use this chemical as a high-purity monomer precursor, contributing to the synthesis of fluoroarene-containing mesogens for liquid crystal display (LCD) formulations. Quality-sensitive manufacturers select this source due to its defined para-hydrogen and ortho-fluorine substitution pattern, which imparts controllable dipole moments and viscosity in the final mesogenic mixture. Processes demand accurate dosing to optimize nematic phase performance and electro-optical switch speed.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for display applications)
    • IEC 62321 (Test methods for certain substances in electronics)
    • ISO 9001:2015 Quality Management Systems
    • IEC 60068 Environmental Testing for Electronic Components

    Typical usage ratio

    • 15–25% by mol in liquid crystal precursor blend, adjusted based on mixture viscosity requirements and display application-specific nematic properties

    Downstream process integration

    • Integrated in stage 1 or 2 synthesis of fluoroarene mono- and di-acrylate mesogens, followed by final mixing into custom LC formulations

    Final product types

    • Active-matrix and passive-matrix LCD panels for consumer electronics
    • Specialty optical films for high-contrast displays

    4. Functional Polymer Manufacturing

    Specialty plastic and high-performance polymer plants utilize this aromatic for synthesizing fluorinated monomers, which confer chemical resistance and surface energy tuning in engineered thermoplastics and copolymers. It functions as a molecular scaffold in the copolymerization process, commonly with vinyl or acrylate partners, to enhance hydrophobicity and flexibility in the final compound. Process engineers precisely manage concentration to ensure target molecular weight and property distribution during melt or solution polymerization.

    Industry compliance standards

    • ISO 1043 (Plastics – Symbols and terms)
    • ASTM D638 (Standard Test Method for Tensile Properties of Plastics)
    • REACH Registration for Industrial Monomers
    • UL 94 Flammability Testing for Plastics

    Typical usage ratio

    • 5–20% by weight in total monomer charge, tuned according to desired polymer fluorine content and bulk mechanical properties

    Downstream process integration

    • Fed into bulk or solution-phase copolymerization upstream of finishing steps such as pelletization and compounding

    Final product types

    • Fluorinated engineering resins for automotive and aviation parts
    • Coating-grade polymer granules for anti-adhesion films and gaskets

    5. Electronic Chemical Synthesis for Semiconductors

    Semiconductor chemical suppliers use this raw material in the preparation of specialty cleaning and etching agents, leveraging its stable fluorine-rich structure to achieve targeted thin-film and substrate cleaning with minimal residue. Integration typically occurs via fluorination and functional group modification in the manufacture of high-performance process chemicals used for semiconductor wafer production and advanced packaging.

    Industry compliance standards

    • SEMI C64 Specification for Advanced Cleaning Chemicals
    • IATF 16949 Automotive Quality Management for Semiconductors
    • IEEE IPC-CH-65B (Guidelines for Cleaning in Electronics Assembly)
    • IPC J-STD-001 (Requirements for Soldered Electrical Assemblies)

    Typical usage ratio

    • 3–10% by weight in formulated etchant or stripping solutions, with value determined by target cleaning efficacy and substrate compatibility

    Downstream process integration

    • Introduced during compounding of wet process chemicals, upstream of quality filtration and packaging for fab use

    Final product types

    • Photoresist stripper solutions
    • Microelectronic wafer cleaning chemicals
    Free Quote

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

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    Certification & Compliance
    More Introduction

    2,3,5,6-Tetrafluorotoluene: A Core Building Block Reshaping Fluorinated Chemistry

    Bringing Decades of Manufacturing Know-How to an Essential Intermediate

    Our team has produced 2,3,5,6-Tetrafluorotoluene for years, watching the landscape of specialty chemicals steadily shift toward higher performance and greater environmental care. We see growing demand for this compound, and that doesn't come as a surprise. Our hands-on experience has shown us its strengths and wide-reaching impacts, especially in the fields of agrochemicals, pharmaceuticals, and materials science.

    2,3,5,6-Tetrafluorotoluene stands out as a unique aromatic compound with a molecular structure that reflects true efficiency. Its molecular formula is C7H2F4CH3. What sets it apart: the fluorine atoms positioned on the benzene ring, which unlocks a set of reactivities and properties that conventional toluene or less-fluorinated analogs simply can't provide. We have worked with a spectrum of fluorinated toluenes, and this one holds its own thanks to that four-point fluorination.

    Experience in Production: Quality That Goes Beyond Specification Sheets

    From sourcing raw materials to the precision fluorination steps, our production lines constantly monitor the process. The molecular purity and handling requirements for 2,3,5,6-Tetrafluorotoluene call for an operator's eye and discipline. We avoid shortcuts and have learned, from batch to batch, how temperature and agitation shifts can impact the isomer ratio or introduce moisture. Our technicians can pick up subtle cues in halogenation that no automated monitor or third-party spec sheet catches. A sample run in our plant regularly hits typical purities above 99.5%, verified by NMR, GC, and moisture analysis.

    Storage practices for this compound matter. Over the years, we've found that stainless steel and inert atmospheres provide the best results. Customers speak up quickly if trace metal impurities drift into the final product, especially in downstream pharmaceutical or agrochemical applications, so we don’t gamble on packaging or transfer steps.

    Functional Advantages that Deliver More Than Just Fluorination

    Other methylated tetrafluorobenzenes exist, but positioning matters. In 2,3,5,6-Tetrafluorotoluene, the arrangement of fluorines on the ring shapes both reactivity and downstream function. We've seen this reflected in the feedback from our partners: different isomers change how products perform in the field, and this one offers a balance not seen in 2,3,4,5- or 2,3,4,6-isomers.

    Fluorination brings a stability that allows for straightforward chlorination or bromination, and the methyl group attached to the aromatic ring aids solubility in many organics. This combination supports both fine chemical synthesis and the development of more advanced crop protection agents. The properties of this compound reduce the number of transformation steps for many downstream products. Less byproduct means fewer headaches in waste management – a recurring theme that those of us on the production line keep top of mind.

    How the Industry Leverages Its Properties

    Repeated requests from pharmaceutical and agrochemical innovators have clarified the need for consistent, high-purity 2,3,5,6-Tetrafluorotoluene. The electron-withdrawing power of the four fluorine atoms shifts the ring's reactivity profile, favoring further substitution at specific positions unattainable from less-fluorinated toluenes. This has allowed our customers to push boundaries with more selective synthesis—for example, building complex active ingredients with lower risk of side reactions.

    As a building block, it offers a streamlined route to more advanced compounds, such as 2,3,5,6-Tetrafluorobenzaldehyde or various functionalized benzoic acids. Several partners in polymer technology have told us they prefer this isomer due to its influence on thermal resistance and chemical inertness in specialty coatings. We have adapted our process scale to handle projects of all sizes, from pilot to commercial rounds, as more companies choose to shift away from chlorine-rich feedstocks.

    Making the Transition to Greener Chemistry

    These days, sustainability is not a buzzword in manufacturing; it's a practical constraint. In the last decade, our plant has made direct changes to reduce emissions and energy use in the fluorination process. The isolation of tetrafluorinated aromatics used to rely on solvents burdened with regulatory and disposal challenges. Through collaborative R&D, we have tested and implemented continuous-flow techniques and new solvent recycling steps, shaving down both cost and waste. For customers concerned with the environmental footprint of their supply chain, these changes in our approach offer real and measurable benefits.

    Supply chain reliability matters more than ever, and 2,3,5,6-Tetrafluorotoluene frequently lands on the critical lists of chemical buyers worldwide. High-quality supply translates directly into time saved for downstream production teams; trace contaminants like unreacted tetrafluorobenzene or over-fluorinated byproducts can destroy yield or complicate isolation. Our operators run regular mock recalls and stress tests on raw material sourcing to prevent disruptions and keep plant runs predictable.

    What Sets It Apart from Other Fluorinated Toluenes?

    Chemically speaking, not all tetrafluorotoluenes behave alike. We've handled nearly every isomer and can say that the electronic characteristics and substitution patterns found in 2,3,5,6- isomer impact nucleophilicity, ring activation, and even volatility. This isomer features a methyl group positioned away from the ends of the ring, influencing boiling point and reactivity, particularly in nucleophilic substitution reactions. That becomes apparent in real production lines: yields tend to be higher, isolation gets simpler, and batch reproducibility improves compared to isomers like 2,3,4,5-tetrafluorotoluene.

    In customer labs, this translates into tangible gains. The methyl group offers a strategic entry point for further functionalization and supports more stable substitution patterns in final products. Over the years, we've seen fewer issues with side-product formation—allowing finished molecules to meet tight specs with less purification. This efficiency in synthesis and post-processing resonates with both R&D chemists and purchasing teams who track raw material throughput and cost per kilo.

    Applications That Shape Modern Chemistry

    The direct uses of 2,3,5,6-Tetrafluorotoluene cut across several vital sectors. Its principal use lies in the preparation of advanced agrochemical intermediates, where precise fluorination boosts efficacy and environmental persistence of the active ingredients. Research groups and pilot plants rely on our material for stepwise conversion into high-value aromatic aldehydes, acids, and further-fluorinated compounds required for next-generation pesticides.

    Pharmaceutical firms depend on it as both a scaffold and as a stepping stone to more complex ring systems, sometimes employing our product as an intermediate in anti-inflammatory or central nervous system therapies. We have collaborated with several who value our tight impurity control, as contamination at this stage can undermine the development of active pharmaceutical ingredients.

    It also finds a home in advanced materials, where the defined substitution pattern enhances the chemical resistance and durability of monomers destined for high-performance polymers, specialty elastomers, or liquid crystal applications. We understand from our customers that this property can expand the performance window of finished goods, from better oxidative stability to increased solvent resistance.

    Investing in Quality and Traceability

    Product quality does not stop at the reactor. We maintain full traceability from precursor to finished lot, going beyond standard documentation. Customers regularly request full analytical profiles, and our QA teams have grown skilled at answering unexpected technical questions—sometimes as mundane as color, sometimes as complex as impurity carryover.

    We operate with reference standards unique to our facility, not simply relying on global commodity specs. Historical data shows us that consistency across shipments eliminates requalification, shortens the time to market for every batch, and keeps production partners loyal. Our plant has fielded complicated questions from auditors focused on both supply reliability and sustainability metrics; our continuous improvement mindset backs up every claim with data.

    Challenges and Real-World Solutions

    Producing high-purity 2,3,5,6-Tetrafluorotoluene comes with its set of challenges, especially when scaling to multi-ton lots. Moisture and oxygen ingress can quickly degrade yield or compromise stability, turning a solid batch into scrap in hours. Over the years, we've tested and refined glovebox sampling, continuous inert blanket systems, and even our drum supplier list, based on lessons learned the hard way.

    Managing effluent and reducing HF emissions in the process became an early focus for us—hauling spent acids for neutralization once took both time and money. Today, we recover and reprocess acids whenever feasible and collaborate with regional partners to close the loop on waste. Steps like this have earned us positive feedback from customers looking for a responsible supply chain.

    On the market side, volatility in demand sometimes leaves excess stock or bottlenecks in availability. Our team addresses this with a blend of inventory planning and frequent forward demand checks with our regular buyers. Sudden market swings get buffered by our safety stock policies and commitment to transparency with our buyers about lead times and capacity.

    Looking Forward: Supporting Innovation with Reliable Chemistry

    What we’ve learned from years of manufacturing 2,3,5,6-Tetrafluorotoluene is that the story extends well beyond the molecule itself. Success lies in a blend of skill, attention to technical detail, and willingness to invest in cleaner, more robust processes. We continuously engage with chemical engineers, R&D scientists, and procurement teams from all over the world to understand evolving demands and resolve bottlenecks before they grow.

    As regulatory frameworks become stricter and market demands evolve, we prioritize direct conversations with customers—offering technical guidance, partnering on custom synthesis trials, and troubleshooting alongside their teams. Our belief is simple: reliable supply enables bolder innovation downstream, and by addressing issues at the manufacturing stage, we create value up the chain.

    A Commitment to the Future of Fluorinated Compounds

    2,3,5,6-Tetrafluorotoluene continues to earn its place as a critical intermediate for innovation-driven industries. Decades in this field have shown us how incremental improvements—tighter control of impurities, lowered process emissions, and more adaptive production scheduling—feed directly into better science and safer products. By investing in the people, processes, and partnerships that shape every shipment, we set a higher standard for specialty chemical manufacturing.

    With every reactor charge, every outgoing drum, and every conversation with a partner on the other side of the world, we reinforce our dedication to quality and forward-thinking chemistry. Every bottle shipped from our plant represents not just a product, but also a series of decisions made to ensure that research, innovation, and global industry can rely on a dependable source for high-purity 2,3,5,6-Tetrafluorotoluene.