|
HS Code |
682368 |
| Chemical Name | 3-Fluorophenylacetonitrile |
| Molecular Formula | C8H6FN |
| Molecular Weight | 135.14 g/mol |
| Cas Number | 348-54-9 |
| Appearance | White to off-white solid |
| Boiling Point | 261-263°C |
| Melting Point | 52-54°C |
| Density | 1.13 g/cm3 |
| Solubility | Slightly soluble in water |
| Flash Point | 126°C |
| Smiles | N#CC1=CC(=CC=C1)F |
| Inchi | InChI=1S/C8H6FN/c9-7-3-1-2-6(4-7)5-8-10/h1-4H,5H2 |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 3-Fluorophenylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "3-Fluorophenylacetonitrile, 25g," with hazard symbols, lot number, and manufacturer information, tightly sealed. |
| Shipping | 3-Fluorophenylacetonitrile is shipped in tightly sealed containers, protected from light and moisture. It is classified as hazardous and handled according to international chemical transport regulations. Appropriate labeling, documentation, and secondary containment are ensured to prevent leakage or spills during transit. Personal protective equipment is recommended during handling and transport. |
| Storage | 3-Fluorophenylacetonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances like strong oxidizing agents. Keep it away from direct sunlight and moisture. Ensure proper labeling and use in a chemical fume hood if handling large quantities. Follow appropriate safety and local regulatory guidelines. |
Applications of 3-Fluorophenylacetonitrile in Industrial Manufacturing3-Fluorophenylacetonitrile is an essential intermediate in several specialized chemical production chains. As a direct manufacturer, we supply this raw material to various segments requiring consistent purity, precise formulation, and controlled production environments. Below we detail the main industrial applications supported by our product, including compliance, process integration, and typical usage ranges based on actual downstream practices. 1. Pharmaceutical Intermediates: Active Pharmaceutical Ingredient (API) SynthesisThe pharmaceutical sector utilizes 3-Fluorophenylacetonitrile as a key intermediate in the preparation of selective serotonin reuptake inhibitors (SSRIs) and other fluorinated phenylacetonitrile-based APIs. Manufacturers incorporate this raw material during the early-to-mid stages of multi-step syntheses, where its aromatic framework and fluorine substituent facilitate the construction of pharmacologically active molecules. The chemical’s profile aligns with GMP-compliant routes, while its controlled impurity profile supports stringent API quality requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Ingredient SynthesisProducers in the agricultural industry use 3-Fluorophenylacetonitrile to synthesize key intermediates for herbicides, fungicides, and insecticidal compounds. Its unique electronic and steric properties contribute to the activity profile of target molecules, supporting both systemic and contact applications. The typical processing involves multi-step coupling and ring closure reactions performed under controlled pressure and temperature to yield final actives with tailored environmental stability. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Organic Electronic MaterialsManufacturers producing functionalized organic molecules for electronic devices leverage 3-Fluorophenylacetonitrile in the synthesis of small-molecule semiconductors and organic light-emitting diode (OLED) precursors. The chemical’s reactivity enables the development of π-conjugated structures, with the fluorine atom contributing to charge carrier mobility and stability in final optoelectronic devices. Formulation chemists adjust the amount used based on target molecular weight and energy band requirements in downstream performance validation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Custom Fragrance & Aroma Ingredient ManufactureFine chemical producers employ 3-Fluorophenylacetonitrile to construct specialty aromatics found in high-end fragrance intermediates. This raw material acts as an aromatic platform for further derivatization such as reduction to aldehydes and alcohols, producing notes valued in modern perfumery and aroma enhancement. The purity and organoleptic neutrality of our product ensures that downstream transformations yield compounds compliant with flavor and fragrance safety requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Nearly every day in our plant, the line between theory and practice vanishes once the batch reactors heat up. For us, manufacturing 3-fluorophenylacetonitrile isn’t an abstract exercise. It’s a hands-on process deeply shaped by years of continuous improvement, unwavering focus on purity, and feedback from customers who turn to us for materials that deliver results under pressure. In our own experience, production runs best when chemistry and operational knowledge move together, and this principle shows itself at every stage of our 3-fluorophenylacetonitrile process.
The backbone of this process: ensuring consistent, reliable product for researchers and manufacturers who expect that each drum arriving at their facility meets precise, predictable standards. This means we watch not only for main actives but for residual solvents, color stability, and trace impurities that often distinguish one supplier from the next. Our judgment comes from regular testing, process adjustment, and close attention to practical factors like safe handling and storage requirements, not just from a shelf full of specifications.
The 3-fluorophenylacetonitrile molecule is more than a checklist entry for chemical catalogs. We’ve seen its role expand steadily—especially in the last decade—across custom synthesis, drug discovery intermediates, and materials research. The introduction of a fluorine atom on the benzene ring at the meta position (3-position) lends this building block a blend of electronic and steric effects that enable transformations not feasible with simple phenylacetonitrile. Substitution patterns create major differences in product reactivity, downstream compatibility, and analytical fingerprint. This isn’t theory to us; repeated batches, scaleup challenges, and customer projects have shown it.
A quick word about model and appearance: our 3-fluorophenylacetonitrile is supplied as a clear to pale yellow liquid—a look shaped by careful control of byproducts at every distillation stage. We track not just the headline chemical assay, but receive feedback on color and residue that tells us a lot about our process quality at real production scales. It’s these practical details—those that don’t make it into simplified specs—that often tip the balance between a trial batch that fizzles or a program that delivers.
Handling fluorinated compounds takes specialized training. Balancing reactivity with worker safety is not just a matter of following rules; it’s a daily discipline. From the start, every batch of 3-fluorophenylacetonitrile must pass multiple checkpoints: starting material tracking, in-process controls for critical impurities, and end-stage vacuum distillation to guarantee not just purity but also consistent volume. Our team relies on automated gas detectors, and we have a routine for glove use, mask fit-checks, and ventilation review. This isn’t one-off paperwork for us; keeping the plant safe comes ahead of meeting schedules, and our regular drills reinforce that commitment.
Customers ask us about purity levels and residual solvent content before any shipment leaves the dock. Typical purity runs better than 99%, and we run GC, NMR, and moisture analyses on every lot. Real-application feedback matters: for catalysis and pharmaceutical intermediates, even minor differences in residuals can slow or spoil subsequent reactions. We don’t look at these checks as burdens but as standards we’ve chosen after years of supporting teams in R&D and pilot operations.
Our clients range from large-scale pharmaceutical synthesis labs to innovators in advanced materials. 3-fluorophenylacetonitrile forms an essential fragment in various bioactive molecules, especially in medicinal chemistry projects exploring new lead compounds or developing structure-activity relationship (SAR) data. Over the years, we've supplied it for anisole and heterocycle modifications, as well as for ligands and building blocks in crop protection chemistry. What sets 3-fluorophenylacetonitrile apart is the way the fluorine atom directs reactivity, making its downstream chemistry more predictable during halogen exchange or cross-coupling procedures. Multiple customers have shared stories of how other isomers (like 2- or 4-fluorophenylacetonitrile) just don't allow the same clean transformations, due to different electronic environments. These are lessons learned under real process development timelines.
Flow chemistry and continuous production setups also prefer our material for its thermal stability under mild heating. Equipment operators tell us that batches with residual acidic byproducts (often seen with less controlled suppliers) gum up reaction vessels or trigger fouling. For us, post-synthesis washing steps are not just a regulatory requirement—they prevent this kind of on-site headache for our customers.
We see our product specification as something that’s shaped by feedback and direct observation, not just written once and reused without thought. Routine analysis at our plant includes purity by gas chromatography, water content by Karl Fischer, and NMR scans for both positional isomerism and minor impurities. Our specs are set with the knowledge of what analytics really matter in organic synthesis, after many conversations with lab supervisors and plant chemists who’ve run our product at scale.
Critical differences exist between our 3-fluorophenylacetonitrile and the bulk product from non-specialist sources. Common complaints from customers who switch include haze formation, delayed filtration in bench tests, or higher levels of hydrolysis byproducts—problems that creep in when production doesn’t stay tightly controlled. We maintain sub-0.2% moisture limits and guarantee no heavy metal contamination, using ICP testing after each campaign. Our approach is to stay deeply involved in the campaign, not just review paper specs.
For research teams, the difference shows up fast. Purity and cleanliness allow for more predictable reaction profiles, reducing byproduct peak areas on chromatograms and saving days or even weeks troubleshooting reaction failures. We’ve had teams report improvements when switching from general commodity product to ours, particularly in sensitive Suzuki-Miyaura couplings, where trace impurities destroy catalytic activity.
Our years supporting both high-volume and specialty users have driven home a basic lesson: successful supply sits at the intersection of chemistry and logistics. A few years ago, after an uptick in requests for larger volumes tied to new agricultural active ingredient programs, we invested in dedicated reactors exclusively for fluorinated compounds, which cuts the risk of cross-contamination. Increased attention to packaging—reducing headspace in drums and adding extra liners—keeps the product fresh even during long-haul shipments. Standard steel drums don’t cut it for high-purity batches; our experience shows that lined polyethylene containers maintain better integrity and resist corrosion during storage.
Global regulations on the transport and labeling of cyano- and fluorinated aromatics change regularly, and staying in step demands constant vigilance. We have a policy to hold periodic training with warehouse and shipping staff, not just because auditors require it, but because we see the direct impact in accident prevention and smoother customs clearance. The reach of our product now touches partners in multiple continents, and every shipment requires us to blend technical care with regulatory know-how.
Pain points for customers rarely trace back to formulas alone. Our technical support team hears from project managers about tight synthesis windows, new reaction screening setups, and the need for fast answers on lot analysis. We treat customer feedback as actionable guidance—if a researcher discovers unusual reactivity or a subtle impurity, our plant team tracks it down, tests retained samples, and adjusts process controls. This level of responsiveness has opened doors to deeper collaboration: pilot-scale runs of new derivatives, custom packaging, and feedback sessions on application data all loop back into our process improvement cycles.
From time to time, new end-uses emerge that challenge us to rethink handling or downstream compatibility. For example, the rise in fluorine-containing agrochemicals has driven demand for acetonitrile derivatives with even stricter limits on halide or transition metal contamination. Instead of dismissing these as niche requirements, we see them as opportunities to learn—modifying glassware, testing new scavengers, or working with university labs to validate impurity profiles in target applications.
Over years of direct production, we have seen that success with 3-fluorophenylacetonitrile rests on small details that others might overlook. Solvent choice during synthesis affects not only overall yield but also long-term storage stability—toluene and DMF traces show up in NMR and raise red flags for strict formulations. Our teams have worked to cut these to undetectable levels, switching to alternative solvents and distillation techniques as new best practices emerge. We use analytic QC not as a checkbox, but as a tool to catch early warning signs that predict future problems.
Strong relationships with raw material suppliers shape our reliability. Shortages in fluorinated benzene feedstocks have taught us to negotiate long-term supply contracts, test new sources, and build contingency inventories. These business decisions grow out of direct production experience, not just market analysis.
Time and again, customers tell us they recognize the benefit in real-world context: improved yield predictability, less downtime for plant cleaning, and more reliable process transfer from bench to kilo scale. The 3-position fluorine brings out reactivity nuances: for example, increased compatibility in palladium-catalyzed carbon-carbon bond formations compared to the 2-position isomer, and less steric hindrance compared to para substitution. These subtle effects, well supported by literature and our in-house data, shape project decisions far beyond a simple catalog listing.
Our experience shows that research teams who move away from generic phenylacetonitrile to our 3-fluoro derivative often simplify their synthetic workflow—cutting out unnecessary protection-deprotection steps, achieving cleaner separations, and running fewer purification cycles. These savings matter, especially in discovery-phase programs where timelines make the difference between patent filings and missed windows.
We take responsibility for every lot that leaves our facility. That means full traceability down to raw batch data, operator logs, and environmental controls. Unplanned outcomes—whether from a failed distillation or shipping mishap—aren’t swept aside, but analyzed and shared with customers if there’s a risk of impact. Feedback from these processes shapes safety upgrades, not just paperwork.
While specifications provide a baseline, our technical service team often works hand in hand with partners developing new compounds, providing reference spectra, MSDS updates, and tailored analytic reports. As a manufacturer, we have the flexibility to adjust lot size, packaging, and even process parameters to respond to changing industry needs. Our adaptability rests on the experience of our plant managers, QC chemists, and technical sales—people who know both the chemistry and the challenges behind it.
Continuous learning forms the heart of our operation. As new process chemistry emerges—such as metal-free coupling or photoredox catalysis—we keep an eye on how our 3-fluorophenylacetonitrile performs in these methods. Early access to pilot data and open lines of communication with end users lets us tweak our process to meet advanced requirements. Each improvement, no matter how small, builds a reputation for reliability that we’ve earned batch after batch, not simply claimed on a datasheet.
Environmental performance matters: we monitor waste, minimize water and solvent usage, and invest in emissions controls that go beyond tick-box compliance. Many customers value traceable chain-of-custody documentation and seek reassurance of responsible sourcing, both for quality and for sustainability. Our long-term plan includes energy-efficient plant upgrades and tighter integration of process analytics to further reduce risk and footprint.
From our side of the fence, producing 3-fluorophenylacetonitrile takes more than a reaction flask and a datasheet. Our story is defined by practical learning, listening to customer experience, and investing in both people and equipment. Through the ordinary routines—running analytic batches at midnight, troubleshooting a reactor jacket, unpacking customer feedback—expertise is built, not borrowed.
For teams that need precision, process stability, and technical backup grounded in real manufacturing, our 3-fluorophenylacetonitrile offers advantages that paper specs alone can’t summarize. We keep learning, keep improving, and stand behind every kilogram as both chemists and partners who share the weight of project deadlines and product outcomes.