|
HS Code |
212190 |
| Productname | Pyridine-3-carbothioamide |
| Casnumber | 22248-63-7 |
| Molecularformula | C6H6N2S |
| Molecularweight | 138.19 |
| Appearance | White to light yellow crystalline powder |
| Meltingpoint | 131-135 °C |
| Solubility | Slightly soluble in water |
| Density | 1.25 g/cm³ (approximate) |
| Pubchemcid | 6976 |
| Smiles | C1=CC(=CN=C1)C(=S)N |
| Inchi | InChI=1S/C6H6N2S/c7-6(9)5-2-1-3-8-4-5/h1-4H,(H2,7,9) |
| Synonyms | 3-Pyridinecarbothioamide |
| Storagetemperature | Store at room temperature |
As an accredited Pyridine-3-carbothioamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Pyridine-3-carbothioamide, 25g, is supplied in a sealed amber glass bottle with tamper-evident cap and chemical hazard labeling. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for Pyridine-3-carbothioamide involves securely packing and shipping in 20-foot containers for safe international transport. |
| Shipping | Pyridine-3-carbothioamide is shipped in tightly sealed containers to prevent moisture and contamination. It is transported according to standard regulations for chemicals, typically as a non-hazardous or low hazard material. Packages should be clearly labeled, protected from physical damage, and stored in a cool, dry place during transit. |
| Storage | **Pyridine-3-carbothioamide** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Ensure it is protected from moisture and direct sunlight. Appropriate safety labeling and access controls should be maintained to prevent accidental exposure or misuse. |
| Shelf Life | Pyridine-3-carbothioamide has a typical shelf life of 2-3 years when stored in tightly sealed containers at room temperature. |
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Purity 98%: Pyridine-3-carbothioamide with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield product formation. Molecular weight 138.18 g/mol: Pyridine-3-carbothioamide with molecular weight 138.18 g/mol is used in organic synthesis laboratories, where it facilitates accurate stoichiometric calculations. Melting point 154°C: Pyridine-3-carbothioamide with melting point 154°C is used in thermal processing applications, where it maintains compound stability during heating. Particle size <50 µm: Pyridine-3-carbothioamide with particle size less than 50 µm is used in catalyst preparation, where it enhances surface area and reaction efficiency. Stability temperature up to 120°C: Pyridine-3-carbothioamide with stability temperature up to 120°C is used in extended storage scenarios, where it preserves chemical integrity and usability. Solubility in ethanol: Pyridine-3-carbothioamide with solubility in ethanol is used in solution-based reaction systems, where it enables homogeneous mixing and efficient reactant distribution. Low water content <0.5%: Pyridine-3-carbothioamide with low water content less than 0.5% is used in moisture-sensitive synthesis, where it prevents undesired side reactions. |
Competitive Pyridine-3-carbothioamide prices that fit your budget—flexible terms and customized quotes for every order.
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Pyridine-3-carbothioamide stands out among specialty chemicals, not just because of its pungent signature or familiar six-membered aromatic ring, but because it brings practical advantages in the field. The molecule, with its core structure based on a pyridine ring at position-3 linked to a thioamide group, has become a mainstay for trusted applications in both research and manufacturing. Seeing it in use can spark curiosity for those outside the chemistry world—though among chemists and process engineers, its value tends to speak for itself, especially in synthesis settings where reliability and straightforward reactivity matter.
Having spent years working alongside formulation teams, I have witnessed Pyridine-3-carbothioamide carve out a particular role, something not easily replaced by alternatives with similar backbones. The thioamide functionality brings a specific nucleophilicity, adding diversity and utility to a compound that might look simple on paper. That simplicity, in reality, gives rise to versatility. In my own experience, the product's physical state—white to slightly yellowish powder—makes it manageable for bench-top manipulation, reduces handling mistakes, and helps avoid the bottlenecks often encountered with liquid reagents.
Looking at real-world results, purity matters, and Pyridine-3-carbothioamide usually comes with high-assay grades, often above 98%. Analytical figures are useful, but what stands out more during a hectic day in the lab is how this purity translates to consistent reaction outcomes. Moisture content and melting point (~142-146°C) remain steady across batches, which is a relief when scaling reactions for pilot production. Keeping color and form stable means less troubleshooting, fewer failed runs, and fewer questions from quality assurance at the final sign-off stage.
The consistency bred from tight manufacturing controls gives peace of mind, yet it’s the chemical robustness that wins loyalty. In sulfur chemistry, reactivity can vary widely from one sample to another, especially with compounds prone to oxidation or hydrolysis. Yet, the Pyridine-3-carbothioamide most chemists encounter doesn’t throw curveballs here—instead, it remains resilient and dependable even in open-flask settings, unless you actively push it with strong oxidants or acids. Not many close analogues can claim such steady performance over multiple years and sources.
Field chemists gravitate toward Pyridine-3-carbothioamide for two big reasons: it helps build heterocyclic scaffolds and enables key intermediates in pharmaceutical research. You find it as a base for hydrazones, thiazoles, and other fused systems that crop up in patents and literature. Medicinal chemistry, in particular, leans heavily on the thioamide function to generate analogues where a sulfur-for-oxygen swap brings altered bioactivity, making subtle but crucial changes to drug candidates.
Some see it as just another bench chemical—an “ingredient”—but that underestimates its importance. For instance, in the pursuit of new kinase inhibitors or antivirals, a single substitution at the 3-position of pyridine changes everything about potency, toxicity, and metabolic stability. Academic groups and pharmaceutical firms don’t simply select it by chance; years of data back up its ability to create tangible progress, whether in an early-stage library or at process scale for active pharmaceutical ingredients (APIs).
Dyes and pigment manufacturers find it handy as a building block for more complex aromatic structures, especially yellow and orange hues. Industrial coatings and polymer systems sometimes integrate derivatives of Pyridine-3-carbothioamide for their chemical stability and straightforward ways to link with other monomers. In these roles, minor changes in impurity profiles or consistency can mean large swings in product quality, which is why seasoned chemists and sourcing professionals rarely gamble with untested alternatives.
Chemists never stop comparing options. Some may ask, “Why not use a similar compound—perhaps a pyridine-2-carbothioamide or a different thioamide altogether?” My own digging, grounded in real-life troubleshooting, keeps circling back to orientation and electronics. Moving the thioamide from the 3-position to the 2- or 4-position on the pyridine ring creates distinctly different reactivity. Reactions that run smoothly with Pyridine-3-carbothioamide can stall or deliver junk when a different positional isomer steps in.
Thioamides, as a group, show a notorious tendency to oxidize, polymerize, or even give off-rotten odor, especially under heat or open air. Yet manufacturers who have responded to repeated user feedback—tightening storage requirements, revising packing to minimize headspace, and using high-purity solvents in recrystallization—have made this one more shelf-stable than its siblings. Years ago, I recall facing persistent decomposition issues with another thioamide, which forced costly batch remakes for a pharmaceutical screen. Switching to Pyridine-3-carbothioamide (with verifiable batch documentation) quickly ended that headache, saving time and restoring credibility to the workflow.
People working on busy lab benches appreciate clear signals about hazards and best practices. Pyridine-3-carbothioamide is not to be underestimated—handling calls for gloves, a fume hood, and careful attention to eye protection because thioamides have a reputation for skin and mucous membrane irritation. Firms that provide detailed safety documentation—including routes of exposure, recommended first-aid steps, and fire reactivity—should be applauded, especially since “minor” mishaps in the lab can spiral out quickly without data to back up safe practices.
Long-term industry veterans remain alert to changing regulations, especially for substances flagged for environmental or human health risks. Pyridine-3-carbothioamide, while not a household name among the public, still moves through regulatory channels—REACH, TSCA, and more. Companies with credibility ensure full chain-of-custody transparency, batch traceability, and up-to-date Material Safety Data Sheets (MSDS). This kind of transparency enables true accountability and allows end-users to audit their supply chains with confidence.
The conversation doesn’t end at product performance. More organizations now ask about the environmental burden of making and moving chemicals such as Pyridine-3-carbothioamide. Experienced buyers know to seek out suppliers who treat waste responsibly and source starting material from facilities with good occupational health standards. Even though this thioamide is not produced in enormous volumes compared to petrochemicals or commodity solvents, efforts to optimize synthesis, recycle solvents, and minimize hazardous reagents all add up.
Seasoned lab managers now press for “green chemistry” alternatives and demand clear answers about residual solvents and byproducts. Pyridine-3-carbothioamide has responded to these shifts, with several vendors offering “low-residual solvent” and “solvent-free” labels where possible. The reality: switching to manufacturers with a record of robust environmental controls does more than look good on paper. It shields all stakeholders from the risk of supply chain disruptions that follow regulatory crackdowns.
Making it on the benchtop is simple enough. Scaling up, as many process chemists can attest, is where the headaches begin. Pyridine-3-carbothioamide, thanks to a relatively straightforward one-pot synthesis from nicotinic acid derivatives and thioamides, bugs engineers less than more finicky heterocycles. The heat management, solubility, and filtration steps have been hammered out by decades of optimization—so even at scale, consistency doesn’t falter.
It’s tempting to blame process hiccups on the molecule, but those setbacks usually come down to starting material impurity or a new supplier cutting corners. Engaged suppliers provide technical support, gram-to-ton lots, and relevant certificates of analysis (CoA) that match what workers actually see in their beaker, not just what marketing promised. The organizations that listen to user feedback and share process improvement data manage to cultivate long-term trust and satisfaction among chemists working at all scales.
No product is perfect. Every lab veteran can point to a failed batch or two, usually tied to poor storage, humidity drift, or contamination at the source. Pyridine-3-carbothioamide is no exception. Keeping it dry, tightly sealed, and away from light stops slow but steady decomposition. I once returned to a neglected jar months after opening, only to find a yellowed solid and uncooperative melting point behavior. Sticking to best practices—using desiccators, dating containers, and tracking open dates—prevents most problems.
One tricky challenge: sourcing from lesser-known suppliers who claim ‘equivalent’ product. Time and again, those shortcuts turn into long days of troubleshooting, failed chromatography, and apologizing to others for wasted effort. Trustworthy sources, peer-reviewed batch data, and technical support hotline access make a bigger difference than flashy branding or minor price discounts. It pays off over the long run, both in peace of mind and real savings.
From my own trajectory—starting as a junior bench chemist, moving through scale-up, and finally coordinating purchases for a pilot plant—one lesson remains consistent: strong supplier relationships beat one-off transactions. For a specialty chemical like Pyridine-3-carbothioamide, open conversations with technical reps unlock helpful tips, document updates, and sometimes even early warnings about supply disruptions or process tweaks. Personal connections, built over years and sometimes cemented face-to-face at trade fairs, lead to honest feedback and mutual respect.
These aren’t abstract concerns. Something as simple as an advance heads-up on shelf-life changes or anticipated purity drifts allowed our team to plan orders, adjust formulations, and avoid costly delays. As industries evolve—pushing for ever-higher standards of transparency, safety, and performance—those partnerships serve as lifelines, especially under pressure to deliver results.
Stepping back, Pyridine-3-carbothioamide remains more than a tool of tradition. Researchers and industry partners continue to seek new synthetic transformations, greener routes, and faster analysis to answer future needs. Investment into catalytic alternatives, improved waste recovery, and automation-friendly packaging all hint at a sector that refuses to be static.
Standardization—paired with technical agility—will determine who thrives. Users who report real-world data, suppliers who act on it, and cross-sector collaborations all build a richer body of shared knowledge. The rise of digital platforms letting chemists cross-reference batch numbers, spectral purity, and even environmental impact will only speed up this process, connecting once-isolated departments into a shared drive for improvement.
Products like Pyridine-3-carbothioamide don’t just appear out of the blue. Every step, from pilot lot to scaled-up production, demands joined-up thinking among suppliers, regulatory teams, and end-users. I’ve seen how responsiveness from manufacturers—even something as simple as batch recall procedures—cut off problems before they reach a critical stage. Accountability on every level, matched by user vigilance, goes a long way.
Ongoing education, both for the veterans and those just starting out, shapes habits that prevent both minor errors and large-scale disasters. Routine refresher courses on hazards, new regulations, and best-practice handling make teams safer and products more trustworthy. Peer-to-peer networks share stories of challenge and success. Information moves faster now than ever—using it well can mean the difference between staying ahead and tripping up.
Pyridine-3-carbothioamide’s staying power comes from a blend of steadfast chemistry, usability, and an industry culture that values reliability over flash. Sourcing matters; relationships matter even more. Experience, supported by consistent data, enables wise decision-making and prevents costly mistakes. Practices evolve, but respect for the chemistry and the people managing it remains at the core. In that sense, the product speaks to anyone who prizes depth over appearance, and work that leads to tangible, safe outcomes.
The next time someone asks why this compound keeps its place in so many protocols and processes, the answer covers more than just structure diagrams and melting points. Its record reflects the careful choices of people who have spent years learning what works—and trusting suppliers who adapt alongside them. For anyone investing in Pyridine-3-carbothioamide, that shared experience, grounded in practicality and attention to every link in the chain, can make all the difference.