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HS Code |
843129 |
| Cas Number | 1121-60-4 |
| Iupac Name | pyridine-2-carbaldehyde |
| Molecular Formula | C6H5NO |
| Molar Mass | 107.11 g/mol |
| Appearance | colorless to pale yellow liquid |
| Boiling Point | 196-198 °C |
| Melting Point | -7 °C |
| Density | 1.131 g/cm3 at 20 °C |
| Solubility In Water | miscible |
| Refractive Index | 1.561 |
| Flash Point | 87 °C |
| Synonyms | 2-formylpyridine |
As an accredited 2-Pyridinecarboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 mL, sealed with a screw cap; labeled with chemical name, hazard information, and supplier details. |
| Shipping | **2-Pyridinecarboxaldehyde** is shipped in tightly sealed containers made of compatible materials, protected from light, heat, and moisture. It is transported according to local, national, and international regulations for hazardous chemicals, typically under UN number 1993 (flammable liquid). Ensure proper labeling, documentation, and handling by trained personnel during shipping. |
| Storage | 2-Pyridinecarboxaldehyde 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 and acids. Protect it from light and moisture. Ensure proper labeling, and store at room temperature or as specified by the manufacturer. Use appropriate secondary containment to prevent spills. |
Applications of 2-Pyridinecarboxaldehyde in Industrial ManufacturingAs a direct manufacturer of 2-Pyridinecarboxaldehyde, we enable a range of advanced downstream transformations across specialized industrial sectors. The following sectors illustrate practical applications, focusing on authentic end-use value, integrated process deployment, and regulatory alignment as documented in real-world manufacturing. 1. Pharmaceutical Intermediate Synthesis for API Production2-Pyridinecarboxaldehyde is widely integrated into pharmaceutical manufacturing, where it acts as a core aldehyde building block in the synthesis of heterocyclic drug intermediates such as cephalosporins, sartans, and anticancer molecules. API process engineers deploy it during selective condensation and cyclization stages, relying on its pyridine reactivity to construct alkaloid scaffolds and pyridyl-based side chains. Each batch adheres to strict traceability protocols to support cGMP validation in final API production. Industry compliance standards
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2. Agrochemical Synthesis of Pyridine-Based Fungicides and HerbicidesDownstream agrochemical producers utilize 2-Pyridinecarboxaldehyde as a reactive aldehyde in the construction of functionalized pyridine rings for contemporary fungicides and herbicides. Its aldehyde group forms essential linkage sites during the synthesis of triazolopyridine and bipyridyl classes, ensuring precise molecular orientation that impacts biological selectivity and field effectiveness. Process control emphasizes residue removal to comply with agrochemical toxicology limits. Industry compliance standards
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3. Specialty Chemical Manufacturing: Fluorescent Probe and Ligand SynthesisR&D divisions and specialty chemical manufacturers use the unique chemistry of 2-Pyridinecarboxaldehyde for fabricating advanced organic ligands and fluorescent labeling agents. Its aldehyde reacts with primary amines or hydrazides to yield Schiff base ligands, which coordinate transition metals in catalysis or biomedical imaging. Controlled dosing ensures minimal off-target reactivity and high labelling yield, critical for downstream analytical application reliability. Industry compliance standards
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4. Corrosion Inhibitor Formulation for Industrial Water TreatmentIn the industrial water treatment sector, 2-Pyridinecarboxaldehyde functions as a key raw material for synthesizing pyridine-based corrosion inhibitors. Manufacturers incorporate it during Mannich base or Schiff base reaction steps to provide amine-pyridine structures known for high steel passivation performance in circulating cooling water and oilfield injection systems. Dosing is fine-tuned to meet anti-scaling and toxicology criteria across different water chemistries. Industry compliance standards
Typical usage ratio
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Making 2-Pyridinecarboxaldehyde demands more than following a set of chemical instructions. Years of handling pyridine-based building blocks have shown just how much this aldehyde stands apart from other aromatic aldehydes and pyridine derivatives. The product’s molecular structure—pyridine with an aldehyde at the 2-position—shapes its behavior in ways that matter, not only to our own production processes but also to specialists relying on its performance in pharmaceuticals, agrochemicals, precision coatings, and modern catalysts.
Our process starts with years of tuning reaction conditions, not only to maximize yield but also to control byproduct profiles and keep common contaminants from interfering with downstream syntheses. Trace impurities like pyridine-3-carboxaldehyde or 2-hydroxypyridine can be major obstacles in fine chemical synthesis, especially where sensitive pharmacopeial standards apply. Consistency requires real-world hands at the reactor, not just a checklist—steady hands that catch small variations in temperature control or solvent purity long before they affect the final batch. It’s easy to see the difference between an aldehyde made for generic intermediate use and a product made for high-purity pharmaceutical inputs.
2-Pyridinecarboxaldehyde appears as a colorless to pale yellow liquid, with a sharp, characteristic odor. At room temperature, it keeps a tight boiling point around 194–197°C and a melting point below 0°C. Laboratory chemical catalogues list this data, but a chemical manufacturer learns what these numbers actually mean in real handling. A lot of buyers underestimate how quickly this aldehyde absorbs moisture from air and the speed at which it reacts with amines or even traces of water, forming imines or hydrates that disrupt reaction profiles. Shipping and storing 2-Pyridinecarboxaldehyde in sealed, inert conditions isn’t just a recommendation—it’s the only way to defend specifications batch after batch.
Batch-to-batch consistency comes from simple habits like pre-drying glassware, tracking solvent moisture by classical Karl Fischer titration, and oxidizing feedstock under strictly regulated conditions. These steps may not make headlines, but failure at these points writes itself into every subsequent step of research. It’s all too easy to spot material produced by shortcutting these habits: color shifts, instability on standing, or increased levels of formic acid due to over-oxidation.
Chemists familiar with heterocyclic synthesis have come to rely on 2-Pyridinecarboxaldehyde for constructing Schiff bases, chelating ligands, and certain nitrogen-containing ring systems found in many biologically active compounds. Pharmaceutical research uses it to install key aldehyde moieties in candidate molecules, while crop protection projects value the ease with which it forms complexes with transition metals. University groups have found it useful in crystal engineering, particularly in supramolecular assemblies where positional selectivity matters.
Customers using the material in medicinal chemistry want more than generic aldehydes—they require lots that won’t trigger unpredictable byproducts or stall coupling reactions. Many have run into trouble with off-brand supplies that include enough 3-aldehyde isomer or oxidized impurity to throw high-throughput screening off-course. Manufacturing for this segment means tuning purification with slow distillation under nitrogen, frequent GC and HPLC checks, and process records that don’t skip details about reagent quality, vessel contamination, or fraction cut points.
Standard models are 99% and 99.5% minimum purity grades. There’s no one-size-fits-all purity; some advanced catalysis applications can tolerate faint impurities, while others—especially peptide synthesis—insist on trace impurity levels down to tenths of a percent. During scale-up, the odor of the product gives hints of quality (and tells you if vent systems need cleaning). Even small differences in stabilization additives or micro-environment packaging can lead to big changes in shelf stability, so attention shifts from wide generalizations to the small practical details—an approach deeply rooted in experience, not in catalog marketing.
2-Pyridinecarboxaldehyde often gets compared to benzaldehyde or other pyridinecarboxaldehydes, especially 3- and 4- positional isomers. Chemically, 2-positioning brings the aldehyde function into direct contact with the nitrogen, making the molecule more reactive in condensation and cyclization reactions. After handling other carboxaldehydes, the distinct reactivity profile stands out the moment you run standard tests. 3-Pyridinecarboxaldehyde offers greater stability but shows less potency in cyclization, making it less attractive for certain drug synthesis tasks. Benzaldehyde, lacking the nitrogen atom, can’t replicate the chelation or hydrogen-bonding tricks that 2-Pyridinecarboxaldehyde performs, and so gets left behind in metal-organic chemistry.
Customers coming from commodity aldehydes sometimes overlook the rate at which 2-Pyridinecarboxaldehyde self-condenses or the specifics of pyridine-nitrogen reactivity. Routine chemical technique isn’t always enough; it calls for a careful pause, handling under low-light conditions, and access to analytical testing, whether you’re working at bench or in pilot plant. Experienced operators recognize the product instantly by its odor, the subtle yellow tint that signals incipient decomposition, or the change in viscosity when the product’s fresh. Our own technicians have learned that relying on off-the-shelf drying agents or standard protocols leaves more residue and inconsistent color than the traditional fractional distillation—a lesson drawn from years of troubleshooting.
Maintaining product quality through the logistics chain brings a different set of challenges. Freight carriers rarely understand why condensation and aldehyde-specific regulations matter, sometimes resulting in cross-contamination or temperature spikes that damage shipment integrity. It’s all about cooperation—whether that means customizing shipment packing or adjusting drum linings so no contact between the product and reactive surfaces happens. Years spent handling feedback from pharmaceutical clients and advanced materials scientists underline just how fast poor logistics management can undo months of meticulous process control. The most advanced plants can’t deliver value if shelf degradation, oxidation, or cross-contamination sneaks in from ignoring these hard-learned lessons.
Our job doesn’t end after the reactor cools and bottles are capped. Regular checks through warehouse visits, temperature recorders during transit, and traceability protocols all stay in place because these steps protect both the customer’s synthesis and our own reputation. Missing a spot in this chain means risking costly regulatory or research setbacks for downstream users, especially in regulated markets.
Making and delivering 2-Pyridinecarboxaldehyde isn’t sterile or flawless. It’s a hands-on process, full of unexpected variables—feedstock variability, summer heat, aging process valves, and staffing changes all shape outcomes. The reality is that most chemical plants, large or small, learn humility early. High-purity aldehydes like this one punish shortcuts in maintenance schedules or skipped calibrations; one week of neglect on a GC detector or a missed chiller service call shows up as inconsistency that trained eyes pick out right away.
Our process teams keep detailed process logs keyed to individual operators, lot numbers, and even ambient humidity, because pattern recognition makes or breaks future batches. Only by comparing real process data across seasons and years does a manufacturer develop an intuition for ideal operating bands. The most confident claims about product consistency always link back to actual process records, not hype or generic assurances.
One overlooked source of variability stems from feedstock suppliers. Even a switch in pyridine vendors can send impurity levels fluctuating. Collaborative work with longstanding chemical partners lets us spot trends and address anomalies before they show up in our own products or those of our customers—a step that matters far more than price when reliability is on the line.
Longstanding collaboration with both university research teams and high-volume industrial buyers provides a constant feedback loop. Some of the most effective incremental process improvements have started with a single research group flagging an unexpected byproduct, or a major client offering their analytics for optimizing purification. Technological change in specialties like organocatalysis, ring-closing reactions, or novel polymerization stems from such open exchanges.
Case-by-case adaptation beats rigid application of so-called “best practices.” Customer partnership teaches which specification parameters have the greatest impact on their finished product yields, and which can be relaxed without loss of performance or regulatory headaches. This level of responsiveness builds reliability over time—something that direct chemical manufacturing relationships can provide, but trading intermediaries rarely support.
Experienced chemical manufacturers grow up with the occupational hazards of volatile, moderately toxic aldehydes. 2-Pyridinecarboxaldehyde isn’t nearly as notorious as hydrazine or phosgene, but its reactivity, volatility, and health risks deserve respect. Standard lab coats and goggles won’t prevent inhalation headaches or derailed shift focus. Facility layout and local exhaust systems make up a critical part of daily operation, given the fumes and sensitivity to air. Hands-on experience shows where theoretical precautions fall short in practice; blending academic guidance with everyday process adjustments works best.
Our safety protocols draw from first-hand accident reviews and near-misses. We see the value in preproduction hazard analyses, not just to satisfy compliance officers, but to develop muscle memory around incident response. The entire crew—from supervisors down to packaging—knows the right routines, because the costs of improvisation show up clearly in industry statistics.
As customers face new challenges—stricter impurity profiles in pharmaceuticals, push toward sustainable solvent systems, and niche applications in supramolecular assembly—manufacturing of 2-Pyridinecarboxaldehyde must keep pace. We have seen firsthand how the same molecular framework that made it useful in yesterday’s coordination chemistry continues to unlock novel uses. One recent trend is the rise of biocatalytic transformations that build on the reactivity enabled by the 2-formylpyridine core, demanding ever-cleaner starting materials and more transparency in supply history.
Instead of standing still, our production methods evolve both in line with technological advances and client-driven guidance. Real improvements show up in quicker impurity detection, lower residual solvent content, and smarter methods for preventing degradation during storage. We learn as much from customers pushing these boundaries as we do from our own plant-floor improvements.
Meeting and exceeding evolving expectations for 2-Pyridinecarboxaldehyde relies on the disciplined application of craft knowledge. Documentation supports consistent results, but daily observation and a habit of tuning process conditions cement reliability. Industry colleagues and serious customers alike have taught us that no written protocol matches the kind of practical know-how earned during maintenance shutdowns or late-night trouble calls.
Choices made in purification, logistics, and routine checks build a product much stronger than what data sheets alone can show. For those inside chemical manufacturing, 2-Pyridinecarboxaldehyde is more than a catalog listing; it’s a vivid demonstration of how the details of daily practice shape broader industry innovation and reliability.