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HS Code |
334175 |
| Iupac Name | N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide |
| Molecular Formula | C13H10N4O2 |
| Molecular Weight | 254.25 g/mol |
| Cas Number | 89856-97-9 |
| Appearance | White to off-white solid |
| Melting Point | 268-272 °C |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 10 grams of N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide, labeled with chemical name and safety information. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide ensures secure, moisture-proof, and efficient bulk chemical transport. |
| Shipping | *N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide* is shipped in secure, airtight packaging to prevent contamination and moisture exposure. It is transported under ambient conditions unless otherwise specified, adhering to all relevant chemical safety regulations. Proper labeling, documentation, and MSDS are included to ensure safe and compliant delivery. |
| Storage | **Description:** Store N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide in a tightly sealed container, protected from light and moisture. Keep at room temperature (approximately 20–25°C) in a dry, well-ventilated area designated for chemicals. Avoid exposure to strong acids, bases, and oxidizing agents. Always follow general chemical safety protocols and reference the compound’s Safety Data Sheet (SDS) for detailed handling and storage guidance. |
| Shelf Life | Shelf life of N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide is typically 2-3 years if stored cool, dry, and protected from light. |
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Purity 98%: N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide with a purity of 98% is used in high-throughput drug discovery assays, where consistent purity ensures reproducible biological activity data. Melting Point 227°C: N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide with a melting point of 227°C is used in medicinal chemistry synthesis, where its defined phase transition supports thermal stability during reaction processes. Molecular Weight 270.27 g/mol: N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide with a molecular weight of 270.27 g/mol is used in structural analysis for ligand design, where accurate molecular mass enables precise computational modeling. Particle Size <50 μm: N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide with particle size less than 50 μm is used in solid-phase formulation development, where fine particle distribution promotes homogenous mixing and dissolution. Solubility in DMSO 10 mg/mL: N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide with solubility in DMSO at 10 mg/mL is used in in vitro assay preparation, where high solubility ensures concentrated and uniform test solutions. Storage Stability at 25°C: N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide with storage stability at 25°C is used in chemical library stockpiling, where ambient stability reduces degradation and simplifies handling logistics. |
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Talking about N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide in our plant, most of the team refers to it simply as “the pyridine double hydrazide.” This compound takes shape from our long-standing work with aromatic heterocycles and hydrazides, two families that surface across pharmaceutical and specialty chemical projects. The structure links two pyridine rings with a carbohydrazide bridge, giving it both symmetry and versatility. Unlike simpler hydrazides that often face solubility or stability issues, this molecule comes with an extra aromatic backbone, making it much more robust in some demanding conditions.
We developed our synthesis route around solid-phase purification steps because we found early that controlling even tiny impurities—unreacted hydrazide or over-oxidation byproducts—became essential for reliable downstream performance. The purity spec we aim for hovers near pharmaceutical standards, not only because our main users expect it, but because we noticed side reactions in catalysis when purity drifts lower than 98 percent. This is a non-trivial decision; running several rounds of crystallization or column work means a real investment in time and solvents. Yet in hands-on feedback from research teams, especially those working on cross-coupling and hydrazone formation, we kept hearing that clean starting material paid off in reaction reliability and interpretability.
Most orders call for gram to multi-kilogram batches, packed in glass or HDPE containers, sealed from moisture and oxygen. Internally, we store it at controlled temperature to keep any degradation at bay. Based on our own long-term stability checks, unchanged samples kept for over a year show retention of purity above 96 percent when sealed, and no change in melting point—a sign degradation isn’t a major risk with our process.
Clients using it for chemical synthesis routinely request documentation about residual solvents, inorganic ions, and heavy metals. We routinely supply residual solvent numbers, and after a hard-learned incident where one batch showed minor chloride pickup, all product now sees a final ion-exchange clean-up step. Analytical data—NMR, LC-MS, IR spectra—comes from in-house runs, not copied certificates. We run these not only to check quality but out of pride; when a senior chemist reported new crystal forms in samples from our partner lab, it kicked off months of study, but underscored the variation that can surface across suppliers who overlook material consistency in pursuit of quick output.
Synthetic chemists ask for this compound because of its coordinating ability and structural duality. The double pyridine motif isn’t just aesthetic; it often anchors transition metal ions more reliably than simpler hydrazides. From years of collaborating with medicinal chemistry groups, we’ve seen this molecule become a staple linker in bifunctional scaffolds, where it serves to connect drug-like molecules in fragment-based design. Its rigid backbone resists hydrolysis, helping downstream partners keep their products shelf-stable during lengthy biological testing.
In some projects, customers point to the molecule’s use as a slow-release agent or masking group for hydrazine moieties. These applications only function when the initial material handles ambient conditions without breaking down. From our own exposure tests, short bursts of humidity or brief exposure to open air don’t change the compound’s mass or NMR profile, which supports these claims made by university and pharma labs. Time after time, we’re reminded of how critical real-world handling studies are—a paper spec sheet never shows you what actually happens on the bench.
Workhorse hydrazides—like isonicotinic or nicotinic hydrazides—have their place in routine organic transformations, but we noticed they often compromise on electronic properties, or polymerize if stored poorly. Some hydrazides will start yellowing or sticking in the bottle after a few weeks, signaling breakdown. With the N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide backbone, we rarely see that, even in intermediate humidity. In feedback from specialty polymer researchers, the symmetry of the molecule and its combined electron-withdrawing and -donating capabilities opens up more nuanced reactivity. For anyone developing organometallic complexes or tuning hydrazones for photophysical research, this structural duality allows them to push their systems further.
Because both pyridine rings sit in defined orientations, the molecule lines up perfectly for directional bonding with metals or with coordinated anions. Less symmetrical hydrazides simply can’t do this. This aspect matters when teams are developing sensors or molecular devices needing precise geometry. If the structure shifts, even subtly, downstream yields drop or device performance weans. We’ve helped teams troubleshoot issues that traced back to poor lot-to-lot consistency from alternate sources. Examining melting point and NMR vs. our reference lots, the culprit often turned out to be isomer impurities—which never leave our plant, thanks to direct hands-on oversight every step.
There’s no shortcut in controlling moisture and temperature throughout production. We’ve learned this the hard way: an uptick in ambient humidity or slightly off-drying can cause batch caking and tougher downstream filtration. Our process involves gentle drying, quite unlike some high-heat protocols that risk altering subtle structural features. Inconsistent crystallization can trap solvent, so keeping the crystallization conditions tight is part of our standard drills. If there are ever batch oddities—discoloration, flow issues—we pull samples and analyze right at the production line rather than waiting for offsite testing. This shaves days off getting answers and keeps problems contained.
Frequently, researchers come calling not about the compound’s molecular weight, but about their difficulties reproducing published results using off-the-shelf samples. Stability in solution plays just as large a role as raw analytical numbers. For teams working in DMSO, DMF, water or THF, our trials indicate that “the pyridine double hydrazide” not only dissolves predictably, but remains clear without precipitating out or yellowing for several days. We run stability tests under variable light and atmosphere—reflecting real operations, not laboratory idealizations—because a researcher’s bench is rarely airless or perfectly dry.
Producing this molecule on a meaningful scale involves careful solvent selection. As regulations change, dichloromethane and similar solvents face deep scrutiny. We spent significant time shifting our process to minimize hazardous waste output, switching purification columns to less toxic fluids, and recycling solvents where possible. While the initial price of eco-friendlier operations appears high, less solvent lost as hazardous waste cuts recurring costs, and meets the evolving environmental standards from both governmental agencies and major clients. Anecdotally, shipments to customers in Western Europe and East Asia now come with requests for solvent usage documentation, even when not required by law.
Our internal QA protocols align with major pharmacopeia recommendations. With the world now eyeing residual impurities, mutagenicity and process byproducts, the pressure builds to let nothing slip. We have had customers—from start-up research outfits to established pharmaceutical firms—send their own auditors or request process walkthroughs. This transparency pays off, as repeat buyers want assurance from the source, not via a chain of resellers. Our audit history supports our claim: technical questions or site visits don’t cause alarm, since every staffer from process engineer to analytical chemist can retrace each step of a given batch.
Every new customer brings different requirements, sometimes outside the standard purity or packing conventions. For one group developing diagnostic devices, particle size distribution made a noticeable impact, so our plant ran targeted grind and sieve steps, then confirmed particle size by laser diffraction. Others ask about custom labeling or barcoding to match their digital inventory. These may sound small, but they trace back to practical needs that only emerge through honest conversations with those working at the bench level. Direct dialogue beats a generic webform or middleman channel every time.
For large-scale users in pharmaceutical R&D, our analytical support extends past what’s printed on a COA. If a new impurity pops up during their own scale-up, we keep communication real and open, sharing intermediate fractions and analytical profiles to troubleshoot together. Years of producing similar heterocyclic hydrazides has made us nimble—if new application data emerges, we offer samples for bench trials, so users decide suitability for their precise circumstances.
Pharmaceutical teams often need linkers or scaffolds able to withstand both solution and solid-phase steps. Some use N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide to anchor bifunctional molecules, connecting two distinct payloads with a chemically stable and easily cleaved bridge. Others exploit its coordination chemistry, where the molecule complexes with metals—serving as a platform for catalytic or sensor design. In some cases, we supply specialty lots with isotopic labels for mechanistic studies or bioanalytical tracking. Not every plant can manage this; our team spent years refining reaction conditions that allow for isotope integration without dropping purity.
Chemical education programs also draw on our material for student training. One notable course used our product while teaching multistep synthesis, reinforcing practical lessons about workup, purification and crystallization. Academic groups value hands-on documentation—stepwise NMR and purity tracking—using lots prepared expressly for teaching, not just routine. It’s a small but real contribution toward upskilling the next generation of chemists.
Scaling this molecule isn’t just about running a larger reactor. Side reactions creep in, heat transfer issues become pronounced, and reaction quenching runs longer than in a one-liter flask. We invested in stirred-tank reactors with real-time temperature feedback, and fine-tuned dosing sequences for reagents. This gives a cleaner product right off synthesis, needing less downstream work. Teams on the floor know that small hiccups—line clogs, pump instability, drift in pH—can snowball into yield drops or purity loss. Our practice involves documenting every deviation and rapid response to minimize knock-on effects.
Loaders and packing crew encounter another challenge: some hydrazides powder easily, but others, including ours, compact unpredictably. Poor powder flow triggers packaging headaches and safety flags. Through trial, we figured out ambient controls that keep material free-flowing, avoiding clumps or dust that might escape containment. We introduced gentle vibration and humidity control in the fill stations to maintain both worker safety and product usability on delivery.
Direct feedback from chemists shapes how we produce and supply N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide. Returning customers often highlight real-world differences they experience between batches from various sources: changes in appearance, batch handling, or even reaction behavior. By collecting and comparing input from both established pharmaceutical groups and start-up research teams, we tailor our process to close the loop on recurring technical needs. Adjustments to crystallization protocols, tweaks to drying phases, and direct support during application troubleshooting form part of an ongoing dialogue—not a one-off improvement.
On multiple occasions, clients have referenced publications that call attention to tiny impurities or new application data, asking for more detailed batch analytics or testing under yet-untried conditions. As a manufacturer that supports innovation, we routinely set aside R&D runs for custom requests, handling small pilot batches for laboratories wishing to branch into new reaction space. Our on-floor chemists and analysts engage in the lab-scale runs, providing notes and troubleshooting insights to optimize the process step by step.
Ordering directly from the maker means skipping the uncertainty that often sneaks in with third-party re-packagers. Every inquiry lands with staff who actually run the reactors and manage packing, giving direct answers rather than generic quotes. All handling instructions, storage advice, and custom modifications build from lived experience, not distant sales scripts.
The difference stands out during out-of-spec events or urgent requests. When a research team contacted us needing an expedited shipment with tailored moisture controls, we walked the order down the line, tracked drying in real time, and packed under nitrogen flush. This led to a repeat order and rare gratitude from an otherwise skeptical end-user. These moments highlight the difference brought by producers who directly shape both the process and delivery, bridging the gap between industrial-scale consistency and research-level adaptability.
Years in chemical manufacturing have taught us that every molecule, especially specialized compounds like N'-(pyridin-4-ylcarbonyl)pyridine-4-carbohydrazide, stands or falls on the details—both in production and in use. Working closely with end-users, scrutinizing each production step, and committing to transparent communication, we build partnerships around more than just product delivery. This approach not only moves chemistry forward for our customers but pushes our own skills and standards higher, reinforcing the link between genuine experience and the highest quality compound the market demands.