|
HS Code |
981212 |
| Iupac Name | pyridine-2-carbaldehyde |
| Common Name | 2-Pyridinecarbaldehyde |
| Cas Number | 1121-60-4 |
| Molecular Formula | C6H5NO |
| Molar Mass | 107.11 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 198-200 °C |
| Melting Point | -29 °C |
| Density | 1.129 g/cm³ |
| Solubility In Water | Soluble |
| Flash Point | 89 °C (closed cup) |
| Refractive Index | 1.556 |
| Smiles | C1=CC=NC(=C1)C=O |
| Pubchem Cid | 11804 |
| Odor | Pungent, characteristic |
As an accredited 2-Pyridinecarbaldehyde 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, tightly sealed with a screw cap, labeled '2-Pyridinecarbaldehyde, CAS 1121-60-4, 100 mL'. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Pyridinecarbaldehyde: 14 metric tons (MT) per 20-foot container, packed in 250 kg drums. |
| Shipping | 2-Pyridinecarbaldehyde is shipped in tightly sealed containers, away from light, moisture, and incompatible substances such as strong oxidizers. It is handled as a hazardous material, with proper labeling and documentation according to regulatory requirements. Temperature control and secondary containment may be used to prevent leaks and ensure safe transportation. |
| Storage | 2-Pyridinecarbaldehyde should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container tightly closed and protected from light and moisture. Store under inert atmosphere if possible. Ensure proper labeling, and handle in accordance with standard chemical safety procedures to avoid decomposition and hazards. |
| Shelf Life | 2-Pyridinecarbaldehyde typically has a shelf life of 12–24 months under cool, dry, and tightly sealed storage conditions. |
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Purity 99%: 2-Pyridinecarbaldehyde with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reproducibility. Molecular weight 107.10 g/mol: 2-Pyridinecarbaldehyde with molecular weight 107.10 g/mol is used in fine chemical production, where precise stoichiometry is critical for product consistency. Melting point −19°C: 2-Pyridinecarbaldehyde with melting point −19°C is used in solution-phase peptide synthesis, where its liquid state at low temperatures improves mixing efficiency. Boiling point 188°C: 2-Pyridinecarbaldehyde with boiling point 188°C is used in organic synthesis workflows, where its thermal stability enables high-temperature reactions. Stability temperature up to 120°C: 2-Pyridinecarbaldehyde with stability temperature up to 120°C is used in enzymatic assays, where it maintains integrity under incubation conditions. Density 1.116 g/cm³: 2-Pyridinecarbaldehyde with density 1.116 g/cm³ is used in analytical reagent preparation, where accurate volumetric measurement enhances experimental reliability. Low water content (<0.1%): 2-Pyridinecarbaldehyde with low water content (<0.1%) is used in moisture-sensitive reactions, where it minimizes side reactions and increases purity of end products. High chemical purity (≥98.5%): 2-Pyridinecarbaldehyde with high chemical purity (≥98.5%) is used in ligand synthesis for coordination chemistry, where contaminant-free synthons yield high-performance complexes. |
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In daily lab routines or in the workshop of a pharmaceutical developer, few tools prove as versatile as 2-Pyridinecarbaldehyde. This compound, carrying the chemical formula C6H5NO, represents much more than a bottle on the shelf. For folks who’ve spent time troubleshooting failed syntheses, the benefits of using a reagent like 2-Pyridinecarbaldehyde stand out as soon as the reaction begins to run more smoothly. Clarity in production methods and quality control tie directly into everything downstream—whether scaling a pilot project or preparing publication-worthy research.
2-Pyridinecarbaldehyde comes as a pale yellow liquid, notable for its distinct, sharp odor. With a molecular weight just under 110 g/mol, it slips easily into many synthetic protocols. Chemists know that an aldehyde group at the 2-position on the pyridine ring opens up a wealth of pathways for creating more complex molecules. In daily practice, that means the compound acts as a key starting material when making pharmaceuticals, agrochemicals, and specialty ligands for catalytic reactions.
Looking at its most common model, the substance finds wide use in both small-scale research and larger manufacturing settings. As a standard, users seek a purity exceeding 98%, and they count on consistent supply. Even small variations in quality can flip a manageable reaction into a headache, so trustworthy product consistency means everything here. For those prepping custom ligands or building intermediates for drug compounds, the little details like water content, residual solvents, and trace metals start to matter more than most people outside the lab imagine.
Fewer intermediates match the track record of 2-Pyridinecarbaldehyde in modern synthesis. From my own time in an academic lab, I recall that several teams reached for this molecule in the hunt for new bioactive structures. It’s not simply tradition or habit; this aldehyde’s chemical behaviors fill roles where other pyridine derivatives can’t take its place. For example, chemists lean on its balance between nucleophilic reactivity at the aldehyde and basicity from the pyridine ring, which helps guide reactions predictably. Reliable reactivity matters most when every batch can’t waste time or expend energy fixing yields.
The compound’s accessible boiling point means straightforward distillation and minimized losses during purification. Unlike some trickier pyridine derivatives, 2-Pyridinecarbaldehyde handles standard storage and transport conditions without excessive fuss. Those practical reasons explain why it has found its way onto purchasing lists for contract research organizations as well as teaching labs.
Day-to-day, 2-Pyridinecarbaldehyde makes itself indispensable in creating customized ligands for transition metal catalysis. Many find its value as a building block for the class of compounds known as Schiff bases. The formation of these bases involves the reaction between the aldehyde group of 2-Pyridinecarbaldehyde and primary amines, yielding products that often serve as ligands for metal complexation. In fact, a number of new catalysts and coordination polymers owe their creation to the flexible backbone provided by this molecule.
In drug discovery, medicinal chemists tap into the reactive site at the 2-position for efficient functionalization. Sometimes, making analogs quickly and reliably determines whether a project will move ahead or stall out in screening. Here, even a modest change—one methyl group swapped in, one halogen shifted—could alter a compound’s biological profile. When those tweaks demand a stable core, reliability in sourcing and handling the main building block counts for everything.
Food safety testing, too, has borrowed ideas from the pharmaceutical space, using derivatives of 2-Pyridinecarbaldehyde as part of detection assays for specific contaminants. Its broad chemical compatibility helps method development proceed without constant adjustment of procedures.
Among pyridinecarbaldehydes, those familiar with organic synthesis will recognize the differences that come from a shift between the 2-, 3-, and 4- positions on the core ring. Moving the aldehyde group from the 2- to the 3-position, for example, changes the electronic landscape dramatically. 2-Pyridinecarbaldehyde carries the aldehyde group close to the nitrogen atom in its aromatic ring, a subtle but crucial arrangement that leads to distinct reactivity.
Chemists appreciate this because certain catalytic pathways favor the 2-isomer’s electronic influence, enabling cyclizations, condensations, or cross-coupling reactions that would lag or fail with the 3- or 4- isomers. There’s also a practical angle. 2-Pyridinecarbaldehyde generally remains more straightforward to handle and purify compared to position-isomers that might carry a higher risk for side-reactions or decomposition under typical lab conditions.
Compared to non-pyridine aldehydes, like benzaldehyde, the combination of aromaticity and the lone pair-bearing nitrogen introduces both new challenges and opportunities. Catalytic systems that require chelating ligands or demand precise orientation around a metal center get a definite boost from this molecule’s architecture. In many cases, users see increased efficiency and control that cannot be matched by basic aromatic aldehydes.
After years of observing order-to-order results, one finds that 2-Pyridinecarbaldehyde’s sensitivity to moisture stands out as a double-edged sword. Keeping the product capped and in a dry space turns into a habit. When exposed to humidity for extended periods, the aldehyde might start to oxidize, affecting performance in key reactions. This detail tends to become obvious at scale, as a single off-batch can disrupt weeks of planning.
Another practical consideration centers on the purity standards set by different suppliers. Not every provider ensures the same level of stringency with respect to trace impurities, often including residual solvents from the original synthesis or unwanted isomers. Researchers who value reproducibility and high yields learn quickly to request up-to-date certificates of analysis and favor suppliers with strong quality control protocols.
On a personal note, I’ve seen a project flounder because a batch contained just enough water to quench a sensitive condensation, and such setbacks stay with you. Product storage and regular quality checks prevent these headaches and let teams focus on discovery and analysis, not repeat troubleshooting.
Working with 2-Pyridinecarbaldehyde, as with many laboratory organics, invites a sense of responsibility. Users respect its volatility and distinctive aroma, always mindful of the flammability risks present with open containers or in high-heat environments. Modern labs invest in dedicated exhausts and prefer to store even small lots in flame-resistant cabinets.
Disposal practices for this compound follow regulations aimed at protecting both workers and environments outside the laboratory. Fresh graduates entering the world of bench chemistry often learn first-hand the importance of documentation and safe disposal, as aldehydes can react to form undesired byproducts in municipal systems. Education and clear protocols help keep everyone on the same page.
The long arc of chemical development has taught experienced researchers that the most innovative science runs only as smoothly as the supplies feeding it. With 2-Pyridinecarbaldehyde, users want a supplier who recognizes the importance of lot-to-lot consistency and transparent documentation. I’ve relied for years on strong vendor relationships to guarantee short lead times, clear communication about batch changes, and regular updates on any new synthesis methods. When a team spends months on an optimization campaign, a sudden change in the reactivity profile because of a new impurity or a subtle difference in handling can cost more than lost time—it can mean losing a competitive edge.
Pharmaceutical manufacturers in particular demand high standards for chemical intermediates. Rigorous in-house and external testing for contaminants becomes the norm, not an exception. A shipment delayed due to failed analysis can mean interruptions in timelines for clinical trial material. On the other hand, analytical and academic labs benefit from transparent documentation and supply chain traceability. These steps close the gap between “checking a box” and conducting world-class research.
Spending years at the bench impresses upon chemists that each chemical brings both risk and opportunity. Proper training in storage, handling, and spill response minimizes injury and keeps costly materials from going to waste. In the case of 2-Pyridinecarbaldehyde, experience shows that stable packaging and clear labeling result in fewer accidents. Newcomers learn fast from mentors who stress never decanting organics over an open bench and always labeling reaction mixtures clearly—lesson learned is a lesson not repeated.
Handling protocols in industry and academia have begun to converge, with audits and periodic retraining reinforcing good habits. It pays to stay current with evolving guidance from regulatory bodies, ensuring that both short-term convenience and long-term safety are supported. I’ve noticed an uptick in green chemistry practices, where the goal is not just effective chemistry but also thoughtful waste reduction. Choice of reagent, including 2-Pyridinecarbaldehyde, fits into this bigger picture.
Analytical chemists often rely on gas chromatography (GC), high-performance liquid chromatography (HPLC), or nuclear magnetic resonance (NMR) spectroscopy for verification. For 2-Pyridinecarbaldehyde, clear, well-resolved peaks on a chromatogram provide assurance that the bottle holds what the label claims. These tools, paired with robust supplier records, offer a strong foundation for trust from the earliest stage of a project to the final report sent to a regulatory agency.
Quality assurance teams set specifications targeting not only assay purity, but also design limits for metals, halides, and other adventitious contaminants. These assurances feed into downstream utility; a poorly characterized lot can ruin a batch of product, while a well-documented source streamlines validation and speeds the release of new formulations.
The global market’s increasing demand for chemical precursors like 2-Pyridinecarbaldehyde puts pressure on suppliers to innovate. One area for potential improvement surfaces in greener, more efficient synthetic methods. Traditional routes for preparing pyridinecarbaldehydes often generate waste streams and involve stoichiometric oxidants. Process chemists now propose catalytic alternatives and closed-loop systems aiming to minimize emissions—approaches that make both environmental and economic sense.
Supply chains, too, move toward transparency. More firms now prioritize end-to-end tracking for batches, allowing users to trace a bottle’s origin and check each step for compliance with required standards. Lab managers and purchasing officers will continue to vote with their budgets, favoring suppliers who provide both consistency and clear documentation about process improvements, sustainability efforts, and corrective actions when issues emerge.
From a regulatory angle, tighter controls on impurities provide developing countries and emerging biotech sectors with the confidence to pursue advanced pharmaceutical research. Training programs focused on best practices for handling and disposal reinforce a culture of responsibility around all high-purity organics, preparing workers to spot potential hazards before they become full-fledged problems.
With every advancement in synthetic methodology, demand for reliable starting materials follows. As scientists, we look for tools that empower us to explore new directions, confident that the fundamentals—chemical purity, predictable reactivity, compliance with safety and environmental norms—are in place. Over the years, 2-Pyridinecarbaldehyde has become a fixture in bench-top and process-scale chemistry because its flexibility and performance meet the standards of both cutting-edge research and mainstream industry.
Labs around the world push into new territory, building on knowledge won through careful observation, smart sourcing, and a commitment to getting the details right. The story of 2-Pyridinecarbaldehyde shows that value comes not just from what’s in the bottle, but from the relationships, experience, and learning that grow alongside a trusted molecule.