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HS Code |
267568 |
| Productname | 2-AMINO-5-HYDROXYPYRIDINE |
| Casnumber | 1121-27-9 |
| Molecularformula | C5H6N2O |
| Molecularweight | 110.12 g/mol |
| Appearance | Light yellow to brown powder |
| Meltingpoint | 241-245°C |
| Solubility | Soluble in water, ethanol |
| Purity | Typically ≥ 98% |
| Density | 1.28 g/cm³ (estimated) |
| Structure | Pyridine ring with amino at position 2 and hydroxyl at position 5 |
| Smiles | c1cc(N)cnc1O |
| Inchi | InChI=1S/C5H6N2O/c6-4-1-2-5(8)7-3-4/h1-3,8H,(H2,6,7) |
| Synonyms | 5-Hydroxy-2-aminopyridine, 2-Amino-5-pyridinol |
As an accredited 2-AMINO-5-HYDROXYPYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-AMINO-5-HYDROXYPYRIDINE is supplied in a 25g amber glass bottle with a tight-sealing cap and chemical hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL container for 2-AMINO-5-HYDROXYPYRIDINE: typically loaded with securely sealed drums or bags, moisture-protected, complying with safety standards. |
| Shipping | 2-AMINO-5-HYDROXYPYRIDINE is shipped in tightly sealed containers under dry and cool conditions. It should be protected from light, moisture, and incompatible substances. Transport must comply with local and international chemical safety regulations, including proper labeling and documentation. Avoid physical damage during transit to ensure product integrity and safety. |
| Storage | **2-Amino-5-hydroxypyridine** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture, direct sunlight, and sources of ignition. Label the container clearly, and ensure it is kept away from food and drink. Follow standard laboratory safety protocols when handling and storing. |
| Shelf Life | 2-Amino-5-hydroxypyridine should be stored tightly sealed, protected from light and moisture; generally stable for at least two years. |
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Purity 99%: 2-AMINO-5-HYDROXYPYRIDINE with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and reduced impurity levels. Melting point 220°C: 2-AMINO-5-HYDROXYPYRIDINE with melting point 220°C is used in high-temperature organic reactions, where it provides enhanced process stability and efficiency. Particle size <10 µm: 2-AMINO-5-HYDROXYPYRIDINE with particle size less than 10 µm is used in catalyst preparation, where it enables uniform dispersion and increased catalytic activity. Moisture content <0.2%: 2-AMINO-5-HYDROXYPYRIDINE with moisture content below 0.2% is used in dye manufacturing, where it minimizes side reactions and improves color consistency. Stability temperature up to 180°C: 2-AMINO-5-HYDROXYPYRIDINE with stability temperature up to 180°C is used in polymer synthesis, where it maintains compound integrity during processing. Assay 98% minimum: 2-AMINO-5-HYDROXYPYRIDINE with assay 98% minimum is used in agrochemical formulation, where it ensures reliable activity and batch-to-batch reproducibility. |
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Anyone who has worked in pharmaceutical research or in advanced materials development has brushed up against compounds that act as silent building blocks—key molecules that spark new reactions or help synthesize something vital. 2-Amino-5-hydroxypyridine stands out as one of those crucial intermediates. Its chemical structure, featuring both an amino group and a hydroxyl group on the pyridine ring, gives it a signature profile in reactions, making it valuable for several applications spanning medicines, agrochemicals, and pigments.
Science doesn’t advance without reliable foundations. In many organic synthesis projects, the presence of both an amino and a hydroxyl group in a single pyridine ring introduces a rare versatility. Experience in a university research lab showed me how this matter-of-fact compound cut down labor in our synthesis routes. In contrast to other pyridines that lacked one of these active groups, 2-amino-5-hydroxypyridine made it noticeably easier to tune reactivity, whether chasing after complex API candidates or mapping new dye chemistries. The specific position of its groups—amino on the 2-position, hydroxyl on the 5—lets it fit into reaction pathways unavailable to mono-substituted variants. Reagents like 2-hydroxypyridine or 5-aminopyridine fall short when broader reactivity is required.
One lesson becomes clear in chemical research: consistency saves money and time. Repetitive purification, batch-to-batch inconsistency, and impurities can derail entire development timelines. Pure 2-amino-5-hydroxypyridine comes as a fine powder, rapidly dissolving in polar solvents, and delivers trustworthy performance from synthesis to formulation. Researchers and process chemists, given a choice, lean toward batches with minimal moisture and reliably low metal content, since these factors play a real role in yield and outcome. Many inferior products contain residual starting material, as well as tough-to-remove byproducts that interfere with downstream steps. Speaking as someone who’s spent months hunting down the source of an unreliable reaction yield, I can vouch for the difference clean material makes.
Pharmaceutical developers appreciate the reactivity of 2-amino-5-hydroxypyridine for building custom scaffolds—especially heterocyclic drugs targeting resistant pathogens. Medicinal chemistry teams often use it to develop complex ring systems found in oncology, neurology, and anti-infective leads. The extra handle provided by the hydroxyl or amino group becomes a docking point for creating libraries of analogues, allowing for rapid lead growth and structure-activity relationship studies. Colorant and pigment manufacturers exploit its hydroxyl group to help anchor chromophore systems, improving color intensity and fastness. Agrochemical teams, by leveraging its dual-functionality, push the boundaries in herbicide or fungicide discovery, especially as older crop protection agents become obsolete due to resistance.
Laboratory and industrial users tend to prefer 2-amino-5-hydroxypyridine for coupling reactions, azo dye precursors, or chelating ligands because its structure avoids common side reactions that plague other close relatives. Where 2-hydroxypyridine might be too unreactive, or 5-aminopyridine too basic, the balanced polarity and nucleophilicity of 2-amino-5-hydroxypyridine makes it more straightforward for late-stage functionalizations.
Chemists often find themselves choosing between compounds that seem almost identical. In practice, those small differences in substitution pattern have big downstream consequences. 2-Hydroxypyridine lacks the electron-donating ability of the amino group, limiting its use in nucleophilic aromatic substitution reactions or in forming certain coordination complexes. 5-Aminopyridine, while reactive, misses out on conjugation and hydrogen bonding enabled by the hydroxyl moiety at the 5-position, which can impact selectivity and solubility.
I remember comparing results using 2-amino-5-hydroxypyridine and 2-amino-4-hydroxypyridine for a dye synthesis; color strength and stability changed noticeably, all because of the spatial arrangement of the functional groups. Positioning on the ring might seem abstract on paper, but yields, shade, and repeatability take a hit in real-world settings if you substitute one for the other. For coordination chemists, the simultaneous presence of donor atoms at 2 and 5-leads to ligand behavior that is both predictable and unique. In contrast, compounds where both groups are ortho (next to each other) or para (across from one another) exhibit different pKa values and binding modes—critical in applications ranging from catalysis to pharmaceuticals.
High-quality 2-amino-5-hydroxypyridine comes measured by established metrics: melting point, moisture content, and heavy metal levels. Most research and industrial users expect a melting point close to published literature values, typically around 210-215°C. Moisture remains a real concern because water’s presence triggers hydrolysis or side-reactions in sensitive syntheses. Labs usually monitor water content with Karl Fischer titration, aiming for under 0.5%. Metal contaminants, often from reagent synthesis, disrupt downstream processes, so manufacturers invest in thorough purification and ICP-OES analysis to push heavy metals below 10 ppm. Genuine suppliers disclose these parameters up front, and analytical labs cross-reference batch certificates independently to verify the claim.
Powder consistency also affects usability: too chunky or fluffy, and accurate weighing becomes tough; too hygroscopic, and material degrades in air. Suppliers tackling these practical problems have an edge—ensuring every batch pours cleanly, stores easily, and delivers the right molar amount each time the bottle’s opened. Experienced chemists keep an eye on product color as well; off-white to beige powder suggests high purity, while darker or grayish material hints at residual impurities or partial degradation.
It’s easy for those unfamiliar with chemical production to underestimate the cascade of trouble a poorly made intermediate can unleash. A kilogram of impure material won’t just cause one bad day—it drags down yields, introduces hidden side-products that show up late in product testing, and can even cause false analytical results. Researchers shoulder this risk, but patients, consumers, and downstream manufacturers ultimately pay for corner cutting up the supply chain.
I’ve seen teams lose patent races because an off-spec batch led to a six-week delay, or compliance headaches arise when a missed impurity caused a regulatory flag. Regulators, including the FDA and EMA, now expect full transparency about the provenance and analytical validation of every reactive intermediate, especially those heading into medicines, pesticides, or pigments with direct consumer impact. Professional oversight, in the form of ISO certification or integrated tracking, gives users confidence from early-stage research all the way through to final product approval.
In one medicinal chemistry project, we leaned on 2-amino-5-hydroxypyridine to couple with advanced mixed carboxylic acids. The speed and efficiency outpaced similar couplings with mono-substituted pyridines, cutting reaction times from hours to minutes. By offering both hydrogen bond donor capability and elevated electron density, this compound enabled routes previously judged too cumbersome or unreliable. Process engineers found fewer byproducts, reducing time spent in column chromatography—always a bottle-neck and cost-driver in scale-up phases.
Those working on dye chemistry recognize another advantage: improved color profiles and stability under light and heat. The pigment derived from this intermediate offered higher color fastness, reducing fading and thereby lowering product returns in textile and plastics applications. This isn’t just a technical win; it has commercial impact. Brands relying on stable colors maintain customer trust and minimize warranty claims over fading or discoloration.
Any conversation about chemical intermediates must address safe use and handling. 2-Amino-5-hydroxypyridine, like most reactive pyridines, demands care in storage—preferably in dry, sealed containers, with limited light exposure to reduce risk of oxidation or degradation. Material safety assessments in the workplace hinge on clear labeling and up-to-date hazard data shared along the supply chain. Leading producers support partners with comprehensive safety documentation and advice covering not just acute risks, but also longer-term issues like environmental fate and workplace hygiene. In a company I consulted for, drills using actual product samples rather than stand-ins highlighted real-world hazards and improved incident response.
Moreover, modern procurement teams value traceability to guarantee ethical and responsible sourcing. In some sectors, this goes further—clients ask for sustainability assessments or minimal solvent footprints in synthesis, which affects supplier choice. Safety isn’t only about the molecule in a flask; it extends to workers during production and to the wider public at the point of use.
Stable supply of specialty chemicals like 2-amino-5-hydroxypyridine isn’t a given. Raw material availability, regulatory scrutiny, and market volatility all create headwinds. In the wake of global disruptions, companies came to appreciate predictable lead times and local supplier relationships. I’ve worked on projects where a delayed or substituted batch put six months of research output at risk. Trusted partners develop contingency inventories and redundant qualified sources to buffer customers from market shocks.
Some buyers assume price alone signals value, but true cost comes from evaluating reliability, response speed, open technical support, and commitment to post-sale collaboration. Partnerships built on long-term goals, rather than transactional sales, are the foundation for tackling the inevitable hurdles that arise in any research or production environment. Holding relationships with suppliers ready to troubleshoot obscure TLC streaks or help interpret spectral data matters on days when the unexpected lands on your bench.
Access to 2-amino-5-hydroxypyridine can be simplified through several targeted solutions. Distributors offering real-time inventory tracking minimize risk of shortfalls. Technical documentation, if kept both up to date and accessible, helps new users avoid mishaps and guarantees correct usage strategies. Batch-level traceability gives process engineers confidence that results today will hold up under full production tomorrow.
For routine users, economy isn’t about buying the cheapest raw material—it’s about total cost over the lifecycle of a project. Investing up front in verified, tested material means fewer process deviations, less need for re-validation, and easier hand-off between lab, pilot, and production scale. Companies win too, as regulatory dossiers completed with high-quality material pass more smoothly through review, unburdened by questions about impurity profiles or uncertain origins.
As drug targets get tougher and materials performance standards rise, research teams rely more on versatile intermediates. Compounds like 2-amino-5-hydroxypyridine, with a reputation built on practical versatility and documented purity, allow chemists to explore new territory. Breakthroughs don’t happen in a vacuum—they build on solid, reproducible work made possible by high-integrity reagents. Laboratories equipped with validated batches avoid unnecessary setbacks and spend their resources where they matter most: on discovery, optimization, and scale-up.
This orientation toward quality and reliability serves broader societal goals. As end-products make their way into medicines, foods, household goods, and industrial processes, consumers benefit from the foundational care applied upstream. Failures traced back to poor-quality intermediates erode trust in brands and industries, and can have real costs—both human and economic. Quality intermediates, properly handled and honestly documented, act as quiet enablers of progress.
Working in both academic and industry labs, I’ve seen that the best outcomes grow from communities of practice—groups who swap notes, flag suspicious batches, and share tips for better yields or purer isolates. Strong partnerships between users and suppliers cultivate spaces where feedback sparks improvements, whether through enhanced detection of trace metals or faster responses to documentation needs.
Standard-setting bodies play their part too, publishing tighter test methods and endorsing quality benchmarks that pull the market forward. Researchers benefit when more detailed characterization keys are made accessible, and when deviations from standard properties are flagged early. Rather than viewing regulations as hurdles, progressive teams see them as milestones, each an opportunity to raise performance and deepen confidence.
Many labs planning to integrate 2-amino-5-hydroxypyridine into their workflows find value in some fundamental questions. Does this batch demonstrate the required minimum purity, verified by NMR and HPLC? How stable is it under typical storage? Are certificate of analysis and safety data up to modern standards? What is the supplier’s track record for resolving batch complaints or supporting process innovation?
Colleagues who develop new methods often set aside reference samples from high-performing lots, using them as benchmarks against future deliveries. This practice avoids costly troubleshooting should a questionable new lot ever enter circulation. About ten years ago, colleagues and I systematically compared lots from three suppliers, identifying a clear leader and helping our group avoid recurring issues from inconsistent batches down the line.
Future advances may come from expanding 2-amino-5-hydroxypyridine’s reach into novel chemical spaces. Teams working on green chemistry want to transition synthesis to less hazardous solvents or renewable feedstocks. Others look to automate verification, leveraging in-line spectroscopy, weight sensors, and environmental controls to track changes from shelf to bench. These initiatives cut errors and help make innovation easier for early-career chemists just getting to know the rigors of reproducible science.
In workshops and symposia, more open sharing of application notes and unsuccessful attempts—what didn’t work, as well as what did—helps the community learn faster. It’s here where high-quality intermediates shine: by reducing unexpected variability, the best products pull hidden knowledge out into the open, letting everyone make faster gains.
Day to day, chemists take pride in delivering reproducible, predictable work, much like craftsmen who demand sharp tools and solid wood. 2-Amino-5-hydroxypyridine stands out to those familiar with the details, not for any flashy claim but for quiet reliability, helping teams meet rising demands on performance, safety, and transparency. Experienced users appreciate both its synthetic versatility and its ability to ease the pressure of compliance in a world where accountability stands tall.
Every project riding on intermediate chemistry deserves a fighting chance at success. Backed by trustworthy quality and a reputable supply chain, 2-amino-5-hydroxypyridine helps projects advance with fewer hiccups. Those of us who have seen research stutter on poor-quality lots know that a commitment to proper sourcing, detailed documentation, and open dialogue remains the real source of progress.