|
HS Code |
547002 |
| Cas Number | 6358-37-0 |
| Molecular Formula | C5H4ClNO |
| Molecular Weight | 129.54 |
| Iupac Name | 5-chloropyridin-3-ol |
| Appearance | Off-white to light brown solid |
| Melting Point | 97-101°C |
| Solubility In Water | Moderately soluble |
| Smiles | C1=CC(=CN=C1Cl)O |
| Synonyms | 5-Chloro-3-hydroxypyridine |
| Purity | Typically ≥98% |
| Storage Temperature | Room temperature |
As an accredited 3-Hydroxy-5-chloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Hydroxy-5-chloropyridine is supplied in a 25g amber glass bottle, securely sealed, and labeled with hazard and product information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-Hydroxy-5-chloropyridine: Typically loaded in 25 kg fiber drums, up to 12–14 metric tons per container. |
| Shipping | 3-Hydroxy-5-chloropyridine is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It is handled as a hazardous material, following regulations for safe transport. Proper labeling, documentation, and temperature control (ambient conditions) are ensured. Protective measures are taken to prevent spills or exposure during transit and storage. |
| Storage | 3-Hydroxy-5-chloropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat, and sources of ignition. Keep it separate from strong oxidizing agents and incompatible chemicals. Properly label the container and avoid excessive moisture exposure. Store at room temperature and ensure access to safety data sheets for emergency procedures. |
| Shelf Life | 3-Hydroxy-5-chloropyridine should be stored tightly sealed, protected from light and moisture; typical shelf life is 2–3 years under recommended conditions. |
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Purity 98%: 3-Hydroxy-5-chloropyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and product yield. Melting Point 150°C: 3-Hydroxy-5-chloropyridine with a melting point of 150°C is used in agrochemical formulation, where it provides thermal stability during processing. Molecular Weight 131.55 g/mol: 3-Hydroxy-5-chloropyridine with molecular weight 131.55 g/mol is used in specialty chemicals manufacturing, where it enables precise stoichiometric calculations for reproducible results. Particle Size <50 µm: 3-Hydroxy-5-chloropyridine with particle size less than 50 microns is used in catalyst preparation, where it allows uniform dispersion and enhanced catalytic activity. Stability Temperature up to 120°C: 3-Hydroxy-5-chloropyridine with stability temperature up to 120°C is used in dye production, where it maintains chemical integrity under process heat conditions. |
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Stepping into a modern chemical lab, you start to notice not just the surge in precision but also the trust researchers put into certain raw materials. 3-Hydroxy-5-chloropyridine is one of those specialty chemicals that stands out for its purpose and reliability. In the realm of heterocyclic aromatic compounds, pyridines with selective substitutions keep pulling their weight in pharmaceutical research and fine chemical synthesis. If you’ve spent any time comparing molecular structures, you’ll see that this particular pyridine derivative occupies a unique address. The hydroxy group at position 3 adds polarity, affecting reactivity and solubility, while the chlorine at position 5 subtly shifts its chemical behavior and opens new pathways in synthesis.
The model under focus here offers a careful balance of purity and manageability. Chemists working at bench scale or scaling up for pilot projects notice when a compound holds a high purity standard, often meeting 98% or higher as demanded by most research protocols. In storage, it comes as a solid, often a pale-yellow crystalline powder. This isn’t just aesthetic — the solid form delivers consistent dosing and measurement, a detail any bench chemist appreciates. In analytical settings, the molecular weight, melting point, and spectral features are always logged. Here, 3-Hydroxy-5-chloropyridine brings with it reliable NMR, MS, and HPLC signatures, which support clear traceability from batch to batch.
If you’re building molecules for agricultural, pharmaceutical, or advanced material use, the way a precursor interacts matters just as much as its theoretical reactivity. What makes 3-Hydroxy-5-chloropyridine catch attention is its dual role in both nucleophilic and electrophilic substitution reactions. Its structural nuances make it an attractive intermediate for crafting more complex frameworks. Medicinal chemists, for example, are finding opportunities in leveraging the hydroxy group’s reactivity for ether formation and the chlorine atom’s amenability to cross-coupling.
The need for versatile building blocks in synthetic chemistry keeps evolving, especially as industry standards grow stricter. Meeting those standards is about more than just a certificate of analysis — it’s about experienced researchers knowing that adding this compound to their toolkit means fewer surprises and repeatable results. A detail I recall from a recent collaborative project: the quality of substituted pyridines, including 3-hydroxy-5-chloropyridine, reduced purification steps and enabled us to keep our focus on developing new scaffolds rather than managing impurities. This experience isn’t unique; it echoes across labs where time and yield hold equal value.
Often researchers ask what sets this compound apart from other chloropyridines or hydroxy-substituted analogues. In short, it’s about the fine tuning of both electron density and steric influence. 3-Hydroxy-5-chloropyridine shows different reactivity patterns compared to 2-chloro-3-hydroxypyridine or 3-hydroxy-2-chloropyridine. Substituent positioning changes how the ring activates toward further reactions, directly impacting how you plan your route in multi-step syntheses. As someone who’s wrestled with alternative routes to form key carbon-nitrogen or carbon-oxygen bonds, I’ve seen how subtle differences in substitution can mean the difference between a clean reaction and a week troubleshooting side-products.
Data from recent journal publications supports this. Studies analyzing the electron distribution in pyridine derivatives point to the unique interaction between hydroxy and chloro substituents at these positions, enabling selective transformation strategies. Commercially, this means you can pivot more quickly between different synthetic goals without shopping for a new reagent each time. The value lies in flexibility and predictability — two attributes that ring true for anyone trying to hit tight deadlines.
Ask an experienced synthetic chemist about daily bottlenecks, and you’ll hear about reagent quality, ease of use, and time savings. 3-Hydroxy-5-chloropyridine stands out in medicinal chemistry programs, particularly during lead optimization phases. In pharmaceutical discovery, there’s often a need to add polar or lipophilic fragments to candidate molecules. This compound allows for site-specific modifications, opening routes to a variety of analogues: ethers, esters, and further substituted aromatics, all from a robust starting point.
Industrial chemists working in agricultural chemicals also spot the value quickly. The hydroxy group lends itself to modification, producing new classes of herbicides or insecticides. The selective presence of chlorine offers metabolic stability, which is increasingly significant as environmental and regulatory pressures shape product pipelines. By using a compound with these dual features, downstream environmental fate studies become more predictable, which reduces hurdles in both research and later commercialization.
One real-world example comes from a team at a contract research organization. They reported significant reductions in byproduct formation when switching from other hydroxy- or chloro-pyridines to this compound. Yield improvements in a challenging etherification step led to more material available for downstream biological testing. For research groups working on tight turnaround cycles, this kind of boost often shifts projects from delays to delivery.
Day-to-day, bench chemists know that consistency in handling matters as much as reactivity on paper. 3-Hydroxy-5-chloropyridine proves stable under common storage conditions, in sealed containers at ambient or cool temperatures. While some pyridine derivatives display volatility or sensitivity to light and moisture, this compound remains manageable without unnecessary precautions. Less time spent managing sensitive storage translates into more productive hands-on work at the bench.
Even so, best practices never go out of style: using clean tools, avoiding cross-contamination, and confirming identity with spectral checks all reinforce the integrity of results. In my own experience, running routine QC checks after delivery ensured that the product performed consistently. This type of dependability supports larger-scale projects, where production timelines hinge on steady supplies and reliable chemical profiles.
Growing attention to safety and environmental responsibility is reshaping laboratory practices worldwide. Chlorinated pyridines sometimes trigger scrutiny due to their persistence or toxicity in the environment. Responsible sourcing and use of 3-Hydroxy-5-chloropyridine requires an awareness of waste handling and downstream impacts. It pays to follow established protocols for solvent reuse, controlled disposal, and use of personal protective equipment.
Leading suppliers now provide extended safety data, making it easier to integrate greener protocols. Research teams that prioritize sustainability find that using a versatile, high-purity compound helps minimize overall waste. For example, the coverage ratio needed for successful reactions is often lower, which cuts leftover material at the end of a synthesis. That’s a small but meaningful step that supports safer lab environments and reduces environmental burden over time.
Chemists find themselves in a race—not against one another, but against time and complexity. Modern synthesis pushes for more efficiency, less cost, and rigorous reproducibility. 3-Hydroxy-5-chloropyridine fits snugly into this picture, especially as high-throughput screening, green chemistry, and data-driven approaches surge forward. Compatibility with a range of solvents—from traditional polar aprotic to emerging green alternatives—adds to its value.
Teams working in combinatorial chemistry note the compound’s reactivity profile lines up with automated screening platforms. Automated liquid handling, parallel synthesis, and even machine-learning-guided optimization can move faster when the building blocks behave predictably. Anecdotally, I’ve found that debugging automated workflows flows much smoother with trusted intermediates. Less variability from starting materials lets teams focus on interpreting results, not chasing down unexpected interactions.
Published studies on related pyridine derivatives outline robust transformation pathways for 3-Hydroxy-5-chloropyridine. In cross-coupling, it responds well to classic palladium-catalyzed reactions, a mainstay in many medicinal and material science syntheses. The hydroxy group’s presence provides modularity — it supports downstream conversion into aryl ethers, alkylated products, or further derivatized structures useful in lead diversification.
This compound also compares favorably in cost-to-performance ratios. Bulk purchasers in high-throughput settings appreciate that, while it sits within a specialty chemicals segment, it balances price with real-world functionality. Analytical labs report clear, consistent spectra, supporting easy verification. These details matter for any researcher tasked with maintaining compliance, managing traceability, and preparing data for regulatory filings.
R&D teams increasingly value building blocks that support unpredictable research paths. With the shifting landscape in both drug discovery and crop science, the utility of adaptable intermediates becomes even clearer. 3-Hydroxy-5-chloropyridine supports both exploratory work at early-stage pipelines and the robust demands of downstream process development. Its stable shelf life and ease of integration with automated systems make it a natural fit for forward-thinking labs.
Preparing the next wave of scientists means handing them tools designed not just for today’s protocols but for the demands of evolving research. Universities and training labs benefit from reliable, well-characterized intermediates that students can use with confidence. There’s a teachable moment in seeing the difference between theory and daily practice—a difference shaped by the right choice of chemical building blocks. Nothing sharpens a chemist’s skills like troubleshooting an unpredictable reagent; nothing frees them to innovate like a compound that behaves just as expected, every time.
Consistency in chemical supply is built on a foundation of experience and documented quality. Third-party audits and validated supply chains help reinforce confidence in product authenticity. Researchers often request full transparency in sourcing and analysis, especially for compounds destined for advanced applications. 3-Hydroxy-5-chloropyridine, supplied with detailed certificates of analysis and clear spectral data, stands up to that scrutiny.
Multiple peer-reviewed articles document the successful use of this compound in synthesis of pharmaceutical candidates and agrochemicals. In open-access reports, scientists detail the selective advantages gained by its substitution pattern—fewer byproducts, shorter synthetic sequences, and improved final product profiles. For labs balancing regulatory loads, having this documentation at hand matters at every audit and milestone.
The momentum propelling modern chemistry often comes from intersections. As synthetic chemistry blends with material science and biochemistry, compounds like 3-Hydroxy-5-chloropyridine find new life beyond traditional roles. In advanced material synthesis, unique pyridine derivatives enable the tuning of optical and electronic properties in experimental polymers and small molecules. Electronic researchers working on OLED or organic semiconductor projects see real promise in substituents that shift absorption and electron transfer characteristics.
Biochemists exploring enzyme modulation and receptor binding profiles find the tailored electronic effects of this compound open new exploratory routes. I remember participating in an interdisciplinary workshop where a team used substituted pyridines, including the hydroxy- and chloro- patterns, to map novel binding pockets. Their findings underscored the subtlety and power of precise molecular engineering—skills supported by compounds that offer both reactivity and predictability.
By building bridges across departments and industries, 3-Hydroxy-5-chloropyridine continues to earn attention in places its original developers may not have predicted. The growing convergence of AI-driven modeling and hands-on experimental work points toward even greater value, as predictive systems increasingly require reliable input data on well-characterized compounds.
No commentary on a specialty chemical is complete without addressing the ever-present hiccup of supply chain interruptions. Global demand spikes, transportation delays, or raw material shortfalls can pose real risks to discovery timelines. Labs driven by commercial or grant deadlines simply cannot afford unpredictable gaps in core material inventory.
One way forward lies in building long-term partnerships between suppliers and end users. Consistent communication about demand projections, flexible batch sizes, and clarity around lead times all help reduce risk. Suppliers responsive to lab needs — providing transparent updates and maintaining responsive quality assurance — stand out as real allies.
Researchers planning for scale-up, whether for clinical material or early-stage product candidates, run detailed compatibility checks on their intermediates. High-purity, stable pyridine derivatives like 3-Hydroxy-5-chloropyridine make for smoother transitions from bench to pilot plant. Those who invest early in robust relationships and thorough product qualification see fewer bottlenecks at critical junctures.
Another solution comes from supporting open data about batch variances and analytical metrics. Many academic and industrial groups now share more QC data along with their published procedures, building a culture of collective quality improvement. This transparency not only supports current work but also guides future users to workflows that steer clear of repeating old mistakes.
Long before automation and AI transformed bench chemistry, the quality of a compound was judged by how it behaved under the unforgiving lens of daily research. My background includes struggling with failed reactions, then switching to a higher-grade starting material and finding the process suddenly clicked. Colleagues recount similar stories — tales of time saved, false leads avoided, and projects rebooted by one simple switch.
That’s not just a mark of better manufacturing but a lesson in trust. Labs that champion meticulous recordkeeping and respect for chemical quality invariably show more progress. With 3-Hydroxy-5-chloropyridine, that trust is built on reliability. Subtle in structure but outsized in impact, its unique profile supports ambitious projects and lessons learned at every scale: from undergraduate synthesis to commercial innovation.
Chemical innovation relies on foundational compounds that do more than check technical boxes. Investment in consistently high-purity intermediates—like 3-Hydroxy-5-chloropyridine—empowers teams to unlock potential in both basic and applied science. Labs that look to the future can rest a little easier knowing that some of the foundational work has already been done: established protocols, verified analytical data, and reliable performance all reduce the friction that slows down new discovery.
As regulations around purity, traceability, and environmental impact clamp down across global markets, adaptable yet dependable building blocks only grow more important. From enabling greener synthesis to reducing process complexity, the right choices made today influence research success for years to come. Those tasked with shepherding innovations from paper to clinic or factory floor know the value of every trusted link in the chemical supply chain.
Selecting the best starting materials has always underpinned great science. 3-Hydroxy-5-chloropyridine has carved out a reputation for bridging theory with practice, supporting creative synthetic approaches and enabling reliable results. Whether you’re chasing a new lead series, designing a catalyst, or building advanced materials, this compound shows the return on investment that comes from thoughtful chemistry paired with practical experience.
In a world hungry for both innovation and dependability, the subtle details matter most. By focusing on proven compounds, researchers pivot away from troubleshooting and toward progress. The continued embrace of precise, reliable intermediates will keep pushing chemistry—and new technology—forward for years to come.