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2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One

    • Product Name 2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One
    • Alias 4-Methylantipyrine
    • Einecs 231-015-6
    • 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

    502153

    Iupac Name 2,4-Dihydro-5-methyl-2-(4-methylphenyl)-3H-pyrazol-3-one
    Molecular Formula C11H12N2O
    Molecular Weight 188.23 g/mol
    Cas Number 89-25-8
    Appearance White to off-white crystalline powder
    Melting Point 162-164°C
    Solubility In Water Slightly soluble
    Density 1.18 g/cm³ (approximate)
    Storage Conditions Store in a cool, dry place, tightly closed
    Synonyms 4-Methylantipyrine, 4-Methyl-2-phenyl-3H-pyrazol-3-one
    Pka Approximately 11.2 (for NH group)
    Hazard Statements May cause eye, skin, and respiratory irritation
    Usage Intermediate in organic synthesis, pharmaceutical research

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

    Packing & Storage
    Packing White, tightly sealed 250g HDPE bottle with tamper-evident cap, labeled with chemical name, formula, hazard symbols, and batch number.
    Shipping The chemical **2,4-Dihydro-5-methyl-2-(4-methylphenyl)-3H-pyrazol-3-one** should be shipped in tightly sealed containers, stored in a cool, dry place, and protected from light. Ensure proper labeling, include a safety data sheet, and comply with all applicable regulations regarding hazardous materials during transit. Handle with appropriate safety precautions.
    Storage Store 2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat sources, ignition, and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling and access for authorized personnel only. Follow relevant safety and chemical hygiene protocols when handling and storing this compound.
    Application of 2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One

    Applications of 2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One in Industrial Manufacturing

    2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One serves as a specialized chemical intermediate in the manufacturing of high-value industrial products. Its primary applications are concentrated in four well-established sectors, each requiring strict adherence to technical and regulatory standards. The following sections provide comprehensive insights relevant to industrial production, regulatory compliance, formulation practices, and final goods across these downstream fields.

    1. Pharmaceutical Intermediates for Non-Steroidal Anti-Inflammatory Drug Synthesis

    Manufacturers use this compound as a critical intermediate in the development of specific pyrazolone-based APIs, especially for non-steroidal anti-inflammatory drug (NSAID) synthesis including phenazone derivatives. The compound is introduced during targeted condensation or cyclization steps, where its chemical structure supports further modifications under controlled conditions. Production plants integrate it after careful assessment of batch traceability and impurity profiling to ensure reliable pharmacopoeial compliance.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients (ICH Q7)
    • European Pharmacopoeia monographs for pyrazolone derivatives
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • Japanese Pharmacopoeia standards for raw pharmaceutical materials

    Typical usage ratio

    • Equals 1.0–1.2 molar equivalents based on targeted NSAID API output
    • Adjustments made per reaction yields and purification recovery rates
    • Common batch sizes: 10 kg to 2,000 kg for commercial production
    • Waste minimization practices use process optimization data for each campaign

    Downstream process integration

    • Charged to reaction vessels after initial solvent charging and in-situ base addition
    • Monitored by HPLC and GC for reaction endpoint and intermediate purity
    • Workup includes aqueous quenching, solvent extraction, and crystallization prior to onward synthesis
    • Integrated with in-line quality control checkpoints

    Final product types

    • Bulk API of phenazone-type NSAIDs
    • Intermediate compounds for final tableting or encapsulation
    • Ready-to-formulate pharmaceutical bases
    • Stabilized granules for solid dosage form manufacturing

    2. Agrochemical Intermediate for Pyrazolone-Based Herbicide Synthesis

    The chemical is widely employed as a synthetic intermediate in the agrochemical sector, particularly for producing selective herbicides incorporating pyrazolone rings. Agrochemical manufacturers rely on its consistent quality and reactivity under high-throughput batch or continuous flow processes, introducing this intermediate prior to functional group modifications. Compliance with regional pesticide legislation, as well as downstream formulation registrations, requires strict in-process documentation and batch release control.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • US EPA Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) compliance
    • ISO 9001:2015 Quality Management Systems for agrochemical manufacturing

    Typical usage ratio

    • 0.8–1.5 molar proportions relative to the next coupling or functionalization agent
    • Process engineers determine dosage based on desired yield and final product purity
    • Common batch scale: 50 kg to 2,500 kg
    • Adjustment based on target technical grade vs. formulation requirements

    Downstream process integration

    • Fed into initial reaction reactors with stringent temperature and pH control
    • Participates in condensation, cyclization, or halogenation as per product requirement
    • Post-reaction, intermediate is isolated, purified by liquid-liquid extraction, and stored under nitrogen
    • Subject to analytical verification including NMR, LC-MS and GC-MS prior to onward synthesis

    Final product types

    • Technical-grade herbicide active ingredients with pyrazolone scaffolds
    • Granular and emulsifiable concentrate herbicide formulations
    • Wettable powder herbicide pre-mixes for field application
    • Custom-formulated selective post-emergence herbicides

    3. Analytical Reagents for Laboratory and Clinical Diagnostics

    Producers of analytical reagent kits incorporate this compound in the formulation of colorimetric and spectrophotometric assays, owing to its chromophoric properties and reactivity towards various analytes. It functions as a coupling agent or indicator in the quantitative determination of compounds such as uric acid or some transition metals. Reagent manufacturers select lots with high purity and confirmed photometric characteristics to meet laboratory traceability and diagnostic quality demands.

    Industry compliance standards

    • ISO 13485:2016 for in vitro diagnostic (IVD) reagent manufacturing
    • CLSI guidelines (Clinical and Laboratory Standards Institute) for analytical performance
    • REACH Regulation (EC) No 1907/2006 for analytical chemicals
    • US FDA 21 CFR 820 for medical device quality system regulation, if used in clinical diagnostics

    Typical usage ratio

    • 0.03–0.3% w/v in final reagent solution, depending on assay sensitivity target
    • Amount tailored to detection method and calibration range required
    • Component stability tested in finished kit at specified shelf life intervals
    • Precise lot-to-lot blending guided by spectrophotometric reference standards

    Downstream process integration

    • Dissolved or suspended in buffered aqueous or alcoholic solutions
    • Combined under controlled light exposure conditions for reagent stability
    • Dispensed into sealed vials or ampules using automated liquid filling lines
    • Incorporated in multi-component test strips or cuvette-based assay systems

    Final product types

    • Uric acid diagnostic test kits
    • Transition metal colorimetric assay reagents
    • Blood or serum analytical chemistry kits for clinical laboratories
    • Educational colorimetric standard solutions for research institutions

    4. Dye Intermediate for Specialty Colorant Production

    Colorant manufacturers utilize this compound as an intermediate for the synthesis of specialized azo and pyrazolone-based dyes. The structure enables targeted diazotization and coupling reactions, producing colorants featuring strong lightfastness and thermal stability required in high-performance textile and printing inks. Compliance with global dye safety standards involves control of reaction conditions, close monitoring of side-reaction contaminants, and downstream purification to ensure batch reproducibility for end users.

    Industry compliance standards

    • Oeko-Tex Standard 100 for dye safety in textiles
    • EU REACH Regulation (Annex XVII) for restricted aromatic amines
    • ZDHC (Zero Discharge of Hazardous Chemicals) guidelines for dye manufacturing
    • ISO 14001 Environmental Management Systems for chemical dye plants

    Typical usage ratio

    • 0.8–1.0 molar equivalents for azo coupling
    • 0.20–0.35 kg per kg finished dye, subject to target shade strength and purity
    • Dosing adjusted per product batch colorimetry and spectral properties
    • Formulators may increase ratio to offset anticipated yield losses in scale-up

    Downstream process integration

    • Introduced into diazotization or direct coupling reactors at tightly regulated temperatures
    • Intermediate is purified via filtration, extraction, and chromatographic methods
    • Blended with other dye intermediates or color boosters as per target colorant profile
    • Pre-formulated dye mass is dried, granulated, or converted to aqueous solutions for application

    Final product types

    • Textile dyes in pad-dyeing and exhaust dyeing operations
    • Printing inks for industrial and digital applications
    • Special effect colorants for plastics and coatings
    • High-performance pigments for technical textiles and automotive interiors
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    Certification & Compliance
    More Introduction

    Introducing 2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One: Direct Insights from Production

    Our Manufacturing Approach to 2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One

    On the production line, every batch of 2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One reflects hands-on care and experience. Every part of its synthesis has taught experienced plant chemists about its unique crystal formation and the subtleties that set it apart from other pyrazolones. As a team that answers for both quality and reliability, we never lose sight of the role that process control plays during cyclization and subsequent purification. This compound, often referred to among our team by its shorthand or structural nickname, reveals a character and consistency that stand up to scrutiny in every batch.

    Understanding the Compound's Structural and Functional Distinctions

    Not every pyrazolone shares the same profile. What distinguishes 2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One starts at its molecular backbone. The 4-methylphenyl group brings a degree of electronic influence that shifts properties significantly compared to unsubstituted or differently substituted relatives. Add to this a methyl group at the 5-position, and you create a molecule with both improved stability and a profile that proves responsive in downstream syntheses. Anyone with hands-on knowledge of this segment of heterocycles knows that tinkerers tweak substituents for these very reasons—drug intermediates, colorants, or even specialty reagents require small differences that affect solubility, reactivity, or processing behaviors in practical settings.

    On our shop floor, the most consistent feedback from long-term clients has focused on both purity and particle habit. Years of producing this pyrazolone for API precursors and pigment intermediates has strengthened the lab’s focus on a clean conversion, sharp melting points and a powder that handles easily without caking or unexpected agglomerates. In contrast, other manufacturers sometimes struggle with off-white tints or trace contaminants; these can become headaches down the line. We have made it habit to invest in additional filtration and drying steps specifically to minimize trace residuals that originate from starting aldehydes or methylhydrazine.

    Applications—Sharing Our Practical Experience

    Chemicals like these define their value in practice—not just on paper. In-house testing teams have worked alongside customers to troubleshoot everything from formulation stability in pharmaceuticals to color-fastness in dyes. This compound frequently enters the scene as either an active intermediate for anti-inflammatory APIs or, in another sector, a core for pigment molecules. Some customers have also realized its worth as an analytical reagent, particularly due to its reliable binding with various metals during detection routines. Our late-shift operators routinely monitor crystallization to deliver a product that remains versatile enough for these varied downstream applications.

    Those using this compound as an intermediate often cite its clean reaction pathway under well-controlled temperature and pH ranges. The methyl and phenyl substitutions help direct subsequent reactions, providing greater predictability—an underappreciated benefit that saves time and cuts waste. Too often, substitutes with different ring substitutions or impurities slow progress and introduce byproducts. By sticking to strict batch recording and materials tracking, we keep the process transparent and reproducible for clients with regulatory and scale-up needs.

    Quality Driven by Chemistry—From Plant Floor to Customer Application

    We have learned that attention to starting materials, time-sensitive handling during condensation, and the right vacuum-drying steps matter immensely. There’s no short-cutting these points; mistakes in any step show themselves later as batch variability, off-odors in finished products, or even failed quality checks. For chemical users in regulated industries—especially pharmaceuticals—the margin for error is razor-thin.

    Some years back, we faced a surge in demand from a customer who required twice our previous average batch volume. Scaling up, the main challenge became keeping every batch at the same high standard. Good documentation and daily adjustment based on batch data enabled the plant to stay ahead. We learned to tweak mixing speeds and cooling rates, which maintained the physical properties our longest-standing customers depend on.

    Not all pyrazolone derivatives used in pigment or chemical synthesis can perform with such predictable reaction profiles. For example, isomeric differences or additional substituents affect both reactivity and handling. We have seen how trace impurities that pass undetected in other suppliers’ materials result in batch failures for the end-user. Rigorous in-process controls, developed after years of operator feedback, now flag even the subtlest deviations in intermediate clarity or byproduct formation.

    Supporting Robust Formulations Downstream

    Clients value the compound’s stability under moderate heat and its tolerance for formulation solvents. An undiscussed lesson we learned relates to shelf life—initially, we underestimated the power of minor formulation tweaks by customers and their impact on storage. A hands-on approach prompted us to extend batch testing protocols, storing product under client-specific conditions, and feeding those results right back into manufacturing guidance.

    Other pyrazolone-based compounds compared side-by-side often reveal issues with stickiness or dustiness, particularly under low humidity. By adjusting our milling and sieving and adding small improvements in drying and air-handling, we deliver a material that flows cleanly—critical for bulk processing and automated dosing. In-house staff regularly audit these steps to maintain consistency.

    Batch Experience Translated into Reliable Product

    Mistakes from inexperience show up right away in this sector—from incomplete reactions to mischaracterized lots. Senior chemists handle weekly reviews of every test record and chromatogram to ensure all critical attributes are met. If any anomaly appears, that batch never leaves the door. This discipline impacts everything from the brightness of finished pigments to the quality control results at major pharmaceutical contract labs.

    Transparency in providing analytical data has proven essential. Over the years, providing clients with HPLC and NMR traces (without being asked) has quieted any worries about batch-to-batch variation. Incoming customers sometimes arrive after facing multiple product failures or unexpected byproducts, seeking material that consistently meets stated criteria. These hard-earned lessons reinforce our resolve to never relax our own batch qualification expectations.

    Practical Solutions for Production and User Challenges

    Fresh feedback loops from clients keep production responsive. Technical teams and production operators regularly examine negative outcomes from the past—like foaming during fermentation or instability in finished API formulations—and adapt the handling or purification routines. Adjustments in solvent ratios or crystallization timeframes sometimes cut process issues by half. New staff join process discussions to internalize what old hands have already learned: this specific compound, with its methyl and phenyl substitutions, rewards careful attention and penalizes carelessness.

    Scale-up sometimes presents headaches, but direct dialogue with formulation scientists helps bypass issues before they escalate. A recent pilot with a pharmaceuticals partner called for producing a larger-than-usual lot. By involving field chemists at the outset, we adjusted cycle times and solvent volumes, avoiding unnecessary losses or variable performance. In another instance, a customer’s pigment batch suffered from shade inconsistency. By working through their dye-bath conditions and sharing real-world drying data from our own QC tests, we identified a solution that restored consistency.

    Real-life problem solving has built mutual trust. These experiences also show why it pays to offer clear batch data and support, not just a product in a package. Plant managers and application chemists keep each other informed about any changes in raw materials; rapid response to feedback ensures problems get traced back and solved instead of allowed to fester.

    Advantages over Related Pyrazolones

    Some might look at a pyrazolone as another commodity, but repeated cycles of analysis and production show the importance of even minor structural changes. Compared to analogues with substitutions at different positions, 2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One outperforms in stability and purity, largely due to its specific molecular build. Comparable materials from generic sources exhibit unpredictability—off-white color or minute residue signals deeper purity shortcomings.

    Several pigment companies and pharmaceutical contract manufacturers have commented that switching to fully characterized lots leads to more robust performance, less re-testing, and fewer rejected batches. Pyrazolones produced without the same level of control often lack in this regard. Yield or color shade problems frequently originate from those small molecular impurities or batch inconsistencies, so persistent attention to batch records and test reports pays off.

    Commitment to Consistent Quality and Transparent Practice

    We commit to making sure every container reaching a client meets the same benchmarks—purity level, handling character, and lot-to-lot consistency. The team that runs these lines draws from long-term manufacturing experience; many have come up through both the plant and quality assurance ranks and carry forward a no-shortcuts mentality. At each stage, open access to analytical practices and batch data means everyone involved can see that raw materials, processing, and final output all meet the high standard expected.

    Across the years of producing this specific compound, the clearest lesson is the wisdom of not compromising process or quality just to move out a higher volume of material. Episodes where others have rushed production have only led to more customer headaches (and sometimes, reversals to our material). Each time, gaining back lost trust has required redoubled transparency and support.

    Continuous Improvement—Learning from Production, Testing, and Application

    Continuous learning forms the backbone of our practice. On the floor and in the lab, new minor tweaks or process improvements are discussed between shifts. It is not unusual for ideas from an application chemist to trigger a double-check of a filtration step or prompt a review of temperature control settings—each change is tracked, reviewed, and documented. Line staff and lab analysts carry shared ownership over product quality; this culture extends forward to all our partners relying on this molecule.

    Listening to both long-term and new clients keeps focus sharp. Regular post-market testing and feed-back driven production modifications mean that improvements are guided by practical field results and not theoretical guesswork. Investment in equipment and operator training keeps both new and old hands ready for unexpected challenges—from raw material changeover to emergent environmental or safety standards.

    Looking to the Future

    Changing regulatory requirements and advances in end-use chemistry continue to shape the way this compound gets produced and delivered. Past experience with solvent replacements and more stringent impurity thresholds has already hardened the team’s adaptability. Open, ongoing dialogue with customers, regulatory advisors, and on-site experts drives continued improvement in both process control and downstream flexibility. Our reputation, built through many years of successful collaboration and a strict adherence to transparent practices, sets expectations high—both for ourselves and for any partner who depends on our 2,4-Dihydro-5-Methyl-2-(4-Methylphenyl)-3H-Pyrazol-3-One in critical applications.

    Conclusion—A Product Built on Experience and Shared Goals

    Years in the field, direct feedback from both plant operators and customers, and a refusal to skip steps have formed a product that stands apart. The compound’s value grows from the reliability and predictability earned batch after batch, shipment after shipment. For us as manufacturers, knowledge gained over years of direct experience becomes a banked legacy—a source of confidence for anyone seeking consistency and transparency in their chemical supply chain. Every drum shipped carries the direct imprint of technical skill and shared commitment to the needs of partners who stake their reputation on our compound, just as we stake ours on making it right.