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Ethyl 2,3,4,5-Tetrafluorobenzoate

    • Product Name Ethyl 2,3,4,5-Tetrafluorobenzoate
    • Alias Ethanol 2,3,4,5-tetrafluorobenzoic acid ester
    • Einecs 319-954-4
    • 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

    962717

    Product Name Ethyl 2,3,4,5-Tetrafluorobenzoate
    Cas Number 380430-34-2
    Molecular Formula C9H4F4O2
    Molar Mass 220.12 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.415 g/cm3 (approximate)
    Solubility Soluble in organic solvents like chloroform, dichloromethane
    Smiles CCOC(=O)C1=CC(F)=C(F)C(F)=C1F
    Inchi InChI=1S/C9H4F4O2/c1-2-15-9(14)5-3-6(10)8(12)7(11)4-5/h3-4H,2H2,1H3
    Refractive Index n20/D 1.448 (estimated)
    Purity Typically ≥97% (commercial grade)
    Storage Store at 2-8°C, keep container tightly closed

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

    Packing & Storage
    Packing Ethyl 2,3,4,5-Tetrafluorobenzoate, 25g, supplied in a sealed amber glass bottle with tamper-evident cap and safety labeling.
    Shipping Ethyl 2,3,4,5-Tetrafluorobenzoate is shipped in tightly-sealed containers to prevent moisture ingress and contamination. Packages are clearly labeled according to chemical safety regulations and protected against breakage during transport. Always store and ship at ambient temperature, away from incompatible materials, and in compliance with all relevant local and international shipping regulations.
    Storage Ethyl 2,3,4,5-tetrafluorobenzoate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep the storage environment free from moisture and sources of ignition. Use proper chemical safety practices and store at recommended ambient conditions, typically at room temperature unless specified otherwise by the supplier.
    Application of Ethyl 2,3,4,5-Tetrafluorobenzoate

    Applications of Ethyl 2,3,4,5-Tetrafluorobenzoate in Industrial Manufacturing

    As a specialized manufacturer of Ethyl 2,3,4,5-Tetrafluorobenzoate, we consistently serve advanced sectors where selective fluorinated intermediates are critical. Below, we outline the practical downstream scenarios for this compound, focusing on real-world manufacturing contexts, critical compliance benchmarks, actual incorporation rates, defined entry points in downstream production, and characteristic end-use products.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Several pharmaceutical companies use this compound as a designated building block for synthesizing fluorinated aromatic intermediates in small-molecule drug discovery pipelines, especially for oncology and CNS disorder therapeutics. It enables the introduction of densely fluorinated aromatic rings, improving physicochemical profiles and metabolic stability in the resulting APIs.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF Monographs for relevant downstream APIs
    • EU EudraLex Volume 4 GMP
    • US FDA 21 CFR Part 211

    Typical usage ratio

    • 0.6–2.0 molar equivalents, adjusted based on specific route and desired fluorination density in each pharmaceutical intermediate

    Downstream process integration

    • Introduced in the aromatic substitution or ester hydrolysis stage of multi-step synthetic routes, usually under inert atmosphere and strictly temperature-controlled reactors during medicinal chemistry or pilot-scale campaigns

    Final product types

    • Active pharmaceutical ingredients for anti-tumor agents
    • Clinical-stage CNS drug candidates
    • Fluorinated analogs of established small molecules

    2. Agrochemical Intermediate Manufacturing

    Manufacturers utilize this material to construct highly fluorinated aromatic skeletons in the synthesis of next-generation herbicides and insecticides. Its controlled reactivity and selective substitution support the production of compounds with enhanced bioavailability and soil persistence, vital for agricultural chemistry.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Ingredients
    • ISO 9001:2015 quality management systems
    • OECD Good Laboratory Practice (GLP)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • 1.0–2.5% by mass of total synthetic feedstock, depending on the final fluorine content and yield targets of the target agrochemical

    Downstream process integration

    • Added during the aromatic coupling step or subsequent transesterification reactions in batch or semi-continuous reactors, with process tracing through HPLC for residual ester monitoring

    Final product types

    • Selective herbicide active ingredients (e.g., fluorinated benzoate derivatives)
    • Fluorinated insecticide core structures

    3. Specialty Polymer Monomer Feedstock

    Industry formulators value this compound for introducing tetrafluorinated moieties into advanced polymer matrices. In performance plastics and high-temperature fluoropolymers, it contributes to greater chemical inertness, reduced dielectric constants, and improved resistance to UV degradation in final goods.

    Industry compliance standards

    • ASTM D5630 – Fluoropolymer Resin Specifications
    • RoHS Directive 2011/65/EU for restricted substances
    • ISO 9001:2015 for quality control in polymer compounding
    • UL 94 for flammability ratings

    Typical usage ratio

    • 1.5–5.0% by total monomer weight, adjusted for desired fluorine content and target polymer performance parameters

    Downstream process integration

    • Blended during the initial monomer charging phase in melt or solution polymerization; sometimes undergoes pre-functionalization before copolymerization in high-shear reactors

    Final product types

    • Fluorinated engineering thermoplastics
    • Hybrid fluoropolymer blends for electronics insulation
    • Specialty coatings for photovoltaic backsheet films

    4. Liquid Crystal Intermediate for Display Technology

    Leading liquid crystal manufacturers integrate this compound in precision syntheses of tetrafluorinated aromatic intermediates to tune polarity and birefringence of advanced LC mixtures. Its structural features allow for refined molecular design improving switching speeds in high-end display applications.

    Industry compliance standards

    • JEITA ED-4701 Testing Methods for Liquid Crystal Materials
    • ISO 9001:2015 process and supply chain documentation
    • IEC 61249-2-21 for restricted substances
    • RoHS and REACH compliance for electrical and electronic equipment

    Typical usage ratio

    • 0.2–1.0% by mass in specific LC precursor formulations, tailored to performance targets for birefringence and melting point in final display blend

    Downstream process integration

    • Employed at the fluorinated aromatic substitution step during synthesis of LC core materials, typically under inert and moisture-controlled conditions

    Final product types

    • Low-voltage nematic LC compounds
    • High-performance display-grade liquid crystal mixtures
    • Specialty LC compounds for rapid-switching TFT LCD panels

    5. Fluorinated Aromatic Compound for OLED Materials

    In OLED emissive layer material development, this compound serves as a key intermediate for synthesizing fluorinated benzene derivatives, enhancing electron mobility and lifetime of emissive molecules in organic light-emitting diodes. Downstream processing leverages its controlled reactivity for targeted substitution and condensation reactions, contributing to advanced device stability and brightness.

    Industry compliance standards

    • IEC 62321 for regulated substances in electronic components
    • ISO 14001:2015 for environmental management during material synthesis
    • RoHS Directive 2011/65/EU
    • JEITA OLED material quality specifications

    Typical usage ratio

    • 0.3–1.5% per OLED batch, optimized for molar conversion and electronic structure in the precursor mixture

    Downstream process integration

    • Integrated in a Suzuki or Buchwald–Hartwig coupling stage with boronic acids or amines, typically under argon with Pd catalysis, followed by purification prior to vacuum deposition or solution casting

    Final product types

    • Emissive layer host materials for OLED panels
    • Electron transport layer precursors
    • Blue and green OLED emitter compounds
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    Certification & Compliance
    More Introduction

    Insight into Ethyl 2,3,4,5-Tetrafluorobenzoate: Practical Uses & Distinctive Features

    Starting from the Shop Floor: Manufacturing Priorities

    Every batch of Ethyl 2,3,4,5-Tetrafluorobenzoate draws on the kind of practical experience built from years at the production line. Our team handles the synthesis from the ground up, paying attention to the right fluorinating steps and precise esterification. In this process, we never lose sight of what matters—clean reactions, consistent yield, and minimizing byproduct formation so downstream handling stays straightforward. The defining aspect is its four fluorine atoms occupying the 2,3,4,5 positions on the benzoate ring, which means dramatic shifts in chemical behavior compared to single-fluorinated or non-fluorinated analogs.

    Within the plant, process tweaks derive from daily reality. Ethylation conditions get tuned depending on the precursor’s reactivity, and fluorine content undergoes routine spot checks via in-house analytics. We’re not guessing at purity—we use validated methods to keep it tight. Whenever someone spots a trace of residual acidity or off-color product from a less-than-ideal run, people gather to troubleshoot and refine the method. Over time, the workflow reflects a tight balance of efficiency, safety, and environmental controls. We’ve learned that rigorous solvent recycling matters not just for compliance but for real cost savings and worker well-being.

    Defining the Chemical: Where Application Shapes Practice

    Ethyl 2,3,4,5-Tetrafluorobenzoate serves as a building block that often goes underappreciated except by those diving deep into specialty synthesis. Drug discovery outfits and crop science companies prize high-purity materials that behave reliably across scale-up. This is not some generic benzoate for vanilla esters—its electron-deficient aromatic system sets it apart. The four fluorines drive up stability in harsh conditions and significantly influence reactivity in further transformations, which is exactly what chemists look for when developing new active ingredients or intermediates for functional polymers.

    We’ve shipped this compound for projects exploring selective cross-coupling chemistry, where the placement of each fluorine has a direct effect on regioselectivity and product distribution. In the plastics modification sector, some clients use it as a precursor for introducing tough fluorinated moieties into materials that demand resilience against aggressive solvents or corrosive agents. Our shop floor sees orders ranging from multi-kilogram runs for pilot plant campaigns, where exacting repeatability gets tested, to small-batch requests destined for narrow, high-value research.

    We handle every request knowing end-users build real projects around reliable timelines and trusted specs. Our in-house technical support doesn’t just know this compound on paper—they’ve spent hours tracking down root causes for single-digit loss in purity or advising on safe solvent recovery. Shipping departments know to take humidity control seriously to prevent hydrolysis and guard against shelf-life reduction.

    Model and Specifications: Practical Details, Not just Data Points

    From operator to chemist to packager, every person working with Ethyl 2,3,4,5-Tetrafluorobenzoate cares about delivering a product that matches the intended end-use. Our batches typically range in the scale most R&D and industrial clients expect, and the product appears as a colorless to pale yellow liquid or oil, depending on batch and storage. We target high assay values as measured by GC and NMR against reference standards, not merely paperwork best guesses. Moisture and residual acid analyses get attention because even microscopic contamination can derail a whole synthesis.

    Every production lot comes straight from our reactor suite, which gets used to handling hazardous reagents safely—fluorinated intermediates take respect, not shortcuts. Tanks, vessels, and lines receive regular passivation and maintenance to ensure no unplanned corrosion sneaks in. Our staff handles in-process and finished lot samples with calibrated equipment, and technical staff scrutinizes every outlier before a shipment ever leaves.

    We’ve learned over years that clients working with this compound usually require narrow impurity profiles rather than just a “good enough” label. There’s always a small overlap with neighboring analogs, like mono- or trifluorinated benzoates, but the physical and chemical properties differ substantially. Volatility, boiling point, and reactivity with nucleophiles—or in palladium-catalyzed functionalizations—stand out as distinctly altered by four contiguous fluorines.

    Field Reports: Usage in the Real World

    Over many cycles of market demand, we’ve noticed key trends in usage. Research chemists and scale-up process teams regularly reach out about this ester for introductions into multi-step synthetic ladders. It’s not just a filler molecule; it often provides both electronic and steric effects that alternative esters cannot. Addition or removal of even one fluorine significantly alters both reactivity and physical handling. We’ve heard feedback from pharmaceutical teams needing the four-fluoro variant for very specific SAR studies, unable to substitute with a trifluorinated or less-substituted ester due to distinct activity profiles observed in advanced screens.

    We field requests from agricultural researchers working on herbicide or fungicide active ingredients, since the four-fluoro pattern has become a staple motif in molecules that must resist metabolic degradation and withstand weathering during field tests. Notably, this benzoate ester stands up to conditions that can degrade less protected analogs. In some cases, we’ve partnered with clients to find safer storage protocols or new transportation methods for field-deployed inventory, adapting drum liners or packaging based on real incidents. This degree of collaboration rarely comes from a purely trading-focused supply chain.

    In our direct experience, requests for custom synthesis often pivot around challenges with alternate benzoate derivatives. Some operations seek only low-impurity material for diagnostic probes, where side products from over-fluorination or migration could throw off critical readouts. Applications in electronics and materials require attention to low residual ionic content, since even trace contamination from production equipment impacts insulation performance or polymer lifetime. Years of back-and-forth with clients have led us to implement more rigorous final filtration and distinct batch segregation to maintain standards at every level.

    Distinct Differences – Not All Benzoates Compete in the Same Arena

    Ethyl 2,3,4,5-Tetrafluorobenzoate consistently draws special attention from formulation chemists and synthetic researchers for reasons rooted in its unique substitution. One immediate difference from common benzoic acid esters lies in its resistance to nucleophilic attack; fully fluorinated rings slow down many common degradation routes, which gives formulators more latitude in extending shelf-life or blocking reactive breakdown in aggressive conditions. Industry peers who work with mono- or difluoro analogs quickly notice milder electronic withdrawal and different spectral signatures, which translate to less stability in real-world applications.

    On the chemical reactivity front, this tetrafluoro pattern shows a decided edge, especially in modern coupling or aromatic substitution methods. Trifluoromethyl or single-fluoro benzoates simply cannot replicate the set of influences that the 2,3,4,5 arrangement imparts to downstream intermediates. We’ve fielded inquiries from process chemists running Suzuki or Buchwald-Hartwig reactions, where this substrate’s predictable reactivity paired with reduced side product profiles means fewer purification headaches at production scale.

    Handling and storage demands also set this product apart. The volatility profile discourages prolonged air exposure, a point trade and distribution outfits often gloss over, leading to quality drifts and headaches for the end-user. In our plant, we control packaging atmosphere and run periodic shelf-life studies to nail down the true behavior in storage so users avoid surprises.

    We learn a lot from conversations with end-users who have tried to substitute non-fluorinated or partially fluorinated benzoates for cost savings. The truth is, in processes demanding robust electronic effects and persistence under thermal stress, cut-rate alternatives simply fall short—be it in lower yields, increased byproducts, or downstream instability. Rather than proposing a one-size-fits-all benzoate, our shop commits to the exact profile required, which usually means keeping the focus on the fully tetrafluorinated pattern for demanding performance.

    Quality Assurance Born from Real Process Challenges

    In our plant, quality assurance goes hand in hand with hands-on production work. Every reaction run draws from a proven sequence of monitoring and rapid adaptation—not just blind automation. We’ve designed each reactor and workup bay to minimize cross-contamination, based on first-hand lessons learned from off-spec incidents in the past. The lessons from a single deviation in fluorination or solvent attack on reactor linings have shaped our protocols into something far more robust than manual or simple automated checks.

    Our senior analysts talk directly with operators and formulation staff, looking at trends in impurity upticks or subtle shifts in chromatogram baselines to forecast and prevent excursions before they affect shipments. This transparency—rare in outsourced or rebranded material—builds trust with long-standing clients who depend on zero-defect deliveries to keep their own production lines moving. The technical team reviews field failure reports or off-grade returns, and we use those details to tune every batch, not just the ones flagged as outliers.

    Beyond standard checks, we carry out routine stress testing at temperatures and humidity levels reflecting real warehouse and shipping conditions. We’ve constructed protocols to catch volatility loss, unintended hydrolysis, or unexpected reactivity with container materials—a safeguard for users who store or transport the product over long distances or under challenging climates. Lab staff rotate through real production lots, not just demo samples, to keep a tight loop between experiment, manufacturing, and market needs.

    Environmental and Safety Aspects: Continuous Improvements from the Trenches

    Making and handling fluorinated chemicals takes experience and a sense of stewardship. We address environmental risk and process safety as a set of daily tasks, not as afterthoughts. The vent systems and emission controls developed in our shop evolved after real-world trials—not paperwork projections—to keep both workplace and community air clean. We track solvent emissions and implement thermal oxidizers or scrubber systems, then verify their effectiveness through independent readings rather than relying solely on regulatory minimums.

    Operators and supervisors spend part of every week training on new safety risks and incident prevention, often prompted by small incidents or industry alerts. We tweak PPE protocols and handling guidelines whenever new data or a fresh challenge comes in, sorting out improvements for tasks like vacuum filtration or pressure transfer. In decommissioning spent process solutions, we target chemical reuse wherever feasible, reducing both disposal loads and costs—lessons that flow directly from finance and compliance audits.

    The move to greener chemistry and improved waste minimization carries weight for us. Ethyl 2,3,4,5-Tetrafluorobenzoate, because of its stability, permits tighter control over effluent composition and reduced emissions during downstream processing. We test every waste stream, aiming to salvage or reuse material rather than send it for costly destruction. We often share findings and best practices with downstream partners aiming for similar improvements.

    While fluorinated compounds rightly raise questions about persistence, our approach backs up responsible stewardship. Regular audits and waste consolidation help minimize open-loop handling, and batch-level documentation means traceability for every kilogram manufactured. Nothing leaves our facility without accounting for impacts on both people and the environment.

    Meeting Today’s and Tomorrow’s Needs: Lessons from Manufacturing and Market

    Demand for Ethyl 2,3,4,5-Tetrafluorobenzoate changes with trends in pharmaceuticals, agrochemicals, and advanced material applications, but certain needs stay constant. Clients look to keep their own innovation timelines intact, not just fill reagent shelves. The bond between manufacturer and end-user goes well beyond transactional ordering. Over years, project scientists have called on us to solve last-minute shortages, investigate batch inconsistencies, or rethink packaging strategies for rough transit.

    Our staff consults regularly with customers considering process scale-up, guiding them through obstacles encountered as bench chemistry meets real-world production. The detailed knowledge acquired from repeated synthesis cycles means we can recommend tweaks or safety checks that avoid costly pitfalls. Sometimes it’s about suggesting a cooling ramp; other times, it’s the right filtration step after watching a filtration collapse in a scaled-up trial.

    With the increased scrutiny across chemical and pharmaceutical production, we’ve responded by building greater transparency into our supply chain and quality reporting. Batch histories, impurity audits, and COA review routines help chemists plan syntheses with confidence, not just cross fingers for a pure delivery. This degree of partnership means clients circle back with feedback to drive improvement in both product and service—elements lacking in packaged “off the shelf” alternatives.

    Facing new regulatory expectations and market pressures, we keep focus on responsible sourcing for critical raw materials, maintaining safety inventory without ties to hazardous or unreliable supply lines. Training investments for plant staff and technical teams ensure no knowledge gap undermines the reliability required by researchers and manufacturers relying on this building block.

    Continuous Refinement Driven by Experience

    Talk about Ethyl 2,3,4,5-Tetrafluorobenzoate sometimes centers around its analytical profile, purity metrics, or end-use applications—details that matter absolutely. Yet, in a real manufacturing setting, the story is one of responding to buyer needs and learning from every challenge. We adapt methods, chase improvements in yield, and above all, bring people up to speed on safe, repeatable production. Every drum that rolls out traces its pedigree to a crew that knows the molecule inside out—through practice, not just protocol.

    Feedback from clients and the experiences of our team drive our process better than any template or generic spec sheet ever could. We don’t simply sell a chemical. We provide the reliability, continuity, and technical guidance that customers depend on, grounded in hard-earned know-how.