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3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole

    • Product Name 3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole
    • Alias Phenylflucarb
    • Einecs 697-002-7
    • 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

    912104

    Product Name 3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole
    Molecular Formula C11H6F6N2
    Molecular Weight 284.17 g/mol
    Cas Number 2251-13-6
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 69-73°C
    Solubility Slightly soluble in organic solvents (e.g., DMSO, acetone)
    Density 1.50 g/cm³ (approximate)
    Structure A pyrazole ring substituted at positions 3 and 5 with trifluoromethyl groups and at position 1 with a phenyl group
    Smiles C1=CC=C(C=C1)N2C=C(C(=N2)C(F)(F)F)C(F)(F)F
    Inchi InChI=1S/C11H6F6N2/c12-10(13,14)8-7(9(15,16)17)18(19-8)11-5-3-2-4-6-11/h2-6H,1H

    As an accredited 3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 25g of **3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole** is securely sealed in an amber glass bottle with hazard and identification labels.
    Shipping **3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole** is shipped in tightly sealed containers, protected from light and moisture. The chemical is handled according to safety regulations and transported as a non-hazardous material under ambient conditions. Packaging ensures stability and prevents leaks, with clear labeling for identification and compliance with local and international shipping guidelines.
    Storage **3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. Keep separate from incompatible substances such as strong oxidizers. Ensure proper labeling, and use appropriate personal protective equipment (PPE) when handling. Store at room temperature unless otherwise specified by the manufacturer.**
    Application of 3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole

    Applications of 3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole in Industrial Manufacturing

    3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole serves as a highly specialized intermediate in several advanced chemical manufacturing sectors. Due to its electron-withdrawing trifluoromethyl groups and aromatic backbone, it plays a critical role in the synthesis of active ingredients and high-value intermediates. Below, we detail its application in established industrial supply chains, focusing on compliance, ratio guidance, implementation process, and final product categories.

    1. Agrochemical Active Ingredient Synthesis

    This pyrazole derivative is utilized in the agricultural industry as a building block for selective fungicides and insecticides, especially where high electron density and metabolic stability are required in the target molecule. Only downstream agrochemical formulators and technical manufacturers use it as a strategic intermediate in active substance development, especially for pyrazole-based crop protection products demanding precise residue and eco-toxicity profiles.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • European Union Regulation (EC) No 1107/2009 on Plant Protection Products
    • US EPA Registration (40 CFR Parts 150–189)
    • China GB 2763 Maximum Residue Limits

    Typical usage ratio

    • 5–25% (w/w) in technical active ingredient synthesis stage; proportions depend on final product yield calculations and impurity control in multi-step synthesis

    Downstream process integration

    • Added at the cyclization or coupling stage for active moiety formation in multi-step batch or continuous agrochemical manufacturing lines

    Final product types

    • Selective fungicides (e.g., pyrazole-based anti-mildew actives)
    • Insecticides for cereals and horticulture
    • Seed treatment actives

    2. Pharmaceutical Intermediate for Antifungal APIs

    As a key structural fragment, this compound is widely adopted in GMP-grade manufacturing sites for the production of antifungal active pharmaceutical ingredients (APIs). Its dual trifluoromethyl groups provide metabolic stability when integrating into triazole or pyrazole antifungal frameworks. Pharmaceutical manufacturers apply it in stringent reaction steps, consistently targeting high-purity outputs with regulated impurity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF Monographs for API synthesis
    • EDQM CEP Regulations for pharmaceutical starting materials
    • Ph. Eur. Guidance for residual solvents and intermediates

    Typical usage ratio

    • 3–12% molar ratio relative to the main backbone; adjusted according to target molecule and step efficiency

    Downstream process integration

    • Introduced in the heterocyclic coupling or condensation step when forming the core structure of antifungal molecules

    Final product types

    • Fluconazole (and other triazole/pyrazole antifungal APIs)
    • Pharmaceutical-grade intermediates for systemic antifungals

    3. Specialty Material Monomer Precursor

    Advanced material producers select this molecule as a functionalized monomer precursor for fluorinated polymers and high-performance coatings. Its incorporation enhances chemical resistance and dielectric properties, fundamental for high-value specialty polymer applications in electronics and chemical processing environments.

    Industry compliance standards

    • REACH Registration (EU Regulation No 1907/2006)
    • RoHS Restriction of Hazardous Substances Directive
    • UL 94 Flammability Testing for polymers
    • ISO 9001:2015 Quality Management for specialty materials

    Typical usage ratio

    • 1–8% by weight as a co-monomer or functional additive, depending on target molecular weight and performance requirements

    Downstream process integration

    • Incorporated by in situ polymerization or grafting during monomer blending and pre-polymer synthesis stages

    Final product types

    • Fluorinated specialty resins for chemical apparatus linings
    • Electronics-grade dielectric coatings
    • Non-stick and anti-corrosive surface technology films

    4. Analytical Reference Material Preparation

    Quality control laboratories and reference standard manufacturers recognize this molecule as a qualified analytical standard and spiking additive for trace analysis and validation in regulated environments. The unique chemical structure offers specificity in chromatographic analysis, enabling reliable calibration and method development for regulated sector analysis of residues or impurities.

    Industry compliance standards

    • ISO/IEC 17025:2017 Testing and Calibration Laboratories
    • USP–NF Reference Standard Guidelines
    • FDA 21 CFR Part 211 for laboratory controls
    • OECD GLP Principles

    Typical usage ratio

    • 0.01–0.1 mg/mL in analytical standard solutions; concentration set by analytical requirements and limit of quantitation

    Downstream process integration

    • Added during preparation of stock standard solutions or as spike-in for matrix recovery studies in QC labs

    Final product types

    • Certified reference materials for chromatography
    • Internal quantitative standards for LC–MS/GC–MS
    • Proficiency testing kits for regulated laboratory accreditation

    5. Crop Protection Formulation R&D

    Advanced agricultural chemical R&D centers employ this compound as a lead scaffold in the discovery and scale-up of new-generation pyrazole herbicides with selective crop safety features. Its structure enables SAR (structure–activity relationship) exploration and patentable formulation innovation under real-world field conditions relevant to international registration dossiers.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • ISO 17034 Reference Material Producer requirements
    • US EPA OPPTS Test Guidelines
    • EU Regulation (EC) No 396/2005 on pesticide MRLs

    Typical usage ratio

    • 1–10% (w/w) in model formulations during biological activity and selectivity screening; precise level based on field test protocols

    Downstream process integration

    • Employed in formulation test batches, SAR screening, and candidate optimization phases prior to upscaling for pilot field trials

    Final product types

    • Early-phase herbicidal formulations and test substances
    • Active ingredient templates for registration samples
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    Certification & Compliance
    More Introduction

    Introducing 3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole: Direct Insights from the Manufacturer

    Our Commitment to Precision Chemistry

    In the world of fluorinated heterocycles, 3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole stands out—a result of focused research, repeated refinement, and persistent hands-on manufacturing experience. Producing this compound starts long before a batch goes into the reactor. We source our starting materials directly, work under strict in-house controls, and never rely on intermediates for quality checks. Consistency at scale presents challenges; impurity profiles shift as production climbs above the kilogram mark. By holding each step accountable to real, measured standards, batch variability rarely becomes an issue.

    What Sets This Compound Apart

    3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole owes its popularity to the unique influence of the trifluoromethyl groups. Two electron-withdrawing CF3 substituents positioned symmetrically at the 3 and 5 spots of the pyrazole core markedly tune the electronic nature of the molecule. These effects pop up in reactions by altering nucleophilicity and stability, giving this pyrazole a reactivity profile that diverges sharply from its monofluorinated or non-fluorinated cousins.

    Other manufacturers sometimes sell similar pyrazoles, but comparing a mono-trifluoromethyl pyrazole or a plain 1-phenylpyrazole to this CF3-laden variant leads to misleading conclusions. Our own control runs show changes in melting point, crystallinity, and spectral purity between the variants. Physical differences directly affect solubility and handling; the strong electron-withdrawing groups stabilize the aromatic system, pushing this molecule into uses that would degrade a less robust analog.

    The material emerges as a solid, off-white with notable thermal stability, and a tightly-defined melting range. We have never encountered significant batch-to-batch shifts, having locked down critical process variables such as water content, acidification rates, and work-up temperatures. Over the years, we have swept away unnecessary purification cycles through optimization. The result—high-purity product with HPLC area purity routinely over 99%. Newcomers notice that differences between competitors often show up in trace impurity fingerprints, not the headline specifications.

    Real Uses: Building Blocks for Modern Chemistry

    Much of our 3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole finds its path into active molecule discovery. The pharmaceutical industry, with its appetite for structure-activity relationships, gravitates to CF3-pyrazoles for their marked metabolic stability and ligand optimization potential. Process chemists push for highly reproducible performance from their starting materials. Our customers in medicinal chemistry programs want this pyrazole for its ability to resist oxidative degradation, holding on to activity in biological screens where less electron-poor heterocycles fade.

    The agricultural sector never stands still. We work with several innovators who benefit from these stable, highly-electronegative motifs as pesticide lead structures. Their synthetic groups appreciate the extra shelf-life and hydrolytic stability, reporting fewer side-reactions during late-stage modifications and easier analytics post-formulation.

    Academic researchers routinely call out the versatility of this molecule as a scaffold for cross-coupling. Trifluoromethylation carves out new synthetic pathways—reactions proceed faster and more smoothly when using the bis-CF3 pyrazole compared to simple phenylpyrazole analogs. We receive regular feedback about cleaner conversions, lower catalyst loading, and higher yields.

    Specifications Rooted in Reliable Practice

    By building and running the manufacturing process ourselves, we maintain tight control over key material attributes. From our reactors to the finished, packaged product, we ensure the particle size, HPLC area purity, melting range, and residual solvent levels are typical for true research-grade chemicals. Material that leaves our site adheres to declared purity and comes with detailed impurity profiling.

    The bis-trifluoromethyl pattern resists hydrolysis and oxidation to a far greater extent than plain pyrazoles. This stability directly translates to easier long-term storage and shipment; fewer breakdown products and less off-target reactivity means lower risk for downstream synthesis. Chemists regularly ask about solubility, and our experience shows the product dissolves reliably in common organics—acetonitrile, dichloromethane, and DMF in particular.

    We've established a production window that allows just enough narrow melting variation to ensure meaningful purity, without going so tight as to unnecessarily exclude perfectly functional lots. Our team regularly benchmarks the physical parameters against international standards, focusing on what actually improves research outcomes.

    Meeting Real-World Challenges

    Producing high-quality, fully characterized intermediates is not a race to the bottom. As manufacturers, pressure to cut corners must be weighed against the reputation impact of an inconsistent product—all eyes turn quickly to the chemical maker if an end-use segment fails. We have run into operational problems in the past: a poorly-designed filtration stage led to slight particulate carry-over, which caused solubility quirks in sensitive assays. That feedback loop, direct from the bench of a process chemist, led us to overhaul part of our work-up line and adjust the filter mesh sizing. We treat these moments as process improvements, not as surface issues.

    Trace solvents persist as an industry-wide difficulty. We employ a multi-step vacuum drying that keeps residual toluene and DMF consistently below trace detection thresholds. Early efforts to over-dry or use higher heat saw more product discoloration—a lesson we learned and applied to our in-line analytical controls.

    Transporting specialty organofluorine products presents another challenge—temperature swings and rough handling can invite degradation even in stable molecules. Our packaging underwent several generations of improvement, moving from generic plastic to thick-walled, inert-lined containers proven to block out moisture and avoid static charge during transit. Not every customer sees these details, but those with reactivity-sensitive targets do.

    Supporting Customer Research and Innovation

    Direct feedback shapes our process almost as much as the chemistry itself. A customer pushing catalytic fluorination sent us a sample with an unexpected impurity artifact picked up after several months’ storage. Examining our supply chain, we identified a minor batch-to-batch difference in the upstream trifluoroacetylating agent that widened a downstream impurity profile. Within a quarter, we switched suppliers and changed the standard for starting material analysis. The next five campaigns ran clean, reinforcing the value of close collaboration between supplier and researcher.

    Startups chasing patentable structures benefit from routes that use our bis-CF3 pyrazole both as a nucleophile and as an electrophile, leveraging the compound’s dual functionality. Their scientists make rapid progress on benzene ring modifications, and we keep open lines of technical support to help with process troubleshooting. In cases where extreme temperature sensitivity or moisture issues arise, we provide application guidance grounded in direct plant experience, not outsourced documents.

    Larger pharmaceutical customers have asked about extended batch reserve programs; our stability data backs up nearly two years shelf life under ambient conditions when sealed tightly. Those working with high-throughput screening platforms appreciate that our QC program overlays both classic NMR and targeted GC-MS profiles before approval.

    Quality Is a Long Game

    A strong supplier-customer relationship only builds with consistent, reliable material. We do not sub-contract reaction steps to third parties; this compounds every aspect of raw material selection, temperature monitoring, and in-process verification. Experienced technicians conduct visual and instrumental inspection of every production lot, flagging anything outside of specification long before it heads to final packaging.

    Our data suggests that relying on in-house crystallization lowers the profile of certain hard-to-remove colored contaminants by more than 60% over outsourced crystallization. Customers running tightly regulated syntheses maintain fewer red-flag incidents and enjoy a smoother regulatory pathway with fully audited batch records.

    Purchasing from the manufacturer means any process change or analytical deviation receives real-time communication. If a customer’s testing uncovers a disagreement, we reach into our batch archive, cross-reference raw data, and collaborate openly, never hiding behind distributors. We have improved solubility by testing in actual customer solvents, not just the typical laboratory fare, returning to synthesis if necessary to tweak parameters and improve the application profile.

    Differences from Other Products: Details Matter

    Plenty of suppliers advertise generic 1-phenylpyrazoles; few are willing to provide detailed impurity analysis and trace lab support. Side-by-side, the dual CF3 modification stands apart for several direct reasons: improved thermal resistance, greater moisture tolerance, and alignment with current trends toward increased fluorination in drug development and agrochemical libraries.

    Researchers confirm cleaner mass spectra, less discoloration on storage, and fewer false positives in downstream reactivity screens when using our material. The distinctive steric and electronic fingerprint of the bis-trifluoromethyl motif unlocks synthetic transformations that more basic analogs cannot match. Single-molecule studies confirm this advantage; spectroscopic datasets reconciled against internal standards repeat the theme.

    We often receive questions comparing our material to vendor-labeled alternatives. Analysis of these samples almost always reveals broader melting ranges and ghost peaks on HPLC—markers of rushed or inadequately washed production processes. By keeping every step inside our own factory, we can promise not only headline purity, but also the less glamorous, crucial elements like consistent solid density and reactivity under standard coupling conditions.

    Optimizing for Your Next Research Step

    We encourage direct, technical dialogue with customers facing bottlenecks or unexpected reactivity. Suggestions drawn from repeated scale-ups in our own plant often translate into better yields and easier handling on the customer end. Our technical team fields questions not only about routine use, but also about extension to new synthetic routes—pyrazole ring functionalization, CF3 exchange, or direct coupling applications.

    Subtle differences in starting material choices impact downstream reactivity. Process screening shows the bis-trifluoromethyl groups suppress competing N-oxidation pathways in high-energy fragment coupling. The chemical community’s drive toward more environmentally robust, easily traceable intermediates sits in alignment with our persistent process improvements.

    Customers pursuing scalable synthesis or custom modifications—such as selective halogenation or improved solubility through pro-drug strategies—find our technical insights grounded in first-hand reaction monitoring. Batch notes returned from multi-kilogram synthesis inform both the way we pack and ship, and the ways we update our written documentation.

    Emerging application fields such as high-performance electronics and specialty coatings continue exploring the pyrazole core, delivered with bis-CF3 groups, for improved reactivity and environmental resistance. This trend helps define next-generation specifications.

    Process Transparency and Ongoing Improvements

    Our team documents every stage of manufacture and shares key insights on request. Experienced chemists scrutinize each lot’s analytical profile to ensure impurities remain within strict thresholds and that unusual peaks are fully explained. Even a small deviation from the expected NMR spectrum receives a full review, and production records are adjusted to close the gap for future lots.

    Our production managers invest in continuous cross-training. By avoiding compartmentalized knowledge, we spot patterns before problems multiply. Plant tours for trusted clients demonstrate first-hand the rigor and transparency built into our approach—something that leaves a lasting impression and recurs in feedback.

    A supply disruption from a main vendor once forced us to pilot an alternative raw supplier. Before shifting, we ran parallel pilot reactions, compared conversion rates, impurity crossover, drying times, and then logged the results. Rolled-back production lines only resumed after full customer notification and approval of the comparability data; that’s a lesson learned the hard way, but it keeps risk low for our clients. Documenting the entire episode provides valuable internal training and a roadmap for prevention.

    Putting Users at the Center of Production

    Beyond the lab and production floor, we learn most from those who use our chemical in tough, real-world synthesis. Experience taught us to probe for more than the standard technical specification. Researchers often care less about headline purity and more about trace ionic residues, lot stability, or unwanted color in downstream processes.

    With the growing influence of automation and high-throughput experimentation, the role of physically and chemically consistent building blocks becomes more important. Developing systems that can dispense, dissolve, and react the same way every time depends entirely on the manufacturer’s QC ethos. Automation interacts poorly with wide melting ranges or sticky, impure solids. Our ongoing plant investments focus specifically on tightening output profiles and lowering inter-batch variability.

    In the eyes of many, sourcing directly from specialist producers provides assurance that process questions—right down to reaction minutia or storage details—are answered by those who know the product best. The benefit of tight feedback across departments, from process chemistry to logistics, cannot be overstated. This dialogue shapes product change, documentation, and future batch design as research markets evolve.

    Upholding Professional Trust

    Reputation in the specialty chemical field builds on reliability, traceability, and open dialogue. Each kilo of 3,5-Bis(Trifluoromethyl)-1-Phenylpyrazole reflects the hands-on experience and the cumulative feedback of clients who have tested and challenged it in diverse applications. We believe that a great product results not just from technical capability, but from commitment to improvement, transparency, and real collaboration. Our approach reflects years at the bench, in the plant, and shoulder-to-shoulder with users at the leading edge of discovery.