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HS Code |
191232 |
| Cas Number | 3984-69-0 |
| Molecular Formula | C5H2ClF3N2 |
| Molecular Weight | 182.53 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 133-134°C (at 760 mmHg) |
| Density | 1.46 g/cm³ |
| Refractive Index | 1.451 |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as dichloromethane, methanol |
As an accredited 4-Chloro-6-Trifluoromethylpyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 100 grams, tightly sealed, labeled with chemical name, hazard symbols, and handling instructions for laboratory use. |
| Shipping | 4-Chloro-6-Trifluoromethylpyrimidine is shipped in tightly sealed containers under standard chemical shipping regulations. It should be protected from light, heat, and moisture, and transported in compliance with local, national, and international dangerous goods guidelines. Proper labeling and documentation must accompany the shipment to ensure safe and compliant handling and delivery. |
| Storage | 4-Chloro-6-Trifluoromethylpyrimidine should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Use appropriate, clearly labeled, chemical-resistant containers and ensure storage in compliance with safety regulations and protocols for hazardous chemicals. |
Applications of 4-Chloro-6-Trifluoromethylpyrimidine in Industrial ManufacturingAs a direct manufacturer with expertise in heterocyclic chemistry, we supply 4-Chloro-6-Trifluoromethylpyrimidine to leading global companies at scale for critical synthesis steps. The following sections detail the material's established, traceable application scenarios in major industrial sectors, with a focus on the specific regulatory, process, and product context in each domain. 1. Crop Protection Active Ingredient SynthesisThis intermediate serves as an essential halogenated building block for the manufacture of advanced pyrimidine-derived herbicide and fungicide actives, such as selective broadleaf weed herbicides, via nucleophilic aromatic substitution leading to downstream functionalization. Compliance with agricultural chemical legislation requires careful raw material verification and trace impurity profiling at each step. Formulators integrate the material predominantly in the first or second stage of multi-step condensation or cyclization reactions when assembling the agrochemical pharmacophore. Application rates typically reflect the stoichiometric requirement plus tight overage management to minimize cost and by-products. Industry compliance standards
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2. Pharmaceutical API Intermediate ManufacturingPharmaceutical companies select this pyrimidine derivative to construct key molecular scaffolds within non-purine dihydropyrimidine inhibitors and novel kinase modulators. The substance acts as a strategic synthon during targeted ring substitution or amide formation under cGMP conditions, enabling the fabrication of registered starting materials and advanced intermediates. All process steps demand full material traceability, impurity fate analysis, and compliance with health authority guidance for intermediates destined for further conversion into APIs, particularly anti-viral and oncology drug candidates. Industry compliance standards
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3. Veterinary Drug Intermediate ProductionAnimal health manufacturers incorporate this compound as a key intermediate when assembling next-generation pyrimidine-based veterinary actives, especially in anti-parasitic and anti-infective molecule development. Formulations leverage the halogen and trifluoromethyl substitution to enhance metabolic stability and bioavailability in final actives. The intermediate enters production at the early stage in multi-step syntheses, requiring stringent adherence to veterinary API-related QC, traceability, and impurity control as prescribed by local and international animal health regulations. Industry compliance standards
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4. Specialty Agrochemical Intermediate SupplyLeading formulators of niche plant growth regulators and seed treatment agents specify this building block for the synthesis of advanced pyrimidine derivatives that exhibit selectivity and controlled release. The material’s unique substitution pattern supports downstream thiol, amine, and aromatic coupling, resulting in multi-functional agrochemical intermediates. Within the specialty agrochemical supply chain, all production steps align with sector-specific export, environmental, and worker safety regulations, and producers adjust the incorporation quantity based on seasonal demand and targeted growth regulator potency. Industry compliance standards
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Experience shapes our approach to every batch of 4-Chloro-6-Trifluoromethylpyrimidine. After years spent behind production lines and in process control labs, we understand what makes a specialty pyrimidine more than just another intermediate. The needs for this compound run deep in the crop science, pharmaceutical, and organic electronics sectors. Our team sees requests from research and high-volume partners alike, so control and consistency form the backbone of our production.
The chemical base—4-Chloro-6-Trifluoromethylpyrimidine—merges an electron-donating chloro group with the highly electronegative trifluoromethyl. This unique structure forms the basis for derivatives that end up in a surprising array of final products. On paper, the CAS number 6631-63-0 signals one molecule among millions. In practice, this model has come to represent reliability for R&D chemists and process engineers who care about clean, traceable feeds.
Years in the plant have shown us that consistency in delivery only happens if you maintain discipline from raw material selections to every packaging run. We provide 4-Chloro-6-Trifluoromethylpyrimidine in lot sizes spanning research-scale bottles to multi-ton drums, keeping impurity limits under 0.5%. This is not an arbitrary standard; the heavy use of downstream substitution reactions means that a surprise contaminant can migrate through a synthesis and endanger critical outputs. Anomalies at the trace level can destroy yields across multi-step syntheses, an expensive and wasteful outcome no chemist wants.
Visual inspection gives a clear, colorless-to-pale yellow liquid. We typically deliver product with a purity of no less than 99.0% (GC), an absolute threshold for those pursuing high-throughput or GMP-compliant work. Materials remain moisture-free, since even small amounts of water cause hydrolysis and shift the halogen balance. Users focused on UPLC-MS or NMR analytics, including those pushing sensitive biotransformation pathways, report back that our batches behave predictably. Over time, this forms trust in the raw material pipeline, which lets researchers stay focused on innovation instead of error tracing.
Nearly every manufacturer promises high quality. We have learned over years of operation that purity goes deeper than a certificate or a spec sheet. Small differences in process steps, timing, or raw feedstock can mean the difference between a straightforward scale-up and a week lost trouble-shooting a runaway impurity profile. Partners in the field have sent us challenging feedback after sourcing from traders or anonymous resellers—sudden problems in their reaction scope, unexpected NMR findings, or product recalls connected to off-spec input chemistry. Each story reinforced what works: a direct line from plant to lab and strong process controls rooted in experience.
Our process maintains traceability through electronic batch records and routine batch reserve samples. Chemical handling follows robust air controls and nitrogen-swept environments because 4-Chloro-6-Trifluoromethylpyrimidine displays light sensitivity and reactivity with ambient moisture. Any product that passes our QA lands in inert-lined containers, helping users avoid post-purchase headaches from decomposition products. These procedures carry real costs in utilities, equipment, and labor. We invest here because we’ve seen too many failures from corner-cutting—both on our own production floor years ago and in tales relayed by end-users who needed a rescue order after a bad batch from a broker.
This intermediate brings real versatility for those facing pyrimidine ring functionalization. It provides two clear reactive sites—the 4-chloro and 6-trifluoromethyl positions—giving users options for nucleophilic aromatic substitution under mild to moderate conditions. Researchers in the agrochemical sector have validated its use in the synthesis of herbicide scaffolds, such as triazolopyrimidine and fluoro-substituted pyrimidines, often gaining better activity and selectivity by exploiting the unique balance of electron-withdrawing and electron-donating effects present here.
Pharmaceutical teams leverage this backbone in a wide range of kinase inhibitors and antiviral programs. The structure resists metabolic oxidation, offering more predictable in vivo clearance profiles. Some groups in OLED and material science have started using 4-Chloro-6-Trifluoromethylpyrimidine for building blocks in high-performance semiconductors and organic frameworks, driven by the hydrophobic and electron-demanding nature of the trifluoromethyl tail. These applications originated in academic bench work but entered commercial production lines, reinforcing our need to keep process variables locked tight.
Working as direct producers, we observe a steady stream of requests for comparisons to similar pyrimidines—especially plain 4-chloropyrimidine or unmethylated variants. Subtle structural differences translate to big changes in reactivity and downstream outcomes. The key difference here is the trifluoromethyl group at the 6-position. This enhances electron withdrawal across the ring and fundamentally changes the available substitution chemistry.
Plain 4-chloropyrimidine tends toward higher reactivity with soft nucleophiles, sometimes resulting in rapid and exothermic substitutions that complicate process scale-up. With the trifluoromethyl addition, our product moderates that reactivity, letting users tune conditions for mono-substitution and limit unwanted side processes. The result is a more forgiving platform for custom synthesis, especially in applications requiring regioselectivity or slow stepwise substitutions.
For those who previously relied on 4,6-dichloropyrimidine or unfluorinated analogs, the shift to this molecule means access to a new set of downstream products—especially in cases demanding unique electronic profiles for improvement of binding specificity or charge mobility. Customers report sharper analytical separation and higher conversion rates in reactions prone to halogen scrambling, delivering cleaner intermediates with less need for post-reaction cleanup. These small differences save time and money at bench scale and are magnified many times during plant-scale operations.
Over the years, maintaining lot-to-lot consistency in 4-Chloro-6-Trifluoromethylpyrimidine posed challenges, especially during commodity surges or upstream raw material bottlenecks. We have faced times where trifluoromethylating agents became scarce due to geopolitical shifts or supply chain interruptions. Lessons from these disruptions taught our team to hold strategic reserves of key precursors and pursue multi-vendor qualification at the raw stock level, well before the global supply chain risk became a news headline.
Adapting to sudden changes requires forethought, not just wishful thinking. Our plant engineers designed flexible synthesis routes that minimize solvent switching and cut down turnaround times if a single intermediate faces a delivery lag. This was not about chasing the lowest costs, but about enabling schedule certainty for clients running continuous process lines or time-critical scale-ups. Whenever customers faced sudden surges in demand—for example, linked to new regulatory registrations or a spike in new product launches—we had material in the pipeline, not empty promises.
Relying on real-time analytics, rather than batch-release paper trails, gave us an edge during unexpected events. Inline GC and moisture probes inside production tanks flagged outliers as they developed, not after the fact. Feedback loops between QA staff and process operators meant that deviations from standard runs triggered immediate corrective actions. Less time spent worrying about what happened last week, more effort invested in keeping this week’s batch on point. This investment in direct QC—trained staff, digital records, and regular proficiency testing—costs more on the balance sheet, but it sure beats lost batches and last-minute trouble-shooting for an out-of-tolerance product.
We've seen clients in pharma and agro spend millions on downstream validations, only to have regulatory authorities question or reject data because of a bad trace impurity in the starting material. With transparent, traceable manufacturing histories, our team works closely with partners to ensure confidence—delivering batch samples, comprehensive COAs, and robust impurity tracking with every lot. End users appreciate traceability, but what matters most is that batches behave the same way every time; reproducibility underpins safety, yield, and regulatory acceptance.
4-Chloro-6-Trifluoromethylpyrimidine stores best under dry nitrogen in amber glass or steel, at room temperature or slightly below. Open drums or bottles draw in moisture quickly, which can start slow hydrolysis that goes unnoticed at bench scale but suddenly derails full process loads. Our crew adopted double-seal packaging with humidity indicators on each drum—small extras that caught attention from process chemists who depend on each package opening in pristine condition.
We recommend using material within six months after arrival for strictest compositional control, but reserve samples from years past continue to meet most analytical standards under correct storage. These recommendations stem from lived experience: routine QA retesting, not just standard documentation.
Dealing direct lets us support customers’ application development and troubleshooting from the source. Sometimes that means walking through a new heterocycle synthesis or helping select the right quenching agent to avoid tricky byproducts. Other times, we support teams who need rapid scale-up of a proven route but no time to revalidate everything from scratch. By keeping the process in-house from start to finish, insights gained through manufacturing flow back into support for development scientists—an edge missing with generic, third-party supply.
We invest in long-term relationships and open problem-solving. Greying engineers and younger chemists alike sit in process debriefs, learning from both failed and successful runs. Feedback becomes process improvement. Every drum shipped means more than moving material—it means standing behind every gram with the knowledge that only comes from seeing the same chemistry, day in, day out, over decades.
Pressure from both customers and regulators pushed us to look for greener, safer, and less resource-intensive ways to make key intermediates. Years ago, legacy routes for 4-Chloro-6-Trifluoromethylpyrimidine relied on heavy metals or aggressive halogenation steps with high waste indexes. Our site team reengineered steps to reduce halogenated byproduct runoff and recycle solvents, cutting both environmental risks and the cost of waste management. Newer steps rely more on catalytic processes with reagent recycling, spurred by both regulatory incentives and a push from our internal environmental teams. We track emissions for every production run, aiming to lower the footprint steadily each year.
Customers benefit from a lighter environmental impact in their supply chain, and we see fewer regulatory bottlenecks as a result. In the end, sustainability does not just mean good PR; it means our product remains available and compliant in every major market, no matter how strict future rules become.
Field experience stays grounded in actual feedback from those who put molecules to the test in full-scale reactions and tightly controlled clinical manufacturing lines. Several partners have told us about abandoned projects suddenly becoming viable with purer, more predictable supply. Others recount yield boosts from single-digit percentages to record-setting runs with no changes in their downstream chemistry. One pharmaceutical developer cut purification cycles in half by switching to our batches, saving weeks in cumulative campaign time across a calendar year. Agrochemical teams, squeezed by seasonal planting windows, leaned on delivery as much as purity—on both counts, reliability underpins their willingness to keep returning.
Direct conversations with process engineers in Latin America and Southeast Asia, regions where supply-chain disruptions recently stung hardest, prove that proximity to the real origin makes a difference. Rapid turnaround and ongoing technical support help customers reduce risk and gain an edge in volatile markets. They know exactly where each drum comes from, what conditions it faced, and who to talk to when challenges arise—an assurance that simply doesn’t exist in the anonymous marketplace.
Demand continues rising across pharmaceuticals, fine chemicals, and materials sciences for fluorinated pyrimidines. Meeting those needs means flexible capacity and strict discipline in both process safety and material quality. Our plant brings both, grounded not in marketing but in decades of practical chemical production that survived both lean times and demand spikes alike.
Adaptability depends on feedback, not guesses. We solicit insights from technical teams, process users, and QC managers—adapting the next production run to squeeze out both risk and cost. By working direct with end-users, we modify packaging, adapt minimum order sizes, or adjust specification points wherever science justifies a change. This is ongoing, practical process improvement, guided by actual experience.
4-Chloro-6-Trifluoromethylpyrimidine occupies an important spot among nitrogen heterocycles—more than a building block, it’s an enabling tool for outcome-driven chemistry. Providing this molecule direct from our controlled plant to your bench or filling line, we hope to offer both the product and the practical understanding that makes each project feasible. Nothing substitutes for knowledge earned at the source and the commitment to improvement that comes with every batch.