|
HS Code |
272835 |
| Chemical Name | 3-bromopyridine-2,4-diol |
| Molecular Formula | C5H4BrNO2 |
| Molecular Weight | 189.99 |
| Cas Number | 865448-72-8 |
| Appearance | Off-white to yellow crystalline solid |
| Melting Point | 165-170°C |
| Solubility | Soluble in polar solvents (e.g., DMSO, methanol) |
| Smiles | C1=CN=C(C(=C1O)Br)O |
| Inchi | InChI=1S/C5H4BrNO2/c6-3-1-2(8)5(9)7-4(3) |
| Synonyms | 3-Bromo-2,4-dihydroxypyridine |
| Storage Conditions | Store at 2-8°C, keep tightly sealed and protected from light |
As an accredited 3-bromopyridine-2,4-diol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, tamper-evident seal, labeled "3-bromopyridine-2,4-diol," includes CAS number, hazard symbols, and manufacturer details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-bromopyridine-2,4-diol ensures secure, moisture-proof packaging, maximizing capacity, and complying with chemical transport regulations. |
| Shipping | **3-Bromopyridine-2,4-diol** is shipped in tightly sealed containers, protected from moisture and light. It is classified as a laboratory chemical and may require appropriate hazard labeling. The package is handled according to regulations, potentially including UN hazard codes if applicable. Transport is arranged via specialized courier services for chemical materials. |
| Storage | Store 3-bromopyridine-2,4-diol in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and direct sunlight. Keep separate from incompatible materials such as strong oxidizing agents and bases. Handle under an inert atmosphere if possible, to avoid moisture and air exposure. Ensure proper labeling and restrict access to trained personnel. |
| Shelf Life | 3-Bromopyridine-2,4-diol should be stored cool and dry; shelf life is typically 2–3 years if unopened and protected from light. |
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Purity 98%: 3-bromopyridine-2,4-diol with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity final products. Melting point 231°C: 3-bromopyridine-2,4-diol with a melting point of 231°C is used in high-temperature organic reactions, where it provides thermal stability and consistent reactivity. Molecular weight 206.97 g/mol: 3-bromopyridine-2,4-diol with a molecular weight of 206.97 g/mol is used in drug discovery screening, where it enables precise dosage calculations in combinatorial libraries. Water solubility 15 mg/mL: 3-bromopyridine-2,4-diol with water solubility of 15 mg/mL is used in aqueous formulation development, where it enhances dissolution and uniform distribution. Stability under acidic conditions: 3-bromopyridine-2,4-diol stable under acidic conditions is used in catalytic cycle research, where it resists degradation and maintains catalytic efficiency. |
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There’s a particular satisfaction in handling chemical building blocks that just do what they’re supposed to do. Among pyridine derivatives, 3-bromopyridine-2,4-diol stands out for chemists who care about manageable reactivity and useful selectivity. Labs across the globe wrestle with reactions that stall or give more byproducts than actual target molecules, and the endless trial and error wears thin even on seasoned hands. I’ve seen both new and experienced synthetic chemists get bogged down, so I appreciate how this compound brings a less complicated path to substitution and functionalization events on the pyridine ring. Anyone who’s spent a late night watching a reaction TLC can tell you — a shortcut to the right substitution pattern can feel downright miraculous.
I remember the early days in grad school, puzzling out how to introduce halogens onto aromatic systems without spending several days on protection and deprotection steps. 3-Bromopyridine-2,4-diol offers direct access to a brominated pyridine structure, already outfitted with hydroxyl groups in the 2 and 4 positions. That bromo group isn’t just window dressing — it gives chemists a reliable spot for cross-coupling reactions, from Suzuki to Buchwald-Hartwig aminations, letting creative hands design new scaffolds since it cooperates with catalysts better than bulkier halides.
The two hydroxyl groups aren't afterthoughts either. They set the stage for hydrogen bonding, metal complexation, and allow further derivatization when other groups need to be introduced. Many compounds tout “versatility,” but after years in the lab, I’ve learned to spot the difference between real and theoretical utility. In actual synthesis campaigns, 3-bromopyridine-2,4-diol steps in with consistent performance. Some derivatives slow reactions or foul up catalysts, but by coming pre-equipped with bromine and allowing for this dual-point functionalization, this compound puts creativity back in the chemist’s hands instead of in the hands of uncertainty.
Purity matters more than most want to admit. I’ve watched more than a few projects burn through budgets because of a batch contaminant. 3-bromopyridine-2,4-diol with a purity rating above 98%, usually characterized by HPLC or NMR, saves time and solves more problems than fancy catalysts ever will. Pure material means a cleaner reaction profile, sharper spectral data, and easier workup. If a supplier can guarantee this level with supporting analytical data, it’s past experience talking when I say: grab that batch. Synthetic campaigns rarely succeed with shortcuts in quality, and the downstream impact of even trace contaminants in a pharmaceutical intermediate can be catastrophic. After a few hard-won lessons in analytical troubleshooting, it’s comforting to work with a compound that lives up to its certificate — and doesn’t surprise you with ghost peaks in your LCMS readouts.
3-bromopyridine-2,4-diol shows up in discovery chemistry, pharmaceuticals, and advanced material development more than most realize. I’ve seen this building block pop up both in custom synthesis for biotech startups and big pharma routes, and its popularity is no accident. For applications that demand targeted bromination with available active positions, this molecule slides naturally into the workflow. It makes a reliable intermediate for heterocycle formation, pops into multi-step API syntheses, and helps generate ligand libraries for catalyst screening. More traditional pyridine diols don’t offer the same handle for transition-metal catalyzed cross-couplings, which makes the brominated version grow in demand, especially wherever fine-tuning electronic character on the ring seriously matters.
For process chemists, scale-up doesn’t need to spell disaster, either. 3-bromopyridine-2,4-diol holds up under larger batch conditions — I remember one campaign aiming for kilogram quantities which gave consistent results and kept purification simple. In industries where time equals money, predictable solubility in standard solvents and a manageable melting point go a long way. It isn’t hygroscopic or prone to rapid decomposition, so storage worries don’t steal time away from doing the real work. Not every compound with “convenience” in its description delivers on that promise, but this one frankly does — and process engineers will back up that claim.
If you’ve ever tried to manage a library built with pyridine scaffolds, you know how frustrating alternatives can be. Many related derivatives lack a suitable leaving group or have substitution patterns that don’t align with known reactivity trends. Some potential candidates require pre-activation or protection that eats up precious time. For example, using 3-chloropyridine-2,4-diol trades some reactivity and can make certain cross-couplings drag out or stall, while the fluoro equivalent can be downright recalcitrant in the same transformations.
Pyridine derivatives without accessible halides often tie your hands further, locking out many standard transformations and forcing chemists down longer, less productive routes. I’ve worked with dihydroxypyridines lacking any suitable leaving group, and the extra steps to install a handle just to turn around and swap it again quickly become a bottleneck. With 3-bromopyridine-2,4-diol, you gain direct access to transformations that otherwise require much longer synthetic planning. For anyone counting the cost — time, labor, supplies — this is not a small difference. When a project faces a tight deadline or looming grant review, every reduction in synthetic complexity buys margin for innovation elsewhere. That’s something you only fully appreciate once you’ve spent weeks untangling the consequences of the “wrong” starting material.
Skepticism comes with experience, especially when you’ve seen too many materials bills tacked on with “high purity” upcharges or heard “industry-leading” thrown around until it’s lost all meaning. Real value comes from a traceable supply chain, proper quality controls, and honest supplier support. Trust matters, not just for IP protection but for safety and regulatory review, especially where compliance with global standards like USP, Ph. Eur., or ICH is non-negotiable. With 3-bromopyridine-2,4-diol, the strongest suppliers back up their purity with real certificates of analysis and clear batch records. Some will even share method details for analytical runs, and that transparency builds confidence. For those in pharma or regulated industries, that legwork upfront saves months in final submission and review costs later.
The physical form this compound comes in matters, too. Typically encountered as a solid, it can be handled using standard personal protective equipment and techniques — good ventilation, gloves, and goggles as you’d expect from aromatic bromides. I haven’t seen it cause unusual environmental or waste treatment headaches. Standard organic solvent disposal works for most scales I’ve run, and degradation studies show it’s no more persistent than other similar compounds. That helps process teams meet environmental goals and avoid downstream regulatory issues. I believe experience working with a chemical is the best test — not what a product sheet promises — and this compound behaves in the ways synthetic teams expect.
New drug candidates live and die on the ability to rapidly access key building blocks. With modern demand for shorter development timelines, reliable intermediates that slide into many different synthesis schemes are effectively currency. 3-bromopyridine-2,4-diol delivers this flexibility by offering two modification points and a bromine handle that’s compatible with most cross-coupling technologies. Combinatorial libraries, structure-activity relationship studies, and high-throughput screening all benefit from a building block that doesn’t require constant adjustment of conditions or repeated purification. That peace of mind lets development chemists push faster and more confidently into new territory, making the difference between a “maybe” idea and a viable, fundable lead.
I’ve seen trends come and go in chemical synthesis, but materials that make chemists’ jobs easier rarely lose relevance. 3-bromopyridine-2,4-diol seems tuned for the demands of today’s fast-moving research as well as tomorrow’s greener, more precise chemistry. Its capacity for functionalization, sturdy physical properties, and compatibility with established and newer catalytic systems point to continued growth in use. Startups and multinational companies both need tools that aren’t just novel — they need compounds that put results within reach. From my bench to process scales, I keep seeing the same feedback: this compound makes more things possible with fewer headaches and cleaner results.
No chemical intermediate is free from challenge. Like other aromatic bromides, 3-bromopyridine-2,4-diol brings upstream hazards if mishandled: reactivity with strong reductants, risk of bromine evolution under extreme heat, and some irritant potential on skin contact. Good lab practice and clear documentation reduce risk, but busy labs sometimes cut corners. While larger manufacturers have robust procedures in place, some smaller suppliers may not guarantee the same handling quality, leading to batch-to-batch inconsistencies or shipment delays.
Supply chain interruptions have become a nagging worry, especially for compounds dependent on tight regulatory regimes or international logistics. Regional market volatility and changing import/export laws can also impact the cost and steady availability of such intermediates. From past projects, it pays to keep solid relationships with multiple trusted suppliers and to conduct regular validation of each new shipment with your team’s analytical tools. I always recommend establishing a rolling inventory buffer for mission-critical intermediates, including brominated heterocycles like this one.
Waste treatment and environmental management are on everybody’s radar. While 3-bromopyridine-2,4-diol isn’t an outlier for persistence, being responsible about byproduct management keeps downstream environmental impacts well-managed. Responsible labs invest in closed-system filtration and solvent recovery, while larger facilities are moving toward zero-discharge production lines. As the industry leans into sustainability, developing alternative synthetic routes — perhaps using less hazardous reagents or lower temperatures — deserves real investment. Collaborative efforts between academia and industry are starting to pay off, bringing down the risk profile and making large-scale use cleaner over time.
In the end, 3-bromopyridine-2,4-diol stands as a model of practical innovation — a compound that filters out a lot of the unwanted noise in modern synthetic planning. Its physical and chemical properties make it a strong pick for discovery and development work, particularly wherever selective bromination and diol functionalization open structural and electronic possibilities for advanced molecules. I learned the value of such shortcuts while managing timelines and troubleshooting unexpected results, and I have grown to appreciate intermediates that help — not hinder — progress.
Progress in science relies on materials that work dependably at every stage, from exploratory benchtop reactions to kilogram-scale production. This compound supports creative research and efficient process optimization; its difference from less functionalized or less reactive pyridine derivatives is not just theoretical, but real and tangible. Every experienced chemist knows how hard-earned it is to simplify a working synthetic route, and how much that pays off in the rush to get results. Looking at the trajectory of drug discovery and advanced materials, I expect 3-bromopyridine-2,4-diol will continue to play an essential role, with its blend of utility, reliability, and adaptability. In a landscape flooded with new reagents, some compounds earn their spot not with flashy claims but through steady, proven value. This is one of them.