|
HS Code |
527088 |
| Cas Number | 349-21-5 |
| Molecular Formula | C7H3F3N2 |
| Molecular Weight | 172.11 |
| Appearance | White to off-white solid |
| Melting Point | 50-54 °C |
| Boiling Point | 233-234 °C |
| Density | 1.38 g/cm3 (estimated) |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CN=CC(=C1C#N)C(F)(F)F |
| Inchi | InChI=1S/C7H3F3N2/c8-7(9,10)5-1-2-12-3-6(5)4-11/h1-3H |
| Refractive Index | 1.468 (estimated) |
| Flash Point | >110 °C (estimated) |
As an accredited 2-(trifluoromethyl)pyridine-4-carbonitrile 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 "2-(trifluoromethyl)pyridine-4-carbonitrile", with hazard symbols and batch information displayed. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-(trifluoromethyl)pyridine-4-carbonitrile involves secure packing, proper labeling, and moisture protection for bulk shipping. |
| Shipping | 2-(Trifluoromethyl)pyridine-4-carbonitrile is shipped in tightly sealed containers, protected from light and moisture. The chemical is typically dispatched as a solid, following all relevant handling and transport regulations for hazardous substances. Ensure the package is clearly labeled and accompanied by Safety Data Sheets (SDS) for safe delivery and compliance. |
| Storage | 2-(Trifluoromethyl)pyridine-4-carbonitrile should be stored in a cool, dry, and well-ventilated area, away from sources of heat and ignition. Keep the container tightly sealed and protect it from moisture and direct sunlight. Store separately from strong oxidizing agents and incompatible chemicals. Ensure proper labeling and use a chemical storage cabinet if available. |
| Shelf Life | 2-(Trifluoromethyl)pyridine-4-carbonitrile is stable under recommended storage conditions, with a typical shelf life of 2-3 years. |
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Purity 99%: 2-(trifluoromethyl)pyridine-4-carbonitrile with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and reproducibility of target molecules. Melting Point 86°C: 2-(trifluoromethyl)pyridine-4-carbonitrile with melting point 86°C is used in fine chemical manufacturing, where it provides optimal processing and handling efficiency. Molecular Weight 172.1 g/mol: 2-(trifluoromethyl)pyridine-4-carbonitrile with molecular weight 172.1 g/mol is used in agrochemical active ingredient design, where it contributes accurate dosage formulation. Particle Size <50 μm: 2-(trifluoromethyl)pyridine-4-carbonitrile with particle size less than 50 μm is used in catalyst development, where it enhances surface area and reaction rate. Stability Temperature up to 150°C: 2-(trifluoromethyl)pyridine-4-carbonitrile with stability temperature up to 150°C is used in high-temperature organic synthesis, where it maintains compound integrity under reaction conditions. Water Content <0.2%: 2-(trifluoromethyl)pyridine-4-carbonitrile with water content under 0.2% is used in moisture-sensitive API production, where it prevents hydrolysis and quality degradation. Colorless Crystalline Form: 2-(trifluoromethyl)pyridine-4-carbonitrile in colorless crystalline form is used in analytical reference material preparation, where it allows accurate spectroscopic characterization. |
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In our years producing specialty chemicals for the pharmaceutical and agrochemical sectors, certain intermediates stand out both in reliability and in the reactions they support. 2-(trifluoromethyl)pyridine-4-carbonitrile, with model identifiers often referred to as TFMP4CN, has marked itself as a solid intermediary in nitrogenous heterocycle chemistry. We focus on quality during the synthesis, starting with raw material selection through purification to the steady analysis holding each batch to not less than 99% purity by HPLC. Pale yellow to off-white powder or crystalline forms, the compound arrives stable, easy to handle, and straightforward to dissolve in most aprotic organic solvents.
Our team values consistency, especially with intermediates like this one. Each batch runs through a rigorous routine: controlled temperature synthesis, waste minimization, and tight storage protocols, ensuring neither degradation nor residual moisture differences between lots. Over time, we have upgraded our reactor setups to extract sharper yields and pressed for greener reagents where possible. What manufacturers end up with is a material truly designed for multiple synthetic applications—a compound not fighting with trace impurities, not weakening over storage, and not showing unexpected peak overlaps in NMR or GC/MS checks.
We see direct requests from both pharmaceutical developers and agrochemical project managers because TFMP4CN aligns with large-scale aims. The trifluoromethyl and cyano groups both influence downstream reactivity: introducing electron-withdrawing character that stabilizes adjacent intermediates and tailors biological activity in target molecules. In real projects, we notice chemists using this compound for:
One synthetic chemist let us know their switch to our material cut down on reaction by-products, which tied directly to time savings downstream—less effort chasing unwanted peak isolation or chromatographic separation. In another process, the predictable reactivity of both the trifluoromethyl and the cyano features led to higher regioselective substitution, raising product yield in multi-step syntheses.
Not all pyridine intermediates behave the same way under modern coupling or cyclization conditions. Our facility has compared TFMP4CN with closer analogs, such as 2-cyanopyridine or 4-trifluoromethylpyridine. The dual substitution—trifluoromethyl at the 2-position, cyano at the 4-position—pulls electron density from two opposed sites, modifying reactivity at both the ring and substituents. This dual effect differs starkly from compounds substituted at a single position or lacking strong electron-withdrawing groups. Reactions like nucleophilic aromatic substitution or cross-coupling benefit: leaving groups activate more predictably, and downstream transformations avoid erratic yields or intractable side products.
Scale-up also sets this product apart. Several other pyridine derivatives face issues with solubility or hydrolytic instability. TFMP4CN handles moisture better in solid form and tolerates multiple organic solvents, which makes it easier to integrate into pilot reactor workflows. Its melting range—neither ultra-high nor too soft—prevents handling headaches, whether a customer receives drums or smaller sealed kegs. In regular solvent screens, we find the material dissolves smoothly into acetonitrile, THF, or even less polar ethers—rare versatility among heterocyclic nitriles.
Our hands-on manufacturing process cuts out surprises. Raw pyridine comes in with trace analysis reports, and we test each incoming drum for metals, isomeric content, and residual solvents. Our team chooses only the lots that fit tight spectral windows. Each stage—nitrile introduction, trifluoromethylation—gets batch-specific monitoring by FTIR and NMR, checked side-by-side with internal reference spectra from previous runs. Some competitors lean on contract blenders or skip hands-on quality assurance, which leads to run-to-run fluctuation and headache-inducing chromatography later. Our customers expect repeatable quality, which means we tune purification strategy for every kilogram.
We stock high-wattage rotary evaporators, jacketed reaction vessels, and continuous-flow pumps for these specialty products. Our personnel know how to quench excess reagents efficiently, and every final lot lands in a moisture-controlled vault before shipment. These steps sound routine, but even a small lapse alters dissolution rate, yield, or shelf life for the end user. With years spent dialing in the process, we avoid product recalls and bypass rework cycles, letting our partners focus on synthesis and scale without interruptions.
Pharmaceutical process chemists gravitate toward TFMP4CN for late-stage diversification. Medicinal chemistry teams aim for quick analog libraries, and the stability under cross-coupling—especially with palladium or nickel—cuts days out of their workflows. In an antimalarial program, one research team reported sharper NMR signals in downstream intermediates, a testament to low trace impurity in the starting material. They matched our COA to their independent analyses, noting overlap in both purity and melting point.
Agrochemical researchers need intermediates that withstand tough process conditions without forming side products difficult to separate at kilogram scale. One customer outlined the comparison with a mono-substituted analog, where background decomposition stained their final product. Switching to our material lifted yield and improved color, reducing purification cycles and offering a more convincing purity spec to their clients. Their own QA tests, run blind with other market options, repeatedly landed our samples at the top for moisture and impurity profile.
Manufacturing trifluoromethylated pyridines demands attention to both workplace safety and external environmental controls. The trifluoromethyl group brings both synthetic benefits and regulatory scrutiny, so we enforce active capture on fluorinated waste streams, recycle solvents within closed-loop systems, and maintain detailed batch traceability, from nitrile raw material through to final product. Our plant has committed to lower solvent emissions, replacing traditional chlorinated solvents with less persistent alternatives once validation completes.
On site, every reaction vessel channels through carbon capture filtration before venting. Routine soil and water samples taken around our facility’s perimeter verify that no fluorinated by-products escape into nearby land or water. Our operators carry out monthly certification on their handling techniques, and outside auditors review every step—from raw material arrival down to blend and pack-out. It takes daily discipline to keep these standards sharp, but the payoff comes in both safer workplaces and in a minimized environmental footprint.
Consistent performance starts at storage. Our experience shows that, though stable, this compound shows best purity over the long-term if kept under argon or nitrogen, and transferred only in dry rooms at humidity under 50%. We ship in impact-resistant, sealed containers. The crystalline product resists caking and clumping, and we include desiccants to catch any stray moisture from the warehouse to your bench. For routine use, we advise researchers to reseal partial containers—simple attention to this step lets the original purity stretch much further.
During transfer operations, our team always works under local exhaust, wearing gloves and safety glasses, following the material safety protocols developed in our own labs. Spills clean up rapidly with absorbent pad and waste funnel, and we collect the recovered powder for fluorinated waste recycling, ensuring no loss into regular solid waste streams. With this compound, a little attention in the handling room translates to fewer surprises during reaction setup and less need for purification tweaking.
We actively partner with academic groups and start-ups pushing boundaries in pyridine-based chemistry. By reviewing their published data and offering our analytic support, we help uncover reaction pathways where 2-(trifluoromethyl)pyridine-4-carbonitrile brings new selectivity or enables unique structural motifs. Collaborators have credited better isolation of intermediates and more robust final product profiles to our tailored material. We work side by side, optimizing both scale and prep—never sending generic stock but checking analytic match whether for milligram runs or multi-kilo pilot lots.
Our own R&D group tracks the latest literature and keeps up with advances in C–H activation, transition-metal catalysis, and green chemistry flows. When novel synthetic methods show merit, we experiment with parallel batches to drive process innovation in-house. Feedback loops back from customers and research labs influence next-generation facility upgrades, automation steps, and trace impurity controls.
Every batch carries the sum of our lessons learned—each error traced, every impurity identified and removed. We’ve seen what happens if trace moisture lingers: yield drops, new peaks crop up on HPLC, product turns from sharp crystal to lump. Reagents chosen carelessly bring colored contaminants or fail to yield high enough conversion in the key reaction, so we qualify all suppliers down to their last detail.
Longer-term, process optimization has made TFMP4CN one of the most predictable intermediates leaving our lines. We have engineered reactor scale-outs and adjusted agitation speeds to minimize local heat spikes, holding consistent temperature during the exothermic stages. Our packaging crews worked through every shipment scenario—solidifying protocols so the material arrives at destination at the same purity as it left the reactor. These quality guardrails mean researchers don’t lose precious time undoing variability—experiments repeat as-planned, project timelines hold, and regulatory expectations get met.
End-users rely on precision at every stage. We see paperwork as important as the powder. Each outgoing drum or flask comes with a full analysis: HPLC trace, NMR, water content by Karl Fischer, melting point, and full impurity profile. Some customers include our certificate directly in their regulatory filings. Having this assurance cuts risk during audits and saves precious time at new drug approval checkpoints. Our own lab equipment receives routine calibration cross-checked against national standards, and analysts train continually in both classic and advanced methods.
Some entrants in the market offer lower-priced options but skimp on analysis or gloss over batch-to-batch quality. Our approach stands firm—we share in-depth data and open our facility for on-site audits. We run confirmatory tests alongside customer QC teams; side-by-side checked samples routinely demonstrate tightest impurity limits, robust infrared spectra, and correct lot color and melting range. Our focus on documentation reflects a wider responsibility to both immediate purchasers and the broader research community counting on reliable building blocks.
Decades of hands-on manufacturing led us to see this intermediate not just as a market product, but as the extension of process know-how, lab discipline, and partnership with user communities. Small tweaks in purification environments, updated reactor linings, better solvent recovery—each step reflects a long conversation with users at the chemistry bench and production line. The most rewarding feedback comes not as awards but as repeat business, long-term contracts, and stories from clients who hit a research milestone using our material.
We never stand still on quality or performance. Our team invests in new production lines, recalibrates equipment to stretch both yield and trace impurity limits downward, and upgrades analytic protocols with every technical advance. Research feedback and batch returns (rare but always teaching something new) shape new standard operating procedures. Our team walks the lines, not just the boardrooms—we see first-hand where chemistry meets manufacturing reality, and those details make all the difference.
We see growing demand for tailored pyridine derivatives across industries, driven by innovations in small-molecule therapy, sustainable crop chemistry, and functional materials. Work in each sector points toward higher standards for both purity and process sustainability. As consumer expectations shift toward traceable ingredients and local compliance, our manufacturing aims to deliver both best-in-class intermediates and transparent supply chain practices.
Every year brings new technical regulations and higher analytic expectations. We prepare for each shift in the marketplace by maintaining discipline in batch production and alignment with real-world synthetic needs. Our plant remains flexible—able to increase throughput, adapt packaging, and pivot supply in response to customer developments. By sharing knowledge and maintaining face-to-face ties with users in industry and academia, we see not just the product but the applications it unlocks: sharper medical breakthroughs, smarter agrotech molecules, and cleaner, clearer production lines.
Across decades and thousands of kilograms, our commitment never changes—championing 2-(trifluoromethyl)pyridine-4-carbonitrile as both a building block and a signal of what responsible manufacturing delivers. Every lot, every shipment, and every client conversation builds toward safer chemistry, smarter processes, and a more reliable supply for chemical innovation.