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HS Code |
636339 |
| Iupac Name | oxazolo[4,5-b]pyridine-2(3H)-thione |
| Molecular Formula | C6H4N2OS |
| Molar Mass | 152.18 g/mol |
| Chemical Class | heterocyclic compound |
| Appearance | yellow solid (assumed, as typical for similar thiones) |
| Smiles | C1=NC2=C(O1)C=CN=C2S |
| Inchi | InChI=1S/C6H4N2OS/c9-6-7-4-2-1-3-8-5(4)10-6/h1-3,9H |
| Melting Point | uncertain, estimated 180-210°C |
| Cas Number | 35202-54-1 |
| Structure Type | bicyclic |
As an accredited oxazolo[4,5-b]pyridine-2(3H)-thione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White HDPE bottle, 10 grams, with tamper-evident cap. Labeled with product name, CAS number, safety warnings, and batch information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for oxazolo[4,5-b]pyridine-2(3H)-thione: Securely packed, sealed, and labeled drums/pallets in standard 20-foot container, ensuring safe international transport. |
| Shipping | The chemical oxazolo[4,5-b]pyridine-2(3H)-thione should be shipped in tightly sealed containers, protected from moisture and light. Appropriate hazard labeling must be applied according to safety regulations. The package should be padded to prevent breakage and handled by trained personnel, complying with relevant chemical shipping and transport guidelines. |
| Storage | **Storage Description:** Store oxazolo[4,5-b]pyridine-2(3H)-thione in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, protected from direct sunlight. Use appropriate chemical storage cabinets if available, and ensure all handling is performed using suitable personal protective equipment (PPE) to avoid exposure. |
| Shelf Life | Oxazolo[4,5-b]pyridine-2(3H)-thione should be stored cool and dry; typical shelf life is 2–3 years under proper conditions. |
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Purity 98%: oxazolo[4,5-b]pyridine-2(3H)-thione with 98% purity is used in pharmaceutical intermediate synthesis, where high-purity ensures optimal yield and minimal side-product formation. Melting Point 178°C: oxazolo[4,5-b]pyridine-2(3H)-thione with a melting point of 178°C is utilized in high-temperature organic reactions, where thermal stability improves process efficiency. Particle Size 5 μm: oxazolo[4,5-b]pyridine-2(3H)-thione with a particle size of 5 μm is applied in solid dispersion formulations, where enhanced dissolution rate increases bioavailability. Stability Temperature up to 120°C: oxazolo[4,5-b]pyridine-2(3H)-thione stable up to 120°C is integrated in catalytic systems, where thermal stability supports consistent catalytic performance. Moisture Content <0.5%: oxazolo[4,5-b]pyridine-2(3H)-thione with moisture content below 0.5% is employed in moisture-sensitive synthesis, where low water content reduces hydrolysis risk. Solubility in DMSO: oxazolo[4,5-b]pyridine-2(3H)-thione soluble in DMSO is chosen for biological screening assays, where high solubility allows precise dosing and homogeneous solutions. Molecular Weight 152.17 g/mol: oxazolo[4,5-b]pyridine-2(3H)-thione with a molecular weight of 152.17 g/mol is used in combinatorial chemistry, where predictable molecular incorporation supports targeted compound design. Assay by HPLC 99%: oxazolo[4,5-b]pyridine-2(3H)-thione with 99% HPLC assay is utilized in analytical reference standards, where high assay accuracy guarantees reliable quantification. Light Sensitivity: oxazolo[4,5-b]pyridine-2(3H)-thione with defined light sensitivity is used in photoreactivity studies, where sensitive detection of degradation profiles is required. |
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Producing oxazolo[4,5-b]pyridine-2(3H)-thione is more than meeting technical standards or filling catalogues. From years in the chemical industry, our focus remains quality at every stage. We take pride in consistency batch after batch, because the smallest difference in a lot can change project timelines or downstream R&D results. In the early days, we learned firsthand how a poorly characterized intermediate could derail an entire synthesis, so we have put strict measures in place for process control and thorough analytical testing.
Oxazolo[4,5-b]pyridine-2(3H)-thione bridges several functional chemistries, sitting at a versatile intersection for pharmaceutical, agrochemical, and specialty material synthesis. Its unique fused nitrogen-oxygen bicyclic structure, paired with a sulfhydryl functionality, gives it reactivity and selectivity not seen in simpler thiones or other heterocycles. Years of handling it in our own syntheses highlighted its advantages: the thione moiety’s nucleophilicity balances well with the aromatic core, allowing access to several scaffold modifications.
We produce this compound in scales that suit both bench research and pilot-scale manufacturing. Rigorous purification steps, including repeated recrystallizations, ensure we achieve high purity — measured routinely by NMR and HPLC. When our process shifted once from ethanol to a mixed solvent system, impurity levels in final lots dropped dramatically. That change came straight from a feedback loop with partners running late-stage intermediates, and it is the kind of adjustment we make, grounded in day-to-day use and feedback rather than abstract theory.
We settled on a specification minimum purity of 98%, using proton NMR and HPLC for every manufactured lot. During one particularly challenging campaign, a subtle contaminant appeared, detectable only by LC-MS — a lesson in how analytical vigilance translates directly to reliability for users. The product appears as a yellowish solid under regular lab conditions, stable during standard short-term handling but prone to darkening under light or humidity. Extra attention goes into packaging: amber glass and low-permeability inner seals significantly extend usable shelf-life.
Quality begins with the raw materials. All starting materials are tested for identity and trace metals before they enter the reactor. Our process features a slow, controlled addition of sulfur sources — this helps avoid over-sulfurization, a pitfall we encountered in early scale-ups leading to high levels of polysulfide side products. Each batch receives a certification sheet with actual manufacturing and QC dates, instrumental data, and retention samples archived for comparison. More than once, a research partner has reached out years later needing access to a sample from a previous year’s lot. Having a good archive system is not a luxury — it is an answer to real-world troubleshooting.
Oxazolo[4,5-b]pyridine-2(3H)-thione serves as a building block in heterocyclic chemistry and more advanced medicinal compound construction. Its core structure offers three distinct points for functionalization, opening diverse substitution routes. Many users in pharmaceutical discovery select this thione scaffold because it tolerates a wide range of reaction conditions, enabling more flexibility during lead optimization or SAR studies. Several customer reports described improved yields over isomeric thione compounds, particularly under mild coupling or cyclization reactions.
Our own applications include adapting this thione as a precursor to sulfenamides, achieved by using carefully chosen amination conditions. The reactivity toward electrophiles outperforms simple pyridine thiones, with faster reaction rates and fewer side products. We have used it as an intermediate in the synthesis of more complex bicyclic heterocycles, and the robust nature of this scaffold means it holds up against a range of oxidants and bases, which is not trivial for more delicate bicyclic ring systems.
Years before, access to this scaffold was limited to either costly imports or DIY syntheses with unreliable yields. We saw a need to standardize and streamline production — bringing it under tighter quality controls, so that every time a researcher opens a bottle, they know what to expect. Increasing consistency cut waste, particularly for academic groups who operate under tight budget constraints. We have received feedback that access to a reliable supply of this compound let several teams advance targets previously abandoned due to unpredictably variable inputs.
In practical terms, comparing oxazolo[4,5-b]pyridine-2(3H)-thione to related heterocycles shows why users keep returning to it as a core scaffold. Compounds such as 2-thioxopyridine or regular oxazole thiones offer only a subset of the reactivity. The fused bicyclo scaffold in oxazolo[4,5-b]pyridine-2(3H)-thione creates a different electronic distribution, allowing unique reactivity under both nucleophilic and electrophilic reaction regimes.
From a manufacturing perspective, making this molecule involves more rigorous control of ring closure steps than more basic lactams or simple thiones. Years ago, attempts to scale with standard conditions led to variable yields and unwanted ring isomers. We adapted by tightening temperature gradients and refining our purification steps, finally achieving predictable output. This focus on process brings peace of mind to formulators and medicinal chemists relying on batch-to-batch uniformity.
We have compared performance in several academic and industrial settings. Standard thione-building blocks tend to decompose in the presence of stronger oxidants, making them less suitable for certain joint synthesis or one-pot transformations. Oxazolo[4,5-b]pyridine-2(3H)-thione demonstrates greater resistance; it keeps its integrity under challenging conditions that cause other thiones to fragment or oxidize excessively. Several university medicinal chemistry labs commented that this stability gave them more room to experiment across broader reaction platforms.
Quality assurance at scale comes from hundreds of repetitions, stubborn troubleshooting, and a willingness to look for failure points. During early pilot runs, we lost an entire batch because a change in water content altered reactivity in an unexpected way. Today, Karl Fischer titrimetry is a standard part of our in-process controls. Consistency, in our experience, depends on understanding both the molecule and the process environment.
We keep records on all process parameters, not just the final output, because subtle fluctuations in temperature or solvent composition can cause impurity drifts. Staff chemists carry out training sessions on new process modifications, emphasizing the ‘why’ behind each parameter — not just rote repetition. The benefit reaches our downstream customers: stable quality means less troubleshooting and more time focused on discovery and application.
There have been cases where a client brought a problem to our team, suspecting the issue was with the product’s purity. Cross-validation showed their other reagent was at fault, but our willingness to help check through HPLC, NMR, and other data saved them further delays. For some it is just chemical supply; for us, each successful outcome reinforces trust and mutual growth.
No synthesis journey is free from setbacks. Scale-up reveals quirks not seen in bench chemistry. One persistent challenge is the thione’s limited light stability. Outgassing from ordinary plastic bottles caused unexpected yellowing over storage. We solved this with improved packaging, moving to tight amber glass containers and desiccant inserts. That one change extended shelf life for several months, minimizing rework or lost samples in customer hands.
Sourcing consistently high-quality starting materials proved another challenge. Early on, low-grade supplies led to “hidden” impurities that passed some basic QC screens but appeared during downstream reactions. Moving to higher-grade precursors — and demanding full transparency from our trusted suppliers — lifted overall product quality. For customers, this means less need for extra purification and more predictable chemistry, something we have seen reflected in batch reports and long-term collaborations.
Manufacturing controls always tie back to real-world use. Several of our large-scale customers encountered bottlenecks when unusual by-product peaks showed up in their own HPLC data. We brought them raw spectral data and collaboratively traced the issue to reaction conditions unique to their process, not ours. Working together, we helped them adjust protocols rather than just pointing fingers or reverting to generic technical support. Practical chemistry wins over theory every time.
Feedback from users remains our most valuable resource. One partner in a European pharmaceutical discovery lab described how the reactivity and shelf stability of our oxazolo[4,5-b]pyridine-2(3H)-thione opened the door to a new series of kinase inhibitors, shortening their optimization timeline by several months. In another case, an agrochemical developer benefited from the compound’s robust performance under varied synthetic conditions, reporting better reproducibility than with other thione or pyridine-based intermediates.
A common thread in feedback: reliable supply and transparent batch documentation eliminated uncertainty for scale-up and regulatory submission. We supply each lot with certificates that list solvent residues, water content, and impurity profiles. This approach grew out of industry needs — regulatory filings can stall if analytical details are missing. We have seen the frustration in blue-chip projects where incomplete supplier transparency caused unnecessary delays, so we resolved years ago to go beyond the usual levels of disclosure.
Researchers working under institutional grant timelines also shared how shipping delays and unpredictably variable purity from other sources hampered their progress. By controlling the entire process — raw materials, synthesis, purification, packaging, and support — we minimize points of failure. We ship with climate-resistant packaging and offer advice for storage and handling.
Every compound has a purpose. Oxazolo[4,5-b]pyridine-2(3H)-thione fills a niche not easily covered by generic thiones or nitrogen heterocycles. In multistep synthesis pathways, its selectivity and reactivity save valuable time and resources. We have seen industrial users cut a reaction step by leveraging its unique functional group layout. For smaller labs, getting the same reactivity out of alternate compounds meant extra purification work, solvent usage, and more waste disposal.
Its structural features foster creativity in medicinal chemistry. The presence of both nitrogen and oxygen in the bicyclic system enables distinct hydrogen bonding and stacking interactions, which have been exploited in crystal engineering and pharmaceutical salt formation. We collaborated with several academic groups integrating this thione into new functional materials — pointing to performance advantages rooted in the inherent electronic structure rather than a single application.
A large-scale agricultural client relied on the compound’s chemical stability to develop actives for crop protection. They found that less decomposition under manufacturing conditions led to higher yields and greater reproducibility, keys to meeting regulatory standards and field efficacy goals.
Manufacturing chemicals at scale is never a static process. We solicit ongoing feedback, not just to catch problems but to evolve the product in line with the needs of those at the bench or on the line. Chemistry rarely rewards those who stand still. Every discovery in improved purification, packaging, or logistics gets introduced as soon as validated. We track emerging synthetic methodologies and remain open to custom modification requests. Adapting our process to shorter cycle times, safer reagents, or upgraded analytics often comes from user-driven need rather than just top-down research.
Our team engages with the wider chemical community. Contributing analytical data to open-access repositories, attending industry symposia, and participating in academic-industry partnerships has helped us anticipate trends in heterocyclic building block demand. More than once, a graduate researcher’s question about alternate substitution patterns has prompted a review of our own synthesis and led to optimization. The cycle of learning flows both ways.
Safety matters as much as performance. We have seen projects run aground due to incompatible handling protocols, so we make storage and hazard guidance a standard part of any collaboration. We recommend cool, dark, and dry conditions. Open discussions with EH&S teams meant our packaging and safety data evolved alongside scientific best practice and regulation.
Disposal and environmental responsibility are not side notes. We advise users about solvent waste and downstream degradation products, and we work with disposal partners to improve environmental profiles at every step of the product’s lifecycle. Our plant maintains full compliance with local and international regulations, built on years of embedding these requirements into process planning and waste treatment procedures.
Oxazolo[4,5-b]pyridine-2(3H)-thione has proven its worth across pharmaceutical, agrochemical, and advanced material research. Its unique scaffold and consistent reactivity enable scientists and engineers to streamline discovery and manufacturing. As chemical synthesis grows more complex, the need for reliable, well-characterized building blocks intensifies. Our experience tells us that consistent supply, high quality, and accessible technical support make the biggest impact on innovation and productivity.
We stay committed to continuous improvement and partnership. Every batch, every inquiry, and every piece of feedback helps refine both product and process. From raw material sourcing to final shipment, our focus remains clear: delivering a trusted, thoroughly characterized intermediate that meets the real needs of modern chemistry. Choosing a supplier with an eye for detail and a record of reliability helps secure successful outcomes — not just for today’s project, but for discoveries yet to come.