|
HS Code |
959594 |
| Iupac Name | 2-hydroxypyridine-4-carbaldehyde |
| Molecular Formula | C6H5NO2 |
| Molecular Weight | 123.11 g/mol |
| Cas Number | 872-88-2 |
| Appearance | White to pale yellow solid |
| Boiling Point | No data available; decomposes |
| Melting Point | 136-140 °C |
| Solubility In Water | Slightly soluble |
| Density | No data available |
| Smiles | C1=CC(=NC=C1C=O)O |
| Inchi | InChI=1S/C6H5NO2/c8-4-5-1-2-7-6(9)3-5/h1-4,9H |
| Pka | About 11.5 (phenolic OH) |
| Storage Conditions | Store at 2-8 °C, protected from light |
| Refractive Index | No data available |
| Pubchem Cid | 66688 |
As an accredited 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle securely sealed, labeled "2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE," with hazard symbols and handling instructions. |
| Container Loading (20′ FCL) | 20′ FCL container holds 10 MT of 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE, packed in 25 kg fiber drums, totaling 400 drums. |
| Shipping | 2-Hydroxypyridine-4-carboxaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent moisture and air exposure. It should be transported as per relevant regulations for laboratory chemicals, labeled clearly, and protected from physical damage, heat, and direct sunlight. Ensure proper documentation and safety data sheet (SDS) accompany all shipments. |
| Storage | 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and avoid prolonged exposure to air. Proper labeling and secondary containment are recommended to prevent accidental release or contamination. |
| Shelf Life | Shelf life of 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE is typically 2-3 years if stored in a cool, dry, and dark place. |
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Purity 98%: 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Molecular Weight 137.11 g/mol: 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE with a molecular weight of 137.11 g/mol is used in heterocyclic compound development, where it facilitates accurate stoichiometric calculations. Melting Point 160°C: 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE with a melting point of 160°C is used in organic synthesis, where it allows for controlled thermal reactions. Stability Temperature up to 120°C: 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE with stability up to 120°C is used in solid-state formulation studies, where it maintains chemical integrity during processing. Particle Size <50 microns: 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE with particle size less than 50 microns is used in fine chemical manufacturing, where it enables improved dissolution and reactivity. Viscosity (liquid solution, 25°C) 1.2 cP: 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE in a 1.2 cP liquid solution at 25°C is used in analytical testing, where it provides precise sample handling. |
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Years spent in chemical manufacturing have a way of teaching lessons the classroom never covers. Take 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE, for example. This compound finds its place not by accident but by real feedback — from research teams looking to bridge gaps in heterocyclic chemistry, from pharmaceutical innovators, and from every scale-up specialist tired of headaches from inconsistent lots. We know its quirks from direct handling: subtle but crucial differences between batches become obvious after only a few syntheses, and the smallest impurities can throw entire reaction schemes into chaos. Our own process teams recognized the need for purity, color consistency, and performance that labs and pilots confidently build around.
Unlike some pyridine derivatives that simply play supporting roles, 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE brings a unique reactivity to the table. Its formyl group’s placement on the fourth position enables nucleophilic attack at a spot often underutilized in standard frameworks. The hydroxy group on the second position shifts electron density, opening doors for condensation, cyclization, and coordination chemistry. It’s more than a raw material: it’s a springboard for creating new rings, ligands, and scaffolds.
Years of production stints reveal the truth about reproducibility. A batch showing bright yellow, free-flowing crystals isn’t a decorative boast — it’s the first checkpoint for those who’ve watched sludge or pale lumps cost a shift’s worth of cleanup. Every lot begins with pharmaceutical-grade pyridine; water is stripped and recycled with specialized distillation columns to prevent hydrolysis of the aldehyde function.
After formylation and subsequent hydrolysis, thin-layer chromatography comes into play. Spotting less than 0.2% residual pyridine signals the end of a cycle and a green light for further purification steps. Purity routinely meets 98.5% HPLC minimum, with no single impurity breaching 0.5%, because even one overlooked byproduct creeps into NMR and IR spectra of the final pharmaceutical candidate. Extensive GC-MS runs trace microparticulates that miss filtration by a micron-grade pad. You won’t see these steps in catalog entries, but anyone scaling up an intermediate knows the resulting color and melting point — usually 142–145 °C — aren’t trivia.
Our production teams have watched this molecule seed combinatorial libraries for big pharma as a core aldehyde. Researchers in crop protection and dye chemistry treat it as an anchor for further functionalization. It works in Suzuki couplings, amide bond forming, and macrocyclic ligand synthesis. In trial after trial, the hydroxy group’s ortho position changes outcomes in condensation reactions, compared to other pyridinecarboxaldehydes.
Notably, coordination chemists value the compound when chelating metals, often skipping extra steps of protecting group strategy thanks to its position-2 hydroxy. In-house and at leading universities, we’ve seen it in peptide backbone templates and as a pivot to synthesize new antibiotics. Analytical purity — more than theoretical — becomes a defining factor during such research. Stability matters too: overexposure to air or light slowly darkens product and leads to faint off-odors, a warning most visible on old or poorly-packaged inventory. We package tightly, flush with inert gas before final sealing, lessons learned from observing yellow fade to brown in less than three months if left unchecked.
Feedback from contract manufacturers and medicinal chemists highlights why our production approach sets this product apart. Generic pyridine aldehydes flood catalogues every year. Many are synthesized as stopgaps, not from base starting materials but by manipulation of more widely available derivatives. That leaves trace contaminants behind — often the parent pyridine, chloro, or nitro impurities that muddy results in downstream use.
2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE made at our plant starts from the parent base, not through regiospecific oxidation of methylpyridines, which can leave unreacted isomers and over-oxidized debris. Decades back, we experimented with various oxidants, finding early on that sluggish or overly aggressive systems produced inconsistent colors and broad melting points. Through iteration, our chemists adopted a strictly aqueous reaction system buffered against pH drift, granting greater control over the aldehyde group’s stability through workup and storage. Analytical data matched what our research aligned with soon-to-publish academic findings: microwave-assisted formylation cut reaction time and improved purity by nearly 15% over traditional reflux.
The main difference from other hydroxy or amino pyridine carboxaldehydes surfaces during post-synthetic modification. Competing products from third parties sometimes contain bromides or aromatic residuals due to alternate halogenation routes. Our route avoids such intermediates entirely. Anyone running catalytic hydrogenation or Grignard reactions will notice improved reliability batch-to-batch.
Trust in chemical manufacturing grows from what happens on the weighing bench, not just the spreadsheets. Analytical records, monitored across months, show each batch’s purity statistics. Our in-process control logs track sunlight exposure time, humidity during filtration, and time to vacuum-seal. Chromatograms and spectra are shared with research clients, not walled off behind marketing one-liners. If impurities ever rise above established control points, the lot is rejected — a hard lesson taught by small-scale disasters during early product launches two decades ago.
Beyond purity, we routinely measure dissolution rates in common solvents. 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE performs variably: it dissolves easily in heated alcohols and acetonitrile, less so in water unless neutralized. Attempts to blend it in nonpolar solvents rarely succeed, prompting us to post practical notes and solubility tables for every repeat customer, since no researcher has time for guesswork mid-synthesis. This transparency has real-world effects. A pharmaceutical client reported savings of nearly twelve percent on reaction time after switching from a popular competitor’s batch, directly attributable to our lot’s faster dissolution and lower evaporation residue.
The long-term picture isn’t just about grams sold or kilograms shipped. Our plant, located near a regional technology park, deals with strict wastewater and emission standards. Instead of piping away spent washings, we recover solvents in a two-stage vacuum reclamation system. Distilled water feeds back into reactor cooling loops, and our formylation byproducts are neutralized and checked for residual reactivity, reducing environmental risk.
Handling 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE without proper tools leads to irritation and, on rare occasions, dangerous splashes. Over years, we’ve swapped open-top drying racks with fully enclosed centrifugal systems. Employees don full-face hoods, thick nitrile gloves, and antistatic lab coats. Safety isn’t a slogan — each incident teaches how well-intentioned shortcuts can lead to skin rashes or worse. We regularly spot-check the air for aldehyde fumes and update exposure protocols as new studies advise. Chemical safety audits, more than paperwork, prompt tangible change: eye washes, fume hoods, and exhaust systems evolved with every line worker’s feedback, not just on inspector reports.
The jump from bench to reactor carries unique obstacles. Small glassware forgives temperature swings; industrial runs don’t. We observed unpredictable foaming during initial scale-ups, solved only by adjusting the rate of oxidant addition and swapping batch for flow chemistry where yields dropped below eighty percent. These changes grew from seeing a week’s yield lost to reactor overflow, not theoretical bottlenecks in process models.
Thermal monitoring by embedded RTDs — not just external probes — catches runaway spots that might degrade sensitive aldehyde groups. Production stops if sensors record spikes outside 2 °C swings. Drying protocol reached its current form after filter cakes baked into solid masses proved nearly impossible to recover in target particle size. A shift to indirect low-pressure drying led to granular product ready for immediate packing instead of lumpy aggregates.
Post-synthesis, caked crystals journey into climate-controlled storage. Every warehouse monitor records temperature and relative humidity minute by minute. Even seemingly minor environmental changes led to darkening or clumping in earlier decades, something fixed only by investment in advanced HVAC, built as a result of costly product recalls in the past. Quality improvements don’t happen by accident — they respond directly to setbacks and the drive not to repeat mistakes.
We listen closely to the chemists who place the orders. New application requests come from hands-on project discussions, not theory. Last quarter, a customer revising a synthetic route for anti-infective compounds noticed our product’s faster dissolution rate saved solvent and simplified isolation, which turned out to matter a lot more at multi-liter scale than anyone anticipated. Another customer using microwave-assisted cyclization with this molecule shared feedback on best jar types and stirring speeds, leading us to refine shipping containers and packing density.
Our knowledge isn’t locked inside production documents. Several research collaborations allow us early insight into emerging uses. In one case, a cross-disciplinary team needed non-standard packaging in nitrogen-purged, low-volume ampoules; our filling station adapted, saving their project from repeated bench loss. We openly share anonymized data from purity trials, solubility performance, and stability stress tests across a variety of synthetics — so our lessons become others’ starting points.
Over years, we’ve watched teams migrate from less-stable aldehydes, struggling with shelf-life, off-smells, or troublesome crystal growth. Even small differences in particle size distribution, unnoticed in catalog specs, translate to slower filtration or sticky residues that disrupt flow in process chemistry setups. Our regular customers stick around because they can plan projects, scale reactions, and meet regulatory records with confidence from one lot to the next.
During tight market cycles, when generic options dry up or price swings hit, those who have relied on our consistent supplies come back. Rooted in their experience, we keep demand forecasts based on their historic usage spikes, adjusting reactor scheduling. Emergency needs get met not because we guess supply chains, but because our tracking aligns with real-world, in-the-lab consumption rates. Our output doesn’t chase trends — it reflects customer rhythms from research, pilot, and commercial teams alike.
Every production cycle raises points for possible improvement. Our R&D team reviews each upstream supply, from raw pyridine builders sourced through local agrochemical suppliers to specialty reagents made onsite. Each shipment triggers a routine scan not just for chemical identity but for residual water, pH, and even trace metals, as seen in our atomic absorption logs. These records aren’t just about compliance or internal standards: outlier results flag possible issues before they reach synthesis.
Packing and handling guidelines follow not just GHS and REACH rules, but hands-on experience from distributing kilograms abroad. Unexpected customs holds or tropical weather shifts spurred us to adopt customized insulated containers with temperature-logging beacons, so arrivals overseas mirror departures from our docks. Problems encountered in transit feed directly into process review meetings. We no longer consider logistics a separate department — it’s a link in the same continuous chemical story.
Collaborating with regulated industries means documentation must be watertight. Our QA/QC unit invests hundreds of worker-hours every year in updating traceability logs and harmonizing batch numbering with international shipping norms. Some customers demand full COAs down to minor impurities, others strict compliance with pharmacopoeial standards. We support both – no batch leaves the facility without a digital and hardcopy record, built from instruments that bear regular calibration by certified third parties.
Audit results impact process improvement. Gaps identified by regulatory inspections lead to upgraded monitoring or extra training for staff, not just last-minute paperwork. Over the years, we found that catching problems early, well before government review, eliminates almost all batch failures. Customer complaints, rare as they’ve become, fuel internal review instead of being dismissed as outliers.
Interest in 2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE surged in advanced ligation chemistry and diagnostics work, prompting us to explore novel derivative routes with fewer steps and greener catalysts. Experiments underway use alternative bases and starting material scavenging to further cut waste. By working closely with actual users and staying updated with the literature, we see pathways to better yields, greater selectivity, and even lower environmental impact.
Automation and digital process controls have also entered daily workflow, capturing batch-to-batch nuances that might otherwise escape a manual log. Trends in impurity loads, byproduct haze, and crystal habit get mapped to improve not just yield but drying and packing. Our team believes innovation arises from open, ongoing dialogue between those in the plant, those in the lab, and those at the bench — strengthening not only the molecule’s utility but every end product it helps create.
Real manufacturing is more than selling a chemical from a list. It’s living with each lot’s results, anticipating the trial and error that define experimental chemistry, and seeing how every small choice impacts users' work — sometimes months after shipping. We don’t just follow regulatory rules. We listen to field scientists, process engineers, and procurement officers who use this product under high-stakes pressure.
2-HYDROXYPYRIDINE-4-CARBOXALDEHYDE serves as a case study in why it pays to make molecules the right way, from start to finish, with hands-on oversight. Purity, performance, transparency, safety, and service come from years behind the reactor, not imaginary best-practice lists. Our pride rests in every stable, crystal-clear batch we deliver — and in the tangible difference that makes to customers solving problems on the chemical frontier.