|
HS Code |
510444 |
| Cas Number | 872-85-5 |
| Molecular Formula | C6H5NO |
| Molecular Weight | 107.11 g/mol |
| Iupac Name | Pyridine-3-carbaldehyde |
| Other Names | 3-Formylpyridine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 196-198 °C |
| Melting Point | 14-16 °C |
| Density | 1.137 g/cm³ |
| Solubility In Water | Soluble |
| Flash Point | 88 °C |
| Purity | Typically >98% |
| Smiles | C1=CC(=CN=C1)C=O |
| Pubchem Cid | 70159 |
| Refractive Index | 1.548 |
As an accredited Pyridine-3-aldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 100 mL of Pyridine-3-aldehyde, tightly sealed with a screw cap, labeled with hazard and product information. |
| Container Loading (20′ FCL) | Pyridine-3-aldehyde is loaded in 20′ FCL containers, ensuring secure, moisture-free, and safe bulk packaging for international shipping. |
| Shipping | Pyridine-3-aldehyde is shipped in tightly sealed containers made of compatible materials, protected from light and moisture. It should be handled as a hazardous chemical, with appropriate hazard labeling and documentation. Shipment typically complies with local and international regulations for flammable and toxic substances, and may require temperature control and secondary containment. |
| Storage | **Pyridine-3-aldehyde** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as oxidizers. Protect from moisture and direct sunlight. Store in a flammable liquids cabinet if possible, and clearly label the container. Keep away from strong bases and acids to avoid decomposition. |
| Shelf Life | Pyridine-3-aldehyde typically has a shelf life of 24 months when stored tightly sealed, protected from light, air, and moisture. |
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Purity 99%: Pyridine-3-aldehyde with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side-product formation. Melting point 55°C: Pyridine-3-aldehyde with a melting point of 55°C is used in agrochemical formulation, where predictable solid-state handling improves production efficiency. Molecular weight 107.1 g/mol: Pyridine-3-aldehyde with a molecular weight of 107.1 g/mol is used in heterocyclic compound manufacturing, where precise molecular mass facilitates accurate formulation. Stability temperature up to 60°C: Pyridine-3-aldehyde with a stability temperature up to 60°C is used in laboratory reagent preparation, where thermal stability prevents decomposition. Moisture content <0.5%: Pyridine-3-aldehyde with moisture content below 0.5% is used in organic synthesis, where low moisture levels reduce unwanted hydrolysis reactions. Low peroxide value: Pyridine-3-aldehyde with a low peroxide value is used in fine chemical production, where oxidative stability preserves chemical integrity during storage. |
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Chemical research and manufacturing have seen sweeping changes in the past decade, as tighter regulations and higher purity standards drive chemists and engineers to scrutinize their raw materials more closely. Pyridine-3-aldehyde is one of those building-block compounds frequently appearing in my experience, whether as a student running a late-night synthesis in a university lab, or later, tracking down reliable suppliers for commercial production. Every time I encounter it, I’m struck by how a seemingly niche molecule can play such outsized roles in fields that rarely overlap in everyday life—pharmaceuticals, chemicals, flavor research, and more.
This compound, known to some as 3-formylpyridine, packs a fair punch given its small structure. Characterized by a pyridine ring with an aldehyde group at the third position, its molecular formula is C6H5NO. In many labs, the substance lands on workbenches as a colorless to pale yellow liquid, with a sharp, somewhat pungent odor—a memorable trait during my first foray synthesizing heterocyclic scaffolds. What’s remarkable is the relatively low boiling point, typically around 200°C, which sets practical expectations for storage and handling.
The specifications for Pyridine-3-aldehyde can feel like a checklist for any seasoned synthetic chemist: purity often exceeds 98% when supplied by reputable sources, and the water content is kept low (commonly under 0.5%) to prevent hydrolysis or side reactions. I still recall troubleshooting a stubborn reaction, only to discover that a barely perceptible excess of water in my aldehyde supply had stalled the process. Over time, these lessons drive home the value of paying attention to supplier certificates of analysis and double-checking the data against independent testing.
Those who work in medicinal chemistry recognize Pyridine-3-aldehyde as more than a simple reagent. Researchers use it to build core structures in a range of drug candidates. Take Alzheimer’s and diabetes research—several pharmaceutical projects seek to install heteroatomic functionalities, and this compound’s reactivity slots in neatly, helping craft molecules designed to modulate biological targets. My time collaborating on a candidate molecule for CNS disorders cemented that aldehyde intermediates like this one aren’t just ingredients; they hold up the project when stability, purity, and timely delivery align.
In organic synthesis, the aldehyde function gives chemists tremendous scope for transformations. Schweitzer’s group, whom I followed closely during my own bench science days, used the compound in selective reductions and as a precursor to oximes and hydrazones. When I worked in industrial settings, I watched colleagues pivot from lab-scale runs to manufacturing campaigns, relying on reliable batches of Pyridine-3-aldehyde to keep yields consistent. Small variations in reactivity or contamination can snowball through these processes. Not every batch is created equal, and the critical eye developed over years of dealing with inconsistent starting materials pays off. Those who buy based solely on price tend to learn that lesson the hard way.
Beyond the pharma and process chemistry worlds, flavor manufacturers sometimes turn to Pyridine-3-aldehyde for subtle aromatic notes, though on a much smaller scale. Its presence in certain flavoring compounds is quite sensitive; only specific grades pass muster, and trace impurities can spoil entire runs. That demand for high purity isn’t an academic obsession but a real economic bottom line, as a ruined batch costs both time and money.
Synthetic routes often call for a choice between positional isomers of pyridinecarboxaldehydes—Pyridine-2-aldehyde, Pyridine-4-aldehyde, and their derivatives. The position of the aldehyde really matters. Subtle differences in chemical behavior lead chemists to prefer one isomer over another, based on the desired connectivity in target molecules. I learned early on that both reactivity and selectivity hinge on details as minor as which carbon hosts a specific functional group.
In large-scale operations, side-by-side hands-on testing often reveals how small changes at the molecular level translate into big differences in product quality. During a pilot run for a new catalyst, our team compared product outcomes using Pyridine-3-aldehyde and its 4-isomer; the 3-isomer consistently delivered better control over regiochemistry, a key step for downstream consistency. Such insights go beyond what catalogs or spec sheets provide, and these first-hand lessons stick with chemists for years.
Compared to common aromatic aldehydes like benzaldehyde, Pyridine-3-aldehyde brings nitrogen into the ring, and that single atom dramatically shifts both electron distribution and overall reactivity. Nucleophilic addition becomes more selective, and opportunities open for pathways that simply aren’t available with standard benzaldehyde. These structural shifts impact not just synthesis planning, but also waste management, purification strategies, and regulatory considerations. One poorly planned substitution can mean headaches for process safety or environmental compliance teams.
Talk to quality managers at a pharmaceutical plant, and you’ll hear the same refrain: source variability plagues specialty chemicals. Pyridine-3-aldehyde, despite its relatively low order volume compared to commodity chemicals, offers case studies in why quality assurance should never be an afterthought. During a recall on an API project, we traced the issue back to a seemingly minor impurity in the supplied Pyridine-3-aldehyde—an impurity that was not consistently screened by some vendors. Testing protocols and thorough documentation aren’t just boxes to tick; they shield companies from costly rework and regulatory violations.
There’s a fine line between affordable sourcing and cutting corners. I’ve watched purchasing managers squeeze vendors on price until only the lowest-cost, least proven players are left. In the worst cases, slight technical deviations in purity—hard to detect with a basic GC—lead to lost batches and sometimes even regulatory censure. These days, larger organizations partner with labs experienced in deep impurity profiling, using advanced techniques like NMR, LC-MS, or even chiral separation when stereochemistry matters. My own preference is to run an extra round of checking, especially when unfamiliar sources come into play. The cost of a single flawed delivery often outweighs the short-term savings from bargain shopping.
Pyridine-based compounds often require thoughtful safety protocols. In my own work, skin contact or inhalation leads to quick reminders about the importance of gloves and fume hoods. While the compound doesn't carry the same notoriety as strong acids or common explosives, it does pose health risks at high concentrations—irration to skin, eyes, or mucous membranes is no joke. Once, an unnoticed spill on a shared bench led to several days of pungent reminders, cutting across even experienced noses. Diligence in labeling, storage, and cleanup becomes second nature over time.
Disposal presents another set of challenges. With growing attention paid to waste streams, especially in regions with strict limits on pyridine discharges, responsible labs and factories segregate, neutralize, or incinerate residues. In a world where trace contaminants can impact everything from wastewater treatment efficacy to regulatory reporting, managing chemical outputs with real care must become part of the organizational DNA.
Consistency in supply chains starts with education. Over the years, I’ve seen that those organizations investing in training not just raw bench chemists, but also procurement, logistics, and compliance staff, sidestep the majority of preventable setbacks. Knowing how to read—and challenge—a certificate of analysis distinguishes veterans from newcomers. Internal quality audits, combined with periodic third-party verification, root out lurking risks before they morph into full-blown crises.
Supplier transparency remains a sticking point in the specialty chemicals world. Those buyers who push for open access to batch-level impurity data, detailed QC records, and auditable handling protocols rarely find themselves blindsided by surprises. I’ve worked with suppliers adapting blockchain-based systems to track shipments, flag excursions, and log exact environmental conditions throughout transit. While no solution is perfect, digital records coupled with actionable alerts prove far more robust than spreadsheets and cursory phone calls. In my view, this shift toward real-time, data-driven supply assurance will only accelerate in coming years.
From an operational standpoint, investing in broader in-house analytical capability gives downstream users faster feedback. Instead of waiting days for outside lab results, immediate validation with state-of-the-art equipment like LC-MS or NMR lets teams catch off-spec material before it enters the production pipeline. I’ve argued for such upgrades at more than one company, pointing not just to higher product quality, but to savings from averted waste and reputational risk.
Each application unlocks new challenges requiring fresh thinking. Medicinal chemists, for example, increasingly customize functionalized derivatives of Pyridine-3-aldehyde to fine-tune drug metabolism or receptor targeting. In the past, modifying core structures would have felt risky, but computational chemistry now enables rapid screening of candidate analogs. I’ve collaborated on projects where dozens of derivatives undergo automated docking or ADME testing, rerouting synthetic plans long before a gram is ever weighed out.
In areas outside pharma, the compound acts as a springboard for advanced nanomaterials, functional polymers, and metal-organic frameworks. Environmental chemistry groups devise new catalysts aimed at cleaner reactions, with Pyridine-3-aldehyde scaffolds at the core. I remember a recent symposium session where researchers presented breakthroughs in solar cell additives, citing unique electronic properties conferred by these pyridine-based molecules. The convergence of fields is no longer a distant aspiration, but an active zone for practical collaboration.
All these advances rely on stable access to well-characterized building blocks. Any progress in synthesis, formulation, or performance tracking rests on foundations built with quality raw materials. That’s why the culture of continuous improvement and traceability around Pyridine-3-aldehyde should remain front and center for developers and users alike.
A decade ago, many industrial players treated specialty chemicals as commodity inputs. It took me a few years in business to realize how shortsighted this approach can be. Product recalls, missed milestones, or failed launches all too often trace back to a flawed starting material that was considered “good enough” at procurement. As the regulatory environment tightens and downstream requirements increase, that margin for error continues to shrink.
A genuine commitment to quality control—with well-documented procedures, reliable partners, and robust analytics—inevitably outpaces price-based decisions. In essence, success across chemistry subfields traces back to respect for the smallest details. Whether it’s a new pharmaceutical lead or an innovative specialty polymer, the attributes of Pyridine-3-aldehyde can make or break that breakthrough. I’ve seen visionary research undone by a supplier’s batch inconsistency, and brilliant commercialization plans halted by unanticipated contaminants. The drive for reproducibility, especially in scale-up, is no longer just a technical issue; it marks the difference between commercial survival and failure.
In the short span of my own career, the expectations attached to specialty reagents like Pyridine-3-aldehyde have evolved. Today’s researchers and engineers must act as stewards not only of their own experimental results, but also of the supply chains and communities impacted by chemical production and use. For younger chemists reading material safety sheets or prepping glassware for the first time, these stories of vigilance and adaptation may seem distant. Yet these values shape outcomes at every stage, from the university lab bench to high-throughput manufacturing lines.
The future will see stronger integration of digital tracking, real-time analytics, and smarter supplier relationships. Each added tool and technique aims to deliver the reliability and transparency required by an increasingly discerning public and a more regulated marketplace. Sharing knowledge about practical roadblocks and effective fixes—instead of relying on dense, jargon-heavy documentation—will help the next generation sidestep old pitfalls and drive innovation further.
Pyridine-3-aldehyde sits at the intersection of science, engineering, and business, enabling significant discoveries and commercial advances across chemistry’s broad canvas. Those who treat this compound as just another name in a catalog risk missing the very real opportunities—and challenges—that come with thoughtful, informed sourcing and use. The best outcomes still rest on respect for foundations laid by careful choices, proven partners, and a culture that prizes precision over expediency. My own journey with this compound, punctuated by both successes and setbacks, confirms that the attention paid at every step ripples through to results that matter. As demands on chemical integrity rise, embracing continuous improvement and open communication with partners shines as not only best practice, but simple common sense.