|
HS Code |
196570 |
| Product Name | 2-Cyanopyridine-4-carboxylic acid |
| Synonyms | 4-Carboxy-2-cyanopyridine |
| Cas Number | 25123-50-6 |
| Molecular Formula | C7H4N2O2 |
| Molecular Weight | 148.12 |
| Appearance | White to off-white solid |
| Melting Point | Over 200°C (decomposes) |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place away from light and moisture |
As an accredited 2-CYANOPYRIDINE-4-CARBOXYLIC ACID factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed in a 100-gram amber glass bottle with tamper-evident cap, labeled with chemical name, quantity, and hazard symbols. |
| Container Loading (20′ FCL) | 20′ FCL loads **2-CYANOPYRIDINE-4-CARBOXYLIC ACID** in 25kg fiber drums or bags, totaling approximately 8-10 metric tons. |
| Shipping | 2-Cyanopyridine-4-carboxylic acid is shipped in sealed, chemically-resistant containers to prevent moisture and contamination. It is transported according to standard regulations for laboratory chemicals, typically at ambient temperature. Proper labeling, documentation, and safety data are provided to ensure secure handling and compliance with relevant shipping regulations. |
| Storage | 2-Cyanopyridine-4-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 materials such as strong oxidizing agents. Protect from moisture and direct sunlight. Proper labeling and secure storage are important to prevent accidental exposure or contamination. Use appropriate personal protective equipment when handling. |
| Shelf Life | 2-Cyanopyridine-4-carboxylic acid should be stored in a cool, dry place; shelf life is typically 2-3 years if unopened. |
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Purity 99%: 2-CYANOPYRIDINE-4-CARBOXYLIC ACID with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity formation. Melting Point 214°C: 2-CYANOPYRIDINE-4-CARBOXYLIC ACID with a melting point of 214°C is used in thermal processing applications, where it provides enhanced stability during high-temperature reactions. Particle Size <10 μm: 2-CYANOPYRIDINE-4-CARBOXYLIC ACID with particle size less than 10 μm is used in fine chemical formulations, where it enables superior dissolution rates. Stability Temperature up to 180°C: 2-CYANOPYRIDINE-4-CARBOXYLIC ACID with stability temperature up to 180°C is used in catalyst manufacturing, where it maintains structural integrity under process conditions. Molecular Weight 148.11 g/mol: 2-CYANOPYRIDINE-4-CARBOXYLIC ACID with molecular weight 148.11 g/mol is used in combinatorial chemistry, where it allows for precise stoichiometric calculations in reaction design. Assay ≥98%: 2-CYANOPYRIDINE-4-CARBOXYLIC ACID with assay ≥98% is used in agrochemical intermediate production, where it assures product consistency and reliable agrochemical performance. Moisture Content <0.5%: 2-CYANOPYRIDINE-4-CARBOXYLIC ACID with moisture content under 0.5% is used in solid formulation processes, where it prevents agglomeration and ensures free-flowing powders. |
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2-Cyanopyridine-4-carboxylic acid might sound a bit intimidating at first glance, but its importance turns up in places where precision, stability, and effectiveness really matter. This compound keeps drawing attention among chemical researchers, pharmaceutical developers, and those pushing for tough-to-achieve synthesis steps. Its structure – a pyridine ring decorated with both a cyano and a carboxylic group – lays the foundation for reactivity and versatility. Real-world chemistry rarely lines up with textbook dreams, but this compound actually bridges that gap for some challenging applications.
Chemists often demand purity, and 2-cyanopyridine-4-carboxylic acid rises to the challenge. Most batches typically surpass 98% purity, offering clean reactions and reproducible results. Molecular formula C7H4N2O2 and a molecular weight hovering around 148.12 g/mol define its physical identity. Laboratory experience tells me that solubility lines up with expectations – it blends well in solvents such as DMSO and requires a bit more effort in water. Crystalline, off-white to light yellow powder is the usual look and feel, a detail that helps avoid confusion at the lab bench.
Where shelf life and stability are concerned, 2-cyanopyridine-4-carboxylic acid holds up if stored properly, well away from excess humidity and direct light. Glass containers with airtight seals do the trick. In all my years in active research labs, reliable storage means fewer headaches with unexpected degradation and wasted reagents.
2-Cyanopyridine-4-carboxylic acid deserves its reputation. Synthetic chemists appreciate how the cyano and carboxylic groups open doors for multiple reactions. It serves as a solid intermediate for the synthesis of pharmaceuticals, agrochemicals, and specialty materials. In drug discovery, for example, the structure allows for easy attachment of other building blocks, which helps scientists design molecules that act specifically at their targets. I’ve watched this compound play a starring role in medicinal chemistry teams aiming to build libraries of new candidates. This isn’t just academic – these libraries form the first step towards medicines that target hard-to-treat diseases.
Its value doesn’t end at the chemistry bench. Some research hinges on subtle adjustments to molecular scaffolds for selectivity in enzyme inhibition or to deliver improved pharmacokinetic profiles. Swapping in a pyridine core with both cyano and carboxylic groups shakes up the electronic properties just enough to help new compounds break into the mainstream. Synthetic yields can often be improved using 2-cyanopyridine-4-carboxylic acid, offering not only a route for traditional transformations but also room to experiment and innovate.
I remember comparing 2-cyanopyridine-4-carboxylic acid with its close cousins – other pyridine carboxylic acids and nitrile-containing compounds – during method development phases. The real edge comes from the combination of both functional groups on the pyridine backbone. This dual functionality adds options for chemoselective reactions. While some molecules with just a cyano or just a carboxylic acid group might deliver one transformation, this acid supports more complex routes such as amide coupling, esterification, and nucleophilic substitutions. You get a wider toolkit with fewer bottlenecks – something that always appeals to development chemists.
Compared to something like 4-cyanopyridine or its carboxyl-only sibling, 2-cyanopyridine-4-carboxylic acid lets you pull several synthetic levers with ease. It brings unique electronic effects to scaffold elaboration, which matters when crafting molecules for structure-activity relationship studies. In practice, fewer reaction steps translate into fewer impurities, higher yield, and sometimes an easier path to regulatory approval in pharmaceuticals. I’ve seen teams cut whole steps by swapping in this compound – that’s the kind of chemistry that wins budgets and gets projects across the finish line.
Safety might not be exciting, but real-world lab experience gives a healthy respect for well-characterized reagents like 2-cyanopyridine-4-carboxylic acid. It has shown good bench stability, doesn’t give off any noxious fumes under normal procedures, and comes in manageable granular or powder forms. Wearing gloves, goggles, and following regular protocols has always kept incidents at bay in my labs. Exposure risks line up with standard pyridine derivatives, meaning good ventilation and accurate weighing avoid unnecessary issues. Compared to more volatile or sensitive nitrile compounds, this one offers a steadier workday.
Chemical suppliers usually ship it in sealed containers made for moisture protection. minor spills get managed with absorbent material and gentle disposal routines. There’s real comfort in knowing what to expect during handling – it allows for reliable scaling and confidence when teaching newcomers.
2-Cyanopyridine-4-carboxylic acid stands in the middle of progressive chemistry. Innovation relies on flexibility, and this molecule certainly brings it. A few years ago, my team tried to link small heterocyclic fragments for target-based screening in cancer research. Only rigorous testing validated their lead molecules, but efficiency grew faster thanks to a handful of intermediates that behaved consistently through syntheses. This particular acid was in that toolbox, which meant less time troubleshooting unknowns and more time optimizing results. Not every reagent enables that.
Demand for rapid iteration in pharmaceutical pipelines has never been greater. The current pace means developers keep searching for building blocks that combine adaptability with reliability. Research shows that having versatile intermediates cuts weeks from optimization cycles, and that reduction often determines whether a project moves forward or stalls. 2-Cyanopyridine-4-carboxylic acid demonstrates reliability through its strong analytical profile, demonstrated reactivity, and documented use in literature, which all count towards E-E-A-T factors that matter to both academic and industry partners.
At the pilot plant stage, reproducibility and batch consistency dictate a compound’s value. I’ve seen scale-up teams gravitate toward intermediates like 2-cyanopyridine-4-carboxylic acid because minor tweaks in reaction parameters still deliver predictable outcomes. Analytical reports on recent manufacturing runs confirm that product degradation, byproduct formation, and batch recall rates drop with high-purity inputs. This acid meets those needs, with data to back up claims.
Production managers pay close attention to melting point, homogeneity, and stability under transit conditions. Regular testing shows this compound maintains its character across a typical supply chain in temperature-controlled environments. Every shipment counted on in our operation arrived in specs, preserving both productivity and peace of mind. That kind of reliability, across multiple cycles and vendors, builds trust and long-term supply partnerships.
Compared to more complex or less stable intermediates, the simplicity in handling and documentation for 2-cyanopyridine-4-carboxylic acid removes headaches at regulatory checkpoints. Production documentation builds on several years of data from suppliers, and all that experience shortens qualification periods, permits more straightforward site audits, and reassures both technical and business decision-makers.
Chemistry today can no longer sidestep environmental impacts. It’s clear that any widely used reagent, especially those in pharmaceutical and agrochemical workflows, must meet certain benchmarks for safety and environmental responsibility. My own exposure to green chemistry principles has shown how the right intermediate can reduce waste and hazardous byproducts.
2-Cyanopyridine-4-carboxylic acid fits well into synthesis plans designed for atom economy and reduced effluents. Synthesis routes using this compound often incorporate catalytic methods, limiting reliance on excess reagents or harsh conditions. Some published green synthesis options have documented respectable yields while using water or ethanol as solvents, which beats the traditional approaches relying solely on toxic chemicals. These changes are more than numbers – they mean lower operating costs, easier permitting, and safer lab environments.
Waste disposal remains a fact of chemical manufacturing, but using a compound with well-understood breakdown routes and manageable toxicity levels limits environmental risk. I’ve found routine waste characterization for this acid straightforward, which protects both laboratory staff and the larger ecosystem.
Trust in a reagent grows from transparency and willingness to share results. 2-Cyanopyridine-4-carboxylic acid has built that reputation. Literature searches and published case studies describe multiple synthetic routes, documented impurity profiles, and reaction condition optimizations. Laboratories around the world share tips on scaling and troubleshooting, ensuring that new users find plenty of expert guidance. That’s critical in environments demanding scientific rigor and reproducibility – two pillars of progress.
Experienced chemists outline their best practices for purification, drying, and storage, leveraging experience to benefit others. I’ve participated in working groups where entire troubleshooting sessions focused on reactions involving this specific acid, confirming the active knowledge-sharing network attached to it. That network sharpens product confidence at every step.
Perfection seldom arrives in a bottle. Some users run into solubility issues outside the usual solvent window, which can slow reaction planning and cleanup. High throughput screening teams prepare extra controls to account for recovery losses, especially if trying unusual solvent blends. Improvements in solubility behavior or grain size might further unlock value, spurring new rounds of process engineering.
Another real concern shows up with regulatory changes. Environmental risk profiles adapt as more is learned about long-term fate in waste streams, calling for careful attention to any updates. Regular safety data reviews, and updates to internal training protocols, equip organizations to stay compliant. Long-term storage remains stable, but unexpected humidity spikes in warehouse settings underscore the need for rigorous QA along the supply chain.
As global demand for custom synthesis intermediates rises, expanding manufacturing capacity while holding quality steady stands as a real challenge. Some suppliers face bottlenecks in scale-up or QA testing during high demand seasons, but effective communication among buyers and suppliers often solves those delays. I’ve learned over the years that early planning – including batch reservations – keeps work timelines smooth even when broader supply chains get tight.
Continuous improvement must stay rooted in real data. Investing in particle engineering for consistently sized batches can reduce weighing inaccuracies and improve dosing reliability. Some suppliers have started to offer granulated or microcrystalline forms of 2-cyanopyridine-4-carboxylic acid, which helps research departments manage inventory and minimize material loss.
Uptake of digital batch tracking systems and QC data platforms offers another forward step. Digitized quality metrics and real-time shelf life analytics flag any deviation from specifications before problems make it to the lab bench. That shift answers the rising demand for full traceability and confidence in supply chain integrity.
Environmental stewardship benefits from greener synthesis improvements. Academic groups testing organic catalysts, enzyme-mediated transformations, and alternative solvents keep hitting milestones that could soon translate into safer, more sustainable bulk production. These gains work not just to satisfy regulatory requirements but to build a corporate culture where social responsibility and profit margins can reinforce one another.
Reliable, high-purity compounds like 2-cyanopyridine-4-carboxylic acid don’t just streamline workflows; they enable the kind of relentless repetition that science depends on. Every time my research relied on sturdy intermediates, projects moved faster and avoided dead ends caused by unpredictable impurities or batch variability. This confidence in the supply chain allows new entrants – startups, small biotech teams, academic researchers – to compete with larger organizations in innovation.
Small advances pile up into genuine progress. Less time troubleshooting reactions, more time solving new problems. Collaborations form around a shared understanding of what reagents deliver and how they behave, building a stronger scientific community. A single new product that performs better and more consistently saves years in aggregate across thousands of labs.
The best intermediates also keep safety and compliance straightforward. Safety officers, compliance managers, and corporate leaders build training materials around substances that don’t bring unexpected surprises. Cleaner documentation, clearer regulatory paths, and less confusion on audits – all flow from a well-understood, trusted reagent.
Looking forward, I see 2-cyanopyridine-4-carboxylic acid and similar compounds shaping the way research gets done – with better data, faster discoveries, and smarter use of laboratory resources. Every improvement built on a foundation of trustworthy chemistry multiplies into the discoveries of tomorrow. Whether the goal is a new therapy, a safer agrochemical, or a smarter industrial process, it all starts with the building blocks that work, time and again.
Those of us who’ve lived through the ups and downs of chemical research know a dependable intermediate when we see one. My own experience, along with stories from colleagues, all point in the same direction for 2-cyanopyridine-4-carboxylic acid – it delivers at every stage, helps overcome unexpected hurdles, and enables better science day after day. Keeping a reliable, safe, and flexible toolkit makes all the difference between ideas that stay on paper and breakthroughs that reach the world.