Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Di-2-Pyridyl Thionocarbonate

    • Product Name Di-2-Pyridyl Thionocarbonate
    • Alias DPT
    • Einecs EINECS 247-302-6
    • 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

    665347

    Product Name Di-2-Pyridyl Thionocarbonate
    Cas Number 2524-64-3
    Molecular Formula C11H8N2OS2
    Molecular Weight 248.33 g/mol
    Appearance Yellow crystalline solid
    Melting Point 61-64°C
    Boiling Point Decomposes before boiling
    Solubility Soluble in organic solvents like dichloromethane and ethanol
    Storage Temperature 2-8°C
    Purity >98%
    Synonyms 2,2'-Dipyridyl thionocarbonate
    Density 1.37 g/cm³
    Smiles C1=CC=NC(=C1)OC(=S)OC2=CC=CC=N2
    Hazard Statements Harmful if swallowed; Causes skin and eye irritation

    As an accredited Di-2-Pyridyl Thionocarbonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Di-2-Pyridyl Thionocarbonate, 5 grams, is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping Di-2-Pyridyl Thionocarbonate is shipped in tightly sealed containers under inert atmosphere conditions to prevent degradation. It should be kept cool, dry, and away from light. Proper labeling is ensured, and transport complies with relevant hazardous material regulations. Shipping is typically done via ground or air, following chemical safety guidelines.
    Storage Di-2-Pyridyl Thionocarbonate should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep it away from sources of ignition, incompatible substances such as strong oxidizing agents, and direct sunlight. Store at room temperature (15–25°C) and handle under inert atmosphere if prolonged storage or high purity is required.
    Application of Di-2-Pyridyl Thionocarbonate

    Applications of Di-2-Pyridyl Thionocarbonate in Industrial Manufacturing

    Di-2-pyridyl thionocarbonate finds targeted use in key industrial sectors as a thiolating and activating agent. Its unique reactivity profile supports specialized transformations, crucial for protocols where selectivity and efficiency are critical. The following sections detail its primary downstream applications in industrial chemistry and manufacturing.

    1. Peptide and Oligonucleotide Synthesis

    Chemical manufacturing of peptides and oligonucleotides utilizes di-2-pyridyl thionocarbonate for the preparation of activated esters, particularly in stepwise thiol coupling and N-terminal thiol protection strategies. The reagent provides precise control for introducing thiol groups to amino acid residues or oligonucleotide backbones, enabling site-specific modification under mild conditions required for sensitive bioactive molecules. Manufacturing procedures demand consistent purity and reactivity to meet pharmaceutical and biotechnological requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP <797> Pharmaceutical Compounding—Sterile Preparations
    • European Pharmacopoeia monographs on peptide APIs
    • ISO 9001:2015 for chemical synthesis process quality

    Typical usage ratio

    • 0.95–1.2 molar equivalents per amino acid/oligonucleotide residue, adjusted by desired thiol functionalization scope

    Downstream process integration

    • Added during resin-bound or solution-phase coupling steps following complete deprotection
    • Employed directly in the activation tank; downstream purification removes by-products
    • Integrated at the side-chain derivatization stage for modified oligonucleotide therapeutics

    Final product types

    • Pharmaceutical-grade peptides for injectables
    • Antisense DNA and RNA oligonucleotides
    • Peptide-drug conjugates (PDCs)
    • Custom research oligonucleotides

    2. Small Molecule API Thiolation

    The compound serves as a key reagent in the synthesis of sulfur-containing small molecule active pharmaceutical ingredients. It enables the targeted conversion of alcohols and amines into thio-esters, facilitating the construction of C–S bonds required in a range of API scaffolds. Controlled addition and reproducible conversion are critical to process yield and regulatory compliance for APIs destined for regulated markets.

    Industry compliance standards

    • FDA 21 CFR Part 211—Current Good Manufacturing Practice for Finished Pharmaceuticals
    • ICH Q11 Development and Manufacture of Drug Substances
    • EU GMP Volume 4 Annex 1 on Sterile Drug Manufacture

    Typical usage ratio

    • 1.1–1.5 equivalents relative to alcohol or amine substrate; adjustment based on substrate reactivity and scale-up batch size

    Downstream process integration

    • Charged directly into C–H to C–S bond-forming stages following precursor activation
    • Incorporated during intermediate transformation in API route
    • By-products isolated in first-stage downstream separation, ensuring purification before crystallization

    Final product types

    • Thioester and thioamide-based APIs
    • Precursor intermediates for antihypertensive drugs
    • Antiviral pharmaceutical actives with sulfur linkage

    3. Bioconjugation for Protein Engineering

    Site-selective protein labeling for diagnostic, research, or therapeutic conjugates relies on di-2-pyridyl thionocarbonate for modification of cysteine residues. The reagent generates activated thiols under mild aqueous conditions, preserving protein conformation and activity during conjugation. This specificity is integral to scalable processes that provide high-performance biomolecular tools suitable for regulated laboratory and clinical applications.

    Industry compliance standards

    • ISO 13485:2016 for production of medical devices and diagnostic reagents
    • USP <1047> Testing for Biologics
    • EN ISO 14644-1 for controlled environments (cleanroom integration)

    Typical usage ratio

    • 0.9–1.3 equivalents per accessible cysteine residue on the protein, titrated by on-site reactivity and product functionalization needs

    Downstream process integration

    • Applied during protein modification prior to antibody-drug conjugation
    • Used in solution immediately following protein purification and buffer exchange
    • Integrated in-line with UV–Vis QC checkpoints for thiol content verification

    Final product types

    • Antibody-drug and protein-polymer conjugates
    • Enzyme functionalization for biosensor manufacturing
    • Labeled diagnostic antibodies
    • Research-grade protein standards

    4. Chemical Synthesis of Polymer Crosslinkers

    Industrial production of specialty polymers, including hydrogel and elastomer crosslinking agents, applies di-2-pyridyl thionocarbonate during the creation of active thiol and dithiol building blocks. It acts as a selective conversion reagent, efficiently transforming diols into dithiols under anhydrous conditions for further reaction with acrylates, urethanes, or maleimides. Careful process control ensures low impurity profiles, essential for performance polymers used in regulated environments.

    Industry compliance standards

    • REACH Regulation EC 1907/2006 for registration and handling of raw chemicals
    • ISO 14001 for environmental management during synthesis
    • ASTM D638 polymer testing protocols

    Typical usage ratio

    • 1.0–1.5 equivalents per hydroxyl group on precursor polymer backbone, adjusted by degree of crosslinking required in final product

    Downstream process integration

    • Fed into batch or continuous reactors immediately prior to dithiol formation
    • By-products removed in solvent extraction prior to downstream polymerization or molding
    • Integrated within dedicated hazardous process containment systems

    Final product types

    • Dithiol-based crosslinkers for hydrogels
    • Biomedical elastomer additives
    • Conductive polymer intermediates
    • Adhesive system crosslinking agents

    5. Synthesis of Chelating Ligands for Metal Recovery

    Producers of specialty ligands for hydrometallurgical recovery of precious and base metals deploy di-2-pyridyl thionocarbonate in the construction of pyridyl-based sulfur ligands. This use supports highly selective ligand frameworks, which coordinate efficiently with gold, palladium, or platinum during ore processing and waste recycling. Manufacturing maintains strict batch traceability to meet the purity and stability requirements for large-scale metal extraction operations.

    Industry compliance standards

    • ISO 9001:2015 quality assurance for ligand manufacturing
    • ISO 14001 for environmental and waste management in metal recovery
    • OECD Guidelines for Testing of Chemicals 107, 117 (partition coefficients)

    Typical usage ratio

    • 1.0–1.4 equivalents relative to the pyridyl precursor; optimization based on target ligand chelation strength

    Downstream process integration

    • Added during ligand functional group introduction post-pyridine framework assembly
    • Employed prior to metal salt exposure in ligand synthesis reactors
    • By-products separated using liquid–liquid extraction for purity assurance

    Final product types

    • Thiopyridyl-metal chelating agents for gold recovery
    • Ligands used in platinum group metal recycling
    • Metal extraction reagents for hydrometallurgy
    • Chemical kits for laboratory precious metal separation
    Free Quote

    Competitive Di-2-Pyridyl Thionocarbonate prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Di-2-Pyridyl Thionocarbonate: Bringing Precision to Thiocarbonyl Applications

    Experience from the Factory Floor

    Making Di-2-Pyridyl Thionocarbonate, which some call DPTC or 2,2'-Dipyridyl Thionocarbonate, starts with a purpose that goes beyond the batch. Our process comes from hands-on adjustments, close attention to raw material purity, and the willingness to refine step-by-step. We see the finished powder as the result of real people giving care to crystallization, drying, and packaging. Each run reflects what our team has learned about keeping particles dry, reducing byproduct formation, and controlling storage environments. This direct experience shapes how we meet the needs of research labs and specialty manufacturers using DPTC for its unique thionocarbonyl reactivity.

    What Sets Di-2-Pyridyl Thionocarbonate Apart

    Inside its flasks and reactors, DPTC shows its real value by balancing reactivity without causing wild side reactions. Many people approach us after running into messy purifications or disappointing conversions with other thionocarbonates. Di-2-Pyridyl Thionocarbonate stands out because its leaving groups—2-pyridyl units—tend not to produce hard-to-remove residues in downstream steps. You won’t smell sulfur lingering on glassware for days. Handling several other thionocarbonate types, we often see sticky intermediates or slow, incomplete reactions. We pick DPTC for projects needing clear, crisp endpoint detection.

    Model and Specifications Built on Practice

    The most requested grade comes as a fine, almost white to pale yellow crystalline powder. Our facilities supply this product with routinely measured purity above 98 percent by HPLC and NMR, reflecting knowledge gained from batch-to-batch QC. Through working hands-on with DPTC, we found moisture to be its greatest enemy. We tackled this with vacuum drying chambers, disposable liners, nitrogen-purged filling, and monitoring every seal. Average particle size measures between 120 to 300 microns because too fine can dust up, while larger granules slow reaction rates. Chemical formula, C11H8N2OS2, is never just a textbook fact to us—it's routine calibration, sacrosanct weighing standards, and the quiet satisfaction of ship-out labels hand-checked by the blenders themselves.

    Practical Uses—Real Chemistry, Real Solutions

    Every season, we supply DPTC for a surprising range of projects. At universities, researchers depend on smooth conversion to thioesters, often preparing activated esters to modify peptides or nucleotides. In process development, our clients use it to couple carboxylic acids with amines under mild conditions. Others find it invaluable for activating thiols without introducing heavy odors or troublesome halide salts. From our vantage point, success in these applications stems from consistent reactivity and bench-top handling safety. We've seen how DPTC blends seamlessly in automated peptide synthesizers and small-scale manufacturing skids, outperforming benzyl, phenyl, and traditional alkyl thionocarbonates where selectivity or ease of purification can make or break a production run.

    Understanding the Limitations—and Getting Ahead

    As with anything on the high bench, Di-2-Pyridyl Thionocarbonate comes with limits. Iron and copper sensitivity, for instance, cannot be ignored. Over the past years, we worked with several chemists running ligation or cyclization reactions—sometimes a change in glassware or magnetic stirrer grade made all the difference. Reactions in water or with excess base can strip out pyridyl units, so we've developed packaging recommendations and advice for customers facing stability challenges. These practical insights help every shipment reach its target lab with as little decomposition as possible.

    Comparisons: DPTC Versus Other Thionocarbonates

    Most of our product research comes from customers eager to compare DPTC with traditional alternatives like S-phenyl or S-benzyl thionocarbonates, CS2-derived agents, and acyl chlorides. The consistent issue: these tend to be more aggressive, less selective, or worse to clean up. Di-2-Pyridyl Thionocarbonate wins out by balancing high conversion rates with the ability to choose milder reaction setups, such as room temperature amidation in DMF or DCM. Years of running comparative tests revealed that residual byproduct management gets less troublesome with DPTC—the 2-pyridyl leaving group dissolves away and can usually be washed out in aqueous workups. In one pharmaceutical client’s scale-up, purification time dropped by nearly half, greatly due to the cleaner side-product profile.

    Batch-to-Batch Consistency: What Experience Teaches

    We’ve ground through more than a hundred runs, watching for shifts in melting point, IR signatures, and TLC performance. Small shifts in heating rate during thionation or awkward solvent carryovers have taught us to tweak not only the process, but also how we schedule maintenance and raw material testing. Trace sulfuric acid from improper thionation costs us time and washes. Real-world labwork shaped our methods, including the way we respond to summer humidity or winter static. Shipment delays, if any, nearly always come back to a careful technician spotting a borderline dryness or shift of color.

    Ensuring Purity and Handling Safety

    Pure DPTC’s stability can deceive. Years of bench work have taught us that any exposure to damp air can provoke unnoticed decomposition, leaving a faintly brown tinge or off-odors. We stress double-sealing and encourage immediate transfer to desiccated storage upon arrival. For safety, we’ve structured our operational checklists around reducing direct skin contact, ensuring only ventilated workspaces are used, and keeping pre-weighed aliquots handy to avoid open scooping. Eye and respiratory protection have stopped minor complaints from becoming bigger issues, particularly in busy labs or pilot plants running multiple reactions at once.

    The Role of DPTC in Modern R&D

    Organic synthesis has changed—streamlined high-throughput workflows and automation now dominate many labs. Di-2-Pyridyl Thionocarbonate is now a fixture in these workflows where predictable reactivity means fewer failed runs and less wasted time. One example stands out: scale-up chemists report more reproducible peptide modifications, without a heavy burden of downstream resin washing. Academic groups have told us about creative routes to thioesters and modified natural products using our product, sidestepping awkward protection and deprotection sequences common with older thionating agents.

    Choosing DPTC: Real Economic and Environmental Gains

    From the shop floor to outgoing quality checks, reducing solvent and energy waste guides our process choices. Di-2-Pyridyl Thionocarbonate fits well in this landscape because it often eliminates the need for halogenated or strongly basic reaction media, saving on both hazardous waste disposal and the cost of complex neutralization. In our own practice, we've trimmed solvent use by 30 percent over five years, driven in part by the ease and cleanliness of workups with DPTC reactions. These direct operational savings matter to every chemical plant manager and lab supervisor.

    Responding to Customer Feedback: Process Improvements

    Real interactions with synthetic chemists have motivated every process tweak we make. One frequent engineer complaint revolved around static buildup in winter, which we answered by switching to anti-static liners and enhanced grounding for our powder funnels. Requests for tighter particle size range led us to invest in new screening mesh and in-line sensors, allowing better batch segregation and more repeatable dissolution rates. Several researchers in peptide modification pushed for documentation explaining how to avoid overactivation—our team worked up detailed guidelines based on reaction logs and customer reports, not just datasheet copy.

    Environmental Considerations and Our Approach

    Waste minimization stands as an ongoing challenge. Some thionating agents require heavy metal cleanups or produce persistent sulfur byproducts. We keep an eye on effluent profiles and work with outside recycling specialists to reduce the environmental impact of DPTC manufacture. By tuning reaction times and keeping our synthesis solvent choices toward green chemistry guidelines, we support both our partners’ compliance and our own site’s long-term sustainability. Efforts toward aqueous recovery and inert atmosphere handling have already reduced our sulfur waste per kilo produced by almost a quarter in the last three years.

    Supporting Advanced Research: The Frontlines of Drug Discovery and Materials Science

    Several major advances in small molecule and peptide chemistry have leaned on Di-2-Pyridyl Thionocarbonate. Collaborations with university teams led to improved ligation steps for bioactive compounds. We’ve watched how newer trends in linker technology, including cleavable bifunctional reagents, draw on DPTC’s reliable leaving group behavior. These partnerships result in peer-reviewed publications and real protocols, validated by our product, giving both sides confidence to share exact quantities, procedures, and troubleshooting measures. Over time, this mutual effort helps move new syntheses out of theory and into scalable processes ready for pilot line-up.

    Meeting Regulatory and Quality Expectations

    In producing DPTC, standards count for more than just certificates. Our in-house quality team routinely calibrates HPLC, checks glassware cleaning logs, and reviews analytical records from each shipment. We stay informed on any updates to REACH and US EPA guidelines regarding pyridine derivatives, ready to adjust documentation as needed. Maintaining a residue-free work area and respecting proper erosion-resistant materials for thionation are lessons learned from years of compliance audits and customer feedback. Each step in our workflow reflects this shared responsibility.

    Real Lessons from Scale-Up and Technology Transfer

    Tech transfer provides a learning curve few academic papers cover. Occasional missteps, like solvent incompatibility or poorly chosen coupling bases, have guided our support for customers tackling multi-kilogram orders. By walking through exact process steps, we translate hard-won lab experience into detailed suggestions—borrowing from both our chemical engineers and QC chemists. Site visits and remote troubleshooting build face-to-face trust that no manual or product spec can replace. In reality, the difference between a successful pilot lot and a costly failure nearly always comes down to adapting the know-how of those making the compound every day.

    Industry Perspective: Why Di-2-Pyridyl Thionocarbonate Matters Now

    The landscape for specialty synthons keeps shifting. Green chemistry, stricter regulatory demands, and a focus on cost efficiency intersect most clearly in how advanced reagents like DPTC are produced and used. We see the pressure customers face to finish projects quickly, document every variable, and maintain tight batch-to-batch consistency. Our commitment lies in bringing the experience of hands-on operators, shift leads, and technical support teams together. The result is a product that delivers not just in textbook conversions but also in the daily workflow of people constantly pushing the boundaries of synthetic chemistry.

    Customer Problem-Solving: Stories from the Bench

    No two customers come to us with identical issues. One biotech group kept losing product yield until we walked them through in-situ monitoring to confirm full conversion. Another pharmaceutical client emailed us pictures of strange off-colors, quickly traced back to an air leak in their old glovebox. These moments matter, not just for the sale, but for the ongoing relationship—our whole production team learns from these stories. In many cases, solutions come from simple tweaks: changing out a desiccant more frequently, switching to a lower-deadspace scoop, or altering the sequence of reactant addition.

    Integration in Automated and High-Throughput Systems

    Integration specialists in the industry now expect reagents to run cleanly in liquid handling robots or automated batch reactors. Our reliability checks focus on flowability, anti-caking, and real-time spectral verification. We've helped several contract research organizations set up DPTC feeds for high-throughput screening, providing not just the product but also guidance on minimizing carryover and fouling. In our experience, the difference between smooth automation and recurring equipment stoppages often comes down to how the reagent moves, how it responds to humidity, and how quickly it re-dissolves for the next cycle.

    Transparency and Continuous Improvement

    Every feedback call, lot review, and batch record feeds into our drive for steady improvement. We publish process updates, notches in operational efficiency, and changes to handling guidelines based on real problems encountered in the field. Our approach relies on transparency—sharing what works, flagging unresolved issues, and inviting customer participation in troubleshooting. By opening up our process details, we aim to build trust, reduce errors, and help our partners avoid the trial-and-error many of us endured in earlier days of DPTC use.

    The Role of Real-World Expertise

    Manufacturing Di-2-Pyridyl Thionocarbonate demands more than a locked-down recipe. The knowledge in each batch comes from years of tuning reaction conditions, listening to upstream and downstream users, and adjusting workflows as regulations, customer needs, and application trends evolve. Scientists and synthetic teams count on us not just for purity and reliability, but for the practical advice that helps them get the most from each gram of material. Ongoing collaboration constantly pushes both the science and production technology forward.

    A Look Forward: Meeting the Demands of Modern Synthesis

    Future demand for more selective, safer, and less wasteful reagents will keep driving our process improvements and support systems. Advances in peptide chemistry, linker technology, and conjugation strategies for new bioactive compounds all lean on building block reagents like Di-2-Pyridyl Thionocarbonate. Our manufacturing team continues to adapt, sharpening our ability to deliver exactly what advanced researchers and manufacturers expect—season after season, kilogram after kilogram, project after project. This ongoing commitment stems not from indirect knowledge or outside speculation, but from the lived experience of the people who make, test, package, and support this product each day.