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Methyl Pyrrolidine-2-Carboxylate Hydrochloride

    • Product Name Methyl Pyrrolidine-2-Carboxylate Hydrochloride
    • Alias Pyrrolidine, 2-(methoxycarbonyl)-, hydrochloride
    • Einecs '627-25-0'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    910974

    Chemical Name Methyl Pyrrolidine-2-Carboxylate Hydrochloride
    Molecular Formula C6H12ClNO2
    Molecular Weight 165.62 g/mol
    Appearance White to off-white crystalline powder
    Solubility Soluble in water
    Melting Point 135-140°C (decomposes)
    Cas Number 55156-17-7
    Storage Conditions Store at room temperature, tightly closed, in a dry place
    Purity Typically ≥98%
    Synonyms Methyl (S)-pyrrolidine-2-carboxylate hydrochloride

    As an accredited Methyl Pyrrolidine-2-Carboxylate Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a sealed, amber glass bottle containing 25 grams of Methyl Pyrrolidine-2-Carboxylate Hydrochloride, labeled with chemical details and safety warnings.
    Shipping Methyl Pyrrolidine-2-Carboxylate Hydrochloride is shipped in tightly sealed, chemical-resistant containers to prevent moisture exposure and contamination. Packages are clearly labeled according to regulatory standards and typically include secondary protective packaging. The chemical is handled under temperature-controlled conditions if required, ensuring safe transit and compliance with all relevant transport regulations.
    Storage Methyl Pyrrolidine-2-Carboxylate Hydrochloride should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from incompatible substances, such as strong oxidizing agents. Store at room temperature or as specified by the manufacturer. Ensure proper labeling and access is restricted to trained personnel to ensure safe handling.
    Application of Methyl Pyrrolidine-2-Carboxylate Hydrochloride

    Applications of Methyl Pyrrolidine-2-Carboxylate Hydrochloride in Industrial Manufacturing

    Methyl Pyrrolidine-2-Carboxylate Hydrochloride serves as an essential intermediate for a limited range of specialized chemical synthesis applications. Its primary industrial value lies in advanced pharmaceutical API synthesis, agrochemical intermediates, and select fine chemical productions. As the direct manufacturer, we supply this material with documented traceability, quality monitoring, and adherence to industry-specific compliance requirements for every application scenario. Below, we highlight genuine sectors where this raw material integrates into production, providing customers with actionable formulations, process insights, regulatory context, and downstream product examples.

    1. Pharmaceutical API Intermediate: Chiral Beta-Lactam Antibiotic Synthesis

    Within advanced pharmaceutical manufacturing, this compound is indispensable during the stereoselective synthesis of certain beta-lactam antibiotics, notably in the construction of chiral intermediates for cephalosporin and carbapenem classes. Integrators utilize this raw material at the protected amino acid stage, introducing it during key condensation steps to yield enantiomerically pure side chains prior to subsequent cyclization. Its precise role connects directly to regulatory controls and process documentation demanded for regulated pharmaceutical API output.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II: Basic Requirements for Active Substances
    • United States Pharmacopeia (USP) General Chapter <1225> Validation of Compendial Procedures
    • China Pharmacopoeia (ChP) for Process Intermediates

    Typical usage ratio

    • 0.12–0.21 molar equivalents per target antibiotic intermediate, with ratio adjusted depending on desired stereochemistry and batch scale

    Downstream process integration

    • Added in condensation step with specific acyl chlorides using controlled pH and temperature to produce key chiral precursors for API assembly; post-condensation, the intermediate advances to cyclization or further protective group manipulations

    Final product types

    • Parenteral and oral cephalosporin formulations (sterile powder, injectable vials, tablets)
    • Carbapenem antibiotics (imipenem, meropenem)

    2. Agrochemical Synthesis: Herbicide Intermediate Production

    Manufacturers of next-generation herbicidal formulations rely on this compound for constructing specific pyrrolidine-dione rings that function as activity-conferring moieties in select active substances. The hydrochloride form guarantees reactivity and purity for scale-up in pilot and industrial campaigns, particularly where downstream herbicidal compounds demand strict residue and impurity management traced to intermediate stages.

    Industry compliance standards

    • US EPA 40 CFR Part 158: Data Requirements for Pesticides
    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 (Quality Management Systems for Chemical Manufacturing)
    • REACH Regulation (EC) No 1907/2006 for registration and safety assessment

    Typical usage ratio

    • 10–20% w/w of total intermediate batch; adjusted by final product purity targets and efficacy screening data

    Downstream process integration

    • Incorporated during cyclization stage with diketone reagents to produce the herbicidal core under controlled base and solvent conditions, prior to derivatization into active ingredients

    Final product types

    • Selective post-emergence herbicides (granules, emulsifiable concentrates)
    • Pre-mixed crop protection agents

    3. Fine Chemicals: Chiral Building Block for Heterocycle Assembly

    Specialty chemical producers employ this compound as a chiral building block in multistep synthesis of value-added heterocycles, including functionalized pyrrolidines for ligand development, electronic materials, and optical isomer separation agents. Deployed predominantly in R&D pilot lines and fine chemical multiplication, the raw material plays a structural role, transferred via downstream reactions with organometallic catalysts or via asymmetric transformations.

    Industry compliance standards

    • ISO 9001:2015 (Fine Chemicals Manufacturing)
    • Chemical Facility Anti-Terrorism Standards (CFATS) for specialty chemical handling
    • Chemistry Quality Assessment Scheme (ChQAS) for research-grade fine materials

    Typical usage ratio

    • 0.5–2.3 g per 10 mmol reaction scale, with ratio dictated by desired yield, catalyst compatibility, and assessed by chiral HPLC purity monitoring

    Downstream process integration

    • Introduced as a nucleophile for asymmetric cyclization at the second or third synthetic stage; subsequent purification involves solvent switching and crystallization before final coupling or functional group installation

    Final product types

    • Enantioenriched heterocyclic intermediates for research
    • Chiral ligands for asymmetric catalysis
    • Specialty fine chemical agents for advanced materials research

    4. Peptide Synthesis: Unnatural Amino Acid Derivative Production

    Advanced peptide manufacturers depend on this raw material for site-specific incorporation of custom pyrrolidine-derived motifs into synthetic peptides, enhancing stability or defining receptor selectivity for pharmacological assays. Customers operate under GMP or research-compliant environments, requiring traceable, specification-tested raw input at the protected intermediate or monomer synthesis stage prior to solid phase chain assembly.

    Industry compliance standards

    • ICH Q11: Development and Manufacture of Drug Substances
    • EU GMP Annex 1: Manufacture of Sterile Medicinal Products (for peptide APIs)
    • USP General Chapter <1047> for Peptide Drug Substances
    • Synthetic Peptide Manufacturing Quality Guidelines (industry consensus)

    Typical usage ratio

    • 0.06–0.14 equivalents per unnatural amino acid building block, refined based on target sequence length and compatibility with Fmoc/Boc protection strategy

    Downstream process integration

    • Used in the pre-activation of side-chain protected monomers, typically as the nucleophilic component during amide bond formation at the monomer or dimerization stage; subsequent coupling with resin-bound or solution-phase peptides

    Final product types

    • Custom peptide fragments for research and pharmaceutical development
    • Conjugated peptide derivatives with improved stability profiles
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    Certification & Compliance
    More Introduction

    Methyl Pyrrolidine-2-Carboxylate Hydrochloride: A Practical Overview from the Factory Floor

    Our Experience with Methyl Pyrrolidine-2-Carboxylate Hydrochloride Manufacturing

    Every day in our chemical facility, we manage the intricacies behind producing Methyl Pyrrolidine-2-Carboxylate Hydrochloride. We take the fundamentals of organic chemistry and turn them into something practical—a compound that finds purpose from lab-scale research to downstream pharmaceutical synthesis. No script or brochure captures how much dedication it takes to ensure every batch supports the real work being done, whether that’s developing advanced intermediates or troubleshooting a new synthetic pathway.

    Unlike commodity chemicals that fill rail cars for basic industry, this molecule occupies a much more focused niche. Our teams navigate stringent quality targets because even the smallest impurity can derail a synthesis further down the line. That’s where our process design matters most. We invested in semi-continuous systems for tight process control. Regular monitoring—beyond what simple batch records demand—lets us spot shifts in purity or moisture content long before those metrics reach a customer’s hands.

    Model and Specifications: Details in Real-World Context

    In most requests, we ship the compound as a crystalline hydrochloride salt, favoring the specifications mid-sized pharmaceutical and fine-chemical companies need. Our typical model offers a purity not less than 98 percent by HPLC, with moisture content held below 1 percent. We keep residual solvents and heavy metals at levels consistently below strict regulatory thresholds. Any color deviation during solidification triggers a root-cause analysis before approval.

    Handling matters just as much as the final assay values. Our packaging team avoids fiber drums and keeps contact surfaces inert, opting for double-lined polyethylene bags within hard plastic containers. This helps maintain shelf-life and prevents cross-reactivity with ambient moisture, which can otherwise shift salt forms or cause compaction. We learned this the hard way through years of working with materials sensitive at a molecular level.

    How Methyl Pyrrolidine-2-Carboxylate Hydrochloride Fits into Chemical Synthesis

    Inside a chemical plant, every product we make gets evaluated by one central standard: how easily does it enable the next step? Methyl Pyrrolidine-2-Carboxylate Hydrochloride serves as a versatile building block. Most of our customers value its status as an intermediate for various custom syntheses. We regularly consult with process chemists designing synthetic pathways for active pharmaceutical ingredients, peptide analogs, or specialty reagents. Much of their work uses N-protected amino acids, and our material supports their protocols by introducing the right chirality and reactivity.

    Some customers use our product for coupling reactions, where the protection afforded by the methyl ester and the hydrochloride salt allow specific reactivity without introducing side reactions. Other users need it as a backbone to construct prodrugs, thanks to its manageable solubility and straightforward deprotection profiles. We’ve even seen applications in green chemistry, where its manageable stability profile supports safer, lower-temperature reactions, saving both energy and waste.

    One point stands out in these discussions: shelf stability impacts usability. We check every drum for caking, discoloration, or even faint odor shifts. If it doesn’t meet the storage conditions that a customer’s lab environment can handle, we know we risk disrupting their workflow. Pulling a batch off the line saves more than just reputation—it saves hours of troubleshooting in plants and labs worldwide.

    Why Our Approach to Quality Control Surpasses Industry Shortcuts

    Scaling up specialty chemicals like Methyl Pyrrolidine-2-Carboxylate Hydrochloride goes beyond meeting crude assay targets and ticking boxes. Our quality team shapes their protocols with input from real customer case studies. We use reference materials sourced from independent bodies, recalibrated against our own internal benchmarks. Every deviation in melting point or IR fingerprint gets immediate attention.

    Some competitors cut time and cost by compromising during purification. That’s a risk we won’t take here—not because it’s easy, but because we’ve seen how downstream chemistry falters when micro-impurities slip through. In one case, a small batch contaminated with a near-invisible by-product led a client’s peptide synthesis to yield only half the expected product. Fixing that lost week of research costs far more than rigorous in-house purification.

    Regulatory compliance pushes us toward ever tighter controls. Rather than treat this as a paperwork exercise, our team embeds real-time batch monitoring, periodic random sampling, and on-site testing. Years ago, before tightening controls, we witnessed first-hand how an out-of-spec batch created downstream analytical challenges. Now, our lab techs are empowered—not only to spot issues but to halt production if anomalies creep in.

    Proactive risk management isn’t just theory to us. Our archives include field reports submitted by chemists who ran our product through high-throughput screens. If a material failed to dissolve properly or deviated in reactivity, our troubleshooting support and process improvements followed. Every report becomes part of our continuous improvement cycle. These side-by-side learnings have made a tangible shift in how we design and manage workflows on site.

    Comparing Methyl Pyrrolidine-2-Carboxylate Hydrochloride with Other Intermediates

    Customers often ask: why choose this molecule over similar esters or salts? The answer lies in real-world performance, not just catalog numbers. We’ve handled methyl esters of other pyrrolidine carboxylic acids and observed notable distinctions. The hydrochloride salt variant we produce consistently shows greater stability during high-humidity storage. Competing free bases often degrade over months, forming by-products that compromise synthetic purity.

    Some labs draw comparisons to tert-butyl esters or free acid forms. We’ve managed parallel pilot runs at customer sites highlighting how methyl ester hydrochloride simplifies reaction setups. The salt dissolves predictably in polar aprotic solvents and maintains manageable pH during coupling steps. By contrast, using a tert-butyl ester requires additional deprotection steps, demanding harsher acid conditions—sometimes pushing other sensitive functionalities beyond tolerance.

    We’ve tracked how these choices impact total process cost and waste generation. Using the hydrochloride salt in place of the free base cuts down neutralization steps, resulting in fewer aqueous washes and less solvent carryover. On top of that, many downstream reactions need precise stoichiometry. Deviations in salt content skew yields and cost extra time diagnosing failed syntheses. We support labs by supplying detailed certificates of analysis covering not just purity, but exact chloride content and residual solvent levels.

    Our technical support sees the downstream impact of switching between analogs. One customer’s move from a methyl ester hydrochloride to an ethyl ester compelled changes to solvent handling and purification, extending overall lead times by days. The methyl ester hydrochloride brought them back to a more reproducible, robust process, ultimately enabling earlier delivery of their API intermediate.

    Customer Feedback: Real-World Insights

    Over the years, our partnerships taught us far more than textbooks about what makes this product valuable. Synthetic chemists appreciate handling a material that resists deliquescence under standard lab environments. Our product stirs smoothly into solution—even after months of storage—without forming clumps or insoluble residues. Customers in the pharmaceutical sector mention improved yield consistency and lower levels of colored side-products when using our hydrochloride compared to similar esters or salts.

    Academic labs look for compounds with reproducible reactivity. We collaborate with leading institutions, running round-robin syntheses to benchmark performance in actual research applications. When their feedback highlighted issues with an older, less pure lot—mainly prolonged reaction times and colored byproducts—we retrofitted aspects of our crystallization process. The result: shorter purification runs, faster intermediate turnover, and more reliable analytical profiles.

    Specialty CROs and scale-up facilities comment on our transparent supply chain. We offer batch histories and real-time tracking, working to reduce back-and-forth about source validation or changing salt forms. Chemists tell us the time saved with full documentation lets them focus on innovation rather than regulatory paperwork.

    Our customer support doesn’t end at shipment. We routinely handle technical queries—everything from pKa values under varied solvent conditions to tips on shelf-life extension in humid climates. These questions have driven us to publish technical bulletins and optimize our shipment conditions to regions with tropical climates, wrapping containers in moisture-barrier films for transit.

    Improvement through Collaboration and Product Stewardship

    We see product stewardship as a living practice. Every error or near-miss drives internal reviews or upstream changes—sometimes through direct dialogues with end-users, sometimes through independent audits. Our site operations encourage real-time feedback, and production planners meet weekly to review technical bulletins and quality incident reports.

    A few years ago, feedback about packaging integrity from overseas transit led us to overhaul our packaging system. Switching to dual-layer bags and vented drums cut moisture ingress incidents to nearly zero. We keep learning—sometimes through hard-won lessons—how supply chain reliability is as crucial as raw specification sheets.

    We also share lessons about regulatory shifts and emerging synthesis technologies. Our clients navigating new impurity guidelines turn to us for process consultation. We’ve supplied supporting documentation for regulatory filings in North America, Europe, and Asia, and made product traceability a key part of our batch release process.

    Supporting Sustainable Chemistry

    Reducing environmental impact is not just about following rules—it’s a responsibility our team takes seriously. We have cut overall solvent usage in final purification steps by re-circulating wash streams, cutting both chemical costs and waste shipments. Efforts to reuse, recycle, and recover solvents have enabled us to shrink our carbon footprint, and those benefits pass along the value chain.

    Energy-intensive steps have come under scrutiny, especially with volatile fuel and electricity markets. By modifying our crystallization cooling profiles and optimizing reactor loading, we minimize rework batches and avoid unnecessary energy spikes. We feed these improvements into new product launches, sharing knowledge with downstream partners who are also chasing sustainability targets.

    We also encourage our supply partners to meet higher standards for responsible sourcing, prioritizing vendors who provide documentation about raw material provenance and ecological impact. These moves may come at a higher up-front cost, but over time, they have lowered batch rejection rates and ensured more stable long-term costs as global supply dynamics shift.

    How We Address Supply Chain Challenges

    Fluctuating market conditions and logistics disruptions test every chemical producer. We’ve faced raw material shortages, port closures, and pandemic-era shipping delays that once would have paralyzed operations. Our response includes holding strategic safety stocks, pre-qualifying alternative suppliers, and investing in local warehousing near major customer hubs.

    Disruptions provided an unexpected benefit: new urgency to digitize our inventory and logistics tracking. We now operate with end-to-end transparency, giving buyers peace of mind about stock availability and shipment timing. Lean inventory management lets us buffer demand spikes without ballooning carrying costs.

    Direct conversations with logistics teams and customer materials managers have helped clarify expectations around lead times, packaging needs, and customs documentation. These exchanges led us to develop language-agnostic labeling, multi-format certificates of analysis, and shipment notifications available in multiple time zones.

    Industry Trends and the Path Ahead

    Our field evolves quickly. Application chemists push for new reactivity, improved salt forms, and tighter impurity controls. We stay in step by investing in staff training and keeping close relationships with technology providers. Adopting new analytical methods—like advanced LC/MS for trace impurity identification—has sped up both troubleshooting and lot release.

    Global regulations never stand still. Both pharmaceutical and specialty chemical customers ask for evidence behind our claims. Data transparency is critical: we publish not just assay ranges, but full chromatograms, impurity profiles, and material trace reports. Our quality records are available for audit, and we routinely participate in customer site visits, offering a view into both lab-scale and plant-scale operations behind every batch.

    There’s growing demand for greener chemistry—milder deprotection protocols, recyclable solvents, lower-waste workups. Our technical team studies new protecting group strategies and partners with research groups focused on reducing process hazards. We see Methyl Pyrrolidine-2-Carboxylate Hydrochloride fitting into these moves: as routes shift from classical chemical transformations to enzyme-catalyzed or solvent-minimized tactics, our molecule continues to add value.

    What Sets Factory-Direct Supply Apart?

    Our advantage rests in maintaining control over every process step, from raw material selection through to final packaging. We trace quality issues to root causes and implement changes without waiting on distant contract producers or trading houses. Our teams get hands-on—troubleshooting unexpected crystallization patterns, validating new analytical methods, and updating workflow documentation in parallel with batch processing.

    This factory-level integration enables short lead times and fast response to custom requests. If a customer specifies a unique particle size or tailored salt form, our site chemists design, trial, and scale the change without layers of middlemen. We’ve run pilot quantities to support everything from medicinal chemistry campaigns to kilogram-scale preclinical studies.

    The factory-direct connection also empowers better risk management. We keep duplicate process trains where possible, avoiding single points of failure. If a major piece of equipment requires downtime, alternate lines can maintain continuity, keeping project timelines intact.

    Our commitment extends past shipping out a drum or bottle. We field technical queries in real time—no deferrals, no ambiguous answers from sales staff without chemistry backgrounds. Whether providing supplementary documentation for regulatory submissions or troubleshooting a stalled synthesis, our team bridges the knowledge gap between production and application chemists.

    Listening and Innovating for the Future

    Product innovation thrives on candid feedback and sustained partnerships. Over the years, direct dialogue with bench chemists helped us refine our purification methods, packaging standards, and support resources. We continue to collaborate with customers advancing new routes, flexible manufacturing concepts, and green chemistry approaches.

    We recognize the complicated, demanding work behind every synthesis that touches our Methyl Pyrrolidine-2-Carboxylate Hydrochloride. Each batch leaving our facility represents dozens of choices, tests, and tradeoffs—all filtered through the lens of practical manufacturing and real-world use. Our approach may not fit a one-size-fits-all template, but it’s built on the lessons and relationships cultivated with experienced chemists around the world. We keep learning, keep improving, and keep listening—because in this industry, that’s how the next generation of innovations come to life.