|
HS Code |
321528 |
| Chemical Name | 2-hydrazinylpyridine |
| Molecular Formula | C5H7N3 |
| Molecular Weight | 109.13 g/mol |
| Cas Number | 505-63-5 |
| Smiles | NNc1ccccn1 |
| Appearance | Pale yellow to beige solid |
| Melting Point | 68-72°C |
| Boiling Point | 309°C |
| Solubility In Water | Soluble |
| Density | 1.20 g/cm³ |
| Pubchem Cid | 11814 |
| Iupac Name | pyridin-2-ylhydrazine |
As an accredited 2-hydrazinylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Hydrazinylpyridine, 25g: Supplied in an amber glass bottle with a screw cap, labeled with hazard warnings and chemical information. |
| Container Loading (20′ FCL) | 20′ FCL: 2-hydrazinylpyridine packed securely in sealed drums or containers, compliant with hazardous material transport regulations, maximizing load efficiency. |
| Shipping | 2-Hydrazinylpyridine should be shipped in tightly sealed containers, protected from light, heat, and moisture. It must be classified and packaged according to relevant hazardous material regulations, ensuring proper labeling for toxicity and potential health hazards. Transport typically occurs by ground or air, following UN guidelines for dangerous goods. |
| Storage | 2-Hydrazinylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition. Store away from incompatible substances such as oxidizing agents and strong acids. Protect from light and moisture. Ensure proper labeling and restrict access to authorized personnel only. Wear appropriate personal protective equipment when handling or transferring the chemical. |
| Shelf Life | 2-Hydrazinylpyridine typically has a shelf life of 2 years when stored tightly sealed, protected from light, moisture, and air. |
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Purity 98%: 2-hydrazinylpyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurities in final drug products. Melting Point 87°C: 2-hydrazinylpyridine with a melting point of 87°C is used in solid-phase organic synthesis, where it enables controlled reaction conditions and product reproducibility. Molecular Weight 109.13 g/mol: 2-hydrazinylpyridine with a molecular weight of 109.13 g/mol is used in catalyst design, where it offers efficient ligand incorporation and precise molar dosing. Stability Temperature 25°C: 2-hydrazinylpyridine stable at 25°C is used in laboratory reagent storage, where it maintains compound integrity during ambient handling. Particle Size <50 μm: 2-hydrazinylpyridine with particle size less than 50 μm is used in fine chemical formulations, where it promotes uniform dispersion and rapid dissolution rates. Aqueous Solubility High: 2-hydrazinylpyridine with high aqueous solubility is used in water-based analytical assays, where it provides consistent assay sensitivity and reproducibility. Reactivity High: 2-hydrazinylpyridine with high reactivity is used in heterocyclic compound synthesis, where it enables efficient ring formation and rapid reaction completion. Storage Stability at pH 7: 2-hydrazinylpyridine stable at pH 7 is used in biological assay development, where it ensures reliable experimental outcomes and minimized degradation during testing. Chromatographic Purity ≥99%: 2-hydrazinylpyridine with chromatographic purity ≥99% is used in reference standard preparation, where it guarantees analytical accuracy and traceability. |
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People working in research or chemical manufacturing often come across 2-hydrazinylpyridine. This compound stands apart with its nitrogen-rich structure, fusing a pyridine ring and a hydrazine group. Chemists know how useful this combination can be—the added reactivity of hydrazine opens many doors for synthesis and analysis. It’s not just another reagent on the shelf; it makes difficult transformations possible, especially when compared to more basic amines or traditional hydrazines. Over the years, its reliability in certain lab reactions has cemented its reputation.
2-Hydrazinylpyridine arrives in a solid form, crystalline and manageable at room temperature. Its structure includes a six-membered aromatic ring blended with a two-nitrogen hydrazine tail. Handling this material always requires precise measurement. The melting point hovers in a reasonable range, and this stability lets chemists work with it without complicated temperature controls. Solubility leans toward water and certain polar organic solvents, allowing mixing into reaction mixtures with little fuss. Chemists who have spent time purifying products understand how helpful these properties are—2-hydrazinylpyridine dissolves when required, yet crystallizes for easy recovery.
In the world of synthetic chemistry, this molecule offers something that more mundane starting materials can’t match. The hydrazine portion brings a double nitrogen punch, reacting smoothly with carbonyls and other electrophiles. For someone working to build complex heterocycles, 2-hydrazinylpyridine often serves as a trusted building block. Many pharmaceutical investigations start with scaffolds made by linking this compound to carefully chosen aldehydes or ketones. The end products, often new rings fused onto the original pyridine, can show all sorts of interesting chemical activity. Medicinal chemists keep an eye on these pathways when designing new candidate drugs.
In addition to building molecules, researchers lean on 2-hydrazinylpyridine for analytical tasks. This compound acts as a derivatizing agent for aldehydes and ketones, helping chemists identify or concentrate trace contaminants in samples. Inspecting reaction progress via thin-layer chromatography or HPLC becomes much easier when compounds form stable hydrazones with clear signatures. For folks aiming to track down elusive intermediates, this reactivity saves both time and effort. Aromatic derivatives tend to show up cleanly on UV-absorbing plates and resist decomposition where less robust reagents might break down.
Hydrazine by itself has always attracted interest, but it’s notoriously unpredictable and hazardous. Chemists appreciate having an option with the same core reactivity minus the extreme risks. The pyridine ring in 2-hydrazinylpyridine doesn’t just offer stability—it guides the reaction in a more controlled fashion. This difference becomes clear once you compare yields in ring-forming reactions or look at the purification steps at the end of a synthesis. Competing hydrazine derivatives sometimes turn out gooey or unmanageable; this compound tends to provide solid, easy-to-handle products.
Another important difference is its selectivity. People working on multi-step syntheses often struggle with unwanted side reactions from less defined hydrazines. The aromatic backbone of 2-hydrazinylpyridine reins in that reactivity, turning what could have been a chaotic process into something much more controlled. Fewer by-products can mean less time spent cleaning up mixtures or running extensive column purifications—both headaches for anyone working to scale up a reaction.
Anyone who’s spent long hours in a chemistry lab knows that ease-of-use counts for a lot. 2-Hydrazinylpyridine’s crystalline form and moderate melting range mean it’s not a spill hazard, unlike some liquid hydrazines that evaporate quickly or soak into gloves. Getting it into solution requires only gentle heating, if at all. Chemists sometimes share stories about unstable hydrazines that refuse to dissolve or produce clouds of noxious gas; the design of this molecule sidesteps many of those headaches without sacrificing utility.
Cost always comes into play for both research and industrial contexts. 2-Hydrazinylpyridine offers an accessible price point for the amount of chemistry it unlocks. Large installations looking to produce kilograms for pharmaceutical synthesis don’t have to pay through the nose for a specialty reagent. Smaller research labs that might use only a few grams find that purchases last a long time, and the shelf life holds up. Few things are more frustrating than opening up a bottle and finding the contents degraded—this compound puts up a good fight against light, moisture, and air.
Waste disposal also deserves scrutiny. Unlike hydrazine hydrate—a notorious pollutant and health hazard—2-hydrazinylpyridine allows for safer collection and neutralization. Waste streams don’t require elaborate neutralization protocols, and solvents from workups respond predictably to standard treatment procedures. Technicians trained to handle hazardous waste get a bit of breathing room, since this compound won’t volatize or leach into common solvent mixtures.
Pharmaceutical development teams constantly look for fresh tools that expand the range of potential therapies. 2-Hydrazinylpyridine slots into this kind of effort, especially during initial explorations of new lead compounds. Its role as a precursor to fused nitrogen-containing rings brings diversity to chemical libraries. Not every molecule from these screens makes the cut, but many candidates would never exist at all without the routes unlocked by this reagent.
Agrochemical researchers keep an eye on it as well. Pyridine-based rings show up in a wide spectrum of fungicides, herbicides, and regulators. 2-Hydrazinylpyridine offers a reliable gateway to these frameworks. Building new variants, testing them against crop pests, and scaling up promising hits—it all starts in the small round-bottomed flasks filled with this crystalline material. The difference between a failed and successful program often boils down to whether the chemistry works on the bench; here, a simple, predictable reagent makes all the difference.
For those in academic research, the flexibility offered by this compound can spark creative thinking in the search for new chemical families. Student researchers, postdocs, and professors who track the latest synthetic strategies can point to countless published works featuring this nitrogen-heavy tool. It not only simplifies certain transformations, it often inspires new routes to once-inaccessible products.
Anyone who has handled hydrazine-based reagents understands the potential risks. Vigorous reactions, fumes, and even burns can result from direct exposure. 2-Hydrazinylpyridine, with its more sedate behavior, proves more cooperative. Standard lab ventilation suffices for routine handling, and the solid form eliminates splattering worries common with liquid analogs. Gloves, goggles, and lab coats remain necessities, but most people won’t need to lock down the whole building while weighing out a sample.
Storage presents another plus. This compound keeps well in sealed glass bottles, out of direct sunlight. It doesn’t pull in so much moisture from the air that you need to chase humidity. For anyone who has spent hours cleaning sticky residue, this lack of hygroscopicity brings real relief. Larger operations transitioning to scaled-up procedures also find the storage straightforward—nothing beyond standard regulatory guidelines for safe chemicals with mild toxicity.
People sometimes reach for phenylhydrazine or unsubstituted hydrazine in synthetic efforts. Phenylhydrazine brings bulk, which sometimes blocks the formation of certain rings by crowding reactive sites. Unsubstituted hydrazine, on the other hand, works quickly but unpredictably, with a tendency to overshoot the mark. After multiple rounds of failed optimization or tricky recrystallizations, chemists notice that even a small tweak to the reagent makes a difference. The pyridine ring of 2-hydrazinylpyridine anchors the reactivity, giving predictable rates and outcomes.
In analytical settings, semicarbazide and other hydrazones sometimes compete for use. Many form weak or unstable linkages, offering poor spectral signatures or decomposing under light. Products from 2-hydrazinylpyridine reactions show strong, well-defined peaks, making qualitative and quantitative analysis more reliable. For years, I watched colleagues fumble with noisy spectra from less robust derivatizing agents. Switching to a sturdier aromatic hydrazine brought clarity to the lab notebook and made write-ups easier to justify.
Inside every laboratory, time and reliability drive choices about which reagents end up on the shelves. 2-Hydrazinylpyridine isn’t simply a placeholder for ‘hydrazine derivative’ in reaction schemes. Its design, blending an electron-rich ring with a reactive nitrogen duo, opens doors that would often remain shut with other chemicals. I’ve seen the shift this brings first-hand: what started as a flash of inspiration on paper crossed over into real, repeatable results. That sort of track record earns repeat orders and builds trust between chemists and their suppliers.
Healthcare research faces relentless pressure to discover and develop new molecules with real-world impact. Every advantage counts. As industry shrinks timelines and expands chemical space, only reagents with proven track records and practical handling survive the transition from bench to pilot plant. 2-Hydrazinylpyridine remains in that select group by marrying versatility with stability, something many new reagents fail to offer at a reasonable cost.
As chemists and industry professionals, we know that sourcing chemicals depends on reliability and transparency. 2-Hydrazinylpyridine benefits from a straightforward synthetic route. Manufacturers can deliver it on schedule without cumbersome purification steps, unlike exotic specialty reagents. This consistency matters, especially for process teams looking to take an idea from screening to kilo lab. Interruptions in supply cost money and hamper innovation.
Environmental concerns require careful thought. Old-school hydrazine production and disposal generated significant hazards; these concerns aren’t abstract when managing a modern facility. The design of 2-hydrazinylpyridine allows for more responsible production and disposal, limiting exposure to the most dangerous byproducts. This change turns risk management into an achievable part of day-to-day operations, not just red tape managed in boardrooms.
Waste stream reduction starts with choosing reagents that resist decomposition, won’t volatilize easily, and react cleanly with targets. 2-Hydrazinylpyridine delivers on these fronts. As regulations tighten around chemical emissions and workplace exposure, facilities gain measurable benefits from switching to substances with safer profiles. Many of us have worked through audits and inspections—every small improvement in waste handling and worker safety spares both time and nerves.
It’s easy to list theoretical benefits, but practical outcomes really drive purchasing decisions. Process chemists, faced with tight deadlines and shifting project requirements, look for reagents that deliver consistent yields and minimize surprises. 2-Hydrazinylpyridine checks those boxes, letting teams focus efforts on the actual targets rather than endless troubleshooting of side reactions or erratic behaviors. The paperwork trailing each batch tells the story: clean isolation, few unexpected peaks on chromatograms, predictable shelf life for recovered intermediates.
Peer-reviewed studies back up these impressions. Publications in medicinal and process chemistry journals note improved efficiency and better selectivity using this compound versus generic hydrazines. These reports find echoes throughout the supply network as both buyers and sellers seek materials with strong support and proven results. Customers demand more than promises; actual measured improvements win business and keep reputations strong.
Every chemical carries some risk, and overly-optimistic marketing erases real dangers. 2-Hydrazinylpyridine, though more manageable than many predecessors, demands the usual personal protective equipment, careful weighing, and respect for its contents. Long-term safety data continue to develop as more facilities handle this molecule at scale. Experienced users recommend periodic review of safety sheets and updated handling guidelines to limit fatigue and accidental exposure.
Sustainability efforts represent another area where ongoing work matters. Chemistry can’t avoid producing waste, but incremental steps move the dial toward greener operations. 2-Hydrazinylpyridine, by producing fewer volatile side products and less problematic waste, fits progressing industry standards. Yet there’s always room for further improvement—finding partners committed to clean synthesis and ethical sourcing becomes part of the equation. As customers ask more questions about carbon footprint and worker safety around the world, chemists will want options to fit these goals.
No single reagent can solve every problem. The real power of 2-hydrazinylpyridine lies in its ability to make tough chemistry easier and more predictable. These advantages give research teams the breathing space to try new ideas without getting bogged down in repeat failures or cleanup. The flow of information from bench scientists back to suppliers—and sometimes even back to regulators—improves with each successful batch. Success breeds more ambitious projects, growing the pool of scientific knowledge and feeding discovery from the ground up.
In classrooms and academic research groups, exposure to robust, reliable reagents builds confidence in young chemists. Students who succeed in the lab early on take on harder challenges in later years. Safe, easy-to-handle materials set up the sort of positive reinforcement that keeps people in the field. As more universities and research centers update their inventories, materials with proven records like 2-hydrazinylpyridine strengthen the next wave of chemical discovery.
Innovation rarely happens in isolation. Collaborations between academic centers and industry groups often depend on shared access to consistent, versatile reagents. 2-Hydrazinylpyridine makes that bridge easier to cross by working well in many settings: small, exploratory syntheses, systematic optimization campaigns, scaled-up process runs. Reliable performance across these diverse demands means information can flow more freely, improving the odds that promising leads survive the transition to commercial reality.
As more research teams take this reagent for a spin, new applications will likely emerge. Medicinal, agrochemical, and materials science fields continuously rethink what’s possible with nitrogen-rich building blocks. History shows that tools like this, when placed in capable hands, spark unexpected findings that ripple outward through science and technology.
Experienced users stress the benefits of integrating this compound into methodical workflow planning. Loading reactions in advance, preparing dry solvents, and setting up straightforward purifications turns the reliable properties of 2-hydrazinylpyridine into real time savings. With common protocols, researchers get stable results batch after batch. This stability feeds back into project planning—timelines tighten, budgets stretch further, and more insight is wrung from each dollar spent.
Process chemists invested in quality control appreciate the predictable impurity profiles associated with this reagent. Tracking batches via spectroscopy or chromatography, quality assurance teams find fewer surprises down the line. This predictability makes regulatory filings smoother, since repeated runs generate the same output in both bench and pilot plant scenarios. People overseeing scale-up operations know the headaches that come with erratic reagents, so gravitate toward those with track records of reproducibility.
Like every reagent, 2-hydrazinylpyridine brings both strengths and limitations. Its solid form makes it handy in the lab, and the controlled reactivity delivers reliable transformations for both synthesis and analysis. Yet it’s not a universal fix-all. People searching for miracles in every bottle may leave disappointed. Its structure won’t fit every niche, and some transformations call for more reactive or entirely different starting materials. For most, though, the advantages outweigh minor shortcomings. It enables tough reactions under milder conditions, sidesteps some of the risks lurking in similar chemicals, and churns out clear, publishable results with minimum fuss.
Trust grows over time. Every day spent handling a compound, every batch that produces good spectra, every bottle that stays viable for a year or more confirms magazine reports and peer journals. Scientists remember which tools worked and which ones didn’t. In case after case, 2-hydrazinylpyridine leaves chemists with reasons to come back for more.
As the chemical industry moves toward greater transparency and responsibility, the ingredients that build our medicines, materials, and crops draw closer scrutiny. 2-Hydrazinylpyridine earns its reputation by helping meet modern standards—cleaner reactions, safer handling, proven outcomes. Continual efforts by suppliers and researchers alike will keep improving the way this compound is produced, distributed, and used. As safety data expands and green chemistry guidelines evolve, options for even safer and more sustainable alternatives will undoubtedly grow.
For now, 2-hydrazinylpyridine offers researchers and manufacturers a practical, reliable path forward—a way to do serious chemistry without getting bogged down in the pitfalls of older, more hazardous compounds. Its story, still being written in papers and patents worldwide, shows how careful design and everyday experience shape the future of science. For those with big questions and tight deadlines, a versatile tool like this often makes the difference between just another lab day and that satisfying breakthrough.