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3,5-Bis(Trifluoromethyl)Pyrazole

    • Product Name 3,5-Bis(Trifluoromethyl)Pyrazole
    • Alias 3,5-Bis(trifluoromethyl)-1H-pyrazole
    • Einecs 251-803-0
    • 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
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    Specifications

    HS Code

    299898

    Cas Number 1722-12-5
    Molecular Formula C7H2F6N2
    Molecular Weight 230.10
    Iupac Name 3,5-bis(trifluoromethyl)-1H-pyrazole
    Appearance White to off-white solid
    Melting Point 116-120°C
    Boiling Point None (decomposes)
    Density 1.62 g/cm³ (calculated)
    Solubility In Water Slightly soluble
    Smiles FC(F)(F)c1cc(nn1)C(F)(F)F
    Inchi InChI=1S/C7H2F6N2/c8-6(9,10)4-2-5(7(11,12)13)15-14-3-4/h2-3H,1H
    Synonyms 3,5-Bis(trifluoromethyl)pyrazole
    Storage Temperature Store at 2-8°C

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3,5-Bis(Trifluoromethyl)Pyrazole, sealed with a screw cap and labeled for laboratory use.
    Shipping 3,5-Bis(Trifluoromethyl)Pyrazole is shipped in tightly sealed containers, protected from moisture and light. It is usually dispatched via ground or air in compliance with chemical transportation regulations. Proper labeling and documentation accompany every shipment, ensuring safe handling and delivery to laboratories or industrial facilities. Store in a cool, dry place upon arrival.
    Storage 3,5-Bis(Trifluoromethyl)Pyrazole should be stored in a cool, dry, and well-ventilated area, tightly sealed in a suitable container, and away from heat, ignition sources, and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. It is recommended to store the chemical under inert gas, such as nitrogen, to minimize degradation and ensure safety.
    Application of 3,5-Bis(Trifluoromethyl)Pyrazole

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

    3,5-Bis(Trifluoromethyl)Pyrazole serves as a valuable fluorinated intermediate in advanced chemical production. Its robust electron-withdrawing structure allows integration into high-performance molecules across demanding industrial fields. We manufacture this specialty raw material for formulation engineers who operate in regulated industries with precise process requirements. Below, we describe real-world downstream applications based on industry standards and technical documentation.

    1. Agrochemical Active Ingredient Synthesis

    Major crop protection formulators incorporate this compound as a key heterocyclic building block for manufacturing next-generation herbicides and fungicides. The electron-deficient pyrazole ring enhances bioactivity and target specificity, supporting constructs for selective weed control and resistance management. Formulation chemists introduce it during the core active ingredient assembly stage and perform further derivatization before final formulation with adjuvants.

    Industry compliance standards

    • ISO 9001:2015 (Quality management for agrochemical manufacturing)
    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006 (EU market registration)
    • US EPA 40 CFR Part 158 (Data submission for pesticide registration)

    Typical usage ratio

    • 0.5–2.5 molar equivalents in core heterocycle coupling stages, adjusted based on target pyrazole-substituted product yield
    • Residual levels in finished formulations below 0.1% following downstream conversion and purification

    Downstream process integration

    • Initial introduction during synthesis of heterocyclic intermediates
    • Coupling with other aromatic or aliphatic partners under copper- or palladium-catalyzed conditions
    • Integration into multi-step active ingredient synthesis, followed by protection/deprotection and isolation
    • Subsequent blending with solvents, wetting agents, and dispersants in technical concentrate formulation

    Final product types

    • Pyrazole-based herbicides (e.g., inhibitors targeting weed-specific enzymes)
    • Novel fungicide actives (e.g., triazole-pyrazole co-structures)
    • Technical-grade active ingredient concentrates for major crop protection brands
    • Formulated suspension concentrates and emulsifiable concentrates

    2. Pharmaceutical Intermediate for Antiviral and Anticancer Compounds

    Our material enables synthesis of highly functionalized pyrazole units that serve as pharmacophores in modern drug discovery. Medicinal chemists use it for constructing structural motifs found in kinase inhibitors, nucleoside analogues, and respiratory antivirals. The high degree of fluorination supports improved metabolic stability and receptor affinity. Production teams rely on strict batch tracking and impurity profiling throughout API routes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211 (Finished pharmaceutical cGMPs)
    • USP/NF Monographs (where applicable for intermediates)
    • European Pharmacopoeia guidelines for advanced intermediates

    Typical usage ratio

    • 0.8–2.0 molar equivalents in stepwise N-arylation and heterocycle-forming reactions
    • Final APIs contain only trace residues (<50 ppm), verified by HPLC or GC-MS

    Downstream process integration

    • Fed into early- or mid-stage reaction vessels for pyrazole ring-building
    • Subject to catalytic amination, halogenation, or acyl substitution, depending on target molecule
    • Isolate target intermediate for further derivatization under GMP protocols
    • Employ process analytical controls to monitor transformation and remove unreacted starting material

    Final product types

    • Antiviral API intermediates (e.g., non-nucleoside reverse transcriptase inhibitors)
    • Oncology drug precursors (e.g., pyrazole-based kinase inhibitors)
    • Test articles for structure-activity relationship screening
    • Clinical trial-scale active intermediate stocks

    3. High-Performance Material Monomer Synthesis

    Engineering plastics and performance elastomers incorporate the compound for fluorinated monomer synthesis. Material scientists value its dual trifluoromethyl substituents for increasing dielectric stability, solvent resistance, and thermal endurance. The compound enters functionalization steps to form monomer blends destined for extreme-environment applications, including aerospace wiring insulation and fuel system seals.

    Industry compliance standards

    • ISO 14001:2015 (Environmental management in specialty polymer production)
    • ASTM D5111 (Standard Test Methods for Polymeric Materials)
    • RoHS Directive 2011/65/EU (Restriction of hazardous substances)
    • UL 94 (Flammability standards for plastic components)

    Typical usage ratio

    • 0.5–1.5 molar equivalents in copolymerization feedstocks, dependent on fluoro-content design
    • Resulting polymer backbone may contain 10–30% by mass derived from the fluorinated building block

    Downstream process integration

    • Mix into precursor monomer slurry prior to controlled radical or ionic polymerization
    • Subject to base- or acid-catalyzed ring opening or substitution
    • Copolymerize with vinyl, acrylate, or urethane monomers in batch reactors
    • Post-treatment purification to remove unreacted monomer by distillation or extraction

    Final product types

    • High-dielectric polymeric insulators for electronics
    • Fluorinated elastomer seals and gaskets for automotive and aerospace sectors
    • Ultrafiltration membranes for aggressive chemical processing
    • Polymer coatings for corrosion resistance

    4. Specialty Fluorinated Fine Chemical Synthesis

    Fine chemical manufacturers utilize this fluorinated pyrazole in multi-step processes where selective introduction of trifluoromethyl groups enables synthesis of advanced intermediates for dyes, liquid crystals, and fluorinated building blocks. By maintaining consistent batch purity, we support chemical synthesis routes requiring precision and low impurity profiles at kilogram and tonnage scale.

    Industry compliance standards

    • Chemical Facility Anti-Terrorism Standards (CFATS) for high-volume reagents
    • ISO 9001:2015 (Process traceability and batch release)
    • Responsible Care® Initiative (Global chemistries stewardship)
    • UN ADR/RID/IMDG codes for hazardous materials handling

    Typical usage ratio

    • 1.0–3.0 equivalents in heterocycle synthesis with further downstream chlorination or alkylation
    • Adjustment based on stoichiometry of final fine chemical transformations

    Downstream process integration

    • Introduction into functional group transformation reactions after condensation or cyclization
    • Employ batch or continuous flow processing for large-scale customization
    • Multi-stage separations to isolate desired functionalized intermediates
    • Rigorous in-process QC for identity, purity, and residual solvents

    Final product types

    • Liquid crystal intermediates for electronic displays
    • Fluorophenyl dyes for photonic and OLED applications
    • Specialty reference standards for analytical laboratories
    • Advanced fine chemical building blocks for research and development
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    More Introduction

    Introducing 3,5-Bis(Trifluoromethyl)Pyrazole: Practical Insights from the Manufacturer

    The Chemistry Behind 3,5-Bis(Trifluoromethyl)Pyrazole

    Making 3,5-Bis(Trifluoromethyl)Pyrazole isn’t just a job in the lab; it’s a core part of our daily operations. The chemical formula, C6H2F6N2, comes to life through each batch, bringing high purity and tightly controlled moisture levels that meet the strictest demands of the fine chemical sector. We control reaction conditions and purification every step of the way, relying on experienced technicians and practical lessons from years of work. You learn quickly what small differences in temperature, solvent ratios, and raw material quality can mean for a finished product’s consistency. Anyone who’s ever run a scale-up through the pilot plant understands the quirks pyrazoles can throw at you. Over many production runs, even tiny trace impurities in precursor materials can show up in the final analysis, so we don’t cut corners selecting our fluorinated starting reagents.

    The compound stands out from its relatives due to the two trifluoromethyl groups at the 3 and 5 positions. These groups dramatically shift the pyrazole’s basicity, solubility, and stability, and those changes keep this molecule in demand for tasks that simpler pyrazoles can’t handle. The electron-withdrawing effects from the CF3 substituents have a clear impact during synthesis — watch the intermediate profiles during NMR and you’ll see it – but in application, those same effects make this pyrazole tough enough for harsh end-use conditions. The molecule resists unwanted side reactions in complex system formulations where others might degrade or discolor. That reliability has kept customers coming back, especially among agrochemical and pharmaceutical developers who simply cannot have off-batch or out-of-spec material derailing their synthesis.

    Product Model and Physical Specifications

    Every drum or tote we ship carries a product batch backed by our own assay and moisture data, not generic numbers from a supplier or repacker. Typical appearance: a white to off-white powder, flowing freely and with minimal clumping thanks to material handling refinements we’ve made over years. Purity runs at or above 99 percent on HPLC in standard lots, with water well below 0.5 percent, commonly under 0.2 percent when required by the pharmaceutical sector. Both single and multi-kilogram packaging lines are maintained in closed systems to keep exposure to air and cross-contamination to a minimum.

    Every batch is tested for residual solvents and heavy metal content. You can request a full impurity profile: NMR, GC-MS, and HPLC data from our QC lab. We maintain these standards not to tick a box, but because we’ve seen what even trace levels of unknowns can do to downstream R&D synthesis. Many of our largest volume users know the headaches of trying to hunt down unknown peaks in their final products, so more than once, we’ve worked with customers to custom-tailor our purification methods. Decades of feedback taught us that each application can demand unique tweaks, and our own plant’s flexibility allows us to deliver on those specifics.

    Usage and Application: Why Producers and Researchers Seek Out 3,5-Bis(Trifluoromethyl)Pyrazole

    Chemists in the knowledge-based sectors know that not every pyrazole performs the same way. The addition of two trifluoromethyl groups changes reactivity and delivers properties that become crucial in both industrial production and research-scale development work. Among agricultural R&D chemists, this molecule forms a trusted scaffold for designing new crop protection agents. The fluorinated pyrazole structure blocks off sites vulnerable to rapid biodegradation, allowing actives to persist through field conditions where non-fluorinated analogs might break down too quickly to be effective. The difference shows up in field test results: longer residual action without buildup of harmful byproducts.

    We have worked directly with process teams at agrochemical firms who rely on 3,5-Bis(Trifluoromethyl)Pyrazole as either the core structure or as a synthetic intermediate. In these cases, purity is more than a specification; leftover residuals from a low-grade supplier can create purification bottlenecks or even cause full-scale re-synthesis. Some groups push beyond standard synthetic routes, using the compound’s unique electronic profile to access new chemical space. The reactivity shift from the dual CF3 substitution opens doors to selective transformations that struggle with regular pyrazoles.

    Pharmaceutical groups reach for this compound when looking for metabolic stability in API candidates. In medicinal chemistry, you need to have faith that the pyrazole will persist in the body long enough to show a response but will not leave behind hazardous metabolites. The physiochemical profile here is a product of careful process design. We’ve fine-tuned crystallization steps and solvent exchange protocols so that each production lot avoids polymorphism and micron-scale amorphous mixing, which can derail formulation studies in pharmaceutical research.

    Our customer base, ranging from global pharma labs to fine chemical blending operations, notes that fully fluorinated pyrazoles like this resist many common formulation problems. The material laughs off attempts at hydrolysis and many oxidants don’t touch it. Its good solubility in a range of aprotic polar solvents makes it a favorite for solution-phase chemistry. Sometimes, during method transfer from lab to production, we’re asked how it compares on dosing or blending against less functionalized pyrazoles. Our direct answer: with 3,5-Bis(Trifluoromethyl)Pyrazole, you see less batch-to-batch performance variability — something that matters when scaling up.

    Why 3,5-Bis(Trifluoromethyl)Pyrazole Outperforms Other Pyrazoles

    Shoppers weighing this molecule against other pyrazoles often focus on price per kilo, but as a manufacturer, we’ve seen plenty of projects stall when a shortcut on starting material quality snowballs into lost time and rework. The added stability from twin trifluoromethyls isn’t a trivia point—it saves headaches in synthesis, storage, and shipping. Non-fluorinated or single-substituted pyrazoles can fall short under stress. You see it in pilot plant observations: color shifts, sensitivity to light, hydrolysis, or poor compatibility during multi-step synthesis.

    Having handled large volumes for pharmaceutical and agrochemical processes, we see that the thermochemical resilience of 3,5-Bis(Trifluoromethyl)Pyrazole translates into fewer surprises. No unexpected off-odors, no gassing-off, and no cryptic decompositions during reaction scale-up. Its wide liquid-solid phase window supports a broader process envelope and underlines its advantage versus lower-substituted variants prone to melting or degradation at modest temperatures. Formulators working with multi-component systems benefit from better shelf stability and less risk of product complaints from the field.

    In the bench-level reaction flask, you can push the molecule through transformations demanding electron-deficient partners, where less substituted analogs would strand you with unreacted feedstock or side products that lower yield and purity. The performance shows up in yield and downstream throughput: less cleaning, less waste disposal, and more predictable analytical profiles.

    From Plant Operations to End User Satisfaction: The Reality Behind Quality Claims

    A specification tells only part of the story. We see the real cost of subpar raw materials showing up as downtime, wasted solvent, and lost labor hours. Several times, we’ve worked with customers to troubleshoot what first appeared as a mystery impurity or reaction blockage. By tracing back through the supply chain, the culprit is almost always something swept under the rug by a trader or third-party source—contamination from reused drums, exposure to humid air during repacking, unintended solvent carryover. Those who choose to work directly with the manufacturer soon notice how fast their own internal troubleshooting times drop. We offer full transparency because over the years, customers taught us that open access to our analytical data and plant records lets their own experts move fast.

    Manufacturing at the source means every batch stays under one roof from raw reagent charging and reaction through drying, milling, and packing. We don’t outsource; our technical team spends as much time fine-tuning on the line as they do in the office. The feedback loop from actual production chemists goes straight into both process improvement and customer troubleshooting. If a problem arises on the customer’s end, we offer real-world advice grounded in what we see every day — not theory, but lessons learned from handling thousands of kilos through all seasons.

    Equipment choice matters more than most realize. Pyrazole chemistry, especially with fluorinated groups, thrives in clean reactors with inert surfaces. We’ve built our plant around this reality: glass-lined and high-alloy steel vessels throughout. Process controls check for oxygen ingress and temperature spikes, as both can trigger product discoloration or off-odor. Even warehouse workers and packers are trained to spot the earliest signs of moisture pickup or contamination, a focus sharpened by real-life cases where a single missed detail cost days or weeks of downstream troubleshooting.

    Meeting Compliance and Safety Expectations

    We’ve been audited by well-known name-brand pharma and crop protection customers, and we welcome it. Safety and regulatory readiness aren’t empty boxes — we document every step so downstream users can supply regulators with confidence. Our workers follow handling and PPE procedures because their own health depends on it, and that culture bleeds into our record of zero regulatory recall incidents in recent memory.

    REACH compliance and hazard labeling standards are built into our operation, but we go further than the minimum. Every container carries the batch-specific quality data needed not only for your safety file, but, more importantly, for real-world traceability in event of incident. By investing in training and facility upgrades, we keep our operation both safe and future-proof against shifting global compliance trends.

    The Human Side of Chemical Manufacturing

    The day-to-day work at the plant means getting hands dirty and thinking on your feet. In one recent case, we uncovered a minor but recurring impurity during a late-stage analysis. Rather than phone in a fix, our team ran through scenario testing on the shop floor and tracked the source to a subtle leak in a vacuum line on a single drying unit. Documentation captured the resolution, and we reached out to all customers receiving lots from that day, offering replacement if needed — not out of obligation, but a shared understanding that downtime hurts everyone. Many customers show appreciation for such open communication; it minimizes their own risk and turns partnership into trust.

    Even with automation, human expertise counts. It’s the experienced operator who catches a shift in product odor or color before sampling, the technician who questions a faint residue on a drum, and the on-site chemist who finds a faster purification by noting a slight difference in crystal shape forming from a cleaner solvent. These details matter. They drive the culture we try to maintain, one where batch records are more than paperwork and each shipment is the result of teamwork across departments.

    Troubleshooting and Customization: Real-World Challenges and Solutions

    Every so often, a user will ask if we can pull back on moisture or tailor the milling for faster dispersion. As the manufacturer, we have access to every lever — drying dwell time, filter bed thickness, grinding fineness, packaging gas. This flexibility isn’t theoretical; it comes from running the equipment and seeing first-hand how each change affects not just that batch, but the next line setup and the operator’s workflow.

    There’s no one-size-fits-all. A commercial-scale user working in high-throughput flow reactors might need lower fine dust for faster pump feeding. R&D-focused customers often request sub-batch quantities to test modifications — we maintain parallel small-batch reactors to handle this. If we spot a recurring request for a tighter impurity profile, our QC team can shift the chromatography method, running longer columns or alternative elution gradients, to meet those needs. Customer feedback drives improvements in our own SOPs.

    In one case, a project stalled because a European end user needed traceable, impurity-free pyrazole after revised regulatory thresholds in certain active matter. Our team stepped in, running troubleshooting calls that revealed a new HPLC peak linked to container storage time. The root cause: a minor reaction catalyzed by residual metal in an old vessel. By swapping tanks and retesting, we solved the issue within two production cycles and documented the fix for regulators. This kind of responsive, manufacturer-driven customization is something distributorships and trading agents can’t deliver.

    Future Trends and Ongoing Commitment to Quality

    Demand for specialized, resilient chemical building blocks continues to rise as the fields relying on advanced molecules grow ever more exacting. 3,5-Bis(Trifluoromethyl)Pyrazole stands in the middle of this change. Sometimes, a new research group will call us for advice on enzymatic compatibility, formulation stabilities, or scale-up bottlenecks — questions that can only really be answered by those handling the molecule from start to finish. We maintain a dialogue with users because every new application teaches both sides something valuable.

    Plant modernization keeps the supply reliable and the product at the edge of current standards. As more crops require new protection agents and more pharmaceutical APIs get built on fluorinated scaffolds, we continue investing in process control, solvent recapture, and analytical upgrades. We’ve chosen to work with supply partners who share a focus on chain-of-custody and responsible sourcing so our customers benefit from continuity and quality.

    Trust in this compound, and any specialty chemical, grows over years of paying attention to details others ignore. Our work with 3,5-Bis(Trifluoromethyl)Pyrazole is guided by the same principle, and we stand ready to answer challenges and adapt with those who rely on it daily.