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HS Code |
814919 |
| Chemical Name | 2-Chloro-3-pyridinecarboxylic acid |
| Molecular Formula | C6H4ClNO2 |
| Molecular Weight | 157.55 g/mol |
| Cas Number | 39469-40-2 |
| Appearance | White to off-white solid |
| Boiling Point | N/A (decomposes) |
| Melting Point | 134-138 °C |
| Density | 1.47 g/cm3 |
| Solubility In Water | Slightly soluble |
| Pka | 3.1 |
| Smiles | C1=CC(=C(N=C1)Cl)C(=O)O |
| Inchi | InChI=1S/C6H4ClNO2/c7-4-2-1-3-8-5(4)6(9)10/h1-3H,(H,9,10) |
| Synonyms | 2-Chloro-nicotinic acid |
| Storage Temperature | Store at room temperature |
| Purity | Typically ≥98% |
As an accredited 2-Chloro-3-Pyridine Carboxylic factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2-Chloro-3-Pyridine Carboxylic is supplied in a sealed amber glass bottle with a secure screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 14 metric tons packed in 560 fiber drums, each containing 25 kg of 2-Chloro-3-Pyridine Carboxylic. |
| Shipping | 2-Chloro-3-pyridine carboxylic acid is typically shipped in tightly sealed containers to prevent moisture uptake and contamination. It should be stored and transported in a cool, dry, and well-ventilated area, away from incompatible substances. Proper labeling and compliance with relevant chemical regulations must be ensured during shipping. |
| Storage | **Storage for 2-Chloro-3-pyridinecarboxylic acid:** Store in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of ignition. Keep away from incompatible substances such as strong oxidizers and bases. Use under a chemical fume hood and ensure proper labeling. Avoid prolonged exposure and prevent environmental release. |
| Shelf Life | 2-Chloro-3-pyridine carboxylic has a shelf life of 24 months when stored in a cool, dry, and sealed container. |
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Purity 99%: 2-Chloro-3-Pyridine Carboxylic with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield production of active compounds. Melting Point 180°C: 2-Chloro-3-Pyridine Carboxylic with a melting point of 180°C is used in agrochemical formulation, where it maintains structural integrity during processing. Molecular Weight 158.55 g/mol: 2-Chloro-3-Pyridine Carboxylic at a molecular weight of 158.55 g/mol is used in heterocyclic compound research, where precise molecular control is required. Stability Temperature up to 120°C: 2-Chloro-3-Pyridine Carboxylic stable up to 120°C is used in catalysis development, where chemical stability enhances reaction efficiency. Particle Size <50 microns: 2-Chloro-3-Pyridine Carboxylic with particle size less than 50 microns is used in fine chemical blending, where uniform dispersion is critical for formulation consistency. Solubility in Methanol: 2-Chloro-3-Pyridine Carboxylic with high solubility in methanol is used in analytical chemistry applications, where rapid sample preparation is facilitated. Residual Water Content <0.5%: 2-Chloro-3-Pyridine Carboxylic with residual water content below 0.5% is used in moisture-sensitive syntheses, where performance reliability is ensured. |
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Strolling through chemical supplier catalogs, a chemist runs across a lot of tough-to-pronounce molecules. Among them, 2-Chloro-3-Pyridine Carboxylic Acid stands out to anyone working on agrochemicals, pharmaceutical intermediates, or fine chemical synthesis. Those who have spent hours staring at reaction schemes can vouch for the particular importance of subtle tweaks in molecular structure—a chlorine on the second carbon of a pyridine ring and a carboxyl group anchoring the third position transform this molecule from an obscure specialty to a go-to intermediate in a crowded lab or production plant. The difference looks modest on a whiteboard, but under the hood it creates multiple opportunities for downstream chemistry.
From personal experience working in small-molecule scale-up, minor substitutions change reactivity in unpredictable ways. 2-Chloro-3-Pyridine Carboxylic Acid (often referred to in shorthand as 2-chloro-3-pyridinecarboxylate or CPCA) drags over unique properties from both its chlorinated and carboxylated branches. The model associated with this product aligns most commonly with a molecular weight in the range of 157 grams per mole, which falls right inside the sweet spot for handling in most synthetic procedures—neither overly volatile nor stubbornly unreactive.
Structurally, this molecule combines the electron-withdrawing effect of chlorine at the ortho position with the versatility of the carboxyl group right nearby. As a result, once you plug this compound into your reaction plan, it behaves differently than a variety of other pyridine derivatives, especially when compared with its closest relatives like 2-Chloropyridine or plain Pyridine-3-Carboxylic Acid. The chlorine atom boosts molecular stability in solution, and the carboxyl group eases transformations via standard condensation, amide formation, or coupling strategies.
Too many times, a project goes astray because a small molecular change is more disruptive than anticipated. In drug discovery and crop protection, even the smallest difference in a precursor can influence yield and downstream scalability. For 2-Chloro-3-Pyridine Carboxylic Acid, the substitution pattern blocks unwanted side reactions—compared with non-chlorinated pyridine carboxylic acids, the chlorine shield on the ring prevents over-oxidation during harsh conditions and cuts down on bench-top tarring. This means less time spent cleaning glassware, more repeatable reaction profiles, and, at scale, fewer run-to-run headaches.
Out of the flask, it generally comes as a pale solid, usually a powder or crystalline mass, which simplifies handling if you measure by spatula or wish to premix with solvents. Lab techs grumble less about clumping compared with more hygroscopic carboxylic acids, which translates to tighter dosage control and less waste during routine batching.
Discussing technical specifications, batch purity usually tops 98%, with trace moisture below 0.5% by Karl Fischer titration—numbers which reflect the care necessary in analytical chemistry for any compound serving as a pharmaceutical or agrochemical intermediate. Think of purity not as an academic boast, but as a real-life buffer against impurity build-up in multi-step syntheses. The trace impurity profile—especially inorganic salts or related pyridine isomers—matters for scale-up, because recyclers and purifiers tally every anomaly.
Anyone who has spent time investigating crop protection will recognize why the right intermediate makes all the difference. This particular molecule, with its chlorinated backbone, fits right into synthetic lines aiming for modern herbicides, fungicides, and select insect growth regulators. The carboxyl group provides a ready handle for building bonds to other functional fragments—a feature those in combinatorial chemistry crave when trying to juggle dozens of modular units. In pharmaceutical settings, 2-Chloro-3-Pyridine Carboxylic Acid can lead directly to key scaffolds in active pharmaceutical ingredients, whether through amide formation, esterification, or coupling with nucleophiles.
Unlike more commonly known benzenoid carboxylic acids, the pyridine moiety puts a basic nitrogen in the ring, offering unique reactivity in palladium-catalyzed cross-coupling or directed ortho-metalation sequences. This allows creative chemists to aim for products that would otherwise demand laborious protecting group strategies or crash out due to low selectivity.
From the perspective of cost-effectiveness and throughput, using this intermediate can shrink process steps and trim spending on reagents and purification. Processes looking to minimize by-products find success here, since the ortho-chloro group increases the selectivity of subsequent halogenations or SNAr (nucleophilic aromatic substitution) reactions. Overreactions fall off, materials move through the plant faster, and process engineers lose less sleep.
Not every pyridine carboxylic acid fits every application. Those who have tried substituting with non-halogenated versions (like plain Nicotinic Acid) probably noticed a bumpier road in both reactivity and physical handling. The chlorine isn’t just decorative—it profoundly alters both solubility and downstream behavior. For instance, 2-Chloro-3-Pyridine Carboxylic Acid remains stable in a broader range of solvents, from acetonitrile to dichloromethane, making it suitable for multi-step campaigns. In the bench environment, it means one can plan longer synthetic runs without factoring significant decomposition into the time budget.
Working in a contract manufacturing organization, time and again, I’ve seen clients try to squeeze costs by opting for general pyridine carboxylates, thinking function beats form. The practical reality proves otherwise: the increased selectivity, lower by-product profile, and improved shelf-life of 2-Chloro-3-Pyridine Carboxylic Acid often save money and time in the end. Partners in drug development or agrochemical formulation frequently circle back to this molecule after encountering bottlenecks using less specialized intermediates.
Physical form also creates a real difference. Compared to oily or sticky alternatives, the easily manageable powder helps with precise weighing and storage. Those in analytical labs appreciate this, especially for quality assurance processes. Stove-top stability cuts risk during shipment and storage, an underappreciated advantage in both global and regional commerce.
Focusing solely on raw materials can blind chemists and buyers to sourcing and stewardship. Because this molecule links directly into pharmaceutical or agricultural pipelines, rigorous attention to vendor quality and traceability backs up every purchase. Those of us in scale-up worry about documentation not as red tape, but as a real safeguard. Analytical certification—NMR, IR, trace metal screening—should arrive alongside the shipment. Reputable suppliers understand the stakes: substandard intermediate might not just cost money, but could put larger projects (and reputations) at risk.
Proper handling in the plant or lab also earns a mention. 2-Chloro-3-Pyridine Carboxylic Acid doesn’t give off acrid fumes like some other chlorinated pyridines. Lab personnel find it less irritating, with standard fume hood precautions and gloves sufficing in most cases. Still, personal protective equipment remains non-negotiable. For larger operations, bulk handling remains straightforward, with robust storage protocols to prevent clumping or accidental exposure.
In our era, regulatory scrutiny on specialty chemicals has only grown, with special emphasis on REACH or similar frameworks. Those planning to use this material in high-throughput or export-oriented processes invest time confirming up-to-date registration and safety information. Input from safety data sheets, hazard labeling, and disposal protocols transcends legal compliance, ensuring safe communities and workplaces—the same values that push chemistry toward better public acceptance.
Anyone working in chemicals for more than a few years has felt the shift toward greener approaches. 2-Chloro-3-Pyridine Carboxylic Acid, while a specialty item, participates in this transition: new suppliers develop processes that minimize waste chloride, recover solvents for reuse, and drive yields with catalytic rather than stoichiometric inputs. The hope is fewer extraction steps, leaner energy usage, and less environmental load. Stories circulate in the industry about process intensification efforts that cut batch footprints and shrink wastewater volumes.
Scale-up sometimes exposes hidden headaches: minor by-products from incomplete reactions or inconsistent crystallization. Savvy chemists and process engineers set up pilot runs, monitor impurity drift, and tweak crystallization with patience gained from long days in the pilot plant. The careful control of solvents, temperature, and filtration means less off-spec material, which has real supply chain impact. In my background with process troubleshooting, small changes—cooler filtration, optimized pH—often make the difference between a two-day clean-up and a seamless campaign.
Growing demand for specialty molecules in pharmaceutical and crop science will demand more robust production models. Digital monitoring, process automation, and data-triggered sampling help maintain batch-to-batch consistency, which is the lifeblood of any intermediate supplier. Buyers looking for 2-Chloro-3-Pyridine Carboxylic Acid shouldn’t hesitate to ask about batch history, shipping times, and laboratory controls. The strongest industry relationships develop around clear communication—not just price points.
Buyers and users who overlook local or international requirements often invite delays. For this molecule, regulatory frameworks can be intricate: compliance with PIC, ICH, or custom export reporting keeps product moving smoothly. Documentation showing absence of controlled substances or persistent bioaccumulative toxins instills confidence along the distribution line. Speaking from personal headaches tied to missing paperwork, clear certificates—from analysis to country-of-origin—build critical trust with both internal and external auditors.
Quality assurance for this class of chemical capitalizes on both analytical data and trustworthy supplier vetting. Laboratories should look beyond just HPLC or NMR for batch approval. Microbial testing, heavy metal screening, and solvent residue checks fill out a picture of material fit for sensitive downstream chemistry. Each certificate is more than a box ticked--it’s assurance that processes relying on tight tolerances won’t grind to a halt.
For partners in regulated industries—whether pharmaceuticals, genomics, or next-generation agrochemistry—a full documentary trail matters. With global movement of both finished product and intermediates, transparency improves predictability, supports smoother import clearance, and lowers the risk of regulatory hold-ups. No one enjoys weeks-long holdups at customs because of missing or incomplete paperwork, especially when production deadlines loom.
The chemical supply world has often lagged behind in customer service, but recent years show a marked improvement for specialty intermediates like 2-Chloro-3-Pyridine Carboxylic Acid. Teams now answer technical questions faster, supply detailed documentation up front, and open discussions about storage, workflow, and application tweaks that help customers optimize use rather than just sell material.
Feedback loops between experienced users and manufacturers create a knowledge base that ripples outward. Customer case studies—non-boilerplate, data-driven—prove vital in refining both process and marketing. Innovation circulates not just in lab notebooks but in direct dialogue between supplier and chemist. New forms, perhaps adjusted for granularity or flowability, sometimes result from straightforward requests based on real-world bottlenecks.
At one point, our own group ran into unanticipated solubility hiccups during scale-up. Vendor engagement made the difference: within days, technical staff brought forward alternate solvent blends, experimental drying conditions, and shared unpublished application notes. An open exchange democratizes innovation, boosting value across the supply chain.
As end-users and downstream manufacturers face tighter margins and increasing regulatory scrutiny, each new intermediate in the supply chain undergoes more thorough vetting. No longer do buyers accept one-size-fits-all solutions. The combination of reactivity, stability, and robust documentation makes 2-Chloro-3-Pyridine Carboxylic Acid stand out. Developers appreciate the faster cycle times and smoother regulatory pathway; analysts value fewer surprises in the impurity profile.
In those companies pushing to replace traditional approaches with modular synthesis, this ingredient supports flexibility and process resilience. Batch reproducibility allows researchers and process engineers to devote time to creative upstream or downstream problem-solving rather than firefighting. The fact that the molecule performs predictably across multiple scales—from flask to ton-scale reactor—means process knowledge gained in the lab transitions more reliably to larger production.
Storage stability, especially under warehouse fluctuations, makes it easier for small operations to stock material without risk of spoilage. Good documentation aligns with modern ERP or track-and-trace environments, transforming what could be a commodity item into a value-adding supply partner.
Changing market forces and accelerating discovery cycles in drug and crop science point toward a growing need for specialized intermediates like 2-Chloro-3-Pyridine Carboxylic Acid. With every new regulation, supply constraint, or technological leap, the need for robust supply networks and trustworthy partners gets more acute.
Industry voices, from bench chemists to regulatory affairs, encourage suppliers to keep pushing boundaries: cleaner processes, sharper analytics, transparent sourcing, and ongoing client engagement. Reformulating intermediates for better performance, tweaking physical properties for tighter operations, and extending technical support create a living feedback loop, not just for the molecule itself but for every stakeholder who relies on it.
In this landscape, intermediates stop being anonymous cogs in a faceless process and become stepping stones that drive discovery and product development. Through rigorous attention to quality, creativity in process engineering, and a commitment to knowledge sharing, the legacy of this specialty chemical keeps growing. For those committed to moving science and industry forward, choosing a partner who treats intermediates like 2-Chloro-3-Pyridine Carboxylic Acid as more than a commodity pays dividends across timelines and project objectives.