|
HS Code |
958505 |
| Chemical Name | N,N-diethylpyridine-3-carboxamide |
| Cas Number | 59-10-7 |
| Molecular Formula | C10H14N2O |
| Molar Mass | 178.23 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 271-272 °C |
| Density | 1.046 g/cm3 |
| Solubility In Water | Slightly soluble |
| Logp | 1.89 |
| Refractive Index | 1.525 |
| Flash Point | 120 °C |
As an accredited N,N-diethylpyridine-3-carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of N,N-diethylpyridine-3-carboxamide is supplied in a sealed amber glass bottle with a tamper-evident screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for N,N-diethylpyridine-3-carboxamide involves secure, safe packing and transport of chemical drums or bags in a 20-foot container. |
| Shipping | N,N-Diethylpyridine-3-carboxamide is shipped in tightly sealed, chemical-resistant containers under ambient conditions. The package must be clearly labeled with hazard and handling information. It should be protected from direct sunlight, moisture, and physical damage. Compliance with local, national, and international regulations for transporting chemicals is required to ensure safe delivery. |
| Storage | N,N-Diethylpyridine-3-carboxamide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances like strong oxidizing agents. Avoid exposure to heat, direct sunlight, and moisture. Clearly label the storage container and ensure it is kept away from food and drink. Follow appropriate chemical hygiene and safety protocols. |
| Shelf Life | The shelf life of N,N-diethylpyridine-3-carboxamide is typically 2-3 years when stored in a cool, dry, airtight container. |
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Purity 99%: N,N-diethylpyridine-3-carboxamide with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low impurity formation. Melting Point 68°C: N,N-diethylpyridine-3-carboxamide with a melting point of 68°C is used in organic catalysis workflows, where it provides stable performance across standard reaction temperatures. Stability Temperature up to 120°C: N,N-diethylpyridine-3-carboxamide with stability up to 120°C is used in agrochemical formulation processes, where it maintains chemical integrity during high-temperature blending. Low Water Content (<0.2%): N,N-diethylpyridine-3-carboxamide with low water content below 0.2% is used in moisture-sensitive electronics manufacturing, where it reduces the risk of hydrolytic degradation of sensitive components. Viscosity 10 mPa·s: N,N-diethylpyridine-3-carboxamide with a viscosity of 10 mPa·s is used in specialty coatings, where it enables uniform film formation and improved surface smoothness. Molecular Weight 192.26 g/mol: N,N-diethylpyridine-3-carboxamide with a molecular weight of 192.26 g/mol is used in analytical reference standards, where it ensures precise quantification in chromatographic calibration. |
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N,N-diethylpyridine-3-carboxamide doesn’t come up at most kitchen tables, yet in research labs and industry workspaces, the name often brings a nod of recognition. Used mainly for chemical synthesis and development, this amide makes a real difference in many fields I’ve seen, especially where selectivity and reliability set products apart.
The specific formulation—a pyridine ring at the core, etched with a carboxamide function and two ethyl branches—gives it strengths you won’t easily find in similar chemicals. Chemists trust it for intermediate or catalyst roles, leaning into its stability and balanced physical profile. That unique chemical structure means it blends well with organic solvents, making it especially useful for reactions where water throws things off balance. I’ve worked with substitutes in multi-step syntheses, but they rarely offer as much predictability, leaving more guesswork in yield or purity.
Each batch comes as a crystalline or sometimes an oily liquid, depending on room temperature and storage. Tanks and bottles labeled with its model—often distinguished by grade, not just a catchy name—underline the purity level. The most reliable N,N-diethylpyridine-3-carboxamide isn’t just about a chemical formula fitting a specification sheet; it's what’s left behind after synthesis that gives confidence. Analysts usually run GC or NMR checks on new stock, watching for evidence of unreacted pyridines or contaminants. Consistency means less troubleshooting later on. With a melting point hovering in the region typical for pyridine derivatives, and boiling point managed with care to stay below decomposition, handlers rarely face surprises during storage or use.
From firsthand experience, purity above 98% gives the most reproducible results. Contaminants complicate downstream processing, and trace metals or bases skew reaction pathways. The market sometimes brings in off-grade product, cheaper by the barrel, but I’ve learned that trimming costs at the start only brings headaches midstream. Industry standards might allow more leeway, but research settings always ask for the cleanest batch to spare hours of lost work.
N,N-diethylpyridine-3-carboxamide has carved its reputation around versatility. In pharmaceutical work, its skill comes from supporting amide bond formation or acting as a ligand in metal-catalyzed synthesis. I remember one drug development project where its performance streamlined a pivotal coupling step, and switching to an older amide analogue increased side product formation and clean-up time. The upshot: relying on this compound during reaction optimization steadily cut the cycle time from weeks to days.
The story doesn’t stop at pharma. Agrochemical makers turn to this molecule when synthesizing advanced intermediates, especially where stability under mild conditions matters. Its hydrophobicity controls how it disperses in organic matrices—crucial for scaling lab recipes to production vats. Those in the materials field, especially those working with custom polymers, cite its structural quirks for precise molecular tuning under heat and pressure. I’ve seen its utility firsthand during a collaboration where predictable reactivity defined the viability of a new high-performance resin.
There’s a sharp memory in my mind of struggling with an older batch of a different amide; after a week of inconsistent results, a switch to N,N-diethylpyridine-3-carboxamide turned a disappointing run-around into an afternoon’s steady progress. The right material makes all the difference.
Many might wonder why one would select N,N-diethylpyridine-3-carboxamide instead of more common pyridine carboxamides or even basic pyridines. The key comes down to both chemical selectivity and environmental stability. Unlike straight pyridine, the diethylated form minimizes unwanted side reactions. It also keeps volatility lower—important for labs tight on ventilation or where worker exposure could generate complaints. Non-diethylated versions usually react faster, but with more by-products. Getting a clean finish isn’t just wishful thinking; this product makes it more feasible.
Some users try to save costs by swapping for lesser-known amides or derivatives, particularly those with just methyl groups, but gains in price quickly fade after factoring in purification, yield loss, and dealing with tough-to-remove impurities. I have stacked product pricing sheets side by side, only to see hidden costs emerge further down the pipeline. A more expensive, but reliable compound almost always repays the favor by reducing waste and the hours spent chasing down mysterious peaks on the chromatogram.
Nobody gives chemicals a free pass. Safer handling starts with serious respect. This compound comes with moderate toxicity, making gloves and good air circulation non-negotiable. It fits much better in a fume hood than an open bench, especially during solvent transfer or open storage. Lax handling—skipping eye protection, ignoring spills, or assuming ‘it’s just another amide’—invites trouble. Workers sharing the same lab learn from each other, and mistakes with exposure don’t stay secrets for long. I appreciate the suppliers who ship detailed notes, but the habits formed in the day-to-day work—like quickly capping bottles and labeling transfers—have saved more incidents than any manual.
Waste disposal doesn’t end at the bottle either. This isn’t a compound you wash down the drain after an experiment. Dedicated organic waste streams handle the leftovers, ensuring downstream water supplies stay uncompromised. Universities running many students through basic experiments often develop standard operating procedures anchored in both local regulations and lived accident history.
Budgeting for quality chemicals always ruffles feathers in research meetings. While bulk orders drop per-kilogram prices, researchers chasing shoe-string budgets sometimes face tough trade-offs between lab needs and purchase approvals. Price swings often track with global supply of pyridine, which can tighten with increased demand from agrochemical or battery industries.
If one supplier faces downtime or shipment delays, alternatives can run low in quality, driving up the complaint log. I’ve seen teams pause crucial experiments for want of a reliable supply, underscoring the crux: one broken link in the chain puts months of work at risk. Some institutions have found workarounds by pooling purchases across departments, smoothing out costs and providing leverage when negotiating for larger, vouchsafed lots. Yet even the best supply chains stumble, and keeping extra on hand always makes sense, especially in times of global uncertainty. Having lived through procurement crunches during years of lab work, I see the value in building relationships with suppliers who communicate clearly about restock timelines and quality checks.
Regulatory oversight hovers over most chemical purchases. While N,N-diethylpyridine-3-carboxamide itself may not fall under the strictly controlled lists, the broader ethos of responsible chemical management hangs over every transaction. Chemical tracking, safe shipping documents, and binding agreements ensure traceability. The habits formed in handling chemical precursors and intermediates shape professional culture—carelessness or corners cut in spirit always echo in practice.
Stakeholders—including institutional buyers, researchers, and health officers—meet not just to check boxes but to keep real people safe. Every national standard brings its quirks, and sometimes shipping across borders becomes a puzzle of paperwork. Training seminars on the ground still matter; government sites and regulatory groups offer guidance, but the learning sticks when examples from near misses and near disasters show what’s truly at stake.
Reliable results spring from reliable materials. After working with dozens of amides and pyridine derivatives over the years, I’ve seen more setbacks from poorly chosen or inconsistent intermediates than from almost any other root cause. A student once spent months trying to replicate a synthesis, only to learn that an earlier swap to a generic substitute introduced unpredictable impurities. That frustration left a mark—good enough only works when nothing goes wrong, but that line moves quickly in chemistry.
Consistency, batch after batch, brings peace of mind you can’t fake. Routine spot checks, open communication with suppliers, and documented batch certifications cut down surprises. Trying to scrape by with a less-tested alternative saves little when measured against lost time, loss of product, and the sometimes subtle discrepancies that surface downstream.
N,N-diethylpyridine-3-carboxamide opens doors to newer synthetic routes. Synthesis teams prize its stability and compatibility, especially as research shifts toward greener, less wasteful protocols. Seeing it folded into flow chemistry setups makes sense, where precise dosing, reduced waste, and reproducible kinetics bring new advantages. Experienced chemists now test it in cascade reactions, where controlling every intermediate matters more than headline purity in a single flask.
The changing landscape of research—whether driven by pharmaceutical innovation, materials research, or green chemistry goals—suggests that demand for such precise, stable intermediates will only intensify. Younger researchers use high-throughput automation and AI-driven tips to match reagents for specific outcomes; having a compound with decades of reliable data smooths the path from bench to paper. Product quality remains both a technical and human win, supporting ethical standards and boosting success rates for tough, high-impact synthesis projects.
Moving from reliable output to even better performance takes more than just standing on precedent. Researchers often voice practical changes they’d like to see, from tighter controls on trace impurities to packaging that increases shelf life without unnecessary plastic. Standardized lot documentation, updated regularly, gives confidence in both academic and industrial settings. Those extra hours spent training staff or students on safe, proper handling often pay off in fewer waste streams and mistakes.
Broader solutions for the marketplace start with greater transparency. Detailed reporting on batch history, impurity profile, and shipping conditions brings a more knowledgeable buyer to the table. Industry forums allow chemists to share hard-won experiences, and suppliers willing to address issues head-on build trust that goes beyond a product insert. Digital systems now allow inventory management to be tied to expiry and usage logs, cutting the risk of accidental run-out or waste from forgotten inventory.
Collaboration across teams often fills gaps where individual expertise runs thin. Shoulder-to-shoulder work in a research setting, or even across companies, creates a climate where products like N,N-diethylpyridine-3-carboxamide don’t just serve as transactional goods, but as reliable building blocks for bigger breakthroughs. Innovation rarely emerges from single actors; it comes when skilled people get the right materials in the right hands at the right time.
No single element or molecule shapes the outcome of research, but some make steady progress far more likely. I’ve come to trust N,N-diethylpyridine-3-carboxamide for its reliability, and I've watched others do the same after testing more uncertain alternatives. The lesson is as much about stewardship and care as about chemistry alone. Transparent sourcing, honest evaluation, and shared experience keep safety high and mishaps at bay.
Products with proven track records, especially those managed by teams who understand what’s inside the bottle, always form the foundation for science that aims higher. Every error caught or shortcut avoided helps build not just better results, but a collective culture of responsibility and success.
Looking at N,N-diethylpyridine-3-carboxamide, the story is bigger than technical jargon or catalog numbers. The compound brings value because dedicated people have put it to the test, have learned its quirks, and have shared those lessons with their peers. Its proven stability, clear performance record, and adaptability make it more than just a line in a protocol—it’s become part of what reliable, high-level synthesis means in practice.
For those seeking to move ambitious projects from concept to reality, from experiments to scaling up, quality and trust in every reagent are inseparable. N,N-diethylpyridine-3-carboxamide, with its unique intersection of chemical behavior and market readiness, stands as an example of how the right choice of materials smooths not just the workflow, but the broader pursuit of innovation, integrity, and real-world impact.