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1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol

    • Product Name 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol
    • Alias 1-methyl-3-hydroxy-5-(trifluoromethyl)pyrazole
    • Einecs 619-541-7
    • 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

    505270

    Chemical Name 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol
    Molecular Formula C5H5F3N2O
    Molar Mass 166.10 g/mol
    Cas Number 69227-27-0
    Appearance White to off-white solid
    Melting Point 92-96°C
    Solubility In Water Slightly soluble
    Chemical Class Pyrazole derivative
    Smiles CN1C=C(C(=N1)O)C(F)(F)F
    Inchi InChI=1S/C5H5F3N2O/c1-10-3-4(5(6,7,8)9-10)2(11)9/h3,11H,1H3
    Synonyms 1-Methyl-5-(trifluoromethyl)pyrazol-3-ol

    As an accredited 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol 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, screw cap sealed, labeled with chemical name, CAS number, hazard symbols, and handling instructions.
    Shipping 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol is shipped in tightly sealed containers, under cool and dry conditions, protected from light, moisture, and incompatible substances. Transportation complies with relevant chemical safety regulations and guidelines, and includes appropriate labeling and documentation. Standard UN/DOT shipping protocols are followed to ensure safe and secure delivery.
    Storage 1-Methyl-5-(trifluoromethyl)-1H-pyrazol-3-ol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Avoid exposure to moisture. Store at room temperature, and handle under proper chemical safety protocols, including the use of gloves and eye protection.
    Application of 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol

    Applications of 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol in Industrial Manufacturing

    As a direct manufacturer, we supply 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol for use in several specialized industrial fields. Our production enables precise sourcing for formulation, quality control, and downstream integration. Below, we outline major application sectors with practical process and compliance details.

    1. Agrochemical Active Ingredient Synthesis

    Many crop protection manufacturers utilize this pyrazole derivative as a core building block in synthesizing selective fungicides and advanced herbicides. The compound’s trifluoromethyl group enhances biological stability and environmental persistence, making it valuable for next-generation formulations targeting resistant pathogens. Process engineers incorporate it during key heterocyclization and functional group substitution steps, where raw material QC and batch tracking are essential. The resulting actives undergo downstream blending prior to bulk formulation.

    Industry compliance standards

    • EPA 40 CFR Part 180 (USA Pesticide Residues)
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 manufacturing system
    • EU Regulation (EC) No 1107/2009 on plant protection products

    Typical usage ratio

    • 5–15% by weight in intermediate active compound synthesis, adjusted depending on target pesticide formula

    Downstream process integration

    • Addition during stage-two condensation and cyclization reactions, monitored by in-process HPLC
    • Purified before formulation blending and microencapsulation

    Final product types

    • Fungicide technical concentrates
    • Selective pre- and post-emergence herbicides
    • Wettable powder and emulsifiable concentrate pesticide products

    2. Pharmaceutical Intermediate Production

    Pharmaceutical manufacturers integrate this compound as a scaffold for synthesizing pyrazole-based drug intermediates. Medicinal chemists value its electron-withdrawing group for tuning bioactivity and pharmacokinetics. It is predominantly used during nitrogen heterocycle construction and late-stage process chemistry, where GMP documentation and traceability are obligatory. Strict analytical test methods verify conformance at each scale-up batch before further derivatization or salt formation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/NF and Ph. Eur. compendial controls where applicable
    • FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • Quality risk management as per ICH Q9 guidelines

    Typical usage ratio

    • 2–8% of total mass in synthetic route for clinical intermediates—proportion selected based on route efficiency

    Downstream process integration

    • Charged during third-step cyclization or amidation in multi-step synthesis campaigns
    • Isolated after flash chromatography for further chemical modification

    Final product types

    • Anti-inflammatory drug intermediates
    • Antiviral agent scaffolds
    • Bulk pyrazole pharma APIs (prior to final salt or esterification)

    3. Specialty Polymer and Coating Additives

    Materials scientists use 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol as a modifier in engineering polymers and high-durability coatings. Its structure contributes to chemical resistance and lowers surface energy in specialty applications like anti-fouling paints and fluoropolymer blends. Chemists add the compound at controlled ratios during solution or melt-phase processes, requiring material registers and REACH conformity for final market approval. The additive’s dispersibility in organic media supports efficient incorporation during resin modification.

    Industry compliance standards

    • REACH Registration and SVHC compliance
    • ISO 14001:2015 Environmental Management
    • RoHS (EU Directive 2011/65/EU) where applicable for electronics coatings
    • ASTM D257 Method for coatings dielectric properties

    Typical usage ratio

    • 0.2–2% by weight in polymeric resin blends; dosage varies by targeted hydrophobicity or solvent resistance

    Downstream process integration

    • Direct metering into reaction vessel during copolymerization or masterbatch blending
    • Dispersed via high-shear mixing under inert gas for reactive coatings

    Final product types

    • Fluoropolymer-based anti-fouling coatings
    • UV-cured resist layers
    • Electrical insulation materials

    4. Analytical and Laboratory Reagent Formulation

    Analytical solution providers and reference labs use this compound as a high-purity standard or derivatization agent in GC-MS and LC-MS method development. Its strong electron-withdrawing capability and heteroaromatic structure enable specific detection of target analytes and enhance chromatographic separation. Chemistry QC teams track batch purity to ≥99% and maintain documentation under ISO/IEC 17025 for traceability. Integration typically involves preparing concentrated stock solutions for calibration and derivatization protocols.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Accreditation
    • ICH Q3A Impurities Testing Guideline for pharmaceuticals
    • ASTM E288-18 Standard for laboratory reagent concentration
    • Analytical purity documented in Certificate of Analysis (COA)

    Typical usage ratio

    • 0.01–0.1% in analytical-grade solution formulations; concentration adjusted per detection requirements

    Downstream process integration

    • Dissolved in acetonitrile or methanol to prepare calibration standards for HPLC/GC
    • Used during derivatization step for specific analyte profiling

    Final product types

    • GC-MS calibration standards
    • HPLC derivatization reagents
    • Certified reference materials

    5. Fine Chemical and Custom Synthesis Starting Material

    Our clients in the fine chemical sector select this functional pyrazole as a starting material to build rare heterocyclic frameworks and design specialty molecules for R&D and pilot scale-up. The compound’s electron-rich nitrogen and fluorinated moiety support efficient ring construction and tailoring of reactivity for target molecule assembly. Operators follow campaign-specific handling SOPs and document all material movements for ISO and local EHS compliance. We ensure zero contamination and batch-specific COAs for such customizable projects.

    Industry compliance standards

    • ISO 9001 Quality Management for custom synthesis
    • OHSAS 18001 (Occupational Health & Safety in specialty manufacturing)
    • REACH pre-registration where applicable
    • National/local fire and chemical handling regulations

    Typical usage ratio

    • 1–10% as primary or secondary reactant in multi-step synthesis pathways, based on molecular target and reaction yield optimization

    Downstream process integration

    • Weighing and addition to round-bottom flasks for batch or continuous synthesis
    • Reacted under inert atmosphere with controlled temperature ramps for final assembly

    Final product types

    • Active pharmaceutical intermediate libraries
    • Specialty heterocyclic compounds for materials science
    • Custom molecule building blocks for contract research
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    Certification & Compliance
    More Introduction

    1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol: Crafting Reliability From the Source

    Experience and Approach in Fine Pyrazole Chemistry

    At our production facility, we handle 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol from the ground up. Decades ago, this molecule rarely appeared outside of specialized research or complex synthesis projects. As direct manufacturer, our teams saw an opportunity to secure consistent sourcing and develop a stable supply line for research, pharma, and agrochemical innovators who demanded control over impurity profiles and batch-to-batch reproducibility. During early attempts, much of the downstream chemistry suffered from irreproducibility and unexpected byproducts, which we traced to variations in precursor quality and uncontrolled conditions during key steps. Experience showed that keeping synthesis under our own roof yielded better consistency and fewer surprises in later evaluations.

    Our technical team relies on a closed, solvent-controlled reaction process. By overseeing everything from raw material handling to cryogenic crystallization, we avoid the inconsistent coloring, occasional contamination, and yield fluctuations that often slip in with outsourced routines or loosely managed intermediates. Technicians constantly calibrate analytical and purification equipment to mirror the evolving needs of our clients’ applications. Without trapping the product to a generic, one-size-fits-all approach, we maintain meaningful oversight of each kilo, tuning each batch to agreed project priorities—clean melting behavior, minimized residual solvents, and crystalline stability over shipment windows.

    Why Quality Parameters Matter in 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol Production

    The pyrazole ring system supports many modern derivatives, but trifluoromethyl substitution at the 5-position presents unique handling and purification hurdles. Early in our development, our laboratory hit roadblocks with solubility shifts and volatile side-products, especially during scale-up. Learning from these setbacks, we introduced staged distillation and incremental cooling stretches, allowing for controlled crystal formation and consistent particle morphology. Not every pyrazole derivative reacts exactly the same way, so we’ve learned not to trust assumptions—especially during drying or storage. Moisture uptake or oxidation, if left unmanaged, can mean failed syntheses a few steps down the line for our customers.

    Instead of only measuring purity by a single HPLC trace or melting point, our team now evaluates multiple physical and chemical signatures. IR, NMR, and residue solvent content remain under constant watch. Teams spot-check each package for caking, discoloration, and even odor changes. Over the years, visiting clients have flagged small differences in solubility when using our material versus competitors. Careful investigation often reveals the impact of stricter residual control or unique post-purification steps we run. Seemingly trivial measures—breaking up early aggregates or double-filtration—have led to longer shelf life and better flow in end-use applications.

    Balancing Process Safety and Consistency

    Safety remains at the core, not only for our operators but for all downstream users. Pyrazole compounds, including the trifluoromethyl variants, can react unpredictably under certain conditions, especially as volumes scale. Our plant has invested in scalable pressure regulation and remote monitoring controls, preventing runaway reactions seen in earlier pilot runs. As global demand rises, process optimization prevents pressure surges, vapor releases, and unexpected impurity formation. Auditing our own runs daily, maintenance managers update workflow and batch records immediately upon any deviation, shutting down questionable equipment for root-cause analysis rather than pushing a risky lot forward.

    While many makers struggle with regulatory hurdles related to energetic intermediates, our site separates hazardous material handling into dedicated modules. This effort pays dividends: customers in pharmaceuticals and high-value agrochemical sectors rarely send back negative feedback on material integrity. During routine stability assessments, importers from Europe and North America have commented on the unmatched uniformity of our shipments over multi-year projects. We attribute this record not to luck, but to living with our product, refining procedures after each incident, and requiring all team members to understand the full system—chemists, handlers, and supervisors alike.

    Applications and Product Integration: End-User Perspectives

    1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol plays critical roles across several innovation arenas. Pharmaceutical groups often seek pyrazole analogs where trifluoromethyl substitutions impart metabolic blocking or target-specific activity, and the 1-methyl configuration sometimes modulates solubility and reactivity for prodrug strategies. In these cases, even trace impurities or unplanned solvent residues can mask or disrupt the desired pharmacological effect. Working side-by-side with R&D partners, we customize batch documentation to include impurity breakdowns beyond regulatory thresholds, letting clients develop new APIs or intermediates with confidence.

    In agrochemical settings, the derivatives built from this molecule commonly boost bioavailability, environmental stability, or target-specific toxicity. The chemical background, informed by frequent field testing data, has allowed us to provide material with a tighter moisture profile and narrower melting range—properties that end up driving formulation yields or product shelf life. Sometimes, process engineers note a formulation challenge, such as variable powder flow or unexpected crystal growth during blending. Years of dedicated troubleshooting with customer teams has taught us that small tweaks in filter timing or hydrodynamics often yield much larger gains than elaborate downstream fixes.

    Beyond large industries, researchers in academia and chemical startups leverage our product insights to accelerate method development, scale-up studies, or mechanistic investigations. Several published case studies and theses, some produced with our technical input, have emerged from these collaborations. As the field pushes for greener or more compact syntheses, the demand for reliable input chemicals only grows. Our clients return to us not only for a molecule, but for the divisible expertise that comes with every drum and kilogram shipped.

    Practical Differences From Standard Pyrazole Isomers and Analogs

    The landscape of pyrazole derivatives is crowded, yet 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol carves out a strong niche. Direct experience with a broad range of analogs lets us draw technical lines between this product and seemingly similar options. For instance, several suppliers push generic 1H-pyrazol-3-ols or non-fluorinated methyl derivatives, but their physical behavior and stability diverge markedly—especially under prolonged shipping or high-shear blending. Trifluoromethyl substitution, while a minor atom swap on paper, introduces broad solubility changes and chemical shifts. Our chemistry teams have documented early on that seemingly minor substitutions dictated solid-state form, powder handling, and reactivity under mild acid or base.

    Clients sometimes request custom pyrazole analogs for comparative studies. We run side-by-side analyses, feeding results back into both plant and customer workflows. In nearly every run, the trifluoromethyl group presents greater hydrophobicity and increased resistance to hydrolytic breakdown, while methylation at the 1-position suppresses some of the nucleophilicity common in 3-ol variants. Compound aggregation, optical stability, and exact melting behavior each arise from the interplay of both functional groups. For applications requiring inert handling, chemical inertia, or clean incorporation into complex matrices, this specific pyrazole offers benefits that similar skeletons fail to match.

    Other manufacturers sometimes overlook these subtleties, shipping isomeric or even mono-fluorinated lots as “close enough” substitutes. Over decades in the trade, we’ve taken in rejected competitor lots, tracing avoided issues back to subtle isomer confusion or inappropriate drying. Markets dealing with small-batch research grade or tons-per-year industrial demand agree: if the specification matches on paper but the performance lags in real-world blending, the difference often comes down to years of manufacturing feedback and adaptation.

    Handling and Storage Insights: Lessons From the Production Line

    After numerous years in pyrazole production, we’ve noticed strong seasonal, atmospheric, and logistical swings impact both the physical and chemical stability of this material. Early batches developed trace yellowing or odor after crossing humid regions, initially baffling clients who relied on generic storage recommendations. Working backward, our team pinpointed trace acid formation and container permeability as key drivers. Now, every outgoing lot is packaged with well-dried liners and labeled with humidity absorption rates. Our warehouses favor dry, shaded storage separated from direct UV and handled with antistatic protocols—simple measures built from mistakes and customer feedback, not from handbooks.

    Long-distance shipments sometimes stretch weeks, so we collaborate with carriers to maintain stable environmental conditions, especially with air or sea transit. Customs delays or regional warehousing often run beyond prediction, so we specify transport-grade packaging, traceable batch labeling, and redundant sealing for each drum. Experience shows that neglecting minor packaging features like liner thickness or seal quality easily offsets any technical advances from the synthesis route itself. After import, users appreciate not only the physical integrity of the product but also timely, transparent support in reshipment or troubleshooting if any deviation pops up.

    Manufacturing Scale-Up and Future-Proofing

    Production scaling doesn’t merely mean larger vessels and more raw feed—real-world scale brings changes in heat transfer, mixing profiles, and crystallization rates. Over many years, we transitioned from lab-bench glassware to closed-loop, automated batch reactors, tracking every process deviation and correlating it with product behavior. Small trials highlighted cooling rate and agitation intensity as major variables affecting both the yield and purity of 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol. By adjusting agitation strength, time of addition, and fractioned temperature ramps, we moved beyond the conventional recipes found in academic papers or trade manuals.

    Repurposing process insight to field application, we helped clients de-risk late-stage scale-up and pilot production. Regular dialogues between process chemists and field users led to faster cycle times and fewer technical holds, especially where final product requirements shifted with new formulation challenges. Instead of locking in a rigid process, we maintain modularity by updating filtration, intermediate drying, and packaging as new guidelines or client needs emerge. This loop between plant, logistics, client, and R&D fuels continuous improvement—anchored by the varied real-world demands rather than static technical brochures.

    Supporting User Innovation

    Many innovation teams thrive on fast-turnaround materials, technical transparency, and accessible documentation. Over the years, we noticed that even seasoned research scientists struggled with slow communication or incomplete origin info from intermediary suppliers. Recognizing this friction, we built support teams who not only know paperwork, but understand ground-level chemical behavior, regional regulations, and pilot scale feasibility. If an R&D group spots an unusual side reaction or application hurdle, our chemists join the investigation, often providing comparative samples, real solubility breakdowns, and troubleshoot documentation that reflects the latest plant reality.

    We also recognize the broader shifts in chemical development: regulators expect more clarity about impurity pathways, sustainability, and batch-to-batch reproducibility. By keeping manufacturing vertically integrated, we can meet new compliance requests much faster and feed those changes into modulated process control and iterative quality improvement. Through workshops, field visits, and joint project reviews, our team picks up lessons that feed directly into product enhancement. Each kilogram tells a story built on years of factory discipline, critical end-user feedback, and the drive to solve not just isolated chemical problems, but the challenge of integrating complex specialty materials into the rapidly changing demands of industry and research.

    Conclusion: The Value of Direct Manufacturing in Specialty Pyrazoles

    Direct experience—gained from daily manufacturing and real-time troubleshooting—anchors our approach and commitment to 1-Methyl-5-(Trifluoromethyl)-1H-Pyrazol-3-ol. This molecule means more than a formulaic entry on a product list: each lot reflects years of process tuning, incident follow-up, and hard-won knowledge about the granular challenges at every point in the supply chain. Most important, these efforts turn into concrete value for partners who count on predictable, high-purity material for cutting-edge applications. As new discoveries push the boundaries of what pyrazole chemistry can offer, we keep our eyes on every practical detail—making sure every shipment delivers, every question receives clear answers, and every new benchmark in performance stands on a foundation of reliability and lived manufacturing experience.