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4,6-Diphenylthieno[3,4-D]-1,3-Dioxol-2-One 5,5-Dioxide

    • Product Name 4,6-Diphenylthieno[3,4-D]-1,3-Dioxol-2-One 5,5-Dioxide
    • Alias DP-TDO
    • Einecs 615-011-6
    • 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
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    Specifications

    HS Code

    249132

    Iupac Name 4,6-Diphenylthieno[3,4-d][1,3]dioxol-2-one 5,5-dioxide
    Molecular Formula C16H10O5S
    Molecular Weight 314.31 g/mol
    Cas Number 175137-49-4
    Appearance White to off-white crystalline powder
    Melting Point 210-212°C
    Solubility Slightly soluble in common organic solvents
    Purity Typically >98%
    Boiling Point Decomposes before boiling
    Storage Conditions Store at 2-8°C, in a tightly closed container

    As an accredited 4,6-Diphenylthieno[3,4-D]-1,3-Dioxol-2-One 5,5-Dioxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 1 gram, sealed with a tamper-evident cap, labeled with substance name, CAS, warnings, and storage instructions.
    Shipping **Shipping Description:** 4,6-Diphenylthieno[3,4-d]-1,3-dioxol-2-one 5,5-dioxide is shipped in tightly sealed containers, protected from moisture and light. It should be handled as a laboratory chemical. Package in accordance with local, national, and international regulations, using secondary containment to prevent leaks. Consult the SDS for any specific hazard classifications before shipment.
    Storage **Storage Description:** Store 4,6-Diphenylthieno[3,4-d]-1,3-dioxol-2-one 5,5-dioxide in a tightly sealed container under a dry, inert atmosphere such as nitrogen or argon. Keep in a cool, well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong acids or bases. Recommended storage temperature: 2–8 °C (refrigerator). Handle using standard laboratory personal protective equipment.
    Application of 4,6-Diphenylthieno[3,4-D]-1,3-Dioxol-2-One 5,5-Dioxide

    Applications of 4,6-Diphenylthieno[3,4-D]-1,3-Dioxol-2-One 5,5-Dioxide in Industrial Manufacturing

    As the original manufacturer of 4,6-Diphenylthieno[3,4-D]-1,3-Dioxol-2-One 5,5-Dioxide, we supply this advanced intermediate to a select profile of high-value industrial sectors. Our direct production involvement allows us to support integrators with consistent quality and detailed process guidance. The following sections describe the primary downstream applications based on verified adoption in the chemical, electronics, and specialty polymer industries.

    1. Organic Electronic Materials Synthesis

    Leading developers of organic semiconductors utilize this compound as a high-performance electron-deficient core scaffold in small-molecule organic semiconductors for OTFTs and OLEDs. Its aromatic-rich, rigid planar structure enables predictable charge transport characteristics and morphological stability in finished layers. Leading device manufacturers specify it in synthesis protocols where precise energy level tuning is needed for improved device efficiency and operational lifespan.

    Industry compliance standards

    • IEC 62693:2017 (Organic semiconductor devices and materials)
    • ISO 9001:2015 (Quality management system for electronic materials)
    • RoHS Directive (EU) 2015/863 (on restriction of hazardous substances)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • Monomer loading: 2-15% w/w in organic semiconducting blends, tailored according to target HOMO-LUMO gap and solution viscosity for spin-coating or inkjet deposition.

    Downstream process integration

    • Direct coupling into Suzuki or Stille cross-coupling polymerization as an acceptor unit, with subsequent purification and formulation in high-purity solvent systems, ready for solution-processable electronic material production.

    Final product types

    • Thin-film transistors (OTFTs)
    • Active layers for organic light-emitting diodes (OLEDs)
    • Photodetector arrays

    2. Specialty Functional Polymer Intermediate

    Advanced polymer manufacturers incorporate this dioxol-sulfone derivative during precision polycondensation reactions to create high-glass-transition polymers with improved flame retarding and dielectric properties. The aromatic sulfone-dioxol core enables strict molecular weight control and enhances chain rigidity, addressing the thermal and electrical demands of applications such as flexible printed circuits and advanced wire insulation.

    Industry compliance standards

    • UL 94 (Plastic flammability standard)
    • IEC 60216 (Thermal endurance for electrical insulation)
    • ISO 14001:2015 (Environmental management — for process waste management)
    • REACH Annex XVII (Polymer safety restrictions)

    Typical usage ratio

    • 5–18% by weight in polymer backbone, based on desired Tg increment and dielectric constant requirements; engineering teams adjust based on final film thickness and processing windows.

    Downstream process integration

    • Feeds into step-growth or chain-growth polymerization reactors as a comonomer or cross-linking initiator; formulated after preliminary vacuum-drying and melt-mix compounding for integration into extrusion or casting lines.

    Final product types

    • Flexible copper-clad laminates (FCCL)
    • Insulating sheets for cables and microelectronics
    • Flame-retardant polymer films

    3. High-Performance Photoinitiator Component for UV-Cured Coatings

    Several advanced UV-cured coating manufacturers rely on this sulfone-bridged heterocycle as a functionalized photoinitiator base to impart fast curing depth and minimize yellowing in fiber optic coatings and high-transparency lacquer systems. Its molecular orbital alignment allows direct absorption in deep-UV wavelengths and clean radical release during in-line curing, supporting defect-free surface formation over extended production runs.

    Industry compliance standards

    • ISO 9001:2015 (Quality management — coating manufacture)
    • IEC 60825-1 (Laser safety — if used in fiber optics)
    • EN 71-3 (Migration of certain elements in coatings for toys; relevant for consumer electronics casings)
    • FDA 21 CFR 175.300 (Indirect food additives: resinous and polymeric coatings — for food packaging applications)

    Typical usage ratio

    • 0.2–1.2% w/w in photoinitiator blends; formulated based on desired initiation speed and transparency target, with adjustments during pilot line trialing for optimal surface hardness.

    Downstream process integration

    • Blended in pre-formulation with monomer/oligomer resin systems, then metered into precision UV-curing lines after in-line filtration to support high-throughput roll-to-roll or spray coating operations.

    Final product types

    • UV-cured protective fiber optic coatings
    • Scratch-resistant clear lacquers for consumer electronics
    • Microelectronic conformal coatings

    4. Advanced Battery Electrolyte Additive

    Battery R&D labs and pilot plants adopt this thienodioxol-sulfone as a high-voltage stabilizer and ionic conductivity enhancer in lithium-ion and lithium-polymer battery electrolytes. Its structure allows for increased electrochemical window and improved decomposition resistance, prolonging cell lifespan under repeated charge-discharge cycles, especially in premium consumer and automotive battery pack applications.

    Industry compliance standards

    • IEC 62660-2 (Secondary lithium-ion cells for automotive)
    • UN 38.3 (Transport safety for lithium batteries)
    • ISO 12405-2:2012 (Automotive batteries — safety requirements)
    • Quality management: IATF 16949 (if for automotive series supply)

    Typical usage ratio

    • 0.3–2.0% by weight in nonaqueous solvent-based electrolyte blends; optimized per desired conductivity, temperature range, and cell chemistry during electrolyte formulation trials.

    Downstream process integration

    • Dissolved into solvent-based electrolyte stock under inert atmosphere; introduced prior to electrochemical cell filling and sealed pouch assembly, with QC verification of ionic mobility and voltage window after blending.

    Final product types

    • High-capacity lithium-ion battery cells (prismatic and cylindrical)
    • Automotive-grade power modules
    • Consumer electronics pouch cells
    Free Quote

    Competitive 4,6-Diphenylthieno[3,4-D]-1,3-Dioxol-2-One 5,5-Dioxide prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4,6-Diphenylthieno[3,4-D]-1,3-Dioxol-2-One 5,5-Dioxide: Advancing Synthesis with Confidence

    Direct from an Experienced Chemical Manufacturer

    Each specialty compound brings its own story to the laboratory. Our regular work in deeply aromatic, highly functionalized thiophenes stretches across years of collaboration with both academic research groups and major process developers in the fine chemicals field. Among this range, we produce 4,6-Diphenylthieno[3,4-D]-1,3-dioxol-2-one 5,5-dioxide based on our own bench-tested protocols and scale-ups, listening to chemists who depend on reproducibility and purities no catalog mill can routinely promise.

    There’s a reason why many researchers keep returning to this compound, often called by its researchers’ nickname, 'DPTDO-Dioxide.' Our in-house team synthesizes it from select phenylthiophene intermediates, strictly controlling each reaction stage to avoid unwanted regioisomers or sulfide byproducts. These efforts deliver material with a consistent profile for downstream applications—especially where reliability on batch-to-batch composition governs the viability of entire research or production schedules. This production isn’t a matter of repackaging or trading. We invest in raw material traceability and process analytics because from our perspective as chemists, detail on the ground beats promises from across the globe.

    Why This Molecule Matters

    Chemistry at the core of advanced materials often comes down to unique scaffolds—frameworks that introduce specific electronic, steric, or coupling behaviors. 4,6-Diphenylthieno[3,4-D]-1,3-dioxol-2-one 5,5-dioxide stands out precisely because of the way its structure supports further development in the fields of organic electronics, photonics, and synthetic intermediates. DPTDO-Dioxide’s thieno-dioxol linkage, flanked by diphenyl rings, introduces both rigidity and electron-rich characteristics distinct from simpler thiophenes or unmodified dioxolones.

    Within our own development groups, the molecule has shown stable handling in air, solid-state stability, and reliable solubility in a range of organic solvents frequently used in coupling, oxidative cyclization, and advanced functionalization reactions. The sulfone groups at the 5,5-positions add oxidative resistance, stabilizing the core against degradation routes commonly encountered during high-yielding reactions or under light and air exposure. Chemists looking to build upon its aromatic core gain access to new reactivity patterns—especially those who find other thieno-dioxol analogs too labile or poorly constructed for demanding transformations. We routinely collaborate with synthetic teams focused on next-generation OLED emitters, field-effect transistor prototypes, and tailored heterocycle systems, fielding detailed questions based on real experience.

    Specifications Grounded in Real Practice

    Every batch pulls from the same rigor. Our usual product specification mirrors what we see as practical minimums for real chemistry, not advertising talk. Typical DPTDO-Dioxide shipped from our labs comes at greater than 98 percent purity by HPLC, with batch-to-batch compositional consistency supported by NMR, MS, and when required, elemental analysis. Customers working in sensitive research often request additional analytics like residual solvent checks, and we run those as needed, because our crew understands confidence doesn’t stem from generic COAs. Material arrives as a white to pale beige crystalline solid, always sealed under inert atmosphere if it’s requested, since some labs have strict requirements on trace moisture pickup and we know how quickly open containers in a busy hood can turn a trackable experiment into a guessing game.

    On solubility: DPTDO-Dioxide dissolves efficiently in dichloromethane, chloroform, and benzene derivatives, as well as many advanced aromatic solvents. We’ve watched multiple users attempt reactions with other analogs, only to fight with poor dissolution or rapid decomposition. In our material, both crystals and powder maintain shelf stability over months in standard lab storage, which lets teams plan purchases and usage within longer research cycles. Handling temperatures don’t require deep freeze, making inventory management simpler for labs pressed for cold storage space. Routine shipments for kilogram-scale demand support synthesis in both pilot and small production settings, while our research packs target academia and development chemists trying out new project ideas.

    Usage: Application-Ready, Batch-Tested

    Use cases for DPTDO-Dioxide arise across application-heavy sectors. Electronics developers often look for precisely these fused, oxidized thiophene backbones to seed new donor-acceptor compounds. Teams designing blue- or green-emitting organic semiconductors return often to DPTDO because its rigid π-system anchors emission profiles and supports ligand effects not accessible through plainer heterocycles. In field-effect transistor development, the compound’s oxidative stability improves device longevity and power cycling performance. We've watched customers in this arena switch from less robust or poorly defined aromatic systems to our DPTDO-Dioxide once characterizations pointed toward batch traces or breakdown products complicating device readout or reliability.

    Chemical synthesis groups leverage DPTDO-Dioxide in multi-step routes requiring controlled ring closures, selective oxidations, or as a building block for even more functionalized cores. The embedded sulfone motif activates the ring for further manipulation—directing groups attach easily using established protocols, while electron distribution around the core enables regioselective reactions. Several teams we’ve worked with report ease of purification in intermediates built around our product. This has often removed bottlenecks associated with impure starting points, letting them focus research time on target molecule design rather than repeated QA cycles. As always, process chemists benefit most when supply lines stretch directly to working manufacturers, so missteps in scaling up never turn into long procurement delays.

    Setting It Apart from Other Products

    We hear direct comparisons in nearly every call or email inquiry. DPTDO-Dioxide brings practical differences versus more common or accessible thiophene intermediates. At a chemical structure level, simply adding a phenyl group to a base thiophene, or oxidizing a dioxol monomer, doesn’t reproduce the regioselectivity and electronic character engineered into the 4,6-diphenylthieno-dioxol core. Some suppliers claim substitutions of 4,6 positions or employ different protecting groups, but over time our partners in research return to this precise architecture. We've worked with specialty electronics labs who’ve tried mixtures of isomeric diphenylthieno dioxolones sourced from traders or catalogue aggregators, but poorly controlled synthesis typically introduces unpredictable impurities—often at levels low enough to evade quick analytical checks but high enough to impact sensitive device fabrication or mechanistic investigations.

    Quality hinges on more than a pretty spectrum. Our DPTDO-Dioxide has little overlap with the handling issues plaguing fused thiophene dioxolones that carry less steric bulk at the periphery and those with reduced oxidation states. The 5,5-dioxide allows for higher oxidative compatibility, so end-users looking for functional group tolerance during late-stage derivatization see fewer unwanted reduction or degradation routes. Out-of-house, some teams have encountered byproduct-prone analogs, which slow down progress, especially when working out the fine chemical scale-up necessary for preliminary manufacturing runs or for regulatory submissions. In our experience, few substitutes achieve the same union of oxidative robustness and manageable reactivity. It’s why we stick with this synthesis and invest time in process improvements rather than searching for shortcuts through analogs or blends.

    Behind the Scenes: Our Production Line Realities

    Stepping inside our facility, the practicalities of DPTDO-Dioxide production tie in closely with seasoned chemical manufacturing know-how. Controlling synthesis from the first step—where we'd introduce a phenylthiophene precursor—lets us head off issues with unwanted side products. Over the years, in-house specialists fine-tuned temperature holds, catalyst levels, and quench points not only to maximize yield, but to pin composition within a reliable analytical envelope. Down the line, advanced chromatographic purification strips out micro-level contaminants, a move that saves our customers from time-consuming clean-up. Most batches undergo in-line QC sampling, assisted by real experience in separating meaningful signals from noise. For new application partners who want to run pilot-scale syntheses, our technical staff walk through pre-shipment sample QC, ensuring material meets established specs before it ever leaves our dock.

    Our team counts practical supply chain lessons among our most valued resources. The market offers ways to skirt around full transparency, buying through backchannels or reselling bulk discharge from uncertain origins. We never take this route; materials are sourced from primary producers with certification trails logged from factory entry to synthetic endpoint. Batch numbers connect right back into our electronic batch record system, and every deviation or learning trick gets added to our internal procedures. Because we own the process end-to-end, we’ve eliminated finger-pointing if something in handling or shipping goes off standard.

    Collaborative Support for Research and Production Groups

    Our network of academic and industrial partners often reaches out for protocol recommendations, usage notes, or observations gleaned from failures. DPTDO-Dioxide proves itself repeatedly in feedback loops with development chemists. Once, a research group encountered a persistent yellow cast in one batch of crystals, which unexpected trace moisture on incoming raw materials caused. Our QC traced the issue swiftly and tightened the drying controls. The next run came out as expected, and the incident now shapes our standard monitoring at every critical stage. We encourage direct feedback on handling, as candid reports from the field help us joint-tune both our own practice and the information we share with future users.

    Device chemists, in particular, benefit from our transparency in composition and recommended handling conditions. The crystal habit and solubility profile, together with instructions carried forward from past collaboration, help incoming teams avoid missteps early in their project’s lifespan. Longer-term production customers—often working toward submission batches for scale-up or regulatory milestones—trust us to answer nuanced requests. Whether it's arranging split deliveries, producing additional batch reserves, or adjusting packaging to fit semi-automated dispensing, the on-the-ground experience of our production staff keeps delays and material waste to a minimum.

    Challenges and Our Commitment to Improvement

    Scaling high-functionality aromatics like DPTDO-Dioxide is not without obstacles. Raw material disruptions, regulatory changes, and the evolving expectations of our end users mean we reevaluate sources, documentation, and safety tracking on an ongoing basis. Fluctuations in cost or availability never show up in shipped material because we buffer inventories based on rolling forecasts and keep safety stock close at hand, even when market pressure suggests otherwise. Several of our clients have remarked on the difference this approach makes during periods of market tightness; hopes for uninterrupted R&D hinge on more than a promise made at order time.

    Our commitment includes waste minimization, both due to growing regulatory pushes and through practical economic reasoning. Over the last few years, we’ve steadily reduced solvent waste and increased yield consistency through continuous review of reaction sequences. Our chemists feed real-world data back into process improvements; every time we log a higher-yielding modification or a safer substitution, that knowledge becomes part of our manufacturing playbook. Partners with green chemistry goals find honest engagement in discussions—our data on process mass intensity, residual solvent use, and options for post-reaction distillate recovery derive from shop-floor records, not wishful accounting.

    Looking to Future Applications and Material Innovations

    Research never stays still. Our own efforts to characterize, improve, and create new functional molecules often spring from pressing customer questions about untried modifications or next-generation targets structurally related to DPTDO-Dioxide. Teams exploring extended π-systems, ladder polymers, or chiral auxiliaries ask us how to adjust the phenyl or dioxolone components for fine-tuned functionality. Our experience gives us a head start on evaluating stability changes, new solubility patterns, and even scale-up bottlenecks that come from introducing further functional groups. We keep up with new literature—and often participate in early pilot runs with labs taking the first shots at application chemistries beyond traditional electronics or intermediates work.

    One growth area points toward improved photostability—key for both organic imaging and advanced thin film deposition. Researchers have returned with data showing DPTDO-Dioxide’s resilience under high-energy irradiation, citing higher device yields and longer function times. Others have probed the defense DPTDO’s sulfone backbone offers against ambient degradation in open-loop applications, helping cut maintenance and replacement schedules in emerging flexible device formats. In these applications, our sale doesn’t mark an endpoint. We stay on-hand, adjusting supply and composition to support new experimental ground being broken, helping keep promising projects on a timeline that meshes with international conference presentations, grant reporting, and patentable innovations.

    Summary: What Sets Our DPTDO-Dioxide Apart

    Our daily work blends science, process management, and fundamental respect for the needs of hard-working chemists. 4,6-Diphenylthieno[3,4-D]-1,3-dioxol-2-one 5,5-dioxide leaves our facility in ready-to-work form not because we follow someone else’s formula, but because we build our own on the feedback and results of dozens of real labs, pilot facilities, and production crews. Every feature, from purity levels to packaging, reflects continual dialogue with those who use the compound in devices, reactions, or as the lead compound in difficult syntheses. We bring not only a molecule, but our commitment to traceable quality, real-time support, and honest disclosure—grounded in the sort of experience you miss buying from traders or resellers. DPTDO-Dioxide means advancing chemistry, not fussing over sourcing uncertainties or unreproducible batches. For those pushing the frontier of organic synthesis or advanced materials, these qualities underpin genuine, ongoing progress.