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L-Serine Benzyl Ester Hydrochloride

    • Product Name L-Serine Benzyl Ester Hydrochloride
    • Alias Benzyl 2-amino-3-hydroxypropanoate hydrochloride
    • Einecs 252-168-8
    • 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
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    Specifications

    HS Code

    583251

    Product Name L-Serine Benzyl Ester Hydrochloride
    Synonyms Benzyl L-serinate hydrochloride
    Chemical Formula C10H14ClNO3
    Molecular Weight 231.68 g/mol
    Cas Number 21626-07-3
    Appearance White to off-white crystalline powder
    Solubility Soluble in water
    Purity Typically ≥ 98%
    Storage Temperature 2-8°C
    Melting Point 151-153°C
    Optical Rotation [α]20/D +16° (c=1, H2O)
    Stability Stable under recommended conditions
    Usage For research and laboratory use only

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

    Packing & Storage
    Packing The 25g L-Serine Benzyl Ester Hydrochloride comes in a sealed amber glass bottle with a white screw cap and detailed labeling.
    Shipping L-Serine Benzyl Ester Hydrochloride is shipped in tightly sealed containers to protect against moisture and air. It is typically packed under inert atmosphere and kept cool and dry during transit. Complies with chemical transportation regulations; handle with appropriate safety measures. Shipping documentation includes safety data and hazard information.
    Storage L-Serine Benzyl Ester Hydrochloride should be stored in a tightly sealed container, protected from moisture and light. Keep the storage area cool and dry, ideally at 2–8°C (refrigerator conditions). Avoid exposure to air and sources of ignition. Ensure the chemical is clearly labeled, and restrict access to trained personnel in compliance with safety regulations. Properly ventilate the storage area.
    Application of L-Serine Benzyl Ester Hydrochloride

    Applications of L-Serine Benzyl Ester Hydrochloride in Industrial Manufacturing

    L-Serine Benzyl Ester Hydrochloride plays a key role in multiple industrial sectors as a critical intermediate for specialty synthesis. As the direct producer, we support established fine chemical, pharmaceutical, and biochemical manufacturers. Our application guidance is based on real-world formulation data and process integration experience.

    1. Peptide Synthesis for Pharmaceutical Intermediates

    L-Serine Benzyl Ester Hydrochloride is widely used in solid-phase and solution-phase peptide synthesis, particularly within drug development pipelines for active pharmaceutical ingredients (APIs). As an N-protected serine derivative, it participates directly in stepwise elongation for both linear and cyclic peptides, allowing for precise sequence assembly. Stringent quality control is essential throughout coupling and deprotection steps, especially when synthesizing pharmaceutical peptides such as hormones, enzyme substrates, or clinical candidates. The material’s purity and reactivity profile support regulatory filings and downstream scaling requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia–National Formulary) monographs for peptide APIs
    • European Pharmacopoeia (Ph. Eur.) guidelines for peptide production
    • 21 CFR Part 211 US FDA cGMP for finished pharmaceuticals

    Typical usage ratio

    • 0.8–1.2 equivalents per step relative to other protected amino acid esters, adjusted for coupling efficiency and resin loading

    Downstream process integration

    • The raw material enters the initial coupling or elongation stage during peptide assembly, followed by sequential deprotection, cleavage, and purification steps; in both batch and automated synthesizers.

    Final product types

    • Pharmaceutical-grade peptides (e.g., oxytocin, vasopressin analogs, peptide API fragments)
    • Clinical development intermediates for peptide therapeutics
    • Research peptides for screening libraries or biomarker studies
    • Enzyme substrates and inhibitors requiring specific serine sequences

    2. Synthesis of Chiral Building Blocks for Fine Chemicals

    Many fine chemical producers use L-Serine Benzyl Ester Hydrochloride as a starting chiral reagent when preparing optically pure intermediates for agrochemicals, pharmaceutical precursors, and flavor compounds. The hydrochloride form delivers stability during storage and handling. Custom hydrolysis and amidation protocols convert the ester to corresponding acids or amides, allowing access to a range of specialty molecules while preserving the L-configuration through the production workflow. Process reliability and enantiopurity must be documented at all stages.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for fine chemical manufacturing
    • REACH Regulation (EC) No 1907/2006 for safe substance use in the EU
    • GMP for starting materials as applied to pharma or food-adjacent products
    • Certificate of Analysis (CoA) with optical purity (enantiomeric excess) verification

    Typical usage ratio

    • 1.0 equivalent as a chiral source, occasionally 1.05–1.10 equivalents to ensure complete conversion, depending on downstream process scale and selectivity

    Downstream process integration

    • Material is typically dissolved in polar solvents for controlled hydrolysis, transesterification, or amidation reactions, becoming a chiral core within multistep organic syntheses.

    Final product types

    • Chiral resolving agents
    • Optically active amines, acids, or alcohols for further synthesis
    • Flavoring agent precursors (e.g., as starting materials for L-serine-based aroma compounds)
    • Pharmaceutical fine chemical intermediates (custom contract manufacturing)

    3. Protected Amino Acid Source in Biotech Research Reagents

    Biotech reagent companies incorporate L-Serine Benzyl Ester Hydrochloride into the synthesis of modified peptides, non-natural amino acids, and enzyme substrates. The protected serine structure ensures selectivity in multistep reactions and minimizes side reactions when generating functionalized biomolecules, markers, and diagnostic substrates. Consistency in batch purity is necessary for R&D, QC validation kits, and large-scale reagent production. Approach to formulation and purification varies based on the bioreagent’s sensitivity and downstream application.

    Industry compliance standards

    • ISO 13485:2016 Quality Management for medical device and diagnostics reagents
    • OECD Principles of Good Laboratory Practice (GLP) for preclinical research chemicals
    • Analytical batch traceability and QA documentation
    • Documentation per customer-specific method validation requirements

    Typical usage ratio

    • 1.0 equivalent in the relevant synthetic reaction, with 5–10% excess for highly functionalized or low-yielding conjugate syntheses

    Downstream process integration

    • Applied as a protected amino acid during key organic transformations in fluorophore labeling, enzyme assay substrate design, or bioconjugate assembly workflows.

    Final product types

    • Modified peptide probes for diagnostics
    • Substrate kits for enzyme assays
    • Custom-labeled amino acids for biomarker studies
    • Precursor components for bioactive reagent kits

    4. API Intermediate in Custom Synthesis Projects

    Contract manufacturers rely on L-Serine Benzyl Ester Hydrochloride for production of protected serine intermediates specified in customer-documented API synthesis pathways. The material’s benzyl ester group enables selective removal under hydrogenolysis, providing precise unmasking of serine residues during the final stages of multi-step synthetic routes. Quality must be controlled for moisture, heavy metals, and optical rotation as these parameters directly impact the regulatory compliance of finished intermediates. Integration into established CDMO workflows reduces variability and supports reliable supply chains for client pharma projects.

    Industry compliance standards

    • EU GMP Part II: Basic Requirements for Active Substances Used as Starting Materials
    • ICH Q3A Impurities in New Drug Substances
    • Certificate of Suitability to the European Pharmacopoeia Monographs (CEP) when required by customers
    • Regulatory batch record retention as per customer’s region

    Typical usage ratio

    • Frequently used at 1.0–1.2 equivalents in protected fragment assembly, with adjustments made during route optimization based on chromatographic yield and purity

    Downstream process integration

    • Feeds directly into protected fragment coupling steps, prior to final deprotection and purification in API manufacturing; often incorporated into continuous flow systems for increased throughput.

    Final product types

    • Advanced protected amino acid intermediates for APIs
    • Peptide and pseudopeptide building blocks
    • Final API fragments awaiting global regulatory filing
    • Reference compounds for process validation
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    Certification & Compliance
    More Introduction

    L-Serine Benzyl Ester Hydrochloride: A Manufacturer’s Perspective

    What Sets L-Serine Benzyl Ester Hydrochloride Apart

    L-Serine Benzyl Ester Hydrochloride may sound like a mouthful, but for those of us in the chemical manufacturing world, the story behind it stays straightforward: this is a compound born out of careful engineering, a precise eye for purity, and a solid understanding of what chemists, formulation scientists, and pharmaceutical companies expect from their input materials. The backbone of this molecule is L-serine, a naturally occurring amino acid, functionalized as a benzyl ester and stabilized with HCl—details that matter as much in bench-scale synthesis as they do on the plant floor.

    In our facilities, product consistency is more than a promise—it’s a daily job. Every batch of L-Serine Benzyl Ester Hydrochloride undergoes scrutiny by trained chemists familiar with both organic synthesis and amino acid handling. Most people have little reason to think about the hurdles involved when producing such an ester salt: sensitive handling of starting materials, robust reaction monitoring, and a final purification step that leaves behind only the compound you need for the next transformation.

    User Experience: In the Lab and on the Production Line

    Researchers and production chemists rely on L-Serine Benzyl Ester Hydrochloride for its versatility. The benzyl ester form shields the carboxylic acid group and brings the molecule into a state amenable to peptide coupling and other synthetic transformations. This protection remains firm during the early, sometimes harsh, synthetic steps, then releases cleanly under hydrogenolysis—a method with broad historical support in peptide and pharmaceutical chemistry.

    Anyone who’s ever tried alternative esters knows the struggle that can arise from byproduct formation or removal difficulty. Ethyl or methyl esters have their place, but the benzyl group offers unique advantages: greater lability to hydrogenation and fewer problems with side reactions. From a process standpoint, the hydrochloride salt offers a straightforward solution to the moisture uptake and stability concerns that sometimes haunt free base forms. It has a crystalline structure that holds up during transport and storage, which makes a big difference in large-scale applications.

    Specifications and What They Mean for End Users

    Our standard offering for L-Serine Benzyl Ester Hydrochloride keeps things uncomplicated: chemical purity goes beyond 98 percent (HPLC), and we deliver a material with steady melting behavior and clear, reproducible NMR signatures. Moisture, a notorious problem in ester salts, is kept to a minimum, sometimes reaching below the detection of common Karl Fischer methods. In one sense, these numbers speak for themselves—yet for the seasoned chemist, the real value comes from the fact that you don’t spend time troubleshooting impurities or arguing with inconsistent yields. Every gram functions how you expect, whether in an automated peptide synthesizer or a custom batch reactor.

    The fine powder format offers an easy match to automated dispensing systems for process-scale synthesis and straightforward handling for manual additions. Flow characteristics, though often ignored in technical writeups, draw notice from anyone trying to minimize static, loss, or clumpy pours at the bench.

    Comparison to Other Products on the Market

    Many manufacturers carry a range of amino acid esters, but those of us who oversee the entire production process notice the subtleties that others miss. With L-Serine Benzyl Ester Hydrochloride, the benzyl protection brings a sweet spot between reactivity and selectivity—key for those making protected peptides or intermediates in complex active pharmaceutical ingredient (API) workflows. Our experience with other serine derivatives, like methyl or t-butyl esters, suggests these lack the same degree of removable protection. The benzyl group, upon hydrogenolysis, disappears cleanly without introducing troublesome byproducts. This efficiency saves time during later synthetic steps and can improve the overall yield of the target molecule.

    Quality assurance forms another dividing line. As primary manufacturers, we maintain direct oversight of all starting materials, solvents, and reaction conditions. Every deviation, no matter how small, means a chain reaction that can foul up large-scale runs or destroy the subtle balances required by high-end pharmaceutical customers. Many labs find that buying directly from the originator of the process rather than a distributor brings not only reliability but technical guidance for troubleshooting and process adaptation.

    Applications That Call for L-Serine Benzyl Ester Hydrochloride

    The most frequent users of our product tend to come from two camps: research and industrial peptide synthesis, and pharmaceutical intermediate preparation. During peptide assembly, the protected serine building block gets slotted into solid- or liquid-phase sequences, inserted with high coupling efficiency. The consistent reactivity and clean removal of the benzyl group enable scientists to push their processes to higher throughput and lower cost per experiment. The residual HCl salt enhances bench stability, an understated advantage that reveals itself when months pass between opening a shipment and its final use.

    Years of feedback show that smaller, less-experienced suppliers often miss the subtle interplay between purity, salt form, and synthetic reactivity. Some might tolerate trace contaminants that seem trivial by NMR but wreak havoc in a peptide cycle. We receive regular updates from partners reporting decreased workup times—fewer purification cycles, clearer product bands on TLC, and drop-in compatibility with modern cyclization or coupling protocols—all direct results of a manufacturer’s continuous process improvements.

    Manufacturing Considerations and What They Mean for You

    Making L-Serine Benzyl Ester Hydrochloride on a commercial scale means paying close attention to batch reproducibility. Temperature, pH, and mixing protocols have drifted to near-mythical status in some discussions, but on the production floor, these are hard realities. Our team logs each handoff and verifies isotopic purity against known standards, ringing alarms whenever a measured parameter veers off the proven route.

    In the early days, we struggled with batch inconsistency, swinging yields, and the occasional unwelcome side product. Monitoring gas flow during benzylation and limiting moisture uptake became crucial—losses here didn’t just increase cost, they created rework and wasted man-hours. Through repeated fine-tuning, we have reached a position where revalidation happens quickly, and unexpected stoppages rarely dent the weekly schedule.

    Solvent recovery and waste management aren’t mere afterthoughts. We have watched the regulations around chemical disposal tighten year by year, and internal controls were added before they became industry mandates. Closed-loop solvent systems, carefully monitored emissions, and a focus on yield efficiency impact the final price to the customer and allow us to minimize our footprint. Sustainable chemistry grows out of practices set during R&D and enforced in the production line, not via after-the-fact pledges.

    Pain Points Solved Through Experience

    Customers contact us with challenges ranging from “How can I avoid product degradation during storage?” to “What special handling reduces batch carryover or cross-contamination?” Through direct conversations, we guide new clients based on issues already faced and resolved in our own labs. For instance, we have learned to recommend vacuum-sealed, light-resistant containers and specific humidity controls—advice many users claim transforms their workflows from frustrating to seamless.

    Feedback underscored the importance of not just selling a chemical but supplying technical partnership. Case reports from biotech clients reveal how a poorly timed shipment of L-Serine Benzyl Ester Hydrochloride from an unfamiliar source sank their production line for weeks, while our in-depth documentation and post-shipment tracking prevented just such disasters. Many find the value in knowing that direct-from-source means traceability, accountability, and guidance that originates from those who know the process inside and out.

    Purity and Analytical Testing: Lessons From the Plant

    Every batch of L-Serine Benzyl Ester Hydrochloride leaves with detailed documentation—HPLC chromatograms, NMR spectra, and moisture analysis. We have learned through experience that published purity specs only go so far in solving clients’ real-world challenges. Often, slightly lower levels of specific impurities spell chaos depending on the downstream reaction. Because our technical staff tests across possible impurity spectra, and not just total purity, we are able to give clear, meaningful guarantees that real users can trust.

    Operational transparency serves as more than a marketing point. Frequent audits from partner companies laid the groundwork for putting batch data online, granting clients secure access to full analytical packages before shipments leave our site. We remember those times when a critical batch faced delay over ambiguous purity data—now, clients see the same test results that our QC supervisors do. This practical approach makes regulatory reviews and scale-up transitions markedly easier.

    Continuous Improvement and New Innovations

    The field never stands still. Requests for new salt forms, higher purities, or adjusted particle sizes reach us regularly. Having an in-house R&D team keeps response time short, allowing us to produce custom grades for researchers exploring serine modifications, small molecule libraries, or emerging modalities. We’ve rolled out tighter moisture specs at the urging of diagnostic kit manufacturers—their precision needs forced us to install more sensitive analytical equipment and to work directly with their teams until every concern was met.

    As manufacturing chemists, we measure each improvement by what it delivers to the next user. Every process change, whether it involves stricter raw material checks, altered packaging, or modified drying protocols, passes through repeated verification. This cycle of feedback and adjustment anchors our ability not just to keep up with market demands, but to guide them.

    Looking Forward: Meeting Tomorrow’s Challenges

    Changes in science often happen quietly, as researchers discover new biological activities, synthetic routes, or regulatory endpoints. L-Serine Benzyl Ester Hydrochloride remains in demand because its role is well-understood, yet open-ended enough to power future discoveries. Requests arrive for non-benzyl ester analogues, for odd isotope labeling, or for high-throughput screening campaigns. Each need pushes us to re-examine process control and logistics—further tuning batch sizes, documentation, and technical support so specific research goals remain achievable.

    We monitor shifts in global regulation and intellectual property, responding by tightening in-house compliance and updating documentation to match local requirements for various markets. No batch ships without an internal check against destinations, intended uses, and routing—from raw serine through to your door. Direct manufacturing means we hold responsibility for quality from synthesis to shipment, and we plan to keep it that way.

    Conclusion: Not Just a Commodity—A Collaboration

    L-Serine Benzyl Ester Hydrochloride may never become a household name outside advanced chemical manufacturing, but we see its value in every satisfied repeat order, each technical inquiry, and the growing list of complex molecules built downstream from our material. Those of us making it stay grounded by the realization that every granule matters: from raw serine to protected intermediates, through to your lab or plant, the details are what define the result.

    As primary manufacturers, we offer knowledge that doesn’t come from a catalog or a product sheet, but from watching production lines in action, solving real-world problems with engineers and scientists, and delivering solutions that last through both expected and unexpected challenges. In short: every shipment provides not just L-Serine Benzyl Ester Hydrochloride, but decades of applied experience—one batch at a time.