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HS Code |
337708 |
| Name | 2,3,6-Trifluorophenylacetonitrile |
| Cas Number | 61726-35-2 |
| Molecular Formula | C8H4F3N |
| Molecular Weight | 171.12 |
| Appearance | White to off-white solid |
| Boiling Point | 242 °C (estimated) |
| Melting Point | 34-36 °C |
| Density | 1.33 g/cm³ (estimated) |
| Smiles | N#CC1=CC(F)=C(F)C=C1F |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Pubchem Cid | 163917 |
| Refractive Index | 1.463 (estimated) |
As an accredited 2,3,6-Trifluorophenylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,3,6-Trifluorophenylacetonitrile is packaged in a sealed amber glass bottle, containing 25 grams, with a secure screw cap. |
| Shipping | 2,3,6-Trifluorophenylacetonitrile is typically shipped in tightly sealed containers to prevent moisture and contamination. The packaging follows regulatory guidelines for hazardous chemicals and should be stored in a cool, dry place during transit. Proper labeling, documentation, and transport via licensed carriers are essential for safe delivery and regulatory compliance. |
| Storage | 2,3,6-Trifluorophenylacetonitrile should be stored in a cool, dry, and well-ventilated area in tightly sealed containers. Protect it from moisture, heat, and direct sunlight. Keep away from incompatible substances such as oxidizing agents and strong acids. Store the chemical under inert gas if possible to minimize air and moisture exposure. Always follow standard laboratory safety protocols when handling and storing. |
Applications of 2,3,6-Trifluorophenylacetonitrile in Industrial Manufacturing2,3,6-Trifluorophenylacetonitrile serves as a key fluorinated intermediate in several regulated specialty chemical synthesis chains. As a manufacturer, we support diverse industrial sectors that require precise integration of this material into their production workflows. Below, we present major industrial segments using this molecule, outlining industry standards, dosage ranges, production stage, and output products specific to each sector. 1. Agrochemical Active Ingredient SynthesisThis intermediate finds application in the targeted synthesis of fluorinated agrochemicals, especially in the production of fungicide and herbicide actives. The controlled introduction of the trifluorophenyl unit at the acetonitrile stage ensures improved biological activity and stability of the final molecules. Large-scale agrochemical producers commonly integrate this raw material into multi-step synthesis beginning with aromatic substitution followed by nitrile functionalization and downstream transformation to carboxylic acid derivatives. Industry compliance standards
Typical usage ratio
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2. Pharmaceutical Intermediate for API SynthesisThis compound functions as a fine chemical building block in the production of certain fluorinated active pharmaceutical ingredients. Its stable trifluorophenyl moiety is crucial for pharmacophores requiring improved metabolic properties. GMP-certified API manufacturers utilize it in multi-stage synthetic routes, particularly for small-molecule drugs where targeted halogenation and acetonitrile insertion enable the requisite chemical backbone for final actives. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Material Additive in Electronic ChemicalsProducers of high-performance electronics materials utilize this compound in the formulation of functionalized polymers, liquid crystal monomers, and specialty resins. The unique electronic characteristics imparted by the trifluorophenyl group enable developers to tailor dielectric properties in advanced material systems. The raw material is integrated through controlled co-polymerization or post-polymer functionalization processes, supporting applications such as photoresist components and dielectric films. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Intermediate for Fine Chemical Synthesis in Dye and Pigment ManufactureThis molecule acts as a key fluorinated intermediate in the synthesis of specialty colorants, especially high-stability dyes and pigments used in demanding end applications such as plastics, high-performance coatings, and UV-resistant inks. The strong electron-withdrawing trifluoromethyl substituents facilitate the development of colorants with superior light and chemical stability. Specialty dye manufacturers incorporate it at defined steps to introduce the required substitution pattern, enhancing product lifetime and customer performance requirements in critical sectors. Industry compliance standards
Typical usage ratio
Downstream process integration
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In the heart of our production site, years of work with specialized nitrile intermediates have shaped a practical understanding of how each product pulls its weight on a chemical line. 2,3,6-Trifluorophenylacetonitrile steps forward as one of the reliable building blocks in the synthesis of advanced agrochemical, pharmaceutical, and material science compounds. Its structure, combining a phenyl ring with three fluorines at precise positions and a reactive acetonitrile tail, fills roles that ordinary phenylacetonitriles miss. Direct input from scale-up chemists and purification teams turns complicated theory into reproducible quality, batch after batch.
The compound comes to life after multistage synthesis brings together simple raw materials under tightly controlled flows of heat and solvent, a process checked by actual people on the line, not just sensors. Workers keep an eye on color clarity, melting point, NMR signals, and impurity ranges. Each kilogram moves from reactor to filtration under lab eyes. The stakes ride on more than just meeting a GC-MS printout; they ride on not causing seeding problems for someone synthesizing a new pyrimidine API or running into resin swelling during material modification.
Hands-on manufacturing puts decisions about reaction route, solvent recycling, and purification order in reach every step. Since we never hand off these choices to a third party or contract shop, adjustments come fast when customer specs make a difference. Experiments with different fluorination routes or tweaks in base strength have given us more than just papers; they’ve taught what stays soluble, where emulsion risks jump, and how quickly the end group hydrolyzes in damp storage. This living knowledge brings flexibility in scale, from a pilot flask to a bulk run, without letting purity standards slip. Customers avoid costly requalifications because the product’s character remains steady.
Laboratories and R&D departments often face mismatches between catalog claims and as-shipped product. From our own expansion years, we know the headaches when you open a drum of supposedly “white powder” that’s more off-pink and clumpy than expected. Over time, we built up our own minimum standards: a purity of at least 98.5% by HPLC, tight limits on single-point moisture, and clear crystalline granulation that doesn’t clog gravity feeders. The remaining fraction, usually trifluorotoluene or trace unreacted starting material, stays below levels that would shift NMR baselines or throw off MS runs. We share full lot COA data because it has value in troubleshooting, not just compliance.
By working with downstream chemists, the team learned long ago that the position of each fluorine atom matters far more than many textbooks suggest. In pharmaceutical research, the 2,3,6-trifluoro substitution pattern delivers a particular electronic push-pull effect. Subtle as it seems, this pattern stabilizes reactive intermediates when forming C–N bonds, especially for heterocycle rings. The difference shows up most in yield improvements, cleaner workups, or in avoiding minor side products that eat up precious column time. When medicinal chemistry managers ask if another fluorophenylacetonitrile will do, the answer depends on how the precursor lines up on their SAR table. But for binding improvement or reduced metabolic loss, the trifluoro pattern keeps getting requested.
During routine rounds of scale-up, you get a sharp feel for how a single change in ring-substitution throws off more than just reaction time. For example, 2,3,6-trifluorophenylacetonitrile stands out against 3,4-difluorophenylacetonitrile and their unmixed cousins thanks to lower electron density on the ring and a distinct resistance to oxidative degradation. What this means in the plant is less concern about unintended brown material forming in the product tray. In end-use, it translates to greater shelf stability, slower hydrolysis in open systems, and less gumming in condensation reactions. Material scientists working on resins or advanced polymers keep turning back to this compound, not out of habit, but out of practical experience – the properties enable clean coupling with other fluorinated monomers, and the product disperses without streaking.
Each time a batch goes out—from first kilo demonstration to full container order—feedback from clients lands back with the process team. Will this batch work with a different palladium catalyst? Has there been any new reactivity during Suzuki coupling stages? Users share, and adjustments happen on the floor in small but important ways. These are not theoretical improvements—they show up in time saved by fewer recrystallizations, better chromatography profiles, or ability to skip an entire protection step in a client’s API route. Our knowledge builds from decades of iterative work and mistakes, not just a pile of certificates. This feedback is as important to us as the raw data from our own labs.
One hard lesson from earlier years involved trouble customers faced when forced to switch suppliers. Grinding bottlenecks came up because some suppliers dilute lots with leftover fractions, or blend non-matching intermediates made in different reactors or even at different plants. By having direct oversight, variability stays low. Chemists on both sides gain confidence in matching earlier trial results, and a feedback loop helps refine both process and performance for new syntheses. It reduces unplanned downtime, lets procurement staff source for longer-term projects, and frees up researchers to try new conditions without the risk of supplier-induced batch variation.
Working with fluorinated intermediates brings unavoidable challenges on the waste and emissions front. Regulations tighten with every year. Direct control lets us close the loop on solvent handling and hydrogen fluoride scrubbing, turning hazards into safe by-products before anything leaves the site. This pushes investment into both local environmental monitoring and staff training. Transparency counts, so emissions data and handling protocols don’t hide behind “confidential business information” labels. Growing experience with greener syntheses and solvent recovery keeps costs and compliance risks in check. If clients in Europe or North America request custom documentation for REACH or TSCA, there’s no paperwork chase; everything traces directly to our own plant data and logs.
The downstream timelines in pharmaceutical development or advanced materials are unforgiving. Each delay, whether from sample retesting or delivery slip, throws off R&D momentum and can mean missed launches. Delivery reliability begins on the factory floor. Stock levels hold steady, and backup production lines give redundancy if technical issues hit. Shorter chains from our reactors to your loading dock beat a web of resellers that only know what their supplier tells them. Buyers can skip redundant QC steps because our process data matches what arrives in the drum. It clears the way for long-term development or just-in-time delivery, instead of lost weeks hunting for replacement material when a batch doesn’t meet mark.
Every few years brings a new application our team did not target during development. Early buyers focused on pharmaceutical and agrochemical projects. Year after year, research into advanced coatings, OLED precursors, and next-generation fluorescent dyes keeps crossing our desk. The clean trifluoromethyl pattern and acetonitrile end keep integrating into larger synthesis platforms. Buyers want both reactivity and physical stability, especially for intermediates heading into high-pressure or multi-enzyme steps. Our on-site teams document each of these new applications, then share updates with recurring clients, supporting both rapid feasibility trials and larger volume campaigns.
As one of the original plant managers said, “No batch is ever identical, but every good batch comes with a reason.” Production only works with people who know what the outcome needs to look and feel like. Over the years, chemists, operators, and QC teams have sharpened a shared sense for what makes genuinely usable product: from how fines flow during drum packing, to what a true low-water content looks like under titration. Ohio or Tokyo, academics or industrials, buyers write in with very practical questions—how does this grade work in a rotary evaporator, will it handle overnight in a glovebox, will it hold under a basic wash step? It only takes one batch shift for a costly project to stall. Having a partner on the other end—someone willing to test and tune—matters more than a stack of printed COAs. The team does not just take orders; they engage with what the next chemist or engineer needs to move forward.
Open data beats marketing: a direct flow of analytical spectra, complete batch records, and impurity logs clears up doubts for clients planning their own registrations or scale-ups. Overseas shipping brings surprises, but nobody likes delayed customs or unexpected flags over trace by-products. Only manufacturers with full lineage control, from raw material intake to sealed product drum, can field unexpected audits or answer tough regulatory questions. We learned early not to hide behind NDAs or vague technical notes—if a client inquires about residue, or if a downstream process throws off smoke, we get on the line to work the details, no finger-pointing. Differences between our 2,3,6-trifluorophenylacetonitrile and catalog samples from jobbers become clear under scrutiny: every peak, every water test, every scale-up record sits ready for actual review—not a marketing summary.
Not every customer comes with a full technical staff or background in advanced fluorination. Our knowledge runs deeper than what makes an appealing brochure. From the early days of navigating key starting materials—managing both cold-chain transport and hazardous handling of fluorinated precursors—the on-site team has solved challenges that never reach the catalog page: solvent recovery on stubborn residues, improved base wash protocols to cut color, new crystallization approaches that keep end-user losses low. These improvements become real cost savings during multi-stage synthesis for those further along the value chain. They also mean new users can address specification questions directly, not through an impersonal channel.
Many skilled chemists found that the way a compound is sealed and shipped makes as much difference as the product itself. Moisture risk, packing geometry, and temperature control have shaped our packaging standards. Secure aluminum-lined drums, vacuum-sealed inner bags, and real-time shipping loggers stop quality problems before arrival: a lesson learned from earlier years, when tins and single liners led to avoidable returns. Each container ships out with tested antistatic liners and QR-linked data paperwork. Transparent chain-of-custody runs through every order—we don’t rely on warehouse repackaging or bulk dilution.
Clients working in scale-up or with advanced functional group chemistry encountered challenges beyond what catalog samples support. Many rely on this specific intermediate because it stands up to both harsh process conditions and downstream scalability. Whether for introduction into multistep pharmaceutical syntheses or coupling with specialty monomers, the precise trifluoro-substitution and clean acetonitrile group ensure no surprises during analytical review. Time-sensitive research projects or long-lead commercial campaigns both gain from confident, specification-backed sourcing. Product quality only comes from producers who stick with both technical progress and honest feedback from those who use the compound under pressure and deadline.
Direct production puts us in constant dialogue with buyers, analysts, and development teams. Feedback drives improvement in handling, batch integrity, and delivery logistics. 2,3,6-Trifluorophenylacetonitrile’s story reflects years of incremental gains—not one big breakthrough, but hundreds of shifts, tests, and scale-ups that raised both quality and reliability. Companies, researchers, and industrial buyers choosing this product receive more than another name on a warehouse shelf. They tap into the experience of those who have handled the full path from raw material to packaged chemical, with eyes on both integrity and practical delivery. Every client’s unique conditions shape ongoing production decisions—whether they need drum lots or new purification scenarios for their end use.
Direct sourcing from a committed manufacturer means better control, clearer data, and practical partnership over the long haul. 2,3,6-Trifluorophenylacetonitrile stands as both a workhorse chemical and a reflection of persistent effort across decades of chemical manufacturing. Improvements, adjustments, and lessons taken over years of production support not just short-term use, but also new, evolving research that points the way toward the next generation of specialty chemicals. Reliable sourcing, real data, and partnership in problem solving will always outlast generic, commoditized supply chains.