|
HS Code |
425816 |
| Chemical Name | 2-Hydroxy-3-Amino-5-Bromo Pyridine |
| Molecular Formula | C5H5BrN2O |
| Molecular Weight | 189.01 g/mol |
| Appearance | Light brown to beige powder |
| Solubility | Soluble in polar organic solvents (e.g., DMSO, methanol) |
| Purity | Typically ≥ 98% (commercial grade) |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 2-Hydroxy-3-Amino-5-Bromo Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, screw cap, clear hazard labeling, chemical name and formula, contains 25 grams of 2-Hydroxy-3-Amino-5-Bromo Pyridine. |
| Container Loading (20′ FCL) | 20′ FCL: 10 MT packed in 200 kg HDPE drums or iron drums, palletized, suitable for safe, international shipment. |
| Shipping | **Shipping Description:** 2-Hydroxy-3-Amino-5-Bromo Pyridine is shipped in tightly sealed containers made of compatible materials, clearly labeled as a laboratory chemical. It should be protected from moisture, heat, and direct sunlight. Transport in compliance with local, national, and international regulations. Handle with gloves and appropriate protective equipment during transit and upon receipt. |
| Storage | 2-Hydroxy-3-Amino-5-Bromo Pyridine should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from heat, light, and incompatible substances such as strong oxidizers. Avoid moisture exposure. Label the container clearly, and handle with appropriate personal protective equipment. Follow all local regulations for safe chemical storage and ensure access to safety data sheets (SDS). |
| Shelf Life | 2-Hydroxy-3-Amino-5-Bromo Pyridine should be stored tightly sealed, protected from light and moisture, with a typical shelf life of 2 years. |
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Purity 98%: 2-Hydroxy-3-Amino-5-Bromo Pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced side-product formation. Melting Point 160°C: 2-Hydroxy-3-Amino-5-Bromo Pyridine with a melting point of 160°C is used in solid-phase organic synthesis, where it provides thermal stability during high-temperature processing. Molecular Weight 205.01 g/mol: 2-Hydroxy-3-Amino-5-Bromo Pyridine with a molecular weight of 205.01 g/mol is used in fine chemical manufacturing, where precise mass control allows accurate formulation. Particle Size <50 µm: 2-Hydroxy-3-Amino-5-Bromo Pyridine with particle size less than 50 microns is used in catalyst preparation, where enhanced surface area increases catalytic activity. Stability up to 120°C: 2-Hydroxy-3-Amino-5-Bromo Pyridine with stability up to 120°C is used in microelectronics material production, where it maintains integrity under process heat. Water Solubility 1.5 g/L: 2-Hydroxy-3-Amino-5-Bromo Pyridine with water solubility of 1.5 g/L is used in aqueous pharmaceutical formulations, where it enables homogeneous dispersion for consistent dosing. Storage Condition 2-8°C: 2-Hydroxy-3-Amino-5-Bromo Pyridine stored at 2-8°C is used in life science research, where controlled storage preserves chemical reactivity over extended periods. Assay ≥99%: 2-Hydroxy-3-Amino-5-Bromo Pyridine with assay value ≥99% is used in reference standard manufacturing, where assay accuracy supports analytical reliability. Moisture Content <0.5%: 2-Hydroxy-3-Amino-5-Bromo Pyridine with moisture content less than 0.5% is used in moisture-sensitive reaction systems, where it prevents undesired hydrolysis. HPLC Purity >99%: 2-Hydroxy-3-Amino-5-Bromo Pyridine with HPLC purity greater than 99% is used in diagnostic reagent formulation, where chemical purity ensures minimal assay interference. |
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2-Hydroxy-3-Amino-5-Bromo Pyridine, often recognized by its CAS number 118964-01-9, holds a solid reputation in research and industry. This compound, with its distinct arrangement of hydroxyl, amino, and bromine groups on a pyridine ring, stands out for more than just its chemistry. The presence of both electron-withdrawing and electron-donating groups on the aromatic ring delivers unique reactivity and practical versatility that a seasoned chemist notices right away. The technical literature describes the off-white to light yellow powder, usually with purity exceeding 97%, as a small but pivotal piece in bigger synthesis puzzles.
Molecularly, this compound weighs in at about 190 grams per mole, with a structure that encourages selective reactions. The hydroxyl at position 2 and the amino at position 3 provide multiple routes for subsequent modifications. That bromine at position 5 isn’t there by accident – it opens doors to cross-coupling reactions, such as Suzuki and Buchwald-Hartwig, by offering a reliable leaving group. This isn’t theory—it’s exactly the leverage researchers want, especially when building complex pharmaceuticals or agrochemicals where precision matters.
Chemistry is filled with small quirks that make or break a synthesis. 2-Hydroxy-3-Amino-5-Bromo Pyridine offers a toolkit rolled into one molecule. My own time in synthesis labs taught me that a well-chosen intermediate saves weeks. With this compound on the bench, there’s less frustration with purification and fewer side reactions compared to similar bromo-pyridines lacking that strategic hydroxy group. This seemingly minor modification changes solubility, increases selectivity, and sometimes makes the impossible route viable.
Other bromo-pyridines or amino-pyridines serve their purposes, but the absence of either the hydroxy or the bromine limits their reach. I recall a run of failed couplings using simple amino-pyridines until introduction of a bromo analogue catalyzed a leap forward. That’s not unique—hundreds of papers have documented similar breakthroughs. The research community consistently turns to molecules like this one for the way they sit at the crossroads of practicality and possibility.
Pharmaceutical development leans heavily on intermediates like 2-Hydroxy-3-Amino-5-Bromo Pyridine. Medicinal chemists don’t waste resources on unmanageable starting materials; they choose intermediates that streamline synthesis and cut down on purification headaches. This particular compound helps build important scaffolds found in kinase inhibitors, antibacterial agents, and CNS-active molecules. The key lies in that combination of functional handles—the hydroxy enables easy derivatization, and bromine invites precise coupling.
Agricultural chemistry benefits, too. Pesticide and herbicide developers often need heteroaromatic frameworks that not only kill pests but break down safely in the environment. If a platform compound brings selectivity in synthesis and opens new functionalization routes, it earns a recurring role in the development pipeline. Researchers in crop protection keep coming back to substituted pyridines for just these reasons.
Some chemists might reach for 2-Amino-5-Bromo Pyridine or its hydroxy-free siblings instead. It’s tempting to grab whatever is cheapest or most available, but these substitutions come at a cost in flexibility. I’ve spent more hours than I’d care to tally purifying byproducts from reactions that started easy but finished with a mess. Missing the hydroxy group means skipping important hydrogen bonding interactions during synthesis, which can tip the scales during later steps.
Consider also plain pyridine derivatives—unsubstituted or mono-substituted compounds aren’t as direct routes to target molecules. Without careful planning, using the wrong intermediate leads to extra steps, lost yield, and more waste. The hydroxy-amino-bromo trio isn’t a luxury—it’s a solution to real synthetic bottlenecks.
Developing pharmaceuticals or agrochemicals involves dozens of steps with tough trade-offs at each stage. Picking the right intermediate feels less like shopping and more like matchmaking: you want reliability, versatility, and compatibility with downstream chemistry. For those who don’t spend late nights reading reaction mechanisms, it’s easy to overlook how much rests on these choices. 2-Hydroxy-3-Amino-5-Bromo Pyridine streamlines several of those steps.
Impurities slip in when a starting material isn’t designed for clean transformations. The hydroxy and amino groups, working together, guide reactions with better precision. That bromine means selective coupling without forcing conditions that wreck sensitive functional groups elsewhere in the molecule. The upshot is a cleaner process, higher yield, and less frustrating troubleshooting.
Environmental regulations push every synthetic chemist to minimize waste and cut out harsh reagents. Every functional group on this molecule helps avoid side products that would end up in waste streams. Cleaner chemistry isn’t a slogan here—it’s a necessary part of convincing regulators and investors that a route is worth pursuing.
Sourcing chemicals responsibly gets more attention than ever. Researchers care about quality, batch consistency, and knowing suppliers meet safety and environmental guidelines. I’ve seen supply chain hiccups disrupt entire R&D programs because a once-reliable intermediate suddenly got caught in regulatory limbo or ran into production issues. The demand for 2-Hydroxy-3-Amino-5-Bromo Pyridine encourages suppliers to invest in reproducible methods and transparent logistics.
Handling this compound in the lab mirrors the way any strong intermediate deserves respect. The amino and bromo groups demand good ventilation, gloves, and eye protection—a practice as standard as it is critical. Nobody likes surprises, especially not with compounds possessing a track record of reactivity. Having reliable analytical data from reputable suppliers means a lab technician doesn’t have to second-guess purity or structure. A strong materials safety culture builds confidence, speeds up workflows, and cuts down on wasted material.
Scientific discovery is as much about dependable supplies as bold ideas. 2-Hydroxy-3-Amino-5-Bromo Pyridine fits into the toolkit of working scientists trying to translate ideas from concept to pilot scale. Every big breakthrough in drug development or crop protection has come out of a thousand small wins—faster reactions, cleaner separations, and, often, a new twist on an old intermediate. That’s the ground chemistry walks on: real progress rooted in practical details.
With the rise of high-throughput screening and automated synthesis, the value of a versatile intermediate only grows. Automation doesn’t forgive inconsistent starting materials or hard-to-control byproducts. As technology pushes the boundaries of speed, chemists still lean on reliable intermediates whose behavior matches published data and in-house experience. The high confidence in outcomes keeps projects under budget and ahead of the curve.
Academic researchers and industrial chemists sometimes speak different languages but face the same hurdles: limited time, uncertain budgets, pressure to innovate. 2-Hydroxy-3-Amino-5-Bromo Pyridine bridges those gaps. Its broad applicability means research teams in academia can test ideas that might seem niche now but serve as the seeds for tomorrow’s commercial products.
Publications have documented the use of this intermediate in synthesizing various heterocyclic frameworks. These frameworks show up in kinase inhibitor libraries and anti-tuberculosis candidates. Collaborations between universities and private companies often start with a common library of fragments—compounds like this one sit at the core. The right intermediate enables a small academic lab to compete with larger teams and deliver results that attract investment or licensing.
Modern synthetic routes can no longer ignore what happens after a process scales up. Substituted pyridines, especially those with halogens and amino groups, must show compliance with evolving regulations around chemical waste and process safety. Choosing an intermediate that streamlines downstream steps, limits toxic byproducts, and supports controlled chemistry aligns with stricter global standards. This helps keep both the lab and the environment safer.
The drive for greener chemistry underpins many new product launches. Designing routes that use fewer steps, generate less waste, or operate under milder conditions benefits everyone from bench scientist to end-user. 2-Hydroxy-3-Amino-5-Bromo Pyridine doesn’t solve every environmental challenge but plays its part by enabling concise, selectivity-driven synthesis with fewer dead-ends or hazardous byproducts. Researchers who work in regulated fields or under constant audit appreciate the built-in predictability.
Chemistry marches forward, but the old saying that quality in equals quality out doesn’t go out of style. As more researchers explore complex targets like multi-target drugs, specialty materials, or next-gen herbicides, the demand for intermediates that keep up with new challenges never slows down. This compound’s place in chemical catalogs reflects years of steady demand, not just as an off-the-shelf product but as a quietly indispensable cog in the wheels of discovery.
Newer methods such as flow chemistry and microreactor designs demand intermediates that perform consistently under specialized conditions. The nuanced balance of reactivity and stability in 2-Hydroxy-3-Amino-5-Bromo Pyridine means it adapts well to these platforms. Labs that switch from batch processing to continuous synthesis need to trust that an intermediate won’t throw a monkey wrench into scale-up. Reliability is not just a bonus—it’s critical.
One ongoing issue that still plagues both large and small labs is access. Researchers in smaller institutions or emerging markets sometimes struggle to source intermediates consistently or at fair prices. This affects innovation across borders, stifling promising new approaches. Open supply chains and transparent pricing from major suppliers help, but progress remains uneven.
Reducing chemical waste remains another major challenge. Process chemistry teams must constantly optimize synthesis to get the most product from the least input. Every extra step creates more solvent use, more handling, more containers to dispose of. Having an intermediate that shaves two or three steps off a route—by enabling coupling, protecting group skips, or direct functionalization—means cleaner results and less to haul away. These practical gains don’t always appear in the headlines, but no one who’s worked at a busy bench under tight safety review takes them for granted.
The bottom line in recommending 2-Hydroxy-3-Amino-5-Bromo Pyridine is rooted in long days and nights troubleshooting failed reactions. Seasoned chemists value not just technical specifications but track record. I remember a series of kinase inhibitor syntheses where this intermediate alone, swapped in for a similar pyridine, improved both overall yield and reaction times. Insights like these aren’t just anecdotes—they play out in countless research groups year after year.
Peer-reviewed studies consistently report good mass balances and cleaner analytical profiles when using this intermediate in cross-coupling reactions. The strategic placement of substituents enables late-stage introduction of sensitive groups. Discussions at conferences often return to “what worked” stories—compounds like this show up again and again when the goal is smooth scale-up or optimized library creation.
A growing number of suppliers now offer this compound, responding to documented demand across pharmaceutical, agrochemical, and academic sectors. Standardized quality assurance and lot-to-lot consistency take center stage as researchers demand more data up front. Analytical results—such as HPLC and NMR—usually accompany shipments, reflecting a push for transparency that benefits everyone along the pipeline. In my experience, this trend reduces uncertainty and speeds up evaluation for new projects.
Distribution networks also must keep up with changing import-export rules, especially as countries adopt newer chemical safety legislation. Suppliers who offer batch traceability and compliance with international guidelines help researchers avoid costly delays or regulatory hiccups. The result is a smoother workflow from idea to bench to product candidate.
Emerging fields such as personalized medicine and advanced materials demand more from intermediates. Variations on the classic substituted pyridine scaffold, like 2-Hydroxy-3-Amino-5-Bromo Pyridine, unleash new options for functionalization and create building blocks tailored for specific biological targets or material properties. High-throughput screening, combinatorial chemistry, and computer-assisted drug design all benefit from reliable access to such intermediates.
Collaborations across chemistry, biology, and data science stand to gain from intermediates that enable modular synthesis. Predictable reactivity helps researchers build compound libraries rapidly, test hypotheses, and move promising candidates toward clinical trials faster. The ongoing need for well-defined, high-purity intermediates won’t diminish as technology marches on.
Ongoing challenges in chemical synthesis can be addressed at several levels. Investing in green chemistry and adopting protocols that minimize hazardous waste pays off in both regulatory compliance and cost savings. Implementing best practices in procurement and storage slashes the risk of contamination or degradation. Training new chemists not only in technique but in evaluating quality keeps research moving efficiently.
Building strong supplier partnerships brings stability to the supply chain. Open dialogue about customer needs, coupled with regular feedback on batch quality, drives improvement. And as automation spreads to more labs, intermediates like 2-Hydroxy-3-Amino-5-Bromo Pyridine may increase in value as their role in streamlining complex workflows comes to the fore.
A compound is only as good as what it enables researchers to achieve. The story of 2-Hydroxy-3-Amino-5-Bromo Pyridine stands out as a testament to the impact of the “unsung hero” intermediates that power real innovation. Whether in a giant pharmaceutical R&D division, a startup chasing a promising new drug target, or a university lab teaching tomorrow’s chemists, this intermediate offers far more than a formula on paper. Its value emerges every time a synthesis goes right, every round of analysis comes back clean, and every breakthrough moves one step closer to real-world use.