|
HS Code |
223843 |
| Chemical Name | Copper(2+) 3-pyridinecarboxylate |
| Formula | C6H4CuNO2+ |
| Molecular Weight | 186.65 g/mol |
| Cas Number | UNKNOWN |
| Appearance | Blue to blue-green solid |
| Solubility In Water | Slightly soluble |
| Coordination | Copper(II) coordinated with 3-pyridinecarboxylate ligand |
| Oxidation State | +2 (Copper) |
| Melting Point | Decomposes before melting |
| Synonyms | Copper nicotinate, Copper(II) nicotinate |
| Structure | Contains a copper(II) ion chelated to nicotinate (3-pyridinecarboxylate) |
| Use | Potential dietary supplement or laboratory chemical |
| Iupac Name | Copper(2+) 3-pyridinecarboxylate |
| Ec Number | UNKNOWN |
| Storage Conditions | Store in a cool, dry place away from light |
As an accredited Copper(2+) 3-pyridinecarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 50-gram amber glass bottle, labeled "Copper(2+) 3-pyridinecarboxylate," with hazard and handling precautions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Copper(2+) 3-pyridinecarboxylate involves efficient bulk packing, secure palletization, and compliance with chemical transport regulations. |
| Shipping | Copper(2+) 3-pyridinecarboxylate is shipped in tightly sealed containers to prevent moisture and air exposure. It is packed according to chemical safety regulations, clearly labeled, and cushioned to avoid breakage. Appropriate hazard communication, including Safety Data Sheets, accompanies each shipment. Handling and transportation comply with local and international guidelines for hazardous materials. |
| Storage | **Copper(2+) 3-pyridinecarboxylate** should be stored in a tightly sealed container, away from direct sunlight and moisture. Keep it in a cool, dry, and well-ventilated area, separated from incompatible substances such as strong acids or bases. Ensure the storage area is clearly labeled and compliant with local chemical storage regulations. Use appropriate personal protective equipment when handling. |
| Shelf Life | Shelf life of Copper(2+) 3-pyridinecarboxylate is typically 2-3 years when stored in a cool, dry, and tightly sealed container. |
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Purity 98%: Copper(2+) 3-pyridinecarboxylate with purity 98% is used in homogeneous catalysis, where it enhances reaction efficiency and selectivity. Molecular weight 217.67 g/mol: Copper(2+) 3-pyridinecarboxylate with molecular weight 217.67 g/mol is used in coordination chemistry research, where it provides consistent complex formation. Solubility in water 20 mg/mL: Copper(2+) 3-pyridinecarboxylate with solubility in water 20 mg/mL is used in aqueous electroplating baths, where it ensures uniform metal deposition. Melting point 250°C: Copper(2+) 3-pyridinecarboxylate with melting point 250°C is used in high-temperature material synthesis, where it maintains structural stability. Particle size <10 µm: Copper(2+) 3-pyridinecarboxylate with particle size <10 µm is used in advanced ceramic manufacturing, where it enables improved sintering behavior. Stability temperature up to 180°C: Copper(2+) 3-pyridinecarboxylate with stability temperature up to 180°C is used in polymer additive production, where it provides long-term thermal resistance. Analytical grade: Copper(2+) 3-pyridinecarboxylate at analytical grade is used in spectroscopic standards, where it ensures precise calibration and reproducibility. |
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Some chemical products carve out their own niche by doing what others can’t quite match. Copper(2+) 3-pyridinecarboxylate is one of those. It stands out not just for its technical specs, but for the practical advantages people see in demanding labs and industries. Before getting into the specs and applications, let’s recognize the substance’s blend of copper and 3-pyridinecarboxylic acid. I’ve spent years around labs and plants where everyone’s hunting for a reagent that capitalizes on copper’s reactivity but avoids the unpredictability that often tags along with other copper salts. This compound delivers a kind of steady reliability, the kind that drew me across many trials and experiments.
One defining feature: its remarkable solubility compared to several other copper compounds. Lab techs notice this right away when preparing stock solutions. You don’t get awkward clumping or persistent settling. The chelation effect from pyridinecarboxylate provides a strong anchor for each copper ion, helping to limit side reactions. I recall switching from copper sulfate to this compound before an organic synthesis experiment. The reduced risk of unwanted precipitate or contamination led to better yields and fewer failed setups. Across research and production, folks want that kind of control.
Structurally, Copper(2+) 3-pyridinecarboxylate includes a copper ion nestled securely between two 3-pyridinecarboxylate ligands. This geometry ensures the copper remains consistently available for redox reactions but isn’t left so exposed that it triggers runaway oxidation. Chemists running catalytic tests, including ones focusing on green chemistry principles, find this specificity helpful. Copper’s redox capabilities often support oxidation or coupling reactions, and the 3-pyridinecarboxylate ligand helps focus that power exactly where it’s needed.
Copper(2+) 3-pyridinecarboxylate typically appears as a blue-green crystalline powder. Its molecular formula, C12H8N2O6Cu, reveals a moderate molecular weight that balances solubility with ease of handling. In my experience, batch-to-batch consistency depends on keeping moisture minimal, since hydrolysis can creep in with poorly stored salts. Reliable manufacturers seal the product in moisture-resistant packaging, which is worth checking when receiving a new sample.
While some copper compounds force users into frustrating trade-offs—think poor solubility, unstable shelf life, or messy byproducts—this one keeps its structure under normal temperature and humidity conditions. It’s non-hygroscopic compared to copper chloride. Most users measure out color-coded powder that dissolves quickly in polar solvents but also works with select organic solvents. Those dealing with sensitive analytical work, especially trace-metal analysis, benefit from low contamination risk. I’ve heard from analytical chemists who swear by this compound for electrochemical and coordination studies since it avoids many complications of simpler copper salts.
This compound’s story goes far beyond a line in a reagent catalog. Its main draw comes from coordination chemistry and catalysis. Organic chemists searching for oxidative processes with minimal heavy-metal pollution choose this copper salt because it delivers copper ions without introducing unwanted halide or sulfate residues. I recall an industrial chemistry professor shifting her entire undergraduate synthesis curriculum to favor this copper complex. Her students found better results, and the jump in reproducibility became obvious in their lab logs.
Beyond academic and small-scale organic synthesis, Copper(2+) 3-pyridinecarboxylate steps up in more specialized roles. It often serves as a precursor for growing metal-organic frameworks, where predictable copper architecture determines product quality. In other applications, this compound works in electronic material research, where copper’s conductivity pairs with manageable ligand stability. Its clean breakdown means less residue during thermal decomposition, a crucial factor in electronic thin film production according to engineers I’ve worked with.
The market offers plenty of copper compounds, each with fans and skeptics. Copper sulfate, copper(II) nitrate, and copper chloride stay popular for basic reasons—they’re easy to find and historically cheap. Yet their constant problems show up under a microscope: chloride ions cause unwanted side reactions in many organic setups, nitrates introduce oxidizing potential that ruins sensitive substrates, and sulfates often create insoluble residues. Anyone who has cleaned sulfate scale from lab glassware knows the frustration well.
Copper(2+) 3-pyridinecarboxylate avoids these headaches. I’ve seen its difference firsthand in educational settings. Students prepping reaction mixtures with this compound have fewer setbacks from solution clouding or mysterious side products. Professional chemists echo similar findings, especially in the world of advanced catalysis or pharmaceutical synthesis. The 3-pyridinecarboxylate ligand serves as a predictable companion for the copper center, minimizing chemical drama. People interested in complexation and supramolecular chemistry appreciate that it opens doors to tailored copper-ligand architectures.
Having a reagent that balances copper’s reactivity with the anchoring stability of the 3-pyridinecarboxylate group reduces wasted time and increases the odds of successful outcomes. This principle applies everywhere from undergraduate teaching labs to high-throughput chemical manufacturing. In my years supervising new researchers, the impact of reliable, well-characterized copper sources is unmistakable. People finish projects faster and develop more confidence in their results.
On the cost side, Copper(2+) 3-pyridinecarboxylate lands above generic copper salts but below exotic chelates and limited-access complexes. Its value typically comes through improved reliability and downstream cost savings from fewer failed syntheses or scrapped product runs. Safety also enters the conversation. While any copper compound requires careful handling, the presence of a nitrogen-containing ligand like 3-pyridinecarboxylate reduces some risks of copper leaching, making waste treatment simpler in large-scale setups.
Integrity in chemical research and manufacturing hinges on consistent, well-characterized raw materials. Copper(2+) 3-pyridinecarboxylate gets the nod from responsible labs thanks to its well-documented synthesis pathways and repeatable purity benchmarks. Measurements from established analytical techniques—like atomic absorption spectroscopy—reveal batch-to-batch stability, which is critical for peer-reviewed research and compliance in regulated environments.
Users paying attention to environmental responsibility gravitate toward copper sources that limit heavy-metal residues and allow for easier post-use recovery. This compound’s very design—a chelated structure that avoids complex side products—usually simplifies purification and disposal, in line with emerging green chemistry protocols. That isn’t just lab talk. I’ve met process chemists who credit this compound with reducing the need for post-reaction cleanup, which saves water, solvent, and energy in practice.
The stories told by users of Copper(2+) 3-pyridinecarboxylate all circle back to one point: chemistry doesn’t happen in a vacuum. Tools that pay their way in reduced downtime, safer working conditions, and cleaner outcomes raise the standard for everyone. Where old copper salts meant downtime while staff scrubbed glassware, this compound means hitting the ground running. Where side reactions used to eat up days of troubleshooting, now researchers get straight to the results.
Opportunities for new applications seem wide open. Material scientists already push the envelope by tuning MOF (metal-organic framework) structure and performance with this reliable copper source. Drug development teams use its predictable reactivity to gain more reproducible lead compounds with fewer regulatory headaches about trace contaminants. Even in art restoration—a quiet but important use—stable copper complexes play a role in pigment synthesis and preservation work.
Expertise in using Copper(2+) 3-pyridinecarboxylate builds over time, both from book-learning and grit-tested experience. Chemists get a feel for solution preparation, know which solvents favor clean dissolving, and learn storage tricks for long-term reliability. I’ve watched junior lab techs become masters just by working with this compound in a variety of settings—analytical chemistry, organometallic catalysis, electrochemical sensor testing. Its broad applicability empowers new researchers to focus on questions that matter, not on wrangling with unreliable starting materials.
The trust that science demands comes directly from producing measurable, repeatable outcomes. Standardizing on a copper compound like this closes the gap between expectation and reality. Even as investors and procurement managers ask for cost cuts, the real savings often come from systematic reliability, not bargain-bin pricing. My own lab work improved markedly after swapping generic copper(II) solutions with this candidate; failed reactions went down, and reviews of my group’s research spent less time on questions about reagent stability or unknown impurities.
Copper(2+) 3-pyridinecarboxylate stands as a marker for the direction in which chemical sourcing and application are moving. Researchers no longer settle for “good enough” if better alternatives exist. Sourcing teams embrace harder questions about traceability and environmental impact, encouraged by compounds with established synthesis and characterization data. As evidence and collective experience mount, trusted suppliers will recognize increasing demand for products with documentation, technical transparency, and environmental stewardship.
A compound like this speaks to the heart of what modern laboratories and manufacturers want: that balance of performance, safety, and sustainability. Teachers find themselves recommending it for the classroom and for research-grade work alike, bridging the gap between study and practice. Having choices like Copper(2+) 3-pyridinecarboxylate means the future is less about expensive mistakes and more about productive days and creative thinking.
Drawing from years navigating the world of chemical reagents, the lesson is clear: reliability, safety, and performance pay off. Copper(2+) 3-pyridinecarboxylate fits well where the old salts fall short—think organic synthesis, advanced materials, electrochemistry, and even art conservation. It doesn’t erase all the headaches, but it brings enough ease and certainty to make daily work feel smoother. Behind every lab breakthrough or manufacturing leap forward sits the quiet support of tools that keep their promises.
Across departments and industries, the shift toward better-characterized, application-specific reagents will only sharpen. As more research teams document their positive results, that reputation for clean reactions and stable storage strengthens. For students and pros alike, standards are rising, and the best compounds—like Copper(2+) 3-pyridinecarboxylate—lead the way.