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HS Code |
817167 |
| Productname | 3-Fluoro-4-(trifluoromethyl)pyridine |
| Casnumber | 57381-86-1 |
| Molecularformula | C6H3F4N |
| Molecularweight | 165.09 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 129-132°C |
| Density | 1.395 g/cm3 |
| Purity | Typically ≥98% |
| Refractiveindex | 1.424 |
| Smiles | FC1=CN=CC(C(F)(F)F)=C1 |
| Inchi | InChI=1S/C6H3F4N/c7-4-3-11-2-1-5(4)6(8,9)10/h1-3H |
| Solubility | Soluble in organic solvents such as dichloromethane and ethanol |
As an accredited 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 3-Fluoro-4-(trifluoromethyl)pyridine, sealed with a tamper-evident cap and labeled clearly. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-Fluoro-4-(trifluoromethyl)pyridine: Securely packed drums or containers, optimized for safe chemical transport and storage. |
| Shipping | 3-Fluoro-4-(trifluoromethyl)pyridine is shipped in tightly sealed containers under ambient or cool, dry conditions to prevent moisture or contamination. The packaging complies with chemical safety regulations, featuring clear labeling and hazard information. Shipping may be subject to local and international regulations due to potential toxicity and environmental hazards. |
| Storage | 3-Fluoro-4-(trifluoromethyl)pyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from direct sunlight, moisture, and sources of ignition. Store under inert atmosphere if specified by the manufacturer. Ensure proper chemical labeling and follow all relevant safety and regulatory guidelines. |
| Shelf Life | 3-Fluoro-4-(trifluoromethyl)pyridine is stable under recommended storage conditions; typically, shelf life exceeds two years when kept cool and dry. |
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Purity 99%: 3-Fluoro-4-(trifluoromethyl)pyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures consistent yield and product quality. Molecular weight 167.06 g/mol: 3-Fluoro-4-(trifluoromethyl)pyridine with molecular weight 167.06 g/mol is used in agrochemical R&D, where precise molecular profiling enables accurate formulation development. Boiling point 110°C: 3-Fluoro-4-(trifluoromethyl)pyridine with a boiling point of 110°C is used in solvent systems optimization, where predictable volatility enhances process control. Refractive index 1.430: 3-Fluoro-4-(trifluoromethyl)pyridine with a refractive index of 1.430 is used in analytical method calibration, where consistent optical properties improve detection accuracy. Storage stability at 25°C: 3-Fluoro-4-(trifluoromethyl)pyridine with storage stability at 25°C is used in bulk chemical inventory management, where long-term stability reduces degradation risk. Low water content (<0.1%): 3-Fluoro-4-(trifluoromethyl)pyridine with low water content (<0.1%) is used in moisture-sensitive synthesis, where minimal hydrolysis risk increases reaction efficiency. Melting point -21°C: 3-Fluoro-4-(trifluoromethyl)pyridine with a melting point of -21°C is used in cryogenic process research, where low freezing point broadens operational temperature range. |
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Working in chemical manufacturing goes beyond formulas and flasks. Day by day, we handle compounds whose impact reaches into laboratories, plant pipelines, and innovation centers worldwide. Among the broad catalog we synthesize, 3-Fluoro-4-(trifluoromethyl)pyridine stands out due to its unique molecular profile and performance history. Knowing this material from the inside—reactor setup to final distillation—we see the details hidden behind catalog entries and distributor listings.
The backbone of this compound, a pyridine ring substituted with both a trifluoromethyl and a fluoro group, gives it a chemical character not found in more basic pyridine analogs. Chemists value this one for routes where increased electron-withdrawing properties and specific substitution patterns are required. We produce it under a tightly controlled environment, avoiding batch inconsistencies that can sabotage downstream yields for our pharmaceutical and agrochemical partners. Our operators don’t just push buttons; they understand why shielding the pyridine nitrogen and carefully introducing the fluorine makes such a difference.
Model and purity matter where reactions are concerned. We see many customers who tried cheaper materials from third-party brokers, only to face sluggish reactivity or persistent byproduct problems in their drug discovery campaigns. With our direct synthesis and rigorous purification, users see fewer side spots on their TLC plates. Repeatable analysis confirms a purity of 99%+, and with every lot we release, we check for trace contaminants—sulfur, metals, or non-volatile residues—that disrupt high-sensitivity projects.
At the bench level, specifications reflect years of trial and error. We stabilize moisture using full vacuum drying cycles, and our operators—real people with skin in the game—swab transfer lines after every major run to prevent ghost peaks in the NMR. Our standard output is a clear liquid under ambient conditions, with a consistent boiling point that confirms batch-to-batch repeatability. Color, odor, and refractive index are not just numbers on data sheets to us; they’re checkpoints that keep us honest, as years of field complaints about off-odors or color shifts have shaped our standard work.
Chemical identity checks use proton and fluorine NMR as well as mass spectrometry. We test every batch ourselves, no farming it out to a third-party lab that doesn’t know our process quirks. The impurities we watch for most closely—unsubstituted pyridines, multi-fluorinated analogs—can sneak in if one step goes off track. Our crews pay attention to GMP documentation, but above all, they fix process problems before filled drums ever leave the gate.
Among pyridine derivatives, 3-Fluoro-4-(trifluoromethyl)pyridine often gets confused with either mono-fluoro or mono-trifluoromethyl analogs. In practice, those aren’t interchangeable. The combined electron-withdrawing effect shifts reactivity just enough to open up unique synthesis pathways. Our downstream partners, especially in the pharmaceutical industry, count on this to introduce specific ring positions for their APIs.
Users sometimes ask for cost comparisons. From where we stand, the savings from using cheaper substitutes often evaporate as soon as downstream reactions start failing or impurity profiles explode beyond regulatory thresholds. Plenty of labs have walked this path: opting for an alternate, then circling back to us with demands for a write-up explaining why their candidate molecules never made it past preclinical. Few alternate pyridines can match both the spectral cleanliness and reactivity of our material. Once the financial and regulatory stakes of late-stage development are on the table, those differences tell the whole story.
A process built for reliability pays off. We have learned, through our own tough experiences, that cutting corners—switching to cheaper precursors or sloppy vessel cleaning—always leads to trouble. Not once in the past decade has a relaxed cleaning schedule failed to creep back into the impurity profile somewhere. On several occasions, a change in minor process parameters led to increased side reactions, visible right away in side-by-side chromatograms.
We don’t just sell this material, we use it as an intermediate for other complex molecules. That feedback loop allows us to spot problems before they show up in our customers’ labs. Our synthesis route avoids harsh conditions that tend to produce tricky-to-remove byproducts like polyfluoro aromatics. Over the years, we have invested in in-line monitoring and precision dosing, leading to a consistent product every time.
Over the past years, several research groups shared their experiences with us. A mid-sized pharmaceutical developer switched to our 3-Fluoro-4-(trifluoromethyl)pyridine when they hit a wall with a generic alternative. Their arylation step required cleaner input to avoid time-consuming purification—by upgrading to our batch, hands-on time at the prep-HPLC dropped by 30%, with a higher isolated yield. In another case, an agrochemical formulator found that minor impurities in a competitor’s material led to plant toxicity at trace concentrations; switching to our product prevented crop loss and regulatory headaches.
Our material meets both exploratory and scale-up requirements. Researchers rely on it to move from milligram-scale lead discovery to multi-kilo pilot campaigns. We help expedite internal tech transfers—our documentation and technical backup come straight from the plant team, not from a marketing slide deck. Relationships matter, and so does clarity in seeing where each batch comes from.
Chemical synthesis isn’t a straight line. A common source of trouble comes from inconsistent raw materials; we faced a string of failed batches years ago traced to a subtle contaminant in the fluorinating agent. The fallout included costly re-runs and lost credibility. We rebuilt our raw material supplier relationships and now audit shipments on arrival.
Waste control has evolved with us. Early syntheses produced unstable byproducts that, left unchecked, worsened over the shelf life. Changing our quench protocol, and integrating faster analytical screens, eliminated a source of instability that would have kept our product off the shelf at quality-driven facilities. Involving production chemists in weekly troubleshooting meetings shrinks time to fix unexpected problems. Nobody sweeps test failures under the rug; we dig for causes until they vanish from the batch records.
We continually review our solvent use, reclaiming and recycling solvents in-house wherever feasible. This reduces environmental footprint and cost, benefitting both our neighbors and downstream users concerned about sustainable chemistry. Any time a process improvement is suggested by our operators—who see every valve and gasket up close—we take it seriously, running controlled trials before switching over to the new practice.
There’s no shortcut to trust. Repeat customers cite more than purity or data sheets—they mention responsiveness, batch traceability, and transparency about process changes. Researchers needing a reliable supply chain and fast troubleshooting get answers from our team, whose hands have actually made and packaged the compound.
Purchasers dealing with inconsistent quality from a reseller often note the difference after switching to source material from the plant where it was made. Time saved chasing batch certifications, chasing downroot causes for failing reactions, and replacing unreliable stock all carry real costs for small and large companies alike. Only source manufacturers see the full story behind each batch.
Synthesizing 3-Fluoro-4-(trifluoromethyl)pyridine has changed with advances in process chemistry. We’re in constant dialogue with academic teams pushing for greener reagents and lower-waste routes. Several process optimizations came directly from outside suggestions, rapidly tested and adopted where they made sense.
As reaction demands shift—tightened impurity specs for clinical trial material, new API candidates requiring gram-scale lots on short notice—we adapt capacity and protocols on the fly. The value of hearing back from users in real time, making changes quickly, and being accountable all along the way cannot be overstated. In an era of tightening regulations and higher standards, being the source manufacturer means carrying the responsibility for each drum and flask, and rarely does a week pass without a lesson that shapes how we move forward.
Every kilogram we ship reflects thousands of micro-decisions, planned process changes, and real hazard controls in the plant. Trust grows not from flashy guarantees but from batch records that match final analysis, and open, honest communication. In an industry where a single impurity spike can end a drug project or fail a public safety regime, there’s no room for mystery-source intermediates or last-minute substitutions.
The relationships we develop with our users go both ways. We learn from their discoveries and struggles, just as they lean on our depth of technical knowledge. There’s no substitute for talking directly to the chemist or engineer who worked through the final distillation, or for access to someone who understands how tiny batch variations ripple through multi-step syntheses.
Experience in manufacturing counts for more than clean paperwork. Each technical bulletin or lot certificate we issue comes backed by operators who have faced, and solved, the problems inherent in scaling reactive fluorinated compounds. By producing 3-Fluoro-4-(trifluoromethyl)pyridine in-house and guarding consistency at every turn, we support researchers not just with material, but with hard-won knowledge from years on the manufacturing floor. We challenge ourselves every day to keep improving—knowing that each small advance we make can turn into a breakthrough for someone many steps down the line. In a field built on precision, careful sourcing means fewer surprises and more reliable results.