2-Pyridinealdehyde

    • Product Name: 2-Pyridinealdehyde
    • Chemical Name (IUPAC): pyridine-2-carbaldehyde
    • CAS No.: 1121-60-4
    • Chemical Formula: C6H5NO
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    Specifications

    HS Code

    846767

    Iupac Name pyridine-2-carbaldehyde
    Cas Number 1121-27-3
    Molecular Formula C6H5NO
    Molar Mass 107.11 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 196-198°C
    Melting Point -19°C
    Density 1.129 g/cm3
    Solubility In Water Slightly soluble
    Flash Point 78°C
    Refractive Index 1.560
    Pubchem Cid 10236

    As an accredited 2-Pyridinealdehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Pyridinealdehyde comes in a 100 mL amber glass bottle with a secure screw cap, clearly labeled with hazard warnings.
    Container Loading (20′ FCL) 20′ FCL can hold about 14–16 MT of 2-Pyridinealdehyde, packed in drums or IBCs, suitable for safe international transport.
    Shipping 2-Pyridinealdehyde is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be handled and transported according to local regulations for hazardous chemicals, typically labeled as a flammable liquid. Proper personal protective equipment (PPE) is required during handling to prevent exposure to vapors or accidental spills.
    Storage 2-Pyridinealdehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as acids, oxidizing agents, and strong bases. Keep it away from sources of ignition, as it is flammable. Store in a chemical storage cabinet designed for flammable liquids, and label the container clearly.
    Shelf Life 2-Pyridinealdehyde typically has a shelf life of 12–24 months when stored tightly sealed, protected from light, moisture, and air.
    Application of 2-Pyridinealdehyde

    Purity 98%: 2-Pyridinealdehyde with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal by-product formation.

    Melting Point 34°C: 2-Pyridinealdehyde with a melting point of 34°C is used in organic catalysis, where controlled phase transition facilitates efficient reaction rates.

    Molecular Weight 107.1 g/mol: 2-Pyridinealdehyde with a molecular weight of 107.1 g/mol is used in heterocyclic compound development, where precise molar calculations enable accurate formulation.

    Stability Temperature up to 40°C: 2-Pyridinealdehyde with stability temperature up to 40°C is used in storage protocols, where thermal stability maintains chemical integrity.

    Density 1.13 g/cm³: 2-Pyridinealdehyde with density 1.13 g/cm³ is used in analytical standard preparation, where consistent density allows reproducible standardization.

    Water Content <0.2%: 2-Pyridinealdehyde with water content less than 0.2% is used in moisture-sensitive synthesis, where low water content prevents hydrolytic side reactions.

    UV Absorbance λmax 310 nm: 2-Pyridinealdehyde with UV absorbance maximum at 310 nm is used in spectrophotometric analyses, where strong absorbance provides high sensitivity detection.

    Refractive Index 1.534: 2-Pyridinealdehyde with refractive index 1.534 is used in optical material research, where specific refractivity aids in advanced materials characterization.

    Boiling Point 188°C: 2-Pyridinealdehyde with boiling point 188°C is used in distillation processes, where adequate volatility ensures efficient product separation.

    Particle Size <5 µm: 2-Pyridinealdehyde with particle size less than 5 micrometers is used in fine chemical formulations, where uniform particle size enhances reactivity and dispersibility.

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    Certification & Compliance
    More Introduction

    2-Pyridinealdehyde: Making Chemistry Work Smarter

    Introducing 2-Pyridinealdehyde

    Many folks in the lab learn pretty quickly that not all reagents are created equal. 2-Pyridinealdehyde stands out in more ways than one, offering real value where precision and versatility matter. If you’ve spent hours tracking down chemicals with reliable purity, you’ll know just how much difference a solid product like this can make. Working with 2-Pyridinealdehyde brings a sense of confidence to chemists who need results they can trust, whether the focus is on research, pilot-scale synthesis, or production work.

    Known Structure, Real Advantages

    2-Pyridinealdehyde packs its punch with the molecular formula C6H5NO and CAS number 1121-60-4. It looks like an aromatic ring with a formyl group at the two position—if you’ve ever messed with aromatic aldehydes, you’ll know this structure opens doors to all sorts of reactions. It comes as a pale yellow liquid with a distinctive scent you won’t forget. People sometimes compare it with benzaldehyde in the storeroom, but its reactivity and selectivity set it in a league of its own.

    Key Details and Real-World Handling

    On the specs front, 2-Pyridinealdehyde usually rolls out with a purity above 98%. This degree of purity saves time, avoids surprises, and brings cost savings in downstream work. In real-world use, I’ve seen this reagent hold its quality even after being opened and handled over multiple sessions. Folks tend to store it cold and keep it away from light—typical for sensitive aldehydes to avoid slow but sure decomposition.

    Weighing out 2-Pyridinealdehyde shouldn’t cause frustration. It’s liquid, which makes transfer and measurement straightforward with a pipette or syringe. It dissolves well in common solvents, like ethanol, ether, and water to a point. For people trying to react it with amines or use it as a building block in heterocycle synthesis, this type of solubility simplifies planning.

    What Sets It Apart?

    Most aldehydes give you that carbonyl group, but here, the attached pyridine ring changes things. It draws in electron density, tuning the reactivity just enough to make the aldehyde group more selective. Organic chemists who build ligands or need to create tailored Schiff bases count on this selectivity—for example, it’s a favorite scaffold when assembling chelating agents. I’ve seen synthetic researchers rely on 2-Pyridinealdehyde when other aromatic aldehydes don’t produce the yield or stability needed, especially in pharmaceutical intermediate preparation.

    Its popularity shows up in real usage. In multi-step synthesis, it often leads to higher yields and easier purification than close cousins like 3- or 4-pyridinecarboxaldehyde. The two-position on the ring just gives it that magic fit for so many condensation, cyclization, and coordination reactions. Yes, some products tout higher flash points or different melting points, but 2-Pyridinealdehyde’s reaction profile remains the key to its value in the lab.

    Use Cases: From the Bench to Industry

    People reach for 2-Pyridinealdehyde in all sorts of projects. I’ve seen teams use it to develop sensors by preparing chromogenic Schiff bases—those color-changing compounds that detect metals or specific anions. Others go straight into chelating ligand synthesis, tying up metals for catalysis or cleanup. Medicinal chemists often dip into the bottle when screening potential drugs, especially when crafting intermediates for alkaloids or other nitrogen-containing compounds.

    The beauty of 2-Pyridinealdehyde is that it makes things easier for synthetic chemists trying to assemble rings or backbone structures. Its versatility shows up when making macrocycles, too, or for functionalizing surfaces for material science. Sparking off cyclizations with diamines often gives cleaner results, and people working in biochemistry can fashion all sorts of tagged biomolecules from it.

    User Trust: Quality, Consistency, and Peace of Mind

    Anyone who’s tried substituting another pyridine aldehyde or going back to plain benzaldehyde tends to notice the difference. Results lack the same reliability. Purity problems lead to inconsistent outcomes, off-smells, or discoloration that can be hard to explain later. With 2-Pyridinealdehyde from established suppliers, I’ve seen fewer headaches, less troubleshooting, and smoother scale-ups. Guaranteed purity means fewer ugly surprises during sensitive downstream processing.

    Handling the liquid itself doesn’t pose special risks, but anyone who’s worked with reactive aldehydes knows about the need for the right storage and gloves. The basic safety measures—ventilation, skin protection, and prompt spill cleanup—apply here, and that helps keep peace of mind for lab managers and bench chemists alike.

    What You Don’t Get From Other Aldehydes

    Benzaldehyde feels like an old standby, but once you need to introduce nitrogen into your product, nothing substitutes for a pyridine aldehyde. Try putting together metal coordination complexes or advancing organocatalyst design, and you’ll see what I mean. The special position of the aldehyde on the ring in 2-Pyridinealdehyde brings higher reactivity toward nucleophiles, letting people tune ligands or adjust flavor profiles for downstream use.

    Some shops pour money into other isomers, like 3- or 4-pyridinecarboxaldehyde. You won’t get the same ring-closure rates or stability with your products. The unique electronics in the two-position give it an identity all its own. Sulfur- and oxygen-centered aroma aldehydes don’t offer the same breadth of utility in catalysis or in bioactive building blocks. That saves both time and budget, which always matters in research and production settings.

    Real Applications and Results

    People often talk about making Schiff bases with 2-Pyridinealdehyde, but this story runs deeper. Think about the times someone needed to trap a specific transition metal in a selective way for an industrial reaction. Standard aldehydes left too much mess and mixed product. With 2-Pyridinealdehyde, the selectivity cleaned up the outcome and cut down purification hours. Even in educational labs, students working on simple condensation reactions get to see major differences in speed and reproducibility compared to alternatives.

    This product slips into so many plans—everywhere from developing new antibiotics and enzymes, to functionalizing polymers for smarter coatings. In rare disease drug pipelines, certain teams rely on it as a key step in introducing N-heterocycles. That’s the kind of impact this single molecule can bring, showing up right at the interface of academic curiosity and real industry needs.

    Clinical and Research Reliability

    Not all chemicals used as analytical standards or intermediates carry the same reputation. 2-Pyridinealdehyde’s high-quality profile supports its use even in sensitive chromatographic and spectroscopic studies. With studies requiring consistent chromophore development or selective tagging of peptides, scientists need this stability to standardize their data. In oligonucleotide labeling, it provides a clean means of introducing aldehyde groups to target molecules.

    Lab staff working in environmental testing also get firsthand benefits. Using 2-Pyridinealdehyde-based Schiff bases to detect trace metals in wastewater, they actually cut down on interference and false readings compared to less selective aldehydes. Over the years, trust for this product has grown, not just on paper but in real-world labs where the stakes are high.

    From Batch to Bottle: Purity Backed By Accountability

    I’ve seen more than one colleague call out the difference good sourcing makes. The market has plenty of low-purity stock; that ends in batch variability and frustration. Sourcing 2-Pyridinealdehyde with specs above 98% offers the reliability chemists bank on. That means clearer NMR and GC spectra, crisper crystallizations, and easier filtration. Those outcomes translate to time savings and dependability, which weighs heavily when every experiment build counts.

    One thing that sets the best offerings apart: open batch records and quality audits. Nobody wants to start an expensive run with a surprise contaminant. In modern labs, any compromise in reagent quality means hours lost and sometimes safety issues. So the product stands as a poster child for how much difference transparency and careful handling make, from manufacturing to the actual weighing and mixing.

    Supporting Greener Chemistry

    More chemistry teams want reagents that support greener practices. 2-Pyridinealdehyde helps by letting researchers use milder reaction conditions and minimize waste. The selectivity enables efficient reactions without piling up by-products, so less solvent and fewer steps go into the process. Folks in scale-up also appreciate the limited need for reprocessing—good for budgets and for sustainable laboratory practices.

    Even in teaching labs, professors pick it for kinetic studies since the reactions can be set up at room temperature, with readily observable results. Less energy and simpler isolation bring the green benefits close to home, and students can see practical results without lots of hazardous side products to manage.

    Special Features: Flexibility For Discovery

    Some products win trust because they offer lots of options. 2-Pyridinealdehyde plays well across fields. Medicinal chemists appreciate the way it inserts nitrogen into scaffolds for potential new leads. Material scientists count on it for cross-linking smart polymers. Environmental testing groups use it for derivatizing trace metals. This flexibility lets groups with limited chemical budgets reuse the same stock for multiple programs, cutting costs and simplifying inventory.

    In my experience, having a bottle of 2-Pyridinealdehyde around means more ideas can move straight to test. This speeds up not just reaction screening, but troubleshooting and method development. Teams can try new ligand or peptide designs or tag different functional groups. The open-ended possibilities spark creativity, which is hard to put a price on in discovery-driven settings.

    Collective Knowledge: Guiding Better Chemistry

    Talking to other chemists, it’s clear that community knowledge backs up the value of this reagent. From the industry side, procurement staff look for the lowest total cost—factoring in quality, lead times, packaging, and repeatability. Project managers appreciate the ability to scale reactions from hundreds of milligrams in a flask to liters in a reactor with no change in product profile. Journal articles and patents keep piling up that mention 2-Pyridinealdehyde, tracking not just chemical progress but the trust communities put in its performance.

    This ongoing feedback loop—where practice informs purchasing, which improves practice again—leads to better processes and conditions for both discovery science and routine production. Decisions about reagents ripple out, shaping what research teams can deliver and how efficiently they work.

    Building A Safer and More Capable Lab

    Safety never goes out of style, and this product plays its part here as well. Clear labeling and comprehensive hazard documentation simplify risk management. The physical properties—manageable vapor pressure, reactivity, and liquid form—make it easier to handle compared to more volatile or reactive aldehydes. Teams that value a smooth day in the lab, from storage to use and waste handling, find real-world gains here, too.

    Choosing reagents with a documented safety track record minimizes downtime and cuts long-term costs. Technical teams doing routine training or onboarding can share clear, real examples of best practices. In research settings where every experiment involves new techniques, that safety margin proves invaluable. And when labs move to scale-up or process development, the predictability sticks around, supporting both quality and compliance with less drama.

    Meeting Tight Timelines and Growing Demands

    The world keeps asking more of both academic and industrial chemistry. Timelines keep getting tighter, and expectations around data traceability and repeatability go up every year. 2-Pyridinealdehyde supports these demands by giving researchers a tool they can trust over the long haul. Unlike niche products with spotty availability, reliable batches keep projects moving, and the transparent documentation lets teams satisfy oversight bodies and regulatory requirements with less paperwork.

    Whether troubleshooting a failing synthesis, speeding up production, or solving data interpretation problems, reliable quality matters. It lets teams focus on bigger questions, driving forward both basic research and targeted innovation. In an environment where every step is measured, from weigh-in to final analysis, that reliability pays off far beyond the lab bench.

    Real Solutions For Real Challenges

    Standing out from the crowd isn’t always about novelty. Sometimes, delivering value comes from doing the fundamentals right—batch after batch. 2-Pyridinealdehyde makes an impact by keeping quality front and center, supporting greener budgets, maintaining clear documentation, and supplying a backbone for all kinds of synthetic projects. Whether tackling new drug candidates, building next-generation materials, or supporting public health monitoring, this product earns its shelf space and helps teams hit their research goals with fewer worries and more control.

    As labs look ahead, priorities keep shifting: more data integrity, more sustainable solutions, and tighter project cycles. Reliable chemical reagents anchor these changes and bring confidence in both routine work and bold new explorations. 2-Pyridinealdehyde fits that bill, offering a mix of consistency, versatility, and user-friendly performance that a new generation of scientists and chemists can appreciate. The next time a tricky reaction, tough scale-up, or ambitious research plan demands a little bit more, this product stands ready to deliver.