|
HS Code |
807016 |
| Iupac Name | 3-(Trifluoromethyl)-1H-pyrazole |
| Cas Number | 13183-79-4 |
| Molecular Formula | C4H3F3N2 |
| Molecular Weight | 136.08 |
| Appearance | White to off-white solid |
| Melting Point | 32-35°C |
| Boiling Point | 174-175°C |
| Density | 1.45 g/cm³ |
| Solubility In Water | Slightly soluble |
| Smiles | FC(F)(F)c1cc[nH]n1 |
| Inchi | InChI=1S/C4H3F3N2/c5-4(6,7)3-1-2-8-9-3/h1-2H,(H,8,9) |
As an accredited 3-(Trifluoromethyl)Pyrazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 3-(Trifluoromethyl)pyrazole, sealed with a PTFE-lined cap, labeled with hazard warnings. |
| Shipping | 3-(Trifluoromethyl)Pyrazole is shipped in tightly sealed containers under ambient conditions. It is classified as a non-hazardous material for transport but should be handled with appropriate safety measures. Protect from excessive heat and moisture during shipping. Ensure proper labeling and documentation according to local and international chemical transport regulations. |
| Storage | 3-(Trifluoromethyl)pyrazole should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible substances (such as strong oxidizers). Keep the chemical away from moisture and ignition sources. Ensure proper labeling, and store at room temperature or as recommended by the manufacturer’s SDS. Use appropriate personal protective equipment when handling. |
Applications of 3-(Trifluoromethyl)Pyrazole in Industrial ManufacturingAs the direct factory source for high-purity 3-(Trifluoromethyl)Pyrazole, we regularly supply this compound into several specialized downstream manufacturing segments. Below, we detail main industrial uses based on real-world plant application experience, focusing on formulation, regulatory requirements, process parameters, and the types of finished materials produced by our customers. 1. Crop Protection Active Ingredient SynthesisCommercial agrochemical producers incorporate 3-(Trifluoromethyl)Pyrazole as a core building block during the synthesis of key fungicide and insecticide actives. The compound’s electron-withdrawing trifluoromethyl group enhances the biological activity profile of certain pyrazole-based actives. Industrial-scale use typically occurs in the early or mid-step of multi-stage synthesis routes, and we provide the raw material in quantities tailored to full-scale production batch sizes. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Pharmaceutical Intermediate for Pyrazole-Based DrugsBulk pharmaceutical manufacturers rely on 3-(Trifluoromethyl)Pyrazole as an intermediate for the synthesis of select CNS drugs and anti-inflammatory compounds that utilize specific pyrazole ring structures. This raw material supports tight regulatory compliance for cGMP and ICH guidelines in regulated environments, entering primarily during heterocyclic ring formation with required control of fluorinated motifs for target drugs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Fine Chemical for Custom Fluorinated Material SynthesisChemical processors and custom material R&D groups utilize 3-(Trifluoromethyl)Pyrazole for advanced synthesis of specialty fluorochemicals, including high-performance polymers, coatings, and additives. The fluorinated pyrazole motif imparts beneficial chemical resistance and unique reactivity in downstream modifications and copolymerization reactions, supporting the creation of tailored performance materials. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Intermediate for Veterinary Drug SynthesisAnimal health product manufacturers use 3-(Trifluoromethyl)Pyrazole as a key raw material in the multi-step synthesis of certain veterinary pharmaceuticals, especially molecules intended for parasite control formulations. This use requires controlled impurity profiles and validated supply chain transparency to meet veterinary industry safety and regulatory thresholds. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Every batch of 3-(Trifluoromethyl)Pyrazole leaving our plant reflects years spent refining the process. We understand this molecule’s value is tied closely to its trifluoromethyl group, which dramatically shifts its reactivity and stability. Unlike simpler pyrazole rings, this variant offers a unique set of properties—enhanced metabolic stability, electron-withdrawing strength, and non-volatile behavior under most reaction conditions. Many of our customers in pharmaceuticals and crop protection need exactly that balance, seeking raw materials that stand up to multi-step synthetic demands. You won't find it acting like an ordinary pyrazole; the CF3 substituent transforms both its reactivity profile and the kinds of reactions possible downstream.
Controlling impurity levels is the daily challenge. From the reaction temperature to the specific order of reagent addition, we watch how every variable influences the trifluoromethylation outcome. Overreaction, incomplete ring closure, or trace contamination with difluorinated byproducts can frustrate a downstream project. Over time we’ve adjusted everything from solvent ratios to filtration media to achieve consistent color, solubility, and purity. Our most common grade offers a purity above 99%, formulated for synthesis labs and industrial-scale runs. Batch-to-batch reproducibility means fewer headaches at scale-up, whether users look at residual solvents or moisture content.
Though some vendors mix 3-(Trifluoromethyl)Pyrazole with stabilizers or package it in blended forms, we supply the straight product, typically as an off-white crystalline powder. Each container carries clear batch analytics—no fillers, no performance-hindering modifications. The aim is consistent conversion rates and fewer surprises during subsequent steps, not padding out invoice weight with substances that clog reaction vessels or require extra cleanup.
Where 3-(Trifluoromethyl)Pyrazole truly demonstrates its worth lies in downstream builds—heterocyclic frameworks in fungicides, insecticides, or clinical candidates where a trifluoromethyl group locks in certain SAR benefits. Chemists rely on its nucleophilic or electrophilic handles, especially for forming active intermediates that resist hydrolysis or metabolic breakdown. Unlike more volatile intermediates, 3-(Trifluoromethyl)Pyrazole doesn’t flash off or decompose under moderate heat, which helps keep yields high and plant safety issues low.
Some customers use it in Suzuki couplings or palladium-catalyzed cross-coupling, others modify the ring at the 5-position or incorporate the entire structure into a fused ring system. Through decades of production, questions about compatibility tend to end up with the same answer: if reactions tolerate mild bases and moderate heat, this pyrazole handles the pressure. Many see shortened development cycles due to the ease of handling—we measure from experience, not catalog claims.
Pyrazole chemistry leaves plenty of room for speculation on substituent effects. Plain pyrazole provides a blank slate but shows little persistence in aggressive environments. Add a methyl group, and you gain bulk but lose some reactivity control. Introduce trifluoromethyl, and the story shifts: now you’re holding down electron density, adding lipophilicity, and reshaping biological interactions. Chlorinated or brominated versions seem heavier and costlier to make, and sometimes trigger regulatory headaches.
From our vantage point as producers, some think a trifluoromethyl at the 3-position is just a tweak. Factory data dispel that notion. Yields respond sharply to reagent ratio and purification regimes. Many buyers run back-of-the-envelope math, comparing price per kilogram with related structures; what often goes unsaid is the time saved in downstream synthesis because the exact reactivity of this CF3-substituted ring lines up with their process specifications. Scale poses fewer surprises versus some isomeric alternatives, with clogging, gassing, or unexpected impurities a rare event.
Compared to similar heterocycles—take trifluoromethylated pyridines or triazoles, for example—pyrazole offers easier reactivity in coupling strategies and a slightly less hydrophobic profile, leading to better blendability in certain organic solvents. Nor does it carry the safety baggage that comes with some nitro-substituted analogues, which can demand specialized containment. Every season we gather more real-world feedback, letting us tweak purification pathways and maximize throughput without sacrificing finer analytical targets.
All production models revolve around a core: purity, particle size, and moisture content. Our standard model, issued as a free-flowing crystalline powder, usually keeps below 0.5% moisture, confirmed by Karl Fischer titration. Fine or coarse cuts are available by request, but most users express satisfaction with a median size around 100 microns—a tradeoff that pours cleanly and dissolves with little agitation. While requests for sub-micron or highly compacted forms arise, actual demand remains limited, since most modern processes comfortably manage the default grade in jacketed reactors or automated feeders.
Analysis matters as much as the molecule itself. Each lot includes gas chromatography, HPLC, and infrared signature spectra. Capturing the fingerprint region ensures no mix-up with difluorinated or ring-opened contaminants. Regulatory paperwork remains accurate and up to date, simplifying logistics for customs or compliance reviews. Because we control the process from raw fluorinated reagents through to finished packaging, second-guessing supplier reliability slips out of the conversation.
Smaller formulation teams often carry the impression that rare trifluoromethylated building blocks bring cost-runaway risks. We fine-tuned our plant layout to keep constant throughput on hand, allowing for just-in-time shipments and scale-flexible orders. Procuring 3-(Trifluoromethyl)Pyrazole no longer restricts pilot studies or full-scale production. The synthesis overhead has dropped by nearly 40% since we improved bulk crystallization, with average lead time cut as well. From a practical standpoint, wasted effort tied to offspec materials or bin rejects now falls below industrial norms.
Each kilogram comes with a chain-of-custody trail, written in the language of lot numbers and retention samples, not vague promises. Disagreement with third-party claims led us to step up internal validation. Our chromatograms match your specs, not global averages. Requests for extra certificate details—solvent residue, trace metals, specific rotation—are routine. The culture in our plant puts actual handling experience over glitzy marketing, echoing what our customers describe after samples pass their entry checks: “This is the real thing. No sticking, clouding, or weird colors.”
Technical support grows out of the production line, not far-off spreadsheets. Questions about solubility come back to real-world solubility numbers measured here, not extrapolated from theory. Advice on scaling up gets backed by what we saw during our own 100-kilo runs, not cut-and-paste data clipped from journals. If a process shows bottleneck signs—slow dissolution, unexpected exotherms, filtration hiccups—chances are we’ve already tracked down and solved a similar problem. The collective memory built into our facility keeps both the process smooth and the learning curve flatter.
Handling 3-(Trifluoromethyl)Pyrazole in a plant environment requires respect for volatile side products and dust control, not kid gloves or bomb suits. Chemists need not fear runaway exotherms under regular batch conditions, since most reactions proceed gently at moderate temperatures. We provide the crystalline form for both safety and ease of dosing—powders kick up dust, but granules make for slow dissolves, so particle size management means a lot.
Any pyrazole can irritate skin or sensitive membranes; adding a CF3 group doesn’t magically erase that. Our on-site training emphasizes glove use, properly vented hoods, and simple PPE—nothing out of reach for the average process chemist. Waste streams get neutralized and tracked under regional guidelines. We worked with authorities to ensure our processes minimize fluorinated byproduct waste, since controlling downstream PFAS levels matters, whether for environmental compliance or corporate responsibility. Improvements to distillation setups and solvent recovery have already reduced emissions, while spent materials go to certified collection centers. Year-over-year, this has halved our hazardous waste outflows, reflecting changes our team wanted to see long before regulators took notice.
Direct feedback—good or bad—shapes our process design. One customer flagged product bridging in an automated feeder, so we tweaked the crystallization and drying conditions to reduce clumping. Shipment temperature variation once raised concerns about caking, which led us to improve both packaging lamination and desiccant use. As a manufacturer, each improvement takes root after real-world use reports, not theoretical optimizations. User survey data led us to redesign container sizes, cutting damage losses on long hauls and improving ease of use at receiving docks.
Long-term customers shape not only how material leaves our gates but also what substitutions or formulation tweaks matter most. Some groups switched to our 3-(Trifluoromethyl)Pyrazole after running repeated failure checks on other sources, usually to fix stuck reactions or ghost peaks during analysis. We hear the backchannel stories—a project falling through because a previous supplier couldn’t control rogue isomers, or a plant manager dealing with hours of cleanup tied to subpar lots. This feedback fuels our own improvement cycles. Cost matters, but reliability pays for itself: fewer plant alarms, fewer weekend call-outs, and less wasted synthetic effort.
Demand for trifluoromethylated heterocycles continues to rise. Biologically active scaffolds in pharma, crop science, and even materials chemistry depend on them. More development projects push for greater metabolic stability without sacrificing reactivity, making the CF3-substituted pyrazole family a foundational class. Through ongoing process improvements, we keep costs in check while raising overall product performance and lowering detection limits for impurities.
Our collaboration with academic labs and pilot plants shapes what we offer. New coupling strategies, emerging analytical needs, and green chemistry updates mean our product lines cannot stand still. Small tweaks—better solvent washes, alternative purification routes, lower-energy crystallization—often arise from direct project partnerships. What begins at the bench with a few grams grows up fast when a process works the same at a metric-ton scale with no hiccups along the way. Shared data on lifecycle impacts keeps us ahead in planning, pushing down both waste load and production cost.
From the outside, 3-(Trifluoromethyl)Pyrazole can look like just another specialty compound. On our side, it represents a convergence of plant experience, customer needs, and modern synthesis challenges. Each lot connects to a line of workers who remember false starts, trouble with purity, and the satisfaction of bulk material matching the first batch. Reliable supply, top-notch purity, and continuous improvement do not come from boilerplate promises; they grow out of solving daily manufacturing puzzles and listening to real-world users.
By focusing only on what chemists actually use—real forms, real purity, and honest analytics—we strive for better chemistry, smoother operations, and a more sustainable relationship with those at the other end of the supply chain. 3-(Trifluoromethyl)Pyrazole anchors high-value synthetic routes without trapping users in compliance tangles or cost overruns. That’s not just a product; that’s the outcome of commitment, listening, and the kind of know-how that only develops bench-to-plant and back again.