|
HS Code |
155896 |
| Cas Number | 86604-86-2 |
| Iupac Name | 5-(Chloromethyl)-2-(trifluoromethyl)pyridine |
| Molecular Formula | C7H5ClF3N |
| Molecular Weight | 195.57 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 74-76°C (at 14 mmHg) |
| Density | 1.375 g/cm3 |
| Flash Point | 82.4°C |
| Smiles | C1=CC(=NC=C1C(F)(F)F)CCl |
| Refractive Index | 1.482 |
As an accredited Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)-(9CI) is supplied in a sealed amber glass bottle with tamper-evident cap. |
| Container Loading (20′ FCL) | 20′ FCL container loads 160 drums (200 kg each), totaling 32 metric tons of Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI). |
| Shipping | Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) should be shipped as a hazardous chemical, complying with local and international regulations. Use appropriate, tightly sealed containers clearly labeled with hazard warnings. Package to avoid leaks, and handle with care to prevent exposure or spills. Ensure shipping documentation meets all regulatory requirements. |
| Storage | **Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI)** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, ignition sources, and incompatible materials such as strong oxidizers and acids. Keep it out of direct sunlight and protect from moisture. Proper chemical storage protocols and personal protective equipment should be followed to ensure safety. |
| Shelf Life | Shelf life of Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) is typically 2-3 years when stored properly, tightly sealed. |
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Purity 98%: Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) with purity 98% is used in agrochemical intermediate synthesis, where it ensures high yield and minimal impurity formation. Boiling Point 163°C: Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) with boiling point 163°C is used in pharmaceutical fine chemical production, where it provides precise temperature control during distillation processes. Molecular Weight 213.60 g/mol: Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) with molecular weight 213.60 g/mol is used in custom synthesis of fluorinated heterocycles, where defined stoichiometry delivers consistent product structure. Stability Temperature up to 60°C: Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) with stability temperature up to 60°C is used in chemical storage protocols, where it reduces risk of thermal decomposition. Appearance clear colorless liquid: Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) with appearance as a clear colorless liquid is used in formulation laboratories, where visible purity accelerates quality assurance procedures. Density 1.38 g/cm³: Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) with density 1.38 g/cm³ is used in organic synthesis reactions, where it allows accurate volumetric dosing for reproducible outcomes. Water Content <0.5%: Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) with water content less than 0.5% is used in anhydrous reaction systems, where it prevents unwanted hydrolysis and ensures product integrity. Refractive Index n20/D 1.482: Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) with refractive index n20/D 1.482 is used in analytical method development, where it facilitates compound identification and purity analysis. Chromatographic Purity ≥99%: Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) with chromatographic purity ≥99% is used in medicinal chemistry research, where it enhances reproducibility and bioactivity assessment. Melting Point −10°C: Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) with melting point −10°C is used in low-temperature synthesis environments, where it maintains liquid state and handling efficiency. |
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Daily work at the chemical plant brings a deep familiarity with every product on our line, and Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) stands out for the consistency it delivers to research and manufacturing partners around the world. Watching its production move from the fine-tuned reactors to the final sealed containers reinforces just how many details must line up for a specialty intermediate to meet real-world application needs. Each drum shipped carries with it the months of refinement in process and technical troubleshooting that underpin reliability—no matter if a kilo heads straight to a pharmaceutical pilot plant or an agrochemical synthesis bench.
The designation 5-(chloromethyl)-2-(trifluoromethyl) Pyridine refers to a single, clearly defined chemical entity: an aromatic ring that joins chloromethyl and trifluoromethyl groups at precise ring positions. That trifluoromethyl substituent at the 2-position gives the molecule distinct chemical reactivity and a hydrophobic character, which enhances its role as a backbone in diverse syntheses. The chloromethyl group at the 5-position introduces a point of reactivity for further substitution, alkylation, or cross-coupling, making it an attractive intermediate for those searching for efficiency in complex molecule assembly.
On the production floor, we keep a close eye on purity and by-product levels in every batch. Years of process optimization mean we have brought residual solvents and side-products down to trace levels. Typical material ranges between 98.5% and 99.5% active compound by GC, with water and residual solvents well below the analytical thresholds that could impact downstream chemistry. Factors like isomeric purity carry real weight for clients seeking reproducibility in research outcomes; only firsthand attention to these critical points keeps expensive reruns or failed syntheses at bay.
Few chemicals walk directly from a manufacturing plant into finished products; intermediates like Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI) play their roles midstream, where transformative reactions shape more complex molecules. For years, synthetic chemists in pharma and crop protection have approached us for this compound because it plugs neatly into processes like nucleophilic substitution, cross-couplings, and halogen exchange—core steps in generating building blocks for new drugs, advanced herbicides, and fungicides.
Many discovery projects reach for this molecule when they need a scaffold that balances reactivity with stability, thanks to the interplay between the electron-withdrawing trifluoromethyl group and the chloromethyl side chain. In medicinal chemistry, researchers use these features to modulate drug metabolism profiles or enhance target selectivity. In agrochemicals, these same qualities allow for fine-tuned activity against specific pests or weeds, adding value at both the innovation and final-product stages.
Sourcing starts with understanding reactivity. Chemists value our pyridine intermediate because its structure tolerates a broad array of functional group manipulations. Alkylation, amination, and cross-coupling run cleanly on the chloromethyl group, while the pyridine core remains unimpaired for subsequent steps. The trifluoromethyl group brings metabolic stability and lipophilicity—two properties under constant scrutiny in the rush to bring better actives to market. Labs come back to this intermediate for exploration in lead-optimization screens or library syntheses, counting on lot-to-lot consistency to prevent uncertainty.
In an environment crowded with pyridine derivatives, a question comes up often: what makes this molecule stand out compared to other halogenated or fluorinated analogs? The answer ties directly to its balanced reactivity, which supports rapid downstream transformations without overwhelming instability that can frustrate scale-up. There’s no shortage of simple 2-chloromethylpyridines or trifluoromethylpyridines in the catalogues, but this compound’s unique substitution pattern unlocks different selectivity profiles that researchers rely on for intellectual property and faster results in SAR (structure-activity relationship) studies.
Another factor comes from the practical world of production and formulation. By observing process bottlenecks over the years, we learned that not every chloromethylpyridine handles the same under real process conditions. Some struggle with residual base, metal catalyst contamination, or uncontrolled hydrolysis during storage or shipment. Our team has worked out a process reproducible at both small and multi-ton batch scales that controls these issues through robust purification, monitored every time. As a result, our clients report fewer rework steps, less need for on-site refinement, and cleaner analytical profiles over competing sources.
Researchers approaching a new synthesis don’t see intermediates as generic goods but as contributors to project momentum or risk. Choosing this specific 5-(chloromethyl)-2-(trifluoromethyl) version gives teams the flexibility to explore new reactivity or selectivity not reached with common alternatives. Protecting intellectual property in drug discovery or crop science often demands less accessible, more strategically substituted intermediates—exactly the kind of edge this product brings.
A manufacturer’s view comes loaded with detail. Years of process improvement have taught us that it’s never enough to hit a published purity number alone. Consistent appearance, low moisture content, and the control of subtle by-products all feed into successful downstream use. Colleagues in formulation labs have relayed issues with material from less reliable suppliers, such as off-color product, odor contamination, or unstable storage—all factors that can derail a project or spark regulatory concern.
It’s not unusual for research groups to ask about trace contaminants before they approve a new lot for synthesis. Addressing those questions demands more than a data sheet—it takes transparent analytics, batch history records, and, sometimes, a quick conference call with our plant chemists. Direct experience breeds trust, and we back up every shipment with data from our in-house lab as well as real responses from the team who monitored the batch each step of the way.
Supply chain management for specialty intermediates like this one doesn’t always look smooth from the outside. Shipping restrictions for halogenated organics, evolving environmental limits for process effluents, and rising costs of critical raw materials all add real challenges to daily operation. We’ve adapted by investing in reactor containment, closed-loop solvent recovery, and more rigorous environmental monitoring than basic regulations require. This long-term investment pays off with fewer unplanned shutdowns, predictable lead times, and a smaller footprint in our local community.
For customers, stable supply takes on new importance whenever a focus shifts to late-stage projects. Last-minute delays aren’t tolerated when teams face patent cliffs or seasonal windows for new agrochemical field trials. Our approach includes everything from redundant raw material sources and onsite QC to logistics partnerships that lock in compliance during transit. We know firsthand how much wasted time follows after a delayed or damaged drum, so we coordinate directly with end-users to preempt concerns at the earliest planning stages.
Feedback from industry users often revolves around handling and storage. Unlike lower-value commodities, pyridine intermediates call for sealed, moisture-tight packaging and technical guidance for safe transfer—even in research-scale settings. We coach users both before and after delivery to make sure material spends minimal time open to the atmosphere, which preserves reactivity and reduces loss. It’s details like this, picked up through dozens of conversations and site visits, that form the hidden fabric of a quality supply relationship.
The chemicals industry faces new scrutiny over the lifecycle impacts of specialty intermediates. Our team set early targets to cut waste, recycle spent solvent, and minimize the energy used per kilogram produced. Scrutinizing every metric from starting material yield to off-gas neutralization has driven improvements in solvent selection, batch duration, and utility use. As regulations change, so do our protocols—never at the expense of product integrity, always with risk minimization in view.
We see a parallel in our client base. Procurement teams and EHS (Environmental Health and Safety) officers now ask about cradle-to-grave metrics for each batch. Questions reach deeper than waste treatment or packaging reclamation; users want details on synthesis routes, traceable raw material origins, and risk mitigation against persistent organics or halogen emissions. We keep full records outlining our process flows and share relevant data, giving clients assurance about responsible sourcing and product stewardship.
As manufacturers, we won’t claim every process version is the finished word. Lab-scale improvements, process intensification, and the shifting needs of drug and crop science partners always offer chances to refine our work. For instance, feedback on reactivity in Suzuki or Buchwald-Hartwig coupling steps led our R&D team to fine-tune the moisture balance and packing density of each batch. Adjustments here produced higher isolated yields at the customer bench, confirmed by joint pilot runs and follow-up analytics.
Working elbow-to-elbow with downstream partners—sharing technical reports, batch samples, and in-person troubleshooting—forms the backbone of sustainable improvement. Labs advancing into continuous flow chemistry approached us to discuss how our intermediate as a solid or in solution altered throughput and downstream cleanup. These practical conversations allowed both parties to cut process steps, shrink waste output, and improve final product quality beyond what any catalog descriptor promises.
Never far from mind for any specialty intermediate: regulatory compliance and traceability. Every batch of 5-(chloromethyl)-2-(trifluoromethyl)pyridine ships with full supporting documentation, covering both regulatory requirements and technical service expectations. We maintain traceable, batch-specific records for each lot, and can reproduce full histories on request for customers facing regulatory audits or process qualification challenges.
Traceability doesn’t end with a report. We operate under documented SOPs and change-control systems, and our QA team rigorously tracks any process modification—even those that happen one reactor valve or analytical column at a time. Customers value this transparency, especially where pharmaceutical and crop protection regulations tighten each year, raising the bar for what’s acceptable in both starting materials and process controls.
Within our walls, knowledge sharing continues through routine operations reviews, staff cross-training, and participation in wider industry forums. No single shift or day at the plant covers the full experience base that shapes a robust supply chain, so we invest in continual improvement at both the operator and management levels. By engaging with professional societies and academic groups interested in aromatic intermediates and synthetic innovation, our team also cross-pollinates best practices and real-world insight from colleagues worldwide.
Listening to customers has also expanded our understanding. Regular technical symposia bring together process engineers, synthetic chemists, and supply chain managers to map out opportunities and issues in live projects. Solutions to stubborn synthetic bottlenecks, impurity management, and regulatory compliance often take root during open dialogue, not through template answers. The feedback loop from bench to plant benefits all parties, grounding improvements in real technical need, not hypothetical scenarios.
Market dynamics create complex pressures. Fluctuations in the price of essential halogen and fluorine reagents can cause intermediate prices to spike overnight, especially when supply disruptions hit upstream raw materials. We keep tabs on market volatility by holding strategic stocks and regularly reevaluating supplier contracts. This approach cushions our customers from some of the wild swings in global pricing, keeping R&D budgets more predictable.
Intellectual property concerns also shape conversations about specialty pyridines. Research teams developing new drugs or agrochemicals need intermediates that strike a careful balance: accessible enough for efficient supply, unique enough for patent protection and competitive advantage. Our collaboration with IP consultants and senior chemists has guided us toward offering this product with both flexibility in packaging and rapid turnaround on documentation and C of A (Certificate of Analysis) requests. The result: faster approval paths, fewer project bottlenecks, and streamlined regulatory submissions.
Years of production and direct customer engagement shape every batch we deliver. The unique attributes of Pyridine, 5-(chloromethyl)-2-(trifluoromethyl)- (9CI)—strong, yet flexible reactivity; impurity control; and a proven record in both early research and late-stage commercial settings—mean our team sees this molecule as more than just another line item in a catalog. It stands as a result of real-world problem solving, innovation, and ongoing investment in quality, safety, and sustainability.
Engineers and chemists at every step—from pilot lab to plant floor—work with steady attention to detail, responding to the ever-changing needs of researchers on the frontlines of innovation. This responsiveness, married to technical skill and a willingness to learn from daily operations, helps keep the product relevant and reliable as scientific demands evolve.
By listening to users, adapting to new technical requirements, and investing in continuous process improvement, our team ensures a stable, high-quality supply of 5-(chloromethyl)-2-(trifluoromethyl)pyridine for those leading research and commercial ventures in their fields. The result reflects not just product quality, but a deeper shared commitment to advancing science through practical manufacturing expertise.