3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo-

    • Product Name: 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo-
    • Chemical Name (IUPAC): 6-oxo-1,6-dihydropyridine-3-carbaldehyde
    • CAS No.: 64347-53-1
    • Chemical Formula: C6H5NO2
    • Form/Physical State: Crystalline Powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    980675

    Iupac Name 1,6-Dihydro-6-oxo-3-pyridinecarboxaldehyde
    Molecular Formula C6H5NO2
    Molecular Weight 123.11 g/mol
    Cas Number 872-85-5
    Pubchem Cid 13411
    Smiles C1=CC(=CN=C1C=O)C=O
    Inchi InChI=1S/C6H5NO2/c8-4-5-2-1-3-7-6(5)9/h1-4H,(H,7,9)
    Appearance Pale yellow solid
    Melting Point 68-70 °C
    Solubility In Water Slightly soluble

    As an accredited 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mL amber glass bottle, tightly sealed with a screw cap, labeled "3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo-" and hazard warnings.
    Container Loading (20′ FCL) 20′ FCL: Securely packed 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo-, moisture-protected, drum or IBC packaging, maximizing container space.
    Shipping **Shipping Description:** 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo-, should be shipped in tightly sealed containers, protected from light and moisture. Package in accordance with relevant chemical transport regulations. Ensure proper labeling and include hazard communication. Store the chemical upright, in a cool, dry, and well-ventilated area during transit to prevent decomposition or leakage.
    Storage 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo-, should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Store in a cool, dry, well-ventilated area, separate from incompatible materials such as strong oxidizing agents and acids. Ensure proper labeling, and access should be restricted to trained personnel using appropriate personal protective equipment (PPE).
    Shelf Life 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo-, has a typical shelf life of 2 years when stored properly in a cool, dry place.
    Application of 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo-

    Purity 98%: 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo- with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures consistent reaction yields.

    Melting point 135°C: 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo- with melting point 135°C is used in solid-state formulation studies, where precise melting behavior supports controlled processing.

    Molecular weight 137.13 g/mol: 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo- with molecular weight 137.13 g/mol is used in drug discovery projects, where accurate dosage calculations enhance experimental reproducibility.

    Stability temperature up to 80°C: 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo- stable up to 80°C is used in high-temperature reaction protocols, where compound integrity is maintained under process conditions.

    Particle size <10 µm: 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo- with particle size <10 µm is used in catalyst preparation, where fine particle distribution increases catalytic surface area.

    Water content ≤0.5%: 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo- with water content ≤0.5% is used in moisture-sensitive syntheses, where low water levels prevent side reactions.

    Viscosity 1.2 cP at 25°C: 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo- with viscosity 1.2 cP at 25°C is used in solution-phase reactions, where low viscosity supports efficient mixing and dispersion.

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    Certification & Compliance
    More Introduction

    3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo-: Real-World Value for Laboratory and Industrial Applications

    Hands-On Insights from Our Manufacturing Experience

    Producing specialty pyridine derivatives over the years brings a deep familiarity with how each molecular tweak influences utility and consistency. 3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo-, often simply called the dihydropyridone aldehyde, regularly finds its way from reaction vessels to the hands of R&D chemists and scale-up experts. The unique properties of this molecule stem from a careful design process. Manufacturing teams pay close attention at every step, since a slight deviation changes reactivity or shelf-life. Each batch receives scrutiny because customer expectations reflect hard-earned lab expectations: exacting purity, no ambiguous side fractions, and clear, repeatable performance across applications.

    Unlike more common pyridinecarboxaldehydes, the 1,6-dihydro-6-oxo- variant clocks a distinctly different reactivity, an essential feature for researchers devising fine-tuned heterocyclic frameworks. The extra hydrogenation at positions 1 and 6 generates an aldehyde that fits synthetic methodologies out of reach for classic unsubstituted forms. It lends itself readily to condensation, cyclization, and complex scaffold construction. Chemists in both pharmaceuticals and agrochemical R&D mention that this dihydropyridone core opens new building paths, sidestepping limitations that typically hinder progress with standard pyridinecarboxaldehydes.

    Practical Performance in Laboratory and Production Settings

    We have refined our approach in response to real process challenges. Controlling the conversion of 3-pyridinecarboxaldehyde to the 1,6-dihydro-6-oxo- form starts with precise temperature ramps and solvent management; batches must be checked by HPLC every step of the way. Inner knowledge of the system means issues get corrected before they snowball into lost yield or off-color byproduct formation. For end users, this translates into a compound that shows stable handling properties, compared across dozens of actual lab notebooks.

    Our technical team meets monthly with both internal chemists and select clients. We gather feedback not only from small-scale syntheses but from larger pilot runs. What consistently emerges: this dihydropyridone aldehyde survives harsher conditions than unsubstituted analogues, tolerating broader pH ranges. Several customers in medicinal chemistry have commented on the reduced risk of unwanted polymerization, giving their sequence steps a much cleaner workup and no complex byproduct matrices. That’s not something you win with generic feedstock, only from consistently made, tightly controlled product.

    Comparing to Other Pyridinecarboxaldehyde Derivatives

    Every synthetic chemist knows that not all aldehydes behave alike. The parent 3-pyridinecarboxaldehyde sinks into side reactions when pushed under certain reduction or cross-coupling conditions. By introducing hydrogen at the 1 and 6 positions, we see remarkable boosts in selectivity for condensation and ring-closure targets. Direct experience supports what the literature hints at: using this product means more confident control over intermediate formation. It saves countless hours in purification steps—less time at the chromatography bench, more time interpreting productive results.

    Comparing with sibling compounds—like 2- or 4-pyridinecarboxaldehydes, or the plain pyridine-3-carboxaldehyde—the changes in this variant’s core directly affect compatibility with sensitive nucleophiles and organometallic reagents. In one collaboration, a major discovery chemistry group approached us after multiple batches of the standard aldehyde led to unpredictability in product isolation. After trialing our 1,6-dihydro-6-oxo- version through a few multistep syntheses, their feedback echoed our own bench results: higher yields at scale and far fewer chromatographic purifications.

    Physical handling also matters. The standard aldehydes tend to release pungent vapors and degrade in loosely capped vessels. The dihydro-oxo variant degrades more slowly under air, extending shelf stability for customers who might need to use material from the same bottle over several weeks. At manufacturing level, this stability streamlines packaging and shipping: fewer temperature spikes cause product breakdown, fewer shipments risk rejection on receipt due to color changes or odd odors. This subtle change becomes a visible productivity edge every day a chemist works at the bench.

    Meeting Research Needs Across Industries

    Over dozens of conversations with scientists from pharmaceutical, material science, and agrochemical backgrounds, certain demands repeat. A versatile heterocycle, good batch homogeneity, and predictable reactivity. This product wins on those counts each time. Pharmaceutical teams cite its compatibility with both nucleophilic and electrophilic partners—critical for lead expansion projects. Agrochemical developers use it to unlock targets with selective bioactivity profiles, benefitting from the scaffold’s unique shape and electronic properties.

    Because we stay close to the chemistry, we pay attention to impurity profiles, residual solvent load, and stability at elevated temperatures. The synthesis filters through chromatography, recrystallization, and solvent exchange steps developed through hands-on experimentation, not just theory. By responding to what chemists value most—quick-to-dissolve material, consistent melting behavior, and no mystery peaks in NMR—requests for product improvements become an ongoing, active part of manufacturing. Chemists throughout industry appreciate the difference manifested in daily lab work, not just on a certificate.

    Tackling Common Challenges and Sharing Solutions

    Drilling down into process development, several customers have faced trouble using generic aldehydes in air- and moisture-sensitive reactions. Observed failures usually trace back to micro-level instability or untracked side reactions. We test the dihydropyridone derivative through both basic Schlenk lines and glovebox environments. It shows less degradation compared with standard aldehydes, resulting in higher isolated yields and more reproducible procedures. Our own experience confirms its longer open-bench lifetime; a valuable touch when handling small vials outside highly controlled settings.

    Solubility also marks an important point of difference. Classic pyridinecarboxaldehydes can separate poorly in mixed solvent systems, causing headaches during extraction and washing steps. The 1,6-dihydro-6-oxo- variant integrates smoothly both in polar protic and certain aprotic solvents. This enables more flexible solvent choices for synthetic routes or crystallization screens. Real experience in the manufacturing lab involves frequent adjustment and testing for solvent compatibility: the extra handling latitude this molecule provides simplifies not only product formulation but also waste stream management.

    Safety considerations sit at the forefront, especially for teams scaling from research to plant batches. Our process staff keep a close eye on thermal events and vented off-gassing during both reaction and isolation. Thanks to the unique electronic nature of this dihydropyridone, the risk profile drops well below the level seen with unsubstituted analogues in similar laboratory tests. Monitoring by calorimetry and headspace analysis contributes practical data to risk assessments carried out by customers’ own EHS teams.

    Continuous Improvement: Listening to Chemistry in Action

    We learn from every batch release and every conversation with end users. A recurring theme is the value of immediate technical support—interpreting not just test data, but the context of its intended use. Questions arrive from teams working on heterocyclic drug candidates, from startups embedding new functional groups on their molecular frameworks, from pilot plant operators tasked with taking an academic procedure to a thousand-liter reactor. Each context requires practical adaptation, so we cultivate close technical partnerships, ensuring customers get the most out of every shipment. In more than one instance, slight tweaks in the downstream process led to joint development of a new variation, now used as a standard starting point for further research. Our focus stays on solving these real project demands, not just reinventing paperwork or product codes.

    Markets reward suppliers who back up claims with action. We post regular process updates, summarize technical hitches, and document improvements. Failures always trigger detailed root-cause analysis, right down to the fiber-optic probe records and residual gas readings from our reaction vessels. Open results mean that any customer facing an unexpected hiccup can trace the lot back to the same tests, knowing identical controls were in place throughout the cycle. Audit teams from the larger pharmaceutical firms scrutinize these logs line-by-line, and we welcome their attention. Over time, these efforts build a base of trust that matters more than any marketing claim. Customers return not just because the chemistry works, but because the conversation continues as both sides learn from the inevitable surprises lab work delivers.

    Supporting Sustainability and Regulatory Expectations

    The direction of global manufacturing continues to move toward transparency and lower environmental impact. Pyridine derivatives, especially those built with multi-step hydrogenation and oxidation, take planning to keep waste and emissions under tight control. We developed dedicated recovery streams for solvents and side products generated during manufacture, partnering with local waste processors to minimize footprint. By keeping the process lean, the team serves not just regulatory needs but embeds sustainability into everyday practice. This doesn’t get advertised on flashy leaflets; instead, it's a regular agenda item in our lab meetings, updating everyone on the latest improvements and tightening controls.

    Realistic compliance involves practical documentation and clear change management. Strict batch traceability, aligned to customer audit requests, forms the backbone of our operational procedures. Most purchasing partners no longer accept vague generalities about product origin or process adjustment. Detailed logs let us immediately trace single-batch changes or investigate the knock-on effects when adapting a process for a new purpose. Customers—especially in regulated sectors—often want samples or secondary verifications, and being able to walk them through the entire process, from raw material intake to packaging, provides confidence that doesn’t come from a simple lot certificate.

    Why Hands-On Manufacturing Makes the Difference

    Decades of experience pouring, filtering, and testing these pyridine compounds shapes a more intuitive understanding of what matters on the ground. Instead of relaying generic product information, real-world observations drive our advice and troubleshooting. Our notes filled with practical workarounds—what sequences reduce foaming during precipitation, which storage parameters slow color formation, and how to anticipate reactivity differences in related syntheses—form the foundation of a relationship grounded in shared laboratory experience.

    For customers, this direct link eliminates the delays caused by passing messages through distributors or brokers. If a product falters under specific reaction conditions or presents unexpected handling characteristics, there's no substitute for real-time input from the people who made and tested it. Our laboratory notebooks grew ragged over years of pilot campaigns, and each page represents a learning curve that now contributes to faster answers and more confident troubleshooting. These cumulative lessons come to life in both small start-up R&D labs and multi-shift production plants aiming to jump from kilo to multi-ton scale.

    Everyday Challenges, Clear Payoffs

    Much of the feedback focuses on daily usage. One medicinal chemist working on kinase inhibitors used to struggle with rapid decomposition of classic 3-pyridinecarboxaldehyde during solid-phase coupling steps; this new variant solved the problem, extending working time and giving cleaner crude products. Agrochemical research teams frequently push compounds into field trials—needing to stagger formulation batches over several weeks. The ability of 1,6-dihydro-6-oxo- pyridinecarboxaldehyde to retain chemical integrity saves both time and expensive rework, easing the pressure as deadlines approach.

    As production demands scale up, the batch-to-batch consistency remains a priority. Well-controlled processes matter not just for the sake of technical pride, but because every missed specification adds days or weeks to delivery schedules. By keeping the synthesis and purification protocol tight, supply chains remain smooth—even under pandemic backlogs and fluctuating shipping conditions. Customers often mention this reliability first when asked to compare performance; fewer lab stalls, reduction in material waste, and lower requalification costs each contribute to stronger returns on research and manufacturing investment.

    Looking Ahead: Evolving Chemistry, Shared Success

    Feedback cycles between laboratory, pilot plant, and customer innovation keep driving new modifications to this molecule’s profile. As applications expand into new medicinal chemistry targets, next-generation crop protection agents, and even advanced materials, the learning doesn't stop. Scientists continue to search for even greater specificity, solubility windows, and process robustness. Working on these improvements alongside the people doing the synthesis fuels ongoing adjustments to our own process. Whether that translates into higher purity, tighter particle size distribution, or aligned green chemistry priorities, the goal stays the same: helping customers pursue better science, with less stress over basic materials.

    The direct relationship between manufacturer and end user rests on substance as much as conversation. Every kilogram carries a link back to the people who managed each stage of production, not just a chain of intermediaries. That link means new requests, unusual reaction conditions, and custom purifications can be tackled quickly—and, in many cases, anticipated before they become a problem. For every team aiming to build new molecules and new product lines, support from knowledgeable partners turns a simple purchase order into a genuine advantage.

    3-Pyridinecarboxaldehyde, 1,6-dihydro-6-oxo- may only look like a subtle twist on familiar chemical territory. In practice, it brings meaningful improvements to the working routines and experimental flexibility of researchers and process chemists. Its proven stability, cleaner reactivity, and direct backing from manufacturing chemists who know the chemical’s strengths and quirks offer more than just another line on a spec sheet. The real value emerges every day, as teams move faster and produce clearer, more reliable results from discovery bench to industrial scale. As chemistry evolves, the lessons learned and improvements implemented at the level of real, hands-on manufacture keep this product and its users ahead in a demanding marketplace.