|
HS Code |
363464 |
| Cas Number | 696-60-0 |
| Molecular Formula | C5H4ClNO |
| Molecular Weight | 129.55 g/mol |
| Iupac Name | 5-Chloropyridin-3-ol |
| Appearance | White to light yellow solid |
| Melting Point | 110-113°C |
| Solubility In Water | Slightly soluble |
| Synonyms | 5-Chloro-3-pyridinol |
| Smiles | C1=CC(=CN=C1Cl)O |
| Inchi | InChI=1S/C5H4ClNO/c6-4-1-5(8)3-7-2-4/h1-3,8H |
As an accredited 5-Chloro-3-hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 5-Chloro-3-hydroxypyridine (25g) is a sealed amber glass bottle with tamper-evident cap and clear labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 5-Chloro-3-hydroxypyridine: Typically accommodates 10–12 metric tons, packed in fiber drums or HDPE bags securely. |
| Shipping | **Shipping Description:** 5-Chloro-3-hydroxypyridine is shipped in tightly sealed containers, protected from moisture and light. Packages comply with relevant chemical transport regulations. Handling instructions and safety data sheets are included. The chemical is labeled clearly with hazard warnings, and temperature control may be required during transit to maintain stability and prevent degradation. |
| Storage | Store 5-Chloro-3-hydroxypyridine in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizers and acids. Label the storage clearly and restrict access to trained personnel. Follow all relevant chemical storage regulations and safety guidelines for hazardous organic compounds. |
| Shelf Life | 5-Chloro-3-hydroxypyridine is stable under recommended storage conditions; shelf life is typically 2–3 years in a cool, dry place. |
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Purity 98%: 5-Chloro-3-hydroxypyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal impurities in the final active ingredient. Melting Point 146°C: 5-Chloro-3-hydroxypyridine with a melting point of 146°C is used in agrochemical formulation development, where thermal stability supports robust processing conditions. Molecular Weight 131.55 g/mol: 5-Chloro-3-hydroxypyridine with a molecular weight of 131.55 g/mol is used in fine chemical manufacturing, where precise molecular mass allows accurate formulation calculations. Particle Size <50 microns: 5-Chloro-3-hydroxypyridine with a particle size below 50 microns is used in catalyst support preparation, where fine particles enhance dispersion and catalytic efficiency. Stability Temperature up to 120°C: 5-Chloro-3-hydroxypyridine with stability up to 120°C is used in dye synthesis processes, where heat resistance ensures consistent reaction performance. Moisture Content <0.5%: 5-Chloro-3-hydroxypyridine with moisture content below 0.5% is used in electronic chemical manufacturing, where low moisture prevents unwanted side reactions. |
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5-Chloro-3-hydroxypyridine rarely draws much attention outside of technical circles, yet behind the name lies a compound that’s quietly changed the shape of chemical synthesis. On its face, the substance looks like any other lab ingredient—white to slightly off-white crystal powder with a mild scent, a chemical formula (C5H4ClNO) that speaks in the language of scientists. Yet for those of us who’ve spent time navigating the ups and downs of process chemistry and organic synthesis, this molecule stands apart for reasons often lost in the product catalogs.
Run your fingers through a bottle of this compound and you’re holding the result of years of careful study in aromatic chemistry. There’s a chlorine atom sitting on the ring, and a hydroxyl group joined at just the right spot. It’s not just about structure—the positioning changes how these rings behave in chemical reactions. In my own work, moving a functional group by even a single atom can mean success or hours of troubleshooting why a target molecule never forms. The placement here grants reactivity that chemists need, sparking transformations that dead-end with less specific substitutes.
Unlike some cousins in the pyridine family, 5-Chloro-3-hydroxypyridine tends to keep itself stable under standard lab conditions. That counts for a lot if your work relies on consistent output from batch to batch. Some related compounds with more volatile functional groups demand extra caution during storage or shipping, costing time and resources. Others drift toward decomposition unless cold and humidity stay under close watch. This compound’s balance of reactivity and shelf-life takes real-world pressure off researchers.
On paper, the uses of 5-Chloro-3-hydroxypyridine often sit under the catchall umbrella of “intermediate.” In reality, it’s the step between raw starting materials and the creation of something valuable, landing in pharmaceuticals, crop protection products, and specialty dyes. You’ll find it floating in the reaction mixture as drug developers work out routes toward next-generation anti-infectives or as agrochemical builders design new molecules that disrupt common pests. From my time in research and scale-up projects, having this intermediate opens up reaction pathways that more convoluted chemical families can’t provide.
There’s also a practical edge. Traditional approaches relying on fully substituted pyridines or ring systems full of sensitive groups often demand fine-tuned temperature controls or rare reagents. By contrast, this compound can survive the rough-and-tumble of a pilot plant or a big production batch. That translates to fewer costly reruns and less trial-and-error in solvent choice or workup.
The batch-to-batch quality of 5-Chloro-3-hydroxypyridine means more than just ticking boxes for purity. From my experience, a purity above 98 percent is not just a marketing number—it closes doors to downstream contamination and speeds up pilot studies. A quick chromatogram reveals expected retention times without ghost peaks that hint at problematic leftovers. Moisture content stays low, keeping the powder from clumping or caking—a frustration nobody wants late on a Friday afternoon.
Molecular weight rests at 129.55 g/mol, a detail most chemists will log in a notebook but only remember when confirming identities post-reaction. Its appearance might vary slightly, depending on trace byproducts or sample history, yet the reliable crystalline texture remains standard for quality lots. Even seemingly small physical differences matter: one shipment I received clumped due to a minor lapse in drying, creating headaches at the slitting hopper and risking uneven dosing. Well-maintained specifications prevent these kinds of production side effects.
In the field, 5-Chloro-3-hydroxypyridine goes beyond being a stepping stone—it’s a linchpin for new pathways in heterocyclic synthesis. Reactivity centers around the activated positions created by its substituents. For example, I’ve seen robust yields in Suzuki cross-couplings that break down when using simple pyridines or those missing the crucial chloro or hydroxyl groups. This flexibility has allowed teams to cut out tedious protection and deprotection steps, saving time, solvent, and money.
In my own pilot runs, scale-up staff regularly commented on the ease of filtering and isolation from standard extractive workups—something that can’t be said of all closely related pyridines. Easy isolation might sound trivial, but in a process setting, subtracting hours from every cycle pays back in capacity and labor cost. Where similar compounds need slurries to be held just above freezing or degassed under nitrogen, this molecule copes without elaborate routines.
Pyridine rings get used everywhere, so it’s easy to assume all similar compounds work alike. My early days in the lab taught me otherwise. Try using 3-chloropyridine or 3-hydroxypyridine instead: reactivity patterns skew, and product distribution climbs out of the expected range. The interplay between the chloro and hydroxy groups makes subtle but meaningful changes in electron density, turning on selectivity for some couplings and knocking down side-product formation in others. It’s the sort of tweak that only emerges after running the same reaction many times—and only with hands-on experience.
Price guides don’t always make these differences obvious, either. Chemically close options may cost a little less up front, but project budgets end up stressed by lost yield or expensive purification steps. I’ve watched project leads switch back to 5-Chloro-3-hydroxypyridine after fighting lower performance for weeks—sometimes paying more on paper to save on hassle and time.
The global supply chain for specialty chemicals has tightened up over recent years, with price and origin playing larger roles than before. Supply interruptions can derail whole development pipelines. I learned through tough lessons that a consistent source of 5-Chloro-3-hydroxypyridine can mean life or death for a launch schedule. Even subtle impurities create unexpected behavior in scale-up environments, where thousands of liters put real dollars on the table. Sourcing from suppliers who publish full certificates of analysis—including not just purity, but data on heavy metals, residual solvents, and stability—has become standard practice for teams aiming to avoid expensive surprises.
Knowing your supplier and reading the traceability reports is less glamorous than the research itself, but I’ve seen teams suffer big schedule slips when batch-to-batch consistency drops. A memory that stands out: months lost chasing product instability down to a subtle contaminant in an otherwise well-passed batch. That was a lesson in the value of tight supply partnerships, not just chasing the lowest price per kilogram.
Addressing the environmental footprint of any chemical used in large quantities matters to both users and communities around production sites. In the case of 5-Chloro-3-hydroxypyridine, synthetic pathways have shifted over recent years to reduce overall waste and cut down on hazardous byproducts. Factory teams I worked with adopted routes using fewer chlorinated solvents, improving workplace safety and cutting disposal costs.
Wastewater management also sharply improves with this compound compared to relatives laden with extra halogens or other reactive substituents. Cleaner effluents mean fewer headaches during audits and smoother permitting from local agencies. Chemists keen to clean up operations turn to it for both reactivity and reduced regulatory drag. I’ve watched companies win contracts and build reputations by focusing on chemicals that support safer practices and greener sourcing upstream.
One lesson that stuck from years in the lab: simple, well-defined compounds cut down on variables and set projects up for faster results. Teams stuck in troubleshooting mode—unexpected color changes, wild temperature excursions, fouling in lines—often find the culprit in using less predictable building blocks. By anchoring more processes around 5-Chloro-3-hydroxypyridine, many projects reduce troubleshooting cycles and keep research timelines tighter.
Beyond the laboratory, production teams count on materials that handle changes in humidity or temperature swings without drifting out of spec. I’ve visited facilities relying on this compound for round-the-clock continuous processes—those lines run smoothly, batch records stay tidy, and interventions drop. This only happens when every shipment lands at the same solid, reliable level that upstream teams agreed on.
No industry goes untouched by supply hiccups or cost pressure. Emerging competitors sometimes offer lower upfront pricing, but the savings erode if product consistency slips, purity drops, or a sudden impurity shows up in final tests. My colleagues and I have worked through transitions where teams tried alternative compounds, betting on nominal chemical similarity only to circle back after unplanned downtime and lost output. Teams that value robust quality, regular analytical checks, and responsive support get more out of this compound—not because it promises magic, but because dependable basics clear the way for progress elsewhere.
Global logistics remain an uneven patchwork, with some regions struggling during unexpected border delays or port closures. Regional storage hubs and more diversified transport solutions limited exposure to these disruptions in my own projects. Close communication between vendors and production planning teams helped keep surprises rare. Transparency about QA and small-batch data keeps both research and operations in lockstep, reducing conflict and accelerating decision-making.
As chemical manufacturing evolves, process engineers keep finding ways to wring more efficiency from less input, and demand for reliable intermediates grows with every discovery in medicine, agriculture, and specialty materials. In this landscape, 5-Chloro-3-hydroxypyridine still holds a place in bench-scale studies and full-scale production alike. New, safer routes keep emerging that lessen risk for workers and the environment, driven both by regulation and by companies competing for contracts that reward best environmental practice.
I remember sitting in meetings with patent attorneys and process R&D managers, teasing apart how small differences in reactivity or stability affected patent strength and profitability. The market gravitates toward building blocks that consistently deliver, and over decades this compound’s spot in the toolbox only grows firmer.
It sometimes takes years in the field to recognize which intermediates truly pull more than their own weight. Through the daily grind—mixing, heating, filtering, testing—some chemicals become trusted friends. For many teams, 5-Chloro-3-hydroxypyridine became that friend, cutting down on uncertainty and letting teams focus on discovery instead of disaster recovery.
Beyond specs and formulas, people want tools that work, suppliers they trust, and materials that stay consistent even as downstream needs change. From my experience manufacturing batches for drug candidates or tweaking the process for agrochemicals, using this compound often led to smoother validation runs and fewer regulatory hurdles. Not every product can offer that—many promise on paper but fall short when the work truly begins.
5-Chloro-3-hydroxypyridine often blends into the long lists of starting materials and intermediates, yet its practical influence on time, cost, safety, and outcomes is easy for those who’ve wrestled with less cooperative chemicals to recognize. Consistent quality, practical stability, and unique reactivity create a product that does more than fill a line item. Its role in efficient, reliable production continues to expand as research and industry race to meet tomorrow’s challenges.