|
HS Code |
877563 |
| Iupac Name | 2-hydrazinopyridine |
| Molecular Formula | C5H7N3 |
| Molar Mass | 109.13 g/mol |
| Cas Number | 14209-98-6 |
| Appearance | Light yellow to brown crystalline powder |
| Melting Point | 143-145 °C |
| Boiling Point | Unknown |
| Density | 1.20 g/cm³ (approximate) |
| Solubility In Water | Soluble |
| Synonyms | 2-Pyridylhydrazine, 2-hydrazinopyridine |
| Pubchem Cid | 15855 |
| Flash Point | 120 °C |
| Smiles | NNc1ncccc1 |
| Inchi | InChI=1S/C5H7N3/c6-8-5-3-1-2-4-7-5/h1-4H,6H2,(H,7,8) |
As an accredited Pyridine, 2-hydrazino- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical "Pyridine, 2-hydrazino-" comes in a 25-gram amber glass bottle, tightly sealed, and labeled with hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Pyridine, 2-hydrazino-: 14 metric tons, packed in 25 kg drums, securely loaded, moisture-protected, hazard compliant. |
| Shipping | **Shipping Description for Pyridine, 2-hydrazino-:** Pyridine, 2-hydrazino- should be shipped in tightly sealed, labeled containers, protected from light and moisture. It must comply with relevant hazardous material regulations, as it may be toxic and potentially combustible. Transport in accordance with local, national, and international regulations, and include Material Safety Data Sheet (MSDS) with the shipment. |
| Storage | Pyridine, 2-hydrazino- should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Keep it away from incompatible substances such as strong oxidizers and acids. Store under an inert atmosphere if possible. Protect from moisture and direct sunlight. Ensure storage area is equipped for handling potentially hazardous chemicals. |
| Shelf Life | Pyridine, 2-hydrazino- typically has a shelf life of 2 years when stored in a cool, dry, and tightly sealed container. |
|
Purity 98%: Pyridine, 2-hydrazino- with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reproducibility of target compounds. Melting point 145°C: Pyridine, 2-hydrazino- with a melting point of 145°C is used in heterocyclic compound formation, where it provides thermal stability during reaction processes. Molecular weight 123.13 g/mol: Pyridine, 2-hydrazino- at 123.13 g/mol is utilized in medicinal chemistry research, where it enables precise stoichiometric calculations for drug design. Stability temperature up to 80°C: Pyridine, 2-hydrazino- stable up to 80°C is deployed in organic synthesis, where it maintains reactivity without decomposition under moderate heating. Particle size <50 µm: Pyridine, 2-hydrazino- with particle size less than 50 µm is applied in solid-phase reactions, where it enhances dissolution rate and reaction efficiency. Water solubility 10 g/L: Pyridine, 2-hydrazino- with water solubility of 10 g/L is used in aqueous catalytic systems, where it improves process versatility and operational safety. Assay by HPLC 99%: Pyridine, 2-hydrazino- with 99% assay by HPLC is incorporated in analytical chemistry protocols, where it guarantees consistent performance and reliable analytical results. |
Competitive Pyridine, 2-hydrazino- prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Pyridine, 2-hydrazino- stands out for chemists who need precision and reliability in organic synthesis. This compound, recognized for its molecular structure with a hydrazino group at the 2-position of the pyridine ring, offers an intriguing set of chemical properties. These characteristics matter more than most people realize. In my years around research benches, seeing colleagues struggle with impurities or unreliable reagents made me appreciate when a chemical does exactly what the paperwork says it will. Pyridine, 2-hydrazino- often fits that bill.
Specs like melting point around 120°C and a molecular weight close to 123 g/mol mark it as manageable for both handling and storage. The colorless-to-pale yellow crystalline appearance gives a direct confidence check, too. If you ever spent time in a lab, you know how much hassle off-color samples bring. Purity often tips above 97% in commercially available bottles, a level that cuts out hours of wasted purification and lets synthetic work move forward without detours. Such reliability isn’t just a selling point; it means deadlines get met and results hold up to peer scrutiny.
Many see pyridine rings as a foundation for pharmaceuticals and agrochemicals, and the 2-hydrazino substitution expands that toolbox. The hydrazino group swings into reactions that build hydrazones, pyrazoles, and various heterocyclic systems. These reactions form the backbone of a lot of custom molecule work, especially when the final goals tie to advanced drug design. In medicinal chemistry, tweaking the pyridine ring, especially at the 2-position, often leads to molecules with interesting bioactivity.
I recall a project with a team trying to dial up antimicrobial action by modifying pyridine scaffolds. We turned to 2-hydrazino derivatives for precise functionalization, crafting molecules with increased selectivity. These derivatives let synthetic chemists build in flexibility through subsequent transformations. Unreactive sites tend to cause bottlenecks in synthesis. By contrast, a hydrazino group opens space for diazotization or condensation, forging routes to novel ring systems without extensive protecting-group work. Cost and effort drop when a molecule offers such straightforward utility.
Not all pyridine derivatives pull their weight. Some substitutions, such as at the 3- or 4- position, change reactivity patterns or simply make downstream modifications a lot harder. For example, 2-amino-pyridine, while important for other uses, does not support the same suite of transformations as the hydrazino analog. The hydrazino group introduces more pronounced nucleophilic character and can participate in condensation reactions even under mild conditions. This makes pyridine, 2-hydrazino- an attractive pick for researchers who want to streamline the creation of more complicated molecules, cutting out repetitive or tricky steps.
From a practical standpoint, it also presents a lower risk of side reactions compared to derivatives with electron-donating groups elsewhere on the ring, which can result in unpredictable by-products. In multi-step syntheses—especially those headed toward sensitive applications—clean chemistry isn’t a luxury, it’s a necessity. My experience tells me that the fewer purification columns and analytical headaches you face, the faster discovery and scale-up both happen. In the pharmaceutical pipeline, each extra purification can add days or weeks to a project, stretching budgets and patience. A reagent that keeps reactions straightforward and pure offers more than a technical advantage—it can change the whole pace of development.
Organic chemistry has always been a balancing act between ambition and reality. Plenty of reaction schemes look great on paper, only to sputter out over scale-up problems or unexpected impurities. Pyridine, 2-hydrazino- entered my radar during a contract research stint. A team was synthesizing novel anti-inflammatory candidates, and finding a way to insert a pyrazole ring efficiently determined whether their work saw publication or wound up shelved. Commercial sources of 2-hydrazino-pyridine proved not only high in consistency, but amenable to scale, driving their patent application forward with weeks to spare.
Another feature worth noting: the straightforward solid form. Powders can sometimes give headaches over clumping or static, especially in humidity, yet pyridine, 2-hydrazino- tends to stay manageable. This practical aspect matters during scale-ups or academic group purchases. More than once, I watched savings evaporate as less stable reagents forced constant reordering due to degradation.
Across the research world, those working on fluorescent probes and new catalysts rely on the unique reactivity of the hydrazino group. Ultrasensitive detection assays for trace biomolecules sometimes turn to derivatives of 2-hydrazino-pyridine. These compounds, when derivatized, provide chromophore or ligand platforms unavailable from other structures. Having the right starting point, or “handle,” as my old mentor used to call it, opens doors to elegant solutions in diagnostics or environmental monitoring.
Lab work has grown more demanding both in quality expectations and safety awareness. Chemical purity is part of the story, but so is predictability in making by-products. Many common pyridine reagents suffer from instability under ambient air or light. Pyridine, 2-hydrazino- shows better shelf stability when stored with minimal moisture exposure, meaning less loss from spoilage. That helps keep project costs in line—a point that gets lost in the wave of paper specifications but never escapes the notice of those running the inventory.
Safety rules in chemical research are far tougher than a decade back. Pyridine derivatives often carry hazards due to toxicity or volatility. Pyridine, 2-hydrazino- isn’t a toy, but its handling profile, compared to chlorinated or nitrosated alternatives, proves less troublesome with proper care and fume hood protocol. The lower vapor pressure—unlike many low-molecular-weight amines—means you won’t be flooded endlessly with odors, and spills pose less of a risk for inhalation. Always wear gloves and goggles, keep your working area organized, and make a habit of keeping the MSDS within reach. Seasoned chemists tend to develop a sixth sense for trouble after a few lab mishaps, so younger scientists can benefit by learning from those stories on safety.
Waste management came front and center in recent years as universities and companies adopted greener chemistry standards. Hydrazine derivatives have faced regulatory scrutiny, so careful planning for disposal and neutralization is vital. My old lab started running satellite waste containers just for hydrazino materials, cutting the risk of accidental mixing that can trigger violent or noxious reactions. Researchers can work proactively with Environmental Health and Safety personnel, scheduling timely pickups and ensuring documentation covers the material’s full lifecycle. It saves time and headaches during audits.
Research organizations and commercial labs depend on steady availability of specialty reagents. Price swings and shortages in chemical markets throw a wrench into research budgets, especially for rare heterocycles or amine derivatives. Pyridine, 2-hydrazino- sometimes faces supply hiccups due to its specialized production routes, often reliant on precursor batch runs and vendor consistency. During a supply gap in 2021, I watched two synthetic projects stall out as teams resorted to either less effective stand-ins or makeshift synthesis from pyridine itself—a detour that cost weeks of effort and still left lingering doubts about product purity.
That experience drove our team to rethink vendor relationships. By building better communication with suppliers and confirming every batch with in-house NMR and HPLC checks, we avoided future hold-ups. For innovative companies, this highlights an ongoing need: reducing dependency on single suppliers and ensuring multiple routes to key reagents. Procurement folks would often joke about “hoarding season,” but in truth, smart stocking and batch verification outplay panic buying every time.
Reliable building blocks form the backbone of innovation. Pyridine, 2-hydrazino- plays an often unheralded but critical role in pushing boundaries, not just in medicinal chemistry, but also in crop protection, materials science, and analytical applications. The same functional group chemistry that makes it useful for pharmaceuticals carries over to dye manufacture and molecular probe design. Each industry rewards agility and reaction efficiency, goals made easier by reagents that deliver consistent results.
Looking across the literature, journals have chronicled the rise of substituted pyridines among modern reaction pathways—especially chemo-selective processes designed for high-value targets. 2-hydrazino derivatives offer a way to join functionality with ring systems that would otherwise require harsh reagents or complicated protections. I’ve heard more than once from process chemists that the best innovations arise not from flashy new reactions, but from everyday molecules that stand up under whatever load a team can throw at them.
Peer-reviewed studies consistently note the versatility of pyridine, 2-hydrazino-, especially in hydrazone and pyrazole synthesis. This backbone appears in fluorescence tagging molecules and cross-coupling partners for polymer chemistry. In teaching laboratories, introducing students to the practical aspects of using such compounds enhances their skill set and readiness for real-world problem-solving. The transition from theory to experiment often stumbles when tools lack reliability. Having reagents like pyridine, 2-hydrazino- in the teaching stockroom helps bridge that gap for young chemists.
The pace of chemical innovation makes the bedrock of reliable reagents like pyridine, 2-hydrazino- even more important. Supply chain turmoil during recent global events exposed the weaknesses of single-source dependencies. Chemists, purchasing officers, and R&D leads need to look at long-term supplier agreements and encourage local production where possible. Underserved regions might benefit from academic-industrial partnerships to scale synthesis of key molecules, making research less vulnerable to fluctuations in global logistics.
Sustainability considerations demand ongoing action. The synthesis and disposal of hydrazine derivatives must adopt best practices to limit environmental burden. Research groups—and especially large organizations—can develop protocols reducing waste and reusing solvents, or even reclaiming hydrazine intermediates before final disposal. Any move in that direction not only cuts costs but strengthens relationships with regulatory authorities, smoothing the way for future research endeavors.
In the classroom, educators can use pyridine, 2-hydrazino- as a case study for teaching both reaction mechanics and laboratory stewardship. By guiding students through the practical choices that come with using, storing, and disposing of specialty reagents, a new generation of scientists builds not just skills but a responsible outlook. These lessons translate straight into research jobs, making graduates better prepared for industry or academia alike.
Why do researchers favor this compound over other pyridines?
It comes down to reactivity, predictability, and adaptability in synthesis. My projects saw more robust yields and less troubleshooting when starting from well-characterized batches of 2-hydrazino-pyridine, especially during multi-step sequences. Other positional isomers simply didn’t provide the same platform for hydrazone or pyrazole construction, resulting in laborious workarounds.
What are best practices for handling and storage?
Secure the reagent in a tightly sealed container, away from excess moisture and light. Standard chemical safety applies: gloves, goggles, and proper fume hood use are musts. For labs dealing with high throughput or long-term storage, invest in desiccators or inert-atmosphere storage cabinets. It saves hassle down the road by preserving sample quality.
How does scale-up typically affect workups or purification?
Scaling reactions often exposes flaws in small-scale protocols. With pyridine, 2-hydrazino-, the solid form stays manageable, and consistent melting points help confirm identity after synthesis or recrystallization. TLC, HPLC, and NMR remain best for tracking purity during both bench-scale and kilo-scale runs. Checking each batch saves headaches if a reaction stalls or stray by-products crop up.
No chemical product exists in a vacuum. Pyridine, 2-hydrazino- holds its place not through fancy marketing but by throwing its weight behind dependable outcomes in sensitive research. Its rise in utility tracks the larger trend of chemistry toward targeted modifications and responsible lab practice. Each year, research pushes for more sustainable, efficient, and economically viable syntheses—and compounds like this one prove that even century-old scaffolds can find new life when steered by practical experience.
By embracing practicality, teamwork, and steady communication between laboratory, sourcing, and safety staff, research groups can ensure this versatile reagent delivers both value and progress. As the field evolves, so too will the standards by which these core building blocks are judged—not just by their specs or price tag, but by the degree to which they enable discovery, learning, and responsible stewardship of resources in the lab and beyond.