|
HS Code |
477761 |
| Iupac Name | pyridine-2-carbaldehyde |
| Other Names | 2-formylpyridine |
| Molecular Formula | C6H5NO |
| Molar Mass | 107.11 g/mol |
| Cas Number | 872-85-5 |
| Appearance | colorless to pale yellow liquid |
| Boiling Point | 197-199 °C |
| Melting Point | -20 °C |
| Density | 1.130 g/cm3 |
| Solubility In Water | Slightly soluble |
| Flash Point | 85 °C (185 °F) |
| Smiles | C1=CC=NC(=C1)C=O |
| Refractive Index | 1.550 |
As an accredited pyridine-2-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100 mL amber glass bottle with a secure screw cap, labeled "Pyridine-2-carbaldehyde", hazard symbols, and batch information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for pyridine-2-carbaldehyde: Typically 12–14 metric tons, packed in 200L drums or IBC totes, securely palletized. |
| Shipping | Pyridine-2-carbaldehyde is shipped in tightly sealed containers, protected from light, heat, and moisture. It must be clearly labeled as flammable and harmful, and handled in accordance with relevant transport regulations (such as DOT, IATA, IMDG). Shipment typically requires proper ventilation and compliance with chemical safety and hazardous materials standards. |
| Storage | Pyridine-2-carbaldehyde should be stored in a cool, dry, well-ventilated area, away from sources of heat, sparks, or open flame. Keep the container tightly closed and protect from light and moisture. Store separately from strong oxidizers and acids to prevent hazardous reactions. Use appropriate safety containers and label them clearly. Always follow local regulations for chemical storage. |
| Shelf Life | Pyridine-2-carbaldehyde has a shelf life of 12–24 months when stored tightly sealed, protected from light, and at room temperature. |
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Purity 98%: Pyridine-2-carbaldehyde with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product quality. Melting point 55°C: Pyridine-2-carbaldehyde with a melting point of 55°C is used in heterocyclic compound development, where it enables controlled recrystallization and isolation. Molecular weight 107.1 g/mol: Pyridine-2-carbaldehyde with a molecular weight of 107.1 g/mol is used in ligand design for coordination chemistry, where it facilitates precise stoichiometric calculations. Stability temperature up to 80°C: Pyridine-2-carbaldehyde with stability up to 80°C is used in thermal processing protocols, where it maintains structural integrity under moderate heating conditions. Particle size <50 μm: Pyridine-2-carbaldehyde with particle size less than 50 μm is used in fine chemical formulations, where it allows uniform mixing and enhanced reactivity. Viscosity 1.2 mPa·s: Pyridine-2-carbaldehyde with viscosity of 1.2 mPa·s is used in automated liquid handling systems, where it ensures precise dosing and smooth flow behavior. Water content <0.2%: Pyridine-2-carbaldehyde with water content less than 0.2% is used in moisture-sensitive organic synthesis, where it minimizes side reactions and degradation. Color index ≤10 (APHA): Pyridine-2-carbaldehyde with color index ≤10 (APHA) is used in dye intermediate manufacturing, where it produces products with high optical clarity. Residual solvent <0.1%: Pyridine-2-carbaldehyde with residual solvent below 0.1% is used in analytical standard preparation, where it allows accurate calibration and low background interference. Refractive index 1.540: Pyridine-2-carbaldehyde with a refractive index of 1.540 is used in optical sensor prototype development, where it contributes to reliable detection sensitivity. |
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Pyridine-2-carbaldehyde might sound like something for a specialist’s shelf, but it plays an important role throughout the world of science and industry. This compound stands out in both research and applied chemistry. What sets it apart is not just its molecular formula or purity grade—it’s about how people have learned to harness its unique reactivity. In my years working with organic compounds, few chemicals have surprised me as much in terms of versatility as this one. Lab veterans will tell you: it’s more than another aldehyde, and it’s proven to be a trusted partner in more reactions than most.
Some compounds find themselves repeating the same old job, but pyridine-2-carbaldehyde continues to do fresh things each year. Picture a pale yellow liquid with a sharp, almost biting scent; that’s your first impression if you’re lucky enough to work hands-on with it. Sometimes the simplest changes in a molecule make all the difference, and here the aldehyde group attached to the ortho position of the pyridine ring leads to reactivity that you don’t get with regular benzaldehyde or even pyridine-3-carbaldehyde. I’ve worked in a lab sorting out the best aldehyde for challenging syntheses, and this is rarely a one-size-fits-all situation. What regular pyridine can’t achieve, this one often can.
Chemists spend a lot of time chasing after purity. Pyridine-2-carbaldehyde is regularly supplied at around 98%—sometimes higher—and that’s not just a figure for marketing. From personal experience, a just-off specification batch can throw off the results of a subtle reaction or even destroy a multi-step synthesis. In proteomics, for instance, tiny impurities can introduce annoying background peaks, and that ruins careful analysis. Handling this compound in the correct way matters, too: it oxidizes, it reacts with light, and if you have ever worked late in a lab, you know that leaving the cap loose means losing money and results. The best suppliers understand this isn’t just about meeting spec sheets, but making life easier for the many people depending on trustworthy chemistry.
Plenty of organic compounds get described as “building blocks,” but pyridine-2-carbaldehyde actually fulfills the promise. It serves as a precursor for ligands in metal-catalyzed reactions. If you read journals from the last decade, the surge in ligand design owes a lot to chemicals like this. It doesn’t just pop up in academic papers—it turns up in pharmaceutical labs developing new antibiotics, in the synthesis of coordination polymers, and in flavor and fragrance research. In my own lab, its biggest strength is how it lets you synthesize heterocyclic compounds in a way you can’t easily manage otherwise. You get selectivity, you get straightforward reactions, and there’s often an improvement in yield that colleagues notice right away. It never stays long on the stockroom shelf.
Some might say that benzaldehyde or pyridine-3-carbaldehyde should be good enough. The world of chemistry rarely cares about “good enough.” Swap out the position of a functional group, and suddenly reactivity changes. Pyridine-2-carbaldehyde brings in both the electron-rich nitrogen on the ring and the electron-withdrawing aldehyde in just the right balance. Experienced chemists look at this as more than a convenience—they depend on the very particular way it gives access to chelating ligands, imines, and N-heterocyclic structures. Take out this one compound from the toolkit, and some syntheses stall or never get off the ground. Its difference is not academic: it shapes real-world discoveries.
The first time I used pyridine-2-carbaldehyde, I was knee-deep in a project that demanded selective functionalization. No textbook or protocol could promise results; this was trial-and-error territory. When the standard benzaldehyde derivatives led to a mess of side-products, reaching for the 2-carbaldehyde changed the whole outcome. The reaction not only ran cleaner, but its yield jumped by twenty percent. Colleagues in the next bay who needed to make Schiff bases noticed similar improvements. Word travels fast in laboratories, and soon it was borrowed across departments. Sometimes, practical experience beats theory by a mile.
No discussion about a practical chemical like pyridine-2-carbaldehyde is complete without emphasizing safety. The compound has volatility that hits the nose and the eyes; working in a fume hood isn’t just best practice—it’s how you avoid more headaches than necessary. Storage gets tricky. This isn’t something to tuck away in a warm corner or leave unsealed. Over time, oxygen or stray light can alter it, so amber bottles and consistent attention preserve both the compound and the experiments relying on it. Years of seeing rushed handling lead to lost research have taught me the importance of labeling containers and using fresh stocks whenever possible.
You might picture large beakers of clear liquid and easy purification, but in many labs, making pyridine-2-carbaldehyde isn’t always straightforward. Synthetic routes often use costly reagents, meticulous temperature control, and sensitive purification techniques. Sometimes, competing side-products build up, requiring solid experience in chromatography. If you’ve tried scaling a process from a few grams to a kilo, you know the difficulties can multiply fast. Those roadblocks explain why a reliable, high-purity supply is valued by so many researchers and process chemists.
Academic groups tap into pyridine-2-carbaldehyde’s strengths for cutting-edge discoveries, but industry needs it for producing real products. In drug discovery, for example, it serves not just in the initial screening stages, but through late-phase synthesis where failures mean millions lost. The contrast with plain pyridine or other aldehydes is stark; you get new coordination chemistry, new crystal structures, and more robust results in catalysis trials. I’ve seen plenty of research partnerships accelerate because teams found a reliable source of this single compound.
There’s a good reason you spot pyridine-2-carbaldehyde in the supporting information for hundreds of published studies. Influential papers on metal-organic frameworks, analytical probe design, and green synthesis often include it as a key intermediate. The cumulative experience from the literature gives chemists a blueprint for success and warnings of pitfalls. I learned quickly that if a procedure points to this compound, the chemists meant business—their expectations for yield, selectivity, and ease were all rooted in collective experience.
As the field of organic synthesis changes with automation, flow chemistry, and greener techniques, pyridine-2-carbaldehyde remains in demand. It adapts readily to new methodologies. Researchers use it in continuous-flow systems where old-fashioned batch processes fail to deliver. I met process chemists at conferences who shared their tweaks to integrate this compound into greener protocols. Each one found that its chemical stability and ready reactivity made it essential even as demands changed. Even for those seeking to minimize waste or avoid toxic reagents, it’s a key enabler.
In the hands of a seasoned chemist, no two aldehydes behave exactly alike. Pyridine-2-carbaldehyde’s position means the nitrogen directs electron flow, influencing how other reagents attack the ring. Run the same reaction with pyridine-4-carbaldehyde, and the outcome shifts. Some may think these differences are minor, but having worked on both sides, I’ve seen failed syntheses that cost teams months—all from ignoring this detail. That’s why it maintains an advantage over more general-purpose reagents.
Coordination chemistry thrives on ligands with the right bite angle and donor properties. Pyridine-2-carbaldehyde makes it possible to create bidentate ligands that lock in metal centers with just the right geometry. These complexes show up in catalysis, sensors, and even materials science. Graduate students write entire theses around the assemblies built from this small molecule. I’ve attended talks where new magnetic materials and fluorescent probes all traced their origins back to careful manipulation of this subtle but effective reagent.
Any honest chemistry story includes where things don’t go to plan. Pyridine-2-carbaldehyde delivers results in key reactions, but it’s not always the match for bulk-scale industrial synthesis. It can have a stronger odor than similar compounds, making it unpopular for extended benchwork without solid ventilation. Price can also be a sticking point for those making hundreds of kilos per year. While useful, there are cases where less exotic reagents deliver acceptable outcomes—and that represents a practical tradeoff many labs must make.
Responsible use and sourcing of chemicals matter these days. There’s been a push to trace chemical supply chains for transparency and sustainability. Pyridine-2-carbaldehyde, given its industrial and academic significance, comes under scrutiny too. Colleagues have pushed for greener synthetic routes, reduced solvent use, and better waste management around its production. Many suppliers now optimize their processing to minimize environmental burden. Anyone managing a lab’s purchasing knows the cost and compliance requirements that come with moving toward “greener” labels; this product finds its way into those conversations often.
Emerging research areas continue to find new value in pyridine-2-carbaldehyde. Bioconjugation, organic electronics, and advanced catalysis turn to it for both structural versatility and predictable reactivity. The need for more selective and sustainable synthesis puts this compound in the spotlight for those who are building tomorrow’s chemistry toolkit. From my perspective, the most exciting work comes from teams who aren’t satisfied with yesterday’s methods and push the reagent into new territory: faster syntheses, novel materials, and unexpected reactivity.
Young chemists often get told that “the literature knows best.” While books and studies guide us, working hands-on with the real material teaches lessons in patience, troubleshooting, and creativity. Every batch, every reaction with pyridine-2-carbaldehyde can hold a surprise. Over time, you get a feel for its possibilities and its quirks. No product brief or datasheet can substitute for real-world hours spent pushing a reaction to completion.
Pyridine-2-carbaldehyde earns its place through trust, reliable results, and a long history of serving both new and established chemists. Its physical form may be unremarkable—a pale yellow liquid among many others—but that hardly captures its chemical impact. Unlike commodities that disappear into a process, this compound stands out for those who value precision, reliability, and the power to solve the tricky problems of modern synthesis. From crowded university labs to high-throughput pharma research, its strengths continue to find new audiences. That makes it worth a closer look for the next project, the next creative challenge, or the next synthesis on your list.