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HS Code |
936907 |
| Product Name | 2-Bromopyridine-5-carboxaldehyde |
| Cas Number | 630423-77-9 |
| Molecular Formula | C6H4BrNO |
| Molecular Weight | 186.01 g/mol |
| Appearance | Yellow to brown crystalline powder |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=NC(=C1)Br)C=O |
| Inchi Key | NSACNQGRMZAUDB-UHFFFAOYSA-N |
| Solubility | Soluble in organic solvents such as DMSO and ethanol |
| Storage Conditions | Store in cool, dry place, under inert atmosphere |
As an accredited 2-BROMOPYRIDINE-5-CARBOXALDEHYDE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Bromopyridine-5-carboxaldehyde is supplied in a 5g amber glass bottle with a screw cap, labeled with hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packaged 2-BROMOPYRIDINE-5-CARBOXALDEHYDE, ensuring safe, efficient bulk chemical transport and compliance with regulations. |
| Shipping | 2-Bromopyridine-5-carboxaldehyde is shipped in secure, tightly sealed containers to prevent leaks and contamination. The chemical is handled in compliance with hazardous material regulations, labeled as a corrosive and potentially harmful substance. Packaging ensures protection from moisture, light, and extreme temperatures during transit, with appropriate documentation for safe transportation. |
| Storage | 2-Bromopyridine-5-carboxaldehyde should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight and sources of ignition. Keep it separated from strong oxidizing agents. Store under inert atmosphere if possible, and protect from moisture. Properly label the container and ensure that only authorized, trained personnel handle and access the compound. |
| Shelf Life | 2-Bromopyridine-5-carboxaldehyde should be stored tightly sealed, protected from light and moisture; typical shelf life is 12–24 months. |
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Purity 98%: 2-BROMOPYRIDINE-5-CARBOXALDEHYDE with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures accurate reaction yields and reduced by-product formation. Molecular Weight 188.01 g/mol: 2-BROMOPYRIDINE-5-CARBOXALDEHYDE of molecular weight 188.01 g/mol is used in heterocyclic compound development, where precise molecular mass allows consistent formulation and reliable scaling. Melting Point 70°C: 2-BROMOPYRIDINE-5-CARBOXALDEHYDE with melting point 70°C is used in solid-state storage for chemical synthesis, where a defined phase transition temperature facilitates handling and processing. Stability Temperature up to 85°C: 2-BROMOPYRIDINE-5-CARBOXALDEHYDE stable up to 85°C is used in high-temperature organic reactions, where stability prevents degradation and maintains product integrity. Particle Size <20 µm: 2-BROMOPYRIDINE-5-CARBOXALDEHYDE with particle size below 20 µm is used in catalyst preparation, where fine particles improve dispersion and reaction efficiency. Assay ≥99%: 2-BROMOPYRIDINE-5-CARBOXALDEHYDE with assay level at or above 99% is used in analytical research, where high assay provides reliable and reproducible experimental results. Moisture Content ≤0.5%: 2-BROMOPYRIDINE-5-CARBOXALDEHYDE with moisture content less than or equal to 0.5% is used in moisture-sensitive synthesis, where low water content prevents unwanted hydrolysis or side reactions. Residual Solvent <0.1%: 2-BROMOPYRIDINE-5-CARBOXALDEHYDE with residual solvent below 0.1% is used in fine chemical manufacturing, where low solvent levels minimize contamination and increase final product quality. |
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2-Bromopyridine-5-carboxaldehyde draws attention among chemists and manufacturers who work with advanced organic molecules. It’s a yellowish solid, modest in appearance, but the real story goes much deeper. With the molecular formula C6H4BrNO, this compound opens pathways for research, pharmaceutical development, and specialty material synthesis. It’s part of a family that often slips past headlines even though it powers progress in labs and development pipelines.
Unlike simpler halogenated heterocycles, 2-bromopyridine-5-carboxaldehyde stands out with its balance of reactivity and selectivity. The pyridine ring, a time-tested backbone in medicinal chemistry, brings both familiarity and adaptability. Add a bromine atom on the second position, and suddenly the molecule offers unique coupling and activation points. The carboxaldehyde group on the fifth position adds another layer of capability, making the compound a versatile intermediate in building more complex architectures. Chemists who appreciate efficiency and flexibility in their reactions notice this difference right away.
For people outside the daily grind of the lab, a specialty chemical like 2-bromopyridine-5-carboxaldehyde might seem tucked away from daily relevance. In practice, it has its fingerprints on many modern pharmaceuticals and advanced materials. Medications treating everything from infections to neurological disorders trace part of their molecular ancestry to intermediates like this one. Drug discovery teams make use of the compound’s reactive positions to assemble candidate molecules, giving them the chance to test novel activities and improve safety profiles. This isn’t theory—countless published syntheses show real-world use.
The unique substitution pattern on 2-bromopyridine-5-carboxaldehyde delivers access to synthetic strategies unavailable with alternatives such as 3-bromopyridine, unsubstituted pyridine, or simple benzaldehydes. For instance, cross-coupling reactions—critically important for forging carbon-carbon bonds—benefit from the bromine handle. Methods like Suzuki and Buchwald-Hartwig reactions become more reliable when working with aryl bromides compared to their chlorine counterparts, thanks to more manageable reactivity. The carboxaldehyde group also sets this molecule apart, opening up selective condensations and cyclizations. That flexibility gives research teams control, a commodity they value above almost everything else.
I’ve watched colleagues reach for 2-bromopyridine-5-carboxaldehyde plenty of times, both in academic and industry labs. Its practical advantages go beyond diagrams in a notebook. The physical stability means it stores without drama. When scaling up, consistency from batch to batch can’t get overlooked. Nobody wants to troubleshoot again and again when a project deadline looms. A well-behaved intermediate saves real money and time, and in industries fighting for each hour and each dollar, those details shape success stories.
The purity and selectivity achieved with this compound directly affect what gets into the pipeline. Better intermediates mean fewer side reactions, cleaner separations, and a smoother road to regulatory approval for complex molecules. That’s not just chemical theory. Chemists know how much a finicky or unpredictable reagent slows things down. Years get spent overcoming one bad impurity or contaminant in process chemistry, and every shortcut toward a cleaner, more reliable result builds confidence in the tools used day in, day out.
Let’s compare 2-bromopyridine-5-carboxaldehyde to some familiar alternatives. 3-bromopyridine and 2-chloropyridine both see their share of use, but each comes with its quirks. Chlorides tend to be less reactive in palladium-catalyzed cross-couplings, demanding harsher conditions and, sometimes, less forgiving yields. Methyl or nitro groups change electronics in ways that might complicate subsequent steps. The aldehyde group on the five-position brings locational specificity for further modifications. This allows organic chemists to design syntheses with fewer steps, reducing waste and improving atom economy. Simpler pathways, fewer purification headaches, and less solvent use make a difference when a process has to leave the benchtop and become a pilot-plant reality.
One common application uses the aldehyde position to install a new substituent, setting the stage for ring closures or further functionalization. Macrocycle formation, heterocycle annulation, or the creation of biaryl systems all benefit from tight control over substituent placement. It’s not just about making something new—it’s about doing it more efficiently and more responsibly. Many research programs seek out green chemistry approaches, and using a reagent that cuts out excess steps fits the bill.
We’re not just talking about a molecule for lab-scale tinkering. Companies focusing on active pharmaceutical ingredients need kilograms or more, with documentation and reproducibility trailing closely behind. The identity, purity, and origin of every batch must be clear. Markets forming around quality intermediates look at both chemical and logistical reliability. To support innovation, producers offer transparent supply chains and quality guarantees, which in turn let research and production teams move ahead with confidence.
Trust plays a massive role wherever regulatory approval looms in the future. For 2-bromopyridine-5-carboxaldehyde, its established status in chemical catalogs means methods to produce it have been honed and standardized. Validated analytical techniques such as NMR, GC-MS, and HPLC confirm purity, and reproducibility in process steps can be demonstrated for anyone who asks. Chemists and QA managers have no patience for uncertainty, so suppliers maintain detailed records and traceability logs for every lot. Companies with an eye on regulatory compliance never take these systems for granted.
For new or reformulated drugs, the provenance of each building block matters for future regulatory submissions. Agencies check for contaminants, residual solvents, and chemical stability. Using a well-known intermediate can speed up the risk assessment and cut down on the surprises that slow down drug approval. That’s not just good business—it enables safer, more effective products to reach patients or customers who need them. You won’t see this compound on consumer labels, but its fingerprints are on countless medicines and specialty materials all over the market.
The conversation around specialty chemicals eventually circles back to sustainability. More and more, manufacturers face expectations from both regulators and customers to deliver products with smaller environmental footprints. 2-Bromopyridine-5-carboxaldehyde finds relevance here by supporting reactions with good atom economy and operational simplicity. Using a brominated intermediate may raise eyebrows about halogenated waste, but process chemists know how to handle and capture byproducts. Modern synthesis routes minimize excess reagents and solvents while maximizing overall yield.
Moving toward greener processes isn’t just a matter of following rules. Waste reduction lets companies save on disposal and raw materials. Selecting intermediates that align with green chemistry principles delivers practical value: shorter processes, milder reactions, and less environmental risk. Over decades of incremental progress, chemists have found ways to make chemical synthesis smarter. In this context, 2-bromopyridine-5-carboxaldehyde fits into streamlined pipelines that value both chemical reactivity and operational responsibility.
Academic researchers reach out for 2-bromopyridine-5-carboxaldehyde when they’re building new heterocyclic compounds or fine-tuning ligand systems in catalysis. The bromo group on the second carbon serves as a reliable handle for attaching bulky or electronically interesting substituents. Publications describing kinase inhibitors, antibiotics, or optoelectronic devices often list this compound in their synthetic schemes. Its straightforward handling and compatibility with common solvents like THF, DMF, and toluene keep it on lab shelves around the world.
On the industrial side, active pharmaceutical ingredient manufacturers rely on intermediates that give consistent results at scale. The path from grams to metric tons brings new challenges—solubility, thermal behavior, impurity profiles, and even packaging. Each of these sets requirements not only for the intermediate itself, but also for the producers who deliver it. 2-bromopyridine-5-carboxaldehyde’s proven reliability satisfies these demands, and it does so because years of experience and optimization support every drum or bottle.
Specialty chemicals extend into electronics and materials science, where pyridine-containing frameworks and molecular scaffolds offer performance advantages. Researchers pushing OLED efficiency or new battery chemistries gravitate toward intermediates with both modularity and reliable supply. They know investment in a single intermediate can yield dividends years down the line, through patent claims or performance benchmarks. A compound with a track record of reproducibility gets adopted more widely, giving rise to new products and discoveries.
Talk to anyone with hands-on experience, and they’ll tell you that physical properties matter as much as reactivity. If a chemical degrades quickly or gives off difficult-to-control vapors, productivity drops. 2-bromopyridine-5-carboxaldehyde offers a measure of stability during storage and use, provided basic safety standards are followed. Sealed containers, cool conditions, and protection from light maintain potency and minimize risks. Proper ventilation, eye protection, and gloves are standard gear for those handling the powder or solutions. This day-to-day practicality helps keep teams safe and avoids drama that can come from more volatile or sensitive compounds.
On larger scales, automated transfer and weighing systems cut down on direct human exposure. Providers furnish detailed safety information and advice, both to meet regulations and to help clients avoid unnecessary mishaps. At every stage, the human factor matters—training and infrastructure keep intermediate chemicals in useful, safe circulation rather than turning them into liabilities.
Behind every bottle or drum of 2-bromopyridine-5-carboxaldehyde, there are decisions shaping quality and supply consistency. The reputation of a supplier grows from transparency and accountability. Production sites using controlled processes, raw materials with proven identity, and careful monitoring at every step pave the road for downstream success. Scientists in both industry and academia learn quickly to avoid unreliable sources, since inconsistent reagents can sabotage research or lead to expensive rework in manufacturing.
Quality certificates and batch records make a difference. Anomalies—like off-colors or uncharacteristic smells—bring production lines to a halt. Regular supplier audits and laboratory checks form the backbone of a reliable sourcing strategy. Experienced chemists keep documentation for every lot, adding a layer of defense against future regulatory headaches. Nobody wants to trace a problem in a finished product back to a missed impurity in an early intermediate.
No chemical exists in a vacuum—supply, regulation, and even geopolitical spice all play their part. Different countries enforce their own sets of rules around shipping and storage. Occasionally, regulatory changes can limit supplies or add lead times. The practical upshot means close coordination between users and suppliers, and sometimes backup plans for sourcing. Security of supply stands out as one reason the best producers invest in documentation, backup logistics, and process redundancies. For 2-bromopyridine-5-carboxaldehyde, the landscape remains robust, but vigilance always pays off.
Prices reflect not only demand, but also the costs of compliance, inspection, and shipping. Unstable pricing or regulatory bottlenecks occasionally hit niche chemicals harder, since fewer producers can weather temporary disruptions. End users track these factors to avoid costly misses in their production timelines. Successful innovation has just as much to do with good planning as with the molecules themselves.
Looking forward, 2-bromopyridine-5-carboxaldehyde’s core strengths promise to keep it in rotation for years to come. Synthesis of new drug candidates, advanced electronic materials, and even specialty ligands for catalysis all pull the molecule in different directions. That broad spectrum creates demand for reliable supply and continuous product improvement, whether that means higher purity, lower metal contamination, or more sustainable synthesis routes.
Challenges linger. Persistent pressure for more sustainable chemistry will continue to shape how companies make and transport all halogenated intermediates. Research groups push suppliers for better environmental profiles and detailed lifecycle data. As regulations tighten and analytical expectations rise, only intermediates with transparent documentation and proven quality will win the loyalty of buyers.
Solutions start with dialogue—between suppliers aiming to exceed expectations and end users who can articulate the trade-offs that matter most to them. Shared experience, published methods, and open channels for quality feedback all help drive progress. Investments in green chemistry, process improvement, and transparent supply chains create ripple effects across the sector, benefiting both established players and up-and-coming researchers.
The story of 2-bromopyridine-5-carboxaldehyde tells us a lot about what moves science and industry forward. Reliable, versatile intermediates bridge the gap between laboratory curiosity and commercial product. They offer more than just molecular building blocks—they give research teams pathways to efficient, clean, and scalable syntheses. On a day-to-day level, they help drive projects to completion, freeing minds and hands for the creative, world-changing part of chemical research.
The lesson from years working alongside this and similar compounds is clear: investing in quality and reliability pays off in every phase, from concept to market. With greater attention paid to how we source, use, and improve specialty intermediates, the pace of innovation only accelerates. 2-bromopyridine-5-carboxaldehyde may not earn a place in the public imagination, but its impact travels quietly through every field that values smarter, safer, and more efficient chemistry. And while the next big breakthrough may wear a different name, it will owe its success to foundational pieces just like this one.