|
HS Code |
526250 |
| Chemical Name | 6-Bromo-2-pyridinecarboxaldehyde |
| Cas Number | 63065-11-2 |
| Molecular Formula | C6H4BrNO |
| Molecular Weight | 186.01 g/mol |
| Appearance | Light yellow to brown solid |
| Melting Point | 72-76°C |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=NC(=C1Br)C=O) |
| Inchi | InChI=1S/C6H4BrNO/c7-5-1-2-6(3-9)8-4-5/h1-4H |
As an accredited 6-Bromo-2-pyridinecarboxaldehyde 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 sealed with a red cap, labeled "6-Bromo-2-pyridinecarboxaldehyde" with hazard symbols and batch details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 6-Bromo-2-pyridinecarboxaldehyde is securely packed in 200 kg drums, totaling approximately 80 drums per container. |
| Shipping | 6-Bromo-2-pyridinecarboxaldehyde is shipped in tightly sealed, chemically resistant containers to prevent contamination and degradation. It is transported under cool, dry conditions, typically as a solid or solution, and handled following all relevant hazardous material regulations. Proper labeling and documentation accompany the shipment to ensure safety and compliance during transit. |
| Storage | Store 6-Bromo-2-pyridinecarboxaldehyde in a tightly sealed container, under an inert atmosphere such as nitrogen or argon, in a cool, dry, and well-ventilated area. Protect from light, heat, and moisture. Keep away from incompatible substances such as strong oxidizing agents and bases. Use appropriate personal protective equipment when handling, and follow local regulations for chemical storage. |
| Shelf Life | 6-Bromo-2-pyridinecarboxaldehyde is stable for at least 2 years if stored tightly sealed, protected from light, and under refrigeration. |
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Purity 98%: 6-Bromo-2-pyridinecarboxaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and yield. Melting Point 63°C: 6-Bromo-2-pyridinecarboxaldehyde with melting point 63°C is used in solid-state organic reactions, where precise temperature control supports consistent product formation. Molecular Weight 186.02 g/mol: 6-Bromo-2-pyridinecarboxaldehyde with molecular weight 186.02 g/mol is used in medicinal chemistry research, where accurate dosing and molecular calculations improve reproducibility. Stability Temperature 25°C: 6-Bromo-2-pyridinecarboxaldehyde with stability temperature 25°C is used in reagent storage for extended durations, where it maintains structural integrity. Low Water Content: 6-Bromo-2-pyridinecarboxaldehyde with low water content is used in moisture-sensitive synthesis protocols, where minimal hydrolysis yields pure compounds. |
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There’s something captivating about molecules that change entire workflows in labs and factories. 6-Bromo-2-pyridinecarboxaldehyde is one of those chemical building blocks that shows up quietly in specialized bottles, but it leaves a strong mark on chemical synthesis and innovation behind the scenes. Chemists who work with heterocyclic compounds or are pioneering new drugs keep running into bottlenecks, especially with how tough it can get when a synthesis hits a dead end. Here, this aldehyde comes into play. Those who have spent hours fine-tuning reaction conditions will appreciate how a small substitution on the pyridine ring can make or break a synthetic plan.
To make it clear, 6-Bromo-2-pyridinecarboxaldehyde isn’t just a mouthful of a name. It sets itself apart thanks to a precise bromine atom and an aldehyde group on the pyridine platform. The bromo tag might look simple, but it’s what chemists look for when designing molecules for next-step cross-coupling or seeking sharper selectivity. The aldehyde group on pyridine is not easy to install, so finding this compound in a pure form shortens the distance between an idea and a tangible outcome in synthesis.
In organic synthesis, finding reliable starting points can be a hassle. 6-Bromo-2-pyridinecarboxaldehyde saves time for research teams because its chemical handle—the combination of aldehyde and bromine groups—brings two powerful entry points for modifying the molecule. In the trenches of R&D, experiments often hit a wall due to poor selectivity or dead ends in functionalization. Trying to add a new group to a picky substrate on a pyridine ring is a real challenge, especially when the game changes depending on the position. This is where experience comes into play. A researcher who has navigated complex multistep syntheses recognizes the edge that comes from starting with a well-placed bromine and aldehyde. It opens the door for Suzuki couplings, Wittig reactions, and condensation reactions right out of the gate.
Friends in the medicinal chemistry field often comment on how tough it is to access unique heterocyclic scaffolds for screening. Lead optimization doesn’t pause for bottlenecks in starting material access. A lot depends on structural novelty, and this building block helps move projects forward without breakdowns in the pipeline. From personal experience, no one wants to spend weeks synthesizing a precursor that ends up acting up in scale-up runs.
In research and manufacturing, inconsistent ingredient quality wastes resources, kills timelines, and sinks confidence in the whole process. Cheaper alternatives sometimes carry more weight in impurities or cause headaches in purification. A clean 6-Bromo-2-pyridinecarboxaldehyde minimizes these issues and keeps outcomes predictable—something every bench chemist or process engineer values. Several academic studies and industrial case reports point to success stories tied directly to reagent grade. Fewer side reactions, cleaner product mixtures, and reliable scaling can make big differences in everything from pharmaceutical API development to high-throughput screening. An experienced hand at the HPLC or the rotavap can spot poorly purified intermediates right away; access to a consistent lot of this chemical streamlines downstream steps.
I remember a project where our team needed to assemble a library of pyridine derivatives for a kinase inhibitor series. Commercial sources of 6-Bromo-2-pyridinecarboxaldehyde brought a noticeable shift in workflow. We spent more time optimizing the main reactions rather than stepping back to troubleshoot supply problems or purify impure precursors. Being able to run parallel reactions using the bromo-aldehyde as a modular core sped up SAR—the structure-activity relationship arms race—by several weeks. Coupling reactions proceeded smoothly, and we shaved unnecessary steps off because the aldehyde group was already in the right spot. Those with years in the lab will acknowledge how rare it is to find a reagent that slashes troubleshooting down to almost nothing.
In pilot plant or scale-up runs, the story changes again. Process chemists face new headaches: yields need to stay up, byproducts down, and regulatory standards get stricter with scale. 6-Bromo-2-pyridinecarboxaldehyde stands up well in these settings, especially when sourced from suppliers who understand impurity profiles and moisture control. Not all halogenated pyridines behave the same way, and small differences in supplier quality can mean less waste and fewer headaches at the isolation step.
A quick scan through catalogs shows pyridine derivatives with all sorts of substitutions. Not every position on the ring offers the same balance of reactivity and selectivity. 6-Bromo-2-pyridinecarboxaldehyde strikes a sweet spot. Bromine at the 6-position makes for selective couplings that would be harder with meta or para positions, especially in the context of late-stage diversification. Aldehyde at the 2-position serves as a solid launching pad for further molecular manipulation—like making imines, oximes, or hitting a reductive amination. By contrast, similar compounds with the substituents out of alignment throw up more barriers in retrosynthesis planning.
I have compared this compound to others such as 3-bromo-2-pyridinecarboxaldehyde and 6-chloro-2-pyridinecarboxaldehyde in both library synthesis and scale-up environments. Subtle electronic effects can bury or enhance reactivity when you swap a bromine for a chlorine. The 6-bromo is harder to dislodge by nucleophiles compared to 6-chloro, and it makes for better leaving group chemistry in certain metal-catalyzed couplings. Those details add up fast, depending on the complexity of the project or the tightness of a timeline.
There has been a burst in demand for advanced heterocyclic intermediates, especially among companies advancing oncology drugs. Companies chasing novel kinase inhibitors or antiviral candidates often require these bromopyridine structures. Product managers working on the supply side invest in partnership with analytical labs to ensure that the chemical meets not just content requirements, but also rigorous limits on possible contaminants. Releasing a batch with residual reagents or solvent traces can trigger regulatory headaches. On the consumer side, scientists want reassurance backed by certificates of analysis showing tight batch-to-batch consistency, low metals, and full transparency around analytical data.
In environments with automation or flow chemistry systems, the robustness of a compound like this comes to the fore. Unlike some finickier aldehyde derivatives or less stable halogenated structures, 6-Bromo-2-pyridinecarboxaldehyde responds well when introduced to continuous processes or in-line quality monitoring. This kind of adaptability adds real value, especially as companies look to cut downtime or ramp up flexibility in small-batch manufacturing.
Years of handling aromatic aldehydes and halogenated reagents bring certain habits for safety and protocol. 6-Bromo-2-pyridinecarboxaldehyde behaves in line with other low-mass aromatic aldehydes—volatile enough to respect, but stable enough not to cause sudden surprises under normal lab conditions. Gloves and protective eyewear stay essential, and I always make sure to keep all halogenated reagents in well-marked secondary containment, just in case. Smells from pyridine aldehydes stand out—sharp but none too acrid—and they remind me to work efficiently at the bench, minimizing unnecessary exposure.
Storage at room temperature, well away from moisture and direct sunlight, preserves its integrity. Many in the community advocate for aliquoting into amber vials if the chemical spends extended time outside original packaging. Regular in-house GC or NMR checks ensure that the quality holds up, avoiding the unpleasant surprise of decomposition tainting an entire set of reactions.
As more startups and academic labs work in fields like medicinal chemistry, agrochemical discovery, and functional materials, the need for modular and reliable heterocyclic building blocks grows. 6-Bromo-2-pyridinecarboxaldehyde fills a unique space here. Historically, many advanced intermediates took time to source and purify, especially for small research groups with tight budgets. Now, improved supply chains and tighter specifications mean smaller teams can dream bigger, knowing the starting material will deliver on its promise.
I’ve heard from colleagues who develop diagnostic agents or ligands for catalysis that this one molecular building block lets them reach more scaffolds in less time. The downstream value appears not just in faster synthesis, but also in the ability to explore more creativity. If a team only has a handful of attempts to get things right, it helps to start on third base rather than at the plate.
Supply chain resilience matters. The events of recent years have shown how fragile logistics can hamstring research or production. Many facilities ran into delays caused by bottlenecks in sourcing key heterocyclic intermediates, so having reliable partners who can deliver high-quality 6-Bromo-2-pyridinecarboxaldehyde makes a sizeable difference. Some regions have pulled ahead by prioritizing local production and trusted supply agreements, minimizing risk of interruption.
On the environmental front, responsible sourcing and minimizing hazardous byproducts remain priorities for both buyers and suppliers. Chemists, especially in larger organizations, look for origin information, transparency around waste management, and assurances that production processes meet responsible care standards. Regulations shift quickly, and organizations keeping ahead of the curve use documentation and supplier screening to enhance compliance. This approach protects not just the end user, but also makes a company more resilient to legal and market shocks.
Strong networks across academia and industry foster better outcomes for everyone involved. One seasoned synthetic chemist shared a story about troubleshooting a key reaction step on a tight deadline. Posting questions to professional forums and reaching out to supplier technical teams delivered answers fast—confirmation of structure by NMR, ideas on alternative workups, and second opinions on whether a minor impurity mattered downstream. It demonstrates that using a widely recognized building block like 6-Bromo-2-pyridinecarboxaldehyde introduces not just practical benefits but also a pathway into global communities.
Suppliers and researchers regularly improve products based on shared troubleshooting and tips. In one instance, a minor tweak in recrystallization solvent recommended by a peer saved a project from a failed batch. That sense of shared knowledge base benefits not just major pharmaceutical companies but also educators running undergraduate research projects. The cycle of iterative improvement connects supply quality, user experience, and new application spaces.
The need for innovative molecular scaffolds only grows as new diseases and novel targets come under investigation. Researchers have started to push the boundaries of where pyridine derivatives can go—materials science, catalysts, sensor technologies, and more. 6-Bromo-2-pyridinecarboxaldehyde appears with increasing frequency in published synthetic pathways and patent filings. This shows a strong demand and continued exploration, backed by a robust foundation of practical use cases.
As someone who has spent years reading chemical literature and cross-referencing progress in real-world labs, I can say this compound’s rising presence represents a shift toward more modular, accessible chemistry. The momentum comes from scientists who value time saved, the flexibility from built-in functional groups, and the confidence that starting materials won’t leave them stranded halfway through a sequence.
No pathway stays static, and newer applications for such versatile intermediates will continue to emerge. It’s worth noting that the strongest advances come from partnerships—whether between supplier and end user, or among scientists who pass on their experiences and recommendations. As automation and regulatory scrutiny become stricter, the demand for intermediates that check every box will only rise.
People working in chemistry know how relentless the pace can be. Every minute spent hunting down pure, reliable starting materials is a lost minute for real discovery. 6-Bromo-2-pyridinecarboxaldehyde isn’t a magic bullet, but its role as a reliable building block snags the attention of those who measure success not just by yields, but by days shaved off grueling projects or by the creative openings found in structure-guided design. Every time a team bypasses a slow, multi-step synthesis in favor of a crisp, ready-to-use bottle, the case for using robust, well-understood pyridinecarboxaldehydes gets a little stronger.
Quality, reliability, and smart design keep projects moving from the planning stage to the finish line. In my experience, having 6-Bromo-2-pyridinecarboxaldehyde at hand brings real confidence to the lab. It offers chemists an edge—practicality in the present, and promise for what’s next.