|
HS Code |
586125 |
| Chemicalname | 5-(Chloromethyl)-2-(trifluoromethyl)pyridine |
| Casnumber | 86604-77-9 |
| Molecularformula | C7H5ClF3N |
| Molecularweight | 195.57 g/mol |
| Appearance | Colorless to light yellow liquid |
| Boilingpoint | 99-101°C at 10 mmHg |
| Density | 1.368 g/mL at 25°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO and dichloromethane |
As an accredited 5-(Chloromethyl)-2-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed with a PTFE-lined cap, labeled with chemical name, hazard symbols, and batch details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 5-(Chloromethyl)-2-(trifluoromethyl)pyridine: Securely packed, typically 160-200 drums, ensuring minimal leakage and safe chemical transport. |
| Shipping | 5-(Chloromethyl)-2-(trifluoromethyl)pyridine is shipped in tightly sealed containers, protected from light and moisture. It is typically packed according to UN regulations for hazardous chemicals, with appropriate hazard labeling. The chemical is transported under controlled temperature and handled by authorized personnel, ensuring compliance with local, national, and international shipping guidelines. |
| Storage | **5-(Chloromethyl)-2-(trifluoromethyl)pyridine** should be stored in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances like strong oxidizers. Keep the container tightly closed and stored in a chemical-resistant, labeled bottle. Handle under an inert atmosphere if sensitive to moisture or air. Use appropriate personal protective equipment when handling. |
| Shelf Life | Shelf life of 5-(Chloromethyl)-2-(trifluoromethyl)pyridine is typically 2 years if stored in a cool, dry, tightly sealed container. |
|
Purity 98%: 5-(Chloromethyl)-2-(trifluoromethyl)pyridine with 98% purity is used in active pharmaceutical ingredient synthesis, where it ensures high product yield and consistency. Molecular weight 197.59 g/mol: 5-(Chloromethyl)-2-(trifluoromethyl)pyridine at molecular weight 197.59 g/mol is applied in agrochemical research, where it provides reliable compound identification and formulation. Melting point 28–31°C: 5-(Chloromethyl)-2-(trifluoromethyl)pyridine with melting point 28–31°C is used in fine chemical manufacturing, where easy handling and controlled processing are enabled. Stability temperature up to 50°C: 5-(Chloromethyl)-2-(trifluoromethyl)pyridine stable up to 50°C is utilized in polymer intermediate synthesis, where thermal stability enhances reaction safety and efficiency. Low water content (<0.5%): 5-(Chloromethyl)-2-(trifluoromethyl)pyridine with water content below 0.5% is used in electronic materials production, where minimal hydrolysis risk improves device reliability. Reactivity: 5-(Chloromethyl)-2-(trifluoromethyl)pyridine with high reactivity is used in heterocyclic compound design, where efficient functionalization supports rapid library generation. Assay ≥98%: 5-(Chloromethyl)-2-(trifluoromethyl)pyridine with assay ≥98% is used in catalyst precursor development, where precise concentration control optimizes catalytic activity. Colorless to pale yellow liquid: 5-(Chloromethyl)-2-(trifluoromethyl)pyridine as a colorless to pale yellow liquid is employed in material science research, where solution-phase processability aids composite fabrication. |
Competitive 5-(Chloromethyl)-2-(trifluoromethyl)pyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
In chemical manufacturing, real-world application always brings us face-to-face with the unique qualities and challenges that a compound can offer. Direct production of 5-(Chloromethyl)-2-(trifluoromethyl)pyridine lets us recognize the nuances that set this intermediate apart from both its analogs and traditional chlorinated pyridines. Over years of active synthesis and hands-on use, the practical advantages, quirks during scale-up, and performance across different industries stand clear.
We synthesize 5-(Chloromethyl)-2-(trifluoromethyl)pyridine using carefully refined batch protocols, tracking the process from raw material sourcing through every quality checkpoint. The resulting crystalline solid displays a characteristic pale yellow color, easy to distinguish in our in-process controls. Regular feedback from customers confirms that the consistent particle size and purity—usually kept above 99% by HPLC—translate to reliable batch-to-batch repeatability, which matters most during downstream synthesis.
In processing, those working with sophisticated fluorinated intermediates notice the impact even of small impurities. Our teams have learned to optimize for minimal formation of double-chlorinated byproducts, which trouble purification lines and disrupt reaction selectivity. With each production run, automation, filtration, and recrystallization cycles are monitored to cut contamination—a practice borne of too many lessons learned by troubleshooting yields at the user end.
The trifluoromethyl group bound to the 2-position on the pyridine ring isn’t just a structural curiosity. In synthesis labs, it creates challenges in halogenation kinetics and subsequent derivatization steps, especially when compared to simpler chloromethylpyridines. Our operators have seen the difference during high-heat workups: the electron-withdrawing effect of CF3 consistently shifts reaction temperatures and rates, requiring close attention to avoid runaway exotherms. The result is a stable compound, resistant to hydrolysis and oxidation. This makes it a reliable player, especially during prolonged storage or if transport schedules lengthen unexpectedly.
End-users of 5-(Chloromethyl)-2-(trifluoromethyl)pyridine often work in active pharmaceutical ingredient (API) synthesis, crop protection agents, and specialty chemicals. Our product gets most attention in heterocyclic assembly, where the reactivity of the chloromethyl group enables efficient nucleophilic substitution. Many have reported that coupling reactions, nucleophilic aromatic substitutions, and Grignard addition steps go more smoothly, with high selectivity for target products. The compound’s nature helps cut side product formation. For those who deal with difficult intermediates, that means smoother cleanups and higher yields, saving time and resource costs.
The presence of the CF3 group has a pronounced effect on pharmacokinetics and biological activity in final molecules, often increasing metabolic stability and bioavailability in drug analogs. We see demand spike wherever medicinal chemistry research intensifies, and product managers request real-world technical support for process optimization, not just catalog samples.
Meanwhile, agrochemical developers value the reliable scale-up from lab syntheses to pilot plants, noting that our process minimizes batch variation in purity and moisture content. This matters during fine formulation work, where development timelines can depend on intermediate stability.
Years of direct handling draw clear technical lines between this compound and alternatives. Some clients compare it to 2-(trifluoromethyl)pyridine or to simple 5-chloromethylpyridine. We’ve seen first-hand the difference in reactivity—especially in metal-catalyzed paths—when the CF3 group stays present. Unlike the non-fluorinated analogs, this compound consistently gives better selectivity in nucleophilic aromatic substitutions, especially with secondary amines or thiols. Fewer byproducts lead to smoother purification, a constant need in both pharma and agro work.
On storage and transport, there’s less hydrolysis and less off-odor development compared to 5-chloromethylpyridine, particularly in high-humidity areas. Our shipments to tropical customers prove year after year that, with tight container sealing and controlled packing, users can avoid expensive breakdown or wastage.
Working with trifluoromethylated products also challenges scale-up techniques. The boiling point and solubility profile differ meaningfully from unsubstituted pyridines. Solid-handling and solvent selection aren’t interchangeable. Those using older protocols for chloromethylpyridine find our support team’s experience with solvent/temperature optimization essential during tech transfer. Subtle shifts in process design—inclusive of distillation cut points and pH adjustment during workup—can mean the difference between robust manufacturing and persistent losses.
Every direct manufacturer faces the question of operator safety and process stewardship. For 5-(Chloromethyl)-2-(trifluoromethyl)pyridine, vapor control and sealed handling has made a clear difference in both health and equipment longevity. Chloromethyl-containing pyridines aren’t casual on mucous membranes or skin. Over the past decade, shop-floor improvements—closed charging, local exhaust upgrades, specialized PPE—have protected operators and cut complaints of irritation. The feedback from our staff aligns with long-term medical monitoring and personal air sampling data. Those new to handling halomethyl pyridines must understand that “standard” organic protocols overlook chronic exposure risks: deliberate engineering and safety culture matter more than one-time training.
Spill response and fire risk mitigation have shaped our choice of packaging. By using tight-seal, chemically resistant drums and unit packs, we give customers confidence that product received at their dock matches the material shipped. Our logistics team keeps up with the evolving regional and international transport rules for halogenated aromatics, ensuring compliance and uninterrupted delivery.
Direct oversight of production brings environmental responsibilities into sharper focus. Waste streams from 5-(Chloromethyl)-2-(trifluoromethyl)pyridine preparation carry residual halides and—without proper scrubbing—risk local emissions. Stepwise improvements in our facilities have cut aqueous chloromethylate contamination using multi-stage scrubbers and targeted neutralization. Regulatory agencies raise the bar every year, and internal self-audits stay one step ahead. Knowing exactly where emissions may occur, and how to contain them, keeps us on the right side of regulation and community safety.
Customers have pushed for documentation of cradle-to-gate environmental impacts. Life cycle data for our manufacturing route, including energy, water, and waste per kilogram made, steers our ongoing investment choices. Where possible, process chemists prioritize greener solvents and recover unused reagents to minimize waste. Every improvement comes from direct observation of shop-floor bottlenecks and dialog with purchasers aiming to green their supply chains, not from abstract target-setting.
Scale-up chemistry carries everyday realities absent from lab-scale success stories. Our journey scaling 5-(Chloromethyl)-2-(trifluoromethyl)pyridine from trails to commercial batches highlighted practical choke points—temperature control, solvent choice, filtration capacity, and product isolation. Bottlenecks that appeared on the periphery soon became central during high-throughput production. Through root-cause analysis and years of de-bugging with both operators and R&D staff, each constraint forced invention or adaptation.
For example, the compound’s solubility profile demands a solvent system with precision to prevent premature crystallization or phase separation during large-scale extractions. We found—through trial and repeat—that slight temperature drift changed recovery yields by several percentage points, not a theoretical concern but a very real impact on product availability. Sharing those lessons with clients shortens their process development cycles, and mutual innovation rises from a basis of honesty, not just compliance.
Walking the factory lines, technical managers see that real assurance doesn’t arise from static specifications alone. Every step of 5-(Chloromethyl)-2-(trifluoromethyl)pyridine’s synthesis undergoes live laboratory and inline analysis: melting point, HPLC purity, residual solvents, moisture, and foreign ion content. Customer audits on our sites rarely surprise us, as transparency runs both ways. Investment in regularly calibrated chromatography, well-trained analytical specialists, and digital batch tracking builds the traceability buyers require—especially in the face of increased regulatory scrutiny.
Batch failure or out-of-spec product triggers root-cause review, not routine discard. From personal experience, close tracking turns isolated events into teachable moments for continuous improvement. Customer feedback catches intermittent problems even top-performing QA lines miss. Direct communication and after-sales visits uncover subtle issues that only manifest during end-use scale-up.
We value critical feedback more than polished praise. Over years of building technical collaborations with pharmaceutical process teams and agrochemical formulators, persistent themes emerge: speed-to-batch, impurity troubleshooting, and practical advice for real-world reactors, not just theoretical guidance. Often, an operator’s query about equipment compatibility, unanticipated residue formation, or unplanned downtime reveals the need for deeper technical support. Drawing from our own experience, we commit specialists to help troubleshoot reaction quenching, crystallization delays, or surprising color change, not just to fill reports but to solve problems end-to-end.
Product stewards who bridge plant operations and customer R&D share knowledge gained from the realities of chemical manufacture—not just from pre-approved scripts. For example, answering questions about scaling up from 10 to 1,000 liters isn’t a sideline but the heart of how evolving needs get met. Tracking regulatory updates, addressing shifting supply patterns, or providing guidance on specialty analytical needs defines the service that manufacturers owe their customers.
No process ever sits still. Keeping 5-(Chloromethyl)-2-(trifluoromethyl)pyridine competitive means regular modernization—not only strengthening production reliability but also anticipating industry’s changing standards regarding traceability and sustainability. New digital tools bring more precise material tracking from raw material receipt to tanker dispatch. Our process engineers adapt digital twin simulations to test changes before risking full-line disruption.
Procurement managers have pushed hard for transparent reporting, especially those supplying to regulated markets where batch-level origin tracking and data access must stand up to regulatory or customer audit. Providing that level of traceability demands more than record-keeping—it relies on genuine process control and clear communication between operators, quality teams, and end-users.
Decades of hands-on manufacturing transform 5-(Chloromethyl)-2-(trifluoromethyl)pyridine from a line item on a chemical inventory to a trusted tool for complex molecule building. Each batch draws on engineering, safety, logistics, and collaboration with end-users looking for consistent results rather than generic catalog promises. The unique combination of a reactive chloromethyl and a stabilizing trifluoromethyl group rewards those who know its intricacies and who seek reliability, from glassware to pilot plant to production line.
Our commitment to quality, open technical engagement, and responsible stewardship grows not from market positioning but from a lived understanding of real-world manufacturing. Each feedback loop, audit, and technical query sharpens our practices and deepens the relationship between manufacturer and innovator. For those seeking more than bare-bones supply, the difference shows in every shipment, every visit, and every successful reaction run.