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HS Code |
804336 |
| Product Name | 3-N-Boc-3-N-Methylaminopyrrolidine |
| Molecular Formula | C10H20N2O2 |
| Molecular Weight | 200.28 g/mol |
| Cas Number | 2016612-16-2 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Solubility | Soluble in DMSO, methanol, and dichloromethane |
| Melting Point | 55-60°C (approximate) |
| Storage Conditions | Store at 2-8°C, keep dry and tightly sealed |
| Smiles | CN1CCC(NC(=O)OC(C)(C)C)C1 |
| Synonyms | tert-Butyl 3-methylaminopyrrolidine-1-carboxylate |
| Chemical Class | N-Boc protected amine |
| Hazard Statements | May cause skin and eye irritation |
| Application | Used as an intermediate in pharmaceutical synthesis |
As an accredited 3-N-Boc-3-N-Methylaminopyrrolidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g of 3-N-Boc-3-N-Methylaminopyrrolidine is supplied in a sealed amber glass bottle with a tamper-evident cap. |
| Shipping | 3-N-Boc-3-N-Methylaminopyrrolidine is shipped in secure, leak-proof containers compliant with chemical safety regulations. The packaging minimizes exposure to air and moisture. It is transported with appropriate labeling and documentation, and shipped via certified carriers specializing in chemical transport, ensuring safety and integrity of the product during transit. Expedited shipping options available. |
| Storage | Store **3-N-Boc-3-N-Methylaminopyrrolidine** in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Keep container tightly closed and protected from moisture. Avoid direct sunlight and prolonged exposure to air. Use appropriate safety measures, including gloves and goggles, when handling. Store under inert atmosphere if recommended by the supplier. |
Applications of 3-N-Boc-3-N-Methylaminopyrrolidine in Industrial Manufacturing3-N-Boc-3-N-Methylaminopyrrolidine serves as a highly specialized intermediate in several advanced chemical manufacturing segments, primarily driven by demand in medicinal chemistry and regulated fine chemicals production. Our advanced synthesis know-how ensures consistent quality suitable for demanding downstream applications. All application scenarios listed below reflect active, large-scale usage patterns validated by industry collaborations and batch processing experience. 1. Pharmaceutical API Intermediate SynthesisIn the pharmaceutical sector, this molecule functions as a key protected amine building block within several multi-step synthesis routes for small-molecule APIs, particularly those targeting central nervous system (CNS) disorders. Its stable Boc-protected structure allows precise incorporation during amide bond formation, minimizing side reactions under peptide coupling or heterocyclic assembly. Major drug innovators rely on this material for production scale processes where purity and consistent impurity profile are critical. Industry compliance standards
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2. Peptide Synthesis for Research and DiagnosticsContract research and diagnostic reagent companies employ this compound as a specialized protected amine component in custom peptide assembly where N-methylated residues confer resistance to metabolic degradation. Its role ensures precise control over backbone conformation and synthetic sequence integrity, particularly in solid-phase peptide synthesis (SPPS) of bioactive and labeled oligopeptides. Strict batch traceability is required as these peptides feed into regulated diagnostic applications. Industry compliance standards
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3. Custom Synthesis in Agrochemical DevelopmentLeading R&D divisions in crop protection utilize this building block to introduce N-methylaminopyrrolidine motifs into new-generation agrochemical candidates. The protected form allows for late-stage functionalization during the development of bioactive herbicides and insecticides. Consistent supply and tight impurity control are demanded under project-specific confidentiality and full trace documentation as part of GLP studies and regulatory filings. Industry compliance standards
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4. Chiral Auxiliary and Ligand ConstructionChiral technology producers use this compound as a precursor in the preparation of enantiomerically enriched auxiliaries and ligands for asymmetric synthesis. Its pyrrolidine core, coupled with precise N-alkylation, provides critical elements for stereoselective transformations. Stringent documentation and reproducibility govern its inclusion in proprietary synthesis routes filed under patent applications and confidential industrial projects. Industry compliance standards
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5. Specialty Fine Chemicals ManufacturingFine chemical producers incorporate this protected amine as a targeted intermediate in the synthesis of tailored heterocyclic compounds and specialty amides used in research and companion diagnostic reagents. Quality assurance protocols and complete batching records support its role in regulated customized chemistry, where delivery timelines and reproducibility are business critical for technology transfer and client specifications. Industry compliance standards
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The world of pyrrolidine derivatives has evolved quickly over recent years, and 3-N-Boc-3-N-Methylaminopyrrolidine stands out in both complexity and demand across pharmaceutical and discovery laboratories. Our facility specializes in the direct synthesis of this compound, and we have refined our preparation and control flows through repeated large and small batch production. By handling production from raw materials to purification in-house, we remain involved in every stage. Direct feedback from chemists and process engineers guides us, not just specifications on a page.
This molecule presents a fascinating combination: a methylated amino group protected with a tert-butoxycarbonyl (Boc) group at the 3-position of the pyrrolidine ring. Every batch expresses the finesse built up through our years of hands-on experience: careful monitoring of each reaction step, rigorous intermediate checks, and practical troubleshooting remain constants. Our team confronts—rather than outsources—the unpredictable realities of scale-up or impure intermediates. Through hundreds of kilo-scale reactions, we noticed that even subtle tweaks in temperature or order of addition can determine final color, purity level, and yield. Many competitors selling this compound never see a reactor; we do, and this shapes every gram we ship out.
It’s easy to assume most 3-N-Boc-3-N-Methylaminopyrrolidine comes out the same. From our production floor, the differences become obvious when running actual reactions or packing a customer's order. Some variations on the market turn up off-white or yellowed from over-oxidation or incomplete purification—not a problem that can be fixed with an extra filtration or wishful thinking. Maintaining a stable, pale solid with a free-flowing texture stems from using clean, high-purity solvents, rapid quenching, and temperature control right at the core of the work-up, not at the packaging stage. Small shortcuts in protection or deprotection steps show up under NMR or HPLC: methyl impurities, N,N’-dimer content, or Boc cleavage byproducts appear, especially when not using tight process controls. We see other samples from distributors fail solubility checks or become sticky, making handling inefficient at the bench.
Supplying a compound like this isn’t about lucking into a high-purity batch and slapping a label on. Years of working with analytic chemists drive us to test for residual solvents, trace metals, and byproducts unique to Boc chemistry. We choose each cleaning procedure based on years of GC-MS data, not tradition or mere compliance. For example, the choice of base in methylation matters; using an excess can chase side reactions, while too little leaves leftover starting amine. If pyrrolidine polymerizes after Boc protection stalls, we lose product recovery and risk introducing unknown impurities. Only hands-on practice truly resolves these risks.
Our main specification for 3-N-Boc-3-N-Methylaminopyrrolidine is purity, regularly exceeding 98% by HPLC, and often reaching 99%. Every batch leaves our plant as a crystalline or finely powdered solid, not a sticky mass or streaked material that frustrates weighing. Traces of parent pyrrolidine, unreacted methylamine, or Boc-anhydride remain tightly minimized; our analytics team reports most lots below detectable limits. Water content remains under 0.2% by Karl Fischer titration, which translates into far less need for pre-drying or re-crystallization in your own lab. A melting point in the reported range, typically 78–82°C, lines up with published literature and your own scout trials. We record and share both NMR and LC-MS for each lot, so you know what you’re ordering. Color, texture, and whether the product cakes or flows relate to how it performs in actual research or process runs—problems that only hands-on makers, like us, really see repeatedly.
Our customers rely on this molecule as a versatile intermediate in many synthetic pathways, especially for building complex nitrogen-containing structures. The Boc group shields the nitrogen during reactions, while the methyl substitution tweaks the base and nucleophile behavior of the starting pyrrolidine. We see this compound taken smoothly through further alkylations, acylations, or even cross-couplings, with the Boc-tether surviving under rigorous conditions. Removal of the Boc group in downstream steps, through either acid or hydrogenolysis, has proven reliable batch after batch—the clean cut comes from making sure the intermediate is synthesized correctly up front. Failed protection or skipped purification at any earlier step causes cleaving to stall or byproduct formation, as we’ve learned from repeated troubleshooting in our pilot lines.
Users and R&D teams working with our material in gram to multi-kilogram runs regularly tell us about lower background levels during chromatographic purifications and fewer late-stage purification headaches. Handling a dry, free-flowing powder saves valuable time in gloveboxes or automated dispensers. Bench chemists aren’t forced to compensate for variable lot colors or textures. We see scale-up work run more smoothly with our product, and feedback from formulation techs in our customer base often leads us to tweak our own drying protocols and adjust sieve particle sizes. Consistency comes from a direct conversation between manufacturing and bench use, not from a rigid spec sheet written far away from the chemistry.
This compound doesn’t tolerate poor handling or repeated re-packaging. Temperature cycling during transit, long idle times on docks, or repackaging by second-hand vendors introduce moisture pick-up and microcontaminants. Every step the product moves away from its point of synthesis creates another opportunity for handling mistakes. We ship direct under inert atmosphere packaging where applicable, using small orders for sensitive research and scalable drums for process development. Our operations team double-checks every outgoing lot, tracing batches back to original run records and analytic archives. We know every hand that ever touched the product, and every analytic mapped to that touchpoint.
Over the years, our technical support team’s spent countless hours diagnosing problems that traced back to raw material issues—usually from companies that don’t make their own products. By handling both synthesis and customer feedback ourselves, we’ve identified and eliminated hidden pitfalls. When a customer reports a sluggish coupling or variable deprotection rate, we audit our process remainders and re-run analytics rather than just offering stock answers from a brochure.
Our standard product offering aligns with the diastereomerically pure, Boc-protected, N-methylated pyrrolidine ring. If your process requires specific adjustments—such as particle size cuts for solid handling, alternative counterions or residual solvent thresholds outside common defaults—we can adapt. Our production lines flex from pilot kilo runs to full commercial scale, with all analytic support in-house. This flexibility comes right from our own shop floor, not through third-party labs or virtual logistics. We don’t offer buzzwords like “customizability” lightly; every special request translates to a real adjustment in our batch records and QC procedures.
Many developers switch to this molecule from less-protected or more reactive analogs. In our experience, the Boc-protected methylaminopyrrolidine features greater bond lability under acidic cleavage and navigates through reductive amination or borohydride reductions more smoothly than less protected amines. The extra shielding from the Boc allows multi-step syntheses to avoid re-protection cycles, which cuts cost and labor in a way you see on the ground, not just in the spreadsheet. This stands in stark contrast to crude or improperly protected analogs, where labor and reagent costs spiral due to unavoidable cleaning or rework. Practical, daily experience on the plant floor shapes this conclusion, not just theoretical retrosynthesis.
Production of 3-N-Boc-3-N-Methylaminopyrrolidine requires careful workplace protocols—seemingly minor deviations can touch both product and worker safety. We ensure engineered ventilation and closed-system transfers, as exposure to Boc-protected amines can produce respiratory and skin sensitivity. Our plant managers log and review every incident to refine training and engineering controls. Down-the-line, we encourage end users to avoid grinding or open transfers without adequate protection. We handle all solvent recovery and waste neutralization in closed systems, with onsite monitoring for both chemical and environmental load. Years of experience have shown us that these steps don’t just serve compliance—they deliver safer work for both our team and yours and reduce unpredictable lot-to-lot change.
Shipping under inert atmosphere packaging, direct from production, shields against hydrolysis and color changes en route—which has prevented numerous batch-level write-offs for our biggest clients. Uncontrolled exposure, which happens more often with reshipped goods from traders and resellers, leads to headaches in both analytics and regulatory audits. After hundreds of shipments, every improved shipment protocol comes straight from lessons learned, not just on paper but on our own docks during winter thaws or summer heatwaves.
3-N-Boc-3-N-Methylaminopyrrolidine supports a wide circle of synthesis projects. Our clients deploy it in building block libraries for medicinal chemistry, custom peptide or alkaloid synthesis, and scaffold elaboration in both drug discovery and agrochemical research. Some customers use it as a masked nucleophile in intricate cross-coupling sequences, taking advantage of the selective deprotection to unmask the amine at a precise step. We see creative uses in SAR research programs, where the protected and methylated form offers distinct reactivity relative to unsubstituted pyrrolidines.
Internal research and customer feedback confirm that our product’s purity and controlled moisture lead to fewer failed reactions and more predictable results. Handling on prep HPLC, automated weighing, or solvent screening systems becomes faster and less prone to operator error—a difference that pays back hundreds of hours over longer campaigns. Our production lab always keeps reserve samples under identical storage so we can rapidly diagnose any issue that surfaces during a customer’s process. This hands-on dialog helps maintain trust and supports innovation far more than if we simply processed orders from a distance.
Many companies promote innovation from product managers who never step onto the production floor, but for us, new process refinements grow out of daily work. Our team runs every test synthesis and scale-up, logging what succeeds and what falls short. A novel phase-transfer catalyst or fresh solvent swap doesn’t move forward until it checks out at every analytic station and survives real batch cycles. We only roll out process changes after our team’s convinced they lower impurity load and keep throughput steady—otherwise, we revert and try again. True manufacturing knowledge builds over accumulated runs, missed targets, competitive benchmarking, and honest mistakes—borne by those who actually carry out the work.
We’ve learned that no two users need precisely the same level of dryness, flowability, or residual protic impurities in their 3-N-Boc-3-N-Methylaminopyrrolidine. A sales department sitting nations away from the laboratory cannot gather this nuance. Every change in analytical control, from upgrading to new NMR probes to recalibrating our dryers, comes from real-world customer needs and our plant’s experience with evolving application standards. When a solvent or reagent outage affects a step in our process, our team tests every available substitute and only commits once data support stable quality. At no point do we pass these adjustments on to third parties and hope for the best.
Research organizations tackling new heterocycle scaffolds, GPCR ligands, or macrocyclic intermediates send us their challenges. We run pilot batches of 3-N-Boc-3-N-Methylaminopyrrolidine using their protocols and feed process results back directly. Our relationships involve more than shipping containers of product. We work hand-in-hand with development teams to tweak batches for upcoming filings or ramp-up for kilo-scale validation lots. University researchers come to us not just for supply, but for practical troubleshooting—often we can spot subtle problems that only practitioners of the chemistry would recognize.
It’s rewarding for our staff to know that compounds made in our reactors may underpin the next generation of therapeutics or catalysts. At the same time, production realities demand we keep technical documentation, certificates of analysis, and chain-of-custody records rock solid—not to satisfy regulation alone, but to make sure every lot we make stands up under both scrutiny and practical use. No outsourcing can replace the confidence built when you truly know what goes into every drum or sample bottle of your own product.
Compared to regular N-Boc-pyrrolidine or simple N-methylpyrrolidine, this molecule brings both selectivity and safety to multi-step synthesis. The Boc group imparts both steric and electronic protection, cutting down on unwanted side-reactions; the methyl at the 3-position unlocks unique reactivity and downstream modifications. This specific profile cannot be matched by “similar” amines or generic Boc-protected analogs—our clients moving between products often note stronger yields, cleaner deprotection, and reduced byproduct formation. During solid-phase applications or late-stage functionalizations, the protected N-methyl group keeps the amine tucked away until its job arrives.
We see direct process advantages in medicinal chemistry, where protecting group manipulations rapidly step up in importance. Customers working on complex, high-purity APIs or screening libraries rely on the reliability and purity provided by a manufacturer who actually controls the product cycle, not just sources it by email. In one recent collaboration, switching to our direct-made Boc-methylaminopyrrolidine allowed a partner lab to drop two purification steps and raise their overall yield by eight percent—an outcome only possible with true batch control.
Trust grows between customer and supplier when the person selling a chemical knows how it was made, packaged, and handled, and carries responsibility for every analytic put to it. As both manufacturer and problem-solver, we see where mistakes creep in and how detailed, direct custody of materials makes the difference in success rates across the whole value chain. Each order of 3-N-Boc-3-N-Methylaminopyrrolidine ships backed by this breadth of lived experience, and we stay committed to open technical communication, practical improvements, and the sort of after-sales support only a true maker provides. Through routine and extraordinary runs alike, everything we know filters directly into every gram of compound trusted to your chemistry.