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1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One

    • Product Name 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One
    • Alias 4-Chloroantipyrine
    • Einecs 220-799-2
    • 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

    265272

    Iupac Name 1-(4-chlorophenyl)-3-methyl-2-pyrazolin-5-one
    Molecular Formula C10H9ClN2O
    Molecular Weight 208.65 g/mol
    Cas Number 89-25-8
    Appearance White to off-white crystalline powder
    Melting Point 166-170°C
    Solubility In Water Slightly soluble
    Density 1.32 g/cm³
    Ph Neutral to slightly acidic in solution
    Logp 1.81
    Synonyms 4-Chlorophenylmethylpyrazolone, 4-Chlorophenazone
    Smiles CC1=NN(C2=CC=C(C=C2)Cl)C(=O)C1

    As an accredited 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White polyethylene bottle containing 100 grams of 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One, labeled with hazard symbols and safety instructions.
    Shipping 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a chemical substance, following standard safety protocols. Transportation complies with relevant regulations, ensuring the package is properly labeled and includes necessary documentation for safe and lawful delivery.
    Storage Store **1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One** in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Ensure labeling and secure storage to prevent unauthorized access. Wear appropriate protective equipment when handling and avoid prolonged exposure to air to maintain chemical stability.
    Application of 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One

    Applications of 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One in Industrial Manufacturing

    As a manufacturer specializing in 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One, we deliver high purity material tailored for core downstream sectors with established technical adoption. Below, we detail specific industry applications, integrating compliance, proportioning guidelines, processing stages, and reference end-product types to support your formulation and scale-up decisions.

    1. Antipyretic and Analgesic Pharmaceutical Synthesis

    This intermediate is crucial in the industrial synthesis of pyrazolone-based pharmaceuticals, particularly within the nonsteroidal anti-inflammatory drug segment. Pharmaceutical groups relying on pyrazolone derivatives for fever and pain reduction incorporate the material at precisely controlled stages, ensuring target compound consistency and safety. Synthesis lines require reliable raw material input to meet regional and international drug quality standards.

    Industry compliance standards

    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (EP)
    • Good Manufacturing Practice (ICH Q7, GMP)
    • China Pharmacopoeia (ChP)

    Typical usage ratio

    • Ranges from 0.5 to 2.5 molar equivalents relative to target API, with ratio adjusted based on desired yield, process batch size, and target impurity profile—determined by structure-activity requirements of downstream drug candidates.

    Downstream process integration

    • Incorporated during early-stage condensation or cyclization reactions; dosing controlled in jacketed reactors under monitored temperature and pH; in multi-step syntheses, material added post-activation of base substrate prior to work-up and purification stages.

    Final product types

    • Metamizole sodium API (Analgin)
    • Phenazone and its analogs
    • Dipyrone derivatives
    • Antipyretic combination tablets and powders

    2. Veterinary Drug Intermediate Production

    Animal health manufacturers use our compound as a building block for specific antipyretic and analgesic veterinary actives, particularly in ruminant and equine sectors. Regulatory oversight for animal pharmaceuticals often parallels human drug compliance, demanding high-purity intermediates to mitigate risks within the food supply chain and protect end-user safety.

    Industry compliance standards

    • Veterinary Drugs Pharmacopoeia (Ph. Vet.)
    • EU Directive 2001/82/EC for veterinary medicinal products
    • GMP for Animal Drugs (China: GB/T 17239.1-1998)
    • FDA Center for Veterinary Medicine (CVM) guidelines

    Typical usage ratio

    • 1.0 – 2.0 equivalents per final API formed, adjusted for synthesis scale and pharmacokinetic requirements of species-specific medications.

    Downstream process integration

    • Charged into continuous flow or batch reactors following solvent pre-conditioning, co-reacted with aldehyde functions or amines under inert conditions to produce the desired veterinary pharmacophore, prior to granulation or sterile filtration.

    Final product types

    • Veterinary NSAID actives (e.g., dipyrone for cattle)
    • Powder and suspension formulations for livestock
    • Antipyretic injection solutions for equine
    • Oral bolus combination veterinary tablets

    3. Dye and Pigment Intermediate Manufacture

    In the colorants industry, this molecule serves as a vital precursor for synthesizing specialty azo dyes and pyrazolone pigments, especially for high-stability applications in textiles and plastics. The manufacturing process relies on precise introduction of the compound during coupling reactions, supporting repeatable hue properties and performance under end-use conditions.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 (Europe)
    • OEKO-TEX® Standard 100
    • EN 71-3 (Safety of Toys – Migration of Certain Elements)
    • ISO 9001 certified QC for pigment/dye production

    Typical usage ratio

    • 10–30% by mol relative to diazo component, depending on pigment intensity, end-use performance specs, and coupling chemistry efficiency.

    Downstream process integration

    • Introduced at the azo-coupling stage directly into alkaline or buffered aqueous systems; followed by filtration, drying, and dispersion blending into granules or powder concentrates for downstream textile and plastic compounding.

    Final product types

    • Pyrazolone-based azo dyes for wool and silk
    • High-lightfast synthetic pigments for plastic molding
    • Color dispersions for printing inks
    • Textile dyeing paste formulations

    4. Analytical Reagent Preparation for Metal Detection

    Laboratory chemical producers formulate this compound into specific analytical reagents used for trace metal detection and spectrophotometric analysis. Its chelating activity with metal ions like Fe3+ or Cu2+ underpins colorimetric methods used in water quality control, mining, and food safety laboratories worldwide.

    Industry compliance standards

    • ISO 17034 for reference materials production
    • OECD Guidelines for the Testing of Chemicals
    • Standard Methods for the Examination of Water and Wastewater (APHA/AWWA/WEF)
    • USP Reagent Grade Quality

    Typical usage ratio

    • Typically formulated at 0.05%–0.2% w/v in aqueous reagent mixture, optimized for the intended detection limit and sensitivity of the test protocol.

    Downstream process integration

    • Dissolved or suspended within buffered solutions during reagent kit assembly; prepared as part of multi-component test mixtures, then aliquoted and sealed under inert atmosphere for distribution to analytical laboratories.

    Final product types

    • Colorimetric test kits for iron, copper and other transition metals
    • Standard analytical reagents for laboratory QC
    • Pre-mixed solutions for spectrophotometers
    • Portable water and food testing strips
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    Certification & Compliance
    More Introduction

    Introducing 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One

    Product Overview

    After years of development and optimization in our facilities, 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One stands as one of the core offerings in our lineup of fine chemicals. The process behind its manufacture has required both a focus on purity and repeatability, learned through decades in the specialty synthesis sector. Sitting at the crossroads of organic and heterocyclic chemistry, this compound brings together a chlorinated aryl structure with the well-documented advantages of the pyrazolone scaffold.

    The compound typically appears as a pale to off-white crystalline powder, a result of careful control during crystallization and purification steps. We have always prioritized achieving tight tolerance specifications for melting point and residual solvent, with analytical checks at each stage. With a molecular formula of C10H9ClN2O and a molecular weight of 208.65 g/mol, the presence of both the methyl group and the para-chlorinated phenyl ring enhances selective properties that cannot be easily matched by structurally simpler analogs.

    Manufacturing Consistency and Purity

    Consistency remains the main focus throughout the entire production process. Each batch undergoes strict quality review, where HPLC and NMR analyses set benchmarks for purity and impurity profiles. Trace byproducts, often originating from incomplete cyclization or side-chlorination, are kept to a minimum. From experience, these side products can impact downstream chemistry, so purging them is a must before we release any material. Our technical team spends hours reviewing analytical data, ensuring high batch reproducibility. Because downstream users are sensitive to impurities during formulation, we do not take shortcuts with isolation and washing steps. This commitment to stringent controls allows our customers in different sectors to integrate this material into their own process flows without unexpected setbacks.

    Over the past few years, we have moved beyond traditional purification with solvent crystallization alone, investing in advanced filtration and drying systems. As a result, our finished material routinely checks in at >99% purity. The minimized lot-to-lot variability we have achieved has not come easy, but it enables smoother process validation and scale-up for our industrial partners.

    Where It Supports Innovation

    The application space for 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One spreads far beyond academia. Our direct cooperation with formulation chemists and process engineers has made clear the unique role this compound plays, especially as a building block for more complex molecules. The combined effects of the chlorinated arene and the pyrazolone ring system enable versatility that’s hard to match in oxidative dye research, ligand design, and pharmaceutical lead optimization.

    Teams in pharmaceutical discovery often choose this molecule when they require a stable, modifiable core. Its reactivity profile, compared to unsubstituted pyrazolones, offers more options during late-stage functionalization. Clients leverage the increased electron-withdrawing effects from the para-chlo phenyl ring to tune solubility, lipophilicity, and even binding selectivity in advanced synthetic routes.

    Specialty dye makers have come to us repeatedly with projects relying on coupling the scaffold to various aromatic or heterocyclic partners. The methyl group attached at the third position on the pyrazoline ring, in particular, opens up further modification without overcomplicating the molecule's overall behavior. Where older, less decorated pyrazolones may fall short on thermal or photostability, this compound stands out, proving to hold up well in accelerated aging trials.

    Some industrial partners see value in its oxidative properties and employ it in analytical chemistry, especially in spectroscopic applications where a robust and predictable chromophore is essential. Compared to structural relatives missing either the chloro or methyl functionality, our product brings better color consistency and a stronger absorbance edge under UV-visible analysis.

    Addressing Common Challenges

    Early on in our production journey, solubility and processability created hurdles. Our plant operators spent several runs fine-tuning crystallization parameters to achieve an optimal balance of particle size and bulk density. It became clear through direct feedback that a more free-flowing material helped downstream dissolution and blending tasks in both lab and industrial settings. Because of this, we standardized on granular sizing that rarely cakes or bridges in drums or sacks, giving better process yield and less downstream labor.

    Some customers would ask why not just use a simple pyrazolone intermediate, skipping the extra steps involved in adding the chloro substituent and the methyl group. Our own comparative small-batch trials, run in partnership with end-users, have shown time and again how these substituents shift properties significantly. The presence of chlorine at the para-position means more than just extra synthetic cost—it shapes everything from reactivity in nucleophilic substitution to resistance against unwanted side reactions in high-heat environments. Both in pilot plants and full-scale production, we tracked much fewer incidents of unplanned byproduct formation using our advanced derivative compared to generic alternatives. That translates into greater confidence and fewer interruptions on the client's end.

    Safe Handling and Storage

    Operating a full-scale synthesis plant instills deep respect for proper handling and process safety. Our standard shipment consists of moisture-tight, inert gas-purged containers, which keep the product dry and chemically uncompromised during longer transit times. While we rarely see material degradation, best results come through cool, dry storage conditions without direct sunlight.

    From plant experience, this product stays quite stable over time; even so, adherence to recommended shelf life and good handling practices (gloves, eye protection, well-ventilated transfers) ensures safety from the moment the container is opened. We commit staff time to deep cleaning of charging vessels and filling lines, preventing cross-contamination and maintaining cleanroom standards during packaging runs.

    Comparing With Similar Structures

    Years of side-by-side laboratory and pilot campaigns have shown the value in this specific substitution pattern. Alternatives such as 1-phenyl-3-methyl-2-pyrazolin-5-one or non-substituted analogs never quite reach the same performance benchmarks in trial synthesis or production blends. The presence of the 4-chloro group delivers a marked improvement in chemical stability, particularly under higher temperature regimes used in pharmaceutical process chemistry.

    From hands-on troubleshooting, we have seen how generic pyrazolones display increased rates of decomposition or isomerization when exposed to demanding process conditions. Our tailored version outperforms, particularly in verticals where downstream modification under stringent conditions is routine. Its consistent appearance and resistance to color change ensure no component-initiated inconsistencies appear in final formulations.

    Even manufacturers in neighboring markets—those looking to scale up their own heterocyclic derivatives—come to us for this compound because standard sources fall short on purity. We have examined off-the-shelf samples from several sources. Many show incomplete conversions, broader impurity bands, or out-of-spec particle size distributions, all factors that impact yield and final product acceptability. The repeat business and referrals we see underscore the trust built through continuous performance.

    Specific Use Cases and Outcomes

    Each day, our process team meets project leads from the pharmaceuticals and agrochemical sectors to review ongoing and upcoming projects. One trend stands out: ever stricter regulatory reviews now demand traceability and reproducibility at every material input step. In several examples, our material has supported validation through full regulatory filings, thanks to complete batch documentation and full-chain traceability.

    A prominent specialty pigment company recently adopted our material to improve both shelf life and hue stability in a new product category. By formulating with our compound, they extended their colorfastness properties well beyond what their original design targets called for, allowing them to claim new application spaces without revalidating their product platform.

    Smaller startups focused on fine chemical synthesis often reach out about scale-up support, aiming to integrate our compound as a modular intermediate. Compared to importing through intermediaries who cannot provide direct process data or rapid technical support, working direct with us means they can troubleshoot alongside our technical staff. Several have cut weeks off their own process tuning cycles, reducing both raw material costs and lead times.

    Working With Our Teams

    Growing this business has required more than building reactors and scaling up filtration. Our staff includes veteran organic chemists and process engineers who have seen it all—from unexpected solubility swings, scale-up exotherms, or loading errors, to on-the-fly process corrections when raw material supply chains hit a snag. We use that collective experience to look out for customers, spotting possible process complications before they take root.

    Joining in early-stage development discussions with clients, we often share insights not just about our own process, but about predictable points of concern in custom synthesis pathways. It pays off. A strong example: after we suggested a different order of reagent addition, a pharma client slashed impurity rates and improved overall step yields by nearly 9%. This kind of back-and-forth comes from directly operating full-scale production, not simply repackaging trade goods.

    Feedback loops drive our operational improvements. Batch audits and customer validation sessions fuel tweaks in purification, drying, and packaging. Not everything about raw material chemistry remains constant throughout the year; humidity shifts, supply stream purity, and even utility constraints mean no two runs are ever quite identical. Our in-plant review system captures these deltas, helping us keep outcome consistency as years pass.

    Future Innovation and Sustainability

    Our commitment goes beyond immediate supply—long-term sustainability and reduced waste drive our ongoing research. In-house, we constantly examine alternative solvents, improved energy recovery systems, and ways to cut down hazardous byproduct formation. Incremental gains come through in reduced solvent use and more efficient batch turnarounds. We gather life-cycle data to see where process improvements push us further toward minimizing environmental impact.

    Efforts behind the scenes have yielded secondary streams for byproducts, with some waste streams repurposed for lower-value technical products. Each new synthesis route is judged not just by cost and purity output but by its environmental repercussions. Technical teams review every tweak for impact well before going live at plant scale.

    Some clients rely on us to meet independent certification standards, especially for green chemistry compatibility. Our process records support those audits, demonstrating that environmental and workplace safety are not just policy lines but operational priorities. As regulatory frameworks evolve, we keep a close dialogue with stakeholders to align new production tweaks with published sustainability benchmarks.

    Why 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One Moves the Industry Forward

    Reflecting on the journey from bench to tonne-scale deliveries, the distinct value of this compound no longer rests just in its chemistry. Years of direct production experience and the need to overcome every challenge honed both the process and the material to high reliability. Those who have adopted this product recognize the reduced project risk, improved output quality, and the simple advantage of working with a manufacturer that understands downstream realities.

    All successful manufacturing hinges on a bridge between what the molecule offers and what the customer process demands. By keeping technical expertise close to the production line and maintaining open communication with our users, we deliver more than raw material: we provide confidence and a genuine partnership in advanced chemistry.

    Contact and Collaborative Opportunities

    If your process would benefit from high-purity, traceable, and reliable 1-(4-Chlorophenyl)-3-Methyl-2-Pyrazolin-5-One, our teams are always interested in deeper collaboration. The lessons built up from every batch support new applications and new efficiencies, helping you focus on innovation, safety, and product launch timelines. From pilot campaigns to ongoing routine supply, each partnership builds on a foundation of direct experience and shared technical language.