6-(trifluoromethyl)pyridine-2-thiol

    • Product Name: 6-(trifluoromethyl)pyridine-2-thiol
    • Chemical Name (IUPAC): 6-(trifluoromethyl)-1λ¹-pyridine-2-thione
    • CAS No.: 349-84-6
    • Chemical Formula: C6H4F3NS
    • Form/Physical State: Powder
    • 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

    841124

    Chemical Name 6-(trifluoromethyl)pyridine-2-thiol
    Molecular Formula C6H4F3NS
    Molecular Weight 179.16 g/mol
    Cas Number 349-77-9
    Appearance Yellow to light brown solid
    Melting Point 56-58 °C
    Solubility Soluble in organic solvents such as DMSO and methanol
    Iupac Name 6-(trifluoromethyl)pyridine-2-thiol
    Smiles C1=CC(=NC(=C1)SC)C(F)(F)F
    Inchi InChI=1S/C6H4F3NS/c7-6(8,9)4-2-1-3-10-5(4)11/h1-3,11H
    Storage Conditions Store at 2-8°C, in a dry, well-ventilated place

    As an accredited 6-(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 The 10g amber glass bottle is tightly sealed, labeled with hazard symbols and product details: "6-(Trifluoromethyl)pyridine-2-thiol, 10g, for laboratory use."
    Container Loading (20′ FCL) **Container Loading (20′ FCL) for 6-(trifluoromethyl)pyridine-2-thiol:** Packed in tightly sealed drums, loaded securely, maximizing capacity, ensuring safe transport, minimizing contamination, and complying with hazardous material regulations.
    Shipping 6-(Trifluoromethyl)pyridine-2-thiol is typically shipped in tightly sealed containers under a dry, inert atmosphere to prevent moisture and air exposure. It is classified as a hazardous material and should be packaged according to relevant safety regulations. Proper labeling and documentation are essential to ensure safe handling and transportation.
    Storage 6-(Trifluoromethyl)pyridine-2-thiol should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry place away from light, heat sources, and incompatible substances like strong oxidizing agents and acids. Ensure proper labelling and store it in a well-ventilated chemical storage cabinet specifically for organosulfur compounds.
    Shelf Life 6-(Trifluoromethyl)pyridine-2-thiol typically has a shelf life of 2 years when stored in a cool, dry, and dark place.
    Application of 6-(trifluoromethyl)pyridine-2-thiol

    Purity 98%: 6-(trifluoromethyl)pyridine-2-thiol with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Melting Point 62°C: 6-(trifluoromethyl)pyridine-2-thiol with a melting point of 62°C is used in organic electronic material development, where it provides thermal stability during processing.

    Molecular Weight 179.16 g/mol: 6-(trifluoromethyl)pyridine-2-thiol with a molecular weight of 179.16 g/mol is used in heterocyclic compound manufacturing, where it enables accurate stoichiometric calculations.

    Stability Temperature Up to 120°C: 6-(trifluoromethyl)pyridine-2-thiol with stability up to 120°C is used in agrochemical formulation, where it maintains structural integrity during formulation blending.

    Particle Size ≤10 microns: 6-(trifluoromethyl)pyridine-2-thiol with particle size ≤10 microns is used in advanced catalyst preparation, where it promotes uniform dispersion and catalytic efficiency.

    Moisture Content ≤0.3%: 6-(trifluoromethyl)pyridine-2-thiol with moisture content ≤0.3% is used in specialty chemical synthesis, where it minimizes side reactions due to low water content.

    Assay ≥99%: 6-(trifluoromethyl)pyridine-2-thiol with an assay of ≥99% is used in fine chemical research, where it guarantees experimental reproducibility.

    Light Sensitivity: 6-(trifluoromethyl)pyridine-2-thiol with low light sensitivity is used in industrial scale-up processes, where it reduces degradation during storage and handling.

    Solubility in DMSO: 6-(trifluoromethyl)pyridine-2-thiol with high solubility in DMSO is used in medicinal chemistry applications, where it enables efficient compound screening.

    Boiling Point 250°C: 6-(trifluoromethyl)pyridine-2-thiol with a boiling point of 250°C is used in high-temperature reaction systems, where it ensures process reliability and safety.

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    Certification & Compliance
    More Introduction

    Introducing 6-(Trifluoromethyl)pyridine-2-thiol: A Synthesis Essential

    Real-World Chemistry, Built around Precision

    Anyone working with heterocyclic intermediates knows the pain points: purity swings, inconsistent physical properties, and the need for specialty functionalities that don't cut corners. Our direct production of 6-(trifluoromethyl)pyridine-2-thiol stems from our decade-long focus on demanding nitrogen-containing aromatics. This compound, with its selective trifluoromethyl substitution on the pyridine ring and thiol group at the ortho-position, draws significant interest from pharmaceutical, agrochemical, and specialty fine chemical researchers. It is not the sort of catalog item that gets tossed into a multipurpose drum. Instead, every batch reflects a commitment to reproducible, reliable synthetic chemistry—one that’s seen from the reactor floor all the way to scale-up discussions and lot-release data reviews.

    Understanding the Demand for 6-(Trifluoromethyl)pyridine-2-thiol

    We’ve listened to countless chemists at scale-up and process development benches pointing to the inefficiencies that emerge from less-refined pyridine thiols. Water content, trace amines, or fluorinated impurities cause headaches during downstream transformations, resulting in wasted runs or labor-intensive rework. Our aim with this product has always been to deliver a material that meets strict impurity profiles, because any compromise travels downstream. For reference, the model designation we use is directly tied to our in-plant lot tracking; nothing leaves our site without HPLC, NMR, and Karl Fischer moisture analysis in line with pharma-industry requirements. The white-to-pale yellow powders we bottle are the direct result of methodical quality control, from raw materials to packed product.

    Specifications Built to Industry-Driven Feedback

    Before we moved to full-scale production, we field-tested specification sheets with contract manufacturers and academic partners. Most arms-length traders see a molecule like 6-(trifluoromethyl)pyridine-2-thiol as a CAS number, a molecular weight, and a set of physical constants. That’s not our approach. Trace metal content, for example, emerges as a concern for catalytic cross-couplings and bioconjugation steps. Residual solvents from the last purification step can derail analytical characterization for high-resolution mass spectrometry. By adjusting both synthetic route and post-processing, we have been able to repeatedly meet or exceed the sub-ppb levels demanded by high-end applications in medicinal chemistry and material science.

    Why Chemists Choose this Compound in the Real World

    The driving force behind the use of 6-(trifluoromethyl)pyridine-2-thiol comes from the unique combination of reactivity and stability. The trifluoromethyl group adds both electron-withdrawing power and increased metabolic stability to scaffolds. For medicinal chemists, this often translates to new SAR space or improved ADME profiles during lead optimization. The thiol handle at position 2 offers a highly reactive nucleophile, suitable for modular elaboration, coupling with activated halides or acyl reagents, and late-stage functionalizations. Unlike more commonplace pyridines or simple thiols, this compound won’t succumb to the same patterns of oxidation or hydrolysis seen in less-engineered sulfur-containing chemicals. Our hands-on experience with real-time stability and reactivity studies has shown why customers say “ours works, theirs doesn’t.”

    Usage Highlights: From Bench to Plant

    It’s rare to have a molecule stay relevant from microgram to kilogram scale. Over the years, our 6-(trifluoromethyl)pyridine-2-thiol has appeared in pilot trials for patented active pharmaceutical ingredients, both as a linker motif and as a strategic building block during fragment-based design. Biologists and conjugation chemists lean on its predictable thiol chemistry for straightforward protein labeling. In specialty materials development, the electron-rich sulfur group interacts favorably with metal centers, opening the door to novel coordination complexes and ligands. Our process engineers have even worked alongside external customers to design solid forms that minimize clumping and improve handling for auto-dispense filling systems. Whether dry-packed or solution-phase, we stick to packing protocols that reflect the core end-use requirement.

    Differences from Other Products—What Experience Teaches

    From a manufacturer’s perspective, meaningful differences almost always come down to batch-to-batch consistency, crystallinity, and impurity clarity. Many competitors take the route of commercial intermediates, blending sources just to meet short-term price pressure. We own every step of the synthesis, including the preparation of all starting pyridines and key fluorinating agents, meaning traceability goes all the way back to primary starting materials. This commitment means we sidestep the kind of off-odor, brown tinge, or variable melting point that plagues off-the-shelf versions. Years ago, we received recurring feedback about a persistent “greasy” characteristic in a competitor’s sample. Reworking our purification to address this not only landed higher purity, but also eliminated caked particles that risked non-uniform distribution in automated reactors.

    Lessons from the Plant Floor: Purity versus Practicality

    Lab-scale synthesis often ignores the invisible hurdles of full-scale chemistry. Theoretical purity from a literature prep doesn’t always translate to an isolatable, storable, and easily weighed sample at scale. We’ve spent entire shift rotations monitoring slow crystallizations, troubleshooting oiling-out issues, and running comparative drying cycles. Each round taught us that trace moisture management played a vital role in shelf-life, and that physical form dictated ease-of-use on automated scales. Reliable analytical backing lets us share full QC documentation, because we know customers need this both for regulatory filing and method validation. We vet every lot against independent analytical standards, sharing COA and method files, so end-users can spot-check and reproduce results with confidence.

    Supporting Data: What Drives Trust

    Not all products come with this level of transparency. From the earliest lots shipped, we’ve attached detailed chromatograms and both NMR and FTIR spectra with every supply. It’s not just about ticking boxes for compliance—customers want rapid troubleshooting, especially as regulatory expectations for trace-level contaminants rise. Following up on reports of minor off-color, we have instituted a retention-sample policy and respond with real-time batch performance data. Our online library now houses anonymized lot summaries, so process chemists can readily access historical batch behavior prior to purchasing. These details become especially valuable in method transfer or tech-pack handoffs between partners.

    Building a Track Record, Not Just a Catalog

    Direct manufacturer involvement in scaling up 6-(trifluoromethyl)pyridine-2-thiol has illuminated just how much seemingly minor specification differences affect end-user satisfaction. Experience forced adaptations in everything from filtration choice to final bottling. Recent conversations with partners migrating from alternative thiolated pyridines revealed that product clarity on method compatibility, blending properties, and volatility had outsized impacts on synthetic throughput. People working at the interface between R&D and production appreciate knowing they can rely on a compound to perform without end-of-batch surprises or difficult material-handling quirks.

    Beyond Bulk: The Edge of in-House Customization

    With our full in-house production, new requests are fielded directly by our synthesis chemists, not shuffled through intermediaries reading from a script. Custom particle sizes, multi-kg campaign volumes, documented impurity profiles, or alternative packing formats—these are adjustments we own in real time. Sometimes customers ask for enhanced dryness specifications. We accommodate with dedicated vacuum ovens and certified desiccant packaging lines. On several occasions, specialized research applications required delivery in custom ampoules for air-sensitive work; we brought these downstream in just a few production runs. Each adjustment cycles back into our production knowledgebase, raising the bar for future deliveries.

    Supporting Process Chemistry: Details That Matter

    Over the course of many collaborations, our team noticed project setbacks emerging from misconceptions around similar thiolated pyridines. For example, the difference made by the electron-donating power of the 2-thiol compared to 3- or 4-positioned analogues is not trivial for heterocycle functionalization. We include commentary in technical notes or customer webinars on anticipated reactivity trends and compatibility concerns. These practical touchstones bridge the gap between a chemical nameplate and tangible productivity at the bench. It’s not uncommon for customers to share application notes with us post-purchase, which circle back to inform our internal guidance and synthesis approach.

    No Substitute for Proven Performance

    Decades in the field clarify that there’s no shortcut to winning long-term customer relationships with a finicky specialty intermediate like 6-(trifluoromethyl)pyridine-2-thiol. Since the product doesn’t conform to a one-size-fits-all mentality, rolling out lines based on direct client requirements builds mutual credibility. Not every supplier is prepared for this depth of engagement; the temptation with specialty intermediates always involves splitting lots, pushing marginal material for small-scale buyers, or generic relabeling to fill gaps. We reject these practices because doing so directly supports reproducible science and robust manufacturing. Each successful batch advances not only our own standards but also raises the expectation for quality industry-wide.

    Recognizing Limitations, Avoiding Over-Claims

    We are upfront about application limits. While the compound has proven valuable in both classic and modern coupling techniques, it isn’t compatible under strongly acidic conditions for prolonged periods, as the pyridine ring can undergo decomposition. Our technical support staff puts forward solvent and storage suggestions rooted in firsthand process development setbacks. Nothing sours a relationship quicker than overpromising, and our technical team commits to providing an honest view of potential challenges when working with sulfur-functionalized heterocycles.

    Path Forward: Meeting New Industry Challenges

    Regulations shift, end-use requirements tighten, and analytical thresholds continue to push downward. Our plant adapts as a matter of course, recently investing in inline process monitoring and upgraded microanalytical equipment to keep pace with trace-level demands. Maintaining flexibility proved critical, as customers began pursuing continuous manufacturing paradigms and automated quality control. More than once, alignment around new delivery forms or scale-up milestones called for pauses, extra sample characterization, or direct customer visits—steps a trader will never take but are second nature for a producer whose name stands behind every drum and bottle shipped.

    Values, Experience, and Customer Outcomes

    Direct manufacturing cultivates a close relationship with the science of synthesis. Familiarity with reaction progression, purification caveats, and post-synthetic handling routines transforms basic raw materials into reliable partners for advanced research. That familiarity is hard-won, in years of failed crystallization experiments and new process iterations. The best validation comes not in certificates, but in the repeated return of project chemists and purchasing managers, who see measurable improvements in yield, ease of workup, and reproducibility. We continue to gather feedback as a fundamental part of our ongoing development process, keeping ears open to the shifting landscape of specialty intermediates.

    Looking Ahead: Supporting Smarter Chemistry

    As new medicines, crop production agents, or materials emerge, the baseline for chemical intermediates like 6-(trifluoromethyl)pyridine-2-thiol keeps evolving. Every new challenge—be it a more robust impurity profile, safer packaging formats, or documentation for regulatory audits—drives us to revisit both process and product. Our role as a chemical manufacturer involves anticipating and solving not only the expected, but also the unforeseen, stumbling blocks in specialty chemistry. The ongoing dialogue with our partners will always shape the next improvements, ensuring research and industry move forward with tools they trust.