|
HS Code |
662784 |
| Chemical Name | 2,5-Dichloro-4-hydroxypyridine |
| Molecular Formula | C5H3Cl2NO |
| Cas Number | 696-23-1 |
| Appearance | White to off-white solid |
| Melting Point | 170-174°C |
| Solubility In Water | Slightly soluble |
| Structure | Pyridine ring with chlorine atoms at positions 2 and 5, hydroxy group at 4 |
| Smiles | C1=CN=C(C(=C1Cl)O)Cl |
| Inchi Key | XJTKRCPGNPHSOA-UHFFFAOYSA-N |
| Storage Conditions | Store in a cool, dry place, tightly closed container |
As an accredited 2,5-Dichloro-4-hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2,5-Dichloro-4-hydroxypyridine, sealed with a screw cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2,5-Dichloro-4-hydroxypyridine: Typically 16–18 metric tons, packed in 25 kg fiber drums with pallets. |
| Shipping | 2,5-Dichloro-4-hydroxypyridine is typically shipped in tightly sealed containers to prevent moisture exposure and contamination. The packaging complies with chemical safety regulations, and containers are clearly labeled. Standard shipping involves ground or air transport with suitable cushioning, and the material should be kept at ambient temperature, away from incompatible substances and direct sunlight. |
| Storage | 2,5-Dichloro-4-hydroxypyridine should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, well-ventilated area. Keep it separated from incompatible substances such as strong oxidizing agents. Ensure proper chemical labeling and access to safety data sheets. Use appropriate personal protective equipment and follow all relevant safety protocols when handling or storing. |
| Shelf Life | 2,5-Dichloro-4-hydroxypyridine is stable under recommended storage conditions, typically maintaining shelf life for at least 2 years. |
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Purity 98%: 2,5-Dichloro-4-hydroxypyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and purity of target compounds. Melting Point 180°C: 2,5-Dichloro-4-hydroxypyridine with a melting point of 180°C is applied in high-temperature organic reactions, where it maintains thermal stability during processing. Particle Size <50 μm: 2,5-Dichloro-4-hydroxypyridine with particle size less than 50 μm is used in catalyst formulations, where it promotes rapid dissolution and uniform reaction rates. Stability Temperature up to 120°C: 2,5-Dichloro-4-hydroxypyridine stable up to 120°C is utilized in agrochemical synthesis workflows, where it prevents decomposition during heating steps. Moisture Content <0.2%: 2,5-Dichloro-4-hydroxypyridine with moisture content below 0.2% is employed in fine chemical manufacturing, where it minimizes the risk of hydrolytic side reactions. |
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Exploring chemicals that shape our everyday products and medicines might sound abstract, but at the heart of many breakthroughs stands a handful of essential building blocks. Among these, 2,5-Dichloro-4-hydroxypyridine holds a unique spot, driven by its distinctive properties and the wide range of reactions it supports. Not every compound threads its way into so many industries and applications, and for anyone working in pharmaceuticals, agrochemicals, or specialty materials, understanding what makes this molecule tick isn’t just useful — it’s essential.
Purity shapes outcome. Sophisticated processes demand compounds that perform predictably, without background interference from contaminants. Most reputable labs supply 2,5-Dichloro-4-hydroxypyridine with over 98% purity, which, from years of my own hands-on synthesis work, usually means fewer headaches downstream. That’s not just a number: skimpy quality can trigger all sorts of issues, from flawed reaction yields to product failures further along the pipeline. Models vary, depending on factors like the intended use and the route a manufacturer takes to synthesize this compound, but one thing sticks: consistency in particle size, color, odor, and the absence of unwanted residues or moisture makes all the difference for chemists chasing reproducible results.
Holding 2,5-Dichloro-4-hydroxypyridine in a vial, what hits you first is its pale yellow color. It rarely clumps, forming a fine powder that dissolves with relative ease in polar solvents. Structurally, the dichlorinated and hydroxylated positions on the pyridine ring behave like a chemical fingerprint, dialing up reactivity where it matters most. In practice, that means a higher chance that critical substitutions or couplings will go through cleanly during synthesis — something any experimental chemist or bulk manufacturer can appreciate. Its melting and boiling points match what you’d expect from a pyridine derivative and lend the kind of durability that industrial processes count on.
The journey of 2,5-Dichloro-4-hydroxypyridine rarely ends at the lab bench. Much of it finds its way into pharmaceuticals, acting as a precursor or intermediate for active ingredients. I’ve seen it employed during early-stage drug discovery, especially in the modification of aromatic scaffolds where chlorine placement or a single hydroxyl group can radically alter a molecule’s effect. Real-world examples show how its specific substitution pattern allows drug designers to fine-tune biological activity, which turns up again in patent filings and published syntheses. I also know research teams use it in oncology and anti-inflammatory research, in part because the dichloro scaffold resists metabolic degradation while the hydroxyl offers a point for further functionalization.
Yet, the reach of this compound doesn’t stop at pharmaceuticals. Crop protection gets a boost from 2,5-Dichloro-4-hydroxypyridine, with agrochemical manufacturers employing it as a stepping stone to herbicides and fungicides that target specific plant processes. These aren’t theoretical uses; digging into journals and patents, the chemical routinely appears in synthetic pathways leading to products now sprayed on millions of acres worldwide.
The straightforward handling of 2,5-Dichloro-4-hydroxypyridine comes up often in synthesis circles. Many experienced chemists — myself included — prefer it for nucleophilic aromatic substitution, where the unique chlorine pattern favors clean, high-yield reactions. The reactivity of the hydroxyl at the para position works in your favor when you’re layering on complexity, initiating further modifications without unwanted side products.
For custom synthesis or scale-up projects, reliability holds the spotlight. Stability during storage, manageable toxicity profiles, and predictable reactivity stand out, making this molecule a frequent choice for teams that need things to work right the first time. I’ve worked on reactions where more “exotic” ring systems failed, but 2,5-Dichloro-4-hydroxypyridine kept delivering reliable results batch after batch.
Stepping into the world of chlorinated pyridines, you’ll find dozens of close relatives, with names differing by a single number or functional group. Still, they don’t all play the same role. Compared to lesser-chlorinated or non-hydroxylated counterparts, 2,5-Dichloro-4-hydroxypyridine combines reactivity and selectivity better than most. The position of both chlorines on the ring boosts its suitability for nucleophilic substitution, which is key for making end-products where specific attachment points spell commercial success or failure.
Some suppliers offer 2,6-dichloro or 3,4-dichloro analogs, expecting similar performances, but I’ve found their reactivity profiles less consistent. The 4-hydroxyl group on this particular molecule allows additional hydrogen bonding, which can make all the difference when designing drugs or fine-tuning process conditions. In side-by-side lab trials, 2,5-Dichloro-4-hydroxypyridine tends to outperform similar compounds in both yield and selectivity, especially in large-scale runs where minimizing byproducts keeps costs in check.
No chemical gets a free pass from scrutiny. 2,5-Dichloro-4-hydroxypyridine, impressive as it is, brings its own set of challenges, especially for scale-up or regulatory acceptance. The main issues I’ve seen involve sourcing, environmental persistence, and the safe disposal of chlorinated byproducts. In smaller settings, impurities or trace contaminants can sneak through, affecting later steps. Since regulations around chlorinated intermediates keep tightening, especially in Europe and North America, producers have worked to streamline purification steps and trace contaminant analysis.
Having spent years troubleshooting reaction bottlenecks, my team and I learned to run pilot-scale validations before full production. Investing in precise analytical follow-up, from HPLC to NMR confirmation, pays off every time. Reducing solvent waste and recycling chlorine-containing wash liquids has become another focus — not just to meet guidelines but because it keeps overall costs sustainable. Chemistry must answer both technical and environmental questions at the same time, and the best teams I’ve worked on always expect regulators to push the bar higher.
Anyone handling halogenated pyridines needs to keep a close eye on safety. While 2,5-Dichloro-4-hydroxypyridine doesn’t explode off the shelf, it poses hazards if not handled with respect. Dust or vapor inhalation, skin contact, and environmental contamination count as real risks. Decent ventilation, gloves, and face shields must become routine. I’ve seen even seasoned chemists become lax and suffer the consequences. Every production run should come with standardized documentation, and safe disposal guidelines shift often as new data emerge.
Waste management forms a big piece of the puzzle. As with similar chlorinated intermediates, neutralizing unused material and treating wash solutions through approved hazardous waste streams protect both the workplace and the wider community. I’ve watched organizations invest heavily in wastewater treatment upgrades just to stay ahead of regulations, not only for compliance but to boost business reputation and keep good folk from walking off the job over ethical concerns.
The chemical world moves quickly, with unexpected shifts hitting demand and raw materials. For a compound like 2,5-Dichloro-4-hydroxypyridine, shifts in pesticide regulation, pharmaceutical targets, or new material applications can send shockwaves through global markets. Rarely does a week pass where I don’t see fresh uses in the scientific literature — sometimes in areas nobody would have guessed five years back.
Take the surge in demand for targeted herbicides with lower residual toxicity. Many new molecules draw on building blocks just like this one, stripping out unnecessary functional groups to give farmers better precision. Pharmaceutical pipelines remain hungry for versatile scaffolds where site-specific substitutions open the door to next-generation treatments. As industries push deeper into sustainable chemistry, this compound’s manageable reactivity may even offer routes to greener synthesis, especially if supply chain partners develop ways to recover or recycle chlorine content.
Recent years have brought shifts in global sourcing and leaner supply chains, especially after supply disruptions shined an uncomfortable spotlight on essential chemicals. Producers who adapt, investing in traceability and reliable logistics, usually come out on top. As demand for sustainable production clicks with cost pressures, companies who can guarantee high-purity, consistently tested 2,5-Dichloro-4-hydroxypyridine will build stronger customer trust. In my experience, buyers pay a premium for documented processes that certify every lot against trace impurities and support green manufacturing credentials.
Open innovation has picked up pace. Cross-industry partnerships between pharmaceutical developers and agrochemical giants often hinge on access to robust, reliable intermediates. More than once, I’ve watched stakeholders from both sides work out deals to co-invest in upstream capacity, sharing risk and guaranteeing supply in an often unpredictable market. The more frequently this compound appears in published patent claims or peer-reviewed journals, the greater its recognized value underlines practical experience.
The days of sourcing specialty chemicals only from local distributors have faded. Today’s buyers demand global reach and trusted documentation, whether ordering 100 grams or half a ton. Established producers, especially those linked to strong international logistics, bring peace of mind, lessening the risk of interruption when geopolitical events or local shortages strike. I’ve seen projects grind to a halt over shipment delays, only to recover thanks to forward-thinking supply partners with regional distribution hubs lined up.
Bulk buyers often stipulate quality agreements covering every point from initial synthesis to packaging and labeling. Such contracts spell out the nitty-gritty, from analytical standards to batch traceability. Smaller, more innovative companies sometimes bypass wholesalers and go straight to primary producers, seeking both price and transparency. The growing focus on sustainability encourages more companies to choose suppliers who invest in traceable, eco-friendly logistics — a trend only gathering steam.
Technical teams keep pushing the envelope in analysis. Decades ago, thin-layer chromatography and melting point checks formed the backbone of compound verification; nobody would accept that today. High-performance liquid chromatography, mass spectrometry, and NMR all work together for identity, purity, and contamination testing. As environments tighten up on impurity allowances, these tools matter more than ever.
Improved analysis speeds up troubleshooting and gives chemists a head start on regulatory submission. Every batch that makes the cut means fewer regulatory headaches and quicker path to market for end products. Having access to complete analytical records builds both team confidence and insurer patience.
Many specialty chemicals draw scrutiny for their role in environmental cycles. 2,5-Dichloro-4-hydroxypyridine, as a chlorinated pyridine, figures into this broader debate. My involvement in industry working groups has shown the tightrope manufacturers walk: keeping costs in check while proving environmental stewardship. Responsible sourcing, green synthesis, and end-of-life planning no longer qualify as “nice-to-haves”; they open doors to regulated markets and win trust from business partners.
It’s hard to overstate how much consumer and investor pressure now steers chemical adoption. Agricultural customers, especially, ask more about field degradation, groundwater residues, and evidence their inputs won’t spark regulatory recalls. While pharmaceutical clients lean harder on documented purity, they also appreciate partners who’ve solved downstream disposal and emission risks for production plants.
This compound isn’t just a commodity. Every step from reaction setup to final work-up demands skill. I’ve mentored young chemists who, despite strong academic backgrounds, discover the quirks of 2,5-Dichloro-4-hydroxypyridine only through hands-on work. Training support, case studies, and open channels between suppliers and users make a clear difference. The best outcomes come from teams who share both successes and rough patches, learning together instead of repeating costly errors in isolation.
Growing demand for remote technical training — whether online seminars or video walkthroughs of challenging synthesis — mirrors the reality of distributed teams and tighter schedules. In my work with international partners, adapting training to local requirements and languages proved a make-or-break factor. As new users join the field and experienced voices retire, investment in skill transfer becomes just as vital as technical upgrades.
Chemistry often feels abstract to those outside the lab, but the impact of a compound like 2,5-Dichloro-4-hydroxypyridine becomes obvious talking with end-users. In one plant, process engineers shortened synthesis routes for a key herbicide by leveraging the reactivity of both chloro groups, reducing waste by almost thirty percent. At a leading pharmaceutical facility, teams integrated this compound into a new cancer drug candidate, mostly because existing intermediates broke down too quickly in metabolic tests.
Smaller specialty chemical firms benefit too. One research manager told me they cut project lead time by switching to a higher-purity grade, which avoided costly rework and data loss. These stories underline a central theme: reliability, performance in the real world, and the support network behind the product go a long way toward deciding success or failure.
Seeing this compound work in practice raises bigger questions for the industry as a whole. How can manufacturing waste be minimised? Are there process changes or greener synthesis routes that maintain performance while answering environmental concerns? These aren’t just marketing questions — they shape research grants, regulatory standards, and public perception.
Some companies now experiment with alternative chlorination methods and renewable feedstocks. Research groups partner with industrial firms, matching new chemistry with built-for-purpose processing plants. Pushes toward closed-loop systems, where waste gets reused or transformed back into valuable inputs, appear in pilot projects and technical journals. Stakeholder buy-in looks stronger for those willing to show solid data, not just good intentions.
Discussing 2,5-Dichloro-4-hydroxypyridine might seem technical, but its ripple effect appears across broad sectors. Everything from the food we grow to the drugs we take and the specialty materials in our devices owes a debt to robust, flexible chemical intermediates. This one, with its well-matched reactivity, straightforward handling, and adaptability, links practical manufacturing to cutting-edge research.
In my time working with varied project teams, no other small molecule has come up so often as both a problem-solver and a launching point for new ideas. As regulations tighten, expectations climb, and sustainability comes to the fore, the challenge for everyone — chemists, manufacturers, and product developers — is clear. Invest in higher standards, better training, stronger supply chains, and open collaboration, and this compound will continue fueling progress where it counts: real-world outcomes that improve lives and create lasting value.