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HS Code |
288594 |
| Chemical Name | 5-Chlorobenzooxazole-2-thiol |
| Cas Number | 2669-88-1 |
| Molecular Formula | C7H4ClNOS |
| Molecular Weight | 185.63 g/mol |
| Appearance | Yellow to brown powder |
| Melting Point | 190-194 °C |
| Solubility | Slightly soluble in water |
| Purity | Typically >98% |
| Storage Conditions | Store in a cool, dry place, protected from light |
| Synonyms | 5-Chloro-1,3-benzoxazole-2-thiol |
As an accredited 5-Chlorobenzooxazole-2-Thiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5-Chlorobenzooxazole-2-Thiol comes in a sealed, amber glass bottle, labeled, containing 25 grams of fine yellow powder. |
| Shipping | 5-Chlorobenzooxazole-2-Thiol is shipped in tightly sealed containers, protected from moisture and light. The package is clearly labeled according to regulatory standards, including hazard warnings. Shipping follows all relevant chemical transport regulations, such as DOT or IATA, ensuring safe handling and delivery, typically under ambient temperature unless otherwise specified by safety guidelines. |
| Storage | **5-Chlorobenzooxazole-2-thiol** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it isolated from incompatible substances such as strong oxidizing agents. Ensure proper labeling and restrict access to trained personnel. Use appropriate protective equipment when handling the chemical. |
Applications of 5-Chlorobenzooxazole-2-Thiol in Industrial ManufacturingAs a specialized manufacturer of 5-Chlorobenzooxazole-2-Thiol, we supply this intermediate to a select range of established industrial sectors where it is essential to advanced chemical synthesis. The following application scenarios demonstrate this raw material’s unique value in real-world downstream manufacturing, supported by industry-specific standards, precise blending guidance, integration stages in process flows, and typical final product forms. 1. Active Pharmaceutical Ingredient (API) Synthesis for Antimicrobial AgentsThis compound serves as a critical sulfur-containing building block in the synthesis of certain antimicrobial drug molecules. Pharmaceutical manufacturers use it to achieve targeted heterocyclic scaffolds, leveraging its reactivity to introduce a 5-chloro-substituted benzooxazole moiety. The material directly enters catalytic condensation steps crucial to API scaffold construction, stringent QC measures applied during both the intermediate and final API production phases. Industry compliance standards
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2. Synthesis of Optical Brighteners for Textile ProcessingIn specialty chemical manufacturing, this raw material enables the introduction of specific sulfur and chlorine functionalities into benzooxazole-based optical brighteners. These brightening agents enhance visible whiteness and UV fluorescence in processed fabrics, and require precise control over intermediate purity. Regulatory compliance is observed at both the intermediate and final product stages as required by textile safety and performance standards. Industry compliance standards
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3. Synthesis of Thiazole-Based Agrochemical ActivesAdvanced pesticide manufacturers employ this intermediate to introduce the required benzooxazole-thiol group in selective fungicides and crop protection molecules, capitalizing on its ability to confer target selectivity and persistence. Production strictly follows global pesticide safety and environmental standards, and the raw material’s introduction stage is controlled carefully to optimize downstream actives’ structure-activity profiles. Industry compliance standards
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4. Electronic Materials Precursor in Polymer Dielectric SynthesisA select group of advanced materials manufacturers incorporate this compound as a monomer precursor during synthesis of polymeric dielectrics and related electronics resins. Its molecular structure helps increase thermal and oxidative resistance of the finished polymers, supporting expanded use in film capacitors, circuit substrates, and high-frequency insulation. The process adheres to electronics and environmental standards, and the raw material must be handled in dry, inert atmospheres during high-purity resin preparation. Industry compliance standards
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Over the past two decades, we have worked hard to create the chemicals that drive new ideas in pharmaceuticals and specialty materials. Among these, 5-Chlorobenzooxazole-2-Thiol stands out. Our deep experience in both research and scale-up has shown us its remarkable potential in multiple industries, especially where accuracy and purity decide the success of downstream chemistry. Through continuous improvement, we have refined each step of the process—from raw material sourcing to final purification—so that customers don’t second guess the quality they’re getting.
Chemists come to us with challenges that need unique solutions. 5-Chlorobenzooxazole-2-Thiol consistently offers a specific reactivity profile that fits custom applications, giving synthesis teams a versatile building block that you can trust under both robust and delicate conditions.
Producing 5-Chlorobenzooxazole-2-Thiol starts with disciplined, analytical work in the laboratory. We believe purity makes or breaks a reaction’s success rate, so our typical batches target a minimum purity of 99%, confirmed using state-of-the-art HPLC and NMR equipment. Other contaminants—trace moisture, residual solvents—are driven as low as possible, not just to meet a test sheet, but to avoid unpredictable activity in the customer’s process.
Physical properties such as melting point and consistent particle size matter a great deal during formulation. Crystalline lots show reliable flow and maintain stability during storage, avoiding issues like caking or premature breakdown. We’ve learned that minor details, like point source variation in batch temperature, can impact the final outcome, so we have automated and validated temperatures across all reactors. Our own chemists keep tight documentation, and every batch leaves with a traceable certificate for audit purposes.
Packaging uses lined containers to protect against humidity and oxidative exposure. We have moved away from cheap or reactive packaging after earlier lessons with shelf-life and color shift, now using medical-grade linings that don’t bleed plasticizers or leach components. Even after months in storage, the product retains its sharp, pale appearance—a quick visual check before the sample ever hits the balance.
Some labs request lots in smaller aliquots for high-throughput work, while bulk buyers in manufacturing prefer sacks or drums. We can support both, as our facility setup accommodates filling lines for a range of volumes. This hands-on handling lets us maintain consistency between 20-gram samples and 100-kilogram bulk shipments.
The manufacturing steps reflect decades of learning from bench-top mishaps and scale-up headaches. Early runs taught us that process water quality changes that seem harmless in small glassware can destabilize entire vessels. We chose to filter and pre-treat all reagents before they reach the reactors, so side reactions stay limited. On the shop floor, careful attention to mixing speeds has saved us from batch heterogeneity that would otherwise come out during drying or milling.
Isolation and drying need close monitoring to ensure the thiol group stays intact and ready for further reaction. Without careful control, the product can darken or lose reactive sulfur, reducing its yield and purity in your own plant. We've invested in closed-transfer lines and low-oxygen atmospheres. Each drum or bottle is sealed in a nitrogen-rich environment for added safety.
Quality assurance doesn’t just stop at the endpoint. Every step—crystallization, filtration, packing—gets a multi-point review. It’s all documented in real-time, which makes regulatory inspections straightforward and gives our clients peace of mind when they allow their own auditors to visit.
Back in our labs, 5-Chlorobenzooxazole-2-Thiol plays a unique role in structure-activity studies and complex molecule assembly. Its appeal boils down to the reactive balance: the chloro group offers selectivity for coupling reactions, while the thiol opens possibilities for modified ligands, sulfur linkages, and heterocyclic core construction. Other similar compounds can’t always offer the same stability or compatibility in one molecule, which means fewer steps, shorter process times, and less waste.
We have seen it work repeatedly in sulfur knock-in reactions for active pharmaceutical ingredients, where competing side reactions threaten to kill yield. The compound's dual functionality lets synthetic chemists explore routes impossible with a mono-functional substrate. This has driven new patents, as well as tweaks to old favorites in pigment chemistry and materials science. Customers often mention its edge in forming metal-thiol complexes with a tighter bond and cleaner profile than comparable thiols.
Our formulation specialists notice that the reactivity window is wide enough for both catalytic and stoichiometric work. This means you can push the process speed or gently coax a stubborn intermediate without losing functional group definition along the way. Teams working in high-stakes pharmaceutical synthesis rely on this flexibility to deliver reliable screens and structure proofs.
Pharmaceutical teams comment on its resistance to oxidation during plant transfer—a seemingly small practical issue that gives added assurance for late-stage intermediates. Materials scientists like the way it resists ring scission and maintains spectral clarity even at elevated temperatures.
Our in-house comparisons include analogues like 5-bromobenzooxazole-2-thiol and 5-chlorobenzooxazole-2-amine. What stands out is the way our compound balances reactivity and stability under a wider range of conditions. 5-bromobenzooxazole-2-thiol sometimes gives sluggish couplings, with expensive transition metals required to drive the process. With 5-chloro, we see a faster kick-off and more complete conversions at moderate temperatures.
Thiol-containing heterocycles have a reputation for instability, especially when sourced from traders or cut with intermediate cuts. We focus on purity and careful process control so our batches avoid the musty odors, uneven melting points, and difficult dissolutions reported for third-party lots. Customers that tried to formulate using other sources noticed more decomposition products, which we tracked to trace oxidants in the raw material chain. Our extra filtration and in-process analytics counteract these weak points.
Some users ask about using other 2-thiol heterocycles instead of ours. The switch can cause issues with electron density, leading to different selectivity profiles in metal-catalyzed couplings and a tendency for over-reaction in sulfur-dependent transformations. We have tried these head-to-head in our pilot plant, and what we see is that 5-Chlorobenzooxazole-2-Thiol reliably delivers manageable selectivity and scalable outcomes—traits that pay dividends during regulatory scale-up.
A good lab practice keeps the product cool, dry, and sealed tight. Those who don’t pay attention might discover color change or lower activity, not overnight but slowly, as small leaks and ambient humidity creep in. A little investment in climate control and tight container handling in storage goes a long way. We noticed the same in our own archive stocks—treat the bottles carefully, and even year-old samples behave nearly as well as freshly packed lots.
Protecting from light and oxygen stays important for long-term shelf-life. Real results from our stability trials show that lots held in vacuum-tight, amber glass last 18 months and more. Thin plastic sometimes lets in air that degrades the critical sulfur content, so we recommend glass or lined metal depending on use case. Analytical labs with busy workflows will benefit from opening smaller aliquots only when needed, to avoid multiple exposures.
Our field team has visited customer sites where mixing older product with fresh led to inconsistent results. Whether in high-throughput screening or kilo-lab synthesis, best performance always comes from using well-kept, single-lot batches. In our own pilot lines, we batch qualify reagents before every campaign to eliminate surprises.
Unlocking new routes to drug molecules or specialty polymers often requires a starting material with precise, predictable reactivity. We have seen some of our partners file new synthetic pathways based on this compound’s dual activity. Its mixed halothiol structure encourages creative shortcutting across multi-step reactions, bringing down total throughput cost and simplifying purification after coupling or ligation.
Some chemists focus on speed—getting from A to B in hours, not days. Here, the optimized crystalline form and clean melt save a step in handling and let them jump straight into solution. Others are more concerned with regulatory compliance and long-term batch reproducibility, especially after repeated FDA or EMA audits. Since our material meets strict impurity thresholds and supports detailed lot tracking, teams don’t lose sleep worrying about the next inspection.
It’s also worth noting the reduction in hazardous waste. Some alternative sulfur sources bring in heavy metals or halogenated byproducts, but tightly controlled manufacturing ensures cleaner mother liquors and minimizes the environmental burden. We’re proud of this, because our plant’s output isn’t just product—it impacts local utilities and waste management downstream. History has taught us that investing up front in analytics pays off on every audit and saves headaches for our clients up and down the supply chain.
Every quarter brings new specs from our pharmaceutical and electronics partners. What worked in 2010 might not hold up under today’s testing or regulatory regimes. We stay close to industry associations and standard-setting bodies, so we can predict changes before our clients are surprised by them. For this compound, in particular, continuous monitoring lets us pick up slight shifts in accepted impurity levels and optimize targeting what matters most.
As more applications demand lower detectible contaminant levels—down to parts per million—we have expanded purification capacity and improved post-synthesis analytics. Feedback from clinical trial chemists led us to refine handling protocols and offer proactive certificates of analysis with every lot. These changes come not from marketing bullet points, but from hearing what practicing scientists struggle with at the bench or in production.
Over time, requests for fresh research samples and specialty blends have allowed us to customize outputs. Some want ultra-fine material for solution-phase work, others need larger lots that hold together for solid-state studies. Customization stays built into our thinking—something large-scale traders can’t or won’t bother with. Whether your problem is scale, purity, or application-specific tweaks, we can support an iterative process to get the right variant on the first order, not after months of frustration.
True value comes not just from what makes it to your flask, but from how it was made. We source precursors from partners we have vetted for both reliability and compliance. Our history with international audits shows that ethical traceability isn’t window dressing; it’s a minimum requirement for regulated markets and export.
Every step in our process—from operator PPE to containment practices—reflects lived experience with chemical handling. We’ve trained teams on what happens when a product leaks, or when reactivity is misunderstood. These lessons shape how we advise clients, and how our containers and labels convey clear, workable instructions for safe use.
Our approach to safety means we document everything, keep chemists informed, and update guidance based on fresh incident data, not just old SOPs. Production never takes shortcuts that risk endangering our teams or your researchers.