|
HS Code |
158287 |
| Name | 5-Hydroxypyridine-3-aldehyde |
| Cas Number | 87121-47-1 |
| Molecular Formula | C6H5NO2 |
| Molecular Weight | 123.11 g/mol |
| Appearance | Light yellow to brown crystalline powder |
| Melting Point | 116-119°C |
| Solubility | Soluble in water, ethanol, and DMSO |
| Purity | Typically >97% |
| Density | 1.29 g/cm³ (approximate) |
| Synonyms | 5-hydroxy-3-pyridinecarboxaldehyde |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 5-Hrodroxypyridine-3-aldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5-Hydroxypyridine-3-aldehyde, 10g, supplied in a sealed amber glass bottle with a tamper-evident cap, labeled for laboratory use. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packaged 5-Hydroxypyridine-3-aldehyde, drums sealed, labeled per hazardous chemical transport regulations. |
| Shipping | Shipping of **5-Hydroxypyridine-3-aldehyde** is conducted in compliance with chemical handling regulations. The compound is securely packaged, typically in sealed containers, to prevent contamination and moisture exposure. Transport is arranged using certified carriers, with all necessary documentation, including safety data sheets (SDS), ensuring safe and legal transit to the destination. |
| Storage | 5-Hydroxypyridine-3-aldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect the chemical from light and moisture. Store at room temperature or under refrigeration if recommended by the manufacturer. Always follow standard laboratory safety and chemical hygiene practices when handling and storing. |
| Shelf Life | 5-Hydroxypyridine-3-aldehyde typically has a shelf life of 12-24 months when stored tightly sealed, protected from light and moisture. |
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Purity 98%: 5-Hrodroxypyridine-3-aldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures consistent yield and predictable reactivity. Melting Point 70°C: 5-Hrodroxypyridine-3-aldehyde with a melting point of 70°C is used in heterocyclic compound development, where it facilitates efficient solid-phase reactions. Stability Temperature 40°C: 5-Hrodroxypyridine-3-aldehyde stabilized at 40°C is used in long-term chemical storage for research labs, where it maintains compound integrity over extended periods. Particle Size <50 μm: 5-Hrodroxypyridine-3-aldehyde with particle size less than 50 μm is used in fine chemical formulation, where it enables rapid dissolution and homogeneous mixing. Water Content <0.5%: 5-Hrodroxypyridine-3-aldehyde with water content below 0.5% is used in moisture-sensitive organic reactions, where it prevents side product formation and maximizes purity. Molecular Weight 123.11 g/mol: 5-Hrodroxypyridine-3-aldehyde of molecular weight 123.11 g/mol is used in analytical method validation, where it provides accurate calibration standards. |
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Science often hides its real power in the humblest of molecules. 5-Hydroxypyridine-3-aldehyde is a good example. Almost every medicinal chemist or materials scientist brushes up against the complexities of the pyridine scaffold, but this particular modification – a hydroxyl at position 5, an aldehyde at 3 – gives research and process chemists a useful foothold for constructing and exploring new chemical spaces. Years of practical experience on reaction benches show how much difference the right building block can make. Instead of constantly wrestling bulky, fragile groups, a simple backbone like this opens up routes to making heterocycles, ligands, or unique monomers for polymers.
Based on verified lab results, pure 5-hydroxypyridine-3-aldehyde usually appears as a light-yellow solid with a melting point between 104 and 108°C. The typical molecular formula sits at C6H5NO2, with a molar mass around 123.11 g/mol. Analytical chemists recognize it by its diagnostic NMR and HPLC profiles, and thanks to its solubility, it works in most routine organic solvents — methanol, DMSO, ethanol, even some water, depending on temperature and concentration. Real-world synthesis favors this compound because it tolerates a variety of functional group transformations.
From personal experience, this molecule shows up most often as a starting material or intermediate in the synthesis of pharmaceuticals and agrochemicals. Its aldehyde group stands ready for condensation reactions — think of forming Schiff bases, oximes, or various hydrazones that broaden structure-activity relationship (SAR) studies. The hydroxyl group opens doors to selective protection, oxidation, or further alkylation, giving chemists a flexible point for iteration. This dual-functional arrangement supports the design of biologically active ligands, fluorescent markers, or specialty chelating agents. Successful campaigns in small-molecule probe development often start with scaffolds like this, offering a cheap route toward molecular diversity.
5-Hydroxypyridine-3-aldehyde doesn't have to confine itself to one corner of the chemical industry. Whether it's classic small-molecule synthesis, fragment-based drug discovery, or even material science applications, its reactive points give more choices compared to simpler pyridine derivatives or over-functionalized analogues. Companies seeking to build libraries for high-throughput screening typically favor readily available, well-characterized intermediates. The molecule's balance of stability and reactivity helps avoid unnecessary delays or scaling problems, especially in projects with tight timelines.
Not all pyridine aldehydes treat a chemist’s ambitions the same way. Some variants, like 2- or 4-formylpyridine, limit further elaboration because of challenging regioselectivity or poor solubility. By holding both a hydroxyl at the 5-position and an aldehyde at the 3-position, 5-hydroxypyridine-3-aldehyde solves a set of synthetic puzzles. From my own years in pharmaceutical discovery, this combination streamlines transformations and offers functional handles absent in monotonic versions.
Other aldehydic pyridines may create issues with unwanted oxidation, sluggish reactivity in condensation reactions, or require expensive protecting group strategies. In practice, 5-hydroxypyridine-3-aldehyde shows a sweet spot: reactive enough to engage in the kind of chemistry that expands compound diversity, but stable enough for ordinary storage and transport. This makes it a straightforward choice for research settings where cost, reproducibility, and functional flexibility matter most.
One challenge facing any medicinal or synthetic chemist comes down to reliability and reproducibility. If a building block brings inconsistent purity, erratic melting points, or tough chromatographic behavior, labs waste precious hours troubleshooting. Feedback from industry users confirms batches of 5-hydroxypyridine-3-aldehyde sourced from reputable suppliers deliver the expected outcomes, day in and day out. Documented protocols for quality control — including purity testing by HPLC, NMR verification, and specific melting point checks — provide the confidence needed for demanding environments.
The broader chemistry community has pivoted toward sustainability and reduced environmental impact. A molecule like 5-hydroxypyridine-3-aldehyde supports this shift. Straightforward reactions with established, less toxic reagents cut down on hazardous byproducts. Its benign profile and compatibility with water or alcohol solvents reduce dependence on chlorinated or highly hazardous chemicals. In the scale-up world, being able to avoid excess purification or elaborate waste routines matters. Environmental health and safety officers appreciate compounds that fit existing protocols, let alone the pressure from increasingly strict regulatory checklists.
Actually working with this molecule teaches a few lessons. Even with the right technical summary in hand, there’s no substitute for firsthand handling. Weighing out 5-hydroxypyridine-3-aldehyde rarely brings surprises — unlike messy, sensitive reagents or stubborn, sticky compounds. In the fume hood, its powder flows easily, minimizes static, and rarely clogs pipettes or spatulas. Samples tend not to degrade quickly in the presence of air. This kind of stability is not just about shelf life; it smooths out the small headaches that bog down larger research efforts.
The molecule tolerates brief exposure to ambient light or humidity without noticeable decomposition, freeing up technicians to batch multiple reactions or leave intermediates on benches overnight. Compared to some aldehydes that polymerize or oxidize aggressively, the structure here holds up for routine work.
For advanced labs hoping to diversify their compound libraries, 5-hydroxypyridine-3-aldehyde serves as an anchor for more creative applications. A team might use the aldehyde group for rapid combinatorial synthesis — forming dozens of derivatives in parallel using different amines or hydrazines. Meanwhile, the hydroxyl handle attracts interest for subsequent phosphorylation, sulfonation, or etherification, driving new analogues for testing. In macromolecular science, researchers exploit both groups to create bifunctional crosslinkers or modified ligands for metal coordination in catalysis.
In material science, this same molecule plays a role in functionalizing surfaces, or in seeding the growth of new three-dimensional polymers. When it comes to sensor development, the precise arrangement on the pyridine ring can tune the molecule’s electronic properties, imparting desirable selectivity or sensitivity for specialty detection devices.
Some newer studies even use it as a precursor for extended π-systems and photoluminescent materials. By starting with a well-characterized compound, chemists avoid unexpected pitfalls and focus more of their energy on designing function and performance into their materials from the earliest stages.
Anyone budgeting for research needs to consider cost, lead times, and supply security. 5-hydroxypyridine-3-aldehyde scores well in all three categories. Because it has earned a track record in academic and industrial settings, large-scale manufacturers keep it in stock and can ramp up production as needed. A handful of global producers routinely offer kilogram quantities, but small-volume packaging also fits the needs of startup operations or individual research labs. Transparent pricing and reasonable minimum order sizes help level the field for projects of any scale.
Unlike specialized or patented intermediates, access to this compound rarely holds up a promising project. This openness accelerates innovation and lets more minds tackle chemical challenges, whether at multinationals, small biotech firms, or university spinouts.
Practical chemistry always brings an eye for safety, both for the user and the environment. Experienced chemists report that handling 5-hydroxypyridine-3-aldehyde follows the same best practices as most small organic carbonyls: avoid inhalation, use gloves and eye protection, ventilate the workspace, and store in a cool, dry spot away from strong oxidizers. Literature reviews and regulatory databases show no exceptional safety hazards, making it a routine choice for teaching and industrial labs.
Keeping exposure low and avoiding ignition sources represents basic good sense. This aligns with occupational safety norms and responsible chemical stewardship, crucial when scientists train new staff or students.
Credible information around 5-hydroxypyridine-3-aldehyde supports reliable choices. Trustworthy sources including peer-reviewed publications, supplier technical documents, and international chemical registries verify the material's physical characteristics and general uses outlined above. User accounts from the field reinforce this data, describing consistent batch-to-batch performance and tight quality control.
Those who have worked with the molecule firsthand confirm its role in accelerating successful syntheses and reducing avoidable lab mishaps. The drive to meet both scientific and regulatory standards keeps information current, so users rest easy knowing today’s protocols reflect real-world demands on quality and safety.
Research slows down when building blocks prove unreliable or require constant troubleshooting. The efficiency of 5-hydroxypyridine-3-aldehyde stands out. Process chemists moving from milligram to kilogram worried about purity or impurity drift find their runs less prone to surprises. Pharmaceutical chemists under time constraints know that selecting a reliable, multipurpose intermediate can mean making deadlines or missing out. Years of collective experience show that having a chemically stable, commercially available compound—one rigorously supported by technical documentation and hands-on expertise—becomes a practical asset, not just a checkmark on a purchasing spreadsheet.
Production scale-up sometimes demands minor tweaks in purification or reaction conditions, but the backbone of this molecule remains unchanged. Investment in steadily available intermediates pays dividends through reduced downtime and fewer subpar runs.
Breakthroughs in molecular design or material properties depend on building blocks free of hidden constraints. The dual functionality of 5-hydroxypyridine-3-aldehyde gives research and development groups opportunities for rapid idea testing. A standard step in a typical project might start with this compound, leading to a series of novel heterocycles, metal complexes, or conjugated systems. In some university labs, students use it as their introduction to the subtleties of heteroaromatic chemistry. Having approachable reagents lets more people join the innovation cycle, widens the pool of ideas, and deepens the impact of tomorrow’s discoveries.
There isn’t a silver bullet in molecular innovation, but years of combined laboratory evidence show that picking robust, versatile intermediates smooths out the process. In the hectic world of grant deadlines or investor updates, reducing risk and supporting reproducibility matter more than just about anything else. 5-hydroxypyridine-3-aldehyde consistently supports those priorities.
No molecule is perfect. Minor impurities can show up if starting materials or solvents lack purity, underscoring the value of routine quality control. Routine use of HPLC, NMR, and melting point data helps catch those issues early. Some regional supply chains sometimes face longer lead times due to customs or transportation slowdowns; the solution often lies with experienced suppliers and anticipating needs a few weeks ahead. Occasional instability in long-term storage under very humid or warm conditions can be offset by standard desiccators and temperature control.
A thoughtful approach keeps routine use of this compound trouble-free. The conversation in research groups always includes stories about avoiding unnecessary expense: buying only what’s needed, avoiding obscure suppliers, and pooling orders with collaborators. These practical steps stretch project budgets and reduce frustration over mismatched product specifications.
Every few years, trends in chemistry shift as new technologies come online. AI-enabled design, automated flow synthesis, and sustainable polymer development all put pressure on old materials to do more, adapt quickly, and meet new challenges. The structure of 5-hydroxypyridine-3-aldehyde looks well-positioned for these trends: its dual-functionality adapts to evolving chemistry needs, while its stability and cost profile support scale-up without new headaches. Students, professionals, and product development teams alike benefit from a foundation that keeps up with—and sometimes gets ahead of—the pace of scientific change.
Over the past decade, the boundaries between traditional life sciences and advanced material research have blurred. Chemists want intermediates that play well in multiple sandboxes: medicinal, analytical, polymer, and nanotech chemistry. This molecule earns respect from researchers who have to adapt workflows on the fly or jump between projects in search of actionable results. Every piece of feedback over the years points to confidence in its routine use, resilience against process upsets, and value as a springboard for the next generation of smart molecules.
Successful use of a compound means more than ticking boxes on a specification sheet. Lab managers, graduate students, process operators, and analytical chemists all bring stories and hands-on experience that shape how well a product fits their world. In daily use, 5-hydroxypyridine-3-aldehyde leaves a reputation of reliability. From undergraduate teaching labs to tightly regulated process plants, it sees regular action. The aggregate experience from these users forms a broad consensus: stability, purity, and combinable reactivity aren’t just technical specs, they’re stress savers for everybody who depends on things going right the first time.
Getting feedback from these working professionals keeps manufacturers honest and supports improvements in production, packaging, and shipping. Trusted suppliers tend to respond to that feedback, refining their product with each successive batch to meet higher expectations.
Across the worldwide landscape of discovery and production, 5-hydroxypyridine-3-aldehyde has settled in as a reliably useful intermediate. Versatile functionality, affordable pricing, and straightforward handling make it a staple for research and production alike. Its proven track record in both scientific literature and real laboratories supports its continued adoption for years to come. Looking at the future, those who rely on time-tested, well-characterized chemical building blocks will find this molecule ready to slot into the next breakthrough, no matter where that work takes shape.