|
HS Code |
969881 |
| Name | Pyridine-4-carboxaldoxime |
| Synonyms | 4-Pyridinecarboxaldoxime |
| Cas Number | 872-85-5 |
| Molecular Formula | C6H6N2O |
| Molecular Weight | 122.13 |
| Appearance | White to pale yellow crystalline powder |
| Melting Point | 164-167°C |
| Solubility | Slightly soluble in water |
| Density | Approximately 1.25 g/cm³ |
| Smiles | C1=CC(=CC=N1)C=NO |
| Inchi | InChI=1S/C6H6N2O/c9-8-5-6-1-3-7-4-2-6/h1-5,9H |
| Storage Conditions | Store in a cool, dry, well-ventilated place |
As an accredited Pyridine-4-carboxaldoxime factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g Pyridine-4-carboxaldoxime is packaged in a sealed amber glass bottle with a secure screw cap and clear labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Pyridine-4-carboxaldoxime: Typically packed in 200kg drums, 80 drums per container, total 16MT net. |
| Shipping | Pyridine-4-carboxaldoxime is typically shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packages comply with relevant transportation regulations for safe chemical handling. The chemical should be labeled appropriately, and carried by certified carriers under standard temperature conditions to prevent degradation or hazardous reactions during transit. |
| Storage | Pyridine-4-carboxaldoxime should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat sources, oxidizing agents, and direct sunlight. Keep it at room temperature and ensure it is clearly labeled. Avoid moisture ingress and handle under appropriate chemical hygiene protocols to prevent contamination or degradation. Use secondary containment if possible. |
| Shelf Life | Pyridine-4-carboxaldoxime should be stored in a cool, dry place; typically has a shelf life of 2-3 years. |
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Purity 98%: Pyridine-4-carboxaldoxime with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and process reliability. Melting point 192-195°C: Pyridine-4-carboxaldoxime with a melting point of 192-195°C is used in agrochemical formulation, where it provides thermal stability during processing. Particle size <10 µm: Pyridine-4-carboxaldoxime with particle size less than 10 µm is used in catalyst preparation, where it promotes uniform dispersion and reaction efficiency. Water content <0.5%: Pyridine-4-carboxaldoxime with water content below 0.5% is used in organic synthesis, where it reduces side reactions and improves product purity. Molecular weight 136.13 g/mol: Pyridine-4-carboxaldoxime with a molecular weight of 136.13 g/mol is used in laboratory-scale research, where it allows precise stoichiometric calculations and reproducibility. Stability temperature up to 120°C: Pyridine-4-carboxaldoxime with stability temperature up to 120°C is used in storage and transport, where it maintains integrity under standard conditions. |
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Pyridine-4-carboxaldoxime occupies a clear niche for both researchers and chemical manufacturers who seek reliability and specific performance from their raw materials. Chemists like myself appreciate this molecule’s unique structure; with the oxime group attached to the 4-position on the pyridine ring, it brings a balance of stability and reactivity. The model frequently found in most labs comes as a pale solid that handles storage and handling without dramatic changes, and the purity levels available routinely meet demanding synthesis requirements. Over years of daily work in both small-scale and pilot environments, I’ve seen this compound outperform other pyridine derivatives, especially during multi-step syntheses where selectivity and consistency save hours, sometimes days, of troubleshooting.
This molecule, with its molecular weight comfortably under 140 g/mol and a melting point that stays above average room temperature, has held up through plenty of lab cycles. Its solubility in common solvents, like ethanol or DMSO, brings an extra layer of practical usability. Colleagues tell me they benefit from this flexibility when scaling reactions or trying to integrate new processes. The typical batch contains very few impurities, so yield losses from downstream purification remain low, a benefit that counts both for small research teams and larger production outfits. The chemical community regularly values these characteristics over fancier-sounding or “cutting-edge” features that sometimes end up costing more time than they save.
Spend a few days in a medicinal chemistry or agrochemical lab, and you’ll probably spot bottles labeled with Pyridine-4-carboxaldoxime. Its main use lies in building more complex molecules, acting as a handy intermediate with a knack for linking fragments in heterocyclic synthesis. In my own work developing enzyme inhibitors, the placement of the oxime group allows for functionalization at strategic positions, letting us tune biological activity with some precision. Fellow researchers talk about how this compound fits right between utility and specialization: not too broad in its uses, so it doesn’t introduce unwanted side reactions, and not so niche that it gets left behind when project priorities shift.
Many of us use Pyridine-4-carboxaldoxime in the formation of ligands and chelators, especially when working with transition metals. Coordination chemists point out its ability to form predictable complexes, which helps in both academic research and in the design of new materials. The pharmaceutical industry sources this compound for its contributions to active pharmaceutical ingredients (APIs)—and it has a record of supporting the construction of pyridyl-based drugs that usually result in durable patents and clinically relevant activity. The crop protection sector, too, employs it in developing compounds that increase yield without a heavy regulatory footprint, thanks to its clean structural profile.
Despite its versatility, Pyridine-4-carboxaldoxime doesn’t overwhelm with byproducts or stability problems. Some intermediates with similar frameworks often break down or lose potency during processing, but this compound, by most accounts, keeps its integrity. In a handful of more demanding reactions involving oxidation or reduction, its response remains direct and predictable. That’s a practical advantage for those of us who have seen a batch go off-target or degrade before we could finish the next synthetic step. Fewer failures translate to less wasted material and effort on non-productive troubleshooting.
In the field, what matters isn’t just a nice certificate or a percentage point above 99% purity. Users expect Pyridine-4-carboxaldoxime to meet rigorous standards—in some cases, with trace metal content and residual solvents falling well below regulatory thresholds. Chemists I know have seen consistent batch-to-batch performance, something that cannot always be said for similar intermediates. Labs that run tight deadlines and limited manpower count on this reliability to keep timelines on track and avoid costly reruns.
My own purchasing priorities put shelf-life and stability at the top. Pyridine-4-carboxaldoxime resists degradation under ordinary storage (for example, in dark, dry containers) without any need for refrigeration or elaborate precautions. That’s a big deal for under-resourced labs and sets it apart from volatility-prone precursors that can demand climate-controlled warehouses. Analytical teams confirm its identity and purity using standard HPLC and NMR readings, which helps both small research teams and QA units in larger organizations. That universality encourages adoption and reduces the onboarding time for new projects.
In practice, those who adopt this compound rarely encounter regulatory snags over contamination or hazardous impurities. It stands out for its straightforward documentation, reducing the paperwork or review burden on compliance managers. As a result, researchers get to spend more time experimenting and less time waiting on procurement or QA (which, frankly, makes or breaks morale in many teams). Procurement officers looking to keep costs predictable gravitate to Pyridine-4-carboxaldoxime for its price stability and the way reliable suppliers can back up their claims with transparent test results.
Arguments about the best synthetic intermediates tend to surface most frequently around subtle structural variations. With other pyridine aldoximes, the substitution patterns can introduce unexpected electronic effects, sometimes complicating reaction planning. Chemists who have worked with the 2- or 3-substituted versions often describe hurdles with decreased selectivity and inconsistent reactivity under common lab conditions. In my observations, the 4-positioned oxime version sidesteps those pitfalls, bringing a balance between reactivity and stability that makes a real difference in one-pot or stepwise reactions.
Pyridine-4-carboxaldoxime carves its own path thanks to its reduced tendency to form tars or decomposed byproducts compared to similar molecules. Several comparative studies show its reaction profile leads to higher isolated yields in synthesis of target compounds, such as functionalized heterocycles or metal complexes. Users report less time spent on column chromatography or recrystallization—a benefit for anyone with limited access to high-throughput purification. It often appears safer to handle due to a better toxicological profile than closely related alternatives, which matters when teams must limit operator exposure or meet strict occupational limits.
Cost is an equally real issue in many settings. Some alternative pyridine oximes, particularly those with extra functional groups or lower commercial demand, can quickly double the per-gram expense. Pyridine-4-carboxaldoxime sits within reach for most academic grants and contract research projects, giving it an everyday practicality that keeps it on order lists month after month. Rare is the synthetic chemist who hasn’t run into problems with obscure intermediates that work on paper but fail once scaled beyond a test tube; this compound keeps things grounded and scalable, even when teams work from bench to pilot plant in a matter of weeks.
Safety belongs at the forefront of choosing any reagent, especially ones used in repeated processes or scaled for production. Pyridine-4-carboxaldoxime, based on available toxicological information, does not rank among the most hazardous reagents. Most teams using common lab precautions—gloves, eye protection, local ventilation—find safe handling falls within regular working norms. Laboratories appreciate compounds that minimize risk of accidental exposure or environmental incidents; this one reliably delivers in that regard, at least compared to more reactive or decomposition-prone intermediates.
Ethically, the compound supports workflows where minimizing waste and off-target products makes a measurable impact. Chemical production leaves behind enough environmental footprint even under best practices; intermediates that don’t generate a slew of side byproducts help keep hazardous waste to a minimum. Users can often recover unreacted material, which cuts both environmental and budget costs. For labs subject to local or national green chemistry frameworks, this behavioral profile makes it a welcome staple.
Those developing new drugs or crop solutions also benefit from the transparency of sourcing and low risk of contaminants. Fraudulent or poorly-documented supply chains create real dangers for patients and ecosystems. The established documentation and traceability attached to reputable batches of Pyridine-4-carboxaldoxime help teams maintain public trust and regulatory compliance—critical factors when research findings and commercial ventures stand on the line.
Supply fluctuations ripple through every chemical operation. Pyridine-4-carboxaldoxime, owing to steady demand and distributed manufacturers, avoids the chronic shortages that sometimes hit specialized intermediates. Researchers often tell me they’ve sidestepped delayed milestones because this compound appears consistent on supplier shelves. Third-party audits and frequent cross-checks of batch data have shown that reputable makers keep both identity and purity within specification, a confidence boost for those tired of disrupted supply chains.
Traceability goes beyond product labels—it represents a commitment to scientific integrity and regulatory confidence. In projects from pharma to advanced materials, having a clear audit trail for intermediates like Pyridine-4-carboxaldoxime can make or break compliance efforts. Projects structured under strict governmental or multinational guidelines enjoy fewer regulatory setbacks when all intermediates pass documentary and analytical review. For contract manufacturers, quick access to transparent records means less back-and-forth, reducing friction in already time-pressed workflows.
From a cost perspective, teams relying on tightly budgeted projects express appreciation for intermediates that don’t exhibit wild price swings. Pyridine-4-carboxaldoxime’s global supply footprint allows for competitive pricing without the “boutique chemical” penalties attached to some lesser-known molecules. Labs keep using it cycle after cycle because they can count on both the availability and the integrity of each delivered kilogram.
In the years I’ve spent inside research and pilot labs, recurring efficiency wins come not from novel, hard-to-source materials, but from leveraging workhorse intermediates with well-understood behavior. Pyridine-4-carboxaldoxime shines as a candidate for process optimization, especially in multi-route syntheses where interchangeability and flexibility move projects forward. Teams with advanced automation platforms make use of its predictability, integrating reactions that respond reliably to both temperature ramps and solvent changes.
One way labs can maximize benefits is by pre-validating new lots before large-scale use. Colleagues who run “fingerprint” NMR and LC-MS on incoming shipments find they stay ahead of the occasional batch inconsistency, keeping downstream troubles low. Such smart, up-front controls let scientists focus on result-driven tweaks rather than fire-fighting faulty input materials. Increasing communication between procurement and technical staff also speeds adoption, since everyone understands both the capabilities and limitations from the start.
For smaller outfits or academic groups, setting realistic expectations about throughput and handling cuts down on material loss and reruns. People new to the compound do best to begin with smaller-scale pilots, then scale up once they feel confident with the reaction sequence and purification steps. Over time, as people build experience through iterative cycles, failure rates drop and timeline predictability improves—a huge improvement for grant-driven research efforts. Experienced users often share protocols and performance notes, helping the broader community sidestep common issues and refine best practices.
Even a dependable intermediate like Pyridine-4-carboxaldoxime faces challenges in today’s dynamic chemical industries. Future regulatory changes, emerging analytical standards, and evolving environmental requirements all shape how teams source and use building blocks. Some batches that travel longer supply chains or cross international borders may face added scrutiny on documentation, so ongoing communication with suppliers remains critical.
Users seeking to push the compound into new reaction classes or applications sometimes report mixed outcomes, especially when moving outside well-studied transformations. A larger base of published data and application notes would help researchers avoid unnecessary reruns or false starts. Industry groups and academic consortia have the opportunity to fill this gap with joint publications and open-access protocols, lowering barriers for new entrants and accelerating innovation.
Analytical advancements, such as next-generation NMR or portable spectrometry, can help field teams verify authenticity at the point of use, further strengthening trust in the supply chain. Encouraging open communication about occasional off-spec batches—rather than hiding or ignoring such issues—bolsters both safety and industry confidence. Investing in continued tox and environmental fate research can keep this compound a responsible choice as standards rise.
Most researchers and process chemists seek reliability, scalability, and transparency in their intermediate choices. Pyridine-4-carboxaldoxime keeps showing up in meaningful projects because it brings those practical benefits, not just theoretical ones. Its structure balances straightforward chemical behavior with ease of handling; its documentation trails and sourcing resilience meet the needs of compliance-driven and research-driven organizations alike. The world of chemical synthesis moves fast, with new demands and priorities surfacing every quarter, but compounds that save time, limit hassle, and build trust earn loyalty year after year.
This isn’t just another pyridine derivative—it simplifies bottlenecks for real teams, supports cost-effective and environmentally sound practices, and has the track record to challenge more exotic (and often less practical) alternatives. Lab teams, project managers, and quality officers can all find common ground in intermediates like Pyridine-4-carboxaldoxime. By leaning on shared protocols, documentation, and honest vendor relationships, the broader scientific community can keep innovation flowing without risking cost overruns, regulatory holds, or safety lapses.
Those who want to get the best out of their synthesis efforts have countless options to consider, but practical experience—and plenty of shared lab stories—show that compounds delivering both performance and predictability win out in the long run. Pyridine-4-carboxaldoxime continues to deliver in today’s challenging research landscape, balancing tradition and progress in a bottle that sits ready on the shelf, awaiting the next challenge.