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HS Code |
513455 |
| Chemical Name | 3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine |
| Molecular Formula | C6H3ClF3NO |
| Molecular Weight | 197.54 g/mol |
| Cas Number | 898566-17-9 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, methanol) |
| Smiles | C1=CC(=C(N=C1C(F)(F)F)O)Cl |
| Inchi | InChI=1S/C6H3ClF3NO/c7-4-2-5(6(8,9)10)11-1-3(4)12/h1-2,12H |
As an accredited 3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine 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, labeled "3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine," with hazard pictograms, batch number, and safety instructions. |
| Shipping | 3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine is securely packaged in accordance with regulatory standards for hazardous chemicals. It ships in sealed containers, protected from moisture and light, typically under ambient or controlled temperature. Appropriate labeling and documentation ensure safe transport, complying with international chemical shipping and safety regulations. |
| Storage | Store **3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine** in a tightly sealed container, protected from moisture, heat, and light. Keep it in a cool, dry, well-ventilated area, separate from incompatible substances such as strong oxidizers and acids. Label the container clearly and handle with appropriate personal protective equipment to prevent contact and inhalation. Dispose of waste according to local regulations. |
Applications of 3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine in Industrial ManufacturingAs an advanced intermediate, 3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine plays a key role in the synthesis of specialty chemicals across the pharmaceutical, agrochemical, and fine chemical industries. Our manufacturing expertise ensures consistent quality for demanding downstream applications where strict process control and regulatory compliance are paramount. 1. Active Pharmaceutical Ingredient (API) SynthesisAPI manufacturers deploy this intermediate during multi-step synthesis of modern fluoroquinolone antibiotics and certain antihypertensive agents. Its pyridine scaffold and halogen functionality allow for robust stepwise transformations, often via selective alkylation or condensation routes. Precise formulation and batch controls are maintained to meet pharmacopeial purity and impurity thresholds, ensuring suitability for large-volume non-sterile and sterile production lines. Industry compliance standards
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2. Agrochemical Synthesis: Herbicide and Fungicide IntermediatesFormulators for crop protection products use 3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine as a specialized building block when producing new-generation selective herbicides and fungicides. The compound’s electron-withdrawing trifluoromethyl group supports enhanced environmental stability in field applications, making it a preferred choice for modern synthesis pipelines. Industry compliance standards
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3. Veterinary Drug Intermediate ManufacturingProducers of veterinary actives rely on this molecule for introducing both halogen and trifluoromethyl groups into pyridine-derived feed medication and companion animal pharmaceuticals. Specialized synthesis processes demand consistent purity for downstream hydrogenation, amidation, or heterocyclic functionalization. Industry compliance standards
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4. Fine Chemical and Specialty Synthesis: Electronic Material PrecursorsManufacturers in the electronics sector leverage this intermediate for the synthesis of high-purity pyridine derivatives required in advanced display panel production, semiconductor chemical vapor deposition, and battery electrolyte additive manufacturing. Strict controls on trace metal content and organofluorine residuals are implemented to prevent device contamination. Industry compliance standards
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Over the past decade, our team has worked with hundreds of heterocyclic building blocks, and few have shaped new development programs quite like 3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine. As a chemical manufacturer that refines every step, from raw material handling to final drying, we've learned that not all pyridine derivatives behave equally in high-performance settings. Synthetic chemists, scale-up specialists, and formulation experts bring different priorities to the table, yet the need for consistent behavior, high purity, and reliable availability remains constant across projects. We developed our process for 3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine to meet the kinds of rigorous standards that research, process development, and commercial operations now demand.
Our batches typically range from a few kilograms in the pilot plant to hundreds of kilograms in full production runs. Every batch starts by validating incoming raw materials from qualified suppliers. Years of hands-on experience have taught us to avoid corners. Early on, we noticed slight impurities in commercial pyridines could compromise selectivity and downstream yields, so we've invested in additional purification steps and robust impurity tracking for each lot. This pyridine derivative leaves our hands only after passing detailed HPLC, GC-MS, and NMR checks conducted in-house. The laboratory never surprises us with a contamination we haven't seen before.
Because most of our volumes serve the pharmaceutical and agrochemical sectors, we've focused on achieving a purity of >99%. Water content is kept at low ppm levels, which has been critical for customers using this intermediate in moisture-sensitive couplings or protection/deprotection sequences. Over the years, we've fielded questions about minor byproducts—the chlorine and trifluoromethyl groups in close proximity might encourage formation of trace side products. Our regular stability studies show this compound retains its profile in long-term storage if kept sealed and away from UV light, and we've incorporated an extra drying cycle for orders destined for particularly sensitive processes.
3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine occupies an unusual intersection between electronic effects and functional group compatibility. The trifluoromethyl group at the 5-position increases electron-withdrawing character across the pyridine ring. This shift makes the molecule far more reactive in palladium-catalyzed couplings, alkylation, or nucleophilic aromatic substitution compared to pyridines lacking such a group. A couple of medicinal chemistry groups pointed out to us that, when using this material as a core in kinase inhibitor programs, they saw cleaner installation of further substituents at the ring’s open positions than with less activated alternatives.
The 2-hydroxy group offers a convenient handle for further derivatization—esters, ethers, or silyl protections fit well into the synthetic strategies we see requested most often. The 3-chloro substituent lends itself to selective displacement under mild conditions, providing a rapid entry point for custom functionalizations. Over the years, we’ve seen the molecule incorporated into insecticide scaffolds, seed treatment products, pharmaceutical intermediates, and fine chemicals for the electronics sector. In each application, customers have come back with stories about how minor changes to the substitution pattern altered the downstream behavior of their compounds—in solubility, reactivity, or stability.
From the perspective of someone who’s weighed, charged, and monitored tanks of this compound through all seasons, physical consistency means more than just a statistic on a COA. At scale, any unexpected behavior — caking, static build-up, variable particle size — can lead to clogs or incomplete dissolution in automated feeders. We granulate our product to a controlled, free-flowing powder. As we discovered during early shipments, this attention to consistency saves untold headaches later in a continuous process. No stubborn lumps, no dust clouds in the blend tanks.
During production, the material’s moderate melting point and volatility require careful temperature control at the filtration and drying stages. A few years ago, a single incident where a drying oven’s probe under-read by 8°C resulted in persistent clumping and a week’s worth of rework—not a scenario anyone wants to repeat. That lesson compelled us to integrate redundant sensors on every production line where this intermediate features. As a result, customers have stopped reporting issues with silting or uneven wetting in their reactors.
We often receive questions about how this compound compares to more classic intermediates such as 3-Chloropyridine, 2-Hydroxy-5-Trifluoromethylpyridine, or unsubstituted 2-chloropyridines. The short answer: the presence of both chlorine and trifluoromethyl groups, combined with the ortho-positioned hydroxy function, delivers a balance of reactivity and selectivity that simple analogues rarely match.
The electron-withdrawing trifluoromethyl group stabilizes the ring, making further functionalization more controlled and less prone to unwanted rearrangements. Compared to unsubstituted 2-hydroxypyridines—where oxidation or polymerization can crop up under harsh conditions—this compound remains more robust in oxidative environments. Likewise, many 3-chloro derivatives without a hydroxy group run into trouble in mild alkaline media, hydrolyzing unpredictably; the hydroxy substitution appears to improve solubility and provides an additional anchor for synthetic transformations, as reported by several of our partners in their published research.
We supply to chemical development labs worldwide, and every feedback loop improves our process. Recently, a company working on biorational crop protection agents reported that their in-line NMR monitors detected a minor spectral impurity not covered in USP or JP monographs. Working closely with their analytical chemists, we re-examined our hydrogen peroxide addition step and fine-tuned the work-up. The next batch cleared their QA checks without a hitch. Collaboration like this sharpens both our product and the quality of downstream innovations we help enable.
On the pharmaceutical front, a major player in small-molecule oncology requested a more detailed residual solvent analysis, pushing us to adapt our GC-FID methods for greater sensitivity to low-level aromatics. Integrating this feedback not only improved our data package but also gave our own internal teams a benchmark for future projects in similarly regulated sectors. Over half our recurring orders now specify custom analytics or extended impurity profiles, reflecting how customers with distinct projects—agrochemistry, medicinal chemistry, materials science—lean on us for more than just material supply.
Production of 3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine, like many halogenated compounds, involves safe handling of chlorinated and fluorinated intermediates. We have steadily phased out older, solvent-intensive crystallization steps, replacing them with distillation and membrane filtration to reduce exposure and waste. Years of operating a closed-loop recovery system for spent solvents have indexed improvements not only in environmental reporting metrics but also in the morale of our production staff—knowing we keep the plant safer and cleaner every cycle.
Local community engagement became more than a buzzword for us after one particularly tough local audit prompted neighbors to ask for more regular emissions transparency. Now, on top of internal batch logs and routine stack testing, we share quarterly environmental data—total VOCs, solid waste, effluents—at monthly meetings with residents and stakeholders. It’s not lost on us that large-scale production of specialty chemicals brings obligations, not just opportunities, to every region we serve.
Any time we release a new lot, whether for a new API synthesis or as an intermediate in crop protection pipelines, our technical team stands behind every drum. If a downstream reaction underperforms, we dive into the batch history, run extra chemistry in the lab, and re-examine every chromatogram. A few years back, a client developing specialty polymers in East Asia ran into gel formation. After a marathon week reviewing data, we flagged a minor change in extrusion rates upstream of our process—data hidden in the early batch logs. Adjusting the rate and confirming particle distribution on the next production run cleared up the issue, restoring the polymer’s performance and timeline.
Experience with multiple sectors drives us to maintain transparent channels with both R&D and manufacturing teams at customer sites. One group using this intermediate to build new OLED materials encountered challenges during scale-up when switching from laboratory glassware to 500L reactors. Working alongside their chemists, our engineering team shared practical tips for mixing order, temperature ramp rates, and anti-caking additive concentrations to make sure the material dissolved as expected. Combining technical exchange with detailed practical experience creates a smoother handoff and higher success rate for both parties.
For new customers, storage and handling advice goes beyond the standard datasheet. The trifluoromethyl group’s chemical resilience doesn’t mean this intermediate should endure wide swings in humidity or temperature. In our warehouse, we keep drums sealed in inert nitrogen when not actively in use. Years spent tracking rejected lots have confirmed that even brief atmospheric exposure doesn’t always yield visible clumping, yet it leads to measurable shifts in trace moisture. End-users who follow similar storage conditions consistently report cleaner reaction outcomes, fewer rejects, and less need for additional pre-treatment.
In long-term storage studies, samples drawn from containers maintained under nitrogen and low RH performed as freshly packed even after two years. By contrast, partially used containers sitting open in high-humidity climates show a subtle yet meaningful uptick in hydrolysis byproducts—a fact that repeats across both academic and industrial reports we’ve reviewed. As a manufacturer, we always prefer to address handling issues at their source. In-house training for new staff now includes real-world examples of storage, blending, and transfer practices that maximize shelf life and minimize unexpected downtime.
We have observed steady growth in demand for heterocyclic intermediates featuring strong electron-withdrawing groups, as regulatory and competitive pressure drive innovation in medicine and agriculture alike. Our chemical development group tracks trends across patent filings and research consortia, spotting new uses for substituted pyridines in both emerging therapies and more resilient crop science platforms. Developers continue to ask for derivatives that combine robust stability with tunable reactivity; 3-Chloro-2-Hydroxy-5-(Trifluoromethyl)Pyridine fits these needs, not simply as a legacy building block but as a platform for new discoveries.
Collaboration remains the engine for improvement in our work. Direct feedback from every facility that uses this material—feedback about clarity, color, purity, reactivity, and problems encountered—feeds straight back to our technical and quality teams. From process tweaks that shave off cycle time, to new analytical protocols that expand our offering to customers in highly regulated fields, every learning creates a stronger foundation for the next iteration. As the market’s needs evolve, so does our commitment to delivering not just chemical product, but the partnership and know-how required to get from concept to completion, batch after batch.