|
HS Code |
834177 |
| Cas Number | 171414-63-4 |
| Molecular Formula | C7H6F3NO |
| Molecular Weight | 177.12 |
| Iupac Name | 3-methoxy-4-(trifluoromethyl)pyridine |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.316 g/cm³ |
| Boiling Point | 180-183°C |
| Melting Point | -6°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Smiles | COC1=CN=CC(=C1)C(F)(F)F |
| Inchi | InChI=1S/C7H6F3NO/c1-12-6-4-11-3-5(2-6)7(8,9)10 |
| Refractive Index | n20/D 1.431 |
As an accredited 3-Methoxy-4-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle labeled “3-Methoxy-4-(trifluoromethyl)pyridine.” Features a secure screw cap and appropriate hazard warnings. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) of 3-Methoxy-4-(trifluoromethyl)pyridine ensures secure, efficient bulk packaging for international chemical transport. |
| Shipping | **Shipping Description for 3-Methoxy-4-(trifluoromethyl)pyridine:** This chemical is shipped in sealed, chemically-resistant containers to prevent leaks or contamination. It should be transported as a hazardous chemical, in accordance with local and international regulations. Containers are securely packed with cushioning material and labeled for identification, hazard warnings, and safety compliance documentation provided. |
| Storage | Store **3-Methoxy-4-(trifluoromethyl)pyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Clearly label the container and keep it away from heat sources and ignition points. Use in a fume hood and ensure proper chemical waste disposal procedures are in place. |
| Shelf Life | 3-Methoxy-4-(trifluoromethyl)pyridine has a shelf life of at least 2 years when stored in a cool, dry, airtight container. |
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Purity 98%: 3-Methoxy-4-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side-product formation. Boiling Point 165°C: 3-Methoxy-4-(trifluoromethyl)pyridine with boiling point 165°C is used in organic solvent preparation, where precise volatility allows controlled reaction conditions. Stability Temperature up to 120°C: 3-Methoxy-4-(trifluoromethyl)pyridine with stability temperature up to 120°C is used in high-temperature catalytic reactions, where stable structural integrity is maintained. Molecular Weight 179.13 g/mol: 3-Methoxy-4-(trifluoromethyl)pyridine with molecular weight 179.13 g/mol is used in agrochemical formulation, where accurate dosing is achieved for effective crop protection. Density 1.32 g/cm³: 3-Methoxy-4-(trifluoromethyl)pyridine with density 1.32 g/cm³ is used in liquid-phase synthesis, where optimal phase separation enhances process efficiency. Refractive Index 1.455: 3-Methoxy-4-(trifluoromethyl)pyridine with refractive index 1.455 is used in analytical standard preparation, where consistent optical properties enable precise detection. Water Content <0.2%: 3-Methoxy-4-(trifluoromethyl)pyridine with water content below 0.2% is used in moisture-sensitive reactions, where low water level prevents hydrolytic degradation. Particle Size <10 μm: 3-Methoxy-4-(trifluoromethyl)pyridine with particle size below 10 μm is used in solid dispersion systems, where fine dispersion promotes homogeneous mixing. Melting Point 42°C: 3-Methoxy-4-(trifluoromethyl)pyridine with melting point 42°C is used in melt-casting technology, where controlled melting facilitates uniform product formation. UV Absorbance λmax 320 nm: 3-Methoxy-4-(trifluoromethyl)pyridine with UV absorbance λmax at 320 nm is used in spectroscopic calibration, where defined absorbance ensures analytical accuracy. |
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In the world of chemical manufacturing, there’s a constant demand for reliable, high-purity intermediates that can drive the progress of new pharmaceuticals and advanced agrochemicals. Among the many options, 3-Methoxy-4-(trifluoromethyl)pyridine has started to catch the attention of both chemists and formulators. This compound combines a pyridine ring with two important modifying groups: a methoxy and a trifluoromethyl, each in a finely tuned position. Over years on our lines, we've seen first-hand how small adjustments in a molecule can go a long way toward improving reaction pathways or end-product stability. From the daily wear on our synthesizers to conversations we’ve had with our clients in R&D, this compound stands out for reliability and adaptability in complex syntheses.
Let’s dig into what makes this molecule interesting. The pyridine ring alone grants notable chemical robustness, which remains an anchor point for diverse transformations. Our in-house analytical team always looks for site-selectivity, and with the methoxy group at the 3-position and the trifluoromethyl group at the 4-position, this arrangement fosters useful electronic effects. These two groups don’t just bring chemical activity—methoxy groups encourage nucleophilicity, trifluoromethyls add both lipophilicity and metabolic stability. Their exact orientation means that downstream reactions—things like cross-couplings or nucleophilic aromatic substitution—run cleaner and with fewer side-products compared to unsubstituted pyridines or even to similar derivatives.
On our production floor, the appeal of 3-Methoxy-4-(trifluoromethyl)pyridine comes down to reproducible results. Over multiple batches, we’ve tuned crystallization and purification steps, squeezing out less than 0.2% water content and maintaining purity over 98% as confirmed by HPLC and NMR screening. We invest in column chromatography and careful distillation steps because any lingering precursor or byproduct can throw off subsequent reactions. Chemists want confidence: nothing ruins a scale-up like finding you’ve introduced a UV-absorbing impurity that mucks up the next stage. Minimal residual solvents and a well-controlled particle size make this product compatible with automated dosing systems, which helps speed up lab and pilot plant protocols.
In our daily dealings with synthetic chemists, we see this compound hit the bench for different reasons. Medicinal chemists make frequent use of it as a core starting material for the construction of central nervous system (CNS) active agents and anti-inflammatory leads. The electron-rich methoxy paired with the inertness of the trifluoromethyl often allows for careful tuning of ADME properties in new drug candidates—a story we’ve followed by supporting collaborators as they optimize molecules for better brain penetration or for resistance to metabolic breakdown. On the agrochemical side, research groups come to us looking for new scaffolds to resist environmental degradation. It’s become apparent from feedback that the trifluoromethyl group grants desired weather-resistance and foliage retention, something not always possible with other functionalized pyridines.
We’ve fielded plenty of questions about solvent handling and compatibility. This material cleans up easily in standard organic solvents. Its low volatility compared to lower-mass pyridines means less loss during transfer and evaporation. Our own teams prefer it in acetonitrile and ethyl acetate, depending on reaction needs. Stability holds up over longer storage times—something many early-stage researchers appreciate when stock compounds sit on shelves for extended periods before analysis starts in earnest.
On the ground, producing 3-Methoxy-4-(trifluoromethyl)pyridine presents challenges many might overlook when reading clean data tables in catalogs. The precursor synthesis, especially introducing the trifluoromethyl group, asks for careful control to avoid byproducts or over-fluorinated contaminants. We’ve retooled reactors and invested in new fluorination equipment to ensure we minimize waste and protect our operators, especially when scaling up from bench runs to hundreds of kilos. Handling pyridine derivatives calls for ventilation and odor control—something that’s easy to forget in R&D, but essential at commercial scales.
Raw materials play a big role. Global supply of fluorinating agents can fluctuate, especially when upstream producers pause for maintenance or environmental upgrades. Flexible purchasing teams stay tuned in to these shifts and keep the necessary stocks, so our production teams don’t get bottlenecked trying to rush orders or hunt for substitutes. Years ago, hiccups in fluorine supply set us back for weeks, and regular communication with suppliers is now a baked-in habit.
After shipping out thousands of kilos and listening to chemists recap their projects, certain differences feel obvious. Direct analogs lack the same level of metabolic robustness. Pyridine itself, or monofunctionalized versions, often show more reactivity than needed, leading to degradative side reactions or instability in finished products. When comparing to closely related 3-methoxypyridines without the trifluoromethyl group, final compounds typically lose out on lipophilicity and resistance to enzymatic degradation, which matters in both medicines and crop-protection agents exposed to harsh environments.
Competition sometimes points to alternative trifluoromethylated pyridines, but customer feedback tells another story. The methoxy group encourages certain palladium-catalyzed couplings and facilitates easier derivatization—and experiments on our pilot lines support these claims with measurable yields, not just theoretical predictions. We’ve also found that in multi-step syntheses, fewer purification stages are needed downstream when starting with this compound, which cuts costs and saves time for our process partners.
Every manufacturer knows that scale introduces new hazards. Unlike bulk pyridine, this product releases a milder odor and, thanks to its solid-state or viscous-liquid form, doesn’t vaporize as quickly. We recommend handling it in well-ventilated spaces, with nitrile gloves and splash protection for operators who have to manage large pours or clean-ups. Our incident logs show that routine attention to PPE and prompt wipedown of drips keeps incidents rare. Storage in airtight high-density polyethylene drums extends its shelf life and protects it from humidity, which otherwise promotes minor hydrolysis over long periods.
Waste streams from clean-up and wash cycles require thoughtful disposal. We maintain on-site reclaiming systems to recover solvents and neutralize traces before they leave our plant. These practices not only keep us in line with local and international safety rules, they also help us keep manufacturing costs in check as waste-related fees rise year after year. In practical terms, our crews benefit from these routines: less exposure, less downtime, and better predictability for production schedules.
In a recent collaboration on a novel kinase inhibitor, our customer’s lead compound suffered acidic instability during late-stage functionalization. Substituting with 3-Methoxy-4-(trifluoromethyl)pyridine tightened up the profile, giving a higher yield and better crystallinity for downstream salt formation. Years ago, a major crop-science inquiry focused on finding a more weather-resistant active for a fungicidal spray. Through multiple runs and tweaks, we saw that trifluoromethyl substitution cut photodegradation by nearly half compared to older pyridine scaffolds. Those savings, in turn, supported the customer’s environmental registration and batch consistency across field trials.
Stories like these underline something we’ve learned time and again: new chemical entities are only as good as the base materials feeding into them. Chemists spend months on design and optimization, but if the building block isn’t pure or stable, the whole project falters. Every time a customer squares away a critical intermediate in their pipeline, our phones ring with new requests for tighter specs or larger batch sizes—a sign that operational reliability generates real-world momentum.
We don’t see product lines like this as static offerings. As downstream industries demand more selective, environmentally aware, and robust molecules, our production approach evolves. We collaborate closely with end users during process validation trials, sometimes altering crystal forms or adopting greener solvents to fit their regulatory or operational needs. Often our chemists join calls with customer labs to troubleshoot sticking points in synthesis, offering advice drawn from experience handling dozens of similar pyridine derivatives.
Increasingly, regulatory frameworks ask for both full chemical traceability and cleaner footprints on every product. Meeting these needs goes beyond simple compliance. Documenting each step of our sourcing, reaction monitoring, and quality checks builds trust over time and saves both us and our customers headaches during audits and filings. Our approach has leaned toward in-process analytical techniques—routine LC-MS checks, and real-time impurity tracking—so we can flag and fix issues before product ever leaves the door.
On the factory floor, new equipment has allowed us to recover more solvents and scrub off-fluorinated materials, reducing both emissions and raw material demand. Installing continuous feed systems has trimmed down the time between lots and improved consistency, a lesson we learned from scaling smaller multipurpose reactors into larger, continuous-batch hybrids. Energy audits and dovetailing with local waste reprocessing centers have helped set a higher bar for sustainability in a sector where legacy practices sometimes hold back progress.
Partnering with universities and research consortia keeps us at the edge of new synthetic routes. Through these relationships, we’ve trialed alternative fluorination reagents that promise to cut costs and minimize hazardous waste. Some experimental routes—like electrochemical activation or gas-phase functionalization—haven't reached full-line implementation yet, but early results point in promising directions. Practicality always leads our decisions—solutions only help if they keep end-use costs down and fit real production schedules.
No manufacturer works in a vacuum. Real-world supply chains remain vulnerable to disruption—shipping delays, regulatory shifts, or upstream chemical shortages. The lessons we’ve drawn from past bottlenecks shape current protocols: holding extra stocks of rare reagents, cross-training logistics staff to reroute orders during volatility, and building in rapid analytical verification for alternate raw material lots. We keep open lines with our most frequent customers, sharing forecasts and risk assessments so nobody gets caught by surprise.
Ongoing trade tension or local regulation changes do ripple through pricing and lead times. Our focus remains on transparent pricing models, plain feedback when things get tight, and quick updates if supply issues look likely. A couple years back, tightness in global fluoroaromatic feedstocks led us to lean harder on our local producers, supporting their upgrades in exchange for forward commitments. Those deals shaved months off fulfillment for pharmaceutical partners locked to tight clinical timelines.
As regulatory expectations raise the bar for molecular safety and sustainability, well-characterized building blocks like 3-Methoxy-4-(trifluoromethyl)pyridine become vital. Over the next few years, we expect to see this compound push farther into both specialty pharma and high-performance materials. Its value doesn’t lie in a single reaction or application—it’s in how it responds to the evolving demands of researchers looking to innovate in crowded fields.
Feedback from our clients continues to drive expansion, not just in output tonnage but in the granularity of support we provide. Routine engagement with formulators, analytical labs, and regulatory specialists shines a light on new challenges we want to help solve, from sharper impurity monitoring to more efficient solvent recovery.
Looking back over the years, this sort of progress comes not just from new machines or certifications, but from meaningful relationships with companies and individual chemists willing to share their hurdles and wins. Every batch we ship, every sample we rush across the world, builds on those cumulative experiences—a reminder that genuine partnership and continual adaptation keep our industry moving forward.