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Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate

    • Product Name Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate
    • Alias ETPC
    • Einecs 682-780-5
    • 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
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    Specifications

    HS Code

    667642

    Productname Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate
    Molecularformula C13H11F3N2O2
    Molecularweight 284.24 g/mol
    Casnumber 151688-92-9
    Appearance White to off-white solid
    Purity Typically ≥98%
    Meltingpoint Approximately 55-59 °C
    Boilingpoint No data available
    Solubility Soluble in organic solvents such as DMSO and dichloromethane
    Storagetemperature Store at 2-8°C, away from light and moisture
    Smiles CCOC(=O)C1=CN(N=C1C2=CC=CC=C2)C(F)(F)F
    Inchi InChI=1S/C13H11F3N2O2/c1-2-20-13(19)10-8-17-18(12(10)9-6-4-3-5-7-9)11(14,15)16/h3-8H,2H2,1H3

    As an accredited Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a secure screw cap, labeled "Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate," batch and hazard info.
    Shipping Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate is shipped in tightly sealed containers, protected from moisture and light. It is handled as a laboratory chemical, with labeling according to applicable regulations. Transport typically follows standard chemical shipping protocols, ensuring safety and compliance during transit. Temperature and hazard information are specified on packaging and documentation.
    Storage Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances like strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature, away from heat and flame. Handle with appropriate personal protective equipment to avoid inhalation, ingestion, or skin contact.
    Application of Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate

    Applications of Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate in Industrial Manufacturing

    Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate is a specialty intermediate that serves as a critical building block in select agrochemical, pharmaceutical, and advanced material manufacturing sectors. As the actual chemical producer, we focus on real-world downstream supply chains where this compound demonstrates indispensable technical utility, and we align with worldwide regulatory requirements to support high-quality industrial output.

    1. Synthesis of Pyrazole-Based Fungicidal Active Ingredients

    This compound enters the synthesis routes of advanced fungicidal agents, notably in the preparation of triazole and strobilurin analogues used in crop protection. During the core construction of heterocyclic actives, the trifluoromethyl-pyrazole scaffold enhances binding selectivity and persistence on target crops. Downstream manufacturers rely on this intermediate in condensed-phase reactions to maintain molecular integrity and to secure consistent performance in large-scale agricultural applications.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO PPP)
    • ISO 9001:2015 Quality Management in Agrochemical Production
    • REACH Registration for Agrochemical Substances (EU)
    • U.S. EPA Active Ingredient Registration Requirements

    Typical usage ratio

    • 0.5%–2.5% by weight in target active synthesis batches, adjusted based on the selected heterocycle construction step and desired substitution pattern of the final fungicidal molecule

    Downstream process integration

    • Introduced during heterocycle assembly at the acylation or condensation stage; often used as a final key intermediate prior to functionalization and formulation into wettable powders or suspension concentrates

    Final product types

    • Fungicidal technical concentrates (TC)
    • Emulsifiable concentrate (EC) formulations
    • Ready-to-use granular agrochemicals
    • Suspension concentrate (SC) fungicides

    2. Active Pharmaceutical Ingredient (API) Intermediate for CNS Drug Development

    Within central nervous system (CNS) drug research and manufacturing, this intermediate supports the assembly of pyrazole-carboxylate pharmacophore cores. Medicinal chemistry teams introduce it during the multi-step synthesis of select antipsychotics and anticonvulsants. Reliable supply and batch traceability ensure that end users meet tight validation standards for preclinical and pilot-scale productions.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 1 for Pharmaceutical Production
    • US FDA 21 CFR Part 210/211
    • Ph. Eur. and USP monographs where applicable (for downstream API)

    Typical usage ratio

    • Range of 0.3–1.1 molar equivalents in medicinal intermediate synthesis, balanced against nucleophilic reagents or alkylating agents in primary coupling reactions

    Downstream process integration

    • Charged as a stage-specific reactant in pyrazole ring functionalization; enters programmed coupling reactions before purification and crystallization of regulated intermediates

    Final product types

    • Regulated CNS drug intermediates
    • Final bulk active pharmaceutical ingredients (API) after downstream synthesis
    • Clinical trial API batches for neurological indications

    3. Agrochemical Insecticidal Intermediate Synthesis

    This material functions in the production of next-generation pyrazole-based insecticides, prized for their ability to disrupt neuro-signal pathways in insects. Agchem companies deploy the intermediate in controlled low-temperature reactions for constructing the insecticidal nucleus before final derivatization and formulation processing.

    Industry compliance standards

    • ISO 17025:2005 for Analytical Laboratories in Agrochemicals
    • AGRO-GMP (China and India, as required for export)
    • U.S. FIFRA Registration (Federal Insecticide, Fungicide, and Rodenticide Act)
    • Global GHS Hazard Communication Alignment for B2B Chemical Supply

    Typical usage ratio

    • Typically used at 1.2–1.4 molar equivalents versus alkyl or aryl partner reagents, optimized according to the coupling efficiency and yield targets of the pilot reactor

    Downstream process integration

    • Added after pre-activation of auxiliary aromatic groups; participates in nucleophilic substitution at the N2 position of pyrazole during batch manufacturing

    Final product types

    • High-purity insecticidal technical concentrates
    • Water-dispersible granules
    • Flowable concentrate insecticide products for row crop and orchard use

    4. Pyrazole-Containing Optical Brightener Formulations

    In specialty materials manufacturing, pyrazole carboxylate derivatives act as cores for optical brighteners used in polymer and textile finishing. By introducing high electron-withdrawing groups, downstream formulators achieve consistent fluorescence and color-stability performance, especially under high-temperature processing involved in plastics extrusion.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for finished finished textiles)
    • REACH Annex XVII for Additives in Consumer Goods
    • RoHS Directive 2011/65/EU (for plastics and electronics)
    • DIN EN ISO 9001 Quality Assurance for Specialty Chemicals

    Typical usage ratio

    • Loaded at 0.1–1.0% by weight in masterbatch compounds, with precise calibration based on the optical absorbance and end-use luminosity requirements

    Downstream process integration

    • Feeds into the melt-phase polymerization or finishing chemical synthesis; blended before compounding with carrier resins or applied during final textile finishing baths

    Final product types

    • Plastic optical brightener masterbatches
    • Bright-whites for woven and nonwoven textiles
    • Additives for high-luminance polymer films

    5. Fine Chemical Building Block for Advanced Material Research

    Research teams and custom synthesis firms select this molecule for stepwise construction of fluorinated pyrazole frameworks in electronic and energy storage materials. Its high reactivity profile is especially well-suited for controlled functionalization in lithium battery electrolyte and conductive polymer prototype development.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for Specialty Chemical Facilities
    • RoHS Compliance for Electronics Applications
    • Chemical control compliance (TSCA, REACH, IECSC) for international shipments
    • Analytical QA/QC standards per downstream customer specifications

    Typical usage ratio

    • Ranges from 0.2–4.5% by weight depending on the complexity of the synthetic module and experimental design for pilot material production

    Downstream process integration

    • Charged at intermediate build or end-stage fluorination cycles in combinatorial synthesis setups for the creation of conductive or highly fluorinated performance compounds

    Final product types

    • Lithium-ion battery electrolyte modifiers
    • Prototype conductive polymer additives
    • Advanced fluorinated intermediates for electronic material R&D
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    Certification & Compliance
    More Introduction

    Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate: A Manufacturer’s Perspective

    In the Lab: Crafting Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate with Precision

    Years spent honing organic synthesis have taught us that certain molecules earn their keep again and again in real applications. Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate stands out as a solid example. Here, each batch starts in reaction kettles we designed specifically to control the tricky points in pyrazole ring formation. The process demands careful temperature and timed reagent introduction, where too fast or too hot wrecks the whole lot. Anyone who has worked with trifluoromethyl pyrazoles knows: each stage must run its course with the right solvent ratios and steady agitation.

    Creating this molecule requires meticulous control over the palladium-catalyzed cross-coupling that joins the phenyl group to the core. A misstep at this stage drains both yield and purity, and the fluorous nature of the -CF3 substituent amplifies the difficulty of keeping side-products under control. Our reaction conditions have evolved with experience, from experimenting with solvent/salt combinations to finally isolating the best pathway for reproducible purity and crystallinity in each batch.

    Specifying the Product: Real Numbers and Consistent Quality

    This compound, usually referred to by R&D chemists under its short-hand or catalog number, forms white to off-white crystalline powders when prepared correctly. We use a melting point as a quick visual indicator for preliminary batch assessment—targeting a narrow window characterizes a clean synthesis. HPLC and NMR go hand-in-hand to confirm the correct skeleton, and we keep water content and residual solvent levels low by design, as traces not only disturb downstream reactions but also frustrate those scaling up for pilot production.

    We keep batches within tight purity specifications. Purity over 98.5% by HPLC minimizes the noise in analytical results and keeps our clients off the troubleshooting steps that come with off-spec material. Moisture content is checked using Karl Fischer titration, and we consistently achieve typical values well under 0.5%. These checkpoints prevent surprises once the material leaves our facility.

    Real-World Uses: More than a Catalog Entry

    This building block doesn’t just sit in a storeroom, it drives forward work in pharmaceuticals, crop protection, and specialty materials. Research teams ask for this molecule by name because the trifluoromethyl group introduces unique electron-withdrawing effects that shift biological activity for leads under investigation. Medicinal chemists often incorporate this compound into larger libraries of heterocycles, trying to unlock new avenues for enzyme inhibition or receptor modulation.

    Agricultural chemistry projects continue to explore pyrazole derivatives’ influence on pest control actives and herbicidal activity. The carboxylate ester at the 4-position opens doors for straightforward modification. We see industrial uses as intermediates, where the arylated backbone combines stability and reactivity, giving formulation chemists room for further functionalization. These aren’t academic exercises—feedback from teams running pilot plant trials confirms the material’s role in scalable, IP-heavy projects.

    How Experience Changes Everything: Common Issues and Real Solutions

    The chemistry behind this compound is not the only thing that matters. How consistently and cleanly it is made directly affects everything downstream. There are no shortcuts to controlling trace metal contamination or trapping difficult-to-remove fluorinated byproducts. For this molecule, we’ve found that slow crystallization—not crash cooling or heavy solvent stripping—yields the best particle size and color.

    One problem our early customers faced involved troublesome solubility. They needed a compound that would dissolve rapidly in polar aprotic solvents, and we achieved this by refining our purification protocol. It took retooling some equipment to better control solvent temperature gradients, but the difference between a granular powder and a waxy lump can make or break time-sensitive campaigns. Many clients thank us for these adjustments, as rapid dissolution means fewer bottlenecks on the day chemists get to work.

    Storage and stability remain practical concerns in every lab. We package this material under dry nitrogen, but storing at ambient doesn’t compromise its stability, as proven by long-term HPLC data stretching back over five years. We share this empirical data with users managing multi-month projects, so they can trust both labeled expiry dates and real-world shelf life, even in humidity swings.

    What Sets This Product Apart: Expertise in Fluorinated Pyrazole Chemistry

    Our familiarity with both the chemistry and the reality of scale means avoiding pitfalls many newcomers face. We do not rely on third-party synthesis; we control everything in-house, from raw fluorinated benzene derivatives to the finished, purified pyrazole ester. This makes trace impurity checks easier to interpret, and batch-to-batch reproducibility remains high. Seeing a consistent NMR signal set, even after years, is our kind of reassurance.

    We don’t treat the trifluoromethyl group as just another substituent. Early runs using off-the-shelf reagents resulted in minuscule but meaningful amounts of byproduct—a halogenated impurity once overlooked in less focused production environments. Direct involvement in selecting, testing, and qualifying starting materials means we get the molecule chemists actually want, not just a number on a chromatogram.

    Differences from generic catalog suppliers show in the details: tighter specification windows, open documentation about impurity profiles, and responsive feedback from actual chemists, not distributors. Our sales team includes people who’ve stood in front of a hotplate for hours, tuning stirring speeds and watching for that moment a clear solution drops crystals of the perfect shape. That experience lets us advise not just on which product to order, but on what to expect—and what could be adapted in formulation or synthesis extensions.

    Supporting Evidence: Why Purity and Consistency Matter in This Case

    At the scale needed for high-throughput screening, unanticipated impurity peaks in analytical runs delay whole programs. We have witnessed this firsthand—one project ground to a halt because an outsourced batch carried over an aryl halide contaminant. Since then, we have made traceability and documentation as integral as the chemistry itself. Our records detail not only origin and chain of custody, but also every solvent lot, temperature readout, and analytical trace. This transparency draws repeat business from those who have faced unexplained results with less scrupulous suppliers.

    Many suppliers operate as intermediaries, sourcing from elsewhere and reselling without ever seeing the inside of their own reactors. That difference tells when a project escalates and the user needs direct access to technical explanations. When a customer finds an unexpected analytical signal, they don’t wait days for a response from an unknown source. Our chemists compare batch data, advise on next-steps for purification, and share relevant spectra on request. This partnership grew from seeing too many teams lose weeks to guesswork forced by lack of support.

    Regulations, Documentation, and Responsible Handling

    Regulatory scrutiny on fluorinated compounds sharpens each year, particularly in pharmaceutical and agrochemical sectors. By keeping full batch histories and maintaining well-documented change-control procedures, we help customers meet both current and anticipated regulatory hurdles. The trickiest parts often involve understanding trace residuals—fluorinated byproducts, low-level arylations, even unexpected transesterification products. Because we’ve manufactured this compound at both research and commercial scale, we advise on which analytical panels reveal trouble most quickly and how to adapt to regional documentation requests.

    Handling fluorinated intermediates calls for respect; we train every operator and maintain engineering controls to reduce exposure to dust and vapors. Nitrogen-blanketed packaging and robust QA documentation support audits and provide peace of mind for customers applying for registrations or preparing master files. We assist with custom documentation packages, from impurity profiles to atypical analytical requests, because we understand how regulatory deadlines impact launch schedules.

    Continuous Improvement: Staying Ahead of Quality Demands

    Feedback from chemists doing real experimental work shaped how we design every production run. Early on, some batches yielded product of suitable purity but marginal flowability, scattering material handling issues across automated systems designed for precise dosing and weighing. Our best solution involved slight tweaks to the particle-size distribution, achieved by controlling crystallization rates rather than simply grinding the product post-synthesis. Adjustments always take time—sometimes measured in weeks, not hours—but the result shows up in fewer customer complaints and more repeat orders.

    Not every improvement is chemical. Managing the logistics of sensitive intermediates means working closely with shippers trained in handling regulated materials. We use custom outer cartons and sealed liners, tracking transit temperature logs to head off the rare—but critical—incident. The result isn’t just regulatory compliance; it reassures users the material inside reflects the same care and precision used in its manufacture.

    Practical Considerations for Users: From Synthesis to Application

    Talking with bench chemists informs many of our practical suggestions for handling this compound. Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate dissolves in most polar organic solvents, especially DMF and acetonitrile, but ethanol and dichloromethane also work well depending on the scale and application. Some customers prefer pre-weighed aliquots for library synthesis or lead optimization campaigns—a practice we support by offering custom packs and sealed bottles minimizing air and moisture ingress.

    Purity and analytical traceability matter from the first reference spectrum through to kilo-lab synthesis. Researchers working in pharmaceutical discovery often run short development timelines, so knowing what to expect from each gram used becomes more than convenience—it serves as the foundation for reliable biological data. Side-by-side comparison with similar pyrazole esters often highlights cleaner baselines when sourced directly from us compared to generic outlets, particularly in UPLC and 1H NMR analyses.

    Scale-up teams working on process intensification have taught us to supply extended CoA data packages, including platinum group metal residue analysis, residual solvent profiles, and heavy metals screening. We understand this isn’t “overkill”—it’s routine good practice. The consequences of a missed out-of-spec result at pilot-plant scale are far greater than in a few gram vials, so we choose to anticipate and support those higher standards proactively.

    What Customers Tell Us: Field Experience and Long-Term Collaborations

    Direct conversations with our clients shape every iteration of how we produce and handle this product. In pharmaceutical discovery groups, synthetic chemists value the sharp melting point and clear NMR spectra for fast reference checks. Agrochemical innovators mention how reliable batches cut down on troubleshooting before screening for bioactivity. We apply their suggestions: fine-tuning drying cycles to produce powders free from agglomeration, or adjusting fill weights to match evolving synthesis scales.

    A number of collaborations grew from solving practical problems—sometimes as simple as refining packaging to reduce static, at other times by working side-by-side on impurity identification once a target molecule advanced to regulatory submission. These relationships reward both sides: customers gain direct access to our manufacturing expertise, and we build a deeper catalog of practical, real-world scenarios that inform our next process improvement projects.

    Looking Forward: Why We Keep Improving This Pyrazole Product

    Chemistry never stands still. As reaction methodologies evolve and analytical techniques become more refined, so do expectations for intermediate quality. Our facility invests continuously in upgraded reactors, new filtration systems, and expanded analytical equipment, because we know our partners will ask for cleaner, faster, and safer products tomorrow than they do today. Each feedback cycle, process tweak, and analytical advance becomes part of our ongoing chemistry—not just in the lab, but at each step along the supply chain.

    The scientists and manufacturers using Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate rely on it to underpin discovery campaigns, optimize active molecules, and support real-world product development. Our commitment is both personal and professional: we built our reputation on providing consistent, clean, and well-documented compounds, and we treat every new order and inquiry as an opportunity to raise the standard further.

    Summary: Experience-Driven Reliability in Pyrazole Chemistry

    Experience counts at every step, from controlling the subtleties of trifluoromethylation to fine-tuning purification and packaging. Our role as the manufacturer gives us direct responsibility—and the leverage to make real improvements—for everyone who uses this molecule. Ethyl 2-Phenyl-3-(Trifluoromethyl)Pyrazole-4-Carboxylate is more than a catalog listing; it’s the result of tireless optimization, listening to actual users, and a clear focus on making a better product year after year.

    For research projects large and small, for scale-up or exploratory synthesis, this pyrazole compound stands as a tested, trustworthy building block. That reliability underpins discovery and progress—just as it underpins everything we do on the manufacturing floor.