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HS Code |
230220 |
| Chemical Name | 2-(4-Fluorophenyl)-Pyrrolidine |
| Molecular Formula | C10H12FN |
| Molecular Weight | 165.21 g/mol |
| Cas Number | 773883-67-1 |
| Appearance | White to off-white solid |
| Solubility | Soluble in organic solvents such as ethanol and DMSO |
| Purity | Typically >98% |
| Smiles | FC1=CC=C(C=C1)C2CCNC2 |
| Inchi | InChI=1S/C10H12FN/c11-9-3-1-8(2-4-9)10-5-6-12-7-10/h1-4,10,12H,5-7H2 |
As an accredited 2-(4-Fluorophenyl)-Pyrrolidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed, amber glass bottle containing 10 grams of 2-(4-Fluorophenyl)-Pyrrolidine, clearly labeled with safety information. |
| Shipping | 2-(4-Fluorophenyl)-Pyrrolidine is carefully packaged in secure, chemical-resistant containers to ensure safety during transit. It is shipped in compliance with all relevant chemical transport regulations, including proper labeling and documentation. Temperature and handling requirements are strictly followed to maintain product integrity during delivery. Express and tracked shipping options are available. |
| Storage | 2-(4-Fluorophenyl)-Pyrrolidine should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep the container tightly closed and clearly labeled. Store the chemical at room temperature, protected from moisture and incompatible substances (such as strong oxidizers and acids). Ensure access is restricted to trained personnel and follow appropriate safety protocols. |
Applications of 2-(4-Fluorophenyl)-Pyrrolidine in Industrial Manufacturing2-(4-Fluorophenyl)-Pyrrolidine is an advanced intermediate that plays a critical role as a structural building block in several specialized chemical synthesis processes. As a dedicated manufacturer, we supply this raw material to downstream industries with tightly defined application scenarios that meet stringent standards for quality, compliance, and process performance. 1. Active Pharmaceutical Ingredient Synthesis for CNS MedicationsPharmaceutical producers utilize 2-(4-Fluorophenyl)-Pyrrolidine as a core intermediate in the multi-step synthesis of central nervous system (CNS) drug candidates, notably within select classes of pyrrolidine-based modulators and antagonists. Process chemists integrate this compound through ring-closing and functional group substitution routes during kilogram-scale batch synthesis under GMP conditions. The precision of its incorporation directly affects yield, impurity profile, and regulatory acceptability of the API. Industry compliance standards
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2. Intermediate for Agrochemical Active Compound SynthesisAgrochemical manufacturers employ 2-(4-Fluorophenyl)-Pyrrolidine as a key precursor in the synthesis pathway of select phenylpyrrolidine-based herbicides and insecticide actives. The compound is introduced at targeted transformation steps to construct heterocyclic scaffolds required for patented agro actives, especially those designed for systemic crop protection. Downstream users demand high batch-to-batch consistency supported by traceable analytical validation. Industry compliance standards
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3. Precursor for Fine Chemical Building Blocks in Organic SynthesisProducers of specialty fine chemicals, including advanced intermediates for dyes, optical brighteners, and performance additives, incorporate 2-(4-Fluorophenyl)-Pyrrolidine as a selective nucleophile and scaffold precursor. Its fluorinated phenyl group confers desirable physicochemical traits to downstream products. These processes necessitate close integration between QC, formulation, and batch documentation under specified ISO protocols. Industry compliance standards
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4. Synthesis of Analytical Standards for Forensic and Clinical LaboratoriesReference material producers and certified laboratory suppliers use 2-(4-Fluorophenyl)-Pyrrolidine as a core structure in synthesizing analytical standards required for legal, forensic, toxicological, and pharmaceutical quality control laboratories. Standard generation relies on traceable raw material input, high-purity control and compliance with intercontinental analytical protocols for the preparation, storage, and shipment of certified reference materials. Industry compliance standards
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It’s one thing to see a chemical structure on paper, but quite another to realize the hours of bench work, fine-tuned temperature control, and multi-step purification behind producing something like 2-(4-Fluorophenyl)-Pyrrolidine. Over the years on the manufacturing line, we’ve learned not to take shortcuts with intermediates that drive pharmaceutical and specialty chemistry forward. When it comes to this compound, our crew knows how much hinges on absolute product reliability: trace impurities unchecked can compromise a whole process chain, and subtle tweaks in synthesis parameters end up making a world of difference in downstream applications.
At our facility, we treat 2-(4-Fluorophenyl)-Pyrrolidine as more than just another name in the catalog. We have spent years evaluating every input and output. The four-membered pyrrolidine ring, carrying its para-fluoro substitution, offers a chemistry-versatile backbone that shapes numerous active pharmaceutical ingredient (API) syntheses and research projects. There is always demand for purity, batch consistency, and robust traceability with this building block, especially since research teams and process chemists rely on reliable sample behavior whether analyzing a five-gram lot or scaling into multi-kilo batches.
Direct handling has shaped how we measure quality. Our 2-(4-Fluorophenyl)-Pyrrolidine typically reaches purity levels that satisfy analytic and preparative uses in leading labs. We screen for color, moisture, and individual impurities by GC or NMR before a drum ever leaves the plant. Over time, we have adopted nitrile gloves, glass-lined reactors, and closed-system filtration to keep everything above-board on the safety and cleanliness front. Chemical processors want minimized bi-product carryover and steady physical properties, so we track melting point, color, and chromatographic profile in every batch history. The compound usually appears as a solid white to off-white crystalline form, which we keep stable during storage and transit.
Our reactors clock in under tight controls—internal temperature monitoring, controlled addition rates, and solvent purification—so the pyrrolidine stays reactive only when it should. The model most common in our output is the para-fluoro variety: the fluoro group in the four-position offers a unique electron arrangement compared to the standard phenyl version, impacting both reactivity and final target compound behaviors. This difference creeps up even in subtle process optimizations, affecting how end users approach coupling reactions, reductions, or further functionalizations.
Plenty of chemical outfits can churn out basic pyrrolidine derivatives. Yet, reliability isn’t built in a year or two, but by fixing every little oversight. Every sticky clamp and slight off-color patch has a story. We’ve seen poorly handled material leading to customer issues with residual moisture or trace solvent, facially minor but disastrous in a high-throughput API plant. For this reason, even after mastering scale-up, our team performs recurrent spot checks and uses in-house analytics before, during, and after crystallization.
Our experience reflects in how closely we measure batch-to-batch consistency. Sometimes, shifts as small as the humidity on the reactor floor can introduce variables. We keep conditions stationary by isolating climate control for pyrrolidine lines; not every competitor invests in these little tweaks, but cumulative data from customer feedback and our own analytical logs have shown that neglecting them triggers phone calls nobody enjoys.
We have watched our 2-(4-Fluorophenyl)-Pyrrolidine support the preparation of newer active pharmaceutical ingredients, especially where biaryl or fluoroarene motifs play pharmacological roles. From chemical start-ups to multinational R&D groups, researchers keep coming back for this compound to seed structure–activity relationship studies, pre-clinical projects, and scaled routes toward fluorinated analogues. One recurring piece of feedback is the convenience—labs spend less time cleaning up downstream impurities when they start with an analytically confirmed building block.
Direct use of our para-fluorinated model brings separation from plain phenylated or hydrogenated pyrrolidines. The fluorine atom subtly shifts the electron density, sometimes leading to cleaner, more predictable coupling in reactions. Those developing new CNS-active compounds or working on next-generation agrochemical actives see notable advantages over the traditional analogs, with the substitution making it easier to adjust solubility and metabolic stability. Our synthesis methods avoid introduction of stubborn by-products sometimes seen in older processes, slashing the effort to refine and filter once the compound hits the customer’s lab.
Our teams have fielded more calls about consistency and reliability on 2-(4-Fluorophenyl)-Pyrrolidine than nearly any other intermediate. Some buyers learned the hard way that quick-and-dirty sources can leave residual solvent or unwanted isomers in batches. From our side, investing in closed handling, solvent recovery, and cross-validated analytics allows us to keep those numbers minimal. We log full batch histories, and both process engineers and QA staff sign off on every certificate—not just for regulatory reasons, but because even small errors in production echo through whole supply chains.
Every plant technician and supervisor has worked runs both during the dog days of summer and in winter’s sharper chills. Minimal fluctuations in atmospheric pressure change the way some batches crystallize. We document these, check the next day’s melting points, and feed back to process development if needed. This hands-on experience means we spot off-specifications early and solve the root without blaming “operator error.” That saves everyone—us and our customers—from the trouble of product recalls or failed downstream reactions.
Manufacturing 2-(4-Fluorophenyl)-Pyrrolidine isn’t just about combining starting materials in the right order. It’s a discipline that comes from learning the limits of each reactor, the quirks of plant utilities, and the patience required to coax high yields. We schedule periodic line maintenance, monitor for kinetic “hot spots” in pre-mix phases, and rotate quality staff to prevent complacency. By keeping up these routines, risks of contamination and process drift stay low. We keep a bench lot aside from every scale-up, so we can answer questions on the spot without handwaving if a customer requests clarification.
In the early days, we struggled with color changes in late-stage crystallization. A few missteps spiked the number of off-white batches. Lining up analytical re-checks and altering solvent purification fixed most of these headaches, and now the process schedule allows for extra filtration steps when things look off. Practical feedback loops like this mean customers stick with our pyrrolidine product year-over-year. No batch moves without direct review—not from a corporate perch, but from chemists who understand what goes wrong on an actual line.
University groups and early-stage pharma often need just enough 2-(4-Fluorophenyl)-Pyrrolidine to develop a synthetic route or check drug candidate properties. Later, as a candidate moves forward, pilot plants and large-scale manufacturing call for bigger, steadier deliveries. Our experience shows that flexibility—offering lots in scalable increments and keeping communication lines open—tends to beat out arms-length sellers who can’t verify lot-level traceability or make adjustments on short notice.
Our staff recognizes that a delayed or non-conforming delivery can halt an entire R&D program. Direct lines of communication mean that our process chemists regularly answer user calls—from “what’s the best solvent for this batch?” to “can you give us residual solvent levels, right now?” It isn’t about ticking off boxes. It’s an unwritten contract between technologists: real-world chemistry rarely follows the marketing script, and customers notice which suppliers respond with technical substance.
The process behind 2-(4-Fluorophenyl)-Pyrrolidine has not stood still. We track our solvent use, run continuous recycling on line solvents, and reduce volatile emissions where possible. Several years back, switching to newer condenser systems dropped emissions and recovered significant product mass. These weren’t driven just by regulations; fielding questions from sharp-eyed QA teams at customer facilities pushes us to keep eliminating inefficiency.
Sustainability isn’t a buzzword for us. Every incremental change where we re-purify wash solvents or install closed-cycle cooling moves the needle for both environmental and economic savings. We share recycling and waste data with larger buyers, helping them demonstrate real environmental improvement up the supply chain. In the grand scheme, these shifts not only make our operation leaner but also reduce input requirement volatility—a key concern as inflation and supply constraints ripple across the industry.
We rely heavily on in-house chromatographers and NMR specialists, who pull samples at multiple production points. Early in our journey, relying on third-party labs for whole-batch release left us vulnerable to delays and interpretative errors. Now, immediate re-testing on site matters more: any deviation from specified impurity thresholds or moisture levels triggers corrective action, not excuses. Such discipline keeps both our operators and our lab chemists in sync.
Customers often ask for expanded certificates—more detailed impurity breakdowns, additional data on trace solvents—and we don’t hesitate to provide them. Feedback reveals that direct manufacturers more eligible to adjust and adapt reporting on the fly tend to win deeper partnerships with pilot-plant and kilo-lab users. Our analytical team also supports user troubleshooting; whether a compound’s behavior shifts in a reaction or a customer requests verification, we keep the lines open.
Years in the industry have shown that purity isn’t just a function of what goes on under the reactor hood. We’ve had lessons in packaging integrity: environmental shifts during transit, punctured drums, or suboptimal sealing leading to subtle moisture ingress. After one summer where a major shipment arrived with caked solid, we adopted improved desiccation and high-barrier liners for this product line. Now each drum or bottle arrives with a tamper-evident seal, accompanied by an internal moisture-scavenging system, not because it’s a regulatory requirement, but because one bad shipment can break trust built over years.
Warehousing staff received cross-training to minimize repackaging errors. In one instance, a mislabeling event nearly risked a batch due for a high-profile client, underscoring the value of layered checks. Every step, from weighing powder to final shipment, gets logged and cross-confirmed. Adopting these extra steps means no surprises for users relying on on-time, as-promised delivery.
Our process doesn’t end with product sent out the door. Users often report back about reaction yields, chromatographic behavior, or even subtle packaging preferences—most of which wouldn’t filter back to a distant trader or re-seller. Sometimes feedback points to adjustments needed in our crystallization cycle or highlights a trend in coupling efficiency. This information shapes both process improvements and our customer relationships.
Researchers have told us about increased consistency in final product yields after switching to our material, cutting back on the need for re-purification. We track these outcomes in house, sharing trends within our team to motivate direct improvements—cutting unnecessary wash steps, tweaking controlled cooling phases, and fine-tuning drying protocols. By remaining open to this practical feedback, we remain responsive both to demanding specifications and to the shifting needs of end users.
From the perspective of the production line, 2-(4-Fluorophenyl)-Pyrrolidine stands out as a reliable gateway to a wide array of advanced syntheses. Its clean, controllable reactivity profile gives medicinal chemistry groups options that simple pyrrolidine or non-fluorinated versions cannot. Many users leverage its benefits in the development of new CNS-active drugs, patent-protected analogues, or next-generation material science studies. The synthesis isn’t always straightforward; specialized handling, slow addition steps, and refined purification all enable its unique performance in final applications.
Its distinguishing character comes not only from the chemical structure, but from consistent physical and analytical characteristics batch over batch. By putting in the effort to keep each lot aligned with user expectations, we take pride in knowing research and production groups trust this compound to push forward drug discovery and innovation. Offering technical transparency, strong quality support, and responsiveness to evolving project needs, our approach ensures that every delivery is both a product and a partnership.
Regardless of shifting demands and tighter regulations, our commitment to producing dependable, high-purity 2-(4-Fluorophenyl)-Pyrrolidine remains grounded in years of plant experience, user-directed feedback, and practical adjustments. We don’t see ourselves as just another cog in a sprawling supply chain. For us, manufacturing this advanced building block is a matter of direct pride, expertise, and continuing collaboration with teams driving real-world scientific progress. Every day, it pays to remember: a single step off course in manufacture ripples downstream to every new product depending on our work. Our hands-on approach, refined processes, and open lines of communication keep this compound a staple in forward-looking innovation.