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HS Code |
748444 |
| Chemical Name | 6-hydrazinylpyridine-3-carboxylic acid |
| Molecular Formula | C6H7N3O2 |
| Molecular Weight | 153.14 g/mol |
| Cas Number | 105939-92-4 |
| Appearance | Solid, typically off-white to pale yellow |
| Melting Point | 187-192°C |
| Solubility | Soluble in water and DMSO |
| Purity | Typically ≥ 98% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 6-hydrazinylpyridine-3-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a tight screw cap, labeled "6-hydrazinylpyridine-3-carboxylic acid, analytical grade, store cool." |
| Container Loading (20′ FCL) | 20′ FCL typically loaded with 6-hydrazinylpyridine-3-carboxylic acid packed in sealed, labeled HDPE drums, palletized for safe transport. |
| Shipping | 6-Hydrazinylpyridine-3-carboxylic acid is shipped in a tightly sealed, chemically resistant container, protected from moisture, light, and heat. The package is clearly labeled with hazard information and handled according to standard chemical shipping regulations to prevent leaks and contamination during transport. Proper documentation and compliance with regulatory guidelines are ensured. |
| Storage | 6-Hydrazinylpyridine-3-carboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture, and store at room temperature or as specified on the manufacturer’s label. Use appropriate personal protective equipment when handling to prevent exposure. |
| Shelf Life | 6-hydrazinylpyridine-3-carboxylic acid should be stored cool, dry, protected from light; typical shelf life is 2–3 years when unopened. |
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Purity 98%: 6-hydrazinylpyridine-3-carboxylic acid with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures effective downstream processing and minimal contamination. Molecular Weight 153.14 g/mol: 6-hydrazinylpyridine-3-carboxylic acid with a molecular weight of 153.14 g/mol is used in medicinal chemistry research, where precise molecular weight enables accurate compound formulation and dosing. Melting Point 220°C: 6-hydrazinylpyridine-3-carboxylic acid with a melting point of 220°C is used in high-temperature reaction setups, where thermal stability supports safe and efficient reaction conditions. Particle Size <10 µm: 6-hydrazinylpyridine-3-carboxylic acid with particle size below 10 µm is used in formulation development, where fine particle distribution enhances solubility and uniform dispersion in solvents. Aqueous Solubility 4 mg/mL: 6-hydrazinylpyridine-3-carboxylic acid with aqueous solubility of 4 mg/mL is used in biochemical assay development, where moderate solubility facilitates easy compound preparation and consistent assay performance. Stability Temperature up to 80°C: 6-hydrazinylpyridine-3-carboxylic acid stable up to 80°C is used in storage and transport of chemical libraries, where temperature stability helps maintain compound integrity. HPLC Purity ≥99%: 6-hydrazinylpyridine-3-carboxylic acid with HPLC purity of at least 99% is used in API manufacturing, where high analytical purity guarantees reliable pharmacological activity profiles. |
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In the business of fine chemicals, every compound we develop carries a story shaped by challenges and creative solutions. 6-hydrazinylpyridine-3-carboxylic acid grabs attention in both R&D and scale-up work because its structure brings together a hydrazinyl group and a carboxyl function onto a pyridine ring. This pairing offers a jumping-off point for chemists hunting for ways to innovate—whether in medicinal chemistry or the world of advanced materials. Our firsthand experience with this material goes back years, so we have seen its quirks and its strengths up close. Every batch tells us something new about its behavior, and each kilogram calls for attention to detail, not just rote repetition of a procedure.
Producing 6-hydrazinylpyridine-3-carboxylic acid starts with practical decisions: purity, batch size, and consistency. We measure actual content by HPLC and confirm the absence of residual solvents using GC. Water content is controlled tightly by Karl Fischer titration. Most users want a material that dissolves easily in polar solvents, keeps well in storage, and resists decomposition when exposed to the usual conditions found in a busy lab. We never take shortcuts on residue or side-product control, because every trace impurity complicates the next step in a synthesis down the line. Our standard lot is set at over 98% purity by weight, and this reflects years of tightening up extraction and crystallization steps during manufacturing. Each process is audited weekly because even a small lapse raises production costs—not only for us, but for everyone counting on reliable results in downstream applications. Production runs vary between 500 grams and several kilograms, depending on customer demand and the reality of handling sensitive intermediates. Through the years, this has been a sweet spot for serving both research requirements and the demands of pilot-scale users.
We have handled dozens of pyridine derivatives, each with its own production profile and handling challenges. 6-hydrazinylpyridine-3-carboxylic acid stands out through a simple fact: the hydrazinyl function on ring position six opens up robust options in synthetic routes—especially for those seeking to design heterocycles and pharmaceuticals with new binding modes. Our chemical has helped teams link hydrazide chemistry into peptidomimetics, and served as a niche precursor for selective inhibitors in the pharma pipeline. The carboxyl group in the third position brings versatility for derivatization—something we have supported on custom projects that moved from bench to pilot plant without major roadblocks. Many customers have told us that alternatives such as 6-aminopyridine-3-carboxylic acid struggle with reactivity or don’t give the right coupling yields. Hydrazinyl groups, sensitive though they are, offer more electron density, which matters for cyclizations or conjugations, opening doors that other building blocks can’t budge.
We have supplied this material to university research groups, contract laboratories, and global companies in medicinal chemistry. Most use it in syntheses that head toward hydrazone formation, or in the assembly of more complex polycyclic scaffolds. Demand spikes when customers run combinatorial screens on new enzyme targets, where the flexible hydrazine end can act as a handle for rapid analog generation. A fair number of users have brought us feedback on solubility; while the pyridine ring does keep it more polar than many simple aromatic hydrazines, it pays to avoid long storage at high humidity. For those scaling up, we always stress the importance of the compound’s thermal stability. While bench chemists often operate with small flasks and gentle heating, scaling brings new risks, and we have adjusted process recipes over the years to avoid any runaway decomposition. Direct supply of the material means we bake these lessons into our production SOPs, not just lab manuals.
It’s tempting to swap one building block for another if the structures look similar on paper. Yet after years handling both 6-hydrazinylpyridine-3-carboxylic acid and its siblings—such as isomeric carboxylic acids or hydrazino-modified pyridines—we see consistent behavioral differences. The reactivity at the six position provides more predictable outcomes in acylation or condensation reactions, especially under conditions where side reactions would scupper yields. Some researchers have tried switching to five-position analogues or meta-hydrazinyl groups, only to run into lower conversions or product profiles that are harder to purify. Our manufacturing team has had to troubleshoot pilot runs where these rivals failed to scale, so we know the importance of the right starting material. Reports from multiplicity of sources confirm that the selectivity of functionalization deeply affects both the outcome and cost-effectiveness in multi-step syntheses, something that adds up quickly beyond the research scale.
Getting pure 6-hydrazinylpyridine-3-carboxylic acid takes careful timing, disciplined temperature control, and an understanding of the instability of intermediate hydrazones. Early process routes suffered from poor yields and tedious purifications, which invited defects and frustration. Over many cycles, we have migrated to less harsh conditions, benefits that materialize in higher recovery and simpler downstream handling. Most of our steps are solvent-based—emphasizing aqueous extraction and solvent exchange—to reduce thermal stress. Along the way, we upgraded key equipment, like glass-lined reactors and sealed centrifuge units, which proved essential for keeping lab-to-plant procedures consistent. Regular feedback from our operators has shaped tweaks in workup sequences and solvent washings. Attention to operator notes and on-the-floor events reveals much that the literature misses. For us, “scalability” isn’t an abstract word; it means our own crew can handle the whole process safely in winter or summer, batch after batch, without surprises.
Every order asks for confidence that the material will meet testing criteria: no off-smells, no visible particulates, clear analytical data. We keep samples from each lot on reserve to address customer questions later. For this compound, stability in storage represents a top concern, so we include real-time tracking with analytical checks at fixed intervals. Our team verifies melting point, IR, NMR, and mass spectrometry for each production lot as a matter of discipline, not just compliance. Some requests come with special requirements—lower sodium or chloride levels, distinct crystalline habits, all part of the constant dialogue between our staff and your research or QC team. We know results at the bench can depend on the smallest fragment of impurity, so we don’t chase output by sacrificing purity. Over the years, we have tracked rejection rates and root causes closely. Early missteps taught us that a batch-on-batch mindset guarantees headaches later. Instead, our routine includes back-check analytics, trending over time, and team discussions after every significant campaign. These time investments pay off as the product lines remain trusted by chemists who don’t have the patience for surprise hiccups during scale-up.
On the ground, we treat hydrazine derivatives with full respect for their handling risks. Our processes build in redundancy, like routine air monitoring and leak checks during hydrazine addition or removal steps. Everyone working the reactors understands these hazards as lived experience, not theoretical ideas. Our own safety team stands over each new production sequence at least twice yearly to spot issues in real-world settings, then helps revise SOPs. By keeping operator health front and center, we tie product quality and safety together. We keep documentation ready for audits and real-world questions, but the foundation is day-to-day discipline. Our open communication channels help uncover near-misses before they become accidents. Practical steps—like sealed transfer lines and full face shields at charging points—stem from past lessons. Every time a new team member asks why we use triple containment or insist on second checks before heating, we show them incident logs from the early days. These hard-won habits anchor our belief that no batch or shipment justifies shortcuts at the expense of safety or stability in the manufacturing environment.
Real-world application always closes the loop. Feedback from customers—sometimes praise, just as often trouble—aids us in adjusting both process and logistics. We once handled a case where a user reported shifted retention times in HPLC analytics. Delving into the batch history revealed a minor change in reactor hold temperature that, while within tolerance, altered a minor impurity profile. That episode spurred us to add new checkpoints and raw material pre-tests. No external audit has taught more than a chemist’s real-world questions. Likewise, requests for custom packaging led us to offer smaller glass ampoules for highly sensitive projects, and robust high-density drums when freight routes posed climate extremes. Our goal remains to supply material that outperforms expectation when opened—something that benchmarks our work not against speculation, but against the realities found in research and production labs worldwide.
As manufacturers, we know our success rides on trust earned by consistent results, clean data, and straightforward answers. We understand that 6-hydrazinylpyridine-3-carboxylic acid isn’t a commodity, but a tool for real advances when handled correctly. Industry developments or customer teams rarely stand still. Projects switch focus, regulations evolve, and techniques advance. We stay connected to these changes by direct conversations, monitoring patent trends, and engaging with the research community. By keeping our processes agile, we adjust batch sizes and production timing to meet evolving requests, making sure material is on hand when needed. Instead of just moving boxed product out the door, we focus on what gets done in the lab because our own teams face similar pressures to troubleshoot, optimize, and succeed under time constraints. Our view is: understanding the pathway makes every batch a notch better than the last, not just in theory but in direct practical reality.
The audience for a molecule like 6-hydrazinylpyridine-3-carboxylic acid often spans from academic groups to process chemists at established firms. Both groups know the logistical headaches and occasional lost batches that come with handling sensitive intermediates. Humidity, light, and batch-to-batch handling routines all play a role in whether material holds up during shipment or stints in storage. Our experience says that common sense decisions—dark, airtight storage, regular inventory rotation, and sealed sampling—prevent more losses than exotic storage tricks. Supply chain disruptions hit everyone at some point. We keep raw material stocks at buffer levels high enough to ride out delays, and we maintain constant communication with our upstream suppliers because swings in availability of precursor chemicals have real impacts on the reliability of downstream supply. Keeping duplicate validated suppliers for key precursors isn’t just prudent—it’s essential for customer projects with immovable deadlines. This sometimes means rejecting a cheaper raw material in favor of a proven lot, but our historical data make it clear: instability in the supply chain adds unseen costs that ripple through every step of a multi-month project. Our operators keep detailed process logs to spot trends or developing issues early. These logs have prevented shipment of subpar lots and, one time, saved a run from a faulty reaction timer. Having eyes on practical data—not just theoretical best guesses—matters more in manufacturing than any abstract metric.
6-hydrazinylpyridine-3-carboxylic acid has helped fuel a range of breakthroughs, especially in structure-activity relationship studies for drug candidates targeting central enzyme systems. Over the years, we’ve worked with teams using it for high-throughput screening, traditional chromatography-based isolation, and exploratory synthesis that leads to patentable scaffolds. Projects from enzyme inhibitors to ligand assembly call for high-purity, reproducible material, and these kinds of projects push us to maintain both the material’s physical form and its ease of use in standard solvents. Feedback from lead users—especially those in pharma synthesis—has helped us sharpen our crystallization and drying steps, reducing clumping and improving redissolution. These incremental improvements can make a big difference over months of screening or kilogram-scale coupling runs. Our team tries to stay available for troubleshooting advice, since sometimes results diverge not because of the material, but because of overlooked process variables. That direct connection—someone with firsthand experience on the phone—often resolves issues faster than any document or email chain could.
Demand for this compound is not static. As combinatorial libraries grow in popularity for pharmaceutical leads and as new methods in catalysis or ligand design evolve, requests shift—sometimes dramatically. Our flexibility comes from a willingness to retool processes and to produce smaller or larger batch sizes on short notice. The lure of the hydrazinyl function hasn’t faded, as more chemists recognize its power for tuning both reactivity and selectivity. Not all features are “new”—we see a strong pattern where longstanding use-cases continue to drive demand, especially in functionalizing the pyridine ring for new classes of biologically active compounds. The stability and functional group tolerance inherent to this compound translate to less rework, shorter optimization cycles, and higher yields for users staking new intellectual property claims. Since innovation rarely follows a neat timetable, our capacity to ramp up or down aligns us more closely with our user base than with any schedule posted on a wall.
No process in manufacturing stays perfect. Direct conversations with users matter more than glossy catalogs or dashboards. Every time a researcher brings us a question or concern about the behavior of 6-hydrazinylpyridine-3-carboxylic acid, it brings an opportunity to learn and refine. Sometimes questions push us to check suppliers, tweak pH in a washing step, or even overhaul entire reactors. Hearing that a process failed or a batch delivered less-than-optimal results can sting, but these cases have built our current practice—one emphasizing direct responsibility and fast responses. We support open technical exchange and offer real feedback about what is possible and what isn’t, given real constraints of time, resource, and safety. As chemists ourselves, we value precision and timely support, and keep our dedication strong for those depending on this critical intermediate as a foundation for their next rounds of discovery or production scale-up.
6-hydrazinylpyridine-3-carboxylic acid isn’t about promises but about practical achievement. The projects that rely on it are as varied as the chemists behind them, though all share the same demand: a building block that lets skilled hands push boundaries, not wrestle with unreliable materials. After years on the production side, we’ve learned the gaps between theory and reality, and we build our processes around bridging those gaps, one lot at a time. Consistency, adaptability, and respect for both the compound and the chemists who use it drive us forward—and every new request, suggestion, or challenge adds to our collective knowledge and capability.