|
HS Code |
248200 |
| Chemical Name | 2-amino-3-hydroxy-5-bromopyridine |
| Molecular Formula | C5H5BrN2O |
| Molecular Weight | 189.01 g/mol |
| Cas Number | 226499-68-5 |
| Appearance | Off-white to light brown solid |
| Boiling Point | No data available |
| Melting Point | 160-164°C |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC(=NC(=C1O)N)Br |
| Inchi | InChI=1S/C5H5BrN2O/c6-3-1-4(9)5(7)8-2-3/h1-2,9H,(H2,7,8) |
| Purity | Typically ≥98% (for commercial samples) |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 2-amino-3-hydroxy-5-bromopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25g amber glass bottle with a tamper-evident cap, labeled clearly with hazard and identification details. |
| Container Loading (20′ FCL) | 20′ FCL container is loaded with securely packaged 2-amino-3-hydroxy-5-bromopyridine, ensuring safe, efficient bulk chemical transportation. |
| Shipping | 2-Amino-3-hydroxy-5-bromopyridine is shipped in tightly sealed containers to prevent moisture and contamination. Packages are clearly labeled according to chemical safety standards and transported under ambient conditions, unless otherwise specified. Handle with appropriate protective measures; shipping complies with relevant local, national, and international regulations for hazardous materials if applicable. |
| Storage | 2-Amino-3-hydroxy-5-bromopyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling and avoid prolonged exposure to air. Use appropriate personal protective equipment when handling. |
| Shelf Life | 2-Amino-3-hydroxy-5-bromopyridine is stable under recommended storage conditions and typically has a shelf life of several years. |
|
Purity 98%: 2-amino-3-hydroxy-5-bromopyridine with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures optimal reaction yield and minimal byproduct formation. Melting point 225°C: 2-amino-3-hydroxy-5-bromopyridine with a melting point of 225°C is used in high-temperature solid-phase peptide synthesis, where thermal stability supports process integrity. Molecular weight 191.02 g/mol: 2-amino-3-hydroxy-5-bromopyridine with a molecular weight of 191.02 g/mol is used in custom heterocyclic compound design, where precise molecular control enables reproducibility in drug development. Particle size <10 µm: 2-amino-3-hydroxy-5-bromopyridine with particle size less than 10 µm is used in fine chemical formulations, where small particle size ensures uniform dispersion and consistent reactivity. Stability temperature up to 160°C: 2-amino-3-hydroxy-5-bromopyridine with stability up to 160°C is used in thermal-resistant coating applications, where reliable temperature endurance improves product durability. Water solubility 0.5 g/L: 2-amino-3-hydroxy-5-bromopyridine with water solubility of 0.5 g/L is used in aqueous synthetic protocols, where controlled dissolution facilitates homogeneous reaction conditions. Ash content <0.1%: 2-amino-3-hydroxy-5-bromopyridine with ash content below 0.1% is used in analytical reference standards, where low residue guarantees measurement accuracy. Residual solvent <50 ppm: 2-amino-3-hydroxy-5-bromopyridine with residual solvent content under 50 ppm is used in active pharmaceutical ingredient (API) manufacture, where negligible solvent presence enhances product safety. pH (1% solution) 6.2: 2-amino-3-hydroxy-5-bromopyridine at pH 6.2 in 1% solution is used in biochemical assay development, where near-neutral pH ensures compatibility with biological systems. UV absorbance λmax 312 nm: 2-amino-3-hydroxy-5-bromopyridine exhibiting UV absorbance maximum at 312 nm is used in photoreactive labeling applications, where specific absorbance enables targeted detection. |
Competitive 2-amino-3-hydroxy-5-bromopyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
A closer look at modern research and industrial labs shows a consistent search for building blocks that can open up new possibilities, push discovery forward, and meet precise needs. 2-amino-3-hydroxy-5-bromopyridine may not win popularity contests, but for those who work with pyridine derivatives, it often finds a place on the shelf thanks to its structure and reactivity profile. People who care about making the most of their time, budgets, and efforts will want to know what sets this compound apart.
Several aspects define this molecule and shape the way it’s put to use. The pyridine core, decorated with both an amino and a hydroxyl group at adjacent positions, along with a bromine at the 5-position, brings three points of chemical appeal to the table: nucleophilicity from the amino, hydrogen bonding and solubility traits from the hydroxy, and halogen reactivity from the bromine. Taken together, these groups let chemists and material scientists plot interesting reaction sequences and transformations that simply aren’t an option with plain pyridine.
This particular substitution pattern speaks to synthetic flexibility. Imagine the hurdles in fine-tuning regulatory pathways or in tweaking the performance of electronic or pharmaceutical intermediates—starting with a pyridine that's already “half decorated,” as many would say, brings down steps and corners. Many labs eye compounds such as 2-amino-3-hydroxy-5-bromopyridine not simply for “filling out” a catalog, but for genuinely enabling new routes. Experience over the years shows that matching a compound’s structure to the right project can trim time, reduce waste, and lead to better yields.
Discussion about 2-amino-3-hydroxy-5-bromopyridine almost always lands on its value as an intermediate. Some specialty pharmaceuticals call for elaborate ring systems that demand careful placement of functional groups before you even begin final cyclization, conjugation, or coupling steps. For instance, this molecule lends itself to Suzuki or Buchwald-Hartwig cross-couplings. Its bromine can serve as a handle for introducing a range of aryl or vinyl groups, which is a staple in the design of new drugs or optoelectronic materials.
Medicinal chemistry efforts, in particular, turn to such building blocks because small tweaks around a ring can lead to big changes in absorption, distribution, metabolism, and even toxicity profiles. The hydroxy and amino groups allow for hydrogen bonding, which may improve solubility or provide key interactions at enzyme binding sites. Every veteran in the drug discovery field has seen a structure-activity relationship plot that pivots on small changes. For every time someone spent months chasing a stubborn molecule, having something like 2-amino-3-hydroxy-5-bromopyridine in reserve offered a shortcut, a way to get to that desired binding pattern without detouring through an extra round of protecting group chemistry.
Material science tells a similar story. Heteroaromatic building blocks serve as the starting points for dyes, sensors, or organic semiconductors. Reliable brominated pyridines often streamline the process of introducing electronic features or tethering functional units to broader frameworks. The decision to reach for this compound—and not a more generic alternative—reflects a tendency among seasoned researchers to invest in starting materials that leave more doors open further down the line.
Take it from years of running reactions in academic and industrial labs: the practical details of a compound sometimes matter more than elaborate description or abstract purity numbers. Most users want reliable melting points and spectra, but stability in the bottle, tolerance to bench conditions, and ease of handling rise to the top when comparing sources. 2-amino-3-hydroxy-5-bromopyridine tends to offer these conveniences. The presence of both hydroxy and amino groups can present handling challenges in some cases, but suppliers who cut corners rarely escape notice—impure lots gum up reactions, increase the need for flash chromatography, and slow down timelines. Those who work with suppliers who are transparent about source and method, and who can provide up-to-date safety and storage advice, escape a lot of headaches that come from second-guessing critical reagents.
From my experience, smart buyers and researchers ask questions about batch consistency, especially when scaling synthesis from milligrams to grams or more. It’s well known that brominated intermediates sometimes run into issues with shelf life or discoloration if impurities lurk, and nothing slows a project more reliably than hearing, “We need to order another bottle—and hope it matches.” Real trust builds around suppliers who meet their own claims, who back up batch numbers with analytical data, and who respond quickly to queries about lot-to-lot variation.
Many labs already keep a few aminopyridines or bromopyridines in rotation. What sets this compound apart is the combination of bromo, hydroxy, and amino in a geometry that lends itself to further transformation. For comparison, plain 2-amino-5-bromopyridine gets used often, but lacks the hydroxy group—introducing that later makes for extra steps, each one eating up time or introducing instability. Meanwhile, starting from 3-hydroxy-5-bromopyridine skips the amino, which is equally valuable in coupling chemistry and biological targeting. Having both groups on board opens doors for patentable new molecules, distinctive cross-coupling patterns, and allows researchers to drop in modifications at points that are otherwise hard to access.
Anyone who’s ever tried to modify a structure after making it knows the pain: each extra transformation increases risk, introduces losses, and eats up chemicals. Choosing a well-designed building block from the start makes more difference than any downstream purification trick can offer. Labs constantly rotate through lists of intermediates to find the best compromise of price, reactivity, and downstream benefit, but for many projects, starting as close to the finish line as possible wins out.
The world of heterocyclic chemistry is crowded with options, and yet demand for specialized compounds like 2-amino-3-hydroxy-5-bromopyridine keeps growing. In past years, requests for such chemicals often stalled due to supply issues or cost, with researchers having to settle for less ideal substitutes, knowing it’d mean more work down the road. People working on time-sensitive projects, especially under budgets that make every purchase count, now gravitate to vendors with proven supply chains and comprehensive data on their offerings.
It’s not uncommon for a single project in drug development, materials science, or chemical biology to cycle through several potential intermediates before settling on the right one. Those starting from a point of structural flexibility—both in terms of available reactive sites and ease of further derivatization—find their way to products like this. The shift in recent years has shown a move away from pure cost-minimization toward more nuanced choices, weighing not just the sticker price but the hidden costs of re-synthesis, repeat purification, or failed runs. Lab directors and procurement managers aim for compounds with transparent origins and batch records rather than hunting blindly through generic catalog sheets.
Having spent a good stretch of time at the bench, I’ve learned to appreciate practical considerations that go well beyond the catalog page. A real test of any chemical comes on a rough day when a reaction needs to run, the clock is ticking, and the margin for error is slim. Compounds that flow free, dissolve properly, and match spectral fingerprints fast become the favorites. I remember one case where three different suppliers sent versions of the “same” intermediate; only one delivered the reliability needed for a published piece of work, and it wasn’t the supplier with the loudest marketing. Purity ranges might look similar on paper, but one poorly washed batch introduces more headaches than anyone enjoys.
The value of robust, accurate Certificates of Analysis can’t be understated. Proper documentation saves resources—not just for regulatory reasons, but for practical troubleshooting. Knowing exactly what’s in the bottle allows for confident planning and less time wasted on unnecessary re-checks. Also, responsiveness from a supplier, especially on product-specific questions or technical support, goes a long way in building loyalty. The world of synthetic chemistry may be grounded in formulas and reactions, but trust and clear communication often prove just as valuable.
Lab professionals know the risk profile of substituted pyridines, especially with halogenated or polyfunctionalized versions. 2-amino-3-hydroxy-5-bromopyridine hasn’t escaped notice when it comes to safety data, and those working with it quickly get used to good lab practices. Gloves, goggles, and fume hoods have become routine. The compound’s structure raises points about potential irritation or long-term exposure, though feedback from occupational health staff and published safety sheets doesn’t earmark it as a major outlier against its close cousins.
Increasing attention to environmental stewardship has influenced sourcing and disposal decisions. More labs—not just those under legal compulsion—now aim to minimize waste or choose vendors committed to green practices. Halogenated intermediates require specialized waste handling, so reducing the per-run usage or switching to more eco-friendly alternatives (when available) represents an ongoing area of improvement. Open communication with suppliers has helped several organizations calibrate their procedures and cut the environmental impact without sacrificing productivity.
Even an ideal intermediate doesn’t eliminate every obstacle. Handling issues sometimes crop up—moisture sensitivity or issues with crystallization occasionally show up when batches sit too long, or when suppliers rush production cycles. Over my years in the lab, I’ve come to rely on internal tracking logs and routine checks of melting point and NMR data to catch “off” batches before they cost weeks. Communication with colleagues about best practices, or directly with vetted vendors on observed batch anomalies, heads off bigger problems.
Supply chain disruptions can impact these specialty chemicals, too. Experienced procurement folks have learned to keep a modest buffer, but without overcommitting capital. Some organizations have started to pre-negotiate delivery schedules with their preferred suppliers. These simple measures help projects move smoothly, even when global supply hiccups threaten to throw plans off track. Relationships matter—a vendor who keeps customers updated and offers real support in times of delay becomes more than just a short-term partner.
A final challenge comes with keeping up with regulatory requirements. Well-documented and fully traceable sourcing gives confidence, not just for intellectual property protection, but in case projects approach late-stage development or scale up. Compliance with documentation isn’t just about crossing T’s and dotting I’s—it enables seamless handoffs between academic, pilot, and commercial teams.
Seasoned researchers keep a running list of “most reliable starting points;” 2-amino-3-hydroxy-5-bromopyridine keeps a place on those lists thanks to its specific utility and performance. While its cost per gram may run higher than bare-bones alternatives, what saves time, trouble, and repeat syntheses ends up being a bargain in the long haul. The ability to run clean, efficient sequences leads to more productivity and, ultimately, better outcomes.
Yet, value isn’t measured just by yield or reaction rate. Researchers pursuing publication or patent protection value intermediates that help build novelty into their target compounds. Unique substitution patterns and uncommonly functionalized building blocks help avoid “prior art” landmines, giving synthetic efforts a real competitive edge. A compound that starts with the right combination of groups can make a routine sequence into a publishable one, or push a stalled development program past the next milestone.
Transparent, detailed product data lets users make smart, context-driven decisions. People who’ve been around the block know manufacturers sometimes advertise only bare specs—pushing for lot-to-lot reproducibility and batch analytics gives lab teams the confidence to take on more challenging work. Partnerships between supplier and customer that go beyond one-time sales drive advances on both sides; suppliers who listen to real-world feedback can refine their processes, reduce product-related setbacks, and improve documentation. This kind of collaboration benefits the larger scientific community.
Newer researchers, and sometimes even institutional buyers, may be tempted to skimp on upfront vetting. The wisdom gained over years in the field shows this rarely pays off. Choosing compounds from reputable sources—even if it means a slightly longer ordering process or a higher unit price—routinely pays dividends in reliability, regulatory success, and ultimately the quality of published or delivered results.
The market for specialty pyridines continues to evolve. Whether in pharmaceuticals, electronics, or advanced materials R&D, the role of smart starting materials becomes more important as demands on efficiency, reproducibility, and innovation grow. More organizations have started integrating compound screening and route optimization at the very start of projects. The more work that can be “front-loaded” by choosing well-considered intermediates, the more time and resources get freed up for true innovation or optimization instead of tedious troubleshooting.
The next years will likely bring more regulation and more demand for transparency, not less. As end markets ask for greener, safer, and better-documented materials, the most successful labs and suppliers will be those who meet that demand willingly. They’ll focus on supporting both experienced and newer scientists with clear documentation, responsive service, and continuous improvement in quality. Trust, clarity, and genuine understanding of the full project pipeline make all the difference.
For those weighing whether 2-amino-3-hydroxy-5-bromopyridine is the right choice, nothing beats honest assessment—of the specific needs of their syntheses, of vendor track records, and of the evolution of regulations and standard lab practices. The extra steps at the decision-making stage pay off. My own career has reinforced how much can be gained by investing time up front, whether in planning new syntheses or choosing which bottle to bring into the lab. And in a world where every research dollar and deadline counts, that kind of careful, experience-driven choice makes a world of difference.