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1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride

    • Product Name 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride
    • Alias 1-Phenyl-5-(trifluoromethyl)-1H-pyrazole-4-carbonyl chloride
    • Einecs NA
    • 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
    VTB
    Specifications

    HS Code

    919960

    Chemical Name 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride
    Molecular Formula C11H6ClF3N2O
    Molecular Weight 274.63 g/mol
    Cas Number 1240607-16-8
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in organic solvents such as dichloromethane and chloroform
    Storage Conditions Store in cool, dry, and well-ventilated area, under inert atmosphere
    Smiles C1=CC=C(C=C1)N2C=C(C(=N2)C(F)(F)F)C(=O)Cl
    Inchi InChI=1S/C11H6ClF3N2O/c12-10(18)8-7(11(13,14)15)16-17(9-5-3-2-4-6-9)8/h2-6H,1H

    As an accredited 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with tamper-evident cap, labeled "1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride, 10g," and hazard pictograms.
    Shipping 1-Phenyl-5-(Trifluoromethyl)pyrazole-4-carbonyl chloride is shipped in tightly sealed, corrosion-resistant containers under an inert atmosphere, such as nitrogen. It is handled as a hazardous material (corrosive, moisture-sensitive), following appropriate chemical transport regulations, including proper labeling and documentation. Temperature control and secondary containment may be required to ensure safe delivery.
    Storage Store **1-Phenyl-5-(trifluoromethyl)pyrazole-4-carbonyl chloride** in a cool, dry, and well-ventilated area away from moisture and incompatible materials, such as strong bases and oxidizing agents. Keep the container tightly closed and protected from light. Use a corrosion-resistant container and clearly label it as corrosive and moisture-sensitive. Handle only in a chemical fume hood, wearing appropriate personal protective equipment.
    Application of 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride

    Applications of 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride in Industrial Manufacturing

    1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride serves as a high-value pyrazole-based intermediate, enabling specialized transformations within select sectors that demand precision in functional group introduction and strict process validation. As an original manufacturer, we support our industrial partners’ requirements for quality-controlled input material, traceable batch production, and reliable fit across tightly defined use-cases. Below, we detail downstream applications for this molecule, focusing on sectors with established and quantifiable integration in large-scale and specialty manufacturing.

    1. Agrochemical Synthesis: Advanced Herbicide & Fungicide Intermediates

    This intermediate is widely adopted within agrochemical production facilities to construct high-performance crop protection agents—particularly next-generation pyrazole derivatives where electron-withdrawing effects are critical for field activity. Leading agrochemical formulators employ this raw material for selective C-acylation steps, introducing trifluoromethyl functionality to the pyrazole core during multi-stage active ingredient synthesis. Formulation chemists reference the molecular scaffold to fine-tune selectivity and degradation rates tailored for global regulatory acceptance.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides (JMPS process)
    • REACH (EC) No 1907/2006 – substances registration & evaluation
    • ISO 9001:2015 Quality Management System (manufacturing stage; audit chain)
    • China GB 4839 and EPA PRN 96-1 for agricultural chemical substances

    Typical usage ratio

    • Bulk technical synthesis: 0.20–0.37 molar equivalent against final target molecule, adjusted for conversion yield in pyrazole coupling

    Downstream process integration

    • Material enters after primary condensation of pyrazole ring; used in acylation or acid chloride transformations prior to specific halogenation/final esterification stage

    Final product types

    • Trifluoromethylpyrazole herbicide actives (e.g., for resistance management formulations)
    • Systemic seed treatment fungicides featuring tailored degradation rates

    2. Pharmaceutical API Intermediate Manufacturing

    The compound’s pyrazole core and acyl chloride group make it especially suitable as a building block for small-molecule pharmaceuticals, specifically for incorporating trifluoromethylated aromatic fragments during advanced synthetic steps. Process chemists in GMP-compliant API plants use it in amidation and esterification steps where rigorous impurity controls, trace element profiles, and lot homogeneity directly affect downstream product registration dossiers. Comprehensive in-process testing and full analytical support align usage with global pharmaceutical regulatory requirements.

    Industry compliance standards

    • ICH Q7 “Good Manufacturing Practice” for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monographs—purity and identity for pyrazole derivatives
    • China Pharmacopoeia (latest edition)—analytical and trace residue requirements
    • FDA 21 CFR Part 211 (US) – Finished Pharmaceuticals (applicable to intermediates)

    Typical usage ratio

    • Process optimization range: 1.02–1.08 equivalent per mol of targeted API substructure, optimized to minimize excess while controlling for process impurities

    Downstream process integration

    • Material is introduced after core motif assembly; used in coupling or acyl substitution reactions under strictly monitored reaction conditions (cGMP monitoring of temperature, reagents & impurities)

    Final product types

    • Pyrazole-containing kinase inhibitors and anti-inflammatory APIs
    • Specialty intermediates in central nervous system pharmaceutical pipelines

    3. Fine Chemical Intermediates for Material Science Applications

    In advanced materials and specialty chemical sectors, this intermediate’s acyl chloride function provides a gateway to tailored functional polymers and fluorinated surface modifiers. Synthesis teams in this segment leverage the reactive site for coupling with nucleophilic substrates, targeting applications where thermal and chemical stability are required. End-use monitoring focuses on consistent active group loading and process repeatability, critical for performance-related downstream products such as advanced fluorinated coatings or high-value monomers.

    Industry compliance standards

    • ISO 14001:2015 (environmental management impact of material intermediates)
    • RoHS Directive 2011/65/EU (when integrated in electronics material pipelines)
    • Japanese Chemical Substances Control Law (CSCL) – handling of new chemical intermediates
    • Quality agreements in accordance with ASTM E2347-19 for specialty chemicals supply

    Typical usage ratio

    • Polymer surface modification: 3–10% by mass in functional monomer blends; concentration fine-tuned by required surface energy and end-use application

    Downstream process integration

    • Loaded in pre-polymer reactor batch, typically after catalyst addition but before chain extension steps; batch-wise analytical controls for conversion and chain length distribution

    Final product types

    • Fluorinated polymer additives for textile or membrane coatings
    • Surface-active intermediates for engineered plastics or elastomers

    4. Veterinary Drug Intermediate Synthesis

    This raw material is adopted in veterinary pharmaceutical production, specifically for synthesizing trifluoromethylated pyrazole derivatives used in advanced anthelmintic and ectoparasiticide agents. Veterinary formulators depend on precise intermediate quality and documented safety data, integrating this compound under stringently validated protocols that meet animal drug safety and global export requirements. It is typically incorporated into synthetic routes that require high selectivity, and finished product registration often depends on validated traceability from intermediate sourcing.

    Industry compliance standards

    • VICH GL10/GL18—Good Manufacturing Practice for Veterinary Products
    • Pharmacopoeia Europaea (Ph. Eur.)—monographs for veterinary APIs
    • US FDA CVM Guidance for Industry (API traceability requirements)
    • ISO 45001 for occupational health in process stages

    Typical usage ratio

    • Veterinary drug synthesis: 0.95–1.10 equivalent in final ring-closing or acylation step, depending on the desired activity spectrum and purity profile

    Downstream process integration

    • Material used in terminal phase of synthetic sequence—often in amidation with key amines or alcohols, supported by HPLC and impurity profiling to meet veterinary regulatory dossiers

    Final product types

    • Trifluoromethylated pyrazole-based anthelmintics
    • Novel ectoparasiticides for livestock and companion animals

    5. Specialty Crop Protection R&D and Pilot Production

    R&D centers in agro-biotechnology and pilot operations integrate this intermediate during the early development and limited-scale validation of custom pyrazole-based active substances—particularly for target site resistance studies and pre-market demonstration batches. Reliable batch homogeneity and extensive analytical support are provided to downstream R&D partners who evaluate field-specific variants and prototype formulations directly reflecting new regulatory guidance and market shifts for targeted biocidal molecules.

    Industry compliance standards

    • CGLP (Current Good Laboratory Practice) for R&D test batches
    • OECD Principles of GLP for field trial substance validation
    • ISO/IEC 17025:2017 for analytical and batch release testing
    • REACH Annex V (test phase exemptions and notification duties)

    Typical usage ratio

    • Pilot & R&D batches: varied from 0.90–1.25 equivalent per batch synthesis step, adjusted per target molecule and reaction efficiency in candidate screening

    Downstream process integration

    • Material added during candidate lead selection phase, typically in manual or semi-automated acylation reactions, coupled with full trace and analytical documentation per research protocol

    Final product types

    • Experimental pyrazole-based plant protection candidates
    • Pre-registration technical concentrates for field efficacy validation
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    Certification & Compliance
    More Introduction

    Introducing 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride: Reliable Building Block for Fine Chemical Synthesis

    The Purpose and Place of a Specialized Intermediate

    In the world of fine and specialty chemicals, purpose-built intermediates make or break an efficient synthesis process. At our production facility, the journey of 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride starts not in a laboratory or trade office, but in the hands of process engineers who have witnessed the growing call for active pharmaceutical ingredients, advanced materials, and modern crop protection chemicals. It takes a combination of intuition and field-tested knowhow to spot the intermediates that bridge lab conception and commercial-scale delivery; this compound stands out as that reliable link.

    Origins: From Concept to Chemical Reality

    Development teams across pharmaceutical, agrochemical, and material science sectors seek out building blocks offering multiple functionalities and the structural rigidity required for targeted synthesis. The 1-phenyl-5-(trifluoromethyl)pyrazole group brings both to the table, leveraging aromatic stability and electronic diversity inherent to the trifluoromethyl substituent. Carbonyl chloride functionality pushes the compound into a realm of high reactivity, perfect for constructing amides, esters, and ultimately, bioactive small molecules. When approached about whether to scale production of this molecule, we spent months evaluating its upstream supply, reaction yields, and shelf-life under typical storage—actual concerns only experienced by those whose daily costs hinge on uninterrupted flow.

    Structure Matters: Practical Impact of Substituents

    It is easy to overlook how molecular structure drives function, but on a shop floor where batch yields and reaction control matter, the details become urgent. The trifluoromethyl group on the pyrazole ring does far more than add complexity: it brings true value in synthesis. This substituent delivers increased lipophilicity and shifts electron density, which profoundly influences reactivity toward acylation and downstream coupling reactions. The phenyl group, chosen for its compatibility with many biologically active frameworks, serves as a trusted anchor. Combined, they make 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride an indispensable tool for medicinal chemists aiming for late-stage diversification.

    Quality Control: Beyond Basic Specifications

    Customers, especially those scaling up processes for regulated industries, rarely settle for surface-level product definitions. Product compliance takes precedence over quantity, and achieving trace impurity levels or batch reproducibility only comes with deep process expertise. We built our protocol around pressure-tested in-process controls. Each batch passes through hands-on monitoring at every critical junction, using modern chromatography tools paired with classic titration checks. Differences are not academic—they stem from direct feedback after more than a decade spent troubleshooting failed couplings and chasing process headaches. We’ve found that the stability of our carbonyl chloride group under storage conditions, and the tightness of our impurity profile, go beyond generic listing and touch daily chemical operations.

    Handling Real-World Constraints

    Every chemist has had a delivery land late, batch purity slip, or downstream reaction grind to a halt from a poorly understood impurity. As a manufacturer, we see first-hand how the shelf-life and moisture sensitivity of carbonyl chloride intermediates can translate to headaches in user hands. Our approach leans on real data, not product claims: tested storage protocols and shelf-life validated by repeated, successful process campaigns. Before certifying a finished batch, samples are exposed to extended temperature and humidity cycles, and only the product demonstrating robust integrity over time ships to users. In one instance, trial partners running multi-kilo synthesis for a new anti-infective required extension of stability beyond conventional durations—we provided real test curves and batch analysis, not theoretical timelines.

    Lab to Kilogram: Consistency Counts

    Production of 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride does not follow a textbook path from bench to plant. Consistency across batches at kilo-scale comes only after error and recalibration, not stock boilerplate. In moving from small-flask samples to campaign lots, common pitfalls hit: variable crystal forms emerging in intermediates, or deviations in acyl chloride content from one drum to the next. Each of these hiccups forced iterative adjustments, whether through reaction temperature profile, solvent choice, or purification technique. Only repeated scale-ups established the robust parameters we follow today. Technical staff often recount the surprise of maintaining purity and reactive group content even after scale-up—achieved by tight documentation and the humility to adjust based on real output, not just following existing literature.

    Applications Driving Demand

    Much of the interest in 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride comes from new molecule discovery programs in both pharma and crop science. Teams engineering new triazoles, amide-linked derivatives, and functionalized heteroaromatics benefit from the reactivity window this intermediate opens. To illustrate, one series of antifungal lead candidates arose only after repeated coupling using our product’s acid chloride group with various substituted anilines. Similarly, crop protection researchers working on next-generation herbicides have used this intermediate to install both polar and nonpolar linkers, balancing water solubility and field stability. We do not just hear about these innovations; we support their development by tweaking supplies to ensure reactivity and reliable delivery.

    Distinctive Features Relative to Similar Products

    Chemical suppliers routinely list rows of structurally related acyl chlorides, but real-world differences stand out most sharply in hands-on production. For example, traditional pyrazole-based carbonyl chlorides lacking the trifluoromethyl group miss key hydrophobic and electronic properties required in certain active ingredients. Our 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride enables coupling reactions under milder conditions, with less need for aggressive bases or dehydrating agents, directly reducing side reactions in vulnerable molecular motifs. We have seen R&D teams switch from conventional aromatic acid chlorides after observing cleaner product profiles and higher isolated yields at similar loading levels. Years of producing both this and related intermediates clarified these distinctions—a discussion not found in catalogs, but proven in repeated, scaled runs.

    Tackling the Challenges of Moisture Sensitivity

    Manufacturing and delivering acid chlorides means meeting the constant challenge of moisture, which quickly deactivates these reactive groups. From day one, our product storage and shipment systems included tested multi-layer barrier solutions, supporting weeks of warehouse time without loss in chloride content. Repeated in-house studies tracked the loss in acidity and increase in hydrolysis byproducts under various climates, not just under ideal conditions. The result: our intermediate remains robust enough for global shipment conditions. If a customer wants bulk lots destined for shipment in high-humidity zones, we provide batch-by-batch hydrolysis rates from retention samples, not best guesses.

    Serving Scale: Process Documentation Meets Regulatory Scrutiny

    Our process documentation draws not from a desire to tick off compliance boxes but from repeated regulatory scrutiny. Large-scale buyers in the agrochemical sector subject both processes and supply chain history to audits aimed not only at tracking origin but also verifying sustained batch quality. Each production record for 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride includes actual deviation logs, batch-specific in-process controls, and demonstrated corrective actions from pilot, scale-up, and full runs. Having lived through real inspections, our production team expects not just requests for certificates, but also for method validations and raw traceability, proof of supply chain security, and full impurity maps. Seasoned manufacturers know: only by building this transparency into every step does trust develop between supplier and user.

    Addressing the Transition from Pilot to Commercial Use

    Process chemists seldom worry about supply constraints at the 10-gram scale, but bottlenecks appear rapidly as synthesis transitions to hundreds or thousands of grams. Spray drying variations, batch-to-batch particulate differences, or tiny shifts in moisture content have real downstream effects—the kind only noticed after several reaction cycles. Through operational experience, we learned to report actual particle size distributions, and control for flow and handling properties, delivering lots with repeatable characteristics. It turns out that fixing these small issues early pays off, avoiding lost product or fouled lines at production scale. Our teams remain available to advise users facing unexpected challenges, always relying on field stories and hard-won lessons rather than generic technical data bulletins.

    Impact on Greener Chemistry

    The carbonyl chloride group has sometimes been labeled “problematic” due to concerns with phosgene use or disposal of chlorinated byproducts. We recognize this and have worked over the years to revisit chlorination and quench practices. Our engineers developed lower-waste conversion steps, cut total reagent excess, and improved neutralization efficiency to minimize discharge. Customers benefit from these steps, especially as compliance teams intensify review of raw material chains. Real reductions in solvent loading and improved recycle rates in our facility follow from years of environmental monitoring—not greenwashing or compliance posturing. By choosing this product, users tap into more environmentally responsible manufacture based on actual improvements, not just claims.

    Standing Apart From Third-Party or Toll Synthesis

    We manufacture this intermediate directly, rarely relying on outside contractors or generic tollers. Many customers have recounted quality swings and delivery hiccups after taking product from intermediaries brokering unknown production sites. Chemical identity, batch numbering, and process traceability are far stronger when managed by those with direct control of vessels, staff, and compliance audits under one roof. Our people know the machinery and chemistry from bottom up—no guesswork or arm’s-length assurances. In conversations with clients scaling clinical trials or new formulation programs, concerns about trace identity are best answered by the same team that actually produces the compound. This is not a marketing point but a day-to-day fact in multi-source environments.

    An Evolving Product: Partnership to Delivery

    Delivering 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride goes far beyond tanks and drums. Many successful launches came after users trialed production lots and provided feedback that led to batch-level improvements. Our technical team maintains direct lines with process chemists, whether it takes offering a rapid remix to correct for a particulates issue or relabeling a batch for improved tracking in a customer’s ERP. In one case involving accelerated shipments for a time-sensitive patent window, production ran continuous overtime, drawing from hot-wash experiences in responding to urgent clinical requests in the past. These stories matter; familiarity with them means living the day-to-day reality of chemical manufacturing, not just reading off a commercial pitch.

    Harnessing Continuous Improvement for Tomorrow’s Goals

    Chemical manufacture demands learning and adaptation. The value of 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride has grown each year, partly due to our production team’s commitment to continuous improvement. Each process run, every analytical tweak, goes back into a living record accessible to our process and QA staff. New requests—whether for different drum types, special purity windows, or alternative analytical reporting—have challenged us to improve actual practice. In time, expanded in-line control and automation will carry these improvements onwards, tightening not just batch-to-batch purity, but also improving delivery and scalability for all partners. Regular customer exchanges and supply partnerships sharpen these capabilities, cementing internal knowhow that cannot be downloaded or delegated.

    The Bottom Line: Value in Experience, Process, and Partnership

    The attractiveness of 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride lies in a unique balance of molecular structure, reliable reactivity, and the hands-on experience of seasoned manufacturing teams. While specifications and molecular diagrams fill catalogs, real quality emerges from dozens of small but critical steps in plant, lab, and shipping office. Day-to-day, our role as manufacturer brings unique insight into which batches will run well, which analytical results matter, what feedback signals a supply chain issue, and how to spot small but important trends in reactivity. Users benefit not from standard claims, but from the disciplined, lived-in approach that direct production experience delivers.

    Looking Forward: Supporting Science and Innovation

    Through direct manufacture, continuous control, and a practical grasp of the needs at various synthesis scales, we help chemical and life sciences developers realize ambitious projects. 1-Phenyl-5-(Trifluoromethyl)Pyrazole-4-Carbonyl Chloride has earned its place as a foundation for innovation thanks to efficient, tuned process work honed daily on our factory floor. Future innovations—from the next breakthrough pharmaceutical to novel crop protection solutions—rely on intermediates produced not by formula, but by steady hands and practiced judgment. In making this compound available and reliable, our team backs real scientific advancement, driven by solutions crafted in direct response to user challenges, not empty promises.