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HS Code |
991502 |
| Chemical Name | 2,3-Dichloro-5-hydroxypyridine |
| Molecular Formula | C5H3Cl2NO |
| Molecular Weight | 180.99 g/mol |
| Cas Number | 117658-18-5 |
| Appearance | White to pale yellow powder |
| Melting Point | 138-142°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place, away from light |
| Synonyms | 2,3-Dichloro-5-pyridinol |
| Inchi Key | LTJYWYHRRTANFW-UHFFFAOYSA-N |
| Smiles | C1=C(C=NC(=C1Cl)Cl)O |
As an accredited 2,3-Dichloro-5-hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g of 2,3-Dichloro-5-hydroxypyridine is packaged in a sealed amber glass bottle with a secure screw cap. |
| Container Loading (20′ FCL) | 20′ FCL: 10 MT packed in 200 kg HDPE drums, 50 drums per container for 2,3-Dichloro-5-hydroxypyridine. |
| Shipping | 2,3-Dichloro-5-hydroxypyridine is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a hazardous material, stored in a cool, dry, well-ventilated area. Proper labeling and documentation are required, and all transport must comply with local and international chemical transportation regulations. |
| Storage | 2,3-Dichloro-5-hydroxypyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances like strong oxidizers and acids. Protect from moisture and direct sunlight. Ensure storage in properly labeled containers, and keep away from ignition sources. Use appropriate personal protective equipment when handling. Follow all relevant safety and regulatory guidelines. |
| Shelf Life | 2,3-Dichloro-5-hydroxypyridine typically has a shelf life of at least two years when stored in a cool, dry, and dark place. |
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Purity 99%: 2,3-Dichloro-5-hydroxypyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product quality. Melting point 125°C: 2,3-Dichloro-5-hydroxypyridine with a melting point of 125°C is used in agrochemical active ingredient formulation, where it provides excellent thermal stability during processing. Particle size <50 µm: 2,3-Dichloro-5-hydroxypyridine with particle size <50 µm is used in catalyst preparation, where it enhances dispersion and catalytic efficiency. Moisture content <0.5%: 2,3-Dichloro-5-hydroxypyridine with moisture content <0.5% is used in chemical synthesis, where it minimizes hydrolysis and by-product formation. Assay ≥98%: 2,3-Dichloro-5-hydroxypyridine with assay ≥98% is used in fine chemicals manufacturing, where it enables precise stoichiometric control for consistent batch quality. Stability temperature up to 90°C: 2,3-Dichloro-5-hydroxypyridine with stability temperature up to 90°C is used in pigment additive production, where it maintains integrity under elevated processing conditions. |
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Anyone who works with heterocyclic compounds knows that subtle differences in structure often mean a lot to chemists and manufacturers. 2,3-Dichloro-5-hydroxypyridine, with its unique pattern of chlorine and hydroxyl substitution on the pyridine ring, tends to stand out for more than just that mouthful of a name. Whether synthesizing fine chemicals or assembling ingredients in crop protection, those two chlorine atoms and a hydroxyl group offer a specific combination that can’t be matched by similar molecules. In my years reading through research papers and chatting with process engineers, this compound comes up for its blend of reactivity and selectivity. Some call it modest, others indispensable; opinions vary, but its place in modern chemistry remains certain.
What draws attention to 2,3-Dichloro-5-hydroxypyridine starts with the six-membered aromatic ring, tweaked just enough by the electron-withdrawing chlorines at the 2 and 3 positions, balanced by a hydroxyl group at the 5 position. This seemingly simple setup changes how it behaves under synthetic conditions. The two chlorines don’t just offer a twist in reactivity; they enhance the molecule’s overall resistance to metabolic breakdown, which plays into its value in agrochemical and pharmaceutical projects. That hydroxyl group, on the other hand, supports targeted derivatization—the process of fine-tuning a chemical’s profile to fit a specific end product.
Folks in the lab who’ve handled batches of this compound know it works best as a pale solid with an expected melting range. I once witnessed a project where a deviation of just three degrees in the melting point signaled an impurity—so small, but in the world of chemical manufacturing, those details often save months of troubleshooting later on. The right quality control processes, such as HPLC and NMR, usually confirm identity and purity, sparing headaches on both research and production scales.
Comparing this compound to other halogenated pyridines, real-world differences become clear. Take its sibling, 3,5-dichloro-2-hydroxypyridine. Similar, but not the same, and the switch in hydroxyl and chlorine placement changes its solubility, reactivity, and downstream application. Chemists know that the differences aren’t just on the surface—they translate to process yields, reaction options, and the spectrum of products that can be built. Years ago, during a scale-up, I saw how 2,3-Dichloro-5-hydroxypyridine’s specific substitution pattern shaved hours off a synthesis, simply because its reactivity aligned better with a chosen coupling partner than its close cousins. These nuances matter for team leads and bench scientists mapping out their synthetic plans.
There’s also the matter of selectivity in reactivity. For manufacturers creating pyridine-based pharmaceuticals, 2,3-Dichloro-5-hydroxypyridine opens doors for installing other functional groups under relatively mild conditions. This flexibility helps muffle costs and streamlines downstream purification, sparing valuable time during pilot and full-scale production runs. Over the years, I’ve learned that ease of purification isn’t always about cutting-edge tech; sometimes, it’s about picking the right intermediate, and this molecule often fits the bill.
In the agricultural chemistry sector, experienced teams prize intermediates that deliver predictable results every time. 2,3-Dichloro-5-hydroxypyridine often finds its way into herbicide or fungicide discovery campaigns. Given its electronic properties, it helps researchers design molecules able to act on vital biochemical pathways in target pests or pathogens, but its real contribution stems from how it enables derivative formation. Crop science depends on innovation, and what I hear from interviewees in development roles is consistent: they need intermediates that support both speed and flexibility. This molecule has a reputation in the community for being a reliable starting point, helping move promising leads through synthesis and testing with fewer unexpected delays.
Pharmaceutical research presents a different landscape full of regulatory hurdles and demands for reproducibility. Here, 2,3-Dichloro-5-hydroxypyridine might not always take the spotlight, but it’s a trusted stepping stone for small-molecule library synthesis, especially for anti-infective and central nervous system candidate molecules. Its halogenated nature assists in bioisosteric replacement—a strategy well-known to medicinal chemists hunting for just the right balance of potency and safety. Several published patents list it as a key intermediate, and stories shared by research chemists often touch on how it helped unlock tricky synthetic routes with minimal fuss.
Beyond agrochemicals and pharmaceuticals, I have met professionals in the dye and specialty chemical sector using 2,3-Dichloro-5-hydroxypyridine as a scaffold for pigment engineering. Their feedback echoes a familiar refrain: reliability, ease of further modification, and the ability to withstand harsh reaction conditions. No fancy lab secrets here—just solid chemistry, plenty of practical know-how, and a clear understanding of what the material can provide.
Product consistency starts at the source. Suppliers who have built a reputation for quality seldom take shortcuts. The best batches show minimal contamination, narrow melting ranges, and stable storage profiles. Users get a product they can trust, which translates to fewer reruns and less wasted material. Handshakes in shipping bays and emails back-and-forth about specs often reveal another side of the business: trust built on shared experience. Customers return to suppliers who keep impurities in check, batch after batch.
In my time working with project managers and supply chain leaders, one lesson stands out—communication cuts down on problems. Labs that rely on this compound typically specify purity of at least 98%, since even small impurities can send downstream reactions sideways. I’ve seen how a single conversation with a supplier, clarified with a certificate of analysis, can prevent a painful and costly standstill during an urgent run. Crafting this sort of institutional know-how only happens with repeated experience and the willingness to adapt standard operating procedures to the specific quirks of a given material.
From a bench scientist’s view, 2,3-Dichloro-5-hydroxypyridine sets itself apart from compounds with fewer halogens or none at all. Its chloro groups crank up the electrophilicity of the ring, making it more eager to undergo nucleophilic aromatic substitution. This ups the efficiency for introducing a range of chemical groups, opening the door to broader diversification. Early-career chemists sometimes learn this lesson the hard way—trying a non-halogenated pyridine, running through the same reaction setup, and ending up disappointed with poor conversions and messy workups.
Researchers after more stability in storage or better tolerance under basic conditions also find this molecule more attractive than many mono-chlorinated analogues. I remember chatting with a materials scientist who spent months optimizing storage protocols for a similar but less robust compound, only to later swap to this one and solve several shelf-life headaches at once. Anecdotal stories like these, echoed across forums and conferences, aren’t trivial—practical experience shapes decisions just as much as published data.
Besides chemistry labs, safety officers and regulatory specialists respect those differences, too. Halogenated compounds often face higher scrutiny when moving across borders or into new application areas. It helps to work with intermediates that offer the desired balance between functionality and manageable compliance steps. Based on conversations I’ve had in compliance working groups, the regulatory paperwork—while annoying at times—tends to move smoother for products backed by dependable documentation and clear, consistent batch analytics. Those who prepare for audits and inventory reconciliation have less to worry about when the product profile stays rock solid year after year.
Every chemical, even the most ordinary-sounding, passes through an intricate net of human decisions and technical adjustments. In order to keep 2,3-Dichloro-5-hydroxypyridine flowing smoothly from benches to reactors, seasoned operators rely on time-tested handling steps. Humidity, temperature, packaging material—each factor acts as a lever. In one facility I visited, a misplaced drum near a steam line shortened shelf life by months, all due to a simple mix-up in warehouse layout. Stories like this underscore why practical details matter so much in daily operations.
People working in production prioritize clear labels and re-sealable packaging to keep the compound dry and uncontaminated. Chemists tend to favor easily opened containers that allow sampling without exposing the full contents to air. Small design tweaks, such as internal liners or moisture-absorbing packets, have become standard for bulk shipments, reflecting years of workplace feedback. Facilities that make room for staff suggestions often find fewer surprises down the line, whether in the quality control lab or at the reactor feed chute.
Field representatives and technical sales staff add another angle. Meeting deadlines with consistent material, answering tough questions about provenance, demonstrating that each batch meets prior commitments—these all matter to customers who expect more than a commodity transaction. In my own time interacting with procurement teams, I’ve seen that technical depth and reliability in supply foster loyalty that price wars alone can’t match.
Modern chemical production can’t escape increased scrutiny over environmental and sustainability issues. Halogenated intermediates demand careful stewardship. Companies and end users look for options that minimize hazardous waste while protecting workers. The market’s shift toward greener solvents and closed-loop systems is real, and organizations that move faster to adopt these innovations often get a competitive edge. I recall the rollout of a wastewater treatment upgrade at a plant handling a range of chloroaromatics, including this compound—one that slashed the chemical oxygen demand by half and helped the plant meet local discharge guidelines months ahead of schedule.
Process engineers who’ve worked with legacy equipment see an ongoing push: retrofitting older batches to reduce emissions, switching to continuous processes that use smaller volumes of hazardous reagents, and installing real-time monitoring. These steps translate into measurable improvements, not just for the environment but for worker morale and long-term operating costs. The best stories come from teams that tackled a known problem—like venting halogenated vapors during drying—and shared their fixes across the company or industry conferences. The cycle of improvement doesn’t end, and 2,3-Dichloro-5-hydroxypyridine, as a widely used intermediate, is at the intersection of these efforts.
Suppliers offering this compound today tend to compete not just on price or purity, but also on how well they document and communicate their environmental and safety credentials. Those working in procurement or sustainability departments weigh these factors heavily when updating approved materials lists or responding to client requests. The best partnerships come when suppliers provide clear breakdowns of solvent use, recovery rates, and steps taken to minimize hazardous byproducts. It pays to be thorough and proactive.
The chemical landscape evolves quickly. As researchers develop more selective herbicides or safer pharmaceuticals, the demands on intermediates like 2,3-Dichloro-5-hydroxypyridine shift too. Advanced analytics and machine learning now support R&D, picking up subtle process variables that once confounded even experienced chemists. Watching teams validate new synthetic routes, I’ve seen how rapid iteration and reliable inputs speed up discovery in ways unimaginable just a decade ago.
Process development increasingly leans into real-time analytics, allowing even minor deviations in intermediate purity or moisture content to be caught and corrected before problems multiply. Teams using 2,3-Dichloro-5-hydroxypyridine appreciate suppliers who go beyond standard lab reports, offering interactive dashboards or trend data. Early warning of new batch characteristics can spell the difference between a seamless campaign and weeks lost chasing a problem to its source. Time really does mean money, and with competition stiffening in every sector, that margin makes a difference.
No chemical is without challenges, and 2,3-Dichloro-5-hydroxypyridine brings its own. Some find occasional production bottlenecks when raw material availability swings or a key supplier drops off the map. Diversifying sources and building solid relationships, grounded in shared knowledge and clear expectations, reduces these risks. Veteran sourcing managers I’ve worked with recommend regular site visits, thorough auditing, and prompt feedback mechanisms to keep things on track.
From the lab bench to pilot plant, those using this compound often tweak their protocols in response to changes in purity, particle size, or hygroscopic properties. Workshops and technical exchanges, both online and in person, foster learning about best practices. I’ve seen how cross-industry collaborations spur progress—a frustrated development chemist learns from a team far afield, adapts their drying method, and solves a thorny stability issue. Open communication keeps these lessons flowing, and industry groups provide the structure for sharing them.
At the site level, safety professionals drive home the importance of clear hazards labeling, proper ventilation systems, and emergency drills. When handled with respect and knowledge, even tricky intermediates integrate smoothly into production and research systems. By investing in ongoing worker training and process monitoring, plants both large and small lower their risk profile and boost confidence among partners and regulators alike.
Technical knowledge only goes so far before it needs grounding in experience. 2,3-Dichloro-5-hydroxypyridine stands as a reminder that even niche chemicals rely on community wisdom, from trusted suppliers to sharp-eyed analysts. Those who work with it every day develop a feel for what works—and what doesn’t—shaping workflows that balance precision, safety, and cost.
No two production lines are exactly the same, and neither are their needs. Some teams optimize for throughput, others for purity, still others for cost control. What unites the best stories across industries is a commitment to sharing information and continuous learning. Those who invest in upgrading systems, documenting lessons, and building relationships with their peers and supply partners rarely regret it.
As the chemical and life sciences fields surge ahead, 2,3-Dichloro-5-hydroxypyridine remains a foundation for discovery and manufacture alike. Its blend of chemical flexibility, robustness, and user-driven improvement keeps it relevant in a competitive, evolving landscape. Keeping an eye on both the technical and the personal stories behind every drum or vial helps guide better decisions at every step of the journey.