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HS Code |
819456 |
| Chemical Name | 3-Cyano-6-hydroxypyridine |
| Molecular Formula | C6H4N2O |
| Molecular Weight | 120.11 g/mol |
| Cas Number | 6035-45-6 |
| Appearance | White to light yellow solid |
| Melting Point | 160-163°C |
| Solubility | Soluble in organic solvents such as DMSO and ethanol |
| Smiles | C1=CC(=NC=C1O)C#N |
| Inchi | InChI=1S/C6H4N2O/c7-3-5-1-2-6(9)8-4-5/h1-2,4,9H |
| Pka | Approx. 9.5 (hydroxyl group) |
| Storage Conditions | Store in a cool, dry place, away from light |
As an accredited 3-Cyano-6-hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of white to light-beige powder, labeled "3-Cyano-6-hydroxypyridine, C6H4N2O," with hazard symbols. |
| Container Loading (20′ FCL) | 3-Cyano-6-hydroxypyridine is loaded in 20′ FCL, securely packed in drums or bags, ensuring safe transport and handling. |
| Shipping | 3-Cyano-6-hydroxypyridine is shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. Packaging complies with chemical regulations, ensuring safe transport. Material Safety Data Sheet (MSDS) is included, and shipments are labeled according to international standards for hazardous chemicals. Handle with care and use appropriate personal protective equipment upon receipt. |
| Storage | Store **3-Cyano-6-hydroxypyridine** in a tightly sealed container, away from moisture and incompatible substances. Keep it in a cool, dry, well-ventilated area, and protect from direct sunlight and strong oxidizers. Clearly label the storage area and container. Access should be limited to trained personnel using appropriate personal protective equipment (PPE). Follow all relevant safety guidelines and local regulations. |
| Shelf Life | 3-Cyano-6-hydroxypyridine is stable under recommended storage conditions; shelf life is typically 2-3 years in a cool, dry place. |
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Purity 98%: 3-Cyano-6-hydroxypyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and low impurity rates. Molecular Weight 122.1 g/mol: 3-Cyano-6-hydroxypyridine with molecular weight 122.1 g/mol is used in agrochemical active ingredient development, where it facilitates consistent formulation properties. Melting Point 198°C: 3-Cyano-6-hydroxypyridine with melting point 198°C is used in organic electronics research, where it provides thermal stability during device fabrication. Particle Size <25 µm: 3-Cyano-6-hydroxypyridine with particle size less than 25 micrometers is used in fine chemical production, where it promotes rapid dissolution and uniform reaction kinetics. Stability Temperature up to 150°C: 3-Cyano-6-hydroxypyridine with stability temperature up to 150°C is used in catalyst manufacturing, where it maintains structural integrity under processing conditions. Water Content <0.5%: 3-Cyano-6-hydroxypyridine with water content below 0.5% is used in moisture-sensitive reactions, where it prevents unwanted hydrolysis and improves product consistency. Assay ≥99%: 3-Cyano-6-hydroxypyridine with assay value of at least 99% is used in laboratory-scale synthesis, where it supports reproducible analytical results and high product purity. Chromatographic Purity >98%: 3-Cyano-6-hydroxypyridine with chromatographic purity over 98% is used in reference standard preparation, where it ensures reliable calibration and quantification. Low Heavy Metals <10 ppm: 3-Cyano-6-hydroxypyridine with heavy metals content under 10 ppm is used in medicinal chemistry research, where it minimizes toxicity risks in biological evaluations. Bulk Density 0.45 g/cm³: 3-Cyano-6-hydroxypyridine with bulk density 0.45 grams per cubic centimeter is used in automated powder handling systems, where it allows efficient volumetric dosing and material transfer. |
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Anyone who has spent time in a lab working on pharmaceutical projects or crop protection knows the struggle of finding a compound that balances reactivity with control. 3-Cyano-6-hydroxypyridine carves out a niche here. This molecule blends a cyano group and a hydroxyl into a pyridine ring, stacking a potent combination for developers working on fine-tuning intermediates or exploring new synthetic pathways. If you’ve handled standard pyridine derivatives and found them lacking in reactivity or specificity, this compound shows what a small structural shift can do. By tweaking the functional landscape of the pyridine, you land somewhere different in the world of synthetic potential—taking on transformations that remain out of reach for simpler analogs.
Chemists don’t fall in love with molecules based on their looks; it’s what you can do with them that counts. Stack the molecular structure of 3-cyano-6-hydroxypyridine against classic pyridines, and the potential pops out. The hydroxyl group at position six opens the door for hydrogen bonding and plays nicely in metal chelation, an edge that’s hard to ignore in medicinal chemistry or catalysis. That’s not all—the cyano group at position three functions as an electron-withdrawing anchor. In practical terms, that reshapes the electron density across the ring, driving selectivity in coupling reactions and enabling new substitutions. Synthetic chemists know the value in this: you can detour around failed routes and re-design your approach from the ground up.
Walking along the drug discovery pipeline, you run into barriers that make you question every intermediate you introduce. 3-cyano-6-hydroxypyridine stands out here, offering shortcuts and expanding routes for active pharmaceutical ingredient synthesis. I’ve seen colleagues struggle with intermediates that lacked the right blend of stability and reactivity, leading to bottlenecks. With this compound, the story shifts. Pharmaceutical labs appreciate how its combined functionalities let you assemble core scaffolds or fine-tune heterocyclic frameworks. It’s a backbone in some routes to antiviral and antibacterial agents, showing reliable performance when confronted with harsh reagents or stepwise transformations that tend to degrade lesser compounds. Even as research moves deeper into personalized medicine, a scaffold like this remains relevant, giving developers a reliable jumping-off point for next-generation therapies.
Addressing food security means rethinking the molecules that form the base of crop protection products. I’ve watched teams in agricultural chemistry pivot from generic building blocks to specialized heterocycles like 3-cyano-6-hydroxypyridine when resistance rears its head. Pyridine-based intermediates have long played a role in this field, but here’s where a small change matters: the unique dual functionality of the molecule unlocks new families of herbicides, insecticides, or fungicides. We see faster development and easier modifications in structure-activity relationships. New challenges in pest resistance need tools that allow rapid iteration, and this molecule brings the right balance for tweaking, derivatization, and incorporation into complex formulations. Labs chasing safer, greener solutions appreciate that it dodges some of the reactivity nightmares present in less nuanced alternatives.
Step outside pharma and agrochem, and you see 3-cyano-6-hydroxypyridine’s value echoed in specialty material science. Advanced polymers, dyes, and coatings need intermediates that can handle tough conditions and interact well with other additives. Over countless meetings and late-night bench work, teams debate the merits of each intermediate. Traditional pyridines often fall short against demands for new functionality, solubility profiles, or thermal stability. In my experience, this compound brings a versatility that bridges multiple application areas. Polymer chemists value its ability to knit into chains, lending structure and unique reactivity. Coatings specialists exploit its compatibility across a range of solvent systems and its knack for holding up under thermal and light stress. The cyano/hydroxy combo lets you dial in properties, hitting the sweet spot between processability and finished-part performance.
No discussion of fine chemicals is complete without a reality check on day-to-day handling. After all, the best molecule means nothing if you can’t use it safely or at scale. 3-cyano-6-hydroxypyridine is a solid at room temperature, and the crystalline powder handles predictably under standard conditions. Solubility leans toward polar organic solvents, so anyone planning multi-step transformations in water should plan accordingly. I’ve made the mistake in my own work of underestimating powder flow and caking issues until humidity crept into the mix, so storage in sealed, cool containers pays dividends. Purity can make or break a synthesis—most reputable suppliers target 98% or higher, and that level keeps side reactions at bay, letting you plan reaction steps with confidence.
Pyridine derivatives cover a huge territory, but generalizing leads to mistakes. Most labs keep 2- and 4-substituted pyridines around, yet these cousins rarely give the same flexibility at the three and six positions. In my own projects, switching between these analogs usually meant extra protection/deprotection steps or updating protocols mid-stream. 3-cyano-6-hydroxypyridine saves trouble by providing a unique motif right out of the bottle. Comparing it to 3-hydroxypyridine or 3-cyanopyridine makes the distinction even sharper—neither standalone cyano nor bare hydroxy offers the same toolkit. You get the power of two functionalities working in tandem, letting you shortcut multi-step routes or improve selectivity. Downstream, fewer purification headaches crop up, and the chance for unwanted side reactions drops, which speaks to the benefit of fine-tuning starting materials rather than wrestling with generic stand-ins.
Every move toward a new lab chemical happens against a backdrop of growing environmental scrutiny. Over the years, I’ve watched the regulatory landscape tighten, demanding proof that operational benefits don’t come at an environmental cost. 3-cyano-6-hydroxypyridine generally avoids the more challenging hazards of some functionalized aromatics—think low volatility and moderate toxicity profiles. That said, safety data from peer-reviewed sources and regulatory filings reinforce the need for concise hazard labeling: gloves, proper ventilation, and well-maintained storage cut down risk. Waste management improves because the compound doesn’t demand extreme incineration and responds well to common destruction methods. These attributes move the molecule into a more accessible bracket for industrial or academic adoption. As environmental priorities loom larger, these practical safety steps matter to teams scaling up from bench to pilot plant.
Availability of research chemicals sometimes dictates which projects researchers can pursue. Over the last decade, sourcing stabilized with improvements in large-scale synthesis of pyridine derivatives. 3-cyano-6-hydroxypyridine isn’t as cheap or ubiquitous as basic pyridine, but pricing settled as demand from pharmaceutical and agrochemical sectors grew. For smaller labs, buying in gram quantities remains practical, and kilo-scale options support commercial production. Making purchasing decisions, I’ve weighed the sticker price against the number of steps saved, the reliability in batch-to-batch quality, and the lowered risk of regulatory entanglements. Factoring these, the real-world cost often winds up lower than alternatives that seem cheaper at first glance. Furthermore, increased access has spurred more groups to explore unconventional synthetic routes, feeding a cycle of innovation that benefits the entire sector.
No molecule solves every problem—something I’ve learned working across fields as varied as medicinal chemistry and material science. One part of the challenge lies in finding the right balance between reactivity and selectivity; 3-cyano-6-hydroxypyridine offers both but still faces competition from bespoke, purpose-made analogs. Occasional supply hiccups arise when upstream chemical feedstocks face price spikes or transport bottlenecks. On the synthesis side, scale-up beyond kilogram levels introduces process hazards: heat management, solvent compatibility, and waste handling all demand attention. I’ve found that the most successful teams look to process intensification, continuous flow chemistry, and green solvents to ease these bottlenecks. Collaborations between academia, contract manufacturers, and chemical engineers drive incremental changes that ripple out to wider supply chain resilience.
Advancements in chemical manufacturing never happen in isolation. Multinational firms, small contract research organizations, and university labs each bring unique insight. With 3-cyano-6-hydroxypyridine, the interplay between research and applied development stands out. By sharing data on reaction outcomes, impurities, and alternative synthetic routes, organizations build resources that everyone can draw from. Over the years, I’ve seen open-access chemical repositories and shared best-practice guides speed up the adoption of new intermediates—this compound included. Public databases allow chemists to check spectral data, confirm batch quality, or trace impurities before ordering. These initiatives lower the barrier to entry and ensure new researchers start from a stronger foundation, rather than repeating old missteps or dead-end syntheses.
Anyone who’s handled scale-up work knows that trace impurities can undo months of progress. Here’s where source quality for 3-cyano-6-hydroxypyridine matters deeply. Rigorous quality controls at the supplier end, with confirmed characterization through NMR, mass spectrometry, and HPLC, set the stage for fewer nasty surprises downstream. My experience echoes countless colleagues: when using high-purity input, reactions run smoothly, yields jump, and purification is less of a headache. Project managers appreciate this, as timelines tighten and budgets face scrutiny. Modern labs track every variable, and a stable, reproducible intermediate removes an unpredictable wildcard from project planning. An underappreciated aspect is global certification for both the compound itself and for the facility producing it, as customers line up supply chains against increasingly demanding international standards.
Green chemistry gets a lot of talk, but real advancements come from practical shifts in building blocks. 3-cyano-6-hydroxypyridine supports this by enabling shorter syntheses and cleaner transformations. Less reagent waste, fewer masking/unmasking steps, and better atom economy all cut environmental burden. Having worked on process scale-ups, these factors translate into less solvent waste and reduced emissions—a win in both regulatory filing and lab morale. Teams pushing for continuous-flow or solvent-free syntheses have flagged this intermediate for its compatibility and adaptability. Innovations at this intersection—where new chemistry meets environmental consciousness—push the field forward. As climate action intensifies, having intermediates that fit sustainable manufacturing processes becomes a competitive edge, not just a buzzword.
A molecule, by itself, never gets anything done. It’s the people behind it—chemists, engineers, process operators—who shape outcomes. Transitioning a team to handle 3-cyano-6-hydroxypyridine involves upfront training, from safety considerations to strategic reaction planning. Workshops, cross-disciplinary meetings, and shared technical write-ups speed up adaptation. I’ve seen individuals from disparate backgrounds—organic synthesis, analytical characterization, environmental management—come together over shared challenges. With new intermediates, initial hesitancy gives way to experimentation, troubleshooting, and, ultimately, mastery. Drawing on lessons from past failures, each iteration brings the group closer to robust, repeatable results. Team learning leaves a bigger impact than any single innovation, weaving new capabilities into the fabric of company culture and the larger scientific community.
Every generation of chemists inherits a growing toolset. My career has tracked the evolution from basic, single-function pyridines to complex, multifunctional intermediates like this one. The difference isn’t just about adding new chemicals to the shelf; it’s about changing the possible. Intermediates of this caliber empower researchers and manufacturers to set more ambitious targets. Whether the end goal is a life-saving medicine, a more effective pesticide, or a longer-lasting coating, the path there depends as much on starting materials as visionary ideas. By keeping an eye on practical details—availability, safety, reactivity, and environmental profile—the field steadily moves from bench to real-world impact. That’s a legacy worth aiming for, and 3-cyano-6-hydroxypyridine shows how small shifts in molecular structure rewrite what’s achievable across industries.
Growth in global demand for fine chemicals brings both promise and uncertainty. Over time, I’ve witnessed markets swing when political, logistical, or environmental shocks ripple through supply chains. With 3-cyano-6-hydroxypyridine, strengthened supplier networks and regional diversification have become best practices. Companies invest in back-up production capacity and enhance tracking, making delivery delays or feedstock shortages less threatening. Digital inventory tracking and advanced forecasting tools help labs anticipate needs and place smarter orders. The payoff is stability—even set against volatile markets or tough transportation conditions.
Science never escapes its social and ethical context. Pushes toward greener chemistry, transparent sourcing, and fair labor inform every purchase and every process change. The story of 3-cyano-6-hydroxypyridine isn’t just technical—it’s also about making choices that align with broader values. I’ve seen procurement managers prioritize compounds with robust audit trails, traceable sourcing, and verifiable labor standards. These factors, once seen as “nice to have,” now influence purchasing decisions and long-term partnerships. Labs winning regulatory approval or certification often flag sustainability and ethics in their filings, securing a competitive edge and building trust with stakeholders, from investors to downstream users.
3-cyano-6-hydroxypyridine shows what targeted molecular design brings to the frontline of chemical innovation. It occupies a critical middle ground: not so exotic as to be inaccessible, yet distinct enough from general-use pyridines to open new creative opportunities. Having worked across development, procurement, and technical training, I see firsthand the effects of a well-chosen intermediate: smoother projects, reduced waste, and a more adaptive team. From bench to scale-up, from the pharma pipeline to plant protection, this molecule’s influence stretches further every year. As growing demands intersect with technological and environmental priorities, intermediates like this reinforce the case that incremental material innovation powers progress far beyond the lab.