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5-Chlorothianaphthene-3-Acetonitrile

    • Product Name 5-Chlorothianaphthene-3-Acetonitrile
    • Alias 5-Chloro-3-(2-thiophenyl)phthalonitrile
    • Einecs 630-719-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    483253

    Productname 5-Chlorothianaphthene-3-Acetonitrile
    Casnumber 405217-42-7
    Molecularformula C12H6ClNS
    Molecularweight 231.70 g/mol
    Appearance Solid
    Purity Typically ≥98%
    Storagetemperature Store at room temperature
    Smiles N#CCc1cc2ccccc2sc1Cl
    Inchi InChI=1S/C12H6ClNS/c13-10-6-8(7-14-5-10)9-3-1-2-4-11(9)15-12(10)14
    Synonyms 5-Chloro-3-(cyanomethyl)thianaphthene

    As an accredited 5-Chlorothianaphthene-3-Acetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 5-Chlorothianaphthene-3-Acetonitrile, tightly sealed with screw cap, labeled for laboratory use only.
    Shipping 5-Chlorothianaphthene-3-acetonitrile should be shipped in tightly sealed containers, protected from light and moisture. It must follow regulations for hazardous chemicals, including labeling and documentation. Shipping should occur via certified carriers specializing in chemicals, with temperature control if required. Ensure compliance with local, national, and international hazardous material transport guidelines.
    Storage Store **5-Chlorothianaphthene-3-Acetonitrile** in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep the container away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling and access only to trained personnel. Follow all relevant safety and chemical storage regulations to prevent accidental release or exposure.
    Application of 5-Chlorothianaphthene-3-Acetonitrile

    Applications of 5-Chlorothianaphthene-3-Acetonitrile in Industrial Manufacturing

    5-Chlorothianaphthene-3-acetonitrile supports advanced synthesis in several regulated industrial sectors. It acts as a key intermediate in chemical formulations where precise structural features and high chemical stability are required. Below, we detail specific downstream manufacturing routes based on current demand and industry practices.

    1. Pharmaceutical API Intermediate for Antipsychotic Agents

    Producers of central nervous system drugs use this material in multi-step chemical syntheses leading to tricyclic antipsychotic active pharmaceutical ingredients. Its chloro-substituted thianaphthalene core provides a critical building block for further derivatizations such as amination and acylation. Multiple patents reference this intermediate for manufacturing agents targeting dopamine and serotonin pathways subject to international regulatory scrutiny.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • US FDA 21 CFR Part 210/211 cGMP requirements
    • WHO GMP guidelines for pharmaceutical production
    • EU EudraLex Volume 4 GMP

    Typical usage ratio

    • Used at 0.8 to 1.15 molar equivalents per API batch, with specific rate adjusted per API target and yield optimization requirements

    Downstream process integration

    • Introduced post-halide activation in the initial condensation step, enabling specific ring closure in API synthesis branches

    Final product types

    • Quetiapine base and its derivatives
    • Pimozide analogues
    • Other tricyclic antipsychotic compounds

    2. Agrochemical Intermediate for Fungicide Synthesis

    Specialty chemical companies incorporate 5-chlorothianaphthene-3-acetonitrile into the production of broad-spectrum fungicide actives. Its aromatic backbone, modified via nitrile transformation, delivers scaffold molecules for protecting crops against soil-borne and leaf pathogens. Integration of this raw material ensures consistent lot-to-lot molecular structure and purity during large-scale production cycles.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 Quality Management for agrochemical production
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • REACH registration compliance (EC No 1907/2006)

    Typical usage ratio

    • Employed at 15–22% by mass in fungicide precursor synthesis; adjusted based on downstream coupling reactions and conversion yields

    Downstream process integration

    • Charged at the early cyclization stage to form heterocyclic active groups, ensuring correct orientation for final bioactive configuration

    Final product types

    • Prothioconazole analog-based fungicide actives
    • Multi-site protective formulations for cereal crops
    • Seed treatment concentrates

    3. Electronic Chemical Synthesis for OLED Precursors

    Manufacturers of organic electronic materials apply this compound for the synthesis of functionalized thianaphthene derivatives, which play a role in developing hole-transport and emitting layers for OLED displays. Here, precise molecular design and purity are critical to maintain electronic properties and reproducibility in device fabrication.

    Industry compliance standards

    • IEC 61249-2-43 standards for materials in electronic assemblies
    • RoHS Directive 2011/65/EU (restriction of hazardous substances)
    • ISO 14001 Environmental Management for chemical processing

    Typical usage ratio

    • Integrated at 5–12% by mass, tailored to the emission wavelength and layer thickness requirements in downstream OLED formulations

    Downstream process integration

    • Fed into Suzuki-Miyaura coupling reactions during early stages of emitter compound assembly, directly influencing the optoelectronic layer performance

    Final product types

    • Blue and green OLED emitting layer materials
    • Specialty hole-transport materials
    • High-brightness display modules

    4. Fine Chemical Intermediate for Advanced Dye Manufacturing

    Producers of specialty dyes utilize 5-chlorothianaphthene-3-acetonitrile for introducing rigid aromatic cores that enhance lightfastness and chemical resistance. The nitrile functionality enables further modifications, such as azo-coupling and sulfonation, driving the creation of colorfast compounds for demanding application environments.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemicals
    • ISO 9001:2015 for dyed product safety
    • REACH compliance for colorant substances

    Typical usage ratio

    • Depends on final dye structure; typically 10–25% by mass in coupling or condensation stages, modulated for chromophore intensity and desired end shade

    Downstream process integration

    • Added after initial diazotization, permitting direct condensation onto target thianaphthene rings

    Final product types

    • Fade-resistant polyester dyes
    • Specialty high-temperature textile dyes
    • Industrial inkjet colorants
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    Certification & Compliance
    More Introduction

    Introducing 5-Chlorothianaphthene-3-Acetonitrile: More Than Just an Intermediate

    Direct From Our Reactors: The Story Behind 5-Chlorothianaphthene-3-Acetonitrile

    Every batch of 5-Chlorothianaphthene-3-Acetonitrile coming out of our reactors results from years spent refining process controls and listening to feedback from industry clients—especially those shaping today’s pharmaceutical and fine chemical landscapes. Unlike the more generic thianaphthene derivatives seen in the market, this molecule presents a unique opportunity for researchers and manufacturers looking to stretch their chemistry into new directions. We make this compound not as a mere extension of existing production lines, but as a response to genuine demand for building blocks pushing the boundaries of both performance and reliability.

    Unique Features Rooted in Expertise

    Let’s talk about what chemistry inside our plant translates to for practical application. The molecular structure—anchored around a 5-chlorine atom on the thianaphthene core, with an acetonitrile side chain at the 3 position—brings together potent reactivity with tailored selectivity. Teams have run repeated lot verifications to ensure a consistent purity of at least 98%. No one in this building is satisfied until we see single, sharp peaks in every high-performance liquid chromatogram. Water content drops below 0.15%, and handling under inert atmosphere means the compound ships in a stable, free-flowing form. These are hard-won margins; we've personally had to retool portions of the synthesis route to minimize unwanted byproducts like dichloro- or unreacted thianaphthenes, simply because we know any deviation affects downstream yields our customers count on.

    How 5-Chlorothianaphthene-3-Acetonitrile Sets Itself Apart

    There’s no confusing this compound with our regular line of thianaphthene acetonitriles. While analogues without the 5-chloro position might save a step in synthesis, they often fall short during late-stage cross-couplings or struggle to deliver regioselectivity. Years ago, we fielded customer reports of instability in non-chlorinated analogues under harsh base conditions—a problem the chlorine handles with resilience. The 5-chloro group, in concert with the thianaphthene sulfur, shapes electronic characteristics that prove critical for chemoselectivity in electrophilic substitutions and Suzuki coupling routes. It’s not just a tweak for the sake of differentiation; it leads to streamlined process development and fewer headaches during scale-up.

    Real-World Application: What Our Partners Achieve

    Most of the product that leaves our plant ends up in the hands of process development teams working on heterocyclic frameworks for advanced intermediates. We’ve watched clients introduce this compound as a core fragment in drug discovery pipelines, where the balance of aromatic stability and cyano-functional group gives access to new chemical space. Some push it into conjugated materials, exploiting the electron-rich backbone for novel optoelectronic behaviors. The difference echoes down the chain—yields stand up, purification simplifies, and waste streams decrease. Our own in-house research crews have measured faster reaction times and stronger selectivity compared to earlier acetonitrile thianaphthenes, thanks to the symbiosis between sulfur and chlorine atoms.

    Specifications Rooted in Reproducibility

    From lot number one, every iteration has started with base chemicals verified by gas chromatography and mass spectrometry. Average melting points hover right where chemistry texts suggest, generally above 98°C. Solubility profiles align with laboratory needs: ready dissolution in polar aprotic solvents such as DMF and DMSO, predictable partitioning when extracted into dichloromethane or ethyl acetate. Trace metal analysis confirms our glass-lined reactors prevent leaching, offering assurance for those pushing toward active pharmaceutical ingredient manufacture. All incoming analytical requests—for example, custom moisture controls or particle size fractions—see an engineer’s hands on deck instead of an automated system ticking boxes.

    Not All Manufacturing Is Created Equal

    Any chemist who’s handled a broad slate of heterocyclic nitriles recognizes the pitfalls of uncontrolled halogenation: off-target substitution or degradation of acetonitrile side chains. Our control strategy stems from iterated small-batch trials, where operators learned to fine-tune temperature ramps and reagent flows. Unlike commodity nitrile operations reliant on bulk reagents, we single-source precursors, test every drum for contaminants, and keep an eye on supply chain impacts from upstream chlorination. Stabilizing the final product also means careful post-reaction handling—we purge oxygen, filter traces of iron, and package under dry nitrogen. Each of these steps comes from learning the hard way which shortcuts do (and don’t) hold up when costs and quality are on the line.

    End Use Cases: What Customers Build

    Workflows spin off countless applications—cross-coupling with boronic acids, regioselective cyanation, and sulfonation all benefit. Research partners have taken 5-Chlorothianaphthene-3-Acetonitrile to synthesize unique building blocks for kinase inhibitors, while others use it to start making rigid core units for advanced organic electronics. A few industrial collaborators feed it directly into multi-step syntheses leading to pigments and specialty dyes, where subtle color modulation comes only from precise aromatic substitutions. We once helped troubleshoot a process glitch for a customer scaling to multi-kilo lots for agrochemical intermediates, tracing inconsistencies to a competitor’s batch with high levels of polyhalogenated impurities—a fault that never appeared in our tightly monitored process.

    A Genuine Commitment to Quality

    Anyone can publish a list of chemical properties, but maintaining reproducibility demands more than technical bullet points. We limit batch sizes to ensure manageable heat loads and complete conversions. Residual solvents never drift out of compliance because we regularly recalibrate stripping protocols and run mock-downstream transformations in our own pilot area. Each shipment arrives in thick-walled, light-proof drums with tamper evidence—concrete measures ensuring receiving chemists deal with the material they expect, whatever the distance it has traveled. Our technical teams don’t treat feedback as noise; after a client reported rate loss in a late-stage palladium-catalyzed reaction, we re-examined every parameter for the next run, even shifting crystallization steps to cut out low-level chlorinated byproducts.

    The Difference in Handling, Storage, and Shelf Life

    We’ve spent time visiting customer labs and factories, watching how the reality of bench work changes based on clean, dry, and free-flowing crystals versus sluggish, impure powders. Recognizing that shelf life matters for process timing and inventory turns, we run accelerated stability checks, confirming that the compound maintains potency for at least 18 months when stored under dry nitrogen at cool ambient temperatures. Most reports of clumping or hydrolysis trace back to substandard packaging or uncontrolled transit; we sidestepped these setbacks early by moving to lined barrels fitted with one-way degassing valves, tested across air, land, and sea shipments under multiple climate regimes.

    Bridging Laboratory Discovery and Industrial-Scale Execution

    There’s often a chasm between small-scale discovery and full-plant production, with unpredictability lurking at the kilo level. We saw early on that laboratory wins around clean spectra and moderate yields could collapse without tight controls on scale. Our R&D efforts do not stop at bench-top synthesis—we work in sync with engineers monitoring pilot runs, capturing variations in heat transfer and agitation that often spell the difference between a usable product and a regulatory headache. By sharing these real-world insights with process partners, we help bridge the challenges of transferring a robust reaction from flask to reactor without shipping surprises or missed delivery dates.

    Supply Chain Realities and Honest Transparency

    Pressures on global supply chains from regulatory, logistical, and market volatility impact specialty chemicals as much as any other sector. We do not outsource quality. Every critical input gets sourced from longstanding partners subject to real audits and repeated analytical checks. Team members track global shipments in real time, and production scheduling stays nimble enough to meet both routine and emergency demand spikes. Years past, logistical hiccups forced us to build robust safety stock to guarantee lead times during port delays and holidays. All these initiatives came from plainly watching what works, not chasing industry buzzwords about lean inventory or “just-in-time” delivery that don’t fit high-stakes chemistry.

    Environmental and Regulatory Responsibility Comes With the Job

    Producing chlorinated aromatic compounds means embracing responsibility for both immediate and long-term environmental impacts. We operate solvent recovery units that minimize emissions and run wastewater through on-site treatment before discharge. Our site rarely generates off-spec waste, but when issues arise, every lot gets documented cradle-to-grave and shipped to reputable incineration partners—no corner-cutting or out-of-sight dumping. Compliance with local and international regulations matters to the future of both the company and the communities hosting our operations. Plant staff routinely undergo training for new health, safety, and environmental protocols, ensuring nobody learns about risks too late to act.

    Continuous Improvement From Feedback Loops

    Early process runs registered occasional color drift and inconsistent flow as particle size varied. Taking that criticism to heart led us to optimize filtration and fine-mill before packing. Technician walkthroughs and hands-on operator training still uncover tweaks to boost efficiency and product homogeneity, straight from those standing over the reactors, not remote consultants. When a process trainee caught a rare case of packaging mislabeling last quarter, the experience triggered a system-wide barcode scanner upgrade—real improvements inspired by workers’ eyes rather than management memos.

    Solutions for Process Bottlenecks and Analytical Needs

    Some customers reach out facing unique issues their own quality teams haven’t resolved, whether it’s reaction stalling or persistence of trace halide under high-stress conditions. Instead of a catalogue answer, we put a synthetic chemist or analytical lead on the phone, reviewing batch sheets and making practical adjustment suggestions. Sometimes, a simple tweak in reaction base or purification solvent resolves persistent troubles due to compound idiosyncrasies—solutions born out of hands-on manufacturing experience, not theoretical guesswork. We invite customer chemists to visit, examine our facilities, and replay scenarios so technical exchanges never become guesswork.

    Supporting Advanced Synthesis: Not Just a Commodity Offer

    Some buyers treat chemical intermediates as interchangeable, tempted by lower-priced generic alternatives. Consistent experience tells us otherwise: each tweak to the starting structure or process affects outcomes in yields, impurity profiles, and overall batch consistency. Our production lines favor predictable output, not just on day one, but year after year. Ingenuity in both equipment maintenance and analytical verification keeps reproducibility high—teams cross-check purification solvents, reaction residues, and shipping documentation every time. We never cut corners on scale-up support or application-specific troubleshooting, so customers’ own work in medicinal or materials chemistry flows without hidden holdups.

    Direct Feedback: How Clients Shape Our Outcome

    One customer's chemist noticed an unusual smell during a distillation step, which pointed to trace volatile impurities missed in our initial gas chromatography protocol. We overhauled the post-synthesis neutralization process, reducing residue to undetectable levels. This example—just one out of dozens—reminds us that only open dialogue and persistent refinement uphold the expectations of both small and large R&D partners. In-house quality monitors welcome all product performance feedback, whether it's a minor observation or a full technical report. These continuous conversations create a partnership, not just a buyer-seller relationship, allowing both sides to walk away smarter with each order.

    Future Directions: Keeping Innovation at the Core

    As research priorities shift—whether toward more complex pharmaceuticals, greener processes, or new classes of optoelectronic materials—the need for reliable, innovative intermediates like 5-Chlorothianaphthene-3-Acetonitrile only grows. We invest in continuous synthesis development, pushing toward even greater purity, lower residual solvent, and more robust packaging for harsh conditions. Our technical team collaborates with outside research labs, sharing knowledge both upstream and downstream so customers never face roadblocks alone. Every discovery—every challenge encountered on our reactor floor—feeds back into deliberate improvements, not just for our bottom line, but for the generation of molecules our customers will dream up next. No product stands still, and we will keep bringing every practical advancement to those who rely on our chemistry.

    Conclusion: Beyond Standard Supply, Toward Real Partnership

    For us, manufacturing 5-Chlorothianaphthene-3-Acetonitrile means far more than converting raw materials into a labeled drum. It’s about translating years of hands-on experience, investments in plant safety, relentless batch verification, and a real commitment to open communication into a product customers can trust every time. We stay grounded in facts, measured by our track record of continual improvement and transparent exchanges with industry partners. Whether your team explores new medicines, develops specialty materials, or scales a process from grams to tons, we stand ready to supply both the compound and the hard-earned insights that make your project a success.