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L-Prolinamide Hydrochloride

    • Product Name L-Prolinamide Hydrochloride
    • Alias prolinamide-hcl
    • Einecs 629-573-9
    • 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

    358678

    Product Name L-Prolinamide Hydrochloride
    Cas Number 7512-59-6
    Molecular Formula C5H11ClN2O
    Molecular Weight 150.61 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 207-212 °C (dec.)
    Solubility In Water Soluble
    Optical Activity Chiral, L-enantiomer
    Purity Typically ≥98%
    Storage Conditions Store at room temperature in a tightly sealed container
    Synonyms L-Prolinamide monohydrochloride
    Ph In Water 4.0-5.0 (1% solution)
    Iupac Name (2S)-pyrrolidine-2-carboxamide hydrochloride
    Ec Number 231-399-6
    Boiling Point Decomposes before boiling

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

    Packing & Storage
    Packing L-Prolinamide Hydrochloride is packaged in a 25g amber glass bottle, sealed, labeled with product details, safety information, and batch number.
    Shipping L-Prolinamide Hydrochloride is shipped in tightly sealed, chemical-resistant containers to prevent moisture absorption and contamination. Packages are labeled with appropriate hazard information and handled per standard chemical safety regulations. Shipping is typically via ground or air, complying with local and international dangerous goods transportation guidelines to ensure secure delivery.
    Storage L-Prolinamide Hydrochloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep the chemical at room temperature and avoid exposure to incompatible substances such as strong oxidizers. Ensure the storage area is appropriately labeled and access is restricted to trained personnel.
    Application of L-Prolinamide Hydrochloride

    Applications of L-Prolinamide Hydrochloride in Industrial Manufacturing

    L-Prolinamide Hydrochloride is a chiral reagent utilized across key sectors in chemical synthesis, pharmaceutical intermediate production, peptide manufacturing, and specialty fine chemicals. As a direct manufacturer, we support advanced processing lines and downstream producers with consistent product quality and regulatory-driven supply chain integration.

    1. Chiral Building Block for Pharmaceutical API Synthesis

    Pharmaceutical manufacturers employ L-Prolinamide Hydrochloride as a vital chiral auxiliary when developing optically active APIs. Its function as a stereochemical controller is essential in asymmetric synthesis routes, allowing selective formation of single-enantiomer pharmaceutical intermediates. The hydrochloride form ensures improved solubility and simplified purification during reaction workup. Typical formulation integrates the raw material at the stereochemistry-defining step, followed by isolation and further derivatization. Consistent performance under strict GMP conditions is critical for downstream yield and regulatory acceptance.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP)
    • European Pharmacopoeia (EP) monographs for intermediates
    • USP General Chapter <823> as applicable

    Typical usage ratio

    • Employed at stoichiometric to slight excess (1.0–1.2 molar equivalents) based on the target intermediate
    • Adjustments depend on process yield optimization and downstream resolution efficiency

    Downstream process integration

    • Charged during the asymmetric induction or coupling step in pharmaceutical synthesis pathways
    • Used in solution-phase or solid-phase API intermediate manufacturing
    • Workup follows with selective extraction and crystallization

    Final product types

    • Chiral pharmaceutical intermediates
    • Single-enantiomer active pharmaceutical ingredients (e.g., beta-lactam antibiotics, antiviral agents)
    • Peptide-based APIs requiring optical purity

    2. Peptide Synthesis: Protecting Group Strategies

    Manufacturers of synthetic peptides and oligopeptides frequently select L-Prolinamide Hydrochloride for its role as a protected prolinamide unit. It participates in stepwise coupling protocols, where its ionic form minimizes racemization and improves solubility profiles in polar solvents. Integration typically occurs during automated synthesizer runs or batch solid-phase procedures, where sequence-specific incorporation maintains integrity. Final resin cleavage and global deprotection steps remove the amide group without impacting main-chain configuration, preserving high yield of desired bioactive peptide chains.

    Industry compliance standards

    • ICH Q11 for Drug Substances
    • US FDA Guidance for Industry: Peptide Drug Products
    • Current Good Manufacturing Practice (cGMP) guidelines (21 CFR Part 210/211)
    • European Pharmacopoeia monographs on synthetic peptides

    Typical usage ratio

    • Incorporated at one equivalent per chain position requiring protected proline
    • Loading levels based on solid-phase resin activity (commonly 0.3–0.7 mmol/g resin)

    Downstream process integration

    • Inserted during Fmoc/t-Boc based stepwise elongation of peptide chains
    • Participates in N-terminal or C-terminal modification steps
    • Removed during global deprotection and selective hydrolysis

    Final product types

    • Active pharmaceutical peptide ingredients
    • Diagnostic peptides
    • Research-grade synthetic oligopeptides
    • Peptide-based drug candidates in clinical development

    3. Fine Chemical Synthesis – Stereoselective Catalysis

    Producers of fine and specialty chemicals use L-Prolinamide Hydrochloride as a chiral ligand or catalyst component in enantioselective transformations. The product offers precise spatial control in catalytic hydrogenation, aldol reactions, and other stereochemistry-critical processes. Its hydrochloride form enhances reactivity in aqueous and biphasic systems. End users dose the material to achieve control over enantiomeric excess, impacting downstream product value. On-site QC confirms batch-wise performance, with direct integration at the catalytic generator or reaction charge stage.

    Industry compliance standards

    • ISO 9001:2015 for quality management in chemical manufacturing
    • REACH regulations for safe handling and processing of intermediates (EU)
    • Responsible Care® management systems for process chemicals

    Typical usage ratio

    • Used at low catalytic loadings (0.5–10 mol% as ligand or auxiliary)
    • Optimal rates determined by substrate:ligand/catalyst screening during process validation

    Downstream process integration

    • Introduced at the beginning of stereocontrolled synthesis steps
    • Dosed as aqueous or polar organic solution to main reactor
    • Recovered where possible after reaction workup

    Final product types

    • Chiral specialty chemicals
    • Synthetic flavors and fragrances
    • Agrochemical intermediates with stereochemical purity
    • Precursors for advanced materials

    4. Research and Development: Reference Standards and Analytical Use

    Chemical research centers and pharmaceutical analytical labs rely on L-Prolinamide Hydrochloride as a purity reference and molecular standard in chiral analysis. Its defined chemical configuration supports calibration of chromatography and spectroscopy equipment, as well as method validation for enantiomeric resolution. Labs purchase the compound in small- to mid-scale lots, performing routine QC checks prior to method development or lot-release analysis. Storage and documentation must meet laboratory GLP protocols, with traceability via Certificate of Analysis.

    Industry compliance standards

    • GLP (Good Laboratory Practice) as defined in OECD Principles
    • ISO/IEC 17025 for chemical and pharmaceutical testing labs
    • FDA and EMA guidelines on analytical method validation

    Typical usage ratio

    • Employed at assay-dependent concentrations (10–100 mg per calibration or test)
    • Adjusted based on instrument sensitivity, standard curve requirements, and detection limits

    Downstream process integration

    • Diluted to standard concentration in solvent
    • Dosed into HPLC, chiral GC, or NMR systems
    • Referenced in purity and identity confirmation of novel samples

    Final product types

    • Certified reference materials
    • Analytical standard solutions for regulatory submissions
    • Calibration blends for chiral separations
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    Certification & Compliance
    More Introduction

    Meeting Real-World Demands: L-Prolinamide Hydrochloride from a Manufacturer’s Viewpoint

    A Closer Look at L-Prolinamide Hydrochloride

    L-Prolinamide Hydrochloride often gets less attention than mainstream intermediates, but this chemical draws a loyal following in research and industry. Every batch leaving our plant carries a clear identity, built on specification, reliability, and a level of practical detail we never overlook. The molecular formula is C5H10ClNO, which describes the pairing of prolinamide with a stable hydrochloride salt. We manufacture this product as a white to off-white crystalline powder, a form most users recognize and trust. Quality tests always focus on purity and moisture, since even trace amounts of byproduct or humidity can unwind sensitive reactions. Our typical lots clock in at over 99% purity, moisture less than 0.5%, and controlled limits on heavy metals. Those numbers don’t exist for show; they keep projects moving forward in labs and factories alike.

    Our journey with L-Prolinamide Hydrochloride started with a goal: eliminate guesswork at the user’s end. Customers voiced frustration with inconsistent flow, sticky samples, or unpredictable spectral signatures. In direct response, we fine-tuned crystallization and drying at production scale, not in one big leap but through rounds of empirical checks, even at the cost of shorter batches. Each specification—particle size, solvent residue, color, odor—came from walking through actual customer feedback. The final result carries clean, sharp IR and ^1H NMR fingerprints. Whether a customer offers comments about chiral purity or physical handling, that feedback shapes the next lot off our line.

    Why Purity and Consistency Matter Beyond the Specs

    We see a broad range of users—academic labs running peptide synthesis, contract manufacturers assembling APIs, and process engineers validating new routes for fine chemical production. In every case, the product’s consistency either greases the wheels or throws a wrench in the work. Purity alone isn’t a trophy; it shortens workup steps, keeps columns from clogging, and makes yields reproducible. A spot of contamination, even if legally within limits, can reduce chiral selectivity or drop isolated yields by a margin that ruins schedules. Our team never just reads batch data—we look for outliers, odd melts, or suspicious color changes that would raise a red flag in our own projects.

    Some users use L-Prolinamide Hydrochloride directly as a chiral building block; others convert it back to prolinamide ahead of downstream transformations. In both cases, our customers benefit when every shipment performs like the last. Peptide chemists care deeply because amide coupling steps expose impurities or salt loadings that dull catalysts. Medicinal chemists run tight timelines, and a failed batch cascades delays across whole teams. Each time we review production or discuss improvements with our R&D group, we focus on these points—because we’ve seen how a small improvement in lot consistency can free up time and cut waste for everyone.

    L-Prolinamide Hydrochloride’s Role in the Synthesis Toolbox

    The structure of L-Prolinamide Hydrochloride holds a special place in synthetic chemistry. The chiral center and the stable amide group invite enantioselective transformations and catalyst research. One key usage we see: development of proline-derived organocatalysts, which set stereo centers in new molecules. Some firms use these for asymmetric aldol or Mannich reactions, vital in the pharmaceutical sector. Others evaluate L-Prolinamide Hydrochloride as a salt form to balance stability and handling in high-throughput screens. We’ve supplied projects ranging from small academic screens to kilogram-scale lots for specialty pharma syntheses. Through all scales, users ask for clarity: lot-to-lot consistency, smooth solubility in water and polar organics, and absolute faith in both structure and chirality.

    Often, a comparison arises with other proline derivatives. L-proline itself, while bulk-available and inexpensive, does not deliver the amide functionality needed for certain coupling chemistries. The methyl ester and benzyl ester analogues present other options but add volatility and risk of byproduct formation. The hydrochloride salt of L-Prolinamide brings specificity: the form is less hygroscopic than free prolinamide and generates predictable pH values in aqueous solution, a benefit for processes sensitive to acid/base balance. It is worth sharing that some users still opt for the free amide if they want direct access to the amine, but feedback points to the hydrochloride as easier to weigh, store, and handle, especially in modern automated labs.

    Key Differences: Standing Apart from the Crowd

    Direct experience teaches that L-Prolinamide Hydrochloride rarely substitutes one-to-one with its analogues. Everything depends on the physicochemical profile, not just the name on the package. The hydrochloride salt flows freely and packs more tightly, making it well-suited for auto-feeding in pilot plants. That flowability can’t always be matched by waxy esters or hygroscopic free bases. In peptide research, many users have remarked that cleaner, crystalline L-Prolinamide Hydrochloride opens coupling strategies previously prone to side reactions. That means less peptide chain deletion or racemization during Fmoc or Boc routes. For industrial processes requiring downstream purification, our product’s controlled specifications make removal of residual chloride and trace metals more predictable—which shortens purification and boosts overall yield.

    There is a tendency in the market to treat amino acid derivatives as commodities, and we’ve sometimes had to work against the view that all lots are interchangeable. Supply chain interruptions or variations between manufacturers can show up during chromatography or crystallization. Our customers have handled situations with competing products where color, consistency, or reactivity fell outside their windows for success. When a project spends months in R&D and a subtle impurity derails the final synthesis step, the frustration travels back up the chain. Testing for compatibility with process solvents, buffer salts, and isolation routines takes more time when a compound starts with unknown variability. In our view as manufacturer, the less time spent “babysitting” a reagent, the faster a project advances.

    Sourcing Challenges and Reliability: Doing It Right

    As manufacturers, we’ve lived through swings in market availability. Raw material shortages, shipping delays, and regulatory changes never make the news for most chemical intermediates, but behind the scenes, they shift delivery dates and project budgets in the real world. Our sourcing team builds relationships upstream to ensure we don’t cut corners on core reagents—pyrrolidine sources, hydrochloric acid quality, drying agents—because the cost of a single substandard input multiplies through every downstream synthesis. We test batches of incoming raw materials, not just to check a box, but because production consistency grows from the ground up. Each run in our reactors comes from verified sources, run with fit-for-purpose equipment, and followed up with full traceability. This approach reduces risk for advanced users by locking in reproducibility.

    We see occasional trends where buyers chase lower prices, only to circle back when a shipment of non-conforming product stalls their workflow. The short-term savings rarely balance the cost of lost time, increased troubleshooting, or revalidating methods. In our experience, strong partnerships with technical and supply teams at client sites foster more progress than a revolving door of faceless transactions. Our R&D group works directly with scientists and engineers at the user end, even traveling to see new installations and monitor pilot runs. This approach surfaces issues faster and has changed our view of what “standard” really means—what might be fine in one context fails in another. Good feedback loops between producer and end user keep us focused on reliability, not just labels or paperwork.

    Supporting Safety and Environmental Considerations

    We keep a sharp eye on safety throughout production and shipping, partly from regulatory requirement but even more so from direct responsibility. Handling hydrochloride salts means controlling airborne dust, monitoring package uniformity, and shipping in containers designed to prevent moisture ingress. Outgassing of hydrochloric acid or off-odors, while rare in high-quality product, mark the difference between careful manufacture and rushed batches. Some shipments head into regulated pharmaceutical plants where batch documentation and audit trails aren’t negotiable. Every detail—label, batch record, spectral data—must tie back the sample to its origin. Our team runs regular safety drills and hazard reviews; this translates to shipments that meet best practice without surprising anyone down the line.

    On the environmental side, our processes prioritize closed systems, solvent recycling, and remediation of waste streams. We track everything from energy use to water consumption, because we know our impact stretches beyond plant walls. Returns, expired lots, and process runoffs are managed in compliance with regional rules and monitored for long-term impact. We’ve shifted to packaging designed for better recyclability and reduced secondary waste. Customers increasingly ask about these details, and open communication about material handling puts everyone in a position to minimize risk and cost. These steps require planning and investment, but they also grow trust between supplier and client—an asset in any field.

    Applications and Insights from the Factory Floor

    Direct contact with end users shapes our approach as much as any quality system. We’ve worked with early-stage pharmaceutical companies running dozens of analogues in parallel; their demand for small, reproducible, and easy-to-handle lots forced us to rethink how we pack, document, and ship. One project using L-Prolinamide Hydrochloride as a key coupling agent for non-natural peptide analogues saw improved yields by shifting from a generic commercial version to our lot—something we didn’t expect until post-reaction testing flagged less byproduct formation and cleaner HPLC traces. Other firms, especially those working on exploratory organocatalyst screens, look for rapid supply at intermediate scale. For them, minimizing backorders is as critical as purity. Because we work directly with these users, small manufacturing adjustments turn into bigger advances at the bench: tighter particle sizes, consistent moisture control, or tailored documentation packages.

    Our plant team regularly faces questions about alternative forms—free base, different salt forms, or custom particle sizes. Some projects benefit from custom batches, especially where unique solvents or downstream reactions are involved. We balance between standardization and customization, knowing that the best impact comes from matching product form to application, not just minimum commercial specs. In rare cases, we’ve helped customers switch forms mid-project, supplying both reference samples and process insights to speed validation. It’s one thing to make a chemical; it’s another to make it fit real-life need. Every delivery window we hit, every batch that passes client QC without a hitch, and every troubleshooting call we field shapes our view of how L-Prolinamide Hydrochloride moves from commodity to critical tool in innovative work.

    Building Trust Over Transaction: Real Experience Counts

    Plenty of companies can ship a product; building trust over several years tells a different story. We’ve kept client projects on track by catching a potential lot inconsistency before it left our plant, or by matching shipment formats to unique storage requirements. Feedback from long-term partners shapes our maintenance, documentation, and packaging—they know that a manufacturer’s job doesn’t stop at the factory door. We’ve adopted real-world suggestions, such as improved lot traceability and clearer analytical data, because our most demanding customers have shown us where old methods fell short.

    Training our staff to understand both the science and the context—the why behind the specs—remains central to how we improve. When we hear frustration about seemingly small defects or scope creep from a customer side, we take those as signals to investigate at the source. Solutions don’t always come from expensive new equipment; sometimes, a better drying stage, closer monitoring of environmental factors, or simple tweaks to documentation procedures deliver outsized results. Our control labs record every relevant test, not for auditing satisfaction, but so that both sides—producer and user—keep a clear line between what’s claimed and what’s delivered.

    Facing the Future: Market Trends and Customer Needs

    The landscape keeps changing. Global supply chains shift, new regulations tighten allowable impurity levels, and user requirements get more specific. We’ve witnessed a surge in demand from precision medicine and advanced peptide design, both fields putting pressure on intermediates to go beyond “commodity” status. L-Prolinamide Hydrochloride holds a unique spot: it crosses boundaries from basic research to applied manufacturing. Many of our users move faster than ever before, and our job is to ensure that the materials on their bench never slow them down. We’ve watched priorities change—ten years ago, cost carried more weight than documentation or traceability; now, process adaptability, compliance history, and sustainability weigh just as heavily.

    To stay ahead, we’ve tied our R&D cycle to actual customer use-cases, not just raw production metrics. Lab visits, method transfer workshops, and post-installation support give us a direct channel from finished product to future improvements. When a client faces a bottleneck due to incompatible salt forms or unexpected side-products, we look for adjustments that work for everyone, not just shortcuts to move more product. We believe the best improvements in chemical manufacturing come from details in process tracking, honest communication about limitations, and the willingness to learn in real time from user experience.

    Working Together—Better Chemicals, Better Outcomes

    Every kilogram of L-Prolinamide Hydrochloride we ship is the product of technical skill and persistent listening. By taking ownership as both manufacturer and problem-solver, we’ve developed a product line that meets the demands of fast-moving fields without sacrificing safety or reliability. We don’t claim to have all the answers, but our focus on direct feedback, robust in-plant analysis, and open collaboration helps us meet the standards users set—not just once, but over and over. The challenges change, and so do the solutions, yet the guiding principle stays the same: a commitment to making every delivery a step forward for chemists, engineers, and researchers who rely on our work.