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Ethyl 2-(Trifluoromethyl)Benzoate

    • Product Name Ethyl 2-(Trifluoromethyl)Benzoate
    • Alias Ethyl 2-(trifluoromethyl)benzoate
    • Einecs 405-070-6
    • 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

    424082

    Product Name Ethyl 2-(Trifluoromethyl)Benzoate
    Cas Number 57851-80-8
    Molecular Formula C10H9F3O2
    Molecular Weight 218.17
    Appearance Colorless to pale yellow liquid
    Boiling Point 110-112°C at 13 mmHg
    Density 1.22 g/cm3 at 25°C
    Refractive Index 1.449-1.453
    Smiles CCOC(=O)C1=CC=CC=C1C(F)(F)F
    Melting Point -22°C
    Storage Temperature Store at room temperature
    Solubility Insoluble in water, soluble in organic solvents

    As an accredited Ethyl 2-(Trifluoromethyl)Benzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ethyl 2-(Trifluoromethyl)Benzoate, 25g, is packaged in an amber glass bottle with a secure screw cap to ensure safe storage.
    Shipping Ethyl 2-(Trifluoromethyl)benzoate is shipped in tightly sealed containers to prevent leakage or contamination. It should be transported in accordance with local and international regulations for chemicals, kept away from incompatible substances, and protected from heat and direct sunlight. Proper labeling and safety documentation accompany each shipment to ensure safe handling.
    Storage **Ethyl 2-(Trifluoromethyl)benzoate** should be stored in a tightly sealed container, placed in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizers and strong acids. Protect from direct sunlight and moisture. Ensure proper chemical labeling and access to appropriate safety measures, including spill containment and fire suppression equipment.
    Application of Ethyl 2-(Trifluoromethyl)Benzoate

    Applications of Ethyl 2-(Trifluoromethyl)Benzoate in Industrial Manufacturing

    Ethyl 2-(Trifluoromethyl)benzoate serves as a critical intermediate in various chemical manufacturing sectors, supporting production lines where fluorinated building blocks are essential. The following sections describe targeted downstream applications with detailed operational insights and compliance references.

    1. Pharmaceutical Intermediate for Anti-inflammatory Drug Synthesis

    Pharmaceutical companies utilize this compound as a precursor in synthesizing selective cyclooxygenase-2 (COX-2) inhibitors and other anti-inflammatory agents. The molecule’s trifluoromethyl group enables specific modifications during the esterification and subsequent reaction steps, contributing to high-purity active pharmaceutical ingredients (APIs). Controlled handling and purity monitoring remain essential during large-scale synthesis to comply with stringent medicinal benchmarks and avoid cross-contamination with other process streams.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for intermediates
    • USP–NF relevant monographs
    • FDA 21 CFR Part 211

    Typical usage ratio

    • Commonly introduced at 5–12% molar ratio relative to main reactant; adjusted by required yield and scale of production

    Downstream process integration

    • Enters early-stage coupling reactions for formation of fluoroaromatic scaffolds
    • Used in flow chemistry or batch reactors prior to hydrolysis and rearrangement

    Final product types

    • COX-2 inhibitor bulk APIs
    • Anti-inflammatory finished tablets and capsules
    • Intermediate precursors for advanced clinical candidates

    2. Agrochemical Synthesis of Herbicidal Active Ingredients

    Specialty agrochemical producers apply this trifluoromethylated ester to generate key herbicidal and fungicidal building blocks. Its chemical stability and compatibility with halogen exchange or amination processes make it valuable for scalable active ingredient fabrication. Careful process control is needed to ensure trace impurities remain within limits set by agrochemical regulations.

    Industry compliance standards

    • FAO/WHO specifications and quality criteria for active substances
    • EPA 40 CFR Part 180 (USA) regarding pesticide tolerances
    • ISO 9001 implementation for chemical raw material supply
    • REACH registration (EC 1907/2006) for European market distribution

    Typical usage ratio

    • Generally 8–20% weight basis in intermediate mixtures; varies with process throughput and downstream conversion rate

    Downstream process integration

    • Incorporated into multi-step syntheses involving halogenation, ester hydrolysis, or amidation stages
    • Processed in reactor trains prior to herbicide formulation blending or granulation

    Final product types

    • Trifluoromethyl-substituted benzoic acid herbicides
    • Seed coating agents and crop protection formulations
    • Pre-emergent selective weed control actives

    3. Synthesis of Specialty Polymers and Fluorinated Materials

    Manufacturers in the advanced materials sector introduce this ester as a fluorinated monomer precursor for producing specialty polymers with improved chemical resistance and thermal stability. The compound supports the formation of high-performance resins used in coatings, membranes, and electronic encapsulants. Quality oversight during polymerization ensures batch-to-batch consistency for downstream electronic or industrial use.

    Industry compliance standards

    • UL 94 for polymer flammability
    • RoHS 2011/65/EU for electronics-related polymers
    • ISO 14001 environmental management
    • ISO 9001 for quality assurance in raw material sourcing

    Typical usage ratio

    • Ranges from 3–10% by weight in copolymer blends; optimized by target polymer architecture and desired material properties

    Downstream process integration

    • Introduced at monomer feed-in step in emulsion, suspension, or solution polymerization
    • Used in conjunction with fluorinated co-monomers and suitable initiators

    Final product types

    • Fluorinated acrylic or methacrylic resins
    • High-performance protective coatings
    • Electronic device encapsulation compounds

    4. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Producers of specialty dyes and pigments implement this compound for introducing trifluoromethyl groups into aromatic chromophores. The reactivity profile aligns with specific acylation or condensation routes, yielding molecules with adjusted absorption and high solvent resistance. Production lines require dedicated purification steps and validation per pigment-grade standards.

    Industry compliance standards

    • EN 71-3 for safety of colorants in toys
    • OEKO-TEX Standard 100 for textile applications
    • ISO 787 General Methods of Test for Pigments and Extenders
    • Global Harmonized System (GHS) labelling for chemical handling

    Typical usage ratio

    • Applied at 2–7% molar input during colorant precursor synthesis, scalable based on chromophore design

    Downstream process integration

    • Engaged in Friedel-Crafts acylation or coupling chemistry forming fluorinated dye intermediates
    • Material enters colorant synthesis reactors before final crystallization and milling

    Final product types

    • Textile dyes with enhanced weather resistance
    • High-purity industrial pigments
    • Solvent-resistant coatings and inks

    5. Electronic Chemicals Precursor for Liquid Crystal Material Synthesis

    Electronics chemical suppliers integrate this aromatic ester in the synthesis of liquid crystal intermediates, particularly for high-performance display manufacturing. The trifluoromethyl group facilitates required dielectric and optical properties, and the material’s purity must meet strict ICP-MS specifications. Supply chain traceability and production documentation are required throughout the electronic materials workflow.

    Industry compliance standards

    • IEC 61249-2-21 for base materials with halogen content limits
    • IPC-6012 for printed circuit board qualification
    • JPCA-ES-01 for electronic substrate chemicals
    • ISO 9001 for advanced material production

    Typical usage ratio

    • Introduced in 1–5% by weight, depending on precise dielectric adjustment needs in the target formulation

    Downstream process integration

    • Used in condensation or alkylation steps building tailored liquid crystal molecules
    • Material fed into syntheses prior to final mixture for LCD or OLED substrate

    Final product types

    • Liquid crystal monomers and blends for flat-panel displays
    • Advanced dielectric layers for electronics
    • Optical-grade synthetic films for high-definition screens
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    Certification & Compliance
    More Introduction

    Ethyl 2-(Trifluoromethyl)Benzoate: A Closer Look Through the Eyes of the Manufacturer

    Day-to-Day Insights from the Production Floor

    Ethyl 2-(Trifluoromethyl)benzoate has become a vital compound in today’s chemical toolkits, with significance underscored in fine chemicals, pharmaceuticals, and advanced material development. Our experience refining every batch of this compound underscores the challenges and rewards of manufacturing specialty chemicals for evolving market needs. Consistency, purity, and reliable supply don’t just happen; behind every drum of material stands a network of careful process control and relentless quality checks.

    The chemical synthesis of Ethyl 2-(Trifluoromethyl)benzoate revolves around balancing efficiency and purity. This compound has the molecular structure C10H9F3O2, packing a trifluoromethyl group onto the benzoate backbone, which not only changes its reactivity but drives its use in specific applications. Over the last decade, we noticed a growing shift toward fluorinated building blocks, due to their impact on metabolic stability and physicochemical properties, especially for pharmaceutical intermediates and agrochemicals. As a primary producer, we have observed firsthand how small tweaks in production have significant effects on both yield and downstream usability.

    Improving Quality: Not Just a Statement

    Our approach to manufacturing starts with raw material selection. Trace impurities in starting compounds can compromise the entire batch, so procurement and incoming analysis form the baseline of quality. We maintain validated supplier relationships and continually monitor input purity, which pays dividends in the predictable behavior of our end product.

    In conventional practice, side reactions—particularly with trifluoromethyl functionality—create challenges by introducing hard-to-remove byproducts. We developed customized purification steps that avoid excessive solvent consumption, ensuring our Ethyl 2-(Trifluoromethyl)benzoate meets purity benchmarks without placing unsustainable burdens on waste treatment operations. Every achievement in waste reduction has ripple effects through our process, demonstrating the real-world impact of sustainable chemistry beyond marketing language.

    Adhering to strict analytical standards forms another pillar of our manufacturing. We employ advanced chromatography to guard against trace impurity buildup batch after batch, confirming purity levels above 99 percent whenever specified. Instrument maintenance and periodic method reviews form part of our internal routines, giving our quality assurance team the confidence to release material that passes not just in-house scrutiny, but also meets the evolving demands of end users who often have applications where failure is not an option. Knowledge gained through regular engagement with partners in pharmaceuticals and research labs reshapes our standards, because we see the downstream impact when our chemistry meets real-world synthesis tasks.

    Why Customers Care About Substitution and Consistency

    A significant part of our customer base comes from pharmaceutical research. Here, Ethyl 2-(Trifluoromethyl)benzoate often appears in the early to intermediate stages of drug synthesis, valued mainly for its ability to introduce the trifluoromethyl group into active molecules. This group lends new properties—like altered lipophilicity and increased metabolic stability—compared to non-fluorinated benzoates, which usually lack those attributes. The presence of the ethyl ester further enhances solubility and provides a clean handle for downstream modifications. Over the years, we have catalogued the fine differences between batches—sometimes as small as moisture content shifts—that can influence reaction kinetics or crystallization in downstream work. Our ongoing communication with bench chemists allows us to tighten our process window.

    Those working in agricultural research notice similar differences. The introduction of the trifluoromethyl group triggers new herbicidal and pesticidal behaviors compared to parent benzoates. These applications require high batch repeatability, with limited tolerance for off-spec materials. We steer every process modification against the backdrop of end application, because even a shift in melting point can derail scale-up on the customer side. We have witnessed delays in time-sensitive projects triggered by variability in upstream intermediates. Drawing on these experiences, we have improved both our specification reviews and certification protocols, collaborating more closely with client-side technical representatives to verify suitability.

    Comparing Ethyl 2-(Trifluoromethyl)Benzoate Against Other Esters and Related Materials

    Distinct from simple ethyl benzoate and other ring-substituted esters, Ethyl 2-(Trifluoromethyl)benzoate incorporates a strong electron-withdrawing group at the ortho position. This structural change does more than alter electronic character; it transforms reactivity and end-use performance. Classic ethyl benzoate finds roles as a fragrance or flavor additive, relying on its stable profile and low toxicity. In contrast, the trifluoromethylated version targets synthetic utility, favored for its unique chemistry and the opportunity it provides in molecular design.

    Direct substitutions—such as switching to the para-isomer or to non-fluorinated analogs—do not reliably deliver the required balance of reactivity and downstream stability. Our in-house chemists have benchmarked substituent effects across more than a dozen esters, confirming that only the ortho-trifluoromethyl analog provides the activation and metabolic profile desired by pharmaceutical and crop protection chemists. Subtle shifts in position or substituent often change more than just the physical behavior; they can create bottlenecks in further modification or harm overall yields in complex synthetic sequences. Clients searching for consistency with an eye to scale-up regularly return to our grade of Ethyl 2-(Trifluoromethyl)benzoate, having experienced inconsistent outcomes with resellers or with different analogs.

    Scalability and Customization: Lessons from Production Experience

    Scale-up in fine chemicals does not follow straight lines. Year over year, we have responded to shifting demand, sometimes producing kilogram batches for research, other times supporting multi-ton runs for pilot plant operations. Every increase in scale brings latent challenges, as minor adjustments that work on the benchtop do not always translate into reliable production at greater volumes. For example, heat transfer issues and increased pressure demands led us to redesign parts of our reactor setup, which reduced batch failures and improved throughput.

    Clients occasionally request tweaks to standard production—whether a tighter moisture limit or removal of trace metals below standard detection limits. Fulfilling these requests forced us to adapt purification and drying protocols, sometimes trading process speed for higher certainty of outcome. Each adaptation tells a story, reminding us that off-the-shelf does not always serve unique applications. Drawing on feedback from analytical and process labs running difficult chemistry, we find it essential to maintain direct support with hands-on chemists so that our customization efforts align with their end goals, not just specifications on paper.

    Ensuring Safety and Compliance Without Cutting Corners

    Direct handling of fluorinated aromatics produces a unique set of exposure risks in the plant environment. Our teams train on both regulatory requirements and in-house safety protocols, because field experience underscores the importance of understanding the hazards beyond what any data sheet describes. For instance, we have witnessed near-misses where basic assumptions about volatility turned out wrong under certain process conditions. Each incident drives us to design safer process containment and better monitoring for hazardous vapors, shielding both our staff and nearby communities.

    Regulatory expectations around traceability and documentation for fine chemicals remain non-negotiable. Batch records, environmental compliance logs, and audit reports shape the daily rhythm of the plant. We maintain these not out of obligation, but from lived experience that lapses—even by accident—jeopardize both client trust and operational licenses. As legislation tightens globally, especially for fluorinated materials, early adaptation gives us and our clients a head start on compliance rather than driving last-minute process changes.

    Customer Relationships: Direct Feedback Drives Progress

    Customer conversations often begin with product properties. They quickly evolve into open-ended discussions about process capabilities and long-term collaboration. We have seen projects pivot around our willingness to explore tighter specifications or alternative packaging, especially in programs where the compound serves as a crucial intermediate. We dedicate teams not just to production but to direct technical support, leveraging years of hands-on troubleshooting. These efforts pay back in both increased loyalty and earlier warnings about shifting customer needs.

    Feedback from the field shapes more than just incremental improvements. When a research group discovered variability in downstream crystallization due to solvent residue, our plant team responded in days—auditing solvent recovery, identifying pinch-points, and offering a tighter finished product specification. These direct interventions moved beyond damage control, resulting in revised SOPs that have since improved outcomes for unrelated clients. We see such cycles repeat across our entire product portfolio; the combination of consistent attention to feedback and operational agility forms the backbone of lasting partnerships.

    Logistics, Shelf Life, and Handling: Practical Realities

    Specialty chemicals like Ethyl 2-(Trifluoromethyl)benzoate do not benefit from just-in-time logistics or mass-market packaging. We have invested in infrastructure—dedicated storage tanks, temperature-controlled warehousing, and rapid-response shipping networks—to protect product integrity across all stages. Issues such as transit exposure, seasonal temperature fluctuation, or improper drum sealing exposed the fragility of some supply chains. Our response has involved tailored drum liners, layered labeling protocols, and active monitoring of transit conditions, which together limit spoilage and ensure full batches reach the user with all properties intact.

    Long-term stability testing remains a core practice, not limited to regulatory-driven programs. We periodically re-analyze retained samples to validate shelf life assurances, learning from each anomaly to refine subsequent batch storage protocols. These internal studies have revealed value in seemingly minor packaging changes, such as incorporating secondary closures or desiccant packets, which extended shelf life in humid regions with no drop in finished product quality. Our real-world logistics experience outpaces paper-based assurances, protecting downstream clients from disruptions that could derail entire projects.

    Supporting the Broader R&D Ecosystem

    Ethyl 2-(Trifluoromethyl)benzoate should not be viewed simply as an isolated compound but as part of a broader shift toward specialty intermediates in research and development. As novel therapies, materials, and crop protection agents depend on advanced building blocks, we see our role expand from supplier to collaborator. Lively exchange between our process chemists and external R&D teams drives faster troubleshooting and sparks new application ideas. We encourage open publication of findings—both successes and pitfalls—linked to our material, accelerating progress for the wider industry.

    We have seen firsthand how shifts in scientific focus reshape demand unpredictably. Sudden interest in fluorinated pharmaceuticals, for example, propelled this compound from niche status to near-essential in multiple discovery programs. Navigating this change called for far more than increased output. It required process redesign, new quality standards, and closer alignment with emerging end uses. Retrospective analysis of these market cycles convinced us that flexibility and dialogue deliver more value than static product lists or inflexible manufacturing schedules.

    Environmental and Community Impact

    Manufacturing fluorinated aromatics traditionally carried a heavy environmental footprint. Over the past several years, we challenged standard practices, exploring alternate solvents, recycling strategies, and energy-efficient operations. Our ongoing investment in emissions control and waste minimization allows us to meet local and international environmental targets with confidence. These practical steps—sometimes incremental, sometimes transformative—produce measurable benefits for surrounding communities and future stakeholders.

    Community engagement extends beyond compliance or impact mitigation. Regular transparency initiatives and conversations with local leaders shape our internal targets. We share updates on waste reduction, energy improvements, and safety milestones not only to satisfy regulatory calls, but to build lasting local trust. We see reduced complaints and stronger community ties as both an outcome of our work and a constant incentive to improve.

    Future Trends: Adapting to New Scientific and Regulatory Landscapes

    Emerging trends in organic synthesis highlight the growing prominence of trifluoromethylated compounds. Enzyme-mediated transformations, green chemistry priorities, and new classes of pharmaceuticals leverage this motif for structure-activity modification. As a core building block, Ethyl 2-(Trifluoromethyl)benzoate not only serves today’s syntheses, but also drives tomorrow’s research. Ongoing collaboration with academic partners and industrial clients gives us early warning as new requirements arise, allowing for preemptive process upgrades.

    With expanding regulation of fluorinated materials, traceability, and safety, we anticipate new monitoring and reporting frameworks—especially for residual fluorine compounds in waste streams and finished products. Anticipating these challenges, our teams already pursue research on lower-emissions synthesis and improved real-time analytical controls, balancing commercial goals with environmental responsibility. No quick fix replaces daily vigilance or investment in continuous improvement, and our approach reflects this reality.

    Conclusion: Commitment Born of Experience

    Producing Ethyl 2-(Trifluoromethyl)benzoate draws not just on technical procedures but on accumulated knowledge from the plant floor to the laboratory bench. Direct engagement with customers, adaptability in production, and a clear-eyed approach to quality, safety, and sustainability mark the full lifecycle of our product. Day after day, decisions on raw material, process parameters, and shipment handling deliver more than another specialty chemical; they support industries pursuing innovation on a global scale.