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HS Code |
672654 |
| Chemical Name | 2-Hydroxy-4-formylpyridine |
| Cas Number | 119193-50-3 |
| Molecular Formula | C6H5NO2 |
| Molecular Weight | 123.11 |
| Appearance | Light yellow to brown solid |
| Melting Point | 107-109°C |
| Solubility | Soluble in organic solvents such as ethanol and DMSO |
| Smiles | C1=CN=C(C=C1C=O)O |
| Inchi | InChI=1S/C6H5NO2/c8-4-5-1-2-6(9)7-3-5/h1-4,9H |
| Pubchem Cid | 3808182 |
| Storage Conditions | Store at room temperature, away from moisture and light |
As an accredited 2-HYDROXY-4-FORMYLPYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-HYDROXY-4-FORMYLPYRIDINE, 5g, is supplied in a sealed amber glass bottle with a tamper-evident cap and detailed chemical labeling. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL):** Packed in 25kg fiber drums, 2-HYDROXY-4-FORMYLPYRIDINE loads approximately 8 metric tons per 20′ FCL container. |
| Shipping | 2-Hydroxy-4-formylpyridine is shipped in tightly sealed containers under ambient or controlled conditions, protected from moisture and light. It is classified as a laboratory reagent, and appropriate labeling, documentation, and handling precautions are applied. Transportation complies with relevant chemical safety regulations to ensure safe delivery and prevent contamination or degradation. |
| Storage | 2-HYDROXY-4-FORMYLPYRIDINE 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 moisture and direct sunlight. Use in a chemical fume hood, and handle with appropriate personal protective equipment to prevent skin and eye contact. |
| Shelf Life | 2-Hydroxy-4-formylpyridine should be stored tightly sealed, protected from light and moisture; typical shelf life is 2–3 years under proper conditions. |
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Purity 98%: 2-HYDROXY-4-FORMYLPYRIDINE with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity levels. Melting Point 155°C: 2-HYDROXY-4-FORMYLPYRIDINE with a melting point of 155°C is used in organic electronics development, where it provides stable processing under elevated temperatures. Molecular Weight 123.11 g/mol: 2-HYDROXY-4-FORMYLPYRIDINE with molecular weight 123.11 g/mol is used in ligand design for coordination chemistry, where it delivers predictable complexation behavior. UV Absorbance 280 nm: 2-HYDROXY-4-FORMYLPYRIDINE with a UV absorbance peak at 280 nm is used in analytical standard calibration, where it allows precise quantification of target analytes. Particle Size <20 μm: 2-HYDROXY-4-FORMYLPYRIDINE with particle size under 20 μm is used in fine chemical formulations, where it improves dissolution rate and homogeneous mixing. Stability Temperature up to 120°C: 2-HYDROXY-4-FORMYLPYRIDINE stable up to 120°C is used in high-temperature catalytic reactions, where it maintains structural integrity and consistent catalytic efficiency. Solubility in Methanol 50 mg/mL: 2-HYDROXY-4-FORMYLPYRIDINE with solubility in methanol of 50 mg/mL is used in chemical assay preparation, where it enables rapid solution preparation and accurate dosing. Water Content <0.5%: 2-HYDROXY-4-FORMYLPYRIDINE with water content below 0.5% is used in moisture-sensitive synthesis, where it minimizes hydrolysis risk and improves product stability. Chromatographic Purity >99%: 2-HYDROXY-4-FORMYLPYRIDINE with chromatographic purity greater than 99% is used in reference material production, where it guarantees reproducible analytical performance. pH Stability Range 4–8: 2-HYDROXY-4-FORMYLPYRIDINE with a pH stability range of 4–8 is used in buffer solution development, where it maintains consistent activity under varying acidic or neutral conditions. |
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Across the landscape of modern organic chemistry, certain building blocks stand out for their versatility and impact on both routine and advanced research. 2-Hydroxy-4-formylpyridine stands with that select group. Over the past few years, I’ve seen it attract attention in countless discussions among researchers, synthesis planners, and analysts looking for reliable chemical tools that do more than just deliver on paper. The compound’s unique profile — sporting both a hydroxy and a formyl group on the pyridine ring — sets it apart not only in structure but in the opportunities it brings to the table. Experiences working in a small lab taught me the value of reagents that adapt to both exploratory and practical requirements, demanding little in the way of compromise.
The model most researchers encounter comes with a proven purity level, consistent melting behavior, and a robust stability that resists the minor mishaps that can plague day-to-day lab routines. Quality assurance takes more than a test result; it relies on clear chromatography, predictable NMR patterns, and batch consistency you can trust across projects. These aren’t just boxes to check. They make the difference between a compound that fits worksheets and one you can count on during a critical synthesis.
Having a hydroxy group on the second position along with a formyl at the fourth gives 2-hydroxy-4-formylpyridine a reactive profile that chemists often call “synthetically privileged.” This configuration invites modification and lets researchers tap into a wealth of routes for ligand design, pharmaceutical intermediate development, and coordination chemistry. Whether it’s acting as a scaffold in medicinal applications, providing a building block for heterocyclic ligands, or slotting into more niche uses like functionalized monomers, the options stretch surprisingly wide.
Traditional pyridine derivatives each have their story. Some, like 2-formylpyridine, show up in standard aldehyde reactions, and many pyridinol derivatives get attention for their biological roles. The specific arrangement of the hydroxy and formyl groups in this model means it offers direct functional handles at two positions, sparing researchers from extra steps otherwise needed for selective activation or protection. I’ve worked on enough multi-stage syntheses to recognize how a well-placed functional group can bring down overall cost and risk. This can often turn a drawn-out project into one that meets deadlines with fewer setbacks.
Other similar molecules often force compromises, either in reactivity, solubility, or availability in high enough quality. 2-hydroxy-4-formylpyridine, by design, drops these hurdles. Its solubility matches the demands of a broad set of solvents — most notably the polar protic and aprotic favorites in organic work. I remember puzzling over certain stubbornly insoluble intermediates, wishing for a product that eased workup and purification. This pyridine derivative answers that call with a clean dissolution profile that speeds up not only the main reaction but the post-synthesis cleanout, saving precious hours.
Chemists care about more than structural novelty. The real test comes through reliable performance in reactions under pressure — whether that’s in the painstaking scale of milligrams or ramping up to the hundreds of grams needed for pilot runs. In my experience, 2-hydroxy-4-formylpyridine brings a practical resilience that many related products simply can’t match. Its chemical stability under normal storage conditions means labs avoid the heartache of unexplained decomposition or color changes leaving you second-guessing your entire week’s work.
I’ve seen this product put to the test in environments where resources run thin, where time is worth more than paper-pushing, and every failed batch leaves a lingering mark on funding and morale. Fewer purification cycles translate directly to cost savings and less solvent waste. Colleagues in pharmaceutical R&D shared similar stories: quicker screening, reduced risk of impurities masking potential activity, and easier scale-up efforts. The straightforward purification opens doors for groups who otherwise might shy away from complex pyridine chemistry, lowering the threshold for innovation in academic and industrial labs alike.
Quality starts and ends with reliable analysis. Every practitioner I know keeps an eye out for suspicious contaminant peaks, inconsistent melting ranges, or fading signals in spectroscopy. This compound makes life easier by offering high-resolution peaks in both NMR and mass spectrometry, confirming purity far beyond the specification sheet. Analytical teams report little headache during initial qualification. Batch traceability and supplier transparency matter for trust, and this particular compound finds favor in procurement teams who need to justify every purchase against strict audit standards.
Over the years, the frustration of discovering silent impurities halfway through a project taught me that no shortcut justifies risking reproducibility. This product comes with documentation verifying each lot, full COA access upon request, and open QR-coded tracking that matches the hygiene standards expected in regulated environments. Labs that focus on GMP or ISO compliance have an easier path to approval when each link in their supply chain delivers this level of verified traceability.
Daily chemical handling brings a blend of routine and vigilance. It’s rare to find a derivative that hits the sweet spot between useful reactivity and manageable hazard. While you always need proper PPE — gloves, goggles, controlled hoods — my experience working with 2-hydroxy-4-formylpyridine stands out for the control it offers without the anxiety that comes with more volatile or toxic reagents. The MSDS recommends all routine precautions, and the compound’s vapor pressure and odor are not overwhelming, making it suitable for both educational and industrial settings with appropriate oversight.
Teams I’ve worked with have minimized exposure risks thanks to a predictable handling profile. Consistent packaging, clear hazard labeling, and well-designed containers let both students and professionals avoid accidents that can otherwise set back productivity. Training new lab staff proves easier when the tools they use fall within the familiar range for safe operation.
Any synthetic chemist knows the pain of a bottleneck step. With this compound, the hydroxy and formyl groups create multiple entry points for conjugation, condensation, and cyclization. In collaboration with catalysis experts, I’ve seen how 2-hydroxy-4-formylpyridine fits well into C–C and C–N bond-forming tricks, delivering derivatives that feed into wider research programs. Drug discovery projects benefit most. Lead optimization, early-stage library construction, and SAR campaigns now have a shortcut to functionally diverse analogs. It’s no surprise the most forward-looking medicinal chemists request this compound by name in their initial screening arrays.
Researchers who focus on supramolecular chemistry leverage the compound’s chelating ability — a direct effect of the neighboring donor sites provided by hydroxy and formyl. Metal coordination studies rely on this to create robust, tuneable ligands. In my graduate days, we struggled with ligands that brought too much or too little reactivity, derailing half a year’s worth of work. 2-hydroxy-4-formylpyridine lets you build systems that capture the sweet spot between lability and strength, essential for creating sensors, catalysts, and advanced materials.
Sustainability looms large for today’s labs, especially as environmental regulations continue to tighten. I remember when switching out stubborn, hazardous compounds felt like an impossible task until a new product gave the same or better results with less fuss at disposal. This pyridine derivative stands above competitors because its synthetic pathways increasingly rely on greener oxidants, fewer halogenated reagents, and milder conditions that reduce both emissions and hazardous waste streams. It provides enough thermal stability to minimize loss during extended reaction times, so fewer wasted runs clog up the workflow or the waste drum.
Production teams see the benefit here: higher atom economy in cross-coupling, fewer incompatible byproducts, and less demand for expensive post-processing. Environmental compliance isn’t just a checkbox — it affects budgets, staff morale, and long-term planning. The environmental health and safety (EHS) officers I spoke with appreciate compounds that fit both risk assessment and life cycle analysis with a minimum of red tape.
Educators see value beyond the technical. Introducing undergraduates to a compound that serves as a springboard for modern heterocyclic chemistry builds skills that stay relevant in both academia and industry. My teaching experience showed that students remember hands-on work with accessible compounds far longer than rote textbook exercises. Safe, reliable, and well-documented, 2-hydroxy-4-formylpyridine lends itself to both demonstration and discovery. Experiments built around its reactivity help young chemists grasp the interplay between structure and function in real time.
Lab instructors gravitate toward tools that require only the usual levels of training and infrastructure. In settings where budgets remain tight, a reagent that lasts on the shelf, avoids exotic hazards, and offers multiple educational outcomes earns a permanent spot in the storeroom. Standard-issue glassware, fume hoods, and stock solvents make the compound a fit within most lab course syllabi, broadening the reach of high-impact chemical education without straining resources.
Bench-to-pilot transition often uncovers flaws in even the most robust compounds. I joined a scale-up team where the biggest challenge was finding cost-effective reagents that didn’t add unforeseen headaches during kilogram synthesis. Here, 2-hydroxy-4-formylpyridine passed scrutiny, with scalable purification and recovery methods that held up from gram to multi-kilogram batches. Its consistent behavior drew praise from production managers who measure success in both yield and downtime.
Downstream partners, from formulation chemists to quality assurance officers, look for reproducible raw material batches. The product’s batch-to-batch data give confidence in continued supply at a professional standard. Having spent time in procurement, I know how supplier reliability ties directly to production targets and downstream obligations. Contract manufacturers favor this level of quality assurance, knowing last-minute corrections can derail shipment schedules for weeks.
Regulatory compliance rarely makes headlines, but it remains non-negotiable for research-intensive industries. 2-hydroxy-4-formylpyridine’s track record in both domestic and international supply chains speaks to its maturity. The compliance documentation stacks up against the standards set by agencies familiar to anyone in the chemical industry. Procurement departments benefit from a transparent chain of custody, clear labeling, and unambiguous batch certification, speeding up approval cycles and audit readiness.
Clinical and preclinical researchers value the ability to link every vial and batch to a corresponding test record, easing the paperwork involved in new compound submissions. This means fewer regulatory bottlenecks, faster project starts, and lower risk of compliance gaps that could slow innovation at the most critical moments.
Trends in chemical research rarely stand still. The movement toward smarter molecules requires a steady supply of intermediates suited for function-driven synthesis, robust analytical controls, and sustainable manufacturing. Based on years of hands-on experience and time spent listening to industry peers, products like 2-hydroxy-4-formylpyridine form the backbone for new discoveries. As research priorities shift toward personalized medicine, greener processes, and faster iteration, the need for reliable, multifunctional scaffolds will only grow.
Investment in this product pays dividends not just in project delivery but in building institutional confidence. Those who shape the next wave of pharmaceuticals, materials, and catalysts look for partners — both products and suppliers — who stand on proven ground. This pyridine derivative isn’t just a line item or a fleeting trend. For labs of every size and ambition, it shapes the present and the future of chemical science.