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HS Code |
603980 |
| Chemical Name | 2-Cyano-3-hydroxypyridine |
| Cas Number | 6832-97-7 |
| Molecular Formula | C6H4N2O |
| Molecular Weight | 120.11 |
| Appearance | Off-white to light yellow solid |
| Melting Point | 151-155 °C |
| Solubility | Soluble in DMSO, partially soluble in water |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=C(N=C1)O)C#N |
| Inchi | InChI=1S/C6H4N2O/c7-3-5-4-8-2-1-6(5)9/h1-2,4,9H |
| Synonyms | 3-Hydroxy-2-cyanopyridine |
| Storage Temperature | Store at room temperature |
As an accredited 2-Cyano-3-hydroxpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Cyano-3-hydroxypyridine, 25g, comes in a sealed amber glass bottle with a secure screw cap for protection. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Cyano-3-hydroxypyridine involves safe, bulk packaging and secure placement to prevent contamination or spillage. |
| Shipping | 2-Cyano-3-hydroxypyridine is shipped in tightly sealed containers to prevent moisture ingress and contamination. The chemical should be stored in a cool, dry place, away from incompatible substances. During transport, ensure proper labeling and compliance with local regulations for handling hazardous chemicals. Use secondary containment to prevent leaks or spills. |
| Storage | 2-Cyano-3-hydroxypyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of heat and ignition. Protect it from light, moisture, and incompatible substances such as strong oxidizers and acids. Label containers clearly and keep them in a designated chemical storage area, with access restricted to trained personnel. |
| Shelf Life | 2-Cyano-3-hydroxypyridine typically has a shelf life of 2–3 years when stored in a cool, dry, and airtight container. |
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Purity 99%: 2-Cyano-3-hydroxpyridine with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurities in the final active compound. Melting Point 129°C: 2-Cyano-3-hydroxpyridine with a melting point of 129°C is used in organic synthesis reactions, where it provides stable solid handling and precise thermal control during processing. Particle Size < 50 Microns: 2-Cyano-3-hydroxpyridine of particle size less than 50 microns is used in catalytic systems, where fine dispersion enhances reaction kinetics and product uniformity. Stability Temperature up to 180°C: 2-Cyano-3-hydroxpyridine with stability up to 180°C is used in high-temperature chemical processes, where it maintains structural integrity and consistent reactivity. Water Content < 0.2%: 2-Cyano-3-hydroxpyridine with a water content below 0.2% is used in moisture-sensitive organic syntheses, where low hygroscopicity prevents unwanted hydrolysis and side reactions. |
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Stepping into a modern chemical lab, I notice shelves lined with glass bottles, each holding compounds with strange names and hidden potential. 2-Cyano-3-hydroxypyridine is a name that doesn’t roll off the tongue, but it has earned its place in research and manufacturing for good reason. This compound stands out because of its versatility and utility as an intermediate in pharmaceutical and agrochemical processes. What I’ve seen is that seasoned chemists pick this molecule not only for its specific reactivity but for the cleaner reaction pathways it brings to the bench.
Chemicals often get lumped together, but 2-Cyano-3-hydroxypyridine doesn’t just blend into the background. Its pyridine ring, a familiar sight for those who have worked with heterocyclic chemistry, features both a cyano group and a hydroxyl group at precise positions on the ring. This arrangement opens up routes for further reactions that similar structures just can’t match as easily. Let’s face it: in a field full of subtle differences, these slight molecular tweaks can save days or weeks in the lab. From my own experience, picking the right intermediate early in a multi-step synthesis can make or break a project.
A closer look at the makeup of 2-Cyano-3-hydroxypyridine points to its most useful feature: the presence of both an electron-withdrawing cyano group and an electron-donating hydroxyl group. This unique blend gives chemists a foundation to target selective reactions. For those unfamiliar, think of it as tuning a radio until only the clearest stations come through; chemists tweak conditions and this molecule responds predictably.
While some other pyridine derivatives can stall out during coupling or substitution steps, this one moves ahead thanks to its structure. In real lab scenarios, that means fewer byproducts and less time hunched over a rotary evaporator or sorting impurities using chromatography. The difference? Less hassle for researchers, but also safer and more environmentally conscious operations all around. No one enjoys losing valuable time — or losing money — fixing avoidable complications.
Product literature can bury buyers in numbers, but most researchers I know focus on purity, appearance, and solubility first. High-purity 2-Cyano-3-hydroxypyridine sets the standard at over 98%, giving you greater confidence that reactions won’t hit snags from mystery contaminants. The compound turns up as a pale yellow to off-white powder, which might sound trivial until you’ve tried working with sticky or impure batches that don’t behave as expected. A well-formed powder means you can weigh out precise amounts and transfer material easily between vessels — simple details that cut frustration on deadline-driven days.
It dissolves in common organic solvents, including ethanol and acetonitrile. That kind of compatibility lets you use it directly in many established protocols. There’s something comforting about not having to reformulate your solvent system just to try out a new intermediate.
2-Cyano-3-hydroxypyridine earns attention largely from its role as an intermediate in synthesizing a range of products. I first encountered it during a project on pyridine-based pharmaceuticals, where its reactive sites made later steps possible without massive overhauls in procedure. Medicinal chemists see value in it because that combination of cyano and hydroxyl groups helps create new molecules with desirable biological activity.
Agrochemical makers also find it valuable. Many pesticide and herbicide formulations draw from chemical frameworks shaped by substitutions on pyridine rings. Having a hydroxyl or cyano group in the right spot can influence how future molecules interact with plant proteins or enzyme systems. From what I have seen, even small changes in these synthetic precursors ripple into big changes in how effectively a finished product performs.
Material scientists explore building up new ligands and specialty polymers starting with 2-Cyano-3-hydroxypyridine. Its adaptability isn’t just theoretical — I’ve watched research teams swap in this compound for other, fussier starting materials, only to find that yields improve and processes become easier to manage. Over time, that is the kind of shift that can change which manufacturers lead markets.
While chemistry often seems locked in a world of research, the downstream effect of using robust intermediates matters more than ever. Sourcing consistent 2-Cyano-3-hydroxypyridine lets labs cut down on repeat experiments and false starts. Imagine chasing a new drug candidate for weeks, only to discover inconsistency or impurity in an early ingredient holds everything back. Lower impurities aren’t just about quality — they influence regulatory approval and public safety.
From conversations with colleagues, there’s widespread agreement that intermediates with well-defined reactivity simplify scaling up promising reactions. In pharma, scaling a synthesis from milligrams to kilograms often kills creative ideas. Successful scale-up hinges on dependability in every intermediate. The purity and consistent behavior of 2-Cyano-3-hydroxypyridine gives projects a better chance of moving out of the lab and closer to production.
Many pyridine-based molecules show up in catalogs and textbooks, and it’s easy to lump them together. But subtle differences add up. Compared to other options like 3-hydroxy-2-methylpyridine or 3-hydroxypyridine, the cyano group on this molecule acts almost like a conductor, changing how electrons flow and enabling specific transformations. What this means is that you can access reaction pathways unavailable through other intermediates. You can make substitutions or extensions on the ring with fewer complications.
In my own troubleshooting, I have found that compounds similar in name or shape do not always perform the same way in coupling or functionalization steps. Reactions with 3-hydroxypyridine, for example, often go in different directions. The extra cyano group in 2-Cyano-3-hydroxypyridine drives certain reactions faster and with more selectivity. It can even withstand tougher conditions, giving you a broader toolkit for synthesis.
This difference shines most brightly in complex syntheses where efficiency matters. Forcing a reaction to work using less-reactive components often leads to lower yields or the presence of tough-to-remove byproducts. Recognizing how one or two atoms swapped on a molecule can flip an outcome is something only gained by hands-on experimentation and failure — and those lessons are hard-won.
Every seasoned chemist knows there are few disappointments greater than discovering a key intermediate degraded on the shelf. 2-Cyano-3-hydroxypyridine, like many sensitive chemicals, deserves proper handling and respect. Storing it in a cool, dry environment avoids clumping and potential breakdown, especially in labs that juggle dozens of open containers. Using tightly sealed bottles cuts down on moisture uptake and preserves the powder’s quality.
Some colleagues working long-term synthesis projects talk about temperature-sensitive reactions. Proper storage ensures results don’t fluctuate from batch to batch. In regulatory or manufacturing settings, these precautions quickly move from afterthought to critical policy — nobody wants their project set back because of degraded reagents. Basic good practice here does more than just save money; it preserves safety and the accuracy of research.
Sustainability isn’t just a buzzword in science anymore. The push to minimize hazardous byproducts has become personal for many working in industry and academia. 2-Cyano-3-hydroxypyridine brings a few practical benefits to those concerned with waste streams. Since it allows for more selective and often higher-yield reactions, the process produces less waste. Reduced waste means less spent on disposal and a smaller environmental impact.
On a related note, the high purity standard translates to fewer needs for lengthy purification steps. Less time, less solvent, less energy spent on “cleaning up” the product downstream. Good choices in the planning stages pay off throughout a project’s lifespan. That sort of thinking is spreading through more labs every year, especially as awareness grows around environmental risk.
Every project faces budget constraints, from university labs to major industry players. 2-Cyano-3-hydroxypyridine may cost a bit more per gram than some generic intermediates. My experience suggests that price differences up front often get wiped out by savings down the line. Shorter, more dependable syntheses mean fewer failed runs, less time lost, and more consistent products. Add in regulatory expectations for traceability and purity, and budget realities quickly align with the need for higher-quality starting materials.
I have watched groups in both academic and corporate settings choose cheaper-but-riskier substitutes, only to find their projects marred by unexpected outcomes or time-consuming troubleshooting. Factoring in hidden costs — wasted time, lost starting materials, repeated purification — makes the case for better intermediates nearly every time.
No major project can ignore the increasing pressure for traceability and documentation around starting materials. 2-Cyano-3-hydroxypyridine’s consistency and clear analytical profile support tracking systems designed to satisfy regulators and internal audit teams alike. Reliable certificate of analysis and validated testing back up the claims on labels.
Regulatory agencies look for transparent sourcing and well-documented chain of custody, especially when projects aim at pharmaceutical or agrochemical registration. Using intermediates with reliable quality history reduces headaches for compliance officers. Skipping this level of care runs the risk of delays, recalls, or lost profit at launch.
Some of the most exciting advances in medicinal chemistry stem from the combination of robust, flexible intermediates and creative teams willing to push boundaries. 2-Cyano-3-hydroxypyridine has quietly enabled researchers to explore new reaction types, faster pathways, and higher selectivity in product design. Keeping this molecule in the repertoire opens doors to unexpected discoveries.
I remember a small team working to streamline the synthesis of a promising antibiotic, only to find a stubborn bottleneck at an early stage. Swapping in 2-Cyano-3-hydroxypyridine cleared it immediately, with better yields and a product profile that passed purity thresholds for preclinical trials. The lesson? Sometimes innovation comes less from new reactions and more from thoughtful choices in starting building blocks.
No chemical should ever be approached without respect for the hazards and responsibilities it carries. In daily operations, good safety procedures apply to 2-Cyano-3-hydroxypyridine as to any compound that might present risks through inhalation, skin contact, or accidental release. Gloves and well-ventilated spaces matter as much as any fancy lab equipment.
People new to the lab sometimes overlook these basics. Those of us seasoned by years of spills, surprises, and lessons learned know that careful handling isn’t paranoia; it’s just smart. Mishaps don’t just threaten individuals — they put entire teams at risk and can halt promising lines of investigation.
Supporting the switch to higher-quality intermediates like 2-Cyano-3-hydroxypyridine involves a few steps. Training is one. Teams who understand the unique benefits and behaviors of their chemicals make fewer costly mistakes. Broadening access to reliable product information builds confidence and speeds up decision making.
Procurement departments should work closer with technical staff to choose sources with legitimate documentation and proven track records. Supply partners willing to maintain consistent standards — and who aren’t content to cut corners — make all the difference. Over the years, building supplier relationships based on shared commitment to safety, transparency, and quality brings a sense of stability to R&D groups regularly facing shifting priorities.
Other fixes come from individual and team initiatives. Establishing clear protocols for storage and handling, conducting periodic in-house purity checks, and keeping up with emerging best practices in hazardous substance management all serve to support safer, more productive work environments.
The world of synthetic chemistry is packed full of options. Yet as regulation tightens and public expectations rise, demand grows for intermediates that deliver reliability, purity, and straightforward utility. 2-Cyano-3-hydroxypyridine bridges the gap between tradition and innovation by providing a stable, versatile platform for new discoveries. Projects seeking both scale and impact will benefit from intermediates with proven track records and clear advantages in real lab settings.
Not all progress relies on radical new inventions. Sometimes, incremental improvements — like selecting an intermediate that actually lives up to its reputation — unlock new opportunities and better results. Having spent my share of late nights running reactions and troubleshooting experiments, I know the value of ingredients that just work. As research challenges grow more complex, I expect 2-Cyano-3-hydroxypyridine to remain an important tool for everyone dreaming up the next breakthrough, in medicine, agriculture, or advanced materials.