|
HS Code |
558786 |
| Chemical Name | 3-Pyridinecarboxylicacid,6-Hydrazino- |
| Cas Number | 20758-41-2 |
| Molecular Formula | C6H7N3O2 |
| Molecular Weight | 153.14 g/mol |
| Iupac Name | 6-hydrazinonicotinic acid |
| Appearance | Solid, powder |
| Melting Point | 259-261°C |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
| Pubchem Cid | 38238 |
| Smiles | NNc1ccc(C(=O)O)cn1 |
| Inchi | InChI=1S/C6H7N3O2/c7-9-5-2-1-4(6(10)11)3-8-5/h1-3H,(H2,7,9)(H,10,11) |
| Density | Unavailable |
| Synonyms | 6-Hydrazinonicotinic acid, 6-Hydrazino-3-pyridinecarboxylic acid |
As an accredited 3-Pyridinecarboxylicacid,6-Hydrazino- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging contains 25 grams of 3-Pyridinecarboxylicacid,6-Hydrazino-, sealed in an amber glass bottle with a secure screw cap. |
| Container Loading (20′ FCL) | 20′ FCL container loading: 3-Pyridinecarboxylicacid,6-Hydrazino- packed securely in drums or bags, maximizing space for safe transport. |
| Shipping | Shipping of 3-Pyridinecarboxylicacid,6-Hydrazino- requires secure, leak-proof packaging to prevent moisture and contamination. The substance should be labeled as a chemical compound, transported according to International Air Transport Association (IATA) and local regulations, with appropriate documentation. Handle with care, avoiding direct contact and exposure to extreme temperatures during transit. |
| Storage | **3-Pyridinecarboxylicacid, 6-Hydrazino-** should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Store at room temperature and ensure proper labeling to avoid accidental misuse. Use appropriate personal protective equipment when handling. |
| Shelf Life | **Shelf Life:** 3-Pyridinecarboxylicacid, 6-hydrazino- typically has a shelf life of 2–3 years if stored in a cool, dry place. |
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Purity 98%: 3-Pyridinecarboxylicacid,6-Hydrazino- with a purity of 98% is used in pharmaceutical intermediate synthesis, where it enables high product yield and consistent chemical reactivity. Melting Point 260°C: 3-Pyridinecarboxylicacid,6-Hydrazino- with a melting point of 260°C is used in high-temperature coupling reactions, where it ensures thermal stability and reliable conversion rates. Molecular Weight 165.16 g/mol: 3-Pyridinecarboxylicacid,6-Hydrazino- with a molecular weight of 165.16 g/mol is used in heterocyclic compound construction, where precise mass balance and reaction efficiency are necessary. Particle Size <50 µm: 3-Pyridinecarboxylicacid,6-Hydrazino- with particle size below 50 µm is used in solid-phase synthesis, where it provides enhanced solubility and reaction uniformity. Stability Temperature 120°C: 3-Pyridinecarboxylicacid,6-Hydrazino- with stability up to 120°C is used in controlled temperature processes, where it minimizes degradation and maintains compound integrity. HPLC Purity ≥99%: 3-Pyridinecarboxylicacid,6-Hydrazino- with HPLC purity of at least 99% is used in analytical applications, where it ensures accurate quantification and minimal interference from impurities. Water Content ≤0.5%: 3-Pyridinecarboxylicacid,6-Hydrazino- with water content no more than 0.5% is used in moisture-sensitive syntheses, where it prevents hydrolysis and increases the reliability of reactions. Assay ≥98%: 3-Pyridinecarboxylicacid,6-Hydrazino- with an assay of at least 98% is used in custom organic ligand development, where high assay supports optimal chelating agent performance. Storage at 2–8°C: 3-Pyridinecarboxylicacid,6-Hydrazino- stored at 2–8°C is used in research laboratories, where controlled storage conditions preserve product stability for extended experimental timelines. Solubility in DMSO >10 mg/mL: 3-Pyridinecarboxylicacid,6-Hydrazino- with solubility in DMSO greater than 10 mg/mL is used in solution-phase screening, where high solubility accelerates dissolution and sample preparation. |
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Out on the blending floor, our team handles raw intermediates every day. Among them, 3-Pyridinecarboxylicacid,6-Hydrazino- stands out due to its structural quirks and the flexibility it brings to advanced synthesis routes. My own experience goes back to our first small-scale batch, where its pale solid appearance quickly attracted queries from neighboring labs. Compared to many aromatic derivatives, this compound combines the pyridine backbone with a reactive hydrazino group at the 6-position, granting it a distinct place in our lineup.
Within our facility, every model lot undergoes detailed process analysis. Our typical production output targets a purity above 98%, confirmed via HPLC and NMR. Crystallinity matters—our in-house crystallization minimizes batch-to-batch variability. Specifics such as melting point, solubility in methanol, and spectral signatures form the backbone of quality control. We package it in moisture-resistant containers to avoid hydrolysis or unwanted condensation, an approach shaped by several seasons of field feedback.
The reactivity profile in our hands never fails to impress. The hydrazino group, oriented at the 6-position on the pyridine ring, opens opportunities for downstream coupling and cyclization reactions that a classic 3-pyridinecarboxylic acid simply does not provide. We form this intermediate using controlled hydrazinolysis, stopping short of overreaction—a technique honed through dozens of optimization cycles.
Walk through our pilot plant and you’ll hear stories of missed yields and eventual breakthroughs. Chemists value this compound during API synthesis. We've worked with research groups turning it into triazoles and larger bioactive frameworks. Unlike generic pyridine acids, the hydrazino substitute acts as an anchoring point for preparing hydrazones—versatile partners in medicinal chemistry. The compound’s performance in condensation reactions allows us to streamline complex builds, shaving days off projects that once dragged on.
Several agrochemical clients ask us for stable hydrazine derivatives. They tell us other intermediates lack the same versatility. We produce tailored batches for those seeking to develop new pest management agents, focusing on the efficiency of the coupling step. In our direct work with formulation scientists, the differences become obvious: competitors’ analogues might falter under higher temperatures, or bring in traces of residual solvents. Our solvent-free approach eliminates these setbacks, giving end users complete freedom to take their synthesis further.
Most chemistry teams approach us after struggling with standard pyridinecarboxylic acids. The 6-hydrazino variant solves issues at multiple points. The classic version often restricts downstream transformation. In our flows, the extra hydrazino group means fewer synthetic steps. Reduction and cyclization run cleaner, with fewer byproducts. In contrast to substituted hydrazino-benzoic acids, our compound delivers both the aromatic nitrogen and carboxyl functionality, producing more robust scaffolds.
We sometimes see confusion over nomenclature—customers try to match product specs with purely numerical codes. One lesson from experience: structure matters more than labels when scaling up. During comparative trials, we observed that aromatic hydrazines lacking a carboxyl group require more aggressive conditions for condensation with aldehydes or ketones, creating purification headaches downstream. Here, the carboxyl handle on the pyridine ring improves reaction control and final isolation.
Traditional pyridines also lose their edge in ligand development. The attached hydrazino group enables direct introduction of functional moieties that enhance metal binding or electronic properties. Our compound provides a shortcut where alternative building blocks call for protecting group strategies, which draw out project timelines and inflate costs. By enabling direct attachment, it supports more efficient ligand synthesis, valued by both universities and specialty catalyst developers.
One hallmark of our operation lies in hands-on oversight. Small tweaks in reaction atmosphere or temperature impact yield consistency. For the 3-Pyridinecarboxylicacid,6-Hydrazino-, humidity during storage becomes critical. Our storage team learned early to add dessicant packs after noticing trace hydrate formation in summer conditions, which customers flagged as melting point anomalies. Adjustments like these, gathered through real-world use, give working chemists more reliable starting points.
We also uphold rigorous documentation. Every batch record keeps a detailed timeline, from raw hydrazine source validation up to packed product. We learned not to underestimate the influence of hydrazine purity on downstream stability—seemingly small changes in input quality altered final color and reactivity. Long before regulatory guidance obliged, we adopted full trace records and retained samples. This gives our customers confidence during audits and regulatory filings, especially those pursuing pharmaceutical approvals.
Our partnerships with analytical labs fostered trust: compounds like this cannot sell on price alone. End users call in with application concerns, and we dig out archived spectra or batch notes to troubleshoot. In one case, an impurity signature traced back to a supplier shift; after realigning our sourcing, we closed the door on that issue. These moments underscore the impact of steady hands and open communication in specialty intermediate manufacturing.
R&D teams frequently reach out for guidance on scaling up from milligram discovery lots to multi-kilo runs. Early on, they discover that model responses in a 10 mL flask might diverge from kilo-scale reactors. We run pilot batches on matched reactors before suggesting parameters. Our engineers assist with heat transfer and mixing aspects, particularly important given the exothermicity of hydrazino group introduction.
We see researchers in crop protection, pharmaceuticals, and new material design draw on this compound’s reactivity. Many clients use the hydrazino functionality for introducing heterocyclic partners, advancing their structure-activity relationship studies. We share our in-house troubleshooting tips, such as solvent swaps to boost solubility or avoid foaming. These practical insights stem from direct experience, gained during both successful and not-so-smooth campaigns.
We constantly monitor applications in photochemistry and chelation science. The unique combination of pyridine and hydrazino features supports photoresponsive ligand development. Teams advancing new LED dyes or metal-chelating agents describe fewer separation steps following the use of this intermediate, in contrast to their previous builds.
Lab safety shapes our procedures. Hydrazino derivatives demand strict protocols during scale-up, especially under high temperature or with strong acids. We moved to closed-system transfers following a minor fume incident—direct lessons etched in memory. Operator training focuses on staging, shielding, and regular monitoring of process temperatures. Material compatibility testing, especially with seals and transfer tubing, keeps us ahead of handling issues.
Many customers rely on full impurity profiles ahead of specification verification programs. We maintain clear, accessible records accessible for audits. Detailed documentation matters: pharmaceutical and crop-science teams face constant scrutiny, and our data support seamless integration into larger compliance frameworks. Open debates with regulatory inspectors informed how we format and store stability studies. For this compound, clear shelf-life data and thermal degradation info drive customer confidence.
In the shipment phase, avoiding moisture pick-up requires double-sealing options, a system we implemented following feedback from clients on multiple continents. Hands-on packing and clear transport labels address customs and shipping hazards. Having seen a border holdup due to ambiguous nomenclature, we tuned bills of lading for clarity—practical adjustments from lived experience, not theory.
Over the years, reaction optimization became essential when using 3-Pyridinecarboxylicacid,6-Hydrazino-. Run-to-run reproducibility can take a hit if the order of reagent addition slips or pH monitoring drifts. We supply in-depth application notes, drawing from repeated bench-scale runs, that highlight common pitfalls and proven fixes. Avoiding over-addition of base keeps yields steady, a subtle point new users often overlook until their workups go awry.
Solubility quirks influence product isolation. Early process development revealed that switching from polar protic to aprotic solvents during crystallization steps dramatically altered purity outcomes. Our chemists consider such variables every day, aware that large-scale batches respond differently than gram-scale trials. Detailed batch reports, including those “unexpected outcome” notes, help customers prepare for their own scale-ups and minimize surprises.
Sometimes, end users run into difficulties due to batch mixing or unaccounted-for solvent residues. Drawing from our own runs, we flag the need for slow addition under efficient cooling to prevent side reactions and uncontrolled foaming—a lesson learned only after a particularly lively foaming incident required a midday system flush. These translated experiences travel with every batch we ship.
Our production lines focus on waste reduction and solvent recycling. The more hydrazines handled, the more acute the waste management challenge gets. Early in product development, we noticed spike in solvent usage for washing and quenching steps. Now, we direct byproduct streams into in-house distillation and solvent recovery units, markedly slashing our footprint. Our research into green alternatives for hydrazinolysis continues, nudged along by both cost savings and regulatory tightening.
Worker safety remains a pillar of daily practice. Our investment in continuous training—eyewash drills, emergency kit use, and handling exercises—pays dividends in day-to-day confidence and minimal incident rates. For compounds like this one, an ounce of real-world preparedness shaves hours off incident management if anything strays off script.
Detailed incident logs have helped us pinpoint root causes behind minor issues, prompting investments in containment upgrades. Real feedback from the operational team drives improvements: say, better PPE choices or adjustments in how pallets are stored on humid days. Sustainable practice does not happen overnight, but our pursuit of minimized emissions and smarter recycling supports ongoing reliability for all partners down the line.
Our customer support lines stay active with calls seeking troubleshooting help or insight about substituting this compound for other intermediates. Sometimes, academic teams face unexpected bottlenecks in mechanistic runs and want an insider’s perspective on how to adapt protocols. Both experienced scientists and newcomers benefit from a transparent account of our own learning curves—mistakes, wins, and all. This is not limited to sales but extends throughout the support we offer, right from bulk synthesis questions to packaging and storage advice.
Drawing from a string of feedback, we understand that hands-on support can break a deadlock. For example, several customers working on hydrazone libraries recounted issues with unanticipated side reactions caused by ambient moisture. After comparing notes with our synthesis team, we compiled brief technical memos outlining methods to reduce such risks, along with real-world yields from parallel temperature trials.
By fostering direct communication with end users, we note recurring patterns quicker. That feedback loop shapes our batch records, packaging tweaks, and even the focus of ongoing process development. Our preparedness to adapt—say, increasing purification checks after an uptick in minor byproducts—flows from treating customer input as a genuine quality driver, not a burden.
Growth in customer demand shapes much of our future planning for 3-Pyridinecarboxylicacid,6-Hydrazino-. Each year, we see new sectors requesting tailored grades—whether for next-generation pharmaceuticals, innovative crop protection, or custom ligands. This feedback spurs updates to in-process testing or agility in our batching schedules. Staying open to new regulatory standards, expanding analytical platforms, and alert to green chemistry initiatives keeps us aligned with fast-changing market demands.
Industry conversations hint at further potential. Collaboration with cross-sector R&D teams opens new reaction pathways for this compound, ranging from construction of new heterocyclic cores to functionalized nanomaterials. In-house chemists push toward more sustainable processes, driving down input demand and supporting end users as they encounter tighter environmental compliance frameworks.
In our company, the voice of every chemist, analyst, and technician matters. This culture of sharing—lessons learned from a thousand crystallizations, surprises in reactivity, and the occasional “what if we try…” experiment—builds confidence across the supply chain. Each lot of 3-Pyridinecarboxylicacid,6-Hydrazino- carries not just a stamp but the know-how of years spent refining, responding, and innovating to deliver compounds that give researchers and manufacturers a crucial edge.