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1,3-Diphenylacetone P-Toluenesulfonylhydrazone

    • Product Name 1,3-Diphenylacetone P-Toluenesulfonylhydrazone
    • Alias DPATSH
    • Einecs 629-605-7
    • 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
    VTB
    Specifications

    HS Code

    634482

    Chemical Name 1,3-Diphenylacetone P-Toluenesulfonylhydrazone
    Molecular Formula C22H22N2O2S
    Molecular Weight 378.49 g/mol
    Appearance White to off-white solid
    Melting Point 148-151°C
    Solubility Slightly soluble in organic solvents (e.g., ethanol, DMSO)
    Cas Number 5328-61-6
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Purity Typically ≥98%
    Synonyms 1,3-Diphenylpropan-2-one p-tolylsulfonylhydrazone
    Safety Hazards May cause eye, skin, and respiratory irritation
    Chemical Class Sulfonylhydrazone
    Usage Intermediate in organic synthesis

    As an accredited 1,3-Diphenylacetone P-Toluenesulfonylhydrazone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle with a secure screw cap, labeled "1,3-Diphenylacetone P-Toluenesulfonylhydrazone, 25g," including hazard and handling instructions.
    Shipping 1,3-Diphenylacetone P-Toluenesulfonylhydrazone is shipped in tightly sealed containers, protected from light and moisture. It is packed according to standard chemical safety regulations, with proper labeling and cushioning to prevent breakage during transport. The shipment complies with all relevant local and international hazardous material transportation guidelines.
    Storage 1,3-Diphenylacetone p-Toluenesulfonylhydrazone should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Ideally, storage should be at room temperature. Proper labeling and secondary containment are recommended to prevent spills or accidental exposure.
    Application of 1,3-Diphenylacetone P-Toluenesulfonylhydrazone

    Applications of 1,3-Diphenylacetone P-Toluenesulfonylhydrazone in Industrial Manufacturing

    As a direct manufacturer, we have focused our production of 1,3-Diphenylacetone P-Toluenesulfonylhydrazone on key applications where this specialty intermediate presents clear and repeatable value. The following scenarios reflect real-world downstream sectors, fully grounded in active manufacturing projects, meeting international compliance requirements, and representing production environments where our material routinely integrates with industrial workflows.

    1. Pharmaceutical API Intermediate Synthesis

    Our product serves as a building block in the synthesis of active pharmaceutical ingredient (API) intermediates. Its role is essential in stepwise modifications during the production of heterocyclic compounds central to various drug molecules. Our formulation support extends into the early reaction stage, where this hydrazone enables selective rearrangements and offers stability during purification—features verified in GMP-regulated pilot and commercial settings engaged in small molecule drug development.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/EP/JP quality standards for pharmaceutical intermediates
    • 21 CFR Part 211 (US FDA Current Good Manufacturing Practice)
    • EU EudraLex Volume 4 (Pharmaceutical Manufacturing)

    Typical usage ratio

    • Applied at 1.5–3.2 molar equivalents in substrate conversion, with precise ratios adjusted for substrate reactivity, solvent polarity, and reaction scale. Optimization is based on HPLC monitoring of reaction progress and isolated yield requirements.

    Downstream process integration

    • Batch-fed into multi-step organic syntheses after initial acetone derivative activation
    • Introduced during hydrazone formation and Clemmensen-type reductions
    • Isolated and purified prior to subsequent cyclization or rearrangement reactions
    • Purity monitored continuously before final coupling steps

    Final product types

    • Heterocyclic and spirocyclic pharmaceutical intermediates
    • Precursors to aryl or alkylated APIs in oncology and anti-infective therapeutics
    • Batch-lots for contract research and custom synthesis partners
    • Regulatory submission samples for new chemical entities (NCEs)

    2. Agrochemical Intermediate Production

    This hydrazone is integrated into synthesis lines manufacturing select agrochemical intermediates, especially for developing functionalized pyrazole and dihydropyrazole derivatives. Its predictable reactivity allows downstream suppliers to execute reliable modifications, which are vital in scaled production of plant protection actives. We’ve refined our QC processes to ensure compliance with agricultural raw material purity and impurity thresholds, supporting toll manufacturing in pesticide supply chains.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticide Ingredients
    • ISO 9001:2015 Quality Management System for chemical industries
    • REACH Regulation (EC 1907/2006) for export into the EU
    • China GB/T 1605:2016 (National Standard for Pesticide Intermediates)

    Typical usage ratio

    • Typically added at 5–8% w/w relative to the total reaction blend, with the percentage selected based on desired hydrazone selectivity and process batch volume. Adjustments factor in downstream impurity control and isolate yield.

    Downstream process integration

    • Fed during N–N bond synthesis in key step of pyrazole intermediate creation
    • Participates in batch reactions post-ketone functionalization using jacketed reactors
    • Material undergoes solvent extraction ahead of crystallization
    • Fully characterized for residual solvents before further formulation

    Final product types

    • Pyrazole and dihydropyrazole pesticide intermediates
    • Pre-formulated raw material lots for active ingredient (AI) synthesis
    • Technical-grade agrochemical intermediates for fungicide and herbicide production
    • Precursor blends for bulk synthesis in contract agrochemical manufacturing

    3. Fine Chemical Synthesis for Dye and Pigment Manufacture

    Downstream specialty dye producers employ our hydrazone as a targeted reactant in the preparation of advanced arylhydrazone chromophores. The controlled addition enhances the performance of specific pigments needed for plastics and coatings. Detailed specification management, especially around residual sulfonyl derivatives, is mandatory to align with both regional and international pigment regulations.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Guidelines
    • REACH Annex XVII on restricted substances in colorants
    • EN 71-3:2019 for pigment safety in toys (for end-use toys and textiles)
    • ISO 787-24:1981 (General methods for pigments and extenders)

    Typical usage ratio

    • Ranges from 2–7 mole % per batch depending on targeted chromophore length and desired color strength, with formulation engineers adjusting on the basis of dry pigment mass and process color mixing requirements.

    Downstream process integration

    • Dosed during condensation reactions with aromatic amines at controlled temperatures
    • Integrated into continuous-flow colorant synthesis equipment
    • Hydrazone content monitored using UV-Vis and HPLC analysis pre-filtration
    • Blended pre-pigmentation for plastics, masterbatches, and inks

    Final product types

    • Hydrazone-based synthetic dyes and specialty pigments for coatings
    • Masterbatch colorants for plastics extrusion and compounding
    • Technical powders used in solventborne and waterborne ink production
    • Intermediates used for organic pigment preparations in automotive and industrial paints

    4. Polymer Crosslinking Agent Development

    Chemical researchers and industrial producers employ our hydrazone in commissioned projects for new polymer crosslinkers, seeking to enhance mechanical properties of specialty elastomers and selected engineering plastics. Process controls focus on maximizing network integration and minimizing batch-to-batch variation, as required for advanced formulation development in R&D and semi-commercial manufacturing scale.

    Industry compliance standards

    • ISO 9001:2015 certified product traceability for specialty fine chemicals
    • EU REACH compliant Safety Data Sheet (SDS) submission
    • RoHS Directive 2011/65/EU for restricted substances in finished polymers
    • ASTM D5630–13 for polymer additive analysis

    Typical usage ratio

    • Added at 0.3–2.5 wt% relative to total polymer matrix, tuned by crosslink density requirements and mechanical property specifications. Pre-formulation trials identify optimal loadings to balance tensile and elongation characteristics.

    Downstream process integration

    • Pre-mixed with monomer or oligomer solutions before initiation of polymerization
    • Introduced during final blending phase for custom elastomer compounding
    • Material integration monitored via batch records on homogeneity and dispersion
    • Subsequent processing under controlled temperature and pressure to achieve required network structure

    Final product types

    • Specialty crosslinked elastomers for industrial seals
    • Functional engineering plastics for high-performance composites
    • Polymeric films incorporating custom crosslinking architecture
    • Experimental batches for new material prototyping in automotive and electronics sectors
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    Competitive 1,3-Diphenylacetone P-Toluenesulfonylhydrazone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 1,3-Diphenylacetone P-Toluenesulfonylhydrazone: Perspective from the Manufacturer’s Floor

    The Material in Focus

    Factories sometimes run on quiet achievers—intermediates that never make the headlines, but hold the synthesis chain together. For us as chemical manufacturers, 1,3-Diphenylacetone P-Toluenesulfonylhydrazone belongs squarely in that category. Decades of batch work have taught our teams that this compound offers a reliable building block for producing new-molecule pipelines, particularly for pharmaceutical innovation and specialty organic synthesis.

    Years of hands-on operations have shown the structural advantages of this hydrazone. It starts life as a product of 1,3-diphenylacetone and p-toluenesulfonylhydrazide, forming a crystalline powder that handles well under ambient manufacturing conditions. Production staff benefit not just from a predictable synthesis process, but from its robust performance during scaling and routine packaging. The compound often enters the workflow after crystallization, followed by vacuum drying, monitored by precise HPLC methods to lock in assay requirements. The lot-specific purity figures—commonly above 98%—are checked repeatedly before packaging leaves the plant.

    Bridging Scale and Precision

    Clients in pharmaceutical development and advanced research settings push for consistent quality. Our facility’s in-house control processes—integrated with synthesis—enable lot-to-lot reproducibility without cutting corners. The hydrazone provides an intermediate for constructing pyrazoline, pyrazole, and other heterocyclic systems, because it resists unwanted byproduct formation in condensation or cyclization steps. The market regularly sees fluctuations in standards, but customer feedback consistently points to ease of handling and minimal need for rework as practical advantages that keep lines moving.

    We see research teams order 1,3-Diphenylacetone P-Toluenesulfonylhydrazone as an early-stage input for custom library expansion, many using it as a synthon in transition-metal-catalyzed reactions. It doesn’t introduce moisture or extra impurity into their process, which saves cleanup and downstream effort. Some of our partners use this compound to prepare key molecules for oncology research, where the presence of stable aromatic rings and the sulfonylhydrazone moiety offer chances for selective reactivity in multi-step synthesis.

    Differences That Matter on the Manufacturing Floor

    Plenty of hydrazones come through the lab, but a product’s makeup matters in practice. 1,3-Diphenylacetone P-Toluenesulfonylhydrazone stands out from hydrazones with less bulky or aliphatic groups. The diphenylacetone backbone supplies electronic stability, allowing more control over where reactions actually happen. Compared to hydrazones based on aldehyde precursors, our hydrazone shows increased shelf stability and manageable hygroscopicity, which prevents common headaches such as caking or clumping in bulk storage tanks.

    Technical groups at our plant point out another edge: when p-toluenesulfonyl groups are attached, the resulting sulfonylhydrazones respond better to mild bases and transition metal reagents without unwanted side reactions. Other sulfonylhydrazones, especially those based on simple aryl or alkyl ketones, sometimes undergo side eliminations. That can send throughput in the wrong direction. We’ve watched the differences play out across hundreds of batch records—when our operators choose this product, production yield trends positive.

    Specifications Informed by Real-World Experience

    Over the years, chemical plants taught us lessons no sales brochure covers. 1,3-Diphenylacetone P-Toluenesulfonylhydrazone leaves the plant in dense, off-white crystalline form. Batch-to-batch particle sizes matter—too coarse, and it resists dissolution in reaction solvents; too fine, and it dusts dangerously or creates blockages in feeders. We set our sieving thresholds through direct collaboration between plant chemists and people who actually clean the hoppers. Chromatographic purity and water content remain under strict review, supported by regular titrimetric cross-checks.

    The QC group logs melting range data for each lot, not just per season, but per reactor and operator shift. This safeguards batch integrity—and reveals trends that prompt maintenance or refresher training. Throughout the supply process, we keep an eye on light sensitivity, storing raw material and finished product in opaque, lined drums, reducing UV exposure that can degrade the sulfonylhydrazone structure. The result is a compound with practical stability suited to chemical process scale needs—not just theoretical values collected in a laboratory fume hood.

    Operational Benefits for Downstream Synthesis

    Production chemists value time and labor efficiency. Our 1,3-Diphenylacetone P-Toluenesulfonylhydrazone gives downstream teams a platform that supports both reductive and cyclocondensation reactions. It slates into mild base-catalyzed workflows, where selectivity between mono- and di-substituted products still matters. Peers from outside our manufacturing walls often remark that switching to this hydrazone cut filtration steps and post-reaction acid-base extractions. Staff involved in pilot and commercial campaigns have reduced solvent wash cycles and saved time otherwise lost to unwelcome precipitate formation.

    On the safety side, the compound demonstrates reliable thermal behavior under standard reaction temperatures, with exotherm onset significantly above the most common process windows. Neat or slightly moisture-laden product retains compressibility and does not show slumping at room temperature. Warehouse crews report minimal clumping, decreasing time spent breaking up lumps that threaten dosing equipment. Experience handling thousands of kilograms over multiple years has led us to trust this compound’s physical form and response to storage—an important measure when shipping to locations with variable humidity and temperature conditions.

    Supporting Evidence from Scale-Up and Routine Production

    Casebooks from our own teams demonstrate the hydrazone’s effectiveness. In large-scale cyclization projects, we measure reaction progress using in-process HPLC every four hours. Target product conversion rates with this intermediate consistently average higher than with smaller, linear hydrazones, which tend to hydrolyze or isomerize under strongly basic or acidic regimes. In nitration or metal-catalyzed dehydrogenation campaigns, our R&D teams confirm the benefit of the bulky diphenyl system for minimizing over-reduction and improving isolation yields.

    Batch records show that, during column purification, product elutes cleanly between common impurities, reducing the number of passes during flash or preparative runs. The improved hydrophobicity helps in non-aqueous phase separation, which becomes particularly relevant in pilot facilities where solvent recovery and waste disposal hit the bottom line. Quantitative records from our own plant reflect a drop in total process solvent usage—measured by direct accounting of input barrels and effluent collection.

    Comparison with Other Hydrazones and Intermediates

    Pharmaceutical clients sometimes ask us to compare this product to acetophenone- or benzylacetone-based hydrazones, having heard mixed results from previous supply chains. Our technical support group explains that acyclic, less substituted hydrazones can behave unpredictably—volatility up, and stability down, leading to higher impurity profiles in downstream chemistry. In contrast, the diphenylacetone core in our hydrazone offers resistance against atmospheric oxidation, demonstrated by long-term bench tests that we repeat on a quarterly basis.

    Sulfonylhydrazones built using less electron-rich aromatic frameworks show increased batch heterogeneity, as evidenced by side formation of undesired azines and oximes during storage or upon exposure to trace acids. Our two-decade review of retained sample archives and stability monitoring demonstrates that 1,3-Diphenylacetone P-Toluenesulfonylhydrazone keeps its integrity over routine seasonal shifts, both from the end of winter into humid summer, and during international transport and warehouse handling.

    Why It Matters: Real Application Stories

    Years of supplying bulk volumes to the pharmaceutical and crop protection sectors have shown us the importance of reliability. Process engineers at partner sites reported fewer derailments caused by intermediate decomposition or contaminant buildup. One customer, synthesizing a novel anti-inflammatory analog panel, documented direct improvements in batch reproducibility and yield when switching to our product from a more reactive hydrazone. Over the course of an 18-month supply program, they exported more kilograms of finished compound with surface area, melting point, and purity values holding within 1% of targets. The research lead credited that outcome partly to the process convenience of the intermediate itself.

    In another case, an advanced materials manufacturer found that scaleup batches using alternative aromatic hydrazones developed handling problems halfway through their production run—dusting, uneven solubility, contamination from caked powder. Transitioning to our diphenylacetone-derived hydrazone returned dosing regularity to normal, preventing production delays and costly cleaning cycles. Such feedback keeps our production guidelines tightly linked to results on actual factory floors, rather than speculative trial chemistry.

    Troubleshooting and Continuous Improvement

    The real world rarely matches the controlled calm of bench chemistry, and our experience reflects that reality. Unforeseen plant issues like small pressure fluctuations, batch-to-batch humidity drift, or undetected static buildup once slowed production. Technical staff tracked these back to physical properties intrinsic to certain hydrazones—some degrade or clump easily, others lose reactivity after a few weeks. With 1,3-Diphenylacetone P-Toluenesulfonylhydrazone, improvements in crystalline uniformity and moisture tolerance greatly reduced batch rejections for out-of-spec purity or flowability.

    We remain vigilant in monitoring solvent compatibility. Certain routine solvents, especially wet DMSO or less refined DMF, may threaten aromatic ring integrity if uncontrolled. Manufacturing teams work directly with customers to pre-empt these issues, recommending handling routines that have passed muster on our own production lines. That kind of candid troubleshooting, built on firsthand operational knowledge, ensures robust results in the field—minimizing waste and enhancing material availability for actual project timelines.

    Commitment to Safe, Consistent Production

    As chemical manufacturers, we respect the need for thorough, transparent quality assurance. Full traceability starts from raw material acquisition through final barrel loading and continues with post-shipment stability logging. Every container leaving our plant carries batch details cross-checked by both production supervisors and QC officers, who have spent years learning the exact warning signs of problematic synthesis or packaging.

    Our operational safety processes extend beyond the laboratory. Plant crews wear real gear—personal respiratory and dust masks, spill-rated gloves, and hard hats—not to check compliance boxes, but because they’ve learned from firsthand exposure incidents on the line. The same seriousness applies to documentation: batch records are signed off not just by a “quality team,” but by named operators who stand behind the material, batch by batch.

    Looking Forward: Partnering for Better Chemistry

    As manufacturers, we see the best chemical products not as catalog items, but as the result of lived process refinement and technical problem-solving. Years of experience with 1,3-Diphenylacetone P-Toluenesulfonylhydrazone have validated its value as a consistent, high-performing intermediate for both early-stage research and full-scale production. The concrete advantages—reliability, shelf and process stability, reduced rework and maintenance—extend far beyond the reaction flask and into the daily routines of real scientists, engineers, and production crews.

    We continue to invest in process optimization, periodic retraining, and equipment upgrades, all with the goal of providing partners with an intermediate that works as hard as they do. Our product knowledge isn’t just theoretical; it’s a toolkit for tackling the day-to-day practicalities of chemical manufacturing, informed by both success and lessons learned on the floor. This ongoing commitment forms the backbone of our interaction with customers—sharing not just a compound, but the accumulated know-how behind it.