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HS Code |
505652 |
| Chemical Name | 1-Benzyl-3-aminopyrrolidine |
| Molecular Formula | C11H16N2 |
| Molecular Weight | 176.26 g/mol |
| Cas Number | 5118-13-8 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 327.5 °C at 760 mmHg |
| Density | 1.04 g/cm3 |
| Melting Point | -6 °C |
| Solubility | Soluble in organic solvents such as ethanol and methanol |
| Purity | Typically >98% |
| Smiles | N1CC(CN)C1Cc2ccccc2 |
| Inchikey | UKRZEQCSFMMLAA-UHFFFAOYSA-N |
As an accredited 1-Benzyl-3-Aminopyrrolidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Benzyl-3-Aminopyrrolidine, 25g, supplied in a tightly sealed amber glass bottle with a tamper-evident cap and clear labeling. |
| Shipping | 1-Benzyl-3-Aminopyrrolidine is typically shipped in sealed containers to prevent contamination and degradation. It should be handled according to chemical safety regulations, with appropriate labeling and documentation. Packages are cushioned and protected from temperature extremes. Shipping may require compliance with hazardous material transport guidelines, depending on destination and quantity. |
| Storage | 1-Benzyl-3-aminopyrrolidine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect the chemical from moisture and light, and keep it at room temperature or as recommended by the manufacturer. Proper labeling and compliance with local storage regulations are important. |
Applications of 1-Benzyl-3-Aminopyrrolidine in Industrial Manufacturing1-Benzyl-3-Aminopyrrolidine serves as a key intermediate in specialized synthetic routes. Its molecular structure enables defined modifications for a range of targeted downstream applications. Below, we outline industrial utilization in pharmaceutical development, agrochemical synthesis, specialty fine chemicals, and advanced material research. 1. Pharmaceutical API Intermediate SynthesisPharmaceutical manufacturers utilize this compound as a crucial intermediate for the production of certain central nervous system (CNS) active pharmaceutical ingredients. The material’s aminopyrrolidine core provides a functional handle for N-alkylation and derivatization. Production lines subject this intermediate to multistep synthesis involving amide formation and selective functional group transformations. Batch records document each synthetic stage per applicable cGMP guidelines, with strict in-process controls for purity and residual solvents, ensuring traceable lot management before conversion into regulated API products. Industry compliance standards
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2. Agrochemical Building BlockManufacturers in the agrochemical sector use 1-Benzyl-3-Aminopyrrolidine to construct novel insecticidal and herbicidal agents. The amine and pyrrolidine functionalities allow coupling with various acyl or sulfonyl chlorides, producing candidate molecules for crop protection. Regulatory batch records log all formulation steps for global registration. Analytical labs run chromatography and spectroscopic methods to verify each intermediate’s identity, while production teams tune process parameters based on conversion rates and impurity profiles dictated by end-use requirements. Industry compliance standards
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3. Synthesis of Specialty Fine ChemicalsFine chemical producers employ 1-Benzyl-3-Aminopyrrolidine for making specialty amine and pyrrolidine derivatives with market positions in fragrance, pigment, and polymer additive industries. Precise stoichiometric control during reductive amination, alkylation, or salt formation steps determines output purity and performance. In-plant laboratories conduct continual monitoring for byproducts and target isomeric ratios. Each campaign documents equipment washes and changeovers per internal SOPs to prevent cross-contamination for customer orders demanding high trace traceability. Industry compliance standards
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4. Advanced Material and Polymer SynthesisResearchers and producers in the advanced materials sector incorporate this compound as a functionalizing agent during custom polymer chain assembly and surface modification routines. The aminopyrrolidine group enables covalent attachment onto polymer backbones or inorganic frameworks, tailoring surface energy, solubility, and binding characteristics. Controlled addition rates and monitoring of chain extension reactions are vital for batch consistency. Analytical QA employs NMR and FTIR to verify functional group integration prior to downstream compounding or formulation. Industry compliance standards
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Crafting 1-Benzyl-3-Aminopyrrolidine in-house has given us a front-row seat to its value and particular character in the world of fine chemicals. Chemistry isn’t just theory, spreadsheets, and stock-keeping units for us. It starts on our own floor, where raw materials arrive and transformations happen right in our reactors. Our team takes pride in knowing that every kilogram we produce carries consistency batch after batch. For years, our technical specialists and production engineers have watched how the structure of 1-Benzyl-3-Aminopyrrolidine finds traction with innovators in pharmaceuticals, custom synthesis, and specialty intermediates. Once you watch this molecule move from pure white powder in a drum to the heart of a reaction, its importance and quirks stand out with a clarity that theory can’t provide.
What sets this molecule apart begins with its chemistry. This compound, built from a pyrrolidine ring bearing an aminogroup at position 3 and a benzyl group at the nitrogen, brings unique structural reactivity. Chemists now frequently seek out molecules like this because the benzyl substitution at the nitrogen gives reactivity that outpaces simple 3-aminopyrrolidines or the pyrrolidine ring alone. The scaffold suits the development of analogs and new materials when a precise balance of reactivity and physical stability matters.
In practice, 1-Benzyl-3-Aminopyrrolidine supports projects that reach far across the life sciences. We have produced this for laboratories focused on central nervous system research, for medicinal chemists building up lead compound libraries, and for contract manufacturers working at all scales. Their feedback draws attention to why, out of the dozens of amine-functionalized heterocycles, this one remains a popular workhorse.
No laboratory ever built a reliable project without reliable material. We run specifications with purity reaching 98% or better by HPLC, accompanied by strict controls on water content, color, and residual solvents. Our in-house batch records speak to this focus, since much of the downstream chemistry depends on trace-level impurities. End-users—especially drug discovery teams—have often noted their sensitivity to inconsistent impurity profiles when screening new molecules. That’s why we vet our batches with GC-MS and NMR in addition to standard analytical documentation.
Crystalline 1-Benzyl-3-Aminopyrrolidine leaves our packaging line as a stable, free-flowing solid. Experience has shown that maintaining tight control over moisture and atmospheric exposure keeps the product fully usable, even after extended storage. The production team learned several years ago that routine ambient air exposure could push the amine to yellowing or off-odors, so every drum is filled under low humidity with repeated checks for oxygen content.
Direct experience with our pharmaceutical partners confirms: the benzyl group on this molecule doesn’t just act as “chemical decoration”—it can steer selectivity in reductive aminations, cyclizations, and alkylations. In a medicinal chemistry context, using this scaffold can reduce multi-step syntheses when compared to the less-substituted analogs, because the protecting group is already built into the molecule.
Some of our clients choose it to explore CNS-active scaffolds or to enhance metabolic stability, both critical attributes in lead-optimization stages. Others are drawn to the ready modification of both the pyrrolidine ring and the benzyl group, giving a versatile path to generate tailored building blocks. This flexibility means fewer laborious protection-deprotection sequences, trimming both cost and cycle time. Having seen hundreds of projects pass through our R&D partnerships, we see how small shifts in the amine’s reactivity profile ripple through to the finished product.
We also hear from chemical suppliers who rely on this compound as an anchor for more complex library construction. The amine at the 3-position reacts cleanly without side-reactions that can plague more hindered configurations. This property simplifies purification and increases throughput in combinatorial contexts or scale-up campaigns.
On paper, the field of aminopyrrolidines looks crowded. In practice, subtle differences mean everything. Switching the benzyl group to the 2- or 4-position or omitting it changes not just the physical characteristics but also the downstream feasibility of certain modifications. Straight pyrrolidine or 3-aminopyrrolidine can work in some syntheses, but they lack the tailored balance this molecule brings. Unprotected amines introduce more side-reactions and demand extra steps for protection prior to selective alkylations. Clients often come to us after running into low yields or lab-scale hiccups with simpler analogs. We see fewer impurities and cleaner analytical profiles at every checkpoint thanks to the benzyl's stabilizing effect.
Comparing to plain benzylamine, the ring’s contribution shows up in solubility, basicity, and metabolic stability. The five-membered ring adds rigidity and shifts the molecule’s behavior in polar and nonpolar systems, which helps with both handling and formulation. The difference isn’t just theoretical: teams working in process chemistry repeatedly report less fouling of reactors, reduced by-product formation, and easier downstream workups in their batch records when using our 1-Benzyl-3-Aminopyrrolidine rather than open-chain alternatives.
Other functionalized pyrrolidines, like those with unsubstituted amines or alternative N-alkyl groups, display higher rates of racemization or unwanted cross-reactivity. Through our collaboration with process development chemists, we’ve validated that the N-benzyl group offers a degree of selectivity unmatched by methyl or ethyl analogs. The difference shows up in better isolation yields and lower solvent volumes during crystallization.
We don’t rely on contract tolling for this product. From purchasing the starting pyrrolidine feedstock to the final QC sampling, it stays under our roof. This degree of transparency lets us intercept issues quickly—we've overhauled purification protocols based on actual output, not just literature suggestions. Our people on the floor blend traditional batch processes with semi-continuous runs, using jacketed glass reactors, inert gas blanketing, and precise temperature ramps controlled by skilled operators. It’s a craft informed by both formal training and years of practical troubleshooting.
Our analytical chemists test every production run against historical lots, ensuring both chemical and physical attributes land inside our published specs. They spot-check random drums from inventory to catch rare shifts in the impurity fingerprint. Having this much in-house control gives long-term repeatability: libraries and production chemists can pull two lots separated by six months and expect the same result from their assays.
Direct experiences with pilot projects prompted us to update both our distillation and filtration stages. When feedback from a long-term partner flagged traces of colored by-products, we responded by fully revisiting wash sequences, packing material, and solvent grades. This type of feedback loop helps us continuously improve real-world compatibility, not just compliance with regulatory paperwork.
One theme echoed by many clients is the role of 1-Benzyl-3-Aminopyrrolidine as a “fixer” or problem-solver in their synthetic sequences. When alternative substrates stalled in test reactions, this molecule often opened a productive route to intermediates with higher purity or better yields. Our process support team, which partners closely with custom synthesis operations, has helped adapt reaction conditions to get the best out of this compound: shorter reaction times, reduced exotherms, and easier workups.
In recent years, interest has grown around its uses far beyond classic pharmaceutical lead compounds. Teams have turned to it for agrochemical intermediates where site-selectivity trumps cost alone, and for next-generation materials where ring flexibility and functional group tolerance limit the available toolbox. High-throughput screening platforms show especially robust results when substituting in this scaffold, as its moderate hydrophobicity and steric construction boost hit rates without complicating downstream isolation.
The product regularly features in patent filings worldwide, signaling its pivotal place in ongoing research and IP development. We see patterns emerge: innovators are not just repeating old steps, but using 1-Benzyl-3-Aminopyrrolidine to sidestep process bottlenecks or to push into new chemical space where simple analogs fall short.
Lab-scale and commercial buyers alike raise key concerns beyond cost: consistent quality and transparent sourcing. Sourcing directly from us—the manufacturer—means traceability right back to procurement of each raw material. That traceability matters once materials reach GMP or ISO-certified environments. Various clients, especially those running multi-ton projects, have shared how they rely on our full documentation chain to satisfy regulatory audits and internal QA checks.
Safety in handling doesn’t end with a material safety data sheet. From process scale-up, we provide support for safe storage, transfer, and waste handling. Chemists in charge of hazardous reactions value clear insight into boiling point, storage stability, and clean disposal. Because the product comes packed under inert conditions and vacuum-sealed when necessary, we’ve seen near-zero incidents linked to atmospheric degradation or off-gassing in our downstream customers’ experience.
As demand ramps up, our own infrastructure has scaled in step. Our largest stainless reactors, routinely cleaned between campaigns, now handle increasing throughput without cross-contamination from previous product lines. Inline monitoring and real-time analytics support early warning if a batch starts to drift from intended parameters, a lesson learned from years of small-scale exploratory work.
Customer conversations increasingly turn to sustainability. Our process engineers have optimized solvent recycling loops within our own operations. Hydrogen and nitrogen streams feed back into plant-wide recovery systems, reducing both external supply dependence and environmental load. Our production lines favor low-toxicity reagents that avoid persistent waste, and our filtration systems are designed for reusable media where possible.
By investing in real-time emissions monitoring, we track the profile of every process vent and minimize unintended releases. Waste minimization is a daily objective for all operators, with strict quotas and incentive programs tied directly to process efficiency. Several client audits have praised our site for going well beyond the regulatory baseline here—reducing the needle-move from compliance to real environmental stewardship.
Researchers with a green chemistry focus ask for Life Cycle Assessment data, and we supply transparent information around our sourcing, footprint, and packaging. This shared commitment matches our own belief in better stewardship, both for our site and in the products we put in chemists’ hands worldwide.
Part of our competitive edge comes from “close to the bench” feedback. Synthesis teams, whether in pharmaceuticals, agrochemicals, or advanced materials, tell us what’s working and what’s not. Their observations fill notebooks on-site and inform real changes—sometimes as minor as switching the grit of a filtration aid, other times as major as substituting an entire solvent family. We actively maintain open channels through technical visits, sample support, and direct consultation on reaction optimization.
For newer users, application support helps ease entry into unfamiliar chemistry. Our technical specialists collaborate closely with R&D teams at every stage of the project, suggesting solvent swaps, pressure ranges, or safe workup strategies to simplify their path to final targets. Knowledge gained from decades of collective troubleshooting, including failed batches and rescue protocols, sets the base for this hands-on support.
Purchasing directly from us, the origin point, puts buyers closer to their product—free from the ambiguity and risk common to the spot-market or opaque supply chains. Our clients value clear answers to questions about batch history, logistics, or future availability. There’s nothing theoretical about the confidence that comes from knowing who made your chemical, how it was stored, and when it will arrive.
More than a number on a bottle, our lot records reflect full traceability. Samples can be matched to corresponding documentation extending from the feedstocks to the exit gate, with each process step logged and verifiable. If an issue arises, real accountability exists: technical staff can walk the production floor, inspect tanks, and consult operational logs within minutes—not days or weeks—something only a true manufacturer can guarantee.
Even in global supply shocks, our ability to adjust production schedules, adapt staff allocation, or reshuffle shipping priorities has held up where more fragmented networks struggled. This backbone, honed through decades of practical challenge, earns us repeat business from both established and emerging innovators.
1-Benzyl-3-Aminopyrrolidine will keep shaping new chemistry for years to come. It’s a testament to the ongoing dialogue between science and hands-on manufacturing. Each day on our site brings fresh insight as new applications emerge, and as challenges shift. Working directly with those pushing the boundaries of drug discovery, materials science, and specialty intermediates, we know this molecule will continue earning its place on the cutting edge—not just as a building block, but as a solution to real problems. Our commitment runs deeper than supply. We’ll keep refining, innovating, and supporting those who transform this compound into new possibilities.