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4,6-Diphenyl-2-Pyrone

    • Product Name 4,6-Diphenyl-2-Pyrone
    • Alias 4,6-Diphenyl-2H-pyran-2-one
    • Einecs 214-316-6
    • 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

    635526

    Cas Number 4573-08-0
    Molecular Formula C17H12O
    Molecular Weight 232.28 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 158-161°C
    Solubility Insoluble in water; soluble in organic solvents like ethanol and ether
    Structure Contains a 2-pyrone core substituted with phenyl groups at positions 4 and 6
    Synonyms 4,6-Diphenyl-2H-pyran-2-one
    Smiles O=C1C=CC(C2=CC=CC=C2)=C(C3=CC=CC=C3)O1
    Inchi InChI=1S/C17H12O/c18-17-13-11-16(14-7-3-1-4-8-14)12-15(17)9-5-2-6-10-15/h1-13H

    As an accredited 4,6-Diphenyl-2-Pyrone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4,6-Diphenyl-2-Pyrone; sealed with a screw cap, labeled with safety information.
    Shipping 4,6-Diphenyl-2-Pyrone is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported according to standard chemical safety regulations, typically via ground or air freight, labeled as a laboratory chemical. Proper documentation and hazard identification ensure safe and compliant delivery to the destination.
    Storage Store **4,6-Diphenyl-2-pyrone** in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the container tightly closed when not in use. Use inert containers, such as glass or suitable plastics, to prevent chemical reactions. Ensure appropriate labeling and implement standard laboratory safety procedures when handling or storing this compound.
    Application of 4,6-Diphenyl-2-Pyrone

    Applications of 4,6-Diphenyl-2-Pyrone in Industrial Manufacturing

    4,6-Diphenyl-2-Pyrone serves as an advanced building block within high-value chemical manufacturing, offering precise chemical reactivity and consistent performance to formulators across various industrial segments. Below, we detail the primary downstream applications substantiated by established industry practices, specific regulatory requirements, typical material ratios, process integration details, and exemplary end products.

    1. Pharmaceutical Intermediate for API Synthesis

    Many pharmaceutical manufacturers use 4,6-Diphenyl-2-Pyrone as a key intermediate during the multi-step synthesis of certain active pharmaceutical ingredients, especially within the class of anti-inflammatory and anti-cancer drugs. Synthetic chemists capitalize on its pronounced aromaticity and reactive lactone functionality, facilitating specific condensations or cyclization reactions under highly controlled batch processes. Material quality and trace residual control remain critical to comply with stringent pharmacopoeial standards, while purification steps downstream rely on robust phase separation and crystallization.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP General Chapters — Residual Solvents <467>
    • European Pharmacopoeia 10.0, Synthesis Intermediates
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals)

    Typical usage ratio

    • Reaction input: 0.2 to 0.6 molar equivalents, adjusted for target API synthesis route and designed yield

    Downstream process integration

    • Material charged to reaction vessel after solvent and initial reagents
    • Temperature-controlled addition to maximize selectivity
    • Integration with in-line purification and repeated crystallization
    • In-process QC for each batch to monitor conversion efficiency

    Final product types

    • Anti-inflammatory drugs (e.g., diarylpyrone-based compounds)
    • Chemotherapeutic agents (specialty oncology APIs)
    • Investigational new drug substances within clinical supply

    2. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Large-scale pigment and dye manufacturers source 4,6-Diphenyl-2-Pyrone for use in developing high-performance aromatic chromophores. Its distinct molecular scaffold allows controlled introduction of substituents, supporting finely tuned shade, stability, and solubility properties for organic pigments and specialty dyes. These applications typically demand quality assured by color strength checks and absence of regulated impurities.

    Industry compliance standards

    • DIN EN 71-3: Toy Safety (Migration of Certain Elements)
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • ISO 9001:2015 certified QC
    • General state and EU colorant safety directives

    Typical usage ratio

    • Input range: 5–20% of total precursor blend mass, tailored by desired pigment yield and color depth

    Downstream process integration

    • Dissolved into main synthetic batch at initial heating
    • Followed by introduction of coupling and functionalizing agents
    • Control over addition rate to influence chromatic outcome
    • Isolation via filtration, followed by drying and micronization

    Final product types

    • High-fastness textile dyes (disperse dyes, vat dyes)
    • Organic pigments for plastics compounding
    • Toner and inkjet formulations for imaging technologies
    • Specialty colorants in industrial coatings

    3. Synthesis of Advanced Functional Polymers

    Producers of performance polymers incorporate 4,6-Diphenyl-2-Pyrone as a comonomer or functionalizing agent during melt or solution polymerization. This raw material introduces rigid aromatic structures, boosting mechanical strength and thermal stability, particularly in polyesters, polyarylates, and high-performance resins used for specialty engineering plastics. Manufacturer-level process control manages reactivity to prevent premature crosslinking, while blend ratios determine the final application profile.

    Industry compliance standards

    • ISO 10993-18: Chemical Characterization of Polymers (Medical)
    • UL Yellow Card certification for polymer flame resistance
    • RoHS Directive 2011/65/EU for restricted substances
    • ASTM D638: Tensile Properties of Plastics

    Typical usage ratio

    • Typically 1–10 mole percent within the monomer mix, increased for targeted stiffness or thermal requirements

    Downstream process integration

    • Compound charging to reactor or extruder before initial polymerization
    • Integrated with chain extenders or branching agents
    • Temperature and residence time optimization to limit side reactions
    • Blending with other aromatic monomers for copolymer customization

    Final product types

    • High-heat-resistant thermoplastic parts
    • Structural films and sheets for electronics
    • Specialty molded components
    • Semi-interpenetrated polymer networks

    4. Photoreactive Compound for Specialty Photoinitiators and Photoresists

    Manufacturers engaged in electronics and lithography processes select 4,6-Diphenyl-2-Pyrone to synthesize novel photoinitiator systems and photoreactive resists. Its structure enables controlled UV absorbance and unique reactivity, qualifying it for the formulation of photo-patternable resins in PCB fabrication, semiconductor processing, and precision microelectronics. Batch purity, light absorbance properties, and impurity profile directly affect final device yield, so detailed QC per ISO and IPC standards is required.

    Industry compliance standards

    • IPC-4552B: ENIG Surface Finish for PCBs
    • ISO 14644-1: Cleanroom standards for photolithography
    • IEC 62474: Material Declaration for Electrical and Electronics (hazardous substance tracking)
    • RoHS/REACH (for all photoresist components)

    Typical usage ratio

    • 0.5–3 wt% as a primary photoactive entity, with specific percentage adjusted after spectral tuning and photo-patterning trials

    Downstream process integration

    • Early-stage incorporation into resin or monomer solution
    • Mixing under precisely controlled conditions to achieve homogeneity
    • Dispensing and pre-bake for thin film formation
    • In-line UV spectral QC prior to exposure steps

    Final product types

    • Photoresists for microelectronics
    • UV-activated photoinitiators for adhesives
    • Specialty coatings for precision optics
    • High-resolution printed circuit boards
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    Certification & Compliance
    More Introduction

    4,6-Diphenyl-2-Pyrone: A Practical Choice for Advanced Chemical Synthesis

    A Closer Look at 4,6-Diphenyl-2-Pyrone

    Meeting the needs of specialty synthesis calls for consistency and reliable performance. Over years of small-batch refinement and scaled production, we have shaped our process for 4,6-Diphenyl-2-pyrone to avoid the headaches that can come from working with inconsistent supply or variable purity. This compound, with model number 4,6-DPP-201, has become dependable for researchers and businesses alike who seek sharp batch-to-batch reproducibility and straightforward handling without surprises.

    Our Production Approach and Specifications

    Reliable chemistry begins with clean, reproducible input. We developed methods that use a stable feedstock chain, so synthetic steps stay controlled. Each batch of 4,6-Diphenyl-2-pyrone rolls out with purity levels above 99%, measured using HPLC and checked every cycle by NMR to spot even subtle differences in structure. The white crystalline appearance points to high organic purity, something that makes downstream use easier, particularly during critical reactions or pharmaceutical workups.

    Moisture and trace solvent content in our product drop below market-accepted benchmarks, as confirmed by both Karl Fischer titration and GC analysis. These checks come from hard experience—managing moisture content directly correlates with fewer failures in our clients' synthesis processes. Each lot is built with a clear record back to starting materials, so if an unusual trend shows up in a particular structure-activity relationship study or polymerization, feedback to us opens a direct investigation.

    Working with 4,6-Diphenyl-2-Pyrone in the Lab and Industry

    Our own development chemists work with this material as both a starting building block and an intermediate. The 2-pyrone ring with its phenyl substitutions lends particular reactivity needed for tailored organic synthesis. We see this compound regularly in projects ranging from ligand design, specialty polymers, and advanced materials, to complex molecule construction relevant for pharmaceuticals and agrochemicals.

    Every kilo matters. Costly setbacks often trace back to trace impurities or inconsistent physical characteristics. For this reason, we invest in constant monitoring and incremental improvements to both the synthetic route and purification. The resulting batches stand up to extended moisture-free storage, without caking or discoloration common with lower-quality material.

    This compound’s melting point is typically reported between 118-122°C, indicating both purity and batch predictability during scale-up operations. We also confirm this window with every run, rejecting any lot that strays outside our established threshold. Chromatographic fingerprinting allows for fast detection of any unexpected secondary components, which supports the strict requirements in regulated applications or, equally, in development laboratories concerned with trace side-products.

    How 4,6-Diphenyl-2-Pyrone Compares in the Market

    Through experience, we've seen how even seemingly minor differences in product grade impact synthesis, especially in the context of catalysis or stepwise derivatization. Lower-purity or off-brand 4,6-Diphenyl-2-pyrone variants can carry residual non-aromatic impurities, residual solvents, or incomplete phenyl substitution, all of which risk introducing side reactions or lowering catalyst lifespans.

    Quality-minded buyers usually spot these pitfalls after a few disappointing experiments. Even in academic setups where small quantities get the most attention, a half-failed reaction invites lost weeks and resource drain. We believe in ensuring customers don’t waste time troubleshooting raw material quality, so our tight specifications for aromatic content, particle size, and residual acidity mean what ships out performs predictably from the first gram to hundred-kilo lots.

    Many new entrants into the specialty organic market focus on lowering headline price, sometimes by reworking side-streams from unrelated production campaigns. We have tested some of these alternatives and found higher levels of tars, discolored organics, and batch-to-batch differences that cause problems down the line. By keeping our production line dedicated for our intermediate-grade and research-grade outputs, we prevent contamination risks found in less controlled setups.

    Sourcing and Sustainability

    Cost pressure across advanced chemicals always looms. Rather than chasing temporary shortcuts, we focus on sourcing starting materials that are traceable, free from restricted or conflict origins, and sustainably managed wherever possible. Any process that generates persistent or hazardous byproducts goes through continuous review—by maximizing recovery and target yield, we've cut both cost and waste volume over the last decade.

    Increasingly, clients ask about the embedded environmental impact of their materials. For 4,6-Diphenyl-2-pyrone, we've re-engineered solvents out of some steps and moved to closed-loop purifications, reducing both emissions and workplace exposure. Investment in energy-reuse and in-plant water purification contribute to this product’s lower waste profile, and we share analysis where customers need to complete their own regulatory or life-cycle assessments.

    The Role of 4,6-Diphenyl-2-Pyrone in Project Success

    Chemists using this building block often tackle difficult target molecules or pursue novel structures with stringent downstream analysis. Whether a customer focuses on new material design, pharmaceutical leads, or catalyst development, success grows from consistency. The 4,6-Diphenyl substitution offers opportunities for both stability and reactivity, supporting both robust scale-up and subtle reactivity tuning.

    Feedback informs new process upgrades each year. For instance, reports of mid-reaction discoloration or trace byproduct formation led us to scrutinize trace impurity profiles in even longer-run purifications. As a result, current process controls minimize potential coupling or hydrolysis side-reactions, not just for the main structure but for those customers pushing the edge of what the molecule can do.

    Some of the most compelling results our collaboration helped achieve have come in advanced drug discovery, where new candidates require not only high-purity core structures but also tight batch consistency for regulatory submission. Incorrect stereochemistry or an unidentified byproduct at 0.2% can derail a full submission package. So, we never ship before comprehensive in-lot analytics resolve within our stricter standards than accepted reference grades.

    Handling, Packaging, and User Experience

    No lab wants to deal with unusable material. To combat common problems, we use moisture- and air-resistant container systems to avoid clumping and reactivity loss. Each package ships with its own lot code, analytics summary, and documented handling recommendations based on our active experience with stability and reactivity.

    Packaging sizes suit a range of users, from gram-scale bench trials up to multi-kilo production. The crystalline solid form resists abrasion and forms stable solutions in typical polar and non-polar organic solvents, so loading into reactors or prepping for isolation steps becomes less labor-intensive than working with similar but more hygroscopic pyrone derivatives.

    Convenience improvements grow out of direct feedback. Several major polymer labs suggested alternate lid types or liner formulations, so we now offer options targeted toward inert-process environments. Clear date-of-manufacture and retention of reserve samples further supports users who may need to compare results over long-term or parallel studies.

    4,6-Diphenyl-2-Pyrone’s Distinguishing Features

    While other pyrone derivatives fill certain roles, this compound holds advantages for both reactivity and product stability. For example, the phenyl groups at the 4 and 6 positions stabilize the core ring and limit unwanted reactivity with electrophiles in pathway steps common in organic transformations. In contrast, alternatives with alkyl groups or replacement at other ring positions often exhibit less thermal stability or greater byproduct formation during multi-step synthesis.

    We have compared performance of similar pyrone products and found 4,6-Diphenyl-2-pyrone outperforms in several key scenarios. In Suzuki-Miyaura couplings or Knoevenagel reactions, the predictable behavior and high melting point create less margin for error—sensitive intermediates and target molecules emerge with higher yield and fewer chromatographic challenges. Its aromaticity and steric profile bring value where selectivity matters, and that extends the reach in novel material or pharmaceutical applications.

    A recurring point from our experience: while high-end competitors may offer results close to ours, gray-market or unvetted sources have never equaled our standards. As a result, our customers continue to request documentation and even samples for comparative studies, reinforcing our approach to verified analytics and transparent sourcing.

    Supporting Your Chemistry: Direct Manufacturer’s Perspective

    As direct producers—not traders or middlemen—we experience firsthand how production scale changes the way you control quality and manage risk. Outsourcing or losing supervision over critical steps can invite variability, especially in batches designed for specialty chemical, pharmaceutical, or material science use. By retaining every step under our own roof, we avoid the pitfalls and delays typical of brokered or relabeled materials, ensuring that you always get a result that matches your project’s requirements.

    From academic labs exploring new pathways, to startups in the materials field, to established contract manufacturers, our philosophy stays consistent: get quality right from the start, confirm every batch with robust analytics, and address real-world production feedback as it comes. This is not an abstract claim—each customer call about reaction outcomes, each request for detailed analytics, and each piece of constructive criticism shapes how we deliver next-generation 4,6-Diphenyl-2-pyrone to fit evolving demands.

    Advanced projects often demand rapid response and unique packaging or analytics solutions. By owning the production chain, we stay flexible to these requests, whether supplying a novel crystalline form, handling regulatory documentation, or offering detailed impurity profiling for audits. Our direct engagement with both bench chemists and industrial process engineers keeps our focus sharp—not just delivering a molecule, but supporting its use from the beaker to commercial scale.

    Continuous Improvement and Collaborative Progress

    Supply only represents half the relationship. For every batch of 4,6-Diphenyl-2-pyrone we produce, customer feedback extends a learning loop that drives future improvements—whether a new purification step to deal with micro-impurities or shifting packaging needs as applications evolve. Over years of collaboration, shared insights reveal new application spaces, from advanced coatings to electronic components, and each improvement returns value both to us and our partners.

    Many improvements come from long-term relationships rather than one-off transactions. For example, a specialty pharma company’s novel use of 4,6-Diphenyl-2-pyrone in custom fragment-based libraries led us to adjust both process parameters and analytics outreach. This cycle—producer and end-user learning in parallel—creates benefits for both, improving future runs and cementing shared progress.

    Our ongoing investment in process analytics—upgrading to more sensitive NMR, automating impurity detection, refining drying times—grew out of watching competitors stall at legacy process limits. By doubling down on innovation, we grant our customers earlier access to next-generation material grades and a clearer window into what to expect on delivery.

    Commitment to Transparent Communication

    Clear information shapes project outcomes. As seasoned chemists ourselves, we aim to maintain straightforward lines of communication: real analytics, honest feedback, and complete transparency on every lot shipped. Each customer gains access to our in-house team—real people with hands-on experience navigating the ups and downs of organic synthesis. The trust we build by showing our process, sharing batch analytics unprompted, or documenting rare anomalies forms the basis of long-term, mutually beneficial business relationships.

    Sourcing 4,6-Diphenyl-2-pyrone directly from a dedicated manufacturer brings users into this loop, bypassing uncertainties often present with generic supply chains. Every gram reflects the shared commitment of our team to chemical integrity, logistical reliability, and real-world applicability for forward-looking chemists and process engineers.

    We share all pertinent information found through our own internal quality testing, and partner closely with regulatory and safety professionals to ensure that every delivery meets and exceeds the necessary standards without adding unnecessary red tape or delay.

    Encouraging Responsible and Efficient Use

    Our long-term customers understand the value of material used with respect—no shortcuts or hidden variables, but a clear path from compound to application. 4,6-Diphenyl-2-pyrone offers both the reliability of a well-studied structure and the practical handling that supports both established processes and new discovery, whether in pharmaceuticals, advanced materials, or specialized reagents.

    Downstream productivity often owes as much to reliable input material as it does to clever chemical engineering. The features that set our product apart—tight control over synthesis, careful purification, and clear, customer-facing documentation—help your process avoid roadblocks. This mindset grew out of our own frustrations with unreliable supply; now, every batch reinforces a track record built on direct experience, rather than marketing claims or generic assurances.

    As industry demands continue to evolve and new applications for 4,6-Diphenyl-2-pyrone emerge, our commitment remains the same: to deliver quality rooted in real expertise, guided by practical needs, and shaped by the open dialogue between chemist and manufacturer.

    Invitation for Collaboration

    We engage deeply with every inquiry—whether from a pioneering startup, an established lab seeking improved yields, or a materials developer looking for robust intermediates. Our best process upgrades and product enhancements grow from active collaboration, critical feedback, and real engagement with the tough challenges that chemists face every day.

    With every kilo of 4,6-Diphenyl-2-pyrone produced and delivered, we renew our promise: to be a partner in progress, not just a supplier, and to ensure your workflow, discovery, or development benefits from hard-earned experience and a relentless focus on quality.