|
HS Code |
627475 |
| Name | 6-chloropyridine-3-carbaldehyde |
| Cas Number | 6358-59-8 |
| Molecular Formula | C6H4ClNO |
| Molecular Weight | 141.56 |
| Appearance | Pale yellow to light brown solid |
| Melting Point | 49-53°C |
| Smiles | C1=CC(=NC=C1C=O)Cl |
| Inchi | InChI=1S/C6H4ClNO/c7-6-2-1-5(4-9)3-8-6/h1-4H |
| Synonyms | 6-chloro-3-pyridinecarboxaldehyde; 6-chloro nicotinaldehyde |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
As an accredited 6-chloropyridine-3-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 6-chloropyridine-3-carbaldehyde is supplied in a sealed amber glass bottle with tamper-evident cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Safely loaded 6-chloropyridine-3-carbaldehyde in sealed drums, secured on pallets, ensuring no leakage or contamination. |
| Shipping | 6-Chloropyridine-3-carbaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It is transported according to regulations for hazardous materials, often accompanied by safety data sheets. The package is labeled with appropriate hazard warnings, and shipping is conducted by certified carriers specializing in chemical transport. |
| Storage | 6-Chloropyridine-3-carbaldehyde should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as oxidizing agents and strong bases. Store at room temperature and label the container clearly. Ensure access for authorized personnel only, following all relevant safety and regulatory guidelines. |
| Shelf Life | 6-Chloropyridine-3-carbaldehyde should be stored tightly sealed, away from light and moisture; shelf life is typically 2 years under proper conditions. |
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Purity 98%: 6-chloropyridine-3-carbaldehyde with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting point 58°C: 6-chloropyridine-3-carbaldehyde with a melting point of 58°C is used in organic synthesis workflows, where it allows for efficient temperature-controlled processing. Stability temperature 25°C: 6-chloropyridine-3-carbaldehyde at a stability temperature of 25°C is used in reagent storage applications, where it maintains chemical integrity during extended storage. Molecular weight 156.56 g/mol: 6-chloropyridine-3-carbaldehyde with a molecular weight of 156.56 g/mol is used in analytical method development, where it enables accurate calibration and quantification. Water content <0.5%: 6-chloropyridine-3-carbaldehyde with water content below 0.5% is used in moisture-sensitive reactions, where it prevents hydrolysis and improves reaction reliability. Particle size <50 µm: 6-chloropyridine-3-carbaldehyde with particle size less than 50 micrometers is used in fine chemical formulations, where it enhances homogeneity and dissolution rates. |
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6-Chloropyridine-3-carbaldehyde stands out in the world of fine chemicals for its unique profile as an intermediate, especially for pharmaceutical and agrochemical applications. This compound belongs to the pyridine family, where substitutions on the ring shape both chemical reactivity and suitability for downstream synthesis. I’ve often found that choosing the right building block for a synthesis plan can spell the difference between a smooth route and multiple dead-ends. This aldehyde, bearing a chlorine atom at the 6-position, brings both versatility and specificity, which makes it a preferred option for many researchers.
The product’s structure can be described as a pyridine ring (which is a six-membered aromatic ring containing one nitrogen atom), with a formyl group (–CHO) attached to the third carbon and a chlorine at the sixth position. This pattern of substitution enhances its reactivity toward nucleophilic addition or condensation, which is one reason chemists value it in synthesizing more complex heterocyclic compounds or coupling reactions. The presence of the chlorine atom often directs subsequent reactions, making selective transformations easier in multi-step synthesis.
In the lab and in commercial plants, 6-chloropyridine-3-carbaldehyde finds its main roles as a starting material for many pharmaceuticals and as a scaffold for insecticides, fungicides, and related products. When I worked on pyridine derivatives for crop protection projects, this compound often served as a branch point—either for halogen exchange or introducing further functionality that paved the way for active ingredients. Its aldehyde group offers strong reactivity with amines, hydrazines, and other nucleophiles, which is vital when you need to build complex molecules quickly and with fewer purification headaches.
Several blockbuster drugs and promising new candidates use chloropyridine-based scaffolds for their bioactive cores. Chemists often turn to 6-chloropyridine-3-carbaldehyde because its dual functionality simplifies the overall route: you can modify the chlorine for further derivatization, while the aldehyde enables quick access to imines, hydrazones, or secondary amines through reductive amination. This reduces the number of synthetic steps, saving both time and resources—values any research manager or process chemist appreciates.
Much of the conversation about 6-chloropyridine-3-carbaldehyde centers on purity, physical form, and consistent quality. Chemists who need kilo-quantities for scale-up look for white to pale yellow crystalline solids, which indicate fewer impurities and reliable handling. Most reputable sources offer the product at purities above 98%, which not only reduces complications during reactions but also helps achieve consistent yields and lower side product formation. Moisture and trace metal content must also be kept low, as these can trigger unwanted side reactions during sensitive transformations.
Melting point and solubility lend practical information for everyday use. This compound typically comes with a melting point in the range that allows for convenient weighing and dosing in synthetic runs. Solubility in organic solvents, such as dichloromethane, tetrahydrofuran, or acetonitrile, means chemists can easily incorporate it into a range of reactions, including those under inert atmospheres or requiring cold temperatures. A detail rarely discussed but important from my own experience: packing and storage matter. Properly sealed, dry containers prevent hydrolysis or oxidation of the aldehyde group, preserving purity over months.
Choosing the right intermediate affects nearly every outcome in synthetic chemistry. I’ve seen many labs wrestle with analogues—like 3-formylpyridine, 2-chloropyridine-3-carbaldehyde, or benzaldehydes. None fits all needs, especially in cases where regioselectivity, downstream function, or reaction compatibility make or break a project. 6-Chloropyridine-3-carbaldehyde brings a specific pattern of reactivity. Its position of the chlorine atom can minimize ortho effects and help with subsequent substitution, a benefit compared to alternatives that might lead to troublesome byproducts or harder purifications.
In pharmaceutical R&D, the target molecule’s biological activity can depend not only on the core scaffold but also on subtle differences in substitution around that core. The 6-chloro group sets up the pyridine ring for later transformations without much steric hindrance, and it can even boost metabolic stability—a factor that has increasing importance in drug development. Chemical engineers appreciate that its formyl group isn’t too hindered, so condensation reactions have higher conversion with less forcing conditions, which directly impacts throughput and energy costs in scale-up environments.
In my years discussing project setbacks and troubleshooting, I’ve noticed quality control issues can bring even the best-designed syntheses to a halt. This product’s popularity has led to more suppliers, but not all meet the same standards. Some offer batches contaminated with moisture, leading to lower yields or unpredictable side products. Ensuring full traceability from raw materials to final delivery ensures that industry and academic labs can consistently reproduce results. Certification according to ISO standards, or compliance with regulations in pharma and agchem, isn’t just a bureaucratic hoop—it gives users confidence in every gram that goes on the balance.
Modern buyers care not just about the chemical structure, but also about broader concepts like sustainability, ethical sourcing, and environmental impact. I’ve personally seen projects where clients demanded life-cycle analyses and assurances that intermediates avoided banned reactors or solvents. The story for 6-chloropyridine-3-carbaldehyde is improving, with some suppliers adopting greener processes. Methods that use recycled solvents, minimize halogen waste, or apply catalytic cross-coupling can lower the footprint. Changes like this don’t just tick boxes; they also make a difference as regulatory scrutiny tightens worldwide.
Scientists who innovate with 6-chloropyridine-3-carbaldehyde sometimes run into limitations that go beyond simple cost. Certain reactions remain sensitive to residual metal impurities or background water (from less-than-ideal packaging or transport). Delays in delivery or documentation gaps can derail scale-ups in regulated industries, where certification and batch records are mandatory. Over the past decade, demand for pyridine derivatives has jumped, leading to market fluctuations and temporary shortages. Long-term partnerships with reliable producers help, but I’ve seen contingency planning become a must—multi-sourcing or stockpiling is now common for key intermediates.
Some chemists also report challenges with shelf-life, as even small amounts of air or moisture can lead to degradation of the aldehyde functionality. One promising direction comes from improved packaging, like moisture-proof vials and inert-atmosphere sachets. For larger users, on-site purification or real-time verification (using spectroscopic methods) helps confirm purity before use. These steps add operational steps, but they save headaches downstream. There’s a growing interest in predictive supply chain modeling, using AI to help forecast shortages before they impact timelines.
From the start of my own chemical training, I learned that seemingly small choices—a particular intermediate, a specific purity grade—often influence the success or failure of larger projects. 6-Chloropyridine-3-carbaldehyde isn’t famous outside specialist circles, but it’s involved in creating products that touch millions, whether as frontline therapies, crop-protection agents, or specialty materials. The core of its importance lies in how it brings flexibility to synthesis, opens doors to new compounds, and supports growing needs for complexity without adding unnecessary cost or operational complexity.
Chemical innovation depends on intermediates with reliable profiles and high purity, which allow researchers to focus on new reactions rather than constant troubleshooting. In my experience, projects using well-characterized batches run smoother, with fewer failures due to inconsistent feedstocks. Suppliers aware of changing regulatory, documentation, and quality demands have become more responsive, actively working with labs to anticipate new challenges. In this way, the practical value of 6-chloropyridine-3-carbaldehyde goes beyond its chemical properties—it represents the kind of steady, incremental progress that fuels big leaps in chemistry and applied science.
Many of today’s most promising pharmaceuticals began as simple ideas, leveraging foundational intermediates like 6-chloropyridine-3-carbaldehyde. Product development cycles move faster now, and researchers face greater pressure to accelerate discovery. A high-quality intermediate isn’t just a commodity; it’s a source of technical confidence. Having worked alongside colleagues in both academic and industrial labs, I’ve seen how the right partner or material can compress months of testing into weeks. Research managers now prioritize robust supply lines to ensure that laboratories can pivot rapidly, especially if a route needs to change or a new analog appears promising in screening.
Feedback loops between intermediate producers and end users are also growing tighter. Suppliers now collect data on how storage, transit, or batch-to-batch variation affects downstream results. This responsiveness keeps projects on schedule and ensures that records meet updated regulatory expectations. Years ago, small inconsistencies might have been chalked up to “lab error,” but today’s quality systems flag even minor deviations for follow-up. This approach doesn’t just support better science; it protects investments and speeds new products to market.
Chemistry continues evolving, and so does demand for compounds like 6-chloropyridine-3-carbaldehyde. R&D trends point toward greater complexity in both pharmaceuticals and agrichemicals, driving interest in high-functionality intermediates. Automation, digital batch tracking, and more widespread adoption of green chemistry all offer paths forward. I’ve personally worked on teams exploring how flow chemistry could produce key intermediates with less waste and tighter controls, reducing costs across the board.
The push toward sustainable chemistry won’t leave intermediates behind. Researchers in both academia and industry are investigating bio-based routes and asymmetric catalysis to minimize environmental impact. Synthetic efficiency, waste reduction, and energy savings will all become central criteria when choosing a supplier. For 6-chloropyridine-3-carbaldehyde, these shifts could mean more localized manufacturing or on-demand production, using smarter process controls and predictive analytics to optimize quality.
The importance of collaboration can’t be overstated. Many successful product launches trace back to partnerships—between R&D labs and intermediate suppliers, between regulatory experts and production engineers. For compounds that require special handling or documentation, having a team of experts with deep practical experience is invaluable. Every successful project I’ve seen benefitted from input on supply, scale, regulatory hurdles, and troubleshooting. By working in concert, teams catch problems earlier, prepare better documentation, and drive innovation faster from concept to product.
6-Chloropyridine-3-carbaldehyde may never earn the same name recognition as the finished medicines and products it helps create, but its impact crosses disciplines and industries. My time in the field taught me that investing in reliable, well-characterized intermediates pays off through better outcomes and fewer surprises at each stage of development. As chemistry moves forward, the focus will stay on safety, quality, and adaptability—not just for legal compliance, but for real-world results that matter in researchers’ and consumers’ lives.
High-quality intermediates will continue to define the pace of discovery. 6-Chloropyridine-3-carbaldehyde, with its fine balance of function and flexibility, stands poised to anchor new innovations for years to come—fueling creative science and helping bring safer, more effective products to the world.