|
HS Code |
266122 |
| Chemicalname | 2-Pyridinecarbothioamide |
| Synonyms | Picolinethioamide |
| Casnumber | 872-88-2 |
| Molecularformula | C6H6N2S |
| Molecularweight | 138.19 |
| Appearance | Yellow to brown solid |
| Meltingpoint | 110-114°C |
| Solubility | Slightly soluble in water |
| Density | 1.29 g/cm3 |
| Smiles | C1=CC=NC(=C1)C(=S)N |
| Inchi | InChI=1S/C6H6N2S/c7-6(9)5-3-1-2-4-8-5/h1-4H,(H2,7,9) |
| Pubchemcid | 189653 |
As an accredited 2-Pyridinecarbothioamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2-Pyridinecarbothioamide (25g) is a tightly sealed amber glass bottle with a printed hazard label and product details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 12 metric tons of 2-Pyridinecarbothioamide packed in 25 kg fiber drums, securely palletized for shipping. |
| Shipping | 2-Pyridinecarbothioamide is shipped in tightly sealed containers, protected from light and moisture to maintain stability. It is classified as a laboratory chemical and must be handled according to appropriate safety guidelines. Shipping is typically done via ground or air, complying with chemical transport regulations to ensure safe and secure delivery. |
| Storage | 2-Pyridinecarbothioamide should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect it from moisture, heat, and direct sunlight. Ensure the storage area is equipped with appropriate spill containment and labeling. Use chemical storage cabinets suitable for organic compounds to minimize risk. |
| Shelf Life | 2-Pyridinecarbothioamide has a typical shelf life of 24 months when stored in a cool, dry place, protected from light. |
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Purity 99%: 2-Pyridinecarbothioamide with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal byproduct formation. Melting Point 146°C: 2-Pyridinecarbothioamide with a melting point of 146°C is used in heterocyclic compound preparation, where temperature stability allows for controlled crystallization. Molecular Weight 138.19 g/mol: 2-Pyridinecarbothioamide with molecular weight 138.19 g/mol is used in fine chemical manufacturing, where consistent mass ensures accurate stoichiometric calculations. Particle Size <100 µm: 2-Pyridinecarbothioamide with particle size below 100 µm is used in solid-phase synthesis, where small particles enhance reaction surface area and uniformity. Solubility in Ethanol: 2-Pyridinecarbothioamide with high solubility in ethanol is used in solution-based catalytic reactions, where complete dissolution leads to efficient reactant interaction. Stability Temperature 80°C: 2-Pyridinecarbothioamide with a stability temperature up to 80°C is used in thermal reaction processes, where chemical integrity is maintained under moderate heat. Moisture Content <0.5%: 2-Pyridinecarbothioamide with moisture content less than 0.5% is used in moisture-sensitive formulations, where low water presence ensures product stability. Assay >98%: 2-Pyridinecarbothioamide with assay greater than 98% is used in analytical chemistry standards, where high assay accuracy supports reliable quantitative analysis. Reactivity Grade: 2-Pyridinecarbothioamide of high reactivity grade is used in sulfur-containing ligand synthesis, where enhanced reactivity promotes efficient coordination complex formation. Bulk Density 0.45 g/cm³: 2-Pyridinecarbothioamide with bulk density 0.45 g/cm³ is used in automated dispensing systems, where consistent bulk properties enable precise volumetric dosing. |
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Walking into a lab and seeing a bottle labeled 2-Pyridinecarbothioamide always sparks a moment of respect, at least for those who've crossed paths with sharp-smelling intermediates and elusive syntheses. This compound doesn't sit in the limelight like some big-name reagents, but its quiet presence fuels a surprising amount of work—especially for chemists chasing after complex molecules or scrupulous quality in their projects.
Chemically, 2-Pyridinecarbothioamide stands out for its structure: a pyridine ring coupled with a thioamide group at the second position. The molecular formula C6H6N2S gives you a clean picture—the combination of an aromatic heterocycle with additional nitrogen and sulfur brings reactivity as well as versatility. More than once, I've watched researchers debate the best use of this material, not because it’s obscure, but because its possibilities keep nudging clear cut answers out of reach.
Specs are everywhere, but what matters when you’re staring at a bottle on the bench? The typical molecular weight lands around 138.19 g/mol. Solid at room temperature, this compound usually appears as a pale, sometimes grayish powder. That form makes handling less mess, which helps during weighing and transfer—a detail that folks managing dozens of syntheses in a week come to appreciate.
Purity remains a top priority, as with most laboratory reagents. The most reliable suppliers offer levels above 98%. Anything lower often hints at cost-cutting or shelf time. In reality, that couple of percent can make or break outcomes, especially with research-scale step reactions.
Melting points serve as a quick check, clocking in typically between 120 and 123°C. In a teaching lab, a sharp melting point feels like a green light—less so when mixed or impure. On more than one occasion, confirming this specification saved hours of troubleshooting down the road.
The textbooks tag 2-Pyridinecarbothioamide mainly as an intermediate. In practice, its job often stretches toward synthesis of ligands, pharmaceuticals, agricultural chemicals, and dyes. Take coordination chemistry: the thioamide’s sulfur and ring nitrogen atoms can latch onto metal ions, creating stable complexes. These then serve in catalysis, materials research, or analytical studies. Working in a lab that dabbles in catalyst development, you quickly notice that not all thioamides handle metals the same way—2-Pyridinecarbothioamide’s arrangement makes for tighter binding in many cases.
Pharmaceutical researchers browse compound libraries and often land on sulfur-containing building blocks for biological activity. This compound’s scaffold pops up in anti-tuberculosis leads, among others. Few things fuel more hope than watching a simple structural tweak turn a lackluster lead into a promising candidate, and the thioamide group plays an unsung role. Sulfur can modulate drug metabolism, impacting everything from half-life to target selectivity. That kind of detail still doesn’t fit on most packaging, but it matters an awful lot at the bench.
In the world of dyes, 2-Pyridinecarbothioamide feeds into production of azo dyes, often as a coupling component. These dyes color textiles, leathers, and sometimes advanced imaging materials. What sounds routine hides plenty of science: the electronic properties of the pyridine ring—and the sulfur’s electron-donating abilities—turn into brighter, longer-lasting shades. Reflection and fastness tests aren’t glamorous, yet any manufacturer who’s dealt with fading yields or unhappy clients knows the impact that a single ingredient can make.
Multiple thioamides sit on the market, each with their quirks. Some, like thiourea, come cheap and handle well—but lack the aromatic bite of a heterocycle. Others include modifications at different positions, altering reactivity or solubility. The fact 2-Pyridinecarbothioamide keeps its sulfur adjacent to the nitrogen-rich pyridine ring directly shapes its behavior. The electron density draws metal ions closer, and the aromatic structure itself transfers electronic effects in a way that lifts performance over some straight-chain analogs.
Years of trial and error have shown me that switching between related thioamides isn’t always a plug-and-play move. Certain catalysts refuse to form or lose efficiency without the precise 2-position connectivity. NMR and IR studies back this up, showing characteristic stretching frequencies and chemical shifts that shift with every minor change. It’s not just about having a sulfur donor; it’s about combining it with the unique push and pull of the pyridine ring.
Nobody wants surprises in the lab—least of all from their reagents. Handling 2-Pyridinecarbothioamide takes the same respect as with most organic chemicals. Gloves, goggles, and proper ventilation stay non-negotiable, as skin contact and inhalation can cause irritation. I recall a colleague who once underestimated a seemingly benign white powder, only to learn the value of reading safety literature the hard way.
Beyond the basics, sourcing from companies who uphold batch consistency and quality checks really matters. Not all intermediates are shipped with the same care. There’s peace of mind that comes from consistent results, whether you’re running an analytical lab or pushing synthetic boundaries. Regular audits, transparent documentation, and responsive customer support all signal a higher standard. Few people sing the praises of supply chain reliability, but if you’ve ever had a project delayed for want of a missing certificate, you know the pain.
What about the waste stream? Thioamide-containing residues and byproducts typically require regulated disposal. Sulfur, nitrogen, and aromatic rings end up flagged as environmentally persistent or hazardous. Partnering with disposal firms—or internal protocols—keeps research moving without regulatory headaches. Looking back, I’ve seen research groups struggle just as much with logistics as with reaction outcomes. No chemist prefers dealing with waste, but ignoring these details can stall progress in more ways than one.
Working with specialty chemicals always means a race against time, budget, and experimental uncertainty. Some of that stress loosens once you find suppliers who look after storage, packaging, and clear documentation. Vacuum-sealed jars or ampoules outperform regular bottles in terms of shelf life—every experienced bench chemist knows the disappointment of opening a clumpy, degraded powder.
Batch testing methods, such as HPLC, FTIR, and NMR, help verify purity and prevent mix-ups. In the early years, I lost hours believing a reaction had failed, when in fact a contaminated bottle had thrown off the results. These mistakes burn lessons deep: reliable reagents don’t guarantee research success, but they prevent avoidable headaches and missteps.
For those scaling from the milligram to the kilogram, packaging size and logistics become as important as purchase price. Buying in small batches saves on loss, while industrial users need the consistency and economies that only large lots can provide. Chemistry finds a thousand work-arounds, but nothing beats predictable supply and honest transparency.
Compared to other thioamides, 2-Pyridinecarbothioamide brings advantages that go beyond cost. The split between heterocyclic and aliphatic structures sets up a hierarchy where aromatic systems edge out others for certain transformations. The added basicity from the ring nitrogen, along with the ability to form chelates, increases selectivity in some catalytic and medicinal chemistry applications.
It’s tempting to chase cheaper, more available options—dimethylthiourea or 4-pyridinecarbothioamide come to mind—but these substitutions sometimes underperform or introduce new issues. Elemental analysis, solubility, or thermal stability may change just enough to threaten reproducibility. I remember a multi-month process where swapping out a single intermediate altered the yield curve across several steps. The so-called ‘small’ substitution echoed through the entire production schedule.
The real question always settles on practicality: will this compound do the job better, safer, or with less fuss? For many, the answer is yes—provided the research calls for its particular set of properties.
No chemical is perfect, and 2-Pyridinecarbothioamide faces the same challenges found in specialty reagents across the board. Shelf stability, global availability, and regulatory hurdles can pose issues for scaling up novel routes or supporting larger projects. Experienced teams address these pressures by choosing high-quality sources and maintaining tight control over inventories.
Improving documentation and traceability helps both suppliers and end users. Robust batch records, COAs, and third-party analysis go a long way to preventing misidentification or unexpected contaminants. In my own projects, routine verification through NMR or mass spec has excised sources of error early, freeing energy to focus on results, not reagents.
Reducing the environmental impact of chemical processes makes for a rising priority—greener synthesis and waste minimization are now in demand, not just a selling point. Researchers engaging in process chemistry or pharmaceutical development now think two or three stages ahead, planning separation and cleanup long before the first gram enters the flask.
Each compound carries its own ‘personality’ built from molecular geometry, electron density, and reactivity. Working daily with 2-Pyridinecarbothioamide, you come to know its quirks: the smell it carries, the way it settles in the jar, the dust that’s more stubborn than expected, and the odd way it marries itself to the balance pan. The most substantial appreciation comes not from spec sheets or catalogs, but from successful syntheses and reactions that finally behave.
Its use as a building block shows up in real-world problem-solving. When a metal-based catalyst needs binding partners that won’t fall apart or cause side reactions, switching to a molecule with a robust aromatic core can salvage weeks’ worth of effort. Lab meetings often include stories about chasing down transient intermediates or finally nailing the conditions for selective complexation. These victories shape the reputation of 2-Pyridinecarbothioamide, one experiment at a time.
Some projects highlight the need for advanced intermediates that withstand harsh conditions—high temperature, low pH, or powerful nucleophiles. Here, a structure like pyridinecarbothioamide outpaces simpler analogs, giving longevity and compatibility. The difference can mean the world to product development timelines.
What pushes a specialty chemical like 2-Pyridinecarbothioamide from ‘nice to have’ into ‘must order’ territory? For me, it traces to repeated proving grounds over years of research and development. Some compounds flicker in and out of fashion; others, like this one, settle into the rotation because they back up promises with results. That track record shapes choices for purchasing and recommending materials to colleagues and industry contacts.
Building trust boils down to more than molecular diagrams and melting points. It involves direct experience, honest supplier relationships, and learning from the inevitable small mistakes that crop up in real laboratory practice. Sharing those stories and approaches with new chemists—mentoring or collaborating on projects—keeps the learning cycle turning.
Science moves too fast for any single intermediate to hold the stage forever, but reliable chemicals with flexible properties serve as benchmarks along the journey. 2-Pyridinecarbothioamide doesn’t make headlines, but it sure makes discoveries possible. That’s value you can measure not just in grams or purity percentages, but in the lessons learned each time it gets weighed out for the next big challenge.