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HS Code |
871806 |
| Product Name | 5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine |
| Cas Number | 63795-51-7 |
| Molecular Formula | C6H5N3O2 |
| Molecular Weight | 151.12 g/mol |
| Appearance | Light yellow to brown solid |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | c1coc(c1)c2nnc(n2)N |
| Inchi | InChI=1S/C6H5N3O2/c7-6-8-9-5(11-6)4-2-1-3-10-4/h1-3H,(H2,7,8,9) |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Chemical Class | 1,3,4-Oxadiazole derivative |
| Hs Code | 2934999090 |
| Synonyms | 2-Amino-5-(2-furyl)-1,3,4-oxadiazole |
As an accredited 5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 10 grams, with tamper-evident cap, labeled “5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine”, CAS, hazard warnings. |
| Shipping | The chemical *5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine* is shipped in secure, sealed containers compliant with chemical safety regulations. It is packaged to prevent moisture, contamination, or degradation, and includes proper labeling and documentation. Shipment typically adheres to standard transport guidelines for laboratory chemicals, ensuring safe delivery to the destination. |
| Storage | Store **5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine** in a cool, dry, well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and clearly labeled. Avoid moisture and incompatible materials, such as strong oxidizing agents. Use appropriate personal protective equipment when handling. Recommended storage temperature is usually at or below room temperature, unless otherwise specified by the supplier. |
Applications of 5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine in Industrial ManufacturingAs an experienced manufacturer, we supply 5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine to specialized industries where stringent process integration and formulation requirements exist. The following sections outline real downstream sectors, detailed compliance norms, established compounding ratios, connection points in production, and finished product categories driven by market demand. 1. Active Pharmaceutical Ingredient (API) Synthesis for Antimicrobial AgentsThis compound serves as a core intermediate in pharmaceutical synthesis, especially for certain heterocyclic antimicrobial agents. Manufacturers incorporate it during the early-stage condensation process to construct novel molecular scaffolds with defined biological profiles. API producers optimize reaction parameters such as solvent selection and purification to maximize yield and purity, ensuring that the downstream biological activity and impurity profiles remain within registration limits for regulated markets. Industry compliance standards
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2. Agrochemical Intermediate in Fungicide DevelopmentFormulators in the agrochemical sector utilize this compound as a building block during synthesis of modern fungicide actives based on the oxadiazole moiety. Chemistry teams design multistep processes integrating this input for introducing the heterocyclic backbone, often under temperature-controlled and pressure-regulated systems to ensure selectivity and reproducibility, with targeted downstream biological assays dictating batch validation and release. Industry compliance standards
Typical usage ratio
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3. Functional Additive in Specialty Coating SystemsManufacturers and formulators in the specialty coatings industry employ this chemical as a functional modifier to impart antifungal and UV-resistance properties to advanced resin systems. Integration takes place during pre-polymer blending or as a post-addition in solvent-based or waterborne formulations, enabling precision adjustment of cross-link density and surface properties suitable for high-performance architectural, protective, or microelectronic coatings. QC labs monitor batch-to-batch consistency using HPLC and FT-IR techniques. Industry compliance standards
Typical usage ratio
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4. Intermediate for Fine Chemical Synthesis in Dye ManufacturingDye producers add 5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine as a synthetic precursor when developing specialty dyes with improved lightfastness and heat resistance required for performance textiles and industrial applications. The material enters multistage synthesis, providing a unique heterocyclic core that confers shade stability and chromophore specificity, with each batch validated against spectral and chromatographic criteria mandated by brand owners and regulatory authorities. Industry compliance standards
Typical usage ratio
Downstream process integration
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Producing 5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine in our plant never feels routine. This compound brings a noticeable challenge in synthesis, demanding close control at several points. We have seen shifts in requests for this material across years, mainly from pharmaceutical researchers keen on heterocyclic cores, but lately there has been a clear uptick from agricultural labs and fine chemical innovators. These changing demands push us to stay at the front of both process design and quality assurance.
One feature chemists mention is the fine balance of stability and reactivity within the molecule itself. It comes down to the fused structure, where the furan ring and oxadiazole system interact. This core gives the molecule distinct properties, opening up routes for further derivatization. Not all compounds in the heterocycle class show this level of synthetic flexibility. Labs looking to build out from the amine position see a significant difference: substitutions react predictably, and side products fall within manageable ranges. Years ago, the focus was on producing basic oxadiazole motifs, but persistent feedback from our clients nudged us to optimize for derivatives where the furan moiety delivers additional electron density and improved pharmacophore profiles.
I remember the first pilot batch we ran that made a mark on internal process meetings. The crystalline nature of 5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine gives it a solid advantage in purification—not every heterocyclic amine can be recrystallized with such clarity. Teams working in older pharmaceutical libraries recall the headaches from amorphous off-white powders, which required multiple rounds of chromatography. Here, the product’s melting point remains sharp and the bulk density consistent between lots, which translates to efficiency in downstream manufacturing. Handling this compound in bulk, there’s no excessive dusting or packing difficulties, making it friendlier from a safety and ergonomic standpoint.
Drawing on conversations with research chemists, it’s clear they value reproducibility. They need assurance every time they order material; surprises sideline whole programs. We have focused on keeping impurity profiles within very strict cutoffs. It’s not by accident that our analytical records show less than 0.2% total impurities—our plant managers run HPLC checks through various steps, ensuring there’s little drift batch to batch. When labs try oxadiazoles from broader suppliers, they sometimes encounter broad peaks or find extra UV absorptions that complicate their studies. This pushes decision makers to return to manufacturers like us who install extensive quality measures through synthesis, not just purification.
Scaling up this specific oxadiazole taught us a few hard lessons. At one point in the process, the oxidation state needs careful control, or byproducts can compromise the amine functionality altogether. We trained operators to recognize subtle shifts in reaction color—those tiny signals save time, money, and prevent costly remediation. Upstream, the furan starting material must meet a tight spec. We source this precursor from partners we’ve tested over the span of years, running small validation lots before taking in a full shipment. There’s no sense running a reactor only to find secondary reactions dropping yield by 5% or more.
Plant infrastructure matters, too. Our reactors feature precision jacket cooling. Even minor temperature lapses can produce unwanted cross-linking on the oxadiazole side. The last time we experimented with equipment borrowed from another line, yields fell and filtration times climbed. We never repeat that error. At every phase, hands-on knowledge from technicians tempers theory from the lab. These lessons cement why direct manufacturers bring a degree of certainty to buyers; we’ve ridden through each bump of scale-up and locked in the tweaks that separate run-of-the-mill batches from high-purity, low-retention-loss material.
Lab groups searching for lead structures often point to this molecule’s amine as a versatile coupling point. This opens several synthetic windows—from forming ureas, amides, or even moving into cross-coupling reactions under Pd catalysis. One of our long-standing partners, a medicinal chemistry team working on new anti-inflammatory scaffolds, banked on this flexibility. They needed to attach bulky aromatic rings while keeping functional group tolerance high. The clean amine position in our product handled acylation in one step, sidestepping byproducts that competitors’ materials started to show when purity slipped. These are not idle anecdotes—each success story fuels confidence for the next generation of research projects.
Some specialty chemical developers bring stories of failed scale-up with structurally similar oxadiazoles. Variations at the 5-position, if produced sloppily, can drag in polymeric byproducts that clog up reactions down the line. With our specific molecule, the electronics of the furan-oxadiazole system promote clean reactivity. Process chemists can plan multi-step syntheses knowing what’s coming from each lot. Reliability matters here—missing a delivery window while hunting for sources of sticky residues and color bodies in off-spec lots costs teams precious funding and momentum. Our philosophy has always placed deep value on eliminating such sources of unpredictability at the manufacturing floor, not outsourcing corrections to late-stage labs or relying on post-facto fixes.
Market shelves brim with various oxadiazole-based intermediates. We’ve handled many analogues ourselves, and the differences are not just academic. Bulk oxadiazole materials with benzene rings at position five can serve in other areas, but they tend to resist derivatization and sometimes bring higher melting points that complicate blending and handling. Furan-substituted variants track better in both solution chemistry and solid-state manipulations. Our production records show this compound’s solubility in common lab solvents enables faster reaction setups and easier workup, a boon for teams looking to streamline pilot runs or speed through SAR cycles.
The purity floor matters. We devote energy to maintaining a near-transparent impurity profile, tracking not only the main product but related process side products. This becomes critical as clients upscale pilot batches—low-level contaminants tolerated in milligram-scale work can cripple kilo-scale campaigns if not managed from the outset. Our analytics team stays nimble, updating methods as we gather structural data from client returns and ongoing internal research. This brings us direct insight on how minute tweaks to temperature or reaction time alter the appearance of trace compounds, helping us leapfrog slower standardization cycles common in trading houses or bulk intermediates brokers.
Our crew approaches every lot of 5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine expecting both routine and surprise. Reactor loading happens early morning, raw material checks continue in parallel. Operators weigh precursors themselves, calibrating balances each week. Once charge-up is confirmed, temperature ramps under direct supervision—not left to overnight timers. Over the years, we’ve changed filtration media twice—an early run of pilot material stuck firmly to old diatomaceous earth, resulting in the switch to a finer paper-based filter that cut processing time by two hours per batch. Each such tweak only became clear through repeated production, not from reading literature reports or relying solely on theoretical specs.
We track every gram of input and output with batch records going back half a decade. Deviations bigger than a percent in yield flag immediate review. Staff feel responsible for their runs, and line managers reward clean records with bonuses. Our leadership takes pride in this ethos. During scale-up for a major client, we ran six consecutive batches over a single week, keeping variance in average particle size below 5%. Consistency breeds trust. Plant workers know product from this reactor ends up in sensitive syntheses—there is no room for shortcutting QC or skipping analytical sign-offs.
This compound has a favorable safety profile at room temperature. Our experience shows careful handling prevents hazards: staffers wear standard PPE including gloves, goggles, and dust masks for handling large quantities. Warehouse protocols trigger regular inspections. We worked with industrial hygienists early on, ensuring ventilation managed any vapors or dust releases, even though on-paper risk remains low. Reactive intermediates in feedstocks receive special scrutiny—trace peroxides are monitored during storage. The goal is simple: protect personnel, prevent spoilage, deliver product that builds confidence in both lab and plant settings. Each incident report triggers improvements to our protocol, drawing from both in-house documentation and industry bulletins on related heterocycles.
We store finished material under nitrogen as a safeguard against prolonged exposure to air, even if stability data suggests little risk under ambient conditions. Our clients’ feedback shaped this practice. Some groups noticed minor color changes after weeks in clear jars; now, we pack material in amber, vacuum-sealed units labeled by lot, with desiccant packs. Direct observation trumps over-reliance on datasheets or abstract risk ratings. Each safeguard layers confidence atop documented stability, keeping costs in check without sacrificing downstream performance.
Producers face ongoing hurdles: supply chain shifts, new regulations, demand for green synthesis. Our plant managers recall specific bottlenecks—once a global furan precursor shortage forced delayed shipments. We responded by qualifying backup vendors, running validation lots to ensure product delivered matched both spec and performance. Constant vigilance on pricing and availability means our customers rarely feel the full brunt of raw material volatility. We learned not to wait for the problem to reach crisis levels. Open communication between procurement and synthesis managers helps spot disruptions early. Changes in environmental compliance brought their own challenges, especially regarding residue waste. We invested in additional solvent recovery and energy-efficient heating to trim both footprint and disposal fees. Feedback from environmental audits shaped several practices now embedded in our daily routine and documentation.
We have seen shifts towards higher regulatory scrutiny for certain intermediates in the oxadiazole family. Facing this environment, we maintain strong documentation, linking every batch to detailed raw material sources, analytical records, and compliance sign-offs. Clients appreciate full transparency: they know what’s in their material from start to finish. No last-minute changes, no hasty substitutions driven by outside market shocks. Many of our clients are multinational labs, subject to regulatory inspection by outside agencies, so shipping anything off-spec isn’t just bad practice; it’s an immediate reputational risk. We treat each order as an audit opportunity—no detail too minor to verify twice.
Recent years brought new groups into the market for 5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine. Agricultural scientists test derivatives for new crop protection ideas, while materials researchers explore the molecule’s furan-oxadiazole linkage for electronic applications. It’s satisfying for our team to ship out high-purity lots knowing their final destination might be a vital new drug candidate or a next-generation material used in smart coatings. This brings responsibility: as applications diversify, so too must our analytical methods and customer support. We don’t lean solely on past success—intense curiosity and regular process reviews keep us aligned with shifting client needs. Our technical staff hold quarterly sessions with outside experts, trading observations on new reaction modes and emerging analytical techniques. Inspiration comes as much from the plant floor as from our partners: lessons travel both ways.
The evolution of this molecule’s market brings opportunities as well as duties. Catering to stricter impurity standards, we doubled down on upstream quality, investing in remote-monitoring systems and periodic recalibration for all sensitive instruments. Waste minimization sits side-by-side with innovation; the goal is not just to deliver a product but to do so with a lighter footprint. We’ve adapted several procedures to move toward greener solvents and reduced auxiliary energy use, guided by both client requests and our own sustainability benchmarks. This mindset ensures our continued ability to deliver, even when uncertainty hits global markets or lab priorities shift unexpectedly.
Making 5-Furan-2-Yl-1,3,4-Oxadiazol-2-Ylamine brings together more than just process chemistry. Every lot shipped reflects diligence, accumulated know-how, and open feedback with end users. From raw material checks to shipping protocols, our approach prizes hands-on manufacturing experience and respect for the real-world needs of customers. Quality comes not just from instrumentation or paperwork, but from continuous corrections and process improvements born from trial, not template. Each batch builds confidence in researchers worldwide, fueling innovation across disciplines. Our team looks forward to seeing where this compound turns up next—whether in the bench-top flasks of a nascent drug program or in the macroscale rollouts of industrially significant materials.