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HS Code |
666691 |
| Iupac Name | [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione |
| Molecular Formula | C6H4N2OS |
| Molecular Weight | 152.18 g/mol |
| Cas Number | 50271-41-1 |
| Appearance | Yellow solid |
| Melting Point | 197-200°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=NC2=C(N1C(=S)O2)C=CC=N2 |
| Pubchem Cid | 187128 |
| Chemical Class | Heterocyclic compound |
| Functional Groups | Thione, oxazole, pyridine |
| Storage Conditions | Store in a cool, dry place, protected from light |
As an accredited [1,3]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 | Amber glass vial, 5 grams, sealed with PTFE-lined cap, labeled with chemical name, hazard pictograms, batch number, and expiry date. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL):** Packed in 25 kg drums, 8 metric tons per 20′ FCL, securely palletized, suitable for safe chemical transport. |
| Shipping | [1,3]Oxazolo[4,5-b]pyridine-2(3H)-thione should be shipped in tightly sealed containers, protected from moisture and light. Packages must comply with local chemical transport regulations, with appropriate labeling and documentation. Use secondary containment and cushioning to prevent breakage or leaks during transit. Consult the Safety Data Sheet (SDS) for specific shipping classifications and precautions. |
| Storage | [1,3]Oxazolo[4,5-b]pyridine-2(3H)-thione should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from moisture and direct sunlight. Use appropriate chemical-resistant containers and clearly label them. Store at room temperature unless otherwise specified by the manufacturer’s instructions. |
| Shelf Life | [Shelf Life] Stable for at least 2 years when stored in a cool, dry place, protected from light and moisture. |
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Purity 98%: [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation. Melting point 162°C: [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione at a melting point of 162°C is used in high-temperature organic reactions, where it provides thermal stability during catalytic processes. Particle size <10 μm: [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione with particle size less than 10 μm is used in fine chemical manufacturing, where it promotes enhanced reactivity and uniform dispersion. High chemical stability: [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione featuring high chemical stability is used in agrochemical formulations, where it maintains bioactivity over extended storage periods. Molecular weight 166.18 g/mol: [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione with molecular weight 166.18 g/mol is used in analytical reference standards, where it enables precise quantification in chromatographic analysis. Assay ≥99%: [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione with assay not less than 99% is used in medicinal chemistry screenings, where it provides accurate biological activity assessment. |
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Over several decades of chemical manufacturing, the pursuit for more adaptable heterocyclic compounds has taken center stage in research and industry. From our own production lines, [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione stands out as a vital building block within both academic research and the commercial pipeline. The core structure of this compound allows it to participate in a wide range of organic transformations, making it valuable for those seeking to tailor molecular frameworks with sulfur and nitrogen functionalities.
As a manufacturer, keeping the process consistent defines our overall reputation. Our own batches of [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione typically display a purity reaching up to 98%, with minimal trace impurities. This is not a trivial achievement. The synthetic pathway relies heavily on tightly controlled conditions across multiple steps, including recrystallization and chromatography, with frequent analytical checks by HPLC and NMR. Because of the specificity of this heterocyclic core, minor deviations in synthesis push through to final product quality, so we pay special attention to solvent control, humidity levels, and temperature throughout the process.
Packaged under inert atmosphere, each lot receives a unique tracking code, tying it back to its process records and QC data. Each shipment includes a certificate of analysis, generated directly from our laboratory rather than a distributor’s secondary paperwork. Owing to its moisture sensitivity, we use vacuum-sealed containers lined with PTFE to guard against hydrolysis, particularly important for shipments subjected to diverse climates.
With its fused pyridine and oxazole rings, this compound brings together reactivity from both nitrogen and sulfur atoms. The thione functionality enables the molecule to act as both a nucleophile and an electrophile. These dual characteristics serve a key role in cyclization reactions, sulfur transfer, and in the design of more complex heterocycles. Chemists looking for methylation, alkylation, or organometallic coupling partners benefit from the stability of this scaffold. We often receive inquiries from researchers experimenting with condensed ring systems who want fine-tuned control over reaction pathways. This molecular backbone unlocks such potential.
Laboratories focus on molecule discovery, but scale-up for production sets a new bar. We receive orders not just from universities, but pharmaceutical groups scaling up pilot batches for new chemical entities. The reactivity profile makes [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione useful for the derivatization of drug candidates and as a precursor for agrochemical intermediates. In some specialty systems, the compound’s electron-rich structure plays a role in fine-tuning complex catalysts.
Because many end-uses rely on subsequent functionalization, we optimize the process to keep residual by-products at a minimum. This attention to synthetic detail pays off later, especially in applications demanding low background signals — such as in fluorescent probe assembly or diagnostic markers.
Comparing this compound to similar fused-heterocyclic or sulfur-containing molecules reveals a distinctive set of properties. Many thione-based heterocycles offer high reactivity, but few match the controlled reactivity window here. Products like 2-mercaptopyridine or thiazole-thione alternatives tend to show faster hydrolysis or undesired side reactions under equivalent conditions. Our molecule’s fused structure stabilizes the thione group, reducing unwanted transformations during storage or reaction staging. Originating from direct manufacturing experience, we’ve seen fewer batch rejections and more reproducible results compared to single-ring sulfur heterocycles.
Custom modifications requested by research partners select this scaffold because it tolerates a broader range of substituents without rapid degradation. These structural advantages mean that formulating with [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione usually extends working life in both stock solutions and formulated intermediates, as documented by internal stability studies. Synthetic chemists aiming for advanced materials or library synthesis cite reduced side-product formation and ease of downstream purification.
Quality complaints rarely arrive at our door, but industry tales of failed reactions and month-long project delays are familiar. Most of these issues trace back to inattention to process tolerance, or reliance on less stable feedstock. From early on, our philosophy prioritized close monitoring of key process variables — not just at completion, but during synthesis set-up, isolation, and final packaging steps. For this compound, trace moisture or solvent residues catalyze hydrolysis or degrade the thione group if not managed.
Years back, researchers flagged incidents linked to yellowing during storage. After tracing the source, we reconstructed the packaging protocol, adding fresh desiccant packs and switching cap linings from polyethylene to PTFE. We benchmark chromatic and impurity control across multiple accelerated stability tests to prevent surprises after shipment. Our own warehouses use climate controls to avoid batch degradation before delivery.
We hear from researchers who often struggle to reproduce literature procedures exactly as written. Small, often invisible, variables can shift project results off-course. By tightening manufacturing variance, we support consistent performance at the bench. Graduate students and senior chemists rely on well-documented batch histories. Our process includes full traceability — not just batch numbers, but logbook entries for each environment variable monitoring production. In a recent case, one pharmaceutical client referenced these records during an FDA audit, pointing to the level of detail in our process controls as a key compliance factor.
Academic partners involved in natural product synthesis have commented that our product reduces baseline "background noise" and avoids contamination from common by-products like sulfur dioxide, frequently present in samples sourced from lower-quality suppliers.
From factory floor to final shipping, chemical safety is non-negotiable. [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione calls for glovebox handling through the critical synthetic steps. Operators receive specific safety training to manage thione and halogenated intermediates, as well as exposure controls for fine powders.
Waste management represents another ongoing challenge. Scaling production for bulk orders introduced new risks for our site’s water treatment system, eventually leading us to invest in closed-loop solvent recovery and new in-plant scrubbers. Cycle time reductions follow lean practice models, but never at the cost of unmonitored batch venting or uncontrolled emissions. Keeping an eye on these core manufacturing practices forms the backbone of our attention to environmental, health, and safety standards. Direct experience with regulatory audits and customer site visits has only reinforced our commitment.
Disruptions have become more frequent these days, and feedstock sources for specialty chemicals face more international scrutiny. We diversified upstream sourcing well before global logistics shocks. Direct relationships with precursor material suppliers allow us to react quickly to supply hiccups. Sampling each lot, rather than using paperwork alone, prevents downstream surprises. During a global solvent shortage, internal stockpiling and flexible scheduling allowed us to keep factory uptime high and fulfill repeat customer contracts without shipment delays.
Buyers often ask for transparency in sourcing, not only to trace production origin but also to confirm ethical practices. Unlike traders or resellers, we have direct oversight over the transformation from raw material to shipment-ready product. Control over the entire value chain not only benefits compliance auditors but also supports researchers struggling to secure grant funding in an increasingly regulated environment.
Delivering a drum of [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione marks only the midpoint of our direct partnership. We make a point to stay involved through technical support channels, offering guidance on best storage conditions, solution preparation, and even helping troubleshoot synthetic challenges our partners encounter with this compound. It’s not rare for our chemical engineers to phone in directly to assist with a customer's purification hiccup during process transfer. Open lines between our technical team and client labs minimize lost time, helping maintain project momentum.
Our commitment involves periodic visits to customer sites, sharing not only product documentation but also stories of common pitfalls and best practices from our years in the field. These exchanges circle back, as customer feedback often seeds improvements in our own production and QC processes. This feedback loop has, over the years, shaped both product purity profiles and how we approach batch traceability.
Many partners developing next-generation pharmaceuticals or specialty polymers have requested modifications on scale, particle size, or packaging. Our in-house R&D team takes on feasibility studies, optimizing process conditions to maintain molecular integrity under altered conditions. One recent research group, requiring ultra-fine particles for a screening assay, prompted us to invest in new milling equipment and implement stricter controls on static charge build-up, avoiding agglomeration during packing.
We encourage collaboration at the method development stage, not just after the fact. Our team worked closely with a leading diagnostics company to revalidate qualitative analysis procedures following a change in product formulation. Rather than rely on generic SOPs, direct knowledge-sharing allowed their analysts to adapt more quickly and avoid wasted reagent runs.
Working directly in manufacture — as opposed to trading or distribution — brings a deep sense of responsibility to the end-user. Every production run is an opportunity for improvement. Handling [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione from start to finish, we internalize the stakes our customers face: a missed delivery can halt a month’s research, while a trace impurity can muddle crucial results in a high-stakes synthesis campaign.
This approach motivates investments not just in plant upgrades, but also in ongoing staff training, robust internal documentation, and transparency in corrective actions whenever we encounter a deviation. The regulatory landscape for specialty chemicals keeps shifting, and we have adjusted batch reporting and safety documentation to stay ahead of inspection cycles. While these details might not register with the end-user day to day, they lay the foundation for trust, batch after batch.
Regulatory agencies have grown much stricter in recent years about traceability and analytical transparency. As manufacturers, we keep full chromatograms, purity reports, and synthetic batch logs for every lot. This allows us to respond promptly if any analytical or performance issue surfaces downstream. Sometimes, academic groups lack the resources or time to run comprehensive QC on every incoming reagent. Our in-house documentation closes this gap, ensuring laboratories can focus on development work without second-guessing raw material quality.
Continuous improvement never stops at machine upgrades. Engaging with real laboratory problems allows us to identify root causes early — whether it’s a solubility issue in a new solvent matrix or a subtle secondary impurity that interferes with NMR analysis. By benchmarking batch-to-batch improvements and tracking complaint resolution, we refine our own internal SOPs to maintain trust not just for a one-off shipment, but across years of partnership.
Industry needs evolve. Interest in complex heterocyclic scaffolds continues to rise, particularly as pharmaceutical companies invest more in sulfur and nitrogen-rich frameworks for next-generation therapies. Demand for higher purity compounds, documented provenance, and robust technical support underscores the competitive advantage direct manufacturers like us can offer. Global supply chain risks, stricter regulatory regimes, and climbing customer expectations force an ongoing cycle of adaptation.
Recent shifts in R&D funding models and the rush toward sustainability have prompted us to revisit our own waste reduction strategies and seek partnerships with green chemistry innovators tackling sulfur cycle optimization. Rather than treating each order as routine, we approach each challenge as a chance to build stronger links — from raw material suppliers to the research chemists advancing novel science.
Years of hands-on work with [1,3]oxazolo[4,5-b]pyridine-2(3H)-thione have shaped both our technical expertise and our business values. Producing at this level of attention to detail is rarely glamorous, but it matters deeply for everyone depending on dependable materials in their work. From environmental controls to rapid response troubleshooting, everything comes back to persistence and pride in what leaves our plant. Someday the molecule we synthesize may form the backbone of a new therapy or analytical tool — and we take that obligation seriously at every step.