|
HS Code |
855753 |
| Product Name | Sodium pyridine-3-carboxylate |
| Synonyms | Sodium nicotinate |
| Chemical Formula | C6H4NNaO2 |
| Molecular Weight | 145.09 g/mol |
| Cas Number | 1003-49-8 |
| Appearance | White to off-white powder |
| Solubility | Soluble in water |
| Melting Point | Decomposes above 230°C |
| Ph Value | Typically 7-9 (1% solution in water) |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Odor | Odorless |
As an accredited Sodium pyridine-3-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sodium pyridine-3-carboxylate is supplied in a sealed, amber glass bottle, 100 grams, with a tamper-evident cap and labeled for laboratory use. |
| Container Loading (20′ FCL) | 20′ FCL: Typically loaded in 25kg bags or fiber drums, totaling about 16–20 metric tons per 20′ container for Sodium pyridine-3-carboxylate. |
| Shipping | Sodium pyridine-3-carboxylate should be shipped in tightly sealed containers, labeled according to regulatory guidelines. Store and transport in a cool, dry place, away from incompatible substances. Ensure packaging prevents leaks or spills. Follow all local, national, and international shipping regulations for chemicals. Use appropriate protective measures to avoid direct contact during handling. |
| Storage | Sodium pyridine-3-carboxylate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers or acids. Avoid exposure to moisture and direct sunlight. Store at room temperature, ideally between 15-25°C (59-77°F). Properly label the container and keep it away from food, drinks, and animal feed. |
| Shelf Life | Sodium pyridine-3-carboxylate typically has a shelf life of 2 years if stored in a cool, dry, and airtight container. |
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Purity 99%: Sodium pyridine-3-carboxylate with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting Point 190°C: Sodium pyridine-3-carboxylate with melting point 190°C is used in high-temperature organic synthesis, where it provides thermal stability during processing. Molecular Weight 143.10 g/mol: Sodium pyridine-3-carboxylate with molecular weight 143.10 g/mol is used in catalyst preparation, where it delivers precise stoichiometric control for reaction scalability. Water Solubility 80 g/L: Sodium pyridine-3-carboxylate with water solubility 80 g/L is used in aqueous formulation of agrochemical products, where it enables rapid and homogeneous dispersion. Particle Size D90 <50 µm: Sodium pyridine-3-carboxylate with particle size D90 <50 µm is used in fine chemical compounding, where it improves blending efficiency and product uniformity. Stability Temperature up to 200°C: Sodium pyridine-3-carboxylate with stability temperature up to 200°C is used in polymer modification reactions, where it maintains functional integrity throughout thermal cycles. Residual Moisture <0.5%: Sodium pyridine-3-carboxylate with residual moisture less than 0.5% is used in electronics-grade material manufacturing, where minimized moisture content protects against hydrolytic degradation. Assay ≥98.5% (HPLC): Sodium pyridine-3-carboxylate with assay ≥98.5% (HPLC) is used in analytical reference standards, where it guarantees reliable and accurate quantification. |
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Sodium pyridine-3-carboxylate, with its distinct place in both research and industrial chemistry, doesn’t usually catch headlines. Yet anyone who spends time in synthesis labs—or moves bulk chemicals for pharmaceutical or specialty material applications—knows its reputation. Some refer to it by its other name, sodium nicotinate. At its core, it’s the sodium salt of nicotinic acid, a molecule related to vitamin B3, but this version brings on a fresh set of uses and practical advantages.
Thinking about the basic chemistry, sodium pyridine-3-carboxylate sits in a league with pyridine derivatives, known for their stable heterocyclic ring and carboxylate function. You see a white to off-white powder, easily soluble in water, holding up under most routing storage and even moderate shipping conditions. The chemical formula, C6H4NNaO2, shows a simple swap—replacing the carboxylic hydrogen with sodium gives added solubility, and that’s where some of the utility comes in. I’ve handled this and similar salts in the lab. You notice the difference right away: the sodium ion makes it less acidic and more user-friendly if you work near neutral pH or need to dissolve the compound without fuss.
The structure isn’t the whole story. Industry labels and specs focus on purity, commonly offering sodium pyridine-3-carboxylate as a solid with a stated purity above 98%. Some producers might chart trace impurities or hydration state, but most reliable suppliers present it as an anhydrous form. Packaging typically avoids the drama that comes from volatile or highly reactive chemicals. I trust it as a stable, storable ingredient that won’t decay or clump, as long as damp air is kept away.
While not every sector recognizes sodium pyridine-3-carboxylate by name, those who depend on precise organic synthesis keep it on hand. In my own research on heterocycle chemistry, sodium pyridine-3-carboxylate became a frequent guest—useful both as a building block and as a ligand. The carboxylate group teams up with metals effortlessly, finding applications in catalyst design, material modification, and systematic pharmaceutical development. The sodium form makes it blend smoothly in aqueous solutions, unlike other pyridine carboxylic acids, which may require neutralization or generate unwanted acidity in sensitive reactions.
Pharmaceutical synthesis leans on this compound for intermediate stages, especially in developing active pharmaceutical ingredients (APIs) that demand tailored heterocyclic scaffolds. Its role reaches beyond pilot labs: some production lines choose sodium nicotinate forms for process efficiency or safety. Food fortification sometimes makes use of sodium salts for more even dispersion in supplements, though in everyday consumer products, the acid form—nicotinic acid or niacin—is more routine. I’ve discussed options with those managing fermentation or vitamin supplement blending, who found the sodium version handy for consistent results in water-heavy environments.
Pyridine carboxylates seem alike if you judge only by their parent structure. In truth, the location of the carboxylate group (the “3-carboxy” part) shapes both reactivity and solubility. Sodium pyridine-2-carboxylate (the ortho isomer) and sodium pyridine-4-carboxylate (the para isomer) share much surface similarity but don’t always fit the same applications. Shifting the group even one atom along the aromatic ring changes how it chelates metals or participates in multi-step synthesis.
From my bench, preparing ligands and functional groups, the difference in coordination behavior becomes evident. The 3-carboxylate position links with metals to form five-membered chelate rings, prized for stability in catalysis or advanced material synthesis. Isomers at the 2- or 4-position shape geometry differently, giving other variants a reputation as niche additives or building blocks. Sodium pyridine-3-carboxylate offers a balance that works across reaction types—sturdy, straightforward, and a “no surprises” option for chemists.
Compared with the free acid (nicotinic acid), the sodium salt wins out on ease of handling in water, reduction of acidity, and compatibility with basic or neutral processes. If a protocol can’t tolerate acidification—think sensitive reagents, enzymes, or certain metal ions—the sodium form slots right in. Even beyond process requirements, those who want to avoid strong acids in formulation or manufacturing settings see this compound as an asset.
Someone might think, “A simple sodium salt—what can go wrong?” My own background in contract research and quality control proved otherwise. Trace impurities or inconsistent hydration can shoot down reaction yields or complicate scale-up. A trustworthy, high-purity batch means fewer surprises and smoother downstream steps. Greater than 98% purity isn’t just a sticker claim, it sets the standard for most synthetic routes and guarantees minor batch-to-batch variation. In specialty applications—making precursors for complex drugs or custom catalysts—those last few percent of purity separate success from expensive rework.
Sterile environments demand an even closer look. Pharmaceutical and food labs need low bioburden and freedom from heavy metal contaminants, since downstream purification can eat up time. Talking with colleagues running GMP (Good Manufacturing Practice) facilities, they lean on analytical certificates showing not just purity but also moisture content and specific identification spectra, like IR or NMR. My own hands-on experience matches this—minor differences in supplier quality sometimes ripple up into big process headaches, and trusted specifications are a lifeline.
Sodium pyridine-3-carboxylate lands in a friendly middle ground—handle it as you would a routine solid, and avoid letting moisture build up. Unlike hygroscopic or volatile organics, the sodium salt behaves reliably, showing no tendency to off-gas or corrode standard lab containers. From storing it sealed at room temperature in poly bottles, I never ran into trouble with clumping or degradation unless it sat exposed for weeks in humid air. Risk of decomposition remains low at standard conditions, a comfort to both small-scale researchers and bulk users moving kilos rather than grams.
Still, proper storage supports product longevity. Water-tight seals and a dry shelf preserve the powder’s flow. Spills—even larger ones in warehouse or pilot plant settings—clean up without special gear or secondary containment. I’ve worked with teams tracking chemical inventories; sodium pyridine-3-carboxylate raised few red flags, neither flammable nor acutely toxic at common exposure levels. Its predictable nature frees up time and energy otherwise spent on safety drills or special ventilation plans.
Concerns about chemical footprints are only rising, and sodium pyridine-3-carboxylate deserves a moment of attention here. Unlike solvent-heavy or highly toxic synthons, sodium salts like this leave manageable residues. Standard waste treatment—acid-base neutralization, dilution, and biological degradation—handles low-concentration streams from lab or production settings. Our team’s waste audits rarely flagged sodium nicotinate as a problem pollutant, though bulk spill scenarios always deserve careful handling and proper reporting.
Direct toxicity to users or environmental risk factors stay low. Oral exposure at typical concentrations doesn’t prompt classification as a major hazard, though, like all specialized chemicals, safe handling habits and standard PPE (gloves, eye protection) form the baseline. Studies on metabolite toxicity highlight low acute effects compared to heavy metals or industrial aromatics. For organizations with ISO 14001 or equivalent environmental management standards, tracking sodium pyridine-3-carboxylate is simple, and process water or byproducts rarely push regulatory limits.
For transport, dry, well-sealed packaging and exposure to standard shipping temperatures don’t create notable risk. My background with chilled and hazardous goods logistics means I appreciate any compound that ships without temperature controls, specialty labeling, or routine spill response. This sodium salt checks those boxes, streamlining both local transport and customs clearance in global supply chains.
Laboratory synthesis claims much of the spotlight. The compound serves as a standard reactant for alkylation, acylation, and complexation reactions. One of the first times I used sodium pyridine-3-carboxylate, we set it up as a ligand donor for transition metal catalysts. The five-membered rings it forms upon chelation stand out for their robustness in both batch and continuous reactions. Colleagues utilizing coordination polymers or molecular sieve development have echoed this—sodium nicotinate derivatives serve as reliable building blocks, reproducible and versatile.
Drug manufacturing finds a friend in this compound for intermediate and side-chain construction. In regulated environments, consistency and low impurity count matter deeply. The sodium form, as opposed to the free acid, plays better with sensitive APIs that react negatively to excess acidity or poor solubility of intermediate reactants. Even clinical trial supply programs see value here, since controlled lots make regulatory documentation easier.
Food and nutraceutical applications, where niacin supplementation targets fortification, sometimes incorporate the sodium salt for ease of blending and dissolution in beverage or supplement mixes. In discussions with product formulators, sodium forms often earn a spot due to the lower risk of pH swings—a real challenge when mixing micro-ingredients with active flavors or sensitive additives. Consumers rarely read this ingredient on a label, but the quality and flow properties of the sodium version appeal to those focused on large-scale vitamin enrichment.
Outside these fields, material science steps up. Metal-organic frameworks and advanced coordination polymers depend on well-characterized sodium pyridine-3-carboxylate to shape pore size, lattice stability, and selective sorption behavior. Teams working in specialty ceramics, battery materials, or environmental capture technologies reap the benefits of its clear reactivity and affordable sourcing. The rise of green chemistry and circular material design only increases interest—predictable, low-toxicity inputs deliver real value for sustainable process planning.
There’s one lesson I’ve learned in both academic and industrial settings: nothing saves time and money more than a trustworthy source. Sodium pyridine-3-carboxylate brings value only when it’s consistently what you expect. Analytical protocols—thin layer chromatography, HPLC, NMR, IR spectroscopy—trace out deviations in purity or identity fast. Good sources provide clear documentation, not just for total purity, but for identified impurities, water content, and spectral fingerprints. In my own work, batches that skipped these details left us chasing shadows when reactions went off script.
The expectation set by the pharmaceutical and food supply chains—clear traceability, tied lot numbers, and reliable performance—now stretches across the board. Laboratories and process engineers alike value clear labeling and responsive technical support. Years ago, I joined a project for scaling up heterocyclic ligand production; supplier transparency about sodium pyridine-3-carboxylate sample history helped save weeks during troubleshooting, cutting through the haze of “what’s different this time?” and getting at the true variable. The investment in a reputable supply line nearly always delivers richer returns than small savings from off-label or irregular product sources.
Even a compound as straightforward as sodium pyridine-3-carboxylate faces occasional challenges. Global supply interruptions, cost pressure, and increasing regulatory demands cause ripples. Supply chain shocks, as seen during disruptions in manufacturing hubs, impact labs and factories far from the original source. I’ve spoken with procurement specialists who weathered unexpected lead times or price spikes, and nearly all adopt the same approach—diversify suppliers, demand full documentation, and maintain better safety stock.
Counterfeit or low-grade product represents a risk not just in pharmaceuticals but also for industrial chemicals. Tracking supplier credibility and reviewing batch certificates protect against poor performance or contamination. Initiatives tying chemical sourcing to blockchain or digital traceability grow each year, letting buyers verify shipments all the way back to the original production lot. In the lab, quick confirmation runs (spot TLC, melting point checks, or rapid NMR) head off problems before scale-up swallows days of work.
Some see an ongoing challenge in refining greener synthesis routes and lowering manufacturing footprints. Sodium pyridine-3-carboxylate production leans on established organic chemistry, but every process update—switching out hazardous solvents, slipping in renewable precursors—feeds into big sustainability goals. Industry groups share research on eco-friendlier dehydration, safer crystallization, or energy-efficient purification as feasible upgrades. Reporting trace solvent use and employing closed-cycle water systems in large-scale plants points the way forward.
The chemical sector’s shift toward sustainability, traceability, and digitalization shapes how compounds like sodium pyridine-3-carboxylate will be produced, monitored, and delivered. Specialty chemicals, no longer the niche domain of a handful of experts, now stand at the foundation of entire emerging industries—clean energy, precision medicine, and tailored materials. I’ve seen small improvements at the supplier end—renewable energy at production sites, digital QA tools, greener solvents—begin to add up, shaping cost, product image, and even compliance with tightening regulations.
Educational outreach matters, too. As younger scientists take the reins in R&D and manufacturing, clear stories and hands-on tips about specialty reagents grow in value. Years ago, I leaned heavily on word-of-mouth wisdom. Today, digital platforms and open-access data close the knowledge gap quickly, letting researchers compare notes on reactivity, formulation, or troubleshooting.
New supply chain models start to put transparency in front. On blockchain-based trade platforms or science-focused procurement networks, buyers can verify not only batch details, but sustainability data, product ethics, and summaries from other users’ lab books. Chemical companies flag green metrics, pushing sodium pyridine-3-carboxylate and other common agents to evolve under the dual pressures of cost and social responsibility. These incremental improvements shape risk management and drive process changes felt by everyone handling this compound—from seasonal contract chemists to plant engineers overseeing 24/7 syntheses.
Sodium pyridine-3-carboxylate doesn’t grab the kind of attention reserved for flashy organometallics or headline-grabbing pharmaceuticals. Instead, it stands as a quiet workhorse—a broad-tool that can meet a host of challenges in both exploratory research and scale-up. My own years working with specialty chemicals repeatedly underscored two facts: details matter, and so do reliable suppliers. This sodium salt proves its value through stable performance, clear sourcing, and adaptability across many industries.
Tracking those differences—across isomers, salt forms, application needs—keeps industry players and researchers from falling into routine or making costly mistakes. Product lifecycle thinking, risk management, and supply robustness all link back to how basic compounds like sodium pyridine-3-carboxylate are sourced, managed, and applied. In an environment where trust, transparency, and science-backed sourcing matter more each year, the humble sodium salt continues to earn its place at the bench, in the process drum, and on the procurement roster.