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HS Code |
436849 |
| Chemical Name | 3-Bromo-5-pyridinecarboxaldehyde |
| Cas Number | 40717-29-3 |
| Molecular Formula | C6H4BrNO |
| Molecular Weight | 186.01 g/mol |
| Appearance | Light yellow to brown liquid |
| Purity | Typically ≥ 97% |
| Solubility | Soluble in organic solvents (e.g., DMSO, ethanol) |
| Smiles | C1=CC(=CN=C1C=O)Br |
| Inchi | InChI=1S/C6H4BrNO/c7-5-1-6(4-9)8-3-2-5/h1-4H |
| Synonyms | 3-Bromo-5-formylpyridine |
| Storage Conditions | Store at 2-8°C, protected from light |
As an accredited 3-Bromo-5-pyridinecarboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 3-Bromo-5-pyridinecarboxaldehyde, clearly labeled with chemical name, CAS number, and hazard warnings. |
| Container Loading (20′ FCL) | Standard 20′ FCL carries 120–160 drums (25 kg each) of 3-Bromo-5-pyridinecarboxaldehyde, securely packaged, moisture-protected. |
| Shipping | 3-Bromo-5-pyridinecarboxaldehyde is shipped in tightly sealed containers, protected from moisture and light, and packed according to hazardous chemical regulations. It is transported as a chemical substance with proper labeling and documentation to ensure safe handling and compliance with international and local shipping guidelines for hazardous materials. |
| Storage | 3-Bromo-5-pyridinecarboxaldehyde 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 strong oxidizing agents. Proper labeling and secure placement in a designated chemical storage cabinet are recommended. Always follow standard laboratory safety guidelines when handling or storing this compound. |
| Shelf Life | 3-Bromo-5-pyridinecarboxaldehyde typically has a shelf life of 24 months when stored tightly sealed, protected from light, moisture, and heat. |
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Purity 98%: 3-Bromo-5-pyridinecarboxaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical yield and reduced side-product formation are achieved. Melting Point 72°C: 3-Bromo-5-pyridinecarboxaldehyde with a melting point of 72°C is used in heterocyclic compound development, where precise thermal characterization ensures reliable crystallization. Molecular Weight 200.01 g/mol: 3-Bromo-5-pyridinecarboxaldehyde with molecular weight 200.01 g/mol is used in agrochemical research, where accurate mass control supports predictable reaction scaling. Stability Temperature up to 35°C: 3-Bromo-5-pyridinecarboxaldehyde stable up to 35°C is used in chemical storage applications, where minimized degradation sustains consistent reactivity for extended periods. Particle Size <100 µm: 3-Bromo-5-pyridinecarboxaldehyde with particle size under 100 µm is used in fine chemical formulation, where improved dispersion enhances reaction homogeneity. Water Content <0.5%: 3-Bromo-5-pyridinecarboxaldehyde with water content below 0.5% is used in moisture-sensitive synthesis, where low moisture enables efficient coupling reactions. |
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Every so often, the right molecule shows up at the right time and quietly gets things moving in research labs. 3-Bromo-5-pyridinecarboxaldehyde brings that kind of reliable, straightforward contribution, standing out for the tasks it takes on in organic synthesis. It doesn’t make splashy headlines. This chemical, with its straightforward formula of C6H4BrNO, slots into plenty of conversations about new molecular design, pharmaceuticals, agrochemical innovation, and advanced materials research.
People usually notice two things about this molecule right away: the bromine and the carboxaldehyde groups, both attached to a flexible pyridine base. This combination doesn’t just look good on paper. Chemists have kept it close for targeted bromination or formylation work, able to move between aromatic substitutions and cross-coupling reactions with relative ease. After handling a lot of different functional building blocks over the years, certain pieces just feel more predictable—3-Bromo-5-pyridinecarboxaldehyde fits that bill. Instead of bringing in extra surprises, it backs up synthetic work, supporting downstream processes where reliability and purity matter.
On the bench, sample purity and reproducibility come before everything else. As a solid with a defined melting point and high chemical purity, 3-Bromo-5-pyridinecarboxaldehyde stands ready for both exploratory routes and scalable syntheses. Versions with purity above 98% have become the standard in most labs—lower-grade material only gets left over when someone is testing crude concepts and doesn’t want to spend too much. Most suppliers now deliver it in various package sizes for gram-to-kilogram orders, giving researchers ample flexibility. Its pale-yellow appearance and crystalline nature make it easy to store, handle, and weigh, especially compared to trickier or more sensitive reagents. The chemical’s stability under standard conditions saves time and stress, avoiding the frantic search for dry ice or glove boxes that come with unstable compounds. With its solid shelf life and minimal volatilization, this chemical fits day-to-day workflows in both academic and industrial environments.
By itself, 3-Bromo-5-pyridinecarboxaldehyde might not impress outside the chemistry community, but its function speaks volumes to researchers. In modern medicinal chemistry, it gives scientists the freedom to run palladium-catalyzed cross-coupling reactions—Suzuki, Sonogashira, Stille, or Heck, just to name a few. The aldehyde makes it perfect for building more complex heterocycles, chain-extended structures, or attaching pharmacophores. Its bromo group opens up the synthesis of diversified pyridine analogs. This single molecule makes possible a whole spectrum of pyridine-based ligands, key drug candidates, and agricultural intermediates that would otherwise be tough to assemble. It allows easy entry into scaffolds crucial for both discovery-phase projects and “scale-up” trials as products inch toward manufacturing.
People new to the field sometimes underestimate how much time a minor impurity or unstable intermediate can waste. Having worked on my share of project timelines and production runs, the dependable nature of 3-Bromo-5-pyridinecarboxaldehyde stands out. It plays well with classic conditions and adapts easily to newer, flow-based chemistry systems. Modular, predictable, and easy to source, it saves weeks of troubleshooting compared to less-characterized analogs.
The greatest endorsement for any building block comes from its track record across projects. Pharmaceutical groups turn to this compound to plug a reactive aldehyde into pyridine-rich drug leads, streamlining the journey to new candidates. Agrochemical research teams see it as a springboard to design molecules that stand up against difficult pests or environmental pressures—often by tweaking the pyridine core. Fine chemical producers depend on it for high-value ligands and dyes, where downstream color chemistry demands crisp reactivity and a clean starting point.
Chemical biology researchers often look for options to precisely dial in functionality on heterocycles, giving them a way to test new enzyme inhibitors or probe molecular pathways. Academic groups teaching advanced synthetic techniques find in 3-Bromo-5-pyridinecarboxaldehyde a molecule that pulls its weight: easy to manipulate, easy to analyze by NMR or mass spectrometry, and easy to recover in reasonable yields. It’s not unusual to see undergraduates getting their feet wet with brominated pyridines, and this compound pops up in more than a few successful lab notebooks.
Sifting through various pyridinecarboxaldehydes and their halogenated cousins, some variations offer unique quirks, but few combine reactivity and dependability quite like the 3-Bromo-5- position. 3-Chloro-5-pyridinecarboxaldehyde brings its own profile, but often yields less in certain couplings and doesn’t always match the selectivity for tougher reactions. 3-Iodo analogs tend to react more aggressively and cost extra, so most groups keep them for rare or specific syntheses—price often tips the balance back toward bromine’s sweet spot. Meanwhile, non-halogenated pyridinecarboxaldehydes don’t open up as many synthetic doors, acting more like islands than crossroads for molecular construction.
Differences extend into the environmental and handling domains, too. Compounds that slip into the air or decompose at the slightest moisture spell more headache than value. 3-Bromo-5-pyridinecarboxaldehyde stays put, stays clean, and fits the intentional, repeatable planning that makes chemistry go faster and smoother. Experience says: projects run by chemists who know their reagents well go smoother, get funded more often, and lead to publications with real impact.
No chemical comes without its own set of hurdles. The biggest hurdle involves regulatory compliance for projects that will scale up beyond the lab. Companies want to know their supply chain can keep up—especially when global demand for building blocks like this ebbs and flows. Reliable sourcing of 3-Bromo-5-pyridinecarboxaldehyde hinges on solid relationships with trusted manufacturers and distributors. Stories still surface of shipments delayed for weeks or material arriving off-spec, throwing a wrench into otherwise smooth development cycles.
Another issue people tackle involves minimizing hazardous waste. With specialty reagents—especially halogenated compounds—the byproducts tend to include persistent organic pollutants. Regulatory expectations on waste handling keep rising, so teams need to plan from the outset to capture and neutralize brominated byproducts. Investment in greener chemistry options and recycling systems continues to spread, but many researchers working under grant deadlines find themselves stuck with “traditional” methods, at least for now.
Price volatility adds another real-world concern. While not as expensive as some rare-earth intermediates or silver-based catalysts, brominated pyridines have seen price swings driven by supply chain hiccups. A few times, the right batch just isn’t available close to home, and teams weigh how soon they need to proceed versus the impact to the budget. This kind of logistical back-and-forth doesn’t just affect research—it feeds into the cost estimates and feasibility analysis that push products closer to the market.
Reagents like 3-Bromo-5-pyridinecarboxaldehyde may not grab attention with flashy branding or wild new reaction types, but they do show up time and again in research that breaks ground. Take, for instance, recent developments in central nervous system drug candidates or the race to tackle new fungal pathogens in crops. In more than a few cases, chemists point to successful routes relying on this molecule’s consistency and adaptability. These breakthroughs don’t happen in isolation; they build, block by block, on tools like this—shaped by criticism in peer reviews, demands on patent timelines, and the pressure of bringing new therapies to patients or new solutions to the environment.
Working in industrial or academic labs, I’ve seen deadlines slip and ideas stall because an intermediate just didn’t behave as predicted. Integrating a chemical with a reputation for reliable coupling, clean separations, and predictable behavior brings real value. Publications based on new methods, product launches in the agrochemical arena, or the transition from small-scale discovery to pilot plant often turn on details no bigger than the right building block in the right spot. Small choices, amplified by experience, drive the larger engine of chemical discovery.
People serious about achieving their R&D goals look for ways to make the most of every intermediate, 3-Bromo-5-pyridinecarboxaldehyde included. First step is always confirming quality—not just what the supplier claims on paper. Real practice means validating melting points, running thin-layer chromatography, and checking spectra before committing to larger batch synthesis. Miss this step and risk dealing with side reactions, wasted solvents, or rejected purification runs. Quality controls, as any veteran chemist will agree, ensure a smooth workflow.
Maximizing value also means considering reaction design from a sustainability standpoint. Traditional protocols sometimes drown in solvents like dichloromethane or rely too much on heavy metals. There’s a push, especially among younger researchers, to re-imagine routes with greener alternatives, like bio-derived or less hazardous solvents, and more efficient catalysts. The bromine atom, while helpful for reactivity, must be managed carefully so that environmental release is avoided. Some labs have begun collaborating with downstream processors to capture waste, neutralize halides, or recover spent reagents for reuse. The industry will only benefit by sharing best practices and reporting honest yields and setbacks in the literature. Openness about what works—failures as well as successes—helps everyone move faster and more safely.
Another step toward smoother integration involves better forecasting for purchasing, by keeping real-time updates on availability and price trends. Some labs have cut the frustration by developing shared chemical inventories or brokering regional partnerships to avoid duplicative, last-minute orders from overseas suppliers. In my own experience, labs that share resources and update inventory databases spend less time chasing packages or explaining delays to funders. Open lines of communication with suppliers have saved projects on more than one occasion, especially when bottlenecks surface without warning.
The safest lab is the one that treats every intermediate seriously. 3-Bromo-5-pyridinecarboxaldehyde needs careful storage away from extremes of heat and incompatible agents. It pays to educate every new team member on personal protective equipment—gloves, goggles, lab coats—and proper ventilation, not just assume everyone knows. Training refreshers prevent accidents before they start, and clear labeling stays essential. Having handled reactive aldehydes and brominated intermediates for years, I’ve learned not to cut corners or rush through protocol set-up. A few extra minutes reviewing hazards and double-checking scales ends up saving both time and resources in the long run.
Work with institutional environmental health and safety staff can clear up questions about disposal and transport protocols. Chemicals like this can attract regulatory attention if not managed well. Cross-checking local regulations, whether in a university setting or an industrial plant, avoids surprise audits and keeps projects on track. Electronic logs, regular inventory checks, and digital waste records have become a regular part of the workflow—tools that help teams avoid costly compliance errors.
3-Bromo-5-pyridinecarboxaldehyde has quietly supported progress across a surprising range of challenges, from basic method development to full-scale drug and agrochemical launches. Teams working together—academic, industrial, and government—continue to uncover fresh synthetic tricks and greener processes building off this one intermediate. There’s no shortage of discoveries left, and chemists who seize collaborative opportunities and share hard-won insights find their work travels farther.
Networks of researchers across institutions have begun pooling analytical data, adding to the public knowledge base. By sharing not just successful experiments but raw data, unexpected results, and purification tips, the learning curve for newcomers dips, speeding up early-stage projects. Online repositories and open-access journals make it easier to track down information on 3-Bromo-5-pyridinecarboxaldehyde, saving repetition of avoidable errors.
Long ties in the field teach that the chemistry community runs on both competition and shared progress. Hard work and openness about reagents—what delivers, what fails, which suppliers respond quickly—keep every lab moving forward. The more the community documents actual field results, the less often research money and talent fall into dead ends.
Looking ahead, the demand for reliable, versatile building blocks like 3-Bromo-5-pyridinecarboxaldehyde won’t slow down. New applications in catalysis, materials science, and pharmaceutical development keep rising. As computational chemistry suggests new targets and high-throughput screening becomes the norm, intermediates able to handle a range of conditions without losing reactivity gain even more value. Future advances around this molecule will likely focus on refining process chemistry, building even cleaner, lower-impact production flows, and finding ways to recycle or reuse spent materials wherever possible.
Sustained investment in education, open-access research tools, and quality assurance will help the next generation of chemists make the most of proven reagents. As someone who’s spent years working with heterocyclic molecules and organizing chemical libraries, I see day-to-day value in tools that work well the first time and stand up under scrutiny. The attention to detail that goes into sourcing, using, and disposing of every gram of compound is what supports discovery—the bold breakthroughs as well as steady incremental gains.
Reliable intermediates make up the backbone of modern chemical discovery. In a field that runs on both speed and care, 3-Bromo-5-pyridinecarboxaldehyde delivers the mix of predictability, adaptability, and clean reactivity that researchers value. Day in and day out, it backs up complex synthetic pathways, fuels advances in targeted drug design and crop science, and proves itself as a trusted partner in the pursuit of new knowledge.
Anyone with experience on the lab floor knows that every reliable intermediate brings down risk, opens up options, and lets teams work smarter. With attention to sourcing, safety, and environmental standards, this molecule will continue to support important work in laboratories around the world. There’s still plenty to do—plenty of chemistry to explore, challenges to tackle, and results to share. 3-Bromo-5-pyridinecarboxaldehyde stands ready for it all, time and again.