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HS Code |
522111 |
| Product Name | 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine |
| Chemical Formula | C7H5ClF3NO |
| Molecular Weight | 211.57 g/mol |
| Cas Number | 796845-74-6 |
| Appearance | White to off-white solid |
| Solubility | Soluble in common organic solvents |
| Purity | Typically >98% |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
| Smiles | C1=CC(=NC(=C1O)CCl)C(F)(F)F |
| Inchikey | MJJNARIELXYSPQ-UHFFFAOYSA-N |
As an accredited 2-Chloromethyl-3-hydroxy-6-(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, sealed with a screw cap; labeled with chemical name, structure, hazard symbols, and batch details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine ensures secure, bulk chemical shipment with proper labeling and safety compliance. |
| Shipping | **Shipping Description:** 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine should be shipped as a hazardous chemical, securely packed in suitable, leak-proof containers. Include appropriate hazard labeling in compliance with local and international regulations. Ship under controlled temperature if required, with documentation (SDS) and emergency procedures available. Handle only by trained personnel to ensure safety during transit. |
| Storage | 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine should be stored in a tightly sealed container, protected from moisture and direct sunlight, in a cool, dry, and well-ventilated area. It should be kept away from incompatible substances such as strong oxidizers and acids. Use proper chemical labeling and secondary containment to prevent accidental spills or leaks. Store at recommended temperature conditions specified in the safety data sheet. |
| Shelf Life | Shelf life of 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine is typically 2 years when stored cool, dry, and tightly sealed. |
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Purity 98%: 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where high chemical stability and yield are ensured. Molecular Weight 213.57 g/mol: 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine of molecular weight 213.57 g/mol is used in agrochemical formulation, where precise dosing and reproducibility are achieved. Melting Point 52°C: 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine with a melting point of 52°C is used in solid-phase preparation processes, where controlled crystallization and processability are important. Stability Temperature 25°C: 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine stable at 25°C is used in bioactive compound storage, where long-term integrity and storage consistency are required. Fine Particle Size <10 μm: 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine with fine particle size under 10 micrometers is used in micronization for inhalation drug development, where uniform distribution and absorption efficiency are enhanced. Water Content <0.5%: 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine with water content less than 0.5% is used in sensitive organic synthesis, where minimal hydrolysis and optimal reactivity are obtained. Storage Condition -20°C: 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine stored at -20°C is used in chemical inventory for reference standards, where compound degradation is prevented. Assay by HPLC ≥99%: 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine with HPLC assay not less than 99% is used in analytical calibration, where high analytical accuracy and reproducibility are provided. |
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Working in our laboratory and plant, we come across plenty of pyridine-based intermediates. 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine stands out for both its chemical complexity and real-world performance. Our experience with this compound—in production, handling, and delivery—puts us in a unique position to talk about what actually matters to end users and research chemists. High-value pharmaceuticals, crop protection agents, and specialty chemical innovation all draw on this core structure, thanks to the reactivity and substitution profile of the molecule.
This pyridine derivative brings three things to the table: a chloromethyl group at the 2-position, a hydroxy at the 3-position, and a trifluoromethyl at the 6-position. Many intermediates feature one or two reactive sites; few offer this blend with such a well-balanced reactivity. The chloromethyl group serves as a handle for further alkylation, while the hydroxy moiety opens up downstream derivatization paths—including esterification, etherification, and more. The trifluoromethyl increases lipophilicity and metabolic stability, which means products built on this skeleton often show improved resistance in biological systems. Manufacturing such a multi-functional scaffold takes both experience and rigorous adherence to process controls.
Making kilogram quantities of 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine calls for process know-how. Micro-scale literature routes seldom scale up without occasional surprises. Early on, we learned that controlling temperature profiles and order of reagent addition shapes side product formation far more than theory suggests. Reagent quality, especially for fluorinated compounds, makes all the difference. Trifluoromethyl sources notoriously drag along impurities that aren't easy to spot in pilot runs but wreak havoc at plant scale. We consistently invest in tighter raw material qualification, then back that up with chromatography and mass spectrometry—no shortcuts.
Customers report most positively about our batch-to-batch reliability. If a recent kilogram order blended seamlessly into an ongoing process without deviation, that's by design, not luck. Achieving high purity—typically exceeding 98% by HPLC—improves yields and reduces downstream isolation headaches. Experienced chemists especially appreciate minimal residual inorganic content and predictable solubility. These characteristics result from both upstream purification and our vigilance around water content during drying. Each production lot ships with a detailed COA and spectroscopic profile, reflecting what we actually measure, not just minimums from an outdated literature source.
We have handled ton-scale operations of this compound with a trained eye for safe transfer and storage. Free-flowing, off-white crystalline solid at room temperature, this molecule handles well under dry conditions and typical containerization. During processing, it's sensitive to prolonged exposure to strong bases and oxidizers; overexposure leads to rapid decomposition and loss of assay. Staff training runs deep, covering both the hazards of halogenated pyridines and best practice in dealing with trace impurities released during work-up. We regularly review safety data and upgrade equipment to minimize personnel exposure and waste, building on field feedback as well as data from our own plant audits.
Pharmaceutical development pushes many intermediates to their limit, and this pyridine finds itself at the center stage of select research projects. Medicinal chemists seek out the compound for heterocyclic synthesis, specifically when exploring new kinase inhibitor scaffolds or fluorinated drug candidates. We see requests from teams building SAR libraries, where the compound’s three distinct reactive sites open up paths that would otherwise each need a separate starting material. Rather than juggling multiple building blocks, research teams count on a single molecule to run parallel modifications.
Crop protection R&D places a different set of demands on our product. The trifluoromethyl group, in particular, attracts agrochemists who want both metabolic stability and strong lipophilicity, supporting the creation of actives that hold up in challenging field environments. We've collaborated on custom syntheses where protecting the hydroxy group allows safe progress through multiple steps, only to deprotect at the last minute—our field specialists often consult on best practices for such sequences, based on hands-on experience in our plant and customer labs.
End users tell us that not all chloromethyl- or trifluoromethyl-functionalized pyridines behave alike. We’ve dialed in the specifications that matter, including melting point, color, HPLC area percent, water content by Karl Fischer, and absence of common structural isomers. Recent customer feedback led us to tighten control of halide impurities and develop rapid-release COA tracking, so supply chain managers access real data before the shipment arrives.
Mass spectrometry and NMR provide fingerprints for verification, but what matters most is how consistently intermediates perform in scaled-up reactors. Many clients prefer our product after direct comparison with alternatives because it slashes purification times, forming byproducts less prone to comigrate with target molecules. We typically receive fewer customer technical queries per batch than bulk suppliers, reflecting fewer surprises at the bench.
Research teams often compare 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine to simpler pyridine derivatives. Standard chloromethyl-pyridines lack the hydroxy group, reducing available derivatization pathways and slowing progress in parallel synthesis. Fluorinated pyridines lacking the chloromethyl site often require additional steps to install equivalent reactivity, lengthening both timelines and budgets. Single-function intermediates, while easier to produce, increase the risk of process bottlenecks as projects scale. By contrast, compounds combining all three groups—in the ratios, purity, and physical form we deliver—let scientists streamline multi-step syntheses, lowering total chemical consumption and sharping focus on the final active or API target.
Forum discussions and customer surveys highlight this reality—researchers equate our product with faster screening turnaround, higher yields in key transformations, and more straightforward analytical workup. Extension labs especially appreciate not having to source three or four precursors and then merge them at risk. Our combined experience, from gram to ton level, feeds back into every batch, allowing us to field unusual customer requests, troubleshoot method issues, and recommend workflow adjustments honed from years of direct plant operation.
Industry expectations are moving toward lower-impact production and responsible stewardship. Over the last three years, we have re-engineered several synthetic steps to reduce consumption of hazardous solvents and minimize halogenated waste. One specific campaign switched from chlorinated solvents to greener alternatives, cutting downstream neutralization requirements in half. Process engineers on our team routinely collect data from each cycle, sharing lessons with both supply partners and customers. No process comes out perfect on the first pass—feedback loops with users drive incremental improvement.
Where regulatory standards pose new challenges—whether on waste water discharge, REACH compliance, or packaging streamlining—we invest in equipment and process validation to stay out in front. Chemists, production operators, analytical staff, and supply chain managers all participate in monthly review sessions. That direct feedback generates real improvements in efficiency, cost control, and environmental footprint—not only for us, but also for partners who require documentation of source material practices when preparing for regulatory submissions or site audits.
A chemical like 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine never leaves the plant as an anonymous commodity; it arrives at a research bench or pilot reactor as a tool for progress and a potential point of failure. Over the years, we have worked with customers troubleshooting reaction stalls linked to minute moisture uptake, learning to modify packaging and handling. Several pharmaceutical groups, running repeated cyclization reactions, encountered color changes and yield drops—on review, we identified trace peroxides from past batches and introduced new in-process scavenging steps.
A few industrial partners, scaling from research kilo-labs up to multi-ton campaigns, asked us to deliver not just the raw chemical but also insights on process safety and bottleneck minimization. Our team spent months jointly developing protocols for safe addition, pressure monitoring, and downstream filtration tweaks. Each success built our understanding—and our willingness to speak the language of both bench chemistry and plant engineering, without defaulting to jargon.
Chemicals that work on paper do not always stand up in reactors now loaded around the clock. Because we actually make 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine in-house, we learn by trial, measured refinement, and attention to real processing variables. We have tested direct incorporation into Suzuki, Buchwald, and various functional group transformations under different conditions. The molecule’s reactivity and thermal durability go beyond theoretical predictions—actual runs taught us how small pH changes or stirring rates alter yield, especially in multistep protection/deprotection series.
Our technical group collaborates with chemists exploring next-generation actives for both agricultural and pharmaceutical applications. We consider every batch a chance to upgrade process hygiene, inform customer documentation, and anticipate strict new standards on purity, handling, or supply continuity. Greater digitalization of production and analytics drives our planning, including real-time tracking and automated lot release systems. These upgrades benefit client innovation speed, letting research move from idea to synthesis to scaled-up validation with fewer hiccups. Each innovation in in-house analytics—be it NMR, LC-MS, or trace metals screening—ripples across every subsequent order.
Direct production and supply bring practical advantages for everyone who needs to pick up the phone or email with a technical query. Our process engineers, plant chemists, and technical support do not treat questions as interruptions to be outsourced but as part of the job. If a customer’s team inquires about batch timelines or potential sulfur inclusion, our answer pulls from live process data instead of theoretical estimates, because we run, staff, and validate the plant lines ourselves.
Fast response to technical, logistical, or regulatory queries improves not only supply dependability but real project momentum. Each time someone requests a custom grade—be it higher purity or a unique particle size—our own staff coordinates the project. Our field experience, from raw material sourcing to finished lot loading, keeps processes tight and feedback quick. Few intermediaries can claim that kind of firsthand, plant-floor exposure to every product shipped.
End uses for 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine continue to advance in complexity. Modern drug discovery and crop protection research both place increased pressure on reactant purity, environmental impact, and reliable delivery schedules. As a manufacturer, we have shifted to accommodate smaller trial-based orders for start-ups alongside the regular contractual deliveries for major established firms. Our facilities support both, drawing on process flexibility built into the reactor lines and a firm grip on batch tracking.
Client networks value real supply transparency—knowing where and how a chemical is made, inspected, sampled, and packaged. We favor open communication about process upgrades, raw material shifts, and any relevant learnings from unexpected plant events. Intellectual property needs remain paramount for many customers, and our operational protocol respects proprietary integrations while still sharing general guidance on best practices. Once a pattern emerges—be it a better solvent swap or a safer handling tweak—we work to pass on the lesson, supporting both customer innovation and our internal culture of continuous improvement.
Every chemical synthesis project carries unique demands, and 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine is no exception. Chemists sometimes request shifts in physical form, custom packaging, or blending with select stabilizers. In these cases, we consult across our R&D and QC teams, probe for unintended side effects, and only then deliver. This direct, in-house approach connects us with development teams at a level that reselling or trading operations simply can’t replicate.
Some of the best results emerge from pilot collaborations: tweaking synthesis to shorten timelines, swapping out reagents to cut regulatory risk, or validating new analytical screens for tighter impurity profiles. Every challenge from customers—be it in process design, analytical validation, or scale-up—adds to our accumulated knowledge. We document these lessons, folding them back into standard operating procedures and sharing feedback with both supply partners and downstream users (always within confidentiality constraints).
All chemical intermediates serve a purpose, but direct manufacturer experience transforms abstract compounds into tools for progress. Our experience with 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine leaves no doubt: detailed plant data, tight quality control, and responsive support matter as much as the molecule’s structure. Effort on our end—fine-tuned purification, meaningful batch analytics, and expert technical service—frequently brings customers back for new projects.
Experience teaches that the more closely process and end-use teams work together, the smoother projects run. If a problem arises with a run—unexpected discoloration, a bad assay, a blocked filter—we cut through speculation with real-time plant insight. No reliance on hearsay, no waiting on a distributor to relay questions to a distant plant. That kind of responsiveness offers real value for syntheses on critical timelines and for projects with novel, complex requirements.
Manufacturing challenging molecules is an ongoing craft. Each batch we produce adds to the collective understanding of what works, what doesn’t, and how real-world process chemistry underpins progress in labs and industries that depend on reliability over theory. From start to finish, our approach with 2-Chloromethyl-3-hydroxy-6-(trifluoromethyl)pyridine reflects this philosophy.