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HS Code |
891403 |
| Chemical Name | 2-Hydroxy-3,5,6-Trichloropyridine |
| Cas Number | 118759-73-2 |
| Molecular Formula | C5H2Cl3NO |
| Molecular Weight | 198.44 g/mol |
| Appearance | Light yellow solid |
| Melting Point | 105-108°C |
| Solubility In Water | Slightly soluble |
| Synonyms | 2-Hydroxy-3,5,6-trichloro-pyridine; Pyridin-2-ol, 3,5,6-trichloro- |
| Density | 1.67 g/cm³ |
| Smiles | C1=C(C(=NC(=C1Cl)Cl)O)Cl |
| Inchikey | HSKZRIBBQQTQPH-UHFFFAOYSA-N |
As an accredited 2-Hydoxy-3,5,6-Trichloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 250g amber glass bottle, with a secure screw cap and hazard labeling for 2-Hydroxy-3,5,6-Trichloropyridine. |
| Container Loading (20′ FCL) | 20′ FCL can load approximately 12 metric tons of 2-Hydroxy-3,5,6-Trichloropyridine, typically packed in 25 kg fiber drums. |
| Shipping | 2-Hydroxy-3,5,6-Trichloropyridine is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It is classified as a hazardous material; therefore, transportation follows relevant regulations (such as DOT, IATA, IMDG) with appropriate labeling. Handle with care, ensuring the package is upright and protected from physical damage during transit. |
| Storage | 2-Hydroxy-3,5,6-trichloropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect it from moisture and direct sunlight. Ensure proper labeling and restrict access to trained personnel. Personal protective equipment should be used during handling and storage. |
| Shelf Life | Shelf life of 2-Hydroxy-3,5,6-trichloropyridine: Stable under recommended storage conditions; typically at least 2 years in a cool, dry place. |
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Purity 99%: 2-Hydoxy-3,5,6-Trichloropyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting point 105°C: 2-Hydoxy-3,5,6-Trichloropyridine with a melting point of 105°C is applied in agrochemical manufacturing, where its thermal stability enhances formulation processing. Particle size <50 microns: 2-Hydoxy-3,5,6-Trichloropyridine with particle size less than 50 microns is used in specialty coatings applications, where it provides uniform dispersion and improved coating homogeneity. Stability temperature up to 180°C: 2-Hydoxy-3,5,6-Trichloropyridine with a stability temperature up to 180°C is utilized in polymer modification, where its robust thermal resistance enables durable material properties. Moisture content <0.2%: 2-Hydoxy-3,5,6-Trichloropyridine with moisture content below 0.2% is used in active pharmaceutical ingredient (API) production, where low moisture prevents hydrolysis and degradation. Assay ≥98%: 2-Hydoxy-3,5,6-Trichloropyridine with assay of at least 98% is employed in fine chemical synthesis, where high assay level guarantees target compound integrity. Solubility in methanol ≥25g/L: 2-Hydoxy-3,5,6-Trichloropyridine with solubility in methanol ≥25g/L is used in laboratory-scale organic synthesis, where superior solubility facilitates rapid reagent preparation. Residual solvents <0.05%: 2-Hydoxy-3,5,6-Trichloropyridine with residual solvents below 0.05% is incorporated in analytical standard production, where low impurity levels ensure reliable analytical results. |
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In chemistry, few compounds offer as much value in both research and industrial settings as 2-Hydroxy-3,5,6-Trichloropyridine. With a molecular formula of C5H2Cl3NO and a molecular weight around 198.44 g/mol, this pale white to light yellow crystalline powder has found its place at the intersection of agricultural innovation, pharmaceuticals, and fine chemicals. At first glance, it might look like just another ring-shaped structure, but those who have spent hours in the lab weighing precise amounts know how much depends on the quality and consistency of such intermediates.
From my own experience in the lab, working with pyridine derivatives never feels trivial. Every minor impurity can set off a chain of unwanted reactions, so purity truly matters. With 2-Hydroxy-3,5,6-Trichloropyridine, the high purity available on the market—often exceeding 98%—has made it a trusted foundation in the hands of chemists focused on reliable results. Researchers rely on a moisture content under 0.5%, and prefer a product that resists caking or clumping, especially during long-term storage in ambient conditions.
Not every chlorinated pyridine offers the same advantage. 2-Hydroxy-3,5,6-Trichloropyridine stands out for the placement of its chlorine atoms and the functional hydroxyl group. This structure increases its reactivity with certain electrophiles, making it an ideal precursor for creating more complex molecules, especially when exact orientation of substituents drives the desired reaction pathway.
Handling pure organic intermediates often brings a set of challenges—for me, moisture absorption and degradation under light have both spoiled plenty of batches over the years. Solid, crystalline form, and a melting point in the reliable range around 145-150°C solve many storage problems for this pyridine. Stability during normal handling means less fuss over storage, which reduces waste and costs over time.
Pick up a bottle of common herbicide, and you might find you’re holding the finished result of dozens of chemical reactions. Trichloropyridine compounds have built a reputation for their critical role in herbicide production, and this particular derivative often acts as an indispensable start. Its consistent performance contributes to the reliable control of unwanted plants in agricultural fields. The supply chain depends on intermediates like 2-Hydroxy-3,5,6-Trichloropyridine, not just as a sourcing line item but as a checkpoint between successful yields and failed batches.
During my graduate years, several teams explored new ways to build active pharmaceutical ingredients by tweaking pyridine structures. Many failed attempts proved that slight changes, such as an extra hydroxy group or a misplaced halogen, could make or break downstream reactions. The trichloro substitution increases hydrophobicity and shifts the electronic balance, opening doors for selective substitution reactions—ideal for developing new drug candidates or improving the cost-effectiveness of generic drugs.
Big names in the chemical industry devote significant resources to improving precursor compounds for efficiency, safety, and environmental impact. Through the years, pyridines like this one have begun to turn up in more than weedkillers. Chemists reach for 2-Hydroxy-3,5,6-Trichloropyridine when synthesizing specialty pharmaceuticals, ligands for catalysts, and some high-performance resins used in advanced manufacturing.
Some of the earliest breakthroughs with chlorinated pyridines involved exploring their antibacterial and antifungal properties. Their robust ring systems resist biological breakdown, which has sparked as much debate as innovation. Environmental stewardship means weighing persistent molecules against their benefits. In lab meetings, the talk shifts from excitement over new reaction routes to discussions of fate and afterlife in water and soil. Real-world chemistry refuses to remain isolated to the flask.
For students picking apart chemical catalogs, many pyridine derivatives can seem interchangeable on paper. But experienced users know the placement of those three chlorines makes a world of difference. Swapping their positions on the aromatic ring instantly changes reactivity, solubility, and even the types of reactions the compound can withstand.
Some competitors to 2-Hydroxy-3,5,6-Trichloropyridine lack the hydroxyl group entirely, shifting their utility more toward electronics or pesticides with different mechanisms. Other isomers, such as 2,3,5-Trichloropyridine, will not accept the same nucleophilic additions or substitutions that one expects from this product. From personal trial and error, I have learned the importance of matching the exact compound to the process to prevent expensive rework and wasted time.
Increasing global demand for food has put herbicides under the spotlight, and every link in the supply chain matters more than ever. 2-Hydroxy-3,5,6-Trichloropyridine finds itself in the crosshairs of regulators, chemists, and farmers alike. Every impurity or change in quality could ripple out to cause failed crop protection or, worse, unintended environmental damage.
Over the years, the best manufacturers of this product have responded to these challenges by improving analytical verification at every stage of production, from starting material inspection to rigorous batch records. My own experience reviewing quality control data shows how tighter process controls and transparent reporting build trust between suppliers, buyers, and researchers. The chemists on the receiving end notice more than just a certificate of analysis—they see the result in the repeatability of their results.
Working with any chlorinated compound means thinking beyond purity. There’s always a need for safe handling protocols and responsible end-of-life treatment. Even a small spill in a poorly ventilated lab can cause headaches—both literal and figurative. Clear labeling and thorough training pay dividends. From my perspective, regular reviews of safety data sheets—often seen as a chore—keep everyone honest and help prevent lapses.
Persistent organic pollutants catch the eye of policymakers because they degrade slowly, sometimes sticking around in soil and water for years. Best practices call for integrating responsible disposal and even closed-loop systems to recycle or neutralize chemical waste. Some groups I’ve worked with have started tracking downstream metabolites, which helps anticipate and limit negative effects before they reach the ecosystem. Not every company has the resources to chase every molecule, so continued dialogue between academia, industry, and regulators becomes vital.
Quality has always been a team effort. Leaders in the chemical trade point to investments in process monitoring equipment, in-line sampling, and not cutting corners with raw materials. As someone who has spent hours trying to identify the origin of an unexpected TLC spot or GC peak, I can't overstate the relief that comes with a consistent product. Some distributors go beyond minimal testing by offering third-party verification. When one batch of 2-Hydroxy-3,5,6-Trichloropyridine performs exactly like the last, the entire chain—right down to the end-user spraying a field—benefits.
Certifications and rigorous supplier audits may seem bureaucratic but prove crucial in a world where a single tainted shipment can damage reputations or even public health. The feedback loop between manufacturers and customers serves all parties. Sometimes a customer will catch an out-of-spec batch before it reaches the market—there’s a sense of community responsibility embedded in these exchanges that protects long-term trust for all involved.
It’s tempting to focus on chemical innovation as a sprint toward the next new molecule, but real progress is measured by building robust supply lines, emergency plans, and a culture of continuous improvement. Unforeseen supply chain hiccups—from shipping delays to regulatory changes—force everyone to be nimble. Experienced buyers now favor relationships rooted in transparency. They regularly review supplier performance, track shipment conditions, and share learnings with peers.
The balance between wider access and environmental protection has grown sharper in recent years. Societal expectations require that chemical producers not simply dump what’s left after extraction, but instead recover, neutralize, or even upcycle waste streams. With global trade regulations tightening, especially for chemicals categorized as persistent or hazardous, keeping one step ahead secures jobs, assures safety, and reduces risk.
Not so long ago, purity testing involved a handful of wet-chemistry techniques and trust in the supplier. Now, HPLC, GC-MS, and advanced spectroscopy let buyers verify every parameter right at the receiving dock. I’ve seen major changes in labs where regular use of NMR or LC-MS became second nature, not just for product development but also verifying raw material consistency. Such rigor turns quality from a box-checking exercise into a competitive advantage.
Automation across production and quality control lines reduces human error and shortens response times. For a compound like 2-Hydroxy-3,5,6-Trichloropyridine, laying in strong analytics means catching off-flavors—literally and figuratively—before they become problems. As more companies digitize their supply chains, traceability improves and recalls become rare events.
The use of advanced intermediates in herbicide production brings up debates over the sustainability of modern agriculture. Every year, farms grow larger and more reliant on chemistry to maximize yields and minimize losses. A compound like 2-Hydroxy-3,5,6-Trichloropyridine becomes a small but vital cog in delivering enough food to a growing population.
New demands from both consumers and governments encourage the shift toward selective, environmentally friendlier formulations. Achieving this means not only choosing better actives but improving the journey of intermediates from lab bench to final product. Practices such as using renewable feedstocks, optimizing reaction conditions for lower waste, and monitoring impact all the way to the field nudge the industry toward a healthier planet.
No review of chemical intermediates stands alone. The drive for alternatives runs strong, prompted by cost, performance, or concern over persistence in the environment. Some research teams explore greener synthesized analogs, swapping out individual groups for less-chlorinated or biodegradable versions. Others push for smarter process engineering, shortening synthetic routes and improving atom economy.
Where 2-Hydroxy-3,5,6-Trichloropyridine holds its ground, it's as much due to its consistent downstream value as to its adaptability in evolving chemical landscapes. From my conversations with industrial chemists, resistance to switching away from the tried-and-true often reflects concern for regulatory re-approval or the challenge in finding a drop-in replacement that delivers the same performance.
My experience suggests that even experienced chemists can sometimes take shortcuts with common intermediates—underestimating potential volatility or exposure risks. Well-designed supplier documentation, regular retraining, and chemical hygiene not only protect staff but sustain productivity. Site audits, feedback mechanisms, and up-to-date chemical inventory protocols serve as front-line defenses.
Team culture also matters. I’ve seen labs where every new shipment gets opened and checked in daylight, not just logged. Peer checks, inventory turnover, and even informal conversations about unexpected results all add up. Such vigilance tends to result in fewer failed syntheses and smoother regulatory compliance—two things that matter to everyone from interns to executives.
My advice for those sourcing 2-Hydroxy-3,5,6-Trichloropyridine is to look beyond the spec sheet. Take the time to understand supplier relationships, typical batch variability, and responsiveness to unexpected events. Don’t hesitate to ask for detailed analytical data, including chromatograms or impurity profiles. Involve your team in supplier evaluations and foster open lines of communication so genuine concerns can surface early.
Stay current with literature, regulatory advisories, and sector-specific best practice papers. These regularly highlight trends or shifts that affect not just price, but reputation and reliability. Collaborative networks—informal or formal—quickly share red flags and problem-solving tips. For a widely used intermediate like this, market knowledge pays dividends.
Efforts to improve 2-Hydroxy-3,5,6-Trichloropyridine continue on several fronts. Some focus on greener synthesis with less toxic reagents. Others look at creating derivatives that maintain core activity while improving biodegradability. In my view, the winning solutions will come from partnerships that blend deep scientific rigor with awareness of global needs.
What gives this compound staying power is not just performance in a reaction vessel, but its track record for enabling progress in key sectors. As industries shift priorities—seeking cost cuts, new capabilities, or a smaller environmental footprint—the demand for trusted, tested intermediates won’t disappear. The lessons learned from handling, improving, and scrutinizing this product echo across the chemical landscape, reminding us that building a responsible future depends on choices made today, batch by batch, and conversation by conversation.