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L-Prolinamide

    • Product Name L-Prolinamide
    • Alias prolinamide
    • Einecs 219-105-5
    • 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

    669426

    Chemical Name L-Prolinamide
    Molecular Formula C5H10N2O
    Molecular Weight 114.15 g/mol
    Cas Number 7531-52-4
    Appearance White to off-white solid
    Melting Point 117-121°C
    Solubility In Water Soluble
    Optical Rotation [α]D20 +65° (c=1, H2O)
    Boiling Point 399.8°C at 760 mmHg
    Density 1.122 g/cm³
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, in a tightly closed container

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

    Packing & Storage
    Packing L-Prolinamide, 25g, supplied in a sealed amber glass bottle with screw cap, clearly labeled with chemical name, CAS, and warnings.
    Shipping L-Prolinamide is shipped in tightly sealed containers to prevent contamination and moisture absorption. Packaging complies with chemical safety regulations and includes proper labeling for identification and hazard communication. During transit, the chemical is protected from extreme temperatures, physical damage, and incompatible substances, ensuring safe and secure delivery to the recipient.
    Storage L-Prolinamide should be stored in a cool, dry, and well-ventilated area, away from sources of heat and incompatible materials. Keep the container tightly closed and protect it from moisture and direct sunlight. Store at room temperature, around 20–25°C (68–77°F), and ensure proper labeling. Follow all relevant safety procedures for chemical storage to prevent contamination and degradation.
    Application of L-Prolinamide

    Applications of L-Prolinamide in Industrial Manufacturing

    L-Prolinamide serves as a specialized chiral building block and crystallization modifier in several precision-driven industrial domains. As a direct manufacturer, we supply L-Prolinamide to downstream partners who require strict adherence to compliance, accurate formulation integration, controlled processing environments, and consistent product quality.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use L-Prolinamide as a stereoselective intermediate to introduce chirality in the asymmetric synthesis of active pharmaceutical ingredients (APIs), particularly in peptide-based drugs and beta-lactam antibiotics. Its integration demands stringent purity checkpoints, as any variance may affect final drug efficacy and regulatory approval. The enantiopurity and chirality offered by the material are essential for producing single-isomer drugs where racemization must be minimized. Batch documentation requirements are rigorous, and traceability is maintained throughout the process chain.

    Industry compliance standards

    • USP (United States Pharmacopeia)
    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EDQM Guidelines for Pharmaceutical Excipients
    • ISO 9001:2015 Quality Management for pharmaceutical intermediates

    Typical usage ratio

    • 0.5–2.5 molar equivalents relative to target chiral core; adjusted based on sequence length or side-chain functionality

    Downstream process integration

    • Enters at the asymmetric synthesis or peptide coupling stage, following solvent deprotection operations and preceding chromatographic purification steps

    Final product types

    • Single-enantiomer APIs (e.g., chiral amines, proline-rich peptide drugs)
    • Beta-lactam antibiotics
    • Small molecule pharmaceutical intermediates

    2. Chiral Ligand Manufacturing for Asymmetric Catalysis

    In the fine chemicals sector, L-Prolinamide functions as a precursor for chiral ligands used in homogeneous and heterogeneous catalytic processes. These ligands facilitate the enantioselective synthesis of agrochemical actives and APIs. Compliance during production focuses on ligand purity, optical activity, and batch reproducibility, as downstream end-users demand tight control over catalyst performance. Documentation for metal traces and residual solvents must align with customer and regulatory audits.

    Industry compliance standards

    • REACH (EU Chemicals Regulation for intermediates and ligands)
    • ISO 17034:2016 for Reference Material Producers
    • OECD guidelines for catalyst testing

    Typical usage ratio

    • 10–25% of total ligand batch mass, or 1.2–1.8 stoichiometric equivalents in ligand functionalization reactions; adjusted for ligand backbone requirements

    Downstream process integration

    • Added at the ligand synthesis step, typically following base activation and prior to coordination with transition metals such as ruthenium, rhodium, or palladium

    Final product types

    • Chiral phosphine ligands
    • Asymmetric hydrogenation catalysts
    • Enantioselective cross-coupling reagents

    3. Peptide and Oligopeptide Synthesis

    Chemical peptide manufacturers adopt L-Prolinamide primarily as an N-terminal capping or chain-terminating agent during solid-phase peptide synthesis (SPPS). Its high purity and low residual moisture content are critical for preventing side reactions that compromise peptide chain integrity. Quality specifications focus on chiral purity, trace organic contaminants, and heavy metal content. Process controls emphasize every addition and cleavage step, particularly when synthesizing protected peptides for clinical trial material or diagnostic use.

    Industry compliance standards

    • GMP (Good Manufacturing Practice, EU Annex 21 for Peptides)
    • ICH Q3A/B Impurity Guidelines
    • FDA DMF (Drug Master File) for peptide intermediates
    • EP (European Pharmacopoeia) for Peptides

    Typical usage ratio

    • 1.0 equiv per N- or C-terminal residue for capping; lower if used as blocking agent in combinatorial libraries

    Downstream process integration

    • Introduced at the resin cleavage or chain elongation stage in automated or manual SPPS, immediately after deprotection and before final cyclization or purification

    Final product types

    • Synthetic peptides for research use
    • API-grade therapeutic peptides
    • Diagnostic peptide standards

    4. Optical Resolution of Racemic Amines

    Manufacturers in stereoselective chemicals production employ L-Prolinamide to induce selective crystallization of optically active amines, separating enantiomers for downstream synthesis. Purity and crystallographic consistency are central QC points, as the efficiency of enantiomer separation directly impacts yield and batch certification. Trace impurity control and optical rotation documentation are essential for customer audits and regulatory submissions.

    Industry compliance standards

    • ISO 9001 for Quality Management Systems
    • FDA 21 CFR Part 211 for manufacturing records and testing
    • Ph.Eur. (European Pharmacopoeia) for optical purity determination

    Typical usage ratio

    • 1.1–1.3 equivalents relative to racemic substrate, depending on target amine solubility and crystal growth parameters

    Downstream process integration

    • Utilized at the enantiomer resolution stage, following production of racemic base and solvent adjustment, and prior to centrifugation and mother liquor recycling

    Final product types

    • Enantiomerically pure amine intermediates
    • Chiral raw materials for further synthesis
    • API precursors for specialty pharmaceuticals

    5. Synthesis of Functionalized Cyclopropanes

    Organic synthesis groups utilize L-Prolinamide as a chiral auxiliary in the ring formation of functionalized cyclopropanes, especially in the agrochemical and fine chemical industries. This purpose hinges on maintaining strict lot-to-lot optical consistency and full adherence to documentation of all reactive intermediates, which are often subject to regulatory review when exported across borders. Storage and handling must restrict moisture uptake, with in-process monitoring during ring closure reactions and post-synthesis extractions to prevent degradation or racemization.

    Industry compliance standards

    • FAMI-QS (Feed Additive and Premixtures Quality System, for agrochemical raw materials)
    • REACH registration for reaction auxiliaries
    • ISO 14001 Environmental Management for synthesis waste

    Typical usage ratio

    • 5–20 mol% relative to starting diazo substrate; precise adjustment based on target enantiomeric excess and ring size

    Downstream process integration

    • Added during the cyclopropanation step following base-catalyzed activation, preceding acid or chromatographic work-up

    Final product types

    • Chiral cyclopropane carboxylic acids
    • Agrochemical actives (such as cyclopropane insecticides or herbicide intermediates)
    • Fine chemical intermediates for API construction
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    Certification & Compliance
    More Introduction

    L-Prolinamide: Our Approach to Precision Chemistry

    Bringing L-Prolinamide from Our Reactors to Your Lab

    Every batch of L-Prolinamide starts with raw materials we carefully source for clarity and purity. Starting raw L-proline, we shepherd every step in-house through controlled hydrating reactions, batch filtration, and drying. These steps remove the guesswork and let us maintain the reliable 99%+ purity specifications so many of our pharmaceutical and fine chemical clients ask for. L-Prolinamide, with its structure closely tied to the cyclized backbone of proline, brings a unique secondary amide group into play, setting it apart from simple amino acids and primary amides in your catalog.

    The Journey from L-Proline to L-Prolinamide

    Proline itself offers value as a chiral building block, but amide formation gives sharper, more controlled reactivity in synthetic schemes. Our controlled amidation process retains the L-stereocenter, backed up by polarimetry and HPLC analysis for every batch. L-Prolinamide appears as a crystalline, white to off-white solid. We do not waste time with unnecessary bulking agents or diluents that dilute your reaction outcomes or leave behind residue.

    Model, Appearance, and Consistency Across Batches

    We manufacture L-Prolinamide in multiple lot sizes, from pilot scale through industrial production. Our main model, LPRA-115, delivers a fine crystalline powder that dissolves rapidly in water and most polar organic solvents. Every batch is checked for particle size distribution and absence of agglomerates—important for high-throughput reactors and automated dispensers. Over the years, we found that consistent crystallinity translates to predictable solubility. That means less downtime adjusting your mixing protocols or cleaning clogged ports.

    Where L-Prolinamide Fits in Your Workflow

    Most clients turn to L-Prolinamide for chiral amide synthesis, peptide intermediates, and as a tool in asymmetric catalysis. Its secondary amide group takes part in hydrogen bonding, which influences protein folding studies, and allows it to act as a launching pad for further N-substituted proline derivatives. Bulk physical properties—melting point, hygroscopicity, and flow—are all measured and published with each lot. Because we run our own reactors and finishing, we can answer direct technical questions about polymorphism, impurities, or process adjustments for your unique applications.

    Technical Validation: From In-House Analytics to External Audits

    We do not rely solely on supplier guarantees or outsourced labs for verification. Instead, we use in-house HPLC, chiral chromatography, and FTIR. Our laboratory benches hold reference spectra for every finished batch, so we can trace even minor deviations if a customer ever notices a difference in color, solubility, or reactivity. Several global pharma clients regularly conduct walkthroughs of our plant and take their own QA samples right off the packaging line. That confidence does not appear overnight. Our staff invest hours resolving the routine pain points we remember from our days working in overcrowded university labs—filter clogging, inconsistent powdering, or off-odors—because our own synthetic chemists run R&D upstairs from production.

    L-Prolinamide Versus Competing Chiral Amides

    Manufacturing L-Prolinamide in-house means full control over the process. We’ve seen what happens when similar products come in from outside traders: unpleasant odors from residual solvents, variable solubility, nonstandard particle sizing, and even mixed stereochemistry sneaking in due to uncontrolled reaction conditions. With L-Prolinamide produced here, every specification starts at the reactor. Our pros monitor for off-ratio reactants, monitor batch color, and keep process logs on actual chemist benches.

    Compared to N-methylprolinamide or racemic forms cut with D-prolinamide, our product offers stereocontrol and batch reliability. Racemic blends confuse chiral catalysts and lead to unwanted byproducts, something anyone who spends months optimizing a new custom route will recognize instantly. L-Prolinamide maintains its L-configuration, with optical purity supported by in-house polarimetry and validated with customer feedback from multi-kilogram runs.

    Typical Usage Across Industries

    The most common use cases for our L-Prolinamide center on asymmetric catalysis and peptide research. Pharmaceutical teams often request L-Prolinamide for use in stepwise solid-phase or solution-phase peptide syntheses, where side reactions from racemization or impure solvents introduce risk cost far beyond a single kilogram of starting material. L-Prolinamide’s amide functionality matches with various activating agents, making it a key starting point for peptide coupling or further derivatization.

    In material science, research into membrane technologies and polymer doping has created new demand for chiral amides. We have scaled our batch process to keep up with requests for kilogram quantities for industrial partners who value consistent powder density and melting behavior, both of which affect their phase separation and membrane formation investigations. Our QA team documents every physical and spectral property, so process scale-up brings no surprises or headaches for in-house QC teams downstream.

    L-Prolinamide’s Role in Advanced Peptide Chemistry

    We have seen growing demand from synthetic peptide houses and academic teams focusing on complex sequence assembly. L-Prolinamide’s amide nitrogen can serve as a site for further protection, acylation, or cyclization, cleanly broadening the library of available unnatural amino acids without introducing extra functional group risk. By keeping enantiopurity high, our product reduces the risk of downstream misincorporation, which often ruins entire peptide fragments and costs weeks in lost research time.

    Our support does not end with shipping a box. We regularly advise industrial customers exploring new catalyst designs or ligands—our chemists answer questions about how moisture content, residual trace acids or bases, or packaging format might affect sensitive reactions. Over years of production, we have engineered packaging and handling protocols that keep L-Prolinamide dry, static-free, and ready for direct bench use.

    Experimentation and Customization—Feedback From the Field

    Researchers have sent us feedback on L-Prolinamide’s behavior in high-throughput screens, automated peptide assembly stations, and even pilot plant-scale hydrogenation. Armed with this data, our production line has tweaked drying conditions or added in-line sieving to remove the frustration of powder clumps that would otherwise cause weigh-scale errors. Some partners requested even finer mesh cuts or extra quality checks on moisture, which we now offer as tailored batch options. Our facility is flexible because each process step—reaction, filtration, drying, sieving—occurs onsite with hands-on technical oversight.

    Rather than relying on a one-size-fits-all approach, we track which lots suit automated dispensing, and which support slow manual addition in custom batch tanks. Our most experienced process chemists inspect every final lot alongside our analytics group before our packaging crew fills containers under nitrogen or dry atmosphere, eliminating the risk of moisture ingress.

    Keeping L-Prolinamide Stable Throughout Shipment and Storage

    From our end, we observed years ago that commercial amides like L-Prolinamide show best shelf life when kept dry and cool, away from acid and oxidizing agents. For this reason, we use double-sealed packaging that resists both atmospheric moisture and accidental acid vapor. Unlike some resellers, we include real-time humidity indicators in every large drum, so facilities staff can verify that the product stayed dry from the minute it left our final QA. Even long-distance shipments for export maintain this guarantee, with customer feedback confirming powder remains free-flowing and unchanged after months in storage.

    Why Direct Manufacturing Matters for L-Prolinamide

    Cutting out trading intermediaries gives us full view over our supply chain and traceability for each drum. We learned, often the hard way, that off-brand or non-OEM L-Prolinamide batches might bring in unintended impurities or stem from inconsistent crystallization techniques. For researchers running delicate chiral transformations, these variables spell disaster. We keep batch records down to gram-level batches—if an end-user in pharmaceuticals, agrochemicals, or polymer development ever finds a problem, we answer with batch-level transparency, not excuses.

    Environment, Health, and Workplace Safety

    As a manufacturer, we balance performance with safe handling and minimal environmental impact. L-Prolinamide’s relatively low toxicity and non-hazardous waste profile means effluent from our plant passes regular third-party scrutiny. Employees wear full PPE throughout reaction, isolation, and packaging, but L-Prolinamide does not pose the same acute risks associated with halogenated solvents or heavy-metal amides. By investing in closed reactor technologies, we keep fugitive emissions low, maintain an excellent accident record, and have yet to receive a citation for poor housekeeping or cross-contamination.

    Feedback from our plant floor shapes our processes. Machine operators signal suggestions for ease of cleaning, powder transfer, or maintenance, which means our safety programs suit both the needs of large-scale chemical handlers and university labs receiving small-scale vials for experimentation.

    Transparency From Factory Floor to End User

    With L-Prolinamide, specifications do not exist as empty claims or marketing copy; they are a daily reality in our plant, built from years of batch records and hands-on troubleshooting. If a fresh R&D customer requests milligram to kilogram scale, we can walk you through the full technical documentation—batch chromatograms, moisture specs, and reference spectra—so your chemistry team knows exactly what to expect before material even leaves our floor. Pharmaceutical and advanced materials teams have equipped us with new technical criteria—trace levels of sodium or chloride, for instance—that we measure and report long before product release.

    Our plant doors have welcomed audits from leading multinationals and boutique research firms, because our confidence comes from daily experience manufacturing in-house, not from paperwork handed down a distribution chain. Those experiences keep us sharp and responsive to every question about physical, chemical, or safety nuances tied to each lot.

    The True Difference: Hands-On Expertise

    L-Prolinamide is not a speculative item shipped through faceless trading desks. With in-house synthesis, batch-to-batch documentation, and a team of working chemists, we deliver reliability along with every container. Over two decades, the direct contact between our R&D, plant, packaging, and analytics teams has created a culture of accountability. If your research, scaleup, or manufacturing demands high-purity L-Prolinamide with full transparency, every drum, jar, or sample vial from our plant meets this expectation.

    No claim stands without backup. We welcome conversation, technical feedback, or custom requests—every experience makes the next batch, and your research results, sharper and cleaner. For those investing in chiral synthesis, advanced peptide chemistry, or specialty materials science, L-Prolinamide, validated by our team and refined over years of hands-on process improvement, makes a measurable difference, from reaction startup to finished product.