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HS Code |
272590 |
| Iupac Name | 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide |
| Molecular Formula | C10H8N2O4S2 |
| Molecular Weight | 284.31 g/mol |
| Cas Number | 54359-40-9 |
| Appearance | White to off-white solid |
| Melting Point | 216-218 °C |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
| Smiles | O=S1(=O)C=CC=CN1SSC2=NC=CC=S2(=O)=O |
As an accredited 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 10 grams of 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide, labeled with hazard pictograms and product information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely palletized 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide, shrink-wrapped, moisture-protected, with proper chemical labeling and documentation. |
| Shipping | **Shipping Description:** 2,2'-Disulfanediylbis(pyridine) 1,1'-dioxide is shipped in tightly sealed containers to prevent moisture ingress and exposure to air. The chemical should be kept cool, dry, and away from incompatible substances. Handle with care according to standard laboratory chemical transport guidelines. Appropriate hazard labeling is required. Transport may be regulated depending on local rules. |
| Storage | 2,2'-Disulfanediylbis(pyridine) 1,1'-dioxide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong acids, bases, and oxidizing agents. Proper chemical labeling and secondary containment are recommended to prevent leaks or spills. Access should be restricted to trained personnel only. |
| Shelf Life | 2,2'-Disulfanediylbis(pyridine) 1,1'-dioxide should be stored cool and dry; shelf life is typically 2–3 years if unopened. |
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Purity 98%: 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product quality. Melting Point 180°C: 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide with a melting point of 180°C is used in organic electronic material fabrication, where it provides thermal stability during processing. Molecular Weight 280.33 g/mol: 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide of molecular weight 280.33 g/mol is used in ligand design for coordination chemistry, where it allows precise stoichiometric control in complex formation. Particle Size <10 μm: 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide with particle size below 10 μm is used in fine chemical formulations, where it enhances solubility and dispersion uniformity. Stability Temperature up to 120°C: 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide stable up to 120°C is used in high-temperature analytical processes, where it maintains integrity and reliability under thermal stress. Moisture Content <0.5%: 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide with moisture content less than 0.5% is used in moisture-sensitive synthesis workflows, where it prevents side reactions and ensures consistent results. Viscosity 1.2 mPa·s (in solution): 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide at a viscosity of 1.2 mPa·s in solution is used in liquid-phase catalysis, where it enables easy handling and homogeneous mixing. |
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At our facilities, the journey with 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide starts in the raw material warehouse and moves through a precise synthesis chain built over years of process optimization. The molecule, with its distinctive disulfide linkage between two pyridine N-oxides, features a structural design that combines chemical stability with unique reactivity. We know this compound by its catalogue model DS-PD-NO2, which captures the focus on purity and consistency essential for downstream work.
Through continuous improvements, we achieve a purity above 98% as determined by HPLC, helping users avoid setbacks caused by unanticipated contaminants. The off-white crystalline powder flows easily, with bulk density and particle size closely monitored to ensure consistent handling in reactors and labs alike. Each batch gets tested for trace metals and residual solvents, since these minute impurities can compromise synthesis or catalytic reactions further in the supply chain.
There’s nothing theoretical about the applications for 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide. Organic chemists often pick it for its reactivity as a mild oxidant, especially in transformation of thioethers and sulfides. The disulfide bridge offers the right balance: stable enough to survive on-shelf but ready to participate in redox cycles at the turn of a stoichiometric dial. In heterocyclic chemistry, its pyridine N-oxide groups act as both electron donors and acceptors, creating unique reaction environments.
On the development bench, we see increasing interest in ligand design for homogeneous catalysis. Here, the flexibility and orientation provided by the disulfide bridge make this molecule stand out among other aromatic N-oxides. Researchers have shared success stories forming complexes with transition metals that show robust activity and selectivity in reactions from carbon-carbon coupling to selective oxidation.
The compound’s ability to coordinate as a bidentate ligand means it can bridge metal centers or chelate more effectively than simpler pyridine derivatives. This property opens the door to application in bioinorganic mimicry, synthetic modeling of metalloproteins, and selective extraction processes. Recent customer projects have even explored its use in molecular electronics and sensor arrays, leveraging the unique redox and electronic features baked into the molecular backbone.
Quality in chemical manufacturing lives and dies by the workflow behind every batch. Here, that starts with high-purity 2-mercaptopyridine N-oxide as our primary precursor. We established a controlled oxidation process, using carefully metered oxidants and temperature control, to link the two moieties while protecting the N-oxide functionality. It sounds textbook, but in reality, finessing the reaction profile—avoiding over-oxidation or incomplete coupling—keeps our process control team on their toes.
The challenge goes further with purification. We developed a crystallization protocol that we refine from customer feedback and our own experience, striking the right conditions for batch reproducibility. Our filtration and drying procedures maintain sample stability without introducing degradation—no use investing time in a high-performing compound if it can’t make it to the client’s door with its integrity intact.
We track a suite of batch-specific data beyond what’s printed on standard certificates. Water content analysis with Karl Fischer titration, residual acid quantification, and microanalysis for elements help us troubleshoot issues from recurring instability to color changes under extended storage. These datasets drive our improvement cycle; if a research lab gives feedback about unforeseen reactivity or solubility changes, we dig into historical batches for clues. Every release gets a certificate built on genuine testing—no generic statements or simple copy-paste certificates. Our QC technicians know both the right time to run a mass spectrum and when a little extra TLC in chromatography will make the difference for a demanding researcher downstream.
In the market, several analogues vie for attention: simple pyridine N-oxides, thioether-linked versions, and other disulfide-bridged aromatic heterocycles. Through side-by-side analysis, our technical team has shown that 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide occupies its own niche thanks to the interplay between the N-oxide group and the disulfide bond. Simple pyridine N-oxides act as weak ligands and don’t support the same redox chemistry; thioether-linked pyridines lack the stability and oxidizability found in this compound’s core.
Our clients working in catalysis or advanced materials demand proof over product claims. We invited several labs to run parallel experiments comparing our disulfanediylbis(pyridine) dioxide to the thioether and mono-N-oxide options in metal-binding and oxidative applications. The results demonstrated longer catalyst lifetimes and higher reaction turnovers, especially in ruthenium and palladium complexes. The product’s extended shelf life and thermal stability also brought practical advantages—technicians could store larger volumes over long project stretches without performance drop, reducing total cost over repeat orders.
Curiosity in the research community powers much of what happens on our production lines. A decade ago, most of the market pull for this molecule came from academic bench labs exploring fundamental coordination chemistry. In the last five years, demand has broadened to include pilot plants developing specialty catalysts and preclinical research groups screening for new pharmacologically relevant scaffolds. Our own team has fielded requests for kilogram-scale custom syntheses to support pre-commercial runs.
Every large-scale order presents unique challenges. Changes in the heat signatures of the exothermic coupling step, concern over potential side-product formation, and stringent moisture control all get logged, analyzed, and incorporated into our scale-up guidelines. Technical support doesn’t end at shipment: our chemists remain available for troubleshooting and optimization. These partnerships matter, as back-and-forth with users often uncovers process refinements—like a tweak in crystallization solvent or a different filtration speed—that can reduce bottlenecks for future runs.
Process safety and regulatory scrutiny have both grown as 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide moves from pure research to the fringes of commercial use. We monitor the literature and regulatory updates closely. While it is not yet heavily regulated, we’re proactive about periodic hazard assessments and best-practice transportation, based on emerging guidelines for disulfide compounds and aromatic N-oxides.
Reliable supply depends on commitment at every level. Most of our technicians have seen dozens of product cycles, troubleshooting everything from stubborn reaction emulsions to crystal clogging in filtration lines. They bring decades of hands-on skills to the table, knowing how to adjust stir rates to yield better batch consistency or tweak solvent polarity based on shifting upstream raw material profiles.
Waste reduction is another focus. Disulfide-containing intermediates can be persistent in water, so we re-route and treat effluent streams, reducing environmental impact and building credibility with auditors and community partners. We switched over to greener oxidants years ago, anticipating the tightening of waste disposal regulations that have since arrived. Staff training helps keep best practices front-of-mind, with regular safety talks and incentives for improvement suggestions directly from the shop floor.
Documentation supports every phase from order to delivery. A chain of signed logbooks, batch records, and analytical worksheets ensure traceability—a practice that’s proved essential more than once, tracing a problem back to a single drum of starting reagent or a shift change where a valve process skipped a step. Our clients don’t see most of those details, but their projects benefit from the reliability these systems provide.
In some markets, traders and resellers may circulate vague quality claims or omit complete test results. Our own approach grew out of frank feedback sessions with synthetic chemists frustrated by hidden details or inconsistent quality. Feedback like this prompted us to overhaul our documentation, sharing batch-specific results rather than one-size-fits-all data sheets. This policy helps clients plan and risk-assess their own processes; they can see not just the nominal purity but the actual impurity profile, water content, and stability benchmarks for the lot they purchase.
We also invest in ongoing product support. As new downstream uses emerge, we review and share stability studies that track how the compound behaves in real-life conditions, not just accelerated aging tests. Open lines for technical questions build trust; chemists know they’ll speak to someone familiar with the product, its quirks under different conditions, and proven workarounds for scale-up and analytical challenges.
Manufacturing 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide comes with a short list of persistent issues. Moisture control tops the list; the N-oxide group absorbs atmospheric water, which can degrade purity and complicate usage in air-sensitive applications. Based on repeated issues flagged from client labs, we transitioned packaging to include multi-layered vapor barriers and desiccant canisters. On request, we offer ampoule sealing for critical applications.
Color formation signals unintended oxidation or contamination. We keep a growing log of case reports, matching discoloration events to handling or shipping problems, and adjust protocols accordingly. Sometimes, small tweaks such as switching from glass to fluoropolymer liners have cut contamination rates more than complex procedural overhauls.
Batch-scale differences can trap unwary users, especially with compounds as sensitive as organosulfur heterocycles. We maintain parallel pilot reactors mimicking both lab and full-scale environments to catch process deviations. This lets us spot small changes in reaction profile that could balloon into big headaches for industrial runs. Working this way requires constant communication between R&D, QC, and production teams—but it’s helped us deliver consistent product even as volumes grew.
For process safety, our in-house protocols run above minimum legal requirements. Real-life incidents in other plants—reactor over-pressurization, inadvertent exposure to oxidants—reinforce the value of layered containment and redundancy checks. We conduct simulated failure drills and regularly review hazard analyses to stay ready for what might go wrong, not just what should.
Success in manufacturing and supplying 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide doesn’t just rest on the right equipment or strict SOPs. It’s rooted in a culture of sharing know-how, both internally and with the scientists relying on our material. More than once, a suggestion from a customer has steered our process development or analysis. Whether it’s a different approach to chromatography or a new application in solid-state devices, these partnerships highlight the dynamic nature of chemical manufacturing.
We view each batch as another chapter in a longer story—one where reliability and transparency build confidence across the supply chain. Our day-to-day work gets measured not just in tons shipped, but in goals met for our partners in research, synthesis, and manufacturing. We stay deeply aware that behind every request is a project on the line, deadlines to meet, and a team depending on trusted materials that work as promised.
New applications for 2,2'-disulfanediylbis(pyridine) 1,1'-dioxide continue to emerge from both academic and private sector labs. As demand grows beyond the bench, we’re scaling up with an eye toward maintaining the consistency and personal support that set us apart in a crowded market. Expansions in reactor capacity, investment in analytical infrastructure, and cross-training for our technical teams ensure we can deliver both quality and scale without compromise.
Every kilogram leaving our warehouse reflects years of refinement—not only of chemical process but of listening to those who use and rely on our product. For each customer, the story of this compound is a collaboration, shaped by their feedback, our team’s dedication, and an ongoing pursuit of reliability and openness. That’s the perspective from the manufacturer’s vantage point: a product that is more than a code or a spec sheet, but a living nexus of science, experience, and partnership.