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HS Code |
479479 |
| Product Name | (R)-2-Methylpyrrolidine Hydrochloride |
| Cas Number | 42042-71-7 |
| Molecular Formula | C5H12ClN |
| Molecular Weight | 121.61 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Melting Point | 171-173°C (decomposition) |
| Solubility | Soluble in water |
| Optical Rotation | [α]D20 +64° (c=1, H2O) |
| Chirality | R-configuration |
| Storage Conditions | Store at 2-8°C, in a tightly closed container |
| Synonyms | (R)-(+)-2-Methylpyrrolidine hydrochloride |
| Structure | Pyrrolidine ring substituted at position 2 with a methyl group, R-stereochemistry, as hydrochloride salt |
| Usage | Chiral building block, pharmaceutical intermediate |
As an accredited (R)-2-Methylpyrrolidine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of (R)-2-Methylpyrrolidine Hydrochloride, labeled with chemical name, formula, purity, and hazard warnings. |
| Shipping | (R)-2-Methylpyrrolidine Hydrochloride is shipped in secure, tightly sealed containers to prevent moisture and contamination. The chemical is packed according to standard safety protocols in compliance with DOT and IATA regulations, labeled as a research chemical, and typically shipped at ambient temperature unless otherwise specified. Handling by trained personnel is required. |
| Storage | (R)-2-Methylpyrrolidine Hydrochloride should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, well-ventilated area, ideally at room temperature (15–25°C). Avoid exposure to incompatible substances such as strong oxidizing agents. Always follow safety protocols and regulatory guidelines for handling and storing hazardous chemicals. |
Applications of (R)-2-Methylpyrrolidine Hydrochloride in Industrial ManufacturingAs a direct manufacturer with extensive expertise in chiral amine synthesis, we supply high-purity (R)-2-Methylpyrrolidine Hydrochloride to institutional and industrial innovators worldwide. Downstream sectors integrate this advanced intermediate into processes requiring strict enantiopurity, compliance-controlled handling, and application-specific formulation in pharmaceutical, fine chemical, and API production. Below we detail real-world application scenarios where this material delivers clear, documented value. 1. Chiral Intermediate for Antiviral API SynthesisPharmaceutical companies utilize (R)-2-Methylpyrrolidine Hydrochloride as a critical chiral building block during the synthesis route of select antiviral active pharmaceutical ingredients. Its high enantiomeric excess enables precise configuration of bioactive antiviral agents, specifically in late-stage amide formation or N-alkylation reactions. Manufacturers require rigorous control during this stage to ensure regulatory compliance for APIs targeting regulated markets. Industry compliance standards
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2. Stereoselective Synthesis of Chiral Agrochemical IntermediatesMajor agrochemical manufacturers integrate this salt into multi-step routes for herbicide and insecticide ingredient precursors where the (R)-enantiomer supports the synthesis of active isomers with targeted biological activity. Control of chiral purity at this stage directly influences the efficacy and safety profiles of final agrochemical formulations. Industry compliance standards
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3. Enantiopure Catalyst Construction for Asymmetric SynthesisSpecialty chemical and pharmaceutical R&D centers employ (R)-2-Methylpyrrolidine Hydrochloride as a core moiety in the manufacturing of chiral ligands and phase transfer catalysts. These agents enable downstream customers to conduct high-yield asymmetric transformations, crucial for next-generation synthetic pathways in both batch and continuous manufacturing environments where reproducible stereochemistry is paramount. Industry compliance standards
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4. Building Block in Synthesis of Specialty Flavors and FragrancesSelect manufacturers in the specialty fine chemicals sector incorporate this chiral amine hydrochloride as a precursor within the synthetic routes of advanced flavor and fragrance ingredients, particularly for products demanding strong enantiopurity with minimal off-notes. Its controlled introduction helps achieve regulatory-acceptable flavor profiles and olfactory precision in accordance with international additive and cosmetic standards. Industry compliance standards
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In the world of chiral building blocks, every intermediate matters. Over years spent in multi-step synthesis, we have become very familiar with the nuances of (R)-2-Methylpyrrolidine Hydrochloride, known for its chiral purity and consistent performance in active pharmaceutical ingredient (API) manufacture. Our in-house team manages each stage, from the initial charge to the final packaging. No part of the process is left unchecked. Our model for this product, batch reference PMP-2R-HCl, reflects decades of continuous improvement. It didn’t happen overnight—consistent feedback from researchers, pilot plant operators, and process chemists shapes every kilogram we produce.
For (R)-2-Methylpyrrolidine Hydrochloride, achieving optical purity above 99% enantiomeric excess forms the foundation of its reliability. Each batch comes highly crystalline, free-flowing, with moisture levels kept well within trace limits by the time it reaches the end user. This constant focus minimizes the need for reprocessing or additional drying steps downstream. The melting point falls reliably within the expected range, a direct result of controlled recrystallization and careful selection of raw inputs. A robust system of analytical verification runs through every stage. We see broad adoption in GMP settings, not just because of paperwork, but because a failed batch could halt multimillion-dollar programs. As hands-on chemists, we scrutinize trace impurities by chiral HPLC, GC-MS, and NMR, giving practical answers to the question: will this material work in scale-up without surprises? That’s our standard—not some abstract notion of “quality,” but actual reproducibility across campaigns.
Process chemists and industrial formulators reach for (R)-2-Methylpyrrolidine Hydrochloride in asymmetric syntheses, especially for creating chiral amine scaffolds in small-molecule drugs. Medicinal chemistry teams use it to unlock enantioselective routes that sidestep the common racemate resolution headaches. Beyond pharma, we get requests from agrochemical innovators working on crop protection agents, where the (R)-enantiomer leads to different biological activity than its (S)-counterpart. No substitute covers the same chiral space with this reliability, so the applications keep growing. Over the years, we’ve partnered with clients optimizing routes to patented APIs, where even a small impurity or incorrect salt form could derail a regulatory filing. We’ve seen the costs of failure firsthand—reactor fouling, crystallization issues, and unreliable downstream reactions. These cases drive us to maintain material that delivers as promised, every time.
Plenty of chiral pyrrolidines and their salts cross our loading docks, but our team pays special attention to the hydrochloride form of (R)-2-Methylpyrrolidine. The plain free base sometimes raises handling headaches, with volatility during transfer and sensitivity to atmospheric moisture. The hydrochloride offers greater stability, less odor, and easier weighing. We have handled orders for both but learned clients prefer the hydrochloride for large-scale operations where consistency saves both time and labor costs. Some competitors sell racemic or unspecified pyrrolidines, often with unclear provenance or inconsistent performance in real synthesis. We faced these same frustrations before launching our own line—facing knock-on effects in hydrogenation or chiral catalyst development. Our process sets the (R)-enantiomer apart: we scale up with true single-enantiomer selectivity, avoiding cross-contamination. The result is cleaner analytics, easier regulatory submissions, and no dangerous guessing about how a given batch will behave.
Producing enantiomerically pure (R)-2-Methylpyrrolidine Hydrochloride at scale brings its own hurdles. Starting with the right chiral precursor is essential; we source inputs from vetted suppliers under signed quality agreements because a low-level impurity in an early intermediate can snowball into a major headache many steps later. We learned early to design crystallization protocols that prevent caking and reduce static electricity, as accidents during charging or milling can turn a clean floor into a hazard zone in minutes. Each lot is dried under precisely controlled vacuum levels, monitored by in-process weighing, not just timers, since ambient humidity still sneaks in. Our finished product never sits on shelves for long—we fill drums and ship promptly, keeping time in storage to a minimum and product as fresh as possible.
We know regulatory filings demand more than a “good enough” COA. Our lot release package includes trace analytics, full HPLC impurity profiles, and verification of optical rotation and absolute configuration. The paperwork is backed by real in-house analytical runs, not outsourced lab printouts. Our customers have leveraged this data to support DMF submissions, pharmacopoeial reviews, and response packages during inspections. Auditors arrive in our facility by appointment every quarter, unannounced sometimes, and walk away without open observations – proof of consistent attention to detail. Most regulatory chemists need to know not just how a material looks, but also how it behaves under stress testing and extended storage. We support these inquiries with accelerated aging studies, salt stability data, and real root-cause analysis if an anomaly appears. Every single batch is fingerprinted and traceable. If an issue arises, we know not just what went wrong, but exactly how to fix it at source without delay—because we have the data to back it up, not empty promises.
Our (R)-2-Methylpyrrolidine Hydrochloride has moved beyond pilot stage into full process validation with branded and generic pharmaceutical production. We’ve navigated questions on batch-to-batch consistency, impurity carry-through, and interfacial compatibility in multi-step sequences. In campaigns where each intermediate weighs on project success, customers came to us after trialing cheaper or off-spec alternatives that either complicated downstream purification or left unexplained byproducts. Through hands-on troubleshooting, we identified subtle batch-variant factors—things that rarely show up in brochures, like filterability, end crystallization texture, or reactivity with borane complexes. Partnerships were built one technical challenge at a time, and we take every call from the plant floor personally. That approachable reputation isn’t a slogan; it keeps improvement moving in real time, not just during annual reviews or contract renewals.
Pharmaceutical firms make up the bulk of our recurring customer base, using (R)-2-Methylpyrrolidine Hydrochloride in the synthesis of complex, chiral “privileged structures” that act as templates for multiple drug classes. With green chemistry on everyone’s radar, our teams methodically reduced the solvent footprint per batch and minimized waste salt byproducts, so clients can report improved process metrics in their own filings. Halide-free alternatives exist for some applications, but for water-sensitive reactions or where easy salt cleavage matters, the hydrochloride stands apart. In probing structure-activity relationships, med chem leaders praise our material’s clean starting profile and lack of unknown peaks by LCMS. Biotech startups leverage it to speed hit-to-lead timelines; established firms lock it into their supply chain after audit. Even in fine fragrance or specialty solvent segments, where small-volume demands still call for reliable chirality, clients return year after year because the downstream chemistry remains predictable—less time lost to troubleshooting, more time spent innovating.
During global shutdowns, strained logistics, and surges in demand, supply resilience became more than just marketing talk. Drawing on internal stock buffers and strategic partnerships, our team kept orders moving without resorting to spot-market intermediates. We offer direct technical support for any formulation questions, process optimization, or trouble in scale-up. Rather than bounce tickets between faceless departments, every inquiry lands on the desk of a chemist with hands-on batch experience—not just a call center operator. Problems get solved quickly, based on firsthand manufacturing and analytical knowledge. Real, documented process adjustments for clients have included specialized particle size requests, moisture-spec customization, and improved anti-caking agents introduced after a batch lost flow due to unforeseen transport delays. Long lead-time planning means our largest customers never worry about unexpected outages or last-minute price jumps. Our business doesn’t chase one-time buyers or speculative orders; recurring partnerships allow us to invest back into process control and technical infrastructure, benefiting every shipment that leaves our floor.
In recent years, several pharmaceutical partners scaled multi-kilo syntheses using our (R)-2-Methylpyrrolidine Hydrochloride in GMP-validated processes. One group previously struggled with inconsistent reactivity during reductive amination, running into failed batches traced back to off-ratio enantiomer purity. Switching to our product, their right-first-time yield improved by double digits, removing the need for additional purification steps. In another instance, a startup with a lean team successfully reduced time-to-candidate-molecule by almost three weeks, thanks to the consistent quality and ready availability of material. Regulatory reviewers remarked upon the cleanliness of final API as well as the traceability of each intermediate—a direct consequence of our traceable documentation and lot-tracking system.
Investment in R&D has not slowed. Our chemists pilot next-generation crystallization technologies that target narrower particle size distribution without raising costs. We run periodic, comparative stability studies across all nitrogen-heterocycle chiral salts to support decisions about which form best suits emerging downstream reactions. The direct connection from plant floor to technical support staff allows us to adapt swiftly to customer feedback, applying the lessons learned in real-world synthesis rather than theoretical process design. Environmental compliance now drives our solvent recovery project, with measurable reductions in carbon footprint per batch thanks to upgraded recovery units and waste segregation strategies. Improved barcoding and in-house data management have all but eliminated order and inventory errors. Today’s refinements become baseline quality for tomorrow—because many customers have come to us through word of mouth, reporting failures or inconsistencies with material sourced from less-experienced suppliers who do not control their process end-to-end.
Years spent producing (R)-2-Methylpyrrolidine Hydrochloride at industrial scale have taught us what matters: no hidden variability, transparency in testing, and close contact with those who actually put our material into reactors, not just procurement staff. Behind every successful synthesis are analysts, plant operators, and troubleshooters who insist on answers that hold up under scrutiny. We serve those expectations by keeping process control close to home and evaluating every improvement not just for speed, but for its technical impact in the long haul. Our approach means customers can build their supply chains with confidence—not empty assurances or lowest-bid temptations, but firm data and real accountability. Whether the next batch goes into a blockbuster drug, a specialty flavor intermediate, or a new agrochemical candidate, our (R)-2-Methylpyrrolidine Hydrochloride stands ready for the challenge—and so do we.