|
HS Code |
824448 |
| Product Name | 2-Hydroxy-3-bromopyridine |
| Cas Number | 4099-87-6 |
| Molecular Formula | C5H4BrNO |
| Molecular Weight | 189.99 |
| Appearance | White to pale yellow solid |
| Melting Point | 95-100°C |
| Boiling Point | 305.3°C at 760 mmHg |
| Density | 1.77 g/cm³ |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., ethanol, DMSO) |
| Synonyms | 3-Bromo-2-hydroxypyridine |
| Smiles | C1=CC(=C(N=C1)O)Br |
| Inchi | InChI=1S/C5H4BrNO/c6-4-2-1-3-7-5(4)8/h1-3,8H |
As an accredited 2-HYDROXY-3-BROMOPYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Hydroxy-3-bromopyridine, sealed with a plastic screw cap and labeled with safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-HYDROXY-3-BROMOPYRIDINE involves secure drum or bag packaging, ensuring moisture protection and optimized space utilization. |
| Shipping | 2-Hydroxy-3-bromopyridine is shipped in tightly sealed containers, suitable for chemicals, with appropriate hazard labeling. It should be transported under dry, cool conditions, protected from heat and incompatible materials. Shipping documents must include safety data information, in compliance with local and international regulations for hazardous materials. Handle with care to avoid spills. |
| Storage | 2-HYDROXY-3-BROMOPYRIDINE 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. Ensure proper labeling and avoid elevated temperatures. Follow all standard laboratory safety protocols and local regulations when handling and storing this chemical. |
| Shelf Life | **Shelf life:** 2-Hydroxy-3-bromopyridine is stable for at least 2 years if stored tightly sealed, dry, and protected from light at room temperature. |
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Purity 98%: 2-HYDROXY-3-BROMOPYRIDINE with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield target compound formation. Melting point 110-113°C: 2-HYDROXY-3-BROMOPYRIDINE with a melting point of 110-113°C is used in agrochemical development, where it facilitates controlled processing at specific thermal conditions. Molecular weight 174.99 g/mol: 2-HYDROXY-3-BROMOPYRIDINE with molecular weight 174.99 g/mol is used in medicinal chemistry research, where it allows accurate stoichiometry in compound library generation. Stability temperature up to 80°C: 2-HYDROXY-3-BROMOPYRIDINE stable up to 80°C is used in catalyst testing, where it maintains structural integrity during reaction screening. Particle size ≤ 50 μm: 2-HYDROXY-3-BROMOPYRIDINE with particle size ≤ 50 μm is used in solid formulation technology, where it enhances dissolution rates in tablet production. Spectral purity (NMR verified): 2-HYDROXY-3-BROMOPYRIDINE of spectral purity (NMR verified) is used in analytical reference standards, where it ensures reliable assay calibration. Solubility in ethanol 25 mg/mL: 2-HYDROXY-3-BROMOPYRIDINE with solubility in ethanol 25 mg/mL is used in solution phase organic synthesis, where it enables homogeneous reaction conditions. Low water content < 0.5%: 2-HYDROXY-3-BROMOPYRIDINE with low water content < 0.5% is used in moisture-sensitive syntheses, where it prevents unwanted hydrolysis reactions. |
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Science shapes more of the world around us than many people stop to realize, and the tools of modern chemistry often go uncelebrated. Anyone poking beneath the surface of pharmaceutical research or advanced materials development eventually comes across specialized building blocks designed for precision and reliability. Among this elite group stands 2-Hydroxy-3-Bromopyridine. Not the kind of chemical people chat about at dinner parties, but quietly, it’s changed the way researchers gather results and organizations develop vital products.
The science behind this compound rests on an aromatic pyridine core, which features both a hydroxyl group and a bromine substituent. While these chemical details might seem dry, their combination opens the door to some impressive applications. Chemists appreciate this product because those two functional groups create different points of reactivity on the ring, meaning this molecule can serve as a unique bridge for building more complex structures—a bit like having a double-ended wrench in the lab’s toolkit when so many standard tools only offer one option.
I spent years watching researchers try to coax molecules into cooperating. You know the scene: hours poured into developing or tweaking synthetic routes just to bring stubborn materials around. Introducing something like 2-Hydroxy-3-Bromopyridine saves that trouble. It doesn’t always get the headlines it deserves, but in hands-on work, efficiency and dependability earn respect fast.
High purity matters in synthesis. It’s frustrating—almost disheartening—to watch a reaction stutter, only to discover impurities in the starting material. Reliable suppliers take pains to ensure a product with purity often greater than 98%, backed up by clear analytical data from techniques such as NMR and HPLC. The appearance? Expect a white to off-white crystalline solid, easy to recognize and handle in most settings. It tends to stay stable when properly stored and handled, so batches behave predictably in the lab.
Talking about molecular specifications, 2-Hydroxy-3-Bromopyridine comes in with a molecular formula of C5H4BrNO and a molecular weight just over 173 g/mol. That’s small enough to keep things flexible for application, but distinct enough to avoid confusion with other common pyridine derivatives.
There’s a sweet spot in research—the place where cost, convenience, and versatility meet. 2-Hydroxy-3-Bromopyridine fills that spot for a number of organic chemists. The coexistence of bromo and hydroxy functionality makes the molecule a prime candidate for cross-coupling reactions. Researchers can introduce new side chains at the bromine site or rely on the hydroxy moiety for further modifications.
This dual personality gives researchers more options for building molecular complexity. For folks in pharma, that spells opportunity. Drug discovery often calls for subtle modifications. Sometimes a single atom changed on a lead compound transforms its bioactivity. Having a molecule with reactivity from both ends means people can explore more possible products in less time and with fewer synthetic steps.
I’ve known colleagues who counted on this compound when mapping out synthetic routes for kinase inhibitors or potential central nervous system agents. The fine-tuned modifications it supports often matter most in the early phases, where speed and flexibility make the difference between making a breakthrough or missing out.
Specialty pyridine derivatives seem similar at a glance, but seasoned chemists know that slight differences create big splits in application. Compare 2-Hydroxy-3-Bromopyridine to more standard halogenated pyridines; the unique marriage of the hydroxy and bromo groups on neighboring positions creates electronic properties and reaction profiles that neither alone could muster.
Try substituting a fluorine or chlorine atom for bromine and you won’t see the same ease in further functionalization, since bromine strikes a balance between reactivity and stability. Go for a pyridinol with a substituent further around the ring and you lose some of the special interplay between ortho-substituted groups. The result: 2-Hydroxy-3-Bromopyridine stands out, not just for what it brings to the table, but for what other, similar-looking molecules can’t do as cleanly.
Pharmaceutical organizations drive a lot of the world’s demand for intermediates like this one. The journey from theory to practice depends on intermediates with reliable activity and well-studied properties. 2-Hydroxy-3-Bromopyridine finds its way into a range of targets, from anti-infectives to oncology prospects. Not every project makes the cover of a medical journal, but the ones that do often build on compounds like this behind the scenes.
In materials science, researchers look for small but powerful chemical handles to build new polymers and specialty materials. People exploring organic semiconductors or materials used in the next wave of electronic devices discover creative uses for these heterocyclic systems. The hydroxy group serves as a launching point for further elaboration, while the bromo site adds versatility in coupling chemistry.
Laboratory scale-up and commercialization always test the mettle of a product. Here, the compound’s solid-state form means ease of weighing and transfer, and its solubility characteristics favor common organic solvents like DMF or acetonitrile—no need for specialty mixing conditions.
Lab professionals weigh not only the technical merits of a substance but also its stewardship and safety profile. There is a certain sense of relief knowing your bottle of a specialty building block comes from a source that can answer questions on hazard rating, toxicity, and recommended handling procedures. Chemistry can’t avoid risk altogether, but it doesn’t need to add new headaches either.
Products with clear supporting documentation put users in the driver’s seat. Those who’ve spent time sorting through cryptic safety docs or ambiguous labels know the value of transparency—knowing exactly what you are working with and how to treat it in the workplace. This sense of reliability means less time second-guessing and more time focusing on the science at hand.
With advanced intermediates, sustainability always looms in the background. Whether tackling waste handling or considering solvent selection, environmentally conscious labs look for intermediates that avoid introducing extra hazards or long-lived waste streams. A building block like this, with a clear profile and established handling protocols, provides peace of mind. Ethical sourcing, responsible waste disposal, and clear lifecycle assessments boost the standing of researchers and manufacturers alike.
In highly regulated environments, traceability and batch consistency build confidence. Pharmaceutical and industrial customers expect suppliers to document the origin, purity, and handling of products through the entire pipeline. Betting on intermediates with dependable supply chains means fewer surprises later, saving time and money during scale-up, technology transfer, or regulatory inspection.
Some compounds fade into the background after a brief moment in the sun, but the real difference-makers show up again and again when innovation demands versatility. 2-Hydroxy-3-Bromopyridine keeps appearing on project maps because of its dual reactivity, handling convenience, and clarity at every purchase.
It’s not hard to recall stories from innovation teams tasked with creating faster, lower-cost, or more potent drugs. Many times those projects run aground on bottlenecks around synthetic modifications. The dual-functionality of this building block can make the difference between a dead end and a breakthrough. Teams that tap into that versatility keep projects nimble and productive.
Not every purchase or transformation goes smoothly. Anyone who’s watched a reaction grind to a halt, or spent days cleaning up side-products, knows the frustration. Sometimes issues stem from batch impurities, storage under the wrong conditions, or old material losing potency. These aren’t unique to this intermediate, but they do crop up and need attention.
What most improves reliability is a combination of good supplier relationships, clear documentation, and ongoing training. Labs that push suppliers for recent, traceable analytical data see fewer surprises than those who treat every batch as interchangeable. Dedicated storage spaces and regular monitoring for degradation help keep materials working as expected. Even beyond the walls of the chemistry department, a culture of accountability trickles down to waste disposal and environmental compliance.
A separate challenge pops up with regulatory filings and technology transfer between facilities. It’s tempting to view intermediates as minor footnotes, but each one becomes part of the larger regulatory story. Recording not only purity and source but also usage in synthesis speeds up audits and improves the overall credibility of a program.
Few people make progress locked away in solitude, and the same goes for chemistry. Teams that openly compare notes on process optimization, analytical troubleshooting, and best practices speed up collective learning. Sharing real-world data about how this compound behaves in new coupling reactions or alternative solvent systems grows the knowledge base faster than isolated trial and error.
Any chemist who’s attended a technical conference or shared protocols on an industry message board knows the satisfaction of contributing a new insight. Better purity checks, improved crystallization methods, and safer handling protocols come about through this sort of back-and-forth. Over time, the growing expertise circles back to benefit not just the core user group but the whole field.
Advanced synthesis means opening new frontiers rather than walking familiar roads. A compound like 2-Hydroxy-3-Bromopyridine clears the way for new analogs in drug research and new functional materials for the electronics and coatings industries. Young scientists notice that compounds allowing quick divergence and easy modification get used more creatively.
Seeing the array of projects that launch from this building block, it’s clear there’s a common thread. Teams want predictability, flexibility, and documentation they can count on. This compound earns its keep by living up to those expectations. The more it enables researchers to take calculated risks—whether that’s a novel reaction type or a rapid screen of possible drug candidates—the more value it builds in both scientific and business arenas.
Decades spent in research and production teach a crucial lesson: the best products solve more than one problem at a time. They minimize risk, speed up work, and free up scientists to focus on their biggest challenges. 2-Hydroxy-3-Bromopyridine demonstrates this by delivering a rare blend of chemical versatility, stability, and ease of handling.
Teams looking to speed innovation don’t want to get bogged down repeating avoidable mistakes. A building block with broad appeal—fitting both classical transition metal catalysis and emerging synthetic methods—naturally gains a dedicated following. This bridges the gap between cutting-edge research and scalable industrial practice, paving the way for rapid progress from concept to prototype to production.
Whether you’re leading a startup on a shoestring budget or optimizing a global pharmaceutical process, the right tools can save more than a line on the expense report—they can change the tempo of discovery itself. Investing in reliable, high-purity building blocks like 2-Hydroxy-3-Bromopyridine often enables smooth transitions between screening, scale-up, and commercial production.
You learn quickly that not all suppliers treat their role the same way. Those who back up their product with detailed specs, batch-to-batch consistency, and responsible documentation earn repeat business. Researchers put value not just on a barrel of chemical, but on the shared expertise and partnership that comes with it.
The heart of organic and medicinal chemistry is about forging connections—literally at the molecular level but also figuratively as researchers collaborate to push the boundaries of knowledge. 2-Hydroxy-3-Bromopyridine offers a rare combination of reactivity and dependability that’s won over its fair share of practitioners around the globe.
The drive to streamline development pipelines and maximize research budgets means each component is scrutinized for added value. In this climate, a reliable, versatile intermediate earns its place not simply on the merits of a tidy molecular structure, but for the ripple effects it creates downstream—in time savings, successful regulatory filings, and, if things go right, potential therapies that change lives. Choosing building blocks is rarely about a name on a label. It’s a matter of trust, preparation, and an ongoing commitment to progress.