5-(Trifluoromethyl)pyridine-2-thiol

    • Product Name: 5-(Trifluoromethyl)pyridine-2-thiol
    • Chemical Name (IUPAC): 5-(Trifluoromethyl)pyridine-2-thiol
    • CAS No.: 22233-56-9
    • Chemical Formula: C6H4F3NS
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    635231

    Chemical Name 5-(Trifluoromethyl)pyridine-2-thiol
    Molecular Formula C6H4F3NS
    Molecular Weight 179.16 g/mol
    Cas Number 139636-56-3
    Appearance Pale yellow to yellow solid
    Melting Point 44-48°C
    Solubility Soluble in organic solvents like DMSO and DMF
    Smiles C1=CC(=NC=C1SC)C(F)(F)F
    Purity Typically >97%
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Synonyms 5-(Trifluoromethyl)-2-mercaptopyridine

    As an accredited 5-(Trifluoromethyl)pyridine-2-thiol 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-(Trifluoromethyl)pyridine-2-thiol, tightly sealed with a screw cap and hazard labeling.
    Container Loading (20′ FCL) 20′ FCL can load approximately 10.4 MT of 5-(Trifluoromethyl)pyridine-2-thiol, packed in 200 kg HDPE drums.
    Shipping 5-(Trifluoromethyl)pyridine-2-thiol is shipped in tightly sealed containers to prevent moisture and air exposure. Packaging complies with chemical safety regulations, including appropriate hazard labeling. During transit, the chemical is protected from excessive heat and direct sunlight. Shipping methods follow all relevant regulations for hazardous materials handling and transport.
    Storage Store **5-(Trifluoromethyl)pyridine-2-thiol** in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and properly labeled. Avoid exposure to moisture and incompatible materials such as strong oxidizers. Store in a chemical-resistant container, preferably under an inert atmosphere like nitrogen or argon if prolonged storage is required.
    Shelf Life 5-(Trifluoromethyl)pyridine-2-thiol should be stored in a cool, dry place; shelf life is typically 2 years under proper conditions.
    Application of 5-(Trifluoromethyl)pyridine-2-thiol

    Purity 98%: 5-(Trifluoromethyl)pyridine-2-thiol with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and low impurity accumulation.

    Molecular Weight 181.16 g/mol: 5-(Trifluoromethyl)pyridine-2-thiol with molecular weight 181.16 g/mol is used in agrochemical active compound development, where it facilitates precise formulation and consistency.

    Melting Point 42-44°C: 5-(Trifluoromethyl)pyridine-2-thiol of melting point 42-44°C is used in organic electronic materials research, where it allows reliable thermal processing and uniform film formation.

    Stability Temperature up to 120°C: 5-(Trifluoromethyl)pyridine-2-thiol with stability temperature up to 120°C is used in catalyst precursor manufacturing, where it maintains composition integrity during high-temperature reactions.

    Particle Size <50 μm: 5-(Trifluoromethyl)pyridine-2-thiol with particle size less than 50 μm is used in fine chemical synthesis, where it enables rapid dissolution and uniform reaction rates.

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    Certification & Compliance
    More Introduction

    5-(Trifluoromethyl)pyridine-2-thiol: A Direct Manufacturer’s Look

    Experience and Craft in Chemical Production

    Chemical manufacturing shifts constantly with industry demand and research directions. Over years on the production floor and in the R&D lab, the realities of synthesis have shaped how we look at molecules like 5-(Trifluoromethyl)pyridine-2-thiol. We work from raw material all the way to packed product, seeing the full journey of every batch. This proximity builds a keen sense for what reaction steps bring out purity and which crude byproducts to avoid, as well as how much waste is worth recycling. In cases where a process seems stable, regulatory changes or supply chain disruptions highlight why detailed control over starting reagents and storage are not just checkboxes, but essential for both safety and quality.

    Specifics of Model and Production Approach

    We produce 5-(Trifluoromethyl)pyridine-2-thiol in batches with careful attention to structural consistency. Molecular formula stands as C6H4F3NS. Our typical model, which many in the industry refer to as closely aligned with CAS 352-35-6, comes from carefully sourced fluorinated compounds and pyridine intermediates. Attention to small details plays out on the bench: one misstep in handling trifluoromethylation causes chain reactions that leave impurities stubborn and hard to remove. Manufacturing at scale calls for reactor setup that provides steady agitation, gradual temperature ramp, and thorough ventilation, since the intermediate steps release sharp, sometimes caustic vapors. We prefer stainless steel reactors for maintaining product integrity and design our filtration steps to capture material that tries to escape with the mother liquor.

    We achieve a material with purity above 98.5%, according to HPLC and NMR testing in-house. Our technicians pulled insights from early pilot runs, tightening the reaction time window and focusing on solvent quality as the single biggest step for yield consistency. It is easy to underestimate how a little leftover water in a batch can throw off the extraction; repeated hands-on trial has taught our process chemists not to take shortcuts. Analytical staff keep a close watch for signs of decomposition, since the sulfur group in the thiol walks a fine line between reactive and stable. Stability holds tightly during refrigerated storage in glass-lined containers, lined to prevent any metal contamination from interfering with subsequent synthesis.

    Applications: More Than Just a Reagent

    Industries request this product for its fine balance of functional groups. The trifluoromethyl side lends both electronegativity and lipophilicity, factors prized in pharmaceutical intermediate work or the construction of specialty agrochemicals. We see customers tune this compound for reactions involving complex aromatic substitutions or for coupling steps where both reactivity and selectivity matter. At the bench or in the plant, small changes to functional group combinations—switching, for example, a methyl group for trifluoromethyl—make a world of difference in both final compound stability and performance.

    Synthesizing more advanced pharmaceuticals often calls for aromatic building blocks that tolerate a range of reaction conditions. 5-(Trifluoromethyl)pyridine-2-thiol steps in because the pyridine core meets stringent electronic specifications, and the thiol group opens further downstream coupling possibilities. For process chemists, predictable behavior during halogenation or oxidation means fewer failed runs and more predictable development schedules. The manufacturing line values not just reactivity, but the way this compound’s byproducts behave—easier phase separation, good filtration, and quick waste treatment. Over the years, feedback from end users has shown that impurities in the thiol region cause headaches further down the synthesis chain, costing both time and lost material. This is why high purity and well-characterized side products remain a point of pride for us.

    Agrochemical researchers and formulation chemists sometimes use this compound as an intermediate, especially in constructing molecules that resist environmental break-down while maintaining a required activity profile. The presence of both pyridine and trifluoromethyl functionalities helps balance biological activity with necessary chemical durability, resulting in formulations that last longer in field trials without leaching breakdown products as quickly.

    Real Factory Challenges and Solutions

    The gap between laboratory curiosity and continuous manufacturing brings problems that catalogs often gloss over. Keeping the trifluoromethyl group intact requires a dry atmosphere during synthesis and a steady flow of inert gas in storage. Years ago, small leaks in the nitrogen line led to decreased shelf life and batch-to-batch variability, even though all other conditions looked right on paper. Catching such issues demands daily vigilance, not just periodic audits. Our maintenance staff now monitor both air-tight gaskets and pressure systems at multiple points.

    Handling effluent poses another challenge, as waste streams from fluorinated syntheses contain persistent materials. Our approach replaces traditional halogenated solvents with more easily treated alternatives. Even so, collection, neutralization, and incineration steps for side products receive detailed scrutiny from both process engineers and outside reviewers. Lessons from early runs, where local fluorine contamination crept into water analysis, led us to strengthen containment and switch to a triple-washout system. This increases both safety and regulatory compliance, serving both our production crew and the communities near our sites.

    When talking about supply chain, upstream sourcing of key starting reagents often experiences unexpected bottlenecks. Not long ago, a worldwide shortage of key fluorinated aromatics slowed production schedules. Building long-term relationships with upstream partners helps manage such risks. We learned, through trial and error, to keep a strategic reserve of both precursor material and finished intermediate, a move that allows us to maintain availability even as markets shift or regulatory rules tighten.

    Comparisons With Related Compounds in Actual Use

    Working with 5-(Trifluoromethyl)pyridine-2-thiol differs from using pyridine derivatives that lack a trifluoromethyl or thiol group. The trifluoromethyl moiety changes how the molecule interacts in both chemical and biological systems. Pyridines without the trifluoromethyl feature characteristically react at different positions and do not carry the same degree of stability under strong acidic or oxidative conditions. In practical use, these differences stand out during no-nonsense batch production: side reactions increase, off-color byproducts pile up, and recovery drops.

    Thiol-free pyridine options miss out on cross-linking capacity, especially for applications undertaking further transformation or metal complexation. The thiol site proves essential when users want to tether this core to other moieties or surfaces, such as when constructing advanced catalysts or tagging agents. From our shop floor perspective, the inclusion of both thiol and trifluoromethyl groups hands formula designers a way to tune reactivity without multiple synthetic steps, avoiding the extra work and waste.

    Other suppliers sometimes offer similar-sounding compounds—often at a discount—produced through secondary step recovery or by repurposing byproducts from other pyridine or trifluoromethyl product lines. We have studied samples from other sources in our own QC lab, and it becomes obvious why direct manufacturing leads to cleaner spectra, fewer unidentified peaks, and better downstream compatibility. Such insights come only after running hundreds of kilograms through both analytical equipment and practical plant use—real experience shapes this conclusion, not a marketing slogan.

    Handling and Safety: Experience in the Real World

    On the ground, handling 5-(Trifluoromethyl)pyridine-2-thiol demands more care than some might expect reading a technical data sheet. The sharp odor of the thiol warns any operator nearby, and staff learn quickly to use personal protective equipment, maintain good ventilation, and avoid cross-contamination with other volatile sulfur compounds. Experience shows that containment hoods require change-out or deep cleaning more often than with simple pyridines.

    Storage containers—especially glass-lined vessels—prevent unwanted side reactions and metal-catalyzed decomposition. We have seen storage trials in both drum and tank configurations, and our long-term data support keeping the product under a dry, inert atmosphere at room temperature or below. Workers follow strict protocols for sample withdrawal, since even a small spill means noticeable odor and a clean-up cycle that interrupts workflow.

    Our accident logs show that slips usually come from distractions during transfer steps or a quick grab for the wrong solvent. We reinforce training so operators always double-check both label and container integrity. Direct and repeated experience on the floor curbs surprises, even when working with an established process. After all, the best results come from smooth, uneventful runs—and those grow out of disciplined, attentive, and well-trained handling.

    Downstream Processing: What Matters in the Plant

    When a synthesized batch moves past QC, plant-scale processing continues to demand vigilance. 5-(Trifluoromethyl)pyridine-2-thiol behaves differently than unfluorinated analogs during crystallization and drying. Its volatility is mild, but thiol odor lingers, so exhaust systems must operate efficiently. Our team found early on that using rotary evaporators under reduced pressure preserved both the thiol integrity and product color, while open-vessel drying led to yellowing and slight decomposition. Experience taught us that even minor overexposure to oxygen or sunlight during this stage dulls the product and complicates further reactions.

    For customers, clean filtering and smooth redissolution for use in organic synthesis matter enormously. We developed grinding and sieving protocols to prevent clumping during storage, and focused on reliable packaging—sealed, moisture-proof drums or foil bags, depending on user volumes. Operators keep a dedicated line for packing fluorinated pyridine derivatives, so as to avoid mix-ups that sometimes occur in multi-product facilities.

    Quality Control: More Than a Checklist

    Running a production site for this molecule reveals that diligent quality control is not just regulatory compliance—it is the key to both plant safety and a good working relationship with end users. We rely on liquid chromatography for both in-process and finished product monitoring, keeping close track of small peaks that signal unwanted byproducts. Our analytic staff spends time correlating slight shifts in spectra with operator logs, learning to spot trends before problems spread.

    Routine cross-checks between on-site and third-party laboratory results ensure objectivity in reporting. We continually upgrade our instrumentation and cross-train staff to interpret ambiguous results with context, not just formulaic comparison to specification sheets. Fielding customer queries and sharing our in-house spectra builds trust and provides reciprocal feedback that improves both sides of the supply chain. Over years, evolving solvent restrictions, shipping regulations, or customer requirements for trace impurity reporting mark not only challenges but also benchmarks for process evolution.

    Shipping and Storage: Practical Solutions

    The practicalities of shipping this product force manufacturers to engineer robust solutions for containment and transit protection. We use lined steel and high-density polyethylene drums for bulk consumers, always with secondary containment to control any accidental leaks or vapor build-up. Our logistics team tracks temperature, ensuring shipments avoid excessive heat even in long transits, and deploys datalogger technology to capture environmental data throughout the journey. Clients operating on several continents can request small-lot pilot batches or full-scale deliveries, with pre-shipment sampling and real-time tracking.

    Long experience with customs clearance and classification of fluorinated organosulfur compounds warns us against paperwork shortcuts. Any omission risks costly delays. We maintain tight documentation and label standards to speed clearance and meet both local and import hygiene protocols. Ensuring the stability of packaged product until receipt at the customer’s door stems from years of troubleshooting—real-time input from both our logistics and technical staff leads directly to these improvements.

    Key Lessons Drawn From Manufacture and Supply

    Experience with this compound teaches lessons that stay with us regardless of shifts in market demand or regulatory favor. We witnessed that plant safety, raw material transparency, and detailed operator training protect not only machine uptime but keep human risk at bay. Supply shocks and volatile raw materials taught us the value of forward planning and investment in long-term partnerships.

    Manufacturing to a high standard means blending scientific rigor with boots-on-the-ground insights. The chemistry of 5-(Trifluoromethyl)pyridine-2-thiol offers opportunity for innovation in end-use development, but only if the product is reliable, traceable, and holds up under scrutiny. These qualities take real-world effort—the kind not visible from a product database or generic write-up. Our long track record, weekly machine logs, operator input, and unfiltered post-mortems on both successes and failures have built the practical knowledge that shapes our current process.

    Research Collaboration and Future Directions

    Open exchange between manufacturers, researchers, and formulators drives both our own methods and improvements in downstream fields. Collaborating with university chemists and startup process teams gives us a window into emerging applications, such as expanded use in electronic materials or as coupling partners in next-generation catalysts. Frequent pilot runs with small changes in reagent profile give real feedback on what works, and just as importantly, what fails under true plant conditions.

    Ideally, as regulation on fluorinated materials tightens, industry-wide effort will streamline safer and more sustainable production routes. We contribute by refining waste treatment, reducing the use of persistent solvents, and publishing our experience with safer alternatives. These measures crop up not as abstract greenwashing but as vital, day-to-day realities in operating a modern specialty chemicals plant.

    Clients who embrace long-term supply relationships benefit most when they share outcome data and process performance. Our openness to share in-process spectra and discuss anomalous results sharpens both our next run and the customer’s synthesis outcomes. These steady, fact-based relationships beat market fluctuations and last beyond short-term order cycles.

    Authority and Confidence Born at the Production Line

    Years of direct production, on-the-ground troubleshooting, and open collaboration with discerning customers shape how we view and supply 5-(Trifluoromethyl)pyridine-2-thiol. Advice emerges from coil reactors, midnight shift logs, and the practical success of our facility crew every single day. Synthetic chemists and process engineers who trust the reality—over slick description—end up with fewer surprises and greater success in their projects.

    The practical authority of a manufacturer comes from clean instruments, clear spectra, low waste, stable shipments, and honest post-mortem of outlier batches. Every kilo of 5-(Trifluoromethyl)pyridine-2-thiol carries this accrued hands-on knowledge, delivering a product that does more than check off a spec—it works, because the people who make it live and breathe its chemistry.