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HS Code |
928576 |
| Name | Pyridine-4-carbaldehyde |
| Synonyms | 4-Formylpyridine |
| Molecular Formula | C6H5NO |
| Molecular Weight | 107.11 g/mol |
| Cas Number | 872-85-5 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 226 °C |
| Melting Point | 15-18 °C |
| Density | 1.131 g/cm3 |
| Solubility In Water | Miscible |
| Flash Point | 104 °C |
| Refractive Index | 1.526 |
| Smiles | C1=CC(=NC=C1)C=O |
| Inchi | InChI=1S/C6H5NO/c8-5-6-1-3-7-4-2-6/h1-5H |
| Pubchem Cid | 10484 |
As an accredited pyridine-4-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 mL clear glass bottle with secure screw cap; white label displaying "Pyridine-4-carbaldehyde, 99%" and hazard information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for pyridine-4-carbaldehyde: Typically packed in 250kg drums, 80 drums per container, totaling 20 metric tons. |
| Shipping | Pyridine-4-carbaldehyde is shipped in tightly sealed containers, protected from light and moisture. It is packed in accordance with hazardous materials regulations due to its flammability and potential health risks. Proper labeling, cushioning, and secondary containment are used, and transport is by approved carriers under temperature-controlled and monitored conditions if required. |
| Storage | Pyridine-4-carbaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from light and moisture. Recommended storage is at room temperature, avoiding temperature extremes. Proper labeling and handling procedures should be followed to prevent spills and exposure. |
| Shelf Life | Pyridine-4-carbaldehyde is stable for at least 2 years if stored tightly sealed, protected from light, at 2-8°C. |
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Purity 99%: Pyridine-4-carbaldehyde purity 99% is used in pharmaceutical synthesis, where it ensures high yield and product consistency. Melting point 105°C: Pyridine-4-carbaldehyde melting point 105°C is used in heterocyclic compound manufacturing, where it enables thermal stability during reaction processes. Molecular weight 107.1 g/mol: Pyridine-4-carbaldehyde molecular weight 107.1 g/mol is used in agrochemical intermediates, where it allows precise stoichiometric calculations. Water content <0.2%: Pyridine-4-carbaldehyde water content <0.2% is used in peptide coupling agents, where it minimizes side reactions and enhances product purity. Stability temperature up to 60°C: Pyridine-4-carbaldehyde stability temperature up to 60°C is used in catalyst development, where it provides reliable handling and storage. Particle size <5 microns: Pyridine-4-carbaldehyde particle size <5 microns is used in fine chemical synthesis, where it improves solubility and reaction kinetics. Residual solvent <0.1%: Pyridine-4-carbaldehyde residual solvent <0.1% is used in API production, where it guarantees pharmaceutical compliance and product safety. UV absorbance at 260 nm: Pyridine-4-carbaldehyde UV absorbance at 260 nm is used in analytical chemistry, where it enables precise detection and quantification. pH stability range 4-8: Pyridine-4-carbaldehyde pH stability range 4-8 is used in buffer formulations, where it maintains chemical integrity under various conditions. Chromatographic purity >98%: Pyridine-4-carbaldehyde chromatographic purity >98% is used in research applications, where it supports reproducible experimental results. |
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Pyridine-4-carbaldehyde has a unique role in chemical synthesis and research. With its structure based on the pyridine ring and an aldehyde group in the para position, this compound stands out for its reactivity and range of applications. Chemists, whether in pharmaceuticals or material science, often search for molecules that can serve as both an intermediate and a reactive agent. Pyridine-4-carbaldehyde delivers on both counts, giving researchers the flexibility needed to synthesize a wide variety of products, from active pharmaceutical ingredients to specialty chemicals for industrial processes.
Its molecular formula, C6H5NO, hints at both stability and reactivity, which is not always easy to achieve in one package. This product typically appears as a yellowish liquid or sometimes a crystalline solid at room temperature, making it straightforward to handle in lab settings. In my experience working with synthetic compounds, I often appreciate those that do not bring unnecessary headaches during purification and storage. Pyridine-4-carbaldehyde tends to hold up well without complex storage requirements, which adds to its practicality in day-to-day research.
Lab technicians and process engineers prize pyridine-4-carbaldehyde for its ability to streamline multi-step syntheses. Many chemical syntheses stumble right from the beginning because starting materials react unpredictably or create troublesome by-products. Pyridine-based aldehydes, especially with the aldehyde at the 4-position, offer a distinct pattern of reactivity. This property makes them favorites in linkers for organic frameworks, in ligand design for catalysis, and in the creation of new heterocyclic scaffolds for drug discovery.
One common application involves condensation reactions, where this molecule willingly forms Schiff bases with a range of amines. I have worked on syntheses in which other aldehydes hesitated or led to impure reactions, but switching to pyridine-4-carbaldehyde yielded cleaner products with fewer side reactions. Its aromatic ring, topped with the electron-withdrawing pyridine nitrogen, increases the electrophilicity of the aldehyde group, enabling chemists to drive reactions efficiently and reproducibly.
Pharmaceutical projects in particular often benefit. Medicinal chemists look for ways to introduce the pyridyl motif into molecules, aiming to boost potency, improve binding to proteins, or modify metabolic fate. Pyridine-4-carbaldehyde offers a reliable entry point. Rather than attempting to retrofit a pyridine ring onto a finished molecule, researchers can use this building block early on, tailoring drugs or probes from the ground up. This approach saves time and cuts waste, which matters both for small start-up labs and established drug companies under pressure to find new leads quickly.
In my lab, I have reached for benzaldehyde, nicotinaldehyde, and pyridine-2-carbaldehyde in many syntheses. Each has quirks that suit specific tasks. What sets pyridine-4-carbaldehyde apart is its balance: it reacts strongly enough for demanding procedures, but not so aggressively that it needs constant babysitting. Benzaldehyde, a classic aromatic aldehyde, lacks the nitrogen atom of pyridine, granting it less flexibility for further derivatization. The pyridine-2-carbaldehyde isomer reacts differently because its nitrogen is closer to the aldehyde, creating steric and electronic effects that can sometimes complicate reactions.
With pyridine-4-carbaldehyde, the positioning of the nitrogen and aldehyde on opposite sides of the ring spreads out electronic effects and avoids crowding in the molecule. This layout influences selectivity, making it easier to control outcomes in syntheses. While some users may reach for simpler aldehydes out of habit, many find that once they have experimented with pyridine-4-carbaldehyde, it unlocks new strategies and product profiles. For custom ligands or advanced pharmaceutical scaffolds, this difference proves far more than cosmetic.
Chemists know the frustration when an experiment fails because the starting material contained unknown impurities. With pyridine-4-carbaldehyde, purity matters a great deal, especially in research pushing the boundaries of what’s possible in drug discovery, catalysis, or new materials. Most suppliers offer this reagent at purities of 97% or higher, which often meets the standard for both academic and industrial research.
Batch consistency also drives reproducibility, an essential principle in science. According to published analytical methods such as gas chromatography and nuclear magnetic resonance, pure pyridine-4-carbaldehyde delivers consistent results and avoids the tailing peaks in chromatography that signal trouble. Working with this compound, I appreciate suppliers who publish clear analytical data and offer certificates of analysis—not just for regulatory paperwork but to confirm that what arrives in the bottle matches what’s listed on the label. Trust in source and transparency builds confidence and saves time chasing down invisible problems.
Global supply chains sometimes create headaches for chemists who rely on materials delivered on time, with reliable specifications. Pyridine-4-carbaldehyde, produced in bulk by several major manufacturers, tends to be available both in laboratory and commercial quantities, so scaling from bench work to pilot or even commercial production poses fewer headaches than for more exotic intermediates. This availability helps ensure projects do not grind to a halt due to unexpected delays in sourcing.
Safety-conscious researchers understand that any compound with aldehyde functionality deserves respect. Pyridine-4-carbaldehyde, like many small aldehydes, carries warning labels for eye, skin, and respiratory irritation. In my years working with it, simple precautions—working in a fume hood, wearing gloves, keeping spill kits nearby—tend to keep risks to a minimum. Reliable suppliers provide clear guidance and standardized documentation, helping labs carry out risk assessments and comply with local and national regulations.
One difference I’ve noticed over the years is that pyridine-4-carbaldehyde lacks some of the volatility and strong odor typical of smaller aldehydes like acetaldehyde or even formaldehyde. This trait makes a practical difference, since background odors or fugitive vapors can make bench work unpleasant and, for compounds like formaldehyde, dangerous at surprisingly low concentrations. While I would never treat pyridine-4-carbaldehyde casually, its physical properties make day-to-day handling much more bearable, which adds to its popularity in research and manufacturing.
Every year, new regulations and corporate guidelines tighten the focus on sustainability in chemical processes. That means not only thinking about what a compound can do, but also about how it is made and disposed of. Pyridine-4-carbaldehyde generally emerges from oxidation reactions on the corresponding methylpyridines, often using reagents that leave fewer toxic by-products than more traditional methods.
For research groups and companies with green chemistry goals, this matters. Fewer hazardous by-products mean easier waste handling and less downstream processing, which cuts costs and reduces environmental impact. Some newer methods even use catalytic oxidation, minimizing the use of stoichiometric heavy metal oxidants that rank high on environmental hazard lists. Adopting these methods, I’ve noticed both an uptick in lab morale and a lessened paperwork burden for hazardous waste tracking.
On the disposal front, care is needed, as with any aldehyde, to ensure that pyridine-4-carbaldehyde does not enter waterways untreated. Still, in comparison with more persistent organic pollutants, it breaks down more readily under typical wastewater treatment conditions. This property, combined with responsible handling, positions it as a relatively sustainable choice among aromatic aldehydes.
Chemistry moves fast, and so do the uses for building blocks like pyridine-4-carbaldehyde. I have followed the literature for years as new research repurposes this compound in unexpected directions. In catalysis, for instance, tailored ligands made from pyridine-4-carbaldehyde can fine-tune the activity and selectivity of metal complexes. These advances matter in making industrial chemistry more efficient, especially for reactions that are energy-intensive or rely on rare metals.
Material scientists have also put pyridine-4-carbaldehyde to work in assembling frameworks that capture gases or filter pollutants from water. Thanks to its chemical functionality, it can link up in predictable, stable patterns, creating porous networks such as metal-organic frameworks (MOFs). These materials show promise for gas storage, separation, and even catalytic applications.
Synthetic organic chemists always look for new routes to challenging molecules. Over the past decade, pyridine-4-carbaldehyde has helped open new doors in heterocycle synthesis, including complicated polycyclic compounds relevant to medicinal chemistry. In my own projects, quick access to this building block has saved weeks or even months, especially compared to older strategies that required multiple steps just to install the right functional groups.
Unlike some chemicals that tie up storage space with their sensitivity, pyridine-4-carbaldehyde tolerates normal conditions for most laboratory and industrial settings. Sealing the bottle tightly, keeping it away from direct sunlight and extreme temperatures—these straightforward measures suffice in most cases. From my perspective, this reliability simplifies lab management, since the product does not require constant monitoring or special cooling.
This compound also ships safely, usually in glass or high-density polyethylene containers of varying sizes. For teams who need to order multiple solvents and reagents, knowing that pyridine-4-carbaldehyde arrives intact, with clear labeling and tamper-evident seals, takes pressure off both procurement and storage logistics. When budgets and timelines are tight, avoiding surprises on delivery day can be the difference between hitting project milestones and missing them.
Wider use of pyridine-4-carbaldehyde runs up against some common drag factors in chemistry: supply fluctuations, price volatility, and less familiarity outside core synthetic teams. Prices can spike during supply interruptions, especially when feedstock chemicals rise in cost. Labs depending on uninterrupted supply may hedge with multiple suppliers or larger inventory buffers.
Broader training and information sharing could help teams new to pyridine-4-carbaldehyde integrate it into their workflows. Detailed case studies from published research, industry case histories, and application notes all contribute to lowering the learning curve. I have seen teams unfamiliar with pyridine chemistry miss key advantages until workshop sessions or joint projects spread practical knowledge. Institutions can encourage cross-team training and make success stories part of onboarding new researchers.
Digital tools now help chemists map compatible reagents and reactions before committing resources to the bench. Expanding searchable databases to include detailed reaction conditions, troubleshooting tips, and downstream uses for pyridine-4-carbaldehyde would help beginners and veterans avoid stumbling blocks and get the most out of each batch.
The rising importance of good manufacturing practice (GMP) standards asks more from chemical suppliers than just delivering a bottle at the right time. Transparency about sourcing, regulatory compliance, and traceability all build trust, especially for labs working toward regulatory filings or commercial launches. Suppliers who demonstrate compliance and publish independent test data win repeat business, as shown by trends in bulk chemical purchasing.
Mislabeling, inadequate analysis, or hidden batch histories can easily derail research or manufacturing. With pyridine-4-carbaldehyde’s applications reaching from pilot-scale production into regulated drugs and materials, chemists and purchasing managers look for partners—not just vendors—who commit to high standards. I recommend labs document supplier performance, set clear expectations, and share feedback both internally and with trusted peer networks.
Small-scale lab wins often stall during scale-up without the right building blocks in place. Pyridine-4-carbaldehyde’s commercial availability in kilogram and ton lots means that synthesis pathways developed for a hundred milligrams translate upward with fewer changes. This property no doubt encourages research teams to consider it for processes meant to graduate from research to manufacturing.
I have watched startup companies leap ahead of better-funded competitors by designing their processes around such scalable intermediates. Teams that select reagents not just for what they can achieve now, but for what the market can reliably provide next year, tend to impress funders and commercialization partners. Pyridine-4-carbaldehyde thus finds a sweet spot for researchers attracted to both practical progress and scientific challenge.
Pyridine-4-carbaldehyde has become a mainstay for chemists looking to innovate efficiently. With its clean reactivity, good availability, and adaptability to emerging green chemistry methods, it not only solves problems but also opens new paths in both academic and industrial laboratories. Its modest hazards, manageable storage needs, and straightforward sourcing make it easy to recommend. For those ready to move beyond traditional aromatic aldehydes in pursuit of new molecules, new materials, or more sustainable chemistry, this is a product that belongs on the bench—and in the planning for the next big breakthrough.