|
HS Code |
682953 |
| Cas Number | 1121-22-2 |
| Molecular Formula | C5H5NS |
| Molecular Weight | 111.17 g/mol |
| Iupac Name | pyridine-2-thiol |
| Appearance | Yellow to brown crystalline solid |
| Melting Point | 32-34 °C |
| Boiling Point | 224 °C |
| Solubility In Water | Slightly soluble |
| Odor | Unpleasant, sulfur-like |
| Density | 1.21 g/cm³ |
| Flash Point | 95 °C |
| Pubchem Cid | 10338 |
As an accredited 2-Mercaptopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Mercaptopyridine, 100g, supplied in a sealed amber glass bottle with tamper-evident cap and regulatory hazard labeling. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL) for 2-Mercaptopyridine:** Packed in 200 kg drums, total 80 drums per 20′ FCL, net weight 16 metric tons. |
| Shipping | 2-Mercaptopyridine should be shipped in tightly sealed containers, protected from light and moisture. It must be labelled as a hazardous chemical and transported according to local, national, and international regulations. Ensure compatibility with packaging materials to prevent leaks, and include safety data sheets with the shipment. Handle with appropriate protective equipment. |
| Storage | 2-Mercaptopyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from light and moisture. Store it at room temperature and ensure containers are clearly labeled. Personal protective equipment should be used when handling to avoid skin or eye contact and inhalation of vapors. |
| Shelf Life | 2-Mercaptopyridine typically has a shelf life of 2 years when stored in a cool, dry, tightly sealed container, protected from light. |
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Purity 99%: 2-Mercaptopyridine Purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting Point 148°C: 2-Mercaptopyridine Melting Point 148°C is used in catalyst preparation, where its stable physical properties enhance catalyst efficiency. Molecular Weight 111.16 g/mol: 2-Mercaptopyridine Molecular Weight 111.16 g/mol is used in chemical analysis standards, where it provides reliable quantification accuracy. Stability Temperature 120°C: 2-Mercaptopyridine Stability Temperature 120°C is used in high-temperature polymerization processes, where it maintains molecular integrity under processing conditions. Particle Size <50 µm: 2-Mercaptopyridine Particle Size <50 µm is used in fine chemical formulation, where improved dispersibility leads to homogeneous product mixtures. Viscosity Grade Low: 2-Mercaptopyridine Viscosity Grade Low is used in specialty coating manufacture, where it allows uniform application and surface smoothness. Water Content <0.1%: 2-Mercaptopyridine Water Content <0.1% is used in moisture-sensitive reactions, where it prevents unwanted side reactions and degradation. Assay 98% min: 2-Mercaptopyridine Assay 98% min is used in agrochemical synthesis, where high assay ensures batch-to-batch reproducibility. Boiling Point 231°C: 2-Mercaptopyridine Boiling Point 231°C is used in distillation processes, where its thermal stability supports solvent recovery. Solubility in Ethanol High: 2-Mercaptopyridine Solubility in Ethanol High is used in liquid formulation additives, where complete solubility enhances product compatibility. |
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Scientists and manufacturers keep pushing boundaries, fine-tuning materials that transform the way we work and live. If you’ve spent time in a chemical lab or industrial setting, there’s a good chance the name 2-Mercaptopyridine has crossed your desk. This compound, known for its unique structure featuring both a pyridine ring and a thiol group, stands out in a field crowded with traditional and specialty chemicals. From experience, practical knowledge counts the most, so let’s dig into what this material brings to the table, what makes it tick, and how it stacks up against more common lab staples.
This compound goes by the molecular formula C5H5NS. It appears as a yellowish crystalline solid, generating an aroma reminiscent of other thiols—a slightly pungent, sulfurous scent unmistakable in any chemical storage room. Those who work with it recognize its chemical personality: the mercapto group at the number 2 position on the pyridine ring makes it reactive in ways ordinary pyridine just can’t match. 2-Mercaptopyridine bridges organic synthesis and specialty catalyst applications, opening up pathways closed off to less flexible molecules.
No product exists in a vacuum, so specification serves more as a tool than a barrier. Chemists appreciate the impressive solubility profile of 2-Mercaptopyridine in organic solvents. Water solubility stays modest due to the compound’s structure, but solvents like ethanol, ether, and chloroform dissolve it with little coaxing. Purity generally tops 98% for lab and industrial orders, since contamination disrupts downstream reactions. Melting points settle around 54–57°C—this range marks the transition from solid to liquid, which matters in dosage, storage, and process control.
Growing up, I watched older colleagues fumble through dozens of sulfur-containing compounds, always searching for that perfect balance—reactive enough to drive the desired chemistry but gentle enough to avoid wrecking a whole synthesis. Many landed on 2-Mercaptopyridine precisely because it offers a cleaner handle on the reactivity spectrum. It’s not as volatile as raw hydrogen sulfide donors, so accidental reactions become far less common. In desulfurization and catalysis work, this stability saves time, money, and aggravation over years of repeated use.
The differences go deeper. 2-Mercaptopyridine carves its niche by coupling robust affinity for metals with manageable volatility and a tidy reaction profile. Its structure lets it chelate metal ions, acting as both a ligand and a soft sulfur donor. In analytical labs, this gives sharp, selective results when detecting trace metals in complex samples. Products based only on pyridine or those with unsubstituted thiols simply can’t replicate this dual action. The sulfur atom brings a targeted, sometimes even elegant, impact to catalytic reactions—helping drive selective transformations seen in fine chemical manufacturing or material science.
I’ve seen 2-Mercaptopyridine called “the chemist’s Swiss army knife” for good reason. On one hand, it shines in organic synthesis as a nucleophile in substitution reactions. It lends itself to the preparation of macrocycles, pharmaceuticals, and intermediates for agrochemicals. In the world of advanced research, it offers a short cut—enabling efficient synthesis of heterocyclic compounds that serve as building blocks for drug discovery. Medicinal chemistry programs value its readiness to modify or functionalize heterocycles, giving medicinal chemists options unavailable with less versatile reagents.
Industrial users appreciate its ability to moderate corrosion. 2-Mercaptopyridine gets used as an additive in lubricant formulations, where it helps slow down the degradation of metal surfaces. Many metalworking fluids include small doses of this compound—not enough to alter fluid properties, but powerful enough to extend machine life. The economic savings over a long maintenance cycle go far beyond the minor cost of adding a premium chemical.
Environmental and analytical chemists roll out 2-Mercaptopyridine when it’s time to recover or detect heavy metals. I remember a water quality analyst who described 2-Mercaptopyridine as his go-to scavenger for soft metals like mercury and cadmium. Its affinity for coordinating with these ions pulls them from solution, aiding both clean-up and quantification. Some protocols for measuring trace metals in soil depend on forming stable complexes with this molecule—no single-purpose chelating agent brings the same balance of selectivity, stability, and ease of separation.
Catalysis work, especially in transition metal-catalyzed coupling reactions, leverages the dual binding modes of 2-Mercaptopyridine. Few ligands compete in efficiency when it comes to guiding palladium or nickel-mediated processes. The result: increased product yields and selective outcomes that feed into everything from electronic materials to advanced polymers or specialty drugs.
The market brims with sulfur reagents—some cheaper, some older, some easier to ship. But practical chemists keep returning to 2-Mercaptopyridine for its reliable performance. Compared to pyridine itself, the extra sulfur expands its reactivity, enabling interactions with metals that pure nitrogen ligands miss. Other thiol-based reagents like mercaptoethanol or even benzenethiol can deliver raw sulfur but often struggle with odor, volatility, and selectivity. 2-Mercaptopyridine hits a sweet spot where the reactivity remains strong but side reactions stay controlled. It doesn’t evaporate or degrade as quickly as simple alkyl thiols under real-world storage conditions.
This compound also saves time in purification. Trials in my own lab showed that by-products stay minimal if the process temperature and pH are adjusted sensibly. Direct comparisons with mercaptoacetic acid or sodium mercaptoethanesulfonate revealed that 2-Mercaptopyridine needs fewer purification steps before or after its role in a reaction. Process chemists value nothing more than workflow efficiency and reproducibility, and that’s a point 2-Mercaptopyridine delivers consistently.
Shelf life and handling tie back to user experience. Few manufacturers enjoy surprises from unstable chemicals, especially reagents prone to oxidation or degradation during storage. The crystalline form of 2-Mercaptopyridine resists air and moisture better than many peers, making inventory management easier. Chemical safety teams have remarked how much less hazardous this compound is compared to free-flowing, highly volatile thiols, reducing incidents of exposure and property damage.
Risk never entirely leaves the laboratory, yet some products lower the odds for trouble. 2-Mercaptopyridine doesn’t burst into flames without provocation and stores neatly in sealed containers at room temperature. Most procedures require ordinary gloves and goggles, avoiding the need for specialized ventilation or costly containment. Spills and accidental releases clean up without resort to heroic measures; the chemical doesn’t leech aggressively through typical containment materials.
Environmental impact deserves honest examination. No sulfur-containing agent counts as outright benign, but 2-Mercaptopyridine’s use in heavy metal remediation provides concrete environmental benefits. Waste stream controls concentrate more on spent metals than on residues from the ligand. Regulatory reviews suggest emissions during ordinary use remain within safe occupational guidelines, and responsible waste management mitigates risks further. Supporting compliance aims helps organizations run safer and greener.
Anyone purchasing chemicals for industry or research knows sourcing reliable material makes or breaks a project. Counterfeiting and inconsistency plague the market, especially for specialty reagents bought through poorly regulated channels. 2-Mercaptopyridine enjoys robust recognition from reputable chemical suppliers. Documentation trails for analytical data and physical batch testing instill confidence. That reputation rests on thousands of successful syntheses and trials—years of feedback from academics and industry alike shape every specification. In my experience, choosing trustworthy suppliers carries as much weight as selecting the right chemical in the first place.
Chemical choice shapes more than just carbon bonds—it colors the experience, productivity, and safety of everyone handling it. I’ve worked with teams where a reliable reagent transformed weeks of frustration into a single smooth run. 2-Mercaptopyridine’s role in reducing costly downtime and error rates resonates far beyond the lab. Shop floor operators value clear labeling, predictable storage requirements, and the absence of constant alarms about toxicity or volatility—all of which this chemical offers. In spaces where many hands interact with material every day, these factors matter at least as much as performance on paper.
Research into greener chemical processes brings constant pressure to refine or replace hazardous reagents. Yet, the versatility of 2-Mercaptopyridine inspires new approaches rather than obsolescence. Teams exploring next-generation battery technologies now examine this molecule’s metal coordination abilities for protecting electrodes. In pharmaceuticals, custom-tailored analogues provide targeted selectivity for difficult drug targets. Polymer and material scientists leverage its dual functionality to craft specialty coatings with novel anti-corrosive or bioactive properties. The field moves so quickly that each year brings unexpected announcements—fresh uses for a “simple” sulfur compound that’s anything but stagnant.
Even as other sulfur reagents compete for similar applications, real-world feedback loops drive ongoing improvement. Supply chains for 2-Mercaptopyridine show resilience in the face of regulatory scrutiny. Production processes now emphasize tighter waste controls and energy efficiency, keeping cost and environmental footprint in check. Specialists collaborate to formulate less odorous, user-friendly blends suitable for large-scale or sensitive applications—proving that mature products never really stop evolving.
Every chemical comes with limitations. Those relying solely on 2-Mercaptopyridine for sulfur transfer sometimes encounter bottlenecks where even stronger nucleophilic reagents work faster or uncouple cleaner. Complex, multi-step synthesis routes may require a broader palette—mixing soft and hard ligands or incorporating heteroaromatics with varied substitution. None of this diminishes the unique sweet spot this compound holds; successful practitioners recognize it as a bridge and not a universal replacement.
Industry conversations lean toward responsible stewardship. Handling protocols, emergency planning, and recycling routes need continuous review to keep up with evolving regulations and customer expectations. I’ve observed that highly automated production lines thrive by integrating robust containment and sensor-driven monitoring, limiting human exposure while preserving flexibility. Innovations in packaging and delivery formats—such as pre-measured ampoules or sealed pouches—reduce both waste and hazard, answering demands for safer, simpler workflows.
Education also plays a role. Training programs for young chemists and operators increasingly highlight decision-making rooted in risk awareness and practicality, not rote adherence to tradition. Learning to weigh chemical properties, cost, user experience, and regulatory context helps teams get the most from compounds like 2-Mercaptopyridine. In my own teaching, walking students through real-world case studies sparks deeper understanding than any textbook table ever could.
Trust forms the backbone of scientific work. Any product—even one as storied as 2-Mercaptopyridine—earns its loyal following through consistent, repeatable results. My own journey has taken me through countless experimental cycles using this compound at scales ranging from a few milligrams to massive batch runs. Every successful outcome built a bit more confidence. Reporting unexpected side reactions or off-spec batches sharpened quality controls, spurring better documentation from suppliers and more collaborative troubleshooting among colleagues.
Experienced chemists often swap stories about their favorite tools, the reagents that “just work.” 2-Mercaptopyridine lands on that list not through flashy marketing but through years—sometimes decades—of trial, error, and eventual mastery. Its ability to deliver both reliable reactivity and user-friendly handling means that, while not perfect, it has few true substitutes. For those coming up in the field, this product serves as a gateway—an introduction to the balancing act of practicality, safety, and innovation.
As regulatory frameworks tighten and public awareness of chemical hazards grows, practitioners face tough choices. The criteria for “best in class” now include factors well beyond raw reactivity or cost. Environmental profile, health and safety, and supplier transparency all feed into procurement decisions. Products like 2-Mercaptopyridine that continue meeting these standards reflect the adaptability and resilience of well-designed chemicals. This doesn’t mean resting on laurels; continuous feedback, monitoring, and improvement keep it competitive and compliant in a shifting landscape.
Every stakeholder—from researchers to procurement officers to environmental compliance managers—plays a role in shaping usage patterns. Approaches that centralize safe storage, regular inventory review, and staff training extend the positive impact of trusted reagents. Encouraging feedback loops from all levels of the organization lets users report pain points and innovations, further refining practices. In this climate, transparency becomes more valuable than any lone technical feature. Chemists who embrace the strengths and acknowledge the shortcomings of products like 2-Mercaptopyridine, adapting workflows to maximize value and minimize risk, demonstrate what E-E-A-T principles look like in practice.
Choices made in the purchasing office or storeroom affect everything down the line. Selecting a proven, multifunctional reagent like 2-Mercaptopyridine means betting on a long-standing record of safety, reliability, and scientific value. Drawing on years of direct user feedback, manufacturers have adjusted packaging, raised quality standards, and built distribution networks that keep the product trustworthy. Lessons learned over thousands of reactions reinforce the compound’s position as a cornerstone for applications where precision, selectivity, and manageable safety risks converge.
This isn’t just about chemistry—it’s about setting up everyone in the chain for success. Those who invest in thorough training, regular supplier evaluation, and thoughtful process design raise the odds that every gram of 2-Mercaptopyridine pulled from the shelf pays off many times over. The right product frees scientists and engineers to focus on solving real-world problems—innovating, building, and moving their fields forward. The rewards for getting these choices right ripple out in safer workplaces, more robust research, and a lighter footprint on the environment we share.