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HS Code |
123057 |
| Chemical Name | 2-Hydroxy-3-aminopyridine |
| Molecular Formula | C5H6N2O |
| Molecular Weight | 110.12 g/mol |
| Cas Number | 13360-65-1 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 184-187°C |
| Solubility | Soluble in water and organic solvents |
| Purity | Typically ≥ 98% |
| Storage Conditions | Store at room temperature, in a dry and well-ventilated place |
| Pka | Approx. 5.6 (hydroxy), 3.8 (amino) |
| Smiles | C1=CC(=C(N=C1)O)N |
| Synonyms | 3-Amino-2-hydroxypyridine |
As an accredited 2-HYDROXY-3-AMINO PYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-HYDROXY-3-AMINO PYRIDINE, 25g, supplied in a sealed amber glass bottle with tamper-evident cap and clear hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-HYDROXY-3-AMINO PYRIDINE: Securely packed in drums or bags, maximizing space, ensuring safe chemical transport. |
| Shipping | 2-Hydroxy-3-amino pyridine is shipped in tightly sealed, chemically resistant containers to prevent moisture ingress and contamination. It should be stored in a cool, dry place, away from incompatible substances. Labels indicating hazardous material are mandatory, and transport complies with applicable regulations to ensure safety during handling and transit. |
| Storage | 2-HYDROXY-3-AMINO PYRIDINE should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizing agents. Protect it from moisture, heat, and direct sunlight. Always store at recommended temperatures, typically room temperature unless specified otherwise, and ensure appropriate labeling and safety measures are in place to prevent accidental exposure or contamination. |
| Shelf Life | 2-Hydroxy-3-amino pyridine typically has a shelf life of 2-3 years when stored in a cool, dry, airtight container. |
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Purity 98%: 2-HYDROXY-3-AMINO PYRIDINE with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and consistent product quality. Melting Point 147°C: 2-HYDROXY-3-AMINO PYRIDINE with a melting point of 147°C is used in organic semiconductor development, where it provides thermal stability during processing. Molecular Weight 110.11 g/mol: 2-HYDROXY-3-AMINO PYRIDINE with a molecular weight of 110.11 g/mol is used in agrochemical compound formulation, where it allows precise dosing and reproducible biological activity. Particle Size <20 μm: 2-HYDROXY-3-AMINO PYRIDINE with a particle size less than 20 μm is used in pigment manufacturing, where it enhances dispersion and color uniformity. Stability Temperature 80°C: 2-HYDROXY-3-AMINO PYRIDINE stable up to 80°C is used in resin modification, where it maintains functional characteristics under elevated curing temperatures. Assay ≥99%: 2-HYDROXY-3-AMINO PYRIDINE with assay ≥99% is used in fine chemical synthesis, where it offers high reactivity and minimal contamination risk. Solubility in Water 15 mg/mL: 2-HYDROXY-3-AMINO PYRIDINE with solubility in water of 15 mg/mL is used in aqueous dye formulations, where it promotes homogeneous mixing and optimal coloration. UV Absorption at 265 nm: 2-HYDROXY-3-AMINO PYRIDINE exhibiting UV absorption at 265 nm is used in analytical standard preparation, where it enables accurate spectrophotometric quantification. |
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Research often feels like a puzzle with a missing piece. For many chemists and process engineers, 2-hydroxy-3-amino pyridine steps in to help complete that puzzle. Drawing from years of hands-on work in medicinal chemistry, it's clear some projects never move forward until you find the right intermediate. This compound, with its distinct hydroxyl and amino groups on the pyridine ring, shapes routes nobody could design with more basic building blocks. It enables synthesis of advanced pharmaceuticals, dyes, agrochemicals, and even specialty catalysts. The real world demands functional diversity, and that's exactly what this molecule offers.
Looking at its structure, the combination of a hydroxy group at the 2-position and an amino group at the 3-position brings big benefits to reactivity and downstream modification. Chemists working in industry and academia alike know how frustrating it can be when a pyridine ring resists every attempt to substitute at a tricky position—but 2-hydroxy-3-amino pyridine opens up several synthetic pathways. Its two functional groups shift reactivity just enough to allow for fine-tuned derivatization. The molecule lends itself well to condensation, acylation, and coupling reactions, and that means more possibilities for people designing next-generation compounds.
On the shelf, this material usually appears as a crystalline solid with a slight tan color. Its melting point sits a bit above many other substituted pyridines, so it stays stable through the temperatures used in most bench chemistry. Water content, purity, and related impurities matter, especially if the compound feeds into a demanding multi-step sequence. Typical lots offer high HPLC purity, with limits on metal and inorganic contaminants that meet everyday quality expectations in lab and manufacturing contexts. The density—noticeable when weighing and mixing—matches what anyone experienced with pyridine derivatives expects: a little heavier than air, not volatile, and manageable with gloved hands.
What sets 2-hydroxy-3-amino pyridine apart is the access it gives to chemistry impossible with plain pyridine or its methylated cousins. In my experience, methylated pyridines tend to block certain transformations, while this molecule opens doors because both the hydroxy and amino groups are easy to protect, deprotect, or swap as reactions unfold. Compared to mono-substituted pyridines like 2-aminopyridine or 3-hydroxypyridine, you have the advantage of dual-site modification, allowing for much richer chemistry. Colleagues in pharma development often mention that this compound fills gaps where neither mono-substituted nor halogenated pyridines can deliver. You see sharper selectivity in metal-catalyzed reactions, and its presence often reduces side-product noise that can derail scale-up.
Lab managers and production supervisors know the headaches that come from unstable intermediates. 2-hydroxy-3-amino pyridine avoids these issues, storing well under standard conditions and keeping its form through shipping and months-long storage. Unlike some nitrogen heterocycles, it doesn’t polymerize or degrade from trace moisture, which means less risk of lost batches and wasted workhours. Technical teams with large inventories appreciate how it keeps a consistent appearance and composition between lots, making it easier to train staff and maintain standard operating procedures.
Medicinal chemistry teams, especially those working on kinase inhibitors, antifungals, or CNS agents, have leaned into this compound as a starting point for scaffold building. I’ve seen more than one early-stage discovery program rerouted to this intermediate because it allows for faster exploration of new structure-activity relationships. Its ability to act as both an electron donor and acceptor unlocks unique pharmacophoric interactions, which medicinal chemists targeting protein pockets can't always achieve with simpler rings. In real terms, breakthroughs in lead optimization often come down to swapping in an intermediate like this and running library synthesis rapidly. As a result, time-to-find-a-winner often drops, budgets stretch further, and collaboration between chemistry and biology tightens up.
With green chemistry and environmental regulation gaining ground, manufacturers need intermediates that won’t throw a wrench in compliance. 2-hydroxy-3-amino pyridine behaves well in solution, so it allows for cleaner workups and less solvent overhead in downstream steps. Unlike some halogenated pyridines, you avoid persistent byproducts that become headaches for wastewater engineers. This directly supports operations working to meet strict emission standards and cut hazardous waste—a practical change that keeps researchers focused on outcomes, not paperwork.
In specialty chemicals, every new performance polymer or pigments project seems to call for a pyridine core modified to order. This compound feeds into established routes for chelating agents, fluorescent tracers, or optical brighteners. I’ve watched teams save months of troubleshooting by choosing this intermediate over less functionalized analogs, bypassing unnecessary protection/deprotection steps and lowering energy input for coupling reactions. Access to both hydroxy and amino handles right on the ring means more efficient cyclizations and cross-coupling reactions—high-value for anyone with scale-up on the horizon.
Crop science increasingly depends on smart chemical scaffolds. Screening libraries built on this molecule can lead to better plant protection agents or herbicides with newer modes of action. In the field-testing phase, researchers appreciate how easy it is to adjust solubility or binding properties by selective modification of this scaffold. Anyone following modern agrochemical patents will have seen an uptick in derivatives based on this framework, especially where improved efficacy and lower environmental persistence matter. Compared to older, more inert intermediates, this compound helps innovation travel from lab bottle to field plot without endless optimization cycles.
Graduate students and principal investigators both value reagents that cut frustration and busywork out of synthesis. With 2-hydroxy-3-amino pyridine, academic labs often skip over bottlenecks that would otherwise require custom synthesis or hazardous reagents. Its solubility profile works for common solvents, so routine purifications rarely bog down a thesis project or side-study. By simplifying routes to complex heterocycles, it keeps research groups competitive, helping them get publications and patents out on time. It also allows for protocol sharing: colleagues can reproduce results more reliably and collaborate across institutions, giving science a lift overall.
Material chemists need building blocks that fit into new frameworks, whether it's for battery components, sensor arrays, or advanced coatings. 2-hydroxy-3-amino pyridine’s bifunctional nature allows straightforward integration into multi-component assembly processes. For anyone trying to match theory to practice in materials synthesis, these dual reactive sites enable rapid tethering to other functional monomers, often lowering the threshold for achieving desired conductivity or optical responses. In collaborative work between industry and universities, this reagent often shows up as a linchpin in novel material prototypes that spin out from basic research.
Chemists care about performance but never ignore safety and waste management. From hands-on practice, the stability of this compound makes life simpler, where spills, storage, and disposal become less hassle than with more reactive solids and liquids. Even larger-scale facilities sidestep the esoteric containment procedures you see with volatile or foul-smelling pyridines. This directly reduces downtime and training costs, freeing team bandwidth for more important tasks. Where regulatory compliance pulls focus, such as REACH in Europe or TSCA in the United States, purchasing teams have reported smoother audits because the impurity and byproduct profiles for this intermediate fall well within existing permit limits.
In decades past, many research labs and plants defaulted to simpler pyridine derivatives, often because those were what catalogs showed or they were the cheapest available. Experience has taught that these older options often drag down yield and drive up the need for purification. This compound—thanks to both hydroxy and amino substitution—offers less chance of site confusion, which can kill a project when scale-up starts. Reviewers on grant panels and in industrial gatekeeping positions increasingly ask, “Why not pick a more functionalized starting point?” The performance gains matter, saving everyone resources in both the short and long term.
Custom synthesis, whether for the latest drug candidate or a pilot batch of high-end pigments, relies on intermediates that don’t throw curveballs mid-sequence. Teams working under tight deadlines prefer intermediates with clear, predictable reactivity. With this compound, the outcomes tend to align with mechanistic expectations, which keeps projects on-track and surprises to a minimum. Crystallization steps give manageable yields, which cuts down on the rework that can send a project off-schedule. This predictability finds plenty of fans in project managers and scientists working with limited budgets and timeframes.
Years of working with both small specialty suppliers and global chemical companies underscore the value of reliable sourcing. 2-hydroxy-3-amino pyridine holds up to scrutiny from purchasing and quality teams. Its purity metrics meet most institutional, pharmaceutical, and industrial standards—without requiring expensive custom lots or extended lead times. Analysts confirm reproducible chromatic and spectroscopic signatures, which matters for in-process checks and release testing. In practical terms, this means less waiting, fewer failed lots, and smoother project workflows.
In recent years, documentation has become as central as the chemical product itself. Regulatory filings and supply chain audits often slow down projects when paperwork lags behind. This product tends to ship with robust analytical support: certificates of analysis, method validation data, and impurity fingerprints that stand up during reviews. In my own project management, audits become much less stressful with this level of transparency. It fosters confidence—even where teams in different countries or regions need compliance assurance for their markets.
Life sciences, specialty chemicals, and advanced materials all press for highly tailored molecules. This compound finds its strongest champions among practitioners who have seen both the limitations and the learning curves with other options. Medicinal chemists, pigment designers, and polymer engineers can tweak their pathways based on its versatile profile. This creates new room for innovation and faster time to commercial or clinical application. Major chemical sectors increasingly flag such high-value intermediates for future-proofing annual research goals.
The blend of reliability and flexibility fits different user profiles. Graduate students can advance their studies without constant troubleshooting and mid-course corrections. Industry veterans cut down on avoidable errors and keep multi-stage syntheses running smoothly. This generates more mentorship and stronger team performance because the risk of unexpected hurdles drops. Experience with this compound teaches that consistency in key intermediates builds technical confidence, both in hands-on work and in strategic project planning.
Solubility happens to be one of the biggest practical considerations when choosing a heterocyclic intermediate. From firsthand lab work, this compound dissolves well in polar solvents—making cleanup fast and recrystallization straightforward. It suspends nicely too, meaning uniform dispersions during addition steps. Reaction times often drop, and downstream purification gets easier compared to similar compounds without this combination of hydroxy and amino substituents. This not only saves consumables but also keeps fume hood usage down. Handling protocols stay simple, with routine personal protective equipment—no special engineering controls necessary for most environments.
Pyridine chemistry keeps evolving. By building on dependable intermediates like 2-hydroxy-3-amino pyridine, future discoveries in health, agriculture, and materials science will move faster. Its adaptability means startups and established companies both find it useful, creating a kind of common ground between entrepreneurship and tradition. The more researchers share results and techniques around this compound, the more robust its applications will become. As academic-industry partnerships take off, expect to see this molecule in more published syntheses, commercial products, and maybe even in the next breakthrough therapeutic or high-performance material.
Every researcher and manufacturer wants reliable, flexible, and trustworthy building blocks to drive innovation. 2-hydroxy-3-amino pyridine fits that bill across diverse chemical applications. Its unique structure opens new doors for synthesis, its material stability reduces risk, and its documentation assures compliance in a world of tightening standards. In the crowded shelf of pyridine intermediates, this one proves its worth not as a commodity, but as a game-changer for those willing to push what’s possible in laboratory and industrial chemistry.