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HS Code |
998681 |
| Chemical Name | 6-Chloropyridine-3-carboxylic acid |
| Cas Number | 6358-36-7 |
| Molecular Formula | C6H4ClNO2 |
| Molecular Weight | 157.55 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 179-183 °C |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC(=NC=C1C(=O)O)Cl |
| Inchi | InChI=1S/C6H4ClNO2/c7-5-2-1-4(6(9)10)3-8-5/h1-3H,(H,9,10) |
| Pubchem Cid | 82597 |
As an accredited 6-Chloropyridine-3-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle labeled "6-Chloropyridine-3-carboxylic acid," features hazard symbols and product details, securely sealed. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 6-Chloropyridine-3-carboxylic acid: Securely packed in fiber drums/paper bags, net weight 5-10MT per container. |
| Shipping | 6-Chloropyridine-3-carboxylic acid is shipped in secure, airtight containers to prevent contamination and moisture absorption. Packaging complies with international chemical transport regulations. The chemical is typically shipped at ambient temperature, unless otherwise specified, and includes appropriate labeling and documentation for safe handling, storage, and customs clearance during transit. |
| Storage | 6-Chloropyridine-3-carboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect it from moisture and direct sunlight. Keep the storage area clearly labeled and restrict access to trained personnel. Adhere to all relevant safety and regulatory guidelines for handling hazardous chemicals. |
| Shelf Life | 6-Chloropyridine-3-carboxylic acid is stable under recommended storage conditions; typically, shelf life is at least 2 years unopened. |
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Purity 99%: 6-Chloropyridine-3-carboxylic acid with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low impurity levels in final drug compounds. Melting point 153°C: 6-Chloropyridine-3-carboxylic acid with a melting point of 153°C is used in solid-phase organic reactions, where it enhances reaction control and product reproducibility. Low moisture content <0.5%: 6-Chloropyridine-3-carboxylic acid with low moisture content below 0.5% is used in agrochemical formulation processes, where it improves shelf-life and stability of active ingredients. Particle size <50 microns: 6-Chloropyridine-3-carboxylic acid with particle size under 50 microns is used in high-precision coating applications, where it provides uniform dispersion and superior surface finish. Stability temperature up to 120°C: 6-Chloropyridine-3-carboxylic acid stable up to 120°C is used in heated batch reactions, where it maintains chemical integrity and consistent reactivity. Assay 98% (HPLC): 6-Chloropyridine-3-carboxylic acid with 98% assay by HPLC is used in specialty chemical synthesis, where it delivers reliable analytical results and predictable reaction outcomes. |
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Chemists and researchers often spend as much time choosing chemicals as they do running experiments. One compound that stands out lately is 6-Chloropyridine-3-carboxylic acid. This molecule has caught the attention of people across pharmaceuticals, agriculture, and advanced material sciences, and for good reason. Precision and repeatability matter so much in the lab. That's why a chemical like this one, with known properties and reliable outcomes, can sometimes feel like a small victory.
With a core pyridine ring, a chlorine atom sitting at the sixth position, and a carboxylic acid moiety at the third, this compound brings distinct possibilities to organic synthesis. The molecular formula, C6H4ClNO2, offers a roadmap for synthetic chemists looking to build complex structures. Purity is never just a number on a label; it’s about trust. High-purity grades of this acid often land above 98%, thanks to careful refinement and dedicated manufacturing controls. That baseline makes a difference in crystallization and reproducibility. A chemist recently told me about an entire reaction sequence that hinged on nothing more than a 0.2% impurity in a similar compound. There’s an important lesson: starting with clean material saves headaches later.
Let’s talk real-world uses. In pharmaceuticals, the aromatic ring forms a solid base for constructing drug candidates. Medicinal chemists appreciate electron-withdrawing groups like chlorine; they tune biological properties and metabolism. The carboxylic acid provides an anchor for coupling reactions. That’s where the action happens: a route to esters, amides, or even new heterocycles. It works as a key intermediate in anti-inflammatory and anti-viral research, and some reports note its presence in multi-step syntheses for experimental compounds.
In crop science, creating molecules that can protect plants without harming the environment poses constant challenges. The structure of 6-Chloropyridine-3-carboxylic acid has been picked for projects developing selective herbicides and growth regulators. Here, its stability and controlled reactivity show their strengths. Down the line, these attributes help keep residues predictable, supporting food safety standards and crop yield.
Those working on electronic materials look for building blocks that offer both structural rigidity and functional handle points. This compound’s architecture, particularly the position of its functional groups, lends itself to further modifications. It can serve as an intermediate for ligands, dyes, or new conductive polymers. When you can count on reproducible reactivity, designing new materials becomes less of a gamble and more of a calculation.
A walk down the chemical supplier catalog reveals hundreds of pyridine derivatives, but not all play the same role. The location of both the chlorine and the acid group in 6-Chloropyridine-3-carboxylic acid does more than decorate the molecule—it shapes its ability to bind, react, and influence biological targets. Sourcing similar compounds with substitution at different ring positions can lead to very different behaviors. For example, a chlorine at the 2-position, or a carboxylic acid at the 4-position, takes you into a new landscape: changes in solubility, electronic effects, and steric influence.
Many pyridine carboxylic acids see use in basic research, but this 6-chloro variant provides a unique intersection between electronic tuning and synthetic versatility. The electron-withdrawing power of the chlorine affects the acidity of the carboxylic group, often enabling specialized transformations. There's value in having a compound that doesn't just sit passively—its presence in a reaction balances stability and reactivity, a factor not always found in other derivatives.
Once the bottle arrives, best practices really kick in. This compound stays stable under normal storage, as long as humidity stays low and light is kept out. Repeated opening and closing of containers introduces risk for hydrolysis, especially when working with high-purity acids. Keeping things dry isn't only about following protocols—it's a matter of keeping experiments consistent and costs down. Refrigeration often stretches shelf life, but storing any acid with proper desiccation becomes a lifelong habit for many in the field.
Lab work often faces scrutiny around waste and environmental impacts. 6-Chloropyridine-3-carboxylic acid, used thoughtfully, lines up well with efforts to minimize unnecessary by-products. Its design supports target-specific transformations, helping to reduce the number of side reactions and unnecessary steps. I remember seeing teams working late, trying to optimize a syntheses that choked out by-products. A well-chosen reagent makes scaling safer and greener. Waste streams drop, and so do disposal costs.
Developments in alternative solvents, reaction miniaturization, and continuous-flow synthesis increasingly favor intermediates that can stand up to both batch and flow conditions. This acid, with its robust structure, doesn’t degrade or react unpredictably when conditions shift. Industries trying to tighten up their environmental profiles see value in these properties. The less one has to track, separate, and clean up, the more attention can go toward what matters: innovation and safety.
No one in research or manufacturing wants to gamble with uncertainty. Rigorous analytical checks—NMR, HPLC, and mass spectrometry—come into play at several points from production through application. Consistency between batches means researchers spend less time troubleshooting and more time moving projects forward. Without getting lost in the weeds, it helps to know that 6-Chloropyridine-3-carboxylic acid often shows sharp, easily identifiable peaks on chromatograms, simplifying checks for purity and helping avoid hidden impurities that plague more ambiguous molecules. Heavy reliance on robust supply chains and clear documentation further reduces risk of error or contamination.
A single batch of an intermediate like this one can quietly influence thousands of downstream results. Consistent melting point, crystal habit, and reactivity—these count far beyond the academic lab. In manufacturing, even slight variations can trigger troubleshooting, lost time, and excess costs. A few tenths of a percent off-spec and the whole process might need adjustment. That's why the manufacturing process leans on validated synthetic routes, controlled crystallization, and spot checks.
From experience, walking into a lab equipped with a bottle from a trusted supplier, there’s a confidence that every hour spent working will give comparable data each time. Compare that to the stress of sourcing a patchwork of chemicals from different vendors—results start drift, and conclusions get shaky. Reliable companies back up their product with stability data, not just shiny packaging. That kind of transparency draws repeat business.
No matter how routine handling becomes, chemical safety deserves attention every single time. 6-Chloropyridine-3-carboxylic acid, like many halogenated aromatics, can act as an irritant. Proper gloves, eye protection, and working under an efficient fume hood take minimal effort and return maximum peace of mind. Good habits stay with you. I have seen minor lapses lead to big problems—a splash here, a spill there—because someone underestimated the risk or grew too comfortable with routine.
Storage choices matter, not only for safety but performance. Acids often interact with metal shelving or poorly sealed lids, so non-reactive containers get the nod. Maintaining clear, up-to-date labeling on all stock helps avoid mix-ups. Cross-contamination creeps up when people skip best practices. Even seasoned chemists have been caught off-guard by an unlabeled jar or a decanted chemical stored in an old bottle. Reliable labeling and segregated storage make life smoother for everyone working in the lab.
Collaboration makes a big impact in science. Teams from pharma, materials, and academic research often lean on intermediary molecules like this one to build custom compounds. The layout and reactivity in 6-Chloropyridine-3-carboxylic acid fit neatly into projects where tailored properties are more than just a nice-to-have—they’re essential. A molecule that can play well in both academic and industrial settings finds itself in more research proposals and development pipelines.
When people talk about research bottlenecks, they often point to scale-up risks, supply interruptions, or unexplained variability. An intermediate with solid track records across small and large batches can open doors to broader collaboration. Shared data, open communication between suppliers and customers, and transparent records keep those doors open. In my own work, consistency from a raw material freed up energy and time for real problem-solving, instead of troubleshooting and repeating failed experiments.
Science rarely sits still. Regulation evolves, market needs shift, and what was niche yesterday finds itself at the center of attention next week. Companies, universities, and contract research outfits rely on intermediates that can flex with new priority lists. 6-Chloropyridine-3-carboxylic acid holds up under these changing currents because practical experience, published data, and years of case studies reinforce its value.
As researchers push tools like automation, high-throughput screening, or AI-guided molecular design, the confidence that comes from trusted building blocks can't be overstated. Each step forward in these technologies multiplies the need for reliable, thoroughly characterized reagents. Chemicals with ambiguous performance or unexplained behaviors end up on the sidelines. This acid, with its well-understood profiles, stays essential as teams ramp up both speed and complexity.
Responsible sourcing is no longer just an afterthought—it’s front and center in decision-making across science and industry. 6-Chloropyridine-3-carboxylic acid, especially from reputable suppliers, comes with a paper trail. From raw starting materials to the finished bottle, transparency in sourcing practices supports not only regulatory compliance but also public trust. I’ve seen teams select one supplier over another simply because of better documentation, safer working conditions for those in the supply chain, or clear environmental practices.
Counterfeit chemicals and unverified purity levels present real risks that don’t show up until disaster strikes. Avoiding those pitfalls takes a willingness to work with certified sources, to demand audit trails, and to stay vigilant against deals that seem too good to be true. Ultimately, the confidence that your reagents come from legitimate sources means your research will be trusted by others—no small thing in a field built on reputation.
The story of 6-Chloropyridine-3-carboxylic acid continues to unfold as new fields merge and boundaries between disciplines blur. Synthetic biology, green chemistry, and nanotechnology each look for reliable, functionally rich launching pads for their innovations. This compound, with its tailored functional groups and track record, can only grow in importance as these sectors mature. The challenge will always be to balance classic chemistry with emerging needs: new reaction routes, sustainability targets, digitalization.
I have watched suppliers respond to these challenges with investments in better purification, full-spectrum analytical testing, and even shorter lead times. On the user side, scientists share their protocols, document new reactions, and push for automation wherever possible. By staying rooted in careful research and hands-on experience, every batch of 6-Chloropyridine-3-carboxylic acid strengthens the bridge between traditional benchwork and tomorrow’s breakthroughs.
After years spent moving between academic research and industry, I find that the value of a compound like this one comes down to more than just numbers on a page. When solutions need to come fast, supply chains wobble, or new ideas hit the pipeline, having a trusted reagent on hand matters more than ever. Each time I’ve had to navigate a tricky synthesis, knowing that my intermediate held up to scrutiny, that its reactions went as planned, and that repeats gave the same results—those moments added up to a better product and a clearer mind.
For those just stepping into the field, or for experienced hands looking to streamline, 6-Chloropyridine-3-carboxylic acid offers more than chemical functionality. It brings predictability, compatibility with modern techniques, and a legacy of successful application across varied challenges. Every bottle, every batch, tells a story of chemistry done right. And in this field, that consistency is worth every penny.