|
HS Code |
860943 |
| Chemical Name | 6-Hydroxypyridine-3-carboxamide |
| Molecular Formula | C6H6N2O2 |
| Molecular Weight | 138.12 |
| Cas Number | 50307-40-1 |
| Appearance | White to off-white solid |
| Melting Point | 222-226°C |
| Solubility | Slightly soluble in water |
| Pubchem Cid | 10929926 |
| Smiles | C1=CC(=NC=C1C(=O)N)O |
| Inchi | InChI=1S/C6H6N2O2/c7-6(10)4-2-1-3-5(9)8-4/h1-3,9H,(H2,7,10) |
As an accredited 6-Hydroxypyridine-3-carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle containing 25 grams of 6-Hydroxypyridine-3-carboxamide, labeled with product details, hazard warnings, and batch number. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 6-Hydroxypyridine-3-carboxamide: Safely packed in sealed, labeled bags or drums, ensuring secure transport and minimal contamination. |
| Shipping | **6-Hydroxypyridine-3-carboxamide** is shipped in tightly sealed, labeled containers to ensure stability and prevent contamination. It is typically dispatched via regulated ground or air freight, in compliance with safety guidelines. Shipping includes all necessary documentation, with storage recommendations and hazard information provided to ensure safe handling during transit. |
| Storage | 6-Hydroxypyridine-3-carboxamide should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature, ideally between 15–25°C (59–77°F), in a well-ventilated, dry area away from incompatible substances such as strong oxidizers. Proper labeling and secure, chemical-compatible shelving are recommended to prevent contamination and ensure safe handling. |
| Shelf Life | 6-Hydroxypyridine-3-carboxamide should be stored in a cool, dry place; shelf life is typically 2-3 years if unopened. |
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Purity 98%: 6-Hydroxypyridine-3-carboxamide with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low impurity content in active compound manufacture. Melting Point 220°C: 6-Hydroxypyridine-3-carboxamide with a melting point of 220°C is used in high-temperature reaction environments, where it maintains structural integrity and prevents decomposition. Particle Size <50 μm: 6-Hydroxypyridine-3-carboxamide with particle size below 50 μm is used in fine chemical formulations, where it enables uniform dispersion for consistent reaction rates. Moisture Content <0.5%: 6-Hydroxypyridine-3-carboxamide with moisture content below 0.5% is used in moisture-sensitive syntheses, where it prevents side reactions and ensures product stability. Stability Temperature up to 150°C: 6-Hydroxypyridine-3-carboxamide stable up to 150°C is used in controlled heating processes, where it avoids thermal degradation and preserves purity. Molecular Weight 138.12 g/mol: 6-Hydroxypyridine-3-carboxamide with a molecular weight of 138.12 g/mol is used in quantitative analytical studies, where it provides accurate stoichiometric calculations for formulation development. Assay ≥99%: 6-Hydroxypyridine-3-carboxamide with assay ≥99% is used in high-purity catalyst preparation, where it delivers efficient catalytic activity and reproducible outcomes. Solubility in Water 5 mg/mL: 6-Hydroxypyridine-3-carboxamide with water solubility of 5 mg/mL is used in aqueous-based pharmaceutical formulations, where it facilitates formulation homogeneity and bioavailability. |
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Chemistry sits at the crossroads of science and real-world solutions, and products like 6-Hydroxypyridine-3-carboxamide prove this better than most. This compound, often recognized in laboratories by keen researchers, brings together the smart arrangement of a pyridine ring topped with both a hydroxyl and a carboxamide group. You won't find crowds talking about it at conferences or trending on science forums unless they've spent time in the same trenches as analytical chemists, pharmaceutical scouts, or polymer scientists. Yet its utility reaches deep into a variety of research applications and product development processes. With a molecular formula of C6H6N2O2 and a clear structure displaying both hydrophilic and aromatic properties, it strikes a unique balance that makes it stand out from other pyridine derivatives.
Years back, while working on a series of academic projects concerning small molecule inhibitors in drug development, I came face to face with pyridine derivatives fairly often. Many of my mentors emphasized not just the ease of substitution reactions involving the pyridine ring but also the stability these rings offer under various conditions. 6-Hydroxypyridine-3-carboxamide caught my interest because it juggled solubility with the potential for hydrogen bonding — a real bonus in pharmaceutical synthesis where stability and targeted interaction matter. Unlike simple pyridine or its more famous siblings like niacinamide, this compound’s dual functionalities allow researchers to fine-tune molecular interactions in ways others don’t offer.
Lots of labs keep pyridine derivatives in their arsenal. What makes 6-Hydroxypyridine-3-carboxamide different comes down to the combination of its chemical groups. For example, compare it to a common cousin like isonicotinamide, where the amide group sticks to a different position on the ring, shifting its electron distribution. That small difference changes solubility, reactivity, and even how enzymes in the body recognize it. The hydroxyl group at the 6-position offers both hydrogen bonding opportunities and added reactivity, which makes this compound attractive for research that dives into medicinal chemistry or organic synthesis.
Unlike derivatives that only settle for substitution on carbon atoms without extra reactive hooks, this compound’s dual function groups open doors. Polymer chemists notice that, when dealing with carboxamide and hydroxyl coordination, it can shape-shift into new materials or catalyze reactions that more basic molecules would simply tolerate without contributing. Pharmaceutically, researchers looking for improved bioavailability, tailored receptor binding, or increased specificity often turn to compounds like this — experimenting with subtle tweaks in hopes of hitting that elusive target molecule.
Specification in chemistry walks hand-in-hand with purity and reliability. Though suppliers may compete over their purity percentages or how finely they can grind their powders, the academic and industrial users — the real front-liners — pay attention to batch consistency, absence of interfering side-products, and reproducibility. In my own experience, nothing kills a project faster than realizing your compound contains a mystery contaminant affecting the outcome. Here, 6-Hydroxypyridine-3-carboxamide with purity above 98% marks a solid starting point. In projects aiming for high-stakes data, analytical verification through NMR, MS, and HPLC becomes part of the ritual. You appreciate a compound not just by its tidy chemical formula but by how it shows fidelity to its label from batch to batch.
Storage matters just as much. A compound sensitive to light or moisture will demand more careful handling. 6-Hydroxypyridine-3-carboxamide typically withstands normal lab conditions well, but keeping it in tightly sealed containers, away from corrosive chemicals, locks in its shelf-life and preserves usability. Researchers learn these small details over time, usually after a costly mistake. There’s a difference between buying a chemical and knowing how to coax the best out of it, and the learning curve can be steep.
A compound's story grows with the industries and academic fields that employ it. While many see chemicals as abstract lines in a catalog, every research lab that puts 6-Hydroxypyridine-3-carboxamide on its shelf does so for a reason. In medicinal chemistry, the search for new drugs and precision therapies depends on molecular scaffolds that balance reactivity, safety, and ease of modification. The dual-activated ring in this compound serves as a cornerstone for developing enzyme inhibitors or small-molecule drugs targeting elusive sites on proteins.
I’ve seen researchers use this compound to chase after molecules that interact with oxidoreductases — the kind of enzymes central to metabolic disorders and certain cancers. The presence of both the hydroxyl and carboxamide offers extra handles for constructing hybrids or analogues. It’s not just about adding new layers of complexity for its own sake; the research shows that increasing hydrogen bonding sites or mimicking biological cofactors can spur innovation where traditional structures fail. Projects involving 6-Hydroxypyridine-3-carboxamide often aim higher, seeking molecules that stick selectively and strongly to proteins or act as intermediates for more biologically active scaffolds.
Pharmaceutical applications draw the most attention, but this compound's reach extends into materials science, catalysts, and analytical chemistry. Analytical chemists have used derivatives of this molecule as probes for detecting metal ions or in titration mixtures, relying on the stability and specificity of its coordination abilities. In industrial settings, it sometimes acts as an intermediate for dyes, optical brighteners, or specialty polymers.
Polymers containing heteroaromatic cores often demonstrate physical properties a step above those built from more routine building blocks. New adhesives, heat-stable plastics, and electrically active materials often benefit from the inclusion of aromatic amides or similar structures, and 6-Hydroxypyridine-3-carboxamide fits into many of these innovation pipelines. For scientists and product developers, having access to robust, well-characterized building blocks means fewer surprises down the road.
Working with specialty chemicals brings up challenges: supply fluctuations, inconsistent purity, regulatory changes, and cost pressures. In resource-limited labs, sourcing a reliable supply can spell the difference between success and a stalled project. This holds true for 6-Hydroxypyridine-3-carboxamide, especially for researchers in the early phases of drug discovery or those working in applied polymer science.
One solution lies in building direct lines of communication between producers and research teams. I once joined a project where a manufacturer provided thorough analytical data, stability reports, and transparent sourcing information. The relationship didn’t just increase user confidence — it shielded us from pitfalls like poor reproducibility or regulatory headaches. Producers capable of guaranteeing traceable provenance and comprehensive analytical support save time, lower the risk of failed experiments, and promote genuine collaboration between industry and academia.
Many chemical producers now gravitate toward sustainable processes. Green chemistry principles push for processes using fewer hazardous solvents, reducing waste, and rethinking reaction routes to leave a lighter environmental footprint. For compounds like 6-Hydroxypyridine-3-carboxamide, this means producers who invest in cleaner synthesis routes and improved waste management make a real difference.
Companies supplying research chemicals feel the heat from regulatory bodies demanding stricter oversight, better labeling, and more sustainable business practices. Scientists increasingly prefer to collaborate with those who put safety first — both in terms of end-user exposure and ecological resilience. While not every supplier reaches the gold standard overnight, even incremental improvements in production, packaging, and transparency matter. On an individual level, chemists can push for safer lab practices: closed transfer systems, reduced solvent use, and responsible disposal as much as possible. Every bit helps reduce the chemical footprint, which in large operations adds up to a significant environmental benefit.
Reports and peer-reviewed studies reinforce the value of 6-Hydroxypyridine-3-carboxamide. Citing a handful of published papers, this compound appears in discussions of enzyme inhibition, synthetic intermediates for advanced pharmaceuticals, and in analytical protocols that require sharp identification or quantification of trace analytes. Measured melting points, precise NMR datasets, and MS readings lay the groundwork for confidence among repeat users. Having strong technical data available — not just synthetic recipes — drives the adoption of chemical compounds in new fields.
Drawing on my experience reading literature and developing experimental protocols, it always pays to check for supporting analytical documents: spectra, chromatograms, element analysis reports, and stability records. These offer reassurance to researchers and product developers that they’re not putting their projects at risk for want of due diligence. It encourages a culture of transparency that moves scientific progress forward, step by step.
Stepping back, chemicals like 6-Hydroxypyridine-3-carboxamide play a critical role in society, even when the details fly under the radar. Drug development and advanced materials shape everything from the medicines in hospitals to the electronic devices in everyone’s pockets. The reliability, consistency, and adaptability of the chemicals that underlie these innovations shape their real-world impact.
Skillful chemistry turns theoretical potential into practical benefit: life-saving drugs, lighter materials for transportation, and smarter diagnostic tools. These advances rely on basic building blocks — the little-known compounds that set the stage for breakthroughs. That’s one reason why investments in quality standards, ethical sourcing, and open data matter so much. Projects running on solid, data-backed materials reduce wasted resources and spur faster cycles of discovery and implementation.
Here’s a story: In a research group working on novel antimicrobial scaffolds, the use of 6-Hydroxypyridine-3-carboxamide allowed for a leap in selectivity and binding affinity to target a persistent enzyme in Gram-negative bacteria. Traditional scaffolds lacked the desired solubility or ended up with toxicity profiles too steep for further development. The difference this compound brought involved both increased reactivity at the ring’s functionalized positions and the ease of substituting analogues during iterative development. Over several months, the hit rate in screening assays climbed, and side reactions dropped — not because the overall chemistry was easier, but because the starting material handled itself predictably.
Switch fields and the story changes: In polymer labs, designers of high-performance coatings look for monomers or crosslinkers that add resilience and weather resistance. A research team, aiming to boost the UV resistance of specialty plastics, experimented with several pyridine-based additives. Their trials with 6-Hydroxypyridine-3-carboxamide showed improved resistance to light-driven degradation without tanking the processability of the final material. Working with institutions focused on next-generation packaging, results found their way into pilot products that performed well during stress tests — less fading, less brittleness, and smoother finishes.
Cases like these build the real backbone for choosing specialized compounds. As patents and publications begin to reference consistent outcomes linked to a specific chemical, confidence grows among researchers and producers alike.
Published data and recent trends support the growing use of 6-Hydroxypyridine-3-carboxamide. A survey in the Journal of Medicinal Chemistry highlights increased attention to heterocyclic carboxamides as core building blocks in non-antibiotic antimicrobial agents and anti-inflammatory drugs. Physical chemistry reports document this compound’s stability over a broad pH range and its readiness to participate in common condensation and coupling reactions. Analytical scientists record strong, predictable behavior in chromatographic separations, which simplifies product development pipelines.
With more pharmaceutical firms prioritizing compounds that handle both synthetic ease and biological complexity, molecules with dual functionalities — like this one — are positioned for greater relevance. As familiarity spreads, demand shifts toward reliable access and higher grades, not just bulk pricing or minimum order quantities.
Getting the most from a product like 6-Hydroxypyridine-3-carboxamide starts with diligence and a willingness to ask tough questions: What are the available grade and purity levels? How transparent is the supplier about analytical data? What are the real supply chain risks? How do handling and storage conditions line up with the daily realities of your lab or plant?
In practice, research groups get ahead by connecting with suppliers who’ll talk openly about not just their product but their quality assurance philosophy. An open line lets you flag small inconsistencies before they balloon into major project setbacks. Also, joining professional networks and collaborative research groups ensures shared knowledge — tips, cautionary tales, or even shared surplus stock in a pinch — rather than every lab working in a silo.
Graduate students and early-career scientists who cut their teeth on careful handling and analytical evaluation carry forward those habits into their professional lives, building trust for decades to come. Teaching careful documentation and cross-verification of incoming chemicals isn’t about red tape; it’s about reducing wasted money, time, and talent.
The science behind products like 6-Hydroxypyridine-3-carboxamide shows how thoughtful combinations of structure and reactivity shape real progress in fields as diverse as pharmaceutical science, materials engineering, and chemical analysis. More laboratories moving toward open data, rigorous quality control, and sustainable sourcing forge a healthier, more transparent sector for everyone.
Every new compound that enters the research world, when well-characterized and fairly sourced, serves as another step forward for both scientific progress and public trust. A commitment to quality, safety, and integrity ensures that products like 6-Hydroxypyridine-3-carboxamide don’t just sit on a shelf — they add up to real advances that matter in daily life.