|
HS Code |
880639 |
| Chemical Name | 2-(Thien-2-Yl)Pyrrolidine |
| Molecular Formula | C8H11NS |
| Molecular Weight | 153.24 g/mol |
| Cas Number | 118589-38-5 |
| Appearance | Colorless to pale yellow liquid |
| Smiles | C1CCNC1C2=CC=CS2 |
| Purity | Typically ≥97% |
| Solubility | Soluble in common organic solvents |
| Storage Condition | Store at 2-8°C, protected from light and moisture |
As an accredited 2-(Thien-2-Yl)Pyrrolidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass vial containing 5 grams of 2-(Thien-2-Yl)Pyrrolidine, securely sealed with a tamper-evident cap, labeled with hazard information. |
| Shipping | 2-(Thien-2-Yl)Pyrrolidine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be transported according to regulations for hazardous chemicals—away from incompatible materials, with temperature control if required. Proper labeling and documentation accompany the shipment, ensuring safe handling and compliance with local and international shipping standards. |
| Storage | 2-(Thien-2-yl)pyrrolidine should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon. Keep it in a cool, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Properly label the storage container and ensure compliance with local chemical safety regulations. |
| Purity 98%: 2-(Thien-2-Yl)Pyrrolidine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reproducible product quality. Melting Point 80°C: 2-(Thien-2-Yl)Pyrrolidine with melting point 80°C is used in solid-state drug formulation, where it provides stable handling during manufacturing processes. Molecular Weight 167.26 g/mol: 2-(Thien-2-Yl)Pyrrolidine at molecular weight 167.26 g/mol is used in custom organic synthesis, where it offers precise stoichiometric calculations for complex molecule construction. Stability up to 120°C: 2-(Thien-2-Yl)Pyrrolidine with stability up to 120°C is used in high-temperature reaction protocols, where it sustains structural integrity under thermal stress. Particle Size <50 μm: 2-(Thien-2-Yl)Pyrrolidine with particle size under 50 μm is used in catalyst preparation, where it ensures uniform dispersion and enhanced reactivity. Water Content <0.5%: 2-(Thien-2-Yl)Pyrrolidine with water content less than 0.5% is used in moisture-sensitive processes, where it minimizes hydrolytic degradation risks. Refractive Index 1.579: 2-(Thien-2-Yl)Pyrrolidine with refractive index 1.579 is used in analytical research, where it aids in accurate spectroscopic identification. Residual Metals <10 ppm: 2-(Thien-2-Yl)Pyrrolidine with residual metals below 10 ppm is used in active pharmaceutical ingredient development, where it guarantees compliance with regulatory purity standards. |
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We’ve been manufacturing 2-(Thien-2-Yl)Pyrrolidine for years, and there’s something rewarding about seeing our batches help researchers push the boundaries of heterocyclic organic chemistry. Years of precise process work and fine tuning have convinced us of this compound's unique role in both research and applied sectors. If you’re reading this as a synthetic chemist or project lead in advanced materials, you probably have your own seasoned opinions about the thienyl-substituted pyrrolidines. Still, our perspective as a company that works daily on the synthesis floor, handling everything from reaction scale-up to purification, adds some on-the-ground context to its introduction.
Our main product model, 2-(Thien-2-Yl)Pyrrolidine, follows a robust standard specification fine-tuned over dozens of production runs. We've maintained batch purities above 98%, with independent HPLC and NMR verification—not just a marketing claim, as every high-purity drum that leaves our warehouse has been tested at least twice. Experience has taught us that even a few tenths of a percent in impurity, especially fewer-than-expected NMR signals, can ruin an entire downstream synthesis. So we built our protocols around removing those elusive by-products, especially thiophene-based tars and trace N-alkyl pyrrole isomers.
Our batches arrive as stable, off-white solids. Moisture control remains vital in our line, since traces from ambient air can sneak in and convert it to the hydrolyzed variant. Factory staff pay special attention to the drying oven schedule, since slight overdrying can cause caking. Each batch passes outgoing QC within 24 hours of production. Storage in inert conditions pays off in consistent reactivity, an observation supported both by our own customers and from updates we receive from long-term partners in Europe and North America.
Unlike many heterocyclic building blocks, 2-(Thien-2-Yl)Pyrrolidine fits a particular set of reactions where substitution patterns and ring strain tweak reactivity in valuable ways. We’ve found its use especially relevant in the synthesis of ligands for organocatalysis, the assembly of advanced functional materials, and targeted medicinal chemistry projects. The thienyl moiety brings pi-stacking properties to larger assemblies. It slots into Suzuki coupling routes without the steric hindrance that can frustrate other aryl-pyrrolidines.
Medicinal chemists have contacted us about its use in fragment-based drug discovery. The core structure offers a useful vector for building out molecular diversity, particularly where classic aniline or cyclohexyl cores show poor bioavailability or metabolic stability. As a manufacturer, we see this clearly in increased demand from pharma R&D divisions during earlier pipeline stages.
In day-to-day manufacturing, we synthesize both thienyl-substituted and phenyl-substituted pyrrolidines. The real difference comes out during recrystallization and solvent handling. 2-(Thien-2-Yl)Pyrrolidine often proves more manageable in bulk, both for isolation and for downstream purification. Its melting point clusters in a range that avoids both excessive loss and troublesome solidification during scale-up.
Contrast this with some of the phenyl derivatives, which have lower solubility profiles and a tendency to separate as sticky tars under slightly suboptimal workups. The handling improvements aren’t just about convenience; they translate into lower loss, easier in-process adjustments, and fewer surprises when running synthesis at tens-of-kilograms scale.
Chemically, the thienyl modification imparts different electronic behavior. Researchers using it in metal complexes note that the resulting ligands exhibit altered electron density relative to their phenyl analogs. This ability to fine-tune donor strength finds practical use in asymmetric catalysis and experimental polymer formation. On the medicinal side, thienyl-pyrrolidines have been explored in lead optimization cycles favoring high CNS penetration and metabolic flexibility—recent work from top academic labs supports what our customers have reported for years.
One trend we’ve witnessed grow involves modular building blocks with heterocyclic substituents that allow further downstream functionalization. 2-(Thien-2-Yl)Pyrrolidine doesn’t just end with one coupling reaction; it has become a favorite among process chemists piloting iterative syntheses and scaffold hopping. In our own plant, optimization for large-scale, high-yielding routes has allowed repeat contracts with biotech start-ups and diversified chemical manufacturers. Reliable supply at scale, without batch-to-batch variability, can mean the difference between a successful library expansion and an entire week’s work lost to purification cycles.
We regularly engage in discussions with the scientists using our material. Common feedback highlights the ease of reaction setup and reproducible coupling yields. In projects involving chiral pool synthesis or metal-catalyzed cyclization, the compound consistently provides clean product profiles, saving both time and solvent. Once, during a collaboration with an advanced materials research group, we jointly optimized a Suzuki-Miyaura coupling protocol to boost yields by eight percent—simply by switching to our latest purified lot, which cut residual metal traces below 0.02%.
From the factory’s standpoint, delivering quality goes deeper than routine paperwork. Years on the floor have taught us that every defect or inconsistency at the production line multiplies during custom synthesis. That’s why we’ve invested in high-throughput chromatography, upgraded column packing schedules annually, and scheduled peer-audited process walkthroughs after every second batch. This hands-on regime ensures that customers don’t encounter off-odors, instability, or unexpected side reactions.
During an internal root-cause review last year, we identified that product aging in poorly sealed packaging led to sporadic spot test failures. As a result, we enjoyed both better shelf stability and significantly fewer customer complaints after redesigning our container seals and rotating stock faster. These factory-floor observations shift the focus from theoretical specification to everyday reliability.
From medicinal chemistry teams designing ion channel modulators to agrochemical developers scaling up new lead candidates, most of our end-users prize adaptability. We’ve seen our product included in pilot programs for hit-to-lead optimization where modular thienyl-pyrrolidines unlocked new bioactive profiles. Academic partners regularly cite improved scaffold rigidity and predictable reaction outcomes—qualities that directly trace back to the purity and stability achieved on our production lines.
Some recent high-throughput screening campaigns sought pyrrolidines with distinct heteroaromatic character, not only for ligand binding studies but also for constructing photoactive chemical libraries. Developers have reported that 2-(Thien-2-Yl)Pyrrolidine’s aromatic profile enhances photostability and modulates excited-state behavior, more so than simple N- or C-alkylated analogs. That sort of feedback helps us focus our next process refinement cycles on areas that matter: minimizing baseline impurities, maximizing crystalline uniformity, and anticipating changes to regulatory priorities.
As product adoption has spread, new synthesis challenges have emerged. One perennial request involves custom quantities and tailored particle sizing—never a trivial task at scale, especially since pyrrolidine derivatives tend to absorb moisture and clump. Our most recent equipment upgrades now allow for improved sieving and encapsulation, resulting in smoother dosing during automated dispensing. We adopted an inline drying system based on direct customer suggestions after seeing delayed mixing in a partner’s continuous reactor.
In our experience, robust supply chains guarantee project continuity. Early on, we suffered from a few bottlenecks related to external suppliers for precursor thiophene. We’ve since integrated redundancy into our procurement, widening our source base, and started direct reactions with upscaled intermediate storage. This change allowed us to keep batch-to-batch consistency and shield customers from the effects of international shipping delays or regulatory interruptions. Years spent troubleshooting these issues taught us the value of adaptive logistics aligned with chemical integrity.
As chemical producers, the responsibility for safety and eco-friendly practice comes with the territory. Throughout the scaling journey for 2-(Thien-2-Yl)Pyrrolidine, we devoted extensive process development into minimizing volatile organic emissions and eliminating hazardous secondary waste. The closed-loop systems we run today not only contribute to regulatory compliance but also improve worker safety on the floor. Recovered solvent recycling from these processes pays off, both for environmental targets and long-term cost control.
Process chemistry specialists at our plant have upgraded operator training to cover thienyl and pyrrolidine-specific risks—knowledge gleaned from decades of safely handling these two classes. These partnerships reinforce a culture where everyone from plant engineers to technical sales recognizes both the value and the risks linked to new product development. Direct experience with safe handling protocols and product-specific training leads to fewer accidents, better quality assurance, and smooth plant operation even as order volumes increase.
We maintain regular dialogue with research institutions utilizing our products. These collaborations don’t stop at providing material—they run into process troubleshooting, joint exploratory syntheses, and ongoing feedback loops. Sometimes, partners uncover subtle forms of product degradation in long-term exposures or unusual solvent conditions; that feedback drives our next-generation process upgrades. We’ve seen this approach pay dividends in forming lighter environmental footprints and improving product reliability.
One notable example came from a multi-center catalyst development project. Researchers pinpointed a minor degradation by-product forming only under UV exposure, a phenomenon rarely noted in standard lab work. With this knowledge, our process engineers revised the post-purification handling and packaging, improving stability across global shipping routes. We continue to rely on similar knowledge exchanges, which ground our manufacturing improvements in actual field use, rather than theoretical risks presumed from literature alone.
The plant team sees firsthand how this product stands up to its cousins, both structurally and operationally. Unlike N-benzylpyrrolidines, which come with batch-to-batch color variability and susceptibility to by-product formation, thienyl-pyrrolidines like this one yield consistently clean spectroscopic and chromatographic signatures. This repeatability gives medicinal chemists more confidence as they scale ideas from milligram test runs to multi-kilogram validation lots. After all, no one likes surprises halfway through a late-stage synthesis—or explaining batch inconsistency to a regulatory body.
Even among the thienyl-substituted pyrrolidines, structural positioning on the ring makes a difference. Our factory settled early on the 2-thienyl isomer because it offered smoother purification profiles compared to the 3-thienyl form. Labs reported easier downstream derivatization and cleaner transformation to secondary or tertiary amines. This alignment of process ease and user benefit is why we focus on this particular isomer, and why our experienced technicians can routinely hit tight impurity specs.
Modern trends in chemical synthesis call for practical yet versatile intermediates. Our experience has shown 2-(Thien-2-Yl)Pyrrolidine answering this call repeatedly—not merely as another heterocycle off the shelf, but as a core feature of microwave-assisted couplings, iterative combinatorial libraries, and bioconjugation strategies. In contracts with gene editing toolmakers, the ease of forming robust linkages to protected nucleophiles turned out to be a project accelerator, while the product’s solubility characteristics allowed for simplified purification cycles—freeing up valuable instrument time for our customers.
It finds favor on the academic side, too, as a teaching tool in advanced undergraduate and graduate courses. We’ve provided technical support to instructors rolling out hands-on experiments, which has revealed an unexpected advantage: reliable, recognizable color and odor make for intuitive process checkpoints, sparing students (and their instructors) the anxiety of product identification typical in beginner syntheses. From this practical angle, we’re proud to contribute not only to innovation at the high end but to new generations training for careers in chemical sciences.
As an actual manufacturer, adjustments never stop. Each new customer project brings unique requirements, prompting us to look for process enhancements in solvent selection, filter design, or drying strategy. Our onsite technical team frequently partners with R&D clients to adapt specs for exotic synthesis routes, whether that means dialing in tighter residual solvent removal or offering tailored crystallization protocols. Continuous improvement comes not from spreadsheets, but from tracking real-world outcomes and chasing down every source of batch inconsistency until resolved.
Data from post-sale returns and application support requests have shaped our investment in active process monitoring. Over the last three years, each quarter has seen reductions in turnaround time and off-spec rejections. Communication from users also prompted us to improve our documentation practices without bogging customers down in unnecessary paperwork—direct, honest reporting on what changes from batch to batch lets development chemists focus on the science rather than troubleshooting product flukes.
Years of industry volatility have reinforced the importance of upstream raw material checks. During the thiophene price spikes of recent years, our purchasing and production leads collaborated closely, building a mix of just-in-time ordering with forward stockpiling for forecasted large-scale orders. We’ve watched competitors struggle with inconsistent sources, which often leaves customers stranded. In contrast, our decision to directly qualify and audit suppliers guarantees that each batch starts with the right foundation, under continuous review for both ethics and quality.
Climate and regulatory changes will always disrupt chemical supply chains. Our operations team applies these lessons proactively, aligning documentation and materials handling so every step—from intermediate formation through final QC—stays transparent. This level of engagement makes it easier for downstream users to validate their own processes, which often translates into more repeat business and trust on both sides.
Our long-standing position as a direct manufacturer shapes every interaction with this product. Whether troubleshooting reaction optimization with a university group or scaling kilogram orders for a pharma customer, we keep field experience at the center of every process improvement. Relationships with end users across four continents ensure that we stay responsive to new trends, regulatory challenges, and scientific advances tied to 2-(Thien-2-Yl)Pyrrolidine.
Staying close to the ground truth means our product development team constantly absorbs feedback, tests hypotheses, and prioritizes production changes that actually matter on the lab bench or factory line. In the world of specialty chemicals, only a manufacturer with this mindset can continually support innovation, adaptability, and reliability—delivering compounds that fuel both cutting-edge discoveries and everyday laboratory progress.