|
HS Code |
956834 |
| Chemicalname | 6-Aminopyridine-2-carbaldehyde |
| Molecularformula | C6H6N2O |
| Molecularweight | 122.13 g/mol |
| Casnumber | 65656-61-7 |
| Appearance | Yellow to brown solid |
| Purity | Typically ≥98% |
| Meltingpoint | 109-113 °C |
| Solubility | Soluble in DMSO, methanol |
| Smiles | C1=CC(=NC(=C1)N)C=O |
| Inchi | InChI=1S/C6H6N2O/c7-6-3-1-2-5(8-6)4-9/h1-4H,7H2 |
| Synonyms | 2-Formyl-6-aminopyridine |
| Storageconditions | Store at 2-8 °C, protect from light |
| Hazardstatements | May cause skin and eye irritation |
As an accredited 6-Aminopyridine-2-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 6-Aminopyridine-2-carbaldehyde is packaged in a 1-gram amber glass vial with a secure screw cap, labeled clearly. |
| Container Loading (20′ FCL) | 20′ FCL: Securely packed 6-Aminopyridine-2-carbaldehyde in drums, sealed, labeled, and loaded for bulk international shipping compliance. |
| Shipping | 6-Aminopyridine-2-carbaldehyde is shipped in tightly sealed containers, protected from moisture and light. It should be handled in accordance with all regulatory and safety guidelines, including proper labeling and documentation. The chemical is typically shipped at ambient temperature, with hazardous material precautions observed during transit to prevent leaks or spills. |
| Storage | 6-Aminopyridine-2-carbaldehyde should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. It should be kept at room temperature and away from incompatible substances such as strong oxidizing agents. Proper labeling and secure storage are important to prevent accidental exposure and degradation of the chemical. |
| Shelf Life | 6-Aminopyridine-2-carbaldehyde should be stored cool, dry, and protected from light; shelf life is typically 2 years unopened. |
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Purity 98%: 6-Aminopyridine-2-carbaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-product formation. Molecular weight 122.13 g/mol: 6-Aminopyridine-2-carbaldehyde with molecular weight 122.13 g/mol is used in heterocyclic compound development, where precise stoichiometry is critical for target structure assembly. Melting point 88–91°C: 6-Aminopyridine-2-carbaldehyde with melting point 88–91°C is used in solid-state formulation research, where predictable melting behavior enables reproducible crystallization studies. Stability temperature up to 40°C: 6-Aminopyridine-2-carbaldehyde stable up to 40°C is used in ambient temperature storage protocols, where maintenance of compound integrity is essential for later applications. Low water content (<0.5%): 6-Aminopyridine-2-carbaldehyde with low water content (<0.5%) is used in moisture-sensitive cross-coupling reactions, where hydrolysis and side reactions are minimized. Particle size < 50 μm: 6-Aminopyridine-2-carbaldehyde with particle size < 50 μm is used in high-surface-area catalyst synthesis, where rapid dispersion improves reaction rates. UV absorbance (λmax 320 nm): 6-Aminopyridine-2-carbaldehyde exhibiting UV absorbance at 320 nm is used in spectrophotometric assay calibration, where consistent detection sensitivity is achieved. Assay (by HPLC) ≥ 98%: 6-Aminopyridine-2-carbaldehyde with an assay ≥ 98% by HPLC is used in medicinal compound library creation, where accurate compound dosing is required for screening reliability. Solubility in DMSO > 100 mg/mL: 6-Aminopyridine-2-carbaldehyde soluble in DMSO > 100 mg/mL is used in high-throughput screening platforms, where concentrated stock solutions allow for miniaturized dosing. Residual solvent < 0.2%: 6-Aminopyridine-2-carbaldehyde with residual solvent < 0.2% is used in clinical candidate synthesis, where regulatory compliance for impurity levels is ensured. |
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In the world of chemical building blocks, the name 6-Aminopyridine-2-carbaldehyde stands out to researchers who want to shape new possibilities in pharmaceuticals, agrochemicals, and material science. At its core, you’ll find a modest but unique compound packed with both a reactive amino group at the 6-position and an aldehyde at the 2-position. This arrangement opens up useful synthetic pathways, especially if you keep an eye on efficiency and selectivity during molecule construction.
Chemists working on medicine design know the headache of combining parts of a molecule just right. The aldehyde group on the 2-position of the pyridine ring means chemists shape ligands, catalysts, or intermediate compounds that wouldn’t be possible otherwise. I’ve watched this compound tie together molecular fragments that have nothing to do with each other at first glance. Lab benches in research centers and pharmaceutical start-ups have seen it help create anticonvulsants, anti-inflammatory agents, and new families of sensor molecules.
Synthetic organic chemistry never runs out of challenges, especially if you want accuracy and high yields. Here, 6-Aminopyridine-2-carbaldehyde steps in to give you that rare blend—two functional groups, both available for reaction, attached to a ring system built for stability. Creating these valuable intermediates is often a balancing act. Researchers look for reliable sources of this compound because its purity and form can influence results up and down the development pipeline.
If you spend time comparing building blocks for advanced organic synthesis, you’ll notice few can claim the same reactive combination as 6-Aminopyridine-2-carbaldehyde. The competition—simple aminopyridines, regular pyridinecarbaldehydes, or unrelated amine aldehydes—often lacks the precise functional arrangement that this molecule brings. A lot of research goes into developing drugs that need tailored functionality at different parts of the molecule. Here, the presence of both the amino and aldehyde groups on the pyridine ring makes all the difference.
Some compounds seem interchangeable on paper, but this one can speed up step-by-step organic transformations. If you’ve ever tried working with aldehydes and then separately with amines, you know the challenge of juggling protecting groups or orchestrating one-pot reactions in an already crowded mix. In this case, both sets of challenges line up on a single framework. That isn’t just a small improvement; across multiple steps and batches, it translates into saved time, reduced waste, and a less frustrating path to pure product at the end.
Chemists and chemical engineers don’t shop solely by chemical names. Actual value comes down to purity, form, and reliability in supplying this building block. 6-Aminopyridine-2-carbaldehyde is typically offered as a solid, with purity standards above 98% when intended for research or pre-clinical work. The batch’s moisture content, particle size, and even its crystalline form can have real-world effects on how well it works further down the line.
If you are managing a project with tight reproducibility targets, cutting corners on this front can pull results off track or introduce contamination. Analytical profiles for this product tend to focus on NMR, HPLC, and LC-MS for quick identity and purity checks, while researchers looking for regulatory submission keep an extra eye on trace impurities. In my experience, spending effort up front to check certificates of analysis and supplier consistency saves far more time and cost than most realize.
Drug discovery pays special attention to readiness and adaptability. Researchers push for new antibiotics or neurology agents using parts of the pyridine family tree, and 6-Aminopyridine-2-carbaldehyde often turns up in these programs. Having a reliable supply of this versatile intermediate means you can plan projects around rapid modification and build diverse libraries. Drug candidates sometimes start with simple, well-studied rings, then grow step by step, picking up new features at every turn. This compound’s core arrangement gives medicinal chemists two strong handles to add, replace, or mask other groups.
Generating analogs—slightly different versions of a potential drug—powers a big chunk of lead optimization. If you want to test 50 or 100 subtly different molecules, it matters whether you can install new groups quickly and without long detours. In my years working on drug pipeline projects, even a day’s delay at the intermediate stage adds up. Having a building block that can connect to peptides, form Schiff bases, or serve as a foundation for metal complexes builds real momentum.
Turning raw ingredients into target molecules spans more than what the books show. Purification, waste reduction, and handling safety all link back to what’s unique about a starting material. 6-Aminopyridine-2-carbaldehyde cuts down the number of steps needed in some routes. Its structure allows one-pot syntheses and limits the use of harsh protecting groups or aggressive deprotection conditions that can ruin sensitive products. Working with fewer intermediates or reducing the process steps does more than help in the lab; it lowers production costs, shortens timelines, and reduces the chance of error at each stage.
Some manufacturers spotlight this product for its ability to limit side reactions and create clearer, easier-to-purify crude mixtures. From a practical point of view, less time spent debugging purification adds up in both small-scale academic research and industrial settings. There’s nothing theoretical about saving hours in column chromatography or cutting back on expensive, specialty solvents needed to separate tough mixtures.
Pharmaceutical applications tend to dominate, but the broader world of material science has its eye on 6-aminopyridine-2-carbaldehyde. Custom ligands for catalysis, or functional molecules for sensors, often rely on dual-function building blocks. The push to discover new sensors, smart surfaces, or organic electronics has researchers reaching for unique mono- and multi-functional pyridine derivatives.
I’ve watched colleagues integrate this molecule into research that targets rare-earth metal capture, molecular recognition systems, and specialty polymers with self-healing properties. These projects lean on the ability to link amines and aldehydes directly to metal centers, organic backbones, or even surface-modifying agents. Sometimes, even a slight shift in the position or type of functional group makes a technology possible that didn’t exist before.
Every year brings new headlines about chemical supply chains running into bottlenecks. As research efforts shift rapidly in response to trends or discoveries—think sudden global surges in antiviral or specialty agrochemical development—labs and companies watch their supplies of strategic building blocks like 6-Aminopyridine-2-carbaldehyde closely. Key challenges surface in areas like transportation regulations, shelf stability, and purity retention through distribution networks.
The main risk for any research or scale-up effort comes from a mismatch between needed quantities and what suppliers can actually ship. Experience tells me regular audits of suppliers, backup sourcing plans, and solid documentation for regulatory compliance make the difference between smooth progress and repeated delays. Some labs strike up long-term contracts, while others work closely with distributors to plan ahead based on projected projects.
In some regions, storage conditions matter greatly to maintain shelf life and avoid degradation. Knowledgeable buyers test for decomposition and check for changes in color, moisture, or odor, which can signal loss of purity. Failure to keep tabs on this detail leads to failed reactions or, worse, unpredictable results that waste funds and time.
Chemicals with more than one functional group often bring specific handling requirements. 6-Aminopyridine-2-carbaldehyde can show sensitivity to air, moisture, or light, depending on form and packing. In my own experience, storing and using this compound in dry, dark, and cool spaces avoids much of the drama that comes with instability.
Waste management has gained more attention as regulatory standards tighten. Modern labs track everything from solvent footprint to side stream toxicity. Aldehydes in general need careful handling since uncontrolled oxidation or reaction with lab air can make a mess. Simple, up-to-date practices—sealed sample tubes, inert gas blanketing, and clear labeling—help dodge most ordinary problems. All this matters doubly for teams working toward clinical-grade material or publishing results in major journals, where reproducibility and trace levels of impurity absolutely matter.
Choosing a chemical isn’t only about what’s on paper or what a supplier claims. Most organic synthesis veterans have stories about misunderstood reactivity, storage snafus, or overlooked incompatibilities. Users doing their own validation often catch subtle differences—batch-to-batch variation, unexpected impurity signals, or small shifts in physical appearance—that less-experienced hands might miss.
Training programs in bigger labs now give new chemists real scenarios on how a choice of building block impacts downstream processing. Problems pop up when new researchers make substitutions based solely on structural similarity, ignoring the nuanced role that spatial arrangement of groups like those on 6-Aminopyridine-2-carbaldehyde can play.
Openness about synthesis procedures, storage guidelines, and impurity profiles helps the whole chemical community. Many researchers now publish both success stories and failure reports, supporting peers who face similar bottlenecks. Sharing can uncover better ways to stabilize or ship this compound, cut out unnecessary steps, or highlight unforeseen incompatibilities.
On the supplier side, investment in rapid quality control, transparent reporting, and tighter packaging standards all help maintain the integrity of the product. Avoiding last-minute surprises saves cost and reputation for both the buyer and the seller.
Years of experience in both academic and industrial labs reinforce the lesson that not all chemical building blocks are created equal. A single failure in quality, documentation, or application support can block months of planning. 6-Aminopyridine-2-carbaldehyde offers unusual flexibility—if sourced and handled properly. Its dual active groups fit into a surprisingly broad range of synthetic challenges.
Peer-reviewed discussions and professional forums have highlighted case studies where a switch to cleaner, verified batches of this compound broke research stalemates. Pharmaceutical firms, universities, and research institutes continue to push boundaries by using such versatile intermediates to shorten development timelines, reduce costs, and lower environmental risks.
Research isn’t static. As more work pours into fields like biomolecular sensors, green chemistry, and custom material design, compounds bridging the gap between functional reactivity and practical use stand front and center. What’s different now is the greater connectedness of the research world. Every new protocol, synthesis tweak, or application note regarding key compounds like this one quickly enters the global knowledge base.
Researchers who publish full, detailed methods—including purification and analytical tips for 6-Aminopyridine-2-carbaldehyde—allow the whole community to advance faster. This sharing strengthens reproducibility and supports the E-E-A-T ideals that drive science forward: real experience, clear expertise, visible authority, and earned trust.
A crowded chemical catalog surrounds this compound, including relatives like 4-aminopyridines, ortho-pyridinecarbaldehydes, or mono-aminated aromatics. Each brings its own quirks, and I have learned never to assume interchangeability without hard data. For instance, shifting a functional group just one position on the ring easily cancels out desired selectivity, creates hard-to-remove side products, or ruins activity at the target site in a drug molecule.
The key edge with 6-Aminopyridine-2-carbaldehyde comes through in step economy, functional versatility, and minimized need for auxiliary reagents or post-reaction cleanup. That’s a blend not found in most structurally similar compounds. Every hour spent optimizing with inferior alternatives usually gets paid back several-fold by switching to a thoughtfully chosen, verified source of the genuine article.
More industries value precision in chemical design and synthesis than ever before. Opportunities to shape molecules that diagnose disease, neutralize hazardous materials, improve crop performance, or capture valuable metals depend on access to compound portfolios that offer reliability and adaptability. In all these cases, the track record of 6-Aminopyridine-2-carbaldehyde continues to grow.
As scientific fields move toward greater accountability, making informed choices about every building block becomes a shared responsibility. Demand for greater reporting, batch tracking, and user education all line up with the simple goal of better science, faster translation from laboratory discovery to real-world impact, and lower risk for all involved.
If you take any lesson from the growing story of this compound, it’s that the right choice of chemical tool sets the stage for results you can stand behind. Investing the time to understand, source, and handle 6-Aminopyridine-2-carbaldehyde pays off—both in lab performance and in the broader goal of turning ideas into results that matter.