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HS Code |
611064 |
| Product Name | 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine |
| Cas Number | 163877-89-4 |
| Molecular Formula | C6H2ClF4N |
| Molecular Weight | 199.54 g/mol |
| Appearance | Colorless to light yellow liquid |
| Density | 1.48 g/cm3 |
| Boiling Point | 130-133°C at 760 mmHg |
| Melting Point | - |
| Purity | Typically ≥98% |
| Refractive Index | n20/D 1.468 |
| Solubility | Soluble in organic solvents |
| Smiles | C1=CN=C(C(=C1F)C(F)(F)F)Cl |
| Inchi | InChI=1S/C6H2ClF4N/c7-4-2-12-1-3(8)5(4)6(9,10)11 |
| Synonyms | 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine |
As an accredited 2-Chloro-3-fluoro-4-(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 of 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine, sealed with a secure screw cap for protection. |
| Container Loading (20′ FCL) | 20′ FCL typically loads 12–14 MT of 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine securely packed in drums or IBCs. |
| Shipping | **Shipping Description:** 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine is shipped in tightly sealed containers, protected from light and moisture. It should be stored at room temperature and handled as a hazardous material under standard chemical shipping regulations. Proper labeling and documentation are required, and transportation should comply with all relevant local and international regulations. |
| Storage | Store **2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep at room temperature or as otherwise specified by the manufacturer. Ensure proper labeling and use appropriate containment to prevent leaks or spills. Follow all relevant safety and regulatory guidelines. |
| Shelf Life | The shelf life of 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine is typically 2–3 years when stored in a cool, dry place. |
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Purity 98%: 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity profile. Melting Point 48-51°C: 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine with melting point 48-51°C is used in agrochemical formulation, where it allows precise solid-state processing and improves formulation consistency. Low Moisture Content ≤0.2%: 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine with low moisture content ≤0.2% is used in heterocyclic compound manufacturing, where it prevents unwanted side reactions and enhances product stability. Reagent Grade: 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine of reagent grade is used in medicinal chemistry research, where it provides reproducible reactivity and reliable assay outcomes. Stability Temperature up to 110°C: 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine with stability temperature up to 110°C is used in high-temperature synthesis processes, where it maintains structural integrity and consistent conversion rates. Molecular Weight 217.56 g/mol: 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine with molecular weight 217.56 g/mol is used in custom library compound development, where it enables precise molar calculations and predictable compound behavior. Assay ≥99%: 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine with assay ≥99% is used in fine chemical production, where it maximizes efficiency and minimizes by-product formation. |
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From our earliest days as a chemical manufacturer, we have committed ourselves to crafting specialty heterocyclic compounds that meet the demanding standards of discovery and bulk synthesis labs. 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine stands out among our products for its consistency in molecular integrity batch after batch. This particular pyridine derivative continues to shape progress in pharmaceutical and agrochemical research, both as a core scaffold and intermediate for larger, more complex molecules. Over the years, tens of kilograms have left our factory, each drum checked and rechecked by our own team—never outsourced, never relabelled—to ensure authenticity and reliability because we know small inconsistencies can cause expensive setbacks downstream.
Every change to a pyridine ring reshapes its electronic landscape. This compound, with its trifluoromethyl anchor at the 4-position, sets itself apart from simpler pyridine analogues: the added electron-withdrawing effect not only boosts chemical stability but also influences compatibility with strong nucleophiles and bases in subsequent coupling reactions. The ortho/para relationship of the chlorine and fluorine atoms alters the ring’s polarity and reactivity, offering an unusually robust platform for designing active pharmaceutical ingredients or fine-tuned crop protection agents.
In the lab and in the plant, we have observed distinct differences in reactivity between this molecule and its lower halogenated versions. A pyridine with only chloro or fluoro groups may come at a lower price, but reactivity and selectivity tell a different story. Chlorine at the 2-position and fluorine at the 3-position combine to create a unique steric and electronic environment, allowing for cleaner and more predictable site-specific functionalization, especially for SNAr pathways and metal-catalyzed cross-couplings.
Prepared and packed in our own on-site facility, our 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine is supplied as a clear to pale yellow liquid at room temperature. We handle this compound under an inert gas blanket to prevent hydrolysis or degradation and have never witnessed significant off-gassing or pressure build-up during normal storage with standard precautions. Our quality benchmarks always include NMR, GC-MS, and Karl Fischer analysis on every batch. Water content remains tightly controlled, and our operators receive regular refresher training on handling fluorinated organics to head off mistakes that jeopardize purity.
Handling protocols are straightforward: this compound won’t corrode equipment or attack elastomers under typical process conditions, and it remains stable in sealed glass or PTFE-lined containers. Our engineers use purpose-built filtration lines to prevent metal contamination, especially when process routes take this intermediate downstream to high-value products. Compared to some brominated or more heavily halogenated pyridines, operators find less vapor phase irritation, but we always stick to tried-and-tested PPE and local extraction on the plant floor. Waste is collected with other halogenated organics, then separated for incineration through licensed hazardous waste channels.
We began producing this molecule in the early 2010s at kilogram scale for a university spinout searching for a high-purity building block for kinase inhibitor research. Process yield was inconsistent during early campaigns, prompting deep process development work involving careful control of temperature in the trifluoromethylation step and a focus on protecting groups in the chlorination stage. With these hurdles cleared, we brought plant-scale manufacturing online and now fill orders ranging from grams for method development to multi-ton drum shipments for ongoing campaigns.
Process stability has always mattered more than simple metrics like yield. Our in-process analytics flag even tiny variances in regioisomer formation or side reactions, so our QC team intervenes early. As a result, isolate quality often exceeds listings published in most commercial catalogues. Our experience shows this extra effort delivers less downtime for scale-up users, as fewer purification steps mean fewer headaches in downstream synthesis, which keeps programs moving on deadline.
Customers searching for new molecular scaffolds turn to 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine thanks to its fingerprint pattern of reactivity. Medicinal chemists rely on it to provide a rigid yet electron-deficient core ideal for bioisosteric replacement or direct elaboration. Its unique pattern of halogen substitution sets it apart from mono-, di-, or tri-halogenated pyridines that lack trifluoromethyl presence. We’ve seen this compound drive lead optimization projects in central nervous system disease pipelines and form the backbone of next-generation fungicides targeting resistant pathogen strains.
One longstanding customer, a European innovator in agrochemical actives, stressed the value of our product’s reproducible purity when producing multi-kilogram lots for late-stage field trials. A single off-spec batch—whether from unknown by-products or regional supplier switches—could set back product registrations by months. We have tackled these risks by certifying each batch internally and with third-party labs on customer request. Delivering peace of mind matters for teams betting their program timelines on quality and reliability.
The world of halogenated pyridines is crowded with close analogues, each offering slight shifts in reactivity and physical character. We often field inquiries about whether 2-chloro-3-fluoro-5-(trifluoromethyl)pyridine or 2-chloro-6-fluoro-4-(trifluoromethyl)pyridine can substitute in an existing process. Years of scale-up campaigns and bench chemistry tell us otherwise: even a small change in the position of a fluorine or chlorine atom can reshape reactivity enough to require full revalidation, expensive method redevelopment, and sometimes even new regulatory filings.
Another key difference lies in downstream transformations: the fluoro group at the 3-position of our compound offers a reliable handle for selective substitution, while keeping metabolic stability high—valuable for pharmaceutical candidates needing resistance to oxidative pathways. The 4-(trifluoromethyl) group not only boosts lipophilicity for agrochemical bioavailability but also enhances the molecule’s process compatibility in continuous flow conditions due to its chemical inertness. For developers aiming for patient or environmental safety, these structural differences can swing a lead candidate from marginal to promising.
We manufacture and ship this pyridine derivative directly from our own plant, taking full responsibility for every lot from raw material to finished liquid. Because we synthesize our own key starting materials, we minimize risk from upstream supply volatility and offer better transparency about every drum’s history. When global fluorochemicals markets tighten, we switch to alternate proprietary supply lines and keep backup raw material on site, never compromising on our agreed timelines.
This direct relationship with end users lets us learn, year over year, how new synthetic pathways and regulatory updates affect specification requests. When a customer requested lower traces of a particular halogenated impurity, we retooled a downstream distillation cut to meet their threshold. Strategic investments in on-site analytics and batch tracking systems mean we can demonstrate both chemical traceability and lot-by-lot documentation to pass audits, a standard catalog traders and middlemen rarely match.
We believe real partnerships mean sharing technical knowledge, not just shipping drums. Each kilogram we produce carries with it insights from process and plant: how to adjust solvents to minimize formation of off-by-one regioisomers, which metal catalysts work best for specific cross-coupling steps off the pyridine core, how to ensure consistent reactivity during process scale-outs. Our customer support team—many of whom have years at the bench—fields questions not just on paperwork, but on real-world process troubleshooting, good manufacturing practices, and optimization for tighter regulatory standards.
We have guided numerous collaborative projects through technical transfer, sharing details about reaction workups, solvent compatibility, and stability on storage that save teams costly repetition and grant reviewers’ trust. Regulatory chemists value our willingness to maintain oversight through validation, keeping impurity profiles in check and providing batch documentation that can stand up to global registration scrutinies.
Producing and handling fluorinated and chlorinated compounds carries heightened duty to both worker safety and environmental stewardship. We design every manufacturing campaign around these values. Equipment is kept to the highest clean-in-place standards to prevent cross-contamination, and staff take part in regular health monitoring and process safety drills. Emissions are scrubbed and containment protocols strictly enforced; our local regulators and fire services audit us regularly, and we’ve always welcomed this oversight.
On the environmental side, we support take-back schemes and offer guidance to customers on waste segregation requirements, safe neutralization, and legal disposal channels—helping them remain on the right side of environmental compliance as rules steadily tighten. We use renewable energy where possible across our site, and ongoing investment in solvent recovery technologies lets us cut down on overall waste year on year. We are transparent about these processes because tomorrow’s customers will only trust suppliers with a visible, verifiable footprint reduction plan.
Shifting global regulations and changing access to key fluorinated reagents affect pricing and availability for everyone using specialty pyridines. Through hard-earned experience, we have seen how sudden trade restrictions or targeted supply shocks force manufacturers to be ready to adapt. We maintain strong ties to both European and Asian precursor suppliers and have expanded on-site production of critical intermediates, so our supply lines are robust even in volatile markets. Sourcing is not just a procurement exercise—it's technical risk management in action.
We also invest in next-generation process development to keep production both safer and more efficient. Where older syntheses used energetically hazardous steps or unsustainable reagents, our technical teams replace them with modern alternatives wherever possible. Recent pilot projects show promising results with low-temperature fluorination methods using greener solvents, and with continuous-flow setups that deliver more consistent product quality at higher throughputs with fewer waste streams.
Manufacturing specialty pyridines such as 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine is never simply a matter of following a recipe. Every batch benefits from years of chemical know-how, technical investment, and direct engagement with process end users. The compound’s unique substitution pattern provides clear advantages over close analogues for anyone developing pharmaceuticals or crop protection molecules that demand both stability and synthetic flexibility. Our team’s dedication to both product reliability and knowledge sharing reflects in each lot shipped, so researchers and plant managers alike can count on both supply and technical support for every challenge their project brings.
New chemical innovation, especially in regulated markets, depends on manufacturers standing behind their products—not just outsourcing and rebadging material. That’s our commitment and our heritage, reflected in every kilogram of 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine we send into the world’s laboratories and production lines.