|
HS Code |
314923 |
| Chemical Name | 6-(trifluoromethyl)pyridine-2-carbonitrile |
| Molecular Formula | C7H3F3N2 |
| Molecular Weight | 172.11 |
| Cas Number | 89855-30-7 |
| Appearance | White to off-white solid |
| Boiling Point | 218-220°C (estimated) |
| Melting Point | 61-63°C |
| Density | 1.37 g/cm3 (estimated) |
| Smiles | C1=CC=NC(=C1C#N)C(F)(F)F |
| Inchi | InChI=1S/C7H3F3N2/c8-7(9,10)5-2-1-3-12-6(5)4-11/h1-3H |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Refractive Index | 1.480 (estimated) |
As an accredited 6-(trifluoromethyl)pyridine-2-carbonitrile 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 6-(trifluoromethyl)pyridine-2-carbonitrile, tightly sealed with a screw cap and labeled for laboratory use. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 6-(trifluoromethyl)pyridine-2-carbonitrile: Secure, sealed drums or bags loaded efficiently, ensuring chemical safety and compliance. |
| Shipping | 6-(Trifluoromethyl)pyridine-2-carbonitrile is typically shipped in tightly sealed containers, under dry and cool conditions to prevent moisture ingress. It is packaged and labeled according to regulatory standards for hazardous chemicals, with proper documentation, and transported in compliance with local and international shipping regulations for toxic and potentially flammable compounds. |
| Storage | Store **6-(trifluoromethyl)pyridine-2-carbonitrile** in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, preferably in a designated chemical storage cabinet. Avoid exposure to direct sunlight and sources of ignition. Follow all standard laboratory safety protocols for handling and storage of organic chemicals. |
| Shelf Life | **Shelf Life:** 6-(Trifluoromethyl)pyridine-2-carbonitrile is stable under recommended storage conditions; shelf life is typically 2–3 years when kept cool, dry, and sealed. |
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Purity 99%: 6-(trifluoromethyl)pyridine-2-carbonitrile with 99% purity is used in high-precision pharmaceutical intermediate synthesis, where it enhances API yield and minimizes by-product contamination. Melting point 56°C: 6-(trifluoromethyl)pyridine-2-carbonitrile with a melting point of 56°C is used in specialty organic electronics manufacturing, where it allows for controlled crystallization and uniform film formation. Stability temperature 120°C: 6-(trifluoromethyl)pyridine-2-carbonitrile with a stability temperature of 120°C is used in agrochemical active ingredient formulation, where it ensures thermal reliability during formulation processes. Particle size <20 µm: 6-(trifluoromethyl)pyridine-2-carbonitrile with particle size less than 20 µm is used in advanced catalyst production, where it promotes homogeneous dispersion and improved catalytic performance. Water content <0.1%: 6-(trifluoromethyl)pyridine-2-carbonitrile with water content below 0.1% is used in moisture-sensitive organic coupling reactions, where it prevents hydrolysis and ensures reaction selectivity. |
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In the field of fluorinated heterocycles, 6-(trifluoromethyl)pyridine-2-carbonitrile has built its own reputation, not because of abstract potential, but because real-world chemists keep returning to it for reliable results. Anyone synthesizing molecules at scale knows perfection remains a moving target, yet this compound consistently produces predictable, clean outcomes when introduced into complex organic transformations.
As factory chemists, our daily work runs deeper than juggling theoretical benefits or summarizing literature claims. Years spent synthesizing, purifying, and shipping this compound reveal where it truly matters. We have handled tons, not just grams or lab-scale flasks. Watching how 6-(trifluoromethyl)pyridine-2-carbonitrile integrates into process flows, how it withstands variable conditions, and how its properties open new synthetic routes, gives a perspective only found in the trenches of industrial chemistry.
On any manufacturing line, the story starts with crystal clarity: purity matters most. With 6-(trifluoromethyl)pyridine-2-carbonitrile, we've seen even fractional impurity levels heighten downstream risk in pharmaceutical and agrochemical ventures. Impurities can sneak into every subsequent derivatization, sometimes throwing off late-stage results. Through continuous process control, HPLC, and robust analytical checks, we consistently produce batches that meet exacting standards, often surpassing 99% purity. The residue on filtration, the appearance under UV, and the chromatogram peaks all tell their story. Repeat customers have pointed out that even after months in storage, the material shows little to no visible decomposition; this stability grows from investments we made at the process design stage, not just in marketing copy.
Those with pilot plants or production-scale ambitions know lab purities rarely transfer seamlessly. Our facilities adjusted temperature profiles, developed custom catalysts, and modified extraction protocols to keep batch-to-batch variation in check, especially when cranking out hundreds of kilograms. The result: a stable supply chain, no sudden spikes in off-spec lots, and no last-minute firefighting. Working directly with API development teams, we’ve observed fewer purification headaches when using our batches—the strongest endorsement any synthetic lab can earn.
An experienced eye spots the trifluoromethyl signal on NMR from a distance. It’s not just another decorative fluorine, but a group that can entirely shift a molecule’s reactivity. In pyridine rings, this group brings electron-withdrawing strength, shaping both nucleophilic and electrophilic substitution patterns. Over time, medicinal chemists gravitate to this motif for its impact on metabolic stability and binding affinity. Agrochemical innovators explore the same feature for pest resistance or weather-fastness.
We have seen this particular scaffold underpin active pharmaceutical ingredients, advanced intermediates, and even specialty dyes. Because the trifluoromethyl sits at the 6-position, it tunes the basicity and hydrogen-bonding—empowering it to behave differently compared to isomeric cousins. Within our customer base, development teams report cleaner routes to next-generation kinase inhibitors and other bioactive targets, as this motif often inserts with high selectivity.
Placing a nitrile at the 2-position on the pyridine core isn't cosmetic. Stepping through one synthetic campaign after another, the nitrile’s value becomes clear. It drives cyclization, fosters amide or carboxylic acid transformations, and opens a gateway to heterocycle diversification. This handle streamlines late-stage modifications, helping research groups shorten step counts and reduce waste. Engineers in our own team have devised efficient hydrogenation and hydrolysis paths, unlocking further downstream products directly from our intermediate.
Many industrial customers shared stories about trying to retrofit less-activated analogs without the nitrile, only for their yields to plummet or their purifications to stall. We have repeatedly watched process chemists circle back to this exact compound, after facing stubborn obstacles elsewhere.
Numbers like melting point, moisture content, and assay values sound reassuring, but anyone who works at scale knows those figures hide their own stories. We've had batches conforming perfectly on paper, yet minor changes in crystal habit or particle size tell us more than spec sheets ever will. Years of hands-on adjustments in drying protocols or crystallization temperature profiles have let us fine-tune flowability and minimize fines carryover. This becomes vital during transfer to reactors or formulation hoppers.
In pharmaceutical settings, a granular understanding of polymorph control and residual solvent levels shows up in audits and documentation. Our team invested in closed-system drying and continuous filtration strategies that minimize unwanted variability. Innovations here lifted our product into a different quality bracket compared to early efforts. When production lines run thousands of vials, even minor process stutters scale up to lost time and product costs. Upstream attention to real-world factors keeps everything else running smoothly.
Chemists don’t search out 6-(trifluoromethyl)pyridine-2-carbonitrile unless their targets demand more than just routine transformations. Over time, we’ve observed our customers gravitate to this intermediate when seeking robust performance under challenging conditions. Medicinal and process chemists continue to describe its use in Suzuki-Miyaura coupling, where the stubbornness of some aryl halides gives way when handled alongside our nitrile derivative.
Many development chemists also harness the site-selective reactivity enabled by the trifluoromethyl and nitrile duo for building complex heterocycles or advanced fragments. Crafting targeted bioactivity or agrochemical selectivity often starts with choices made at the intermediate stage—and this is a favored choice where thermal and chemical stability can make or break a synthetic route. On our end, we hear repeatedly about step reductions, cleaner cleavages, and robust downstream manipulations that owe their success to the reliability offered here.
In analytical research, the distinctively sharp signals in NMR and MS allow rapid tracking in multi-step synthesis, freeing up project capacity rather than eating up hours on troubleshooting. When the real-time need for rapid turnaround trumps academic neatness, choosing our grade keeps whole teams on schedule.
Many in the field compare this molecule with simpler fluoropyridines or pyridines bearing other functional groups. We’ve compared head-to-head—sourcing, handling, and converting the methyl, fluoro, and cyano analogs through dozens of reactions. The stability brought by the six-position trifluoromethyl simply outpaces others, particularly under oxidative or high-temperature conditions. The nitrile boosts versatility, rapidly unlocking a broader horizon of downstream options via imidate, amide, acid, or amine pathways. These functional levers are less accessible with simple 6-fluoropyridine or 2-methyl analogs.
From airflow in the drying oven to the residues on the glassware, the difference lands in small but significant ways. Practicing chemists recognize the boost in reaction selectivity and yield, choosing this intermediate when project failure isn’t a viable option. Our own teams notice that using less robust analogs in scale-up experiments resulted in more frequent rework and unanticipated byproduct formation, leading to costly troubleshooting and batch recall.
Producing a specialty intermediate like this calls for attention far beyond the reaction vessel. Compliance with international standards for residual solvents, trace metal content, and REACH-related documentation comes from repeated inspection and audit cycles. Our batches cross borders for clinical research, regulatory active ingredient testing, and large-scale contract manufacturing—each setting its own hoops to jump through. Decades of chemistry experience reinforce the lesson: keeping quality high at the source always beats scrambling when regulators come knocking.
Over time, we’ve implemented real-time monitoring of critical process parameters, enabling data-driven corrective action if even subtle deviations appear. Our documentation package travels with every shipment, detailing everything from spectral verification to batch history and shipping traceability. Nobody wants phone calls about missing paperwork or mismatched certification. Avoiding delays and rejection at customs or inspection comes from this persistence and attention to detail.
No large-scale chemical product tells a clean, linear story. A few years ago, we handled a batch where trace chlorinated byproducts spiked unexpectedly high. The cleanroom sensors and vigilant QC chemists spotted off-hue crystals at the drying stage. Rapid root cause analysis backtracked the issue to a minor solvent contamination. Instead of quietly blending away the evidence, we held the entire lot, reprocessed it, and upgraded our solvent supply chain. That decision paid off in the long run: our partners and customers didn’t face unplanned impurities, and we strengthened our reputation for transparency. This isn’t a selling point plucked from a brochure—it’s daily practice earned through hard experience.
We’ve also adapted our drying and packaging processes following years of data showing that even marginal exposure to ambient humidity during transfer slightly increased hydrolysis products. These aren’t details that show up in glossy marketing, but in real production life, those adjustments protect customer projects and save both headache and money. Constant feedback from buyers, chemists, and regulatory auditors drives our process evolution: persistent small optimizations yield the steady product quality others often chase but rarely catch.
Raw materials for fluorinated building blocks fluctuate in price and availability. For 6-(trifluoromethyl)pyridine-2-carbonitrile, we forecast purchasing 12–18 months out, building redundancy across geographic regions. Years of supply chain vigilance mean that surges in raw material cost or shipping slowdowns cause less disruption. We run regular scenario planning in both scheduling and logistics.
For customers organizing multi-ton campaigns or multi-year research contracts, knowing their supply won’t suddenly blink out is more valuable than shaving a few cents per kilo off the rack rate. Teams running short of this intermediate face project delays that ripple all the way to clinical trial launches or field study windows. Working out direct, transparent relationships with fluorochemical and solvent suppliers keeps our ship steady even through unexpected global events.
Certain powder handling systems or larger packaging options have come directly from feedback at partner manufacturing plants. The goal: minimize transfer loss, speed up charging, and keep worker exposure as low as possible. Changing up drum linings and neck diameters sounds dull unless you’ve watched a busy crew lose precious hours and kilos in awkward transfer operations. Every process tweak or supply contract adaptation carries with it a decade’s worth of conversations with users and factory engineers.
Our direct customers range from multinational pharmaceutical groups to university research labs and contract formulation outfits. A unique feature of this market: researchers constantly push the boundary on what’s possible, then discover their best-laid synthetic plans grind to a halt due to intermediate or impurity issues. Time and time again, we’ve been pulled into troubleshooting sessions, running parallel batch tests in our plant to mirror customer issues. Sometimes it means tweaking crystallization; sometimes re-optimizing filtration or switching solvents. These stories usually end with a learning that becomes standard practice, not just for us but baked into our broader customer support.
Scientists in the know often request targeted analytical profiles or customized impurity thresholds. While meeting these bespoke requirements taxes our QC staff, the knowledge cycles back into our production and gives every subsequent batch a higher standard. Direct dialogue with process development teams steers us toward better solutions—whether it’s reducing trace chloride carryover, tuning particle size for automated feeders, or embedding secondary containment measures for operators. Long-term users appreciate that we don’t just sell kilos; we share data, methods, and troubleshooting advice based on actual manufacturing reality, not internet speculation.
Many customers in this chemical class report hard lessons with goods sourced from traders or brokers. Often, these intermediaries lack deep knowledge of actual manufacturing steps or supply conditions. In contrast, coming direct to a manufacturer—one who has run continuous process improvements and suffered the consequences of their own mistakes—means getting not only a product but all the accrued hard-fought know-how. We talk chemistry, not box-ticking logistics.
Regular visits from purchasers and technical teams let them walk our lines, check our logs, and conduct joint risk assessments. This transparency saves time and builds trust deeper than third-party “quality assurance” promises can reach. Our bulk buyers even deploy their own process engineers to test pilot lots on site, catching potential integration issues before full-scale scaling. This kind of partnership only emerges when molecules are made, not traded.
Fluorinated compounds draw their share of environmental scrutiny, yet ignoring sustainability only kicks the can down the line for the next operator. Real progress here happens at the plant: we continually refine recycling and abatement setups, monitor effluent closely, and keep solvent recovery rates high. Our goal is to remain ready for shifting environmental regulations—long before changes become mandates.
Our production teams have phased out less responsible reagents and process aids wherever possible, redirecting waste streams into closed-loop purification. These choices directly impact not only our own bottom line but also the compliance risk and sustainability targets of our downstream customers. Environmental responsibility is no longer a badge, but a requirement for ongoing viability in this sector.
Meeting evolving needs isn’t about stacking features onto a product description. We’re in the lab and on the factory floor, debugging syntheses side-by-side with users running new applications or hitting regulatory roadblocks. Requests for unique blends, tighter impurity controls, or tailored analytical packages prompt rethinking of historic methods rather than one-size-fits-all “solutions.”
The future of a specialty intermediate like 6-(trifluoromethyl)pyridine-2-carbonitrile doesn’t rest on yesterday’s chemistry degrees or patent filings. Success emerges from repeated trials, honest mistakes, and every feedback loop between our technical teams and the scientists driving innovation at the user end. Only by bridging process realities and research goals do we all get ahead.
So much of the world’s value in synthetic chemistry hides in the work nobody sees—running the 17th process check at midnight, shipping early samples to beat development targets, defending analytical standards before regulatory audits. These stories speak louder than the glossiest catalog entry or web listing. Our teams respect these unwritten truths, keeping an ongoing conversation open with every customer, researcher, or operator who relies on our work.
Having lived through the real complexity of industrial fluorinated intermediates, we understand what separates a usable product from just another reagent on the shelf. The best results start with honest dialogue, high standards on the processing floor, and a commitment to continuous improvement rooted in experience, not empty promises.