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5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione

    • Product Name 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione
    • Alias 5-Heptyl-1,3,4-oxadiazole-2-thiol
    • Einecs 248-859-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    384629

    Iupac Name 5-Heptyl-1,3,4-oxadiazole-2(3H)-thione
    Molecular Formula C9H16N2OS
    Molecular Weight 200.30 g/mol
    Cas Number 10451-06-8
    Appearance White to off-white crystalline powder
    Melting Point 77-80°C
    Solubility Slightly soluble in water, soluble in organic solvents such as ethanol and DMSO
    Boiling Point Decomposes before boiling
    Smiles CCCCCCCc1nnc(s1)=S
    Synonyms 2-Thioxo-5-heptyl-1,3,4-oxadiazoline
    Logp Estimated 3.6

    As an accredited 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione, 10 grams," chemical hazard symbols, and secure screw cap.
    Shipping 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione is shipped in tightly sealed, chemically resistant containers under standard ambient conditions. Packages are clearly labeled, handled by trained personnel, and compliant with relevant regulations. Transport is via ground or air, with documentation ensuring traceability and safety during transit. Special handling instructions are provided if required.
    Storage Store **5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione** in a tightly sealed container, away from moisture, direct sunlight, and incompatible substances such as strong oxidizers. Keep in a cool, dry, well-ventilated area at room temperature. Use appropriate chemical storage cabinets and label clearly. Minimize exposure to heat and handle under inert atmosphere if necessary to prevent decomposition or unwanted reactions.
    Application of 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione

    Applications of 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione in Industrial Manufacturing

    5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione serves as a key functional additive and intermediate in several high-value specialty material sectors. By leveraging its distinct structure and thione reactivity, downstream manufacturers achieve targeted improvements in product performance, processing efficiency, and regulatory compliance. Below, we detail focused industrial scenarios where this raw material delivers measurable advantages.

    1. Sulfur-Containing Corrosion Inhibitors in Oil & Gas Production

    5-Heptyl-1,3,4-oxadiazole-2(3H)-thione provides targeted sulfur donor groups for advanced corrosion inhibitor formulations used in downhole and topside oilfield environments. Its selective adsorption on ferrous metal surfaces slows pitting and uniform corrosion, particularly under high-salinity and high-sulfide loads. Typical use focuses on continuous injection treatments for pipelines, storage tanks, and water injection systems handling sour crude and produced brines.

    Industry compliance standards

    • NACE MR0175/ISO 15156 (Materials for use in H2S-containing oil and gas environments)
    • API RP 932-B (Corrosion Control in Refineries)
    • REACH (for additive registration and use in Europe)
    • ISO 9001:2015 (Quality management for chemical formulation facilities)

    Typical usage ratio

    • Formulation concentrations: 0.5–2.5% by weight, adjusted according to fluid phase, chloride content, and system metallurgy

    Downstream process integration

    • Dosing during batch or continuous blending of corrosion inhibitor concentrates for field deployment
    • Addition post-neutralization and emulsion breaking stages
    • Compatibility checks performed with demulsifiers and scale inhibitors during final QC

    Final product types

    • Pipeline corrosion inhibitor packages
    • Topside vessel protection chemicals
    • Wellbore tubular treatments for sour service

    2. Rubber Vulcanization Accelerators in Industrial Elastomers

    5-Heptyl-1,3,4-oxadiazole-2(3H)-thione acts as a sulfur-supplying accelerator in the vulcanization of natural and synthetic rubbers, enhancing crosslink formation for improved mechanical properties, thermal aging resistance, and elasticity. Rubber compounders incorporate it to fine-tune cure kinetics and final modulus in thick-section profiles, conveyor belts, and molded gaskets exposed to aggressive chemical and heat cycles.

    Industry compliance standards

    • ASTM D3182 (Rubber compounding and processing standards)
    • EN 1420-1 (Rubber and plastics hoses and tubing for food and beverage)
    • FDA 21 CFR 177.2600 (Rubber articles intended for repeated use—where applicable)
    • ISO/TS 16949 (Automotive-related quality management systems)

    Typical usage ratio

    • Dosage: 0.3–1.0 phr (parts per hundred rubber), adjusted based on polymer type and sulfur donor requirements

    Downstream process integration

    • Direct addition during compounding with other accelerators and antidegradants in open mills or internal mixers
    • Incorporation before final blending and extrusion
    • Quality control via curing curve analysis and dynamic mechanical testing

    Final product types

    • Industrial hoses and chemical handling tubing
    • Automotive molded seals and grommets
    • High-performance conveyor belting

    3. Functional Additive in High-Performance Lubricant Formulations

    In the specialty lubricant sector, this oxadiazole-based compound provides extreme pressure (EP) and anti-wear performance through active sulfur chemistry, reacting at contact surfaces during boundary lubrication. Lubricant blenders utilize it in gear oils, compressor fluids, and metalworking lubricants to reduce galling and micro-welding under high load, ensuring extended service intervals and minimizing downtime in critical equipment.

    Industry compliance standards

    • DIN 51517 (Lubricants—Lubricating oils for machinery)
    • ISO 11158 (Industrial lubricants—ISO VG classes and performance)
    • ASTM D2266 (Four-ball wear test for lubricants)
    • EHS registration for safe use in closed lubricant systems

    Typical usage ratio

    • Typical concentration: 0.05–0.3% weight in finished lubricant, optimized via tribological testing depending on base oil group and additive interactions

    Downstream process integration

    • Solubilization in base oils alongside other EP agents and antioxidants during base blend make-up
    • Addition before vacuum dehydration and filtration steps to maintain additive integrity
    • Final performance validation based on load-wear index and corrosion inhibition

    Final product types

    • Heavy-duty gear and transmission oils
    • High-pressure hydraulic fluids
    • Metalworking fluids for cutting and forming operations

    4. Photostabilizer Intermediate in Specialty Polymer Additives

    As a precursor for synthesizing oxadiazole-class photostabilizers, this molecule forms the backbone for UV-absorbing additives integrated into high-value polymers. Chemical manufacturers convert it via controlled cyclization and substitution to tailor spectral absorption in films, fibers, and molded parts for outdoor use, preventing yellowing, embrittlement, and property loss.

    Industry compliance standards

    • EU REACH (Polymers and additive registration)
    • ISO 4892 (Plastics—Methods of exposure to laboratory light sources)
    • FDA 21 CFR 175.300 (Resinous and polymeric coatings)
    • RoHS (Restriction of Hazardous Substances for electronics-facing polymers)

    Typical usage ratio

    • In final photostabilizer synthesis: 1 molar equivalent as core intermediate; in masterbatch, photostabilizers are dosed at 0.2–0.8% polymer weight depending on UV durability targets

    Downstream process integration

    • Chlorination, etherification, or acylation of the oxadiazole core, followed by purification
    • Incorporation of final additive into plastics compounding stage via masterbatch concentrates
    • Stabilizer function verified by accelerated weathering and mechanical retention testing

    Final product types

    • UV-resistant polyethylene and polypropylene films
    • Outdoor-rated polycarbonate sheets and panels
    • Automotive exterior trim and lighting covers
    Free Quote

    Competitive 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione: Perspective from the Manufacturer

    Introducing a Specialized Compound

    Working on the synthesis floor every day, our team interacts constantly with chemical transformations that challenge both patience and precision. One molecule that has earned a place on our production line, and a degree of respect in our technical discussions, is 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione. A mouthful to pronounce, but this compound brings a distinct performance profile to advanced organic synthesis and fine chemical applications.

    Unlike bulk precursors churned out on high-volume lines, this molecule takes more finesse. Our process engineers designed a synthesis route that eliminates batch-to-batch yield drops. Yield consistency—backed by ongoing quality checks—provides downstream manufacturers with reliable input batches without unexpected performance swings, which can make all the difference in multistep synthesis or device fabrication.

    Bridging Lab Discovery and Commercial Production

    It’s easy to overlook the gulf between a high-purity sample from a university bench and the stable, kilogram-scale lots demanded by specialty manufacturers. Years ago, some of our customers approached us after repeated setbacks with inconsistent intermediate concentrations, tough crystallization steps, and sample decomposition during shipment. Our staff chemists and operators spent months re-engineering the process to solve these pain points. We solved recrystallization quirks and watched over every step to avoid unwanted oxidation or ring scission.

    Our commercial route for 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione achieves high purity levels, with staff running hands-on analytical checks through NMR, GC-MS, and HPLC each batch. No algorithm can replace human oversight here; one flash of a strange signal on the chromatogram sets off lab alarms and gets resolved by the same people who run the reactors. Over the years, we’ve found that this hybrid approach—technology backed by a core team’s tacit operating experience—prevents mishaps and surprises for specialty orders.

    What Sets This Compound Apart?

    We have shipped dozens of similar oxadiazole analogs over the years—each with their own subtle differences. Among heterocyclic thiones, this heptyl chain attached at the five position adds a unique balance of hydrophobicity and compatibility with hydrocarbon blends. That means customers exploring new molecular architectures for electronics, specialty coatings, or pharmaceutical candidates see a more predictable behavior profile—no sudden phase separations or unpredictable solvent incompatibility.

    Many thione compounds run into handling issues due to instability or moisture sensitivity. Past attempts from competing lines left scientists frustrated, watching their samples degrade mid-experiment. Experience taught us how to tune purification and packaging to head off this pitfall. We deploy precision-vacuum packaging protocols straight on the production floor—operators monitor packing lines closely, minimizing weighing and transfer steps. Our logistics team stores the final product in low-humidity zones and runs time checks to prevent sitting inventory from aging past its peak.

    Specifications Matter—But So Does Field Knowledge

    For technical teams measuring melting points and solubility parameters, our 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione routinely achieves tight specifications demanded by end users. Purity routinely hits above 99 percent. Moisture and impurity controls clamp below critical thresholds; we see our clients’ downstream conversions run more cleanly as a result. The formula itself, C9H15N3OS, offers a fine balance between molecular weight and ring stability, making it easier to build on or modify than shorter chain analogs. Small differences in carbon chain length or ring substituents can have outsized influence on behavior—and we have witnessed more dramatic failed runs with shorter or longer alkyl chains.

    We have received reports from polymer research teams experimenting with 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione as a crosslinking modifier that blends more smoothly with polyolefins or step-growth polymers. Organic electronics labs have tapped this compound for its resistance to oxidative breakdown in shelf-life studies, allowing for experimental devices that maintain dielectric properties under real-world stress.

    Our technical staff keeps close tabs on user feedback, adjusting process parameters and collaborating on joint projects. Each batch we ship carries the hard lessons of failed experiments—mistaken catalyst ratios, incomplete ring closure, and overexposed thione under light—rolled into a more reliable, repeatable product.

    Supporting Novel Applications

    By partnering directly with industrial chemists, we see breakthroughs in uses for this compound every year. A team in advanced adhesives needed a low-polarity, sulfur-containing ring that could act as a UV-stabilizer backbone without compromising blend clarity. Feedback on compounded dispersions highlighted minor haze and poor flow when they tried commercial alternatives—their switch to our 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione led to clear matrices and robust UV resistance.

    Pharmaceutical developers experimenting with new sulfhydryl-containing intermediates often struggle with batch impurity control when working with delicate thione rings. Our operating staff tackles this challenge by monitoring byproduct residuals and tweaking isolation parameters. Having immediate access to run history and a direct line to the chemists behind the process enables fast iteration and troubleshooting—attributes not found in oversized facilities or off-the-shelf suppliers.

    Distinct Differences from Standard Products

    Those accustomed to common thione analogs may not expect the subtle, real-world benefits provided by the five-carbon heptyl chain. Lab trials with shorter (butyl or pentyl) groups reveal earlier phase separation, unpredictability in concentrated blends, and oxidative instability. Lengthening the chain beyond seven carbons, meanwhile, causes solubility headaches and shelf-life problems. This compound’s signature lies in the sweet spot between compatibility and stability—it integrates into diverse chemistries without bringing along handling headaches.

    Several commercial researchers using off-brand stock materials have experienced higher rates of oxidative polymerization and degradation—once they switched to our 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione, those problems dropped off. This isn’t just a matter of catalog numbers, but of decades of refinement and customer-driven feedback poured back into every lot.

    Quality Control Backed by Practical Realities

    Having watched what failures look like—from mis-labeled shipments to botched crystallization during hot summers—we put our energy into prevention rather than paperwork. Structural confirmations on each batch, hands-on checks by the same chemists who handle the reactors, and short time gaps between synthesis and shipment reduce degradation and mix-ups. No batch gets released without detailed reviews from more than one set of hands and eyes, a regime we built only after learning the hard way.

    Process tweaks happen on the fly based on live operator comments. That agility can’t be found in hands-off, scaled-up traders whose only interface is an order screen. Expert judgment, both on the process line and in packaging, prevents dozens of little mishaps that often don’t show up in the final specification sheet—but show up loudly in downstream user headaches.

    Facing Supply Chain Realities

    Transporting fine chemicals in varying climate zones can tip a decent product into disappointment, with thiones especially prone to decomposition. Our facilities—located close to shipping routes but shielded from humidity swings—give us an edge that only years of logistical missteps could have taught.

    We tailored our logistics to the quirks of 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione. Insulated containers, moisture barriers, cold-shipment flags, and coordinated timing make sure each lot arrives as functional as the day it left the reactor. Fragile compounds expose the difference between a hands-on manufacturer and a faceless supply chain—one poorly planned hold on a tarmac can undo weeks of careful synthesis.

    Scale-Up Challenges Meet Problem Solvers

    Scaling up oxadiazole thiones exposed a dozen unpredictable twists. From prototype glassware in bench-scale synthesis to the larger vessels in our main production hall, reactor fouling, yield dips, and trace byproduct spikes forced us to innovate batch by batch. Instruments alone never solved these problems; veterans on the team noticed patterns in foam formation, scorching hazards, and filtration oddities that don’t show up in technical papers.

    We continually revisit and revise our process diagrams, learning from pilot-scale flops. Those lessons, recorded in operator notebooks and morning briefings, shape every run, every deviation logged, and every decision made about solvents or purification steps. No process ever truly finishes evolving—we remain ready to adapt to new science or user needs as the compound finds novel homes in research and industry.

    Technologists and Chemists: The Feedback Loop

    By holding regular discussions with researchers in the field, we notice new trends and challenges ahead of standard order forms or technical reports. Recently, a customer in conductive polymer development asked for tighter controls on trace solvent residues. Our process engineers jumped at the challenge, modifying reactor venting and implementing fresh drying checks—delivering purer lots that passed once-troublesome spectral checks.

    Pharmaceutical teams need clean, impurity-free materials—our analytical staff picks up feedback, shares spectral anomalies with the process crew, and never waits for annual audits to drive improvement. Our tight team culture—melding synthetic skill with practical troubleshooting—lifts us above a one-size-fits-all supplier. We’ve seen that most innovations in specialty chemical production grow from cumulative, field-driven changes, not committee room mandates.

    Sustainability Learnings and Manufacturing Responsibility

    As environmental regulations shift, we face new imperatives for waste reduction and process greenification. Some years back, our team switched to less hazardous solvents during intermediate steps after a review of emissions and downstream handling risks. Tweaking to less aggressive reagents dropped solvent waste and cut the volatile emissions load, allowing us to recycle side-stream products safely.

    Our long-term relationships with local waste handlers and solvent recyclers—built through years of coordinated pickups and open data sharing—give us a unique operational perspective. Many in-house staff have taken on-site safety and environmental steward roles, keeping risk controls tight and community trust strong.

    Supporting Scientific Discovery—From Bench to Bulk

    We often see scientists push the envelope on what 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione can achieve, whether in catalytic cross-coupling, photovoltaic research, or as a tailored intermediate in medicinal target syntheses. The line between lab-scale innovation and process-scale consistency remains narrow—without flexible, engaged manufacturers, that gap widens. Our team sees the role of the manufacturer as a true partner, not just a box-checking supplier. The questions, stubborn technical hurdles, and unexpected requests scientists toss our way make each week different from the last.

    As new fields demand custom molecules with defined behaviors—where one contaminant or structural difference can set back months of research—an experienced, flexible, and proven manufacturing team brings peace of mind. Our journey with 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione doesn’t just offer a product; it represents a learning curve personalized for each application, built on mistakes avoided, problems solved, and solutions discovered together with the field’s top thinkers.

    Joining Innovation with Dependable Chemistry

    From lab notebook sketches to full production, each lot of 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione we deliver carries more than a batch number. It embodies years of incremental troubleshooting, user stories, field-tested packaging, and continual listening to real-world challenges. We value this compound not because of its molecular structure or a product code in the catalog, but for the bridge it builds between synthesis floor experience and scientific progress.

    Whether destined for organic optoelectronics, advanced polymer blends, or the pages of academic journals, our process puts stability and transparency above one-off transactions. We hold ourselves not just to numbers on a spec sheet, but to the day-to-day realities of our partners in research and manufacturing.

    Conclusion: Experience Sets the Standard

    From the first experimental batches to today’s commercial lots, 5-Heptyl-1,3,4-Oxadiazole-2(3H)-Thione has educated every member of our staff in the art and science of specialty chemical manufacturing. The compound becomes more than an intermediate; it’s a canvas for collaboration, a source of operational pride, and a daily challenge to innovate and improve.

    As science races ahead, our team stands committed to meeting new goals and puzzling out new applications for this unique molecule. Every project, order, and challenge adds another layer to our shared legacy—one that wins respect not just from our customers, but from every hand that shapes, tests, and ships a chemical that enables new frontiers in industry and research.